MANAGEMENT OF
UNCONTROLLED
HAZARDOUS
WASTE SITES
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NATIONAL CONFERENCE ON
MANAGEMENT OF
UNCONTROLLED
HAZARDOUS
WASTE SITES
OCTOBER 31 -NOVEMBER 2, 1983
WASHINGTON, D.C.
AFFILIATES:
• U.S. Environmental Protection Agency
• Hazardous Materials Control Research Institute
• U.S. Corps of Engineers
• U.S. Geological Survey
• American Society of Civil Engineers
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PREFACE
Under the Comprehensive Environmental Response, Compensation and Liability Act of
1980 (CERCLA or "Superfund"), a Trust Fund, administered by the U.S. Environmental
Protection Agency (EPA), was set up to help pay for cleaning up the hazardous waste sites
threatening the public health or the environment. EPA has inventoried almost 16,000 such
sites, however, to be eligible for cleanup under "Superfund", a site must be included in the
National Priorities List (NPL).
In October 1981, EPA published an interim priority list of 115 sites and in July 1982, ex-
panded the eligibility list adding 45 sites for a total of 160 sites. EPA published a list of 418
sites as a proposed rule in December 1982, including 153 of the 160 sites previously publish-
ed. Times Beach, Missouri, was proposed in March 1983, bringing the total proposed to 419.
After a period of public comment, EPA published the NPL as a final rule in August 1983.
At the same time, EPA proposed 133 new sites in its first NPL update.
The papers presented at the National Conference on Management of Uncontrolled Hazar-
dous Waste Sites update the significant technology and information necessary to identify
and evaluate uncontrolled hazardous waste sites and control and mitigate the consequences
from those sites on the National Priorities List. Because of its importance, this Proceedings
also includes a listing of the 406 sites on the NPL and the 133 sites in the proposed update.
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ACKNOWLEDGEMENT
The National Conference and Exhibition on Management of Uncontrolled Hazardous
Waste Sites was made possible through the involvement of many individuals and organiza-
tions. We would like to express our thanks and appreciation to all who assisted.
U.S. Environmental Protection Agency
Hazardous Materials Control Research Institute
U.S. Corps of Engineers
U.S. Geological Survey
American Society of Civil Engineers
The Program Committee is comprised of knowledgeable individuals cooperating to pro-
duce an effective and informative program. These individuals are:
Harold Bernard, Hazardous Materials Control Research Institute
Bill Hanson, U.S. Environmental Protection Agency
Steven Ragone, Ph.D., U.S. Geological Survey
Don Sanning, U.S. Environmental Protection Agency
George Schlossnagle, Ph.D., U.S. Corps of Engineers
Harold J. Snyder, Jr., U.S. Environmental Protection Agency
Jerry Steinberg, Ph.D., American Society of Civil Engineers
Anthony Tafuri, U.S. Environmental Protection Agency
The concentrated effort necessary to publish a Proceedings of this size and scope in the
time allotted is certainly 'above and beyond'. Our special thanks to Dr. Gary Bennett, Pro-
fessor of Biochemical Engineering, The University of Toledo, and Hal Bernard, HMCRI,
whose editing allowed for a more uniform Proceedings; to the typesetters and graphics team
who managed to meet the impossible deadlines set; and to the staff of HMCRI, in par-
ticular, Beverly Walcoff, Project Manager, for coordinating the many aspects and activities
of this Conference.
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CONTENTS
SUPERFUND MANAGEMENT
Directions in Hazardous Waste Cleanup: Choices
in Superf und Implementation 1
Sylvia K. Lowrance, Esq. & Elaine G. Stanley
Corps of Engineers Superf und Quality Management 5
George W. Schlossnagle, Ph.D. & Noel W. Urban
Superfund Responses to Threatened Drinking Water
Resources , 8
Marcia Fine Silcox & Verna J. Montgomery
Analysis of Mining Sites on The National
Priorities List 13
Brian L. Murphy, William W. Beck, Jr. &
Dennis F. Unites
Lessons Learned by the Corps of Engineers on Two
Superfund Remedial Projects 17
Brian V. Moran & Joseph R. Turner
Advances in Mapping Organic Contamination:
Alternative Solutions to a Complex Problem
Michael R. Noel, Richard C. Benson & Paul M. Beam
Ova Field Screening at a Hazardous Waste Site ,
Brian J. Jacot
A Semiquantitative Program for Rapid Screening of
the Elemental Components of Hazardous Waste Material..
David A. Leighty, Duane S. Chase & Danton
D. Nygaard
ERT's Air Monitoring Guides for Uncontrolled
Hazardous Waste Sites
Rodney D. Turpin
On-Site Air Monitoring Classification by Use of the
ERT Two-Stage Collection Tube
Rodney D. Turpin
Use of Detector Ratios for Contaminant Screening by
High-Pressure Liquid Chromatography
David H. Powell, Ph.D., Albert L. Shroads, John J.
Mousa, Ph.D. & Stuart A. Whitlock
.71
.76
...79
.82
.85
.86
SITE INVESTIGATION
Waterway Decontamination—Four Case Studies 21
John C. Henningson
Study of Subsurface Contamination with Geophysical
Monitoring Methods at Henderson, Nevada 28
Eric G. Walther, Ph.D., Douglas LaBrecque, Dennis
D. Weber, Ph.D., Roy B. Evans, Ph.D. &
J. Jeffrey Van Ee
Refined Strategies for Abandoned Site Discovery
and Assessment 37
Charles R. Fellows & James H. Sullivan, Ph.D.
Investigation of Soil and Water Contamination at
Western Processing, King County, Washington 43
Hussein Aldis, John Osborn & Frederick Wolf
SCREENING
Protocol for Identification of Reactivities of
Unknown Wastes 54
C.D. Wolbach, Ph.D.
Techniques for Identification and Neutralization of
Unknown Hazardous Materials 63
Charles E. Hina, Al B. Garlauskas & Timothy D. Carter
Geophysical Investigations of Abandoned Waste Sites
and Contaminated Industrial Areas in West Germany 68
Rainer H. Feld, Dr. Rer. Nat., Manfred Stammler, Dr.
Rer. Nat., Gerald A. Sandness, Ph.D. &
C. Scott Kimball
SAMPLING & MONITORING
Delineation of Underground Hydrocarbon Leaks by
Organic Vapor Detection
Mohsen Mehran, Ph.D., Michael J. Nimmons &
Edward B. Sirota
Real Time Monitoring of Low Level Air
Contaminants from Hazardous Waste Sites
Michael B. Amster, Nasrat Hijazi, Ph.D. &
Rosalind Chan
Determination of Airborne Volatile Nitrogen
Compounds Using Four Independent Techniques ....
Paul F. Clay & Thomas M. Spittler, Ph.D.
Field Measurement of PCB's in Soil and Sediment
Using a Portable Gas Chromatograph
Thomas M. Spittler, Ph.D.
.94
.98
.100
.105
GEOHYDROLOGY
Downhole Sensing Equipment for Hazardous Waste
Site Investigations
William M. Adams, Ph.D., Stephen W. Wheatcraft,
Ph.D. & John W. Hess, Ph.D.
Groundwater Systems and Hazardous Waste Sites—
A Basic Conceptual Framework ,
Boyd N. Possin
.108
.114
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Improved Methods of Flow System Characterization ...
Joseph L. Devary, Ph.D.
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Health and Safety Considerations: Superfund
Hazardous Waste Sites 285
Kathleen S. Roos & Patricia A. Scofield
Dual-Purpose FTIR: Qualitative Analytical Screening
Tool and Quantitative Site Monitor 291
Kurt W. Eastman
Off-Site Assessment of Air Emissions from Hazardous
Waste Disposal Facilities 293
Charles E. Schmidt, Ph.D. & M. W. Eltgroth, Ph.D.
REMEDIAL RESPONSE
Clean-Up of Shope's Landfill, Girard, Pa 296
Robert D. Mutch, Jr., James Daigler & James
H. Clarke, Ph.D.
Approach Towards Establishing Interim Hazardous
Waste Cleanup Criteria 301
Richard A. Dime, Ph.D., Marwan M. Sadat, Ph.D.
& Jorge Berkowitz, Ph.D.
Training Resources for Superfund 304
Benjamin Taylor, Ph.D., George W. Schlossnagle,
Ph.D. & Noel Urban
Site Security and Waste Removal Activities at an
Abandoned Hazardous Waste Site 310
Michael A. Barbara, Thomas J. Morahan &
Robert W. Teets
Status of REM/FTT EPA Contracts 313
Paul F. Nadeau, William T. Dehn & Paul Goldstein
Expeditious Completion: A Forgotten Goal 320
James C. Scott & Robert B. Pearce
Hazardous Wastes Worker Health and Safety
Guidelines 322
Lynn P. Wallace, Ph.D. & William F. Martin
Navy Management of Abandoned Hazardous Waste Sites 326
Lt. (jg) Lily-Ann Openshaw, CEC, USN, Elizabeth
B. Luecker & Cdr. John P. Collins, Ph.D., CEC, USN
Price Landfill: Interim and Long-Term Remedial
Actions : 358
James R. Wallace, Salvatore Badalamenti &
Robert N. Ogg
COST
The Application of Computer Models to the Evaluation
of Hazardous Waste Management Options for
Uncontrolled Hazardous Waste Sites 362
Rosalie T. Matthews
The Impact of Limited Competition on Removal
Project Cost Budgets 366
Gregory A. Vanderlaan
Remedial Action Management and Cost Analysis 370
James D. Werner, Edward J. Yang, Ph.D. & Eric Nagle
Costs of Remedial Actions at Uncontrolled Hazardous
Waste Sites—Impacts of Worker Health and Safety
Considerations 376
James J. Walsh, John M. Lippitt & M. Scott
PUBLIC PARTICIPATION
Public Awareness Programs 383
George M. Fell
Institutional Challenges of the Superfund
Community Relations Program 386
Anthony M. Diecidue, Daphne Gemmill & Edwin Berk
How Onsite Assessments Can Help Achieve
Successful Site Cleanup 389
Nancy R. Tuor & Nancy J. Jerrick
Why Government and Industry Have Failed at Public
Participation Programs at Superfund Sites 392
Lois Marie Gibbs
CASE HISTORIES
Coal Tar Containment & Cleanup, Plattsburg,
New York 331
Stewart N. Thompson, Anthony S. Burgess, Ph.D. &
Dennis O'Dea
Emergency Removal Action at the Bankrupt Crystal
Chemical Plant, Houston, Texas 338
E. Wallace Cooper
The Case History of the BT-Kemi Dumpsite 342
Peter Solyom
Investigation of Subsurface Discharge from a Metal
Finishing Industry 346
George W. Lee, Jr., Richard D. Jones, G. David
Knowles & Scott J. Adamowski
A Dual Purpose Cleanup at a Superfund Site 352
William R. Adams, Jr. & James S. Atwell
Remedial Activities at the Miami Drum Site, Florida 354
Vernon B. Myers, Ph.D.
RISK/DECISION ANALYSIS
The Role of Removal Actions at Uncontrolled
Hazardous Waste Sites: Case Studies 395
Joanne Wyman, Ph.D., Jann Buller, Cheryl Hawkins
& Steve Heare
Risks, Costs and Public Policy: Determining
Acceptable Cleanup Levels 398
J. O'Neill Collins, J.D. & Philip C. LeClare, Ph.D.
Comparative Risk Assessment: A Tool for Remedial
Action Planning 40!
Joseph V. Rodricks, Ph.D.
Risk Acceptability for Handling, Analysis and
Disposal of Dioxin in a Laboratory 405
Chia Shun Shih, Ph.D.
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STATE PROGRAMS
Management Plan for Hazardous Waste Site
Cleanups In New Jersey
Mar-wan M. Sadat, Ph.D., Michele Ma tea &
Anthony Farro
The Development of the Massachusetts Contingency
Plan for the State Superfund
Yee Cho
State of Texas Superfund Program and Review of
Two Specific Sites
James W. Tremblay & J. Chris Lippe
The States and EPA: An Evolving Partnership
Under Superfund
Jan Wine & Heather Burns
LEGAL LIABILITY
Minimizing Liability Exposure When Contracting
Hazardous Waste Services
John C. Robbins
Legal Mechanisms for Defining Appropriate Extent
of Remedial Action
Randy M. Molt, ESQ.
Liabilities at Common Law for Groundwater
Contamination
Edward I. Selig, Esq.
.413
.420
.423
.428
.431
.433
.437
Compensating the Third Party for a Superfund
Cleanup Failure
Julie C. Becker & David Van Slyke
.442
POST-CLOSURE
Indicator Methods for Post-Closure Monitoring
of Ground Waters 446
Ihor Lysyj
Post-Closure Monitoring Research Needs for
Hazardous Waste Disposal Sites 449
John D. Koutsandreas, Peter J. Mavraganis
& William A. Bailey, Ph.D.
Failure Predictions for the Post-Closure Liability
Trust Fund Analysis 453
Gaynor W. Dawson, C. Joe English & Peter Guerrero
Superfund and RCRA Closure/Post-Closure:
An Illinois Perspective 459
Robert G. Kuykendall
EXHIBITOR LIST 461
NATIONAL PRIORITIES LIST AND
UPDATE/AUGUST 1983 467
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DIRECTIONS IN HAZARDOUS WASTE CLEANUP:
CHOICES IN SUPERFUND IMPLEMENTATION
SYLVIA K. LOWRANCE, ESQ.
ELAINE G. STANLEY
U.S. Environmental Protection Agency
Office of Emergency and Remedial Response
Washington, D.C.
INTRODUCTION
The enactment of the Comprehensive Environmental Response,
Compensation, and Liability Act of 1980 (CERCLA)', was hailed
as the beginning of a new era in environmental law: a bold, new
non-regulatory program. Unlike its major predecessors (Clean
Water, Clean Air or Resource Conservation and Recovery Acts),
it does not establish general standards of behavior for the regu-
lated community. Rather, it creates a program to comprehensive-
ly address past, present and future releases of a broad range of
toxic materials. More specifically, CERCLA grants discretion and
authority to undertake either response or enforcement actions to
achieve cleanup of any release of a hazardous substance into the
environment.2
There is a tendency by many who are affected by its provisions
to interpret CERCLA narrowly. According to this perception,
CERCLA is a statute designed to achieve cleanup of existing un-
controlled waste sites, either through direct Federal funding or
through enforcement efforts. The scope of the program established
under the Act is far broader, however.
Since the definition of release is so broad5 and the number of
covered substances so large,4 the Act actually authorizes action
following almost any incident at which chemicals are present or
emitted. The statute even allows response, in some circumstances,
where there is a permit under other environmental laws or where
a chemical is already regulated under other laws.5 Congress' intent
was to provide a mechanism to respond to problems posed by past,
unregulated, inadequate waste disposal, as well as to provide a
"safety net" which would allow response to incidents that would
not, or could not, be responded to in any other fashion. The
Congress, through this grant of authority, sought to anticipate the
unanticipated. Yet, the cost of having this broad authority is the
flexibility needed to make decisions on program priorities that
allow sound program management while maintaining capability to
respond to ever-increasing needs.
The breadth of the program, along with the vast administra-
tive discretion, is the single greatest challenge to those agencies
charged with implementing the program. Given finite resources,
the USEPA as the lead Federal agency for Superfund has had to
make fundamental choices in how to implement the law.
This is not the only challenge to program management, how-
ever. In addition to the response and enforcement authorities,
Congress enacted other, far-reaching provisions:
(1) Section 104 (i) requires the establishment of an Agency for
Toxic Substances and Disease Registry. Among the responsi-
bilities of this Agency are: (1) establishment of a registry of per-
sons exposed to toxic substances, and (2) providing medical care
and testing in the case of public health emergencies (including
chromosomal testing and epidemiological studies and perform-
ing research to determine the relationship between exposure to
toxic substances and illness).6
(2) Section lll(b) of CERCLA allows the Fund to be used for
payment of claims for injury to or destruction or loss of na-
tural resources resulting from a release or threat of release of a
hazardous substance. Section 107 of the Act imposes liability for
loss of natural resources up to $50,000,000.'
In this paper, however, the authors focus only on the decisions
required to develop an effective response program.
CHOICES AT THE OUTSET
The Agency's first option was to set the basic direction for the
statute's implementation, decision-making made more complex by
the sweep of the legislation and the lack of institutional prece-
dent. Of necessity then, these first-round decisions came down to
choices between broad directions and themes. These choices were
quickly made and were based on general policy considerations and
political philosophy rather than on any analytic framework or prec-
edent.
HUSBANDING THE TRUST FUND
Many of the most significant decisions involved the use of mon-
ies in the Hazardous Substances Response Trust Fund, the so-
called $1.6 billion Superfund [funded by taxes on the manufacture
or import of specified petroleum and chemical feedstocks (87%)
and by appropriated general revenues (13%)]. Out of these op-
tions, the theme of conserving or husbanding Fund monies
emerged. One major decision was to utilize the enforcement and
response authorities sequentially rather than concurrently, the "en-
forcement first, clean up later" mode. Thus, under the aegis of
Agency enforcement officials, a phased and lengthy system of for-
mal notification, communication and negotiation with the broadest
range of parties responsible for a problem that could be identified
was developed and implemented.8
The information on responsible parties was not readily avail-
able; many site owners or operators did not keep records of who
brought wastes to the site; it required a search to identify gen-
erators of such wastes. Such information needed to be complete-
ly verified prior to any but the most initial notice, a task of great
complexity at sites with multiple responsible parties. Thus, for
each site, a substantial amount of time was absorbed by these
SUPERFUND MANAGEMENT
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activities prior to any decision to "release" it for Fund-financed
study or other actions. The exception to this approach occurred
when an emergency situation arose necessitating the use of the re-
moval authorities.
A second decision was to limit funds for activities other than
enforcement or actual site work. Taking this approach would con-
strain, or eliminate altogether, important "support" or capability
building activities such as health and safety training for State and
local personnel, equipment purchases, laboratory analytic services,
general technical assistance, State and Regional contingency plan-
ning programs and other similar activities.
A third decision was to narrowly restrict, through regulation,
policy and operations the use of "removal" actions. These actions
are unilateral Federal responses to an "emergency" resulting from
a release of hazardous substances. A policy and operational direc-
tion was imposed to limit such actions to actual or ongoing emer-
gencies rather than include potential or likely emergencies. This
approach spawned allegations that a "body count" was required
in order to elect Superfund emergency response. It also produced
instances where more funds were being spent during an "actual"
emergency than would have been required for a preventative "po-
tential" action. Similarly, the National Contingency Plan (NCP),
the major program regulation, established a two level hierarchy of
removals; in addition to the "immediate" or emergency removals,
it created a new "planned removal" concept for actions at sites
not on the National Priorities List which required expedited but
not immediate attention.' This category allowed an opportunity for
more extensive planning, for competitive procurements and for a
10% State cost-share, all of which could reduce the amount of
Fund monies required.
Finally, another decision further emphasized the desire to max-
imize least cost options combined with environmental and public
health considerations in developing cost-effective solutions; that
was the decision to adopt an iterative, open ended process of
analysis and evaluation of alternative long-term remedies. This
process, as outlined in the NCP10, is not tied to environmental
standards, previous solutions or precedents but requires a discrete
site-by-site analysis for each remedy. The assumption was that
sites present unique physical environmental problems that seldom
resemble each other and, hence, that information and analysis are
not easily transferable or general standards applicable or easily
extrapolated. A remedy was to be tailored to each site. Although
the process might be lengthy, funds would be spent with a greater
certainty of success at that site.
RESULTANT POLICY DIRECTIONS
The direction of the program was established to conserve Fund
monies and to limit the universe of potential sites. Development
of policy positions and program guidance for several important
areas followed. Alone, these areas do not limit or set a particular
direction, but in each case, presented with options, the selection
of policy was consistent with Fund conservation. Important policy
in the areas of Federal facilities, mining wastes and radioactive
sites serves to illustrate how the goal of conserving Fund monies
was met.
Congress, in CERCLA, clearly tried to address the fact that in-
active hazardous waste sites could and do exist on Federal facil-
ities. It precluded use of Trust Fund monies for remedial action at
such sites." The approach initially selected was to extend the spirit
of the exclusion to all Superfund type activities and leave such ac-
tions to the affected Federal agency. Only in the ambiguous case
of a release, possibly but not definitely related to a Federal facility,
was listing on the National Priorities List (NPL) allowed; no other
response was taken. USEPA's responsibility in the Federal facil-
ities area was limited to providing the advice and technical support
to other agencies as needed to develop their own cleanup programs.
During that time, no funds were spent for any type of response at a
Federal facility; subsequently, the Agency has indicated its intent to
list on the NPL all Federal facilities that qualify under the same
system as non-Federal sites. ^cor-i A
Radioactive releases also received some attention in CEKCLA;
specific exemptions from CERCLA response authority are given to
sites subject to the financial protection requirements of the Atomic
Energy Act or to 25 sites designated under the Uranium Mill Tail-
ings Radiation Control Act.12 This exemption was by policy ex-
tended to cover sites with current licenses from the Nuclear Regu-
latory Commission (although the licensee is not subject to financial
protection requirements)."
Mining sites present a more complicated issue of jurisdiction
under CERCLA. CERCLA includes certain mining wastes in its
definition of hazardous substances; however, the list of RCRA
wastes incorporated by reference in CERCLA excludes mining
wastes." Some argue that this precludes inclusion of mining wastes
in the CERCLA definition of hazardous substances. Arguments
can be made that some constituents of mining wastes were in-
cluded under other definitions of "hazardous substances" or as
"pollutants and contaminants." The interpretation of the applic-
ability of the RCRA exclusion or of the applicable definition
affects the Agency's ability to enforce and recover costs from par-
ties responsible for the release. An approach was selected that
emphasized the pursuit of all possible enforcement options. How-
ever, actual Fund response to such sites was not approved until
it became apparent that enforcement options failed.
The impact of the decisions on mining, radioactive and Federal
sites was to shift the burden of response to other sectors of govern-
ment in lieu of the Superfund. But these other programs and agen-
cies were not originally charged with the goals of Superfund and,
therefore, were not mobilized to meet the public demands for
cleanup.
Program management decisions also implemented these de-
cisions. The National Priorities List (NPL) is mandated by Sec-
tion 105 of CERCLA as a list of at least 400 of the highest priority
facilities among known response targets." Gross estimates of the
average cost of a remedial project ($6.5 million) and of the amount
of Fund monies available for remedial action ($1.1 billion) lead
USEPA to conclude that, at the most, the Fund could be stretched
to cover 170 sites. Two decisions were driven by this analysis:
(1) limit the NPL to as close to 400 sites as possible and (2) do not
start any type of work at sites that cannot be completely funded
based on projected available funding. The practical effect of these
decisions was to artificially limit the universe of sites for States
and USEPA to use as public response targets. This approach linked
the decision on whether a release merited Superfund action to the
availability of funds. It also reduced the generalized impact of
the program, setting up competition for scarce dollars which fav-
ored States with readily available funds for cost-sharing.
Finally, a management choice affected the speed of response.
The decision to manage the program centrally from USEPA Head-
quarters deviated from past Agency practice of delegation of auth-
ority to the ten Regional Offices. This direction was taken osten-
sibly to ensure consistent policy implementation, set selected prec-
edents, facilitate monitoring and control expenditures. Central-
ized management, however, was criticized for causing delay in
approval of Superfund projects.
RESPONSE VERSUS PROBLEM IDENTIFICATION
The second theme that emerged from the program direction can
be characterized as short-term versus long-term goals, response
versus research or the definition of the problem. The decisions
made again can be characterized as limiting or short-term. One im-
portant choice was not to allocate funds for broad rather than
site-specific health activities on the causation of health problems
by types of hazardous substances or other occurrence in classes of
situations. Funds for activities such as development or expansion
of lexicological data bases were not forthcoming. The decision
not to fund expanded data bases stemmed also from a second
choice: that of delineating a limited universe of problems.
SUPERFUND MANAGEMENT
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National estimates of potential Superfund sites varied widely
during the debate leading to passage of the law; the moist wide-
ly cited number was 30-50,000. However, given the uncertainty of
the real universe, a provision for a one-time notification was in-
cluded in the statute. This resulted in notification of about 7,000
sites which when combined with other existing inventories re-
sulted in a 1982 estimate of 11,000 sites. An assessment of what was
actually present at all these sites would clearly stretch the Fund; on
the assumption that the "worst" sites had been discovered and
were in the inventory, it was decided to focus efforts on working
through but not adding to the inventory. (Since then, sites have
continued to be added for a current total in excess of 16,000. With
additional funds earmarked for State use in FY 83 and FY 84 for
just this purpose, it is estimated that the inventory may climb to
as much as 22,000-27,000 sites.)
FUTURE CHOICES
The pressure for priority setting choices in the Superfund pro-
gram is likely to become even more acute in the years to come. Sev-
eral major issues which will impact the use of finite resources are
beginning to emerge.
Foremost of these new issues is victim compensation. There has
been interest in providing third party compensation for damages
caused by hazardous substance releases for several years. The issue
has become one of some importance since a CERCLA-mandated
task force of attorneys representing several major legal associa-
tions published a report supporting an administrative compensa-
tion system for victims of toxic torts.''
There have been at least six bills introduced in Congress on this
topic to date. Many of these bills provide not only for compensa-
tion of personal injury, but also for property damage and other
economic loss. Many of the bills establish a separate fund for use
in compensating victims. Others, however, allow use of Fund
monies from the Superfund itself.
The impact of such a scheme on the Superfund program could be
massive. Under these circumstances, USEPA would be required to
make tradeoffs between cleanup and containment (the objective
of which is to prevent harm to third parties) and compensating
victims for damages that already occurred. This fundamental
choice, together with the concomitant increased workload, could
further constrain a cleanup program. USEPA decisions on when
and where to respond could be linked to third party compensa-
tion as well.
If the agency decides that a release merits Fund-financed re-
sponse, it may act as a catalyst for the bringing of third party
claims for alleged damages resulting from the release. Conversely,
if claims are brought for damages resulting from a release to which
the Fund is not prepared to respond, the claim could lead to in-
creased pressure to respond. In either case, a victim compensa-
tion program would add to the difficult fund management choices
already confronting government.
Another major issue that has a fundamental impact on how
Superfund will be managed in the future is the contamination of
the nation's groundwater. Of the 546 sites listed on USEPA's Na-
tional Priorities List (NPL) 75% have groundwater problems. The
Agency recently formed another Groundwater Task Force to iden-
tify options for dealing with this problem. Releases resulting in
groundwater contamination can come from many sources, some of
which are covered by CERCLA. How the Agency addresses this
problem will have a profound impact on the Superfund program.
If other means are effectively mobilized to prevent future
groundwater contamination as well as some current contamina-
tion, it could substantially reduce the drain on Superfund re-
sources. If not, the Superfund will have to balance these very
costly groundwater cleanup needs against other demands.
Finally, the major institutional issue confronting the Superfund
is State capability to manage cleanup programs. The States' ad-
ministrative, technical and financial capability to handle cleanup is
crucial. USEPA looks to the States to handle many incidents
without Fund-financing. Even when a release merits Federal fi-
nancing, States are encouraged to take the lead in responding. At
a minimum, CERCLA requires a State contribution of 10% of the
remedial action costs.
CERCLA provides no funds to support State programs; any
funds provided to a State for administrative expenses must be
linked to response at a particular site. This lack of program fund-
ing causes an acute problem in development of State programs.
Without strong State programs, it is doubtful that the Federal
Government will be able to hand over the Superfund program to
the States in the near future. In the financial area, an initial
USEPA study indicates that there could be as much as a $22
million short-fall in State revenues needed to meet the minimum
State match required by the Superfund statute.
A recent change in USEPA's cost sharing policy does not elim-
inate the problem, it merely defers it to a later phase of response.
USEPA has modified its policy regarding State cost-sharing on
remedial actions and now requires only the statutorily required
cost-share on remedial construction. Moreover, the Agency is
considering modifications to its policy on operations and main-
tenance to allow the Fund to pay for a greater share of these
costs. States must address this problem now to avoid future de-
lays in remedial response.
CONCLUSIONS
After several years of experience with the Superfund program, a
new direction is emerging at the USEPA. Rather than seeking to
conserve fund monies for exceptional incidents, USEPA has im-
plemented or is considering the implementation of several policy
changes that would result in full implementation of CERCLA's
response, enforcement and health-related authorities.
Expedited Cleanup
First, the USEPA no longer requires exhaustion of all enforce-
ment remedies prior to undertaking fund-financed cleanup. The
agency was severely criticized in many cases for allowing negotia-
tions with responsible parties to last many months without any
Fund-financed activity taking place. Under newly emerging pol-
icies, it appears that where there is a question of whether or not
responsible parties will clean up, the USEPA will proceed with a
remedial investigation and feasibility study while negotiations are
completed. After the studies are completed, the agency will select
the remedy it considers most appropriate. Responsible parties will
then have the option of implementing the remedy or the fund will
proceed with cleanup and bring a cost recovery action.
New management at USEPA has started to delegate more
authority to USEPA Regional Offices, an action which is expected
to expedite response. In May 1983, USEPA delegated authority
to Regional Offices to spend up to $250,000 for immediate re-
moval actions. Delegations of some components of the remedial
program are under consideration. Crucial to the success of this
delegation is appropriate program guidance by USEPA.
There was little such guidance during the first few years of the
program. Based on experience gained in the early years, however,
the Agency has made it known that it plans to issue guidance in
some of the most difficult program areas.
How Clean Is Clean?
The issue of "how clean is clean?" or how to determine the
appropriate extent of remedial action is one of the most difficult
issues confronting the Superfund program. Unlike other environ-
mental programs, Superfund response often involves many chemi-
cals affecting water, soils and air. In many cases, there are no en-
vironmental standards for the contaminants. Compounding this
problem is the fact that many of the remedies being pursued are
pushing .the state of the art of response technology. In order to
meet these challenges, the USEPA is developing guidelines for
undertaking a remedial action. As part of these guidelines, USEPA
is considering an approach that will utilize promulgated standards
SUPERFUND MANAGEMENT
-------
where they are appropriate. Where standards do not exist, USEPA
is exploring a risk analysis methodology.
New Sites Added
Many initiatives are underway which will fundamentally affect
the speed with which response is initiated as well as the number
of releases made eligible for fund-financed work. When promul-
gating the final NPL, the Agency also proposed 133 additional
sites for the list." It is likely that subsequent updates will signif-
icantly expand the number of sites on the list as states complete
their investigations of suspected problem sites.
In addition to opening up the potential for a NPL contain-
ing significantly more than 400 sites, USEPA has taken several
other steps that could contribute to an expanded number of Super-
fund needs. First, in the preamble to the final NPL, the Agency in-
dicated that it may be appropriate to list Federal facilities. This
would require an amendment to the National Contingency Plan.
Second, the agency has decided that sites containing mining waste
will be treated as any other sites for purposes of taking Fund-
financed response action. This means that enforcement efforts
need not always take precedence over the option of Fund-financ-
ing. Finally, the Agency has also indicated that it is considering
allowing listing of sites on an additional basis, when the site pre-
sents a serious public health threat through direct contact poten-
tial but does not score sufficiently high on the Hazard Ranking
System to be placed on the NPL under current policy.
Philosophical Change
Each of these proposals indicates a willingness on the part of
USEPA to separate decisions concerning the merit of a proposed
fund-financed action from the issue of whether funds are actual-
ly (or will be) available if action is deemed appropriate. This appar-
ent change in philosophy leads inevitably to the issue of whether the
agency will take the additional step of examining the response
thresholds it has established in the National Contingency Plan.
The tightly drawn criteria for eligibility for fund-financed removal
or remedial action have been criticized for not allowing enough
flexibility in the removal area to allow expeditious response to
immediate problems. It remains to be seen whether the Agency
will re-examine the criteria for taking emergency and nonemer-
gency removal actions, with the objective of allowing greater re-
sponse flexibility.
Finally, unlike previous policies designed to encourage State in-
volvement early in the response process through cost-sharing
requirements for planning activities, USEPA's recently announced
policies regarding State involvement appear to take account of the
need to foster State program development. Finally, the Agency is
also embarking on a program to assist States in managing their
fiscal resources for Superfund actions. All of these actions point
to a realization that, in order to deal with an increasing superfund
workload, the agency must not only adopt policies to encourage
State involvement, but also assist the states in developing their
capabilities to do so.
Most importantly, the realization is emerging that the prob-
lems Superfund was designed to resolve are every bit as complex
institutionally and environmentally as seen by the original drafters
of the statute. These problems do not lend themselves to con-
strained, short term solutions. As the problems continue to ma-
ture, it is likely that policies will continue to evolve in response
to these problems.
REFERENCES
Pub. L. 96-510, 94 stat. 2767 (1980), codified at 42 U.S.C. §9601
el. seq.
§I04(a) and §106, CERCLA.
CERCLA section 101(22) defines "release" as "any spilling, leak-
ing, pumping, pouring, emitting, emptying, discharging, injecting,
escaping, leaching, dumping, or disposing into the environment, but
excludes (A) any release which results in exposure to persons solely
within a workplace, with respect to a claim which such persons may
assert against the employer of such persons, (B) emissions from the
engine exhaust of a motor vehicle, rolling stock, aircraft, vessel, or
pipeline pumping station engine, (C) release of source, byproduct, or
special nuclear material from a nuclear incident, as those terms are
defined in the Atomic Energy Act of 1954, if such release is subject
to requirements with respect to financial protection established by
the Nuclear Regulatory Commission under section 170 of such Act, or,
for the purposes of section 104 of this title or any other response
action, any release of source byproduct, or special nuclear material
from any processing site designated under section 102(a)(l) or 302(a)
of the Uranium Mill Tailings Radiation Control Act of 1978, and
(d) the normal application of fertilizer;"
4. CERCLA section 101(14) defines "hazardous substances" as "(A)
any substance designated pursuant to section 311 (t>)(a)(A) of the
Federal Water Pollution Act, (B) any element, compound, mixture,
solution, or substance designated pursuant to section 102 of this Act,
(C) any hazardous waste having the characteristics identified under or
listed pursuant to section 3001 of the Solid Waste Disposal Act (but
not including any waste the regulation of which under the Solid Waste
Disposal Act has been suspended by Act of Congress), (D) any toxic
pollutant listed under section 307(a) of the Federal Water Pollution
Control Act, (E) any hazardous air pollutant listed under section 112
of the Clean Air Act, and (F) and imminently hazardous chemical
substance or mixture with respect to which the Administrator has taken
action pursuant to section 7 of the Toxic Substances Control Act.
The term does not include petroleum, including crude oil or any frac-
tion thereof which is not otherwise specifically listed or designated
as a hazardous substance under subparagraphs (A) through (F) of this
paragraph, and the term does not include natural gas, natural gas
liquids, liquefied natural gas, or synthetic gas usable for fuel (or mix-
tures of natural gas and such synthetic gas);"
5. Section 104 of CERCLA provides authority to respond to Federally
permitted release; as long as the release falls within the narrow defi-
nition of Federally permitted release under section 101(10) of the Act,
however, there is no liability imposed under section 107 for the release
and no reporting requirements.
6. See §104(i) of CERCLA.
7. See §11 l(a)(l) and (b), and §107 (a) and (c) of CERCLA.
8. See 106(c) guidelines FR
9. 40CFR300.
10. 40 CFR 300.68.
11. Section §lll(e) of CERCLA which prohibits the use of Trust Fund
monies for remedial actions and §107(g) which request Federal agencies
to comply substantially and procedurally with CERCLA.
12. See section 101(22) of CERCLA.
13. 48 FR 40661, Sept. 8, 1983.
14. See section 101(14)(c) of CERCLA.
15. 48 FR 40658, Sept. 8, 1983.
16. See CERCLA §301(e).
17. 48 FR40674, Sept. 8, 1983.
SUPERFUND MANAGEMENT
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CORPS OF ENGINEERS
SUPERFUND QUALITY MANAGEMENT
GEORGE W. SCHLOSSNAGLE, Ph.D.
NOEL W. URBAN
Office of the Chief of Engineers
Washington, D.C.
INTRODUCTION
The U.S. Army Corps of Engineers (USAGE or Corps) and the
USEPA entered into an interagency agreement in Feb. 1982. The
purpose of the agreement was to define Corps assistance to USEPA
for implementing the Comprehensive Environmental Response,
Compensation and Liability Act of 1980 (CERCLA). Based upon
the agreement, the Corps has primary responsibility for the de-
sign and construction of all Federal lead Superfund remedial ac-
tions. In that role, the Corps acts as the government's contracting
officer and exercises review and approval authority for all design
and construction activities for remedial actions. In addition, the
Corps provides technical assistance to USEPA during remedial in-
vestigation and feasibility studies. Upon USEPA request, the
Corps may provide other support such as oversight to enforce-
ment-managed design and construction activities and biddability
and constructability reviews for state lead projects.
The effective management of the quality of the environmental
and chemical data during the Corps activities is integral to the
successful accomplishment of the Corps Superfund mission. To
assure the quality of environmental and chemical data, the Corps
has assigned responsibilities and developed procedures during
Superfund activities. These are stated in a draft Engineer Regula-
tion (ER 1110-2-XXX) entitled, "Environmental and Chemical
Quality Management for Superfund Activities," July 26, 1983.
The draft ER presents a generic quality management plan (GQMP)
which will be used as a basis for development of site specific qual-
ity management plans (SSQMP), contract specifications and the
construction contractor quality control plans (CQCP) for each
Superfund project.
PURPOSE
During Corps Superfund projects, field operating activities of
the Corps, design architect-engineers (AEs) and contractors will
collect, analyze and document environmental and chemical data.
As a goal, the data should be scientifically and legally defensible.
One of the principal reasons data are taken is to ensure proper
payment for contract services. Work on a Superfund project may
include the removal of hazardous materials from a site. Payment
is partly based upon the concentrations and amounts of specific
materials which are removed. To ensure proper payment, the Corps
needs reliable checks on what is actually leaving the site. Similarly,
work on a site may include biological, chemical or physical treat-
ment of the material and site. The Corps needs to monitor the
actual performance of these processes in the reduction of the haz-
ard and, if applicable, to monitor any permitted discharge from a
site which may occur.
Even though the primary reason for the Corps' concern with the
quality management of environmental and chemical data is the
monitoring of contract performance, this does not diminish the
Corps' concern for health and safety factors. Environmental data,
such as air monitoring, is accomplished on-site to ensure a safe
and healthy work environment for government and contractor per-
sonnel. In addition, cost recovery is of principal concern to
USEPA. USEPA may need to use the data collected at a site to
support its litigation efforts to recover costs. It is the Corps' ex-
perience that much of data to be used in litigation efforts are
collected before design and construction activities; however, if
additional data are needed to support cost recovery efforts,
USEPA has the opportunity to review and supplement our
SSQMPs to ensure the Corps' quality management procedures
are adequate to meet USEPA's objective.
DEFINITIONS
Quality Management (QM)—All control and assurance activities
to achieve that quality which is established as necessary during the
development of the site specific quality management plan
(SSQMP).
Quality Assurance (QA)—The means by which the Government
assures that quality control activities are sufficient and function-
ing through reviews, inspections and tests.
Quality Control (QC)—The construction contractor's or archi-
tect engineer's (AEs) management and control of his own work,
his supplies, his testing agencies and his subcontractor's activ-
ities to comply with contract requirements.
Generic Quality Management Plan (GQMP)—The GQMP as out-
lined in Table 1 is the developmental framework for the site spe-
cific quality management plan (SSQMP). The Corps Superfund
Design Division, Missouri River Division (MRD), Omaha, Ne-
braska is responsible for developing the SSQMP using the GQMP
as guidance.
Table 1
Outline of the Generic Quality Management Plan (GQMP)
I. Title Page
II. Table of Contents
III. Project Description
IV. Project Organization and Responsibility
V. Quality Management Objectives
VI. Sampling Procedures
VII. Sample Custody
VIII. Reports
A. Daily Contractor
B. Contractor Quality Control Project Summary
C. Site Specific Quality Management Final Report
IX. Calibration Procedures and Frequency
X. Data Analysis and Reporting
XII. Performance and System Audits
XIII. Preventive Maintenance
XIV. Assessing Data Precision, Accuracy and Completeness
XV. Corrective Actions
SUPERFUND MANAGEMENT
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Site Specific Quality Management Plan (SSQMP)—A working
document prepared during the design phase of federal lead remed-
ial actions using the GQMP as a guide. The SSQMP clearly de-
fines a specific project organization including identification of
quality control and quality assurance responsibility for each Corps
organization, the AE, construction contractors and others who
may be involved. That portion of the SSQMP which refers to the
construction contractor's quality control (CQQ, and contract
technical specifications will be incorporated in the Invitation for
Bids (IFBs) as part of the contract provisions under "Contract
Quality Control." Site specific information will include the iden-
tity of hazardous materials.
Contractor Quality Control Plan (CQCP)—A working plan devel-
oped by the construction contractor based upon the contract tech-
nical specifications. The plan is developed after award of the con-
tract and will be approved by the Constructions District before
the work commences on-site. The document will contain an effec-
tive plan for environmental and chemical data quality control.
The contract technical specifications will also require the contrac-
tor to prepare a CQC Project Summary at project close-out. An
outline of the CQCP is provided in Table 2.
QUALITY MANAGEMENT RESPONSIBILITIES
Office of the Chief of Engineers (OCE)
The Chief, General Engineering Branch, Directorate of Engi-
neering and Contraction, Office of the Chief of Engineers, Wash-
ington, D.C. acts as the designated program manager for Super-
fund activities with responsibility for overall Corps policies, pro-
cedures, execution activities and coordination with Corps field
operating activities. Primary responsibility for all aspects of the
Corps Superfund and for all necessary headquarters level coordina-
tion with USEPA and other agencies lies with the Program Man-
ager for ongoing activities. In addition, the Chief provides tech-
nical assistance to the Design Division, Missouri River Division
(MRD), during the development of the SSQMP and the technical
Table 2
Outline of the Contractors Quality Control Plan (CQCP)
I. The construction contractor's quality control organization.
II. Names, number and qualifications of personnel to be used for this
purpose.
HI. Authority and responsibilities of all quality control personnel.
IV. Schedule of inspections.
V. Proposed analytical methods to be used including names of tech-
nicians performing each method.
VI. Proposed sample collection, handling, storage, transfer, and record-
ing protocols, including chain-of-custody procedures.
VII. Method of performing, documenting and enforcing quality control
operations of the prime contractor and subcontractors including
inspection and testing.
VIII. A copy of a letter of direction to the Contractor's representative
responsible for quality control, outlining his duties and respon-
sibilities, and signed by a principal officer of the firm.
Validated Corps Laboratories—Selected Corps laboratories will be
used in support of Superfund projects. The laboratories will pro-
vide technical assistance to the Superfund project construction dis-
trict in the supervision of quality management. Laboratories will
be validated using a two step procedure. The first step is a review
of the laboratory analytical capabilities. The second step is plac-
ing the laboratory in a performance evaluation program.
provision, Contractor Quality Control and other assistance on
other design aspects. The Chief provides technical assistance to
the Construction Division personnel during the construction phase
of all projects.
The Chief, General Engineering Branch, validates laboratones
in specific technical areas for Superfund activities. Division labor-
atory validation should commence before the division laboratones
assume technical supervision on QM for the district. The Chief,
General Engineering Branch, also audits project Quality Manage-
ment to ensure effective management of environmental and chem-
ical data.
Design Division
The design division for Superfund activities is the Missouri
River Division (MRD), Omaha, Nebraska. MRD has tasked its
division laboratory to develop the site specific quality manage-
ment plans (SSQMPs). MRD is responsible for insuring that con-
tract specifications in the Invitation for Bids contain all contractor
quality control elements identified in the SSQMP that are the re-
sponsibility of the construction contractor. MRD coordinates all
QM efforts with the applicable construction division, the Water-
ways Experiment Station (WES) and OCE; however MRD re-
mains as the final approval authority for the SSQMP and contract
specifications.
Construction Division and District
The Corps division supervising the construction district is the
construction division. The Corps district assigned the responsibil-
ity to administer the construction contract is the construction
district. The construction district assigns the Resident (or Area)
Engineer as the QM Officer who is responsible for coordinating
all QA and QC during a Superfund project. Technical problems
with implementation of the SSQMP are coordinated with MRD.
The construction district administers Superfund contracts. Accord-
ingly, the construction district also evaluates and approves the
Contractor Quality Control Plan (CQCP) with concurrence by the
construction division, design division and OCE. The CQCP and
SSQMP will be used as background by the validated laboratories
to assess the effectiveness of QM during specific Superfund ac-
tivities. Work will not begin until an approved CQCP has been
accepted by the Contracting Officer. Changes from the approved
CQCP will be coordinated with the design division and validated
laboratories. The construction district will prepare a final summary
report of environmental and chemical QA and CQC. The report
will be attached to a construction contractor quality control (CQC)
project summary and located in project files. Photocopies of all
documentation concerning data collection, analysis and report-
ing will be included as an appendix to this report.
Validated laboratories are used to provide technical assistance to
the construction district in the technical supervision of QM dur-
ing Superfund activities. Validated laboratories are typically Corps
division laboratories, and for a specific Superfund effort, the val-
idated laboratory would be the construction division's laboratory.
In the event the construction division does not have a laboratory,
as is the case of the Corps' North Atlantic Division (NAD), an-
other Corps laboratory will be designated to assume the role as
division laboratory.
GENERAL PROCEDURES
There are normally four phases of Corps involvement during
Superfund activities: 1) Predesign technical assistance; 2) project
acceptance; 3) design; and 4) construction.
Predesign Technical Assistance
During the site investigation and feasibility study stages, the
Corps will provide technical assistance to USEPA. The Missouri
River Division (MRD) will evaluate data and project documents
for technical adequacy for design alternative selection and deter-
mine additional data requirements for the design phase. Frequent-
SUPERFUND MANAGEMENT
-------
ly, some data (usually chemical data) may not be available until a
later date. As part of the review, MRD will review the environ-
Table 3
Checklist for Review of Site Specific Quality Management Plan (SSQMP)
and Contractor Quality Control Plan (CQCP)
1. Are project objectives and the use of sampling and analysis data clearly
stated?
2. Is the importance of QA and QC clearly stated?
3. Has a person been designated as having the responsibility for QA and
CQC?
4. Is the organizational structure in place to accomplish QA and CQC?
5. Do personnel have adequate education and experience to produce
quality data?
6. Is specialized training necessary for working with the hazardous
materials associated with the project?
7. Does the construction contractor have the personnel to accomplish the
sampling and analysis in a timely manner required by the project?
8. Does the construction contractor have adequate sampling equipment?
9. Are appropriate sample containers specified?
10. If in situ measurements are required, is appropriate instrumentation
available? Are requirements stated?
11. Are plans in effect for field calibration, maintenance and performance
checks?
12. Will documentation of these checks be available?
13. Are descriptions of sampling procedures provided? Are standard
methods to be used?
14. Are provisions made to avoid sample contamination?
15. Are sampling site locations clearly defined? In the case of drum
sampling, are all or some of the drums to be sampled?
16. How many duplicate samples will be taken? Are provisions made for
split samples?
17. Are background samples to be taken?
18. Are provisions made to assure that samples are representative?
19. Are field notebooks used to record site observations and field data?
20. How will field data be verified?
21. Will laboratory analyses be provided by a mobile laboratory on site,
or must samples be transported?
22. If samples are transported, do samples meet U.S. Department of
Transportation and USEPA regulations? Has chain of custody been
considered?
23. If preservation of samples is required, will USEPA approved preser-
vation methods be used?
24. Will standard methods analysis be used (i.e., USEPA, ASTM, etc)?
25. If non-standard methods are used, what validation procedures have
been used to assure the integrity of the method?
26. Will the procedures used result in data that meet required detection
limits, accuracy and precision?
27. How many duplicate analyses will be run? Spiked samples? Split
samples?
28. Is the instrument calibration system described?
20. Are calibration standards traceable to NBS?
30. When will the data be validated?
31. Is the statistical treatment of the data described?
32. Is provision made for the CQC Daily Report, the CQC Project Sum-
mary, and the SSQM final Reports?
33. Is provision made throughout the project to apply quality control
measures and take corrective actions?
34. Has the ultimate fate of samples taken for analysis been considered?
35. Are provisions made for distribution and review of all required
reports?
36. Is the technical supervision role by validated laboratories identified?
37. Has safety been properly considered? Is this plan in conformance with
the Contractor Accident Prevention Plan and the Site Specific Safety
Plan as discussed in EC 385-1-192?
mental and chemical data to assess the quality of data provided.
Review of data from the site investigation and feasibility study
stages will address the following questions with regard to QA:
•Where do the data come from (i.e., USEPA, states, USGS, Con-
tractor)?
•Were the data generated under acceptable quality controlled
conditions?
•Have the data been examined by USEPA to assess the quality
assurance?
•Is information available on sampling procedures and analytical
methodologies?
•Were chain-of-custody procedures in effect during sampling and
analysis?
•How complete is the data set? Will additional data be provided?
•What is the source of the additional data?
The QA review and recommendations will be incorporated with
other review comments and forwarded to OCE for review and
exception comments. Once the OCE accepts the USEPA project,
appropriate elements of the GQMP should be implemented.
Project Acceptance Phase
Normally, USEPA will forward a selected project to OCE
(DAEN-ECE-B) for acceptance. If accepted, it is assigned to the
appropriate Corps field operating activity (FOA).
Design Phase
During the design phase, AE contractors on Superfund projects
will be required to make their laboratory facilities available for
Corps inspections. In addition, the Design Division will be respon-
sible for preparation of each site specific quality management plan
((SSQMP) and the contract technical specifications, using the
generic quality management plan (GQMP) as a guide. Review of
the SSQMP will occur at the 60% design review or other appro-
priate review level, and the technical specifications will be reviewed
at the time of final design. Final approval of the SSQMP and tech-
nical specifications will be made by the design division (MRDs)
with concurrences required as specified previously.
Construction Phase
The construction contractor will prepare the written Contractor
Quality Control Plan (CQCP) based on the technical specifica-
tions. The CQCP must contain an effective plan for environ-
mental and chemical data quality control. The checklist presented
in Table 3 should be helpful during the review of the CQCP
and also the SSQMP. The appropriate Corps FOA will inspect
the contractor's chemistry laboratories using validated Corps lab-
oratory resources. The contract technical provisions will require the
contractor to permit government inspection of the contractor's
laboratory facilities. The contractor's laboratory facilities will be
inspected and approved before performing any chemical analyses
required by the construction contract. Laboratories may be on or
off the construction site. Subsequent inspections to determine con-
formance with the CQCP plan will be made by a validated Corps
laboratory as necessary.
CONCLUSION
The Corps realizes that successful mission accomplishment of its
Superfund role is dependent upon an effective environmental and
chemical quality management program integrating the various as-
pects of quality assurance and quality control. To achieve this,
the Corps has developed a three stage process. First, a generic
quality management plan was developed as a guide for all Super-
fund projects. Secondly, for each Superfund project, the design
division will develop a site specific quality management plan using
the generic quality management plan as a guide. And thirdly, the
site specific quality management plan will be used by the Corps
in its quality assurance role and the Construction Contractor will
use elements of this plan found in the contract specifications to
develop its contractor quality control plan.
SUPERFUND MANAGEMENT
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SUPERFUND RESPONSES TO THREATENED
DRINKING WATER RESOURCES
MARCIA FINE SILCOX
VERNA J. MONTGOMERY
Booz, Allen & Hamilton, Inc.
Washington, D.C.
INTRODUCTION
America's supply of drinking water can be seriously threatened
by industrial and agricultural effluents and improper disposal of
hazardous chemical wastes. Many of the environmental statutes
and regulations respond either directly or indirectly to these poten-
tial drinking water problems. Some, like the Safe Drinking Water
Act', provide preventive drinking water quality standards for meas-
uring the safety of potable water. More recent statutes, like
CERCLA2 (Superfund), provide the USEPA with a responsive
tool to meet the various challenges of groundwater contamina-
tion and persistent organic chemicals. Embodied in CERCLA are
a number of authorities not available in other statutes and activ-
ities designed to ensure drinking water quality in the face of haz-
ardous waste contamination threats. In fact, a major impetus for
the passage of CERCLA was the evidence of a growing threat to
drinking water.
In this paper, the authors examine the role of CERCLA in pro-
tecting and preserving drinking water resources. They examine the
statutory and regulatory provisions of four statutes that are applic-
able to drinking water and the differences in those provisions,
and they provide an analysis of Superfund activities to date, iden-
tifying patterns of drinking water contamination and response.
The paper is concluded with a discussion of the managerial implica-
tions of drinking water pollution and response.
STATUTORY PROVISIONS FOR THE
PROTECTION OF DRINKING WATER
Over the past 12 years, the USEPA has initiated several regula-
tory programs which, in full or in part, address the problem of
toxic substance pollution of surface water and groundwater. The
most prominent of these programs are:
•Clean Water Act of 1977' (amending the Federal Water Pollu-
tion Control Act of 1972)
•Safe Drinking Water Act of 1974'
•Resource Conservation and Recovery Act of 1976*
•Comprehensive Environmental Response, Compensation and
Liability Act of 19802
The regulated pollutants and the types of Federal and state re-
sponses vary with each statute. Because of the potential scope of
drinking water damages and their direct impact on public health
and welfare, each of the four major environmental statutes out-
lined in Table 1 has an important role to play. The general attri-
butes of each statute and the responsive (post hoc) and preventive
actions, the surface water and groundwater provisions and the var-
iation in regulation of specified chemicals and in engineering con-
trols are compared in the table.
Clean Water Act
The 1977 Clean Water Act's predecessor, the Federal Water
Pollution Control Act, was enacted in 1972 with three primary
goals:
•Protection of fish and wildlife in and around water by July 1, 1983
•Protection of water quality for recreational purposes
•Elimination of the discharge of pollutants into navigable waters
by 1985
To achieve these goals, USEPA established water quality stand-
ards based upon water use (including seafood consumption and
drinking), effluent guidelines based upon Best Practicable Tech-
nology (BPT) methods and a permitting program to regulate the
discharge of pollutants into the water. States share in the imple-
mentation of this program by instituting the water quality stan-
dards and developing state management plans for the quality of
both surface and groundwater.
The primary focus of this Act is to protect against surface water
contamination by industrial and municipal effluents. However,
CWA Section 311 provides Federal authority to respond to re-
leases of oil and hazardous substances into the navigable waters
and shores of the United States by establishing a fund to finance
cleanup activities. This section does not provide for response
activities involving groundwater or release incidents that are multi-
media in nature. CERCLA, particularly in its removal program,
builds upon the foundation of CWA Section 311 to provide re-
sponse authority for hazardous waste releases to non-navigable
waters and other media.
Safe Drinking Water Act
The Safe Drinking Water Act (SOWA) of 1974 established na-
tional drinking water quality standards for public drinking water
supplies. Primary public health standards were instituted for drink-
ing water, as were secondary standards for regulating the appear-
ance, taste and odor of drinking water. In addition to these water
quality standards for municipal drinking water supplies, are two
important provisions:
•Control of underground injection of wastes that may contam-
inate potable groundwater resources
•Designation of certain aquifers as sole source suppliers of drink-
ing water to a particular area.
The SDWA for the first time establishes Federal standards on
groundwater quality vis-a-vis underground injection. The preven-
tive focus of the Underground Injection Control (UIC) program
ensures that the design, construction, operation and abandonment
of injection wells will be conducted in a manner that does not allow
pollutants to migrate from the disposal well to the aquifer Tech-
SUPERFUND MANAGEMENT
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Table 1
Comparison of Drinking Water Provisions of Major Statutes
ACT
CLEAN WATER ACT
(CWA) formerly
the FEDERAL
WATER POLLUTION
CONTROL ACT of
1972 (FWPCA)
SAFE DRINKING
WATER ACT
(SDWA)
RESOURCE
CONSERVATION
AND RECOVERY
ACT (RCRA)
COMPREHENSIVE
ENVIRONMENTAL
RESPONSE,
COMPENSATION
AND LIABILITY
ACT (CERCLA)
DATE OF
PASSAGE
1977
1971*
1976
I960
RESPONSE
TYPE
Responds to
exceedence
of NPDES
standards
Responds to
exceedence
of MCL
Standards
Prevents
contaminat ion
through UIC
program and
sole source
aquifer
designation
Responds to
exceedence
of MCL
Standards
Responds to
releases or
threats of
releases
through
di recti ves
of NCP
MEDIA
FOCUS
Surface
water and
groundwater
Surface
water and
groundwater
Groundwater
Surface
water and
Groundwater
STANDARDS
National
Pol lutant
Di scharge
El iminat ion
System
(NPDES)
National
Ambient
Water
dual i ty
Criteria
(NAWQC)
21 Maximum
Contaminant
Levels (MCL)
5 Health
Advisories
No standards
eval uat ion
criteria for
igni tabi 1 i ty
corros i vi ty ,
react ivi ty ,
toxici ty
Nat ional
Contingency
Plan (NCP)
sets forth
no numerical
standards
REGULATED
POLLUTANTS
Conventional
pol lutants e.g.
suspended sol ids,
oil/grease, pH,
fecal col iform
129 toxic
pol lutants
Non-convent ional
pol lutants
e.g. ammon i a ,
ni trogen,
phosphorous
Col iform
bacteria
Heavy metals
Certain
chlorinated
organics
96 process
wastes
'(OO chemicals
Hazardous
substances as
defined under
RCRA, FWPCA,
CAA, TSCA and as
promulgated under
CERCLA
RELATION TO
DRINKING WATER
1 ndi rect
Direct
Ind i rect
Di rect
CONTROL
SOURCE
In ambient
water
At tap
At municipal
supply
At source
At source
At municipal
supply
At tap
nical standards and permitting provisions foster this objective. Mit-
igative provisions for previously contaminated water are not pro-
vided under the UIC program.
Resource Conservation and Recovery Act
In an effort to prevent contamination of the nation's ground-
water from practices other than underground injection, the Re-
source Conservation and Recovery Act was enacted in 1976. Under
this Act, waste disposal into landfills, lagoons, ponds and pits is
regulated with proper design and operation standards being re-
quired. Specific groundwater quality standards, based upon the
Maximum Contaminant Levels set forth under SDWA, were in-
stituted for facilities licensed under RCRA to act in conjunction
with the waste disposal facility permitting, operation and closure
standards.
The enactment of RCRA provided a preventive structure for
ensuring proper operation, maintenance and closure of hazardous
waste facilities. Despite the promise that RCRA holds for preven-
tion of future drinking water contamination, it could not provide a
response capability to protect water resources now threatened.
CERCLA, however, has this potential.
Comprehensive Environmental Response,
Compensation and Liability Act
Since the enactment of the CWA, SDWA and RCRA, the
amounts and types of contaminants that can enter an aquatic or
subterranean environment have increased dramatically. An esti-
mated 28 million to 54 million metric tons of Federally regulated
hazardous wastes were generated in the United States in 1980.s
In 1980, as a direct result of increased attention to the problems
of abandoned hazardous waste sites, Congress enacted the Com-
prehensive Environmental Response, Compensation and Liability
Act also known as Superfund. This legislation creates a $1.6 billion
Trust Fund to be used to cover the costs of responding to releases
or threatened releases of hazardous substances into the environ-
ment. Just as RCRA prescribes a regulatory mandate, CERCLA
sets forth a Federal and state response authority.
CERCLA is likely to be the major environmental initiative of the
decade, and, although not a drinking water statute per se, it does
contain provisions for protecting and preserving drinking water re-
sources that fill some of the gaps left by other statutes. It repre-
sents the first Federal statute to focus specifically on response to
SUPERFUND MANAGEMENT
-------
environmental and public health threats posed by releases of haz-
ardous material in ail environmental media including groundwater.
Using it, the USEPA can respond to multi-media threats and in-
cidents in non-navigable waterways and has express mitigative pro-
visions. As such, CERCLA provides the specific definitions and
other statutory language that make direct reference to the known
threat of hazardous waste contamination of drinking water.
A particular sensitivity to the importance of groundwater and
drinking water has been evident since the statute's inception in
1980. For example, while each of the major pieces of legislation
outlined above contains an imminent hazard provision relating to
groundwater, only CERCLA provides the broad authority to pro-
tect public health, welfare and the environment from groundwater
pollution.
Another example of CERCLA's direct concern with drinking
water can be seen in the definitions outlined in CERCLA Section
101:
•Groundwater defined as water in a saturated zone or stratum or
beneath the surface of land or water
•Natural resource defined to include water, groundwater and
drinking water supplies
•Removal defined to include among others, the provision of alter-
native water supplies
•Remedial action defined to include among others, the provision
of alternative water supplies
In addition to its definitions, Superfund's primary operational
regulation and guidance, the National Contingency Plan6 (NCP),
provides more specific direction on the importance of preserving
and protecting potable water resources. The NCP imparts the
various powers and responsibilities of the Federal agencies during
CERCLA response actions. It contains both explicit and implicit
instructions for handling and evaluating drinking water contamina-
tion threats from hazardous substance releases. Specifically, the
Hazardous Ranking System outlined in the NCP is used as a
measure for examining five potential exposure pathways for con-
taminants at sites to be considered for the National Priorities List.
Two of these pathways, groundwater and surface water, relate
directly to drinking water contamination threats and can be iden-
tified by the existence or likelihood of a hazardous substance re-
lease, the characteristics of the hazardous materials released and
the composition and size of the threatened population.
To determine how a groundwater contamination threat impacts
a population, USEPA's hazard ranking algorithm considers the:
•Use of the aquifer, assigning low values to unusable aquifers
and high values to aquifers that provide the only drinking water
source
•Distance from the nearest well to the hazardous substance (max-
imum distance is three miles)
•Size of the population served
The contribution of groundwater and surface water contam-
ination to site listing on the National Priorities List (NPL) is signif-
icant. Of the 418 sites on the NPL, 347 groundwater and 60 sur-
face water (though not necessarily drinking water) impacts were
noted.7 The following section describes specific examples of
CERCLA's emphasis on response to threats of groundwater and
surface water contamination by hazardous substances and outlines
the implications these findings suggest.
CERCLA RESPONSE TO DRINKING WATER THREATS
The potential importance of Superfund activities in solving
drinking water problems had been underscored during the enact-
ment of the statute as well as early during phases of program im-
plementation. As Superfund moved from implementation into its
current status as a fully operative program, it was obvious that
drinking water concerns would continue to play a role...but the
question remained, to what extent? In trying to answer these ques-
tions, current program information was analyzed. The effort des-
cribed herein examined manual data bases and documents. It was
hoped that an informal survey might demonstrate:
•The scope and pattern of CERCLA-related drinking water con-
tamination
•The nature and use of actual or proposed mitigative activities
This analysis might then provide program managers with a set of
trends or implications that might be useful in future planning and
resource allocation. The analysis is based upon comparisons of re-
moval actions with remedial actions and descriptions of the dif-
ferent types of water resources injured by hazardous wastes or
addressed by Superfund. These findings are presented in the next
section.
Methods of Analysis
Superfund activities are generally classified as removal or re-
medial actions. Removal actions are designed to reduce threats of
imminent hazards. A six month/$l million limitation is placed on
all actions taken to protect human health and welfare, stop the
hazardous release and minimize the environmental damage. A re-
medial action is taken when the threat is not emergency in nature
and will require a more long-term and costly solution. To draw a
basic picture of drinking water problems and Superfund solutions,
two useful program documents were identified:
• The Removal Tracking System (RTS) reports are generated regu-
larly to aid the Emergency Response Division (ERD) in tracking
immediate and planned removal actions. The specific data source
for this report is the weekly Summary of Removal Activities.
•Remedial Action Master Plans (RAMPs) are written as part of the
investigation phase of each National Priority List site response.
They describe actual findings at the site as well as anticipated
mitigative activities.
The RTS reports examined for this analysis included all removal
actions completed or in progress since the inception of the Super-
fund program through May 15, 1983. In addition, while RAMPs
will be prepared for all 419 National Priority List sites, a random
sample of 26 RAMPs was evaluated for the purpose of this paper.
The following section details the findings.
Water Source Variation
Drinking water can be derived from surface water—ponds,
rivers, lakes and streams that are usually purified chemically and
delivered through municipal systems or from saturated under-
ground geologic formations known as aquifers. Groundwater may
or may not be disinfected and may be supplied through municipal
systems or through privately owned wells. In this paper, the authors
examine how often surface water and groundwater that might be
used as drinking water were impacted by hazardous waste sites
addressed under Superfund. Of 131 removal sites, 28 sites (21%)
noted drinking water threats. At remedial sites, the 26 RAMPs
evaluated noted potential drinking water threats at 11 sites (42%).
The findings on the type of water source threatened by hazardous
waste at those sites are shown in Figure 1.
There has always been a substantial emphasis on groundwater
pollution in conjunction with hazardous waste. Under contract to
USEPA, Booz, Allen & Hamilton prepared a preliminary analysis
of 221 remedial sites in May 1983, to evaluate, among other things,
the extent of groundwater threats. The analysis showed that 145
sites (66%) had verified or suspected groundwater contamination.
The actual use of the groundwater for drinking water was not
noted. However, the impact on surface water cannot be ignored
(Figure 2). Surface water threats are particularly evident, as might
be expected, in the removal setting where emergency activities are
common. It may also be indicative of the cost differential in meet-
ing remedial and removal action needs. Since groundwater clean-
up is so costly and time consuming, it may not be feasible within
the $1 million statutory removal ceiling or the six month statutory
limit.
Groundwater and surface water threats often appear together,
especially in remedial incidents, thus demonstrating the broad
geographic and intermedia hazard posed by waste constituents As
10
St'PERFtND MANAGEMENT
-------
noted earlier, one of CERCLA's important attributes is that multi-
media focus.
Type of Contaminants
The importance of CERCLA's ability to respond to toxic pollu-
tants in or near drinking water sources is emphasized by the types
of pollutants discovered during remedial response actions at Super-
fund sites. The contaminants noted in the sample of RAMPs for
remedial sites with possible drinking water involvement are shown
in Figure 2. Iron, which is a natural water contaminant, and tri-
chlorolethylene, an industrial solvent, were noted at more than half
of the sites on which this report is based. Heavy metals such as
cadmium, arsenic, chromium and lead were each found in a third
of the sites. Phenols were seen more often than other organics and
organics were generally noted in less than 15% of the sampled
remedial sites.
Figure 1
Drinking Water Source Threats at Sample Superfund Sites
The situation was surprisingly different for removal actions, as
shown in Figure 3. Here, unspecified solvents and other organics
including pesticides and PCBs were most often described. The only
chemical types named in both remedial and removal sites are
phenols and benzene. There is also likely overlap in the unspeci-
fied solvent categories. In removal statistics, no heavy metals are
shown and there is a much narrower range of specified pollutants.
A contributing factor to this disparity could be that the substantial
heavy metal involvement at remedial sites results from the nature of
the inoperative facility that requires long-term remedial action.
Remedial sites showed nearly twice as many different pollutants as
a group. This is attributable to the differences in specificity in the
RAMPs used in the remedial analysis and the Removal Summary
used in the removal analysis. Caution should therefore be used in
interpreting these results.
Testing and Abatement Actions
After determining that significant threats to drinking water exist
at Superfund sites, it was important to examine the types of in-
vestigative and mitigative action now under consideration or under
way. In the final portion of this analysis, the type and frequency
of testing and abatement actions for drinking water threats were
examined. The varied types of response actions described in the
RAMPs or the Removal Summary are listed in Table 2. The most
prevalent activity at both removal and remedial sites was sampling
and analysis, a vital component in determining the appropriate
mitigative measure.
There was some mitigative action to date. Removal sites relied
heavily on source containment activities such as drum removal or
lagoon stabilization to prevent threats from being magnified or
realized. Other types of mitigative activities varied widely from
simple bans on water use or provision of alternative water to com-
plex engineering actions such as construction of channels and dams
to contain leachates. More of these complex, construction or en-
gineering actions were noted in the remedial plans, again pointing
to the statutory cost and time limitations on removal actions.
55 — |
50 -
40 —
B
«
| 35 —
|._
E 15 -
10 —
5 —
Z
i
|U
^ i
Sg «
OQ
5^
BENZENE
CADMIUM
O
§
1
CHLORIDE.
/
t
8
§3
It
>
CYANIDE
i
71
/ — :
I
„.
|
UJ
5
PHENOLS
•»
I
i
TETRACHl
ETHYLENE
TOLUENE
y 71
Q
8
TOTAL DK
SOLIDS
%
a
R
TRICHLOR
CONTAMINANTS
Figure 2
Water Contaminants at Remedial Sites
SUPERFUND MANAGEMENT
11
-------
CONTAMINANTS
SOURCE
REMEDIAL ACTION MASTER PLANS (RAMPS)
REMOVAL SUMMARY MATRIX
Figure 3
Water Contaminants at Removal Sites
Table 2
Types of Frequency of Drinking Water Testing and Abatement Actions
ACTION TYPE
Sampling and analysis
Upgradient pumping, discharge
Source containment, removal
Provision of alternative water 3
Tie-in to municipal system 1
Water treatment
Ban non-essential water use 2
Groundwater treatment 2
Drainage channels, dams 3
New well construction 1
•Remedial actions thai are contemplated.
••Removal actions that have occurred or will occur.
SOURCE:
Remedial Action Master Plans (RAMPs)
Removal Summary Matrix
FREQUENCY
Remedial* Removal*
(11 sites) (28 sites)
8 8
3
16
3
3
3
IMPLICATIONS
As Superfund gains momentum and more sites and incidents are
addressed, it will be important for program managers to be able to
predict the type and number of responses that will be required. In
so doing, they will be able to allocate resources and personnel
most efficiently and expeditiously.
Although drinking water problems are only one of the many en-
vironmental results caused by improper hazardous waste disposal,
the scope of drinking water threats is broad. And, while a number
of statutes will continue to be used to treat or prevent drinking
water degradation, Superfund must play a vital response role.
Alternative drinking water provision or treatment costs are only a
portion of the total cost, but they can be substantial—especially
when source removal and engineering efforts are required to con-
tain pollutants that might enter drinking water supplies.
The technical components of Superfund response actions will
need to be sensitive to the drinking water issue. Methods of dealing
with the heavy metal and organic solvent contaminants are seen as
vital. Moreover, the threat to surface water, especially in removal
incidents, cannot be ignored. It is often stated that half the U.S.
population takes its drinking water from groundwater: this means
that half the nation relies on surface water. Therefore, protection
and improvement of both sources is critical.
The variety of Federal environmental statutes outlined in this
paper shows an increased attention to the linkage between drink-
ing water and waste issues. However, there is a vital need to inte-
grate the existing regulations into a consistent and comprehensive
protection program for both surface water and groundwater. Cur-
rently, water quality standards vary from statute to statute and
from state to state. Maximum contamination limits are utilized
under RCRA and SDWA, while CWA and the broader response
authority under CERCLA require different quality standards for
similar contamination situations. An effort should be made to pro-
vide a water protection program that respects:
•Consistent water quality standards
•Variety of contaminants that enter aquatic and subterranean
environments
•Availability and cost of technology to address contamination
problems
•Federal and state response authorities
This program could evolve by amending the existing statutes or
through the development of a comprehensive national policy to
assess and protect the quality of groundwater and surface water for
existing and projected future uses and for the protection of the
public health and the environment.
REFERENCES
1. Safe Drinking Water Act (SDWA), 40 USC 300f-300j-q et. seq.
2. Comprehensive Environmental Response, Compensation, and Liability
Act (CERCLA), 42 U.S.C. 9601-9657 et. seq.
3. Clean Water Act (CWA), 33 U.S.C. 466 et. seq.
4. Resource Conservation And Recovery Act (RCRA) 42 U.S.C. 6901-
6986 et. seq.
5. Technologies and Management Strategies for Hazardous Waste Con-
trol, Office of Technology Assessment, Mar. 1983, 8.
6. National Oil and Hazardous Substances Contingency Plan, Federal
Register, 47, July 16, 1982, 31100, 40 CFR 300.
7. Annon., Hazardous Waste News, 5, Jan. 3, 1982, 1.
8. Booz, Allen & Hamilton and ICF, Inc., "Preliminary Steps Toward
a Superfund Drinking Water Policy," Feb. 1982.
12
SUPERFUND MANAGEMENT
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ANALYSIS OF MINING SITES ON
THE NATIONAL PRIORITIES LIST
BRIAN L. MURPHY
WILLIAM W. BECK, JR.
DENNIS F. UNITES
TRC Environmental Consultants, Incorporated
East Hartford, Connecticut
INTRODUCTION
On Dec. 20, 1982,418 sites were placed on the National Priorities
List (NPL).1 This was the culmination of an effort by USEPA
and numerous state agencies to identify the hazardous waste dis-
posal sites in the United States which present the greatest risk to
human health and/or the environment.
Sites believed to present a hazardous waste problem are desig-
nated for the NPL by a two step procedure:
1. The states nominate sites for the NPL. Under the Comprehen-
sive Environmental Response, Compensation and Liability Act
(CERCLA), which established this procedure, each state must
have at least one site on the NPL.
2. An intendedly objective scoring system developed by the
MITRE Corporation for USEPA (the "MITRE model") is
then used to select sites. MITRE model scores are furnished by
the states with their nomination. In reality, USEPA or its con-
tractors did the scoring for the states in many cases.
The USEPA has estimated that there may be 10,000 to 20,000
hazardous waste sites potentially covered by CERCLA. Of these
690, or about 5%, were nominated for the NPL. Thus, the win-
nowing process in Step 1 is much greater than in Sept 2 (418/690 =
61%). For mining sites, 31 locations were nominated, of which 17
sites were selected. Presumably, like the other sites, the mining sites
nominated represent only a small fraction of the total popula-
tion.
The second step of the listing process is the comparison of Mitre
Model scores to compose the NPL. The model calculates scores
for five "pathways" of potential human exposure: groundwater,
surface water, air, direct contact and fire and explosion. The first
three pathways are combined (by taking the square root of the sum
of the squares) into an overall "migration" score. The migration
score is essentially the determinant for listing on the NPL. Accord-
ing to the National Contingency Plan (Federal Register, 47, July
16, 1982, 31180), placement of sites on the NPL is based primarily
on the migration score. The fire and explosion and direct con-
tact scores may be used to determine if emergency attention is
needed.
The score for each of the three migration pathways is the pro-
duct of scores for three "factors":
1. The existence or likelihood of a release. An "observed re-
lease" which is basically a measurement of concentration above
background at any location automatically produces the maxi-
mum score.
1. Times Beach, Missouri has since become the 419th site and further additions to the list were
expected on Aug. 1,1983.
2. A "characteristics" score which is the sum of scores for quan-
tity and toxicity/persistence for water pathways and quantity,
toxicity, and reactivity, and incompatibility for the air path-
way. The score for "quantity" is determined by the total vol-
ume of waste while the score for parameters like "toxicity/
persistence" is determined by the most toxic and persistent com-
ponent.
3. The characteristics of the population or sensitive environment
at risk, such as distance to point of exposure and number of
people involved. Potential scores for population factors are
much larger than for purely environmental factors.
In this paper, mining sites are defined by whether the practices
at the site would qualify an operator for membership in the Amer-
ican Mining Congress (AMC). These practices include extraction,
smelting and refining but not fabrication into a final product. Only
sites where mining practices are responsible for most of the Mitre
Model score are analyzed. Under these criteria, the 31 mining sites
analyzed, including 17 NPL sites, are shown in Table 1.
In this paper, the authors are concerned solely with the techni-
cal validity of the listing process. Legal issues, such as the pro-
priety of including mining sites in Superfund, are not considered.
Nor are site-by-site characterizations a primary concern; this is
done only to the extent necessary to provide perspective on the
validity of the Mitre Model results.
NOMINATION OF SITES BASED ON
EXTENT OF EXISTING INFORMATION
In generating Mitre Model scores to be submitted for a site's
nomination, a general result is: the more information available
the higher the score. This result is as true for sites not causing any
significant harm to the environment as it is for genuine problem
sites.
The Mitre Model score rises with the available information for
the following reasons. The instructions for using the model specify
that where there are no data for a factor, it is assigned a value of
zero. Further, where data are lacking for two or more factors, the
entire pathway score (air, groundwater or surface water) is set to
zero. Finally, the maximum score for any pathway can only occur
for a measurement, or other conclusive evidence, of a concentra-
tion above background (irrespective of whether or not the concen-
tration is significant in terms of health standards and criteria).
Most of the 31 mining sites nominated for the NPL have prior
studies; some have a history of USEPA and/or state negotiations
and, in a few cases, consent decrees. Further evidence that these
sites are well known is the fact that all of the 17 NPL sites and ten
SUPERFUND MANAGEMENT
13
-------
Table 1
Sites Analyzed
NPL Sites
1. Anaconda Smelter
Anaconda, MT
2. Bunker Hill Smelter
Smelterville, ID
3. California Gulch
Leadville, CO
4. Celtor Chemical
Humboldt County, CA
5. Central City—Idaho Springs
Clear Creek and
Gilpin Counties, CO
6. Commencement Bay
Tacoma, WA
7. Homestake Mining
Milan, NM
8. Iron Mountain Mine
Shasta County, CA
9. Milltown Reservoir
Milltown, MO
10. Mountain View Mobile Homes
Globe, AZ
11. PaJmerton Zinc
Paimerton, PA
12. Silver Bow Creek
Silver Box and
Deerlodge Counties, MT
13. Tar Creek—Kansas
Cherokee County, OK
14. Tar Creek—Oklahoma
Ottawa County, OK
15. United Nuclear
Churchrock, NM
16. U.S. Titanium
Nelson County, VA
17. Whitewood Creek
Black Hills, SD
Recommended by States but Not NPL Sites
Mining Activity'
Copper smelter
Lead and zinc smelter
Metal mines
Metals reclamation mill
Gold mines
Metal smelting
Uranium mill
Copper mines
Copper mines and smelter
Asbestos mills
Zinc refinery and smelter
Metal mines and mills
Lead and zinc mines
Iron and zinc mines
Uranium mill
Mine and refinery
Gold mines and mill
18. Alder Mill
Twisp, WA
19. Anaconda Copper
Weed Hts, NV
20. Anaconda Refinery
Great Falls, MT
21. ASARCO Globe Facility
Commerce City, CO
22. Blackbird Mine
Cobalt, ID
23. Gateway Mill site
Gateway, CO
24. Hendricks Mine
Boulder, CO
25. HoldenMine
Holden Village, WA
26. LomaMill
Loma, CO
27. Placerville Tram
Placerville, CO
28. RioTinto
Mountain City, NV
29. Sawpit Tram
Sawpit, CO
30. Silver Mountain Mine
Lomis, WA
31. Vanadium Mill Site
Vanadium, CO
Metals mill
Copper mine
Copper and zinc refinery
Metal recovery (smelting)
Mine
Vanadium mill
Radium and flourspar mill
Metals mine
Vanadium mill
Vanadium tram/ore bin
Copper mine
Vanadium tram/ore bin
Gold and silver mine
Vanadium mill
of the 14 additional sites have "observed" (that is, measured re-
leases) in some route category. Although a site may be well kn°^n
for some environmental impact, it may not be in an area scored by
the Mitre Model. For mining sites, for example, acid mine drain-
age and its effect on aquatic life are often of concern; this is the
case at eight of the 17 NPL sites. No score is given for acidity in the
Mitre Model.
The routes which contributed to scoring at the 31 sites are shown
in Table 2. Unlike groundwater and surface water, the air route
only contributes when there is a measured release (rather than a
likely release). The reason the air pathway does not occur for the
non-NPL sites is that they generally do not have as extensive
measurements as the NPL sites. Almost all mining sites consider
both groundwater and surface water pathways in the scoring with
the highest scores generally being obtained for the groundwater.
Overall structure of the model in combining source, release and
population information is shown in Figure 1. The information re-
quired is designed to be readily available rather than self consis-
tent.
To gain some insight into what distinguishes the NPL from the
non-NPL sites, a sensitivity analysis was performed for each
parameter occurring in each pathway score. This was done by de-
creasing each parameter score by 50% and calculating the overall
change in the total score. An example will make this procedure
clearer. At the first entry in Table 1, the Anaconda Smelter Site
in Anaconda, Montana, the total migration score is 58.7. In ob-
taining this result, "quantity of waste" in the groundwater path-
way was scored as 8 points. Had quality of waste been scored as
4 points, the migration score would drop by 6.0 points to 52.7.
For the parameter "toxicity/persistence" in the surface water path-
way, a score of 18 was recorded. Had this score recorded as 9
points, the migration score would drop by 2.7 points to 56.0.
Hence, the overall score is more sensitive to the value of the first
parameter. The results when all pathways are combined so that
"observed release" represents any of the three pathways, etc., are
shown in Table 3. The different pathways were combined because
they basically all behave the same way.3
Table 2
Mitre Model Scoring
NPL Sites (17)
Considered
Highest Score
Non-NPL Sites (14)
Considered
Highest Score
Air (%)
41
18
0
0
Groundwater (%)
94
65
100
71
Surface
Water (%)
88
18
100
29
Table 3
Sensitivity Analysis for 17 NPL Sites
Parameter Importance
1st 2nd 3rd
"Observed release" 16 1
Distance to well or
intake/population 12 5
Toxicity, persistence 4 11
Quantity 1
Water/land use
Containment 1
4th
2
1
2
8
3
1
5th
4
3
4
6
1
2 lrm is the mining diMiviu niajnh responsible for the Mure Model score At some sites, non-
mmmg u>cs A!VO contribute ic» (he wore- At other siies, ihe use has now changed from lhai listed.
3. Numbers may add 10 more lhan |7 horizontally, because more than one pathway is con-
sidered.
14
SUPERFUND MANAGEMENT
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QUANTITY FROM TOTAL VOLUME
• OF SPOILS OR TAILINGS.
IRRESPECTIVE OF TOXICITY
TOXICITY FROM MOST HAZARDOUS
MEASURABLE COMPONENT.
IRRESPECTIVE OF QUANTITY
MEASUREMENT FOR
OBSERVED RELEASE
AT SITE, IRRESPECTIVE
OF LEVEL ABOVE BACKOROUND
POPULATION WITHIN
3-4 MILES, IRRESPECTIVE
OF EXPOSURE LEVEL
Figure 1
Overview: Mitre Model Methodology
IF A CHEMICAL DUMP >10,000
DRUMS WITH DIOXIN, ETC.
OH A MINING SITE
MAXIMUM SCORE
•WASTE
CHARACTERISTICS'
NOMINATION
MAXIMUM SCORE
•OBSERVED RELEASE'
NPL LISTING
(MINING) COMMUNITY POPULATION
MORE THAN 100 PEOPLE
WITHIN 3-4 MILES
Figure 2
National Priorities List (NPL) Overview: Mitre Model Logic
The fact that the maximum number of sites occurs along the
diagonal in Table 3 indicates a consistent pattern of parameter im-
portance. Whether or not there is an observed release is almost al-
ways (16 times out of 17) the most important factor; popula-
tion factors and distance to well or intake are usually the second
most important factor and so on.
This picture of how the Mitre Model works can be simplified
even further by just considering the top four parameters in Table 3
and recognizing that for parameters such as distance to well/pop-
ulation served or distance to stream/population, the population
portion of the parameter is a good indicator of this whole fac-
tor (of course, it is the whole factor for the air pathway) since peo-
ple require wells or surface water.4
Results are shown in Table 4 for the rule: "Observed release,
population greater than 100 and (near) maximum toxicity, persis-
tence and quantity in any one pathway produces an NPL site/
—failure to satisfy these conditions does not."
The two sites not satisfying this rule are of particular interest.
Alden Mill has the highest score of any non-NPL site, higher than
several of the NPL sites, but the score is based on "unproven"
arsenic content of the waste. This may be why it is an exception to
the selection rule and was not listed. The NPL site not satisfying
the rule is Celtor Chemical. It scores maximum on toxicity, persis-
tence and quantity and has a population nearby of more than 100,
but it is an inferred rather than an observed release. It has the
second lowest score5 of the NPL sites and, in fact, is lower than the
score for Alden Mill. The Celtor Chemical site scores fairly high on
direct contact, however, and is said to be a children's play area on
the Hoopla Indian Reservation. Although the direct contact hazard
to children does not enter into the migration score calculation, it
may be the reason why this site is an exception to the selection
rule.
Table 4
Percentage of Sites Satisfying the Selection Rule
NPL Site6 94% (1 site not an observed release, 16
satisfy the rule)
Non-NPL Sites 6% (13 sites satisfy the rule, 1 does not)
MINING SITE CHARACTERISTICS LEADING TO LISTING
In summary, the way the Mitre Model treats mining sites can be
represented by the equation:
Mitre Observed Quantity Population
Model = Release x Toxicity, x Score
Score Score Persistence
Score
As illustrated in Figure 2:
•Mining sites almost automatically receive the maximum quantity,
toxicity, persistence score based on total amount of tailings,
spoils, slag or discharge and on the presence of the small amounts
(relative to bulk water) of metals, etc. Of the 31 sites, 26 had max-
imum or next to maximum scores in some pathway for this factor.
•A mining site which is nominated for the NPL will tend to have
maximum score for an "observed release" in at least one path-
way (27 of the 31 did) because only sites that have been previous-
ly studied tend to be nominated and any concentration measure-
ment above background (no matter how small) constitutes an ob-
served release.
•With maximum scores in these two areas, the total score will be
high enough for listing on the NPL unless there are virtually no
people in the area. Twenty-five out of the thirty-one sites had
more than 100 people within three or four miles.
WHY 14 SITES WERE NOT LISTED
The specific reasons, in terms of the three factors comprising
the rule, why the 14 non-NPL sites failed to score high enough for
listing is shown in Table 5. Results are given only for the highest
scoring pathway.
Lack of an observed release and little or no population nearby
are the most common reasons for low scores. Of the five cases
where quantity and toxicity/persistence scores were not (near) max-
imum, two of the sites were tram sites and the quantity of waste
was actually relatively small. At another two of the five sites, the
toxicity and persistence scores were based on sulfuric acid and cy-
anide rather than trace metals in the waste. Had the scorer
selected metals, maximum toxicity/persistence scores would have
been achieved.
4. The population figure used is the figure mentioned in scoring that pathway at that site.
5. The lowest scoring NPL site is the Mountain View Mobile Homes asbestos site.
6. One NPL site has next to maximum score in the dominant pathway for the toxicity/persis-
tence parameter. Score in this pathway is based on copper rather than cadmium which was used
in the other pathway and which would have produced a maximum score. All the others score the
maximum in these categories.
VALIDITY OF MODEL APPLICATION TO MINING
After reviewing the 31 sites nominated for the National Priorities
List, the authors of this paper are convinced that what distinguishes
SUPERFUND MANAGEMENT
15
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Table 5
Reasons Why 14 Mining Sites Nominated Were Not Selected for the
National Priorities List—Properties of Highest Scoring Pathway
Sice
No.
18
19
20
21
22
23
24
25
26
27
28
29
30
31
TOTAL
No. Obs.
Release
X
X
X
X
X
X
X
X
8
Less Ihan
(New) Max.
Quantity &
ToxiciCy
X
X1
X'
X'
X1"
5
Population Less
than 100
Within 3-9 Miles Other
X X'
X
X
X
X
X
6 1
7, "Unproven Arsenic Content of Waste," see tent.
8 Tram site
9, Based on sulfunc acid not metals.
lO.Ba^cd on cyanide solution not metals.
NPL sites from non-NPL sites is not primarily degree of hazard.
Rather, the distinction is based mainly on how much prior study
has been done at a site and how rural the surroundings are. It
could be argued that both of these factors correlate to some ex-
tent with degree of hazard. This is true, but the model then must
be viewed as assessing risk in an extremely indirect way.
As has been noted, special characteristics of mining sites that
contribute to high Mitre Model scores are the large amounts of
waste involved and the presence of trace metals in the waste. These
characteristics tend to produce maximum scores in one of the three
scoring areas—groundwater, surface water or air. Thus, scores in
the other two areas which are too small to produce listing at a
chemical dump may be sufficient to list a mining site.
It is concluded that the Mitre Model is not a useful tool for
assessing or ranking hazards at mining sites because the score is
produced by factors which have little to do with the actual haz-
ards at the site. The Mitre Model seems to have been developed
with chemical dumps in mind. In that context, its scoring system
may be more useful. For example, maximum quantity of waste may
indicate more than 10,000 drums of chemical present rather than,
as for mining, more than 2,500 tons of spoils, slag, or tailings.
Maximum toxicity at a chemical dump may indicate presence in
concentrated form of very toxic or carcinogenic compounds rather
than, as at many mining sites, the normal and unconcentrated ele-
ments in the earth at the site.
16
SUPERFUND MANAGEMENT
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LESSONS LEARNED BY THE CORPS OF ENGINEERS ON TWO
SUPERFUND REMEDIAL PROJECTS
BRIAN V. MORAN
U.S. Army Corps of Engineers
Directorate of Engineering & Construction
JOSEPH R. TURNER
U.S. Army Corps of Engineers
Construction Division
Huntington, West Virginia
INTRODUCTION
In implementation of the Congressionally mandated program for
cleanup of the Nation's most serious hazardous waste sites, the
USEPA and the U.S. Army Corps of Engineers signed an inter-
agency program management agreement in February of 1982.
Under that agreement, and on specific request from USEPA, the
Corps is managing Superfund program remedial action design and
construction contracts, and, additionally, is providing several
forms of Superfund-related technical assistance to USEPA.
Corps involvement is triggered through USEPA's three-tiered
lead role determination process. In this process, as many are aware,
USEPA first determines whether a private party or organization
is liable for cleanup and asks that entity to do the necessary work.
If that request does not produce positive results, then, in a second
approach, USEPA determines whether the state in which the
is located can and will do the cleanup. If the state declines, Fed-
eral-lead cleanup is designated, and USEPA requests that the
Corps undertake management of appropriate remedial action,
(design and construction).
With Federal lead remedial projects, the Corps' primary respon-
sibility under the interagency agreement is to serve as manager for
remedial action design and construction, acting as the Federal gov-
ernment's contracting officer. Included in this role is the procure-
ment and management of the services of architect-engineer firms
involved in project design and of construction firms engaged in ac-
tual site cleanup and material disposal work.
Secondary Corps responsibilities include providing technical
assistance to USEPA through reviews of USEPA-managed feas-
ibility studies and, on request, reviewing site cleanup plans for
state-lead remedial actions. The Corps also served, in one recent
case, as USEPA's on-site "oversight," representative at a remedial
project being cleaned up by the waste generator. The Corps under-
stands that there is a good possibility that it will be called on to do
more of this type of "oversight" review and monitoring work in
the future.
Throughout the program, overall guidance, policy and funding
for Corps support remains with USEPA.
Before the Corps begins work at a hazardous waste site, sev-
eral things have already been settled by USEPA, the state in-
volved and others. Decisions about cost recovery have been made;
public participation has been arranged; assurances on site main-
tenance have been given, National Environmental Policy Act doc-
uments have been initiated and permits and real estate rights have
been obtained.
During the preliminary site investigation and feasibility study
phases of a cleanup action, the Corps provides technical assis-
tance which assures that the proposed action USEPA has selected
is technically feasible and can, in fact, be engineered and con-
structed. The Corps would not accept management of a cleanup
action if it thinks it can not reasonably be designed, constructed,
operated and maintained.
The Corps is also responsible for developing, at each site, a site
safety plan based on information contained in the remedial in-
vestigation and feasibility study. This plan covers the health and
safety of personnel involved in site design and in the actual cleanup
operation. It also covers the health and safety of populations in
the immediate site area. Implementation of this plan is shared be-
tween USEPA and the Corps. Corps responsibility is limited to de-
sign and remedial action personnel, while USEPA coordinates all
actions involving off-site populations. In addition to development
of the site safety plan, the Corps is responsible for environmental
monitoring during the design and construction phases; preparation
of site operation and maintenance manuals; facility start-up; oper-
ator training; and for assisting USEPA in the implementation of
community plans.
LESSONS LEARNED FROM THE LEHIGH ELECTRIC
AND CHEM-DYNE PROJECTS
Lehigh Electric and Chem-Dyne were the first two major Corps
Superfund projects. The Lehigh site involved the cleanup of poly-
chlorinated biphenyls (PCBs), PCB contaminated equipment,
transformers, capacitors and debris. (Figure 1) The site was form-
Figure 1
The Lehigh Electric Site was an electrical equipment storage and repair
facility. Large quantities of PCBs were spilled and released at the site.
SUPERFUND MANAGEMENT
17
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erly a transformer repair facility which contained numerous trans-
formers, many of which contained high level PCB fluids. The site
is located in Old Forge, Pennsylvania and is enclosed by a fence
surrounding the zone of contamination estimated at 6.4 acres. This
contaminated zone covered not only the Lehigh Electric and En-
gineering Company, but also adjacent properties.
The first phase of the project involved surface removal of waste
materials and demolition of existing structures. This phase was
completed on time and under budget. A second "Phase II" Le-
high project is now being undertaken to remove contaminated soils
and restore the site to its original condition.
The Chem-Dyne project involved removal of a wide assortment
of inorganic and organic chemical wastes and sludges, demolition
of contaminated tankage and buildings, as well as contaminated
soils removal. This site is located near the center of Hamilton, a
city of 65,000 residents, approximately 20 miles from downtown
Cincinnati. At one time, over 30,000 drums were stored at Chem-
Dyne, a site that was supposed to recycle this hazardous material.
(Figure 2).
Figure 2
The Chem-Dyne site formerly contained some 30,000 drums of
hazardous wastes.
l»
Figure 3
The hazardous nature of chemicals on site calls for a contractor with
specialized expertise and proven experience in hazardous waste cleanup.
The most notable incidents connected with this site have been
two major fires and a fish kill in the nearby Great Miami River
that extended for 37 miles. The Chem-Dyne operation soon be-
came a huge receiver of hazardous waste materials and served some
of the nation's largest companies before going bankrupt in 1980.
As a result of completing these projects, the Corps has pro-
gressed further along the "learning curve" in developing its exper-
tise for management of cleanup of abandoned hazardous waste
sites. The following information highlights the numerous contract-
ing and implementation considerations that the Corps has learned
from those projects which will be incorporated into future Corps
USEPA Superfund remedial projects. The "lessons learned" in-
formation from these projects is broken down into three categor-
ies. Contracting Considerations, Operating Considerations and
Regulatory Considerations.
Contracting Considerations:
•Working relationships, including responsibilities, should be estab-
lished with all agencies involved prior to advertising for bids.
•Responsibilities for all state and government agencies involved
should be resolved prior to initiation of site cleanup. At Chem-
Dyne, a few contract modifications were requested which could
easily have led to conflict had the Corps not previously discussed
proper procedures for each agency to accomplish its responsibil-
ities. It is important, also, that the cleanup contractor understand
he is working only for the Corps of Engineers while on site and
not for any other agency. Other agencies should present any pro-
posed modifications or other comments to the Contracting Offi-
cer in the lead Corps district for discussion and implementation.
•Many cleanup contractors are accustomed to bidding cleanup/re-
medial work on a time and materials basis.
The lump sum method of bidding these projects, if utilized,
can pose problems to prospective contractors due to unforeseen
conditions encountered. Therefore, contract provisions should
be included which allow methods of reacting to unknown site
conditions. Contract language should always be specific as to ex-
actly what is to be removed/disposed of under contract. Con-
centrations of contaminants to be removed must also be defined
as accurately as possible in the bid packages.
•Property boundaries under USEPA jurisdiction should be well de-
fined in the contract. At Lehigh, contaminant boundaries dif-
fered from contract boundaries. Project boundaries should
normally be the contamination boundaries.
•All required rights of entry should be obtained prior to advertis-
ing for bids for site work. At Chem-Dyne it was necessary to post-
pone the bid opening because of questionable rights of entry. This
postponement caused much community concern. Prior to in-
itiation of cleanup contract work, all necessary rights of entry for
this project had to be obtained. This precedent of obtaining the
necessary rights of entry prior to advertising will be standardized
for future Federal Corps Superfund cleanups.
•Contaminant testing procedures should be clearly defined and al-
ways conform to accepted procedures. Testing to be done by A.E.
vs. contractor firms should also be clearly defined. In many in-
stances, contaminant testing should be priced as unit cost items,
since testing costs are often a significant percentage of total costs
and are related to other unit costs test items.
•Bid packages should include aerial photographs and on-site
photos of disposal areas, when possible, to provide prospective
bidders with visual information on what can be anticipated at the
site.
•Disposal options—Local constraints which may preclude lower
cost disposal options for wastes, such as local industrial waste
landfills (thereby driving up project costs), should be investi-
gated.
•Although usual Corps contracting procedures require local labor
use, local labor is usually unsatisfactory for doing this type of
project due to the specialized nature and hazards involved. (Fig-
ure 3). For future projects, however, the Corps is exploring the
possibility of expanding the field of prospective bidders to in-
clude local construction contractors for the less serious, lower
risk sites.
•Safety—Sufficient and adequate safety equipment must be avail-
able for both on-site government personnel and official visitors
and should be specified in the bid package.
SUPERFUND MANAGEMENT
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•Personnel productivity levels should be considered when writing
contract documents which involve mandatory use of specialized
safety equipment such as "moon suits" and self contained breath-
ing apparatus.
•The contractor's industrial hygienist is expected to check during
the site evaluation to see whether the protective equipment spe-
cified in the contract is appropriate. Corps division and district
personnel with expertise in industrial hygiene and occupational
health will review the contractor's safety evaluation before
changes are allowed in the contract. If changes are necessary,
contract requirements and costs must also be adjusted.
Operating Considerations:
•Early attention must be given to public affairs and public aware-
ness prior to on-site activity. At Chem-Dyne, the USEPA and the
Ohio EPA had been active for several years in community rela-
tions programs. As the bid opening approached, however, addi-
tional pressure was applied by local population to clean up the
site safely and promptly. The local clamor soon attracted na-
tional press attention which continued throughout the project.
Normally, two news articles a day were published concerning ac-
tivities at the site. Only during the right of entry problem and the
bid protest issue did the press tend to be somewhat critical.
Public relations and the division of work were well established
during the project. The public expected the safest methods to be
used and to be kept fully informed as work progressed. When
the first load of hazardous waste left the site, a public gathering
cheered its exit from the Chem-Dyne facility.
•On-site testing and monitoring procedures should, as much as
possible, follow standard, recognized methods. Equipment and
procedures should be chosen which produce results that are both
accurate and useable within design parameters. Limitations of
test procedures and equipment should be known and factored in-
to site specific actions.
•The importance of QA/QC (quality assurance and quality con-
trol) must not be underestimated. Based on the Corps' Lehigh
experiences, it has developed general guidance for QA/QC to in-
clude formats for site specific QA/QC plans.
•Detailed records must be maintained for all wastes removed (Fig-
ure 4) and kept track of by: color coding, manifests and ADP
system (large projects).
•At Chem-Dyne, it was realized that weight measurement pay-
ment by the ton would be more appropriate measurement than 55
gal drum equivalents due to the large quantities of waste to be re-
moved from the site.
•At Chem-Dyne, a detailed grid system and alphanumeric coding
system was designed for tracking the waste drums. These data
were then entered into a Corps computerized data management
system specifically tailored for this purpose.
•The formulation of a good safety program is a must for a haz-
ardous waste site. At Chem-Dyne, the site is located near the
center of a city of 65,000 people. Private homes and factories
overlooked cleanup operations and safety procedures were con-
stantly under the surveillance of local residents. Any potential
incident or release of contamination quickly kindled an interest
in site safety and off-site safety. At Chem-Dyne the fear of fire
was very real with local residents, since several fires had occurred
during operations of the facility. Because of this, the public was
very interested in the air monitoring system, which was designed
to detect hazardous gases leaving the site.
•Safety—Health physicals should be specifically tailored to each
project, reflecting potential exposure to contaminants of con-
cern. Tests should also be sensible. For instance, serum PCB
testing at Lehigh (as originally proposed) would have had little
value since PCB accumulates in fatty tissues, not blood.
•Security guards are not currently allowed on site in the exclusion
areas. Since situations could arise where they may need to go into
these areas, future contracts will normally provide safety training
to these personnel so they may proceed.
•Emergencies (Chemical exposure/injury, fire/explosion, environ-
mental accident)—Arrangements must be made with local and
state emergency response personnel prior to construction to in-
sure that response personnel are trained and equipped to handle
all possible on-site emergencies. The site specific safety plans
prepared by the Corps will include an analysis of the types of emer-
gencies possible at the site, the procedures to be followed in the
event of such an emergency and the local and state emergency
response personnel which may be necessary to support cleanup
activities and protect persons on and off-site. As part of the site
specific safety plan, a safety expert should be readily available,
or on call, to make timely safety decisions which may affect pro-
ject operations. Local police and fire departments, ambulance
teams and hospital emergency rooms may need additional emer-
gency and personal protective equipment, or their personnel may
need specific training to provide the proper support needed in case
of an emergency.
•Qualitative air monitoring is currently performed only during
working hours with "after the fact" laboratory analyses. A more
appropriate technique would be to employ a continuous real
time" monitoring direct reading system that would also provide
instantaneous data at different areas on the site during non-work-
ing hours. This is particularly important where a site is in close
proximity to a residential area where the immediate safety of the
local populace is of concern.
•Training materials and courses available in the hazardous waste
handling and disposal field should be well documented and made
available to Corps of Engineers lead districts. To meet this need,
a Superfund Training Manual is now available to all Corps dis-
tricts. Lead district personnel will use this manual as a guide, but
must pursue training rigorously as there is much competition for
training spaces.
Regulatory Considerations
•It is important to have a working knowledge of USEPA, State
and local regulations in order to avoid regulatory conflicts dur-
ing the course of the project. For example, some state regula-
tions are more stringent than Federal regulations. Potential con-
flicts should be identified and resolved prior to initiation of con-
struction.
•Before construction, it is important to ensure through USEPA
regional offices that all necessary permit applications, USEPA
RCRA Hazardous Waste Program are understood and complied
with. These requirements should be coordinated with the USEPA
regional offices prior to initiation of construction.
Figure 4
Detailed records must be maintained for all wastes removed.
SUPERFUND MANAGEMENT 19
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•Who signs the "Hazardous Waste Manifest" must also be de-
fined in bid documents. The specifications for Chem-Dyne clean-
up stated that the cleanup contractor would be responsible for
signing the "Hazardous Waste Manifest" as the generator, thus
accepting responsibility under the requirements of RCRA for the
wastes.
Even with this clear statement in the contract specifications,
it was necessary to direct the contractor to sign the manifests.
Evidently cleanup contractors are reluctant to sign these "Haz-
ardous Waste Manifests" as the generator because of the inherent
Figure 5
Load contents being verified before leaving site. Accurate manifest
preparation is important.
liabilities. The question of "who is a generator" at a Superfund
remedial project is a tough one with which both USEPA and the
Corps are currently struggling.
•Documentation requirements must be agreed upon with USEPA
and the state agency at the earliest possible date. At all hazardous
waste site cleanups, litigation is at some stage with site owners,
operators and generators. At Chem-Dyne, over 200 parties are
involved for both surface cleanup and subsurface contamina-
tion. USEPA and Ohio EPA have asked for extensive documen-
tation from the Corps as to the location and condition of each
drum. It is necessary to use a computer to realistically manage
this information for 8,500 drums. (Figure 5).
SUMMARY
These are some of the most important lessons the Corps has
learned to date on administering Superfund remedial projects.
The Corps is certainly "further along the learning curve" than it
was a year ago. Undoubtedly, however, much more will be learned
as the Corps undertakes its role in the Superfund program.
The Corps is proud of its involvement in this critical program
for cleaning up the nation's abandoned hazardous waste "toxic
time bombs." It believes that its experience in design and con-
struction management will insure cost-effective cleanup of these
sites in an environmentally safe manner.
ACKNOWLEDGEMENT
Mr. David Deeds and Mr. Ken Zimmerman, Corps of Engi-
neers Huntington District, for their contribution of information
concerning the Chem-Dyne project, and Mr. Edward Cox and
Mr. Dennis Dubreil, Corps of Engineers Baltimore District, for
their contribution of "lessons learned" on the Lehigh project.
20
SUPERFUND MANAGEMENT
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WATERWAY DECONTAMINATION—FOUR CASE STUDIES
JOHN C. HENNINGSON
Malcolm Pirniejnc.
White Plains, New York
PROBLEM DEFINITION
Many of the nation's rivers are contaminated by significant levels
of toxic and/or hazardous organic chemicals. In addition, many
ports and harbors have substantial contamination by heavy metals.
The nature of contaminants, amount and areal extent vary greatly
as indicated in Table 1. These conditions often result in significant
risks, impacts and economic effects.
The extent of exposure and impacts for such contamination is
often much greater than that associated with upland uncontrolled
abandoned sites. Currents, tidal movements and storms exacerbate
the original contamination of sediments by industrial outfalls.
Storm surges are difficult to predict and may result in significant
redistribution greatly increasing the costs and decreasing the
feasibility of complete cleanup.
In this paper, the author utilizes four examples to clarify the
unique problems associated with waterways contamination. In par-
ticular, the possibility for catastrophic loss or redistribution of con-
taminated sediment would seem to warrant special consideration
and a high priority for cleanup.
HUDSON RIVER, NEW YORK
The study area is illustrated on Figure 1 and includes the upper
40-mile reach of the Hudson River from Albany to Fort Edward
and the lower 140 miles to New York City, which is tidal. The
primary source of the polychlorinated biphenyls (PCB) was the
General Electric Company in the Fort Edward-Hudson Falls area.
The material was discharged directly via an effluent stream to the
river and, in addition, contaminated solid waste and drums were
put in a number of landfills throughout the study area. Some initial
dredging of PCB-contaminated bed materials has been undertaken
in order to maintain the navigation channel in this part of the river.
Approximately 200,000 yd.3 of material were removed in 1977 and
1978, using state funds and funds from a settlement with General
Electric. This has provided significant experience with regard to
dredging equipment capabilities and sediment/contaminant loss
rates. These losses have been estimated in several cases, but this
dredging project provided the opportunity to monitor and test
specific containment methods.
The Hudson River from New York to Albany is a tidal estuary
and is a significant fishery or nursery area for striped bass and
shad. The area above Albany to Fort Edward is a series of pools
formed by eight dams and locks. The pools facilitate navigation of
the Champlain Barge Canal and several of the dams provide
hydroelectric power. In the past, the river has been used extensively
for the transportation of timber and bankside processing of wood
Table 1
Examples of Contaminated Waterways
Location
Illinois
Indiana
Massachusetts,
Connecticut
Massachusetts
New York
New York
New York
Virginia
Virginia
Washington
Wisconsin
Wisconsin
Wisconsin
Name & Type of
Waterway
Waukegan Harbor
Grand Calumet River and
Indiana Harbor Canal
Housatonic River
Acushnet Estuary
Hudson River & Estuary
Oneida Lake
Niagara River
James River/Chesapeake Bay
Shenandoah River
Commencment Bay
Fox River
Sheboygan Harbor
Milwaukee Harbor
Nature & Extent of
Contamination
PCB; source to Lake
Michigan
PCB; source to Lake
Michigan
PCB; over 100 miles of river
PCB
PCB; over 150 miles of river
& New York Harbor
Mirex
Dioxin
Kepone
Mercury
Various contaminants
PCB; source to Lake
Michigan
PCB; source to Lake
Michigan
PCB; source to Lake
Michigan
products in local lumber mills. The PCB problem first came to light
after an additional dam was removed at Fort Edward in 1973. This
was a timber crib dam in imminent danger of failure. After removal
and subsequent flooding in late 1973 and 1974, approximately
900,000 yd3 of material scoured downstream. At the time the dam
was removed, no one realized that the sediment in the former pool
behind this dam was heavily contaminated with PCB.
Before action could be taken, a 100-year flood occurred in 1976
which moved over 300,000 additional yd3 of highly contaminated
material [< 1,000 mg/1 PCB] downstream into over 40 "hotspots"
exceeding 50 mg/1 (Figure 2). It is fortunate that the upper river is
composed of a series of dams and pools which trapped most of this
material before it reached the estuary.3 However, another storm of
similar magnitude may result in even greater redistribution and
make river cleanup unfeasible.
The contamination in the Hudson River System has caused the
closing of commercial fishing for most species and advisories
against consumption of sport fish by recreational fishermen.' In
SITE INVESTIGATION
21
-------
0 oTLy (
HI TDIl lUTt
PCI lECUUTItt
rioted iiu
Hi COIfS V (
FCIUU CHIMEL
•IIIUUCE OICOCIU
HUDSON RIVER BASIN
(FORMER SITE OF
GENERAL MOTORS
FOUNDRY)
Figure 1
Hudson River Basin Map
Of (irilOrioui COlSdrmoi
I If II I4IC tl»l I 1111
Figure 3
Location of Outboard Marine Corporation Plant and PCB Outfalls
in Relation to Slip #3 and the North Ditch
SLIP NO.3
SLIP NO.I
LARScN
r HAS I ME
WAUKEGA.N
PORT
DISTRICT
CREATES THAN SCO PPM
•lil 50-500 PPM
LESS THAN 50 GREATER
THAN 10 PPM
10 PPM OR LESS
LAKE MICHIGA.1
Figure 2
Map of PCB-Contaminated Areas in the Hudson River
Figure 4
Extent of PCB Contamination in the Waukegan Harbor
SITE INVESTIGATION
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addition, the contamination of sediments has made the
maintenance of navigable waters difficult and expensive since
highly contaminated dredged material must be placed in upland
sites suitable for such materials.2 Furthermore, the continued
utilization of the river as a public water supply has been the subject
of considerable controversy.'
Several alternatives have been evaluated for reclaiming this reach
of river. No action is unacceptable, since as long as the PCBs are in
the sediment, they are subject to movement and flushing
downstream. There is enough PCB, over 400,000 Ibs in this reach
of river, to serve as a source of PCB in contamination of fish in the
lower river virtually forever. As long as it is there, there will be an
uptake into the fish resulting in levels in the flesh of over the FDA
limit of 2.0 ng/g. Dredging seems to be the only practical remedial
action. In the review of the feasibility of dredging, a number of fac-
tors were considered: the technology that is currently available,
emerging dredging technologies, the costs of various dredging
systems, the environmental effects associated with various systems
and the factors that would have a bearing on whether a remedial
program could be implemented—including financing and manage-
ment of the system.
In 1980, the U.S. Congress provided for the utilization of funds
under Section 201 of the Clean Water Act to clean up the Hudson
River. The USEPA is currently opposing this approach and recom-
mending that a more appropriate mechanism would be the Super-
fund. The net result has been a lack of the approvals necessary to
take decisive action and an increased risk of catastrophic loss of
PCB to the estuary.9 This congressional appropriation of $20 x 106
will be lost unless action is taken by Sept. 1983.
The USEPA has initiated preparation of a Remedial Action
Master Plan (RAMP) to define the approach to developing feasible
remediation alternatives. Unfortunately, the RAMP and subse-
quent feasibility studies cannot be completed prior to the deadline
for existing fund allocations. Therefore, several private groups and
New York State have recently filed legal action against the USEPA
to release the funds.
WAUKEGAN HARBOR, ILLINOIS
Waukegan Harbor is located on the west shore of Lake Michigan
at Waukegan, 36 miles north of Chicago and 47 miles south of
Milwaukee (Figure 3). Waukegan, a city of 65,259 people (1970
census), encircles the irregularly-shaped harbor. It is a busy fishing
and charter boat area and prides itself on being a "Salmon
Capital." The area of the harbor, exclusive of the mouth, is ap-
proximately 37 acres. Water depths vary from 14 to 25 ft with some
shallower spots near boat launching locations and in the far upper
reaches of Slip No. 3."
In order to maintain the navigational use of the harbor, the U.S.
Army Corps of Engineers traditionally dredged an average of
30,000 yd3 of sediments per year near the main entrance channel.
With the exception of the removal of a small amount of uncon-
taminated material (contaminated to less than 1 ppm) from the
southeast corner by the Waukegan Port Authority, no dredging has
been performed in the harbor since PCB contamination was
discovered in 1975."
The total volume of contaminated sediments in the harbor is
estimated to be 168,000 yd3 containing up to approximately 275,000
Ibs of PCBs. Harbor sediments consist basically of: 1) a top soft
"muck" layer, 2) an underlying sand layer and 3) a generally im-
pervious silty clay layer. The muck layer varies from 0 to 10.5 ft in
thickness. Available data have shown that this layer is con-
taminated at all depths and at any given location in the harbor.
Contamination is highest in Slip No. 3 (as high as 500,000 ppm or
'50% PCBs) and decreases toward the harbor mouth, where concen-
trations drop to the 5 to 10 ppm range. The sand layer varies from 0
to 9 ft in thickness. The contamination level of this sand is less than
5 ppm, except below the old OMC outfall in Slip No. 3. The
underlying gray silty clay is generally impervious, but may contain
some gravel, sand or thin organic seams that could allow PCB
penetration. PCBs have been found to be less than 1 ppm in this
layer, except immediately below the Slip No. 3 outfall.4
The zones of harbor contamination exceeding 500 ppm, 50 ppm
and 10 ppm PCBs respectively, are shown on Figure 4. The high
concentrations found in Slip No. 3 suggest that nearly pure PCB
hydraulic fluid must have been deposited from the OMC outfall in-
to harbor sediments during the years of maximum PCB fluid
leakage. These PCBs have now spread out into the harbor through
the muck layer.*
PCB contamination of fish caught in the harbor averages 18
ppm, and two groups of lake trout collected in the lake near
Waukegan had 3.4 ppm and 5.4 ppm average concentrations,
respectively. When these levels are compared with the FDA tem-
porary tolerance limits of 5 ppm and proposed limits of 2 ppm, it
suggests that all fish caught in Waukegan Harbor, and some caught
in the nearby area of the lake, are unfit for regular consumption.4
The levels of PCBs in the waters of the harbor, the nearshore
areas and even the lake itself are higher than the water quality
criteria currently recommended by USEPA. These elevated levels
are of great concern because of their effect on fish contaminant
levels and human health due to the high bioaccumulation factors.
PCB levels in the open waters of Lake Michigan range from 5 to 10
ng/1 and, typically, up to 50 ng/1 in nearshore waters. This is
substantially above the USEPA recommended levels of 1 ng/1 or
less, designed to reduce levels in fish to those acceptable for human
consumption. Levels in Waukegan Harbor are much higher, rang-
ing from less than 100 ng/1 in the harbor channel to several thou-
sand ng/1 in Slip No. 3."
A second area of excessive PCB contamination by OMC, in addi-
tion to the harbor sediments, has been found in the nearby "North
Ditch" and in the soils of the adjacent parking lot for OMC
employees. The North Ditch is a small tributary approximately
1,500 ft north of the harbor, which drains 0.11 mi2 of property
owned by OMC and the North Shore Sanitary District. About 40%
of this area has an impervious surface (roads, railroads, buildings
and parking lots). Upstream from OMC, North Ditch drains an
area of landfill (which served as a disposal site for urban debris)
composed of sandy material. It then crosses the Elgin, Joliet and
Eastern Railway Company tracks via a 36 in. culvert, before enter-
ing OMC property.4
The North Ditch apparently received the largest portion of all
PCBs discharged from OMC between 1959 and 1972. These PCBs
may be found in very high concentrations; as much as 25% PCBs
(250,000 ppm) had been found in surface sediments near the OMC
outfalls and 38% PCBs in underlying sediments as early as 1977.
Concentrations as high as 24,000 ppm were found 7 ft below the
ditch. The worst areas are immediately downstream of OMC's
former outfalls which carried the heaviest PCB load from the old
die cast building. Downstream surface concentrations stay above 50
ppm almost to the lake. Based on data gathered through 1977, it
was estimated that approximately 4,500 yd3 are contaminated at a
level higher than 50 ppm PCBs, and 6,300 yd3 at a level above 10
ppm.4
High soil concentrations of up to 14,000 ppm PCBs were also
found just south of the North Ditch and only 500 ft from the lake
in OMC's parking lot area. Six other samples exceeded 1,000 ppm.
Contamination of groundwater, in levels ranging from 2 to 680
fig/\, was found in sampling conducted by OMC's consultant on
the OMC site in 1977. Concentrations of PCBs that have been
found in soils on OMC property are higher than the level at which
PCB contaminated materials are required by USEPA regulations to
be contained in a secure landfill approved for PCB disposal.4
The North Ditch discharges PCBs to the lake during its regular
flow and during rainstorms. OMC's consultant estimated, in 1977,
that roughly 7 to 8 Ib/yr were entering the lake through this route.
In USEPA's view, there is the possibility that the ditch could,
under special conditions, produce large additional releases of
PCBs.4
Finally, the slow migration of PCBs through the contaminated
soils results in a gradual release of PCBs into shallow groundwater
SITE INVESTIGATION
23
-------
aquifers which are believed to be discharging into the lake. As
PCBs are probably spreading through the groundwater and soils,
this source is believed to be increasing.'
To date, no less than three separate evaluations have been con-
ducted to determine the most feasible course of action for
remediating the problems in the vicinity of the OMC plant. The
range of alternatives which have been considered include: no ac-
tion, stabilization in place, removal and disposal on-site and
removal and disposal off-site. Suboptions involving portions of the
harbor and/or the North Ditch were also considered. The projected
costs of remediation have ranged from $2,000,000 to $40,000,000.'
Following the detection of contamination in 1975, the State of Il-
linois and OMC initiated negotiations. In 1978, after negotiations
broke down, the U.S. Attorney filed a suit on behalf of the
USEPA. Subsequently, the State of Illinois and Monsanto, the
PCB supplier, have also become parties to legal action. In late
1982, additional negotiations occurred between OMC and the
USEPA; however, these were also terminated. It appears that the
determination of responsibility for cleanup costs will depend upon-
the outcome of litigation which may take years. As a result,
cleanup may have to be implemented through the Superfund pro-
gram. However, it has now been over 7 years since the problem was
identified. In the interim, no substantial action has been taken to
stabilize or remove this source of contamination to Lake
Michigan.'
NEW BEDFORD HARBOR
New Bedford Harbor is a major port located at the mouth of the
Acushnet River on Buzzards Bay in southeastern Massachusetts
(Figure 5). It supports an extensive fishing industry as well as other
commercial and industrial activities. Available data indicate that
the sediments, water column and aquatic organisms in the harbor
area contain high concentrations of PCB. Until 1977, PCB was
used by two industries in New Bedford; Aerovox, Inc. and Cornell-
Dubilier Electronics Corporation. PCB was discharged directly to
harbor waters from these industries and indirectly via the New Bed-
ford municipal wastewater treatment plant.'
ff.
Aerovoi
ACUSHKET
LEGEND
Includes areas nitri PCB
concentrations > 500*E/t
Areas «itn PCB concentrations
> 50>itti PCB concentrations
> 10/ng/g and < 50>Kg/£
Isolated samples > 50/1 g/j
NOTE: All concentrations are
given in nicroirans per
gran («g/E) oased on
dry neignt.
ACUSHNET RIVER ESTUARY
&-, PCB CONCENTRATIONS
New Seolorn
Sewjjt Treatnent
Plant OutfaUs
Figure 5
New Bedford Harbor Study Area
Figure 6
Acushnet River Estuary PCB Concentrations
The Massachusetts Department of Public Health has placed
restrictions on the taking of lobster, finfish and shellfish in the New
Bedford Harbor area due to PCB levels in these organisms ex-
ceeding the Food and Drug Administration (FDA) limit of 5 jig/g.
In addition, dredging necessary for harbor development projects is
impeded due to the difficulty of disposing of sediments containing
high concentrations of both PCB and heavy metals.'
As indicated in Figure 6, PCB concentrations in the sediment of
the northern portion of the upper estuary (Zone la) generally ex-
ceeded 500 /ig/g (dry weight) with concentrations greater than
10,000 /ig/g measured at several sampling stations in the vicinity of
a former PCB discharge point. Sediment PCB levels exceeding 50
/tg/g are present in the estuary (Zone la) as far south as Pope's
Island, in the northwest corner of the outer harbor (Zone 2) and in
the vicinity of the New Bedford wastewater treatment plant outfalls
(Zone 2). Sediment PCB concentrations of 10-50 /ig/g occur in the
peripheral areas of the inner harbor (Zone Ib) with lower values in
the navigation channel. PCB levels in the 10-50 /tg/g range are also
24
SITE INVESTIGATION
-------
found in the sediment along the west shore of the outer harbor
(Zone 2) near a second, former PCB discharge point.6
In addition to high PCB levels in river and harbor sediments,
data also indicate that the sediments contain significantly high
levels of heavy metals such as copper, chromium, lead and zinc.
Copper has been measured at concentrations greater than 8,000
/tg/g, in the upper estuary (Zone la), while lead and zinc have been
measured at levels exceeding 1,000 /*g/g.6
Water column samples collected in the study area indicate PCB
levels as high as 4.0 ^g/1 in harbor waters. These levels were
measured in the upper estuary in the area of the highest sediment
PCB concentrations. In general, water column PCB concentrations
appear to decrease below detectable levels in the south, although
detectable levels of PCB have been found near the New Bedford
wastewater treatment plant outfall.6
Due to high tissue levels of PCB, Zones la and Ib are closed to
all fishing activities, Zone 2 is closed to the taking of bottom-
feeding finfish and lobster and Zone 3 is closed to lobstering only.
Aquatic organisms exhibit the highest PCB levels in Zones la and
Ib and decreasing levels seaward. A majority of the finfish sampled
in the inner harbor (Zone Ib) have PCB levels exceeding the FDA
limit. Lobsters represent an important recreational and commercial
fishery in the study area. PCB levels in this species appear to fluc-
tuate seasonally, with higher tissue levels being detected in spring
lobster samples in comparison with fall samples. This may be due
to a seasonal lobster migration pattern in and out of more con-
taminated areas. These fluctuations may also result from the poten-
tial effect of spring flood flows on water column concentrations
and, in turn, organism PCB concentrations. In the spring of 1982
approximately 75"% of the sites samples in Zone 3 exceeded the
FDA limit of 5 /tg/g wet weight.6
Based on the evaluation of available data, it was concluded that
conceptual programs for the removal of PCB-contaminated sedi-
ment should be developed. Several recent studies of PCB-
contaminated waterways have shown removal of contaminated
bottom material by dredging to be the most technically and
economically feasible remedial action. Malcolm Pirnie, Inc. for-
mulated five dredging program alternatives. Alternatives 1, 2 and 3
are remedial dredging programs designed to remove the most PCB-
contaminated sediments. Alternatives 4 and 5 address dredging re-
quirements for harbor development projects in harbor areas with
less PCB contamination:
•Dredge sediments containing greater than 500 /tg/g PCB with dis-
posal at a secure upland site (Hot Spot I Project).
•Dredge sediments containing greater than 50 /*g/g with disposal at
a secure upland site (Hot Spot II Project).
•Dredge sediments containing greater than 10 /*g/g PCB with dis-
posal of sediments containing 50 /ig/g PCB or greater at a secure
upland site, and shoreline disposal of sediments containing less
than 50 /tg/g (Hot Spot III Project).
•Allow implementation of channel improvement dredging, bridge
excavation and initiation of small-scale harbor development pro-
jects through removal and shoreline containment of the PCB-
contaminated sediment volumes involved (Harbor Development
Project C).
•Allow implementation of channel improvement dredging, bridge
excavation and initiation of larger-scale harbor development pro-
jects through removal and shoreline containment of the PCB-
contaminated sediment volumes involved (Harbor Development
Project D).
The areas of greatest PCB contamination are in Zones la, Ib and
2. Contaminated sediment volumes for inner and outer harbor
dredging alternatives (Zones la, Ib and 2) are indicated in Table 2.6
The anticipated benefits to be derived from dredging programs
are related to the two primary issues involved:
•Reductions in PCB levels in aquatic life generally, and specifically
in organisms of commercial and sport fishing importance.
•Lifting of regulatory constraints on harbor development projects.
Reductions in PCB concentrations in aquatic organisms will be
related to, among other factors, the extent to which PCB-
contaminated bed materials are removed, the effects of this
removal on PCB levels in the water column and the levels of PCB in
the remaining undredged harbor areas.
Regulatory constraints on harbor development projects will be
reduced by the provision of containment sites for the PCB-
contaminated fraction of the bed materials in areas being con-
sidered for channel improvement dredging, bridge excavation and
various other construction and development projects.6
After considerable discussion between the Commonwealth of
Massachusetts and the USEPA, it appears that the USEPA will
take the lead in any cleanup. A draft RAMP has been completed
and circulated for public comment. The RAMP recommends a
complete Feasibility Study involving additional extensive sampling
before a remedial action program is initiated. It is clear that several
more years may pass before an actual cleanup is implemented.
Table 2
PCB-Contaminated Sediment Volumes
(Based on Available Data)
Typical PCB
Concentration in
Dredged Area
Cumulative Volume
of Dredged
Material
yds3
Hot Spots I
Hot Spots II
Hot Spots III
10J
120,000
300,000
900,000
Project
REMEDIAL DREDGING PROJECTS
_500' 70,000
_502 2,200,000
_10' 4,400,000
HARBOR DEVELOPMENT PROJECTS
Project A: Channel _10! 80,000
Improvement Dredging
Project B: Proj. A +
Bridge Excavation
Project C: Proj. B +
Small Scale Harbor
Development
Project D: Proj. C +
Large Scale Harbor
Development
NOTES:
1. PCB concentration based on measured PCB values in top 2 ft of sediment.
2. PCB concentrations based on surface samples ( 0-4 in. depth) only, due to insufficient data at
greater depths.
3. Approximate concentrations based on minimal sampling; must be verified with detailed sampling
on a site-by-site basis.
Niagara River, New York
The Niagara Falls area became the focus of national attention as
a result of the indications of serious chemical contamination in the
vicinity of the Love Canal area in 1975 and 1976. However, prior to
that time "questionable water quality" conditions in the Niagara
River had been of concern.7 The concern in the late 60's and early
70's focused on industrial wastewater discharges. Now that most of
these discharges are under control, interest has focused on other
sources of contamination and the contaminated sediments on the
river bottom.
According to the USEPA, inactive hazardous waste disposal sites
are believed to be a major source of persistent chemical substances
in fish in the Niagara River. No less than 155 sites have been iden-
tified within three miles of the river.8 This extensive list of potential
sources makes the determination of the extent of contamination
and appropriate remediation difficult. Until all sources which con-
tribute to a specific area are known, the long-term benefits of
cleanup may be questionable since recontamination is possible.
The concerns and investigations associated with remediating
problems related to the Love Canal site will serve to illustrate the
complexity of the decision-making process. The location of the
Love Canal with respect to the general Niagara River area is shown
in Figure 7.
SITE INVESTIGATION
25
-------
1 Site ConUlnnwnl
3 Black and Bergholtz Creeks
5 Ground-water Monitoring
(Broad Area)
7 Lin SUUona/Sanlury and Slonn S
2 North Storm and Sanitary Sewer.
4 South Storm and Sanitary Sewer.
6 102nd Street Outlall Sediment
Figure 1
General Site Location Map for the Niagara Falls/Love Canal Area
Between 1942 and 1952, over 21,000 tons of chemicals—acids,
chlorides, mercaptans, phenols, toluenes, pesticides,
chlorobenzenes, benzylchlorides, sulfides, sulfydrates—were
disposed of at the site of an abandoned canal in Niagara Falls, New
York. This site was later sold and portions were developed for
residential use. As a result of unusually wet weather -during the
1970's and the possible disturbance of the original soil cover, these
contaminants were found to have migrated from the dumpsite to
basements of nearby homes and to the surface.
The alarmed response of residents led to NYSDEC studies in late
1977, and subsequently to initial remedial measures, including
leachate collection and treatment systems, a clay cover and fencing
off of some areas. A July 1982 report by USEPA concluded that
the leachate system has halted lateral transport of contaminants
through the soil and that the area is habitable except for lots adja-
cent to the canal. Houses on these lots have already been de-
molished.
Now it appears that prior to containment, contaminants left the
site via storm drainage and sanitary sewers. Contaminants have
been found in sewers and sediments deposited at storm sewer out-
falls. Malcolm Pirnie is currently studying five areas surrounding
the Love Canal site, including associated contaminated storm
sewers, sanitary sewers, creeks and a delta into the Niagara River
from a stormwater outfall. In each area, Malcolm Pirnie is deter-
mining the extent of contamination, identifying contamination
pathways, assessing effects of contaminant migration and develop-
ing and evaluating remedial measures to prevent further con-
tamination.'
The areas under study are illustrated in Figure 8. In Jan. 1983, an
intensive three-week sampling program involving over 25 scientists,
engineers and technicians was conducted to determine the extent of
contamination. Over 1,000 samples were taken including water,
sediment and waste deposits. The potential presence of dioxin re-
quired development of site-specific sampling and laboratory
analysis protocols. These data are being evaluated and a range of
remedial alternatives are being developed. The report is scheduled
for late summer 1983.
This work is being funded by the Federal Superfund and im-
plemented under a cooperative agreement between the state and the
USEPA. It is anticipated that the costs will eventually be borne by
responsible industries or other parties as a result of litigation or set-
tlement. This way be complicated by the presence of seven addi-
tional sites nearby which may also contribute to the contamination
of the area, sewers and waterways.1
CLEANUP FINANCING
A major problem in expediting the cleanup of waterway con-
tamination is funding. The seven most probable mechanisms for
financing the cleanup of contaminated waterways are listed below:
Figure 8
Love Canal Superfund Projects—Niagara Falls, New York
•Direct action by industry or other "Responsible Parties"
•Clean Water Act, Section 115, In Place Toxicants
•Clean Water Act, Section 201, Wastewater Facilities Construction
Grants
•Clean Water Act, Section 311, Emergency Spill Cleanup
•Superfund
•State Funds
•Extension of U.S. Corps of Engineers Responsibilities for Water-
way Maintenance
The most desirable is direct action by "responsible parties."
However, in most cases lengthy litigation occurs before a settlement
is achieved. In the interim, storms or other mechanisms may cause
substantial redistribution of contaminants. The litigation with
responsible parties with respect to Waukegan Harbor has gone on
for over seven years and still has not been resolved. The legal ac-
tivities associated with the Love Canal and other sources to the
Niagara River have a similar record.
Section 115 of the Clean Water Act directs the USEPA to iden-
tify the location of in-place pollutants and authorizes removal and
disposal. Fifteen million dollars was authorized, but has never been
appropriated. This work would be done in conjunction with the
U.S. Army and, therefore, is related to an extension of the Corps
of Engineers responsibilities as noted below. It does not appear that
Congress will take any action to implement funding for this financ-
ing option in the near future.
In New York State, the U.S. Congress provided for the utiliza-
tion of funds under Section 201 of the Clean Water Act to clean up
the Hudson River. The USEPA is currently opposing this approach
and recommending that a more appropriate mechanism would be
26
SITE INVESTIGATION
-------
the Superfund. The net result has been a lack of the approvals
necessary to take decisive action and an increased risk of
catastrophic loss of PCB to the estuary.10
Some funds have been allocated from Section 311 to study the
problem in Waukegan Harbor." However, the extent of such funds
is limited and cannot facilitate cleanup on a broad nationwide
scale. This mechanism appears to be intended for emergency
response to spills rather than contamination resulting from long-
term industrial discharges. In addition, a special congressional ap-
propriation of $1.5 million was passed in 1980. However, this is not
enough to complete a cleanup.
In most cases, contaminated waterways are clearly abandoned
uncontrolled hazardous waste disposal sites. Waukegan Harbor,
the Acushnet Estuary and the Niagara River sediment deposits have
been earmarked for the receipt of monies from Superfund.
Hopefully, this program will accelerate from its present pace so
that these problems may be dealt with in a timely fashion. The most
difficult problem is the allocation of priorities between upland sites
and waterway contamination such as the Woburn Landfill and the
Achushnet Estuary in Massachusetts, or the Love Canal versus the
Hudson River in New York.
Some states, such as New Jersey and New York, have established
state superfunds. However, it is unlikely that the available funds
can remedy extensive waterway contamination. For example, the
cost of cleaning up the major hotspots in the Hudson River will ex-
ceed $20,000,000.
On James River and Chesapeake Bay, the Corps of Engineers
has financed limited studies to evaluate certain cleanup efforts re-
lated to maintenance dredging.11'12 An expansion of Corps authori-
zation beyond normal maintenance may be an effective mechanism
for accelerating waterways cleanup.
CONCLUSIONS
The contamination of sediments in the nation's waterways is a
major problem. The redistribution of contamination by currents,
tides and storms often makes the potential risks and impact on
natural and economic resources greater than for upland sites. In
some cases, the potential for catastrophic releases of contaminants
may warrant that greater priority be given to waterways contamina-
tion than for many upland disposal sites. The remedial methods for
contaminated sediments have been evaluated extensively, and the
most feasible action is usually to dredge concentrated areas before
redistribution can occur and place the dredged material in secure
upland disposal sites. Unfortunately, such actions are relatively
costly and compound the difficulties in assessing priorities.
The cleanup of an extensively contaminated waterbody such as
the upper Hudson River may be several times more costly than
stabilizing an upland abandoned uncontrolled waste disposal site.
Several possible mechanisms are available for financing cleanups.
However, the delays associated with many proposed programs have
greatly increased the risk of irretrievable loss of contaminated
materials due to storms or other catastrophic events less common
to upland sites. It is recommended that a higher priority be con-
sidered for allocating resources to the cleanup of contaminated
waterways in recognition of the special risks and potential impacts
associated with such problems.
REFERENCES
1. Malcolm Pirnie, Inc., "Draft Environmental Impact Statement PCB
Hot Spot Dredging Program, Upper Hudson River, New York," for
NYS Department of Environmental Conservation, White Plains, New
York, 1980.
2. Malcolm Pirnie, Inc., "Draft Environmental Impact Statement and
10-Year Management Plan, Hudson River Federal Channel Mainten-
ance Dredging," U.S. Corps of Engineers New York District, White
Plains, New York, 1981.
3. Henningson, J.C. and Thomas, R.F., "Hudson River Cleanup," Pro-
ceedings of the Workshop on Environmental Decontamination, Oak
Ridge National Laboratory, Oak Ridge, Tennessee, 1979.
4. USEPA, "The PCB Contamination Problem in Waukegan Harbor,"
Chicago, Illinois, 1981.
5. Malcolm Pirnie, Inc., Technical Memoranda in Support of Litigation,
prepared by R.P. Brownell and J.C. Henningson, White Plains, New
York, 1982.
6. Malcolm Pirnie, Inc., "Final Report: The Commonwealth of Massa-
chusetts Acushnet River Estuary PCB Study," Massachusetts Di-
vision of Water Pollution Control, White Plains, New York, 1982.
7. Malcolm Pirnie, Inc., "Engineering Report, Van De Water Plant
Raw Water Intake," Hamburg, New York, 1975.
8. Malcolm Pirnie, Inc., "Background Information, Health and Safety
Training Program, Love Canal Remedial Project, Five Engineering
Investigations," Niagara Falls, New York, White Plains, New York,
1982.
9. Malcolm Pirnie, Inc., "Agreement with the New York State Depart-
ment of Environmental Conservation (Scope of Services) for Site In-
vestigations and Remedial Alternative Evaluations for the Five Task
Areas, Love Canal Site in Niagara Falls, New York," White Plains,
New York, 1982.
10. Knickabocker News, "New Twists May Block Dredging of PCBs,"
Albany, New York, August 28, 1982.
11. Haller, D.L., "Demonstration of Advanced Dredging Technology-
Dredging Contaminated Material Kepone James River, Virginia,"
Norfolk District, U.S. Army Corps of Engineers, undated.
12. Vann, R.G., "James River, Virginia Dredging Demonstration in Con-
taminated Material (Kepone) Dustpan versus Cutterhead," Norfolk
District, U.S. Army Corps of Engineers, undated.
SITE INVESTIGATION
27
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STUDY OF SUBSURFACE CONTAMINATION WITH
GEOPHYSICAL MONITORING METHODS
AT HENDERSON, NEVADA
ERIC G. WALTHER, Ph.D.
DOUGLAS LaBRECQUE
DENNIS D. WEBER, Ph.D.
Lockheed-EMSCO Environmental Program
Las Vegas, Nevada
ROY B. EVANS, Ph.D.
J. JEFFREY VAN EE
U.S. Environmental Protection Agency
Environmental Monitoring Systems Laboratory
Las Vegas, Nevada
INTRODUCTION
The geophysical program of USEPA's Environmental Mon-
itoring Systems Laboratory in Las Vegas (EMSL-LV) has as one
objective the demonstration and evaluation of geophysical methods
for detecting and mapping subsurface-contaminants.
The use of these methods is part of a cost-effective approach to
groundwater monitoring. Cost-effective assessments of subsurface
contamination include three phases: (1) preliminary site assess-
ment, using aerial photography, onsite inspections and other in-
formation to approximate hazardous waste site boundaries and
contaminant source locations; (2) geophysical surveys to pinpoint
sources of contamination and to help define plumes of conduc-
tive contaminants; and (3) confirmation of groundwater contam-
ination through monitoring well networks designed with the help of
the geophysical surveys. The spatial characterization of ground-
water contaminant plumes can make possible the efficient loca-
tion of monitoring wells and reduce the costs and risks in explor-
atory drilling.
In the past, investigation of subsurface contamination has de-
pended upon: (1) drilling to obtain information on the geologic
setting; (2) monitoring wells for samples of groundwater; and (3)
laboratory analyses of soil, groundwater and waste samples. Dur-
ing the past decade, extensive development in remote sensing geo-
physical equipment, field methods, analytical techniques and asso-
ciated computer processing has greatly improved the geologist's
ability to characterize hazardous waste sites and subsurface con-
tamination. Some geophysical methods offer a means of detecting
contaminant plumes, groundwater flow direction and speed and
buried wastes or other sources of contamination. Some can be
used for measurements of contaminants and moisture movement
within the unsaturated zone; others offer a way to obtain de-
tailed information about subsurface geology. The capability to
characterize the subsurface rapidly without disturbing the site
offers benefits in terms of less cost, less risk and better understand-
ing of site conditions.
EMSL-LV geophysical programs fall into three areas: (1) sur-
face-based survey methods for horizontal-plane-mapping of con-
taminant plumes; (2) downhole sensing techniques to obtain in-
formation on the vertical structure of site geology and hydro-
geology, the speed and direction of groundwater flow and the
vertical extent of contaminant plumes; and (3) surveys utilizing
borehole-to-surface methods to obtain information on the move-
ment of fluids from injection wells.
The EMSL-LV objective of demonstrating the evaluating the use
of geophysical methods in assessments of groundwater contamina-
|Site Selection]
+
I Site Layout |
.
[ Electromagnetic Induction Survey I |
Resistivity Survey |
| Well Drilling I |
._.
| Organic Vapor Survey I |
.+
I Complex Resistivity Survey 11
Laboratory Complex Resistivity Measurements |
I Complex Resistivity Survey II |
*
[Well Drilling II |
*
[ Soil Sampling |
V '
| Well Water Sampling |
| Organic Vapor Survey II |
[Ground Penetrating Radar Survey |
V
I Downhole Complex Resistivity |
| Complex Resistivity Survey IJT|
z
I Electromagnetic Induction Survey II
| Report [
Figure 1
Technical design of the study
tion has three different but related subparts: (1) the testing of ex-
isting geophysical methods in groundwater assessments; (2) the
integration of conventional and geophysical techniques to' develop
SITE INVESTIGATION
-------
new, cost-effective monitoring procedures; and (3) the develop-
ment of new geophysical equipment. Testing of existing methods
focuses on the application of geophysical techniques and equip-
ment used in mineral and petroleum exploration to groundwater
problems. Existing surface-based methods currently receiving
attention include conventional resistivity, electromagnetic induc-
tion, ground-penetrating radar, magnetometry, seismic reflection
and refraction and complex resistivity (also called spectral in-
duced polarization).
Technical Design
The technical design started with site selection (Figure 1). The
site needed to have contaminated groundwater with a conductivity
contrast to the surrounding rock sufficiently large to allow ob-
servation with the electrical methods to be tested. Several can-
didate sites around the nation were evaluated before choosing the
Henderson site near Las Vegas.
Electromagnetic induction was selected as the first method be-
cause it was expected to be easy, rapid and inexpensive. Con-
ventional resistivity followed in order to check the electromagnetic
measurements with another electrical method. All electrical meth-
ods were expected to respond well to the known high concen-
trations of total dissolved solids in the groundwater. Resistiv-
ity offered the opportunity to both profile horizontal variation
along a transect and measure the depth variation at selected
positions.
Organic vapor concentrations could have been surveyed anytime
but were convenient to schedule following the electromagnetic and
conventional resistivity surveys. The complex resistivity surveys
were conducted in sequence because they logically followed con-
ventional resistivity. Next followed the soil and water sampling
and analysis in order to develop data for the evaluation of the
geophysical measurements. A second organic vapor survey was
conducted to check different techniques.
1
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Aquatic and
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Complai Rasiitivitf
Survay 1
(Contractor)
Zongi Enginiiring and
Raiaarch Orginiiatiaa
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(Subcontractor)
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Program!
Radio Fraquancy
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uses
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Figure 2
Study Organization
Figure 3
General location map (taken from Tinlin et al. 1983)
Surveys too recent to be presented here include ground penetrat-
ing radar, additional surface complex resistivity, downhole com-
plex resistivity and additional electromagnetic induction measure-
ments. The institutions involved in these surveys are shown in
Figure 2.
Site Description
The general location of the Henderson site is shown in Figure 3.
A source of groundwater contamination is the industrial complex
shown at the bottom of Figure 4. The federal government con-
structed some of the facilities during World War II to refine mag-
nesium ore. Over the years the facilities have accommodated
companies manufacturing products ranging from titanium to pesti-
cide intermediates.
A plume moves downgradient in the unconfined aquifer from
the industrial area, through the study area and to Los Vegas Wash,
flowing under industrial, municipal and private residential prop-
erty. This plume path was suggested by the pattern of total dis-
solved solids (TDS) concentrations shown in Figure 4.
Hydrogeology
The geologic cross-section along the transect is shown in Figure
5. The cross-section was developed from the 23 wells drilled along
the transect during Mar. 1983 and shows the elevation of the
ground, water table and aquiclude. The ground slope is low along
the transect and similarly low perpendicular to the transect, slop-
ing down toward the north. The high water table between Sta-
tions 610 and 613 is caused by the recharge from Alpha Ditch,
which carries 1.4 x 10" to 3.1 x 10" mVday of cooling water along
Pabco Road from the BMI industrial complex to Las Vegas Wash.
This cooling water contains only 755 mg/1 total dissolved solids
making it less saline than the surrounding groundwater.15
SITE INVESTIGATION
29
-------
Pittman Aru ^
Total Disaolv*d Solidi
Concentration! of Saturated
Sand and Gravel
Figure 4
Groundwater quality based on total dissolved solids (adopted from
U.S. Bureau of Reclamation 1983)
METHODOLOGY
The first electromagnetic induction instrument used by Technos
was a Geonics EM-31 containing a transmitter and receiver in one
portable unit. The apparent conductivity was read at each 15 m in-
terval from an analog meter.
The EM-31 was used in both the vertical and horizontal orien-
tations at heights above ground of 0, 0.3, 0.6, 0.9, 1.2, 1.5, 1.8 and
2.1 m in order to obtain a vertical sounding of apparent conduc-
tivity at Stations 620, 625, 637.5, 639, 647, 651 and 675.
The second instrument was a Geonics EM-34-3, which required
two people to operate. For horizontal profiling, this instrument
was used with an intercoil spacing of 10 m and with the coil axes
alternately oriented vertically and horizontally. Coil spacings of 10,
20 and 40 m, and both vertical and horizontal orientations were
systematically used to obtain a vertical sounding of apparent con-
ductivity at the same stations used for the EM-31.
Normally, the coils were oriented with the line connecting the
centers being parallel and directly above the transect line. Some
measurements were taken with the line between the coil centers
oriented perpendicular to the normal orientation. These measure-
ments were intended to measure lateral homogeneity of the appar-
ent conductivity.
With its coil axes vertical, the EM-31 has a median depth1 of
2.7 m. The median depth is the depth above or below which one-
half of the measured signal is generated. The secondary magnetic
field is the signal for electromagnetic induction. If the instrument
is turned 90 ° around its boom axis, the median depth decreases to
about 1.5 m. The EM-34-3 has a median depth of 0.86 loop sep-
arations with the coil axes vertical and 0.38 loop separations with
the loop axes horizontal.
The median depth agrees with the penetration depths of similar
instruments used in mineral exploration. McNeill' defines penetra-
tion depth as the depth above which 75% of the measured signal
is generated. Under ideal conditions, structures can be detected at
the penetration depths which are about double the median depths.
The resistivity measurements at Henderson were made with a
Bison Model 2390 which has separate transmitting and receiving
units, signal enhancement through stacking and adjustable fre-
quency. The transect was profiled by using the Lee-partitioning
version of the Wenner electrode array, centered at each 30 m sta-
tion used for the EM-34-3. The "a" spacings were set at 6 and 15
m in an attempt to get penetration depths similar to those obtained
with the EM-31 and EM-34-3 according to McNeill.' The injected
currents were 20 and 50 mamp at the 6 and 15 m spacings, respec-
tively. The steel electrodes were inserted 0.2 m into the ground, and
0.5 1 of water was poured around each to reduce the contact re-
sistance with the soil. Soundings were conducted at selected sta-
tions to develop information on the variation of conductivity with
depth. The stations were 620, 637, 647, 649 and were selected to
cover the entire transect. Two orthogonal soundings were con-
ducted at 637 to explore horizontal directional dependence; one
was oriented north-south, the other east-west. All other soundings
were oriented east-west.
The soundings used "a" spacings of 0.3, 0.45, 0.6, 0.9, 1.5,
2.1, 3.0,4.5, 6, 9, 15, 21, 30, 60 and 90 m.
1660-
Scale in Feel
Scale in Meters
500
Test Well
Figure 5
Hydrogeologic cross-section of the transect
SITE INVESTIGATION
-------
The Lee-partitioning arrangement has an extra potential elec-
trode at the center of the array from which the distance to each of
the other potential electrodes ia a/2. The apparent resistivity was
computed from:
pa = 4?ra
(1)
for each side of the array, where V is the potential difference
measured between the center and one other potential electrode and
I is the current. This arrangement provides twice as much data as
the conventional Wenner array. The two apparent resistivities com-
puted for each setting of the array give a measure of horizontal as
well as vertical variability.
Different equipment and methods were used for each of the two
complex resistivity field surveys although they both used the dipole-
dipole array. Laboratory measurements of complex resistivity were
arranged on soil cores from the contaminated zone in order to
quickly get a rough estimate of the phase response over the wid-
est available range of frequencies.
ZERO (Zonge Engineering and Research Organization) Survey
The ZERO survey used an "a" spacing of: (1) 30 m for survey-
ing 853 m of the transect between Stations 618 and 646; and (2)
15 m for 213 m of transect between Stations 631 and 638 (Figure
5).
ZERO originally proposed to conduct this survey using a square
wave transmitter current and analyzing the received signal for the
first five odd harmonics as well as the primary frequency. Three
primary frequencies at 0.125, 1 and 8 Hertz would be used to give
a total of 18 frequencies ranging from 0.125 to 88 Hertz. Use of
the higher harmonics requires that they be normalized by the actual
harmonic content of the transmitted waveform. To do this, the
transmitter current is sampled through a hardwire link between re-
ceiver and transmitter (Figure 6a) and recorded simultaneously
with the input signal. Both signals would be fast-Fournier-trans-
formed and the received signal normalized by the transmitted
signal.
As will be discussed in the results section, radio frequency noise
forced a change of equipment configuration. In the alternative
configuration, only the primary frequency is measured (Figure 6b).
In this case, adequate synchronization of the receiver and trans-
mitter is achieved using crystal clocks. ZERO investigators believed
that phase differences as small as 0.2 milliradians could be meas-
ured with this configuration.
Phoenix Geophysics Survey Methodology
Phoenix Geophysics used the dipole-dipole array with 7.5 m di-
poles to survey from Station 618 to Station 654 and from Sta-
tion 668 to 674. Using the dipole-dipole array with 3 m dipole
lengths, Phoenix also surveyed from 655.4 to 634. Both profiles
used interdipole spacings of n = a to n = 6a and eight frequencies
increasing by factors of four from 1/16 Hertz to 1024 Hertz.
The Phoenix Geophysics equipment included a seven-channel re-
ceiver. One channel measures the transmitter waveform through a
hardwire link, and the remaining six channels measure the six re-
ceiving dipoles. In this configuration, an entire diagonal of the
pseudosection is measured simultaneously. Timing is controlled by
a crystal clock in the receiver which in turn controls the transmitter
through the hardwire link.
USGS Laboratory Complex Resistivity Methodology
At Station 643, a hollow stem auger was used to drill to the soil
sampling depths. At the surface and each succeeding 1.5 m depth,
the soil sample was taken by driving 0.6 m lengths of 2.5 cm
diameter PVC pipe into the ground. The pipe was not capped, but
placed immediately into plastic bags which were heat-sealed and
labelled. After being air freighted to Denver, a 20 cm3 volume of
each sample was placed in a cylindrical Teflon sample holder and
the electrical properties measured as described in Hunt et al.4 In-
. ComploK Resistivity t
(PDP-8orGDP-12)
400 Cyda Engloa
(tranamrnar)
Data ProcaiaJng
Track
(OOP-12 Trued Mounud
Moda Shown)
Figure 6a.
Harmonic data collection configuration (taken from ZERO brochure)
b. Oiscrata-Froquancy C.R.
(Two-Dipoto Acquisition) 1
400 CrO* Engina
(transmrnar)
Noli: Not 10 Scala
Tranamlttar
Truck
Figure 6b
Discrete frequency complex resistivity configuration
(taken from ZERO brochure)
stead of filling the ends of the sample holder with water, the three
spaces in the holder were filled equally with soil from the PVC
pipe. The Teflon membranes were removed because no metallic
minerals were expected in the soil. These changes allowed measure-
ment of the samples in their natural state.
The current was applied to the sample, and the frequency was
varied from 10"3 to 106 Hertz. The resulting potential difference
was measured, allowing the computation of apparent resistivity and
phase.
Special attention was focused on phase because it was expected
to provide the most information on the presence of contaminated
groundwater and, perhaps, indicate a difference between inorganic
and organic contamination.
Organic Vapor Methodology
Benzene, chlorobenzene, dichlorobenzene and chloroform were
known to be present at the site from previous studies.5'12 An inde-
pendent method was needed to survey the organic concentrations.
The two organic vapor surveys used different methodologies,
and the second survey included the testing of a new gas sampling
device.
Technos Methodology
Twenty-eight holes 10 cm in diameter were rotary drilled along
the transect (not shown in Figure 5). None of the holes were cased,
allowing vapor to transfer into the hole from the surrounding
earth. Eight of the holes collapsed because the sand and gravel was
loose. This prevented the drillers from reaching the water table, the
intended depth. A 1.5 m section of 10 cm PVC casing was placed
at the top of each hole with a collar of soil on a plastic sheet. The
casing was capped in order to allow the accumulation of vapor in
the hole.
The organic vapor analyzer was a Foxboro Century VOA128
portable gas chromatograph with flame ionization detector. The
output is the equivalent methane concentration in parts per million
with a minimum detectable concentration of 0.5 to 1 ppm. Accur-
ate measurement of organic gases other than methane requires that
the equivalent methane concentration be multiplied by a correction
factor. This instrument detects all organic vapors, but with a differ-
ent sensitivity to each. At Henderson, the mix of organics in the
liquid or vapor phase is unknown.
The procedure at each of the 28 holes was to: (1) remove the
cap; (2) replace it with a similar cap having a hole through which
SITE INVESTIGATION
31
-------
Tygon tubing was passed to the analyzer; (3) push the tubing
through the hole until the end reached the sampling depth of 2-3 m;
and (4) read the meter for the equivalent methane concentration
while raising the tubing a half meter or so. This procedure was used
twice (once within one hour after drilling and then again about 24
hours later).
Desert Research Institute Methodology
The Desert Research Institute used specific gas indicator tubes
made by Draeger. These tubes are colorimetric, containing a reac-
tant that changes color linearly in distance along the tube in pro-
portion to the concentration of the gas being measured. The
sampled volume of air is a specified constant in order to make the
concentration directly measureable from the length of color
change.
DRI used a hollow stem auger drill to reach each depth to be
sampled. The iron custom-made sampler (Figure 7) was then
pushed 0.3 m into the soil at the bottom of the 1.5 m deep hole.
The sampler was withdrawn 1 cm to open the inlet for the soil gas.
A second iron tube holding the Draeger gas sampling tube was
lowered down inside the first tube. O-rings were used to close the
air path between the two iron tubes. Soil gas was drawn through
the Draeger tube and tubing connected to a bellows pump at the
top of the hole. After pulling the specified volume of soil gas
through the indicator tube, the entire sample holder was with-
drawn from the hole. The Draeger tube was removed from the
holder, and the length of color change was measured.
-Hammering Cap
-Iron Pipe
u
0
Sampling Pipe
Draeger Gas Detection Tube
O-rings
-Iron Sampler and Tip
Figure 7
Soil gas sampler
a. Configuration for hammering sampler into soil
b. Placement of sampling pipe with Draeger tube into the sampler
The indicator tubes were also used in an experiment designed
to facilitate reading the color change while pumping. The samp-
ler was imbedded in the soil as described above, but it held no
indicator tube. Instead, tubing ran from the top of the sampler
to the indicator tube above ground. Another piece of tubing con-
nected the other end of the indicator tube to the bellows vacuum
pump. Before placing the Draeger tube in the line just before the
pump, the bellows were pumped to clear the volume in the iron
sampler and the tubing, replacing the air with several volumes of
soil gas. The bellows were pumped enough to cause a measur-
able color change in the indicator tube. The total volume of
sampled soil gas was calculated from the number of strokes and
the stroke volume of 100 cm3.
The DRI survey also suspended an indicator tube on tubing in
order to measure the benzene concentration just above the water
in the head space of each cased well. The soil gas sample volume
was 2 1. The DRI methodologies only measured benzene with the
indicator tubes, while Technos measured total organic vapors as
equivalent methane.
RESULTS
The results of the electromagnetic induction surveys are pre-
sented by instrument. The first survey was conducted with the
more portable and fast instrument, the EM-31.
EM-31 Results
The apparent conductivity measured with the EM-31 and vertical
coil axes is shown in Figure 8. The conductivities were high enough
to induce a nonlinearity that required correction. The EM-31 with
coil axes vertical has a median depth of 2.7 m. These EM-31 data
are dominated by the unsaturated zone because the depth to water
varies from 2 to 11 m as shown in Figure 5.
The EM-31 indicates the lowest conductivities are west of Hydro
Conduit Corp where pumping of gravel pits lying 61 m north of
the transect has dropped the water table below 9 m.
Between Stations 654 and 667 a short parallel transect about 61 m
north of the transect was used to obtain measurements outside
Hydro Conduit Corp. This change in transect axis probably ac-
counts for the discontinuities in the field data.
Figure 8
EM-31 profile with vertical axis dipoles1
Figure 9
EM-34-3 profile with horizontal axis dipoles and a = 10 m"
32
SITE INVESTIGATION
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j,ii nj,i n i^n in 111tjj11 ijji 11^111 ijj m^i n ijj i
Sultan Number
Figure 10
Resistivity profile, a = 6 m'
imm iniHMMiiiiiMiiuiiiiM ii inn il
Station NumlMT
Figure 11
Resistivity profile, a = 15 m"
EM-34-3 Results
The apparent conductivity profile measured with a coil separa-
tion of 10 m and horizontal-axis coils is shown in Figure 9. No data
were taken around Hydro Conduit Corp. In this configuration,
the EM-34-3 has a median depth of 3.8 m, only 30% greater than
the EM-31. The 30 m sampling interval of the EM-34-3 survey
missed some of the fine details of the EM-31 survey, but the re-
sults are similar. Between Stations 617 and 635 the EM-34-3 shows
apparent conductivities 30% greater than with the EM-31. This
difference is probably caused by the influence of a relatively con-
ductive saturated zone at depths of 3.7 to 4.6 m which is barely de-
tectable by the EM-31 but moderately detectable by the EM-34-3.
The reciprocal of apparent resistivity is plotted as apparent con-
ductivity to facilitate comparison with the apparent conductivity
measured by electromagnetic induction. The apparent conductivity
profile obtained with a 6 m "a" spacing which had a median pene-
tration depth of 3 m is shown in Figure 10. The apparent conduc-
tivity obtained with a 15 m "a" spacing which had a deeper med-
ian penetration depth of 8 m is shown in Figure 11. These conven-
tional resistivity profiles agree with the electromagnetic induction
profiles.
ZERO Survey Results
The radio frequency interference was so intense as to nullify the
measurements made with the ZERO harmonic data configuration
(Figure 6a). Various electrical filters were devised, but did not ade-
quately reduce the noise. Two radio station transmitters were
noted nearby, one of them transmitting 50 kw at 720 kilo Hertz
from towers 2 kilometers east of the transect. This carrier frequen-
cy was received by the hardwire between the transmitter and re-
ceiver acting as an antenna. These unusually high noise levels prob-
ably saturated the preamplifier, causing the components to act in a
nonlinear fashion and thereby demodulating the AM radio signal
to produce audio frequency noise (50-20,000 Hertz).
Electrical noise was reduced by replacing the unshielded twin
lead cables with coaxial cables and grounding the outer lead. After
all these attempts over five days failed to reduce the noise suffic-
iently, the system was changed to the discrete frequency configur-
ation shown in Figure 6b. Overnight freezing of the ground caused
a delay some mornings to allow thawing of the ground and stabil-
ization of the electrical signal.
Between Stations 643 and 633 (Figure 5) the 30 m dipoles show
rapidly increasing apparent conductivity with decreasing interdi-
pole spacing. This indicates a highly conductive zone shallower
than 12.6 m, the median depth at n = a. Between Stations 637 and
633 the 15 m dipoles show a conductor at n = a and 2a. It appears
that the conductor lies about 6 m deep at 634 and dips to the east.
Between Stations 631 and 623 the apparent conductivity is relative-
ly uniform, ranging from 125 to 200 mmhos/m.
Only the phase for 30 m dipoles with n = a will be discussed here
because:
(1) the median depth shows n = a to be most representative of the
plume
(2) the 30 m data had to be filtered to be interpreted whereas the
15 m data were too few to be filtered
(3) the electromagnetic coupling is smallest at n = a. This coupling
is the inductive/capacitive effect of the transmitting system on
the received signal. The decoupling corrections by ZERO were
less than one milliradian.
Phoenix Geophysics Survey Results
Phoenix Geophysics also experienced problems due to the un-
usually high radio frequency interference at the site. Measure-
ments by USEPA showed that most of the interference was caused
by commercial radio stations and the peak amplitude was 1 volt at
720 Hertz at the input of the Phoenix receiver. Low pass resis-
tance/capacitance filters reduced the noise to an acceptable level.
Unfortunately, the filters caused a phase shift in the input signal at
high frequencies, depending on the contract resistance of the elec-
trodes to the ground. Although the high frequency data were there-
fore unreliable, the low frequencies, which were of greater interest,
were unaffected.
The phase response from 1/64 to 1024 Hertz taken with 7.5 m
dipoles and n = 3a at Stations 622 and 644, representing uncontam-
inated and contaminated groundwater, respectively, are compared
in Figure 12. The shape of the curve taken at 622 is typical of clay-
bearing sediments. At high frequencies, high phase values are
caused by electromagnetic coupling and plot almost on a straight
line. At lower frequencies, polarization effects appear as a broad
smoothly varying curve with a peak of 10 mradians at 4 Hertz.
The measurements made at Station 644 differ. At high frequen-
cies, the electromagnetic coupling increased due to the higher back-
•—• Station 622
o—oStation 644
= 100
10-
1/64 1/16 1/4 1 4 16 64 256 1024
Frequency (Hertz)
Figure 12
Comparison of the spectral phase response of contaminated Station 644
and uncontaminated Station 622
SITE INVESTIGATION
33
-------
ground conductivities. However, below 1 Hertz the phase drops off
rapidly to zero in agreement with lab measurements by Sill." Thus,
the low frequencies should best indicate contamination.
USGS Laboratory Results
The apparent resistivity varied from 1.5 to 7.1 ohm-meter, was
highest in the 0 to 0.6 m sample and lowest in the 3-3.6 m and 4.5-
5.1 m samples. The phase varied from about 0.1 to 177 mradians,
being highest at a frequency of 0.01 Hertz in the sample from
3-3.6 m. In general, the greatest phase angles were measured at
this frequency. The phase signatures showed enough variation at
low frequencies to suggest the need to conduct field measurements
down to a frequency of 1/64 Hertz.
These laboratory phase measurements are different from the
field measurements of ZERO and Phoenix Geophysics. Table 1
shows the USGS median and mean phases measured at 1, 0.5,
0.2, 0.1, and 0.05 Hertz.
Table 1
USGS Phase Measurements at 1,0.5,0.2,0.1 and 0.05 Hertz
Depth
(meters)
0-.6
1.5-1.7
3-3.6
4.5-5.1
6-6.6
Phase (mrad)
Median
11.7
15.6
26.9
71.1
58.6
Mean
15.4
18.7
38.5
68.6
49.7
The largest phase angle measured by ZERO was only 4.6 mrad-
ians between Stations 620 and 643 at 1/8 Hertz. Of the 167 phase
measurements made along this part of the transect, 95% were
less than 3.5 mradians. The largest phase measured by Phoenix
Geophysics was 5.6 mradians for the 792 measurements made with-
in 15 m of Station 643 at which the soil was sampled. Ninety-
nine percent of these readings were less than 3.5 mradians. There-
fore, these field phases were 2 to 10 times less than the laboratory
phases.
The difference may be caused by: (1) the large change in scale
between the laboratory measurements on 2.5 cm samples and the
field measurements on 3-30 m "a" spacings; and (2) a change in
sample composition due to loss of organic or water vapor. De-
gassing is a common problem in water and soil sampling, and may
have been due to: (1) air spaces around the samples; (2) plastic
bags that were not sealed air tight; and (3) samples that were not
cooled for shipment. Improved sampling methods which would
insure sample integrity are under consideration.
Organic Vapor Results
The measured equivalent methane concentrations are shown in
Figure 13. Most (75-95%) of the organic vapor was benzene, ac-
cording to the chromatograms. There was a small chlorobenzene
peak. If the vapor was only benzene, then the concentrations in
Figure 13 should be multiplied by 1.5 in order to get actual ben-
zene concentrations.2 The actual organic vapor concentrations may
have been higher than the plotted concentrations because: (1)
above ground air could have moved down into the hole and into
the sampling tube; and (2) some sampled organics could have
adsorbed on the inside wall of the Tygon tubing.
The profile agrees well with those from electromagnetic induc-
tion and resistivity. The three peaks suggest lateral inhomog-
eneities. The water table is close to the surface along this transect
and the soil is loose, allowing little chance for the organic vapor
to move much laterally as it leaves the liquid phase. Therefore,
the surface profile is probably a reasonable representation of the
subsurface liquid location.
The benzene concentrations measured by Desert Research Insti-
tute at the 2m depth and in the wellhead space are shown in Fig-
ure 14. The concentrations are measurable between Stations 633
and 649, where the electrical methods also show a response. These
data agree well with those of Technos" for the part of the transect
having measurable benzene vapor. The Technos concentrations
were higher despite the possibility of sorption loss and dilution
by above ground air. One reason may be that the Technos meas-
urements were made in the head space of uncased holes, allowing
organic vapor transport from the earth through the entire wall
area of the hole above the water table. The uncased holes had an
average wall area of 0.88 mj, far greater than the slotted area
allowing organic vapor transport through the walls of the cased
holes. Desert Research Institute found the benzene concentration
immeasurably low in some wells, using the indicator tubes in the
head space of the wells with slotted casings from top to bottom,
e.g., Station 643 in Figure 14.
Organic Vapor Maaiuramanu
Pinman Lateral Transact
£'"',*' ''i' " '«' ''A' "4111T4"
s : : £ s s s
Sution
.»
•10
Figure 13
Soil gas profile obtained by OVA"
Figure 14
Benzene measurements
The benzene concentrations measured by Desert Research Insti-
tute with the soil gas sampler at 2 m may also be low because air
from above ground may have been drawn through the 0.3 m of soil
above the soil gas inlet and diluted the soil organic vapor.
The well at Station 645 was pumped as usual before taking a
water sample. The benzene in the head space was measured sev-
eral times thereafter as shown in Table 2. It seems that the pump-
ing of the groundwater caused a release of organic vapor and the
initial high concentration. The benzene concentration seems to
have then declined to an equilibrium based on the normal rate of
transfer of organic vapor from the water and surrounding soil.
34
SITE INVESTIGATION
-------
Table 2
Benzene Concentrations in Well 645
Time After Pumping (hours)
Concentration (ppm)
Few minutes
27
52
172
420
38
22
18
Figure 15
Apparent conductivity measured by Phoenix Geophysics at n = a and
a = 7.5 m (median depth = 3 m), total dissolved solids, and water table
depth as a function of station number.
«
-------
contaminated with organics or inorganics in order to develop a
better understanding of the frequency dependent signatures of the
output variables.
All of the methods need to be implemented at a site contam-
inated only with organics in order to separate the effects of organ-
ics and inorganics.
REFERENCES
1. Edwards, L.S., "Modified pseudo-section for resistivity and IP",
Geophysics 42, 1977, 1020-1036.
2. Foxboro Century, "Instrument literature," 1983.
3. French, R.H., Mifflin, M.D. and Edkins, J., "Soil Storage in Lower
Las Vegas Valley," Report from Desert Research Institute to U.S.
Bureau of Reclamation, 1982.
4. Hunt, G.R., Johnson, G.R., Olhoeft, G.R., Watson, D.E. and Wat-
son, K., "Initial report of the Petrophysics Laboratory," U.S.
Geological Survey Circular 789, 1979.
5. JRB Associates, Inc. Henderson Industrial Complex, USEPA Con-
tract 68-04-5052, Directive of Work 23, June 1981.
6. Klein, J.D., Pelton, W.H. and Washburne, J.C., "Spectral in-
duced polarization survey, Pittman and Sunset Transects, Henderson,
Nevada," Report to Lockheed Engineering and Management Services
Co. 1983.
7. McGillem, C.D. and Copper, G.R., "Continuous and Discrete Signal
and System Analysis:" Holt, Rinehart and Winston, Inc., New York,
1974.
8. McNeill, J.D., "Electromagnetic terrain conductive measurement at
low induction numbers," Technical Note TN-6, Geonics Limited,
Oct. 1980.
9. Mooney, H.M., Handbook of Engineering Geophysics, Volume 2:
Electrical resistivity. Bison Instruments, Inc., 1980
10. Sill, W.R., "Induced polarization in clay-bearing sandstones and the
effects of oil saturation," Research Report, Institute of Geophysics
and Planetary Physics, University of California, San Diego, 1964.
11. Sill, W.R., UURI presentation to Lockheed-EMSCO Environmental
Monitoring Department, 1983.
12. Stauffer Chemical Co., Second Quarterly Report, Sept. 1982.
13. Technos, "Geophysical Investigation of the Henderson Site Plume,"
Report submitted to Lockheed-EMSCO, Jan. 1983.
14. Tinlin, R.M. and Zonge, K.L., "Feasibility of using complex re-
sistivity to monitor groundwater contamination," Report to
USEPA, 1983.
15. U.S. Bureau of Reclamation, "Colorado River Basin Salinity Con-
trol Project, Point Source Division, Las Vegas Wash Unit, Nevada.
Pittman Verification Program," Draft Verification Plan Report, Apr.
1983.
16. Vingoe, P., "Introduction of electrical resistivity surveying," ABEM
Geophysical Memorandum 5/72, 1972.
17. Zohdy, A.A., Eaton, G.P. and Mabey, D.R., "Application of sur-
face geophysics to groundwater investigation, Chapter Dl" in Tech-
niques of Water Resources Investigations of the United States Geo-
logical Survey, Book 2, Collection of Environmental Data, 1974.
36
SITE INVESTIGATION
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REFINED STRATEGIES FOR ABANDONED
SITE DISCOVERY AND ASSESSMENT
CHARLES R. FELLOWS
JAMES H. SULLIVAN, Ph.D.
Water and Air Research, Inc.
Gainesville, Florida
INTRODUCTION
Assessment of abandoned hazardous waste sites typically in-
volves field efforts to help determine severity and extent of con-
taminant movement. Work scopes for site appraisal are usually
developed after limited efforts to identify wastes disposed of at the
site and general site environmental characteristics. There is a need
for better methods to develop appraisal work scopes. This need is
indicated by a significant amount of technically inappropriate or
inefficient work scopes which have been developed at various sites.
There are no universal assessment strategies that may be
automatically applied to adequately identify or characterize suspect
hazardous waste disposal sites. Furthermore, standardized con-
tamination assessment protocol is not appropriate due to the exten-
sive variability of site-specific factors. These factors include
disposal practices, waste substances, site environment and types of
human or environmental resources that are at risk.
Although a universal site appraisal method is not feasible, it is
possible to develop a formal framework within which successful
site appraisals can be developed. The essence of such a framework
must be accurate consideration of potential human and en-
vironmental significance of an individual site. This has been par-
tially addressed by site ranking models which characterize and
categorize sites in a systemized but somewhat arbitrarily defined
manner. The typical purpose of such ranking models is to reduce all
information about a site to a single number. This number may be
compared to values for other sites in order to prioritize resource
allocation for site investigations. While filling an important need in
the site assessment process, such ranking models do not define the
best strategy by which individual sites can be assessed or
characterized.
Here is a systemized approach to site appraisal intended to guide
development of field work scopes which are technically adequate
yet free of requirements for unneeded or unusable information.
Systematic site appraisal includes four basic considerations which
are discussed in detail in the following section:
•Defining which substances at sites pose threats to human health or
environment; this involves identifying which chemical substances
are toxic, how they are toxic, to which environmental component
they are toxic and at what level they are toxic.
•Defining in situ factors which may impact the fact of specific
contaminants of concern.
•Identifying waste movement patterns so that monitoring schemes
are used which encounter waste substances during sampling.
•Selecting appropriate analytical methods which accurately quan-
tify contaminants, but strictly according to the rationale defined
in the first item above.
Performing initial site assessments by rote may result in inade-
quate site management and may poorly utilize financial resources.
It is important to alert waste site investigators to some of the inade-
quate strategies that have been formulated in the past and to pro-
pose an appraisal system that helps eliminate repetition of these and
similar recommendations.
Actual sampling and monitoring recommendations are presented
and critiqued in this paper, but clients, locations and investigating
contractors remain anonymous. This is done to avoid problems and
delays associated with obtaining permission to publicize sites. The
need to reveal all aspects of site information for scientific scrutiny
is offset by the need to relay essential facts about certain sites for
the purposes of rapidly developing the issues presented in this
paper.
Material presented here has come from over a dozen studies at
different locations and the critiqued recommendations have been
made by individuals from over half a dozen organizations. Similar
recommendations can be found in many publicly released studies
involving assessment of abandoned hazardous waste sites.
SYSTEMIZED APPROACH TO SITE APPRAISAL
Four essential aspects of successful site appraisal are presented
below. These are interrelated and, in practice, often cannot be
totally segregated. However, they are presented individually for
purposes of explanation and consideration.
Rigorous Definition of Potential Hazard
This aspect of site appraisal is presented first because all other
aspects depend upon it. Specific threats to human health and/or
environment must be carefully and rigorously defined. Rigorously
is a key word because all too often investigators tend to lose sight of
the specific problem, i.e., the potential threat, when analyses for
site evaluation are selected. Only by defining problems carefully
can appropriate analyses be performed to confirm or deny problem
existence. This involves defining which substances at a site are toxic
or potentially toxic. Then the investigation must specify how these
substances are toxic, to what aspect of the environment they are
toxic and at what level they are toxic.
In order to adquately assess a suspect uncontrolled waste site, it
is necessary to know types of waste potentially present. This often
proves to be the most challenging aspect of site appraisal. It is com-
mon to experience difficulty in determining exactly what wastes
were disposed of at a given site. However, if rigorous appraisal is to
be accomplished, stipulation of actual waste substances using
technical judgment, as needed, must be made. There is a great
tendency to consider an almost infinite assortment of potential
SITE INVESTIGATION
37
-------
wastes, but this leads to elaborate site assessment work which often
cannot be tolerated due to limited resources. In lieu of reliable
documentation of materials placed at a site, review of significant
waste contributions and/or contributing processes must be used to
deduce a limited number of highly probable site constituents.
Once specific site constituents are determined, the level of con-
cern for each chemical substance must be defined. This level is the
concentration at which a contaminant poses a health or en-
vironmental risk. Defining this level is sometimes difficult even for
regulated or water quality criteria compounds and can be much
more difficult for other chemicals. However, only by defining a
concentration level of concern can answers be provided for the
question of whether or not a threat exists. Also, this level
establishes analytical detection limits.
Threats to human health can involve death, illness, localized ir-
ritation, aesthetic concerns, reproductive dysfunction or long-term
manifestations such as cancer. Threats to the environment take
many forms including habitat destruction, plant or animal toxica-
tion or bioconcentration of contaminants. Wastes may threaten
community structure or stability by being toxic to juvenile forms of
certain species. A final justification for rigorous hazard assessment
is as follows.
Site assessments involve a series of investigating organizations
with one group implementing recommendations of another
organization. Consequently, unless a well-defined perceived risk is
presented along with a comprehensive plan for its evaluation, the
recommended monitoring plan may be changed and a poor assess-
ment performed.
Interactions Between Wastes and Site Environment
To adequately assess a suspect uncontrolled site, it is necessary to
understand the environmental fate of wastes at the site. Waste
substances can interact with other wastes, water and with strata in a
multitude of ways. Of these interactions, those among different
wastes usually can be predicted with the least amount of confidence
because extent of mixing of wastes within the site cannot be de-
fined. Well mixed sites are rare.
Reactions between wastes and water (percolation and ground-
water) fall into both physical and chemical categories. After
disposal, wastes may dissolve totally or only certain constituents
may be solubilized. Waste constituents may react, be precipitated
by, or chelate with naturally occurring chemicals in ambient water.
Physically some wastes will tend to form layers that float on the
ground water table while others tend to sink into it.
Wastes will interact with earth strata and change in
characteristics, and in doing so negate, change or create new health
and environmental threats. Hydrophobic wastes tend to sorb to
earth materials either irreversibly or with some continual desorp-
tion. Some wastes might be chemically neutralized by some strata
like acids by limestone or oxidants in organic soils. The biological
component within the ground may affect decomposition by utiliz-
ing waste organics as carbon substrates or may affect biotransfor-
mation, for example, DDT to DDD or DDE. Volatilization of both
sorbed and dissolved materials can also occur.
Defining fate of contaminants of concern permits substantial
narrowing of site assessment work scope. Fewer sampling points
(e.g. wells) and fewer analyses can abe used to determined contami-
nant movement. At some sites, insufficient information about
aquifer characteristics may preclude assessment of contaminant
fate. In these cases broader, more costly monitoring must be used.
Therefore, gathering information about in situ factors and making
technical judgments regarding contaminant fate are essential to a
refined assessment method.
Contaminant Migration Appraisal
During this step of the appraisal system, physical characteristics
of the site are evaluated to identify existence and locations of
potential migration routes. Routes of interest are those related
directly to threats posed by individual wastes. When developing
sampling schemes, it is important to maintain an awareness of
possible waste movement in the environment. For example, if dur-
ing rigorous definition of potential hazards only potable wells
screened far below the groundwater surface have been identified as
possibly threatened, then screened portions of proposed monitor-
ing wells should not intercept near-surface groundwater layers.
This concept is expected to be controversial because it forces focus-
ing of consideration rather than "shotgun" style testing. Nonethe-
less, if hazard definition has enabled a focus solely on deeper
aquifers, then attempts to detect contamination in shallow aquifer
zones should be avoided.
Specifying Appropriate Analytics and Sampling
Even if all other steps are performed well, the end result of a site
assessment may be less than worthwhile if inappropriate analytical
methods are used. All analytical methods have finite limits of preci-
sion and accuracy and may be affected by various kinds of in-
terferences.
Different tests for the same analyte will probably have different
levels of complexity, different sets of interferences, different detec-
tion limits and, of course, different costs. Methods that measure
groups of chemical species, e.g., methods for oil and grease or
phenolics, may suffer from systematic errors by not measuring all
the species equally.1'2
It is therefore important that method selection be dictated by the
nature of the specific threats at the site under consideration. This
means that:
•An analytical method must be sensitive enough to detect a con-
taminant concentration at, or preferably below, the level of con-
cern.
•The selected method should be specific enough for the contam-
inant of concern.
As an example, the use of the Total Organic Halide (TOX)
method for detection of pesticides in water can be considered. Al-
though this test will measure halogenated pesticides, it will also re-
spond to all other halogenated organics. If detected in a sample,
further testing would be required to identify and quantify any such
pesticide, if it were actually present. Additionally, if DDT were the
chemical of concern, the TOX test would be a poor choice since the
solubility of DDT in water (about ljtg/1) is about five times lower
than the sensitivity limit of this method.' Therefore, DDT could re-
main undetected and still pose a threat to the environment or
human food chain.
The use of indicator analytes can speed up and reduce costs of
site assessments. When a single component of a waste is used as an
indicator analyte, it is important that the substance be an ap-
propriate measure of contamination. It is also important that its
measurement allow an accurate assessment for all associated con-
taminants of concern. One example of a poor indicator analyte is
the use of lead as an indicator of leaded fuel contamination.
Methods for lead analysis are relatively routine, provide adequately
low detection limits and are relatively inexpensive. Tetraethyl lead
(TEL) has a fresh water solubility of about 0.25 mg/1 or about 0.16
mg/1 as lead." At saturation, TEL would exceed the interim
primary drinking water standard for lead by about three times.5 If,
by water movement and associated natural processes, TEL-
saturated water were diluted 5 or 10 times and then sampled, it
would yield lead values that would not exceed potability standards
and that would not be distinguishable from water containing lead
as a naturally occurring contaminant.
A better indicator analyte for petroleum fuels like leaded
gasoline is benzene. Such fuels are manufactured to specifications
for properties such as volatility, flash point and octane rating. Con-
sequently, actual chemical composition may vary greatly. Data ac-
quired by this author for three different gasolines, both leaded and
unleaded, showed benzene to comprise slightly over 1 % in all three.
Benzene solubility is about 0.8 g/1 or over 3,000 times greater than
TEL solubility.4
38
SITE INVESTIGATION
-------
Benzene would not be expected to be a naturally occurring con-
taminant. The published USEPA detection limit for benzene is 0.2
/ig/1 which is well below the 6.6 /tg/1 criterion for a lifetime cancer
risk of one in 100,000.'
If benzene-saturated water were diluted 10,000 fold, a sample
would yield a benzene concentration corresponding to a lifetime
cancer risk of greater than one in 10,000. In the previous example,
the lead value would have been about one-third the drinking water
standard with only a ten-fold dilution. Benzene would appear to be
a better general indicator of fuel contamination, especially for
threats involving taste and odors, carcinogenicity and chronic tox-
icity to aquatic organisms.
Rigorous hazard assessment (as discussed above) involves defin-
ing which component of the environment is at risk. This then dic-
tates what samples should be collected. When possible, samples
should be taken from the component that poses the potential
threat. For example, if pesticide contamination of fish is the
perceived threat, water or sediment sampling and analysis would
not be adequate since fish may bioconcentrate some pesticides up
to 100,000 to more than 1,000,000 times ambient levels.8'9 Using
water and sediment samples for indicators of food chain con-
tamination requires that the results must be extrapolated for
evaluation of the food organisms. If no pesticides are detected,
they may still be present and concentrated to levels of concern in
fish. If pesticides are found in water or sediment, site assessment re-
quires that concentrations found will be assumed to be static with
regard to time and sampling locations. However, further monitor-
ing may be necessary to adequately evaluate the actual amount of
pesticides in the system.
When formulating sampling instructions, care should be taken to
be specific about factors that may influence the assessment.
Seasonal rainfall, ocean tides, land development, well screening
depths, composite sampling and determination of dissolved or total
analytes are some of the factors that may pertain to a given site.
Another factor to be considered is that no two laboratories
follow the same procedures for all routine analyses. Before sampl-
ing it is important to communicate with the analytical laboratory
which methods are to be used, what detection limits are necessary
and the nature of the quality assurance and control data that are
desired.
AN EXAMPLE OF SYSTEMIZED SITE APPRAISAL
As a way of further explaining the concepts of the systemized ap-
praisal system discussed above, an example is given. Consideration
of uncontrolled petroleum disposal/leak sites will show a diversity
of problems that may be encountered and suggests the manner in
which they may be successfully evaluated. Such uncontrolled sites
may result from above- or below-ground leaks, fire fighting train-
ing activities, vehicle maintenance, traffic accidents and past waste
disposal practices. This type of site is usually easier to evaluate than
other types of waste sites since the waste is generally one or two
kinds of fuels and not a combination of poorly documented spent
wastes. Even though it is relatively easy to evaluate, the following
discussion will demonstrate that a broad range of factors must be
considered in order to successfully assess a site containing these
wastes.
Rigorous Definition of Potential Hazard
Petroleum fuels are variable organic mixtures,10'11 and different
distillation fractions may be blended together. Sometimes ad-
ditives, like tetraethyl lead and tetramethyl lead, may be used to in-
crease the octane rating. Information about the quantitative com-
position of even specific lots of motor fuels is rare.
Petroleum fuels contain alkanes, benzene, toluene, xylene and
naphthalene along with other less water soluble aromatics.
Benzene, toluene and xylene were estimated to make up about 87%
of the water soluble components in one type of jet fuel, JP-412.
These lower molecular weight fractions are believed by some to be
the fraction more toxic to aquatic organisms.'3 Of the chemicals
listed above, the two that pose the most cause for concern are
benzene and the organolead compounds.14 Benzene is a carcinogen
and is probably the most toxic of the soluble aromatics, while lead
is a toxic pollutant and is one of the interim primary drinking water
metals. Benzene has been found in both leaded and unleaded
gasoline between 1.1% and 1.2% and is water soluble to about 0.8
g/1. Leaded gasoline has been known to contain 3 g/gal of lead
although the fresh water solubility of tetraethyl lead is about 0.25
mg/1 or about 0.16 mg/1 of lead.
The threats posed by petroleum fuels are varied. Petroleum fuels
may impact taste and odors to potable waters in addition to causing
lead and benzene contamination. One gallon of gasoline containing
3 g/gal of lead can contaminate about 16,000 gal of water to the 50
/ig/1 lead standard. Tetraethyl lead saturated water would exceed
this interim primary drinking water standard by about a factor of
three.
Since there is no drinking water standard for benzene, some
judgment must be made for an acceptable concentration in drink-
ing water (i.e., defining a concentration of concern). Among other
human health effects, benzene is a carcinogen. The criteria concen-
tration which corresponds to a lifetime cancer risk of 1 in 100,000 is
6.6 jig/1. If a lifetime cancer risk of 1 in 10,000 is judged acceptable
and a linear extrapolation to 66 /tg/1 is made, 1 gal of gasoline could
contaminate about 120,000 gal of water.
Benzene saturated water would probably cause taste and odor
problems impairing potability and would require orders of
magnitude dilution before it could be considered safe. Tetraethyl
lead saturated water would only require about a three-fold dilution
to be acceptable by the lead standard.
Environmentally, petroleum contamination may produce
chronic and acute toxic responses in aquatic organisms, changes in
behavior, flesh tainting in commercially important species and
bioaccumulation in food chains.12'13'16 Lead toxicity to aquatic
species and water hardness have been found to be inversely and ex-
ponentially related. Guidelines for 24-hour averages are 0.75 and 20
/tg/1 for water hardness of 50 and 200 mg/1 as CaCo3>
respectively.14 Because of this relationship, the hardness of the
threatened water should be considered when deliberating on the
concentration of concern for lead. It should be noted that the
Water Quality Criteria'4 guidelines are for total recoverable lead
and not specifically for organolead which might be expected to be
more easily bioaccumulated.
Water Quality Criteria guidelines for benzene in the aquatic en-
vironment are less specific but indicate that acute toxicity may oc-
cur at or below 5 mg/1 in fresh or saltwater. In a review paper on
the effects of oil on marine organisms, Moore and Dwyer present
data showing that larvae of all species in the main bay under study
were killed by the soluble aromatic fraction at concentrations of
between 0.1 and 1.0 mg/1.'3 Generally, it appears that adult
organisms experience sublethal or lethal effects at between 1 to 10
mg/1. They cite another study that found feeding, reproduction
and social behavior of fish and lobsters to be adversely affected by
soluble aromatics fractions at concentrations of between 10 and 100
jig/1. They further discuss bioaccumulation of soluble hydrocar-
bons and provide a simple example showing a 50 /*g/g accumula-
tion by an oyster from an ambient concentration of 1.25 jtg/1.
Some organisms will lose some accumulated aromatics if exposure
is discontinued.
Two other issues involving a waste fuel disposal/leak site should
be considered. One is the explosion or fire hazard caused by the
build-up of fuel vapors in underground structures, and the other is
consideration of feasibility of recovering fuel floating on ground-
water. This option should be considered even if no threat exists
since the cost of recovery might be less than the value of the
recovered fuel.
Interaction Between Waste Fuel and Site Environment
In the above discussion, the fuel components of concern are
identified as lead, water soluble aromatics of which benzene might
SITE INVESTIGATION
39
-------
be the most threatening, flammable vapors and the recoverable
bulk of the spillage.
Fuel spilled on or in the ground would saturate soil and tend to
migrate downward to the groundwater table. This migration would
occur either as organics solubilized in recharged water from the soil
sorbed fuel or as bulk fuel if sufficient quantity had been released.
Upon reaching the water table, the soluble fraction would migrate
downgradient with the groundwater. Bulk fuel would form a
floating layer on top of the water table. Water soluble constituents
would be released to water at the fuel/water interface and to subse-
quent recharge water percolating through a fuel-saturated layer.
Environmental factors affecting individual fuel components in-
clude the biological decomposition of fuel organics which is ac-
complished mostly by aerobic bacteria." Straight chain paraffinic
hydrocarbons are decomposed most readily while the aromatic
fraction are metabolized very slowly. When exposed to sunlight,
tetraethyl lead can be photo-degraded but otherwise has stable
molecular structure."
Migration Assessment of Waste Fuel
Assessing potential waste movement typically requires site-
specific information. However, several general issues are discussed
to indicate assessment procedures. The fuel components of concern
may migrate from the spill locationby movement of a floating layer
on top of the groundwater table, by dissolution into the ground-
water and subsequent migration with groundwater flow and/or by
volatilization. Petroleum fumes may pose a hazard either on or off-
site but most likely only if confined to an enclosed space.
Since fuel may form a floating layer it is important to consider as
potential migration corridors the trenches in which pipeline and
cables have been placed and then backfilled." Such situations
become especially important when these backfilled trenches in-
tercept the groundwater table since the backfilled material may
have a greater hydraulic conductivity than the original undisturbed
material.
Various geophysical methods may be employed to delineate areas
of a subsurface fuel layer, while the use of wells may be needed to
assess the soluble contaminants or to supply additional information
about subsurface fuel layers. Organic fume sensors or combustible
gas indicators are available to assess the hazard posed by volatile
fuel components.
Appropriate Analytics and Sampling
Before formulating recommendations for sampling and
analytics, final selection of the waste fuel component of concern
must be made. Both lead and benzene are candidates. Of the two
major contaminants, benzene is the better indicator analyte since:
(1) it can be found over a detectable range of at least six orders of
magnitude; and (2) benzene is unlikely to be found as a naturally
occurring contaminant. Published detection limits for conventional
lead1 and benzene methods' are similar (1.0 and 0.2 /ig/1, respec-
tively) although the cost of analysis is several times greater for
benzene.
Use of an oil and grease extraction with subsequent gravimetric
or infrared detection is not appropriate since all or some of the
soluble organics will be lost.1-2 Additionally, these procedures have
detection limits greater than the concentration of concern and are
not specific for the contaminant of concern.
Sampling for either organolead or volatile hydrocarbons should
be accomplished in a manner which avoids placing the sample in a
partial vacuum or bubbling gas through the sample.!° Collection of
soil samples, when potable water is threatened, is only appropriate
for sites of recent contamination where insufficient time has elaps-
ed to allow contaminants migration to the water table.
The greatest threats posed to aquatic life by petroleum fuel are
by lead and the soluble aromatic fractions. Bioaccumulation of
these substances may cause tainting of flesh and/or possible food
chain contamination.
The analytical rationale for assessing the threat to aquatic life is
similar to that for potable water assessment. Lead, however, may
pose a relatively greater threat to aquatic life. Hardness of the
threatened water influences the choice of the appropriate test(s) to
be performed." Benzene analysis by gas chromatography allows
quantification of other water soluble aromatics at little or no addi-
tional cost.
Appropriate samples include water for assessing the threat to the
aquatic organisms. Tissue samples from selected species may be ap-
propriate if food chain contamination were at issue and sufficient
time had elapsed since fuel release for bioaccumulation to have oc-
curred.
Fires and explosions may endanger human life and property.
These risks can be appropriately evaluated with instruments that
measure volatile organic vapors. Appropriate in situ measurements
can be performed in confined spaces where build up of fumes might
occur.
Regarding possible recovery of petroleum products, the initial
issue may be to evaluate the amount of free product available for
recovery. This layer is appropriately measured by determining the
thickness of the fuel in monitoring wells by using water finding and
gasoline finding pastes on a measuring tape.17 Screening in such
wells should include the interval in which the fuel layer would be
floating upon the water table. Accurate estimation of the total
amount of fuel requires adjustment of the measured fuel thickness
in a well to allow for capillary pressures in the fuel saturated
medium (soil) and medium porosity.31 Geophysical methods can
also be used to assess fuel volume, delineate fuel layer boundaries,
and to assist in siting monitor and recovery wells.
Summary
Waste fuel, disposed of or leaked at a site, can present a signifi-
cant hazardous waste contamination problem. However, when
compared to sites receiving many different wastes, this situation is
relatively uncomplex. Yet, successful site appraisal requires that a
wide spectrum of factors be considered. The preceding paragraphs
indicate this process.
REFINING PAST ASSESSMENT STRATEGIES
The following recommendations are presented as examples of
rudimentary strategies. These strategies would have allowed better
site assessment if the proposed appraisal system had been applied.
Generally it appears that many inappropriate recommendations
have been made due to either lack of a precisely defined threat or
lack of a thorough understanding of the analytical methods re-
quired. In many instances, inappropriate analysis of soils or
sediments were made instead of directly assessing water contamina-
tion. In most cases, the specific threat was never clearly stated nor
were rationales for the recommendations presented.
Strategy No. 1—Fire Protection Training Area
Situation: A diked pit has been used since the mid-1950's for fire
fighting training activities. Prior to the mid-1970's training ac-
tivities were held monthly during which "contaminated fuels and
some combustible waste chemicals were burned." Since the
mid-1970's, only uncontaminated jet fuel has been burned on a
quarterly basis in quantities of about 500 gal. An underdrain
system with an oil/water separator exists, but the installation date
is not known. The nearest receptor is a creek about 800 ft away
which is used for recreation. The nearest well is about 5,000 ft
away. The most definitive statement of the threat posed by this site
was that the site was "considered to have a moderate potential for
environmental contamination."
Actual Recommendation: Take soil samples at regular intervals
and at any interface from each of six soil borings. Prepare a water
extract of each soil sample and analyze extract for: 12 metals, TOC,
pH, oil and grease, cyanide, phenol, PCBs, dissolved solids,
fluoride, nitrate, four insecticides, two herbicides and radium. In-
40
SITE INVESTIGATION
-------
siiui ana sample four wells if soil boring observations indicate the
presence of contamination.
Refined Strategy: Since this site was still in use as a fire fighting
training area and no concern was expressed about human contact
with the soil surface, it will be assumed that no such human health
threat existed. The greatest threat is from contaminant migration
off-site to the nearby creek. Any materials in the soil have had suf-
ficient time to leach into the groundwater. Therefore, analysis of
soil extracts is unwarranted. Assuming 20 soil samples, eliminating
soil testing saves about $10,000.
Well installation and sampling would provide data on the
medium of concern, i.e., the groundwater. Because this site was
used for 25 years, well placement near the pit would be appropriate
as would siting of wells further away from the pit and between the
pit and the creek. It might be expected that the nonfuel related
substances listed above were disposed of in common containers
with other wastes and that the composite was burned at this site.
Contaminants of concern are: water soluble petroleum aromatics,
halogenated organic solvents, phenolics, oil containing PCBs and
organolead. Appropriate analytics would be PCBs and purgeable
aromatics by G.C., TOX, phenolics by 4-AAP and, possibly, lead
by AAS.
Strategy No. 2—Well Siting
Recommendation: Generalized policy was stated that for each
site recommended for groundwater monitoring, four wells would
be used. Of these, one would be upgradient and three would be
downgradient.
Refined Strategy: Use of upgradient or background wells can
help to distinguish natural contaminant concentrations from
elevated levels. For example, if excessive lead loading to relatively
soft water is occurring it might be caused by naturally occurring
lead dissolution rather than from landfill leachate. Upgradient
wells can also provide valuable data for calculating direction and
speed of groundwater flow as well as other useful information
(e.g., pH, specific conductance).
However, situations exist where a universal well siting strategy is
not appropriate. Migration of spilled PCB oil to a potable well is an
example. Since PCBs are not naturally occurring substances, an
upgradient well would provide little useful information unless the
site location was in doubt. Financial resources might be better used
(e.g., installing another downgradient well).
Strategy No. 3—Food Chaiji Assessment
Situation: A landfill received both industrial and municipal
wastes over a 30-year period. When this landfill was closed, a
recreational area was created including a large pond which is partly
situated into an area formerly occupied by landfill wastes. This
pond was later stocked with various species of game fish. The pond
is used intensively by sport fishermen but has never required
restocking. Concern exists about the possibility of bioaccumulation
of pesticides and PCBs by these edible fish.
Recommendation: Sample and analyze pond water and sediment
for pesticides and PCBs.
Refined Strategy: Since a self-sustaining fish population exists
and an elapse time of years should have allowed for the bioac-
cumulation of the substances of concern, the medium of concern,
i.e., the fish, should be sampled directly. Select species with dif-
ferent food preferences (e.g., bottom feeders, like catfish, fish con-
sumers such as bass) and analyze edible tissue composites of in-
dividuals for pesticides and PCBs.
Strategy N o. 4—Landfill Contaminants
Situation: Two landfills may have received waste oils, solvents,
paints, pesticide containers and petroleum products in addition to
municipal wastes. The potential threat posed by these sites was not
stated although potable water was not threatened.
Actual Recommendations: Install one well at each site, sample
wells and analyze for TOC, COD, seven pesticides and two her-
bicides.
Refined Strategy: Since the nature of the threats posed by these
sites is not known, no adequate strategy may be suggested. Tests
for pH, TOC and COD were probably intended as indicators of
landfill leachate. Since the TOC and COD tests are general tests
and would, in the case of landfill leachates, be measuring the same
major constituent, i.e., organic carbon compounds, recommenda-
tion of both tests is a poor strategy. Selection of pH, specific con-
ductance and TOC would provide additional information related to
dissolved ionic substances and thus would be a better strategy to
identify landfill leachate. Analysis for TOX would provide infor-
mation on halogenated solvents.
Strategy No . 5—Photographic Waste Sites
Situation: At two sites, "significant" quantities of spent
photographic solutions containing silver were disposed of either by
overland discharge or via an underground drain field. These sites
received wastes for about 15 years during a period of high levels of
photographic laboratory activities. This disposal practice ended in
the mid-1960's. It was stated that if shallow groundwater became
contaminated, silver migration to a river could occur. The river is
located about 3,600 ft away from the nearest site. Depth to shallow
groundwater is less than 10 ft.
Actual Recommendation: Collect a composited soil sample from
each site and analyze for silver content. Each composite should
consist of three soil subsamples and should be collected from
various depths near or below the drain field from one site and from
the upper 10 cm at the other site. One background soil sample
should be collected and analyzed if the average silver concentration
for area soil is not available.
For each site that has soil concentrations of silver "several times
above background levels," two monitoring wells should be in-
stalled and quarterly sampling for silver should be performed. Well
placement should be adjacent to and further downgradient from
the site.
Refined Strategy: Soil sampling for silver is inappropriate
because:
•A significant quantity of silver was known to have been disposed
of between 15 and 30 years. If significant groundwater contam-
ination were going to occur, it should be apparent by now.
•The total soil content of silver will not indicate what silver frac-
tion is or will become mobile.
•Defining the background soil levels of silver on a single sample is
a tenuous approach.
•The concentration of concern, i.e., "several times above back-
ground" appears to be an arbitrary limit.
•These composited samples will effectively dilute the silver from
each subsample by a factor of three. If only one subsample is
actually taken from contaminated soil the apparent level of con-
tamination will be proportionally reduced.
Groundwater sampling is indicated. Well placement should be
immediately downgradient and farther downgradient from site.
Remove any suspended solids before sample preservation and
analysis.
Strategy No. 6—Organics Waste Site
Situation: During the 1960's and 1970's this one-half acre site
received various wastes including hardfill, metal spools, waste oil
and solvents. It is about 15 ft from the tidal zone of a bay and is
located on very sandy soil. Contaminants of concern were de-
scribed only as "waste oil, waste solvents and drums" and the
threat was defined as contaminant migration potential to the bay.
Actual Recommendations: Install four wells, one upgradient and
three downgradient, and, at a minimum, sample groundwater for:
chloride, iron, manganese, phenol, sodium, sulfate, pH, specific
conductance, total organic halogen and total organic carbon.
Refined Strategy: Since the contaminants of concern are oil and
solvents, and since this site is only about 15 ft from a tidal, seawater
bay, the inorganic analyses are inappropriate and probably cannot
distinguish landfill leachate from infiltrated seawater. Since the site
SITE INVESTIGATION
41
-------
area is small and distance to the bay is short, three downgradient
wells can be installed with a high degree of confidence that at least
one well will intercept any leachate plume. Recommended analyses
should be TOX, TOC, phenolics and purgeable aromatics. Specific
conductance and pH tests should also be performed to help discern
total flushing effects on the groundwater regime. An upgradient
well should be installed to assess inland spread of contaminants by
tidal action. More information is required to determine the op-
timum number of downgradient wells.
CONCLUSION
Formulation of assessment recommendations is often difficult
due to lack of information. At times, no amount of historical
record searching or scientific literature reviewing will eliminate this
problem. It is in such situations that rudimentary assessment
strategies are most justified.
In cases where adequate information is available or can be
assumed with a high degree of confidence, a more refined assess-
ment strategy is worthwhile. Systemically the first step is to clearly
define the environmental or human health threats and to identify
the contaminants of concern. After identifying interaction between
contaminants of concern and site environment, a site monitoring
plan should be formulated to assess all potential migration routes.
Lastly, appropriate analytical methods should be selected to quan-
tify the contaminants of concern to a level below the predetermined
concentration of concern and to provide an answer as to whether or
not a health or environmental problem exists.
With the exception of indicator analytes or group determina-
tions, the chemical analyses should be directed to the problem con-
taminant and the medium (e.g., water, fish) in which it will pose the
problem. Indicator analytes are conservative waste constituents
that may be used as tracers to reveal waste migration. Such in-
dicators should be relatable to the contaminants of concern. Group
determinations, such as total recoverable phenolics or total organic
halogens, should be elected only after verifying that limits of detec-
tion are adequate to assess the specific problem at hand.
Refining assessment strategies should help to provide better
evaluation of problems posed by specific sites. Data interpretation
becomes more straight forward, and financial resources are con-
served and better utilized.
REFERENCES
1. USEPA, Methods for Chemical Analysis of Water and Wastewater,
EPA-600/4-79-020, March 1983.
2. American Public Health Association, Standard Methods for the Exam-
ination of Water and Waste Water, 15th Edition, 1981.
3. USEPA, "Total Organic Halide-Interim Method 450.1," Environ-
mental Monitoring and Support Laboratory. Cincinnati, Ohio, 1980.
4. Roderer, G., "On the Toxic Effects of Tetraethyl Lead and Its De-
rivatives on the Chrysophyte Potesioochromonas malhamensis,'
Envir. Res. 23, 1980, 371-384.
5. Code of Federal Regulations, Title 40, Subchapter D, Part 141.11(b).
6. USEPA, Parameters Handbook for the Nationwide Urban Runoff
Program, Water Planning Division, Washington, D.C. 20460,
October 1979.
7. USEPA, "Methods of Organic Chemical Analysis of Municipal and
Industrial Wastewater," Method 602, EPA-600/4-82-057, July 1982.
8. Metcalf, R.L., "Biological Fate and Transformation of Pollutants in
Water," in Fate of Pollutants in the Air and Water Environmental.
Part 2. Chemical and Biological Fate of Pollutants in the Environ-
ment., I.H. Suffet, Editor. John Wiley and Sons, Inc., 1977.
9. Southworth, G.R. et a/., "The Risk of Chemicals to Aquatic Envir-
onment," pg. 85-153 in Environmental Risk Analysis for Chemicals,
R.A. Conway, Editor. Van Nostrand Reinhold Comp., New York,
New York. 1982.
10. DiCorcia, A., Samperi, R. and Capponi, G., "Gas Chromatographic
Analysis of Gasoline and Pure Naphtha Using Packed Columns,"
J. of Chromatography, 160, 1978, 174-175.
11. Petrovic, K. and Vitorovic, "Recognition and Qualitative Characteri-
zation of Commercial Petroleum Fuels and Synthetic Fuels by a Gas
Chromatographic Fingerprinting Technique," J. of Chromatography,
119, 1976, 413-422.
12. Fisher, J.W. et at., "Biological Monitoring of Bluegill Activity,"
Water Resources Bulletin, 19, 1983, 211-215.
13. Moore, S.F. and Dwyer, R.L., "Effects of Oil on Marine Organ-
isms: A Critical Assessment of Published Data," Water Res., 8, 1974,
819-827.
14. USEPA, "Appendix A-Summary of Water Quality Criteria." Federal
Register 45, No. 231, 79324-79341, Nov. 28, 1980.
15. Marshall, E., "EPA May Allow More Lead in Gasoline," Science,
215, 1982, 1375-1378.
16. Malins, D.C. and Hodgins, H.O., "Petroleum and Marine Fishes:
A Review of Uptake, Disposition, and Effects," Envir. Tech. 15,1981,
1272-1280.
17. American Petroleum Institute. "Underground Spill Cleanup Man-
ual." API Publication 1628, June 1980.
18. Sittig, M., Handbook of Toxic and Hazardous Chemicals. Noyes
Publications, Park Ridge, New Jersey, 1981.
19. Kramer, W.H. "Ground-Water Pollution from Gasoline," Ground-
water Monitoring Review, pg. 18-22, Spring 1982.
20. USEPA, Handbook for Sampling and Sample Preservation of Water
and Wastewater, EPA-600/4-82-029, Sept. 1982.
21. de Pastrovich, T.L. et al., "Protection of Groundwater from Oil
Pollution," CONCAWE Report Nr. 3/79, (Oil Companies' Interna-
tional Study Group for Conservation of Clean Air and Water-
Europe), Den Haag, Apr. 1979.
42
SITE INVESTIGATION
-------
INVESTIGATION OF SOIL AND WATER CONTAMINATION
AT WESTERN PROCESSING, KING COUNTY, WASHINGTON
HUSSEIN ALOIS
Ecology and Environment, Inc.
Seattle, Washington
JOHN OSBORN
FREDERICK WOLF
Environmental Services Division
U.S. Environmental Protection Agency
Seattle, Washington
INTRODUCTION
Western Processing began .operations in 1957 as an animal by-
products and brewer's yeast processor. Since then the operation has
expanded to include the handling of solvents, flue dust, battery
chips, acids, cyanides and a wide variety of industrial waste. The
company has Interim Status as a storage facility for hazardous
materials as regulated by the Resource Conservative and Recovery
Act (RCRA). It has no state or local permits for discharge to a
sewer, to surface water or to the ground and groundwater.
The site is located within the City of Kent but about four miles
north of the central business district. It lies in Section 1, Township
22N Range 4E, Willamette Meridian, the entrance is at latitude
47°25'37"N, longitude 122 °14'31"W and the address is 7215 South
196th Street (Figure 1).
The facility occupies about 13 acres on which there are a small
laboratory, a solvent recycling plant, a fertilizer plant, bulk storage
tanks, drum storage areas, piles of flue dust, construction debris
and large cement-block above ground storage lagoons for liquid
wastes, cooling water and process water. Mill Creek, also known as
King County Drainage Ditch #1, runs across the northwest corner
of the site from south to north. Along the eastern boundary the
Kent Bicycle Trail occupies a former railroad right-of-way, along
which run a high voltage power line and a drainage ditch. Beyond
these, to the east, is the Burlington Northern Railroad. Access is
from South 196th Street along the northern boundary (Figure 2).
The site lies in the flood plain of the Duwamish/Green River.
The area is very flat, with an average elevation around 20 ft above
mean sea level.
During May 1982, the USEPA conducted a stream survey
around Western Processing.1 Twenty-six of the priority pollutants
were found in the surface waters around the site, all of which were
subsequently found on-site.
During June 1982, the Municipality of Metropolitan Seattle
(METRO) sampled surface water upstream and downstream of
Western Processing in Mill Creek. A marked increase in heavy
metal content, mostly zinc, was noted.
As a result of these findings and an on-site inspection, the
USEPA issued an order under Section 3013 of RCRA to require the
owner to conduct such monitoring as would be reasonable to ascer-
tain the nature and extent of hazard to human health or the en-
vironment presented by the site. After the site owner had declared
himself unable to carry out the necessary monitoring, a court order
was obtained to enable the USEPA and its contractors to in-
vestigate the site.
GEOLOGY AND HYDROLOGY
The Green River valley lies within the Puget Sound Lowland
which consists of a broad plain of glacial sediments cut into by a
network of marine embavments. The Green River valley was
formerly one of those embayments and is filled with sand, gravel,
silt and clay brought down by the White, Green, Black and Cedar
Rivers.2
During the course of the investigation, the Western Processing
site itself was found to be underlain by sand, silt, gravel, clay, peat
and artificial fill. In places as much as six to eight feet of fill were
recorded, and in Well 22B battery casings were reported mixed with
silty sand from 15 to 24 ft. Clay was encountered in a number of
boreholes at depths from 6 to 15 ft, being more common under the
northern part of the site, at Wells 1A, 2, 4, 5, 6, 7, 8, 9, 10, 11 A,
12, 14, 17 and 20, but absent from Wells 18, 22B, 23, 24, and 25B
(Figure 3). The clay is gray to bluish gray in color and contains
organic material. It was probably laid down in a lake, or lakes,
which were common the Green River valley, and varies in thickness
from 1 to 4 ft. The most common materials encountered in
boreholes were fine sand, light brown or grayish brown, and silt,
gray to grayish brown, often mixed with some clay.
The water table was found at very shallow depths, ranging from
3 to 12 ft and averaging 6 ft from the surface. At Well 19, which
was installed in a depression north of South 196th Street, the water
flowed out at the surface. Water level measurements taken on Nov.
15, 1982 (Table 1) suggest that the relatively permeable material at
the surface within the facility and the lack of vegetation have
resulted in a higher rate of percolation of rain into the ground than
in surrounding areas. This appears to have created a groundwater
"high" or mound under Western Processing (Figures 4 and 5).
Although the predominant flow directions of groundwater are west
and north to Mill Creek, the mound would cause flow to the east
and even south within the site for a short distance as well. The flow
at Well 19 is probably a response to this local increase in hydraulic
head under a confining clav laver.
There are higher hydraulic heads in the shallow wells of adjacent
pairs such as 11 A, 11B and 17A, 17B (Table 1). This indicates that
the groundwater mound has created a hydraulic head which is driv-
ing groundwater down into the aquifer at least to levels below 30 ft,
since flow is always from higher hydraulic head to lower.
A berm along the east side of Western Processing now prevents
most surface runoff in that direction. Surface runoff from the site
was observed during the site investigation going west to Mill Creek
or out of the front gate and down into a depression outside the nor-
theast corner of the site.
SITE INVESTIGATION
43
-------
Figure 1
Western Processing, Kent, Washington
PRELIMINARY SITE INVESTIGATION
AND SITE SAFETY
Table 1
Water Table Elevations, November 1982 and May 1983
The toxic nature of many of the materials handled by Western
Processing required the development of a safety plan prior to any
on-site work. An ambient air characterization of the site was per-
formed on Sept. 23 and 27, 1982, to determine what respiratory
hazards might be present.
On Sept. 23, the field team members entered the site wearing self-
contained breathing apparatus and measured the air quality at 26
sites (Figure 6) using a Century Systems Organic Vapor Analyzer
(OVA), Model 128, and a Photoionizer, HNU Model PI 101. Sta-
tion 17 showed 4-5 ppm, the only site above a background level of 1
ppm. Shallow holes were dug by hand at a number of locations to
see if disturbed soil released volatile organics. Soil samples were
taken from these locations to determine what substances were pre-
sent. The soil samples from Stations 17 and 20 showed detectable
but not quantifiable levels of several volatile organic solvents.
On Sept. 27, the field team returned to the site to install High Vol
samplers with activated charcoal tubes. Four were installed on-site
at Stations 3,11,17 and 20 and two off-site at Stations 27 and 29 in
an attempt to collect organic vapor from the normal breathing
zone. Sampling was for a period of four hours only. None of these
tubes showed detectable levels of organics when analyzed at the
laboratory of Ecology and Environment, Inc., Buffalo, New York.
On the basis of the soils data, and because of the presence of bar-
rels and tanks of waste on-site, it was decided that all personnel
would wear air purifying respirators with combination particulate
and organic vapor cartridges when working on-site. As part of the
safety precautions, it was required that the breathing zone around
any hole being dug by drill or backhoe be monitored at all times
with the OVA or photoionizer.
All personnel leaving the site were decontaminated with steam
cleaner and detergent solution. All equipment entering or leaving
the site was steam cleaned. Wash water from these decontamina-
tion operations was collected into 55-gal Department of Transpor-
tation approved drums. After analysis they were removed to an ap-
proved waste disposal site.
Observation
Well
Number
1A (shallow)
IB (deep)
2
3
4
5
6
7
8
9
10
11A (shallow)
11B (deep)
12
13
14
15
16
17 A (shallow)
17B (deep)
18
19
20
21
22A (shallow)
22B (deep)
23
24
25A (shallow)
25B (deep)
26
27
28
29
Water Table
Elevations
(Feet Above Mean Sea Level)
November 1982
13.55
12.86
14.37
18.35
12.37
15.17
14.19
14.59
13.39
11.35
12.09
14.83
12.94
14.10
11.91
Cap Rusted On
15.29
13.73
16.39
12.72
15.86
14.35
15.88
12.80
13.90
13.77
14.05
13.34
13.81
13.85
14.48
14.51
....
May 1983
15.19
14.40
15.65
19.41
13.76
16.62
15.79
16.26
15.28
12.21
12.50
16.53
14.97
15.72
13.70
—
17.24
13.69
18.20
14.57
18.25
—
17.23
15.24
15.68
14.72
16.30
16.17
16.03
15.89
16.13
15.13
12.46
15.01
44
SITE INVESTIGATION
-------
Figure 2
Site Plan,
I-III Waste Ponds
Figure 3
Monitoring
Wells Locations
• MONITORING WELL
>]•
Figure 4
Water Table,
November 1982
Figure 5
Water Table,
May 1983
SITE INVESTIGATION 45
-------
Figure 6
Ambient Air
Sampling Locations
Figure 7
Soil Sampling
Locations
Figure 8
Priority Pollutant
Metals in Soils (ppm)
-1000- 1000 ppm contour
30,175 TOTAL PP METAL IN SOIL
11M
1433 "1" 30GB
i WESTERN 2
-------
CD'""
SeiHhlMthST.
Figure 10
Total Priority Pollutant
Volatiles in Soils (ppm)
Figure 12
Non-Priority Pollutant
Solvents in Shallow
Groundwater (mg/1)
Figure 11
Total Priority Pollutant
Volatiles in Shallow
Groundwater (mg/1)
Priority Pollutant Acid
Extractibles in Soils (ppm)
19 TOTAL P.P. VOUTILES
• MONITORING WELL
*-ESTIMATED FLOW DIRECTION
SITE INVESTIGATION 47
-------
Figure 14
Priority Pollutant Acid
Extractibles in Shallow
Groundwater (mg/1)
Figure 15
Total Priority Pollutant
Base/Neutral Extractibles
in Soils (ppm)
t UONITOR1NQ WELL
-100- 100 mj/l CONTOUR
SAMPLING PROGRAM
Well Installation and Soil Sampling
As a result of the USEPA and METRO surveys and an on-site in-
spection, the USEPA began a site investigation.
Sampling sites were proposed on the basis of the known site
history and from review of archival imagery, that is, aerial
photographs dating from 1960 through 1980. A number of wells
were installed around the perimeter, and a number of two level
wells (Stations 1, 11, 17, 22), were put in a line down the center of
the site to investigate changes in hydraulic head with depth. Re-
maining locations were selected as being on the site of former
lagoons, waste piles, spills, etc., or between such sites and the prob-
ably receiving waters to the north, west and east of the site (Figure 2).
The USEPA was initially informed that the site had been raised
with demolition debris and that they must be prepared to find con-
crete, brick, reinforcing bars, etc., below the surface. It was pro-
posed, therefore, to use a backhoe to dig through the fill, an ex-
cavation method that could handle such material and also expose
the depth and type of fill. Holes deeper than the reach of the
backhoe were to be drilled with a cable tool rig. The first two holes,
at Well 1 and at Well 11, were dug with the backhoe but exposed no
demolition debris; instead, sand and silt were common.
At Station 11 the level of volatile organics in the air around the
backhoe pit was greater than 1000 ppm. For this reason, and
because the site owner claimed that the backhoe pits were creating a
hazard for his employees, it was decided to sample soil and install
wells with the cable tool only. Later it was decided to bring a soil
sampling drill rig on-site to sample soil with a small diameter (3 in.)
solid stem auger, and to install well points in the holes.
The initial holes were dug and wells installed in the first week of
October. The soil sampling rig was brought on-site Oct. 12. On-site
drilling was completed by Oct. 26. Because of the methods used,
none of the soil samples is of undisturbed materials. Contamina-
tion from levels other than that being excavated was minimized by
carefully cleaning up the hole before sampling, in the case of the
backhoe and auger, and by driving down steel casing behind the bit
to shut off the upper part of the hole when the well was being con-
structed using the cable tool rig. Samples taken with the cable tool
from below the water table were scraped off the bit. For a summary
of soil samples taken from well locations, see Table 2. Each soil
sample was collected into two 8 oz wide mouth glass jars with
teflon-lined lids. The soil was scooped with a gloved hand into the
bottles. Between each sampling an outer disposal vinyl glove was
discarded and an inner butyl rubber glove washed in clean water,
brought on to the site by the field team.
Nine samples were also collected with a hand auger, on Oct. 25,
along the east side of the site. Seven came from between 1 to 2 ft
below the surface of a berm of material scraped off Western Pro-
cessing's yard and heaped up along its east side to prevent run-off
into a ditch outside the east fence. The remaining two samples came
from within the ditch at the north end of the site where a pipe pro-
trudes through the berm and boundary fence and where the
material in the ditch is stained as if by spilled material (Figure 7).
These were handled in the same manner as the other soil samples.
Eleven samples of surface soil were collected Nov. 18 from what
appeared to be spill sites (Figure 7). These were scraped up with the
sample container and pushed into the bottle with the teflon-lined
lid. The outside of each sample container was washed before being
packed.
Backhoe and cable tool holes had 4 in. PVC casing and slotted
screen set in them, the screen was surrounded with a gravel pack of
pea gravel and a mixture of bentonite and sand placed around the
casing to provide a seal up to the surface. The 3 in. holes drilled
with the solid stem auger had stainless steel well points on 2 in.
black iron pipe driven down into them. Both wells and well points
48
SITE INVESTIGATION
-------
Table 2
Summary of Soil Sampling Locations
— Jen — Method of — r
Number Drilling S
IA back
IB
2
3
4
9
6
7
8
9
1 0
1 1 A
1 IB
| 2
13
I 4
19
16
1 7A
1 78
IB
19
20
2 |
22A
228
23
24
25A
25B
26
27
28
29
30
ab!
uge
uga
uge
uge
uga
uga
abl
uga
ack
abl
uga
uga
abl
uga
abl
abl
abl
uge
*
ab 1
abl
abl
abl
abl
abl
uga
uga
uga
uga
oa
tool
too 1
oa
tool
tool
tool
tool
tool
too 1
tool
tool
tool
tool
tool
-rhod of
mp 1 1 ng
ackhoa
uger
ugar
uger
uger
ug«r
uger
uger
ugar
ackhoa
ugar
ugar
ugar
abla tool
abl a tool
ugar
ugar
ugar
"s? +
!„!
ugar
ugar
ugar
ugar
uger
ugar
ugar
Uaptn'to Mai ! —
Point ((t. )
12
30
12
12
19
12
12
12
16
19
1 «
12
29
9
1 2
16
19
i;
30
16
6
I ij
| •
27
19
I •
16
26
16
12
12
12
~HJe
3
X
x
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
pths ar Mhicn samp 1 as were co 1 1 acted i TT. j
6 9 12 1518 21 24 27 30
xxx
XXX X
X
X
X X •
X X
X
X
X X
X X* X
X X
X X
X X X X X
X X
xxx
X X
X X
X X
X
X X
X X
'Samples collected at 8 ft. and 10 ft.
—No sample collected since soils were documented in adjacent hole.
Table 3
Cl and TDS Results
Well*
01
01
02
03
04
05
06
07
08
09
10
11
11
12
13
14
15
16
17
17
18
19
20
21
22
22
23
24
25
25
26
27
28
29
30
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Water
Depth
Shallow
Deep
Shallow
Shallow
Shallow
Shallow
Shallow
Shallow
Shallow
Shallow
Shallow
Shallow
Deep
Shallow
Shallow
Shallow
Shallow
Shallow
Shallow
Deep
Shallow
Shallow
Shallow
Shallow
Shallow
Deep
Shallow
Shallow
Shallow
Deep
Shallow
Shallow
Shallow
Shallow
Shallow
Transfer Blank
Transport Blank
Lab #
45150
45151
44154
46153
44155
44156
44157
44158
45152
44160
44161
45153
45154
44159
44150
44163
45164
44164
45155
45156
45163
44151
44165
44166
45157
45158
45162
44167
45159
45160
45161
46150
46151
46152
51150.
44152
44153
C1(mg/1)
101
77
224
1500
127
1737
599
388
136
1899
5968
1508
1819
150
49
2553
1670
1144
3394
782
386
205
739
1202
396
2202
590
11
303
34
814
768
5447
2548
5
1 u
1 u
TDS (mg/1)
1232
563
2146
19832
1716
20356
6300
2574
3288
10828
33074
12580
14650
1952
568
19852
9406
14712
19652
4636
2254
1782
3340
4626
2062
6128
3456
652
1170
280
2026
3544
18564
10780
144
5
8
Shallow = 6-16 ft j" = less than limit of detection
Deep = 26-30 ft
then had a 6 in. steel casing cemented in around the top of the well
and capped with a padlocked steel cap. All wells were surged and
bailed or pumped to yield relatively sediment free water as part of
well completion. The depth from which water samples were taken
depended on the depth at which the well screen was set.
Groundwater Sampling
After all monitoring wells had been installed and water levels
measured, they were all pumped with a Robb Air Pump until either
three times the volume of water standing in the casing had been
discharged or the well was dry. The first three wells pumped, Nos.
2, 13, and 19, were pumped onto the ground. Later water pumped
from wells was collected into drums and stored with the wash water
from the decontamination station. To reduce cross contamination
to a minimum, the pump and its discharge line were submerged in
potable water from the City of Kent fire hydrant and run for 5 min
between each well.
Each well was allowed to recharge and then sampled with a
stainless steel bailer which had been washed with distilled water and
rinsed with reagent grade acetone and then with pure methanol
followed by distilled water again. The bailer was then allowed to
dry. The bailer was lowered into each well on a monofilament line.
A new line was used for each well. On-site wells were sampled from
Nov. 1 to 12, 1982. Off-site wells were sampled on Nov. 15, 1982.
The bailer's and sampler's gloves were rinsed twice with the
water being sampled and then the sample containers were rinsed.
Each prelabeled container was then filled and its outside washed
off with potable water before it was placed in an ice chest. Two
half-gallon brown glass bottles with teflon-lined lids were collected
for extractible organics analyses, two 40 ml glass vials with teflon-
lined lids for volatile organics and two 1000 ml polyethylene con-
tainers for heavy metals and for cyanide analyses. An additional
500 ml polyethylene container was filled to be checked for total
dissolved solids and chloride (Table 3). At the time of sampling the
conductivity and pH of the water was checked (Table 4).
SITE INVESTIGATION
49
-------
Table 4
Conductivity and pH Readings
Well t
1A (shallow)
18 (deep)
2
3
^
5
6
7
8
9
10
11A (shallow)
11B (deep)
12
13*
14
15
16
17A (shallow)
17B (deep)
18
19*
20
21
22A (shallow)
22B (deep)
23
24
25A (shallow)
2SB (deep)
26
•Off-site wells
shallow well (12-16 fi)
deep well (28-30 fl)
PH
6.70
7.55
6.58
13.00
6.68
9.36
7.50
No Data
No Data
6.80
4.58
4.84
4.79
No Data
6.42
5.15
No Data
5.61
6.26
5.02
No Data
6.30
7.53
No Data
6.55
5.96
6.79
No Data
6.47
6.68
6.33
Conductivity
(Mlcromhos)
2000
1400
35.5
>7500
1700
>7500
>7500
No Data
No Data
4800
>7500
5500
>7500
No Data
No Data
>7500
No Data
>7500
1100
4000
No Data
No Data
3300
No Data
420
4500
4500
No Data
1600
300
1700
RESULTS AND DISCUSSION
Because of the number of samples (170, with blanks), and the
large number of parameters checked, it is impossible within the
scope of this report to discuss them all. Selected samples, generally
those most contaminated, are discussed, together with the blanks
and the background well (Well 30).
The transport blank, which was supposedly organic-free water
and went unopened from the USEPA laboratory to the contract
laboratory, shows four volatile organics at trace concentrations
(*? 5 to 20 /tg/1), and trichloroethylene at 76 /tg/1. These could have
been in the water or from the container. The transfer blank, which
consisted of the same water run through the bailer into a fresh con-
tainer, showed no volatiles, but picked up 140 /tg/1 of zinc. It seems
likely that the volatiles were in the water but that the zinc came off
the bailer. For this reason, as a precaution, only levels of zine 700
ftg/l will be regarded as clear indication of contamination in water.
The rinsate from empty soil sample bottles showed insignificant
levels of some metals, but had 88 /tg/1 of methylene chloride.
Although this may be from the laboratory rather than the con-
tainer, levels of methylene chloride in a soil sample of > 500 /tg/kg
will be considered questionable evidence of contamination. In
general, contaminants in groundwater or soil found at levels less
than five times these found in the appropriate blank are regarded as
suspect and are shown in parentheses on the tables.
The pea gravel used by the driller in well construction showed
traces of some metals and cyanide, but the potential impact on
groundwater from the wells is negligible. The City of Kent water
used by the driller was sampled and shows low levels of impurities.
Only methylene chloride was significant (56 /tg/1) and, again, may
have come from the laboratory, but levels of methylene chloride of
>250 /tg/1 should be regarded as suspect, where found in ground-
water.
Conductivity and pH of groundwater can be useful measures of
inorganic ions in the water and of the presence of acids or alkalis.
These parameters were monitored for most of the on-site wells
while they were being sampled (Table 4). For conductivity, the
numbers range from 35 to >7500/tmhos. Uncontaminated ground-
water at Lakewood, Washington, for comparison, ranged from 130
to 290 /tmhos and any figure over 1000 would indicate pollution.
The pH values ranged from 5.02 to 13.00, with the latter being
classifiable as a corrosive waste by RCRA criteria.5
Because of questions raised about organics, mainly the pesticide
and base/neutral extractibles groups, being carried by sediment in-
to groundwater samples, particular note should be taken of water
samples from those wells installed where the soils were heavily con-
taminated with these organics. The water in these wells show very
low or no levels of these compounds and is evidently largely free of
contaminated sediment.
Results
Because of the high levels of contamination encountered,
generally only those instances where the soil exceeded 1000 mg/kg
(ppm) dry weight of inorganics, or 1000 /tg/kg (ppb) of organics are
discussed. For the same reason, only levels about 1000 /tg/1 of
organics or inorganics in groundwater will be referred to except
when comparison with blanks or the background well (Well 30) is
called for. These levels have no regulatory significance but are used
as indicators of gross contamination.
In all, 87 priority pollutants were detected on or close to the site,
67 of them in quantifiable levels. Twelve other hazardous materials
were noted, 11 at quantifiable levels. Twenty-one of those com-
pounds are considered carcinogens and 28 are considered suspected
carcinogens.
One or more inorganic priority pollutant exceeded 1000 ppm in
soil in 59 out of 130 samples (45%) and exceeded 1000 /tg/1 in
groundwater in 28 out of 35 wells (80%). The percentages of
samples in which organic priority pollutants exceeded 1000 /tg/1 in
water or 1000 /tg/kg in soil are 67.6% and 38.5%, respectively.
Twenty out of 29 shallow wells and three out of five deep wells had
one or more organic priority pollutants exceeding 1000 /tg/1, and
nine out of 20 surface soil samples and 41 out of 110 borehole soil
samples had one or more priority pollutants exceeding 1000 /tg/kg.
Nineteen soil samples were classifiable as hazardous waste by
RCRA definition, as were seven groundwater samples. Contami-
nant loading in soil and water, both on-site and downgradient from
it, showed marked contamination in every case, ranging up to soil
containing levels of priority pollutant metals of 9% or more.
It is clear that there has been widespread spillage, leaking or
dumping or organic chemicals at this site, including material con-
taining at least 36 priority pollutants in relatively high levels.
There is no doubt that the Western Processing site has created
serious soil and groundwater contamination and is contributing to
air and surface water contamination.
Inorganics
The total dissolved solids (TDS) and chloride results (Table 3) are
a good general index of pollution. When compared to Well 30 as
background, all the on-site or near site wells are at least twice as
high in chloride and TDS and range up to 1000 times greater in
chloride at Wells 10 and 28 and over 100 times greater in TDS in
Wells 3, 5, 10, 11, 14, 16, 17 and 28.
Of the inorganics measured, aluminum, iron, manganese and
boron were relatively common elements. Water from 21 wells ex-
ceeded 10,000 /tg/1 in one or more of these pollutants and ranged
up to 510,000 /tg/1, compared to levels of undetected (C200), 4600,
1200 and 1200 /tg/1 of these elements in the background well, Well
30.
Of the priority pollutant metals, zinc was the most common.
Twenty-one water samples exceeded 1000 /tg/1, ranging up to
510,000 /tg/1 in Wells 18 and 28. For comparison, Well 30 had 32
/tg/1. Thirty-three soil samples exceeded 1000 mg/kg ranging up to
81,000 mg/kg in surface soil sample No. 5. It seems clear that zinc
has been leaching out of the soil into the groundwater.
Other notably elevated metals analyses were: chromium in six
wells, with levels up to 65,000 /tg/I (in Well 14); copper in eight
50
SITE INVESTIGATION
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wells, with a high of 13,000 /tg/1 (in Well 5); nickel in 11 wells, with
a high of 280,000 /tg/1 (in Well 10). Background levels are:
undetected; undetected; and 210 /tg/1 respectively, (in Well 30).
The two most toxic metals after mercury, which does not appear
to be a problem at this site, were cadmium and lead. These exceed-
ed 1000 /tg/1 in seven wells with lead at 3300 /tg/1 in Well 3 and cad-
mium at 60,000 /tg/1 in Well 10. For comparison, the background
well (Well 30) showed 1000
/tg/kg (1 ppm). All 18 samples affected were soils, the most con-
taminated of which was surface soil sample No. 8 with approx-
imately 5.1% by weight of priority pollutants, including 2.0% of
phenanthrene and 1.6% pyrene.
The sample results in excess of 1000 /tg/kg (Ippm) are listed in
Table 6.
The acid extractibles were all phenolics, and six of these were
found at levels about 1000 /tg/1 or 1000 /tg/kg. The most important
compound was phenol, itself, which was found in 12 wells and 13
soil samples. The highest concentration was in Well 27 which had a
surprising 4,100,000 /tg/1. Of the soil samples, the most con-
taminated (Well 22, 12-15 ft) contained 65,000 /tg/kg.
Table 6
Base/Neutral Extractibles in Soil (>1 ppm)
Compound
Acenaphthene
Hexachloroethane
Phthalates (as a group)
Benzo-[ a]-anthracene
Fluor anthene
Naphthalene
Benzo-k-f 1 uoranthene
Chrysene
Anthracene
Fluorene
Phenanthrene
Pyrene
Number of
Samples
3
1
14
1
7
3
1
4
1
4
9
8
Highest
Value Found
5090 ppm
1.8 ppm
860 ppm
200 ppm
234 ppm
5.2 ppm
130 ppm
1210 ppm
1.6 ppm
8600 ppm
20,000 ppm
16,000 ppm
tConcentration of soluble metal in the test extract
•Standard for Chromium = 5,000 >ig/l
Standard for Cadmium = 1,000 p%/\
Standard for Lead = 5,000 j»g/l
To summarize the highest levels of phenolics: pentachlorophenol
was found in two soil samples including a surface sample with
17,000 /tg/kg; 2,4-dichlorophenol was found in five soil samples,
the highest level found being 7900 /tg/kg between 3 to 6 ft in Well
10; 2,4-dimethylphenol was in two wells, the higher level being 1100
Mg/1 in Well 12, and in six soil samples including a surface soil con-
taining 11,000 /tg/kg; 2-nitrophenol was found off-site in Well 27 in
the extraordinary concentration of 1,300 /ig/1; and 4-nitrophenol
was found in Well 15 at 3200 Mg/1.
After the base/neutral extractibles, the volatiles group was the
most heavily represented. Nine different priority pollutants oc-
curred at levels > 1000 /tg/1 or 1000 /tg/kg. The highest level of any
volatile found was 720,000 /tg/1 of methylene chloride in Well 15.
Methylene chloride was also found at high levels in 12 other wells
and nine soil samples. Trichloroethene was even more widespread,
being found in 18 wells and eight soil samples. The most con-
taminated well was Well 15 again, with 210,000 /tg/1. The most con-
taminated soil was also from Well 15 at 3 to 6 ft (580,000 /tg/kg).
Toluene was found in water from seven wells within the range of
1000 to 22,000 /tg/1 with the highest level in Well 17. Of the six soil
samples in the 1000 /tg/kg range the highest was also from Well
17 at 3 to 6 ft, and registered 394,000 /tg/kg.
Chloroform was found in that same sample (Well 17, 3-6 ft), at
18,000 /tg/kg, and in five groundwater samples, with the highest
reaching 27,000 /tg/1 (Well 15). This well had the highest level for
1,1,1-trichloroethane at 340,000 /tg/1 while three others had high
values also. Not surprisingly, of two soil samples contaminated
with the same compound the higher was from Well 15 at 3 to 6 ft,
(174,000 /tg/kg). 1,1-dichloroethane was found at high levels only
in two water samples, the higher again being from Well 15 (33,000
SITE INVESTIGATION
51
-------
jig/1). Trans-l,2-dichloroethene was also found at high levels only
in water. Of five wells affected the highest was Well 21 (390,000
/ig/1). Lastly, ethylbenzene was found at significant concentrations
in three soil samples, the worst being from Well 17 at 3 to 6 ft
(37,000 /ig/kg).
Besides these priority pollutants, which were selected as in-
dicators of industrial pollution as the result of a consent agreement
requiring the USEPA to create a list of the most common such
materials, there were many other hazardous substances. Twelve of
these materials, acetone, benzoic acid, benzyl alcohol, 2-butanone,
dibenzofuran, 2-hexanone, 2-methyl naphthalene, 2-methylphenol,
4-methylphenol, styrene, 2,4,5-trichlorophenol and o-xylene, were
noted; one or more occurred in 69 soil samples and 23 groundwater
samples. For example, acetone occurred in soil in levels up to
17,000 /tg/kg (Well 17), and was found in groundwater in the same
well at 130,000 /ig/I. 2-butanone was also found in the soil in Well
17, at up to 580,000 /tg/kg, and in the water at 460,000 /ig/1.
Numerous other compounds were identified with varying degrees
of assurance, and their levels estimated by Ecology and Environ-
ment, Inc. For example, 2-oxazolidinone, 2-(2hydroxypropyl)-5-
methyl occurred quite commonly, reaching a level of 60,000 jtg/kg
(Well 9, soil, 6-9 ft).
Carcinogens
A number of known and suspected carcinogens were detected on
and around the Western Processing site. The 21 known carcinogens
found are listed in Table 7. The 28 suspected carcinogens, including
two not on the priority pollutant list, are listed in Table 8.
Table 7
Known Carcinogens* on USEPA Priority Pollutant List
Table 8
Suspected Carcinogens* on USEPA Priority List
Pollutants Found On-Slte
Pollutants Not Found On-Slte
Arsenic
Benzene
Benzo(a)anthracene
Benzofblfluoranthene
Benzolajpyrene
Beryllium
Cadmium
Carbon Tetrachlorlde
Chloroform
Chromium
l,2-D1chloroethane
Gamma BHC (Llndane)
Nickel
PCB-1016
PCB-1221
PCB-1232
PCB-1242
PCB-1248
PCB-1254
PCB-1260
Vinyl Chloride
Acrylon1tr1le
Benz1d1ne
B1s (Chloromethyl) Ether
N-N1trosod1methylam1ne
N-N1trosod1-N-Propylm1ne
TCDD
Toxaphene
•National Toxicology Program (5)
Total Contaminant Levels
To give a better idea of the overall impact of the site, tables were
constructed showing the total load of contaminants in selected
water and soil samples. Analyses from six on-site wells, one
background well (Well 30) and one downgradient well (Well 28,
Figure 3) were tabulated. Thirty-two priority pollutants were found
in the on-site wells in measurable quantities. Twenty priority
pollutants and five hazardous materials were found in the downgra-
dient well, all of which were found on-site. Only four priority
pollutants were found in significant levels in the background well.
Total contaminant levels (both priority pollutant and others),
together with chloride, total dissolved solids and pH (where
measured) were identified.
Priority pollutants are usually measured in parts per billion in
water samples. Some are thought to have effects on human health
even at these levels in drinking water. Carcinogens are generally
Pollutants Found On-S1te
Pollutants Not Found On-S1te
Acenaphthene
Acenaphthylene
Anthracene
Benzo(k)fluoranthene
Benzo(gh1)pery1ene
B1s(2-Chloroethyl)ether
Chlorobenzene
Chrysene
1,2,5,6-Olbenzathracene
(Perylene)
DieldHn
4,6-D1n1tro-0-Cresol
Fluoranthene
(Benzo(k)fluorene)
Fluorene
Heptachlor
Hexachlorobutadlene
Hexachlorocyclopentadlene
Hexachloroethane
Indeno (l,2,3-CD)pyrene
Naphthalene
N-N1trosod1phenylam1ne
Phenathrene
Pyrene
1,1,2,2-Tetrachloroethane
2,4,6-Trlchlorophenol
1,2-Trans-D1chloroethylene
Non PP Hazardous Materials
(partial 11st)
Dibenzofuran
Styrene
Alpha BHC
Chlordane
2-Chloroethyl Vinyl Ether
2-Chloronaphthalene
3,3-D1chlorobenz1dene
Heptachlor Epoxlde
P-Chloro-N-Cresol
•Soderman. J.V. 1982(6)
thought to have no threshold below which they have no effect. Of
the on-site priority pollutants, eight are considered carcinogens and
four are suspected carcinogens.
Total contaminants in the selected wells ranged from 53,323 /tg/1
to 1,359,982 Mg/1 (averaging 709,393 /tg/1). The background well,
in contrast, has a total contaminant load of 956 /tg/1. Interestingly,
the well most highly contaminated with priority pollutants was Well
27, outside the site. Because of the high levels of phenol and
2-nitrophenol, the priority pollutant loading is 5,683,500 pg/l.
The analytical data for the soil samples showed total contami-
nant levels even higher than for water, particularly in the case of the
inorganics. Selected soil samples showed lead up to 8.4% in one
sample, zinc up to 8.1% and several organics above the 1% level.
Total contaminant loads for these samples ranged from 0.02% to
an astonishing 9.93%.
The distribution of hazardous material in the soils and ground-
water showed some interesting patterns. Priority pollutant metals
in surface soils and average levels in borehold soils exceeded 1000
ppm over most of the site (Figure 8). Only at the northwest corner
of the site around Wells 1, 2, 4, 6, 7, 8, 11 and 12, and at the south
end of the site around Wells 24, 25 and 26 were lower levels en-
countered. This agreed quite well with the distribution of total
priority pollutant metals in shallow groundwater (Figure 9). This
was in excess of 100 mg/1 off the northeast corner of the site in Well
19 and 29, and in the middle of the site around Wells 10, 11, 14, 17,
18, 27 and 28. Levels were surprisingly low below the south part of
the site and also in Well 16. The top 15 ft of soils in this well av-
eraged an astonishing 4.6% lead, the highest in any well, but the
lead level in the groundwater was only 470 /ig/1.
The sum of all the volatile priority pollutants in soils from each
well suggests that there were at least two major spill locations on-
site, at Wells 15 and 17 (Figure 10). The distribution of volatiles in
the groundwater suggests that there may well have been several
more spills, upstream of Wells 21, 27, and possibly 14, for example
(Figure 11).
52
SITE INVESTIGATION
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Non-priority pollutant solvents showed similar distribution with
the exception of Well 15 (Figure 12).
The sum of the total priority pollutant acid extractibles (phenols)
found in soil samples, does not yield a clear picture (Figure 13).
Levels of from 2 to 102 ppm are scattered over the site from the
south end north to Well 10. The groundwater picture suggests a
major source may be the lagoons along the west side of the site,
near Well 27. Other sources may be the "Reaction Pond" and
burial sites or spills near Wells 17, and 5 (Figure 14).
Distribution of priority pollutant base/neutral extractibles in
soils extends south from Well 11 almost to the south end of the site.
Concentrations in the surface soils range from non-detected to
5.8% (Figure 15), within this area. Evidently these compounds are
relatively strongly adsorbed on soils, because only very low levels
were found in groundwater.
REFERENCES
1. Aldis, H., "Survey of Drainage and Industrial Development around
Western Processing, Kent, Washington." Memorandum from Ecology
and Environment, Inc., to Environmental Protection Agency, TDD 10-
8203-04B, July 1982.
2. Mullineaux, D.R., "Geology of the Renton, Auburn, and Black Dia-
mond Quadrangles, King County, Washington," Geological Survey
Professional Paper 672, 1970.
3. U.S. Government Printing Office (GPO), "Guidelines Establishing Test
Procedures for the Analysis of Pollutants; Proposed Regulations" in
Federal Register, 45, 1980, 33122.
4. U.S. Government Printing Office (GPO), "Guidelines Establishing Test
Procedures for the Analysis of Pollutants; Proposed Regulations" in
Federal Register, 45, 1980, 33127.
5. "National Toxicity Program: Second Annual Report, 1982 List of 88
Known or Suspected Carcinogens," U.S. Department of Health, Edu-
cation and Welfare, Public Health Service, RTF, North Carolina 27709.
6. Soderman, J.V. ed, CRC Handbook of Identified Carcinogens and
Non-Carcinogens: Carcinogenicity-Mutagenicity Database. Two vol-
umes, CRC Press, Inc., 1982.
SITE INVESTIGATION
53
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PROTOCOL FOR IDENTIFICATION OF
REACTIVITIES OF UNKNOWN WASTES
C.D. WOLBACH, Ph.D.
Acurex Corporation
Energy & Environmental Division
Mountain View, California
INTRODUCTION
Under the Superfund program numerous locations containing
large quantities of hazardous wastes have been identified. These
sites may present long-term danger to the local environment and
possible immediate danger to personnel involved in cleanup. A
major effort in any cleanup is the bulk recontainerization of haz-
ardous materials located in leaking drums or tanks or stored in
holding ponds. This step is usually performed to allow shipment
to intermediate storage or ultimate disposal. However, many ma-
terials are incompatible with each other and when mised can re-
sult in immediate undesirable reactions or intermediate-term re-
actions that can produce dangerous results.
Work has been or is being performed to identify what types of
materials have compatibility problems and the potential results of
their mixing.''2i3 These efforts are primarily theoretical studies in-
corporating chemistry of pure compounds. One study has classified
materials into several reactivity groups, identified potential prob-
lems with mixing different groups and specified a logical series of
procedures to avoid mixing of incompatible materials.1 The docu-
ment ("A Method for Determining the Compatibility of Haz-
ardous Wastes") classifies wastes by chemical class and/or general
reactive properties and lays out a sequence of activities to deter-
mine the compatibility of two wastes. The key elements of this
document are a compatibility chart and a flow diagram for its use.
However, the study presupposes a knowledge of the composition
of the waste materials. Such information is often available from
generators of hazardous waste but is seldom available during re-
medial action at an abandoned site.
The need to test mix two wastes on a small scale is emphasized
even if the compatibility chart indicates compatibility. Other work
has been directed toward field tests for one or two specific re-
action hazards or chemical characteristics.4'5'6 These efforts address
only the most immediate and catastrophic effects of incompatibil-
ity. Cleanup personnel are left with no way of estimating the short-
term (minutes to hours) or long-term (days to weeks) effects of mix-
ing and recontainerizing unknown materials.
PURPOSE
Because comprehensive and organized field-usable procedures
identifying general categories of wastes are lacking, the USEPA,
Office of Research and Development, Municipal Environmental
Research Laboratory (MERL) at Cincinnati, OH initiated this pro-
ject to identify and assemble the technology necessary to fill this
void. The purpose of this project was to establish sequences of
simple test procedures that would enable workers in the field to
classify hazardous wastes according to their chemical reactivity
when no prior knowledge was available regarding their com-
position. The chemical reactivity classifications (reactivity groups)
would then be used to predict which waste materials could be
mixed safely by applying the compatibility chart in Reference 1.
Specifically, the goals of this project were to identify, if possible,
field-usable procedures to classify wastes into the reactivity groups
developed in Reference 1; test identified procedures against rep-
resentatives of their respective reactivity groups; establish a pro-
tocol for the use of the procedures; assemble a field test kit; and
demonstrate the ability of the protocol and kit to function in the
field.
There are 41 reactivity groups for which tests were desired. They
are numbered 1 through 34 and 101 through 107 (Table 1). These
are called the reactivity group numbers or RGNs. The tests used to
classify a sample waste into the correct RON had to be simple
enough that users with minimum training could apply them. The
associated protocol had to be logical and contain a minimum of
complex decisions.
The environment in which these classification test procedures
will be utilized requires certain limitations on the schemes, test
procedures and equipment to be used. The following limitations
were specifically addressed during the course of this study:
•The procedures must be safe and easy to perform by nonpro-
fessionals. To maximize the safety of the test procedures, only
small amounts of the test materials are used, and materials of ex-
treme reactivity are identified early in the testing sequence. The
simplicity of the test procedures was verified by using nonpro-
fessionals to perform the tests in the latter part of the program.
•The procedures must give definitive, objective results. Test ma-
terials were analyzed as unknowns and by different analysts to
verify objectivity of observations.
•The equipment must be standard, readily available, portable
and require minimal utility hookups, since the tests will be ap-
plied in remote field locations. For this reason, the test equipment
is entirely self-contained (i.e., requires no utility hookups, etc.)
•The procedures need to be performed as rapidly as possible, since
numerous waste samples will require testing. For this reason,
abbreviated classification schemes are proposed as a time-saving
measure.
•The test procedures must be performable with slightly restricted
manual dexterity, since they may be performed in areas where
protective clothing is required.
•The test procedures must be reproducible.
54
SCREENING
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Table 1
Reactivity Group Definitions
Reactivity
group no. Reactivity group name
1 Acids, mineral, nonoxidizing
2 Acids, mineral, oxidizing
3 Acids, organic
4 Alcohols and glycols
5 Aldehydes
6 Amides
7 Amines, aliphatic and aromatic
8 Azo compounds, diazo compounds, and hydrazines
9 Carbamates
10 Caustics
11 Cyanides
12 Dithiocarbamates
13 Esters
14 Ethers
15 Fluorides, inorganic
16 Hydrocarbons, aromatic
17 Halogenated organics
18 Isocyanates
19 Ketones
20 Mercaptans and other organic sulfides
21 Metals, alkali and alkaline earth, elemental and alloys
22 Metals, other elemental and alloys in the form of powders,
vapors, or sponges
23 Metals, other elemental and alloys as sheets, rods, mold-
ings, drops, etc.
24 Metals and metal compounds, toxic
25 Nitrides
26 Nitriles
27 Nitro compounds
28 Hydrocarbons, aliphatic, unsaturated
29 Hydrocarbons, aliphatic, saturated
30 Peroxides and hydroperoxides, organic
31 Phenols and cresols
32 Organophosphates, phosphothioates, phosphodithioates
33 Sulfides, inorganic
34 Epoxides
101 Combustible and flammable materials, miscellaneous
102 Explosives
103 Polymerizable compounds
104 Oxidizing agents, strong
105 Reducing agents, strong
106 Water and mixtures containing water
107 Water reactive substances
SCOPE
Fifty-eight compounds were selected from a listing (Appendix 1
or Reference 1) of materials likely to be found in hazardous waste
disposal facilities. The compounds were selected to represent as
broad a range of chemical reactivity as possible. All of the reac-
tivity groups, except RON 25 (nitrides), from the compatibility
chart in Reference 1 are represented by the 58 test compounds.
Test procedures were identified from literature sources
and arranged into test schemes to classify waste materials into re-
activity groups. The test procedures were applied to the 58 test
compounds. In the development of the test schemes, each of the
test procedures was applied to the test compounds and results were
compared to those expected. The test schemes and procedures were
then applied to the 58 test compounds anonymously, and the re-
sults were used to classify the "unknown" test compounds into
reactivity groups.
All equipment and reagents used in the test schemes were as-
sembled into a field test kit. A manual for the use of the test
schemes, including detailed instructions for conducting the test
procedures and directions for use of the flow diagrams, is included
in the kit.
A mixing device was assembled and evaluated for its ability to
detect reactivity by gas and heat evolution. The design of the de-
vice is a simplified version of similar devices reported earlier in the
literature."
At the conclusion of the study, the field test kit was employed
in a 1-week field evaluation at the USEPA Combustion Research
Test Facility located in Jefferson, AK. The tests were applied to
29 actual wastes during the field evaluation.
PROTOCOL DESCRIPTION
The protocol resulting from this project consists of 28 tests or
procedures. These tests are grouped into six procedure sets (PS)
which are briefly summarized in Table 2. The procedure sets are
organized into a logical sequence depending on the gross physical
characteristics of the sample (Figure 1). The individual tests within
a procedure set are also logically organized to minimize the num-
ber of tests required for classification. Procedure set 1 is shown in
Figure 2 as an example of the process.
Procedures Sequence
The test procedures are organized into a scheme for the classifi-
cation of unknown hazardous wastes into reactivity groups. Pre-
liminary procedures classify the material as acid, base, oxidizing,
reducing, or water-reactive, and primarily organic or inorganic.
The results of preliminary tests are used to give direction to sub-
sequent testing procedures which are used for further classification,
ultimately into reactivity groups. The scheme is organized in a man-
ner to identify materials with high reactivity or unusual hazards
early in the testing sequence. In some cases, information gained in
the early stages of testing can be used to classify the material and
eliminate the need for further testing or to provide cautions to be
applied in subsequent testing activities (i.e., explosive hazard).
The sequence in which test procedures are carried out is shown
schematically in Figure 1. The testing sequence begins with a visual
examination of the waste material to classify it as a solid, sludge,
slurry or liquid. This examination may give a strong indication of
its identity (i.e., metal).
Table 2
Procedure Sets
PS
Title
Information obtained
1 pH and Redox Tests
2 Solution-Reactivity and
Special Functionality
Tests
3 Falme Test
Sodium Fusion and Ferrox
Tests
Organic Functionality
Tests
Inorganic Functionality
Tests
Acidity, basicity, oxidizing and
reducing potential
Identification of sulfides and cy-
anides, reactivity and solubility in
acids and solvents, reactivity with
water, presence of water
Combustibility, classification as
organic or inorganic, identification
of explosives
Identification of oxygen, nitro-
gen, phosphorus, sulfur, and
halogen in organic waste materials
Presence of specific organic
functional groups
Presence of elemental metals,
heavy metal compounds, and
inorganic fluorides
Depending upon the phase of the waste material, preliminary
testing is initiated. If the waste is a liquid, slurry or sludge, PS 1
is carried out first. The rationale for beginning with PS 1 is that
the chance for extreme hazards due to acidity and/or redox poten-
tial may be greater for liquids than for solids and these hazards
are most easily identified. If the material is found to be strongly
SCREENING
55
-------
PROCEDURE SET ?
*
LIOI
FILTER
J1D
SOLID
PROCEDURE SET 2
PROCrDUK SET 3
Figure 1
Sequence of procedure sets
O
[ I
STMI
STOP
CMUKUf
D
CLASSIFY
INTO RGN
CCNOUCT pH
AHO 1EDOI TESTS
_
Figure 2
Procedure set 1—pH and redox tests
56 SCREENING
-------
acidic and/or oxidative, the need for further testing is virtually
eliminated (strong acids and oxidizing agents are incompatible
with most other classes of wastes).
The test procedure continues with solution-reactivity tests and
flame tests to determine the material's solubility/reactivity char-
acteristics and to identify the waste as organic or inorganic. For
organics, functionality tests (PSs 4 and 5) are performed to class-
ify the waste into specific RGNs. For inorganics, PS 6 is con-
ducted to identify specific RGNs.
PS 1—pH and Redox Tests
Early in the testing sequence, pH, oxidation and reduction tests
are performed on a waste material or its aqueous solution using
specified test papers. These tests identify some of the most reac-
tive of the RGNs (those with the most limited compatibility char-
acteristics). Specific RGNs identified are as follows:
•RON 1—Nonoxidizing mineral acids
•RON 2—Oxidizing mineral acids
•RON 3—Organic acids
•RGN 10—Caustics
•RON 104—Strong oxidizing agents
•RGN 105—Strong reducing agents
PS 1 is shown in Figure 2. Classification into RGNs 1, 2, or
104 virtually eliminates the need for further testing since these
RGNs are incompatible with most wastes. In addition, classifica-
tion into RGNs 10 and 104 or 10 and 105 has similar compat-
ibility characteristics.
PS 2—Solution-Reactivity and Special Functionality Tests
These procedures are conducted to determine the reactivity of
the waste material with water, acids and bases and the solubility
of the waste material in aqueous acid, base and four organic sol-
vents. The first procedure is the treatment of the waste material
with water. Most water-reactive materials are identified (and
further testing is suspended). The solubility of the material in
water is noted. Liquids are tested for the presence of water (RGN
106), and all waste materials are tested for sulfide and cyanide
(RGNs 33 and 11, respectively). Finally, the material is treated
with an aqueous base, a series of acids, and four solvents. The
following RGNs are determined in PS 2:
•RGN 11—Cyanides
•RGN 33—Inorganic sulfides
•RGN 106—Mixtures containing water
•RGN 107—Water-reactive substances
In addition, clues are given regarding the gross identity (reac-
tive, inert, organic, inorganic) of the waste material.
PS 3—Flame TEsts
Observation of the behavior of a material upon ignition can pro-
vide a great deal of insight regarding its composition. Results
(observations) upon ignition are characterized by one of the follow-
ing descriptions:
•Burns violently
•Burns (with or without smoke)
•Produces a colored flame but does not burn
•Melts but does not burn
•Evaporates or sublimes but does not burn
While these observations are somewhat subjective, after the train-
ing period with an experienced chemist, most observers will be
able to make a distinction between organics, inorganics and free
metals using the flame test. RGN 102 (explosive) is determined
directly by means of the flame test.
PS 4—Ferrox and Sodium Fusion
The classification of a material as primarily organic or inorganic
is made in PS 2 or 3. PS 4 is conducted if it is determined that the
material is organic and provides elemental analysis information.
This procedure set consists primarily of two tests: sodium fusion
with specific tests for nitrogen, sulfur, phosphorus and halogen;
and the ferrox test to identify organic materials containing oxygen.
In addition, specific optional tests are included to differentiate be-
tween classes of hydrocarbons.
The waste material is first subjected to fusion with sodium
metal. The metal is thus decomposed, and heteroatoms form sod-
ium sulfide (sulfar), sodium cyanide (nitrogen), sodium phosphate
(phosphorus) and/or sodium halide (halogen). Positive tests for
sulfur, nitrogen or phosphorus are followed by appropriate spe-
cific functional group tests (PS 6). If tests for sulfur, nitrogen or
phosphorus are negative, the ferrox test is conducted to deter-
mine the presence of oxygen. A negative ferrox test indicates the
material is a halogenated hydrocarbon (RGN 17 determined by
sodium fusion) or a hydrocarbon. Specific optional tests are in-
cluded to distinguish between aromatics (RGN 16), alkenes (RGN
28) and alkanes (RGN 29). Since compatibility characteristics of
RGNs 16, 28, and 29 are similar, it is likely that tests to distin-
guish these three RGNs are unnecessary.
PS 4 provided for the classification of five RGNs specifically.
These are as follows:
•RGN 16—aromatic hydrocarbons
•RGN 17—halogenated organics
•RGN 28—unsaturated aliphatic hydrocarbons
•RGN 29—saturated aliphatic hydrocarbons
•RGN 32—organophosphates, phosphothioates, and phos-
phodithioates
Elemental composition information is provided which is utilized
in PS 5, discussed in the following paragraphs.
PS 5—Organic Functionality Tests
Elemental analysis information obtained in PS 4 is used as a
starting point for PS 5. This set of procedures includes specific
tests for 17 reactivity groups. PS 5 contains three major parts:
tests for functionalities containing sulfur, nitrogen and/or oxygen.
If the ferrox test (PS 4) is positive, tests are conducted for func-
tional groups containing oxygen. Three of these (RGNs 3, 30, and
34) are very reactive, but information already obtained in PSs 1 and
2 is used in the classification into these RGNs. Other reactivity
groups containing only oxygen (RGNs 4, 5, 13, 14, 19, and 31)
are less reactive and have similar compatibility characteristics.
Separate optional tests are provided for determining the presence
of these RGNs, but they may be eliminated and materials with
positive ferrox test placed into a compolsite group representing
all of these RGNs.
If the sodium fusion results indicate the presence of nitrogen
in the waste material, tests for functional groups containing nitro-
gen are conducted. Like the RGNs containing only oxygen, three
RGNs (8, 9, and 18) are much more reactive than the others. Tests
are therefore conducted for RGNs 8, 9 and 18 and optional tests
for RGNs 6, 7, 26, and 27 are provided.
If sulfur is present (from the sodium fusion), RGNs 12 and/or
20 are indicated. These can be distinguished by individual (op-
tional) tests. The compatibility characteristics of these two RGNs
are similar, however, and conducting tests to distinguish them is
probably not necessary.
In summary, 17 RGNs are determined in PS 5:
•Oxygen functional groups
RGN 3—Organic acids
RGN 4—Alcohols and flycols
RGN 5—Aldehydes
RGN 13—Esters
RGN 14—Ethers
RGN 19—Ketones
RGN 31—Phenols and cresols
RGN 34—Epoxides
RGN 30—Peroxides
•Nitrogen functional groups
RGN 6—Amides
RGN 7—Amines
RGN 8—Azo compounds, diazo compounds and hydrazines
SCREENING
57
-------
RGN 9—Carbamates
RGN 18—Isocyanates (no test)
RGN 26— Nitriles
RGN 27—Organic nitro compounds
•Sulfur functional groups
RGN 12—Dithiocarbamates
RGN 20—Mercaptans and other organic sulfides
PS 6—Inorganic Functionality Tests
PS 6 includes tests for metals and other inorganic species not
identified in PSs 1 and 2.
Solids are tested for metals using phosphomolybdic acid. The
form of the metal (sheets, powder, etc.) is determined by inspec-
tion. Alkali metals are determined by their water reactivity. If the
material is not an elemental metal, it is dissolved (using HNO3 if
necessary). This solution (or liquid waste) is tested for the presence
of heavy metal compounds (RGN 24) and for fluorides (RGN 15).
The reactivity groups determined in PS 6 are the following:
•RGN 15—Inorganic fluorides
•RGN 21—Elemental alkali and alkaline earth metals
•RGN 22—Elemental metals in the form of powders, vapors or
sponges
•RGN 23—Elemental metals in the form of sheets, rods, mould-
ings, drops, etc.
•RGN 24—Toxic metals and metal compounds
A test has not been identified for RGN 25, nitrides, but these
compounds fit into the explosives class (RGN 102), determined in
PS 3.
Determination of Compatibility
After completion of the appropriate test procedures, a waste ma-
terial is classified into one or more reactivity groups based upon
the test results. At this point, the compatibility chart from Refer-
ence 1 is consulted to determine the potential effects of mixing with
wastes of other classes. In cases where compatibility is indicated,
wastes are initially mixed on a small scale to verify compatibility
before attempting full-scale mixing.
RESULTS AND DISCUSSION
During laboratory verification of the protocol, over 750 individ-
ual functionality test observations were made (PS 4, 5, and 6) on
blind samples. Fifteen false positive results and two false negative
Table 3
General Summary of Functionality Test Results
Sodium fusion
Cytnide/thlocyanate
Phosphate
Ha tide
Ferroa test
pH
ScMff's test
Hydro* mate
Iodine test
Ferric chloride
Copper chloride
B«eytr' i test
Phoipho*otybdiC 1C id
Suifid*
T
ame e con
Organ c nitrogen compounds
Organ c phosphorus compounds
Organic halogen compounds
Organic Oiygen compounds
Acids (organic)
Alcohols
Aldehydes
Esters
Ethers
Phenol s
Amides and/or nitrites
DUhio arbamates
orga tc Sul fide*
Elemental metals
ests
40
40
40
40
40
40
40
40
40
40
22
22
22
22
22
22
13
3
10
16
results positive
IB 0
2 0
2 0
10 1
3 2
3 0
1 0
6 1
3 6
2 1
5 0
« 1
1 0
1 3
4 0
2 0
1 0
3 0
5 0
10 0
16 0
negative
0
0
0
1
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
results were recorded. A summary of the reliability of the test pro-
cedures employed as applied to the reference compounds is shown
in Table 3. In light of the multiple functional!ty of many of the
reference compounds, the frequency of false positive and false neg-
ative observations is considered to be acceptable.
Results of Blind Analyses of the Reference Compounds
The test schemes were evaluated by subjecting the reference com-
pounds to the schemes. The reference compounds were submitted
as unknowns after concealing their identities and assigning num-
bers to them. Testing was carried out following the sequence in-
dicated in the schemes and assigning RGNs based on the individual
test results.
The experimentally determined RGNs for each compound are
summarized in Table 4 for the purpose of comparison with their
known RGNs. Several of these compounds exhibited properties
during testing which were inconsistent with their assigned RGNs
(Appendix 1 of Reference 1). After evaluation of the1 chemical
structure of these compounds, it was discovered that some of the
RGNs were incorrectly assigned, and these were corrected. The
RGN changes are indicated in Table 5.
Two blind test runs (A and B) were conducted by two different
technicians to determine the reproducibility of the results. The
second set (B) of blind analyses was carried out by a technician
who was not involved in the development of the test procedures
and had no specific training in chemical analysis. He was given the
test kit instruction manual and also a draft of the USEPA report
on which this paper was written. Instructions on how to use the
test equipment and the critical points of each test, e.g., interpreta-
tion of the flame test in terms of flammability, explosiveness,
combustibility and residue were given. Some initial assistance was
given in interpretation of the precipitate formation or color devel-
opment for certain tests. Aside from this, all reference compounds
were carried through the test scheme and assigned RGNs without
further assistance.
Potassium cyanide and dimethylaminazobenzene were not sub-
mitted to the blind tests to prevent unnecessary exposure as recom-
mended by the Acurex safety officer. Several other compounds
were also eliminated because sufficient quantities for testing were
not available, as indicated in Table 4. Of the remaining reference
compounds (test run A), seven were assigned incorrect RGNs or
no RGN could be determined. For three of these compounds, the
results are explained by their chemical behavior during testing.
Chromium was not detected as elemental metal because of its ex-
treme insolubility under the test conditions. Barium iodide, barium
oxide and barium cannot be detected as barium sulfide, and
toluene diisocyanate showed positive amine and ester test results,
while the isocyanate group was not detected because no qualita-
tive test method was available.
Other difficulties included the detection of water reactivity
(RGN 107) which was defined as reaction with visible gas evolu-
tion or spattering. This resulted in nondetection of RGN 107
for three compounds: barium oxide, toluene isocyanate and chlor-
ophenyl isocyanate. In addition, polymerizable compounds were
not detectable. Several materials (chromium trioxide, cadmium
and barium) reacted violently during the flame test, although
they are not considered explosives.
The comparison of results from both test replicates show good
correlation of most RGNs. The individual functionality tests also
showed good agreement, with 18 disagreeing individual test results
out of the 261 individual determinations.
Results of Blind Analyses of Other Pure Compounds
Two sets of unknown laboratory chemicals were tested by
following the test scheme. Six unknowns were mixtures of two
compounds designated HWC (hazardous waste combination)-X,
1-6; 12 unknowns were single compounds designated HWC-X,
11-22. The RGNs determined from testing as compared to their
actual RGNs are presented in Table 5. Out of the 12 single un-
58
SCREENING
-------
Table 4
Results of Duplicate Blind Analyses of the Reference Compounds Using the Test Schemes
Compound
Chromium oxide
Cadmium
Sodium
Arsenic pentasulfide
Chromium
Copper
Lead
Nickel
Barium
Barium iodide
Barium oxide
Calcium hypochlorite
Selenium di ethyl -
dithiocarbamate
Hydrof 1 uorosi 1 i cic acid
Peracetic acid
Fluoboric acid
Hexafluorophosphoric acid
Hydrofluoric acid
Trinitrobenzoic acid
Picric acid
Dipicrylamine
Aminoproprioni tri le
Aminobenzothiazole
Benzoyl peroxide
Cyanoacetic acid
Toluene diisocyanate
Hydroxyl amine *HC1
Malathion
Parathion
Ethyl zimate
Vinyl acetate
Brotnoxynil
p-Chl orophenyl i socyanate
Styrene
Ethyl ene glycol-
monomethyl ether
Polypropylene
Propyleneoxide
Methyl methacrylate
Ethyl acrylate
Mercaptobenzothiazole
Lannate
Hydroxyacetophenone
Mercaptoethanol
b-Butyl acrylate
Acrolein
Di acetone alcohol
Aldicarb
Polysulfide
Hexene
Decene
Tepa
Acetamide
Naphthalene
Di phenamide
n-Decane
RGN(s)
2a,24,104a
22.24
10f, 21, 102, 105,107
24a,33
23,24
23,24
23,24
22,24
10,21,24^,107
24a
10,24a,107a
10f,104
12,24
1,15
3,30b,104f
2f,15
2f,15
1 15
3f,27,102
3,27b,31b,102
7,27,102
7,26
7
30,102
3,26
18d,107a
105
13f,32
27e>f,32
12,24
13,103°
13e,f,17,26e
17,18d,107a
16,28,103d
4,14e
29,101a
34d, 103d, 107
13,103d
13,103d
20
9
19,31
4e,20,105f
13,103d
5,103d
4f
28
28
7f,32
6
16
6
29
RGN(s)
(experimental )
Run A
24,102
22,24,102
10,102,107
33
ND
23,24
23,24
22,24
10,21,102,107
ND
10
10,104
12
1,15
3,104
2,15
2,15
1,15
3
3,102
102
6/26,7,14°
7
13C,30,102
3,6/26
7°, 13°
ND
3,13,32
4C,32
12,14°
13
17
17
16,28
4
29
4,107
4C,13
13
7°, 20
9
19,31
20,105
ND
5
19
ND
3,20
28
28
32
6/26
16
ND
29
RGN(s)
(experimental }
Run B Comments
104,2 Reacts like explosive, color interference
22,24 Reacts like explosive
Reacts like explosive
--
ND Some acid reaction, insoluble under test
conditions
23,24
23,24
22,24
10,21,24,102,107 Reacts like explosive
104
10,22
10,104
12,19
1,15
3 Eliminated from scheme after PS 1
2,15
2,15
1,15
3,6/26c Eliminated from scheme after PS 1
3,27,31 Eliminated from scheme after PS 3
3C,31C102
6/26,7
7,6/26°
30,104,102
3
9 May hydrolyze during test
32 pH 3
27,32,6/26°
12,14
13
13,17,26,107a
9°, 17, 6/26°
16,28
4,14
107 Hydrolyzes to alcohol
13
13
20
9
19
20
13
5
4,19
17°, 32°
20,14
28
28
--
6/26
16
6/26
29
ND: No RGN determined
-- Not done, insufficient sample
6/26: Same test for either RGN
aNot detectable by test used
*>Not tested for this RGN due to elimination from scheme
°Incorrect RGN
dNo test available for this RGN
eRGN not detected
fCorrected RGN
SCREENING
59
-------
Table S
Results of Blind Analysis of Selected Pare Compounds
and Binary Mixtures
Hazardous
-sste
Combination
Compound
RGN(s)
(known)
RGN(s)
(experimental)
Two (2) Components
1 Picric acid, ethylene glycol 4b,Ha,31,27J, 3,102
monomethyl ether 102
2 Mercaptobenzothtazole 20,4&,19,105 20,19,7,105
dtacetone alcohol
3 Styrene. hydroxyacetophenone 16J,103,4,19, 4,19,31,32C,16,
31,2811 28
4 Bromoxynll. vinyl acetate 17 ,26°,13.103d 9,17,13
5 Mercaptoethanol. hexane 4,20e,28a 4, 20
6 Chlorophenyl, (socyanate 17,18d.107° 17,19C,6/26C
Single Compounds
11
12
13
14
15
16
17
18
19
20
21
22
Iodine
Sodium borohydride
Sodium diethyldi thiocarbamate
Stannous sulfate
Benzole acid
Bromobenzene
Phenyl hydrazlne
0-N1troan!Hne
Pyrogal lol
Tin (granules)
fliphenyl
Hydrofluoric acid
104,2
105
12
24,105,1
3
17
8
7,27°
3,31,105
22,24
16
1,15,106
104,2
105,14<:.102,17C
12
1,24,105
3.19C
17
14C.8
7
3,31,105
22,24
16
1,15,106
aNot tested Tor this RGN due to elimination from test scheme
bRGN not detected
cIncorrect RGN
dNo test available for this RGN
known compounds tested all RGNs were correctly assigned for
nine compounds and for the remaining three the most significant
RGNs were assigned. Four RGNs were incorrectly assigned (false
positive) and one RGN was not detected. For the six unknown
mixtures, the RGNs were only partially identified because several
of the tests which would identify functional groups of the second
component of the mixture were not conducted according to the
test scheme in the following instances: (1) in the presence of
certain functional groups, (2) at a specific pH (less than 3) or (3)
where the mixture exhibited explosive behavior during the flame
test. Nevertheless, the most significant RGNs were assigned for
all of the six mixtures.
FIELD EVALUATION OF THE PROTOCOL AND TEST KIT
A field evaluation of the test kit was conducted Mar. 8 to 11,
1983 at the USEPA Combustion Research Facility in Jefferson,
AK. Twenty-five hazardous waste samples were collected from
two sites prior to the field evaluation by Richard Carnes, USEPA's
Technical Advisor for the project. Four of the samples had two
distinct layers. The layers were separated and analyzed individual-
ly, bringing the total number of samples analyzed to 29. The
gross identity of the waste materials was known to the technical
advisor but not to the field crew until after the testing was com-
pleted.
The tests were performed outside (day 1) on a temporary ply-
wood working surface and in a trailer with a counter (days 2 and
3) because of inclement weather. The wind was gusting from 20 to
30 mph, and the temperature was in the mid-30s (°F). It is be-
lieved that these conditions simulated field conditions closely.
Only two significant difficulties were encountered in performing
the tests under field conditions. The first was that several of the
samples contained two phases, and the kit was not equipped with
a separatory funnel or equivalent device. Based on this exper-
ience, several small separatory funnels were added to the test kit
equipment list. A second problem encountered was performing the
tests under adverse weather conditions; the wind was a problem.
Under windy conditions, reagent bottles and sample vials tipped
over and the flame was difficult to maintain and control. Overall,
the tests proved relatively easy to perform under field conditions.
A list of the samples, including the composition and a summary
of results, is presented in Table 6. Twenty-eight of the 29 samples
were categorized correctly (according to the impartial judgment of
the on-site project technical advisor) in the field evaluation. Sam-
ple 6E was described as "waste solvents with amines" but was
characterized as RGNs 10 (caustic), 24 (metal compounds), and
106 (water). Upon contacting the source of this sample, it was
found that, indeed, the authors had accidentally been given the
water layer of a two-layer system. Amines dissolved in the water
would account for the caustic (RGN 10) description and could act
as a chelating agent to carry heavy metals into the water. An-
other sample, 3D, was described as ethanol wash (two layers).
The upper layer was identified as aromatic hydrocarbon (RGN
16), but only water (RGN 106) was detected in the lower layer.
Two oil samples containing PCBs (samples 16E and 17E) were
identified only as aromatic hydrocarbons. The PCB levels in these
samples was not known, but was assumed to be low (trace level)
in which case the chloride was present at too low a level to be de-
tected.
Sample 8DU was identified as organic, but examination was not
carried beyond the flame test. The flame test results indicated to a
technician that the material might be an explosive. Further testing
would have been at the discretion of a qualified supervisor. In fact,
the material was the organic layer from the still bottom of a sol-
vent recovery refinery. The lower (water) layer was found to con-
tain metals. Thus, the flame behavior of 8DU was probably due to
burning metallic materials in the sample.
Sample 3E, a waste naphtha, was found to have sulfur present,
but no sulfur compounds were identified. Sulfur is not uncommon
in naphtha, either as elemental sulfur or as organic sulfides.
Organic sulfur groups other than mercaptans, thiocarbamates and
disulfides are not detected by the methods used in the test scheme.
The failure to identify sulfur-containing organic species may also
indicate a difference in sensitivity between the test for sulfur and
the specific functionality tests. The same conclusion can be reached
from the results of sample 10E. A positive nitrogen response was
obtained, but no nitrogen compounds were detected in this waste
sample.
A carbon tetrachloride waste sample (4E) was found to contain
aromatics and organic acids as well as being in RGN 17 (chlor-
inated organics).
Two minor shortcomings of the test schemes were pointed out
by the field evaluation. The test schemes are organized so that
aqueous liquids are not tested for organics. The sodium fusion
procedure and a number of specific organic functionality tests are
not amenable to aqueous solutions. For compatibility purposes,
the classification of aqueous organics as aqueous mixtures would
probably suffice. For purposes of predicting optimum destruction
technology, the inability to detect organics in water may be a seri-
ous limitation.
During the field test, approximately 40 man-hours were spent
in actual sample analysis. Since 29 phases were analyzed, the aver-
age analysis time was approximately 1.3 hr/sample. This average
analysis time is expected to be acceptable in field applications.
60
SCREENING
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Table 6
Description of Samples Tested and Summary of Results of the Field Evaluation
Sample3
ID
2D
3DU
3DL
4DU
4DL
5D
6D
70
8DU
SDL
IE
2E
3E
4E
5E
6Eb
7E
8E
9E
IDE
HE
12E
13EU
13EL
14E
15E
16E
17E
Sample
Identification
Dirty PCE
TCE still bottoms, oil ,
hydrocarbons
Ethanol wash and oils
Ethanol wash and oils
Toluene in thinner wash
Toluene in thinner wash
MEK, xylene, and solvents
Acetone and MEK
MEK from paint
manufacturing
Still bottoms from solvent
recovery refinery
Still bottoms from solvent
recovery refinery
Organochlorine waste streams
Wastewater from storage tank
Waste naphtha
Carbon tetrachloride
MIBK with waste solvents
Waste solvents with amines
Thiocarbohydrazide with f^S
Spent caustic
Ethyl ene di chloride still
bottoms
Waste solvents, waste ink
Waste varnish
Water base insecticide
Oil base insecticide
Oil base insecticide
Tribromocumene
PCB oil , high level
PCB oil , low level
Silicone oil (with PCB's)
Sample
description
Yellow-brown liquid
Dark brown emulsion very small upper layer
Brown liquid (upper layer of two layers)
Pale brown liquid (lower layer of two layers)
Pale yellow liquid (upper layer of two layers)
Pale brown liquid (lower layer of two layers)
Very light tan emulsion
Light purple emulsion
Green-brown emulsion
Dark brown slurry (upper layer of two layers)
Pale yellow liquid (lower layer of two layers)
Very dark (opaque) viscous liquid
Tan liquid (very small amount of dark brown
1 iquid on top)
Light brown clear liquid
Dark brown clear liquid
Light pink clear liquid
Light brown clear liquid
Red-orange clear liquid
Clear colorless viscous liquid with small
amount of black particulate
Very dark blue liquid
Dark gray viscous liquid
Light brown clear viscous liquid
Milky white opaque viscous suspension
Yellow clear liquid (upper layer of two layers)
Cloudy light yellow liquid (lower layer of two
layers)
Opaque red-brown viscous suspension
Light yellow-green clear liquid
Light orange clear liquid
Very light yellow-green clear liquid
Ri
Predicted
17
17
16,28
4,106
16
106
16,19
19
19
b
b
17
106
16,28, or 29
17
19
7
33,105,106
10,106
17
b
16
106C
d
d,e
16,17
16,17
16,17
16,17
SN(s)
Found
4,17
16,17
16
106
16,19
106
4,16,19
19
16,19
102
24,106
17
10,24,106
4,16,31
3,16,17
4,19,31
10,24,106b
10,33,105,106
10,106
17
13,19
16
106d
16
106
16,17
16,17
16
16
aSources of hazardous waste samples are being kept anonymous at the request of the
project technical advisor
DSee discussion
cNot well defined by waste description
dAlso found to contain organics
eWater not predicted by waste description
SCREENING
61
-------
CONCLUSIONS
As with any new protocol or methodology, there are areas re-
quiring further work. For the protocol as it relates specifically to
the RON classification system put forward in Simmons, et a/.,"
there are four RGNs for which specific class tests have not been
identified: isocyanates, epoxides, nitrides and polymerizable ma-
terials. Two weaknesses were found in the RON classification
system: (1) the failure to identify levels at which a particular RON
may pose a problem, and (2) the lack of a classification for water
solutions containing high levels of soluble organics. These weak-
nesses are mirrored in the current protocol in that detection lim-
its have not been established and a procedure for identifying
organics in water has not been defined. Finally, although it was
originally hoped that the procedure would be so simple and so ex-
plicit that almost any technician could successfully use the kit and
protocol, it is recommended that users have some minimal train-
ing (approximately 1 week).
The protocol and kit were used successfully to identify 28 real
waste samples in the field. Specifically,
•36 of 41 predicted RGNs were identified
• 13 unpredicted RGNs were found
•One mislabeled sample was found
•The average analytical time was 1.3 hr/phase
ACKNOWLEDGEMENTS
This work was funded by the USEPA Municipal Environ-
mental Research Laboratory in Cincinnati, OH under contract
68-02-3176, assignment 38. The Project Officer was Ms. Naomi
Barkley to whom much credit goes for keeping the needs of the
end user in view. Special thanks are due our Technical Advisor,
Mr. Richard Carnes of the EPA Industrial Environmental Re-
search Laboratory in Cincinnati. He first suggested the project,
furnished much of the background information, arranged for use
of the USEPA Combustion Research Facility at Jefferson, AK for
the field testing and furnished the waste samples. Finally, the
major work of testing the protocol and assembling and testing the
kit was performed by Dr. Richard Whitney, Ms. Ursula Spanna-
gel and Mr. Ron Scholtz.
Portions of this paper were presented at the USEPA Ninth
Annual Research Symposium Land Disposal, Incineration and
Treatment Of Hazardous Waste, May 2-4, 1983, Ft. Mitchell, KY
and appear in the proceedings under the title "Field Scheme for
Determination of Waste Reactivity Groups" by U. Spannagel,
R. Whitney and D. Wolbach.
REFERENCES
1. Hatayama, H.K., Chen, J.J., de Vera, E.R., Stephens, R.D. and
Strom, D.L., "A Method of Determining the Compatibility of Haz-
ardous Wastes," EPA/600/2-80-076, USEPA, Cincinnati, Ohio,
1980. NTIS PB No. 80-221005.
2. Lynn, J.P. and Rossow, H.E., "Classification of Chemical Reac-
tivity Hazards," National Technical Information Center, Alexandria,
Virginia, 1970.
3. ASTM Committee D34 report in progress (personal communication:
B.C. Malloy, Chairman).
4. Dahn, C.J., "Chemical Compatibility and Storage Considerations
for Process Systems Hazards Analysis," J. of Hazardous Materials,
4, 1980, 121-127.
5. Myers, L.C., "The Chemical Reactivity Test—A Compatibility
Screening Test for Explosives," J. of Hazardous Materials, 4, 1980,
77-87.
6. Turpin, R.D., "Oxidation/Reduction Potential Field Test Kit for Use
at Hazardous Material Spills," Proc. Hazardous Material Spills
Conference, Apr. 1982, 225-230.
7. Cheronis, N.D. and Entrikin, J.B., Semimicro Qualitative Organic
Analysis, Interscience Publishers, Inc., New York, 1960.
8. Feigl, F., Spot Tests in Inorganic Analysis, Elsevier Publishing
Company, New York, 1972.
9. Feigl, F., Spot Tests in Organic Analysis, Elsevier Publishing Com-
pany, New York, 1966.
10. Rand, H.C., Greenberg, A.E. and Taras, M.J., "Standard Methods
for the Examination of Water and Wastewater," 14th ed., Amer-
ican Public Health Association, Washington, D.C., 1978.
11. Simmons, B.P., Tan, I., Li, T.H., Stephens, R.D. and Strom, D.L.,
"A Method For Determining the Reactivity of Hazardous Wastes,"
USEPA, Cincinnati, Ohio, 1982 (Preliminary).
62
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TECHNIQUES FOR IDENTIFICATION AND NEUTRALIZATION
OF UNKNOWN HAZARDOUS MATERIALS
CHARLES E. HINA
AL B. GARLAUSKAS
TIMOTHY D. CARTER
Samsel Services Company
Cleveland, Ohio
INTRODUCTION
In Feb. 1983, a pre-demolition inspection of an abandoned
building on the east side of Cleveland, Ohio revealed the presence
of a large number of containers of chemicals. Investigation by the
Ohio Environmental Protection Agency (OEPA) and the USEPA
determined the following:
•The building had once housed a pharmaceutical manufacturing
facility
•Over 3,000 containers of chemicals and pharmaceutical prepara-
tions ranging in size from Ig to 25 kg were present
•About one-third of the containers were unlabeled or otherwise
unidentifiable
•Among the labeled materials were explosives such as picric acid,
organic and inorganic peroxides, and water reactive materials
such as aluminum chloride, sodium metal and calcium hydride
•The owner disavowed any responsibility for the building or its
contents
Because of the hazard, the USEPA assumed responsibility under
Superfund legislation for removal and disposal of the chemicals
and pharmaceutical preparations.
Landfilling was selected as the most economical disposal alter-
native for these chemicals providing that the chemicals could be
altered to make them suitable for burial. In order for chemicals and
wastes to be disposed of in a secure hazardous chemical landfill,
OEPA regulations require that the chemicals be segregated into one
of six disposal groups. The groups which are based on reactive pro-
perties are described in Table 1. Excepted materials that may not be
placed in a landfill are summarized in Table 2. Since the labeled
materials included a number of excepted items, it was decided the
characteristics of the unlabeled materials would have to be iden-
tified to a degree that would permit safe handling and disposal.
In this paper, the authors describe the procedures employed to:
identify any excepted chemicals among the unlabeled materials,
segregate the remaining unlabeled materials into one of six disposal
groups and destroy or neutralize the excepted materials sufficiently
to permit landfill disposal.
ANALYTICAL PROCEDURES
Based on the definitions and requirements of the excepted
materials and disposal groups listed in Tables 1 and 2, a number of
characteristics had to be determined for each of the unlabeled
materials. The characteristics necessary to identify excepted
materials included: explosiveness, oxidizing capacity, air reactivity,
water reactivity and pyrophoric activity. Because of the nature of
Table 1
Description of Disposal Groups
Disposal
Group
Group A
Group B
Group C
Group D
Group E
Group F
Description
Inorganic acids: hydrochloric acid, sulfuric acid
Elements and inorganics that do not liberate gaseous
products when acidified: sodium chloride, barium sulfate
Very strong organic acids: trichloroacetic acid, trifluorace-
tic acid
Inorganic alkalines: sodium hydroxide, potassium
hydroxide
Elements and inorganic chemicals that liberate gaseous
products when acidified: potassium cyanide, sodium sulfide
Heavy metal compounds and elements: copper sulfate,
mercury, iron, zinc
Organic compounds: including organic acids (Ref.
Group A exceptions) but excluding organic bases: acetone,
mineral oil, glucose, cured phenolic resin, chloroform
Organic bases: triethanolamine, pyridine. Aqueous
ammonia solutions: ammonium hydroxide
Inorganics oxidizing agents: potassium nitrate, sodium
nitrite
Amphoteric metal compounds and elements: arsenic
trioxide, selenium, beryllium, lead, aluminum, tin,
antimony and vanadium
the operations at the site, it was decided that pathogenic or infec-
tious materials were of no concern.
In order to segregate the non-excepted materials into one of the
six disposal groups, the following characteristics had to be deter-
mined: acidity/basicity, organic/inorganic, oxidizing activity, acid
reactivity and base reactivity. To determine these characteristics
and segregate the unknown materials, 10 tests were employed:
Air Reactivity
Burn Test
Water Reactivity
pH
Organic Peroxide
Organic Base
Inorganic Oxidizer
Aggressive Inorganic Oxidizer
Acid Reactivity
Base Reactivity
SCREENING
63
-------
NEUTRALI IE
i
NOT ACID'REACTIVE NOT ACID'REACTIVE
BASE REACTIVE NOT BASE REACTIVE
Figure 1
Flow Chart for Disposal of Unknowns
Table 2
Excepted Materials that Cannot Be Landfilled
According to OEPA Guidelines
•Shock sensitive materials: Class A & B explosives, picric acid, mercury
fluminate, azides, some low molecular weight ethers, other.
•Extremely aggressive oxidizing agents: peroxides, perchlorates, persul-
fates, chlorates, other.
•Materials that react violently with air or water to produce heat and
flame: sodium metal, lithium metal, phosphorus, organic acid chlorides,
hydrides, carbides, sodium-potassium alloys, grignard reagents, alumi-
num trichloride, antimony pentachloride, phosphorus trichloride.
•Pressurized containers: gas cylinders, aerosol cans.
•Radioactive materials of any type.
•Pyrophoric materials of any type.
•Pathogenic or biologically infectious materials of any type.
The flow chart in Figure 1 shows how the results of the tests were
used to identify the excepted materials and segregate the remainder
into one of six disposal groups. The initial steps in the identification
process were a determination of air and water reactivity, identifica-
tion of explosive materials and separation of the inorganic
materials from the organic materials.
The explosives were burned, and the residue was retested to
determine extent of destruction. When the destruction was com-
plete, the residue was further tested to determine into which
disposal group the residue should be placed. The organic materials
were analyzed to identify those which were peroxides or organic
bases. The peroxides were neutralized, and the residue was retested
to identify the proper disposal groups.
Inorganic materials were tested to determine pH acid and base
reactivity and oxidizing capacity. Inorganic materials identified as
oxidizers were further tested to determine if they were aggressive
oxidizers. Aggressive oxidizers were destroyed, and the residue re-
analyzed to determine into which disposal group the residue should
be placed.
Reagents
All analytical reagents were prepared with analytical reagent
grade chemicals:
•6N sodium hydroxide
•6N hydrochloric acid
•Manganous chloride saturated solution of MnC^' 4H2O in
concentrated hydrochloric acid
•Titanium sulfate reagent mixed Ig TiO2 with 20 g KHSO4,
heated the mixture until transparent, cooled the melt rapidly,
ground to a powder, dissolved the powder in 500 ml of 18N sul-
furic acid and filtered through a sintered glass filter
•Nickel dimethyl glyoxime reagent - Solution A: Dissolved
810mg of dimethyl glyoxime in 100ml 95% alcohol. Solution B;
Dissolved 770mg NiSO4 in 100ml distilled water. Mixed 50ml of
each solution and shook vigorously. Filtered the mixed reagent.
The clear filtrate was used for the test.
Analytical Methods
Air Reactivity:
Each of the unknowns which were enclosed were carefully op-
ened and observed for emission of fumes or gases. Since many of
the containers were without tops and the material in many of the
64
SCREENING
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containers with tops had become caked, care was taken to expose
the potentially reactive material below the surface.
If, on opening, the material emitted fumes or gases, it was con-
sidered to be air reactive. The contents of containers which released
pressure when opened and exposed to the atmosphere were also
considered air reactive. None of the unknown materials ignited
when the containers were opened.
Burn Test:
20 to 50 mg of a solid unknown were transferred to a stainless
steel spatula and heated in an open flame. If the material was a li-
quid, a stainless steel loop holding a drip of the unknown was
employed.
If the sample ignited violently at some point in the heating pro-
cess, it was considered to be explosive. If the sample burned slowly
but evolved large quantities of fumes, it may also have been ex-
plosive. If the material burned with a flame, it was considered to be
organic. Exceptions to this guideline are inorganics such as
phosphorus or sulfur. These inorganics, however, are easily
detected by the manner in which they burn (slowly) and the fumes
generated. If the material did not burn, but charred or turned
black, it was suspected of being organic. If, on continual heating,
the char burned off, the unknown was considered to be organic. If,
however, the residue did not burn off, the material was considered
to be inorganic. Most of the unknowns melted, but melting was not
considered as an indicator characteristic.
Water Reactivity:
The unknown (l-2g) was added to a beaker containing 10-15 ml
of distilled water. The sample was observed for temperature change
and evolution of gas or fumes. The solubility of the material was
also noted.
Materials which evolved gases or fumes or ignited were con-
sidered to be water reactive. Materials which produced a
temperature change were not considered to be water reactive unless
the water approached boiling temperature. Temperature change
was, however, useful for identifying the material. For example,
strong acids and bases tend to be exothermic (emit heat) while com-
pounds such as thiosulfates tend to be endothermic (absorb heat).
The solubility of the materials was noted as being very soluble,
slightly soluble or insoluble. While solubility was not indicative of
water reactivity, it helped to characterize the unknowns. Clear
organics, such as chloroform or carbon tetrachloride, test as an in-
organic in the flame test. Because these compounds were insoluble
and immiscible in water, it indicated that they were organics.
pH Test:
The residue from the water reactivity test was used for the pH
measurement. If the sample dissolved but did not generate heat,
electronic measurement was used. If the sample did not dissolve,
was organic or evolved significant heat, wide range pH paper was
used to estimate the pH. Narrow range pH paper was then used to
measure the pH to within 0.2 pH units.
A pH of 2 or less indicated that the material was acidic and a can-
didate for Disposal Group A, while pH of 9 or more indicated that
inorganics were candidates for Disposal Group B and organics for
Disposal Group D. When the pH ranged between 2 and 9, no deci-
sion could be made as to the Disposal Group in which a material
should be placed. A number of organics, particularly the oint-
ments, salves, oils and greases did not dissociate sufficiently to pro-
duce a definitive pH value. These materials were called neutral.
Organic Peroxide:
Two drops of liquids or 50-100 mg of solid organics were
transferred to a test tube. Titanium sulfate reagent (1 ml) was
added and the color change noted. A yellow color indicated the
presence of organic peroxides. If no color change occurred, the
sample was placed in warm water (55 °C) for 2-3 min. Since many
of the organic materials were colored or reacted with strong sulfuric
acid to produce a yellow to amber color (sometimes red), a sample
blank was also run. The sample blank consisted of the same
amount of sample to which 1 ml of 18N sulfuric acid was added.
The sample blank was processed in the same manner as the sample.
Since almost all peroxides react with titanium sulfate in 18N
sulfuric acid, the formation of a yellow color was evidence that the
material was a peroxide or contained traces of peroxide. The
unknowns which did not produce a yellow color were not con-
sidered to be peroxides.
Organic Base:
Two drops or 50-100 mg of the unknown material were trans-
ferred to a spot test plate and 2-3 drops of nickel dimethylglyoxime
were added. Formation of a red precipitate indicated that the
material was an organic base.
Materials forming a red precipitate with nickel dimethylglyoxime
were placed in Disposal Group D. All ammonium hydroxide and
basic ammonium solutions gave a positive test. A number of
organics which had a greater than 8.5 did not give a positive test.
These materials are probably dyes and color indicators and are not
considered organic bases, although they exhibit a basic pH in
aqueous solution. Many materials that had an almost neutral pH in
aqueous solution gave a positive organic base test.
Inorganic Oxidizer:
50-100 mg of solid or two drops of liquid inorganic material were
placed in a test tube. Drops of concentrated hydrochloric acid were
added until any effervescent reaction ceased. 2 ml of the
manganous chloride reagent were added. A black or brown
manganic precipitate was indicative of the presence of an oxidizing
agent. If no precipitate was formed immediately, the sample was
placed in a warm water bath (50 °C) for 2-3 minutes. If no brown or
black precipitate appeared upon warming, the material was not an
oxidizing agent. If the material was brown, black, dark-colored or
reacted with hydrochloric acid (silver salts for example), a sample
blank consisting of sample and concentrated hydrochloric acid was
prepared. The sample was then compared to the blank to determine
if a positive oxidizer test had occurred.
Vogel2 indicates that nitrate, nitrite, ferricyanide, chlorate,
bromate, iodate chromate and permanganate give positive reac-
tions. Barium dioxide, dichromates and bismuthates also gave a
positive reaction. The materials that did not produce a brown or
black coloration or precipitate were not classed as oxidizers.
The speed at which the brown or black color was formed and the
quantity of color or precipitate was an indication of the strength of
the oxidizer. Permanganates, for example, reacted immediately and
produced a dense black precipitate. The materials which gave a
positive oxidizer test were further tested to determine whether they
were aggressive oxidizers.
Aggressive Inorganic Oxidizers:
50 to 100 mg of the unknown were dissolved in 1 ml concentrated
sulfuric acid. Evolution of the greenish-yellow gas chlorine dioxide
was indicative of the presence of chlorates. If no chlorine dioxide
was evolved, the sample was heated. Evolution of white fumes was
indicative of the presence of perchlorates. Permanganates, while
not producing chlorine dioxide or white fumes, reacted violently
with sulfuric acid.
Oxidizers which did not produce chlorine dioxide, white fumes
upon heating or react violently with concentrated sulfuric acid were
not considered to be aggressive oxidizers and, thus, were placed in
Disposal Group E. Aggressive oxidizers were neutralized then
retested.
Acid Reactivity:
One to two grams of the unknown were added to 10-15 ml of
distilled water and 2 ml of 6N hydrochloric acid were added. The
evolution of heat, vapor or gas indicated that the material was acid
reactive.
Materials that produce heat upon acidification are generally
strong bases, although some amphoteric materials such as
aluminum, arsenic and bismuth containing compounds produce
heat as well as precipitate. Evolution of gas is indicative of car-
SCREENING
65
-------
bonates, sulfides, sulfites, chlorites, cyanides and arsenites. Evolu-
tion of gas may also indicate that the material is a metal such as
zinc, ion or arsenic. Differences in solubility, appearance and pH
of the materials being tested were used to assist in determining what
type of compound was being tested. A negative reaction may in-
dicate that the material could be a neutral salt such as sodium
chloride, phosphate or sulfate.
A material which is acid reactive was not placed in Disposal
Group A but was placed in either Disposal Group B or F, depen-
ding on its base reactivity.
Base Reactivity:
One to two grams of the unknown were added to 10-15 ml of
distilled water and 4 ml of 6N sodium hydroxide added. The evolu-
tion of heat, vapor or gas was indicative of a positive base reaction.
Some materials such as heavy metals and amphoteric metals may
form precipitates with or without evolution of heat.
Materials that produce heat upon addition of strong base are
generally strong acids although, as noted above, some amphoteric
compounds may react with evolution of heat. All ammonium com-
pounds and some amphoteric compounds will evolve gas or vapors.
A negative reaction may indicate that the material is a neutral salt
or that it is a basic in nature.
A material which was based reactive was not placed in Disposal
Group B but was placed in Disposal Group A or F depending on its
acid reactivity.
NEUTRALIZATION OF EXCEPTED MATERIALS
The explosive materials were burned in small quantities until no
readily combustible material remained. Water and air reactive
materials were slowly added to 10 times their weight of water. The
pH of the resulting mixture was adjusted to approximately 7. The
organic peroxides were neutralized by mixing with 10 times their
weight of 20% sodium hydroxide. The peroxide-hydroxide mixture
was stirred intermittently until a negative reaction for peroxide was
achieved. Aggressive oxidizers were mixed with concentrated
hydrochloric acid, then gently heated to expel gases.
RESULTS
A total of 1302 unlabeled materials were analyzed. This number
included the residues from neutralization of the excepted materials.
The distribution of the unlabeled materials among the disposal
groups is shown in Table 3.
Table 3
Distribution of Unlabeled Materials Between the Six Disposal Groups
Disposal
Group
No. of Drums
No. of
Unlabeled
Materials
75
B C D E F
8 17 31 1
196 699 137 52 29
Unlabeled materials (1,188 in number) were packed into drums.
The remainder of the unlabeled materials were used up during the
analyses leaving no separate residue.
Very few problems were encountered in analysis and in determin-
ing to which disposal group each belonged. Minor problems were
presented by the many colored materials which in some cases in-
terfered with easy interpretation of the reactions. These problems
were overcome by the use of sample and reagent used.
Disposal Group A:
Most of the 75 items in this group had a low pH but, more im-
portantly, were base-reactive. Nine of the Group A items were
organic materials with pH values of less than 2 and were strongly
base reactive. Several of the items in Group A were neutral base
reactive salts; these were ammonium salts as evidenced by evolution
of ammonia gas when the base was added. Also included in Group
A were several neutral salts which were neither acid nor base reac-
tive.
Disposal Group B:
The pH of the 1% items in this group ranged from 4 to 14, and
about half of the materials were acid reactive. The majority of the
items that were acid reactive were apparently hydroxides as
evidenced by generation of heat when reacted with acid. Many of
the materials produced gas when reacted with acid. Most of the
compounds were carbonates and bicarbonates, although two were
suspected of being cyanides. A number of metals such as iron and
zinc were also present.
Disposal Group C:
This was the largest group, encompassing 699 items. There was a
great deal of variance in this group, although all contained carbon,
were not air or water reactive and were not organic bases or perox-
ides. Some items had pH values as high as 13 but did not produce a
precipitate when treated with nickel dimethylglyoxime reagent.
Many of these items were probably indicators.
Disposal Group D:
All of the 137 samples in this group produced a red precipitate
when treated with nickel dimethylglyoxime reagent. A number of
the items had pH values as low as 4.5, indicating that pH was not
an indicator of the basicity of a material. Materials that were
suspected of being compounds such as ammonium hydroxide,
thanolamine, morpholine and pyridine produced immediate dense
precipitates when reacted with the nickel dimethylglyoxime
reagent. Approximately 30 chemicals, however, required up to 30
sec to form the typical red precipitate. The delayed reaction may
have been in part due to low solubility, but most likely the material
was a weak base such as diphenylamine.
Disposal Group E:
All of the 52 chemicals in this group were inorganic oxidizers.
Most of these were nitrates, although some were ferricyanides,
dichromates, bromates and iodates. Two matrials suspected of be-
ing bismuthates were also included in this group because
bismuthates are oxidizers. Bismuth compounds were normally
placed in Disposal Group F.
Disposal Group F:
Many of the 29 chemicals in this group were metals. The metals,
all of which were both acid and base reactive, included materials
suspected of being bismuth, lead, selenium, aluminum, arsenic, tin
and antimony. Included in this group were neutralization residues
from an air and water reactive material suspected of being arsenic
trichloride and three items suspected of being aluminum
trichloride.
The excepted and reactive materials that were neutralized or
destroyed are listed in Table 4. These materials were fairly easy to
destroy and required only time for the reaction to go to completion.
Both the organic and inorganic peroxides required 3 to 4 days after
mixing for neutralization to be complete. Of the materials listed in
Table 4, sodium metal, calcium hydride, calcium carbide, one con-
tainer of sodium peroxide and one container of aluminum chloride
were labeled. All the other materials were unlabeled.
DISCUSSION
The testing procedures described in this paper were designed to
separate a large number of unknown materials into compatible
disposal groups. Specific identification of each material was not re-
quired, although for a number of inorganic materials it was pos-
sible. Most of the materials could not be totally identified even
though they were suspected of being pure compounds. Mixtures
were only identified as far as it was necessary to place them into one
of the disposal groups.
Since the procedure was not designed to identify specific com-
pounds, there are a number of types of materials for which this
procedure is not applicable. Highly toxic or carcinogenic materials
66
SCREENING
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Table 4
Summary of Excepted Materials
Item
Bromine
Sodium Metal
Calcium Hydride
Calcium Carbide
Sodium Peroxide
Phosphorous
Chlorate
Arsenic Trichloride
Aluminum Trichloride
Air Reactive Liquids
Hydrogen Chloride Gas
Cylinder
Organic Peroxide
Organic Explosives
Qty.
3000g
900g
454g
454g
850g
35g
30g
lOOg
1800g
500ml
BOOOg
200g
Reacted with
Sodium Hydroxide
Water
Water
Water
Water
Burned
Hydrochloric Acid
Water & Sodium Hydroxide
Water & Sodium Hydroxide
Water & Sodium Hydroxide
Water & Sodium Hydroxide
Sodium Hydroxide
Burned
No.
Con-
tain.
ers
1
2
1
1
2
3
2
1
4
2
1
11
6
such as dioxin which should not be landfilled are beyond the scope
of this procedure. This procedure is applicable to situations similar
to the one encountered where the general nature of the waste
materials is known. It may also be employed to segregate total
unknowns into disposal groups provided that specific tests are per-
formed to determine the presence and concentration of materials
that cannot be landfilled.
The methods used to neutralize or destroy the excepted materials
were based on the nature of the materials, the relatively small quan-
tities present and use of available reagents and equipment.
REFERENCES
1. Vecera, M. and Gasparic, J., Detection and Identification of Organic
Compounds, Plenum Press, New York, 1971.
2. Vogel, A.I., A Test-Book of Macro and Semimicro Qualitative In-
organic Analysis, Longmans Green and Co., London, England, 1965.
ACKNOWLEDGEMENT
In this paper, the authors have summarized the results of a pro-
ject performed under contract to USEPA, Region V, Eastern
District Office, Mr. Daniel A. Papcke, Project Officer.
SCREENING
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GEOPHYSICAL INVESTIGATIONS OF ABANDONED WASTE
SITES AND CONTAMINATED INDUSTRIAL AREAS
IN WEST GERMANY
RAINER H. FELD, DR. RER.NAT.
MANFRED STAMMLER, DR. RER.NAT.
Battelle-Institut e.V.
Frankfurt am Main, West Germany
GERALD A. SANDNESS, Ph.D.
C. SCOTT KIMBALL
Battelle Pacific Northwest Laboratories
Richland, Washington
INTRODUCTION
According to a conservative estimate of the "Umweltbundes-
amt (DBA)" in Berlin (West), approximately 1000 uncontrolled
and abandoned dump sites containing toxic and hazardous material
are suspected in West Germany. In a program sponsored by the
Federal Ministry for Research and Technology (BMFT) and tech-
nically administrated by the UBA, Battelle-Institut e.V., Frankfurt
and Battelle Pacific Northwest, Richland have investigated aban-
doned waste sites in West Germany using modern geophysical
methods.
The program is evaluating the following methods of investiga-
tion:
•Ground probing radar (GPR)
•Electromagnetic induction (EMI)
•Magnetometer (Mt)
It is measuring the ability of each method to detect the boun-
daries of disposed waste, to locate contaminated groundwater
plumes and to determine the plume flow direction to allow the
effective placement of monitoring wells. Locating buried materials
(drums, containers or bulk wastes) is of importance in the evalua-
tion of the hazard potential.
Results of geophysical surveys together with the chemical, geo-
logical and hydrological analyses will permit the design and imple-
mentation of suitable remedial action plans.
THE SITES
Of the 11 sites which have been investigated to date, results of
three will be presented in this paper.
Sprendlingen
In 1964, the Prael GmbH began to operate a chemical wastes
dump in a clay pit at Sprendlingen. The dumping of chemicals was
stopped in 1974. Later, the remaining sections of the pit were filled
with refuse. In 1980, that part of the site which was believed to
contain chemical wastes was covered with a clay-cap and seeded.
The groundwater in the village of Sprendlingen was found to
be contaminated by various organic and inorganic substances.
Consequently, monitoring wells were drilled; however, no correla-
tion could be established between the groundwater contamination
in the village and the data from the monitoring wells.
Although it was known that the fluvial sediment in this region
consists of complex layering of clay and gravel, it was not real-
ized that this could lead to a well defined and complex system of
plumes. Such a system of plumes, however, would have explained
why water wells that were situated less than 100 m from each
other would have completely different readings and why higher
contamination was found at distant wells than at some of the wells
next to the dump site.
The geophysical survey was performed at the outer north part of
the site. Radar probing was used to detect the boundaries of the
site which were not registered.
Magnetometer measurements were made in order to determine
whether metallic objects were present in the fill. The purpose of the
electromagnetic induction measurements (EMI) was to detect con-
taminated groundwater plumes which were believed to move
through the fields next to the dump site in the direction of the
village.
Munchehagen
The former waste disposal site of the Bosinghaus and Stenzel
GmbH is located in an old clay stone pit near the village of Munch-
ehagen. The site was utilized until 1975. Various chemical wastes,
partially packaged in drums, were dumped in a controlled manner
in lagoons separated from each other by clay dikes. The pit was
filled to the upper edge of the dikes. In order to enlarge the volume
of the pit, the heights of the dikes were increased.
Several years after the site's closure, contaminants were found
outside the dump area, migrating into a nearby forest. Subse-
quently, the trees in a highly contaminated zone died.
The side was covered by a clay stone layer, and a drainage sys-
tem was installed. However, the seepage could not be brought
under control and started to affect the contaminant concentration
of the leachate of the adjacent new disposal site.
To detect the position of the dikes and lagoons, radar prob-
ing was utilized. Magnetometer measurements were performed to
separate the regions where a high metal content would lead to the
assumption that drums with toxic wastes had been buried. EMI-
probing was used to determine regions of varying conductivity.
Hamburg-Feldhofe
The site at Feldhofe in Hamburg is a small (4000 mj) lot where
waste was dumped near the remains of an old house and a nearby
pond. The property was abandoned by the owner. Authorities were
only recently informed by citizens living adjacent to the site that
drums with unknown contents had been disposed there some time
ago. By probing at suspected locations based on information from
local citizens, several drums filled with chemicals were found. The
site has to be cleaned up due to the projected reconstruction of a
railway bridge overpassing the site.
68
SCREENING
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Combined magnetometer and radar measurements were used to
monitor the area.
METHODS
Ground Probing Radar
The radar system consists of several antennas which transmit
radar signals at frequencies between 80 and 900 MHz. According
to the soil conditions, the desired penetration depth and resolu-
tion, the appropriate probe is chosen. The probe is moved over the
area to be surveyed at a constant speed. The reflected signals are
recorded on magnetic tape and are computer analyzed. Depending
on the condition of the ground and the transmitted frequency,
the penetration depth is 3 to 5 m.
Reflectors are geological formations and structures and objects
in the ground. Good reflectors are metals and saturated clay. Those
structures which are situated below very strong reflectors cannot be
detected. Interfaces between dump sites and the surrounding areas
show up well, as the reflection pattern normally changes signifi-
cantly going from undisturbed to disturbed ground.
The recorded radar signals are vertical slices of tracks.1 These
slices show the position of the probe on the horizontal line and the
signal travelling time corresponding to the relative depth on the ver-
tical line. Computer corrections are made for background noise
and invariant signals. Programs for a more detailed signal analy-
sis are available.
An additional option is to compute color coded horizontal slices
(maps).2 These maps give overall information about the distribu-
tion of reflectors.
Electromagnetic Induction
The instrument for electromagnetic induction (EMI) consists of
a transmitter coil and a receiver coil.3 The two coils are spaced at a
defined and fixed distance from each other.
The electromagnetic field of the transmitter coil induces an al-
ternating current in the soil. This current induces a secondary elec-
tromagnetic field. The receiver coil compares the secondary field to
the primary field. The integrated conductivity of the soil is cal-
culated by a microelectronic device in the instrument. The pene-
tration depth is approximately 1.5 times the coil's distance. The
instrument used in this investigation was the EM31 by Geonics
Ltd.
The signals can be recorded for grids with spacing of 1 to 5 m be-
tween traverses. Conductivity maps can be computed using tech-
niques similar to those described for radar probing.4
Magnetometer
A magnetometer measures the variations of the earth's mag-
netic field dur to ferromagnetic objects in the ground. Magneto-
meters are used to locate single objects such as ammunition and
drums5 or to map certain geological formations.' Magnetometer
surveys of disposal areas can detect drums and other metallic
objects.
Computer techniques are used to map the magnetic anomalies.
Thus, information on the overall distribution of ferromagnetic
materials on the site is obtained.2
DATA COLLECTION AND ANALYSIS
The methods of data collection and analysis were the same for all
three sites.
The radar probes were hauled by a small four wheel drive ve-
hicle. In all cases a 100 Mhz GSSI antenna was used.
The data generated were digitalized and preprocessed by a micro-
processor system and stored on magnetic tape. Depending on the
dimensions and shape of the site, data were collected on each
traverse ranging in length from 30 to 100 m. The distance between
two traverses was normally 1 m.
The magnetometer data were collected on the same grid as the
radar data. They were preprocessed by a microprocessor and stored
on a semiconductor memory unit.
The EMI data were collected either on a 5 m or a 2 m spacing. A
Geonics Ltd. EM31 instrument was used for all terrain conduc-
tivity measurements. The depth of these measurements is approx-
imately 6 m. The data were recorded by hand.
Dataprocessing was carried out on-site on a computer installed in
a van. The radar profile was displayed on a screen. Color-coded
maps showing the radar, EMI and magnetometer intensities were
generated, thus permitting an on-site check of the recorded data
quality. In a case of unsatisfactory quality, a repeat run was per-
formed.
The final processing took place at the central computer facilities.
The color-coded maps were calculated and copied on film using a
Dicomed D163 colorgraphics device. For the radar data, the verti-
cal profiles were also displayed in order to permit a visual inter-
pretation of detailed features in the ground. Vertical profiles
give more information about specific single objects and their depth
than maps which show only an overall distribution of features for
a chosen depth interval.
RESULTS
Sprendlingen
At Sprendlingen, an area of 10,000 m2 was surveyed by ground
penetrating radar and magnetometer. Using the EMI instrument,
30,000 m2 were investigated.
At the north side of the area, the boundary between the waste
filled clay pit and the adjacent fields could be clearly identified by
the radar data. The central part of the site shows various regions
of high radar reflectivity which could be related to metallic ob-
jects. The map of the magnetic anomalies shows that there are
several separated regions with a high content of metallic materials.
The EMI-data maps show the regions of very high conductivity
which can partially be related to the magnetic anomalies. The other
regions are believed to contain electrically conductive non-ferro-
magnetic materials.
From the regions of high conductivity in the waste dump, a con-
fined zone of higher conductivity leads into the surrounding fields
and continues toward the village of Sprendlingen. Approximately
50 m away from the edge of the dump, it splits into two plumes
approximately 5 to 20 m in diameter. Both streams move toward
the village location where the most contaminated groundwater
wells were found. These very confined regions of high conduc-
tivity are now believed to be relatable to a stream of contaminants
along layers of higher permeability in the ground.
Munchehagen
The radar maps of the Munchehagen dump site show various
separated zones with high radar reflection intensities. The largest
area of high intensity appears to be at the south end of the site.
The interpretation of the radar data is difficult, as the site has
been covered with a 60-100 cm layer of clay stone which was very
wet when the measurements were made, and wet-clay has very
high attenuation for radar signals.
The magnetometer measurements, which are not affected by the
clay layer, show several large magnetic anomalies believed to be
lagoons filled with metal objects such as drums. The maps of the
EMI-data show features similar to the ones found in the maps of
the magnetic anomalies. The EMI-maps, however, show additional
regions where non-metallic waste of high conductivity has been
dumped. The conductivity maps and the maps of the magnetic
anomalies show that the site consists of confined areas with differ-
ent kinds of wastes.
Hamburg-Feldhofe
The radar maps for Feldhofe show two regions of high density
of radar reflection separated by a zone where only a little re-
SCREENING
69
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flection occurred. For this site, a visual interpretation of the radar
profiles (Figure 1) was made to obtain more information about
the distribution of single objects.
With this method a number of single metallic and non-metallic
objects could be located. The metallic objects are concentrated
at four different locations. One of them is the region where drums
filled with chemicals had already been found. The magnetic
anomalies are related to these regions and match the radar data.
Figure 1
Radar profiles for Feldhoffe (Hansestadt Hamburg). The horizontal lines
of the profiles indicate the position of the radar probe; the vertical lines in-
dicate the travel time of the reflected radar signal. The profiles have been
corrected for background noise and invariant features.
CONCLUSION
The results of the data analysis show that radar, EMI and
magnetometer measurements, when used together, give detailed in-
formation about objects, different structures within the waste site
and the interface between excavations and undisturbed soil. In
addition, EMI data help to detect contaminated plumes when the
conductivities of the contaminants and the uncontaminated soil are
different. Differences of some millimhos/m are sufficient.
Detection of specific objects is best accomplished by the analysis
of radar profiles of each track since these profiles contain the
depth information.
In all cases, large quantities of data have to be handled. The
computer-assisted data analysis improves the detection probabil-
ity significantly.
ACKNOWLEDGEMENT
The authors would like to thank Dr. Konnecke for his help in
the data analysis and Mr. Kaul for his help in the data acqui-
sition. They also wish to thank the staff of the regional and state
agencies of Rheinland Pfalz, Niedersachsen und Hansestadt Ham-
burg for their cooperation. The support by the Bundesminister
fur Forschung und Technologic is gratefully acknowledged.
REFERENCES
1. Bowders, J.Y., Koerner, R.M. and Lord, A.E., "Buried Container
Detection using Ground Probing Radar", /. of Hazardous Materials,
7, 1982, 1-17.
2. Sandness, G.A., Dawson, G.W., Mathieu, T.J. and Rising, J.L.,
"The Application of Geophysical Survey Techniques to Mapping of
waste in Abandoned Landfills," Hazardous Materials Risk Assess-
ment, Disposal and Management, Miami Beach, 1979.
3. McNeil, J.D., "Electromagnetic Terrain Conductivity Measurements at
Low Induction Numbers," Technical Note TN-6 Geonics Ltd., 1980.
4. Feld, R. and Stammler, M., "Systematische Untersuchung von Altlas-
ten Teilabschlubbericht zum Projekt "Sondierung von kontaminierten
Standorten" UBA/BMFT, BF-R-65.385-1 (1983).
5. Universalsuchgerat Model! EL 1303, Information leaflet of Vallon
GmbH, Eningen, W. Germany.
6. Green, R. and Stanley, J.M., "Application of a Hilbert Transforma-
tion Method to the interpretation of Surface-Vehicle Magnetic Data,"
Geophys. Prospect. 23, 1975, 18-27.
70
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ADVANCES IN MAPPING ORGANIC CONTAMINATION:
ALTERNATIVE SOLUTIONS TO A COMPLEX PROBLEM
MICHAEL R. NOEL
RICHARD C. BENSON
PAUL M. BEAM
Technos, Inc.
Miami, Florida
INTRODUCTION
The authors' objective in this paper is to outline a systematic
approach for mapping the extent of subsurface organic contam-
ination to provide improved:
•Technical site assessments
•Monitoring well network designs
•Remedial action plans
•Risk assessments
In the first section of the paper, the major variables which will
influence contaminant behavior and, therefore, must be considered
in determining an appropriate mapping approach are reviewed.
The discussion draws attention to factors which can influence how,
where, when and with what to map organics in the most cost-effec-
tive manner. In the second section, a classification scheme divides
organic contamination into three types: (1) floaters, (2) mixers
and (3) sinkers. In the third section, various alternatives and con-
siderations applicable to mapping these types of contamination are
discussed.
No single method will be appropriate in mapping organic con-
tamination at all sites. Therefore, a sound systematic approach
that incorporates an understanding of the contaminants and their
behavior along with the impact of the local hydrogeologic con-
ditions and cultural features is needed. In addition, a knowledge of
the various technical methods available to assist in solving the prob-
lem is also necessary. Using the above resources, it is possible to
provide rapid, cost effective and accurate descriptions of the distri-
bution of subsurface organics.
VARIABLE TO CONSIDER
Each site possesses an interrelated set of variables which must
be considered in order to develop the most appropriate mapping
scheme. These variables are related to the type, source and cir-
cumstances of organic contamination as well as the site's access-
ibility and hydrogeologic parameters (Table 1). These factors con-
trol where and how far the contaminants will migrate. They also
influence the selection of methods most applicable to mapping their
extent.
Types of Organics
Each organic compound has unique characteristics. In terms of
mapping their extent and predicting their subsurface movement,
some of these characteristics are most significant. For example,
knowing the contaminant is a low density hydrocarbon will prob-
ably focus attention on the upper portion of the aquifer since these
types of organics would tend to float. However, if the contam-
inant were a high density chlorinated hydrocarbon, the attention
may be focused deeper in the aquifer since these organics would
tend to sink.
Table 1
Variables to Consider in Mapping
•Contaminant Related
Density
Volatility
Viscosity
Solubility
Mobility
•Source RElated
Electrical Conductivity
Concentration
Size of Input Area
Volume of Contaminant Input
Depth of Input
Rate and Duration of Input
•Hydrolgeologic Related
Geologic (Heterogeneity and Anisotropy)
Permeability
Water Table Depth
Flow Direction
Background Water Quality
Soil Types
Confining Layers
•Site Related
Accessibility
Cultural Development
Safety
•Resource Related
Time
Money
Another significant parameter is viscosity. Under identical geo-
logic conditions, the volume of product retained by the soil will be
about four times greater for a light fuel oil of high viscosity than
for gasoline that has a low viscosity.1 In the case of light fuel
oil, more emphasis might be directed toward the soils in the vadose
zone, whereas with gasoline the focus would probably be at the
water table. Viscosity also influences the lateral area which might
be considered in the investigation since gasoline would spread
further than fuel oil.
Solubility is obviously another important parameter to consider
in mapping. Lighter hydrocarbons such as gasoline are approx-
imately two orders of magnitude more soluble than the heavier
hydrocarbons such as lubricating oils.2 In the case of gasoline con-
tamination, therefore, greater consideration must be given to con-
tamination below the water table (soluble components).
Mobility of organics is a broad encompassing term which lumps
the various chemical, biological and physical retardation mech-
anisms together to describe how far a contaminant may migrate.
This type of information can be used to determine the potential
lateral and vertical boundaries of the investigation area.
Volatility effects the mobility of an organic, and it also provides
a means of detection with organic vapor analyzers (OVA).
SCREENING
71
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Source Related Variables
Several source related variables have a significant bearing in
mapping the extent of organic contamination. One of the most im-
portant is the electrical conductivity of the contaminant plume.
For example, most pure organics will have little or no electrical
conductivity associated with them. On the other hand, experience
has shown that the same organic contaminants leaking from a dis-
posal lagoon or evaporation pit will typically contain enough im-
purities to produce an electrical conductive signature in the plume.
In these instances, electrical geophysical techniques can be em-
ployed to map the plume's extent.
Concentration is another source related variable that should be
considered. In the case of a halogenated (dense) hydrocarbon, the
contaminants from a concentrated source would have a greater
tendency to sink than those from a dilute source. Another factor
of concentration is the ability of some organic solvents to struc-
turally alter (shrink, dessicate) clay and make a confining layer
more permeable.3'4 This alteration would most certainly be more
severe if the organics were concentrated as opposed to being dilute.
Another group of variables associated with the source are the cir-
cumstances under which the contamination occurred. Factors such
as the area over which the contaminant was introduced (widespread
or point source), rate and duration of input (long term pipe leak or
short term drum spill), volume of contaminant (one drum or large
tank) and depth at which the contaminant input occurs influence
where and how far mapping will extend.
Contaminants leaking from the surface will have to travel
through the vadose zone and may not reach the water table. Con-
taminants leaking below the surface allow a greater percentage of
the leaking contaminants to reach the ground water.
Hydrogeologic Variables
Two of the most significant and all encompassing hydrogeologic
variables that affect mapping are horizontal and vertical geologic
variations (heterogeneity and anisotropy). Whether it pertains to
stratigraphy, structure, permeabilities or soil types, the site's heter-
ogeneity and anisotropy will determine the accuracy of any map-
ping program.
Both natural variations in permeability (e.g., gravel versus clay
versus fractured rock) and man-induced variations (e.g., buried
utilities and sewers) will influence the potential pathways and dis-
tances the contaminants can migrate.
Other groundwater parameters worthy of consideration include
depth to and fluctuation in the water table, flow direction and
background water quality. The depth to water table will determine
which mapping techniques are appropriate. Fluctuations in the
water level will also effect the thickness of an oil layer in the
aquifer.' Knowledge of the local groundwater flow direction is crit-
ical to focus attention in the proper area. The background water
quality is necessary as a standard of comparison regardless of map-
ping techniques.
The soil type can affect the performance and application of cer-
tain mapping techniques as well as influencing the mobility of
organics in the form of attenuation. In mapping a high density con-
taminant which has migrated downward with gravity, the topog-
raphy of the lower confining layer becomes very important since
this can control lateral contaminant migration.
Site Variables
Accessibility is important because it can affect the density of cov-
erage of a mapping technique and determine whether or not cer-
tain techniques are feasible. Likewise, safety considerations are
important site variables that can slow and even limit the mapping
program.
Resources
The resources of time and money are two variables that have to
be considered in every site investigation. The tradeoff between cost
and levels of accuracy and confidence must be considered to devel-
op a cost-effective mapping approach.
CLASSIFICATION OF ORGANIC CONTAMINATION
The multitude of situations that can and do result by combin-
ing the wide range of variables complicates the mapping of organ-
ics. Because of this complex scenario, the approach to mapping or-
ganic contamination must be site specific. In order to present a
summary of approaches, three forms of organic behavior will be
discussed. These categories are based upon three modes of migra-
tion in an aquifer:
•Floaters
•Mixers
•Sinkers
Conceptual models of these forms of organic contamination are
shown in Figure 1.
"Floaters" are the low density hydrocarbons which have typical-
ly leaked or spilled as pure product from pipes and tanks and which
tend to migrate in the saturated zone at the top of the water table
(Figure 1A). Some of the more common hydrocarbons that are
constantly threatening aquifers include gasoline, jet fuel and lubri-
cating oils.
"Mixers" are the water soluble organic components which more
or less migrate through an aquifer in a manner similar to the
ambient ground water. One of the most common and widespread
"FLOATERS"
•MIXERS"
"SINKERS"
Figure 1
Conceptual Models of Organic Floaters, Mixers and Sinkers
72
SCREENING
-------
is trichloroethylene (TCE). Typical sources of mixers include land-
fills, industrial complexes and leaking evaporation ponds and la-
goons. Mixers also include the dissolved organic components re-
sulting from floaters and sinkers (Figure 1).
"Sinkers" are the high density halogenated hydrocarbons whose
migration can be strongly influenced by gravity. Because of their
density, they may flow in a direction different than the ambient
groundwater (Figure 1C). Some examples of dense hydrocarbons
include carbon tetrachloride, tetrachloroethylene, chloroform and
1,2,4-trichlorobenzene.
APPROACHES TO MAPPING ORGANIC CONTAMINATION
The traditional approach to detecting and mapping organic con-
tamination has been by direct sampling and observations via bore-
holes. This approach provides a direct sample from which highly
qualitative and quantitative data can be acquired. One draw-
back is that budgets and schedules control the number of wells
and hence the degree of coverage. In addition, the wells may be
located so that they provide information which is not represen-
tative of site conditions and lead to inaccurate conclusions. Fur-
thermore, safety considerations and accessibility constraints may
dictate that a drilling program cannot even be implemented.
Drilling will be required at all sites to provide monitoring or
remedial action. In some cases, the only way to detect organics
will be through dirlling and direct observations. Depending on
the situation, a number of alternative, more effective solutions
to mapping organic contamination exist. Some of these alterna-
tives can be used to indirectly delineate the extent of the organ-
ics. In other cases, they can provide information that helps pre-
dict the migration of organic contaminants.
Floaters
There are several alternatives to mapping floaters. Depending
upon the situation, some may be more applicable than others.
One of the most successful approaches is the use of portable organ-
ic vapor detectors such as an OVA, HNU, explosivity meters and
Draeger tubes. These tools can be applied in a variety of ways to
measure in situ organic vapors which can then be used to infer the
presence of organic contamination.
Since volatilization tends to be inhibited by overlying material,
access to the gas "envelope" associated with a floater will have to
be provided. This access can sometimes be provided in the form of
manholes or utility vaults. It could also be provided by hand-aug-.
ering small 1 to 3 in.-diameter holes or inserting small diameter
probes into the soil. In culturally developed areas, the holes can be
installed in grassy medians or, if necessary, a hand drill can be used
to puncture the pavement or asphalt.
Aside from the groundwater level, the depth required to inter-
cept the vapor envelope will depend largely upon the permeabil-
ity of the soils, the vapor pressure of the organic contaminants
and, to a certain degree, the continuity and/or thickness of the free
product layer. Measuring vapors immediately after augering versus
allowing time for the hole to equilibrate is another factor to con-
sider.
Another approach to mapping floaters is through the use of elec-
trical geophysical methods such as electromagnetics (EM) and
resistivity (RES). Both of these techniques measure the ability of
subsurface soil, rock and groundwater to conduct an electric cur-
rent. Since hydrocarbons like gasoline and oil are insulators (very
poor conductors), it would be expected that their presence would
inhibit current flow thereby decreasing the apparent electrical con-
ductivity.
The practical application of EM and RES techniques to map-
ping floaters is controlled by signal to noise ratios and the ability
of the investigator to properly acquire and interpret the data. In
order to determine if these techniques are appropriate at a site,
the processes which produce a detectable conductivity contrast
(with respect to background) must be understood.
The most significant factor influencing the detection of floaters
with EM and/or RES is the amount of water which is displaced
by the hydrocarbon product. Because water has the greatest in-
fluence on increasing terrain conductivities, its absence or relative
displacement will produce the most significant decrease in con-
ductivity.
The displacement of groundwater can result from a variety of
mechanisms. The mechanism that probably creates the greatest de-
crease in conductivity is the depression of the capillary zone and/or
water table by a lens of floating hydrocarbons. The amount of de-
pression is controlled by factors such as rate of product loss (faster
rates generally produce greater depressions), specific gravity of the
product, slope of the potentiometric surface (low gradients gen-
erally produce thicker accumulations) and the permeabilities of
the soils (lower permeabilities generally produce thicker accumula-
tions).
Other mechanisms which displace water relative to background
areas are associated with residual saturation of soils with product.
Depending upon the viscosity of the product and the retention
capacity of the soil, a certain amount of product will be tied up by
the soils. If the water table rises, some of the product bound in the
soil will remain in the pore spaces below the water table. Com-
pared to background areas, this will produce a decrease in conduc-
tivity because the pore spaces contain relatively less water. The
amount of product bound in the soil beneath the water table would
be greater for high viscosity fluids such as fuel oils than for lower
viscosity gasolines. Likewise, fine grain materials would retain
larger amounts of product than highly permeable coarse grained
materials.
The residually saturated (with product) soils above the water
table produce an insignificant decrease in conductivity. This is be-
cause mostly air (zero conductivity) instead of water is displaced
by the product (zero conductivity). The water which is present in
the soil as moisture appears to be resistant to displacement by oil
(at least initially) because of surface tension. This non-displaced
soil moisture is still able to conduct a current and, therefore, little
decrease in electrical conductivity occurs.
The residual saturation of oil in the vadose zone would become
more influential in changing the apparent conductivity after a rain-
fall. In background areas, percolating rainwater would increase the
moisture content of the soils and, hence, the conductivity. Rain-
water percolating over a residual plume, however, would have to
overcome the product's surface tension in order to displace it. In
this case, a greater non-conductive anomaly with respect to back-
ground would be expected over residually saturated soils after a
rainfall.
Both the RES and EM techniques have advantages and limita-
tions in mapping floaters. A non-conductive oil layer produces a
greater anomaly with RES than EM measurements. However, with
RES the anomaly becomes less apparent in highly resistive geologic
materials than in highly conductive materials. This is not the case
with EM where the anomalous response (percent change from
background) appears to be relatively independent of background
conductivities. Because the volume of material which is measured
by RES is large compared to EM (due to the larger dimen-
sions of the electrode array), the detectability of smaller plumes
with RES would be less than with EM. Furthermore, since elec-
trodes must be inserted into the ground with RES, its use would be
limited in culturally developed areas (concrete covered areas). Not
only does the electrode problem not exist with EM, but also data
can be acquired quicker and continuously to provide much finer
resolution.
Another geophysical technique which may be appropriate in
mapping floaters is ground penetrating radar (GPR). The mechan-
ism that allows GPR to detect floating hydrocarbons is the de-
pression of the capillary zone and/or the water table. In back-
ground areas, the capillary zone can range in thickness from a few
inches to several feet depending upon the permeability of the soils.
In the capillary zone, the gradual decrease in water content toward
SCREENING
73
-------
the land surface produces a very non-discrete interface that is some-
times difficult to detect by GPR. However, a layer of hydrocarbons
that compresses the capillary zone would produce a much more dis-
crete and detectable interface compared to background areas.
If the situation was such that the water table was depressed by an
oil layer, a dip in the water table surface could also be observed.
The major limitation of the GPR techniques is that its penetra-
tion and overall performance is highly site specific. Its depth of
penetration generally decreases with increasing silt/clay content.
However, many floating organic problems occur in areas with a
shallow water table where GPR can still be used effectively. In
areas with coarse grained sediments, GPR penetration becomes
significantly improved.
Aside from indirectly detecting floating hydrocarbons with the
approaches described, mapping features which may control the
contaminants migration would help predict their movement. Float-
ers are strongly influenced by local hydrogeologic and cultural
features. Through the use of some geophysical techniques, natural
features such as buried permeable channels can be quickly iden-
tified. The existence and location of clay lenses which may trap
or perch product layers in the vadose zone can also be mapped.
These types of hydrogeologic information can be a significant help
in developing an understanding of the setting and, therefore, place-
ment of monitor and recovery wells in more effective locations.
In addition to natural features, many cultural features can in-
fluence the flow of hydrocarbon products. High permeability back-
fills, such as utility and pipeline trenches, offer excellent migration
paths. These features can be located by personal communica-
tion and site utility plans or with detection techniques such as GPR,
EM, metal detectors and magnetometers which can be employed
for locating pipes, cables and trenches.
Mixers
Depending upon the source of the organics migrating through
the aquifer, the approach will vary. Organic contamination which
comes from landfills, disposal lagoons or industrial complexes
usually will be associated with other contaminants containing free
ions and salts which will give the plume a conductive signature. In
these instances, the electrical techniques of EM and RES can often
be used to map the extent of contamination. An example of this
technique is shown in Figure 2 which illustrates coincident signa-
tures acquired using EM, RES and OVA techniques along a tran-
sect crossing an organic-rich plume. The application of EM and
RES techniques to map contaminant plumes has been widely used
and is the subject of many technical papers.5'6'7-8
Typically, investigators think that the use of electrical techniques
is limited to mapping inorganic contamination. While it is true that
the plume constituents which effect conductivity are inorganic
(e.g., Na, Cl, K, Ca, SO4, etc.), knowing where the inorganic con-
taminants are can be of great assistance in determining the extent of
organic contamination.
In some cases, the migration extent of organic and inorganic
contamination is the same. In others, the organics may have been
attenuated enough by various physical, chemical and biological
mechanisms, that the map of inorganics presents a worst case pic-
ture of the extent of organics. In these instances, knowledge of re-
tardation factors can help determine where the organics would be
within the non-conservative inorganic plume.
In other cases, the relatively soluble and refractory organics may
migrate much further than the inorganic components through dis-
persion processes. In these instances, knowledge of the inorganic
plume's extent, shape and direction can be used to predict the loca-
tion of the organics through extrapolation.
In organic contamination, plumes in which there are no con-
ductive signature determinations of groundwater flow rates and
directions should be used to locate monitoring wells. Mapping
natural geologic features with techniques such as EM, RES, GPR
and seismic can often aid in these hydrogeologic assessments and
provide insight as to where the contaminants may migrate (Fig-
I I 6 I 8 J 8 8
SMM Nu*v (ft M i DO)
Figure 2
Coincident Electromagnetic, Resistivity and Organic Vapor
Analyzer Data across Conductive Organic-Rich Plume
View: NE
Figure 3
Three-Dimensional Representation of Continuous EM Data over Fractured
Rock. Peaks (high conductivity) represent moisture filled fractures in
otherwise dry bedrock.
74
SCREENING
-------
ures 3 and 4). The location and/or distribution of sand and clay
lenses, fracture zones and buried relic stream channels will in-
fluence contaminant flow patterns. Knowing where these natural
features are in advance can help ensure that monitor wells are
placed in locations which will most likely intercept the contam-
inant plume.
Figure 4
Ground Penetrating Radar Data Identifying a Buried Stream Channel
which contained more Permeable Sands and Gravels than surrounding
material.
Sinkers
If the contaminant plume has a conductive signature, the appli-
cation of EM and RES methods as previously described can be
used to map sinkers. If no conductive signature exists, natural
geologic features which may control the migration of the dense
plume can be mapped with geophysical techniques such as EM,
RES, GPR and seismic.
Because 'of the density factor, these plumes may respond more
to gravity than to potentiometric gradients. Therefore, any in-
formation concerning the depth, slope and topography of lower
confining layers such as bedrock or clay will help predict the con-
taminants behavior. For example, a dense contaminant plume was
identified migrating beneath a stream which served as a normal
groundwater discharge zone. The contaminants continued to mi-
grate beyond the stream and beneath a large hill, defying the
shallow hydraulic gradients produced by the topography. Because
of their density, the contaminants were migrating by gravity down
the slope of a bedrock confining layer.
CONCLUSIONS
In order to monitor and/or remediate organic contamination
effectively, it is essential to realize the overall extent of the con-
tamination. Acquiring this information is seldom a straightfor-
ward task. Therefore, approaching the problem in a methodical
manner will be most effective.
The approaches to mapping organic contamination are numer-
ous. Depending upon the type and source of organics, circum-
stances of input and hydrogeologic and cultural features, certain
approaches are more applicable than others. Understanding the
contaminants and their behavior within the local hydrogeologic
setting is necessary. Knowledge of the various technical approaches
available to assist in solving the problem is also needed. The most
cost effective mapping plan will systematically evaluate the relative
influences of the site parameters and, from the alternatives avail-
able, develop the most appropriate approach. Using the above re-
sources and approach, it is possible to provide a cost effective and
accurate description of the distribution of organics contamination.
REFERENCES
1. Shepherd, W.D., "Practical Geohydrological Aspects of Groundwater
Contamination," Proc. National Symposium on Aquifer Restoration
and Ground Water Monitoring, Columbus, Ohio, May, 1983.
2. Study Group: Water and Petroleum, "Evaluation and Treatment of
Oil Spill Accidents on Land with a View to the Protection of Water
Resources," 2nd ed., Federal Ministry of the Interior, Bonn, West
Germany, 1970.
3. Coons, W., Wright, J., Zordan, T. and Ellison, R., "Geochemical
Considerations for Hazardous Waste Facility Design," presented at:
Second Geotechnical Conference and Exhibit on Design and Con-
struction, Las Vegas, Nevada, Apr., 1982.
4. Anderson, D.C., Brown, K.W. and Green, J., "Organic Leachate
Effects on the Permeability of Clay Liners," Proc. National Con-
ference on Management of Uncontrolled Hazardous Waste Sites, Oct.,
1981,223-229.
5. Noel, M.R., Benson, R.D. and Glaccum, R.A., "The Use of Con-
temporary Geophysical Techniques to Aid Design of Cost-Effective
Monitoring Well Networks and Data Analysis," Proc. National Sym-
posium on Aquifer Restoration and Ground-water Monitoring, Colum-
bus, Ohio, May, 1982, 163-168.
6. Glaccum, R.A., Noel, M.R., Evans, R.B. and McMillion, L., "Corre-
lation of Geophysical and Organic Vapor Analyzer Data over a Con-
ductive Plume Containing Volatile Organics," Proc. National Sym-
posium on Aquifer Restoration and Groundwater Monitoring, Colum-
bus, Ohio, May, 1983, Preprint.
7. McNeill, J.D., "Electromagnetic Resistivity Mapping of Contaminant
Plumes," Proc. National Conference on Management of Uncontrolled
Hazardous Waste Sites, Nov., 1982, 1-6.
8. Greenhouse, J.P. and Slaine, D.D., "The Use of Reconnaissance
Electromagnetic Methods to Map Contaminant Migration," Ground-
water Monitoring Review, 3, No. 2, 1983, 47-59.
SCREENING
75
-------
OVA FIELD SCREENING AT A HAZARDOUS WASTE SITE
BRIAN J. JACOT
Fred C. Hart Associates, Inc.
New York, New York
INTRODUCTION
The Comprehensive Emergency Response, Compensation and
Liability Act (Superfund) provides for emergency and remedial
cleanups of hazardous waste sites. Now that the Superfund pro-
gram is being implemented nationwide, site owners are turning
to the private sector for independent site characterizations and
remedial alternatives. Since there is an understandable sense of
expediency involved with regard to the cleanup of these sites, an
intense, multi-disciplinary study must be conducted within a lim-
ited time frame. It is, therefore, essential that in-field screening
be performed to identify problem areas where additional analyses
may be warranted. In this paper, the author describes the use of
an organic vapor analyzer (OVA) in performing these field screen-
ing procedures at a large hazardous waste landfill.
BACKGROUND
The landfill studied is located at the top of a large hill covering
30 acres, of which approximately 19 acres are covered by fill ma-
terial. In addition to the active landfill area, a portion of the west-
ern side of the property has been excavated for cover material.
An access road to the site enters from the southeast corner.
The property has been the site of waste management activities
since the late 1930s. Waste management was conducted in accor-
dance with the accepted practice of the time. Up until the late 1950s
or early 1960s, waste was burned at the site. Subsequently, in
response to public concern with air pollution, landfilling began.
Since the mid-1960s, the site has received only municipal waste
from several surrounding communities.
The intent of the study was the acquisition of additional infor-
mation about the site, in particular, the geology and hydro-
geology. As the study progressed, efforts focused on two main
areas: (1) the assessment of the risk of groundwater contamina-
tion attributable to the site, and (2) the development of the best
engineering approach to remedy the discharge of leachate into local
surface waters.
With those goals in mind, the field investigation included: the
implementation of a test boring program, the digging of test pits
and trenches, testing the integrity of existing wells, water level mea-
surements in existing and newly installed wells, measuring surface
runoff, seed mapping, sampling and analyzing leachate collected
from wells screened in the landfill, an electrical resistivity survey
and field screening with the OVA.
INTENT
Field Screening was conducted at the landfill with an OVA dur-
ing a three day period in 1982. The intent of this field screening
was twofold: (1) to screen natural groundwater seeps and water
from existing observation wells to detect the presence of volatile
organics, and (2) to assist in the characterization of leachate as a
possible groundwater contaminant.
METHODOLOGY
The OVA is a highly sensitive instrument designed to measure
trace quantities of organic vapors in air. It utilizes a portable
hydrogen flame ionization detector similar to those utilized in
laboratory gas chromatographs (GCs) and has similar analytical
capabilities.
The OVA has two modes of operations: (1) the survey mode,
and (2) the GC mode. When used in the survey mode, the OVA
is an efficient and accurate indicator of total compound concen-
trations on a continuous sampling basis with a response time of
one to two seconds. The OVA performs in the GC mode of oper-
ation when a sample is injected onto the GC column. This causes
the various gas components in the sample to separate as contact is
made with the material in the column. Each component of the
sample gas mixture elutes from the column at a different time to
enter the flame ionization detector chamber, providing its own
measurable response. Although the GC option allows for qual-
itative and quantitative analysis of specific components, that de-
gree of analysis was beyond the cope of work for this study.
On Dec. 1 and 2, 1982, a perimeter site survey (Figure 1) was
conducted to measure total airborne hydrocarbons. Leachate seeps
and landfill runoff were the primary targets of the investigation.
Surveys of wells FW-1 and FW-2 were also conducted. In addition
to field screening, the OVA was used to monitor hydrocarbon
concentrations encountered during the drilling of wells FW-1 and
FW-2. This procedure was used to advise the drillers and super-
visory personnel of safety precautions in case high concentrations
of non-methane hydrocarbons were encountered.
Sample Collection
On Dec. 3, GC analyses were performed on a total of 14 samples
collected at leachate seeps, landfill runoffs and observation wells
(Figure 1). A description of each sample location is given below:
Sample No. Sample Location
#1
#2
#3
#4
Landfill runoff adjacent to excavation area
Landfill runoff 200 ft downstream of excavation
stream
Landfill runoff 400 ft downstream of excavation
area
Major landfill runoff stream at culvert
SCREENING
-------
#5 Major landfill runoff stream 200 ft downstream of
culvert
#6 Major landfill runoff stream 400 ft downstream of
culvert
#7 Leachate seep on southern boundary of landfill
FW-1 Leachate from well FW-1
FW-2 Leachate from well FW-2
W-l Water from well #1
W-2 Water from well #2
W-3 Water from well #3
W-4 Water from well #4 (before evacuation)
W-4b Water from well #4 (after evacuation)
Wells FW-1 and FW-2 were installed by Fred C. Hart Asso-
ciates and screened directly in fill material while wells W-l, W-2,
W-3 and W-4 were existing wells screened in low permeability till,
approximately 20 to 30 ft below the base of the landfill.
Laboratory Analysis
The analyses were conducted in a laboratory at the local waste-
water treatment plant. All samples were collected in 40 ml VOA
vials. Approximately one-third of each vial was left unfilled for GC
headspace analysis. The vials were heated in a hot-water bath to
induce the volatilization of any organics into the headspace.
RESULTS
Preliminary Survey
Detailed results of the perimeter site survey are given below:
Figure 1
OVA Field Screening
For the purposes of this study, a 250 ul gas tight syringe was
utilized for all the GC analyses. The samples were prescreened by
injecting a 50 ul aliquot of the headspace of each of the 14 samples
directly into the flame ionization chamber, bypassing the GC col-
umn. This technique allows for the efficient use of time since a
sample can be designated as "dirty" or "clean" in a matter of
seconds. When using this technique, care must be taken when in-
jecting the sample into the flame ionization chamber. The sample
must be introduced to the chamber slowly so as not to put out the
flame. Any sample which shows a positive response on the OVA
meter is considered "dirty" and requires further analysis.
Of the 14 samples prescreened, sample numbers 2, 3, W-2, W-
4 and W-4b showed no hydrocarbon contamination. A GC analy-
sis was performed on each of the remaining 9 samples suing a 200
ul injection onto a G-24 column. The "G" column is an all-pur-
pose, medium polarity column and is the best column which can
be utilized for these types of analyses.
11:00 a.m.
Location 1
11:00-11:05 a.m.
Location 2
11:07-11:13 a.m.
Location 3
11:14-11:20 a.m.
Location 4
11:21-11:26 a.m.
Location 5
11:27-11:33 a.m.
Location 6
11:33-11:40 a.m.
Location 7
11:40-11:50 a.m.
11:50 a.m.
OVA startup, westerly winds 5-10 mph, OVA
background at S.W. corner of landfill 1-2
ppm.
Large leachate seep area along western
boundary of landfill showed no readings over
background.
Stream flow area along northwestern
boundary of landfill showed no readings over
background.
Major runoff stream flowing off northern
boundary of landfill showed a number of ele-
vated readings in the 5-10 ppm range. A high
heading of 60 ppm was noted at the rock out-
crop.
Readings along the northwest boundary in-
creased to the 5-20 ppm range as downwind
side of landfill was approached.
Large leachate seep area along western
boundary of the landfill (active area) showed
readings continuing in the 5-20 ppm range.
Readings began to drop to background levels
as southwest corner (upwind) of the landfill
was approached.
Large leachate seep area along southern
boundary of the landfill showed readings in
the 3-5 ppm range with isolated spikes of up
to 50 ppm. One small seep showed readings of
30 ppm. This reading was reproducible.
OVA shut down.
Generally, readings upwind of the landfill were at background
levels of 1 to 2 ppm. Readings along the sownwind perimeter of the
landfill were in the range of 5 to 20 ppm. These elevated read-
ings were due to methane being generated at the site. In addition,
a survey of the hillside surrounding the entire landfill showed no
readings above background.
Total hydrocarbon readings during the drilling of FW-1 and FW-
2 were in excess of 1,000 ppm, the upper detection limit of the
OVA. Gas chromatograph scans done at these test borings re-
vealed the major constituent to be methane. However, a number of
samller peaks in the 10-50 ppm range were also noted at each test
boring. Based on the results of the monitoring during the drilling
of wells FW-1 and FW-2, the drillers were advised to wear respir-
atory protection.
GC Headspace Analyses
The strip chart recordings of the GC scans are provided in Fig-
ure 2. The vertical scale indicates retention time and is approx-
imately 1 in. = 6 min. Each peak is an identifiable volatile organ-
ic compound.
Of the nine contaminated samples identified by the prescreen-
ing procedure, sample #1 was the only sample which showed meth-
ane to be the only contaminant. Sample No. 5, 6, FW-1 and FW-2
showed a number of other volatile contaminants with retention
times of 1 min or less. These are probably indicative of C2-C
hydrocarbons (e.g., butane, propane, etc.). Sample No. 4, 5, and 6
taken from the major landfill runoff stream showed consistent con-
tamination peaks with concentrations increasing nearer the landfill.
SCREENING
77
-------
Samples FW-1 and FW-2 showed by far the highest degree of
contamination, with several major volatile organic constituents
noted on each GC scan. The retention time of these contaminants
was indicative of aromatic hydrocarbons or halogenated com-
pounds. These compounds are normally associated with industrial
solvents. The concentrations of these contaminants were generally
in the 1 to 10 ppm range.
Based in part on the results of the OVA GC analyses, it was de-
cided that additional laboratory GC/MS analyses were warranted
in order to accurately qualify and quantify the leachate contamina-
tion. For this purpose, samples were collected from wells FW-1 and
Table 1
Concentrations of Volatile Organics al Wells FW-1 and FW-2 (pg/l)
Benzene
Chlorobenzene
Chloroethane
1,1 -Dichloroethane
1,2-Dichloroethane
Ethylbenzene
Methylene Chloride
Tetrachloroethylene
Toluene
1,2-Trans-dichloroethylene
Trichloroethylene
Trichlorofluoromethane
Vinyl Chloride
Ortho-Xylene
Meta & Para-Xylenes
Acetone
Methyl Ethyl Ketone (MEK)
FW-1
544
14
49
10
2,500
28
13
16
415
302
6,810
7,850
FW-2
5,520
16
629
12
2,650
10
10
386
225
100
17
Figure 2
OVA Strip Chart Recordings
FW-2 which were screened directly in the landfill leachate. The re-
sults of these analyses are shown in Table 1.
Benzene, toluene, acetone and methyl ethyl ketone, were de-
tected in FW-1 or FW-2 at concentrations of approximately 2 to 8
mg/1. These compounds, or compounds exhibiting like retention
times, and their concentrations were predicted through the OVA
GC analysis.
CONCLUSIONS
Given the right working conditions and required amount of time,
it is possible to qualify and, to a certain degree of accuracy, quan-
tify the contaminant peaks resulting from the OVA GC analyses.
However, in most investigatory studies that degree of analysis is
not feasible. It is generally more important to identify areas or
zones of contamination and, in some cases, to characterize that
contamination for future laboratory analyses.
The OVA is an extremely useful and practical instrument, and its
utilization should be considered for all potential hazardous waste
site characterizations. It has a wide range of applications, depend-
ing on site specific objectives. In the context of this study, results
of the OVA field screening procedures provided for the efficient
use of resources in successfully designing a remedial program for
the cleanup of a hazardous waste site.
78
SCREENING
-------
A SEMIQUANTITATIVE PROGRAM FOR RAPID
SCREENING OF THE ELEMENTAL COMPONENTS OF
HAZARDOUS WASTE MATERIAL
DAVID A. LEIGHTY
DUANE S. CHASE
DANTON D. NYGAARD
Instrumentation Laboratory
Analytical Instrument Division
Andover, Massachusetts
INTRODUCTION
The characterization of the metal content of hazardous materials
or hazardous waste has been made easier by the use of the induc-
tively coupled plasma spectrometer (ICP). Early polychromator (or
"fixed") units had a predetermined number of channels designated
for a given set of elements, and these systems could not easily be
changed to analyze a new element. Screening various hazardous
materials requires the ability to determine almost any metal on the
periodic table.
The next generation of ICP, the sequential plasma that can be
programmed to determine any element at any wavelength desired,
fills a very important need in the environmental and waste monitor-
ing field. These sequential instruments can be optimized to quan-
titatively determine the metal content of any type of hazardous
material. However, if only one unknown sample has to be analyzed
for a large number of elements, the calibration of a sequential in-
strument is not fast or cost effective. An easier method for quickly
and semiquantitatively determining what elements are contained in
a sample needed to be created.
Instrumentation Laboratory has developed a program that can
be quickly calibrated and is totally versatile as to element and line
selection. This program, called Multiquant, can be used to deter-
mine if any metal of interest is in a given sample to ±25% ac-
curacy. This approach to analysis is very cost effective when screen-
ing hazardous wastes.
The principle of Multiquant is based on taking a few calibration
elements and predetermining the ratio of these "header" element
line intensities to the intensity of a "dependent" line. The intensity
ratio is usually constant for elements with lines of similar
wavelength and degree of ionization. Once the ratio has been deter-
mined, a program can be developed containing both header and
dependent lines. Only the header lines are calibrated. The header
line intensity is multiplied by the predetermined ratio, and the cor-
responding number is used as a calibration value for the dependent
element. Three or four elements are routinely used to calibrate 29
elements. Header and dependent lines can be added or deleted as
desired. Up to 78 elements can be listed in the program. Quick
calibration is possible because only four header lines are involved.
Another feature of Multiquant is the ability to automatically
record the spectra at each wavelength listed in the program. A
typical plot and the information printed with the graphics are
shown in Figure 1. The ability to graphically record each
wavelength automatically is a powerful tool for the determination
of background and spectral problems and for methods develop-
ment. Line selection for a complex matrix can be tedious, as several
n i
Date
2G47
- x
B SEP B2
0B: 55: 51
Time—'
ZN 213.BB R
Wavelength -/
ZN Z13.BG
I /Sample
9BB 10.25
"^-Counts [_
Concentration
213.85
213.95
Figure 1
Spectral Recording
lines may have to be investigated to find an element's interference
free wavelength.
The Multiquant program can be modified to contain any number
of spectral lines for a given element. A standard line selection pro-
gram can be generated for a given set of elements and, when used in
conjunction with the automatic video printout, can perform the
methods development for a given sample quickly and efficiently.
The advantages of the Multiquant program are summarized in
Table 1.
INSTRUMENT PREPARATION
The Multiquant program, as shipped, consists of four header
lines and 26 dependent lines. Before any modification, the program
can be used to obtain analyses of ±300% accuracy. By optimizing
each peak position ("trimming" the line) once, and by initially
readjusting the elemental ratios for a particular instrument, the ac-
curacy of the data obtained can be improved to ± 25%. The stan-
dard Multiquant program used for this investigation was optimized
as described above, and the elemental lines are listed in Table 2.
The four lines used to calibrate all of the elements are listed in
Table 3.
Analyses were carried out by first calibrating the program using
the three element standard, and then simply running the sample.
A sample can be quickly analyzed using the Multiquant program.
If no CRT or hard copy graphics are available, a sample can be
analyzed for 29 elements in less than five minutes. If hard copy
graphics are desired, an analysis can be completed in less than 11
minutes.
SCREENING
79
-------
Table 1
Multiquant Advantages
•Standard program allows for the rapid determination of 29 elements in a
sample, based on a three element calibration
•Program can be easily modified to allow analysis of up to 87 elements
based on operator selected element calibration
•Provides a fast method to determine elements in a sample to ± 25%
accuracy
•Automatic display of emission intensity versus wavelength to provide
visual identification of spectral interferences
•Automatic operation from the optional autosampler providing printed
results and video copies of spectra for each sample
•Program requires no hardware changes
•Calibration easily updated
•Can be used for line selection
Niagara River
Water
NBS #1566
NBS #1571
Table 4
Sample Preparation Methods
USGS GXR-3 Fe/Min Rich
Ore
NBS #1645 River Sediment
Oyster Tissue
Orchard Leaves
LiBo2 Fusion: 1.5g Flux 0.5 g sample;
20 min fusion time @ 1100°C
Acid Digestion: HNO3/HC104/H2SO4/
HF; 4 hr digest time heat to near
dryness
Preserved with small amount of acid
Dry Ashing: heat at 400 °C for at least
12 hr; dilute in 5ft HC1
Dry Ashing: heat to 400 °C for at least
12 hr; dilute in 5% HC1
1,000,000
Table 2
Elements in Multiquant Program
Element
Ag
Al
As
B
Ba
Ba
Be
Bi
Ca
Cd
Co
Cr
Cu
Fe
Li
Mg
Mn
Mo
Na
Ni
Pb
Pd
Pt
Sb
Se
Si
Sr
Tl
V
Zn
•••BC" is loa
Wavelength (nm)
328.07
396.15
193.70
249.77
455.40
233.53
313.04
223.06
317.93
214.44
230.79
205.55
324.75
259.94
670.78
285.21
257.61
202.02
589.59
231.60
220.35
340.46
265.95
206.83
196.03
251.61
407.77
351.92
290.88
213.86
uion of background correction point: left, right, or both sides of peak.
BC*
L
L& R
L
L
L
L
L
R
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
L
Table 3
Elements Used for Multiquant Calibration
Element
Ba
Ba
Cu
Zn
Wavelength (nm)
233.53
455.40
324.75
213.86
Concentration
5
5
10
10
(mg/1)
GXR3
USGS Rftnnol MrarM
10
10'
• Multiquint
O Sundird ICP Arulyiit
100 1.000 10.000 100.000 1.000.000
10* Iff" 104 10s 10*
Canified Concentration
Figure 2
Concentration of Metals in a Reference Material
10,000-r
.1,000 •
z 100
10 too i.ooo
Certified Concentration
Figure 3
Concentration of Metals in River Sediment
10.000
80
SCREENING
-------
100n
1 10 H
Niagara River Water
(Spiked Niagara River .Water Sample)
10
Standard Plasma
100
Figure 4
Concentration of Metals in Niagara River Water
2071
5 MflY 83
16= 17: 35
PB 220.35 A
PB 220.35 fl
PB 220.35 A
0
220.11
220.21
Figure 6
Spectral Interference of Al and Pb
10.000 n
10
100 1,000
Certified Concentration
10,000
Figure 5
Concentration of Metals in Oyster Tissue
SAMPLE PREPARATION AND ANALYSIS
Several standard materials were obtained from various sources
and prepared for ICP analysis. The materials and their respective
sample preparation methods are listed in Table 4. Each material
was analyzed by both Multiquant and a standard ICP program in
which each element was calibrated. All standard ICP analyses were
carried out using an IL Plasma-200 ICP with the exception of the
Niagara River water which was analyzed using a polychromator
ICP spectrometer.
RESULTS
Even though the Multiquant program utilizes only four lines for
calibration, the data obtained using the program are quite accurate.
The plots for a variety of elements in several matrices are shown in
Figures 2 to 5; the results are excellent. For many applications,
these data are accurate enough to eliminate the need for further
quantification. The Multiquant specification of ± 25% accuracy is
easily surpassed for most of the determinations.
For the Multiquant program to be effective, the ratios of the
various line intensities have to remain relatively constant no matter
what the matrix. If the ratio is matrix dependent, then it would be
necessary to matrix match the Multiquant calibration solution with
a given sample. All of the results listed in Figures 2 to 5 were ob-
tained using the standard Multiquant calibration solution; no at-
tempt was made to match the calibration solution and the blank.
The data indicate that the matrix has little effect on the ratio values
for the various elements. Using only one standard matrix enhances
the capability of Multiquant to be used quickly on any type of
hazardous waste sample.
The automatic graphics can be used to good advantage with the
Multiquant program. If a special interferent or background pro-
blem is suspected, the autoscaling wavelength plots can be quickly
consulted to determine the best course of action. Another
wavelength can be selected using the Multiquant or the final
analytical program. The Zn line is shown in Figure 1; no in-
terference is apparent at this wavelength. The curve shown in
Figure 6 indicates that a wing broadening spectral interference of
Al on Pb occurred at the 220.35 nm wavelength.
If the concentrations of only a few elements in a sample have to
be determined but the sample still must be investigated for a large
number of metals, the quantified elements can be header elements.
Since the header lines are actually calibrated, the measurement ac-
curacy for these elements will be the same as the standard analytical
program, ± 2%.
CONCLUSIONS
Instrumentation Laboratory's Multiquant program fills a real
need in the hazardous waste management field. Fast, cost effective
screening of liquid samples can be carried out without tedious in-
strument calibration. As seen from the data presented, the Multi-
quant program can be quite accurate and may eliminate the need
for further quantification. The automatic plotting routine permits
quick assessment of spectral and background problems as well as a
fast methods development technique for line selection. The infor-
mation obtained from the Multiquant program can be a valuable
aid to the monitoring and measurement of hazardous materials.
SCREENING
81
-------
ERT'S AIR MONITORING GUIDES FOR
UNCONTROLLED HAZARDOUS WASTE SITES
RODNEY D. TURPIN
Environmental Response Team
U.S. Environmental Protection Agency
Edison, New Jersey
INTRODUCTION
The USEPA's Environmental Response Team (ERT) tfas es-
tablished in October 1978 to provide technical assistance to On-
Scene Coordinator's (OSC), Regional Response Team (RRT),
National Response Team (NRT), USEPA Headquarters and~Re-
gional Offices, as well as other Government Agencies in the area
of emergency environmental issues, such as chemical spills and
uncontrolled hazardous waste sites.
In this paper, the author describes the air monitoring guides
used by ERT for the initial monitoring/classification of site con-
ditions. He describes, also, the objectives of using total atmos-
pheric gas/vapor concentrations, on-site/off-site analysis of organ-
ic gases/vapors, sampling, collection media and specific contam-
inant identification.
The following are only a few of the many factors involved in
developing a site specific air monitoring program: equipment avail-
ability, collection media, flow rates, analytical protocol, analysis
time, detection limit, wind speed, ambient temperature, atom-
spheric conditions and operational cost. In addition to all these
factors, where does one start monitoring and what logical ap-
proach does one follow?
OBJECTIVES
A number of air hazards may be present at a site including:
•Combustible gases that can lead to fires and explosives
•Oxygen deficiency
•Radiation
•Toxic organic and inorganic gases or vapors
Procedures for assessing the first three hazards are relatively
straightforward and are documented in occupational safety and
health literature. If the types of gases/vapors are known, they can
be measured with properly calibrated instruments or standard in-
dustrial hygiene procedures. When little is known of the contam-
inants present or concentrations of individual constituents, the
analysis problem is more difficult.
The objectives are simply to obtain reasonable balance between
cost, personnel requirements, accuracy, detection limits and analy-
tical cost, analytical turn around time and analytical laboratory
availability. USEPA's approach achieves a reasonable balance be-
tween these factors by the use of direct reading instruments (DRI)
and off-site laboratory analysis by an accredited American Indus-
trail Hygiene Association laboratory.
Two types of field instruments, flame ionization detector (FID)
and photoinoization detector (PID), are capable of detecting most
volatile organic compounds in drums, tanks, soil and water. They
can be used to make the initial site survey and to collect contin-
uous air monitoring data during response operations.
Since the field FID and PID are small portable instruments, they
cannot be expected to yield results as accurate as laboratory in-
struments. They are relatively easy to use to detect total organic
concentrations of known contaminants in air, but the interpreta-
tion of data becomes more difficult when trying to identify the
components of a mixture.
The following is a list of equipment necessary to perform all
phases of the ERT five step Air Monitoring Guides:
•Portable Photoionization Detector
•Portable Organic Vapor Analyzer (GC/FID)
•Low Flor Personnel Sampling Pumps (10 cc/min to 100 cc/min)
•High Flow Personnel Sampling Pumps (200 cc/min to 3 1/min)
•Tenax Thermal Desorption Collection Tubes (metal)
•Carbon Sphere Thermal Desorption Collector TuBes (metal)
•Carbon Filled Glass Sampling Tubes (150 mg and 600 mg)
•Paniculate Cassettes
•Cool Packs
•Thermal Storage Containers
FIELD PROCEDURES
In general the FID and PID instruments can be used for four of
the following five steps. Each of the steps for detecting gas/vapor
contaminants builds on the previous step and helps to further char-
acterize the concentrations measured by the two instruments. The
fifth step (Particulate Sampling) is totally independent of the
previous four steps and is based primarily on knowledge of the site.
Determine Background Concentrations
To establish background levels of air pollution in the vicinity of
a hazardous waste site or spill, the initial air monitoring step should
be to collect samples in upwind areas not suspected of containing
air contaminants. It is important to avoid locations such as free-
ways, active industrial sites, etc., that are readily accessible but
may not give a true picture of prevailing conditions in clean areas
nearby. Depending on the situation, monitoring may be done in the
area adjacent to the site to determine if contaminants are leaving
the site.
In addition to setting up air pumps with appropriate collection
media in the background area, FID/PID direct reading instrument
readings should be taken.
82
SCREENING
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Determine Concentrations On-Site
The initial on-site survey is conducted with FID/PID direct read-
ing instruments (DRI's) to determine general site ambient con-
ditions and/or to locate the "so-called" hot spots. In addition,
data obtained with DRI's during the survey must be compared with
the background data.
The total gas/vapor concentrations should be measured near any
suspected contaminated area (both at ground level and breathing
zone), being careful to avoid transient contaminants such as heavy
equipment exhaust. If possible, another survey should be made at
the background station and a rough sketch made of the site.
Site Area Samples
On-site air monitoring may be performed from two to four times
daily depending on several factors such as wind speed/direction
and temperature. The number of sampling stations/locations as
well as sampling train vary with atmospheric conditions. In addi-
tion to a control (background) station, there should be stations ith-
in the suspected contaminated area(s) and downwind near the site
boundary. They should be set up where total gas/vapor concen-
trations are the highest or suspected of being present.
The stations consist of a personnel monitoring pump with an
appropriate collection medium. The type of pumps, medium and
flow rates will vary. For example, personnel sampling pumps with
a flow rate of approximately 100 cc/min, thermal desorption tubes
(carbon spheres/Tenas) and an Organic Vapor Analyzer with a
programmable thermal desorber are commonly used. The sampling
pumps are run at about 100 cc/min for sufficient time to collect
15-301. Samples are desorbed and analyzed on-site with a field FID
to determine the number of peaks and total concentrations.
Initially, morning and afternoon samples should be collected to
establish a baseline both on-site and background. Total gas/vapor
concentrations should be measured at the start and finish of each
sample collection. A suggested format for reporting/calculating
total gas/vapor concentrations is shown in Figure No. 1.
1. Volume sampled by "MDA Accuhaler 808" Personal Sampling Pump:
Volume sampled (cc's) = final stroke count—initial stroke count
X cc's/stroke*
X Multiplier factor for orifice used**
'Specified on pump itself
**Specified in operations manual and Table 1
SAMPLE CALCULATION:
At beginning of sampling period, Accuhaler stroke counter reads
16292.9. At the end of sampling period, it reads 16632.9. What is the
volume of air sampled?
Volume sampled (cc) = 16632.9 -16292.9
X 5.7 (cc/pump stroke)
X 1.1 (multiplier for orifice)
Volume Samples = 2131.8 cc or 2.1 1
2. Reporting Format
a. Total GC Mode: Time Weighted Average (Using OVA Thermal
Desorber)
TWA (ppm) = Volume desorbed (1) X concentration (ppm)
Volume collected (liters)
= 0.300 (L) X 22 (ppm)
2.1 (liters)
= 3.14 ppm as CH4 (methane)
b. Peaks: GC mode
•four peaks observed (none measured)
^attached chromatograph
Figure 1
Table 1
Multiplier Factor for "MDA Accuhaler 808"
Personal Sampling Pumps
Calibration at
20 cc/min
Orifice Color
Yellow
Orange
Red
Brown
Purple
Blue
Green
Black
Normal Flow
Rate-cc/min
100
50
20
10
5
2
1
0.5
Volume/Stroke
Multiplier
1.1
1.06
1.00
0.99
0.97
Reference:
Instruction Manual, Accuhaler, Personnel Sampling Pump Models 808 and 818
MDA Scientific, Inc., Elmdale Avenue, Glenview, IL 60025
Table 2
Organic Solvents Identified by P&CAM Analytical Method No. 127
ORGANIC
SOLVENT
Acetone
Benzene
Carbon tetrachloride
Chloroform
Dichloromethane
p-Dioxane
Ethylene dichloride
Methyl ethyl ketone
Styrene
Tetrachloroethylene
1 , 1 ,2-trichloroethane
1 , 1 , 1 -trichloroethane
(methyl chloroform)
Trichloroethylene
Toluene
Xylene
MOLECULAR
WEIGHT
58.1
78.1
154.0
119.0
84.9
88.1
99.0
72.1
104.0
166.0
133.0
133.0
131.0
92.1
106.0
Reference:
NIOSH Manual of Analytical Methods
U.S. Department of Health Education & Welfare
Public Health Service Center for Disease Control
National Institute of Occupational Safety & Health
DHEW (NIOSH) Publication No. 77-157-A.
Identify Specific Contaminants (if needed)
When specific information is needed on the contaminants, addi-
tional personal monitoring pumps should be run, this time with
both thermal desorption tubes (Tenax/carbon spheres) and carbon
filled glass tubes. Generally, when total gas/vapor reading and the
number of peaks obtained in the previous step is low, a 150 mg
carbon filled glass sampling tube should be used and operated long
enough at a flow rate of 100 cc/min to pass 15 to 301 of air.
When total gas/vapor reading and the number of peaks iden-
tified previously are high, a 600 mg carbon filled glass sampling
tube should be operated long enough at a flow rate of 1/2-2 1/min
to pass 90 to 1501 of air.
If desorption equipment is not available for routine monitoring,
100 mg carbon filled glass sampling tubes should be collected rou-
tinely every 2-3 days depending on site activities and atmospheric
conditions) and analyzed off-site until sufficient background data
have been collected. Off-site analysis should be conducted in
accordance with the National Institute of Occupational Safety and
SCREENING
83
-------
Health (NIOSH) P&CAM Analytical Method No. 127 by an ac-
credited American Industrial Hygiene Association laboratory. Or-
ganic solvents used in this analysis are shown in Table 2. Samples
should be held by the laboratory for possible gas chromatography/
mass spectrometry analysis until the On-Scene Coordinator re-
leases them.
If other than organic solvents are suspected, then the NIOSH
Manual of Analytical Methods (Vol. 1-7) should be consulted for
the appropriate collection medium and air flow rates.
If the recently developed ERT 2-stage tube field tests are suc-
cessful, then the numbers of 150 mg/600 mg carbon tubes as well
as other widely used media may be reduced. This tube was devel-
oped using state-of-the-art technology with the objective of
developing convenient screening media for air samples at sites
where unknown/multiple contaminants may be present. Since this
tube has only been used twice in the field at the writing of this
paper, a conclusion can not be drawn at this time. More de-
tails are contained in the author's other paper in these Proceed-
ings: "On-Site Air Monitoring Classification by Use of the ERT
Two-Stage Collection Tube."
Identify Paniculate Contaminants (if needed)
Samples for particulates may be collected at any time. Since the
collection medium vary tremendously, the NIOSH Manual of
Analytical Methods (Vol. 1-7) should be consulted for those meth-
ods routinely used in industry.
CONCLUSION
Although this paper describes the initial ERT Air Monitoring
Program it does not address an entire occupational and/or public
health air monitoring program. The use of this program in con-
junction with a complete occupational health and safety program
has proven to be extremely useful.
ACKNOWLEDGEMENT
The author expresses his appreciation to all members of
USEPA's Environmental Response Team for their many contribu-
tions and constant updating of the Air Monitoring program and
his indebtedness to Philip Campagna, ERT-TAT Leader, Weston-
Sper, Edison, NJ. for his many contributions and many long hours
of hard work and assistance during site monitoring responses.
84
SCREENING
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ON-SITE AIR MONITORING CLASSIFICATION BY USE
OF THE ERT TWO-STAGE COLLECTION TUBE
RODNEY D. TURPIN
Environmental Response Branch
U.S. Environmental Protection Agency
Edison, New Jersey
INTRODUCTION
The USEPA's Environmental Response Team (ERT) was
established in Oct. 1978 to provide technical assistance to Federal
On-Scene Coordinators (OSC), Regional Response Team (RRT),
National Response Team (NRT), USEPA Headquarters/Regional
Offices and other government agencies in the area of environ-
mental emergency issues such as chemical spills and uncontrolled
hazardous waste sites.
In this paper, the author describes the two-stage air sampling
tube developed jointly by ERT and Oil and Hazardous Ma-
terials Spills Branch, Edison, N.J. The project was based on state-
of-the-art technique with the objective of developing a convenient
screening medium for air samples at sites where unknown and
multiple contaminants may be present. In this paper, the author
describes the tube development, sampling rates and method of an-
alysis. Since the tube has only been used twice in the field at this
time, the conference presentation will include the advantages and
disadvantages of the two-stage collection tube but no results.
PROJECT SCOPE OF WORK
Imagine a 20 acre site Anywhere, USA, with 5,000 to 10,000 un-
identified 55 gal drums, four unlined waste lagoons containing
unidentified liquids adjacent to a housing development. You have
been asked to conduct an emergency air monitoring program.
What collection medium (Tenax, Carbon, Silica Gel, Florisal, etc.)
and sampling pump air flow rate (10 cc/min, 50 cc/min, 100 cc/
min. 1-1/min, 2 1/min) would you select? What would be the
appropriate sampling volume? What is the minimum analytical
turn around time? What is the appropriate analytical protocol?
What would be the total number of samples collected per station?
These are just a few of the questions to ask oneself if given this
assignment. Obviously, the more information you have to eval-
uate, the less difficult the assignment. Thus, the reason for the
two-stage tube which was developed to provide a quick profile of
compounds encountered at a typical hazardous waste site.
In order to keep this project at a minimum cost and devel-
opment period, the project was restricted to three tube config-
urations with each having three separate stages:
Tube A—Consisted of a polyurethane foam first stage, Tenax/
GC second stage and an activated carbon third stage.
Tube B—Consisted of a polyurethane foam first stage Chromosorb
102 second stage and an activated carbon third stage.
Tube C—Consisted of a polyurethane foam first stage, Porapak
second stage and an activated carbon third stage.
EVALUATION PROCESS
The evaluation consisted of the following phases:
1. Tube A, B, and C were spiked directly with the following chem-
icals: Arochlor-1254, chlordane, tricresyl phosphate, isopropyl
alcohol, nitrosoamine, aniline, naphthalene, ethyl benzene,
methyl isobutyl ketone, bis (2-chloroethyl) ether, dichloro-
phenol. The tubes were kept at room temperature overnight
and thoroughly desorbed for gas chromatography/mass spec-
trophotometer (GC/MS) analysis.
2. Based on the results from phase one, a tube was selected for
further evaluation which consisted of generating a known con-
centration of contaminants at different humidities in a calibra-
tion chamber. Tubes were collected at various flow rates and
analyzed by GC/MS to evaluate desorption efficiency.
Like many short-term projects based on state-of-the-art tech-
niques, the scope of work was modified as the results from the
evaluation phase were generated. In fact, the finished prototype
tube consists of a 2-stage collection tube with the first stage con-
sisting of Tenax-GC and a Chromosorb 102 second stage.
FIELD APPLICABILITY
As stated earlier, due to a project delay, the tube has only been
used twice in the field at the end of summer 1983. The study indi-
cates there are two optimum flow rates for the 2-stage tube: 50
ml/min for 200 min and/or 10 ml/m for 100 min. Between the
optimum flow rate and the analytical method, it is apparent that
all the chemicals identified in the Tube Evaluation Process sec-
tion will not be collected by the two-stage tube. Such chemicals as
tricresyl phosphate, isopropyl alcohol, chlordane, Aroclor 1254
and naphthalene may not be easily identified during field activities.
CONCLUSION
If the two-stage tube performs in service as well as in the eval-
uation study, it appears that response teams will be able to collect
fewer air samples, obtain faster results and identify many of the
low-level organic air contaminants. With this information,
response personnel will be better able to identify and develop a site
specific air monitoring program.
ACKNOWLEDGEMENT
The author expresses his appreciation to all members of the
USEPA's Environmental Response Team for their many contribu-
tions and constant updating and his indebtedness to all members
of USEPA's Oil and Hazardous Material Spills Branch, Edison,
NJ as well as ERT-TAT and EERU members for their contribu-
tions.
SCREENING
85
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USE OF DETECTOR RATIOS FOR CONTAMINANT
SCREENING BY HIGH-PRESSURE
LIQUID CHROMATOGRAPHY
DAVID H. POWELL, Ph.D.
ALBERT L. SHROADS
JOHN J. MOUSA, Ph.D.
STUART A. WHITLOCK
Environmental Science and Engineering, Inc.
Gainesville, Florida
INTRODUCTION
Two important aspects of contamination assessment of hazar-
dous waste sites are qualitative indentification of the chemical
species present and quantitative evaluation of the extent of con-
tamination. Because of its excellent specificity, gas
chromatography/mass spectrometry (GC/MS) is generally
employed for qualitative identifications; however, this technique is
not economically viable for the extensive quantitative evaluations
needed to map contamination profiles which can require hundreds
of analyses.
Less expensive analytical procedures such as GC or high-pressure
liquid chromatography (HPLC) may be preferable for more exten-
sive studies. Specific detectors and relative peak retention times are
generally used in GC and HPLC analyses to confirm compound
identities; however, these techniques provide a minimum of
qualitative information. Detector ratios have been used to increase
the qualitative specificity of these chromatographic techniques.
Baker et al.' showed that by using relative retention times, only
9<% of 101 drugs of forensic interest could be distinguished;
however, use of a combination of retention times and a single ab-
sorbance ratio allowed identification of 95% of the drugs. Giles et
al.' used two fixed-wavelength absorbance detectors at 254 and 280
nanometers (nm) for the detection of polynuclear aromatic
hydrocarbons (PHA).
Although rapid-scan absorbance detectors are currently
available, the use of detector ratios is a relatively inexpensive way
to increase the specificity of HPLC procedures. The statistical
variability of these ratios is critical for qualitative identification. In
this paper, the authors present a method for analysis of selected
munition-related compounds and PAH and the statistical variabil-
ity of various detector ratios for 25 compounds.
Ratios were determined for spiked samples of distilled water con-
taining 100 mg/1 of sulfate and chloride to mimic a natural water
(referred to as standard water). Confidence intervals for the com-
pound detector ratios were calculated according to Dixon and
Massey' for samples analyzed with and without a silica-gel column
cleanup.
The ratios were determined for a range of spiked samples with
concentrations varied by a factor of 20 in the range of 1 to 100 fig/\.
Detection limits for each analyte were determined by the statistical
procedure of Hubaux and Vos.4 The analytes and quantitative
detection methods are listed in Table 1.
The tested concentration ranges in natural and standard water
for each analyte are listed in Table 2. The method is very sensitive,
with the lowest detectable concentration of 100 pg/1 for chrysene.
The detection limits (DL) in standard and natural water, calculated
according to Hubaux and Vos,4 are listed in Table 3.
The detection limits for standard water samples cleaned by silica
gel chromatography are listed to indicate the quality of the cleanup
technique for each analyte. The analytes were also spiked into a
sample of lake water and analyzed for a comparison of the ratios in
a natural matrix with those obtained in the artificial standard water
matrix.
The silica gel cleanup step provides a mechanism for eliminating
possible interferences from highly polar compounds such as fatty
acids and carboxylic acids that may be present in the extract.
Detector ratios were determined for both absorbance ratios of
various wavelengths and absorbance/fluorescence ratios for com-
pounds that also fiuoresced.
Table 1
Analytes and Quantitative Detection Methods
Analyte
HMX
RDX
1,3,5-TNB
1,3-DNB
3,5-DNP
2,4,6-TNT
2,6-DNT
2,4-DNT
Naphthalene
Acenaphthylene
Acenaphthene
Phenanthrene
Anthracene
Fluoranthene
Pyrene
Chrysene
Benzo(b)fluoranthene
Benzo(k)fluoranthene
Benzo(a)pyrene
Indeno(l,2,3-cd)pyrene
Quantitative Detection
Method
UV (230 nm)
UV (230 nm)
UV (230 nm)
UV (254 nm)
UV (254 nm)
UV (254 nm)
UV (230 nm)
UV (254 nm)
UV (280 nm)
UV (280 nm)
UV (280 nm)
UV (280 nm)
UV (254 nm)
UV (280 nm)
UV (280 nm)
UV (280 nm)
Fluorescence (y ex 290 nm,
y em> 350 nm)
Fluorescence (y ex 290 nm,
•y> 350 nm)
UV (254 nm)
UV (280 nm)
86
SCREENING
-------
Table 2
Tested Concentration Ranges in Natural and Standard Water
Analyte
HMX
RDX
1,3,5-TNB
1,3-DNB
3,5-DNP
2,4,6-TNT
2,6-DNT
2,4-DNT
Naphthalene
Acenaphthylene
Acenaphthene
Phenanthrene
Anthracene
Fluoranthene
Pyrene
Chrysene
Benzo(b)fluoranthene
Benzo(k)fluoranthene
Benzo(a)pyrene
Indeno(l ,2,3-cd)pyrene
Concentration Range
fog/1)
2.0 to 40
2.0 to 48
1.9 to 38
2.2 to 44
3.6 to 73
2.0 to 40
2.3 to 46
2.0 to 40
4.1 to 82
6.6 to 131
1.5 to 48
1.5 to 30
1.2 to 24
0.4 to 8.0
1.9 to 38
0.10 to 2.0
0.10 to 2.1
0.21 t04;l
0.22 to 4.5
0.28 to 5.8
Table 3
Detection Limits in Standard and Natural Water*
Analyte
HMX
RDX
1,3,5-TNB
1,3-DNB
3,5-DNP
2,4,6-TNT
2,6-TNT
2,4-DNT
Naphthalene
Acenaphthylene
Acenaphthene
Phenanthrene
Anthracene
Fluoranthene
Pyrene
Chrysene
Benzo(b)fluoranthene
Benzo(k)fluoranthene
Benzo(a)pyrene
Indeno(l ,2,3-cd)pyrene
•Calculated according to Hubaux and Vos'
Standard
Water
fog/1)
15
6
6
6
11
6
9
6
27
22
10
5
2
0.9
8
0.4
2
1
0.8
2
Standard
Water
(After
Silica Gel
Cleanup)
fog/1)
11
8
6
8
28
11
12
7
33
35
12
5
5
1
6
0.5
0.3
0.8
0.9
2
Natural
Water
fog/I)
10
6
6
11
34
7
7
7
21
28
10
5
5
2
7
0.3
0.6
1
2
2
The analysis rate is quite adequate for fast turnaround,
screening-type analysis. After instrument calibration, which re-
quires approximately 6 hr, one analyst can analyze four extracts in
an 8 hr day. One analyst can perform approximately eight extrac-
tions in an 8 hr day.
EXPERIMENTAL PROCEDURES
Instrumentation
The HPLC instrumentation (Figure 1) is a gradient elution
system with two columns connected in series with a variable-
wavelength, ultraviolet (UV)-visible absorbance detector; a 254-nm
absorbance detector; and a fluorescence detector.
An Altex Model 322 dual-pump liquid chromatograph is used as
the gradient pumping system. After mixing, the elution solvent is
passed through a guard column [5 cm by 4.6 mm] packed with silica
gel (Fisher, 60 to 200 mesh) to presaturate the mobile phase with
silica and, therefore, extend column life. The mobile phase is then
passed through a 0.25 /tin filter to remove entrained particulates.
Water Jacket
.nalytical Column*
V*ri«bl« UV
D«t«ctor
254-nm UV
Detector
Detector
Figure 1
HPLC Screening Apparatus
An Altex Model 500 autosampler is used as the injection system,
and a guard column (5 cm by 4.6 mm) packed with Pelliguard LC-
CN pellicular packing (40 ;tm) is present in the system. Both the in-
jector and the guard column are maintained at room temperature.
The silica precolumn and filter are maintained at the same
temperature (52 °C) as the analytical columns, which consist of an
Ultrasphere CN 5 /*m column [25 cm by 4.6 mm inner diameter
(ID)]. The column temperature is maintained at 52°C by use of a
circulating water bath (Fisher Scientific Model 80) and a column
water jacket from Altech Associates. Any of the commonly
available column thermostats capable of handling two columns
may be substituted. The Ultrasphere CN column is the first column
in the series after the injector, followed by the Ultrasphere ODS
column. The mobile phase consists of various percentages of
methanol varying from 30 to 90% in pH = 3 phosphate-buffered
water. The elution program for HPLC screening is shown in Figure
2.
The column effluent is passed through three detectors in series,
each connected by means of low-dead-volume unions and a
minimum length of 0.25 mm stainless steel tubing. The order of the
detectors is as follows:
1. Perkin-Elmer LC-75 variable-wavelength spectrometer with
autocontrol.
SCREENING
87
-------
2. Altex Model 153 fixed-wavelength detector set at 254 nm.
3. Per kin-Elmer Fluorescence Spectrometer Model 650-S.
Each detector is connected to a Spectra Physics Model 4100 in-
tegrator. An Altex Model 420 microprocessor is used to control the
pumps and signal the variable-wavelength detector. The
microprocessor initially signals the autosampler to load the sample
loop. The autosampler then flushes the sample loop for 60 sec, in-
jects the sample onto the analytical column and signals the three in-
tegrators to start. After 10 minutes, the microprocessor sends a se-
cond flag to the autosampler to reset it prior to the next injection.
At 60 min, the microprocessor signals the Perkin-Elmer LC-75 with
autocontrol to switch detection wavelength from 230 to 280 nm.
This wavelength is reset to 230 nm at 135 minutes by another signal
from the microprocessor. At 137 minutes, a second signal to the
LC-75 resets the detector for the next injection. The retention times
for each analyte are listed in Table 4.
Table 4
HPLC Retention Times
Figure 2
Elution Program for HPLC Screen
Analyle
HMX
RDX
1,3,5-TNB
1,3-DNB
3,5-DNP
2,4,6-TNT
2,6-DNT
2,4-DNT
Naphthalene
Acenaphthylene
Acenaphthene
Phenanthrene
Anthracene
Fluoranthene
Pyrene
Chrysene
Benzo(b)fluoranthene
Benzo(k)fluoranthene
Benzo(a)pyrene
Dibenzo(a,h)anthracene
Indeno( 1,2,3-cd)pyrene
Retention Time (min)
9.2
13.0
16.8
20.8
26.9
29.3
35.0
36.1
84.5
89.1
95.7
97.5
98.8
102.2
103.4
108.2
112.9
113.3
114.0
116.8
117.9
Extraction
Samples are allowed to warm to room temperature and are
poured into a 21 glass or Teflon® separatory funnel with Teflon®
stopcocks. The pH is checked with wide-range pH paper and ad-
justed to less than 3 with 6N HC1. Reagent-grade Nad [100 g] is
added to the sample, which is then shaken to dissolve the salt. The
sample is extracted three times with 100-milliliter (ml) aliquots of
methylene chloride. A portion of the extract is saved for possible
further cleanup. The remainder of the extract is concentrated to 0.5
ml on an 80 °C water bath using a Kuderna-Danish concentrator
apparatus. The solvent is exchanged to acetonitrile, and the final
sample is diluted with pH = 3 phosphate-buffered water to approx-
imately 30"% acetonitrile concentration, the extract is transferred to
a 1 ml septum-sealed vial for HPLC analysis.
Sample Cleanup
If it becomes apparent during the HPLC analysis that the sample
cleanup is necessary for proper qualitative identification of the
sample components, the following procedure is used to help
remove possible interferents. The cleanup procedure is necessary
when components are found with the proper retention times but
without the correct detector ratios or when large broad-band in-
terferents are noted in the chromatogram. The sample cleanup
steps are described below.
The methylene chloride extract is passed through a silica gel Sep-
Pak® at a rate of approximately 5 ml/min, and the eluate is col-
lected in a 20 ml Kuderna-Danish receiver. The sample extract
storage vial is rinsed with 5 ml of 50% methanol in methylene
chloride. This extract is passed through the silica gel Sep-Pak® ,
and the eluate is collected in the 20 ml Kuderna-Danish receiver.
The sample is concentrated, and the solvent is exchanged to
acetonitrile. The final solvent is made up to 30% acetonitrile in
pH = 3 phosphate-buffered water.
Calibration
A minimum of three instrument calibration standards and a
blank are run at the beginning of the analysis. One of these stan-
dards is duplicated at the conclusion of the analytical run to verify
constant instrument response. The normalized integrator areas ver-
sus micrograms/milliliter of each standard is plotted to obtain a
working curve.
Analysis
Fifty microliters of the extract are injected onto the HPLC col-
umn. The peak response for the components of interest on each of
the three detectors is measured. Peak heights rather than areas are
used because they are less subject to interferences. Determination
of the concentration of the components of interest is conducted ac-
cording to the calculation section described below.
Qualitative identification of the components of interest is out-
lined in Figure 3. Detector ratios are calculated for unknown sam-
ple components and compared to the ratios obtained during the
calibration run. The ratios obtained during documentation should
serve as guidelines for the magnitude and variance of the expected
ratios. The absolute value of the ratios may vary somewhat on dif-
ferent instrumentation, especially on ratios involving fluorescence,
because only a relative intensity on a particular instrument is
measured. The absorbance ratios should be more consistent among
different instruments because the absorbance is a property
measured in a more rigorously defined manner than fluorescent in-
tensity.
If the retention time and the ratios match those for one of the
standards, the presence of that particular analyte in the sample is
confirmed. If peaks are found for which the retention times match
but the ratios do not match any of the standards, sample cleanup is
conducted. The cleaned fraction is then analyzed by HPLC, and
the same criteria are applied for compound verification. A detector
ratio is considered positive if it falls within the 95% confidence in-
terval for the ratio obtained during documentation for that par-
ticular analyte.
SCREENING
-------
Figure 3
Logic Flowchart for Qualitative Identification by
HPLC Screening Procedure
A = 230 nra
i
o
A - 280 run
I 1 ~~~~~~~
0 50
RETENTION TIME (mln)
—I
120
Figure 4
HPLC Chromatogram of a Standard Water Sample Spiked at the 10X Level Using a Perkin-Elmer LC-75
SCREENING
89
-------
SB-
T~
50
120
RETENTION TIME (mln)
Figure 5
HPLC Chromatogram of a Standard Water Sample Spiked at the 10X Level Using a 254-nm Detector
e.
1
y.
1
M
RETENTION TIME (mln)
120
Excitation A - 290 nm
Emission X • Filter O350 nm)
Figure 6
HPLC Chromalogram of a Standard Water Sample Spiked at the 10-DL Level Using a Fluorescence Detector
90
SCREENING
-------
Table 5
Absorbance Ratios and Detection Limits of Analytes in Standard Water without Silica Gel Cleanup
Compound
HMX
RDX
ATNBA.
135TNB
13DNB
NB
35DNP
Tetryl
246TNT
26DNT
24DNT
12DNT
Naphthalene
Acenaphthylene
Acenaphthene
Fhenanthrene
Anthracene
Fluor anthene
Pyrene
Chrysene
Benzo(b) fluor anthene
Benzo(k) f luoranthene
Benzo(a)pyrene
Dibenzo(a ,h)anthracene
Indenod ,2,3-cd)pyrene
Detector
Wavelength
(nm)
230/254
230/254
230/254
230/254
230/254
230/254
230/254
230/254
230/254
230/254
230/254
230/254
280/254
254/F1***
280/F1
280/254
280/254
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
254/280
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
Mean
Absorbance Lowest
Ratio* Concentration
+ 95% CIt for Ratio (ug/L)
b.6 + 0.80
3.0 + 0.25
2.8
3.6^0.29
1.9_+ 0.26
0.70
1.7 + 0.58
3.14
2.3 + 0.43
1.5 + 0.95
1.2 + 0.31
0.852
1.6 + 0.8
21 + 12
36^5.0
1.3 + 0.28
0.53^0.13
0.35jf 0.13
29 _+ 5.9
!!_+ 1.6
0.0082^0.014
220^56
1.5^0.31
2.2 + 0.64
0.55 + 0.16
1.2 + 0.39
0.46 + 0.16
7.9^1.5
3.8 + 1.0
0.43^0.15
15 + 1.3
6.6^2.5
0.99 + 0.42
0.97^0.27
0.99 + 0.56
1.3^0.47
0.39 + 0.16
0.50 + 0.23
1.6 + 0.70
1.3 + 0.58
2.0 + 0.83
12 + 6.4
0.62 + 0.39
6.9^2.2
0.89 _+ 0.27
1.6 + 0.34
1.4 + 0.32
4.0
2.0
N)tt
1.9
2.2
M)
3.6
ND
2.0
2.3
2.0
ND
4.1
41
41
6.6
1.5
1.5
6.1
6.1
12
12
12
0.4
0.4
0.4
1.9
1.9
19
0.40
1.0
1.0
0.21
0.21
0.21
0.21
0.21
0.21
0.45
0.45
0.45
0.75
0.75
0.75
0.58
0.58
0.58
Target DL
(ug/L)
4.0
4.0
ND
3.8
4.4
ND
7.3
ND
4.0
4.6
4.0
ND
8.2
8.2
8.2
13
4.8
3.0
3.0
3.0
2.4
2.4
2.4
0.8
0.8
0.8
3.8
3.8
3.8
0.20
0.20
0.20
0.21
0.21
0.21
0.41
0.41
0.41
0.45
0.45
0.45
1.5
1.5
1.5
0.58
0.58
0.58
Documented
DL**
(ug/L)
15
6
ND
6
6
ND
11
ND
6
9
6
ND
27
—
—
22
10
5
—
—
2
—
—
0.9
—
—
8
—
—
0.4
—
—
2
—
—
1
—
—
0.8
—
—
ND
—
—
2
—
—
Retention
Time
(minutes)
9.2
13.0
14.3
16.8
20.8
24.8
26.9
29.5
29.3
35.0
36.1
52.5
84.5
—
—
89.1
95.7
97.5
—
—
98.8
—
—
102.2
—
—
103.4
—
—
108.2
—
—
112.9
—
—
113.3
—
—
114.0
—
—
116.8
—
—
117.9
_
*Determined from peak height
tCI = Confidence interval (n
measurements **DL = Detection limit calculated according to Hubaux and Vox (1970) ***'
= 20) tt Not determined due to co-elution, interference, or instability problems
Fluorescence measured at wavelengths greater than 350 nm
SCREENING 91
-------
Table 6
Absorbance Ratios and Detection Limits of AnaJytes in Standard Water with Silica Gel Cleanup
Compound
1HX
RDX
135TNB
13DNB
35DNP
246TNT
26DNT
24DNT
Naphthalene
Acenaphthylene
Acenaphthene
Phenanthrene
Anthracene
Fluoranthene
Pyrene
Chrysene
Benzo(b)fluoranthene
Benzo(k) floor anthene
BenzD(a)pyrene
Dibenzo(a.h) anthracene
IndenoU, 2, 3-cd) pyrene
Detector
Wavelength
(nn)
230/254
230/254
230/254
230/254
230/254
230/254
230/254
230/254
280/254
254/Fltt
280/F1
280/254
280/254
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/n
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
2SO/F1
Mean lowest
Absorbance Concentration
Ratio* for Ratio
+ 95% CIt (ug/L)
6.6^2.2
3.0^0.63
3.6 + 0.79
1.9 ±0.29
1.6 + 0.68
2. 3 ±0.76
1.7 _+ 0.89
1.1 _+ 0.55
1.6 ±0.62
22 ±16
37 ±6.0
1.4±0.71
0.52 ± 0.47
0.35 ±0.05
31 + 12
10 +4.7
0.0084 ±0.011
230 ± 72
1.9 + 2.5
2.3 + 0.56
0.53 ±0.13
1.2 + 0.30
0.48 ±0.17
7.8±1.4
3. 7 ±0.97
0.40 ±0.046
16. 2 ±5.9
6.0 + 5.0
1.0 + 0.46
0.94 + 0.30
0.96 ±0.38
1.4 + 0.71
0.39^0.26
0.53^0.26
1.8 + 0.52
1.3^0.51
2.0^1.2
13^3.7
0.61 + 0.28
7.7 + 2.9
0.88^0.38
1.6^0.77
1.4 jf 1.0
4.0
2.0
1.9
2.2
3.6
2.0
2.3
2.0
4.1
41
41
6.6
1.5
1.5
6.1
6.1
12
12
12
0.4
0.4
0.4
1.9
7.7
7.7
0.40
1.0
1.0
0.21
0.21
0.21
0.41
0.21
0.41
0.45
0.45
0.45
1.5
1.5
1.5
0.58
0.58
0.58
Target
DL
(ug/L)
4.0
4.0
3.8
4.4
7.3
4.0
4.6
4.0
8.2
8.2
8.2
13
4.8
3.0
3.0
3.0
2.4
2.4
2.4
0.8
0.8
0.8
3.8
3.8
3.8
0.20
0.20
0.20
0.21
0.21
0.21
0.41
0.41
0.41
0.45
0.45
0.45
1.5
1.5
1.5
0.58
0.5&
0.58
Doc merited
DL**
(ug/L)
11
8
6
8
8
11
12
7
33
—
35
12
5
—
—
5
—
—
1
—
—
6
—
—
0.5
—
—
0.3
—
—
0.8
—
—
0.9
—
—
H)***
—
—
2
—
—
Retention
Time
(minutes)
9.2
13.0
16.8
20.8
26.9
29.3
35.0
36.1
84.5
—
89.1
95.7
97.5
—
—
98.8
—
—
102.2
—
—
103.4
—
—
108.2
—
—
112.9
—
—
113.3
—
—
114.0
—
—
116.8
—
—
117.9
—
—
"Deicrmmed from peak heights measurements
*CI Confidence intenal (n = 20)
"DL = Detection limn calculated according to Hubaux and Vos (1970)
ttFluorescence measured at wavelengths greater than 350 nm
"*ND ^ Not determined due 10 interference problem
92
SCREENING
-------
Table 7
Comparison of Absorbance Ratios for Natural Water
Versus Standard Water
CALCULATIONS
Determine the concentration of each analyte according to the following
formula:
HMX
RDX
1,3,5-TNB
1,3-DNB
3,5-DNP
2,4,6-TNT
2,6-DNT
2,4-DNT
Naphthalene
Acenaphthylene
Phenanthrene
Anthracene
Fluoranthene
Pyrene
Chrysene
Benzo(b)fluoran-
thene
Benzo(k)fluoran-
thene
Benzo(a)pyrene
Indeno(l,2,3-cd)
pyrene
Detector
Wavelengths
(nm)
230/254
230/254
230/254
230/254
230/254
230/254
230/254
230/254
280/254
254/FI"
280/F1
280/254
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/F1
280/F1
280/254
254/FI
280/F1
280/254
254/FI
280/F1
280/254
254/FI
280/F1
280/254
254/FI
280/F1
280/254
254/FI
280/F1
Standard Water
Absorb. Ratio
± 9SVo CI*
6.6 ± 0.80
3.0 ± 0.25
3.6 ± 0.29
1.9 ± 0.26
1.7 ± 0.58
2.3 ± 0.43
1.5 ± 0.95
1.2 ± 0.31
1.6 ± 0.8
21 ± 12
36 ± 5.0
1.3 ± 0.28
0.35 ± 0.13
29 ± 5.9
11 ± 1.6
0.0082 ± 0.014
220 ± 56
1.5 ± 0.31
2.2 ± 0.64
0.55 ± 0.16
1.2 ± 0.39
0.46 ± 0.16
7.9 ± 1.5
3.8 ± 1.0
0.43 ± 0.15
15 ± 1.3
6.6 ± 2.5
0.99 ± 0.42
0.097 ± 0.27
0.99 ± 0.56
1.3 ± 0.47
0.39 ± 0.16
0.50 ± 0.23
1.6 ± 0.70
1.3 ± 0.58
2.0 ± 0.83
0.89 ± 0.27
1.6 ± 0.34
1.4 ± 0.32
Natural Water
Absorb.
Ratiof
6.8
2.9
3.5
1.9
1.8
2.3
1.8
1.2
1.5
23
35
1.2
0.34
31
11
0.006
223
1.3
2.4
0.57
1.4
0.44
8.9
3.9
0.43
16
7.1
0.89
1.1
0.96
1.2
0.40
0.46
1.8
1.2
2.2
0.98
1.4
1.4
Concentration Oig/g) =
(Vs)
(1)
where: A = Concentration (jig/ml) of analyte found in the
sample by comparison with the appropriate
standard curve (/ig/ml)
Volume of total extract (ml)
Volume of initial sample extracted (1)
•Confidence interval (n = 20); rates determined by peak heights.
tNatural water ratio determined from a 5-DL-level spiked sample not cleaned by silica gel.
"Greater than 350 nm.
Vt =
Vs =
The concentration is corrected for recovery by dividing by the
slope of the regression line for observed value versus target value
for spiked samples.
The mean detector ratios, 95% confidence interval and lowest
level (/tg/1) at which these ratios could be accurately measured due
to instrumental sensitivity limitations are presented in Tables 5 and
6. Example chromatograms are presented in Figures 4, 5 and 6.
DISCUSSION
Good agreement is noted between the ratios obtained for samples
with and without silica gel cleanup. The 95% confidence intervals
are calculated based on 20 measurements and indicate that these
ratios should be quite useful for qualitative confirmation of com-
pound identities. A comparison of the ratios obtained from spiked
samples of natural water with those obtained for the standard
media is shown in Table 7. All of the ratios for the natural media
are well within the confidence interval obtained for standard
media. These results demonstrate the utility of detector ratios for
the confirmation of compound identities in actual media. The use
of these ratios provides a relatively inexpensive method for increas-
ing the specificity of HPLC procedures.
REFERENCES
1. Baker, J.K., Skelton, R.E. and Ma, C.Y., J. Chromatography, 168,
1978, 417-427.
2. Dixon, W.J. and Massey, F.J., Jr., Introduction to Statistical Analy-
sis, McGraw-Hill, Inc., New York, 1969.
3. Giles, J.W., Somack, R. and McKay, V.S., "Detection and Identifica-
tion of Polynuclear Aromatic Hydrocarbons by HPLC." Presented at
the American Chemical Society Annual Meeting, Washington, D.C.
1979.
4. Hubaux, A. and Vos, G., Anal. Chem., 42, 1970, 840.
SCREENING
93
-------
DELINEATION OF UNDERGROUND HYDROCARBON LEAKS
BY ORGANIC VAPOR DETECTION
MOHSEN MEHRAN, Ph.D.
MICHAEL J. NIMMONS
EDWARD B. SIROTA
D'Appolonia Consulting Engineers, Inc.
Irvine, California
INTRODUCTION
The concern over leakage of petroleum products from
underground tanks and pipes, stems from both economic and en-
vironmental considerations. Matis and Osgood2 have reported
gasoline leaks from less than 10 to more than 1000 gallons.1'2 In
1976, the costs of cleanup operations have been reported to be in
the range of $1 to $100/gal of product spilled.1 Recent experience
of the authors indicates costs can range to more than $1000/gal
leaked with no recovery of any free product. A large percentage of
this cost is incurred during the investigation phase in order to
delineate the extent of product migration. For example, the cost of
a drilling and abatement program for the product gasoline pipeline
leak in Glendale, California, assumed by Western Oil and Gas
Association was approximately $700,000. This is only part of the
cost of the total recovery, most of which was assumed by other par-
ties involved.4
In addition to high costs for product recovery, the environmental
consequences resulting from migration of various phases (liquid,
vapor and dissolved) of hydrocarbons can be serious. Soil con-
tamination by the liquid phase (free product) can last for long
periods of time. Removal of the contaminated soil is perhaps the
most environmentally acceptable but most costly method of mitiga-
tion. Hydrocarbon vapor can migrate through the soil pore space
into underground structures and cause undesirable odors and ex-
plosions. The hydrocarbons dissolved in groundwater can migrate,
laterally and vertically, to large distances away from the source
causing contamination of downgradient water supplies.
Efficient investigation of leaks is a key to cost-effective product
recovery and the prevention of extensive areal contamination and
associated economic consequences. The authors' purpose is to pre-
sent a method by which the probably extent of a free product plume
from underground hydrocarbon spills can be delineated by measur-
ing the organic vapor concentration in the soil pore space. This
method of delineation can reduce the extent and, thus, the cost of
drilling programs that are required to map underground hydrocar-
bon contamination.
PETROLEUM PRODUCT MIGRATION
IN SOIL-WATER SYSTEMS
As gasoline leaks from underground facilities into the soil, a cer-
tain amount adsorbs on the soil particles while the excess migrates
under the influence of gravity and capillary forces. A continuous
supply of gasoline for an extended period of time will result in the
flow of liquid large distances away from the source. The vertical
migration of free product, however, will be prevented if the water
table is encountered. In this case, free material will migrate laterally
on top of the water table and in the general direction of the ground-
water gradient. During this process a portion of free product in
contact with the water table will dissolve in the water and subse-
quently be transported downstream. The dissolved phase will be
subject to mass flow of water, dispersion and physicochemical
phenomena such as adsorption and biodegradation.
The vertical migration of the free product generally produces a
wetting zone,' the shape of which depends on homogeneity and
isotropy of the medium. A portion of the free product in both the
flowing and adsorbed phases is subject to evaporation. This pro-
cess is also dominant when free product reaches the water table or
any geologic barrier such as clay layers. The gaseous phase of
gasoline migrates through the pore space by the diffusion-
convection process. Migration of gasoline in the vapor phase
depends on properties of the medium and thermal gradients.
PRODUCT MIGRATION IN THE VAPOR PHASE
Transport of gasoline vapor in the soil pore space is governed by
the processes of diffusion and convection. Diffusion is the result of
thermal motion of the molecules subject to a concentration gra-
dient. Convection is the result of a pressure gradient causing mass
flow in the gaseous phase. Although transport of the vapor phase
in soil is a three-dimensional phenomena, for illustrative purposes
only one dimension will be considered.
The governing equation describing the migration of the vapor
phase can be written as:'
3C _
7F '
where
C
t
DO
y
3 C 3C
S" ~ V TT—
) j, 2 o 3y
= concentration of gas
= time
= diffusion coefficient
= distance
= interstitial gas velocity
(1)
Neglecting the mass flow and assuming isothermal conditions,
the equation (1) will be reduced to:
3C
which includes the effects of diffusion only.
(2)
94
SAMPLING & MONITORING
-------
Considering a two-dimensional contaminated space as shown in
Figure 1, in which case the x dimension is infinitely long, the
assumption of one-dimensional vertical migration can be valid.7
For the conditions shown in Figure 1, the initial and boundary con-
ditions are given as:
c
c
12
3y
Co
c.
1
y> o
y - h
C • o
t> o
t> o
(3a)
(3b)
<3c)
where
C0 = initial concentration of gas in the pore space
Q = concentration of gas at the soil-air interface
h = depth to the bottom of the contaminated zone
Solution of the equation (2) subject to initial and boundary condi-
tions (equation 3) is given by:'
Cos
Ca + (Co * V -4 I
(2n+l)ny
(-Dn
D (2n-H)2n2t
n"o
(4)
2h
The concentration profiles for various values of D0t/h2 are given
in Figure 2 to illustrate the decrease in concentration as the distance
from the source increases.
Without describing the mathematical details of two-dimensional
transport of vapor, from the above discussion it should be clear
that concentration of vapor is expected to decrease both vertically
and horizontally as a function of distance from the contaminated
zone. This, of course, is based on the assumption that the medium
is homogeneous and isotropic. Vapor detection methodology and
interpretation presented herein are based on the above assumptions
and mathematical descriptions of gas flow.
DIRECTION OF
SURFACE WIND
t I t t 4
Figure 1
A two-dimensional representation of soil contaminated zone
(After Thibodeaux7)
ORGANIC VAPOR DETECTION
Detection of petroleum vapor from seeps and leaks dates back to
nineteenth century oil explorations. Geophysical methods are
among the most accepted methods used for exploratory purposes.
These methods are generally costly, and other methods, such as gas
geochemistry, are consequently becoming increasingly more attrac-
Figure 2
Vapor concentration in the contaminated zone (After Thibodeaux7)
live. A conventional method of measuring hydrocarbon gas uses a
soil-gas sampler which extracts the sample to be used for subse-
quent analysis. This has the disadvantage of not taking into ac-
count the rapid changes due to meteorological factors. Also, a
limited depth is attainable in this method. Another method is col-
lecting the soil sample and sealing the sample into a gas-tight con-
tainer for later analysis.
However, a new method has recently been developed at the Col-
orado School of Mines' using an integrative device equipped with
activated carbon. A shallow hole of 6 to 10 in. is drilled, and the in-
strument is kept in the hole for one week or two weeks prior to ex-
traction and subsequent laboratory analysis.
The method of organic vapor detection presented uses the same
concepts of gas geochemistry with one exception. Measurements
are made of the instantaneous concentration of gas released from
the pore space.
Instrumentation
The organic vapor detection surveys described utilized an
Analytical Instruments Development Corporation (AID) Portable
Organic Vapor Meter, Model 580. The AID 580 is a battery-
powered, portable gas sampler with a photo-ionization detector.
The instrument uses a small air pump to sample as much as 0.5
1/min. The gaseous sample is subjected to high intensity ultra-violet
light from a krypton lamp with an ionizing energy of 10.0 eV.
Water and low molecular weight hydrocarbons such as methane,
ethane, propane, methyl alcohol and some freons will not ionize
and, thus, will not be detected by the instrument. The ionized sam-
ple produces an ion current which is proportional to concentration
and is measured by the instrument's picoammeter. The photo-
ionization detector has a linear range from 0 to 2,000 ppm with a
minimum resolution of 0.1 ppm.
The AID 580 is not species specific and will detect a variety of the
hydrocarbons present in gasoline vapor. Instrument accuracy is
dependent upon calibration with known concentrations of a known
organic vapor. As employed in the surveys presented in this paper,
each set of concentration measurements at a given location and on
a given day is relative to a butadiene calibration standard and a
constant instrument sensitivity setting.
Procedure
Each hydrocarbon vapor detection survey consists of drilling a
predetermined, uniform pattern of 1 in. diameter, 15 to 18 in. deep
holes with an electric roto-hammer. Immediately upon the roto-
hammer bit removal, a 4 in. long casing is temporarily inserted into
the borehole in order to minimize asphalt dust and surface at-
mospheric hydrocarbon sampling interference. A small diameter
(less than 0.2 in. diameter) polyethylene tube is inserted through the
temporary casing top to conduct the sampling.
SAMPLING & MONITORING 95
-------
As the sample is withdrawn, there is generally an increasing series
of readings until a maximum reading is obtained, after which the
readings decline. The peak instrument reading is the record of
observation.
Following the reading, the casing and sampling tube are
withdrawn, cleaned and purged before the next measurement.
Depending on the site, 20 to 30 vapor detection holes are usually
drilled. Before, during and following vapor hole measurement,
background ambient hydrocarbon vapor concentrations are noted.
The background concentrations are subtracted from the borehole
readings to obtain net vapor concentration.
The vapor detection holes are placed in a predetermined pattern
and sampled in a cartesian or radial grid system. Additional holes
are drilled and sampled when gradients are measured. Holes are
backfilled after the survey is completed.
Data Analysis
The relative concentration values obtained from the instrument
are used as input to a computer code called "SURFACE II". This
code is capable of interpolating and extrapolating the input data to
arrive at isoconcentration lines. The plotting technique used in
SURFACE II requires a minimum number of 10 data points. As
the number of data points increases, the accuracy of data presenta-
tion by isoconcentration lines also increases.
Factors Affecting Measurement Reliability
Parameters affecting evaporation of gasoline through the soil
pore space can be categorized into two groups, the environmental
factors and the properties of the medium. The environmental fac-
tors include temperature, barometric pressure, relative humidity
and wind velocity at the soil surface. The properties of the medium
affecting gasoline evaporation consist of soil moisture, soil struc-
ture, organic carbon content and type, thickness and porosity of
the pavement.
The authors' experience in organic vapor survey shows that cool,
calm and cloudy days provide favorable environmental conditions
for high reliability. Low moisture content and high porosity are
among the most important media properties producing reliable
measurements.
CASE STUDIES
The organic vapor detection method discussed has been used at a
number of gasoline leaks to delineate the areal extent of free pro-
duct contamination. The method has been successful in some cases
and not so successful in others. The three cases presented here will
provide a better understanding of the capability (Cases A and B)
and limitation (Case C) of the method.
The characteristics of the sites, pertinent to the subject, are sum-
marized in Table 1. It should be pointed out that most of the infor-
mation given in Table 1 is obtained after performing the vapor
probe survey.
Case A
This case involved a gasoline station underlain by a mixture of
sand, silt and clay to a depth of 11 ft and decomposed granite
below that. The decomposed granite is a confined aquifer under
artesian head which raises the piezometric level to a depth of 9 ft.
As shown in Figure 3, the vapor survey indicated high concentra-
tions coinciding with a borehole into the gasoline storage tank
backfill where free gasoline was observed. Three other boreholes
revealed no gasoline on the groundwater. No gasoline was detected
in soil samples from the three boreholes. The relatively low organic
vapor readings outside the immediate vicinity of the tank area cor-
roborate the absence of gasoline in the surrounding soil.
The artesian head of the groundwater could contain the free
gasoline plume in the relatively porous sand backfill of the tank pit.
The low organic vapor measurements at the site periphery is consis-
tent with the fact that no gasoline plume was detected off-site.
Table 1
Site Characteristics
Cue
Vol. of
Leak
(gal.)
< 1,000
Porosity
(*)
Av. In slla
Moisture
Content
Depth lo
Ground-
water (ft)
Stratigraphy
Sandy Clay (0-11 ft)
{Decomposed
Granite (11 ft and
below) 28 10 11
B 1.1302 Sill and Silty Sand 25<'> < 10<'> 8
C 2.500 Silty Clay (0-5 ft) varies 5 13
Silty Sand (5-13 ft)
Clay (13-18 ft)
Sandstone (18 ft and
below)
(1) Estimated from soil texture
(2) All hydrogeologic and geotechnical data indicate that less than 2,500 gal could have been lost.
Case B
The gasoline station is located on an alluvial plain, comprised of
a complex stratigraphy of interfingering layers and lenses of gravel,
sand silt and clay. A surface layer of silt and sand lies on a deeper
layer of silty clay encountered at depths varying from 10 to 20 ft.
The site is underlain by a moderately sloping semi-perched water
table sloping generally to the south. The shallow (8 ft), semi-
perched groundwater does not appear to be pumped in the vicinity
of the site. As shown in Figure 4, the vapor survey indicated
elevated concentrations immediately south of the storage tanks.
This was consistent with the presence of free product in borings im-
mediately adjacent to and south of the east storage tank. Borings
B-l and B-2 contained 13 in. and 20 in. of free product, respective-
ly, at the beginning of the investigation. Vapor probe readings at
the station periphery indicated no evidence of elevated organic
vapor concentrations off-site. Though petroleum hydrocarbon
odors were noted in other boring during drilling, no free product
was detected at the other borings outside of the immediate
underground tank area. The organic vapor survey in this case pro-
vided initial evidence of a localized plume and guidance for
borehole location.
Figure 3
Isoconcentration lines obtained from organic vapor survey in Case A
SAMPLING & MONITORING
-------
Figure 4
Isoconcentration lines obtained from organic vapor survey in Case B
MCVLfT*
LESEND
V|2 VAPOR DETECTKW POINT
B-2 BORING
Figure 5
Isoconcentration lines obtained from organic vapor survey in Case C
CaseC
This gasoline station is underlain by a clay layer overlying a
sand/silt layer which overlies a clay layer of relatively low
permeability. A dense sandstone formation underlies the site at a
depth of about 27 ft. Groundwater was found at a depth of 13 ft
and is considered to be a local perched ground water table.
Organic vapor probe measurements are shown in Figure 5.
Measured vapor concentrations were generally uniform over most
of the site with the exclusion of the three areas of relatively lower
concentrations.
No free product was encountered in any of six boreholes on the
site. The surface soils emitted an organic humus odor from all
boreholes. Gasoline odor was observed only at one borehole near
the gasoline storage tanks. The high organic vapor probe readings
at the site were attributed to the organic content of the near-surface
clay layer. Use of the vapor probe under such conditions may give
inconclusive indications.
CONCLUSIONS
Under favorable conditions, organic vapor detection provides a
rapid and economical means of locating approximate areal extent
of underground hydrocarbon contamination. The technique can be
implemented by one person, and it is possible to drill up to 40 holes
in one day. The magnitude and location of isoconcentration lines
can be used for guidance in drilling observation wells. This tech-
nique of delineation of underground hydrocarbon leaks can reduce
the cost of drilling programs that are required to map underground
hydrocarbon contamination.
The conditions that are most favorable for providing reliable
results are as follows: high water table, homogeneous and isotropic
geologic material, coarse-grained material, absence of underground
structural barriers, dry unsaturated material and fresh product.
In situations when the top soil consists of a dense clay layer
deeper than the reach of the drill, the result may not be reliable.
Under these conditions, the clay cap would prevent migration of
the vapor phase to the surface. Temperature and wind play a
significant role in performance of the instrument. Cool and calm
days are ideal. Turbulence in the air will cause rapid exchange be-
tween the probe surrounding and the air which will result in
unreliable readings. Interference from other sources such as surface
spills and gasoline station islands could also cause unreliable
results. The sensitivity of the instrument, per se, and its perfor-
mance relative to environmental factors, dictate the need for a con-
sistent and knowledgeable field observer.
REFERENCES
1. Matis, J.R., "Petroleum Contamination of Groundwater in Mary-
land," Ground Water, 9, (6), 1971, 57-61.
2. Osgood, J.O., "Hydrocarbon Dispersion in Groundwater: Significance
and Characteristics," Ground Water, 12 (6), 1974, 427-436.
3. Hall, P.L. and Quam, H., "Countermeasures to Control Oil Spills
in Western Canada," Ground Water, 14 (3), 1976, 163-169.
4. Williams, D.E. and Wilder, D.G., "Gasoline Pollution of a Ground-
water Reservoir—A Case History," Ground Water, 9 (6), 1971, 50-54.
5. Schwille, F., "Petroleum Contamination of the Subsoil—A Hydro-
logical Problem," The Joint Problems of the Oil and Water In-
dustries, ed. Peter Hepple, Elsevier, Amsterdam, 1967, 25-53.
6. Rolston, D.E., Kirkham, D. and Nielson, D.R., "Miscible Displace-
ment of Gases through Soil Columns," Soil Sci. Soc. Amer. Proc., 33,
1969, 488-492.
7. Thibodeaux, L.J., "Chemodynamics," John Wiley & Sons, New York,
1979.
8. Carslaw, H.S. and Jaeger, J.C., "Conduction of Heat in Solids,"
Oxford University Press, London, 1959, 96.
9. Klusman, R.W. and Voorhees, K.J., "A New Development in Petrol-
eum Exploration Technology," Mines Magazine, 73, March 1983.
SAMPLING & MONITORING
97
-------
REAL TIME MONITORING OF LOW LEVEL AIR
CONTAMINANTS FROM HAZARDOUS WASTE SITES
MICHAEL B. AMSTER
TRC Environmental Consultants
East Hartford, Connecticut
NASRAT HIJAZI, Ph.D.
ROSALIND CHAN
TRC Advanced Analytics Canada, Inc.
Thornhill, Ontario
INTRODUCTION
The Silresim Chemical Corporation was a chemical waste
reclamation facility in Lowell, Massachusetts. When the site was
abandoned in early 1978, approximately one million gallons of
hazardous materials were left in drum and bulk storage. This ma-
terial was removed in 1981. Odor complaints were received from
neighbors; these complaints persisted over the years.
To ascertain the existence of an air contamination problem, TRC
Advanced Analytics was contracted by the Department of En-
vironmental Quality Engineering (DEQE) and the USEPA to
address two major issues at the Silresim site and its environs. The
first was to qualitatively identify as many pollutants as possible
emanating from the site. The second was to compare the "air qual-
ity" in terms of pollutant types on the site to the air quality up-
wind and downwind. This enables the Study Group to determine
whether or not the Silresim site is contributing any air pollutants
to the general neighborhood.
PROCEDURE
The investigation was conducted on site using the SCIEX®
TAGA® 3000 (Trace Atmospheric Gas Analyzer). The TAGA®
in its mobile form, installed in a CMC motor coach, is capable
of continuous, real time monitoring of gas and vapor phase ma-
terials at both source and ambient concentration levels. The ana-
lytical component of the TAGA® system is based on the prin-
ciples of atmospheric pressure chemical ionization (APCI) coupled
with ion detection by mass spectrometry (MS).'
A schematic of the main components of the TAGA® 3000
system is found in Figure 1. Ambient air with its contents of trace
volatile pollutants is drawn into the analyzer by a pump at con-
trollable flows between 0.5 to 4 I/sec through 22 mm (OD) all-
glass sampling line. The trace pollutants are ionized by a corona
discharge of a point-to-plane type which generates stable ion cur-
rents (controllable between 10~7 and 10"15 amps) of either positive
or negative reactant ions. The formed ions are electrically drawn
toward a plate containing an orifice which separates the atmos-
pheric pressure region from the high vacuum region necessary for
mass spectral analysis. During the transit to the orifice, the ions
pass through a chemical ionization region and an inert gas curtain.
In the chemical ionization region, the primary ions (derived from
water and oxygen for the positive and negative ion mode of the
APCI/MS) react with trace compounds present in ambient air
through a series of ion molecule reactions to form ions represen-
tative of the various trace compounds.
The TAGA! 3000 system is a single mass spectrometric tech-
nique capable of identifying m/z peaks that differ by 1 amu.
In the positive ion mode analyses, protonation or charge trans-
fer is possible leading to the MH+ or M+ peak respectively. In the
negative ion mode analyses, hydride abstraction is most common
leading to the (M-H)- peak. With the single mass spectrometric
technique, two or more compounds residing at the same m/z peak
will not be distinguished.
The three techniques which can provide clues for tentative com-
pound assignments are:
•Ion Molecule Chemistry—A chemical ionization reagent is added
to the ambient flow to enhance the signal representing the trace
compound. For example, when small quantities of ammonia are
added to the source, NH4+ reagent ion is formed, and the amide
and amine chemical classes are highlighted.1
•TAGA® 3000 Collision Induced Dissociation—Use of both high
and low declustering potentials can distinguish between the parent
ion, and the fragment ion, and the fragment ion or water cluster,
since a moderately declustered spectrum with no fragments or a
fragmented ion spectrum may be obtained.
•Tandem Mass Spectrometry which can be achieved with the
TAGA® 6000 MS/MS system—The technique consists of two
stages of mass analysis. A primary mass analyzer selects ionized
chemical components from a complex mixture and a second mass
analyzer identifies the products of collision-ally activation decom-
position (CAD) of these preselected ions.3
Tentative assignments made on the basis of the above informa-
tion are confirmed or rejected on the basis of standard spectra of
the appropriate reference standard.
Cl REAGENT QAS
GAS MEMBRANE
OUAORUPOLE MS e « • «
1—
ATMOSPHERIC PRESSURE .
SOURCE REGION
Figure 1
Schematic of the Atmosphere Pressure Ion Source and
the Mass Spectrometer Region
98
SAMPLING & MONITORING
-------
TAGA® Quantitation
The calibration method is a relatively simple procedure of doping
air with ultra-trace concentrations of specific vapors. A small vol-
ume (approximately 0.5 ml) of compound under test is placed in a
10 or 20 ml syringe and by carefully depressing and then retract-
ing the plunger, the inside of the syringe barrel is coated with a thin
film of the sample. Within a few minutes, the vapor of the com-
pound has reached equilibrium with the air in the syringe. The com-
pound vapor/air mixture may then be injected in the TAGA®
air inlet stream by means of an automated syringe drive unit.
Knowing the vapor pressure of the compound, the temperature,
the atmospheric pressure and the injection rate, the concentration
of the component in real air may be calculated.
Data Acquisition by Single MS System
The data system integrated into the TAGA® includes a PDF
11/03 mini-computer with an interactive graphics terminal and
realtime display, data collection and printout.
The field experiments were restricted to the use of the APCI
ionization source and were conducted as follows:
•Positive and negative ion mode scans in the mass-to-charge range
of 2 to 250 atomic mass units were conducted on each sampling
site. Four locations were chosen on the Silresim site, and seven
off-site locations were chosen for ambient air monitoring.
•On-site calibration for the most significant peak(s) in the mass
spectra of the above was conducted
•Targeted compound analysis on and off the Silresim site
•Half-hour time weighted average (TWA) on targeted chemicals
•Selected soil and water samples from the Silresim site were
analyzed for headspace at ambient temperatures
RESULTS
Positive and negative mass spectral scans were conducted at four
locations on the Silresim site and at seven off-site locations within
the residential community. Oxygen based chemicals, such as
phenols, total phthalates/phthalic anhydride were present at insig-
nificant levels (•*: 1 ppb). Nitrogen based organics such as pyridine,
methyl pyridine and C3-amine were also present at very low con-
centrations (<1 ppb). However, a detailed assessment and inter-
pretation of the data show that dimethyl formamide will consti-
tute the most significant air contamination problem on the site.
The identification of m/z 74 as dimethyl formamide was confirmed
by taking advantage of the two-stage cluster breakup of the single
MS system with reference to the pure standard.
On-site calibration for dimethyl formamide was conducted. The
calibration curve shows a saturated response at approximately 50
ppb. The concentrations (ppb) of dimethyl formamide for the
various sampling sites are shown in Table 1.
Further air monitoring around the Silresim facility and Lowell
area has temporarily pinpointed a neighboring industry as a poten-
tial source of dimethyl formamide. The half-hour TWA concen-
trations at the Silresim site, the neighboring industry and the resi-
dential community are 2.18 ppb, >50 ppb and 8.0 ppb respec-
tively.
CONCLUSIONS
The major odor problems experienced by the citizens of the
neighboring Silresim site appear to be attributable to dimethyl
formamide. No significant amounts of benzene, alkyl benzenes,
PAH, phenols or amines were detected in the vapor phase at the
Silresim site.
The major source of DMF discharge appears to be a neighboring
industry (>50 ppb). Minor amounts of DMF were found on the
residential community air (8.0 ppb) and the Silresim site air (2.18
ppb).
REFERENCES
1. SCIEX® Publication—"Mobile Mass Spectrometry: A New Tech-
nique for Rapid Environmental Analysis".
2. Hiajzi, N.H., Chai, R. and Nacson, S., "A Methodology for Mon-
itoring Air Pollutants on Industrial Landfill Sites," 75th APCA Con-
ference, New Orleans, La., June 1982.
3. SCIEX® Publication—"TAGA® 6000 MS/MS: A Versatile System
Approach to Problem Solving by Tandem Mass Spectrometry."
Table I
Time-Weighted Averages for Dimethyl Formamide
UATK
Mar. 14, 1903
Mar. 15, 1983
Mar. 17, 1VII1
AMIIIKNT A lit
SITK 1
10. 09 AH
0.12 ppb
SITK 'I.
10:45 AM
0.48 ppb
SITK '1
11: 15 AH
0.55 ppb
Mi-.KKNNA I
n'KKKPK
2:31 I'M
0.02 ppb
IHIWNWIMII
NAI'I.K ST.
5:03 I'M
3.77 ppb
AMBIENT AIK
SITE 3A
9:30 AM
7.63 ppb
ARROW
PARKING I.OT
IO:Vi AM
< 0.05 ppb
WASHINGTON &
LEVERETT ST.
ll):/ir> AM
4.33 ppb
F.NO OF
ELLSWORTH ST.
12: IV I'M
3.2 ppb
SITE 4
"MOT SI'OT
AREA"
lifiH I'M
1»'50 ppb
CHEI>ISFOHI) I
AVI-HUI; n
4l4') I'M
5.4 ppb
HOLIDAY I III!
PARKING LOT,
TEWKKSIIUIIY.MASS.
li:<>7 I'M
0.63 ppb
SOIL IIKADSI'ACF. (20°C)
S-l
0.011 |i|il>
S-2
11.50 |>|>l>
S-3
H.'i'l ppli
S-4
(l.2:i |'|'l>
S-5
0.0:i pph
S-fi
II. Id p|il>
WATER IIEADSI'ACE (20°C)
SITE I
0.23 ppb
SITE 2
0.0'j ppb
SAMPLING & MONITORING
99
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DETERMINATION OF AIRBORNE VOLATILE NITROGEN
COMPOUNDS USING FOUR INDEPENDENT TECHNIQUES
PAUL F. CLAY
NUS Corporation
Bedford, Massachusetts
THOMAS M. SPITTLER, Ph.D.
U.S. Environmental Protection Agency, Region I
Lexington, Massachusetts
INTRODUCTION
In this paper, the authors describe the results of an air monitor-
ing study conducted during the spring of 1983 in the vicinity of a
hazardous waste site. The precision of four analytic techniques is
compared, and some problems associated with air monitoring at
hazardous waste sites located in urban areas are described. Since
there are legal proceedings pending for the waste site, and since the
results of the study implicated two nearby industrial facilities which
are voluntarily taking steps to reduce their air emissions, specific
names are not used. Of greater interest and importance are the
descriptions of the techniques which were used and the data which
resulted.
Study Area Description and History
The study area is located in a moderately sized city where a varie-
ty of manufacturing facilities are located. The initial focus of this
air monitoring study was centered upon a five acre site formerly oc-
cupied by a chemical recycling facility which principally conducted
solvent reclamation.
The facility operated for several years until 1977, when the owner
filed for bankruptcy. As a result of a variety of operational and
regulatory problems, approximately 23,000 drums of various spent
chemicals had accumulated at the time of the facility's bankruptcy.
Over the next several years, the state environmental agency remov-
ed all of the drums of wastes and, in addition, removed the remain-
ing wastes which were stored in about 50 above-ground tanks.
Waste removal was completed in 1981.
The state environmental agency also subcontracted a limited
hydrogeologic investigation which revealed that widespread soil
contamination, most likely caused by poor waste handling prac-
tices, existed at soil depths ranging from a few inches to several feet
below ground surface. The principal soil contaminants detected
were a variety of volatile organic compounds, including 1,1,1-tri-
chloroethane, trychloroethylene, ethylbenzene, tetrachloro-
ethylene, toluene, methyene chloride and trichlorofluoromethane.
Concentrations ranged from 1 to over 330 mg/1.
Although the site is situated in a predominantly industrial area,
about 450 private residences exist within a one-half mile radius of
the site. A number of area residents have complained about odors
which they believe emanate from the site.
Summary of Previous Air Monitoring
In the summer of 1982, the state air quality agency, assisted by
EPA, conducted an ambient air study on and around the site. Air
samples for volatile organic compound analysis were collected by
using portable pumps to draw ambient air through stainless steel
tubes filled with activated charcoal and Tenax sorbent. The char-
coal and Tenax tubes were taken to a laboratory for thermal
desorption and subsequent gas chromatograph/mass spectrometer
(GC/MS) analysis. A number of grab samples were also obtained
and injected directly into a Photovac, Inc. portable gas
chromatograph for analysis in the field. The results of the GC/MS
analysis revealed that the air directly above, upwind and downwind
of the site contained total concentrations of volatile organic com-
pounds including benzene, toluene and tetrachloroethylene at less
than 10 ppb. The literature suggests that such concentrations of
these compounds are typically present in urban air from a variety of
sources.' The conclusion drawn was that the site was not a source
of volatile organic air contamination.
In the late fall of 1982, the state environmental agency arranged
for a one-day air monitoring demonstration to be performed by a
mobile real-time system known as the TAGA 3000, owned by MDS
Analytics of Ontario, Canada. The TAGA 3000 unit performed
several time-weighted scans at and around the site.
The data reported to the state environmental agency indicated
that the air in the vicinity of the site was contaminated with a varie-
ty of nitrogenated and oxygenated compounds, including C-2, C:3
and C-4 amines (isomers not identifiable) and phthalates/
phthalic anhydride. The total amine concentration was approx-
imately 400 ppb. Subsequently, the data were released to the public
along with a synopsis of the potential health effects for the com-
pounds.
Increased public concern about air quality prompted USEPA, in
the early spring of 1983, to initiate a comprehensive air monitoring
study in order to verify or refute the data reported as a result of the
fall study. The NUS Corporation (under Contract No. 68-01-6699)
was tasked by USEPA to design and coordinate a comprehensive
study in conjunction with the USEPA New England Regional
Laboratory (NERL). As preparations for the work took place, two
major factors were under consideration. First, the compounds
reported to be present in the air at the site by the first TAGA 3000
study had never been reported as major contaminants in the soil of
the site; and second, the concentrations of the C-2, C-3 and C-4
amine compounds reported appeared to be unreasonably high for
ambient air.
GENERAL APPROACH
The study focused first upon obtaining the services of the TAGA
3000 system to repeat the monitoring techniques carried out in the
fall of 1982 and second upon identifying one or more techniques
100
SAMPLING & MONITORING
-------
which could be carried out independently, but simultaneously with
the TAGA 3000 work. Since volatile nitrogen compounds were the
contaminants of interest, considerable emphasis was placed upon
the identification of sampling and analytical techniques specific for
those compounds. Consequently, a senior scientist from the Ther-
moElectron Corporation, a company specializing heavily in
research and development of the sampling and analysis of nitrogen
compounds, was consulted. The ThermoElectron Corporation
holds several patents for both nitrogen compound sampling media
and nitrogen compound analysis. The primary techniques involved
the TAGA 3000 system and the ThermoElectron Corporation
methodology.
To supplement these two primary techniques, it was also deemed
necessary to conduct additional sampling and analysis for volatile
compounds known to be present in the contaminated soil of the
site. Thus, preparations were made to obtain air samples through
Tenax sorbent tubes for subsequent thermal desorption and
GC/MS analysis. As a fourth methodology, several portable gas
chromatographs, including a highly sensitive photoionization
detector (PID) GC and a GC employing a flame ionization detector
(FID) were used to analyze air grab samples obtained during the
time of sorbent tube sampling.
SAMPLING AND ANALYSIS TECHNIQUES
TAGA 3000
The TAGA 3000, Atmospheric Pressure Chemical Ionization/
Mass Spectrometer (APCI/MS) System, is a mobile, self-contained
system which allows real-time sampling and analysis of ambient air.
Sampling is accomplished by means of a high capacity air pump
which draws ambient air into the system at flow rates ranging from
0.5 to 10 I/sec. Analysis is performed using an APCI system which
enables ionization of trace gas molecules at atmospheric pressure,
using the ions produced in a primary ionization process from air as
reagent ions. To increase the selectivity for specific compounds, a
reagent, such as ammonia, can be added to the carrier gas in the
system. This results in increased selectivity for airborne nitrogen
containing species, such as amines.2 This particular system was
used during both the fall of 1982 and the spring of 1983 studies.
Following ionization, the reactant ions are separated according
to mass-to-charge ratios and detected by a signal handling system
over a dynamic range of from 1 to 107 ion counts per second. An
on-board computer system manages the data. The TAGA 3000
system allows data acquisition which includes scanning over a
mass-to-charge range for unknown species. A limitation of this
system is the inability to distinguish among species having the same
mass-to-charge ratio. At this writing, a TAGA 6000 system has
been developed which reportedly overcomes this limitation.
However, it was not used in this study.
N-Nitrosamine-Specific Sampling and Analysis
Sorbent cartridges used for sampling were Thermosorb/A™ car-
tridges provided by the ThermoElectron Corporation. Samples
were collected using portable sampling pumps calibrated at flow
rates in the range of 1.5 1/min. Following sampling, the cartridges
were eluted with 1.8 ml to 3 ml 1% potassium hydroxide in
methanol solution. Analysis was accomplished by injecting aliquots
of the solutions into a chromatographic system employing a
TEA™ Model 610 Nitrogen Analyzer.3
Tenax Sorbent Sampling and Analysis
Stainless steel tubes filled with Tenax were pre-cleaned, and
samples were collected using portable, battery driven sampling
pumps calibrated at flow rates of 200 cmVmin. Following samp-
ling, the tubes were thermally desorbed and aliquots of the desorb-
ed sample injected into a GC/MS system for analysis.
Grab Sampling and Analysis
At several specific locations ambient air grab samples were ob-
tained by puncturing the septa of 125 ml bottles which had
previously been evacuated and sealed. Aliquots of the samples were
then analyzed using a portable gas chromatograph with FID.
CONTAMINANT IDENTIFICATION
The study took place over a period of 10 days, which included
five actual sampling days, with time for initial analyses, interpreta-
tion of data and adjustment of work scope. The first day of samp-
ling was focused upon the chemical waste site, with air samples col-
lected on-site, upwind and downwind of the site. To determine
wind speed and direction, a permanent, recording wind direction/
speed indicator was installed at the site security trailer. Sampling
and analysis methodologies included the following:
•The TAGA 3000 system, which performed 30 min. time-weighted
average scans for species having mass-to-charge ratios corre-
sponding to the C-2, C-3, C-4 amines
•Thermosorb/A™ cartridges, with 30 min. composite samples
collected over the simultaneous 30 min. period
•Tenax sorbent tubes with simultaneous 30 min. composite samp-
ling
•Intermittent ambient air grab samples injected directly into a
portable GC with PID.
The second day of sampling employed the TAGA 3000 system
only and was principally directed toward obtaining ambient air
data for residential areas further removed from the disposal site. It
was also on this day that the attention of the study was shifted
toward contaminant sources other than the waste site, and that the
identity of the principal airborne contaminant was established.
The circumstances surrounding the redirection of the study are
described as follows. During the 30 min. scan at a location directly
on the waste site, the TAGA 3000 system recorded a high ion count
signal for a 74+ mass-to-charge (m/z) ion species which had been
identified previously as a C-4 amine. Through the application of an
ion cluster breakup process, a fragmented ion spectrum was ac-
quired which closely matched the fragmented ion spectrum of
N,N-dimethylformamide (DMF).2 A consultation with several state
agencies revealed that two industrial facilities within the site vicinity
reported DMF to be a major constituent of their volatile emissions
to the air.
Consequently, the third day of sampling was directed toward ob-
taining confirmation that the industrial facilities, and not the soil of
the disposal site, were the principal sources of the DMF in the study
area. Two industrial sources were identified. A fourth and fifth day
of sampling were conducted to determine the relative levels of con-
taminants emitted by each of the two industrial facilities.
The data obtained from the third day of sampling established the
reliability of nitrogen compound-specific sorbent/analysis and
Tenax/GC/MS methods. Therefore, the TAGA 3000 system and
the portable GCs were not used on the fourth and fifth days.
RESULTS OF SAMPLING AND ANALYSIS
The results of the sampling and analysis are presented in Tables 1
through 4. The data are presented in a tabulated format for each
day of sampling during the study. Sampling locations are described
as being upwind or downwind of suspected sources.
Day 1
The data for the first day of sampling, which included the TAGA
3000 system, Tenax sorbent tubes followed by thermal desorption
and GC/MS analysis and Thermosorb A sorbent followed by sol-
vent elution and GC analysis are shown in Table 1. The data ac-
quired by injecting grab samples of air directly into a portable PID
GC during the sampling time agreed with the GC/MS data and are
not included.
Day 2
The data obtained on the second day of sampling, which in-
volved the TAGA 3000 system only, are shown in Table 2. A
number of 30 min. time-weighted scans were performed at loca-
SAMPLING & MONITORING
101
-------
Table 1
N,N-Dimethyl Formamlde (DMF) and Additional Compounds 30-Minute Samples, Day 1
CONCENTRATION
LOCATION OF DMF
TAGA THERMO- EPA
3000 ELECTRON NERL
At Waste
At Waste
At Waste
Site 0.12 NS NS
Site 0.*8 ND, 1.9(D) NS
Site 0.55 Trace,1 TraceJ(D) ND2
Upwind of 0.02 2.0, Trace'(D) ND2
Waste Site
Downwind of 3.77 NA ND2
Waste Site
CONCENTRATION OF
ADDITIONAL COMPOUNDS
TAGA THERMO- EPA
3000 ELECTRON NERL
» NS
» DMA: ND,
TEA: ND,
* DMA: ND,
TEA: ND,
* DMA: ND,
TEA: ND,
NA
ND(D)
ND(D)
ND(D)
ND(D)
ND(D)
ND(D)
NS
NS
Benzene: <1
Toluene: 3
Xylene 0.9
Benzene:
Toluene:
Benzene
<1
1
<1
Toluene: 2
Xylene: 0.*
1,1,1-TCE: 1
Fluoro-
trichloromethane: 0.5
TCE: 0.9
Key:
NO - Not Detected
NS - Not Sampled
NA - Not Analyzed
(D) - Duplicate Sample
DMA » Dimethyl Amine
TEA - Triethyl Amine (unconfirmed)
1.1,1 TCE - 1,1,1-Trichloroethylene
Notes:
TAGA 3000 Scan for pyridine, methyl pyridine, C-3-Amine, phenol, total phthalates/phthalic anhydride all present at less than 1 ppb.
1. Detection limit 0.6 ppb.
2. Detection limit 20-50 ppb.
All ThermoElectron samples collected on Thermosorb A Sorbent.
TAOA 3000 values are 30 min. time-weighted.
EPA and ThermoElectron values are for 30 min. composite samples.
All concentrations in ppb.
Table 2
Results for 30 Min. Time-Weighted Scans (TAGA 3000 only)
Day Two, N.N-Dimethyl Formamide (DMF)
Location
At waste site, unsettled wind
Residential area, south of site,
unsettled wind
Residential area, west of site,
unsettled wind
Residential area, east of site,
unsettled wind
At waste site, downwind of Facility A
Residential area, southwest of waste
site, unsettled wind
2 miles from waste site
DMF
Concentration (ppb)
7.63
< 0.005
4.33
3.2
>40
5.4
0.63
Notes:
TAGA 3000 Scan for pyridine, methyl pyridine, C-3 amine, phenol, total phthalates/phthalic
anhydride, all present at less than 1 ppb.
TAGA 3000 System is saturated by DMF concentrations > 40 ppb, as determined by calibration
plot.
tions in residential areas surrounding the waste site. The afternoon
on-site scan was particularly significant, as it was during that time
that the presence of DMF was first suspected.
Day 3
The data for the third day of sampling, which included the
TAGA 3000 system, Tenax sorbent tubes followed by thermal
desorption and GC/MS analysis and Thermosorb A sorbent
followed by solvent elution and GC analysis, are shown in Table 3.
An additional technique used was the grab sample/portable GC
analysis technique using evacuated vials and an FID/GC. These
data are not included in Table 3, but are presented in Table 5 to il-
lustrate the correlation of results among the four techniques.
Sampling during the third day purposely took place during the
operation hours of one of the two industrial facilities, (designated
A and B), which were first identified as sources of DMF emissions.
Days 4 and 5
Sampling on Days 4 and 5 was designed to characterize air emis-
sions both when industrial facility A, which did not operate 24
hours per day, was closed, and when industrial B, which operated
24 hours per day, was active. Additional samples were also ob-
tained at the waste site in order to provide further verification that
the site was not the source of DMF. The data are reported in Table
4.
DISCUSSION
Day 1—
The results of the sampling and analyses using all of the previ-
ously described techniques revealed that concentrations of volatile
compounds, including volatile nitrogen compounds, were present
at barely detectable levels at sampling locations directly on the
waste site, downwind and upwind of the site. The highest concen-
tration detected was for DMF at about 4 ppb. Although the loca-
tion was downwind of the disposal site, that particular sampling
location was also located downwind of industrial facility B, which
was a source of DMF emissions.
102
SAMPLING & MONITORING
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Table 3
Concentrations of N,N-Dimethyl Formamide (DMF) and
Additional Compounds, 30-Min. Samples, Day 3
Concentration of
Additional Compounds
EPA
NERL
2700
TAGA
3000
•2
Thermo-
Electron
DMA: 500,
375 (D)
EPA
NERL
Toluene:
340
Xylene:
840
Concentration
of DMF
Location
TAGA Thermo-
3000 Electron
Downwind >40' 2600,2800
Facility A (D)
TEA: 19,
16 (D)
Upwind of 8.0 6,4 (D) ND3 '4 DMA: 0.8, Toluene:
Facility A 3 (D) 2.7
TEA: ND, Xylene:
ND (D) 14
KEY: (D) Duplicate Sample; DMA—Dimethyl Amine; TEA—Triethyl Amine (unconfirmed)
Notes:
1. TAOA 3000 system is saturated by DMF concentrations > 40 ppb, as determined by calibra-
tion plot.
2. TAOA 3000 reported pyridine, methyl pyridine, C-3 Amine, phenol, total phthalates/phthalic
anhydride <1 ppb. Additional contaminant tentatively identified as triethyl amine, concentra-
tion relatively low.
3. Detection limit is 20-50 ppb.
4. Same as Note 2, except m/z 102+ species (thought to be triethyl amine), not detected.
TAOA 3000 values are 30 minute time-weighted averages.
EPA and ThermoElectron values are for 30 minute composite samples.
5. Concentrations in ppb.
Table 4
Results of Day 4 and 5 Ambient Air Sampling, Analyses Conducted
by EPA/NERL and ThermoElectron Corporation
Sampling
Time
4hr
Contaminant Concentrations (ppb)
EPA/NERL
Benzene: 2
DMF: ND2
Toluene: 220
DMF: 740
Xylene: 10
Ethylbenzene: 2
Toluene: 160
DMF: 230
Toluene: 2
DMF: ND2
Toluene: 8
DMF: ND2
ThermoElectron
DMF: Tracel
DMA: Tracel
DMF: 402
DMA: 250
DMF: 470
DMA: 250
DMF: ND1
DMA: ND1
DMF: 17
DMF: ND1
Location
At Waste Site
Downwind of 4.5 hr
Industrial
Facility B
Same as above 30 min.
Downwind of 30 min.
Waste Site, up-
wind of Facility A
Downwind of 30 min.
Facility A, Facility
not operating at
this time
KEY: ND—Not Detected; DMF—N,N-Dimethyl Formamide; DMA—Dimethyl Amine
Notes:
1. Detection limit is 0.6 ppb
2. Detection limit is 20-50 ppb
Day 2—
The series of 30-min. time-weighted scans conducted by the
TAGA 3000 system did not reveal any significant concentrations of
volatile nitrogen compounds, with the exception of one location.
Coincidentally, that location was on the waste site in a position
directly downwind of industrial facility A. At the time, wind direc-
tion was steady and wind speed was about 8-10 knots. It was at this
location that the ion fragmentation process described earlier iden-
tified DMF as the principal airborne contaminant. The data is
reported as greater than 40 ppb since calibration curves subsequent-
ly plotted for the TAGA 3000 system response to DMF revealed
that the system becomes saturated at concentrations exceeding 40
ppb of DMF. Of greatest significance was that the data, together
with the available background information about nearby industrial
facilities' emissions, indicated that the waste site was not the source
of volatile nitrogen contaminants.
Day 3
Prior to the 30 min. sampling runs for which data are reported in
Table 3, the TAGA 3000 system was used in a mobile scanning
mode. The system was set up to display continuous total ion counts
for the 74 + m/z species believed, at this point, to be DMF. The
continuous scan was performed while driving from a point about
0.5 mile from industrial facility A to a location approximately 300
ft directly downwind of a visible plume being emitted from the
facility's ventilation system. The total ion count display rose steadi-
ly as the facility was approached, with the highest, steady values
recorded at the downwind location.
Subsequently, 30 min. samples were obtained at the downwind
location and at upwind location (Table 3). The data from these
samples confirmed the facility as a source of significant DMF emis-
sions and, additionally, revealed that significant concentrations of
other volatile compounds were being emitted. A fourth technique,
for which data are not presented in Table 4, involved grab samp-
ling/direct injection to a portable FID GC which was previously
described. A correlation for selected compounds obtained by the
four techniques at the downwind and upwind locations is shown in
Table 5
Correlation of Data for Selected Compounds, Day 3
(State Environmental Agency, USEPA/NERL, ThermoElectron
and TAGA 3000)
DMF
Concentration
Xylene Toluene
2860
2700
2600
2800 (D)
NS
ND5
6
4(D)
8.0
1680
840
NA
NS
14
NA
NA
280
340
NA
NS
27
NA
NA
Location
300 ft Downwind from
Facility A
State Agency1
EPA2
ThermoElectron3
Upwind of Facility A
State Agency
USEPA2
ThermoElectron3
TAGA 3000*
Legend:
NS = Not Sampled
DMF = N,N-Dimethyl Formamide
NA = Not Analyzed for
(D) = Duplicate Sample
Notes:
1. State Agency samples were instantaneous grab samples obtained during the 30 min. period.
2. EPA samples were 30 min. samples.
3. ThermoElectron samples were 30 min. samples.
4. TAGA 3000 value not reported for upwind location, as system becomes saturated above 40 ppb
concentration.
5. USEPA detection limit 20-50 ppb.
Table 5. The data for downwind sampling show excellent agree-
ment for higher concentrations among three techniques: the grab
sampling and portable GC analysis; Tenax sorbent followed by
thermal desorption and GC/MS analysis; and Thermosorb A sor-
bent followed by solvent desorption and GC/nitrogen-specific
detector analysis. As noted on Table 5, data are not reported for
the TAGA 3000 system at this location since the concentrations ex-
ceeded 40 ppb. For the upwind location where trace levels of com-
pounds were detected, the agreement between the TAGA 3000
system and the nitrogen-specific sampling and analysis was ex-
cellent. Grab samples were not obtained at this location. The con-
centrations of DMF were below the limit of detection (20-50 ppb)
for the Tenax/GC/MS analysis.
Days 4 and 5—
Comparison of the data from the two techniques shows excellent
agreement for DMF concentrations (Table 4). Also, the two
methods are complementary in that a volatile nitrogen compound
(DMA) not detected by the Tenax/GS/MS technique is detected at
SAMPLING & MONITORING
103
-------
significant levels by the ThermoElectron technique. Similarly,
significant concentrations of xylene and toluene were detected by
the Tenax/GC/MS system and not by the ThermoElectron system.
CONCLUSIONS
Of the four independent techniques applied simultaneously dur-
ing this study, it was determined that three techniques provided ex-
cellent agreement for concentrations of DMF above 40 ppb in-
cluding: sampling with Thermosorb A sorbent followed by solvent
desorption and analysis by GC with a nitrogen-specific detector;
sampling with Tenax sorbent followed by thermal desorption and
GC/MS analysis; and analysis of grab samples with a portable FID
GC. Correlation between the laboratory and field instrument data
further supports the reliability of the portable instruments widely
used by USEPA and its contractors during field investigations.
At concentrations of DMF < 40 ppb, excellent correlation was
achieved using the TAGA 3000 system and sampling with Ther-
mosorb A sorbent followed by solvent elution and GC analysis with
a nitrogen-specific detector.
This study also demonstrated that the design of ambient air
monitoring programs for hazardous waste disposal sites must
carefully consider the potential for contaminant contribution from
other sources in urban areas. The limitations of the sampling and
analytical procedures contemplated must be carefully evaluated
and, wherever possible, alternative, independent techniques should
be employed to ensure the reliability of the data.
REFERENCES
1. Singh, H.B., Salas, L.J., Smith, A. and Shigeishi, H., "Meas-
urements of Some Potentially Hazardous Organic Chemicals";
Atmos. Env., 15, 1980, 601-612.
2. Report to NUS Corporation, March, 1983. MDS Analytics,
Thornhill, Ontario.
3. Formal Report Of Analysis for N-Nitroso Compounds. April,
1983. ThermoElectron Corporation, Waltham, Massachusetts.
104
SAMPLING & MONITORING
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FIELD MEASUREMENT OF PCB'S IN SOIL AND SEDIMENT
USING A PORTABLE GAS CHROMATOGRAPH
THOMAS M. SPITTLER, Ph.D.
U.S. Environmental Protection Agency, Region I
Lexington, Massachusetts
INTRODUCTION
With the recent increase in activity at hazardous waste sites
where cleanup and remedial action is underway, there has emerged
a need for rapid analytical methods for assessing contamination in
water, sediment and soil. Of special interest, because of its
widespread use and disposal, is the group of materials known as
PCBs (polychlorinated biphenols).
EQUIPMENT AND METHODOLOGY
In the USEPA, Region I laboratory at Lexington, MA, chemists
have developed a rapid field method for measuring the presence of
PCBs in soil and sediments. The analytical technique is GC/EC
(gas chromatography using the linearized electron capture
detector). The column is held in an insulated isothermal chamber.
If preheated using AC power, the oven can maintain 200 °C for 8
hr on battery operation. The GC has three on-board lecture bottles
of gas. These have been manifolded so that 0.14 m3 of 5% methane
in Argon can be taken into the field. At 30 cmVmin, this allows
the GC to operate for approximately one week. The batteries can
be recharged overnight for 8 hrs of use.
For PCB measurement, the author employed a 1.2 m x 0.32 cm
stainless steel column packed with 3% SE-30 on 800/100 mesh
chromosorb W-HP. The column was held at 207 °C, and most in-
jections were made using 1-3 ul of a hexane extract of soil or a stan-
dard sediment test sample. Flow was held at 30 cmVmin. These
conditions permitted elution of the six major peaks of Arochlor
1254 (Figure 1) in about 8 min.
Field samples were prepared for analysis by weighing out 400 mg
of soil into a 2 cm3 septum vial. When less accuracy was needed,
no balance was utilized and sample size was estimated by volume.
To the soil were added 100 ul of water, 400 ul of methanol and
500 ul of technical grade hexane. The sample was agitated for about
20 sec by hard shaking or by holding the vial to the tip of a vibrat-
ing engraver. Finally, a dilution was made if a high PCB level were
anticipated. If not, the top layer in the vial was sampled with a 10
ul syringe and a 1-3 ul sample was injected into the GC.
Various solvent mixtures were tested for extraction efficiency.
The test sample was a bone dry sediment standard containing 24.6
ppm of Arochlor 1242. This reference material was prepared by the
EPA facility in Cincinnati several years ago and is a real sediment
from New Bedford Harbor which has been homogenized and
carefully assayed for PCBs. Data in Figure 2 show recovery of 1242
from this sample using: (1) hexane alone, (2) hexane and water
(1:1), (3) hexane, water and ethyl ether, (4) ethyl ether and water,
(5) ethyl ether, water and methanol, (6) methanol and hexane (1:1)
0.8 ng 1254
.1x512 sens.
Mln.
10
Figure 1
Field Chromatogram of Arochlor 1245 Extracted from Soil
and (7) water, methanol and hexane (1:4:5). This last combination
appears to give the best recovery. When added to a dry sample in
the order shown, the effect of the water is to wet the sample, thus
permitting extraction of PCB by methanol. The extracted PCB is
partitioned almost exclusively into the hexane from the aqueous
methanol. Final recovery is calculated from initial weight and hex-
ane volume.
QUALITY CONTROL
The recovery of 1242 from the sediment standard in comparison
with a hexane standard of pure 1242 is shown in Figure 3. Although
other peaks are present, it is evident from the three starred peaks
that recovery of the 1242 is almost complete. Results of subsequent
tests by various chemists on the USEPA staff and on the FIT team
range from 80% to 105% recovery of 1242.
AROCHLOR STANDARDS
Several standard Arochlors are shown for purposes of pattern
recognition in Figures 4, 5 and 6. Reproducibility was demon-
strated by making repeat injections of 1016 and 1242 and changing
the output attenuation.
The sensitivity of the method is shown in Figure 7. This test was
an injection of 43 pg of chlordane at a sensitivity setting of 1 x 32.
The baseline noise was still low enough that 5-10 pg could be readily
determined. This figure also illustrates the usefulness of a field
SAMPLING & MONITORING
105
-------
Hexane
Hexane
H20
Hexane
MeOH
Hexane
H20
Et20
4ng 122!
1x512 sens
3ng 1016
Ix[5l2 sens.
4ng 1242
1x512 sens.
Figure 4
Reference Chromatograms of Arochlor 1221, 1016& 1242
4ng 1248
1x512 sens.
0.8 ng
|x 128,sen
1254
Figure 5
Reference Chromatograms of Arochlor 1248 and 1254
Figure 2
Extraction Efficiency of Various Solvent Combinations
method for measuring any other chlorinated compounds of in-
terest.
PRECISION
The choice of 400 mg of soil is obviously arbitrary. It is used in
order to keep the entire cleanup step within a 2 cm3 vial. A test of
replication was done on one field sample contaminated with about
20,000 ppm of 1254.
Three samples of 50, 54 and 54 mg were weighed into separate
vials, extracted and then diluted 1:1000 into hexane in a separate
vial. The three Chromatograms are shown in Figure 8. Two peaks
were quantified to demonstrate how reproducible a measurement
can be, even in a field sample.
QA Sample
1242 Std.
o Contam.
4ng 1260
Ix 512 sens.
Figure 6
Reference Chromatogram of Arochlor 1260
0.43 ng
1x256 sens.
43 pa
x 32 sens.
Figure 3
Rcco\er> Efficiency of Arochlor 1242 from Sediment Standard
Figure 7
Sensitivity of Field Method to Chlordane
106 SAMPLING & MONITORING
-------
FIELD EXPERIENCE
On the first day of field use, the author analyzed 40 soils and
about 10 QC samples in 6 hr. This time period even covered lunch
and 40 min. downtime when the field generator ran out of gasoline.
Most runs were completed in less than 9 min. and many very low
level samples had the run aborted after about 4 min when it was evi-
dent that the second major 1254 peak was almost totally absent.
Concentrations were calculated on the spot from periodic standard
runs and PCB levels ranged from less than 0.2 ppm to 24,000 ppm
of 1254.
CONCLUSIONS
Aside from the obvious savings of analysis time, sample handling
and costly delays when resampling would be required, this field
technique has two key benefits:
•It permits an on-scene cleanup coordinator to make informed
real time decisions on excavation and removal of PCB contam-
inated soil, thus reducing costly second and third trips to remove
material missed in a prior visit.
•It prevents excessive excavation and costly trucking and disposal
of low level contamination by allowing a coordinator to know
exactly when enough high level contamination has been removed
to effect thorough cleanup of a spill or disposal site.
Figure 8
Replication of Field Measurements of Contaminated Soil
SAMPLING & MONITORING
107
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DOWNHOLE SENSING EQUIPMENT FOR HAZARDOUS
WASTE SITE INVESTIGATIONS
WILLIAM M. ADAMS, Ph.D.
STEPHEN W. WHEATCRAFT, Ph.D.
JOHN W. HESS, Ph.D.
Desert Research Institute
University of Nevada System
Las Vegas, Nevada
INTRODUCTION
Subsurface information is required to determine hydrogeologic
conditions of hazardous waste sites, to locate contaminant plumes
and to monitor for leaks from disposal facilities. Available down-
hole sensing instruments were surveyed to determine their potential
use in hazardous waste site investigations. This survey included
traditional geophysical logging equipment and various geochem-
ical sensing equipment for downhole logging and in situ monitor-
ing.
Most downhole logging systems available today were developed
for the petroleum, geothermal or mineral exploration markets. A
limited number of systems have been marketed for groundwater
exploration. The criteria used in the development and evolution of
all those systems are different from those appropriate to hazardous
waste sites, where holes will generally be less than 100 m in depth
and as small as 5 cm in diameter. For example, high temperature
and high pressure requirements are negligible for such shallow
holes. However, the downhole environment could be corrosive.
Traditionally, downhole geophysical instruments have emphasized
the rocks or soil matrix rather than the water. Typically, bore-
holes were open rather than cased with PVC or Teflon.
Hazardous waste site downhole sensing efforts have four objec-
tives:
•To determine lithology, porosity and structure
•To locate zones of saturation
•To identify physical and chemical characteristics of fluids
•To measure groundwater flow velocity and direction
Corresponding to each objective, there are one or more sensing
methods. For each objective, those subsurface methods that are or
will soon be available for holes of greater than 100mm in diameter
are listed in Table 1. The analysis of the data logged to produce
the desired objective information is described by several
authors. '•2'M
Based on professional judgment, four downhole sensors were
chosen for further investigation of their applicability to hazardous
waste site problems. A logging system which could address these
four objectives includes:
•Induction logger
•Natural gamma logger
•Fluid conductivity and temperature logger
•Thermal groundwater flow meter.
Potentially suitable equipment is available today except for the
induction sonde. The other three are presently being evaluated by
the Desert Research Institute.
In this paper, the authors propose draft specifications for a log-
ging system dedicated to holes less than 100m in depth and as small
as 5cm in diameter. These are given first in functional form, then
in terms of existing construction and design standards. This paper
is restricted to consideration of the saturated zone and to solid-
waste sites; spills are excluded. The work described herein is the
first part of a research program that will involve the evaluation of
existing equipment and services by field trials and laboratory study.
Those findings may indicate that additional instrumentation devel-
opment is appropriate.
In order to determine what types of technologies are available
and their suitability for gathering the data required to decide on site
selection and characterization or to design a monitoring network,
the Desert Research Institute has conducted two surveys; one of
the literature and the other of the marketplace.
HAZARDOUS WASTE SITE PROBLEM
Assessment of the real or potential impact of a hazardous waste
site is a problem in three physical dimensions plus time. The pro-
cesses of selecting a site on or in which to place a waste storage
facility and of assessing active or abandoned sites require the hy-
drogeologic characterization of the sites. Information is needed on
stratigraphic succession and facies changes beneath the site. Assess-
ment of existing groundwater contamination requires measurement
of the vertical as well as the horizontal extent of contaminant
plume.
In order to obtain this information in a cost effective manner,
an integrated three-phased approach is used. First, a review of all
available data is conducted. Second, surface and downhole geo-
physical data relating to the site are collected and combined with
lithologic logging and water sampling. Third, the monitoring pro-
gram is designed, including the locations and sampling intervals of
the up and downgradient groundwater monitoring wells and other
subsurface monitoring equipment.
A waste facility is sited on the surface of or in the ground; leach-
ate may move downward and away from the site. Four common
facility types that require monitoring of groundwater in the upper-
most aquifer are landfills, surface impoundments, waste storage
piles and land treatment areas. A facility overview depicting all
four types of disposal facilities is shown in Figure 1. Shown are the
boundaries of the waste management area and the facility, includ-
ing the up and downgradient monitoring wells. All four of these fa-
cility types require the same basic subsurface knowledge to prop-
erly locate the facility and design the groundwater monitoring net-
works. In characterizing the sites, hydrogeological information is
required for each. This information may include the stratigraphy,
the spatial distribution of porosity and permeability, any signifi-
108
GEOHVDROLOGY
-------
c_— .«»«,uiii. U1 ainsuuupiiy, cauon excnange and sorptive capaci-
ties of clay constituents, the distributions of the types of clays and
groundwater flow velocities and gradients.
Once a site has been characterized, a groundwater monitoring
network is designed. The features of the network should depend
upon: (1) the quality of the containment barrier(s), (2) the prob-
able detection time of a leak through the barriers and (3) the prob-
able transit time of a leaking fluid to the facility boundary. For
example, in a landfill having a single liner, a minimal network is
considered to include at least three wells, one in the direction from
which the water in the uppermost aquifer is coming and two in the
direction to which the water is flowing. These are called the up-
gradient (or background) and downgradient wells respectively and
are shown schematically in Figures 1 and 2. Suitable monitoring
instrumentation must be installed in each well and data gathered
and reported as appropriate.
Shown in Figure 3 is a three dimensional cross section below a
single liner landfill indicating the importance of data on vertical
and horizontal permeabilities. Layer Kj is an aquitard separating
the aquifers K,,, K,, Kj, K3 and K,,. The downgradient monitoring
well would have to be designed to sample in the proper zone(s) (in
this case horizontal permeabilities K0 and K4). Completion zones
for the monitoring wells can be determined from lithologic well logs
and geophysical logs. Information on the lithology and fluid chem-
istries is important in determining what chemical parameters to
measure in the monitoring well. Such processes as cation exchange
and mineral precipitation and solution can affect the chemistry of
the leachate reaching the monitoring well.
Upgradlent (Background)
'Groundwater Monitoring Well
Figure 1
Hazardous Waste Facility Overview
Upgradlant
Monitoring Wall
Downgradlant
Monitoring Well
Direction of Groundwater Flow •
Groundwater Flow
Figure 2
Schematic of Typical Landfill with Single Liner (not to scale)
Figure 3
Effects of Permeability Variation on Pollutant Movement
The problems involved in hydrogeologic characterization of
monitoring waste disposal sites require subsurface technical infor-
mation, which may not be readily available. Indeed, the instru-
ments that are available to gather each type of data are not well
known. In particular, the suitability of the existing technology to
provide data appropriate to the field situation described above is
questionable.
OBJECTIVES OF DOWNHOLE SENSING
At present, hazardous waste site borehole sensing has four ob-
jectives:
•To determine the lithology of the strata intersected, the geolog-
ical structure of the strata and the spatial distributions of porosity
and permeability
•To locate the zones of saturation in three dimensions
•To obtain estimates of the physical and chemical characteristics
of the fluids in the rocks
•To measure or estimate the velocity and direction of the ground-
water flow in the uppermost aquifer and to determine the nature
of the water movement
These data are required to determine hydrogeologic conditions
of hazardous waste sites, to locate contaminant plumes and to
design and operate groundwater monitoring programs at waste
sites. The hydrogeologic information is used to define the upper-
most aquifer, determine the groundwater gradients and to deter-
mine the probable contaminant pathways. This information is then
used to locate the up and downgradient monitoring wells, includ-
ing the proper sampling zones.
LITERATURE SURVEY
A wide range of equipment and techniques already exist for geol-
physical and geochemical exploration and investigations. However,
these have been developed for oil, mineral, groundwater or geo-
thermal exploration. Some, such as selecting dam sites or design-
ing foundations for structures, have evolved for engineering work.
To find those publications which might describe suitable pro-
cedures, a computer literature search was conducted on the follow-
ing files: DOE Energy-74-82, NTIS-64-82, Water Resources Ab-
stracts-68-82. Pollution Abstracts-70-82, and Claims/U.S. Patent
Abstracts-? 1-82. (The search statement, in terms of keywords and
connectives, is available from the authors.)
This search identified 953 citations. A scan of the abstracts of
these citations showed that those methods or tools that had been
developed for other purposes are not optimum for collecting data
in a waste site environment. Often, as in the case of oil well tools,
the problem is that the tool diameter is greater than the diameter
of the hole. Similarly, a sonde that is 10 m in length gives very lit-
tle data in a hole that is only 20 m in depth.
GEOHYDROLOGY
109
-------
Tible 1
Downhole Sensing Methods
Objective
Location of Zones of
Saturation
Physical and Chemical
Characteristics of
Fluids
Stratigraphy
and Porosity
Flow and Direction
Subsurface Methods
Electric Log
Temperature log
Neutron log
Gamma-Gamma log
Electric log
Temperature log
Fluid Conductivity log
Spontaneous Potential log
Specific Ion Electrodes
Fiber Optics
D.O., Eh, pH probes
Formation Resistivity log
Induced Polarization log
Natural Gamma log
Spectral Gamma log
Thermal Neutron log
Cross Borehole Radar
Cross Borehole Shear
Resistance log
Acoustic-Transit Time log
Acoustic-Amplitude log
Acoustic-Wave Form log
Neutron log
Induction log
Spontaneous Potential log
Flowmeter
Tracer
Differential Temperature log
Water level
MARKETPLACE SURVE
A survey of the marketplace was conducted to ascertain the
present availability of equipment for subsurface sensing at haz-
ardous waste sites. A letter was sent to some purveyors of geophy-
sical and geochemical equipment or techniques, as chosen from
advertising in such journals as Ground Water or Geophysics.
The results of this survey are presented in Table 2. In the begin-
ning, the expectation was that a data base would be created. Due
to the limited response, the data base has not been created at this
time.
DISCUSSION OF SURVEY FINDINGS
From the 171 letters sent out, there were 21 returns (13%), which
was much smaller than expected. This may indicate that geophysi-
cal equipment manufacturers are not yet aware of the hazardous
waste market. There are about 20,000 hazardous waste sites in the
coterminous United States, each of which will most likely have
some type of monitoring program.
Another feature that is evident from Table 2 is the variety of
responses. That is, very few vendors are competing in exactly the
same service or equipment capability. There are often differences
in dimensions, accuracy, costs or precision that constitute signifi-
cant variations among the vendors.
DRAFT SPECIFICATIONS OF INSTRUMENTS
Functionally, the need is for measurements that can contribute
to achieving the objectives mentioned earlier. Specifically, sug-
gested design parameters for logging boreholes to monitor waste
sites or to evaluate prospective sites are given in Table 3. These
design parameters are only draft specifications; as experience is
obtained in using logging equipment for exploring or monitoring
hazardous waste sites, modification will be appropriate.
Table 2
Manufactures of Downhole Equipment
ACOUSTICAL
Sh«arw
)D Vtfoiiiy
Sonic U>f
Liin* Spaced Same
~~SoftT7 "SjndV
"~Sh**r^i7t "V* focTtV
" v." ft7
" u* 11 ~<7iT«rc~~fooT~
IS.I,
_JJ
98.t "
ik >:
U >M
5oT«"
IM
-ft"
110
GEOHYDROLOGY
-------
Table 2 (continued)
S - sonde diameter (on)
D - cable length (m)
U - unknown
X - available
1 1
CO
a.
""
v o> z n
=' 3 S g
i « s"!
r
»
i-
r-
O O O
o o A
-1 -- X
O "- X
n" 5"
o
rt
*
0 S
3 n
• 3
n
*
1 s i
1 I s
T • 1 • °
\ i "' !
0. • O
5* ?.
" *
— 3
* ?.
a. !*
£•
o
u>
c
K
n
H
f
•
ELECTRICAL
Focused
Sonde
•TR
ol.terlog
inticy Log ~
Self Potent tat
32
279
40
200
50.8
254
1.5
254
"54 54~
Fluid Resistivity
41
U
29
254
120
U
NUCLEAR
Natural Gai
78
762
Gamma Gamma Dens i ty 60
U
Dual Gamma Gaoaoa 60
Density U
Gamma Ray Spectrometer 50.8
U
Natural Canna Ray
Spectrometer
(Gamma) U U
Dens ity Boreho le 1 14
Compensated Lagging U
Neutron-Neutron 35
Porosity U
Dual Thermal Neutron 63
U
Neutron 92 U
U U
Epic he row 1 Neutron 92
Logging U
Log
Sidevill Neutron
Poroaity Log
Depth Probe 84
92
U
50 U 43
U
50
43
U
43
U
111
U
FLOW AND DIMENSION
Caliper
60
U
78
762
102
127
32
254
Caliper
From the foregoing surveys, from experience and from atten-
dance at numerous exhibits associated with professional confer-
ences, the authors are aware that equipment, especially borehole
instruments, usually requires interconnections between units in
order to achieve flexibility of system application. Standardiza-
tion of interconnections (i.e., a policy of "plug compatibility")
would enhance flexibility. Already there is some standardization in
the industry, as in the use of the NIMS specifications for sizes
of console units. Standardization of the interconnections would
also provide a significant benefit to the consumer, viz., he would
have the ability to interchange parts between manufacturers. For
example, any logging system uses a sensor, a cable, a processing-
storage unit and a display unit. The consumer would benefit from
being able to interconnect units purchased from various vendors.
STANDARDIZATION OF DISPLAY FORMAT
In the oil industry, the well logging is usually provided by a third-
party support company. Besides the techical specialization, this
condition has also evolved because of the licensing requirements
for handling radioactive materials such as those used in some log-
ging sondes. There are conditions which may cause a similar devel-
opment in the logging and monitoring of hazardous waste sites.
For example, it is reasonable to require quality assurance of the
sampling. With more than one person using the document (the
logs), a standardized format is desirable.
Surprisingly, a Standard Hydrocarbon Well Log Form has only
recently been published by the Society of Professional Well Log
Analysts.' Standards for calibration of instruments and processing
GEOHYDROLOGY
111
-------
Table 2 (continued)
1 > i i
» C 3
1 s j
~
1 1
9
*
o
I
o i x — _
3 » • n
n "" ** c
3-
3
i
A
*
2 : I
I I
w*
f
V
•
•<
SO.8
127
130
UOO
Every effort has been made to assure accuracy of these data; however, the
jjthors and sponsors recommend confirmation with the respective manufacturers
disapproval or approval.
Table 3
Draft Specifications for Downhole Logging
POWER: Battery operated: Minimum of 8 hr continuously. Battery-
charger operating from 115 VAC, 230 VAC and/or 12 VAC [for field
operation.]
WEIGHT: Total less than 200 kg. Each piece less than 25 kg [for porta-
bility and shipping). Each piece packed for shipping less than 30 kg [so
can travel as excess baggage]. [Each area or well accessible by vehicle.]
SIZE: To fit, when assembled, in rear of small 4WD vehicle [for min-
imizing set-up at well site].
CABLE: Length to 120 m [to allow vehicle to be a distance from the well
head). Seven conductor.
DEPTH INFORMATION: Mean precision less than 2 cm; mean accuracy
less than 4 cm.
DATA LOG RELATIVE TO DEPTH: Mean deviation of less than 4 cm;
standard deviation of the deviation less than 8 cm.
TEMPERATURE RANGE: Operating 0 to 30°C. Shipping or storage:
- 25 °C to + 55 rC.
SONDE DIAMETER: To run in a smooth casing of 5 cm ID and having
meximum of ten-degree gradual change in slope over 10m.
SONDE LENGTH: Able to measure data to within 1 m of the bottom of
the hole.
WINCH: Optional power-drive; capable of being manually operated [for
emergency break-down situations).
SONDE PRESSURE: Sonde pressure rated to 100 m minimum.
ELEVATION: Equipment to operate between -75m and -I-3,000m.
PANEL DISPLAYS: Battery Voltage (optional). Depth (optional). Ver-
tical Velocity of Sonde (optional). Data (analog and/or digital). Sonde
Temperature (optional). Sonde Pressure (optional). Time (analog or dig-
ital) Month, Day, Hour, Minute, Second or Julian.
MANUALS: Operator's Manual. Maintenance Manual. Schematics [to
assist in field repairing]. Parts List.
SERVICE AND MAINTENANCE: Third-party availability.
GEOHYDROLOGY
-------
of samples of cuttings had been published earlier.6'7 A group com-
posed of representatives from manufacturers and users or potential
users should propose similar standards for the work involved in ex-
ploring for waste sites and for monitoring existing waste sites.
SUMMARY
Subsurface information is required to characterize sites, to locate
contaminant plumes and to monitor for leaks from disposal facil-
ities. From two surveys, one of the technical and scientific litera-
ture, including patents, and the other of the brochures and pamph-
lets provided by organizations in the logging business, it appears
that problems of the hazardous waste industry have not yet ade-
quately been addressed by the logging industry. Three out of four
downhole sensor types identified as applicable are available today.
The fourth, an induction logger, is not available for use in shallow,
small diameter holes. Presently, the Desert Research Institute is
testing and evaluating the thermal flow meter, natural gamma log-
ger and the fluid temperature and conductivity logger. A suitable
induction logger is under development by several manufacturers.
Various subsurface sensing equipment and techniques can
address the need for such information gathered from boreholes less
than 100 m in depth and as small as 5 cm in diameter. At present,
a limited number of such systems applicable to hazardous waste
sites exist. The vendors of logging equipment do not appear to be
following a "plug-compatible" policy. Calibration of instruments
and software must be standardized as the first step toward intro-
ducing quality assurance into geophysical exploration and geo-
physical monitoring. Such quality assurance has already evolved,
for instance, in water quality analysis.
ACKNOWLEDGEMENTS
The survey work described in this paper is being performed
under Cooperative Agreement No. CR810051-01-0 between the
Desert Research Institute and the USEPA. Appreciation is ex-
pressed to Leslie G. McMillion, the Project Officer, for his direc-
tion of the project and for his significant contribution to the prepa-
ration of this paper.
REFERENCES
1. Asquith, G.B., "Log Analysis by Microcomputer," PennWell Books,
Tulsa.Ok.,1980.
2. Merkel, R.H., "Well Log Formation Evaluation," Course Note Series
#14, AAPO, Tulsa, OK.
3. Asquith, O. and Gibson, C., "Basic Well Log Analysis for Geolo-
gists," AAPG Methods in Exploration Series, 1982.
4. Hilchie, D.W., "Applied Openhole Log Interpretation," published by
D.W. Hilchie, Inc., Box 785, Golden, Co., 1982.
5. S.P.W.L.A. Standards Committee, 1982, "Standard Hydrocarbon
Well Log Form," Transactions, Twenty-Third Annual Logging Sym-
posium, Volume II, Corpus Christi, Tx., 1982.
6. S.P.W.L.A. Standards Committee, "Standard No. 2 on Instrument
Calibration," Society of Professional Well Log Analysts, First Edition,
June 1981.
7. S.P.W.L.A. Standards Committee, "Standard No. 2 on Cuttings
Samples Processing," Society of Professional Well Log Analysts,
First Edition, June 1981.
OEOHYDROLOGY
113
-------
GROUNDWATER SYSTEMS AND HAZARDOUS WASTE
SITES—A BASIC CONCEPTUAL FRAMEWORK
BO YD N. POSSIN
Ecology and Environment, Inc.
Buffalo, New York
INTRODUCTION
Decision makers who must deal with the relative seriousness of
the groundwater contamination hazard posed by individual haz-
ardous waste sites often find themselves at a loss as to how to make
such judgments. This is especially true during those long periods of
time between the initial discovery that a given site might be posing
a groundwater threat and the eventual development of detailed,
site-specific hydrogeological data.
Attempts are often made to fill these knowledge gaps with avail-
able information pertaining to the presence and orientation of the
underlying aquifers or the speculated distribution of subsurface
permeabilities, e.g., the too-often heard declaration, "Ground-
water follows the path of least resistance." In other cases, the
lack of field data is accepted as a lack of any data.
In the USEPA's Hazard Ranking System' (HRS), for example,
the mere presence of a contaminant in concentrations above back-
ground in groundwater within a mile or two of any public well in
any direction, is sufficient to markedly increase the groundwater
subscore. There is no way to account for the direction of ground-
water contaminant migration within the HRS. It is the author's
opinion that this approach can, and should, be refined.
A FUNDAMENTAL HYDROGEOLOGICAL CONCEPT—
THE GROUNDWATER FLOW SYSTEM
Over the past 20 years, theoretical hydrogeological research
has provided a very useful, regime-oriented context within which
to conceptualize groundwater flow.2'3 That concept is known as the
Groundwater Flow System (GWFS).
Groundwater is analogous to, and in fact inseparable from, sur-
face water. A familiar concept is the surface water watershed which
consists of a drainage network of stream channels bounded by a
topographic surface water divide and having one outlet, the main
stream channel, at the lower end of the watershed. Not nearly so
familiar, however, is the concept that each surface water watershed
has associated with it a groundwater watershed, more properly re-
ferred to as a shallow, or local, GWFS. All of a shallow GWFS's
water enters the ground (recharges) in the watershed and eventually
moves into (discharges) the surface stream draining the watershed.
Thus, underlying every perennially flowing stream's watershed is a
shallow GWFS.
The lateral boundaries of a shallow GWFS are generally con-
tiguous with the overlying watershed's surface water divide. The
upper boundary of a shallow GWFS is the water table surface (a
surface beneath which all interconnected soil* and rock pores are
•In this paper, the term "soil" is used in (he engineering ralhcr than the agricultural sense and
refers to all earth materials that are not rock; i.e . all unconsolidated materials are referred to
»S "soil "
filled with water) and the lower boundary is a surface below which
groundwater is moving in a direction which will cause it to dis-
charge at a point outside the surface water watershed.
The existence of a "shallow" GWFS means that there must also
be a "deep" GWFS. Figure 1 shows a cross section, perpendicular
to the main direction of flow, through three perennial streams, a
main stream and two of its tributaries. The water table surface is a
subdued replica of the land surface. The degree of this replication
is largely a function of climate, specifically, the amount of precip-
itation available for groundwater recharge. Each stream is under-
lain by its own shallow GWFS. However, some of the water
entering the ground in the highest uplands, the regional recharge
areas, flows underneath the shallow, local flow systems and moves
directly to the main stream. This is an example of a deep or regional
GWFS. The main stem serves not only as a local discharge point,
but also as a regional discharge point.
On a volume per unit time basis, most of the water which moves
through the ground moves in shallow GWFSs. As a result, shallow
GWFSs sustain streamflow and, thus, background water quality in
flowing streams during non-precipitation periods. Shallow GWFSs
similarly provide water to and are important in controlling the
quality of inland freshwater lakes. Much of the groundwater
withdrawn for human consumption comes from shallow GWFSs.
Shallow GWFSs are relatively easy to contaminate by surface
dumping of hazardous substances because their upper surface, the
water table, is commonly separated from the land surface by only
a few feet of porous, unsaturated soil or rock. However, the rela-
tively rapid rate of groundwater flow moving through them can
result in self-cleaning periods as short as a few years.
GWFS SENSITIVITY TO CONTAMINATION
The deep GWFS has a much larger cross sectional area than all
the overlying shallow GWFSs combined (Figure 1). In fact, in
terms of the total volume of the earth's groundwater, most ground-
water is contained within deep rather than shallow GWFSs.
However, it has just been stated that most of the water moving
through the ground moves in shallow GWFSs. Is this a contra-
diction? It is not because the water in deep GWFSs moves much
more slowly than water in shallow GWFSs. This occurs because
the ratio of recharge zone surface area to total system volume is
much smaller for deep systems than for shallow systems. There-
fore, the amount of water entering a deep GWFS is much smaller
relative to its size than the amount of water entering a shallow
GWFS.
Unfortunately, the resultant slow flow rates mean that deep
GWFSs, once contaminated, are not self-cleaning in terms of
human lifespans. Although their relatively small recharge areas
114
GEOHYDROLOGY
-------
RECHARGE DKCMAIVGI
»«« ARE.
-SHALLOW FLOW-
^SYSTEMS ~
TWO
LOCAL REGIONAL
DISCHARGE RECHARGE
IEA AREAS
Figure 1
Typical Groundwater Flow System Configuration
help protect them from contamination, they are still vulnerable
because they are often penetrated by wells which can greatly alter
the GWFS configurations by drawing in contaminated waters
from overlying shallow GWFSs which can serve as potential ver-
tical conduits for contaminants if improperly constructed.
THE AQUIFER
The reader may have noticed that the discussion has proceeded
thus far without reference to that familiar term "aquifer," (which
is another fundamental hydrogeological concept) and its com-
panion, "aquitard." This has been done deliberately, as a matter
of emphasis. Whether or not a particular geological formation is
an aquifer or an aquitard, merely describes the relative ease with
which water will enter a well which penetrates that formation.
Aquifers are not water pipes—their various orientations do not
exercise the primary control on which way groundwaters move.
As shown in Figure 1, the primary control on groundwater move-
ment is topography, not geology. This is a critical point in under-
standing the application of hydrogeological concepts to hazardous
waste site contamination. Groundwater contamination is a dy-
namic problem, requiring an understanding of which way and at
what speed the groundwater moves. Fundamentally, groundwater
movement is not defined by aquifer/aquitard orientation, but
rather by GWFS orientation.
HOW TO APPLY GWFS CONCEPTS
To determine the potential adverse impact a hazardous waste
site has on the surrounding area's groundwater resources, the pri-
mary task is to ascertain the site's location in relation to the under-
lying GWFS. To do this, first locate the site on the appropriate
USGS topographic quadrangle map. Determine the watershed
configuration of the perennially flowing stream which drains the
area occupied by the site. The zone that is most susceptible to
groundwater contamination from the site is the area between the
site and the flowing stream.
If the site is located relatively close to the stream, as com-
pared to the watershed boundaries, the potential for widespread
contamination is less. There are two reasons for this. First, the
potential contaminant flow path is relatively short. Second,
groundwater flow in GWFS discharge areas is upward (Figure
1). This upward component of movement precludes the possibil-
ity of any downward migration of contaminants dissolved in the
groundwater.
Conversely, if the site is located closer to the watershed boun-
dary, the potential for widespread groundwater contamination is
much greater. The groundwater flow path is long and the vertical
component of movement is downward. If the site is located on a
major upland separating major watersheds, it is even possible that
contamination of a deep GWFS may occur.
Another critical point to note is that flowing streams con-
stitute a hydraulic boundary. Normally, contaminants which orig-
inate in a given GWFS migrate to the downgradient discharge
zone, but no further. Therefore, contaminants originating on one
side of a flowing stream's watershed do not have the potential for
affecting groundwater quality on the other side of the watershed.
VARIATIONS
There are two important variables which can modify the gen-
eralized concept displayed on Figure 1: one is natural and one is
man-caused. The natural variable is climate. Infiltrating precipi-
tation is the source of groundwater for most GWFSs. In rela-
tively arid climates, infiltration is very low and the degree to
which the water table replicates the configuration of the land
surface is markedly reduced. The effect of this is that, in arid reg-
ions, GWFSs are much larger in areal extent than in humid reg-
ions and the differentiation of flow into layered shallow and deep
GWFSs is less common. Nevertheless, the general rule still ob-
tains: groundwater flows toward the nearest perennially flowing
stream.*
The major man-caused variable is groundwater pumpage. A
pumping well is, in essence, a new groundwater discharge zone.
If it is a high-yield well, or if it is one of a cluster of lower yield
wells, it can dramatically change natural GWFS configurations.
For example, a pumping well located on one side of a flowing
stream can conceivably induce contaminants to cross beneath the
stream from the other side, thus creating an exception to the gen-
eral rule that flowing streams act as a hydraulic barrier to such
movement.
Another more dramatic modification occurs when many wells
are installed and pumped such as in the Chicago metropolitan
area." A hundred years ago all deep wells drilled in Chicago were
flowing artesian wells, indicating strong regional discharge area
conditions. With such a strong potential upward hydraulic pres-
sure, it would have been virtually impossible to have contam-
inated the deep aquifers from surface sources at that time.
However, over the years, so many wells have been installed and
pumped in and around Chicago, that the artesian conditions have
been completely reversed and the potential for groundwater (and
contaminant) movement is now downward.
None of these problems need be overwhelming when apply-
ing GWFS theory to preliminarily evaluate the potential ground-
water contamination problems that might be caused by a given
site.
The information needed is almost always available. Topographic
and climatological data are available for the entire nation. Ground-
water pumping information for major wells, including locations
and discharge rates, is almost always available in state or local
government files. There are few, if any, parts of the United States
where an experienced hydrogeologist or water resources engineer
cannot apply GWFS theory and quickly evaluate the potential
scope of a groundwater contamination threat posed by any given
hazardous waste site.
SUMMARY
An understanding of fundamental GWFS concepts leads to the
following conclusions:
•In order to determine the eventual destination of contaminants
carried by groundwater, it is imperative that the location of the
contaminant source relative to the underlying GWFS be under-
stood.
•In order to protect drinking water aquifers from surface-gen-
erated contamination, it is necessary to identify the configura-
tion of the GWFSs that flow through them.
•Since GWFS configuration is primarily controlled by topography,
climate and man-made pumpage, and since detailed topo-
*In arid areas it is important to distinguish the source of streamflow. If it is high mountain snow-
melt or reservoir storage, then the stream is not a groundwater discharge zone and ground-
water does not flow toward it.
GEOHYDROLOGY
115
-------
graphical climatological and pumpage information is readily
available for most areas, it is almost always possible that the
potential nature, scope and severity of groundwater problems
can be understood by decision makers well before detailed field
investigations are performed.
Groundwater movement is not mysterious. The principles gov-
erning the manner in which groundwater transports contaminants
are fairly well understood. This does not mean that groundwater
contamination problems caused by hazardous waste sites and other
sources are not complex. They are, but the complexities do not
arise when reaching an understanding of the ways in which the
contaminants have dispersed; they arise when attempts are made
to remove, neutralize or isolate the contaminants from the ground-
water.
These problems must be distinguished, however, from the prob-
lems of initially identifying the scope of the contamination. Any-
one well versed in GWFS theory and with a modicum of "real
world" experience in the field, is well equipped to make timely,
useful evaluations of groundwater contamination potential using
nothing more than commonly available information.
ACKNOWLEDGEMENT
The author is indebted to Dr. David A. Stephenson of Water
Resources Associates, Inc., formerly of the University of Wiscon-
sin, for instilling in him GWFS theory at a time when it could
not be found in the textbooks.
REFERENCES
1. MITRE Corporation, Uncontrolled Hazardous Waste Site Ranking
System—A. Users Manual, prepared for the USEPA, June 1982.
2. Toth, J., "A Theoretical Analysis of Groundwater Flow in Small
Drainage Basins," J. of Geophysical Research, 68, 1963, 4795-4812.
3. Freeze, R.A. and Witherspoon, P.A., "Theoretical Analysis of
Regional Groundwater Flow. 2. Effect of Water-Table Configuration
and Subsurface Permeability Variation," Water Resources Res., 1,
1965,563-576.
4. Sassman, R.T., Benson, J.S., Mende, J.S., Gangler, N.F. and Col-
vin, V.M., Water-Level Decline and Pumpage in Deep Wells in the
Chicago Region, 1971-1975, Circular 125, Illinois State Water Survey,
Urbana.IL., 1977.
116
GEOHYDROLOGY
-------
IMPROVED METHODS OF
FLOW SYSTEM CHARACTERIZATION
JOSEPH L. DEVARY, Ph.D.
RONALD SCHALLA
Battelle, Pacific Northwest Division
Richland, Washington
INTRODUCTION
Because hydrologic characterization of hazardous waste sites is
difficult and expensive, it is important to use field data efficiently
in modeling subsurface flow and transport. Conventional ap-
proaches to hydrologic data processing (e.g., hand-contoured
maps), are often too subjective to provide the most efficient and ac-
curate use of the data. Improved methods to characterize flow
systems can help private firms and government agencies control
costs and achieve better results.
LIQUID TRENCHES
LANDFILLS
METERS 0 300
FEET 0 900
Figure 1
Location of Potential Hazardous Waste Disposal Sites at the Site
In this report, the authors discuss the application of a
geostatistical technique known as kriging and an elementary
hydraulic conductivity inverse technique to better characterize the
flow system for hazardous-waste sites. These techniques have been
successfully applied to a remedial action project for the United
States Army Toxic and Hazardous Materials Agency (USA-
THAMA).
The site in question is a highly industrialized facility located in
the southeastern United States. During the last five years, the site
has been investigated with regard to surface water and potential
groundwater pollution from industrial wastes. Following a series of
studies in 1979 through 1982, it was determined that hazardous
waste constituents, particularly volatile chlorinated hydrocarbons,
had entered the groundwater and appeared to be migrating from
two former disposal areas. A map of the site indicating the major
disposal areas which may be probably sources of contamination is
shown in Figure 1.
The following plan was developed to evaluate the hazardous
waste migration problem:
•Characterize both the site and regional hydrologic flow systems
•Evaluate the extent of groundwater contamination
•Develop numerical simulation models for groundwater flow and
transport
•Design effective remedial action plans based on evaluation of
alternatives using the transport models
In this paper, the authors primarily report on the site
characterization activities (first two items) which are used to
develop the numerical models for flow and transport. The evalua-
tion of sophisticated remedial action measures (e.g., dewatering
wells, emplacement of impermeable barriers, etc.) requires fully
calibrated numerical models.
GEOHYDROLOGY OF THE DEPOT
The site lies within the Valley and Ridge Province of the Ap-
palachian Highlands with elevations from approximately 600 to
1000 ft. The largest portion of the site is underlain by silicious
dolomite, limestone and shale of Cambrian to Ordovician age. Well
developed fractures, sink holes and solution channels typical of
karstic terrain have been found in these deposits.
The current conceptualization of the local groundwater system
consists of four layers:
•Upper clay-rich semi-confining layer
•Sand and/or gravel aquifer
•Fractured solution-channeled bedrock aquifer
•Lower confining zone of unweathered bedrock
GEOHYDROLOGY
117
-------
KRIGING AND GEOSTAT1STICS
Geostatistics and kriging are statistical techniques that can be used
to estimate a surface from spatially-distributed data. They were
developed in the early 1960s primarily by the French mathematician
George Matheron to solve mining estimation problems. In the last
several years, hydrologists and ground water modelers have utilized
geostatistical techniques to analyze hydrologic field data8'9'12'25.
Kriging is a statistically based interpolator of irregularly spaced
data. To krige an estimate of a variable (e.g., potentiometric head)
at a particular location (xj where no field measurement is
available, the following steps are required:
•Select the boreholes (with data) nearest the location to be esti-
mated; typically, between 8 and 16 neighboring boreholes are
used in the interpolation procedure. Let HI, H2-... Hn denote
those measured values (Figure 2).
•Determine the weights (i.e., the kriging weights) to be used for
the averaging process; the kriging weights depend on the drift
(overall trend) of the data and the covariance (variogram or gen-
eralized covariance) that corresponds to data fluctuations super-
imposed on the drift. Let X,, X2, .... Xn denote the kriging weights.
•Derive the kriged estimate by calculating a weighted average of the
nearest-neighbor values using the kriging weights; the kriged
estimate at x0 is given by:
H*(x0)
(1)
1=1
\
/
•\
* = xi
O = x0
Figure 2
Kriging Estimate at Point X0
•The variance corresponding to the estimation error is cal-
culated using the kriging weights and covariance:
KID)
(2)
t-1
i-1 j-1
where KJJ is the generalized covariance evaluated at the ith and jth
well borehole locations.
The kriging weights [\] minimize the error variance V2 [H*(\o
of Equation (2) subject to the unbiased condition
E[H«(Xo) - H(xo)] = 0
The covariance expression K of Equation (2) is the generalized
covariance of an intrinsic random function."
A full discussion of kriging theory, including drift and gener-
alized covariance estimation, may be found in several literature rc-
A STREAMTUBE HYDRAULIC
CONDUCTIVITY INVERSE TECHNIQUE
To accurately simulate contaminant transport, it is necessary to
estimate the Darcian velocity field. Potentiometric head data are
typically plentiful and accurate; kriged potentiometric surfaces
based upon head measurements are generally realistic interpreta-
tions of the flow system. Unfortunately, hydraulic conductivity
measurements that are derived from pump tests often exhibit
tremendous variability with very little spatial correlation with
observed hydraulic gradients. Significant errors in calculated
hydraulic conductivity usually result from media heterogeneities
and the fact that pump tests do not usually stress the system over a
large enough area to be truly representative of macroscale flow.
Researchers have resorted to "inverse techniques" to infer
realistic hydraulic conductivity distributions from available poten-
tiometric head and hydraulic conductivity data.3'5-14'20'22-24'26-29
The inverse technique which we have used was designed by
Nelson20-21, Cearlock et al.2 and Rice26 and involves scaling a
known hydraulic conductivity value along a streamtube according
to the convergence or divergency of flow. The approach requires a
digitized potentiometric head surface to generate a flow net and a
known hydraulic conductivity value for each streamtube. This ap-
proach is ideal for preliminary site characterization activities
because a numerical groundwater flow model is not required.
FLOW SYSTEM CHARACTERIZATION
As previously discussed, the groundwater sources for the region
encompassing the site were grouped into four layers: (1) an upper
semi-confining layer (shallow system), (2) sand/gravel, (3) frac-
tured bedrock aquifers (deep system) and (4) a lower confining
layer. The groundwater flow and transport activities involved
calibrating a three dimensional finite-element model to simulate
flow in the upper three layers. The geostatistical activities were con-
centrated in the deep aquifer where the contamination was most
widespread, and, therefore, the majority of monitoring wells (50-
deep vs. 24-shallow as of April 1983) were bored into this deep
unit. Although the authors did krige a realistic potentiometric sur-
face for the shallow system, only the work on the deep unit will be
discussed.
Locations for wells bored into the deep hydrostratagraphic unit
(50 wells) are shown in Figure 3 and Figure 4 is a hand-drawn con-
tour map of potentiometric head (Apr. 1982) as interpreted by the
project hydrogeologist. The potentiometric surface generally con-
forms to the topography with a convergence of flow along the
eastern Depot boundary. Geostatistical data analysis techniques
were applied to evaluate the hand-interpreted potentiometric sur-
face and help select additional well locations for the next phase of
drilling.
First the validity of the Apr. 1982 potentiometric data were
checked. This involved kriged estimates of potentiometric head at
existing well locations using head measurements from surrounding
wells. Six data errors were discussed that could be attributed to
transcription errors and incorrectly surveyed well locations. Three
wells were discovered that were initially assigned to the wrong
hydrostratigraphic unit.
A contour plot of the kriged potentiometric surface based upon
the Apr. 1982 measured head data is shown in Figure 3. The hand-
interpreted surface (Figure 4) and the kriged surface (Figure 5) have
the same general southeasterly flow characteristics. However, the
two surfaces do not agree along the southwestern and eastern site
boundaries. Because head data did not exist in these two regions,
the kriged surface could not match the hand-interpreted version.
The standard deviation of the kriging error is approximately 1 .Om
along the southwestern and eastern site boundaries, which shows
that the kriged and hand-interpreted surfaces are significantly dif-
ferent in these regions (the differences are greater than 3 x sigma =
3.0m).
Based on this evaluation, 10 new wells were screened into the
deep aquifer to more fully characterize the flow system (Figure 6).
118
GEOHYDROLOGY
-------
a
y
• OLD WELLS
METERS 0 300
FEET 0 900
Figure 3
Deep Unit Well Locations (April 1982)
METERS 0 300
FEET 0 900
METERS 0 300
FEET 0 900
Figure 4
Hand-Drawn Potentiometric Contour Map for the
Deep Unit (April 1982)
Figure 5
Kriged Potentiometric Surface for the Deep Unit (April 1982)
The well locations were based upon those regions where:
•The kriged surface differed most significantly from the hand-
interpreted surface
•The kriging uncertainty was largest
•The contaminant plume needed to be more accurately character-
ized.
Unfortunately, it was not possible to drill a new well off-site to
verify the existence of a postulated high permeability flow channel
along the eastern boundary of the site.
A time-equivalent set of potentiometric head measurements were
collected in Mar. 1983, including the 10 new wells of the deep
stratigraphic unit (Figure 6). Differences between the Apr. 1982
(Figure 5) and Mar. 1983 (Figure 7) kriged potentiometric surfaces
are discussed below.
•The Mar. 1983 kriged surface was significantly smoother and
more regular in the northwestern region of the site than the Apr.
1982 surface. This resulted from reclassifying several wells which
were originally thought to be cased in the deep stratigraphic unit.
•The flow channel east of the site boundary was more clearly de-
lineated in the Mar. 1983 kriged surface. The inclusion of a re-
cently discovered offpost well (192 m), located in the deep unit
approximately one-half mile east of the site, causes the converg-
ence of streamlines.
Note that the inclusion of two additional well values in the
southwestern corner of the site to the Mar. 1983 data has not ap-
preciably changed the flow pathways. These data confirm that flow
in the deep stratigraphic unit is actually under a ridge across the
southern site boundary and is not confined to the installation. This
occurs because the bedrock stratigraphic layer does not conform to
the surface topography. This last point is important to the design of
a remedial action plan because contaminant sources are located in
the southwestern corner of the site (Figure 1).
GEOHYDROLOGY
119
-------
!. o
Q
y
a -.•• '
V- ,' .
• OLD WELLS
o NEW WELLS
METERS 0 300
FEET 0 900
Figure 6
New Well Locations for the Deep Stratigraphic Unit
Figure 7
Contour Plot of the Kriged Potentiometric Surface (March 1983)
120 GEOHYDROLOGY
Figure 8
Flownet of Deep Stratigraphic Unit Based on
Kriged Potentiometric Surface (March 1983)
Figure 9
Transmissivity Surface Utilizing Measured Data (mVday)
-------
The flow-net that was derived from the Mar. 1983 kriged poten-
tiometric surface for the deep aquifer is shown in Figure 8. The
contour plotting and streamline generation routines of the VTT
(Variable Thickness Transient) ground water flow code' were used
to produce the flow-net. Notice that the streamlines converge into a
flow channel east of the site boundary. The exact placement of this
flow channel is still uncertain because head data from wells east of
the channel does not exist.
The next step in system characterization was to determine a
hydraulic conductivity distribution that would conform to the
flow-net of Figure 8. Figure 9 is a kriged contour plot of the
transmissivity data that had been derived from pump tests. The
transmissivity data showed over three orders of magnitude of
variability (range = 0.01-550 mVday) with very little correlation
between transmissivity values and the flow-net. To be physically
realistic (conserve flow), transmissivity values must be high in
regions of low hydraulic gradient and low in regions of high
hydraulic gradient.
To remedy the situation, the streamtube hydraulic conductivity
inverse technique was applied to the kriged flow-net of Figure 8.
Observed transmissivity values in the 10-35 mVday range were used
as initial values for six streamtube analyses for the region. No
recharge or discharge was assumed along the streamtubes, and a
uniform depth for the deep stratigraphic unit was specified. The in-
ferred transmissivities along these six streamtubes were statistically
interpolated (kriged) to the entire region (Figure 10). The hydraulic
conductivity distribution for the deep aquifer was then derived
from the inferred transmissivity surface by dividing the
transmissivity values by the aquifer thickness.
This inferred hydraulic conductivity surface served as the basis
for the first simulation runs of three-dimensional groundwater
flow. Figure 11 is the predicted potentiometric head for the deep
stratigraphic unit utilizing the inferred hydraulic conductivity
distribution for the deep unit and regional determinations of boun-
dary flux, recharge and hydraulic conductivity of the shallow
hydrostratigraphic unit. The accuracy of Figure 11 demonstrates
that the use of geostatistical techniques to derive the flow-net and
an elementary streamtube inverse technique to determine the
hydraulic conductivity distribution enabled better calibration of the
three-dimensional flow model for the site.
As an epilogue, a second phase of drilling which was completed
in June 1983 discovered a zone of high transmissivity along the
eastern site boundary. Returns of gravels up to 3 in. in diameter
were obtained from the 4 in. test hole, thus indicating a zone of
very high hydraulic conductivity for the postulated flow channel.
This reinforces the inferred transmissivity distribution of Figure 11
and perhaps shows that the flow channel is closer to the eastern site
boundary than expected.
CONCLUSIONS
The important benefits that kriging offers for processing
hydrologic data, as exemplified by the current study, are:
•Objectively identifying the need for additional field measurements
•Selecting optimal well locations for defining the flow system
•Determining the value of subjective inferences made by hydro-
geologists
•Establishing data validity
•Producing "best fit" contour plots from irregularly spaced field
measurements
•Reducing the time and cost required to update computer simula-
tions of surfaces as new data are acquired
•Reducing data uncertainty to acceptable levels
Figure 10
Inferred Transmissivity Distribution Using the
Streamtube Inverse Technique
Figure 11
Predicted Potentiometric Surface Using Three-
Dimensional Flow Model
GEOHYDROLOGY
121
-------
Furthermore, by using inverse techniques in conjunction with the
kriged potentiometric surface and available hydraulic conductivity
data, a mass-conserving flow system is created that conforms to
measured Held data.
REFERENCES
1. Bond, F.W., el a/., "Variable Thickness Transient Groundwater Flow
Model-User's Manual." EPRI CS-2011 Project 1406-1, Prepared for
Electrical Power Research Institute by Battelle, Pacific Northwest
Laboratories, Richland, Washington, 1981.
2. Cearlock, D.B., Ktpp, K.L. and Friedrichs, D.R., "The Transmis-
sivity Iterative Calculation Routine—Theory and Numerical Imple-
mentation." BNWL-1706, Pacific Northwest Laboratory, Richland,
Washington, 1972.
3. Chavent, G., Dupuy, M and Lemmonier, P., "History matching by
use of optimal control theory." Soc. Petrol. Engin. J. 15, 1975, 74-86.
4. Chiles, J.P., "Geostatistique des Phenomenes Non Stationnaires."
These de Docteur-Ingeniur, University de Nancy, Nancy, France, 1977.
5. Cooley, R.L., "A Method of estimating parameters and assessing
reliability for models of steady state ground-water flow." 1. Theory
and numerical procedures, Water Research, 13, 1977, 318-324.
6. Delfiner, P., "Linear estimation of non-stationary phenomena,"
In Advance Geostatistics in the Mining Industry, Reidel, Dordrecht,
Holland, 1975, 49-60.
7. Delfiner, P. and Chiles, J.P., "Conditional simulations: A new Monte
Carlo approach to probabilistic evaluation of hydrocarbon in
place," Ecole des Mines de Paris, Fontainbleu, France, 1978.
9. Devary, J.L. and Doctor, P.G., "Pore velocity estimation uncertain-
ties," Water Resources., 18, 1982, 1157-1164.
10. Devary, J.L., "Permian Potentiometric Analysis," PNL-Pacific
Northwest Laboratory, Richland, Washington, 1983.
11. Freeze, F.A. and Cherry, J.A., Ground-water, Prentice-Hall, Inc.,
Englewood Cliffs, New Jersey, 1979.
12. Gambolati, G. and Volpi, G., "Groundwater contour mapping in
Venice by stochastic interpolators. 1. Theory," Water Resources
Res. 15, 1979, 281-290.
13. Gelb, A., Applied Optimal Estimation, M.I.T. Press, Cambridge,
Massachusetts, 1979.
14. Marsily, de, G., "De 1, identification des systemes hydrogeologiques,
Tome I: Synthese, Doctoral es Sciences Dissertation, Universite P. et
M. Curie (Paris VI), 1978.
15. Matheron, G., "Les Variables Regionalissees et leur Estimation,"
Masson and Cie, France, 1965.
16. Matheron, G., "Elements pour une Theorie des Milieux Poreus,"
Masson and Cie, France, 1967.
17. Matheron, G., LewKrigeage Universel," Les Cashiers du CMM;
fasc. 1 Fontainbleu, France, 1969.
18. Matheron, G., "The intrinsic random functions and their applica-
tions," Adv. in Applied Probability. 5, 1973, 439-705-711.
19. Mejia, J.M., "On the synthesis of random field sampling from the
spectrum: An application to the generation of hydrologic spatial pro-
cesses," Water Resources Res., 10, 1974,705-711.
20. Nelson, R.W., "In-place measurement of permeability in heteoro-
geneous media 1. Theory of a proposed method," J. Geophysical
Res., 6, 1960, 1753-1758.
21. Nelson, R.W., "In-Place Measurement of Permeability in hetero-
geneous media 2. Experimental and computational considerations,"
J. Geophysical Res., 1961.
22. Neuman, S.P., "Calibration of distributed parameter groundwater
flow models viewed as a multiple-objective decision process under un-
certainty," Water Resources Res., 9, 1973, 1006-1021.
23. Neuman, S.P., "A statistical approach to the inverse problem of
aquifer hydrology: III. Improved solution method and added per-
spective," Water Resources Res. (in press).
24. Neuman, P. and Yakowitz, S., "A statistical approach to the inverse
problem of aquifer hydrology: I. Theory," Water Resources Res.
25. Olea, R.A., "Optimum Mapping Techniques Using Regionalized
Variable Theory," Kansas Geological Society, 1975.
26. Rice, W.A., "Error uncertainty analysis of a direct inverse technique
with application to the Hanford Site." Submitted as M.A. Thesis,
University of Washington, Seattle, Washington, 1983.
27. Volpi, G. and Gambolati, G., "On the Use of a Main Trend for the
Kriging Technique in Hydrology." Advances in Water Resources, 1,
1978, 345-349.
28. Wilson, J.L. and Dettinger, M., "Steady State Versus Transient Par-
ameter Estimation in Ground-Water Systems." Paper presented at
Specialty Conference on Verification of Mathematical and Physical
Models in Hydraulic Engineering, Amer. Soc. of Civil Eng., Univ. of
Md., College Park, Aug. 9, 1978.
29. Wilson, J.L., Kitanidis, P. and Dettinger, M., "State and Parameter
Estimation in Ground-Water Models." Paper presented at the Chap-
man Conference on Applications of Kalman Filter to Hydrology, Hy-
draulics and Water Resources, AGU, Pittsburgh, PA. May 1978.
122
GEOHYDROLOGY
-------
EVALUATION OF GROUNDWATER HYDRAULICS
WITH RESPECT TO REMEDIAL DESIGN
WARREN V. BLASLAND, JR.
RICHARD D. JONES
GEORGE W. LEE, JR.
GUY A. SWENSON, III
O'Brien & Gere Engineers, Inc.
Syracuse, New York
INTRODUCTION
In a hydrogeologic investigation of the Kingsbury landfill,
O'Brien & Gere Engineers, Inc. documented groundwater con-
tamination attributed to discharges from the refuse. In order to
abate significant current and future releases or migration of haz-
ardous wastes from the site, a remedial design involving in-place
containment was developed by O'Brien & Gere.
The remedial design consisted of a groundwater cutoff wall
keyed into a clay layer beneath the site and a low permeable cap in-
stalled over the refuse. The purpose of this in-place containment
design is to effectively isolate the site from the hydrogeologic en-
vironment and thereby mitigate off-site migration of contaminated
groundwater.
An analysis of the projected post-construction groundwater hy-
draulics of the site was an integral part of the remediation de-
sign process and provided necessary documentation of the effec-
tiveness of the proposed remediation to state regulatory officials.
This analysis of the projected post-construction groundwater hy-
draulics provided:
PRE-REMEDIATION CONDITIONS
3oSo So «io3o noom So IK i«5onlo
SECTION K4
POST-REMEDIATION CONDITIONS
4OO tOO too TOO MO MO OOO IIOO ItOO I3OO I4OO
SECTION K4
LEBEMD
Figure 1
Pre-Remediation and Post-Remediation Cross-Section
GEOHYDROLOGY 123
-------
•An evaluation of the remedial design effectiveness in isolating the
site from the hydrogeologic environment
•An evaluation of the potential off-site migration of contam-
inated groundwater and its potential impacts on the surrounding
hydrogeologic environment
•Information critical to the design of the remediation measures.
BACKGROUND
The Kingsbury landfill site is located in eastern New York. The
site lithology consists of up to 70 ft of landfilled material depos-
ited upon a proglacial deltaic sand formation (Figure 1). The sands,
from less than 10 ft to about 70 ft thick, overlie a continuous
lacustrine clay formation. This clay formation increases in thick-
ness from less than 10 ft along the western border of the site to
over 70 ft along the eastern border of the site. Along the western
border of the site, a till formation composed of clay, silt, sand and
gravel sized particles underlies the clay. The groundwater table is
located in the sand formation and the lower portion of the landfill
material. Both the clay and till are also saturated.
The remedial design developed for the site consists of a cap with
a low hydraulic conductivity, 1 x 10~7 cm/sec or less (Figure 1),
and a groundwater cutoff wall (Figure 2). The cutoff wall must
have a hydraulic conductivity of 1 x 10~7 cm/sec or less and be
keyed into a continuous geologic unit with an acceptably low hy-
draulic conductivity. At the Kingsbury site, the clay and till have
acceptably low hydraulic conductivities and form the continuous
confining unit beneath the site.
METHOD OF EVALUATION
The analysis of the projected post-construction hydraulics for
this site utilized basic equations for steady-state groundwater flow
and a simplified model of the site groundwater hydraulics. This
simplified model of the site recognized that groundwater could
flow into and/or out of the site through three potential paths:
•The site cap
•The groundwater cutoff wall
•The confining unit at the base of the site.
The potential groundwater flow into and/or out of the site
through each of these three paths was evaluated independently
under steady-state conditions. Following these independent cal-
culations, the values of inflow and outflow were summed in a site
groundwater budget. Since the groundwater table within the re-
mediated site is expected to eventually reach some near equilib-
rium level where the net inflow into the site equals the net out-
flow from the site, sequential calculations assuming different
groundwater table elevations (193 ft and 195 ft) within the site were
used to estimate this equilibrium groundwater elevation. To more
accurately approximate the site conditions, the site was segmented
for the individual calculations. The analysis was conducted for the
worst-case conditions as a conservative method of accounting for
the approximate nature of the calculations.
This analysis of the projected post-construction groundwater hy-
draulics was performed manually using analytical steady-state
groundwater flow equations to demonstrate that the equations and
techniques for such an analysis are readily available to consul-
tants. Computer models of varying degrees of sophistication may
be used in similar analyses. However, their availability is more re-
stricted and the sophistication and expense involved with computer
modeling may exceed that which the site groundwater hydraulics or
client requires.
ASSUMPTIONS
The groundwater hydraulics of most hazardous waste sites are
complex and are accurately evaluated with transient equations for
LEGEND
~—— ntorauo ainrr MU.L
K4: MCTION LIME
0 BORINGS rr OTMCftS
H WILLS COMFICTCD UTH
NOVCUK* IM2
Q WRINGS COMICTCO tfTCH
NOVCHKK P«4!
« WCLLS COUH.CTCD KFCTf
NOVtuKU on
* WRINGS COMM.ETIO BtfORC
NOVCMeC* I*U
CONTOUR WTCTVWJ CVCrtT
9'AaOVt WAN tUt LIVCL
KINGSBURY
Figure 2
Site Plans
124
GEOHYDROLOGY
-------
Efl wojj
NOVtMMA
AFTM
€J BOmNGS CCWPLCTIO ATTCM
NOrtMWH- l>«2
fl> WCLU o)*«n-rrtD BCFO«
HOVCHMI* WW
9 KMIMC9 COMPETED BCTOUt
NOVtMKff IM2
dtOUNCMMTCH COKTDUH UHC
0/M/W
OMOUffOVMTU fUM DffHtTMH
OJWTOVIt MTIRUMJ 1HOWM
AM IN FttT MOW MUM
MA UVCL.
<=
9CALI ID FCET
Figure 3
Groundwater Elevation Contour Map in Sand
groundwater flow. Consequently, assumptions are necessary to
allow analysis using steady-state equations. The principal assump-
tions that are made in this analysis are:
•Steady-state conditions exist
•The geologic formations are homogeneous
•The geologic formations are infinite in horizontal extent
•Uniform, homogeneous and isotropic materials will be used for
remedial construction
•Remedial construction will be performed as per design
The first three assumptions relate to the analysis of ground-
water hydraulics by analytical equations. These assumptions enable
steady-state analytical equations to be used in the analysis rather
than complex transient equations. While the use of analytical equa-
tions for an analysis of the post-construction groundwater hydraul-
ics is less precise, such an analysis does provide a reasonable
approximation of the groundwater hydraulics. When the site
groundwater hydraulics are considered over a 10 or 20 year span of
time, the groundwater hydraulics approximate steady-state con-
ditions. The last two assumptions relate to the remedial construc-
tion and serve the same purpose as the assumption of homogeneous
and isotropic geologic formations.
In addition to the principal assumptions already presented, cer-
tain site specific assumptions were made. It was assumed that the
groundwater elevations in the sand outside the limits of the ground-
water cutoff wall were similar to those existing in Dec. 1982 (Fig-
ure 3), with some modifications to account for mounding along the
upgradient portion of the site. This assumption was considered
valid and conservative since data was from a wet season. It was also
assumed that the groundwater heads measured in the clay and till in
Dec. 1982 (Figure 4) were representative of long-term heads in
those formations. Since the clay and till formations have very low
hydraulic conductivities, their hydraulic heads will be representa-
tive of long-term head rather than short-term fluctuations.
CALCULATIONS
Infiltration Through the Site Cap
Precipitation is the principal source of groundwater recharge
in the vicinity of the Kingsbury site. It is estimated that regional
groundwater recharge in the vicinity of the site is equivalent to
about 9 in. of rainfall per year.1 In order to minimize the potential
groundwater recharge to the site, a cap of very low hydraulic con-
ductivity (1 x 10~7 cm/sec or less) is included in the remedial de-
sign. In order to evaluate the potential infiltration through the cap,
a water budget was calculated for the cap using averaged precip-
itation, runoff and evapotranspiration data. The calculations
followed methods described in the USEPA publication "Use of the
Water Budget Method for Predicting Leachate Generation from
Solid Waste Disposal Sites".2 These calculations indicated that in-
filtration into the cap could potentially occur during eight months
of the year. Since the cap is designed to have a hydraulic conduc-
tivity of 1 x 10~7 cm/sec, or less, the infiltration could only pene-
trate to a depth of about 2 cm in eight months. Using an assumed
value of soil moisture storage for the clay cap of 2.1 cm, the stor-
age capacity of the 2 cm of soil is about 0.6 cm. A 15 cm vege-
tated soil layer overlies the clay cap, consequently evapotranspira-
tion will undoubtedly use this water during the months of high
evapotranspiration.
An analysis of a hydrologic budget for the site cap indicates that
no groundwater recharge will reach the site through the cap.
Inflow and Outflow through the Groundwater Cutoff Wall
The second path where inflow and/or outflow could occur is
through the groundwater cutoff wall. The groundwater cutoff wall
is designed as a low permeability (hydraulic conductivity 1 x 10~7
cm/sec, or less) barrier to groundwater flow. If the flow rates of
the cutoff wall are compared to the flow rates in the more perme-
able sand of the site, the cutoff wall would appear relatively im-
permeable. However, no material is actually impermeable, and
GEOHYDROLOGY
125
-------
some groundwater flow will occur through the cutoff wall. There-
fore, this flow must be accounted for in the site groundwater
budget.
The potential groundwater flow through the cutoff wall was
examined using Darcy's equation for flow:
Q =
-Si! A
dl
(1)
where
K =
dh =
dl =
hydraulic conductivity
the difference in hydraulic head on either side of the wall
the length of the groundwater flow path (the width of the
wall)
A = the vertical cross sectional area of the wall (A = LH,
L = length of wall, and H = height of the wall in con-
tact with groundwater)
Sections of the cutoff wall where potential inflow can occur in-
clude areas where the hydraulic head outside the cutoff wall is
higher than inside. Areas where potential outflow can occur in-
clude areas where the hydraulic head outside the cutoff wall is low-
er than inside (Figures 2 and 3).
In order to evaluate the potential groundwater flow, the cutoff
wall was divided into several sections depending on the magnitude
and direction of the head difference across the cutoff wall. Calcu-
lations were made for each section, summing the inflow and out-
flow rates for all sections to arrive at an estimate of the total poten-
tial inflow and outflow to and from the site through the cutoff
wall (Table 1). A negative notation in the calculations indicates
groundwater flow out of the area within the limits of the cutoff
wall and a positive notation indicates inflow to the area within the
limits of the cutoff wall.
For the calculations, the height of the cutoff wall in contact with
saturated sand was determined from test boring data and Figures
3 and 5. The calculations indicate that groundwater inflow to the
site will occur along the western portion of the site and that ground-
water outflow will occur along the eastern portion of the site.
Inflow and Outflow through the Base Confining Layer
The third path of the site groundwater inflow and outflow is
the confining layer, clay and till, at the base of the site. The hy-
draulic conductivity of the clay, 3.9 x 10~7 cm/sec, and the clay
and till combined, 3.3 x 10~6 cm/sec, are acceptably low to be used
as a confining unit in in-place remediation; however, groundwater
will flow into and out of the site through this unit. This flow was
determined and accounted for in the site groundwater budget.
The calculations of the potential groundwater inflow and out-
flow utilized a simple flow net, Figure 6, and the equation:3
Q_ mkdh
(2)
where:
m =
K =
dh =
n =
L =
the number of flow tubes in the flow net
the hydraulic conductivity
the difference in head in the clay between the inside and
outside of the cutoff wall
the number of divisions of head in the flow net
the length of the section considered
Sections of the area of investigation where potential inflow
through the confining layer can occur are areas where the hy-
draulic head in the clay outside the limits of the cutoff wall is higher
than inside. Sections where potential outflow can occur are areas
where the hydraulic head in the clay inside the limits of the cutoff
wall is higher than outside (Figure 4).
In order to more accurately evaluate the potential flow, the area
of investigation was divided into several sections depending on the
LEGEND
0 KMHM* H OTHCItt
B W£LU COMPUTED
NOVtMCR IH1
G KMMGS COMPLETED VTCH
NOVEMKft UK
9 WELLl COMMUTED KRME
9 HMWi COMPLETED KPDK
110'
•n OMTouji LW
<=
12/23/82
WOONOWATM FLOW OIMCTION
CONTOUR WTEIMIU MMM Mi
• 1ZT MOVE HEM tt* ICVCL
KINGSBURY
Figure 4
Hydraulic Head in Clay Contour Map
126
GEOHYDROLOGY
-------
Table 1
Kingsbury Site
Calculations of Potential Inflow and Outflow through the Groundwater Cutoff Wall
Equation Used: Q
v dh .
K -n- A
K hydraulic conductivity 2.12 x 10 gpd/ft (1 x 10 cm/sec)
dh head difference across cutoff wall
dl width of cutoff wall =2.5 ft.
A vertical cross sectional area of cutoff wall (Length x Average Height)
ASSUMED SITE EQUILIBRIUM GROUNDWATER ELEVATION
LENGTH OF SECTION
SECTION ALONG CUTOFF WALL
A L
B L
C L
D L
E L
F L
G L
H L
I L
350
550
435
900
150
150
150
100
700
ft.
ft.
ft.
ft.
ft.
ft.
ft.
ft.
ft.
ASSUMED EXTERIOR
GROUNDWATER ELEVATION
210.
195.
185.
0 ft.
.0 ft.
,0 ft.
175.0 ft.
182,
187
195
205
215
.5 ft.
.5 ft.
.0 ft.
.0 ft.
.0 ft.
193 ft.
AVG. HEIGHT
28.9
27.3
43.5
50.9
33.6
39.3
51.3
50.0
46.5
ft.
ft.
ft.
ft.
ft.
ft.
ft.
ft.
ft. '
dh
17.0 ft.
2.0 ft.
-8.0 ft.
-18.0 ft.
-10.5 ft.
5.5 ft.
2.0 ft.
12.0 ft.
22.0 ft.
TOTAL INFLOW
TOTAL OUTFLOW
a
146 gpd
25 gpd
-128 gpd
-699 gpd
-45 gpd
-27 gpd
13 gpd
51 gpd
607 gpd
842 gpd
-899 gpd
195 ft.
AVG. HEIGHT
28.9 ft.
27.3 ft.
45.5 ft.
52.9 ft.
35.6 ft.
41.3 ft.
51.3 ft.
50.0 ft.
46.5 ft.
dh
15.0 ft.
0.0 ft.
-10.0 ft.
-20.0 ft.
-12.5 ft.
-7.5 ft.
0.0 ft.
10.0 ft.
20.0 ft.
fl
129 gpd
0 gpd
-168 gpd
-807 gpd
-57 gpd
-39 gpd
0 gpd
42 gpd
552 gpd
723 gpd
-1071 gpd
Table 2
Kingsbury Site
Calculations of Potential Inflow and Outflow through the Base Confining Layer
Equation Used: Q = ^- L
K hydraulic conductivity
m number of flow tubes in the flow net 5
n number of divisions of head in the flow net 6
dh head difference between the interior and exterior of cutoff wall
L Length of the perimeter affected
LENGTH
OF SECTION ALONG ASSUMED EXTERIOR
SECTION CUTOFF WALL PERIMETER
J L
K L
L L
M L •
N L
0 L
P L
Q L
250
550
500
350
300
335
600
550
ft.
ft.
ft.
ft.
ft.
ft.
ft.
ft.
GROUNDWATER
207.
202.
197.
192.
187.
182.
177.
172.
ELEVATION
5
5
5
5
5
5
5
5
ft.
ft.
ft.
ft.
ft.
ft.
ft.
ft.
K
(gpd/ft')
7 x 10
7 x 10
8.2 x
8.2 x
8.2 x
8.2 x
8.2 x
8.2 x
TOTAL
TOTAL
-2
-2
lO'3
io-3
ID'3
ID'3
lO'3
io-3
INFLOW
OUTFLOW
ASSUMED EQUILIBRIUM GROUNDWATER ELEVATION
193 ft. 195 ft.
dh
14.5 ft.
9.5 ft.
4.5 ft.
-0.5 ft.
-5.5 ft.
-10.5 ft.
-15.5 ft.
-20.5 ft.
9,
211 gpd
305 gpd
15 gpd
-1 gpd
-11 gpd
-24 gpd
'•64 gpd
-77 gpd
531 gpd
-177 gpd
dh
12.5 ft.
7.5 ft.
2.5 ft.
-2.5 ft.
-7.5 ft.
-12.5 ft.
-17.5 ft.
-22.5 ft.
9.
182 gpd
241 gpd
9 gpd
-6 gpd
-15 gpd
-29 gpd
-72 gpd
-85 gpd
432 gpd
-207 gpd
GEOHYDROLOGY
127
-------
LEGEND
TOP OF O.AY CONTOUK UNC
aOKINCS IT OTHERS
«u.s comrrco AFTER
NOVEUKR IM2
BOOIW5 couriETED trnm
NOVEMER n«Z
VELLS COMPLETED KTOK
NOVEMBER IM2
SORING* COMPLETED BEFORE
CONTOUR INTERVALS SHOWN
ME M FEET AIOVE MEAN
SEA LEVEL.
KINGSBURY
SCALE IN FEET
Figure 5
Top of Clay Elevation Contour Map
magnitude and direction of the head difference. Calculations were
made for each section, summing the inflow and outflow rates for
all sections to arrive at an estimate of the total potential inflow
and outflow through the base (Table 2). A positive notation in the
calculations indicates that groundwater flows into the area within
the cutoff wall, and a negative notation indicates outflow from
the area within the cutoff wall.
The above calculations indicate that groundwater inflow into the
site will occur along the western portion of the site, and ground-
water outflows will occur along the eastern portion of the site.
SITE GROUNDWATER BUDGET
A groundwater budget is a summation of the total groundwater
flow into and out of an area of investigation. The net change in the
water budget indicates whether groundwater is being added to or
subtracted from storage within the study area. When the total in-
flow equals the total outflow, there is no net change in storage
within the study area, the groundwater budget is in equilibrium
and an equilibrium groundwater elevation within the site will be
achieved.
The Kingsbury site projected post-construction groundwater
budget was calculated for various assumed constant groundwater
elevations (193 ft and 195 ft) within the limits of the cutoff walls.
For each case, the volume of total inflow and outflow was
summed. A positive net change in the water budget indicated that
groundwater was being added to storage within the limits of the
cutoff wall. As a result, the groundwater elevation within the site
would rise. A negative net change in the water budget indicated
that groundwater was being removed from storage, and the
groundwater elevation within the limits of the cutoff wall would
Figure 6
Flow Net
fall. A best fit method was employed to estimate the equilibrium
groundwater elevation within the limits of the cutoff wall, where
inflow equalled outflow, and there was no change in storage or the
groundwater elevation (Table 3).
The projected post-construction groundwater budget for the
Kingsbury site indicates that a groundwater elevation within the
limits of the cutoff wall between 193 ft and 195 ft will result in a
balanced groundwater budget. For design purposes, this equilib-
rium groundwater elevation is therefore assumed to be 195 ft. The
groundwater inflow to the site and the outflow from the site at
equilibrium are estimated to be about 1200 GPD.
128
GEOHYDROLOGY
-------
PROPOSED CUTOFF WALL
sm
GROUNDWATEft FLOW OMCCTION
(GENERALIZED)
BORINGS Sr OTHERS
WELLS COMPLETED AFTER
NOVEMBER IM1
BORIN6S COMPLETED AFTER
NOVEMBER 1*12
WELL] COMPLETED BEFORE
NOVEMBER I»B2
BORINS1 COMPLETED BEFORE
NOVEMBER IM3
CONTOUR INTERVALS EVERY
9T ABOVE MCA* SEA LEVEL
KINGS6URY
POST - CONSTRUCTION
GROUNDWATER FLOW MAP
SCALE IN FIET
Figure 7
Post-Construction Groundwater Flow Map
Table 3
Projected Post-Construction Groundwater Budgets
Rate of Inflow at Equilibrium Elevations
Source of Inflow
Inflow through cutoff wall
Inflow through base
TOTAL INFLOW
193 ft.
842 gpd
531 gpd
1373
Rate of Outflow at Equilibrium Elevations
Source of Outflow 193 ft.
Outflow through cutoff wall - 899 gpd
Outflow through base - 177 gpd
TOTAL OUTFLOW - 1076 gpd
NET BUDGET +297 gpd
195 ft.
723 gpd
432 gpd
1155gpd
195 ft.
-1071 gpd
207 gpd
• 1278 gpd
123 gpd
CONCLUSIONS
An analysis of the projected, post-construction ground water hy-
draulics of a site indicated that the estimated groundwater flow
through the site would be approximately 1200 gpd. Prior to remed-
iation, the groundwater flow through the site was estimated to be
78,000 gpd using the equation Q = KiA, where K = hydraulic
conductivity of the sand (about 75 gpd/ftz), i = the hydraulic
gradient (0.033 ft/ft), and A = the vertical cross-sectional area
(900 ft by 35 ft = 31,500 ft2). Therefore, the remedial design
would result in a 98% reduction in the flow of groundwater
through the site. This major reduction shows that the remedial de-
sign will effectively isolate the site from the hydrogeologic environ-
ment (Figures 1 and 7).
Since the remediated site will only cause the regional ground-
water to flow around the site rather than reduce the regional flow,
any contaminated groundwater leaving the site will undergo signifi-
cant dilution at about a 1 to 65 ratio with the regional ground-
water flow. In addition, the outflow that occurs will occur along
the entire downgradient side of the site which has a length of about
1000 ft; therefore, the outflow per linear foot will be roughly 1.2
gpd. The potential for off-site migration and impact would, there-
fore, be significantly reduced considering the area over which the
release should occur and the dilution that does occur.
Finally, the projected post-construction, equilibrium, ground-
water elevation of 195 ft within the site is significantly above the
elevation of the ground surface on the east side of the site. This
elevation indicated that a portion of the site would have to be built
up so that the groundwater would not impact the structural in-
tegrity of the site cap and compromise the remedial design. In this
manner the post-construction groundwater hydraulics analysis
provided valuable information used in the actual remedial design.
REFERENCES
1. O'Brien & Gere Engineers, Inc., "Kingsbury—Fort Edward Sites En-
gineering Report," Revised, Nov. 1982.
2. Fenn, D.G., Hanley, K.J. and DeLeare, T.V., "Use of the Water Bal-
ance Method for Predicting Leachate Generation From Solid Waste
Disposal Sites," EPA-530/SW-168, 1975.
3. Freeze, R.A. and Cherry, J.A., Groundwater, Prentice-Hall, Inc., 1979.
GEOHYDROLOGY
129
-------
EVALUATION OF VARIOUS GEOTECHNICAL AND
GEOPHYSICAL TECHNIQUES FOR SITE
CHARACTERIZATION STUDIES RELATIVE TO PLANNED
REMEDIAL ACTION MEASURES
RICHARD G. DiNITTO
NUS Corporation
Bedford, Massachusetts
INTRODUCTION
With the current emphasis on cleanup and restoration of haz-
ardous waste sites throughout the United States, there is an immed-
iate need to quickly and cost-effectively evaluate: (1) if previous
site characterization studies have been adequate in defining the
problem, (2) if proposed remedial actions will sufficiently contain
or reduce the contamination and (3) what additional techniques
can be employed to provide the necessary additional data. Previous
investigations of many sites have addressed only overburden con-
tamination or have inadequately assessed the bedrock aquifer
regime.
If the bedrock aquifer is or potentially will be contaminated,
then site characterization studies need to evaluate the overall dis-
tribution of contamination, both vertically and horizontally, the
presence or absence of till and the configuration and structure of
the underlying bedrock. Several case studies of sites where planned
or implemented remedial action studies inadequately addressed the
entire contaminant distribution and migration routes will be pre-
sented.
Data from various geotechnical and geophysical techniques can
greatly aid the investigation in identifying the appropriate remedial
measures to be implemented or additional studies required before
remedial action is taken at sites where the bedrock aquifer is or
could be contaminated.
These techniques will be evaluated in relation to various case
studies. Emphasis will be placed on illustrating how the techniques
have been successfully and unsuccessfully utilized in assessing site
conditions for initial site characterizations and for remedial plan-
ning. In addition, an overview of each technique, its limitations,
surficial terrain constraints and usefulness by geologic settings will
be addressed.
BEDROCK AQUIFER CONCERNS
Investigations performed by the author in New England and
previous studies by others1'2'3 have shown that bedrock aquifer
contamination is a significant problem, especially in areas where
the majority of drinking water wells are in bedrock. Bedrock
aquifer contamination is frequently attributable to contaminant
migration downward to the overburden-bedrock interface (Figure
1), even when the contaminants may be less dense than water. It
appears that the mechanism which causes this downgradient migra-
tion is the hydraulic loading of recharge water (such as percola-
tion of precipitation) to the saturated zone. This natural loading
may force contaminants into deeper portions of the aquifer.4-5
The pressures exhibited by the soil materials and the groundwater
itself will generally prohibit the contaminants from displacing
groundwater and rising back to the surface of the water table.
A simple method for evaluating the potential for downward mi-
gration is to install multi-level wells to determine vertical hydraulic
gradients. An observed downward vertical gradient indicates that
contaminants disposed of in that area would probably migrate
downward into the aquifer with the movement of groundwater.'
Typically, recharge areas are characterized by downward vertical
hydraulic gradients and groundwater flow. If the majority of con-
taminants are denser than water, then a stronger downward migra-
tion of the contamination may be expected. When there is an up-
ward vertical hydraulic gradient, as in areas of groundwater dis-
charge, or when there has been a large spill of compounds, such
as hydrocarbons, the contaminants will be observed primarily near
or at the water table surface. Even in the case of hydrocarbon
spills, a small fraction (up to 15 mg/1) of some hydrocarbon com-
pounds, such as benzene, toluene and xylene may enter the ground-
water as soluble components.6'7
The downward migration of contaminant plumes is important
because the plumes may reach the bedrock-overburden interface
and enter the bedrock aquifer. Only a continuous, thick and rela-
tively impervious overburden stratum, such as clay or till separating
the bedrock from previous overburden, would prevent contamina-
tion from affecting the bedrock aquifer. However, till layers are
not continuous above bedrock in most glaciated terrains and in the
presence of organic compounds the till may be structurally altered
to become more permeable.' In a recent study in eastern Massa-
chusetts, significant organic contamination(>0.5 mg/1) was de-
tected in one soil boring throughout a 50 ft till layer."
The movement of a contaminant plume that has reached the bed-
rock-overburden interface will be controlled by three factors:
•Bedrock surface topography
•Vertical and horizontal hydraulic gradients
•Extent and/or zonation of bedrock fractures
The bedrock surface topography can channel contaminant flow
in the same way that surface waters are controlled by the surface
topography. The contaminant flow will be further controlled by
hydraulic gradients. Vertical hydraulic gradients in bedrock re-
charge areas will determine, to a certain degree, the amount of con-
tamination that will enter and migrate through bedrock fractures.
Lastly, bedrock fractures play a significant role in contaminant
flow patterns. The common orientations, density, vertical and hori-
zontal extent and interconnection of fractures are important char-
acteristics that need to be evaluated to properly assess the bedrock
aquifer regime and its potential flow patterns. Since the greatest
130
GEOHYDROLOGY
-------
BEDROCK/TILL
Figure 1
Cross-section of a contaminant plume that has migrated to the bottom of the overburden aquifer. The existence of such a plume could contaminate the
bedrock aquifer. All wells shown are multi-level.
amount of groundwater flow is through rock fractures,'0 primary
porosity will not be addressed in this paper.
PREVIOUS STUDIES
Many sites in New England have been evaluated and assessed for
remedial activities in the past two years. In several cases, actual
long-term remedial programs, such as interceptor/barrier wells,
leachate collection and treatment systems and a variety of contain-
ment measures have been planned and implemented. The public
perception that sites aren't being cleaned up quickly enough or that
sites are being "studied to death" has often led investigators to a
"quick and dirty" approach to site assessments. This approach
usually fails to address the entire contamination problem, especial-
ly in relation to the bedrock aquifer regime. Described below are
three case histories which show how inadequate site assessments
have led to remedial designs that would prove to be ineffective
for long-term remediation.
Case Study—One
At a site in southeastern New England, a hydrocarbon spill
which occurred during the past decade has contaminated several
downgradient bedrock wells (Figure 2). At the time of the spill,
only overburden wells existed downgradient of the source of the
spill. Many of these wells were contaminated, but in the last ten
years have been renovated by natural flushing of the aquifer or by
the microbial degradation of the hydrocarbons in the aquifer.
Information gathered during an initial site assessment suggested
that the hydrocarbon contaminants would not affect the bedrock
aquifer because a till layer was present above the bedrock in the
vicinity of the residences. It was also assumed that the hydrocar-
bons would remain primarily on the surface of the water table.
Therefore, in an attempt to avoid future problems, several residen-
tial owners had bedrock wells installed. However, subsequent test-
PBOPOSED MmlER »EU
- MONITORING WELLS
ing has shown that hydrocarbon contamination exists in nearly all
of the bedrock wells and has remained over the past several years.
A second site assessment was performed which recommended
that barrier wells in the overburden be installed between the source
of contamination and upgradient of the residential wells (Figure 2).
An investigation performed by the author had shown that the
source of the spill, a storage tank, lies only a few feet above frac-
tured bedrock.
The absence of a semi-confining layer allowed contaminants to
migrate directly to the bedrock surface and into the bedrock
aquifer. Dissolution of the hydrocarbons in groundwater is the
probable source of contamination seen in the downgradient bed-
rock wells.
The recommended barrier well system in the overburden may
fail to intercept contamination within the bedrock fractures. The
fact that contamination has remained in the bedrock aquifer for
several years indicated that biodegradation is not an important
mitigating factor in this case. For the barrier well system to be
effective in removing hydrocarbon contamination from the bed-
rock aquifer, some bedrock wells would have to be incorporated
into the barrier well system.
Figure 2
Cross-section of a site in southeastern New England and approximate
contaminant distribution (dotted area) in bedrock.
Figure 3
Cross-section of a site in southeastern New England showing the known
distribution of contamination (dotted area).
Case Study—Two
A remedial assessment was performed to determine the ade-
quacy of current and planned remedial measures at a landfill lo-
cated in southeastern New England. The landfill had been built
on top of floodplain, river terrace and glaciofluvial deposits (Fig-
ure 3) along the edge of a large buried bedrock valley with ground-
water flowing through the site from the northwest to the southeast
and east. Inadequate cover materials have not prevented liquid
GEOHYDROLOGY
131
-------
wastes disposed of in the landfill from percolating into the ground-
water. This movement of contaminants has been observed both in
the form of leachate breakouts along the toe of the landfill and in
the groundwater sampled from monitoring wells downgradient of
and along the landfill's edge.
Present and planned remedial actions at this landfill include a
clay and/or plastic liner to cap the site and a leachate collection
system installed to a depth of 10 to 15 ft around the downgrad-
ient edge of the landfill. Most of the monitoring wells installed at
or around the site were placed at depths not exceeding 20 ft. One
well was placed to a depth of over 40 ft, and several wells were
placed to depths below the floodplain and alluvium deposits. The
contaminant distribution (Figure 3) shows that contaminants were
migrating to deeper portions of the aquifer. Indeed, much of the
contamination observed in the shallow wells was from a depth of 15
to 20 ft.
The planned remedial actions fail to address contamination that
exists at depth. The contamination migrating to deeper portions
of the aquifer may be controlled by the buried bedrock valley
topography and may potentially impact bedrock and deep over-
burden wells on the other side of the river. To date, no studies
have been performed to evaluate the long-term effects of deep
contaminant migration and bedrock aquifer degradation.
Figure 4
Cross-section of a site in central New England showing the proposed
effect that a slurry wall would have.
Case Study—Three
In central New England, a disposal operation located over a sand
and gravel aquifer discharged more than 200,000 gal of waste into
the ground (Figure 4). The waste severely degraded the aquifer
and within years after the operation began, contamination began
discharging into a nearby river. Two factors prompted an immed-
iate field investigation: all downgradient residences are serviced
by private wells; and the contamination discharging into the river
was becoming a health threat to abutting residences. The field in-
vestigation was conducted to determine the extent of contamina-
tion and to evaluate and select appropriate remedial options.
The study concluded that an immediate remedial option should
be the emplacement of a slurry wall around the area of significant
contamination and that the wall should extend to bedrock. The
depth to bedrock was based almost entirely on refusal depths in
till under the assumption that till is both relatively impermeable
and represents an approximate depth to bedrock. The single bor-
ing that was drilled into bedrock was in an area where till was thin-
nest. The bedrock core retrieved was highly fractured.
As a result of the failure to identify the actual depth to bedrock,
the initial slurry wall design was inadequate in mitigating con-
taminant migration. Further site characterization identified that the
bedrock surface sloped to the west in the area where the slurry wall
was to be installed. Failure to initially define the actual bedrock
surface led to a redesigning of the slurry wall so that it would ex-
tend to the bedrock surface, thereby increasing costs.
TECHNIQUES FOR EVALUATING
THE BEDROCK AQUIFER REGIME
The need to assess the bedrock aquifer regime will be based on
several factors:
•Environmental impact if the bedrock aquifer becomes contam-
inated
•The chemistry of the contaminants disposed of at a given site,
such as densities, solubilities, natural biodegradation factors and
adsorbability to soil particles
•The disposal practices and proximity to bedrock recharge terrains
•The quality of contaminants disposed and released to the environ-
ment, and the timing of the release: continuous, at intervals or
a single spill
•The present horizontal and vertical extent of contamination
•The subsurface stratigraphy, with particular emphasis on the ex-
tent and thickness of confining layers such as till or clay
A previous paper by this author and others described an ap-
proach to assess these factors that would enable the investigator
to determine the potential for bedrock aquifer contamination.1
In many sites where remedial actions are planned or antic-
ipated, an initial site assessment should have been performed to
address all of the above factors. For some of these sites, the initial
assessment is summarized in a Remedial Action Master Plan or
RAMP.
The RAMP also suggests what remaining site characterization
studies (referred to as remedial investigations) might be under-
taken before feasibility studies and remedial actions are performed.
It is during the remedial investigation that a proper assessment of
the bedrock aquifer regime would be conducted.
If, through an evaluation of the factors described above, a
potential exists for bedrock aquifer contamination, then additional
work should be performed to further characterize the bedrock
aquifer. There are many geotechnical and geophysical techniques
available to the site investigator. When selecting these techniques,
the overall goal or objective of a site assessment should be kept
in mind. Improper application of these techniques can greatly in-
crease project costs and extend completion deadlines, overshadow-
ing the usefulness of the data acquired.
Surface Measurement of Bedrock Fractures
Since most of the groundwater flow in bedrock is through rock
fractures, it is of tremendous importance to identify and locate
these fractures. Measurement of bedrock fractures from the sur-
face is a relatively quick and inexpensive technique for estab-
lishing fracture orientations and characteristics. Two methods can
be employed: fracture pattern analysis and fracture trace analysis.
The former requires that individual fractures be measured from
surface bedrock exposures, while the latter traces potential frac-
tures from aerial photographs.
Fracture pattern analysis is the more favored of the two methods
in delineating overall bedrock fracture characteristics since a three-
dimensional aspect (strike and dip) is obtained. Several good refer-
ences are available that describe in detail how to measure and plot
individual fractures"'12 and will not be discussed here. The desired
product of a pattern analysis is a stereo net pole plot (Figure 5).
The stereo net plot indicates the preferred fracture orientations
and their relative frequencies for the area studies. These data (pri-
marily the dips) can be compared to bedrock cores, if available, to
evaluate the depths at which commonly observed orientations in
surface exposures occur. Changes in preferred orientations of frac-
tures at depth may represent fractures that exist outside the area in-
itially studied at the surface or may represent large-scale fracture
zones that could not be perceived from individual surface outcrops.
Projection of surface data to the subsurface becomes less reliable
when there are no core data with which to compare. Expanding the
study area of surface measurements is preferred if core data are un-
available.
This technique has been employed successfully at several sites in
New England. In most cases, it was observed that the preferred
132
GEOHYDROLOGY
-------
CONTOUR DIAGRAM Of THE POLES TO 1
JOINTS- EAST CENTRAL WOflUflN, MA.
CONTOUR DIAGRAM Of THE POLESTO 29 FAULTS
EAST CENTRAL WOOUflN. MA.
Figure 5
Contour Diagrams for bedrock joints and observable faults from surface
exposures. The joint pattern does not exhibit any major fracture
orientations. The faults have a preferred orientation with a trend of
N55E and a dip of 85 ° NW.
orientations of fractures (as joints and faults) were similar to the
pattern of contamination distribution observed in bedrock wells.
This similarity strongly suggests that contaminant migration is
being controlled by a set of fractures. In one study, the fracture
pattern analysis was unsuccessful in predicting contaminant flow
patterns. Incomplete assessment of the contaminant sources, a lack
of existing monitoring well and local residential well data and water
quality analysis are believed to have played a role in the unsuccess-
ful application of this technique.
Costs associated with a fracture pattern analysis are primarily
based on the size of the area to be studied and the cost of the field
geologist. An important advantage of this technique is that the
work can generally be performed in-house by most geotechnical
firms. A study area size of five square miles and located in a glaci-
ated terrain with two dozen outcrops, where 300 to 500 measure-
ments are to be taken, can be completed within one week at a prob-
able cost of between $800 and $1,300.
The second method of surface fracture measurements employs
aerial photography for tracing individual bedrock fractures and
fracture zones. The concept is to trace, from aerial photographs,
lineaments in the surface topography where bedrock is not ex-
posed and individual fractures from bedrock where it outcrops.
It is assumed that significant water-bearing fractures would be
more easily eroded, thereby producing a topographic lineament
that is observable from photographs. Indeed, many significant
fracture zones can be observed as lineaments on the standard
United States Geological Survey topographic quadrangle maps or
on aeromagnetic maps. A major disadvantage with this technique
is that the data obtained are only two-dimensional. The three-
dimensional aspect of fractures and their structural relationships
are not evaluated. In addition, man's constant reworking of the
landscape and the extensive glacial overburden common in New
England can obscure many fractures.
The cost of a fracture trace analysis will depend on whether the
work will be subcontracted or performed in-house. The interpre-
tational experience needed in working with stereo aerial photog-
raphy may result in the need to subcontract the work. Assuming
the same site characteristics for the fracture pattern analysis dis-
cussed above, subcontract costs for fracture trace analysis will
range from $1,000 to $1,400.
Vertical Seismic Profiling
Vertical seismic profiling (VSP) is a new seismic technique avail-
able to the groundwater industry.13 The technique utilizes an array
of detectors set in a borehole to produce a three-dimensional
image of subsurface structures such as fractures. A seismic source
or shot point (explosives, weight drop, etc.) is used at some distance
J 1
X
. „ ^ ^ SPUNCEt
PHACTUdC ZONE -
Figure 6
Diagram depicting how Vertical Seismic Profiling works (left) and the
seismograph recording generated (right).13
from the borehole (Figure 6). As the seismic wavefront travels
downward, it will compress bedrock fractures. The compression
of a fracture produces a secondary wavefront that travels through
the fracture until it encounters the borehole where it generates tube
waves that travel vertically in the borehole and are measured by
the array of detectors. The seismograph trace recordings would
then produce a wave pattern that resembles a less-than symbol «"),
with the pointed end representing the origin (fracture) of the tube
waves.
The orientation and approximate permeability of the fractures
can be obtained by generating seismic readings from successive
shot points located at varying distances and directions from the
borehole (Figure 7). The mathematical derivation of fracture
permeabilities from the seismic data will not be discussed here,
but it has been shown that these permeabilities have compared ex-
tremely well with standard borehole permeability tests when con-
ducted in the same borehole. The reader is referred to the two
developers of this technique for more detailed information.13
The applicability of VSP to hazardous waste site investigations
and to remedial planning studies is still under investigation. This
technique has been successfully utilized in New England to iden-
tify fracture zones that have been transmitting contaminated
groundwater to bedrock supply wells. Orientations and perme-
abilities of these zones have been determined and are currently be-
ing evaluated to locate the source of contamination. Additionally,
the known subsurface orientation of these fractures will allow
future remedial studies to accurately locate test wells to intercept
contaminated water.
GEOHYDROLOGY
133
-------
COHFtllMKMAL 1 Wl»> "AVI COU»IUH»Al I TU»E WAV!
Id ««T TIUCM I UOOUI.I VMIU UOOUU VALUM I nMMAHUlV
-rums WAVE rnoM ZONE
i- WAVE
Figure 7
Diagram depicting the use of various shot points along source lines
radiating out from the borehole to determine the fracture orientation
and approximate permeability."
VSP will be extremely useful in remedial planning stages
(remedial investigations and feasibility studies). Significant cost
savings may be realized if recovery, interceptor or barrier wells
can be accurately located. Also, the effectiveness of other remed-
ial alternatives can be more completely assessed. The primary lim-
itation associated with VSP is that boreholes into bedrock need to
be distributed over the entire study area to insure maximum re-
liability of the seismic data.
If boreholes do not exist, or are relatively scarce, new holes
would have to be drilled which would increase the cost of the study.
The use of existing bedrock wells will help reduce the need for
drilling additional holes. Otherwise, data from one borehole would
have to be projected through the subsurface without having sup-
porting data from nearby wells. Typically, fractures can be mapped
horizontally by VSP to a radial distance from the borehole equal to
approximately one-half the depth of the borehole itself.
Pumping/Drawdown Tests
In attempting to evaluate whether contamination in bedrock is
being controlled by a specific fracture zone or by a random set
of fractures, a pump and drawdown study can be performed. In-
itial work, to include a fracture pattern analysis and a review of
the regional geology, will identify the common orientation of frac-
tures and the possible existence of fracture zones. A standard pump
test is performed, but with the emphasis on measuring the draw-
downs in monitoring wells or in other existing wells surrounding
the pumping well. Critical factors in designing such a study are:
•The pumping well should be placed within the suspected fracture
zone or in an area with similar fracture orientations
•Monitoring wells should be placed within and parallel to the frac-
ture zone and perpendicular to the zone
•As a minimum, each well location should include a well that is
screened only in bedrock and one that is screened only in the over-
burden
It is preferable that the bedrock well extend at least 100 ft or
more into the rock to insure proper fracture interception, and
that the wells be placed at varying distances from the pumping well.
The actual numbers, locations and depths of the wells would de-
pend on site conditions and project objectives. Local existing wells,
if accessible and if used in the drawdown study, will decrease
drilling costs and will expand the monitoring network. From the
drawdowns measured in each well, the investigator can evaluate the
primary migration pathways of groundwater and contamination
and can determine possible source areas of that contamination.
Knowledge of whether contamination is migrating within a single
fracture zone or, alternatively, through random fractures, will
mandate what remedial alternatives would be effective in controll-
ing the contamination.
Schuller and others1 approached a bedrock aquifer contamina-
tion problem in a manner similar to that discussed above. Their
study confirmed the existence of a fracture zone that was acting as
a conduit for contamination. The pump test had produced an elon-
gated cone of depression parallel to the suspected fracture zone.
Remedial action taken at that site has been successful.
Other Techniques
Several other techniques are also available including seismic re-
fraction surveys, electrical resistivity surveys, magnetics and gravity
measurements and packer tests in bedrock wells. Seismic refrac-
tion surveys have been used extensively in the glaciated Northeast
for delineating depths to bedrock. Determinations of the bedrock
seismic velocities have proven to be helpful in evaluating the poten-
tial for fracture zones in areas where insufficient surface data exist.
The use of electrical resistivity in conjunction with seismic refrac-
tion holds promise in estimating relative depths of significant bed-
rock surface fracture zones.
The use of gravity and/or magnetic measurements has not been
widely employed for glaciated terrains for bedrock aquifer assess-
ments, and more work is needed to assess their usefulness. Aero-
magnetic maps have been useful in locating structural geologic line-
aments such as fracture zones that can't be observed from surface
exposures of bedrock. This application is especially helpful where
overburden is thick.
REFERENCES
1. DiNitto, R.G., Norman, W.R. and Hanley, M.N., "An Approach to
Investigating Groundwater Contaminant Movement in Bedrock
Aquifers: Case Histories," Proc. of National Conference on Manage-
ment of Uncontrolled Hazardous Waste Sites, Nov. 1982, Washing-
ton, D.C., 111-117.
2. Gruber, P.O., "Evaluation of Ground-Water Contamination Asso-
ciated with the Use of Organic Solvents at Romansville, Pennsyl-
vania," Abstracts with Prog., The Third National Symposium and
Exposition on Aquifer Restoration and Ground Water Monitoring,
NWWA, Columbus, OH, May 1983.
3. Schuller, R.M., Beck, Jr., W.W. and Price, D.R., "Case Study of
Contaminant Reversal and Groundwater Restoration in a Fractured
Bedrock," Proc. of National Conference on Management of Uncon-
trolled Hazardous Waste Sites, Nov. 1982, Washington, D.C., 94-96.
4. Freeze, R.A. and Cherry, J.A., Groundwater, Prentice-Hall, Inc.,
Englewood Cliffs, NJ, 1979.
5. Faust, C.R., "The Use of Modeling in Monitoring Network Design,"
Proc. of the Second National Symposium and Exposition on Aquifer
Restoration and Ground Water Monitoring, Columbus, OH, 1982,
156-162.
6. Yaniga, P.M., "Alternatives in Decontamination for Hydrocarbon-
Contaminated Aquifers," Ground Water Monitoring Review, V.2,
No. 4,1982,40-49.
7. Chaffee, W.T. and Weimar, R.A., "Remedial Programs for Ground-
Water Supplies Contaminated by Gasoline," Abstracts with Prog,,
Third National Symposium and Exposition on Aquifer Restoration
and Ground Water Monitoring, NWWA, Columbus, OH, May 1983.
8. Josephson, J., "Protecting public groundwater supplies," Environ.
Sci. Tech., 16, 1982, 502A-505A.
9. Cook, D.K. and DiNitto, R.G., "Evaluation of the Hydrogeology
and Groundwater Quality of East and North Woburn," Ecology
and Environment, Inc., Woburn, Massachusetts, 1982.
10. Sowers, G.F., "Rock Permeability or Hydraulic Conductivity—An
Overview," in Permeability and Groundwater Contaminant Trans-
port, ASTM STP 746, T.F. Zimmie and C.O. Riggs, Eds., America!
Soc. for Testing and Materials, 1981,65-83.
11. Billings, M.P., "Structural Geology," Prentice-Hall, Inc Englewood
Cliffs, NJ, 1972.
12. Lahee, F.H., "Field Geology," McGraw-Hill Book Company New
York, 1961. y
13. Vertical Seismic Profiling Technique was developed for hydrogeologic
investigation use by Edward Levine of Weston Geophysical Corpora-
tion of Westboro, Massachusetts, and Professor M. Nafi Toksoz,
Director of MIT's Earth Resources Laboratory.
1J4
GEOHYDROLOGY
-------
A MODEL BASED METHODOLOGY FOR REMEDIAL ACTION
ASSESSMENT AT HAZARDOUS WASTE SITES
SCOTT H. BOUTWELL
BENJAMIN R. ROBERTS, Ph.D.
STUART M. BROWN
Anderson-Nichols & Co., Inc.
Palo Alto, California
T.Y. RICHARD LO
Stanford, California
INTRODUCTION
In the past, selection and design of remedial actions for uncon-
trolled hazardous waste sites has largely been accomplished
through field data collection, simple analyses and engineering
judgement. Such approaches are generally satisfactory for most
sites. There is a subset of sites, however, where conditions are so
complex that simple analyses may not provide enough guidance to
allow for the proper selection and design of remedial actions.
Given the high economic costs to government and industry
associated with site cleanup combined with the future societal cost
of inadequate actions, it is important that effective, economical
actions be chosen. Thus, there is a need for a remedial action
assessment methodology which is flexible enough to provide the
appropriate level of analysis and accurate enough to provide con-
fidence in the decisions made.
Recently, several studies involving the evaluation of remedial
actions at uncontrolled hazardous waste sites have been success-
fully accomplished using relatively sophisticated models. Examples
are the La Bounty landfill in Charles City, IA1, Love Canal2 and
a site in Gloucester, Ontario.3 These studies provide a motivation
for the development of a methodology composed of sophisticated
models which can address the diverse nature of waste sites. Such a
methodology, by expanding on the capabilities demonstrated in
these studies, could accurately represent remedial action impacts on
the entire hydrologic system (land surface, unsaturated zone and
saturated groundwater zone).
It is clear from experience to date that two levels of sophis-
tication are needed in hazardous waste site and remedial action
assessments: (1) simplified, "desk-top" methods (e.g., nomo-
graphs, analytical equations and hand-held calculator programs)
for use where resources such as data, time, money and user exper-
tise are limited and, (2) comprehensive numerical models for use on
complex sites that will require costly remedial actions. Conse-
quently, a methodology is being developed.that provides: (1) a
comprehensive modeling capability by interfacing sophisticated
models for the three hydrologic zones, (2) flexibility by incorpor-
ating simplified, "desk top" methods which require limited
resources in their application and (3) guidance on when to apply
each method. In this paper the authors focus on the first issue:
the selection and interfacing of sophisticated models.
OVERVIEW OF THE MODEL-BASED METHODOLOGY
The proposed model-based methodology consists of three key
elements: a set of sophisticated models (one for each hydrologic
zone); a date base structure and associated programs to transmit
information between models and link the models together; and a
set of instructions (referred to as "unit operation modules") for
modifying and using the models to simulate the effects of alterna-
tive remedial actions. The authors developed a system of inde-
pendent, but linked models because such a structure allows: (1)
use of one or more models independently where modeling of all
three zones is not needed and (2) increased user understanding
and confidence because each model can be implemented and ver-
ified separately.
Such a structure requires a model linkage technique which pro-
vides transfer of information between models at their boundaries
(e.g., the water table boundary between the unsaturated and
saturated groundwater zones). Given the diversity of hazardous
waste site conditions and potential remedial actions, guidance on
the proper application of the model system to remedial action
assessment is essential. This is provided through the unit operation
modules.
SELECTION OF MODELS FOR
REMEDIAL ACTION ASSESSMENT
The identification of candidate numerical models for each
hydrologic zone was based on the following criteria:
•Model time frame
•Ability to represent multiple spatial dimensions
•Representation of key physical and chemical processes
•Capacity to represent the changes in geometry and processes
caused by specific remedial actions
Final selection of specific models for each of the hydrologic
zones was based on the data structure of the model and its com-
patibility with other selected models, the extent of past model
testing and validation and the quality of available model documen-
tation. These criteria and the selected models will be discussed in
this section.
Contaminant transport processes and chemical interactions vary
substantially between zones in the hydrologic system. As shown
in Figure 1, the hydrologic system can be divided into zones
(surface water, unsaturated groundwater and saturated ground-
water) plus an atmospheric zone. Key contaminant transport pro-
cesses within these hydrologic zones include advection, dispersion,
sorption and degradation in all zones. Runoff, evapotranspira-
tion, erosion and infiltration occur in the surface zone.
Transport processes between zones include infiltration or seep-
age from surface to unsaturated zones and leaching from un-
saturated to saturated zones. The construction of a waste site in
the system alters some of these processes, and the installation of
GEOHYDROLOGY
135
-------
Atmospheric
f Precipitation
Evapotranapiration
Surface Water
Unsaturated
Ground Water
Saturated
Ground Water
Surface Seepage
I Leachate Evaporation
Contaminated Groundwatef
Contaminated
Sediments
Bedrock
Figure 1
Hydrologic Zones and Processes Near Waste Disposal Sites
(After JRB, 1982)
remedial actions causes other changes. Inter-zone transfers of
water and contaminants may be influenced by pumping or injec-
tion wells, interception trenches or impermeable barriers. Table
1 is a matrix which summarizes the effects of 15 remedial ac-
tions on these key processes.
Model time frame must be dynamic so that variations in the
hydrology, process changes over time due to the installation of
remedial actions and the movement of contaminants may be rep-
resented. Time step size will vary with the zone and will be shortest
in the surface zone where hydrologic changes are rapid. Spatial
representation must be a minimum of two dimensions in the sat-
urated zone to represent remedial actions such as impermeable
barriers and complex flow conditions. In the unsaturated zone,
one dimension may be adequate to represent most actions, but
two dimensions will be required to simulate sloping french drains
or clay layers with perched water tables.
Remedial action representation in the models is also dependent
on the ability to model heterogeneous properties such as hydraulic
conductivity and adsorption and to vary spatial resolution where
abrupt changes in geometry or materials occur. For example, an
impermeable barrier requires an abrupt decrease in hydraulic con-
ductivity and an in situ treatment bed requires an abrupt increase
in material properties related to adsorption and/or degradation.
These changes are summarized in Table 1.
The data structure of a model (i.e., the way information is in-
put, stored and output by the model) determines the way in which
models for the three zones will be linked. If individual model struc-
tures are not compatible, linkage of models into an integrated
system is difficult. Model testing and documentation ensures that
selected models operate correctly and can be readily implemented
and used efficiently.
Twelve candidate models were selected for evaluation based on
the above criteria. A matrix comparing models to evaluation cri-
teria is shown in Table 2. The ability of a given model to represent
a specific remedial action can be assessed by comparing the model
requirements shown in Table 1 with model capabilities in Table 2.
Many of the models have similar capabilities but model validation,
case studies and documentation varies.
One model or model package for each zone was selected based
on the above criteria: HSPF (Hydrologic Simulation Program
Fortran) for the surface zone, Femwater/Femwaste for the un-
saturated zone and FE3DGW/CFEST for the saturated zone:
•HSPF' is a watershed hydrologic model which also simulates
erosion, chemical transport in overland flow, streams and lakes
and infiltration of contaminants. HSPF's multiple land segment
and river reach approach allows the representation of hetero-
genous land surface and river properties as lumped parameters.
A key capability is the model's very flexible data structure and
data base management system.
•Femwater/Femwaste' is a two-dimensional, vertical plane, finite
element model which incorporates both variable time steps and
variable spatial resolution. This allows the simulation of complex
boundary conditions, abrupt permeability changes and variations
in infiltration from the surface over time. It also provides a flex-
ible input and output data structure.
•CFEST7 is a two-or three-dimensional, finite element model which
incorporates variable spatial resolution and allows the simulation
of complex boundary conditions and abrupt changes in hydraulic
conductivity typical of remedial actions. Wells and drains can be
simulated efficiently. In addition, CFEST can simplify data input
by performing steps such as grid generation automatically.
DEVELOPMENT OF THE REMEDIAL
ACTION MODELING SYSTEM
The modeling system which has been developed relies on com-
munication between the three models to provide simulation of con-
taminant transport through the three hydrologic zones. Informa-
tion which must be transferred parallels the movement of the con-
taminant between zones (Figure 1). Between the surface and un-
saturated zones, contaminant and water infiltrates downward from
rainfall or surface storage. Leachate reaching the groundwater
table moves from the unsaturated zone into the saturated zone.
Groundwater and contaminants may reenter the surface zone
through recharge to streams and lakes.
Remedial actions may also result in transfers. For example, con-
taminated groundwater can be pumped to the surface, treated and
136
GEOHYDROLOGY
-------
Table 1
Remedial Actions and Processes Matrix
Gradi ng
Revegeta t ion
Surface Water Diversion
and Collection
SUBSURFACE CONTROL
Capping S Top Liners
Seepage Basin & Di tches
Subsurface Drain /
Ditches / Bottom Liners
Impermeable Barriers
Ground Water Pumping
Interceptor Trenches
Permeable Treatment Bed
Biorecl ama t ion
Chemical Injection
Solution Mining Extractio
Excavation / Hydraul 1C
Dredgi ng
GAS MIGRATION CONTROL
Glossary: Legend:
P = Permeability Mitigates Process in
A = Permeability, Adsorption, Relation to No Action
Degradation & Dispersion + = Enhances Process in
S = Single Segment Relation to No Action
M = Multipl e Segments
L - Lateral
V = Vertical
then applied to the land surface (see Table 1). The boundary con-
ditions and source/sink terms in the models must account for
these transfers, as shown in Figure 2. Infiltration in HSPF becomes
a flux boundary condition in Femwater/Femwaste, while leachate
movement through the bottom boundary of Femwater/Femwaste
becomes a flux boundary condition for CFEST. A pumping well is
a sink term in appropriate nodes in CFEST and a source term in
HSPF if land application is used.
Two approaches to linking the models were considered: (1) a
direct coupling of the model equations such that computations
in all three zones are performed simultaneously and (2) a "soft
linkage" which transfers information sequentially between models.
Under soft linkage, the models are run in order (surface, un-
saturated, saturated) for all time with no transfer of informa-
tion against the natural direction of water movement. Any such
feedback must be computed in advance and checked subse-
quently against actual model results. This may involve iterative
application of the models.
Matching of boundary conditions between models must also be
checked to ensure that model results are consistent. For example,
soil moisture is computed in different ways in HSPF and Fern-
water, but must match. The soft linkage approach, as illustrated
in Figure 2, was chosen because a direct coupling of the models
would be unnecessarily complex and expensive to develop and im-
plement.
Linkage between the three models is implemented through two
bridge programs which accept time series data from one model,
modify it as needed and output it to the next model. Data mod-
ifications include: (1) temporal aggregation or disaggregation to
match model time step requirements, (2) spatial averaging or inter-
polation to match boundary value points, (3) unit conversions and
(4) changes in formats required by the programs. Verifying the
validity of transferred data is left to the user.
EVALUATION OF REMEDIAL ACTIONS:
UNIT OPERATION MODULES
Unit operation modules are a set of descriptive instructions for
the simulation of remedial actions using the developed model sys-
tem. They provide guidance for model parameter and structure
adjustment including:
•Computational element sizes and placement
•The use of flux, head and concentration boundary conditions
•Process-related parameters such as sorption coefficients, hy-
draulic conductivities and degradation rates
GEOHYDROLOGY
137
-------
Table 2
Model Review Matrix
SMFACCJODtl
wsw UM!
CKAMS (WD* / Corp.
Of £««.)
ins* TWUTt D_nw_ KWCI
FM1ATEI / rCNWASTC7 (QWH.!
TitriT / NiTiUi (lit / fiatullc)
S[NTMA / FCCTM (Baca)
SATMUTtD ZOUt HOOEl
rEiu / rrw (om.)
SWITI (|nltr«)
KTN (Inttra)
fOKW / CFEST (BatUllr)
AT171D (OfHI)
PUSM CrtcUtt 1 Lonnqufit)
Footnotn:
1. All *o<
i *rt umtttd/ lUtt
t eonildvr volatnitatlo*.
i. HwflM*! / Transport fedtl.
(«)
Legend:
Mitt pit land i
iMpagt (handling of
ftcp*ft pond)
ODCiBMAtatloA - onlj for flow aodtl.
not for traMport cod*.
Ihir'i Outdo • only for flow avdil,
not for trantport cotf*.
t.T, AND »h,
CLIMATE W
TIME SERIES
1 fc>
LAND ^
APPLICATION
HSPF
W
INPUT
PARAMETERS
NET INFILTRATION (MODEL LINKAGE)
LEACHATE 0 AND C (MODEL LINKAGE)
INPUT PARAMETERS
GROUND WATER FLO* AND CONCENTRATION
Figure 2
Sequential Execution of the Model System
The modules are written to provide an overview of each re-
medial action, modeling instructions, a list of affected boundary
conditions and model parameters and typical parameter ranges for
the action. Additional information related to the use of the unit
modules in conjunction with existing costing procedures as well as
the evaluation of design life and failure mode considerations, is
also included. Based on past studies4'8, the remedial actions which
are currently represented by unit operation modules are listed in
Table 1.
Groundwater pumping and/or injection are frequently consid-
ered remedial actions which have the potential to remove or
immobilize contaminant plumes in the saturated zone. Some of the
key model-related information which would be included in the unit
operation module for ground water pumping is shown in Table 3.
A check list of the important processes and zones affected which
indirectly indicates which models must be used to evaluate the
action is provided in Table 1.
CONTINUING DEVELOPMENT EFFORTS
While the modeling system provides a powerful methodology for
remedial action assessment, experience with the individual models
and with the system is limited. In the coming year, the model sys-
tem and assessment methodology will be applied to several exist-
ing sites presently being evaluated by USEPA. Model results will
be compared to field observations on the performance of selected
actions. Modifications will be made to the modeling system based
on the results of the test applications. The methodology will also
be used in the site evaluation process. The results of these appli-
cations will be used to refine model system application procedures
and provide additional guidance for remedial action assessments.
Simplified methods, including hand-held calculator programs,
analytical expressions and nomographs, will also be tested, as
appropriate, on the existing sites. Comparisons between the per-
formance of the model-based methodology and the simplified
methods will be made.
138
GEOHYDROLQGY
-------
Table3
Unit Operation Module for Groundwater Pumping
(An Abstract of Module Contents)
Purposes: 1) lower water table to prevent saturation of the waste site,
2) reverse pressure gradient to prevent contaminant movement toward a
discharge zone, 3) reduce pressure differences between leaky aquifers to
prevent contaminant movement and 4) create, through pumping/injec-
tion well pairs, a closed flow path which precludes outward contaminant
migration and captures the contaminant plume.
Design Variations: 1) pumped water is usually treated before reinjec-
tion or surface recharge, 2) off-site disposal of pumpage may be possible
and 3) may be used in combination with impermeable barriers and seep-
age ponds
Affected Zones: saturated zone; unsaturated zone if seepage ponds are
used for recharge; surface zone if land application is used
Models Required: CFEST: HSPF if land application is used for re-
charge; Femwater/Femwaste if recharged water contains contaminants or
seepage ponds are used to recharge treated water
CFEST Modifications: use of a series of sink or source nodes to repre-
sent wells; recalculation of heads; adjustment of element boundaries as
needed to represent a new water table configuration
Femwater/Femwaste Modifications: modification of land surface
(infiltration) boundary conditions to represent seepage ponds (constant
head boundaries); adjustment of bottom element boundaries to represent
new water table
HSPF Modifications: creation of land segments and addition of source
terms where land application of pumped groundwater occurs
Changes in Model Parameters: HSPF—none; Femwater/Femwaste—
increase hydraulic conductivities in elements bounding seepage ponds;
CFEST—none
Modeling Issues: discontinuities in head caused by wells and seepage
ponds may cause numerical instability unless smaller elements are used in
the vicinity of these actions (Femwater and CFEST)
ACKNOWLEDGEMENTS
This project is sponsored by the USEPA, Solid and Hazardous
Waste Research Division, Cincinnati, OH, USEPA Contract No.
C8-03-3116, Work Assignment No. 5. Mr. Douglas Ammon is the
Technical Project Manager; Mr. Lee Mulkey is the Project Officer.
REFERENCES
1. Cole, C.R., "Evaluation of Landfill Remedial Action Alternatives
Through Groundwater Modeling", Proc. National Conference on Man-
agement of Uncontrolled Hazardous Waste Sites, Washington, D.C.
Nov. 1982.
2. Silka, L.R. and Mercer, J.W., "Evaluation of Remedial Actions for
Groundwater Contamination at Love Canal, New York", Proc. Na-
tional Conference on Management of Uncontrolled Hazardous Waste
Sites, Washington, D.C., 1982, 159-164.
3. Geological Testing Consultants, "Gloucester Special Waste Disposal
Site: Hydrostratigraphic Interpretation and Remedial Measures Assess-
ment Using Mathematical Modeling Techniques", Draft Report, 1982.
4. JRB Associates, Handbook of Remedial Action at Hazardous Waste
Disposal Sites, USEPA, Cincinnati, OH, EPA 62516-82-006,1982.
5. Johansen, R., et al., User's Manual for the Hydrological Simulation
Program—Fortran (HSPF), Release 7.0, USEPA, Athens, GA, EPA
60019-80-015, 1981.
6. Yeh, G.T., "Training Course No. 1: The Implementation of Fem-
water (ORNL-5567) Computer Program—Final Report", NUREG/CR-
2705, 1982.
7. Gupta, S.K., et al., "A Multi-dimensional Finite Element Code for the
Analysis of Coupled Fluid, Energy, and Solute Transport (CFEST)",
PNL 4260, Battelle Pacific Northwest Laboratory, Richland, WA,
1982.
8. SCS Engineers, "Costs of Remedial Response Actions at Uncontrolled
Hazardous Waste Sites: Final Report", 1981.
GEOHYDROLOGY
139
-------
LIMITATIONS OF SCALED AND SINGLE-VALUED
DISPERSION COEFFICIENTS IN DESCRIBING POLLUTION
MIGRATION IN STRATIFIED AQUIFERS
ROBERT S. FARRELL
Department of Civil Engineering
University of New Hampshire
Durham, New Hampshire
ARTHUR R. DAY*
Office of Solid Waste
U.S. Environmental Protection Agency
Washington, D.C.
INTRODUCTION
The dispersive properties of an aquifer are to a large degree a
function of the spatial distribution of hydraulic conductivity. The
changes in dispersivity caused by vertical changes in hydraulic con-
ductivity in a layered aquifer are examined in this study for non-
reactive contaminants. A complete discussion of this study is
presented by Farrell.'
At large scales, dispersivity (or the dispersion coefficient, where
the dispersion coefficient = dispersivity times seepage velocity) is a
fitted parameter in a solute transport model used to calibrate the
model with actual site contamination data. The magnitude of the
dispersion coefficient is proportional to the scale of observation.
Anderson1 points out that large scale dispersivities must be con-
sidered to be apparent dispersivities and are partly determined by
the nodal spacing and model used. Unfortunately, there is no true
physical understanding of dispersivity on the local or regional scale.
In this study, the authors examine the sensitivity of calculated
dispersion coefficient values to variations in the vertical distribu-
tion of hydraulic conductivity. This is initially performed through
numerical simulation of solute transport in various layered aquifer
systems along a given flow line. These results are compared with
data from a field study by Pickens and Grisak.' The results indicate
substantial limitations in the use of dispersion coefficients in
layered aquifer modeling.
THEORETICAL BACKGROUND
Two independent methods have been used to estimate dispersion
coefficients (aside from laboratory-scale tests or rigorously con-
trolled field experiments). Dispersion coefficient values can be
fitted to the advection-dispersion equation using known relative
concentration data. They are also estimated for layered aquifers by
deriving a constant from the distribution of hydraulic conductivity.
This section describes both methods.
Once dispersion coefficients have been estimated, breakthrough
curves can be computed. These curves show the relative concentra-
tions of a given contaminant with distance from the source. Several
types of breakthrough curves are discussed in this paper.
The one-dimensional form of the advection-dispersion equation
developed by Bachmat and Bear2 describes the relationship of the
dispersion coefficient and groundwater flow:
DL - V _£ = ± G(x.t).
(1)
where DL is the dispersion coefficient, c is the solute concentration,
x is the distance from the source, V is the seepage velocity and G is
the mass gained or lost. This equation is discussed by Freeze and
Cherry4, and Fried.' The equation neglects molecular diffusion.
Equation 1 can be solved analytically for various simple boun-
dary conditions. For the following conditions:
C(0,t) = C0at x = 0
C(0,t) = C0 at t >0, and
C(oo,t) = at t>0,
the following solution is obtained:4
c
Co
_ 1 fERFC/x+V*t
2 I
+ EXP/V*x\ ERFC x + Vfrt
\DL )
(2)
•This paper «a* co-authored b> Arthur Da> in his pmate capacity No official support or endorse-
ment bs the I'SEPA is intended or should be inferred
where C/C0 is the relative concentration (dimensionless), DL =
dL*V (dL is the longitudinal dispersivity) (L2/T), t is the time since
spreading started (T), x is the distance from the source (L) and V is
the seepage velocity (L/T). The relative concentration 0.5 occurs at
the mean travel distance (x).
A second method to determine the dispersion coefficient is given
by Pickens and Grisak.6 The results are dispersivity values that are
time and distance dependent as a function of the mean travel
distance from the source of contamination:
dL = C*x, (3)
where dL is dispersivity (L), C is a dimensionless constant depen-
dent on the hydraulic conductivity distribution and x is the mean
travel distance (L). Pickens and Grisak' used field data to deter-
mine composite concentration breakthrough curves for full aquifer
thicknesses (later referred to as continuous curves). This was done
using weighted averages for hydraulic conductivity, layer thickness
and measured relative concentration at the sampling point for each
layer.
METHODS
This study was divided into two phases. In phase one, numerical
simulation techniques were used to compute breakthrough curves
for a variety of layered aquifer systems. These techniques were
developed for this study by Farrell as a solution for Equation 2
(which is a derivative of the advection-dispersion equation dis-
cussed above). A DEC-10 computer was used to solve the equation
140
GEOHYDROLOGY
-------
while an Apple III was used to preprocess the data and to perform
statistical analyses.
The simulations were generally restricted to the range of 2 to 100
ft downgradient from the source. Three sets of simulations were
performed. In the first (called the Uniform Distribution Set), the
number of aquifer layers was varied from 2 to 40. The hydraulic
conductivity values of individual layers were constant throughout
the layer; specific values ranged from 1 to 60 ft/day. Porosity and
hydraulic gradient were held constant. This allowed the effects of
layering to be isolated.
In the second set (called the Normal and Skewed Distribution
Set), three aquifer systems with 40 layers were studied. The
hydraulic conductivity distribution of these layers was normal
(forming a bell-shaped curve), skewed right (the median is to the
right of the mean) and skewed left (the median is to the left of the
mean). The skewed left case is also referred to as a log normal
distribution.
The third set (called the Field Data Set) was developed using ex-
perimental data presented by Pickens and Grisak6 for a single well
test. These data were taken as representing 18 layers (18 samplers
were uniformly distributed vertically through the aquifer in the
field test). The hydraulic conductivities of these layers were ten
times greater than those used in the other two sets of simulations.
Three types of breakthrough curves were calculated for each set
of simulations. A "continuous curve" (labeled CCZ on the figures)
results from the weighted averaging of the relative concentrations
of each layer of the aquifer at a given time or distance. This curve
depicts the vertically integrated concentration determined in
monitoring wells that sample the entire aquifer thickness. Pickens
and Grisak6 refer to this type of curve as a composite curve.
A "homogeneous curve" (labeled CCOH on the figures) results
from the weighted averaging of hydraulic conductivity, porosity,
seepage velocity and the dispersion coefficient for each layer. This
curve represents the response expected from a single-layered system
with the same average parameter values as the layered system.
The "iterated curve" (labeled CCOCC on the figures) is the solu-
tion of the advection-dispersion equation using the same aquifer
parameters as for the homogeneous curves except for the dispersion
coefficient. The dispersion coefficient is used as a fitting parameter
in an attempt to match the homogeneous and continuous curves at
every point.
A minimum dispersion coefficient, MINDL, for all times and
distances of interest was determined. This parameter was the
minimum dispersion coefficient that provided the best match be-
tween a continuous curve and a relative concentration determined
by the advection-dispersion equation. Unlike the iterated curve
solutions which determine the appropriate dispersion coefficient
for each point of interest, the MINDL value is the single value for
the dispersion coefficient that minimizes the difference in relative
concentration between two entire curves.
Phase two of this study compared dispersion coefficients deter-
mined by the simulations described above with values estimated us-
ing methods presented by Pickens and Grisak6 for similar aquifers.
This was done to both check the accuracy of this alternate
methodology and to evaluate the utility of the simpler method for
multi-layer aquifers.
RESULTS
Uniform Distribution Simulations
Typical breakthrough curves for the Uniform Distribution Set
of simulations are shown in Figure 1. All iterated curve values are
equal to the continuous curve values near the source (where C/C0
= 1.0). Between this region and the mean travel distance, the
iterated values are above the continuous curve values. It was not
possible to fit the iterated curve to the continuous curve by
manipulating the dispersion coefficient over a range of 0 to 100
ftVday. A low point in the iterated dispersivity coefficient values
occurs near the mean travel distance (C/C0 = 0.5). Beyond this
distance, the iterated curve can be matched to the continuous
TIME = 100 DAYS
A ccz
O ccocc
* CCOH
o.o
0 20 40 80 80 100
DISTANCE FROM SOURCECFEET3
Figure 1
Breakthrough curve for 40 layers, uniform distribution
curve. However, the values for the dispersion coefficient necessary
for this first increase and then decrease to zero as the curve ap-
proaches a relative concentration of zero away from the source.
The dispersion coefficients needed to match the iterated curve to
the continuous curve increase with time at a fixed point. This in-
crease is linear (Figure 2) after the mean travel distance has passed a
point of interest (in this case, 10 ft from the source). However, the
dispersion coefficient decreases to zero with increasing time when
all points are considered.
Another scale effect is observed when time is held constant, and
MINDL is determined. MINDL as a function of time up to 120,000
days is shown in Figure 3. The slope of the curve from 10 to 1000
days is linear (0.01 ft Vday2). The curve becomes asymptotic at
greater times.
Normal and Skewed Distribution Simulations
Typical breakthrough curves for 100 day simulations are
presented in Figure 4 for a right skewed distribution. These curves
show relationships common to all the Normal and Skewed
Distribution Simulations.
The homogeneous breakthrough curves for these simulations are
more similar to the continuous curves than are the homogeneous
curves for uniform distributions. This is reflected by lower values
for MINDL. The iterated curves also more closely match the con-
tinuous curves compared with the pairings in the uniform distribu-
tions. The right skewed distribution iterated curves matched the
continuous curves at 18 of 19 points evaluated.
The relationship of MINDL with time is shown in Figure 5. This
relationship illustrates another scale effect. However, the relation-
GEOHYDROLOGY
141
-------
IS .
DC
tt^doy
ti .
TIME = 100 DAYS
m m 3M
TIME (DAYS)
MEAN TRAVEL TIME
40.9 DAYS
Figure 2
Linear change in DC that occurs after the mean travel time has passed a
distance of 10 feet from the source (for 40 layers)
lUNDL
TIME (DAYS>
Figure 3
Change in MINDL with changing time for distances from 2 to 600 feet
ship is not linear for the skewed distribution, as contrasted with the
relationship observed for uniform distribution simulations at early
times (Figure 3). The curves for the skewed and log normal
distributions appear to be asymptotic at much earlier times than in
the uniform distributions.
The results indicate that trends in the change in the dispersion
coefficient for iterated simulations with distance are similar to the
trends noted earlier for the uniformly distributed systems.
Field Data Set
The data used in these simulations are taken from Pickens and
Grisak* and have a random distribution of hydraulic conductivity.
The dispersion coefficients for the various layers studied are log
normally distributed.
Using Pickens' and Grisak's methods' for determining the scal-
ing effect for changes in dispersivity with mean travel distance
results in the following relationship for random stratification:
dL = 0.1116»x (4)
Typical breakthrough curves for 1.4 days are presented in Figure
6. These curves indicate relationships for changes in the dispersion
coefficient for iterated simulations similar to those observed for the
40-layered, normal and skewed distribution systems previously
described. The iterated dispersion coefficients needed to match the
continuous curves are much larger than those needed for the nor-
CCZ
ccocc
CCOH
0 20 40 80 80 100
DISTANCE FROM SOURCECFEETD
Figure 4
Breakthrough curves, 40 layers, right skewed distribution
mal and skewed systems, however. This is a function of the higher
seepage velocity of the aquifer described in the Field Data Set.
The dispersion coefficients determined from the iterated simula-
tions range from 0 to greater than 100 fWday. The continuous and
iterated curves match where the relative concentration is near 1.0
and 0.5 and at distances greater than the mean travel distance. The
dispersion coefficients needed to match the iterated curve to the
continuous curve at distances greater than the mean travel distance
became greater with increasing time.
Another scaling effect is shown by the change in MINDL for
constant times over distance. This relationship is sensitive to the
position of the mean travel distance and the mean travel time (t) at
early times. MINDL determined without consideration for the
position of the mean travel distance is shown in Figure 7a.
Figure 7b was prepared so that the mean travel distance was
always one of the distances at which the iterated and continuous
curves were matched. The function for the line in Figure 7b is:
MINDL = 0.08 + 3.42f(L2/T), (5)
or in terms of dispersivity:
dL = 0.004 + 0.183 F(L) (6)
If written in terms of mean travel distance (x), these become:
dL = 0.04 + 0.01 x (L) (7)
Another scaling effect is shown by the values from the iterated
simulations needed to match the continuous curve at the mean
travel distance. In Figure 8, it can be observed that:
DL = 0.07 + 0.217 5T(L2/T), (8)
of in terms of dispersivity:
dL = 0.002 + 0.117x(L). (9)
Equation (9) is similar to equation (4), which was determined using
Pickens' and Grisak's methods. However, at any distance greater
than that shown on Figure 8 (i.e., 60 ft), the dispersion coefficient
142
GEOHYDROLOGY
-------
.1.
.1
MINDL
ftfday
./NORMAL
U U III HI Ml
TIME (DAYS}
Figure 5
Changes in MINDL determined over all distances with changing times
1.0 -i
o.e -
TIME = 3.0 DAYS
7£
10.3
A. CCZ
UJ CCOC2
X CCCW
DC'S
0.0
2T
ioo.o
0 20 40 00 80 100
DISTANCE FROM SOURCECFEETD
MINDL
SLOPE - 3.42
X
DAYS
HINM. DETERMINED VTTH MEAN TRAVEL DISTANCES
HINDI
FT?DAY
SLOPE - S.7I
DAYS
MINDL DETERMINED WITH FIXED DISTANCES
Figure 7
Changes in MINDL with time for fixed distances
DC
DL - 9.97 * 8.2l7»t
H -8.882 + 8.1l7»t
45
eo
HEAN TRAVEL PltfAIICE CfwO
Figure 6
Breakthrough curves, Pickens and Grisak's data
Figure 8
The change in DC with the change in the mean travel distance
GEOHYDROLOGY 143
-------
sI ope = 1.17
ZO 4O 60 80 ICC
DISTANCE FROM SOURCE (feet)
Figure 9
Plot of DC values at C/Co equal to 0.25
necessary to obtain agreement between the two breakthrough
curves could have been any value. This is because any solution to
the advection-dispersion equation must pass through a relative con-
centration of 0.5 at the mean travel distance.
Another scaling effect found in determining dispersion coeffi-
cients is shown in Figure 9. At a fixed relative concentration of 0.25
(ahead of the mean travel distance), the values of the iterated
dispersion coefficient are described by the linear function:
DL = 9.7 + 1.17x(L2/T). (10)
CONCLUSIONS
Homogeneous simulations of the advection-dispersion equation
do not compare favorably with continuous simulations. The
presence of layering is a major factor in determining the shape of a
continuous breakthrough curve, although the exact number of
layers is not very significant. Homogeneous simulation integrate
the properties of individual layers into a single averaged value for
the entire aquifer.
The position of the mean travel distance is a major factor in the
ability to match an iterated simulation curve to a continuous curve.
Before the mean travel distance has passed a point of interest, it is
almost always possible to fit an iterated simulation curve to a con-
tinuous curve by varying the dispersion coefficient. However, this
iterated dispersion coefficient may be quite large (e.g., greater than
100 ftVday). Once the mean travel distance has passed a given
point, it is impossible to fit an iterated curve to the continuous
curve over the distance between the source and the mean travel
distance. Consequently, scaled and single-valued dispersion coeffi-
cients cannot be used with the advection-dispersion equation to
describe pollution migration in a stratified, permeable aquifer
unless the mean travel distance or mean travel time of the con-
tamination has not yet reached the point of interest.
The minimum dispersion coefficient (MINDL) used in the
advection-dispersion equation to approximate a stratified layer
solution as a function of time is linear at early times and asymptotic
thereafter. The point at which this change occurs is a function of
the hydraulic conductivity distribution of the system.
There are four important effects of scale in estimating the disper-
sion coefficient. The first (Figure 2) shows that dispersion coeffi-
cients determined at given distances from the source vary with time.
The second effect is the change in the minimum dispersion coeffi-
cient with time (Figure 3). At early tunes, the change is linear, but it
does not reach an asymptotic value as time increases. The third ef-
fect (Figure 8) is the linear change in the dispersion coefficient
needed to match the iterated curve to the continuous curve at the
mean travel distance. At short distances, this relationship agrees
well with Pickens' and Grisak's results. However, this comparison
is misleading, because as the value of the continuous curve ap-
proaches a relative concentration of 0.5, any dispersion coefficient
can be used to match the continuous and iterated curves.
The final effect of scale (Figure 9) is the linear change in the
iterated dispersion coefficient at fixed values of the relative concen-
tration through times ahead of the mean travel distance.
This study demonstrates that the relationships described by
Pickens and Grisak' can be applied only to distances close to the
source. Their methods cannot be applied to multi-layer aquifers for
any significant distance from the source.
REFERENCES
1. Anderson, M.P., "Using Models to Simulate the Movement of Con-
taminants through Groundwater Flow Systems". Critical Reviews in
Environ. Control, 9, 1979, 97-159.
2. Bachmat, Y. and Bear, Jr., "The General Equations of Hydrodynamic
Dispersion in Homogeneous, Isotropic, Porous Mediums", /.
GeoPhys. Res., 69, 1964, 2561.
3. Farrell, R., "Dispersion Coefficients in Layered Geologic Systems",
Thesis, Univ. of N.H., Durham, N.H., 1983.
4. Freeze, R.A. and Cherry, J.A., Groundwater, Prentice-Hall, Engle-
wood Cliffs, NJ, 1979.
5. Fried, J.J., Groundwater Pollution, Elsevier Scientific, Amsterdam,
1975.
6. Pickens, R.W. and Grisak, G.E., "Scale-Dependent Dispersion in a
Stratified Granual Aquifer", Water Res. Res., 17, 1981, 1191-1211.
7. Pickens, R.W. and Grisak, G.E., "Modeling of Scale-Dependent Dis-
persion in Hydrogeologic Systems", Water Res. Res., 17, 1981, 1700-
1711.
144
GEOHYDROLOGY
-------
USE OF A DIGITAL MODEL TO EVALUATE
HYDROGEOLOGIC CONTROLS ON GROUNDWATER
FLOW IN A FRACTURED ROCK AQUIFER
MORRIS L. MASLIA
U.S. Geological Survey, Water Resources Division
Doraville, Georgia
RICHARD H. JOHNSTON
U.S. Geological Survey, Water Resources Division
Atlanta, Georgia
INTRODUCTION
The flow of groundwater through fractured rocks at a 15 acre
chemical waste disposal site (Hyde Park landfill) located north of
Niagara Falls, New York, was investigated using computer simula-
tion.
Underlying Hyde Park landfill from top to bottom are: (1) low-
permeability glacial till, (2) a moderately permeable fractured rock
aquifer—the Lockport Dolomite and (3) a low-permeability unit—
the Rochester Shale (Figure 1). The groundwater flow system can
be described as horizontally layered geologic units bounded on
three sides by groundwater drains: (1) the Niagara River Gorge (to
the west) which is eroded below the Rochester Shale, (2) the canal
of the Niagara Power Project (to the north) that is excavated into
the Rochester Shale and (3) the buried conduits of the power pro-
ject to the east that fully penetrate the Lockport Dolomite in the
reach near Hyde Park.
Water infiltrating the landfill from the surface moves initially
through low-permeability glacial till and thence into low porosity,
fractured dolomite that appears to have moderately high horizontal
hydraulic conductivity. The nearly impermeable Rochester Shale
may effectively provide a base to the groundwater flow system ex-
cept possibly near the Niagara Gorge where the shale is vertically
jointed.
Simulation was used to test three hypotheses related to flow in
the fractured rocks underlying Hyde Park landfill. A finite element
Galerkin technique was used to discretize the following equation
and solve for saturated-unsaturated flow assuming steady-state
conditions.
A. [KCKXX ah) d_ (KrKzz ah) = 0
dh dx dz dz
(1)
KM and K^ are defined as the principal components of the aniso-
tropic hydraulic conductivity tensor at saturation, h is the hydraulic
head (elevation head, z, plus pressure head, p) and Kr is the relative
hydraulic conductivity (0
-------
•RLTITUOE OF HflTER TflBLE
605 EOUIPOTENTIflL LINE.
INTERVAL IS 5 FEET
^475
425>-
-|150
H425
400-
-400
0 400 800 1200 1600 2000 2400 2800 3200 3600 4000 4400 4800 5200 5600 S000 6400 6800 7200 7600 8000
CROSS SECTIONAL DISTANCE FROM NIHGRRfl RIVER, IN FEET
Figure 1
Hydrogeologic units, depth and location of observation wells, and average 1979-1981 groundwater levels (from Maslia and Johnston, 1982).
are highest in the upper unit of the Lockport, ranging from about
1 to 5 ft/day.
•A groundwater divide exists east of the landfill, indicating that
all groundwater originating near or flowing beneath the landfill
will flow toward and discharge in the gorge.
•The zone of highest velocities (and presumably greatest potential
for transporting chemical contaminants) includes the upper unit
of the Lockport and part of the lower unit of the Lockport Dolo-
mite between the landfill and the gorge. The time required for
groundwater to move from the landfill to the gorge in the Lock-
port Dolomite is estimated to be 5 to 6 years.
REFERENCES
1.
of
Aral, M.M. and Maslia, M.L., "Unsteady Seepage Analysis
Wallace Dam," ASCF, 109, 1983, 809-826.
2. Bouwer, H., "Unsaturated Flow in Groundwater Hydraulics," J. of
the Hydraulics Div., ASCE, 90, 1964, 212-243.
3. Ibid., Ground Water Hydrology, McGraw Hill, New York, 1978.
4. Elder, V.A., Proctor, B.L. and Kites, R.A., "Organic Compounds
Found Near Dump Sites in Niagara Falls, New York," Env. Sci.
Tech., IS, 1981, 1237-1242.
5. Freeze, R.A., "Influence of the Unsaturated Flow Domain on Seep-
age Through Earth Dams," Water Resources Res., 7, 1971, 924-941.
6. Ibid., "Three-Dimensional, Transient, Saturated-Unsaturated Flow
in a Ground-Water Basin," Water Resources Res., 7, 1971, 347-366.
7. Freeze, R.A. and Witherspoon, P.A., "Theoretical Analysis of
Ground Water Flow: Effect of Water Table Configuration and Sub-
surface Permeability Variation," Water Resources Res., 3, 1967,
623-634.
8. Gardner, W.R., "Some Steady-State Solutions of the Unsaturated
Moisture Flow Equation With Application to Evaporation From a
Water Table," Soil Science, 85, 1958, 228-232.
9. Interagency Task Force on Hazardous Wastes, "Hazardous Waste
Disposal in Erie and Niagara Counties, New York," New York De-
partment of Environmental Conservation, 1979.
10. Johnston, R.H., "Water-Bearing Characteristics of the Lockport
Dolomite Near Niagara Falls, New York," USGS Professional Paper
450-C, 1962, C123-C125.
11. Ibid., "Ground Water in the Niagara Falls Area, New York," New
York Water Resources Commission Bulletin GW-53, 1964.
12. LaSala, A.M., "New Approaches to Water-Resources Investigations
in Upstate New York," Ground Water, 5, 1967, 6-11.
13. Neuman, S.P., "Saturated-Unsaturated Seepage by Finite Elements,"
/. of the Hydraulics Div., ASCE, HY12, 1973, 2233-2250.
14. Reeves, M. and Duguid, J.O., "Water Movement Through Saturated-
Unsaturated Porous Media: A Finite Element Galerkin Model," Oak
Ridge National Laboratory Report, No. 4927, 1975.
15. U.S. District Court, Buffalo, New York, Reply Brief of the United
States of America; Testimony of L. Miller, R.H. Johnston, K. Davis,
D.B. Twedell, F. Rovers and E.G. Anderson: Civil action no. 79-
989, v. II, 1981.
16. Zienkiewicz, O.C., The Finite Element Method, London, McGraw-
Hill, New York, 1977.
146
GEOHYDROLOGV
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LEAK DETECTION TECHNIQUES AND REPAIRABILITY
OPTIONS FOR LINED WASTE IMPOUNDMENT SITES
MURIEL JENNINGS WALLER
RAJIV SINGH
EarthTech, Inc.
Baltimore, Maryland
INTRODUCTION
There is a pressing need to develop reliable, non-destructive
monitoring techniques to determine if a significant leak exists in
hazardous waste impoundment liners before escaping leachate can
seriously damage the groundwater. Needed also are better tech-
niques to economically locate precisely where a leak is occurring in
a liner.
Once a leak is located, it then becomes necessary to either effect
acceptable repairs to the liner or to close-off the site and remove the
existing waste to a safe impoundment location. Both leak detection
and liner repairability can be considered to be developing
technologies. The purpose of the authors writing this paper is to
present the result of two USEPA projects, the first to develop leak
detection techniques and the second to investigate the problem of
liner repairability. Liner repairability and leak detection must be
regarded as a three part problem:
•Location and definition of the size and nature of the failure
•Accessibility of the leak or failure in order to effect repairs
•Availability of a proven repair technology specific to a given liner
system
LINER REPAIRABILITY
The purpose of the repairability program was to conduct a state-
of-the-art review of current liner repair techniques being utilized in
all types of emplaced liner systems including natural soils, admixes
and synthetic (including asphaltic and bentonite) membranes. This
broad review has been followed by a ranking matrix exercise and
concludes with a series of laboratory evaluations of various repair
methods. This yields preliminary data on the technical and
economic feasibility of remedial repair to in-service systems and
establishes the direction of future research.
The use of man-made or altered natural materials of low
permeability to line waste disposal impoundments has been shown
to be a feasible method to prevent the escape of liquid waste com-
ponents and leachate from disposal sites and the subsequent con-
tamination of surface or groundwater. However, if liners are to ac-
complish this objective, information is needed to evaluate and
monitor liner performance and to effect cost-effective, technically
adequate repairs once problems have been demonstrated in both
existing and planned lined impoundments. The eventual goal of
this leak detection program is the location of leaks (to an accuracy
of 1 ft2). Additional research is being performed to better define
and predict the application and use of liners in the field including
the problem of degradation of liner materials from long term ex-
posure to chemicals and environmental influences and preplace-
ment and placement procedures to assure optimum field perfor-
mance. Now that an extensive data base on liner performance and
leak detection techniques is being developed from which logical
engineering decisions regarding the application of lining materials
can be made, it is necessary to evaluate existing repair techniques
and, based on this information, to develop new, more effective
techniques where necessary.
Currently, some repair techniques are being applied in the field
to effect localized repairs to liner systems. These vary widely,
depending upon the type of liner being repaired, the extent of the
problem and the expertise involved in design and implementation
of the repair. The success of these repairs is also widely variable.
However, in all cases the repair of in-service liner systems is highly
complex, and dependent upon a number of variables. The
availability of rapid and cost-effective methods for sealing existing
impoundments will allow the acceptable uses of lined impound-
ments to increase. At the same time, the effective life-time of such
systems will be extended. In addition, such a capability will con-
tribute to the ability to solve a pressing environmental problem that
currently cannot be treated consistently and effectively.
Objectives
The objective of the proposed program is to develop information
on current liner repair techniques and then, based on the results of
a ranking matrix exercise, to select and evaluate a variety of liner
repair methods under laboratory conditions. The final develop-
ment of this program will be criteria by which the technical and
economic feasibility of the repairability of a variety of in-place liner
systems under a number of conditions can be assessed. These broad
goals are being met by the following:
•State-of-the-art review
•Development of a ranking matrix
•Documentation of technology
•Development of a ranking criteria
•Laboratory evaluation
The Leak Repair Problem
The nature and occurrence of liner leaks vary widely, depending
upon the type of liner employed, the waste impounded, significant
weather exposures and maintenance and installation problems. A
leak may vary from a puncture or seam failure in a membrane liner
to large scale cracking from subsidence problems in soil or admix
liners and finally to widespread degradation of liner impermeability
due to improper matching of wastes to impoundment materials.
Anderson and Brown at Texas A&M have exposed compacted clay
BARRIERS
147
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liners in simulated conditions to a variety of solvents and have
achieved permeability values as high as 10~4 cm/sec.
In addition, depending upon the nature of the wastes impounded
in a given liner system, the impoundment may be accessible from
the surface through draw-down of fluid levels. In other cases, the
only method by which to access a leak may be by locating the point
source of a leak underneath a liner and reaching it through the use
of innovative directional drilling and injection techniques. Finally,
the treatment of choice for a given liner failure will have to be
matched to each specific liner material to assure the integrity of the
repair and the repair technique itself must be evaluated to insure
that both strength and low permeability will be maintained
throughout the service life of the liner.
Other important factors influencing liner repairability in the field
include site specific problems. These range from swelling of mem-
branes due to exposure to leachates, the use of dissimilar materials,
poor preparations in attempting to effect a repair, the presence of
water pressure or other structural stresses, to the effects of leachate
on soil pH that may make patching, plugging or filling a leak more
difficult.
Cost factors, too, will play a vital role in the feasibility of liner
repair. In cases where it may be possible to drain a fluid impound-
ment, the cost/benefit trade-off will be between the cost of drain-
ing and replacing the liner versus the cost of effecting widespread
repairs. In other cases, where vital water supplies are threatened
and physical removal of the hazardous material to a secure site is
dangerous or impossible, the costs of repair, however great, are cer-
tainly orders of magnitude lower than the possible social costs to an
affected community.
Obviously, the problem of liner repairability is both diverse and
complex. Ultimately, it would be ideal to be able to select from a
matrix the optimum leak repair technique for a given liner, climate,
soil and waste type. However, given the complexity of the problem,
each repair solution will probably be a problem unto itself, requir-
ing site specific analysis and design.
Emplaced Liner Systems
A wide variety of materials are available for the emplacement of
impermeable barriers under or around waste impoundments. A list
of potential materials for lining waste storage and disposal
facilities1 is available. For the purposes of this program, the dis-
cussion is limited to three broad classifications of liners:
•Soil and clays
•Admixes
•Polymeric membranes
Three broad classifications of repair techniques are also being
considered:
•Patching
•Mechanically plugging
•Sealing with soil grouts
Each liner type is treated in detail in "Lining of Waste Impound-
ment Disposal Facilities.'"
Laboratory Evaluations
The objectives of this task are to evaluate each of the techniques
identified for further investigation at the outset of the program.
The outcome of this work will be the information to provide
technical and economic assessment of existing repair technology,
identify gaps in existing techniques and point the way to future
research.
Broad goals of the laboratory evaluation are:
•An assessment of field seaming procedures for in-place repairs,
including those recommended by manufacturers, as well as
"tricks-of-the-trade" applied by practitioners in the field
•The feasibility of drying out and repairing a dried out piece of
previously exposed liner
•The reliability of a variety of adhesive bonds after exposure to
several leachates under both shear and peel testing
•Preliminary injection parameters for various repair compounds:
epoxy resins, silicones, chemical and paniculate grouts
•Durability over time of the same compounds (by destruction
testing)
•The feasibility of conducting repairs under several different con-
ditions, as in leachate impregnated soils or in the presence of
running or stagnant water
Although this program is seen as exploratory in nature, the im-
portance of conducting the first stages of laboratory evaluations of
liner repair systems under controlled conditions with the total pro-
cedure exposed to view cannot be overestimated. Once these issues
are well understood, work can begin on attempting field repairs in
difficult-to-access environments, underneath or at the bottom of
in-service impoundments. For this task, the following are being
considered:
•Plugging tests with epoxies on each polymeric membrane selected
for testing
•Exposure of simulated repairs in polyethylene liners to at least
three conditions including several waste types and weather con-
ditions
Each repaired liner will then be tested for strength in both peel
and shear modes to measure the strength of the adhesive and the
strength of the seam. The peel strength of a seam is more sensitive
to aging and exposure than the shear strength test. In many cases,
the peel values will drop considerably without resulting in ap-
preciable loss to shear strength. Whereas, in shear strength test-
ing, values remain relatively even until failure occurs, at which
point they drop precipitously. Therefore, for durability studies, it
is particularly important to use peel tests to evaluate seams or
patches. The results of these limited tests can then be compared to
seam strength values already established in tests on non-exposed
liners.
•Bench scale grout durability testing to compare the durability of
several candidate grouts selected from the literature review when
exposed to contaminants
•Further tests conducted on samples of degraded clay liners to
evaluate their repairability by plugging, grouting and underseal-
ing means
•Use of soil samples from landfill liner simulators which have been
exposed to chemical waste leachates for a six-year period to the
range of grout tests. An attempt will also be made to effect small
scale repairs upon the cored soils remaining in the simulators.
•Execution of the Ranking Matrix encompassing the results of the
laboratory evaluations as well as the literature review. Labora-
tory protocols are currently being developed.
LEAK DETECTION
Time-domain reflectometry and acoustic emission monitoring as
techniques for monitoring leaks in waste impoundment liners have
been studied under controlled field conditions in a 0.4 hectare li-
quid impoundment site. These non-destructive techniques have
proven to be successful in detecting leaks under certain specified
conditions. A detailed description of the test site and results ob-
tained for tests conducted under controlled conditions are dis-
cussed herein.
The study was conducted at an artificial liquid impoundment site
located at South West Research Institute in San Antonio, Tx. The
liquid impoundment site covers an area of 0.4 hectare. The site is
2 m deep and is lined with a 2 mm thick high density polyethylene
liner. The TDR and acoustic emission techniques were evaluated
for their usefulness in a 15 m x 15 m triangular section of the pond.
Both techniques being evaluated by EarthTech required that a liner
be placed on a pad of coarse-grained material such as sand or
gravel. The toe-to-toe distance of the inside of the square pond was
46 m. A 1 in 3 slope was used on the inside of the berm and a 1 in 4
slope on the outside of the berm (where it existed). There was a 2.4
m wide road used for access around the pond along the top of all
the berms.
Plan and profile views of the pond are shown in Figure 1. To
create optimum conditions for evaluating the TDR and acoustic
emission techniques, an additional 60 cm of clay on the floor of the
pond were excavated as shown in Figure 1. Drain tiles were placed
148
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ISOM —.
9
it
15-OM
45-Ok
VALVE
1*95 M-M-6 4
SUMP
-I5M
CLAY
SECTION A-A
Figure 1
View of the Waste Impoundment Site
in the excavated area. A 10 cm diameter perforated polyvinyl
chloride drain tile was used and wrapped with a filter fabric to keep
the soil from clogging the drain tile. The drain tiles were connected
to a 2,000 1 commercial concrete sump placed 20 m south of the
outside toe of the berm. Sand and gravel were placed directly on the
clay soil in the excavated triangular area. For TDR evaluation,
three sets of horizontal transmission lines with lengths of 5, 11 and
17 m and with each line length having five sets of conductor spac-
ings of 10, 20, 30, 50 and 100 cm were placed in the sandy soil 30 cm
below the liner. Holes simulating leaks ranging from 5 to 20 cm
diameter were placed over the center of each of the different
lengths of transmission lines. In addition, vertical TDR lines were
placed near the leak holes to measure the horizontal spread of the
. fluid in the sandy soil.
Both techniques required slightly different soil conditions. Thus,
there were three sets of holes for each system (Figure 2). For time
domain reflectometer experiments, sandy soil with some fine grain
soils was placed along the transmission lines just below the TDR
holes. This was done to allow a horizontal spread of the fluid. The
acoustic emission monitoring experiment required a very permeable
soil with a wide range of grain sizes to be placed under acoustic
emission monitoring holes. This was done to enable flow rates be-
tween 0.2 -1 I/sec to exist in the soil. The holes through the liner
were constructed of 4.8 cm outside diameter high-density polyethy-
lene tubing.
The leak points were plumbed to enable the control of flow of
water through the system. The quantity of water flowing through
the system was measured by a flow meter.
Time Domain Reflectometer Transmission Line Layout
The TDR system used three sets of transmission lines running
diagonally across one corner of the pond as shown in Figure 3. The
transmission line lengths were 5,11 and 17m. Each set of transmis-
sion lines had center-to-center spacing of 10, 20, 30, 50 and 100 cm.
These transmission lines terminated at a 1 mm thick fiberglass
board. This board connected these copper transmission lines to a
300 ohm twin lead which was brought up on both sides of the berm
via raceways for monitoring purposes. All the 300 ohm cables were
cut to the same length to reduce the time necessary to set up the
TDR system and to obtain the data to a minimum.
Acoustic Emission Monitoring
Three sets of holes were placed in the liner for acoustic emission
monitoring tests. Each of these holes was located over the center of
the horizontal TDR transmission lines. Six sets of acoustic sensors
were placed in the soil under the liner. Four of these sensors were
placed directly below the leak points, and two sensors were placed
further away from the leak. All the sensors were placed horizontal-
A-E HOLES
TOR HOLES
ISOM
Figure 2
Location of the TDK and AEM Holes
ANCHORS FOR
TOR LINES
RACEWAY FOR
300 A TOR
LINES
SPACERS FOR
TOR LINES
Figure 3
Horizontal Transmission Lines for Time Domain
Reflectometer Monitoring
BARRIERS
149
-------
ly about 15 cm below the surface of the gravel. The sensors placed
directly below the leak source monitored the spectra of the sound
produced as the water flowed in the soil. The sensors placed away
from the hole monitored the background noise level. In addition,
three sensors were placed in the water above the liner during the
course of the tests. Of the three sensors, one was placed farthest
away from the leak point; this measured the background level of
the noise in the area. Another was placed 15 cm from the acoustic-
emission hole that was being tested. The third acoustic emission
sensor was hung from the rope stretched diagonally from the two
berms. The depth and position of the sensor were varied depending
upon the particular test being carried out.
For the same experiment, the TDR response was plotted against
time in Figure 5 after each of four applications of 4 1 of water on
the llm long transmission lines having a conductor spacing of 10
cm. The TDR response changed most rapidly within 3 min after the
water was added and then initially decreased or dried at a rate of
about 5% of the wetting rate and then at a slower rate thereafter.
The drying rate was not linear. In unsaturated soils the soil surface
tensions holds water, and thus the water content does not im-
mediately return to zero. The soil reached saturation after the se-
cond 41 of water were added. Insufficient time for drying was given
before the application of the third 41 of water were added, and thus
one did not see a change in the TDR response.
Measurement Technique
TDR
The time domain reflectometer measurement technique was car-
ried out on all the transmission lines, both vertical and horizontal,
before any water was added. Then the transmission lines around
the hole through which water had been added were monitored at
short intervals. This provided a picture of TDR response along the
transmission line versus time after a known volume of water was
added through the simulated leak in the liner.
Acoustic Emission
The measurement technique included monitoring four sensors at
a time. Initial tests were conducted to establish the background
noise levels for sensors buried below the line. Once such a level was
established, the sensors monitored for a test included: (1) a sensor
situated directly below the simulated leak hole—this monitored the
exact noise amplitude, (2) a sensor located at a fixed position 15 cm
above the liner near the simulated leak point, (3) a sensor which
had flexibility to move in either the vertical or horizontal direction
and (4) a sensor above the liner located a distance further away
from the leak for monitoring the prevalent background noise level.
A series of attenuation measurements was conducted to establish
the values for attenuation for signals propagating through water in
a shallow pond.
Results
TDR Field Results
A series of tests was carried out at the model waste impoundment
site to determine the size of leak from a liner that could be detected
using transmission lines placed in coarse grained soil under the
liner. In the following text, two sets of results are presented to show
the effects of permeability, grain size and soil moisture on the
detection capability of the system. These two tests were conducted
during two different phases of the experiments: (1) the first was
conducted prior to emplacement of the liner when the permeability
of soil was 0.02 I/sec, with soil-water content at 22% and fine
grained material spread around the horizontal lines; (2) the second
tests were conducted after emplacement of the liner.
In the interim between the first and second sets of tests, the site
soils had undergone removal and drying on three separate occa-
sions due to unseasonably wet weather in San Antonio. The soil
permeability was thus increased to 0.1 I/sec since the subsurface
material suffered a major loss of fine grained material. Soil-water
content was \0%.
In both cases, water was applied through the 10 cm diameter leak
points. For case one, the TDR response varied as a function of
position along the 11 m long transmission line (Figure 4). The
dashed line shows the before-wetting response for easy comparison
with the after-wetting response. The TDR response dropped at
about the 5 m position after 4 1 of water were added. The TDR
response decreased because the dielectric constant of the wet soil
was greater than that of the dry soil. The impedance decreased as
the dielectric constant increased.
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,
Before
welting
Alter
wetting
Approx. Position (meter)
Figure 4
The TDR Responses before and after Adding 4 1 of Water to the 11 m
Long Transmission Lines at the Waste Impoundment Site
•o
TMC M imrrie
Figure 5
Variation of the Amplitude of the TDR Response versus
Time after Water Was Applied
For case two, the change in TDR response on the 11 m long
transmission lines for a conductor spacing of 10 cm after 8 1 of
water were added through the simulated leak point is shown in
Figure 6. The change in the TDR response was much smaller than
the responses observed in case one. In addition, only one or both
sets of vertical transmission lines placed directly below the leak
point detected any water at all. It was also determined from the ver-
tical transmission line measurements that it took only 2 min for a
water front to move down past the horizontal transmission lines.
These results indicated that the soil was very permeable and that the
wetting front was not moving out horizontally more than 5 cm. In
spite of this, close inspection of the TDR response showed a change
as seen by the hatched area in Figure 6.
150
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LEAK POINT
8 IIUr» of wotir oddid
0 mln
3mln
Figure 6
The shading shows the change on the llm long 10 cm spacing
transmission line after 8 1 of water was added
The TDR response began to change at 14:30 hours, about 2.5
min after the addition of 8 1 of water. The level of the TDR
response varied beginning at the location where the simulated leak
was located, 4 m from the start of the transmission lines. The TDR
response returned to near its original before-wetting response in
about 15 min. These changes in the TDR response were small com-
pared to those observed in case one. These changes in response
were also observed in both 17 m and 5 m long transmission lines
with conductor spacing of only 10 cm.
The results of the above series of tests confirmed the laboratory
results.2 TDR systems can detect leaks when the anomaly size is
equal to or greater than half the spacing between the conductors of
the transmission line.
Despite the fact that in case two the soil was drier, the high
permeability of soil prevented horizontal extent of the anomaly to
be greater than 5 cm. As such, the response obtained was less ob-
vious.
Acoustic Emission
Results for acoustic emission monitoring included: (1) estab-
lishing the level of background noise level of the system, (2)
measuring the noise levels when water flows through the soil and (3)
determining the attenuation values of sound when propagating
through water in a shallow pond.
Background Noise Characteristics
The spectral characteristics of the background sounds were
monitored regularly throughout the tests. The spectra of the
background noise measured with one sensor located in the soil and
the other sensor located 10 cm above the liner with 1.6 m of water
in the pond are shown in Figure 7. The sensor in the soil picked up
10 times more noise at frequencies below 50 Hz than the sensor in
the water. This was because low frequencies propagate very well in
the ground.
The spectra of the background of the noises observed with the
sensor positioned 10 cm above the liner with 1.6 m of water in the
pond are shown in Figure 8. The amplitude of the background
sounds did not vary by more than 60 to 200 mV. This variation in
amplitude is essentially the limit of the measurement precision
throughout all of the experiments discussed; thus we concluded
that the background noise level remained constant throughout all
the tests in the field model waste impoundment site.
Noise Spectra When Water Flows through the Soil
The spectra of the sounds as the water flowed at 0.3 I/sec with in-
creasing time are shown in Figure 9. The average background
sound level is shown in all of the spectra presented as a reference.
As the time increased after the start of the water flowing, the sound
amplitude decreased. In fact, after a minute of water flowing in the
soil there were little or no sounds produced compared to the back-
ground sound level. The high sound amplitude just after the water
began to flow probably was caused by air bubbles moving through
the soil pores. Fine grained particles also increased the sound
amplitude produced as water flowed through the soils.
« 10-
i ,
001
SOIL
0 100 200 300 400 500 600 TOO 800 900 1000
FREQUENCY (HERTZ)
Figure 7
Spectra of Background Noise with AE Sensors Above and Below
the Liner of the Pond with 1.6 m of Water
~3> 200 sS> «55555 So TOO «ooJEo~
FREQUENCY(HIRTZ)
Figure 8
Spectra of the Background Noises Observed During the Tests at the
Model Pond Site in San Antonio
BARRIERS
151
-------
30
10 -
3 -
003.
~IOO 200 300 400 500600 700 800 9OO 1000
FREQUENCY (HERTZ)
Figure 9
Spectra of the Sounds as Water Flows at .03 I/sec through Soil
versus Time after Start of Leak
30'
10-
3-
0-1-
0-03
100 ZOO 300 400 500 600 700 800 900 OOO
FREQUENCY (HERTZ)
The sound spectra as water flowed at different rates through the
soil were measured at different time intervals after the valves were
opened. During the time interval just after the water began to flow,
the amplitude of the sounds increased as the flow rate increased as
shown in Figure lOa. The frequency range of the sounds also in-
creased as the flow rate increased. After the water had been flowing
for 30 sec or so, the amplitude of the sounds did not vary
significantly with the water flow rate as shown in Figure lOb. These
results were expected as the turbulent flow of water alone was not a
significant source of sound energy. However, more sound energy
was expected as the flow rate of water mixed with air and soil in-
creased. It is also not surprising that the frequency range of the
sounds increased as the flow rate of the water mixed with air and
soil increased.
The spectra of the sound produced just after the water began to
flow and the sensor position was varied with respect to the
simulated leak in the liner are shown in Figure 11. In addition, a
stationary sensor 15 cm from the leak was installed to monitor the
amplitude of the sounds from the leak. The results showed that it
was rather difficult to detect the sounds from the leak at a range
greater than 1 m at this model waste impoundment site.
Additional experiments were conducted to examine the effect of
turbid water flow through soil. The results indicated that sound
amplitude increased as fine grained material was added for a short
while and then decreased to background noise levels. This was due
to the fact that fine grained particles in the water tended to get
caught in the soil pores near the hole in the liner. This decreased the
flow rate considerably and consequently the sound levels de-
creased.
The results discussed above confirmed the results that Davis2 ob-
tained in controlled laboratory conditions; water alone flowing
through soil does not produce significant sound energy. Sounds are
produced when water mixed with fine grained soils or air flows tur-
bulently through soils.
The attenuation tests conducted at the waste impoundment site
showed that the attenuation valves were 1 dB/m. This was due to
the fact that much of the energy was being lost as waves at the
water surface. This result confirmed the results obtained by
Rubano,5 which stated that attenuation increased as depth decreas-
ed.
Figure 10A
Spectra of Sound as Water Flows at Different Rates for a Time
Period 0-13 Seconds After the Start of the Leak
30
10-
Id
o
X
<
I-
0-1-
0-03
0-6 lltvi/iie
0 100 ZOO 300 400 800 600 700 BOO 900 1000
FREQUENCY (HERTZ)
30
ID-
o
2 '•
Ul
o
? I.
o.
Z 0-3.
<
0-1-
bocfgflund
0 100 200 300 400 300 600 700 800 900 1000
FREQUENCY (HERTZ)
Figure 11
Spectra of the Sounds Produced from Water Flowing in Soil as the
Distance of Sensor from the Leak Is Varied
Figure 10B
Spectra of Sound as Water Flows at Different Rates for a Time
Period 30-60 Seconds After the Start of the Leak
CONCLUSIONS
A time domain reflectometry technique using transmission lines
placed under sandy soils can detect leaks with dimensions that are
152
BARRIERS
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about the same size as the spacing between the transmission lines
that are about 20 m long. The technique looks promising for leak
detection and monitoring at small (<: 0.4 hectare) impoundment
sites.
Turbulent flow of water mixed with either soil grains or air flow-
ing through soils will produce sounds that can be detected by
acoustic emission monitoring. The maximum practical range over
which sounds can be detected is in the order of 1 m. This technique
can be implemented in planned sites by emplacement of transducers
beneath the site; an added advantage of this technique is that it can
also be used from the surface in existing sites to locate leaks non-
destructively.
Further tests using improved signal processing techniques are
necessary to make the acoustic emission monitoring and time do-
main reflectometry techniques practical and economical for detec-
ting liner leaks.
Both TDR techniques and acoustic emission monitoring tech-
niques are presently well understood and await further develop-
ment and field application. At the conclusions of the liner
repairability program, it is anticipated that current knowledge and
technology related to the repair of liner failures in situ will be
understood. In addition, further development and application of
repair techniques evaluated in the course of the program will even-
tually allow appropriate repair measures to be taken in time to pre-
vent or minimize environmental damage when a liner failure occurs
without the need to remove the impounded waste and completely
replace the damaged liner.
REFERENCES
1. Davis, J.L., Singh, R., Stegman, B.C. and Waller, M.J., "Innovative
Concepts for Detecting and Locating Leaks in Landfill Liner Sys-
tems," Final Report to USEPA, Cincinnati, OH, Contract No. 68-
03-3030, (In press).
2. Davis, J.L., "Application of the Time-Domain Reflectometry (TDR),
Technique for the Measurement of Electrical Properties of Soils and
Other Geologic Materials," Final Report to Geological Survey of Can-
ada, Contract NO. OSQ81-00158, June 1982.
3. Haxo, H.E., Jr., "Testing of Materials for Use in the Lining of Waste
Disposal Facilities," Special Technical Publication No. 760, Ameri-
can Society for Testing and Materials, 1982.
4. Matrecon, Inc., "Lining of Waste Impoundment and Disposal Facili-
ties," Final Report for Municipal Environmental Research Labora-
tory, Office of Research and Development, USEPA, 1980.
5. Rubano, L.A., "Acoustic Propagation in Shallow Water Over a Low-
Velocity Bottom," J. Acoust. Soc., 67, 1980, 1608-1613.
6. Topp, G.C., Davis, J.L. and Annan, A.P., "Electromagnetic De-
termination of Soil Water Content: Measurements in Coaxial Trans-
mission Lines," Water Resources Res., 16, 1980, 574-582.
7. Waller, M.J. and Davis, J.L. 1981, "Assessment of Innovative Tech-
niques to Detect Landfill Liner Failings," Report to USEPA, Cin-
cinnati, OH, Contract No. 68-03-3209.
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CLAY BARRIER — LEACHATE INTERACTION
DAVID C. ANDERSON
STEVEN G. JONES
K.W. Brown and Associates, Inc.
College Station, Texas
INTRODUCTION
Interactions between clay barriers and leachate components may
cause deterioration of the barrier's ability to contain the leachate.
Two important dynamic clay barrier properties that may be af-
fected by interactions with leachate are:
•Effective pore volume: the pore space that transmits leachate per-
colating through a clay barrier
•Permeability: the rate at which leachate percolates through a clay
barrier at a given hydraulic gradient
Either a decrease in the effective pore volume at a constant
permeability or an increase in the permeability of a clay barrier will
result in an early appearance of leachate in the subsoil. Increased
permeability of a barrier would result in an increased rate of
leachate migration. A decrease in the volume of pores transmitting
the leachate at a constant permeability would result in a decrease in
the time it would take for the leachate to move through the barrier.
A decrease in effective pore volume would occur if a clay barrier
experienced shrinkage cracking. The leachate would preferentially
move through the crack instead of through the whole clay barrier
matrix. This would result in leachate breaching the clay barrier
earlier than would be expected with a given permeability where the
leachate moved uniformly through the clay barrier.
Two of the most important potential failure mechanisms that in-
volve barrier-leachate interaction are:
•Dissolution and piping: dissolution of clay barrier constituents
that bind particles together and the subsequent piping (move-
ment of clay particles with the percolating leachate)
•Development of soil structure: pulling together of soil particles
into aggregations of many particles resulting in the formation of
large interaggregate pores
By understanding the mechanisms by which clay barriers fail, it
may be possible to alter leachate to lessen its impact on the dynamic
properties of the clay barriers. Knowing leachate components likely
to affect barrier properties makes it possible to identify wastes that
require pretreatment. Discussions of these two clay barrier failure
mechanisms and the leachate components that may cause these
failures follow.
DISSOLUTION AND PIPING
If a strongly acidic or basic leachate moves into a clay liner, it
may initially dissolve substances coating the liquid-conducting pore
walls. These coatings include soil binding agents such as native
organic matter, calcium carbonate and iron oxide polymers.
Dissolution of binding agents releases soil particles for migration
through pore spaces within the rigid soil matrix. The diameters of
the pores from which the particles were released would, therefore,
increase.
However, whether the permeability of the clay barrier increases
or decreases will depend on the fate of the migrating particles. If
the particles migrate (pipe) through the clay barrier, then the
permeability may increase. If the particles lodge in pore constric-
tions thereby clogging the soil, the permeability will decrease. For a
barrier to fail due to exposure to acidic or basic leachates, there
must be both dissolution and piping.
Piping begins on the underside of a clay barrier where released
particles can migrate into substrata containing larger pore
diameters. The soil pipe then progresses upward through the clay
barrier until it forms an opening into the impoundment or landfill.
Clay particles have been shown to migrate through soils containing
less than 15% clay.' Consequently, soils adjacent to clay barriers
should be evaluated for their ability to facilitate piping in the bar-
rier.
Both organic and inorganic acids react with and dissolve portions
of compacted clay soils. Acids dissolve aluminum, iron and silica,
eroding the lattice structure of clays and releasing undissolved
fragments for migration in a percolating leachate.2 Organic acid
wastes have been shown to dissolve smectitic, illitic and kaolinitic
clay minerals.3
Bases also have been implicated in the dissolution of clay
minerals and the removal of silica from the crystalline structure of
clay. Many organic bases may be too weak to dissolve clay
minerals, but dilute solutions of strong inorganic bases have been
shown to be sufficient to dissolve clay minerals.*
DEVELOPMENT OF SOIL STRUCTURE
Soil structure is the spatial arrangement of soil solids and voids.
In clayey soils, the arrangement and spacing of the plate-like clay
particles play a dominant role in this structure. Clay barriers that
are either placed as a slurry or compacted at above optimum water
content tend to have a massive structure which is made up of small
interparticle pores with few aggregations of clay particles and few
large interaggregate pores.
An aggregated structure develops in native soils partially as the
result of climatic cycles such as wetting and drying. Clay particle
surfaces may be dehydrated during prolonged dry spells. When the
layers of interparticle water are removed, these particles form more
tightly packed aggregations accompanied by the formation of large
interaggregate pores. In addition, clayey soils often develop large
cracks during dry spells. Both interaggregate pores and large cracks
represent a shift in the pore size distribution toward larger pores,
154
BARRIERS
-------
which may result in permeability increases and decreases in the ef-
fective pore volume of the clay barrier.
Structural development of clay barriers can be characterized as
the pulling together of groups of clay particles into aggregates. Ag-
gregations are caused by increased cohesive forces between in-
dividual clay particles. When repulsive forces are overcome by at-
tractive forces, the clay particles will tend to flocculate (aggregate),
resulting in the formation of relatively large interaggregate pores.
Forces of attraction are strongest close to clay surfaces and
diminish rapidly with increasing distance from the surfaces.
However, these attractive forces do not vary significantly with
changes in leachate chemistry.5
Forces of repulsion between adjacent clay surfaces are primarily
electrostatic. Negatively charged clay particles are neutralized by
positively charged cations that adsorb to clay surfaces. Where a li-
quid is also adsorbed to clay surfaces, cations tend to swarm
around in the liquid layer, forming a positively charged cloud
around the clay particles. Adjacent positively charged clouds repel
each other, resulting in an equilibrium spacing between the clay
particles. Interparticle spacing, therefore, is a function of the
thickness of these cationic clouds. Characteristics of a liquid that
affect cationic cloud thickness and, therefore, forces of repulsion,
are salt concentration, dielectric constant, dipole moment and
molecular size (diameter of individual molecules). Effects of salt
concentration and dielectric constant are schematically represented
in Figure 1.
AQUEOUS SYSTEM
(SALT
CONCENTRATION)
HIGH
MEDIUM
LOW
ORGANIC LIQUIDS
(DIELECTRIC
CONSTANT)
A
B
C
LOW
MEDIUM
HIGH
terparticle spacings. At small interparticle spacings, attractive
forces are greater than repulsive forces and clay particles tend to
flocculate.7 Flocculation of clay particles caused by changes in the
cationic cloud thickness may transform a massive, structureless and
slowly permeable clay barrier into an aggregated and more
permeable barrier.
A situation analogous to the decrease in repulsive forces that ac-
companies an increase in interparticle salt concentration occurs if
interparticle water is displaced by an organic liquid that has a lower
dielectric constant than water (Figure 1). Simply stated, the dielec-
tric constant represents the ability of a liquid to transmit charge.8
As this ability decreases (i.e., decreasing dielectric constant), the
layers of liquid surrounding the clay particles and containing the
cationic cloud must be decreased for the negatively charged clay
surfaces to be neutralized.
Since most organic liquids have dielectric constants substantially
lower than that of water,9'10 the interparticle spacing of clay par-
ticles in a clay barrier permeated by organic liquids would be ex-
pected to decrease. For instance, if a waste liquid high in propanol
replaced water, the interparticle spacing would decrease (Table 1).
If the dielectric constant of interparticle liquid decreased below a
certain value, a structureless and slowly permeable clay barrier can
be transformed into an aggregated one with increased permeability.
Both dipole moment and molecular size of a liquid affect inter-
particle spacing by affecting the number of liquid layers that will
adsorb to clay mineral surfaces. The number of adsorbed liquid
layers increases with increasing dipole moment and decreasing
molecular size.3 This interplay between dipole moment and
molecular size explains the initial increase in spacing from
methanol to ethanol (Table 2). These two alcohols have a small
enough molecular size to adsorb in two layers. However, members
of the homologous series of alcohols larger than ethanol are
restricted to adsorbing in one layer. Thus, from ethanol to pro-
panol, there is a decrease in interparticle spacing corresponding to
the decrease to one adsorbed layer. Interlayer spacing increases
above propanol due to the increasing thickness of the one adsorbed
layer.
FORCES
OF
REPULSION
FORCES
OF
ATTRACTION
DISTANCE BETWEEN
CLAY PARTICLES
Figure 1
Forces between clay particles as affected by salt concentration
and dielectric constant of the interparticle liquid
As the salt concentration increases in the liquid layer surround-
ing a clay particle, the thickness of the cationic cloud decreases,
resulting in a decrease in electrostatic repulsion and interparticle
spacing. A direct relationship has been noted between salt concen-
tration and interparticle spacing in clay minerals.6 Both distilled
water and low salt concentrations give large interparticle spacing
values while higher salt concentrations give progressively smaller in-
LEACHATE COMPONENTS
Both permeability and effective pore volume may be affected by
solvents and solutes in a leachate. While low permeabilities may be
obtained with clay barriers permeated by pure water, studies have
shown that this may not be the case with clay barriers permeated by
organic liquids or water containing a high concentration of certain
solutes.
Table 1
Interparticle Spacing of a Clay Mineral Immersed in Water-Propanol
Mixtures with Various Dielectric Constants9
Dielectric
Constant
Liquid
Water
100%
70%
40%
30%
20%
0%
Mixture
Propanol
0%
30%
60%
70%
80%
100%
(25 °(
78.5
57.7
36.4
30.7
26.1
20.1
Interparticle
Spacing
(nm)
0.93
0.89
0.85
0.78
0.78
0.45
BARRIERS
155
-------
Table 2
Interlayer Spacing of Smectite with a Homologous Series
of Normal Monohydric Alcohols"
Normal
Monohydric
Alcohols
Methanol
Ethanol
1 -Propanol
1-Butanol
1-Pentanol
2-Methyl-2-bulanol
Cyclohcxanol
Interlayer
Sparing
(nm)
0.74
0.79
0.45
0.46
0.46
0.54
0.54
Thickness of
One Layer
(nm)
0.37
0.39
0.45
0.46
0.46
0.54
0.54
Number of
Adsorbed
Layers
2
2
Leachate composition depends on waste composition and site
climatic conditions. The initial liquids released from a waste
(primary leachate) may bear little resemblance to the subsequent
leachate generated by rainwater percolating through the waste
(secondary leachate). Leachates may be subjected to climatic cycles
of concentration by evaporation and dilution by rainfall. In addi-
tion, many wastes undergo biochemical and geochemical changes
that may dramatically alter leachate chemistry. All these factors
should be considered when evaluating clay barrier-leachate com-
patibility.
These leachate components are divided into organic liquids and
aqueous leachates (Figure 2). Following is a review of the literature
on the effects of potential leachate components on clay barrier
permeability and effective pore volume of clay barriers.
ORGANIC LIQUIDS
Liquids placed in land storage and disposal facilities have, in the
past, included a wide assortment of organic liquids. However, the
majority of papers describing leachate consider only water as the li-
quid phase. Water is viewed as the carrier liquid and organic
chemicals are considered to be present in only trace quantities.
Leachate may, however, contain a mixture of water and miscible
organic liquids. Leachates may also be composed of immiscible
organic liquids containing only traces of water. Storage or disposal
of either an organic waste or sludge with an organic liquid phase
may result in exposure of clay barriers to organic liquids released by
the waste.
The first evidence that clay minerals may be much more
permeable to organic liquids than to water was published over 40
years ago in a study of clays used in ceramics,'2 That study conclud-
ed that differences in both clay particle arrangements and interpar-
ticle spacing were at least partly responsible for the clay being be-
tween 100,000 and 1,000,000 times more permeable to organic li-
quids than to water.
Huge quantities of organic liquids are used and eventually
discarded by a wide variety of industries. Organic solvents are used
to dry clean clothing, clean metal surfaces of manufactured goods
before the final painting and in the day-to-day cleaning of
machinery. Other major sources of waste organic liquids are oily
sludges that accumulate and must be periodically removed from in-
dustrial process vessels (such as still bottoms) and oil storage tanks.
In the following discussion, these organic liquids have been divided
into four classes: acidic, basic, neutral polar and neutral nonpolar.
Acidic Organic Liquids
In a study to determine the effect of organic acids on clay soil
liners, four compacted clay soils with diverse mineralogical and
chemical properties were permeated first by water to establish their
baseline permeabilities and then by glacial acetic acid." All four
soils showed initial permeability decreases when permeated by the
concentrated liquid organic acid. However, two of the clay soils
eventually underwent substantial permeability increases. Initial
Figure 2
Leachate components: Types of organic liquids and
solutes of aqueous leachate
decreases in permeability were thought to be due to partial dissolu-
tion and subsequent migration of soil particles. These migrating
particle fragments were thought to lodge in the liquid-conducting
pores, thus decreasing cross-sectional area available for liquid flow.
Permeability increases seen in two of these soils were thought to be
due to progressive soil piping that eventually cleared the initially
clogged pores.
Because of across-the-board piping that occurred with acid
treated clays, it was thought that any strong acid capable of dissolv-
ing soil components might increase the permeability of clay bar-
riers. Neutralization of acids and bases prior to their disposal may
be the best safeguard against clay barrier failure in these cases, pro-
vided the resulting salts do not adversely affect permeability.
Basic Organic Liquids
In a study of the effect of organic bases on clay liner permeabili-
ty, four compacted clay soils were permeated by water followed by
the organic base aniline." Permeabilities were stable to water, but
increased when the soils were permeated by aniline. There were no
signs of migrating soil particles in any effluent samples collected
from the four aniline-treated soils. Apparently, aniline was too
weak a base to cause significant dissolution of clay soil com-
ponents.
However, examination of the soils after permeability testing in-
dicated that the organic base causes extensive structural changes in
the upper half of the clay soils. The massive structure of the four
soils was altered by aniline into an aggregated structure character-
ized by visible pores and cracks on the surface of the soils."
Neutral Polar Organic Liquids
Many common industrial feedstocks and solvents are neutral
polar organics such as ketones and alcohols. Polarity generally in-
dicates that a chemical has a high water solubility, and consequent-
ly these liquids may be present in aqueous leachate over a wide
range of concentrations. These organic liquids are often disposed in
relatively concentrated form" and thus may, in some cases, be the
predominant liquid when a leachate reaches a clay barrier.
In a study of the effects of neutral polar organics on clay soils,
four compacted clay soils were permeated by water followed by
acetone." All four soils had relatively stable permeabilities to water
but eventually exhibited large permeability increases after permea-
tion by acetone. Initially, there were significant permeability
decreases in all four soils below 0.5 pore volume, but large
permeability increases subsequently occurred. The explanation
given for these permeability sequences was:"
•The higher dipole moment of acetone (2.74 debyes) relative to
water (1.83 debyes) initially caused the soils to swell and, hence,
undergo permeability decreases.
156
BARRIERS
-------
•The higher molecular volume of acetone (73.5 cm3 mol~') relative
to water (18.4 cm3 mol"1) subsequently caused the soils to shrink
and, hence, undergo permeability increases.
Permeability increases were attributed to the development of an ag-
gregated structure in the initially massive clay soils, since examina-
tion of the soils after acetone treatment revealed extensive
shrinkage and cracking.
Laboratory and field studies were conducted to evaluate the ef-
fect of an acetone-bearing waste on the permeability of three types
of clay liners.14 While clay liners tested in the laboratory and field
all showed initial permeability decreases, large permeability in-
creases eventually occurred in all the liners.
Another study of the effect of acetone on the permeability of
compacted clay soils also noted initial permeability decreases." Un-
fortunately, these studies were terminated before 0.5 pore volume
of acetone had passed through the soils, which is the point where
permeability increases occurred in both of the other studies exam-
ining the effects of acetone on permeability.
A methanol and water solution (20% H2O) was similarly used as
the permeant liquid for four clay soils after baseline permeabilities
were established with water." While the methanol-permeated soils
underwent large permeability increases, there was no initial
permeability decrease as with the acetone-permeated soils. Lack of
an initial permeability decrease was thought to be consistent with
the lower dipole moment of methanol (1.66 debyes) relative to
water. Final examination of the methanol-permeated soils revealed
development of large pores and cracks on the surface of the treated
soils."
Another study examined the intrinsic permeability (normalized
for differences in viscosity and density of the liquids) of three clay
soils to two neutral polar organic liquids and water" (Table 3).
Alcohol-treated soils exhibited intrinsic permeabilities over one
order of magnitude greater than the water-permeated clay soils.
Etyhlene glycol-treated soils had intrinsic permeabilities over five
times greater than water in two cases and over 10 times greater in
the third soil.
Neutral polar organic liquids are soluble in water and may,
therefore, be substantially diluted after disposal. Neutral nonpolar
organic liquids, however, are generally immiscible and hence re-
main in concentrated form after disposal.
Table 3
Intrinsic Permeability of Three Clay Soils
to Water and Four Organic Solvents'
Intrinsic Permeability (cm2)
Lake Bottom Fanno
Clay (Illite & Nicholson (Montmorillonite
Permeant Liquids
Nonpolar-aromatic
(xylene)
Nonpolar-aliphatic
(kerosene)
Polar-glycol
(ethylene glycol)
Polar-alcohol
(isopropyl alcohol)
Water
Kaolinite)
1.4 x 10~8
1.0 x 10~9
2.4 x ID"9
6.4 x 10~9
5.1 x 10-'°
(Vermiculite) & Mica)
2.9xlO~9 1.5 x 10~7
2.9 xlO~9 1.6 x 10-7
1.4x10-'° 6.3xlO-8
6.8x10-'° 9.3xlO-8
4.3x10-" 1.6x10-'
Neutral Nonpolar Organic Liquids
Most nonaqueous liquids that are disposed in landfills are neutral
nonpolar organics. This class includes waste oils and many of the
discarded industrial solvents. Common nonpolar solvents include
aromatic (e.g., benzene and xylene) and aliphatic (e.g., heptane)
compounds.
Benzene and water were used as permeant liquids to measure the
depth of penetration with time through a compacted clay subsoil.11
Approximately 90 cm columns of the clay subsoil were compacted
to 95% of standard proctor density. Test liquids were placed over
the compacted soil, and air pressure was applied to the top of the li-
quid to stimulate a hydraulic head of approximately 7 m and a
hydraulic gradient of roughly 24. The depth of penetration with
time for water and benzene when the clay liner was compacted at
optimum moisture content (31% by weight) and for benzene when
the clay liner was compacted at 20% and 10% water content by
weight is given in Table 4.
Shortcomings of the study included the following: (1) no actual
permeability values were given, and (2) the report lacked an ade-
quate characterization of the clay subsoil. However, the following
conclusions can be drawn from the study:
•When compacted at optimum moisture and 95% of standard
proctor density, the clay subsoil was approximately 100 times
more permeabale to benzene than to water.
•When properly compacted to a thickness of approximately 90 cm,
the clay subsoil was found to be a suitable surface impoundment
liner for tap water but not for benzene.
•When compacted at optimum moisture and 95% standard proctor
density, the 90 cm thick compacted clay, subjected to a hydraulic
gradient of 24, would begin to leak benzene in approximately
36 days.
•When compacted on the dry side of optimum moisture but still
at 95% standard proctor density, the clay subsoil would be sub-
stantially more permeable to benzene than if it had been com-
pacted at the optimum moisture content.
•When permeated by benzene rather than tap water, the clay sub-
soil had a substantially reduced effective pore volume.
In another study, permeabilities and breakthrough curves were
determined for four compacted clay soils permeated by water and
then xylene." All soils showed stable permeabilities to water but
underwent large permeability increases (100 fold) when permeated
with xylene. The small fraction of a pore volume (<0.25) that was
passed before breakthrough indicated that xylene greatly decreased
the effective pore volume of the clay soils. Examination of the soils
revealed massive structure after permeation by water and highly ag-
gregated structure after permeation by xylene.
Table 4
Depth of Penetration with Time for Benzene and Tap Water
Percolating through a 90 cm Column of Compacted Clay11
Permeant
Liquid
Tap water
Benzene
Benzene
Benzene
Compaction
Water Content
(% by weight)
31
31
20
10
Elapsed
Time
(Days)
100
36
32
0.63
Depth of
Penetration
(cm)
2.4
90.0
90.0
90.0
Table 5
Void Ratio and Permeability Relationships for Calcium and Sodium
Saturated Clays Permeated by Water and Naphtha"
Clay
Calcium
Saturated
Sodium
Saturated
Void
Ratio
1.72
3.75
WATER
Permeability
(cm sec~l)
1.6 x 10-9
5.2 x 10-H
Void
Ratio
1.52
1.31
NAPHTHA
Permeability
(cm sec 1)
6.4 x 10-5
3.8x 10-5
BARRIERS
157
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Laboratory and field studies were conducted to evaluate the ef-
fect of a xylene paint waste on the permeability of three types of
clay liners." Large permeability increases occurred in both the
laboratory and field studies.
Intrinsic permeabilities of three clay soils to xylene, kerosene and
water were evaluated in another study" (Table 3). Xylene treated
soils showed intrinsic permeability increases of from 1.5 to 2 orders
of magnitude over values obtained with water. Kerosene caused in-
creases of from 0.5 to 2 orders of magnitude over water.
Permeabilities of sodium and calcium saturated clays permeated
by water and naphtha were evaluated in another study" (Table 5).
Permeabilities of the two clays to naphtha were six and four orders
of magnitude, respectively, greater than when permeated by water.
These permeability differences occurred 'in spite of substantial
reductions in the void ratio for the clays treated with the nonpolar
liquid. Permeability differences were thought to be at least partially
due to the inability of naphtha to form an immobilized liquid film
on the clay mineral surfaces.
Another study noted that nonpolar compounds such as xylene
may greatly increase the permeability of compacted clay soils by
causing the formation of shrinkage cracks." This study inaccurate-
ly listed the equilibrium permeability for xylene-treated soils as the
low permeability values obtained prior to the formation of the
shrinkage cracks and solvent breakthrough. The authors then plot-
ted the artificially low permeability values for neutral nonpolar li-
quids versus their dielectric constants and arrived at the following
faulty conclusion: "All clay soils were more permeable to water
than to organic solvents.""
Intrinsic permeability of a clay loam to oil was found not be be
significantly affected by the exchangeable sodium percentage (ESP)
of the soil (Table 6)." The intrinsic permeability of the soil to water
was found to be 3-4 x 10~9 cm2 and 2-3 x lO"10 cm2 at ESP values
of 0-5 and 20-25, respectively. However, the intrinsic permeability
of the soil was 1-3 x 10 -"" cm2 to the light oil regardless of the ESP
of the soil.
Another study gave permeabilities and breakthrough curves for
four compacted clay soils permeated by water and then heptane.13
All soils showed stable permeability values to water but underwent
large permeability increases (100 fold) when permeated by heptane.
Heptane also caused a reduction in the effective pore volume of the
clay soils (breakthrough occurred at -C0.25 of a pore volume).
Following large initial increases, permeability increases slowed to
near constant values. The constant permeabilities eventually
reached by the soils were thought to be related to the limited ability
of aliphatic neutral nonpolar organic liquids to penetrate interlayer
spaces of the clay minerals. In contrast, neutral polar organic li-
quids can penetrate interlayer spaces. Soils treated with polar li-
quids showed more nearly continuous permeability increases and
less of a decrease in the effective pore volume of the clay soils."
Thus, it would appear that both permeability increases and effec-
tive pore volume reductions are most severe with nonpolar organic
liquids.
Table 6
Intrinsic Permeability of a Clay Loam Soil
to Oil and Water at Two ESP Ranges"
Intrinsic Permeability (cm2)
Pcrmeanl Liquid
Water
Light Oil
ESP = 0-5
3-4xlO-»
1-2 x 10-8
ESP = 20-25
2-3 x 10-|0
2-3 x lO-8
AQUEOUS LEACHATES
Most hazardous waste leachates are water-based solutions con-
taining an assortment of organic and inorganic solutes. The effect
these constituents have on the permeability of a clay barrier may
depend on the concentrations of the constituents. At very low
solute concentrations (distilled water), the permeability of a clay
barrier usually decreases substantially. One soil with 12% clay ex-
hibited a stable permeability during treatment with a landfill
leachate (1.6 x 10~* cm sec"1)- However, it underwent a 64 fold
reduction in permeability (to 2.5 x 10~6 cm sec"1) when subse-
quently treated with distilled water.20
While strongly concentrated leachates may increase permeability,
no examples were found in the literature where very dilute aqueous
solutions caused substantial permeability increases. One potential
exception may be water that contains low concentrations of strong
surfactants. These compounds could increase the (intrinsic)
permeability of a soil by decreasing the surface tension of water."
Acidic and Basic Aqueous Solutions
Both acids and bases can dissolve clay liner compounds. Dissolu-
tion of clay minerals and soil binding agents can release particles
for migration through soil. The result may be either permeability
reductions through pore clogging or permeability increases through
particle piping. One other mechanism of permeability increase with
these reactive solutes could be disruption due to the release of gases
from chemical reactions within the soil core.
In one study, three clay soils packed in columns were permeated
by either 0.1 N hydrochloric acid or sodium hydroxide." The acid-
treated soils broke into thin lenses which finally expanded into
separate clumps near the top of the soil cores. Near the bottom of
the columns, the soils underwent enough shrinkage to separate
from the column walls and allow unrestricted flow of the acid. In
another column test, permeability of three clay soils decreased after
they were permeated by 0.1 N sodium hydroxide. However, less
than one pore volume of the base was passed through these cores.
This small amount reduced the usefulness of the findings for inter-
preting long-term effects on the permeability of the clay soils.
Two strongly basic and two strongly acidic wastewaters seeped
through two simulated clay liners in a "relatively short time.""
The 2.4 cm thick liners were constructed with one of two commer-
cially available bentonite clays mixed with beach sand. The two
basic wastes (slop water of pH 12 and spent caustic waste of pH
11.3) seeped through the clay liners in 2 to 3 days, respectively. The
two acidic wastes (stainless steel pickling liquor composed of nitric,
hydrofluoric and acetic acids at pH 1.5, and another unidentified
acid waste at pH 4.8) seeped through the clay liners in 3 and 17-44
days, respectively. It has been suggested, however, that the sand
from San Francisco Bay used for the base soil was not washed, and
that the clay "would not have hydrated properly due to the
presence of the salt in the admix.""
Other studies have been conducted on the permeability of clays
to aqueous solutions of acids and bases. One showed that 1% solu-
tions of either sodium hydroxide or hydrochloric acid caused 400%
and 250% increases, respectively, in the permeability of soils mixed
with 1% bentonite.25 The permeability increases occurred during
the passage of 15 pore volumes of the acidic and basic solutions.
Another study showed large permeability increases when mont-
morillonitic clays were permeated by either strongly basic (5.0 N
NaOH) or acidic 2.0 N chromic acid) solutions.26 When kaolinitic
or vermiculitic clays were permeated by these solutions, however,
the clays underwent permeability decreases.
Leachate from the disposal of organic wastes can be expected to
go through a stage of acidic pH due to the production of acids as
organic decomposition by-products.27'28 During this low pH stage,
as much as 95% of the total chemical oxygen demand (COD) in a
leachate may be in the form of organic acids,29 while the COD of
leachate may be as high as 900,000 mg/l.)0 Organic acids found in
leachate include acetic, propionic, butyric, valeric and caproic.
158
BARRIERS
-------
Although no studies could be found that specifically evaluated the
influence of aqueous solutions of organic acids on the permeability
of clay liners, these acids are widely used to increase the permeabili-
ty of wells used in oil production.31'32'33
Salts in Aqueous Solutions
The permeability of clay soils is affected by the chemical species
and concentration of salts in solution and on the exchange sites of
the clay. These permeability-salt relationships may also vary in
magnitude and reversibility for clays of different mineralogy and
with differing amounts of soil binding agents. The following gen-
eralizations may aid in understanding these complex relation-
ships:34
•Permeability decreases with decreasing concentrations of salts in
the soil solution.
•Permeability decreases with increasing percentage of sodium oc-
cupied cation exchange sites on a soil.
•Permeability reductions described in 1 and 2, above, are usually
greater in soils with high contents of swelling clay minerals
(smectites).
•The effects described in 1 and 2, above, are usually negligible
in soils high in binding agents such as iron or aluminum hydrous
oxides.
The low permeability associated with sodium salt affected soils
are often increased by the addition of gypsum (CaSO4). In one
study, large permeability increases were obtained when the soil salt
concentration was increased by adding gypsum." The addition of
10 metric tons of gypsum per hectare of clay loam soil yielded a salt
concentration in the soil solution of 20 meq/1. This resulted in a
permeability increase of two orders of magnitude (from 5 x 10~4
to 5 x 10"4 tol 5 x 10-2 cm/hr).
Another study examined the influence of high salt concentra-
tions (3.1% Nad + 3.6% NajSOJ on the permeability of two
simulated clay liners constructed os smectitic clays (sodium sat-
urated and organic polymer-treated) and a sandy soil.36 Permea-
bility of the organic polymer-treated smectite was unaffected by the
concentrated salt solution, but the sodium saturated smectite (na-
tural bentonite) underwent a 100 fold permeability increase (from 1
x 10~6 to 1 x 10~4 cm sec"1) in just seven days.
In a later study, the influence of an aqueous solution of 10%
ammonium chloride on the permeability of three smectitic clays
was examined.37 These clays were described as: (1) natural benton-
ite with no contaminant resistance; (2) bentonite which had in the
past demonstrated a degree of resistance; and (3) bentonite that
was highly contaminant resistant. After seven days at a perme-
ability of approximately 1 x 10"7 cm/sec, all three clays showed no
effects of the strong salt solution. However, after the end of a 28
day period, two of the clays (1 and 3) had completely failed while
the third clay (2) was still maintaining the permeability it had on
day one. This study indicated that permeability or seepage behavior
of a clay exposed to contaminants should be evaluated as a func-
tion of pore volume displacements rather than time. While the two
clays that failed had done so after passage of 0.5 of a pore volume,
the third clay was still performing well after passage of 2 pore
volumes.
Salts of heavy metals (0.015 N PbCl2 and HgCl2) produced
erratic changes in the flow rates of three clay soils." Compared
with flow rates for deionized water, the heavy metals decreased the
flow in one clay, increased flow by as much as 100% in a second
clay, and increased flow by as much as 400% (for mercury) and
3,000% (for lead) in a third clay soil. The report concluded that
addition of any salt tends to increase the permeability of clay.
Effects of two metal salt solutions (copper sulfate and zinc chlor-
ide) on the permeability of a compacted smectitic clay soil were
evaluated in another study.2' A slight increase in permeability of
the clay soil was noted with the copper sulfate solution and zinc
chloride caused the second simulated clay liner to completely fail.
The salt concentrations used in these studies were not reported.
Organic Chemicals in Aqueous Solutions
Any organic chemical may be present in aqueous leachates at
concentrations up to its maximum solubility. Organic solutes found
in aqueous leachates include the entire range of organic chemicals
found in hazardous waste streams. These may include low concen-
trations of nonpolar and potentially much higher concentrations of
polar organic chemicals.
While dilute solutions of organic chemicals may be expected to
affect clay barrier permeability less than concentrated organic
liquids, there is little information concerning the effects of various
concentrations. One study found that a solution of 0.01 N phenol
had no affect on two clays but slightly decreased the permeabil-
ity of a third clay." In another study, organic rich wastewater was
thought to cause the formation of highly permeable channels in
clay subsoils.3' These channels were described as vertically
oriented, 2 to 60 cm in diameter, inverted cone-shaped bodies with
much lower bulk densities and 2 to 18 times the permeability of
the surrounding soil.
CONCLUSIONS
Two mechanisms by which leachate can disrupt clay barriers are
as follows:
•Dissolution of soil binding agents by acidic or basic leachates
followed by piping of the clay particles out of the barrier
•Development of soil structure due to the effect of organic liquids
or salts on the balance of forces between clay particles
Information indicating that clay barriers may be much more
permeable to organic liquids than to water has been in the scien-
tific literature for over four decades. High concentrations of acids,
bases or salts may also increase the permeability of clay barriers.
This information should be considered where remedial action and
disposal options are being evaluated for wastes that may release
leachates containing these components.
Prior to the placement of any containment barrier, compatibil-
ity tests should be conducted. These tests should include evalua-
tion of the permeability of the containment barrier with whatever
leachate is to be contained. In addition, it is advisable to determine
whether the leachate will alter the effective pore volume of the
barrier.
REFERENCES
1. Hardcastle, J.H. and Mitchell, J.K., "Electrolyte Concentrations-
Permeability Relations in Sodium Illite-Silt Mixtures", Clays and
Clay Minerals 22, 1974, 143-1544.
2. Grim, R.E., Clay Mineralogy. 2nd ed. McGraw Hill, New York,
1968.
3. Malcolm, R.L., Leenheer, J.A., and Weed, S.B., "Dissolution of
Aquifer Clay Minerals During Deep-Well Disposal of Industrial
Organic Wastes". Presented at the International Clay Conf. Mexico
City, Mexico, July, 1975.
4. Nutting, P.E. "The Action of Some Aqueous Solutions in Clays of
the Montmorillonite Group", U.S. Geological Survey Professional
Papers 197, 1943,219-235.
5. Van Olphen, H. Clay Colloid Chemistry. John Wiley and Sons, Inc.,
New York, 1963.
6. Weiss, A. "Interlayer Swelling as a General Model of Swelling
Behavior". ChemicalBer. 91, 1958, 487-502.
7. Yong, R.N. and Warkentin, B.P., Soil Properties and Behavior.
Elsevier Publishing Company, New York, 1975.
8. Bockris, R.D. and Reddy, A.K., Modern Electrochemistry; Volumes
1 & 2. Plenum Publishing Company, New York, 1970.
9. Barshad, I., "Factors Affecting the Interlayer Expansion of Vermi-
culite and Montmorillonite with Organic Substances", Soil Sci. Soc
Am. Proc. 16, 1952, 176-182.
10. Murray, R.S. and Quirk, J.P., "The Physical Swelling of Clays in
Solvents", Soil Sci. Soc. Am. J. 46, 1982, 865-868.
11. MacEwan, D.M.C., "Complexes of Clays with Organic Compounds:
I. Complex Formation Between Montmorillonite and Halloysite and
BARRIERS
159
-------
Certain Organic Liquids", Transactions of the Faraday Society 44,
1948, 349-367.
12. Macey, H.H., "Clay-Water Relationships and the Internal Mechanism
of Drying", Transactions. British Ceramic Society 41, 1942,73-121.
13. Brown, K.W. and Anderson, D.C., Effects of Organic Solvents on the
Permeability of Clay Soils. U.S. Environmental Protection Agency,
Washington, D.C. EPA-600/2-83-016, 1983.
14. Brown, K.W., Green, J., and Thomas, J., "The Influence of Selected
Organic Liquids on the Permeability of Clay Liners", In D.W. Shultz
(ed.) Land Disposal, Incineration, and Treatment of Hazardous
Waste (Proceedings of the Ninth Annual Research Symposium).
EPA-600/9-83-002, 1983.
15. Green, J.W., Lee, G.F., and Jones, R., "Clay Soil Permeability and
Hazardous Waste Storage", JWPCF8, 1981, 1347-1354.
16. Schram, M., "Permeability of Soils to Four Organic Solvents and
Water". M.S. Thesis, University of Arizona, Tucson, Arizona, 1981.
17. White, R., "Remolded Soil Samples from Proposed Waste Landfill
Site North of Three Rivers, Texas". Trinity Engineering Testing
Corporation, Report #76791. Corpus Christi, Texas, 1976.
18. Buchanan, P.N., "Effect of Temperature and Adsorbed Water on
Permeability and Consolidation Characteristics of Sodium and Cal-
cium Montmorillonite" Ph.D. Dissertation, Texas A&M Univer-
sity, College Station, Texas, 1964.
19. Van Schaik, J.C., "Oil: Water Permeability Ratios as a Measure of
the Stability of Soil Structure", Can. ofSoilSci. 54, 1974, 331-2.
20. Chan, K.Y., "Changes to a Soil on Irrigation with a Sanitary Landfill
Leachate", Water, Air, and Soil Pollut. 17, 1982, 295-304.
21. Letey, J., Osborn, J.F., and Valoras, N., "Soil Water Repellency
and the Use of Non-Ionic Surfactants". Contribution #154, Cali-
fornia Water Research Center, 1975.
22. Sanks, R.L., LaPlante, J.M., and Gloyna, E.F., "Survey—Suitabil-
ity of Clay Beds for Storage of Industrial Solid Wastes", Tech-
nical Report EHE-76-04, CRWR-128, Center for Research in Water
Resources, University of Texas, Austin, Texas, 1975.
23. Haxo, H.E., Jr., "Evaluation of Selected Liners When Exposed to
Hazardous Wastes", In Proc. Hazardous Waste Research Symposium.
EPA-600/9-76-015, 1976.
24. Kingsbury, R., Private Communication, 1981.
25. D'Appolonia, D.J., "Slurry Trench Cut-off Walls for Hazardous
Waste Isolation". Engineered Construction International, Inc. 1981.
26. Coia, M.F., "The Effect of Electroplating Wastes Upon Clay as an
Impermeable Boundary to Leaching" M.S. Thesis, Duke University,
Durham, North Carolina, 1981.
27. Pohland, F.G., Sanitary Landfill Stabilization, Leachate Recycle, and
Residual Treatment. U.S. Environmental Protection Agency, Wash-
ington, D.C. EPA 600/2-75-043, 1975.
28. Hoeks, J. and Borst, R.J., "Anaerobic Digestion of Free Volatile
Fatty Acids in Soils Below Waste Tips", Water, Air, and Soil. Pollut.
17, 1982,165-173.
29. Harmsen, J. "Identification of Organic Compounds in the Leachate
of a Waste Tip", Note #1227. Institute for Land and Water Man-
agement Research, Wageningen, The Netherlands, 1980.
30. Monsanto. Hazardous Waste Leachate Management Manual.
(DRAFT) pp. 3-11. USEPA Contract #68-03-2550., U.S. Environ-
mental Protection Agency, Cincinnati, Ohio, 1980.
31. Hurst, R.E. "Chemicals Find Growing Use in Oil Fields", Chem.
Eng. News 48, March 9, 1970, 10.
32. Johansen, R.T., Powell, J.P., and Dunning, H.N., "The Use of Non-
Ionic Detergent and Citric Acid for Improving Cleanout Procedures
of Water-Input Wells in Secondary Oil-Recovery Projects" U.S.
Bureau of Mines, Information Circular #7797, 1951.
33. Sinex, H.E., Jr., Dissolution of a Porous Matrix by Slowly Reacting
Flowing Acids". M.S. Thesis, University of Texas, Austin, Texas,
1970.
34. Bresler, E., McNeal, B.L., and Carter, D.L. "Saline and Sodic Soils:
Principles Dynamics Modeling", Advanced Series in Agricultural
Sciences. Volume 10, Springer Verlag, New York, 1982.
35. Loveday, J., "Relative Significance of Electolyte and Cation Ex-
change Effects when Gypsum is Applied to a Sodic Clay Soil", Aust.
J. Soil Res. 74,1976,361-371.
36. Hughes, J., "Use of Bentonite as a Soil Sealant for Leachate Control
in Sanitary Landfills", Soil Laboratory Engineering Report Data 280-
E, American Colloid Company, Skokie, Illinois, 1975.
37. Hughes, J., "A Method for the Evaluation of Bentonites as Soil
Sealants for the Control of Highly Contaminated Industrial Wastes",
Proc. of the 32nd Industrial Waste Conference at Purdue University.
Lafayette, Indiana, 1977, 814-819.
38. Simpson, T.W. and Cunningham, R.L., "The Occurrence of Flow
Channels in Soils", J. of Environ. Qual. 11, 1982, 29-30.
160
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EVALUATION OF SIMPLIFIED TECHNIQUES FOR
PREDICTING MOISTURE BREAKTHROUGH OF SOIL LINERS
DANIEL J. GOODE
GCA/Technology Division
Bedford, Massachusetts
INTRODUCTION
The USEPA is considering incorporating an alternative design
concept into proposed regulations for hazardous waste disposal
(Part 264, Subpart K) to allow construction of liquid storage im-
poundments with a single natural soil bottom liner of sufficient
thickness to prevent liquid breakthrough during the operating life
of the impoundment. At closure, liquid waste is to be removed
along with the depth of bottom liner contaminated as a result of li-
quid waste seepage. The goal of incorporating this concept into the
regulations is to provide flexibility to the prospective owner/
operator in selecting a means of storing hazardous wastes onsite
prior to ultimate disposal.
The USEPA is considering the use of a transit time equation to
provide a simple method of estimating necessary bottom liner
thickness as a function of the design impoundment life. Other tech-
niques for prediction of soil liner breakthrough are available and
under study. These include the Green and Ampt infiltration model,
Philip's quasi-analytical solution, a linearized unsaturated flow
solution and numerical techniques.
The transit time equation under consideration is derived from
Darcy's equation for one dimensional, steady state, saturated flow
in porous medium. Other basic assumptions include the use of total
(versus effective) porosity and constant hydraulic conductivity in-
dependent of moisture content. This technique does not incor-
porate the variation of hydraulic conductivity with moisture con-
tent or the high capillary suction gradients that can exist in un-
saturated soils. Simple modifications to this equation incorporate
use of effective porosity and a capillary suction at the liner bottom
which reduce the equation's error.
The Green and Ampt1 model of infiltration applies Darcy flow
theory to the saturated zone above an advancing moisture front.
The effect of capillary forces is incorporated through a suction or
negative pressure head at the moisture front. Thus, the driving
forces are gravity and the difference in pressure head at the soil sur-
face and the negative pressure head at the moisture front. The
resulting governing equation has an analytical solution which
relates breakthrough time for a given liner thickness. Parameters
for the Green and Ampt model are determined from unsaturated
soil properties.
Philip,2'3'4 developed a quasi-analytical solution for nonlinear in-
filtration and applied this technique to infiltration into a clay soil.
A series solution is developed by combining several ordinary dif-
ferential equations for a transformed coordinate system. This
technique involves numerical integration for each different soil and
requires definition of the soil's unsaturated properties.
The nonlinear governing equation for unsaturated flow can be
linearized by using constant values of soil specific moisture capacity
and hydraulic conductivity. This linearized equation has an
analytical solution for infiltration into a single soil layer. The con-
stant soil properties are determined by curve fitting of the analytical
solution to data from field or laboratory column tests.
Due to the nonlinearities of the unsaturated flow equation,
general analytical solutions have not been obtained. Numerical
techniques are available to solve the unsaturated flow equations.
These techniques, namely finite difference and finite element
methods, retain the nonlinearity of the liner column matrix with
piece-wise continuous approximate representations and allow
nonuniform soil properties and initial moisture distributions.
Available programs range from basic flow to coupled heat and
moisture transport with vapor transport and moisture hysteresis.
MODELS OF FLOW THROUGH SOIL LINERS
The flow domain for liner breakthrough (Figure 1) consists of: a
layer of liquid in the impoundment of depth h£(L); a natural soil
DATUM
JL
IMPOUNDED
LIQUID
FILL
•^SATURATED,".
•»:.*. ZONE • .•."'
Figure 1
Flow domain for liner breakthrough
BARRIERS
161
-------
liner of thickness d (L); a layer of underlying site soil, which may or
may not be saturated; and a constantly saturated groundwater layer
of the same site soil. For this study, only vertical processes are con-
sidered. Horizontal flow may be significant at the edges of the sur-
face impoundment, but this will reduce the rate of vertical move-
ment.
Initially, the site soil moisture profile is in static (no-flow)
equilibrium with the water table or saturated zone. Vertical fluxes
due to evapotranspiration and/or natural infiltration are ignored.
This liner is homogeneous and initially has a constant moisture con-
tent, 00, over its entire thickness. The impoundment is then filled to
a depth h>.
After the impoundment is filled, the flow system is not in
equilibrium, and liquid will flow vertically down from the im-
poundment into the liner and eventually into the site soil and
saturated groundwater zone. The author's goal is to simulate this
flow and predict the liner thickness required to prevent leachate
from reaching groundwater during the impoundment's design life.
A brief description of the mathematics of the transit time equation,
the Green and Ampt infiltration model, Philip's quasi-analytical
unsaturated flow solution, a linearized unsaturated flow solution
and numerical solutions are presented below.
Transit Time Equation
The transit time equation under-predicts the rate of liner
breakthrough,' but it can be modified to include the effects of:
•Effective porosity instead of total porosity
•Negative fluid pressure at liner bottom
which reduce this error. These modifications are not an attempt to
change the basic assumptions which are:
•Steady state Darcy flow
•Fully saturated flow
•Advective transport only
•Homogeneous liner
The steady state saturated vertical flow equation in the liner can
be written:6
K ir = o
dz
(1)
where K [L/T] is the vertical saturated hydraulic conductivity, =
p
— + z [L] is the piezometric head, p [F/L2] is the fluid pore pres-
y
sure, -/[F/L3] is the fluid's specific weight and z [L] is the vertical
Cartesian coordinate, positive upward. Hydraulic conductivity is a
function of both the porous medium matrix and the pore fluid.
Applying fixed pressure boundary conditions to the liner top and
bottom, the velocity of flow, (V[L/T], through the liner according
to Cogley' is:
v - -
(2)
where ne [ - ] is effective porosity, d [L] is the liner thickness, h< [L]
is the ponded fluid depth and hd [L] is capillary head at the liner
bottom. Assuming a design life, t, the design thickness (to just con-
tain fluid) is:
V t - t —
(3)
Rearranging and solving for d gives:
\l/l
This expression is identical to the unmodified transit time equation
if the fluid pressure at the liner bottom is zero (hj = 0) and effec-
tive porosity (nj is replaced by total porosity, n.
These two modifications,
•Effective porosity instead of total porosity
•Negative fluid pressure at liner bottom
both increase the design thickness, d, for a given design life.
Green and Ampt Wetting Front Model
Green and Ampt' derived a simple model of infiltration which
has been proposed as a design model for liner reliability. The soil
moisture profile is conceptualized as a square wave moving down
the soil column (Figure 2). Above the wetting front, the soil is fully
saturated, while below the wetting front the moisture content is
equal to its initial value, 6;. Assuming the pressure head at the front
is a suction, \f/c, [L] due to the partial initial saturation, Darcy flux
q [L3/T] in the saturated zone' is:
(5)
where Lp [L] is the depth of penetration of the wetting front from
the liner top. Conservation of volume of the pore fluid requires:
dL
q - (n-8.) j^
Combining (II) and (12) and integrating:
n-9. f
-^
(6)
(7)
The design liner thickness is equal to d = Lp, when t equals the
design life.
The Green and Ampt model approximates the dynamics of the
liner infiltration event. Its major shortcomings are divergence at
large times and the difficulty in estimating ^c. Esimates of \j/c which
are too low (more negative) yield thicker liners. Techniques for
estimating \l/c have been presented by several authors including
Neuman' and Brakensier.9
IUKI IOTTOM
Figure 2
Definition sketch for Green and Ampt infiltration model
Unsaturated Flow Analysis
The governing equation for one-dimensional unsaturated flow in
the vertical direction can be written:'
d8 3
(8)
in which ^ E 0 - z [L] is matric potential or capillary pressure head,
where <*>[L) is piezometric head; e [-] is volumetric moisture con-
162
BARRIERS
-------
tent; K(^) = kr(\t) K, [LT~'] is unsaturated hydraulic conductivi-
ty, where Kr(^) [ - ] is relative hydraulic conductivity, and K [LT ~ ']
is saturated hydraulic conductivity; z [L] is the vertical coordinate,
positive upward; and t [T] is time. This equation is developed from
conservation of mass. The first term represents the change in
storage of liquid mass and the second term is mass flux divergence,
or the change in flux over space. The second term contains fluxes
due to the pressure gradient (K(^) 2E-) and gravitational potential
. The flux term is developed from Darcy's law for porous
media flow:
3z
(9)
in which q [LT '] is flux. Implicit assumptions of equation (8) are
that the fluid and soil matrix have constant densities, and that
moisture transport is unaffected by the vapor phase. Vapor effects
can be important when considering flow resistance during rapid in-
filtration,10 but its effects are minimal in fine grained soils over
long times.
At the top of the liner column, z = 0, the liquid pressure is con-
trolled by the level of liquid in the impoundment (Figure 1). The
water table boundary condition at the bottom of the soil column is
assumed to be controlled by local groundwater flow and unaffected
by the small amount of liquid discharging through the liner.
Liquid is held in the pore space of an unsaturated porous
medium by capillary and adsorptive forces." In a soil column at
static equilibrium, these surface tension forces between the liquid
and solids are equal to the force of gravity pulling the liquid down.
In general, the smaller the pore size, the more weight these forces
can support. For the liquid to be at static (no flow) equilibrium, the
piezometric head must be constant, = ^ + z = constant over the
entire column. Thus, the capillary pressure head varies linearly with
the negative of height:
^ = * constant ~ z (10>
at and below the water table > = zw and \j/ = 0, and above the
water table:
in
cm).
BARRIERS 163
-------
Hydraulic conductivity is a function of both the soil and the fluid.
Hereafter, hydraulic conductivity will refer to properties of the soil
fluid system when the fluid is the proposed impoundment leachate.
Recognized effects of chemicals in liquids on the soil matrix are not
addressed here. For a given soil, the hydraulic conductivity is
dependent on the moisture content or capillary pressure in the soil.
As a function of moisture content, , the hydraulic conductivity
function shows little hysteresis6'14 and since, as stated above, (\l/)
hysteresis for this infiltration problem is ignored, the hydraulic
conductivity of a function of capillary pressure can also be deter-
mined as a unique relationship. The relationship between hydraulic
conductivity and capillary pressure head for a sandy and a clayey
soil is shown in Figure 4.
Philip's Solution
A quasi-analytical solution to the governing equation of vertical
infiltration (8) was developed by Philip.4 The reader is referred to
that work for a complete description of the technique.
Philip's solution is developed through a perturbation on a trans-
formed differential equation. The solution is for depth at a given
time:
-z =
a2t + a3t
3/2
(15)
in which the parameters lj, &2, ... are a function of moisture con-
tent and unsaturated soil properties. In general, these parameters
are determined by numerical integration. At large times, high order
terms become important but the profile shape does not change. For
this situation, a "profile at infinity" solution is used.
Philip's solution requires the unsaturated moisture
characteristics and unsaturated hydraulic conductivity curve for the
soil and only simulates one semi-infinite homogeneous layer. On a
finite liner, this solution is accurate until the moisture front begins
to affect the bottom of the liner. Philip's solution cannot incor-
porate the draining effect of the underlying sand layer.
Transient Linearized Approximate Solution
Linearization of the highly nonlinear transient unsaturated flow
equation (8) can yield analytical solutions which can, in turn, be
used to evaluate liner reliability. Although inherently an approx-
imation, this technique captures much of the dynamics of the in-
filtration event. Moore" has previously recommended this tech-
nique for impoundment liner evaluation.
The governing equation for unsaturated flow is highly nonlinear
due to the dependence of and K on \l/. These nonlinearities can be
removed and a solution obtained by rearranging:
.
3t d6
46
and substituting D* - ^ K and K* = ZZ
in: d0 d0
11 . D* JLt . K* ii . o
3t ,2 3i
(16)
resultin8
(17)
Applying boundary conditions \l/ = h at the top (Z = 0), where h is
the depth of ponded liquid, and initial condition ^ = ^j where ^i is
the initial fluid pore pressure head, the solution is:'
fe
KM
'
where erfc is the complimentary error function." Unlike the pro-
posed transit time equation or the Green and Ampt model, the
transient linearized solution results in a continuous profile of soil
moisture which is physically more accurate (see "Actual" moisture
content curve in Figure 2). Thus, there is no sudden increase in
moisture content or reduction in suction pressure at the liner bot-
tom. Rather, moisture content gradually increases from the initial
value to saturation as the wetting front advances. This is consistent
with the experimental observation that moisture flows out the bot-
tom of the column before it is completely saturated." Since there is
no explicit breakthrough, physically or mathematically, one must
define this concept in terms of relative changes in moisture content
or pressure. A common choice is 50%, but significant leachate may
have already reached the liner bottom at this time. A standard
value of (\l/- \l/{)/h - ${), such as 0.1 or 10%, could be chosen to
represent breakthrough.
The major fault with this method is in determining D* and K*
since the terms which define them vary over several orders of
magnitude during saturation. More" has outlined a method for
determining K** and D** for the moisture content form of the
linearized governing equation. (Note K** and D** are not
numerically equivalent to K* and D* due to different governing
equations.) Saturated conductivity is used for K**, and D** is
determined by curve fitting results of laboratory column tests. It
has not been verified that results of short-time small-scale
laboratory tests can be adequately scaled to represent field
behavior, and the fitted D** is a function of time and length. This
method does approximate the dynamic characteristics of the in-
filtration event, specifically high capillary forces and decreased
wetting front velocity with time.
Numerical Simulation of Unsaturated Flow
Finite Difference Methods (FDM) have been successfully applied
to a wide range of groundwater flow problems. In application to
the vertical unsaturated flow equation, the vertical column is di-
vided into a row of short vertical segments or elements called a grid.
For mesh-centered grids, the values of capillary pressure head (ifr)
are evaluated at nodes which are located at the ends of each seg-
ment. For a block-centered grid, these nodes are located at the
center of each segment. Likewise, solutions in time are obtained by
breaking time into discrete steps. Solutions at new times are ob-
tained (at the nodes) using the previous solution(s). In general, the
accuracy of this method improves as the grid spacing (Az) and the
time step (At) decrease in size. Freeze and Cherry" describe the ap-
plication of FDM to vertical unsaturated flow. An application of
FDM to liner design is presented below.
MODEL COMPARISONS
The liner models described above are compared in the simulation
of breakthrough in a clay soil. Results for the numerical (finite ele-
ment) and Philip's solution are from Milly." Philip's solution has
been verified by comparison with laboratory column tests and
serves as the "correct" result.
The liner material simulated is Yolo light clay. This material is
not a particularly effective liner but has been well studied and is
presented for comparison. The soil properties are: porosity, n =
0.495, initial moisture content, <£j = 0.237 and saturated conduc-
tivity, K = 1.23 x 10"5 cm/s. The liquid depth in the impoundment
is h^ = 25 cm. Breakthrough is defined by the ratio of suction
pressure reduction at the liner bottom to the difference between in-
itial pressure and the top boundary pressure. Results of the
numerical and quasi-analytical solutions are plotted for 10% and
50% reduction in suction at the bottom of the liner to illustrate the
conservative effect of choosing values lower than 50%. Design liner
thickness is plotted versus design life or a semi-log scale in Figure 3.
The unmodified transit time equation (<}) and the modified tran-
sit time equation (D) are applied to the liner. The additional
parameters needed for the modified form are taken as: nc = n =
0.495, for the top curve, liner bottom pressure head, hd = - 10cm,
and for the bottom curve hd = - 100 cm. Results of the Green and
Ampt model (o) are plotted for two values of wetting front suction
head, the top line is ^c = -10 cm and the bottom line is ^c =
- 100 cm. The coefficients for the linearized unsaturated flow solu-
tion are determined by fitting to the numerical results, D* = 10'2
164
BARRIERS
-------
and K* = 3 x 105. This model's breakthrough results [(^
(h - ^) = 0.1] are plotted for one set of parameters (A).
As shown in Figure 3, solutions differ over a wide range. The un-
modified transit time equation underestimates liner thickness for
given design life. The modified solution is also sensitive to hj, a
parameter which is an artifact of the approximation involved and
cannot be determined from field data. This error would be even
more pronounced for a heavy clay, with lower conductivity. The
Green and Ampt and linearized equation models are both sensitive
to parameters which, again, are artifacts of their respective approx-
imation and are difficult to accurately estimate from soil property
data. If the parameters can be accurately determined, these tech-
niques may yield usable results. Results of the numerical model
agree with Philip's solution.
APPLICATION OF A NUMERICAL MODEL
The FDM has been applied to vertical unsaturated flow by many
authors. Freeze20 investigated natural recharge and discharge
mechanisms. Brutsaert21 used a two-dimensional vertical model in a
study of soil moisture flow beneath drains and irrigation ditches.
Cooley22 investigated flow to a pumping well using an axisymmetric
two-dimensional vertical model. For one-dimensional vertical flow,
the FDM has been verified by, among others, Green et al." and
Ragab et al."
SOILINER", an available computer program for finite dif-
ference modeling of vertical unsaturated flow, can be applied to
design a hypothetical liner illustrating the utility of numerical
techniques in complying with regulatory requirements. The discus-
sion and results below are not restricted to this computer code but
would be similar for any numerical model which solves the
nonlinear unsaturated flow equations.
For this study, the spatial domain of the vertical unsaturated
flow equation is the soil column from the impoundment liner top to
the water table. This domain includes the liner and the underlying
site soil. This domain is discretized into several nodes for which
subscript i represents the node number. Values of the state variable,
matric potential, \l/, and soil properties hydraulic conductivity. K(^)
and moisture capacity, C(\f>), are approximated by values at a node
i: ^;, KJ and Q. K; and Q are functions of ^. These values are used
to approximate the derivatives in the governing equation. The first
term in (8), representing pressure driven flux, can be replaced by:
at
n+1
At
(22)
iz
11\ L
(19)
in which Az = Zj + 1 -z, is the node spacing and
>l/2
>l/2
(20)
are the geometric mean conductivities between nodes. The gravita-
tional flux term can be expressed as:
K. , - K.
i+l i-l
2Az
(21)
Equations (19) and (21) are centered difference approximations.26
The temporal domain of the vertical unsaturated flow equation is
time, ts»0, after infiltration into the liner begins. Time is broken
down into time level subdomains in which superscript n represents
time level. The continuous properties and matric potential are
again approximated by values at discrete time levels:
^n, Kn and c". The storage term in (8) can be written:
Both sides of (22) contain terms which must be evaluated at the cur-
rent timestep, tn + ', and depend on the solution ^n + 1, thus (22) is
implicit in ^n +1
Substitution of the finite difference approximations into the
governing differential equation results in a system of nonlinear
algebraic equations which can be solved to give, the matrix potential
at the nodes points at any time step. Since the conductivity and
moisture capacity terms depend on the solution, an iterative pro-
cedure must be used at each time step, resolving the equations until
the soil properties for that time step remain constant. Pinder and
Gray26 discuss solution techniques for this system of equations.
During numerical solution of the governing equation for vertical
unsaturated flow, the specific moisture capacity C(^) and un-
saturated hydraulic conductivity K(^) must be determined. The
values must be evaluated for each value of matrix potential at the
node points. There are two general methods for incorporating these
continuous curves into the numerical model. The first is by specify-
ing a table of points from the data curves. The computer program
then interpolates between these tabular values when needed for ad-
ditional points. The second method is to directly compute soil
properties using functional relationships or equations.
Hypothetical Liner Design Problem
A temporary surface impoundment for storage of hazardous
wastes is to be constructed in a sandy soil with a shallow water table
5 m below the land surface. Site soil will be excavated to sufficient
depth to install a natural soil liner. The top of the liner will corre-
spond to the original land surface. The impoundment depth will be
1 m. This impoundment will be used to store hazardous liquids for
5 years at which time the liquids will be removed and all con-
taminated soils excavated. Use of a numerical model to simulate the
hydraulic performance of this liner allows an accurate estimation of
the required soil liner thickness and the extent of release at closure.
The site soil is a sand with a saturated hydraulic conductivity of
9.44 x 1C-3 cm/s and a porosity of 0.287 [data from Haverkamp et
al.]" The material for the soil liner is a heavy clay with a saturated
hydraulic conductivity of 1 x 10 ~7 cm/s and a porosity of 0.5.
These values are similar to a compacted bentonite clay and are
more restrictive to flow than the Yolo light clay. The unsaturated
conductivity and moisture characteristic curves for these two soils
are shown in Figure 4. The site soil moisture is initially in static no
flow equilibrium with the water table. Under these conditions, the
pressure head at any point is the negative of the elevation above the
water table. For example, at an elevation of 300 cm above the water
table, the pressure is \j/ = - 300 cm. The clay liner is initially at a
saturation of 50% which corresponds to a moisture content of 0.25
and a pressure head of - 500 cm.
The Green and Ampt infiltration model can be used to estimate
the depth of infiltration into the clay after 5 years. A wetting front
pressure head of - 32 cm is estimated using techniques presented
by Neuman.8 The depth of infiltration is obtained by interatively
assuming a depth and solving (7) for time. The predicted depth is
obtained when the calculated time is 5 years. For infiltration into
the liner soil, the calculated depth is about 175 cm. The accuracy of
this depth is shown below during numerical simulation.
For numerical simulations, the soil column from the liner top to
the water table (5 m deep) is discretized into 120 elements as
follows: the first 5 cm are divided into 10 elements, the next 25 cm
into 25 elements; the next 50 cm into 25 elements; the next 120 cm
into 30 elements; and the final 300 cm into 30 elements.
Within each block of elements, the node spacing is constant. The
computer model automatically computes time step such that the
maximum change in pressure between time steps is less than 25 cm.
In addition, the maximum allowable time step is 11.6 days. The
fully implicit time stepping scheme is used.
BARRIERS
165
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1.i 2.1 3.8 4.1 C.I
Figure 5
Pressure versus time in liner with initial moisture content of 0.25
MOISTURE CONTENT
.8 .1 .2 .3 .4
i i i i_
.5
S
B
IA
£ u>
u w-
N §
m
i
B
HIJ
B
B
S
T-
B
B
in-
M.6 doyi
116 doyt
6ytort
Figure 6
Moisture content profile in liner with initial moisture content of 0.25
Three simulations are presented below to illustrate numerical
simulation of liner breakthrough and the general flexibility of this
technique. The first simulation is a straightforward infiltration
problem. The second simulation shows the effect of installing a
liner which is initially wetter than that used in the first simulation.
The third simulation incorporated a sand layer within the liner and
shows the impact of this design on breakthrough time.
The results of simulation of moisture movement into the liner
system with a liner thickness of 180 cm are shown in Figures 5 and
6. The capillary pressure at several locations in the liner as a func-
tion of time is given in Figure 5. Moisture moves into the soil at a
rate which decreases with time, reaching a depth of 45 cm in about
0.5 year and reaching a depth of 90 cm after about 1.5 years.
Likewise, at a point 135 cm below the liner top, the soil does not
approach saturation until over 3.5 years. The pressure at the bot-
tom of liner increases in early times because the initial pressure con-
dition is lower than the pressure in the underlying sand, thus
moisture actually moves up into the liner. The pressure at the bot-
tom of the liner first responds to infiltration from the impound-
ment after about 5 years and is approaching its steady state value at
6 years.
A plot of the moisture content profile in the clay liner and
underlying sand at several times during infiltration is shown in
Figure 6. Before the wetting front reaches the bottom of the liner,
moisture is flowing up into the clay from the sand due to the initial
pressure gradients. The infiltration profile at 5 years just reaches
the bottom of the liner. The profile at 6 years is essentially in steady
state and will remain unchanged as long as the boundary conditions
do not change.
At the end of 5 years, liquid is flowing out of the bottom of the
liner at a discharge rate of 3.78 x 10~4 cm/day or 0.54 ftVday/
acre. For an impoundment 1 acre in area, 0.54 ft3 of liquid flows
out of the liner in one day. Whether this rate is large enough to
represent breakthrough of the liner is not clear. At this time, the
moisture content in the clay at the liner bottom is 0.275. The rate of
discharge to the water table at 5 years is zero. Thus, although li-
quids are leaking through the liner bottom, they are not yet
reaching the saturated groundwater.
One year later, the discharge rate at the liner bottom has in-
creased to 1.36 x 10-2 cm/day or 19.5 ftVday/acre. By this time,
the sand has hydraulically responded to infiltration and the
discharge to the water table is also 19.5 ftVday/acre. The moisture
content in the clay at the liner bottom is 0.31. At 6 years, this
system is essentially in steady state and the moisture content at the
liner bottom will not increase significantly.
The increase in moisture content in the sand which occurs
because of this infiltration between year 5 and year 6 is insignificant
(Figure 6). The sand is so much more conductive to flow than the
clay that only a small change in pressure gradients is sufficient to
move all leakage from the liner down to the water table.
The effect of initial moisture content in the soil liner can be in-
vestigated by simply changing the initial specifications on the clay
soil liner. The results of simulation on the same liner system with an
initial moisture content in the liner of 0.30, which corresponds to a
pressure head of -200 cm, are shown in Figure 7. The fact that
pressure gradients will be less in this case might suggest that
breakthrough would occur slower. However, as shown in Figure 7,
the pressure at the liner bottom begins changing after 4 years as op-
posed to 5 years above. This is because the unsaturated hydraulic
conductivity is higher at this higher initial capillary pressure, and
there is less pore space which must be filled by the advancing
moisture front. This liner reaches equilibrium after 5 years. Figure
7 also shows that the initial pressure gradient at the liner bottom
has been reversed from that above. In this case, the pressure in the
liner is higher and the initial flow is down into the site soil, thus
reducing pressure at the liner bottom.
Figure 7
Pressure versus time in liner with initial moisture content of 0.30
166
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Use of the numerical model allows simulation of complex liner
systems and variable boundary conditions. For this third simula-
tion, the liner consists of a 60 cm thick layer of the site soil between
two 60 cm layers of the liner clay. In addition, this simulation in-
corporates a change in the impoundment depth from 100 to 200 cm
after 2 years. The liner moisture content profile at three times dur-
ing infiltration is shown in Figure 8. Before the moisture front
reaches the sand layer, it has no effect on infiltration and the curve
is identical to Figure 6. The profile at 1.6 years, after the moisture
front has reached the sand layer, is down to about 1.5 m below the
liner top. This compares to less than 1 m with a homogeneous liner.
Leachate entering the sand layer quickly move vertically down to
the interface between the sand and clay. This interface could serve
as an effective leachate collection point. The sand layer does not
completely saturate until about 3 years after construction, at which
time the system is essentially in steady state. Steady state discharge
from the bottom clay layer into the underlying site soil is higher for
this liner design, with a value of about 40 ftVday/acre, due in part
to the increased impoundment depth.
MOISTURE CONTENT
.8 .1 .2 .3 .A
r
(_;
N g
CLAY
SANO
CLAY
116 DflVS
•—• 1.6 YEflR
— 5 YEflRS
Figure 8
Moisture content profiles in a three layer liner
The initial liner design, a homogeneous layer 180 cm thick,
resulted in release of potentially hazardous liquids to the un-
saturated zone above the water table after 5 years. If the design goal
was a liner that released zero liquid at this time, the model could be
run with a thicker liner, examining the flow rate at the liner bot-
tom. In addition, the numerical model can easily simulate different
designs with various soil layers and the effect of variable boundary
conditions. Soil properties may also vary from one node to
another, thus allowing simulation of a liner with variable soil prop-
erties. The numerical model is also valuable in predicting the steady
state moisture profile and discharge rates from the liner for any
configuration.
CONCLUSIONS
Simplified techniques for estimating liner thickness are not suffi-
cient for many cases of soil liner design. The unmodified transit
time equation results in a liner which is insufficient to contain
hazardous liquids during the design life. Modifications to this equa-
tion reduce this error but do not incorporate the physical
characteristics of the breakthrough problem, namely high initial in-
filtration rates and variation of soil properties with saturation.
The transient Green and Ampt infiltration model does simulate the
variation of infiltration rate with time. A wetting front suction
head must be used for accurate results, and this parameter must be
determined from unsaturated soil properties. Nonetheless, this
technique may be sufficient for situations of one homogeneous
liner when initial breakthrough is the only concern. This model will
not predict the liner behavior after breakthrough has occurred.
Philip's quasi-analytical solution for unsaturated flow requires
numerical integration over unsaturated soil properties and, as
above, cannot incorporate liner behavior after breakthrough.
The linearized unsaturated solution requires determination of
equation parameters which are not physical soil properties and
which may show scaling problems from laboratory to the field. If
the goal of simulation is only the liner's behavior up to
breakthrough, and the liner can be considered a single
homogeneous soil, the Green and Ampt equation can predict a
relatively accurate design thickness for relatively little computa-
tional effort.
For the general analysis of flow through liners, numerical pro-
cedures are the only technique with sufficient flexibility to simulate
a wide range of physical situations. Numerical methods can incor-
porate many different soil types or a soil with properties that vary
in space. Numerical models are not limited in the temporal varia-
tions which can be incorporated. A model such as the one described
above could be used to simulate hydraulic behavior of the liner dur-
ing its entire life, including simulation of the site soil after the liner
layer is removed and the site closed. Because of this generality and
flexibility, numerical methods in conjunction with unsaturated soil
properties are suggested as effective tools in soil liner design.
ACKNOWLEDGMENTS
Portions of this study were funded by the USEPA's Office of
Solid Waste under contract 68-02-3168. Arthur Day was OSW's
project officer for these tasks. Charles Young was project manager
for GCA/Technology Division. Russell Wilder and David Cogley
reviewed the manuscript.
REFERENCES
1. Green, W.H. and Ampt, G.A., "Studies in Soil Physics I: The Flow of
Air and Water Through Soils," J. Agric. Sci. 4, 1911, 1-24.
2. Philip, J.R., "The theory of infiltration: 1. The infiltration equation
and its solution", Soil Sci., 83, 1957, 345-357.
3. Philip, J.R., "The theory of infiltration: 6. Effect of water depth over
soil," So/7 Sci., 85, 1958, 278-286.
4. Philip, J.R., "Theory of infiltration", in V.T. Chow, ed., Advances in
Hydroscience, Vol. 5, Academic Press, New York, 1969, 215-297.
5. Cogley, D.A., Goode, D.J. and Young, C.W., "Review of the transit
time equation for estimating storage impoundment bottom liner
thickness", GC A/Technology Division Final Report prepared for
USEPA Office of Solid Waste under Contract 68-02-3168, 1982.
6. Bear, J., Hydraulics of Ground-water, McGraw-Hill, New York, 1979.
7. McWhorter, D.B. and Nelson, J.D., "Unsaturated flow beneath
tailings impoundments", J. Geotechnical Eng. Div., ASCE, 105
(GT11), 1979, 1317-1334.
8. Neuman, S.P., "Wetting front pressure head in the infiltration model
of Green and Ampt", Water Resources Res. 12, 1976, 564-566.
9. Brakensier, D.L., "Estimating the effective capillary pressure in the
Green and Ampt infiltration equation", Water Resources Res. 13,
1977, 680-682.
10. Parlange, J.Y. and Hill, D.E., "Air and water movement in porous
media: compressibility effects, Soil Sci., 127, 1979, 257-263.
11. Hillel, D., Soil and Water—Physical Principles and Processes, Aca-
demic Press, New York, 1971.
12. Morel-Seytoux, H.J., "Two-phase flows in porous media", in V.T.
Chow, ed., Advances in Hydroscience, Vol 9, Academic Press New
York, 1973, 199-202.
BARRIERS
167
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13. Dane, J.H. and Wierenga, P.J., "Effect of hysteresis on the prediction
of infiltration, redistribution and drainage of water in a layered soil,"
J. of Hydrology, 25, 1975, 229-242.
14. Mualem, Y., "A new model for predicting the hydraulic conductivity
of unsaturated porous media", Water Resources Res., 12, 1976, 513-
522.
15. Moore, C.A., "Landfill and Surface Impoundment Performance
Evaluation Manual", Submitted to the USEPA, Office of Water and
Waste Management, by Geotechnics, Inc. SW-869, Sept. 1980.
16. Crank, J., The Mathematics of Diffusion, Clarendon Press, Oxford,
1956.
17. Mclntrye, D.S., Cunningham, R.B., Vatanakul, V. and Stewart,
G.A., "Measured hydraulic conductivity in clay soils: methods, tech-
niques, and errors". Soil Sci., 128, 1979, 171-183.
18. Freeze, R.A. and Cherry, J.A., Groundwater, Prentice-Hall, Engle-
wood Cliffs, NJ, 1979.
19. Milly, P.C.D., "Moisture and heat transport in hysteretic, inhomo-
geneous porous media: a matric head-based formulation and a nu-
merical model", Water Resources Res., 18 1982, 489-498.
20. Freeze, R.A., "The mechanism of natural groundwater recharge and
discharge: 1. One-dimensional, vertical, unsteady, unsaturated flow
above a recharging or discharging groundwater flow system",
Water Resources Res., 5, 1969, 153-171.
21. Brutsaert, W.F., "A functional interation technique for solving the
Richards equation applied to two-dimensional infiltration problems",
Water Resources Res.. 7, 1971, 1583-15%.
22. Cooley, R.L., "A finite difference method for unsteady flow in vari-
ably saturated porous media: application to a single pumping well",
Water Resources Res., 7, 1971, 1607-1625.
23. Green, D.W., Dabiri, H. and Weinaug, C.F., "Numerical modeling
of unsaturated groundwater flow and comparison of the model to a
field experiment", Water Resources Res., 6, 1970, 862-874.
24. Ragab, R., Feyen, J., Hillel, D., "Comparison of experimental and
simulated infiltration profiles in sand," Soil Sci., 133, 1982, 61-64.
25. Goode, D.J., et at., "Documentation and User's Manual for
SOILINER: Vertical Unsaturated Flow", GCA/Technology Division,
Bedford, MA (in preparation), 1983.
26. Pinder, G.F. and Gray, W.G., Finite Element Simulation in Surface
and Subsurface Hydrology, Academic Press, New York, 1977.
27. Haverkamp, R., Vauclin, M., Touma, J., Wierenga, P.J. and
Vachaud, G, "A comparison of numerical simulation models for one-
dimensional infiltration", Soil Sci. Society of America J., 41, 1977
285-294.
168
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DEVELOPMENT OF CONTAINMENT TECHNIQUES AND
MATERIALS RESISTANT TO GROUNDWATER
CONTAMINATING CHEMICALS
HANNO MULLER-KIRCHENBAUER, Prof. Sc.D.
WERNER FRIEDRICH, Dipl.-Ing.
Institute for Soil Mechanics and Foundation Engineering
University of Hannover
Hannover, Federal Republic of Germany
HANSJURGEN HASS, Sc.D.
Dynamit Nobel AG
Troisdorf, Federal Republic of Germany
INTRODUCTION
In 1970, approximately 50,000 disposal sites were registered in
the Federal Republic of Germany. Two percent of these seem to
contain hazardous wastes and need appropriate treatment so that
the groundwater and the surroundings shall not be affected.1 Addi-
tionally, there are further unregistered intrusions from earlier times
and from World War II such as bombed factories and oil or
chemical storage.
Clearly the best way to correct pollution at these sites is to dig
them up and to refill the pits with clean material. However, in the
case of very deep contamination or of intensively settled surround-
ings, the dig and refill procedure is neither technically nor
economically possible. This has resulted in an intense search for
alternative solutions in recent years.
Progress has been made with encapsulation techniques.2'3
Although this concept can be successfully used, there are many
special conditions that have to be considered; these are discussed in
the following sections.
CONVENTIONAL SEALING OF CONSTRUCTION
PITS AGAINST WATER
Before encapsulation was used, the technology of sealing con-
struction pits to avoid dewatering was developed.
Such waterproof pits have been needed in cases listed below:
•Deep construction pits beside pile foundations in soft soils. De-
watering is not acceptable in order to avoid the settling of soft
soil and damage to piles.
•Deep pits in coastal areas, where dewatering can cause a rise in
the salty groundwater level and disappearance of the sweet
groundwater.
•All cases where dewatering can cause risk to the drinking or in-
dustrial water supply.
Encapsulation has been used as a sealing procedure in Europe to
prevent the inflow of high water quantities to the pits. The founda-
tion levels protected by sealing can finally be drained by pumping
out small water quantities allowed in by the residual permeability of
the sealant. As the only stability requirement, the hydraulic uplift
has to be measured so that the bottom sealant cannot be lifted
thereby avoiding hydraulic failure. This stability condition means
that the bottom sealing has to be situated relatively deep below the
foundation level; consequently, relative precise boring and grout-
ing equipment have been developed.
For the containment technique, as well as guarding against
polluted water, there are two alternatives: (1) natural and (2) ar-
tificial bottom sealing (Figure 1). In every case, the vertical screens,
which are mostly small slurry trenches with different backfills, have
to reach the bottom sealant and penetrate it for a certain distance to
achieve good contact. The artificial bottom sealant consists of a
grouted layer.
For all parts of such encapsulations, the boring, grouting and
control techniques as well as the grouting and slurry materials and
their preparation, mixing and installation have to be completely
developed and checked.
Example 1: Thin Slurry Screen Together With a Tight
Natural Layer
Natural Ground-
water Level
.'.'.'• '.'• '. •' • • ; Sand-'-' .'•'.•••' "••-'.-•'•
Example 2: Slurry Trench Wall Together With a
Grouted Layer
Natural Ground -
water Level
.owered Groundwater Level
— Slurry Trench •
.Wall •• .
• Sand
-Grouted Layer
Figure 1
Alternative Containment Techniques
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169
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Unfortunately, these techniques can fail very easily if the relevant
conditions (the chemistry of the milieu in which the sealant is
placed; the fluid which the sealant has to withstand) change. The
grout and slurry mixtures have to be compatible with the in situ
chemicals.
As stated, these sealing methods have been recently applied to
the encapsulation of pollutants.4'5 In these cases, the intended seal-
ing is not directed against water coming from the outside to the in-
side, but against the pollutants flowing from the inside to the out-
side.
ENCAPSULATION AGAINST POLLUTANTS
The essential components of a system for sealing against
pollutants are shown in Figure 2. This is the way they are used in
Europe as amelioration measures for contaminated areas. Due to
economic constraints, the vertical elements are generally con-
structed with small slurry trenches although normal slurry trenches,
pile walls or grouted walls would be possible.
Primary Contamination
Secondarily
Displaced
Contamination
Artificial Bottom Sealing
(Grouted Layer)
Type 1 : Artificial Bottom Sealing
Primary Contamination
Secondarily
Displaced
Contamination
-.'.' '. '•: '•',.- Tertiary Penetration of the '.
Cohesive Layer
Type 2 . Tightening Natural Soil Layer
•If the natural or artificial bottom sealing layers are penetrated,
tertiary contamination takes place.
•For all encapsulations, one must suspect that secondary contam-
ination can have occurred before construction measurement or
after construction together with tertiary migration (Figure 2).
•The conventional bentonite-based slurry mixtures as well as the
mainly silicate-based grouts change their Theological behavior if
they directly contact contaminating chemicals. Thus, viscosity
yield limits, strength and permeability of the grout are affected
after installation.
D'Appolonia has pointed out the changes in the permeability of
bentonite backfills due to the presence of different chemicals.'
Similar results have been found by the authors.
As a result of these differences and resulting problems, the con-
ventional encapsulation technique cannot be transferred directly to
pollutant containment without modification. For the desired ap-
plication the following conditions must be considered:
•It should be ensured that solutions of contaminants contact the
seals in concentrations as low as possible. This can be achieved by
placing drains inside of the contained volume so that the internal
water level is lower than the external one and the hydraulic gradi-
ent is in the direction from outside to inside (Figure 3). No con-
centrated pollutants, under normal conditions, will migrate from
inside to outside. Only the solutions secondarily displaced can
flow back from outside to inside. In the special case of complete
encapsulation, secondary and tertiary intrusions are also con-
tained. The seal can only be percolated by water.
•Independent of the mentioned ideal case, short-term outward
directed percolation cannot be excluded. This situation can be
caused by heavy rainfall or by extreme dryness.
In the first case, the internal water level rises; in the second case,
the external level decreases; in both cases, the seepage direction
changes from inward to outward. That is the reason, therefore,
that the backfills have to be resistant against the percolating
chemicals.
•Backfills and grouting materials have to react correctly with the
chemically loaded milieu and have to build up the desired reduc-
tion of permeability against water as well as against contaminants.
As pointed out in the next section of this paper, new chemicals
and chemical admixtures must be developed.
•The preparation, grouting and slurry trench techniques have to
be checked against the changed Theological behavior of the mix-
tures.
•A special problem is caused by gravity as pollutants sink without
external gradients. If that process is to be stopped by a reverse
gradient, directed up, one must reach a certain value which can be
calculated using the procedure shown in Figure 4. Tests of that
calculation are part of an ongoing research program at the In-
stitute for Soil Mechanics at the University of Hannover.
Primary Contamination
Figure 2
Principles of Encapsulation
In contrast to simply sealing against external groundwater, most
published papers dealing with encapsulation of pollutants have not
discussed the following important aspects:
•Pollutants can sink to areas deeper than the original contamina-
tion level or be displaced horizontally; hence they can build up
secondary contamination.
•The sinking can occur without any external hydraulic gradient,
being caused only by gravity and capillarity effects.'
•Numerous contaminating chemicals—for example chlorinated
hydrocarbons—can penetrate silt and natural clay layers as well as
grouted layers treated with certain injection materials; this can
also occur without external hydraulic gradients.
Lowered Internal
Groundwaler Level
— Small Slurry Trench
- ' ' '\ ,' ,'/'•*< ' / ,',','/ / ' / 'Cohesive Soil
Secondarily Displaced
Contamination
^ To the Inside Directed Row Lines
Lowered Groundwater level Inside of the Encapsulation
Figure 3
Encapsulation with Lowered Internal Groundwater Level
170
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Waler Reservoir
Overflow
Overflow
Contaminant
Saturated Sand
Contaminant
Saturated
Cohesive Soil
Clean Cohesive
Soil
Water Saturated
Sand
Waler Sampling
Region ol
Streamlines
Have to Be
Absorbed By
the Drainage
Well
Streamlines
Separation Line
(No Flow Across
This Line )
>1 [heap + (d + All)--^11
L 7\v J
3.
>1 fhCap + (d + Al), _^1
L TW
q =
UP
1 -JL
7T
Ah>7,
heap : Capillary Elevation
AY : Difference Between the Specific Weights of the Contaminant and
of Water
•yw : Specific Weight of Water
Figure 4
Determination of the Retarding Gradient
•If tertiary contamination exists below the bottom sealant before
construction, that can also affect the groundwater. In such cases,
a deep drainage system can remove a certain part of this natural
groundwater flow. This can be measured so that no stream line
crossing the polluted area continues to the tailwater (Figure 5).
That problem is also being investigated at the Institute for Soil
Mechanics at the University of Hannover.
The purpose of such a deep drainage system is not for the usual
dewatering and lowering of the groundwater surface, but to
withdraw the minimum amount of water to prevent further
chemical displacement to the downstream side.
If the flushing of the subsoil is useful, higher water quantities can
be pumped.
Chemical Aspects of Grout Mixtures
It is necessary to divide the suitable gel-developers into two main
silicate groups: (1) grout-mixtures which produce consolidation gels
and (2) those which have a pure sealing character. In both cases it is
more or less a question of water-containing silica-gels. Other gels,
based on organic polymers or on monomers being polymerized,
should not be utilized in connection with ecological problems.
In time, the consolidation gels should form a Si°2 skeleton which
would improve the mechanical properties of the penetrated grain
system. The use of such grouts should, therefore, be restricted to
applications where strengthening properties are required. The
transformation of a gel into a crystalline lattice is called "aging";
the liberation of gel-water is called "syneresis". Within 160 days,
consolidation gels have syneresis values of about 30-40 gr water per
100 gr of gel.
A sealing gel is applied under the same conditions as consolida-
tion gels. However, the gel should not develop into a SiVlattice but
q : Required Quantity of Pumped Water
uo : Current Velocity of Groundwater
yia : Are Shown in the Figure
Figure 5
Drainage Well System to Prevent Further Contaminant
Displacement to the Downstream Side
should remain as a light gel in equilibrium with the groundwater for
as long as possible in order to maintain its gel structure. These gels
essentially have lower solid contents and, therefore, more water
than consolidation gels; thus they typically have very low syneresis
values in the range of 5-7%.
Grouting gels, based on waterglass, are produced by the use of
so-called reactants which are mainly hydrolysable organic com-
pounds such as organic esters or amides. Their effect occurs due to
hydrolysis in which the equilibrium alkalinity is consumed, thus
producing water-insoluble silica phases. The extent of the transfor-
mation or hydrolysis is referred to as the "degree of
neutralization".
The typical sealing gel which is produced by waterglass and
sodium aluminate is developed by a totally different mechanism. It
is distinguished by a low silica content, high water-absorption abili-
ty and good long-term stability. Long-term stabilty is very depen-
dent upon the polymerization ability of the reactive components,
i.e., the silicate and the aluminate. DYNAGROUT T is such an op-
timized, highly stabilized reactant based on sodium aluminate.
Whereas in the past the technological effect of the consolidation
gels has been the main consideration, they have also been used in
diluted form as sealing gels. Today, ecological considerations are
strongly influencing the choice of gel systems. When, for example,
organic esters or amides are used as reactants, their degradation
products, such as organic alcohols, amines and salts of carbonic
acids are contained in the syneresis water. Additionally, it is
necessary to consider that, if the gel forming reaction is incomplete,
the reactant can escape into the environment. In the case of silicate
and aluminate gels, excess reagent has no deleterious effect on the
environment. Indeed, aluminate is used in several countries in the
treatment of potable water. Other reaction products are not formed
during the gel-formation. The mechanism taking place during the
gel development is not based on a splitting of the reactant, but on a
process described as an electrochemical-caused gelation of a col-
loidal system.
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171
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Attempts to minimize the environmental effects of traditional
consolidation gels by using very dilute systems often results in gels
which show both poor consolidation and ineffective sealing.
The development of the new reactants DYNAGROUT SP and
DYNAGROUT SB by DYNAMIT NOBEL shows a new approach
to the problem wherein the organic component is chemically built
into the silicate gel. The resulting organically modified silica gel is
thereby strongly hydrophobized, has an essentially improved adhe-
sion to the sand and the organic groupings can be neither dissolved
out nor washed out. The use of all of these waterglass based gel-
systems puts a certain burden on the environment from alkali
hydroxide. However, the influence on the environment is mini-
mized when the effects of dilution and absorption by the surround-
ing soils are taken into consideration.
The penetration of chemical pollutants into the soil and the
possibility of a remedial action by the methods in question is shown
in Figure 6. It can be seen that a horizontal gel seal can come into
contact with pure contaminants (A) or with aqueous solutions of
these contaminants in groundwater (B).
In order to reproduce these effects, a grouted sand was per-
colated in a test cylinder (Figure 7). The hydraulic gradient was ap-
proximately 30. The apparatus was designed to eliminate side-
streams. The tightness of the gel-sand mixture was tested against
the attack of the following pollutant solutions:
•15% by wt. potassium-ferrocyanide solution
•5% by wt. sulfuric acid solution
•8.4% by wt. phenol solution
•0.01% by wt. trichloroethylene solution
The gel was formed with DYNAGROUT T on the basis of 15%
by volume waterglass.
Slurry Trench
Ground
Water
" • \ c
\ - -
brouted Layer
I Adsorbed Contaminant in the Unsaturated Zone
II Capillary Zone
III Contaminant in Phase in the Saturated Zone
IV Solution of ihe Contaminant
A Contact of Grout with Contaminant in Phase
B Contact of Grout with Solution of the Contaminant
C Contact of Wall with Contaminant in Phase
D Contact of Wall with Solution of the Contaminant
Figure 6
Encapsulation Slurry in Contact with Pollutants
The development of the permeability of the gel sand mixture over
a period of approximately 1200 hours is shown in Figure 8. Under
these conditions DYNAGROUT T gels remained tight against an
all the tested materials. Under attack by sulfuric acid, the tightness
even increased.
Another testing apparatus is shown in Figure 9. Under a lower
gradient of about 15, the evaluation of pure liquid organic
• Chlorinoted Hydrocarbon
Figure 7
Test Equipment for Aqueous Solutions
: -10
3-15
——'—[—'—'—'—'—r—
Test Solution
+ * Water
K, [FelCNIt]-Solution 1SV. b.wl.
H,SO, - Solution 5V. b.wl.
Phenol-Solution 8.4V. b.wl.
Perchloroethylene 0,01 '/• b. wt.
Grout
DYNAGROUT T/ Wolergloss 15V. by Vol.
I
500 -, ... n. i 100° uo°
Elapsed Time [hrsj
Figure 8
Permeability Test Results with DYNAGROUT-based Gels
chemicals is possible. This apparatus was also used to measure the
action of concentrated aqueous solutions of the described
chemicals. The behavior of the DYNAGROUT T gels investigated
in this test apparatus corresponds to the results found in the
previously mentioned test unit.
With the inner tube of this glass apparatus filled with pure per-
chloroethylene, the K-value increased from 10 ~7 to 10 ~3 m/sec
within the first 200 hours; this data show that a gel of this composi-
tion is not stable in contact with a pure chlorinated hydrocarbon.
Degeneration of the gel occurs and the chemical breaks through.
This result should be considered as an example for the break-down
of a usual efficient gel-seal.
The next area to be investigated is the mechanism of these
degeneration effects of the gel-sand compound.
Attempts to find silicate-based gels which would be more stable
than DYNAGROUT T gel were based on the idea of changing the
character of the T-gel from hydrophilic to hydrophobia. In both
cases of SP and SB reactants, two gel developers have been
discovered which, when built into the silica-gel structure, form
hydrophobizing groupings. The mechanism of gel formation com-
prises the splitting of the reactant, the electrochemical coagulation
of the colloid-sol and the incorporation of the major part of the
reactive components in the gel.
Gels so formed were tested in the glass apparatus (Figure 9).
They were treated with water, with aqueous solutions of phenol
and sulfuric acid, with pure perchloroethylene and trichloroethy-
lene and also with diesel oil. The DYNAGROUT SP and SB gels
had a waterglass content of either 15 or 28% by volume. The
172
BARRIERS
-------
Grouting Material
Glass Cylinder
Contaminant
Water
Gel-Saturated Soil
Perforated Bottom
Volume with Negative
Water Pressure
Figure 9
Test Equipment for Pure Chemicals
development of the K-values in 1200 hours is shown in Figure 10.
Aqueous solutions behave similarly to DYNAGROUT T-based
systems when in contact with these gels, but in contact with pure
chemicals the new gels experienced no breakdown; on the contrary,
they become even tighter. DYNAGROUT SB behaves even better
than DYNAGROUT SP when contacted with perchloroethylene
(Figure 11).
Chemical Aspects of Backfill Materials
Materials generally used in the construction of small slurry walls
and respective slurry trenches are: powdered limestone, powdered
clay ore bentonite, cement and water. If such mixes with K-values
of 10~5 to 10~7 m/sec are penetrated not only by water but also by
chemicals, the swelling properties of the clay minerals will especial-
ly be changed. By an exchange effect, polaric and ionogenic
chemicals are introduced between the plates of the clay lattice. The
crystallization of the cement gel phase is also disturbed, resulting in
a reduction of the final strength of the wall.
The shrinkage of the clay minerals increases the permeability of
the slurry wall, permitting an additional attack from sulphates and
lime-aggressive carbonic acid which is often present in ground-
water; this can result in a total destruction of the wall. Conversely,
the presence of particulate matter in the groundwater fills the pores
and helps to reduce these effects.
The correct use of DYNAGROUT T and DYNAGROUT SB,
however, in the producing of these slurries will result in the follow-
ing advantages:
•The Theological behavior is improved
•The water-retaining capacity is enhanced
•The fluidity of the mixes is improved
-£--5
-15
Grout
DYNAGROUT SP/
Watergloss
15V. by Vol.
Test Solution
• • Water
• • Phenol-Solution lea. 8V. b.wt.)
• • Perchloroethylene
• • Perchloroethylene| Walerglass 28V.)
o o Trkhloroethylene
O 0 Diesel Oil
o o H2SO, (5V. b.wl.)
500 1000
Elapsed Time [ hfs]
Figure 10
Stability of DYNAGROUT-based Gels
1400
: -5
o
1
1
Grout
DYNAGROUT SP resp.
DYNAGROUT SB/
Waterglass
15V. by Vol.
Test Solution
* •* Water
J J Perchloroethylene
> DYNAGROUT SP
DYNAGROUT SB
0 500 r n 1000 KOO
Elapsed Time |_nrsj
Figure 11
Stability of Different DYNAGROUT-based Gels
•The tightness of the cured mixes against water and aqueous pol-
lutants is increased
A simple test unit for a fast measurement of the permeability is
shown in Figure 12. The same equipment used for testing gels was
also used. The permeability decreased by about two orders of
magnitude, i.e., only 1 to 10% of pollutant which permeates
through a conventional mass will run through walls compounded
with the mentioned admixtures (Figure 13). As with the gels, these
admixtures are chemically bonded to the slurry components. Ac-
cording to the tests they cannot be hydrolyzed and cannot be
washed out.
The work discussed in this section is part of a research program
of DYNAMIT NOBEL AG which will be supported by the "Ger-
man Ministry for Research and Technology". The government's
interest in this field involves the possibility of immobilizing toxic
wastes in the subsoil by utilization of these techniques, processes
and materials.
CASE HISTORY
In West Berlin, chlorinated hydrocarbons have been found
(Figure 14) down to a depth of 8 to 9 m, mainly in the sand layers.
From about 10 m downwards, marl had been found sometimes
changing with thin sand beds. The marl layer from 9 to 11 m depth
could be considered as a natural sealing stratum. Underneath, only
low concentrated tertiary intrusions have been determined.
As an amelioration system, the principle illustrated in Figure 3
was recommended. The system consisted of vertical sealing screens
with modified bentonite-cement backfill with an upper and a lower
drainage system. The proposal has been accepted by the West
Berlin government and special site tests are presently being done to
BARRIERS
173
-------
Water Saturated Sand
Figure 12
Principle of the Percolation Test
200
pso
a
B 100
£
SO
Cfmtnl - Benlonttt - Slurry
Bfntonilt 2.iV. b.wl.
Limtilont Powdtr 16.5V. b.wl
Ctment 10.7V. b.wl
Wolff tO.1V. b wl
OYNAGROUT SB o> SP
Slurry without Addilivr
< Slurry with 05V. SB
> Slurry with 05V. SP
50
100 ISO
Elapsed Tlrrw [hrs]
200
250
Figure 13
Permeability of Cement-Bentonite-Slurries
upp*r Ltvrl w
Fug Orommg
Low Lr*ri v»ms
m
i-on'
&I.X.,
090
j»
100
voo
no
«.»
»»tKh 11.80
)V5O
1700
if
"_•*
~
&
i
£
FJ*ig *
Fm» Sand
Cloy, kondy
F**$orx)
ClOT.Mti-tdy Tfih
Ftn* So«d i
- n
Mori
Sand
Mori
/
i 1
:
/ 0 Grownd Surloc*
o Not\xol Orounowairf Lrwrl
^7L»wprt>d Org(M»ning Cotw»>v* So>* /
Smo«l SK/rr
j
\
1r»txh
Figure 14
Principle of the Containment in West Berlin
•250-
c
o
0)
Q-
C
150-
100-
50-
40-
30-
20-
10-
Tri £
Trichloroethylene
Without
Additive
Tri / H20
Without
Additive
H20
With
Additive
Tri/ H20
With
Additive
H,0
0 10 2030^.050
Elapsed
100
Time [hrsj
Figure 15
Permeability Test Results with Conventional and Modified Bentonite-
Cement Backfills Loaded with Water or Trichloroethylene
determine the appropriate procedures to handle the modified
backfill with conventional equipment.
The permeability results of tests with conventional and modified
backfills loaded both with water and with trichloroethyiene solu-
tion are shown in Figure 15.
REFERENCES
1. Lieckfeld, C.-P., "Beerdigt auf Zeit," Natur, No. 4, April 1983.
2. Evans, J.C. and Fang, H.-Y., "Geotechnical Aspects of the Design
and Construction of Waste Containment Systems", Proc. 3. National
Conference of Management of Uncontrolled Hazardous Waste Sites,
Washington, D.C. 1982.
3. Spooner, P.A., Wetzel, R.S. and Orube, W.E., "Pollution Migration
Cut-Off Using Slurry Trench Construction", Proc. Third National
Conference on the Management of Uncontrolled Hazardous Waste
Sites, 1982.
4. Heitfeld, K.-H., Dullmann, H. and Krapp, L., "Erfahrungen mil
Dichtungswanden fur Mulldeponien und Baugruben", Proc. 2. Nat.
Tag. In g.-Geol., Fellbach 1979.
5. Schirmer, H., "Sanierung und Erweiterung einer Abfalldeponie durch
eine umschlie^ende Dichtungsschlitzwand", Wasser und Boden 11,
1980.
6. Schwille, F., "Die Ausbreitung von Chlorkohlenwasserstoffen im
Untergrund, erlautert anhand von Modellversuchen", Ber.D.Bunde-
sanstalt fur Gewasserkunde, Koblenz, 1982.
7. D'Appolonia, D.J., "Soil-Bentonite Slurry Trench Cut-offs", J. of
the Ceotech. Eng. Division, ASCE, 106, N o. GT4, 1980.
174
BARRIERS
-------
THE HYDRAULIC CONDUCTIVITY OF SILICATE
GROUTED SANDS WITH VARIOUS CHEMICALS
ARTHUR E. LORD, JR., Ph.D.
FREDERICK C. WEIST
Department of Physics
ROBERT M. KOERNER, Ph.D.
FRANCIS J. ARLAND
Department of Civil Engineering
Drexel University
Philadelphia, Pennsylvania
INTRODUCTION
Although antiquity (even the Bible) lists the use of grouting
materials, modern usage can be traced to 1802 where a suspension
of clay and lime was used to strengthen a masonry wall in Dieppe,
France.1 Portland cement was first used as a grouting material in
1838 in the construction of the first Thames tunnel in England.' In
1886, Jeziorsky patented the first chemical grout (sodium silicate
and calcium chloride). In the mid-1950s, many organic chemical
products suitable for use as grouts were developed. Cement grouts
(being cheaper) are used much more than chemical grouts,
although chemical grouts are widely used in Europe.
The basic reasons for grouting are the following:
•Increase strength
•Decrease compressibility
•Decrease permeability
The use of most interest here is the decrease of permeability with
special emphasis on stopping the flow of various hazardous
chemicals moving within leachate or the ground water flow regime.
Indeed, there is a very strong effort currently underway toward
mitigating the effect of contamination of groundwater, rivers and
lakes by hazardous materials leaking from waste disposal sites.
Cutoff walls of various types are being used to intercept the flow
between the landfill site and the potentially pollutable water. Types
of cutoff walls used in geotechnical engineering and heavy con-
struction work, which are usually adopted to make seepage cutoff
walls, are the following:
•Cement grout type wall
-Cement
-Cement/clay
-Cement/fly ash
-Cement/clay/fly ash
•Chemical grout type wall
-Silicate
-Acrylamide and polyacrylamides
-Phenoplast
-Lignosulfite
-Aminoplast
-Some combinations of above
-New products (e.g., acrylate)
•Slurry walls
-Soil/bentonite backfilled trench
-Geomembrane liner in a backfilled trench
•Sheet pile walls
-Interlocking steel sheets
-Tongue and groove precast concrete panels
-Tongue and groove timber
The time dependent reaction of these cutoff wall materials with
various chemicals is, in general, unknown. It is thought (usually
without experimental justification) that a number of these materials
are quite durable and impermeable to most chemical agents and en-
vironmental conditions. However, there has been very little work
on the durability of these wall materials when in a possibly cor-
rosive chemical environment. In retrospect, however, it was also
thought that the clay materials commonly used at sanitary landfill
sites for liners would be impervious to most chemicals. However,
some very significant recent work performed at Texas A & M
University showed this thinking to be quite false. In this work, it
was shown that most organic solvents (acetone, xylene, methanol,
etc.) will permeate readily through clay liners.2'3'4 The object of this
study is to see if a similarly adverse behavior also occurs in
chemically grouted walls.
PERMEABILITY AND CHEMICAL
COMPATIBILITY OF GROUTED SOIL
Neither compatibility nor permeability have been extensively
studied in grouted soils. For example, there are no ASTM or NSF
standards on measuring either property, and literature is relatively
scarce. There is, however, a standard for permeability testing of
soils, per se.' While a few studies have been done for water
permeability of grouted soils, no studies of permeability of
chemicals were found during the literature search.
Below is a summary of available material concerning the water
permeability of the various grouts (chemical compatibility will be
mentioned where available):
Cement-Type Grouts:
In the New Orleans Conference on grouting,6 a section is devoted
to cement grouting and the point is made that the material should
be quite impermeable (permeability $ 10~9 cm/s) to water and most
other materials. The exception is sulfates and some acids which are
known to strongly attack Portland cement. These authors believed
that cement type grouts should be quite permanent to most en-
vironmental situations. More work definitely needs to be per-
formed concerning the stability of cement grouted soil in contact
with various chemicals.
Resin-Type Grouts:
Work done on the acrylamides7'8 indicates that these materials
also have low permeabilities (f 10~9 cm/s). They should be relative-
ly stable under action by various chemicals,8'9 but specific
permeability data were not presented for the various chemicals.
Silicate-Type Grouts:
More work has been done on the water permeability of these
grouted soils than any other grouting material. The Tallard and
BARRIERS
175
-------
Caron FHA Reports" deal with silicate grouts in considerable
detail. The permeability is approximately 10~5 cm/s when well-
cured, but can increase to 10~3 cm/s if water flows through con-
tinuously. Studies of these "leaching" experiments are described in
Tallard and Caron." The permeabilities are also briefly mentioned
in articles dealing mainly with mechanical properties"-12. The
permeabilities to various chemicals are not included.
Slurry Walls:
The permeability has been given by D'Appolonia" as about 10~7
cm/s. D'Appolonia's article also indicates some of the com-
patibilities of slurry wall materials with various chemicals, but the
list of chemicals is not extensive.
EXPERIMENTAL APPROACH
For all tests in this study, the grout used had the following com-
position: 40% sodium silicate, 40% distilled water, 10% calcium
chloride (accelerator) and 10% ethyl acetate or formamide (reac-
tant). The soil used throughout was an Ottawa sand, which is a
rounded quartz sand of average particle size of 0.42 mm. It is the
medium sand size category and classified SP by the Unified Soil
Classification system.
Samples used for chemical compatability and quality control
mechanical testing were made in a split mold cylinder of size 3.34
cm diameter by 7.1 cm long. Samples used for permeability
measurements were made in an intact permeameter cell of the same
size.
For the chemical compatibility tests the samples were cut to 1.3S
cm length and were placed in 100 ml beakers and covered with the
particular chemical. The top was then sealed with parafilm and/or
aluminum foil (Figure 1. A list of the chemicals used is found in
Table 1. Only one grouted sample was used for each solution, ex-
cept for the sodium hydroxide solution where duplicate grouted
samples were immersed in separate but identical solutions.
For both types of tests, appropriate amounts of the above grout
mixture and Ottawa sand were thoroughly mixed and then com-
pacted into molds with a Harvard compactor. The void ratio
(volume of voids/volums of solids) was about 0.88. From grout
overflow during compaction, it was estimated that about 70% of
the voids were Tilled with grout. The samples were them mold-cured
for two weeks in air. Note should be made that the preferred
method of grouting samples in the laboratory is by forcing the
grout through the soil voids with pressure." However, the simpler
procedure used here produced samples with unconfined compres-
sion strength as high12-14 and water permeabilities to within at least
an order of magnitude10-11 of those produced by the pressure
method. Because the present work deals with chemical aspects, and
not mechanical aspects, it was felt that the simpler sample prepara-
tion was satisfactory.
Permeability measurements were performed in standard Soil Test
K 620 falling head permeameters of cell dimensions given above. At
least two, and sometimes four, samples were run for each chemical
investigated. The permeability was determined using the following
equation:
k - 2.3
U°810 (h)
(1)
where
k = coefficient of permeability (cm/s)
A | = sample cross section (cm2)
A2 = standpipe cross section (cm2)
L = sample length (cm)
At = time increment (s)
h,, = initial water height reading (cm)
hf = final water height reading (cm)
Two pore volumes of distilled water were allowed to flow
through the sample to evaluate its water permeability before the
particular chemical was used as permeant. Permeability
measurements were made as a function of pore volumes of liquid
passing through the samples until the individual tests were con-
cluded.
Figure 1
Photograph of a portion of the grouted sand samples
being tested for chemical compatibility
Figure 2
Grouted sand samples being tested for compatibility with four organic
solvents. From left to right: acetic acid, ethylene glycol, methanol and
acetone. The photographs were taken after 5 month's immersion.
CHEMICAL COMPATIBILITY TEST RESULTS
Of particular interest is the fact that all of the organic solvents
tested had no visible effect on the grouted sand samples. See Figure
2 where the photographs were taken after five months of immer-
sion. This is important because organic solvents were found to raise
the permeabilities of clay liners to a point where they would be
unattractive as liners or barriers for high solvent type wastes.2-3-4
Hence, silicate grouted material would be attractive in the
manufacture or repair of cutoff walls for these common type
wastes.
A complete range of pH's from 1 to 13 was used (Table 1). The
acidic (low pH) solutions had no observed effect on the grouted
sand; however, the basic (high pH) solutions did attack the grouted
soil samples (Figure 3). The pH of 12 (NaOH solution) completely
destroyed the integrity of the sample in less than one hour.
Disintegration of silicate grouted samples occurs at any pH > 8,
although it is slower at the lower pH values in this range. The time
176
BARRIERS
-------
Table 1
List of Chemicals Used in Compatibility Studies
Chemical
A. BASES
Sodium Hydroxide Solutions
10%, 50%, 100% (by vol.)
Sodium Hydroxide Solutions
pH'sof8,9,10,11,12,13
Ammonium Hydroxide
pH'sof8,9,10.11,12,13
B. ACIDS
Sulfuric Acid Solutions
pH'sofl,l,2,3,4,5,6
85% Phosphoric Acid Solution
Hydrochloric Acid
10% Hydrochloric Acid Solution
Acetic Acid
C. ORGANIC SOLVENTS
Acetone
Methylene Chloride
Ethylene Chloride
Ethylene Glycol
Heptane
Xylene
Methanol
D. SALTS
Saturated Potassium Chloride Solution
Saturated Sodium Dichromate Solution
Saturated Ferric Nitrate Solution
Saturated Ferric Chloride Solution
Saturated Ferric Chloride Solution
Saturated Sodium Chloride Solution
E. OTHERS
Mineral Oil
70% Isopropyl Alcohol
Cyclohexane
Saturated Oxalic Acid Solution
Saturated Potassium Permanganate Solution
Distilled Water
Philadelphia Tap Water
Time of
Immersion
(Months)
9
5
4
6
6
6
6
6
6
9
9
2
2
1
1
9
6
6
2
2
6
6
of disintegration as a function of pH for both sodium hydroxide
and ammonium hydroxide solutions is shown in Figure 4. The time
for disintegration was arbitrarily taken as the time needed to
observe an easily noticeable number of sand grains on the bottom
of the beaker. (This leads to a large underestimation of the
disintegration time at pH values in the vicinity of 7, because, due to
simply physical erosion, there are always some grains in the bottom
of the beaker.) The disintegration time is a strong function of pH,
decreasing markedly at high pH values. The basic form is to be ex-
pected since basic solutions are known15-16 to destabilize the silicate
"polymer".
PERMEABILITY TEST RESULTS
The permeability results for five common organic solvents are
shown in Table 2. The pertinent properties of these liquids are
given in Table 3. The results are tabulated in terms of percentage
change in permeability after passage of three pore volumes of the li-
quid (after the great majority of the water was displaced by the li-
quid) and the permeability of water through the sample. The
organic solvents which had such a devastating effect on the clay
materials have very little effect on the permeability of the silicate
grouted sands. In fact, the changes seen in Table 2 are strictly in ac-
cordance with the inverse of the kinematic viscosity (viscosity) of the
density
Table 2
Effect of Organic Solvents on the Permeability of Silicate Grouted Soil
_ — __ _ initial ~ Initial
X Change in Permeability Permeability Permeability
After Passage of Three of Liquid of Water
Liquid Pore Volumes of Liquid (cm/aec) (cm/sec)
Acetone
Sample
Sample
Sample
Sample
Methanol
Sample
Sample
Ethylene
Sample
Sample
1
2
3
4
1
2
Clycol
1
2
+ 5.5
+ 16
+ 13
0
+ 5
+ 5.9
-12.7
-12.7
1
2
2
1
2
1
1
1
.8 x
.5 x
.3 x
.3 x
.0 x
.7 x
.1 x
.1 x
1C'*
10-*
10-*
10-*
10-*
_A
10
10"5
io-5
9
x
1.4
1.
7.
1.
1.
1.
1.
1
5
3
1
2
3
io-5
X
X
X
X
X
X
X
10-*
10-*
ID'5
10-*
-A
10
10-*
10-*
Acetic Acid
Sample
Sample
Xylene
Sample
Sample
1
2
1
2
+ 5.8
+ 3.4
0
0
5
5
1
1
.2 x
.8 x
.9 x
.5 x
io-s
ID'5
10-*
10-*
9.
1.
1.
1.
8
2
5
2
X
X
X
X
io"5
10-*
10-*
10-*
Figure 3
Grouted sand samples being tested for compatibility with basic
solutions. Sodium hydroxide solutions of pH values (from left to right):
8, 10 and 12. The photographs were taken after one day of immersion.
Table 3
Properties of Organic Solvents Used in Study (water also included)
Net*
Acetic
Acid
Methuiol
Acetone
Ethylene
Clycol
Xylene
Denilty
et 20*C
U./C-3)
1.05
0.79
0.79
1.11
0.87
VUcoelty
•t 20'C
(Centipolee)
1.28
0.54
0.33
21.0
o.ei
Klneutlc Viecoelty
(Vlacoslty/Denelty)
(cP/«./c«J>
1.21
0.61
0.417
18.9
0.9J
Dielectric
Conetant at
20*C
6.2
31.2
21.4
3S.7
2.4
Weter
Solubility
•t 20-C
(»/!>
-
-
.
0.20
BARRIERS
177
-------
various permeating liquids (Table 3). For example, acetone has a
low kinematic viscosity, hence a high permeability; ethylene glycol
has a high kinematic viscosity, hence a low permeability. This is an
indication that the sample is changing very little during the
permeability tests.
Permeability measurements were also made using ammonium
hydroxide (pH = 12.6) as the permeating liquid. The work on
chemical compatibility showed that high pH solutions such as this
would destroy the mechanical integrity of the sample within an
hour. It was reasoned that loss of integrity would lead to dramatic
increases in permeability in a very short time. However, the pro-
ducts of decomposition of the grouted sample clogged the
permeameter, and meaningful results were difficult to achieve. In
one series of tests, breakthrough was achieved before clogging oc-
curred; in an other series, the apparent permeability only increased
by a factor of eight after the passage of 15 pore volumes of am-
monium hydroxide.
£ 200
a
H
00
«
l>
c
100
(a) Response of Sodium Hydroxide
00^°
7 9
pH
II
13
200
100
(b) Response of Ammonium Hydroxide
II
13
PH
Figure 4
Initial disintegration time for sodium silicate grouted sand samples in
sodium hydroxide and ammonium hydroxide as a function of pH. The
time is in the vicinity of 7 due to simple physical erosion.
After using all the organic permeants, the grouted sand had to be
"chisled-out" of the permeameter cell, indicating that there were
no edge paths for the permeant to follow. After using ammonium
hydroxide, however, the grouted sand was very easily removed
from the permeameter cell.
CONCLUSIONS
The permanent containment of leachates from chemical and
hazardous waste sites is a problem of growing national awareness
and concern. When such a situation is found to exist, the usual
remedy is thought to be a bentonite clay backfilled-slurry con-
structed cutoff wall. These walls, extending down to an acquiclude
or to great depths beneath the zone of seepage, have the same
vulnerability to leachale attack as do clay liner materials. Since
clays have been shown to be susceptible to certain chemical attack,
an alternate method is a chemically grouted cutoff wall which
generally uses a sodium silicate based grout. The obvious question,
on which this paper is based, is what effect to chemicals have on the
hydraulic properties of grouted soils?
The paper addresses the question via two types of tests: (1) the
compatibility of grouted sand samples immersed in chemicals, and
(2) permeability tests using the same chemicals. Using a wide range
of chemicals it was found that only in one instance did breakdown
of the samples occur. When using basic solutions (particularly
when the pH ^ 8) the samples visually disintegrated and the
permeabilities markedly increased.
Thus, it appears that sodium silicate grouted soils can perform as
adequate temporary seepage barriers or be used in sealing localized
liner or cutoff wall leaks, except as noted above. This statement
strictly applies only for the time scales involved in these ex-
periments. Silicate grouts are known to suffer from "synereris",
which is a separating out of the water over long times with con-
comitant increase in permeability. Also, this study looked only at a
silicate grout. The grouts listed in the Introduction all have dif-
ferent properties of strength and permeability.
ACKNOWLEDGEMENT
The author would like to thank Mr. Joseph P. Welsh of the
Hayward Baker Company for helpful discussions, suggesting the
commonly used silicate grout material and supplying some of the
ingredients. Mr. Donald Byrnes performed some of the preliminary
studies.
REFERENCES
1. Karol, R.H. and Welsh, J.P., "Chemical Grouts," Encyclopedia of
Chemical Technology, Vol. 5, 3rd Edition, J. Wiley & Sons, Inc., New
York, 1979, 368-374.
2. Anderson, D.C., Brown, K.W. and Green, J., "Organic Leachate Ef-
fects on the Permeability of Clay Liners," Proc. Conference on the
Management of Uncontrolled Waste Sites, 1981, 223-229.
3. Anderson, D.C., Brown, K.W. and Green, J., "Effect of Organic
Fluids on the Permeability of Clay Soil Liners," In: Land Disposal of
Hazardous Waste, Proc. Eighth Annual Research Symp., EPA Re-
port 600/9-82-002, 1982, 179-190.
4. Anderson, D., "Does Landfill Leachate Make Clay Liners More Per-
meable?" Civil Engineering, ASCE, Sept. 1982, 66-69.
5. ASTM Annual Book of Standards, Part 19—Soil and Rock; Building
Stones, ASTM D 2434-68 (Reapproved 1974), ASTM Phila., PA,
Baker, W.H., ed., 1982, 373-379.
6. Proc. ofConf. on Grouting in Geotechnical Engineering, ASCE, New
Orleans, LA, Feb. 1982.
7. Dorion, G.H., Burkhard, H. and White, M.L., "The Permeability of
Sand Stabilized with a Chemical Grout," Bulletin ASTM 250, 1960,
34-35.
8. Clarke, W.J., "Performance Characteristics of Acrylate Polymer
Grout," Ref. 6, 418-432.
9. Berry, R.M., "Injectite® -80 Polyacrylamide Grout," Ref. 6,
394^02.
10. Tallard, G.R. and Caron, C., "Chemical Grouts for Soils," Vol. 1—
Available Materials; Vol. 2—Engineering Evaluation of Available
Materials, Reports No. FHWA-RD-77-50 and FHWA-RD-51, 1977,
U.S. Federal Highway Administration.
11. Karol, R.H., Chemical Grouting, Marcel Dekker, NY, 1982.
12. Clough, G.W., Kuck, W.M. and Kasali, G., "Silicate Stabilized
Sand," J. Geotech. Engin., ASCE 105, 1978, 65-82.
13. D-Appolonia, D.J., "Soil Bentonite Slurry Trench Cut-Offs," /. Geo-
tech. Engin., ASCE 106, 1980, 399^17.
14. Warner, J., "Strength Properties of Chemically Solidified Sands,"
J. Soil Mech. and Found Div., ASCE 98, 1972, 1163-1185.
15. Her, R.K., The Colloid Chemistry of Silica and Silicates, Cornell
Univ. Press, Ithaca, NY, 1955.
16. Vail, J.G. and Willis, J.H., Soluble Silicates, Their Properties and
Uses Volume I: Chemistry, Reinhold Publ. Corp., New York, NY
1952.
178
BARRIERS
-------
EFFECTIVENESS OF IMPERMEABLE BARRIERS FOR
RETARDATION OF POLLUTANT MIGRATION
ROBERT C. KNOX, Ph.D.
Environmental and Ground Water Institute
University of Oklahoma
Norman, Oklahoma
INTRODUCTION
One of the most popular current methods of containing con-
taminated groundwater is through the use of subsurface im-
permeable barriers. These barriers can take one of three forms:
slurry walls; grout curtains; or steel sheet-piles. Successful opera-
tion of these barrier systems depends upon three basic criteria.
First, the barrier must be truly impermeable and remain so even
upon exposure to the contaminated groundwater. Second, there
must exist an underlying impermeable formation, at a reasonable
depth, to which the barrier can be connected. Third, an adequate
connection between the barrier and the underlying formation must
be assured.
In this paper, the author presents the results of the analysis of the
movement of contaminated groundwater under or through an im-
perfect barrier. The first phase of the analysis consists of the
development of an analytical solution for the flow of groundwater
under a barrier and a simple numerical integration technique for
developing concentration breakthrough curves. This simple solu-
tion algorithm was applied to the cases of variable recharge rates
and lengths, variable depths of penetration of the barrier and
anisotropic soils. The second phase of the analysis involves apply-
ing a numerical solute transport model to analyze the performance
of a barrier with and without the effects of hydrodynamic disper-
sion, in the presence of a layered soil and of a fully penetrating but
partially permeable barrier.
ANALYTICAL SOLUTION
One of the first steps in this research was to find or develop an
analytical solution to the groundwater flow equation which could
be used to calibrate and confirm the accuracy of a subsequent
numerical computer model. Because of the specificity of the prob-
lem, it was decided to develop an analytical solution.
The problem to be analyzed is that of flow of contaminated
groundwater under an impermeable barrier (Figure 1). The equa-
tion governing the steady state flow of water through an isotropic,
homogeneous media (in terms of the stream function) is given by:
62*
6x2
= 0
(1)
x, y = horizontal and vertical directions respectively and ¥ is the
stream function that describes the flow paths for steady flow
through the aquifer. This is the well known Laplace equation.
One method for solving the equation is called the separation of
variables technique. A general solution by this technique has been
developed by Kirkham and Powers.1 The analytical solution par-
ticular to the proposed problem will be generated by substituting
the appropriate boundary conditions into the general solution
below.
y(x,y) « A + Bx + Cy + Dxy
sinh
( or
cosh
sn
{ or
cos
n(b+ or)
y
x
n(c+ or)
y
(2)
where
A, B, C, D, En, «, b, c = constants, and
n = 1,2,...
By substituting the boundary conditions shown below for the
specified problem into the above equation, one can generate a
specific solution for the distribution of the streamlines in the
aquifer.
B.C.I
B.C.2
B.C.3
B.C.3
B.C.5
* = *0
* = 0
* ={f (
* = *Q
* = *„
x = 0
x = 0
x = s
0-cx< s
o< ycb
b
-------
These substitutions yield the following dimensionless equation
(8)
Y + XY +
(4)
-2 slnh(mrN(l-X))sln(mtY)sln(n*B)
(n7°2 sinh(nirN)
Solving for *jj yields
Numerical Flow Model
The next step in the research was to develop a numerical model
for calculating the dimensionless streamline distribution and incor-
porating flexibility to handle situations other than that depicted in
Figure 1. The model was calibrated with the analytical solution
developed above.
The governing equation for groundwater flow through an
anisotropic, homogeneous media is
S2f
+ K
KAY2
2(KAyz+Ax2)
,+*,
' 1+1,1 Ti-l,j)
(9)
This equation can be programmed on a computer using an
iterative alternating direction solution procedure to converge upon
the solution for *jj at the nodes of an artificial grid representing
the 2-dimensional aquifer. The program can calculate a value of
(5) *iC,T for nocle (i>J)bv Usin8its four surrounding nodes. A new value
of * for node (i,j) is calculated by a relaxation equation of the form
where
Kx = hydraulic conductivity in the x-direction
Ky = hydraulic conductivity in the y-direction
Dividing both sides of the equation by Ky and remembering that
= */*o, X = x/s and Y = y/d, yields
old
Letting K = Kx/Ky (d/s)2 be the aspect ratio, yields
contaminated recharge (C0,c)
(6)
(7)
////// s / / / / / / / s /
Figure 1
Hypothetical aquifer-barrier system subjected to
steady-state contaminated recharge
i.j
calc _ old
- y }
> . T . . /
(10)
The relaxation factor accelerates the convergence of the method.
A convergence criterion of 0 was input to the model to increase ac-
curacy. So, the process is controlledjpy an iteration limit (ITER =
30) The end result is a dimensionless * distribution for all the nodes
in the grid.
SOLUTE TRAVEL TIME UTILIZING
PLUG FLOW ANALYSIS
Development of pollutant breakthrough curves can be ac-
complished by considering the kinematics of the flow field in Figure
1 as was done by McLin.2 This type of analysis ignores the effects
of dispersion and inherently assumes that vertical flow effects can
be ignored for the elongated (width/depth ratio ^ 4) aquifer. In
essence, the assumption is that the contaminated recharge travels as
"plugs" (Figure 2). By definition, the flow between two
streamlines must remain constant. The time for a particle to flow
from one point (sj) to another (82 is equal to the volume of water in
the flow field divided by the volumetric flow rate. Using a unit
dimension in the third direction, the time becomes equal to the area
of flow divided by the areal flow rate. From Figure 2 this time can
be expressed by
(ID
where Q = d*
Using the following substitutions to non-dimensionalize the
equation:
A0 = SD, the cross section of the aquifer,
*0 =«S,
e = recharge rate,
A(*) = A(*)/A0, a dimensionless area, and
^ = i'/'i'o, a dimensionless streamline
yields
The continuous derivatives of the above equation can be replaced
by their finite difference approximations. This yields
nSDdA(f)
eSd?
C/tc
(12)
180
BARRIERS
-------
where tc = n D/e is defined as the solute response time for the
aquifer. If the numerical model can generate the distribution of the
dimensionless ¥, one can numerically integrate to determine the
relationship of* vs. A(^). The sjppe of this curve can then be deter-
mined to generate the dA(¥)/d* term needed.
C/Co
1.0 '
Figure 2
Illustration of plug flow
If one considers the flow of the contaminant to be "plug flow"
as outlined in Figure 2, the outflow concentration can be generated.
If each of the stream tubes in Figure 2 carries one tenth of the con-
taminated recharge (e) at a concentration C0, then the average con-
centration of the outflow at any time will depend on the number of
stream tubes that have arrived at the point of outflow. More
specifically, if two of the stream tubes have arrived, the average
concentration C, at the point of outflow, will be equal to 0.2C0.
The relationship in terms of an equation is
C'/2C0 = * (13)
Hence, pollutant breakthrough curves (C/C0 vs t/tQ) can be
generated from the known distribution of * in the aquifer.
Problem 1: Full Recharge, Varying Depths of
Penetration, Isotropic Soil
The first, and probably the simplest, problem to be examined is
that of full length recharge and varying depths of penetration of the
barrier in a homogeneous, isotropic aquifer. Conceptually, this
situation is equivalent to placing a barrier right next to a source of
contaminated recharge.
Plotted in Figure 3 are the pollutant breakthrough curves for no
barrier and for two different depths of penetration of the barrier.
All three of the curves show a fictitious immediate response in the
form of a relative concentration (C/C0) increase. The curves also
show that as the depth of the barrier increases, the initial response
of the system decreases. In other words, the two "with barrier"
cases show a time lag before a dramatic response over that of the
"no barrier" case. The curves also show that the "with barrier"
cases actually catch and then surpass the "no barrier" case in terms
of relative concentration.
The time lag for the "with barrier" cases can be explained by ex-
amining the ¥ distributions under the barrier (Figure 4). As might
be expected, the placement of a barrier significantly increases the
flow distance for the near streamlines. The far streamlines are af-
fected less by placement of the barrier. The increase in flow path
distances explains the time lag seen in Figure 3.
The reason for the deeper barrier actually overtaking the
shallower barrier and the no barrier cases in terms of relative con-
centration over time can be explained by the spacing of the
Figure 3
Pollutant breakthrough curves for aquifer subjected to full recharge
Figure 4
Streamline distributions for 50% and 90% penetration barrier
streamlines around the opening in the barrier in Figure 4. The
Cauchy-Riemann conditions state that velocity (specific discharge)
vectors are proportional to the rate of change of * in the or-
thogonal direction.
t«* and
«y
Y a IT O»
y y 6x
(14)
Since the streamlines are closely spaced near the opening, the
velocities in both directions are increasing. Notice that, for the
deeper barrier, the velocity gradient around the opening is steeper
and its effects are felt further into the aquifer. Although the travel
distances for the deep harrier are increased, the contaminant is ac-
tually subjected to a more intense velocity gradient and, as such,
will overtake the cases of shallow or no barrier with their mild
velocity gradients. Flow in the deep barrier case overtakes the other
cases at a relative concentration of about 0.4 (Figure 3). This
phenomenon may or may not be significant depending on what
relative concentration is considered critical. This critical concentra-
tion will be pollutant specific.
Problem 2: Variable Length of Recharge
One of the variations imposed on the aquifer was changing the
length of the recharge area. A comparison was made for full
recharge and recharge over the outer 3/4, 1/2 and 1/4 of the
aquifer. Conceptually, this is equivalent to placing the barrier
downgradient from a source of contaminated recharge.
BARRIERS
181
-------
Note that although moving the barrier further away from the
source of recharge provides a greater initial time lag, this increased
lag can only be attributed to the increased travel distance and not to
the performance of the barrier. The effectiveness of the barriers is
diminished by placing them downgradient. Plotted in Figure 5 are
the pollutant breakthrough curves for the deep barrier for the four
different lengths of recharge. Although the barrier placed furthest
downgradient provides the greatest time lag, it actually has the
greatest rate of concentration increase and overtakes the barrier
placed right next to the source at a relative concentration of about
0.7. The explanation for this phenomenon is that placement of a
barrier downgradient from the recharge allows the flow pattern to
become established before entering the area of influence of the bar-
rier.
Problem 3: Anisotropic Soil
Another variation imposed on the aquifer was to place
anisotropic soils within the aquifer. Two cases will be examined.
First, the soil will be assumed to be highly conductive in the
horizontal direction (Kj'^Ky). Conceptually, this is equivalent to
a highly stratified soil, perhaps layers of sand and gravel between
layers of clay. The second case will be that of a soil highly conduc-
tive in the vertical direction (Ky» KJ. Conceptually, this is
equivalent to a highly fracured soil.
C/Co
1.0 -
-R«charg» Ow*r Outer 1/2
-R»crt»rgo Over Oul«r 1/4
1
Figure 5
Pollutant breakthrough curves for 90% penetrating barrier
at variable recharge lengths
Figure 6
Pollutant breakthrough curves for no-barrier and 90% barrier
in horizontally conductive soil
Figure 7
Pollutant breakthrough curves for no-barrier and 90%
penetrating barrier in vertically conductive soil
The approach used was to apply an overall directional conduc-
tivity reflecting the ability of the soil to transmit water in that direc-
tion. Also, because the hydraulic conductivities for this model are
incorporated in an aspect ratio (K = (Kx/Ky)(D/S)2), only the ratio
of horizontal conductivity to vertical conductivity is needed.
Hence, if a conductivity ratio of 10 (Kx/Ky = 10) is used, this im-
plies that the aquifer has a greater propensity to transmit the water
laterally than vertically.
Plotted in Figure 6 are the pollutant breakthrough curves for no
barrier and a deep (90%) barrier in a horizontally conductive
(Kx/Ky = 10) aquifer subjected to full length recharge. These
curves follow the pattern established previously, i.e., the deep bar-
rier provides an initial time lag but eventually overtakes the no bar-
rier case. The interesting aspect of these curves, however, is the
very gradual concentration increase at the higher values of C/C0.
What is happening is that the furthest streamtubes (the streamtubes
that must travel furthest downward) are having trouble moving ver-
tically downward initially. Hence their time of arrival under the
barrier is being delayed.
Plotted in Figure 7 are the same curves except the soil is now
dominated by vertical conductivity (Kx/Ky = 0.1). These curves
show a more gradual rate of concentration increase. This
phenomenon reflects the fact that the streamtubes are dropping
vertically with relative ease but are having trouble moving laterally.
Since the difference in horizontal distance (x-direction) each
streamtube must travel is greater than the distance difference in the
vertical direction, the streamtubes will tend to arrive in proportion
to the horizontal distance which they must travel. This accounts for
the gradual rate of concentration increase.
ANALYSIS BY NUMERICAL SOLUTE
TRANSPORT MODEL
This phase of the analysis involved applying the Konikow-Brede-
hoeft (K-B)3 numerical solute transport model to the proposed
problem to examine three phenomena. First, the effects of disper-
sion on the pollutant breakthrough curves were examined. Second,
the effects of keying the barrier into a relatively impermeable yet
not totally impermeable formation were analyzed. Finally, the
behavior of a totally penetrating but semi-permeable barrier was
assessed.
Problem 4: Effects of Dispersion
Plotted in Figure 8 are the pollutant breakthrough curves at 90%
depth for the no-barrier case and three dispersive cases for a 90%
penetrating barrier. The aquifer is 100 ft deep and 500 ft wide.
The first thing to note about Figure 8 is that the placement of a
partially penetrating barrier in the aquifer is ineffective in terms of
182
BARRIERS
-------
T (y.ori)'
Figure 8
Pollutant breakthrough curves for an elongated aquifer
retarding pollutant migration. The no-barrier case shows an almost
immediate response to the contaminated recharge. However, the
with-barrier cases only provide time lags on the order of one year
over that of the no-barrier case. Moreover, the rate of concentra-
tion increase under the barrier is as great as, if not greater than,
that of the no-barrier case. In essence, all the barrier does is provide
a small initial time lag. The actual numerical values of these time
lags is not important because the input data is hypothetical, but the
relative behavior of the barrier to the no-barrier case is important.
It shows that partially penetrating barriers are not completely effec-
tive in retarding pollutant migration.
Problem 5: Layered Soils
One means of alleviating the problem of a partially penetrating
barrier would be to construct an adequate key into an im-
permeaable formation. If an impermeable formation does not exist
at a reasonable depth, one would probably not use a barrier.
However, if a relatively, yet not totally, impermeable layer exists at
a reasonable depth, one might key into it. Plotted in Figure 9 are
the breakthrough curves for a partially penetrating barrier (90%)
and a barrier that has been keyed into a formation only slightly less
permeable than the overlying aquifer (Klayer = 0.1 Kaquifer). The re-
sults are quite dramatic. Not only does the impermeable layer delay
the initial appearance of contaminant under the barrier, but it also
decreases the rate at which the concentration of the escaping con-
taminant increases. This effect is even more pronounced for deeper
aquifers.
Figure 10
Pollutant breakthrough curve for barrier keyed
to impermeable layer (50 ft)
Figure 9
Pollutant breakthrough curves for barrier keyed
to impermeable layer (25 ft)
Figure 11
Pollutant breakthrough curves adjacent to a
semi-permeable barrier at 30% depth
Plotted in Figure 10 are the same curves for an aquifer twice as
deep as that of Figure 9. The time lag is approximately twice that of
Figure 9 and this is explained by the fact that the contaminant must
travel twice the distance vertically before attempting to penetrate
the layer.
The above phenomenon has practical significance because it im-
plies that barriers might be useful at future facilities where an ar-
tificial impermeable layer (such as a clay liner) has been placed. In
these situations, an adequate key can be assured by simply sinking
the barrier down past the liner. Such is not the case with deep im-
permeable bedrock where one must be concerned with both the
quality and depth of penetration of the key into the bedrock.
Problem 6: Semi-Permeable Barriers
Another problem that has plagued barriers is that the im-
permeability of the wall itself cannot be assured. Steel sheet-piles
are not initially water-tight, and grout curtains and slurry walls are
both subject to permeability increases upon exposure to certain
contaminants. Plotted in Figure 11 are the concentration
breakthrough curves at 30% depths on the left side of the barrier
for two different barrier permeabilities. The barrier is fully
penetrating but possesses a permeability only slightly less than that
of the aquifer. Insuring the impermeability of the barrier appears to
be a more critical factor than insuring an adequate key. Note that
keying the barrier into a semi-permeable layer was extremely effec-
tive in retarding pollutant migration.
A fully penetrating barrier (Figure 11) does not perform effec-
tively unless the permeability of the barrier is at least two orders of
magnitude lower than the adjacent aquifer (Kbarrier = Kaquifer).
This is reasonable because there exists a significant stress in the
horizontal direction, while stresses in the vertical direction are
minor, i.e., in this situation the tendency is for the pollutant to
migrate laterally more than downward.
BARRIERS
183
-------
C/Co
1.0 -
Figure 12
Comparison of simple and K-B models
COMPARISON OF MODELS
By imposing a constant head difference across the impermeable
barrier, a constant flow through the opening in the barrier is
developed. Since the aquifer is assumed to be at steady state condi-
tions, the flow through the opening in the barrier must be equal to
the amount of recharge coming into the aquifer. The recharge rate
the aquifer is subjected to is the recharge flow divided by the length
of the aquifer. With this known recharge rate, it is possible to use
the simple analysis and calculate the response time (tc = —) for a
given aquifer. With a known tc, the pollutant breakthrough curves
can be converted to include an absolute time (t) rather than a
dimensionless time parameter (t/tc). This will allow for a com-
parison of the results of the simple plug flow model and the
sophisticated K-B model.
Plotted in Figure 12 are the pollutant breakthrough curves for
the 100 ft deep, 400 ft wide aquifer. Two of the curves were
generated by the K-B model and they reflect the case of no disper-
sion and mild dispersion. The third curve represents the results
generated by the simple plug flow model, converted to an absolute
time scale by the process outlined above. The curves illustrate that
the simple model tends to predict an earlier first arrival and a more
gradual concentration increase of pollutant under the barrier. An
interesting aspect of Figure 12 is that the results of both the K-B
model and the simple plug flow model are not significantly dif-
ferent. This same trend was found when converting the simple plug
flow model results to a comparable basis with the K-B model results
for other depths of aquifers. Hence, it is concluded that the simple
model not only gives an accurate prediction of the general behavior
of these barrier systems, but can also provide fairly comparable ac-
tual values relative to the results of the K-B model if the parameter
tc can be calculated.
CONCLUSIONS
The first phase of the analysis utilized a simplified (plug flow)
model to examine the travel of pollutants from a source of con-
taminated recharge through an aquifer and under a partially pene-
trating impermeable barrier. The model was applied to a variety
of simple input conditions. From this analysis the following conclu-
sions can be drawn.
• The most efficient use of barrier technology is to place the bar-
rier directly adjacent to the source of contaminated recharge.
Placement of the barrier downgradient has been examined under a
variety of conditions and, in each case, was found to be less effec-
tive than an adjacent barrier. Placing a barrier downgradient allows
the pollution front to become established and approach the gap in
the barrier as a wall. Hence, concentration increase under the bar-
rier is quite dramatic following a small initial time lag. The initial
time lag is due solely to aquifer geometry. When these facts are
coupled with the added consideration that placing a barrier
downgradient will increase its total length (and cost), it becomes
obvious that this is less than optimum application of the
technology.
• Unless a perfect connection can be made between the barrier
and the underlying impermeable formation, the barrier does not
provide complete containment. The barrier will provide an initial
time lag before the appearance and increase in concentration of a
contaminant under the barrier. However, this positive attribute is
counterbalanced by the fact that the concentration under a partially
penetrating barrier will actually increase faster than the outflow
concentration in an aquifer with no barrier. This phenomena will
be significant depending on the pollutant and the relative concen-
tration considered to be critical.
• When an aquifer with a waste source is highly conductive in
the vertical direction, the effectiveness of a barrier is practically
negligible. Conversely, aquifers conductive in the horizontal direc-
tion are more amenable to barrier technology. This is because the
pollutants tend to run laterally initially until they reach the barrier.
They then must travel vertically downward to get by the barrier. In
essence, the barrier dramatically increases the flow path distance
the pollutant would normally follow.
• The numerical model and analysis employed in this phase of
the research was relatively simple, quick and economical. However,
the results generated only provide information on the general
behavior of barriers. The results would be hard to apply to a field
problem unless specific parameters, such as aquifer response time
(tc), could be related to input data, such as hydraulic conductivity.
Additionally, the simple numerical model does not handle some of
the more complex variations such as dispersion, layered soils or
semi-permeable barriers.
As a result of the second phase of the analysis, a number of addi-
tional conclusions can be drawn about the general behavior of bar-
riers. Because the input data was hypothetical, no specifics can be
discussed, but the trends can be outlined. The conclusions are:
• The effects of dispersion on the overall behavior of barrier
systems is negligible. The general pattern of an initial time lag prior
to first appearance of contaminant, followed by a rapid increase in
concentration and concluded with an assymptotic approach to in-
put concentration is followed whether the pollutant is dispersive or
not. Dispersive pollutants tend to arrive earlier than non-dispersive
pollutants, but this factor is not significant when one considers that
the time lags are on the order of fractions of years.
•The ability to key a truly impermeable barrier to an im-
permeable formation, be it totally or only moderately im-
permeable, dramatically improves the performance of the barrier.
If an adequate key cannot be assured, barriers are a poor (and ex-
pensive) choice of groundwater pollution control.
• The placement of a barrier that is not dramatically less
permeable than the native aquifer material is ineffective. Moreover,
the contaminant tends to first penetrate the upper parts of a semi-
permeable barrier, and this fact should be considered in the design
of monitoring networks for barriers. Monitoring these systems only
at full depth may not detect the movement of contaminant out of
the upper layers.
REFERENCES
1. Kirkham, D. and Powers, W.L., "Physical Artifices for Solving Flow
Problems", Advanced Soil Physics, 1st Ed., John Wiley and Sons,
1972, pp. 85-130.
2. McLin, S.G., "Lumped Parameter Hydrosalinity Model", Ph.D.
Dissertation, New Mexico Mining and Technology Institute, 1980,
Socorro, New Mexico.
3. Konikow, L.F. and Bredehoeft, J.D., "Computer Model of Two-
Dimensional Solute Transport and Dispersion in Ground Water", Book
1, Chapter 2, 1978, Techniques of Water Resources Investigations of
the United States Geological Survey, Washington, D.C.
184
BARRIERS
-------
FUNDAMENTALS or SYNTHETIC MEMBRANE LINER
SELECTION: A PRACTICAL PROTOCOL FOR SPECIFIERS
J. BRIAN AINSWORTH
Schlegel Lining Technology, Inc.
The Woodlands, Texas
INTRODUCTION
Subtitle C of RCRA creates a "cradle to grave" hazardous waste
management system whose intent is to protect human health and
the environment. With rare exception, the regulations as currently
promulgated require the use of a synthetic liner at least 30 mils
(0.76 mm) thick in hazardous waste surface impoundments, waste
piles and landfills.
Yet it is unfortunate, and of probable risk to human health and
the environment, that no one profession has taken that body of
knowledge and experience called "liner technology" as its own.
The science-based fundamentals of synthetic liners are to be found
in a number of disciplines including civil, chemical and mechanical
engineering; polymer formulation or rubber compounding;
geology, hydrology and hydrogeology; and, occasionally, business
administration.
It is urgent that specifiers and permit writers extend their
understanding of containment technology and the role that a liner
plays within a containment system. New liner technologies are in-
creasingly available, while some older lining concepts have been
called into question. Recent technological advances in the produc-
tion, supply and installation of synthetic membrane liners have, for
example, provided liners that resist thermal deterioration; are inert
to chemical attack, including organics; and are capable of with-
standing severe loading and other physical forces.
Designing a containment system for the future as well as for to-
day's legal requirements is now necessary. Specifying a liner for
that containment system is a complicated task, one that goes
beyond the token use of a 30 mil thickness or naive acceptance of a
manufacturer's or installer's unsubstantiated promise of "trust
me."
It is imperative that liners be viewed and evaluated as part of a
system designed to contain hazardous wastes. This evaluation in-
cludes the selection of the liner material and the installation of the
liner, all within the context of the uses to which the liner will be put
during its intended life.
Evaluation of liner properties is a key procedure. It has been
pointed out by others' that the essential factors to consider in
selecting an appropriate liner include:
•The compatibility of a liner with supporting and surrounding
environmental elements at the site
•The compatibility of the specified wastes or waste leachates with
liner materials
•The period of time that the liner will be expected to contain the
specified wastes.
It is the author's intention that this paper itemize those in-
fluences on a liner for a specific application at a given site, that will
affect the performance and service life of a containment system.
This discussion of the many factors that will have varying degrees
of impact on liner performance, and thus the containment system
in its entirety, is also intended to provoke specification writers to
issue much more detailed and far more demanding performance re-
quirements for lining systems.
STRENGTH AND THICKNESS
The ability of a synthetic liner to resist puncture and tear, both
during installation and during the service life of a facility, is
especially critical. Puncture of a liner can occur through a number
of means including falling objects, equipment moving on the liner,
ice forces, wind and wave action, abrasion and movement against
sharp-edged protrusions. Tear is encountered when a damaged
area, such as a small hole or rip, is subjected to tensile stress that
propagates the damage.
Reliance on the USEPA requirements for a 30 mil minimum
thickness is totally inadequate for protecting a liner from puncture
and tear. It is this author's considered opinion, derived in part
from field experience in replacing punctured and failed thin liners,
that a minimum thickness of at least 80 mils is necessary to sustain
the many predictable loadings that a liner can be expected to en-
counter.
The author also believes a lining system should be designed to
minimize the risk of puncture and tear. The converse design ap-
proach is to settle for the least permissible thickness to reduce
short-term costs, even though this approach often, and erroneous-
ly, assumes that incremental liner thicknesses will result in in-
cremental costs.
Two methods for increasing a synthetic liner's resistance to punc-
ture and tear are available to the design engineer: selecting a high-
strength material or increasing the thickness of a given liner. In
those cases where the design engineer must exercise extreme cau-
tion, usually because of the nature of the facility, it is prudent prac-
tice to opt for both alternatives to afford a factor of safety as high
as possible.
Puncture Tests
Schlegel Lining Technology has performed puncture and tear
resistance testing on various synthetic membrane lining materials
currently available on the market2 (Figures 1, 2 and 3). The purpose
of this testing was to determine the relationship between puncture
resistance and tear resistance vs HDPE liner thickness and to com-
pare the strength of various liner materials by measuring their
respective tear resistance values.
The test procedure used for the puncture resistance testing was
the Swiss Standard SIA 280/14. In this test, a steel bolt of specified
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dimensions and weight is allowed to fall onto a liner specimen. The
height is varied until the critical drop height is found; i.e., the
greatest height from which the steel bolt is dropped and causes no
liner puncture for five individual trials.
The tear resistance testing was conducted in accordance with the
German Standard DIN 53 515. In this test, a Graves angle test
specimen is subjected to tensile stress using a testing speed of 20
in./min; this relatively high testing speed allows for an accurate
simulation of rapid tearing as would be found in actual site condi-
tions.
There is a linear relationship between puncture resistance and
liner thickness and between tear resistance and liner thickness
(Figures 1 and 2). Figure 3 shows a comparison of tear resistance
and thickness for various synthetic membrane liners. This com-
parison shows how different materials afford different resistance to
tear, with HDPE essentially a magnitude of order above the next
closest lining material. These curves clearly illustrate that the design
engineer can opt for a high safety factor by specifying a thick liner
of the appropriate material.
There are many predictable forces with puncture and tear poten-
tial that the synthetic liner must withstand. These loads can be
delineated in the following areas:
Installation Procedures and Problems
Vehicular, equipment and pedestrian traffic on or about the
liner, particularly during installation, must be considered. Methods
for unrolling the liner and laying it out should be specified, in-
cluding the permissibility of traffic on the liner. Methods of field
seaming the liner and the allowable equipment and pedestrian
loading at that time must also be considered. Large, heavy seaming
equipment working on thin mil liners should generally not be al-
lowed.
I
[j
£
o
TESTING ACCORDING TO SIA 280/14
O
O «o
O
z
cc
TESTING ACCORDING TO DIN S3 515
LINER THICKNESS (mm)
Figure 2
Tear Resistance Testing
Tearing Force vs. Thickness for HDPE Liner
Ul „_
CC *°
n
TESTING ACCORDING TO DIN S3 515
40 50 50 70
LINER THICKNESS - MILS
LINER THICKNESS (mm)
Figure 1
Puncture Resistance Testing
Critical Drop Height vs. Thickness for HDPE Liner
Figure 3
Tear Resistance Testing
Tearing Force vs. Thickness for Various Synthetic Membrane Liners
Consideration must be made for other trades working on or
about the synthetic liner. Situations such as the construction of
contiguous roadways or the construction of pipe trestles or racks
above and across lined basins are factors in this category. Heavy
tools falling from a great distance or sparks from welding and cut-
ting equipment must be considered in the design. Liners that cannot
tolerate any and all of the anticipated loadings should be excluded
from the specifications.
Subgrade Conditions and Earth Covers
The subgrade must be properly prepared for the placement of a
synthetic membrane liner. The ability of the liner to tolerate the
puncture forces generated by stones, rocks, roots and other sharp-
edged protrusions in the underlying soil, when subjected to a load
from above or below, is a major consideration. The puncture
resistance of a liner is a direct measure of its ability to resist these
forces. With thin liners, a layer of sand or very well graded soil is
required; using a thicker lining, however, generally results in the
opportunity to use screened in situ materials for the liner sub-base,
resulting in a cost savings to the owner.
The placement of an earth cover on a synthetic membrane liner
following its installation serves to protect the liner from the move-
ment of heavy equipment or unplanned and unpredictable high
loads. The supply and placement of an earthen cover over a liner
requires careful and close inspection. The proper grades of material
are required and should be rigidly inspected prior to and during
placement. The specifications for the supply and placement of the
subgrade must also apply to the covering material. Sharp-edged ob-
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jects in the cover material can puncture a liner from above, as those
in the subgrade can puncture it from below. Any suspect areas
should be uncovered, inspected and repaired as necessary.
Underlying Soil Stability
Localized differential settling of the basin floor and side slopes
can exert forces on a synthetic liner. It can be expected that minor
amounts of differential settling and ground shifting (seismic activ-
ity) wil occur. Specifications should anticipate this event by calling
for: a tensile strength of the liner at yield of greater than 1500
lb/in.2, and an elongation of at least 10% before reaching the yield
point. By specifying these properties, certain inconsistencies in the
subgrade can be tolerated.
If there is even minor sloughing of the soil on the side slopes
under the liner, this earth movement could tear the liner as it
migrates down the slope behind the liner.
A major contributing factor to the movement of soil on a slope
behind a liner is excess moisture in the soil. This can be caused by:
an improperly graded top of berm which then allows moisture to
permeate through the anchor trench and berm area; overfilling of a
basin with inadequate overflow protection; or a tear in the liner on
the slope, allowing water to impinge directly on the earthen slope,
with head pressure forcing it quickly into the side slope.
Hail, Rainfall and Wind Loads
Weather conditions that produce violent thunderstorms,
hailstorms, or severe wind loads are serious considerations in the
selection of a liner. A severe thunderstorm, for example, could
puncture a thin liner and a hailstorm is even more likely to cause
damage. These types of storms must be coped with both during and
following installation. During the time that a liner is being in-
stalled, weather presents a more severe problem because generally a
broad area of the liner would be exposed to the storm. Following
commissioning of a basin, only the exposed liner berm area would
be susceptible to damage from storms.
High wind loads are an additional problem. All possible precau-
tions should be taken to protect the liner from wind damage during
installation. Planning the layout pattern of the liner and providing
for proper ballasting and protection during installation are impor-
tant procedures. Shut-down operations such as weekends and
holidays must be accommodated.
It should not be viewed as anachronistic that a specifier enter in-
to the scheduling and sequencing of operations. Establishment of a
well-planned course of action and strict adherence to it is prudent
during lining installation.
Following installation of a synthetic liner in the basin, wind can
pose further problems. If the basin is to be left empty for an ex-
tended period of time before plant startup, or if it will be drained
on a regular basis due to plant process operations, necessary
ballasting and protection against the wind are again required. A
strong wind blowing across an empty basin generates an uplift force
on a synthetic liner. Ways to design against this include proper
ballasting or providing vent holes at the top of the berms.
Ballast
Ballasting of a synthetic liner in a large basin is generally required
both during and after installation. Many means of ballasting are
available, including sand bagging, covering the entire floor with a
layer of water or soil, piling soil in strategic areas, placing rubber
tires filled with grout and placing concrete ballast blocks.
Considerable thought should be put into a proposal for a
ballasting operation. The possibility exists for the occurrence of an
adverse chemical reaction between a rubber tire and the consti-
tuents of a basin. In arid regions, a layer of water used as ballast in
the bottom of the basin is not possible. If a heavy soil cover is used
over the bottom of a basin and is not subsequently removed, it
lessens the working volume of the basin.
Thermal Exposure
Synthetic liners tolerate varying ranges of temperatures; newer
liner technologies in particular have generated liners capable of
tolerating temperatures as high as 190°F and as low as -74°F.
Fluid temperature within the basis is of prime importance but the
exposed liner on the berm of an impoundment experiences tremen-
dous sun loads and a corresponding rise in temperature. In many
areas of the country, such as the Southwest United States, this fac-
tor cannot be ignored. On some polymeric membrane liners,
sunlight acting in conjunction with ozone can cause shrinkage or
liner embrittlement.
The fluid temperatures within a basin can generally be predicted
or calculated during the initial design. Many times the term "am-
bient temperature" is used. Generally, and probably accurately,
this temperature can be expected to be less than 100°F, although in-
vestigations into the actual temperature of the contents of the basin
must be conducted and considered. Two key items for assessment
are: (1) the possibility of an exothermic chemical reaction occurring
within the basin, and (2) the concentration of salts in a basin that
might result in the formation of a crude solar pond.
An exothermic chemical reaction could cause the instantaneous
temperature to be greater than 150°F. This localized temperature
would be detrimental to many liners. Further, a slow build-up of
salts in a basin could contribute to the formation of a crude solar
pond. Temperatures in the bottom of a solar pond have been
known to approach 200 °F, a level that is far beyond the ability of
many liners to withstand.
It is difficult to design against these two problems. Unless strict
controls to prevent the dumping of unexpected and unplanned
chemicals are maintained within the plant or unless temperatures in
a pond are monitored on an intermittent basis, the possibility of
subjecting a synthetic membrane liner to a high localized
temperature exists. This unwanted event should be designed for by
selecting a liner material that will tolerate temperatures in ranges to
be reasonably expected.
Startup Procedures
Initial filling of a basin requires vigilance. Items such as splash
pads, diffusers and other means of alleviating water forces on the
liner during filling should be considered.
Proper design requires specifications for a puncture resistant lin-
ing able to withstand the anticipated forces of falling water, ap-
propriate design of the piping network and the inclusion of con-
crete or earth cover in strategic areas.
Subsequent Cleanout Operations
If the basin will be cleaned on a periodic basis, the forces to
which it will be subjected during these operations must be con-
sidered. A suction hose or submersible trash pump, small rubber-
tired equipment with a front end bucket or possibly a dredging
operation are all processes that could be used to clean the basin.
The impact of these processes upon the liner should be considered.
Ice
In northern climates, two forces can occur from the formation of
ice in a basin. The first is the lateral pressure exerted on the side
slopes of the basin when the entire surface freezes. The second oc-
curs in the springtime; large chunks of ice, broken off from the
main body, can be driven by wind and wave action into the slopes
creating localized point source forces on the liner. The location of
the basin with respect to wind direction and wind velocities must be
considered; prevailing winds, frequencies and maximum velocities
should be studied. The possibility of strategically siting a basin to
shelter it from wind forces as much as possible should be in-
vestigated.
The specification for the side slope gradient should be analyzed.
By employing a relatively "mild" slope, such as 3:1 (horizontal-
vertical) or greater, the lateral pressure of a solid ice cap on a basin
is eased due to the ability of the cap to "ride up" on the slopes and
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never impinge on the liner in a direction perpendicular to the slope.
This same phenomenon occurs with ice chunks driven or carried
into the liner during the spring breakup of the ice cap; the more
gradual the slope, the easier it is for the water to carry the ice up the
slope instead of directly into it.
A Final consideration in ice loading is a determination of the
tendency of the ice to adhere to the synthetic liner. If adherence is
possible it occurs more frequently with rough textured liners; this
process increases the adverse effect of the ice on the liner. If an ice
cap forms across the entire basin, portions of the ice cap around the
perimeter can actually "hang" on the liner and readily tear it when
spring breakup occurs.
Abrasion
Wind-blown sand can abrade the liner at the top of the berm
area. The dumping of bottom ash or fly ash slurried with water can
cause abrasion in the inlet areas of the basin or in areas where ex-
cessive wind and wave action occur. Few formal sources of abra-
sion resistance tabulations for liners have been generated; however,
various pipe manufacturers fabricate pipe made of the same
material as some synthetic liners (HDPE and PVC). Some pub-
lished data exists from these sources.
Process Uses of the Basin
Liquid level fluctuations, amount of agitation and mixing, heavy
equipment movement and wind and wave action must also be con-
sidered. The installation of floating aerators or submerged aeration
equipment or mixing via high velocity pumping or influent chan-
nels, are all factors that can cause uplift forces on the basin floor
and varying amounts of wind and wave action on the slopes.
The puncture resistance of the synthetic liner plus the soil stabil-
ity of the side slopes are the parameters of specification for these
applications.
Recreation Uses of the Basin
Recreational uses of a very large basin or water reservoir can pro-
duce forces on the liner that must be considered before its selection.
If the upstream face of a dam is lined with a synthetic membrane,
such forces as extreme wind and wave action, floating logs, debris
and ice all must be considered.
Economy of Volume
The term economy of volume describes how a change in gradient
on a side slope from a shallower one to a steeper one positively af-
fects the working volume of a basin in two ways: (1) if steeper
slopes are employed, the user realizes a much greater basin volume
for the same land area, and (2) if steeper slopes are used, the same
volume can be realized for a smaller land area as compared to
shallow slopes over a greater land area.
Clearly, if realizing economy of volume is desired, two elements
are necessary. The first is that the earthen subgrade be able to
maintain its stability at the desired slope; slopes steeper than 1.5:1
are generally not encountered. The second is that the synthetic
membrane liner be able to support its own weight and not elongate
when installed on a steep slope.
Vandalism and Wildlife
Vandalism at any facility is always possible; particularly suscepti-
ble areas would be the berm and top portions of a liner. The effects
of wildlife must also be considered; the penetration of animal
hooves, again primarily in the berm areas, is a definite possibility.
The prime method of preventing these problems includes proper
security and fencing. As a contingency measure, however, a liner
having a high puncture resistance can also be specified.
Burrowing Animals and Plant Penetration
Small rodents and burrowing animals sometimes use a liner as a
food source and are able to gnaw through it. Further, some types of
synthetic liners are susceptible to the penetration of roots and
plants. Linings containing plasticizers or other possible rodent food
sources should not be specified; rodent populations are difficult to
control, and rodents can gnaw through a liner in unexpected loca-
tions making it very difficult to isolate any leakage.
LINER CHEMICAL COMPATIBILITY
In addition to assessing and specifying physical properties re-
quired to meet the service needs of the facility, it is also absolutely
necessary to assess the chemical compatibility of a synthetic mem-
brane liner in order to specify an appropriate material. The com-
pilation of a complete list of chemical constituents and their con-
centrations that could come in contact with the synthetic membrane
liner is required. A design engineer must consider each of these con-
stituents on a case-by-case basis to determine the ability of a syn-
thetic liner to withstand the effects of the chemicals in contact with
it.
All the waste fluids that could contact the liner should be
categorized and characterized. Items that should be considered in
this characterization include fluid temperature, pH and concentra-
tion of organics. Initial liner selection or rejection can be made
from knowledge of the chemicals.
The problem of synergism of the various chemicals, however, is a
more complex one. Synergism involves many unknowns. Predict-
ing synergistic reactions requires a vast amount of knowledge; it is a
seemingly impossible task to predict any and all combinations of
chemicals that might contact the liner. A waste that one day might
have an innocuous effect on a liner could the next day, in conjunc-
tion with an additional chemical, have a disastrous effect on the
same liner. Clearly, the most efficient means of designing around
this problem is to select a lining that tolerates and withstands any
and all combinations of chemicals envisioned.
An effective and common procedure to determine the general
compatibility of a synthetic membrane liner is to consult a matrix.
Matrices showing the types of liner materials and a variety of in-
dustrial and hazardous wastes are easily obtained. By consulting a
matrix, one can quickly learn what families of chemicals or hazar-
dous wastes are detrimental to a given synthetic membrane liner.
The intent, of course, is to select a lining material that is compatible
with all families of chemicals and hazardous wastes that it can be
expected to encounter during its life.
A more specific measure for determining the chemical com-
patibility of a synthetic membrane liner is an immersion test. In this
test, a sample of the synthetic membrane liner is immersed in the
anticipated waste (one side immersion only per USEPA Method
9090) in the concentrations that can be expected. Certain physical
parameters of the liner material are then monitored and recorded as
the test proceeds. The key parameter monitored during the test is
the weight change of the sample. Values that are generally deter-
mined following the planned time of soaking are weight gain, ten-
sile strength at yield and break and elongation at yield and break.
During the test, an indication of a gain in weight by the sample
means the synthetic liner is absorbing the chemical with which it is
in contact; generally, the elongation properties of a synthetic liner
are adversely affected when a severe weight gain occurs. If a weight
loss occurs, it is an indication that the chemicals in contact with the
liner are dissolving it; in this case, it can be expected that there will
be a definite drop in the tensile strength both at break and at yield
and elongation both at yield and at break.
Schlegel Lining Technology has developed its own 28-day immer-
sion test, run at 158 °F and employing total immersion of the sam-
ple. The purpose of this is to accelerate the results that would be ex-
perienced during a test run at ambient temperature on only one side
of the liner. The maximum allowable weight gain or loss, and the
maximum allowable drop or increase in tensile properties, have
been standardized by Schlegel Lining Technology for in-house use.
If a given chemical waste affects the lining material adversely at
this elevated temperature, however, it is rejected from considera-
tion as a lining material, even though anticipated exposure might be
only to an ambient temperature waste. Selected examples of such
chemical compatibility testing are as follows:
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Example 1
Test: 28 days, 158°F
Liquid Sample: Oily Waste Water Containing High Amounts of
Sulfates and Chlorides
Liner Material
HOPE
CSPE
PVC
CPE
% Weight Change
Chloride Solution Sulfate Solution
0.12 + 0.90
20.2 + 19.3
1.46
17.1
15.8
22.5
Example 2
Test: 28 days, 158 °F
Liquid Sample: Aqueous Brine Solution
Liner
Material
CSPE
HOPE
Example 3
Test: 28 days,
Liquid Sample
Liner
Material
CSPE
% Weight
Change
+ 2.58
(Not stabilized
after 28 days)
+ 0.08
°7o Change in
Tensile B
+ 39.1
1.87
% Change in
Elongation B
- 30.8
HOPE
Example 4
Test: 28 days,
Liquid Sample
Liner
Material
PVC
194 °F
: 20% Aqueous Phosphoric Acid Solution
% Weight % Change in % Change in
Change Tensile B Elongation B
+ 8.83 + 102 - 26.4
(Not stabilized
after 28 days)
+ 0.14 - 0.78
0
158°F
: Sodium Cyanide Leachate Solution
HDPE
Example 5
Test: 28 days,
Liquid Sample
Liner
Material
XR-5
HDPE
% Weight
Change
+ 7.46
(Not stabilized
After 28 days)
+ 0.13
% Change in
Tensile B
- 11.3
1.30
% Change in
Elongation B
- 5.65
158°F
Mostly water, containing heavy metals, organic
solvents, organic acids, alcohols and aldehydes
% Weight % Change in % Change in
Change Tensile B Elongation B
+ 2.73 + 31.9 + 8.57
+ 0.29 + 0.11 0
These examples clearly illustrate the effects of different
chemicals at elevated temperatures on various synthetic liners
available on the market.
LINER SEAMING METHODS
How a liner is seamed, whether in the factory or the field, is
critical to a system's performance. Although this author is unaware
of any published study ranking lining system failure mechanisms,
common sense and knowledge of the propensity for human error
suggest that seam failures are very likely a leading cause of lining
system failure. Specifications for a seam should state not only a
joining technique, but also a quantification of seam strength,
which is a function of the base material's strength and a quality
control program for testing seams.
There are eight methods for joining seams:
(1) Adhesive seams are joined with a chemical adhesive system
that bonds together two separate membrane surfaces. The chemical
adhesive system is an additional element to the seam system and,
thus, must meet all the criteria of the application such as chemical
resistance, temperature extremes, etc. Generally, when using
adhesives, a two-component system is employed. This requires care
in mixing. When the adhesive is applied, the residence time before
bonding is critical as well as the pressure applied and timing of
pressure. These variables may be difficult to control in the field.
(2) With a bodied solvent seam, lining material is dissolved in a
solvent which softens and bonds the liner surfaces together. This
method is essentially an adhesive system made up from the parent
material. Problems of application timing and pressure, as men-
tioned for adhesive seams, do exist, and the amount of solvent used
is critical. Again, field application requires care.
(3) Dielectric seams are made when a high frequency dielectric
current is used to melt the surfaces of a membrane material so that
the surfaces can be homogeneously bonded together under
pressure. This process is used most often to fabricate factory
seams, because the use of high frequency current is more difficult
in the field. The timing and the amount of pressure is critical.
(4) For extrusion welded seams, a bond is obtained between two
flexible membranes by extruding a molten ribbon of the parent
material between overlapped liner pieces, followed by applied
pressure. This is a relatively straight-forward task in the field.
(5) Solvent seams use solvents to soften the surfaces to be bond-
ed; generally, pressure is then applied to the seam. Under field con-
ditions, the application of the solvent and timing and pressure can
be a difficult task.
(6) A chemically adhesive tape may be used to bond liner surfaces
together. This tape system adds an additional element to the seam
system that must be assessed for the application. Taped seams are
not commonly made in the field and have all the hazards associated
with adhesive seams.
(7) To make thermal seams, high temperature air or gas is applied
between the two surfaces to be bonded until the membrane surfaces
melt, at which time pressure is applied to create a homogeneous
bond between the two surfaces. Timing and pressure must be
carefully controlled.
(7) Vulcanized seams are formed when the areas to be bonded are
unvulcanized materials that are cured together with heat and
pressure. This method is applicable only for thermoset materials.
A lining system owner or operator may plan to install such a
system in several stages or may wish to have the option of enlarging
his facility at some future time. This not infrequent situation will
affect the selection of a material, because some liners do not have
the capability of joining new materials to old. A liner that
undergoes complete vulcanization after exposure to the sun, for ex-
ample, cannot be amended. On the other hand, there are liners to
which new materials can be seamed at any time.
LINER SERVICE AGREEMENTS
AND COST PROJECTIONS
When one or more lining materials have been selected as the
material(s) that the specifier is confident will withstand the broad
range of physical and chemical attack envisioned during the life of
the basin, the service life and concomitant long term costs must be
determined to complete the liner selection process. Both the liner
service agreement (warranty) and long term costs enter into this
cost selection phase.
Liner Service Agreements
A synthetic liner must be able to withstand severe physical stress-
ing and chemical attack. Even the most intelligent specifier,
however, might overlook some design details or future intended use
and service work may be necessary.
A well written, detailed warranty statement is an advantage to
both the customer and the membrane liner supplier and installer.
By delineating all parameters at the outset, the customer knows
what he can expect in terms of repairs and the supplier knows what
agreements he must uphold. Vague warranties with bland promises
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must be scrutinized closely and rejected by the customer where ap-
propriate.
Key items to be included in a service agreement include: length of
time it is in force, hazards covered and not covered, breadth of the
statement (liners can fail from a wide range of factors), expediency
of repair and cost. Some warranties contain a section that could be
termed a "full warranty" and a section that could be termed a "pro
rata warranty."
Generally, the full warranty protects the customer completely for
a specified time, as long as the customer is not guilty of negligence
or misuse. However, it would be wise to define exactly what is in-
cluded in the so-called "full warranty"; the technical specifications
must closely define all wastes, temperature, concentrations,
volumes and frequencies that are to be expected. Many warranty
statements include the terminology "customery use" or "use for
which it was intended." If the job specifications closely define these
normal or intended uses, the customer is protected. Failure to
define and categorize could create a loophole for an unethical sup-
plier.
Pro rata warranties are a current phenomenon in service agree-
ments. In essence, both the supplier and customer pay for repairs,
in proportion to the length of time a lined basin has been in service.
On the surface, it is a reasonable arrangement where, in effect, the
supplier/installer is rewarded for properly installing the synthetic
membrane liner and providing first-class workmanship.
Failure to define the intended purpose of the basin and its consti-
tuents, however, could again allow an unethical company to shirk
its responsibility and fail to bear its share for repair of the damage.
In the preceding discussion the terms "manufacturer" and "in-
staller" have been used interchangeably. Very often, however, the
liner manufacturer simply sells his product to a liner installer (fre-
quently an excavation company that actually dug the basin), who in
turn marks up the price and installs the liner. A subsequent liner
failure results in a disagreement over repair responsibility.
The customer calls to report a failure of the liner, and invariably
the first party it is reported to implicates the second party involved;
the liner is not repaired (or it requires an exorbitant time period to
replace it) and legal battles ensue. This causes nothing but delays,
frustration and expense for the customer who is left with the battle
of fighting the regulatory authority in charge of protecting the en-
vironment. The customer pays for the inabilities of others.
A specifier should insist that the entire lining package be pro-
vided and installed by a single, responsible, stable business entity.
Then, if a failure occurs, a single party is responsible for liner
repairs, whether related to manufacturing problems or installation
deficiencies. The customer benefits with more control over the
situation and a greater likelihood of repairs being made in a timely,
low or no cost manner. If the financial integrity of the manufac-
turer/installer is questionable, it is certainly in order to require
100% Performance and Payment Bond, for as long a period as
practicable. Any company incapable of providing the necessary
bonding and financial security should be immediately eliminated
from consideration. A customer must be assured of having repairs
made on an equitable and timely basis.
Liner Cost Projections
Long term cost projections are difficult to make but are a
necessary task in attempting to assess the efficacy of a lining
system. The initial reaction of a customer is generally to accept the
lowest cost bid. Unfortunately, this myopic viewpoint totally ig-
nores long term security. Opting for thin mil liners, installed by
under-capitalized installers, is not a cost efficient means of pro-
viding a secure impoundment for long term service.
Leaks occurring in a lined basin can be costly and require a great
deal of time and effort to repair. Costs that occur in repairing a
liner can include: pumping, demucking, sludge disposal (including
permits), loss of revenue from normal basin uses, fines to
regulatory agencies for failure to protect the environment and costs
of cleanup operations. Clearly, these costs can be expensive for one
leak in a liner. Adding these repair costs to the initial low cost in-
stallation can quickly drive the cumulative cost far in excess of the
initial installation cost for a thicker liner capable of withstanding
the forces a synthetic membrane liner experiences during operation.
LINER QUALITY ASSURANCE PROGRAM
Although a complete discussion of this subject is beyond the
scope of this paper, certain highlights of any Quality Assurance
(QA) program should be noted.
A raw material supplier should be required to provide and certify
all the technical aspects of his product. Upon receipt of the raw
material by the membrane manufacturer, these parameters should
be rechecked in the manufacturer's facility before production
begins.
During membrane liner production, QA should be monitored
closely to ensure that the liner meets all specifications required.
Tolerance ranges should be established, clearly defined and
adhered to. Lining material not meeting the specifications must be
scrapped.
The lining installation itself requires exacting QA standards. No
liner, regardless of its production QA, is useful until it is seamed
and installed properly. Again, standards of proper temperature for
joining, proper weather for joining and the use of skilled tech-
nicians to properly join and test the panels must be established and
maintained.
Adherence to each of these stages of QA will result in an integral
lining system capable of containing the hazardous wastes for which
it was designed.
CONCLUSIONS
Synthetic liners are subjected to a broad spectrum of mechanical
and chemical attack during their service lives. Some of these factors
can be predicted during the design phase of the specifier; others
are difficult or impossible to predict or envision. Therefore, the
specifier should select a synthetic liner of at least 80 mil thickness
that exhibits a wide range of chemical compatibility.
REFERENCES
1. USEPA, Office of Solid Waste and Emergency Response, "Lining of
Waste Impoundment and Disposal Facilities", p. 2, SW-870, Revised
Edition, Washington, D.C., Mar. 1983.
2. Etter, D., "Puncture Resistance and Tear Resistance of Plastic Liners",
Schlegel Engineering GmbH, Hamburg, West Germany, 1979.
3. Clarke, R.T., Jr., "Uses For Synthetic Membrane Liners In Retarding
The Movement of Contaminated Groundwater From Hazardous Waste
Sites", Schlegel Lining Technology, Inc., The Woodlands, Texas, 1983.
4. "USEPA, Hazardous Waste Management System; Standards Ap-
plicable To Owners and Operators of Hazardous Waste Treatment,
Storage and Disposal Facilities; and EPA Administered Permit Pro-
grams", Federal Register. 47, July 26, 1982, 32274-32388.
5. VanderVoort, J., "The Containment of Hazardous and Chemical
Wastes By The Use of Polymeric Flexible Membrane Liners", Schlegel
Lining Technology, Inc., The Woodlands, Texas, 1981.
6. VanderVoort, J., "Comprehensive Quality Control in the Geomem-
brane Industry", Schlegel Lining Technology, Inc., The Woodlands,
Texas, 1983.
190
BARRIERS
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THE "ENVIROWALL CUT-OFF" VERTICAL BARRIER
SALVATORE V. ARLOTTA, JR.
Wehran Engineering Corporation
Middletown, New York
INTRODUCTION
The migration of polluted groundwater or leachate from con-
taminated sites or waste disposal areas, especially abandoned sites,
is an environmental problem of national proportions. A new and
unique concept called the "Envirowall Cut-Off" has been devel-
oped to construct a vertical, impermeable barrier to prevent this
migration.
"Envirowall Cut-Off" is a hybrid cut-off wall. It is constructed
with high density polyethylene (HDPE) and sand backfill and is
installed by using the slurry trench construction method. Once in-
stalled, a very low permeability, composite, vertical barrier is es-
tablished with several unique engineering properties.
The overall concept and construction methodology was demon-
strated during a full scale construction test at a sanitary landfill in
New Brunswick, New Jersey during the Fall of 1982. The test was
planned to demonstrate the feasibility of the techniques and ma-
terials used to construct the Envirowall Cut-Off under generally
difficult (by design) conditions. The test also demonstrated the
major advantages of the Envirowall Cut-Off over other types of
cut-off wall construction.
WALL CONSTRUCTION
The Envirowall Cut-Off essentially functions as a cut-off wall
with redundant features for controlling horizontal seepage. One
hundred mil HDPE sheet is used to form an envelope which lines
the walls of an excavated trench. The bentonite slurry used during
construction keeps the trench stable for placement of the HDPE
sheet and sand backfill and also forms a filter cake on the walls of
the trench. This filter cake further decreases the permeability of
the composite in-place barrier. The sand backfill, besides serving as
ballast, provides an internal, porous medium for monitoring seep-
age and, if necessary, withdrawal of intruding pollutants.
MIGRATION PREVENTION
The prevention of groundwater contamination by the seepage of
pollutants is often the major focus of the engineering effort for
remedial measures at a chemically contaminated site. Many var-
iables enter into the picture. Some of these variables are:
•Quality and direction of the groundwater flow
•Characteristics of the waste
•Hydrogeological characteristics of the site and adjacent areas
•Human health risks involved
When the site is a landfill, the prevention of subsurface migra-
tion of leachate from the site is usually the goal in order to pre-
vent environmental degradation. A thorough study of the geology,
groundwater regime and soil conditions is required to select the best
method of preventing subsurface seepage of pollutants or migra-
tion of leachate. If leachate enters the groundwater, the polluted
groundwater will migrate, following the hydraulic gradient of the
water table.
To prevent leachate from moving laterally via the groundwater,
an impermeable barrier or cut-off wall must be constructed per-
pendicular to the groundwater hydraulic gradient. Depending on
site stratigraphy, cut-off walls are often keyed into an underlying
soil stratum of low permeability to effectively seal off the sub-
surface horizontal migration of contaminants. This is often done at
landfill sites or hazardous waste disposal sites as a remedial meas-
ure.
LEACHATE GENERATION
Typically, a certain percentage of precipitation which falls on a
landfill eventually ends up percolating through the waste, which is
often buried, to form leachate. Any contaminants which are picked
up in the leachate through contact with waste will be transported
with the leachate.
Some landfill sites contain hazardous toxic compounds which
can be leached out of the waste and eventually contaminate the
groundwater. Two types of leachate are involved:
•Flowable constituents of the waste
•The flowables generated from infiltration or percolation as men-
tioned above
These are usually referred to as primary and secondary leach-
ate, respectively. The majority of industrial hazardous wastes are
produced as liquids and, therefore, can easily become primary
leachates. Both the solute and solvent phases of leachate can affect
the permeability of the natural ground, of liners or of cut-offs.
Wastes can be classified either by source (i.e., municipal refuse,
industrial and chemical process waste, dredge spoil, etc.) or by
physical class (i.e., organic, aqueous-inorganic, aqueous-organic,
etc.). Physical classification is more useful when assessing likely
effects on liners or cut-offs. Organic fluids associated with indus-
trial wastes which are often placed in a disposal facility cover a
spectrum of types.
WASTE CONTAINMENT STRUCTURAL FAILURES
Recent research has indicated possible concerns for soil struc-
tures, such as clay dikes, cut-offs and liners, which are used for
containment of wastes. Failure mechanisms fall into four major
categories:
BARRIERS
191
-------
r~
emutiD SUKFACC
FILL
-AND-
REFUSE
_ MEADOW
MATERIAL'S
Figure 1
Excavated Trench before Placement of the Liner
GROUND 51/«/MC£
SLURRY
(BENTONITE)
• HOPE LINED
- WATER AND SAND FILL
Figure 2
Cross-Section of the Trench with Liner
1. Dissolution
2. Syneresis
3. Piping
4. Desiccation
It is important to evaluate the materials for containment in
relation to the wastes. Generally strong acids, strong bases, salts
and highly ionic wastes are aggressive toward soils.
ENVIROWALL ADVANTAGES
The Envirowall Cut-Off has several advantageous features when
used as a vertical barrier to form a cut-off wall. The Envirowall
Cut-Off, when used for environmental control, combines some of
the ideas of clay and of a soil bentonite cut-off wall and adds the
capability for monitoring performance and withdrawal of contam-
inants from within the cut-off wall. The HDPE envelope pro-
vides a stable, low permeability (10~12 cm/sec) membrane and,
when installed in the trench, provides improved resistance to perm-
eation and low overall permeability for the Envirowall Cut-Off
system.
Construction
The slurry trench construction method allows installation of the
Envirowall Cut-Off in areas with difficult site conditions and to
relatively deep elevations. The bentonite slurry used in the con-
struction maintains the stability of the trench during the installa-
tion of the Envirowall Cut-Off HDPE envelope. The slurry also
develops a filter cake on the walls of the trench, which provides an
additional low permeability bentonite and soil layer.
The Envirowall Cut-Off is constructed in a similar manner as the
soil bentonite cut-off wall. A narrow trench is excavated and filled
with bentonite slurry to stabilize the trench walls during construc-
tion. The HDPE envelope is fabricated above ground to fit the
dimensions of the trench. Sheets are cut and seamed to form a U-
shaped envelope and set with ballast weight to provide an initial
submergence into the trench. The envelope is lifted and set in the
trench. Water and sand are pumped into the envelope to develop
negative buoyancy and to form the HDPE to the shape of the
trench (Figures 1 and 2).
Monitoring
The sand also provides a medium for placing a system of mon-
itoring or withdrawal wells within the cut-off wall envelope. Sand
backfill is an important component of the Envirowall Cut-Off.
Water quality within the wall can be monitored through the sand
on a long-term basis. If leakage is ever noted by detection of con-
tamination in a monitoring well, the porous sand medium can be
pumped to evacuate and control the contaminated water and pre-
vent further migration beyond the Envirowall Cut-Off.
The sand is graded to provide a high permeability medium with-
in the envelope, ideally with a higher permeability than the sur-
rounding soil in which the cut-off wall is excavated. Small diameter
piezometers or monitoring wells are placed in the sand backfill.
Piezometric head can be routinely observed and water quality
samples extracted for testing.
When piezometers are installed within the homogenous sand
medium contained in the envelope, continuous monitoring of
piezometric head would indicate the condition of the liner. This
would require that the water level within the envelope be adjusted
initially to an elevation below that of the site. In this way, a net
positive head into the Envirowall Cut-Off is established (Figure 3).
100 Ull_ SCHLESEL
HOPE SHEET
— MONITORING WELL
EXISTING
/— WOUND sunrtct
SOIL PERMEATED 73*
WITH BENTONITE^ j
BENTONITE FILTER CAKE
WATER LEVEL AT SITt
WATER LEVEL INSIDE OF
ENVELOP HONITOREO
CLAY LAYER <*->.
KOMOCK »
PIEZOMETER IN SAND
N T.S.
Figure 3
Piezometer in Sand
N.T.S.
192
BARRIERS
-------
If leakage of the HDPE membrane were detected, the gradient
would be into the envelope and a rise in piezometric head would
occur, providing a simple indicator of membrane integrity.
Water quality monitoring could also be undertaken to determine
the type and characteristics of any substances entering the en-
velope. If the envelope were damaged such that a high rate of
leakage occurred, the high permeability sand medium could also
be pumped. A series of withdrawal wells or well points, likewise
within the sand, could be used to extract any contaminated liquid
entering and maintain a net gradient into the liner. This provides
a redundant safety feature beyond the initial establishment of a
low permeability barrier (Figure 4).
- WITHDRAWAL WELLS
Figure 4
Withdrawal Well Operation
N.T.S.
Effluent Removal
In the case where the waste is very aggressive toward the ben-
tonite filter cake and HDPE such that the integrity of the mem-
brane is reduced considerably, the sand medium with withdrawal
wells or well points simulates a control structure for dewatering.
This is especially beneficial where existing soil conditions at the
site are not conducive for establishing an efficient pumping sys-
tem for withdrawal. Collected effluent would then be discharged
for treatment. The effectiveness will depend on the spacing of
the wells within the sand.
Where conditions are such that the sand and withdrawal wells
are being used to control seepage from a site, the Envirowall Cut-
Off will approximate a fully penetrating slot drain or line sink,
and a solution for drawdown can be obtained using equations
based on this type of drainage concept.
Assuming equilibrium conditions under unconfined flow from a
line source and with a vertical slot penetrating a homogeneous
isotropic stratum and bounded at the base by a horizontal imper-
vious stratum, and further assuming the Dupuit-Forchheimer con-
ditions apply to the hydraulic gradient, then the flow through a
vertical element to the sink can be described by Darcy's Law:
Q = kiA
, . dh
and: i ='—; A = hx
dy
substituting given: Q = khx —
dy
(1)
(2)
(3)
which describes the basic relationship for drawdown and flow. The
flow (Q) would be equal to the withdrawal rate within the Enviro-
wall Cut-Off (Figure 5).
FULL SCALE TEST
A full scale construction test project of the Envirowall Cut-Off
was performed at an existing sanitary landfill in New Jersey in the
fall of 1982 to demonstrate the overall construction procedure for
ORIGINAL
GROUND
WATER LEVEL
IMPERVIOUS BASE
Figure 5
Idealized Flow from a Line Source to a Fully Penetrating Slot
fabricating the HDPE envelope and placing it into a trench filled
with slurry by backfilling with sand. The project was conducted
in three phases:
1. The excavation of a triangular-shaped trench filled with the
bentonite slurry mixture through the landfill waste
2. The cutting and seaming of HDPE material to form an envelope
with the prescribed geometry
3. The placement of this HDPE envelope in the trench and sub-
sequent backfilling with sand and water
The high density polyethylene (HDPE) envelope was fabricated
by Schlegel Lining Technology, Inc. and later submerged by ICOS
Corporation of America into a trench excavated to a triangular-
shaped plan. This full scale test introduced several potential ad-
vantages of the Envirowall Cut-Off over other types of cut-off
walls and demonstrated the techniques and materials which could
be used in the construction of Envirowall Cut-Off under realistic
conditions.
Indeed, the test site was an inactive portion of a working land-
fill. The trench was excavated approximately 22 ft, passing through
approximately 10 ft of previously deposited solid waste and ex-
tending down into the underlying foundation of meadow mat
(organic peat) which generally occupied the landfill site.
The trench was excavated by a backhoe in triangular plan creat-
ing sharp corners to check the workability of the 100 mil HDPE
membrane to accommodate very angular corners. Each side of the
trench was excavated a distance of 51 ft. The triangular configura-
tion used in the test project presented an example of extreme hand-
ling conditions and provided a good idea of the problems pre-
sented in this new type of construction. The entire envelope was
prefabricated from 33 ft wide rolls of HDPE above ground to
conform to the triangular-shaped plan (Figure 6).
Various shapes and sizes were cut and seamed for the one piece
envelope using the Schlegel extrusion welder. Two corners of the
envelope were preconstructed using a corner jig. The third corner
of the triangle was a closure system which consisted of two inter-
locking HDPE pipes. Experience indicated that it was beneficial
to perform as much of the fabrication as close to the trench as
possible to minimize excessive movement of the liner. This re-
duced the potential for abrasion and handling damage.
The trench was filled with sodium montmorillinite bentonite
slurry having a viscosity of approximately 40 sec by Marsh Fun-
nel. The slurry stabilized the walls of the trench until the prefab-
ricated HDPE envelope was ready to be placed.
A 3 ft diameter HDPE pipe and a 0.5 ft diameter HDPE pipe
were welded on each of the two outer edges of the envelope. These
two pipes were used to form an interlocking joint at the third
corner of the triangle. The 3 ft diameter pipe was slotted as the
envelope was submerged into the trench on the last triangular leg.
This pipe joint would later be bonded by pressure grouting.
BARRIERS
193
-------
SAND AND WATER FILL
SIDE A « 51 FT.
SIDE 8 » 72 FT.
SIDE C * 51 FT.
Figure 6
Plan View of the HOPE Liner in Place
N.T.S.
A crane was used to move the 100 mil HDPE into position for
seaming and fabrication. Continuous support was provided for the
envelope with lifting bars and battens to keep it from bending and
wrinkling.
The entire fabrication process required several days for this first
installation. As fabrication of the envelope neared completion and
was made ready for installation, the trench was checked and
cleaned of any debris which might have inhibited the installa-
tion. A clam shell was used to remove any objects that might be
protruding from the walls or collecting at the bottom of the trench.
Cranes were again used for the lift of the liner into the trench.
Using the spreader bars to lift each envelope side and keeping
them straight, the cranes worked together to set the membrane en-
velope in place above the trench. The side with the 3 ft pipe at-
tached was lowered into the trench first; water was pumped into the
envelope so that this initial side was lowered sufficiently to allow a
front-end loader to begin filling with sand. An overflow trench was
prepared in one corner of the trench to handle the slurry that was
displaced as the envelope was submerged. The pipe joint was then
made by sleeving the 0.5 ft diameter pipe into the 3 ft diameter
pipe, making the envelope continuous.
Sand continued to be dumped into the envelope at a rapid pace
until it was completely submerged. The membrane expanded well
to conform to the shape of the trench. The test program was term-
inated at this point. However, at a remedial site, monitoring wells
and piezometers would be installed in addition to pressure grout-
ing the sleeved pipe joint. Also, the excess membrane above grade
would be welded to completely enclose the sand medium within
the envelope, thereby protecting it from the weather or accidental
contamination from above grade. If a site is scheduled to be capped
with an HDPE membrane, the butting outside edges of the capping
membrane and the top of the envelope can be jointed by welding to
complete the enclosure of the site.
The test project made the Envirowall Cut-Off concept a reality
and demonstrated the feasibility of installing a composite cut-off
wall at a landfill site.
194
BARRIERS
-------
SPENT ACID AND PLATING WASTE
SURFACE IMPOUNDMENT CLOSURE
FRANK D. HALE
O'Brien & Gere Engineers, Inc.
Syracuse, New York
CORNELIUS B. MURPHY, JR., Ph.D.
OBG Technical Services, Inc.
Syracuse, New York
ROYDEN S. PARRATT
Renshaw Bay Corporation
E. Syracuse, New York
BACKGROUND
Since 1958, a surface impoundment had been used as a
depository for process wastes from a steel rod and wire manufac-
turing company. A plan view, shown in Figure 1, illustrates the
cellular arrangement of the impoundment constructed using ex-
isting alluvial clay soils. The surface impoundment was expanded
as the manufacturing facility grew; as a cell was filled with
wastewater, a higher dike was constructed encompassing a larger
surface area. The total volume of the impoundment in 1983 was
estimated at 33,000,000 gal, with a surface area of 13.4 acres.
An Industrial Waste Survey conducted in 1981-82 indicated that
alkaline cleaners, hydrochloric acid, zinc plating solutions,
chromate conversion coating solutions and wastewater from the
pickling line were discharged to the impoundment. The principal
contributor was the pickling operation where waste pickle liquor
and caustic rinses were generated. The liquid impoundment was
analyzed (Table 1).
PROPERTY UNE-»(
PROPERTY LINE -
A treatment facility which would eliminate the need for the sur-
face impoundment was being designed in 1982. These facilities were
expected to be operational by the fourth quarter of 1983. Conse-
quently in Nov. 1982, consideration was given to closing the surface
impoundment. In addition, the water level was rising to a point
where continued discharges to the impoundment was not prudent.
Table 1
Concentrations of Various Chemicals in the Impoundment
Chemical
Arsenic
Barium
Cadmium
Calcium
Chloride
Chromium (hex)
Chromium (total)
Cyanide (free)
Cyanide (total)
Floride
Iron
Lead
Magnesium
Concen-
tration
(mg/1)
0.024
0.5
0.058
435
1729
0.005
2.57
0.01
0.05
46.7
1933
0.4
75
Chemical
Mercury
Nitrate (as N)
Nickel
Orthophosphate
pH
Potassium
Selenium
Silicon
Silver
Sodium
Sulfate
Suspended Solids
Zinc
Concen-
tration
(mg/1)
0.0004
1.0
1.75
0.7
1.75 unit
81.6
0.002
94
0.05
596
6150
41
191
Figure 1
Surface Impoundment Site Plan
As the recipient of listed hazardous wastes, namely "spent pickle
liquor from steel finishing operations," the surface impoundment
was regulated as a Treatment, Storage or Disposal Facility under
the Resource Conservation and Recovery Act of 1976. Data col-
lected during the Industrial Waste Survey indicated that corrosivity
was the only characteristic of either the sediments or the overlying
water which would qualify as hazardous per RCRA criteria. The
concentrations of lead and chrome in the acidic impoundment
water were less than the USEPA's EP Toxicity Limit of 5 mg/1 as
was the EP extract from impoundment sediments.
As the impoundment did receive the "listed" hazardous waste
"KO6, spent pickle liquor from steel finishing operations," the
contents and contaminated soil was regulated as a hazardous waste
until "delisted" pursuant to 40 CFR 260.20 and 40 CFR 260.22.
Consequently the handling of the liquid contents and contaminated
soils was dictated by RCRA. Projected delays in the approval of
TREATMENT
195
-------
the "delisting" petition resulted in the submittal of a Closure Plan
which assumed the materials were hazardous wastes.
The first step in the closure of the site required the removal of the
free liquid in the impoundment. Given the specific conditions, the
most attractive discharge point was the available sanitary sewer
system. The advantages included dilution of the high total dis-
solved solids, minimal permitting requirements and ready access to
a suitable sewer. Discharge to the sanitary sewers required com-
pliance with the sewer use ordinance (Tabale 2).
Table 2
Sewer Use Ordinance Discharge Limits
100
Chemical
PH
Boron
Cadmium
Chromium (hex)
Chromium (tri)
Iron
Nickel
Lead
Zinc
Discharge Limit
6-9 units
1
2
2
10
15
3
0.1
2
Based on the comprehensive sampling and analysis, it was deter-
mined that iron, sulfates, chlorides and zinc were the principal
ionic components. In addition, the average concentrations of 0.4
mg/1, 191 mg Zn/1 and 1933 mg Fe/1 were in excess of the cor-
responding limits for discharge to the sewer. The existing pH of less
than 2 also was not suitable for discharge to sanitary sewers.
An evaluation of alternatives for the removal of the metals of
concern by physical/chemical process, disposal of sludge and
subsequent closure of the surface impoundment was initiated. The
criteria used to evaluate these alternatives included compatibility
with program objectives, technical feasibility, ease of implementa-
tion, potential for regulatory agency acceptance and estimated
costs.
TREATMENT TECHNOLOGY
Various treatment methods such as chemical precipitation, ion
exchange, electrochemical oxidation and reverse osmosis are
available for the removal of chemical constituents from
wastewaters.' Initial screening indicated that chemical precipitation
was the most attractive approach. Neutralization of the highly
acidic wastewater in the impoundment could be accomplished with
hydrated lime (CafOH)^, sodium carbonate (Na2CO3), limestone
(CaCo3) or sodium hydroxide (NaOH).
Zinc and lead have minimum solubilities (Figure 2) with respect
to the hydroxides at a pH of 9 to 10.' At these hydrogen ion con-
centrations, the iron content would also be within sewer use limita-
tions. Combined neutralization of the 33,000,000 gal in the im-
poundment and subsequent precipitation of the metals at a pH of
approximately 9 therefore, appeared to be the most technically and
economically feasible alternative.
Preliminary tests conducted by the manufacturer indicated that
agricultural limestone could increase the impoundment pH only to
5, even at limestone dosages as high as 23 g/1. As much as 5 g/1
hydrated lime was required to further raise the pH to 9. Hydrated
lime alone could neutralize the raw water to pH 9 at a dosage of ap-
proximately 10 g/1.
It was apparent that the chemical make-up of the liquid in the
impoundment was such that a number of physical/chemical reac-
tions were involved. An extensive laboratory investigation to arrive
at optimum combination and dosages of chemicals would have
been time consuming and costly and would have defeated the pur-
pose of minimizing total costs. Hence, a more rational approach
i.o
o.i
0.01
0.001
0.0001
Figure 2
Solubilities of Metal Hydroxides as a Function of pH
from USEPA 440/1-82/091-b
was followed. This consisted of the simulation of chemical treat-
ment using a chemical equilibrium program and verification of the
computer simulated results with bench scale tests.
COMPUTER SIMULATION
An aqueous chemical equilibrium model, MINEQL, developed
by Westall, et a/.2 and modified at Syracuse University, was used to
evaluate treatment chemicals and operating pH. MINEQL solves
for the concentration of various soluble and precipitated chemical
species from mass action and mass balance expressions by the
Newton-Ralphson interactive technique. The effects of ionic
strength and temperature on the thermodynamic equilibrium con-
stants are incorporated in the computation. A detailed description
of the computer algorithm is given by Westall, et al.1 The input to
the model includes temperature and the total concentration of ca-
tions and anions.
Four combinations of chemicals: (1) hydrated lime, (2) calcium
carbonate and hydrated lime, (3) caustic and (4) calcium carbonate
and caustic were simulated. Two general conditions were
evaluated, an open condition and a closed condition. The open
condition simulates a system at equilibrium with the atmosphere,
whereas a closed system does not interact with the atmosphere. The
predicted pH values from the computer simulation for the open
and closed system are presented in Tables 3 and 4.
The results of CaCo3 computations confirmed preliminary find-
ings that CaCo3 would not increase the pH above 5.3-5.9 in a
1%
TREATMENT
-------
Table 3
pH from Computer Simulations of Titrations for
System Open to Atmosphere
(1)
CaC03
Dose pH
9/1
0 1.8
2 2.1
6 2.5
8 7.5
10
(2)
Ca(OH),
Dose pH
9/1
0 1.8
2 2.1
6 7.5
8 7.5
(3)
8 g/1 CaC03;
and Ca(OH).
Dose pH
9/1
0 7.5
2 7.5
6 7.5
(4)
NaOH
Dose
9/1
0
1
3
4
5
6
7
pH
1.8
2.1
2. 1
2.2
2.4
3.0
8.0
8.9
'(5)
8 g/1 CaCO,;
and NaOHJ
Dose pH
9/1
0 7.50
1 7.6
2 7.6
3 7.7
4 7.7
5 7.8
6 8.00
7 8.9
Table 4
pH from Computer Simulations of Titrations for
System Closed to Atmosphere
(1)
CaC03
Dose
9/1
0
2
4
6
8
10
pH
1.8
2.1
2.2
2.5
5.6
5.6
(2)
Ca(OH)?
Dose pH
9/1
0 1.8
2 2.1
4 2.3
6 11.8
8 11.8
(3)
8 g/1 CaC03;
and Ca(OH),
Dose
9/1
0
1
2
3
4
5
6
7
PH<
5.9
6.0
6.1
6.4
7.4
7.8
8.2
11.6
(4)
NaOH
Dose
9/1
0
1
2
3
4
5
6
7
PH
1.8
2.5
3.5
4.1
7.2
7.7
8.0
9.0
(5)
8 g/1 CaCO,;
and NaOHJ
Dose
9/1
0
1
2
3
4
5
6
7
pH
5.9
6.0
6.2
6.5
6.6
6.7
6.9
7.5
closed system. This is similar to a short term laboratory test. The
maximum pH was attained at a minimum CaCO3 dosage of 8 g/1.
An open system would allow the pH to rise to about 7.5 at the same
CaCO3 dosage. The reduction in the Zn and Pb concentrations was
significant but inadequate. At pH 7.5, Zn concentrations were
estimated at 34.7 mg Zn/1 and 0.27 mg Pb/1. This suggested that a
higher pH would be required to achieve the limits.
Utilizing Ca(OH)2 to neutralize the impoundment contents also
resulted in variable results depending on whether the system was
open or closed. An open system resulted in a maximum pH of 7.5;
consequently, the metal concentrations were unacceptable. The
closed system required between 4 and 6 g/1 to raise the pH above
9.5. At a dosage of 6 g/1 the resultant pH was 11.8, and the key
metal concentrations were 0.56 mg Zn/1 and 0.002 mg Pb/1. Diffu-
sion of CO2 from the atmosphere into the treated liquid would
depress the pH. In most applications of Ca(OH)2 this diffusion is
insignificant.
A test utilizing pretreatment with 8 g/1 of CaCO3 followed by
Ca(OH)2 resulted in no pH change in the open system. This was
due to movement of CO2 into the solution. The closed system
resulted in a pH rise. However, the amount of Ca(OH)2 required to
raise the pH to 9 was similar to the test case with no CaCO3
pretreatment.
Sodium hydroxide at a dosage of 7 g/1 would be required to raise
the pH to 9. Interaction with atmospheric CO2 had little effect on
the required dosage.
The fifth system tested utilized 8 g/1 CaCO3 followed by NaOH.
This system under closed conditions precipitated CaCO3 and the
pH increased with NaOH addition. Under both closed and open
conditions, over 7 g/1 NaOH was required to raise the pH to 9.
In situations where calcium or carbonate compounds were to be
used to neutralize impoundment contents, the equilibrium with the
atmospheric significantly affected chemical requirements. A system
which was allowed to equilibrate, after 8 g/1 of CaCO3 addition,
with the atmosphere (open system) would contain very little CO2.
Subsequent alkalinity addition under relatively closed conditions
would optimize chemical dosages for these materials. Such a com-
bination theoretically required 8 g/1 CaCO3 and approximately 0.2
g/1 Ca(OH2) of NaOH to neutralize the raw waste to a pH of 9. The
actual Ca(OH)2 dosage would be expected to be somewhat higher if
the CO2 supersaturation in the impoundment after CaCO3 addition
is not completely relieved.
As a result of the MINEQL computer evaluation, it was deter-
mined that certain combinations of chemicals and reaction times
were likely to be effective in neutralizing the impoundment and
reducing soluble metal components to acceptable concentrations.
Preliminary costs, presented as Table 5, were determined to focus
laboratory verification on the more cost effective alternatives.
Table 5
Projected Chemical Costs for Surface Impoundment
Neutralization from Computer Simulation
Cost
Treatment Dosage (g/1) ($/MiIlion Gal)
CaCo3 8 not effective
Ca(OH)2 6 2200
CaCO3, then Ca(OH)2 8/6 3170
CaCo3, equilibrate, Ca(OH)2 8/0.1 1010
NaOH 7 15170
CaCO3, then NaOH 8/7 16140
CaCO3> equilibrate, NaOH 8/0.1 1190
LABORATORY EVALUATION
Based on the computer model simulation, the following systems
were tested using samples obtained from various points on the sur-
face of the impoundment:
a. Single stage Ca(OH)2
b. Pretreat with CaCO3, polish with Ca(OH)2
c. Pretreat with CaCO3, polish with NaOH
The bench scale tests conducted in the laboratory utilized con-
ventional jar test equipment with field tests conducted using 10 1
containers. A titration with NaOH was used to verify model predic-
tions. The results, presented in Figure 3, indicated that 5.5-6.0 g/1
NaOH would be required.
Figure 3
Neutralization Requirements from Bench Scale Tests
TREATMENT
197
-------
Single Stage
The computer model results suggested a theoretical Ca(OH)2
dosage of 6 g (Ca(OH)2/l under expected conditions. After 10 min.
of mixing, 6 g Ca(OH)2/l resulted in a pH of 7.3 whereas 10 g
(Ca(OH)2/l resulted in a pH greater than 12. These experimental
results indicated that with the waste stream, the actual dosage re-
quired was greater than the predicted 6 g/1 but less than 10 g
Ca(OH)2/l.
A 10 1 test was conducted at 8.0 g Ca(OH>2/l to obtain larger
volumes of sample to work with. The 8.0 g Ca(OH)2/l treatment
resulted in a pH of 9.0 after 15 hr. The difference between the
predicted dosage of 6 g/1 and observed dosage of 8 g/1 was at-
tributed to mixing efficiency and CO2 infiltration. Supernatant
metals were measured at 0.15 mg Zn/1 and less than 0.2 mg Pb/1.
A completely mixed sample dosed at 10 g Ca(OH)2/l was used to
conduct a settling test in a 100 ml graduated cylinder. The results,
presented in Tables 6 and 7, suggest a settling velocity for this treat-
ment of 0.5 cm/min., equivalent to a surface overflow rate of 170
gal/day-ft2. Allowing the material to settle further resulted in a
final sludge volume of B% (v/v).
Pretreatment with CaCO3 Polish with Ca(OH)2
Impoundment contents treated with 10 g CaCO3/l are used as a
starting material. The pH was 4.0 after 15 hr of equilibration. After
39 hours of equilibration, the pH had risen to 5.0. When aerated
for 2 hr after 39 hr of equilibration, the pH increased to 5.5. Ex-
amination of the titration curves presented in Figure 3 illustrates
the significant impact the residual CO2 had on chemical re-
quirements. As expected, the closer the CaCO3 solution was to
equilibrium with the atmosphere, the lower the Ca(OH)2 require-
ment to reach a target pH of 9.0.
Analyses conducted on the supernatant indicate that at a 3 g
Ca(OH)2/l dosage, metal concentrations were 0.2 mg Zn/1 and less
than 0.1 mg Pb/1. The supernatant cleared rapidly with settling test
results suggesting a settling velocity of 2.7 cm/min. or 950 gal/day-
ft2. The residual sludge volume after polishing treatment, when
combined with that expected from the CaCO3 pretreatment, was
comparable to that observed for the Ca(OH)2 treatment. Solids
production was estimated to be 8550 mg/1 or 37 tons/million gal
for both stages of treatment.
Pretreatment with CaCO3, Polishing with NaOH
A 15 hr settled supernatant of a 10 g CaCO3/l pretreated sample
was treated with NaOH. A dosage of 1.5 g NaOH/1 resulted in a
pH of 8.6, whereas a pH of 9.2 was achieved with a dosage of 2.0 g
NaOH/1. A sample which had been stored for a longer period
resulted in a pH of 10.3 at a dosage of 2.0 g NaOH/1. These results
indicated that residual CO2 in the CaCO3 pretreated sample con-
sumed considerable alkalinity. Analyses of supernatant samples
resulted in metal concentrations of 0.03 mg Zn/1 and less than 0.1
mg Pb/1. Supernatant TSS was determined to be 90 mg/1.
The sample was resuspended and the interface height reported as
a function of time. The results, presented in Table 7, suggested a
settling velocity for the solids of approximately 0.5 cm/min.,
equivalent to a surface overflow rate of 170 gal/day-ft2. The NaOH
sludge volume was greater than that observed for the Ca(OH)2
treatment mode. The sludge production was 5700 mg/1.
Table 6
Laboratory Evaluation of Chemical Treatment
Pretreatment
— —
-
-
10 g/1 CaC03
10 g/1 CaC03
Treatment
10 g/1 CaC03
8.0 g/1 Ca(OH)2
6.5 g/1 NaOH
20 g/1 CaCO /6 g/1 Ca(OH)
3 g/1 Ca(OH)2
2 g/1 NaOH
Final
pH
(S.U.)
3.0
9.5
11.5
7.1
10.5
10.3
Supernatant
TSS
(mg/1 )
1400
162
-
130
90
Zn
(mg/1 )
72
0.15
0.25
0.04
0.20
0.03
Pb
(mg/1 )
0.3
0.1
0.1
0.1
0.1
0.1
Sludge
TSS Vol.
(mg/1) (%)
3100
6200
-
5480
5700
(a)
10
27
-
20
25
40
a. Sludge volume measured after 15 hours.
Table 7
Sludge Volumes after Chemical Treatment
Pretreatment
None
None
None
10 g/1 CaCO
10 g/1 CaCO
Treatment
12 g/1 CaCO
6 g/1 Ca(OH)
10 g/1 Ca(OH)
3 g/1 Ca(OH)
2 g/1 NaOH
Final
pH
4.8
5.5
11.3
9.5
10.3
Sludge Volume (%)
5 min
100
70
90
25
94
10 min
52
40
76
20
73
30 min 60 min
10 9
20 12
44 32
19 16*
46 31
Comments
Fines, settle slow
Fines, settle slow
Few fines
Clear supernatant
Clear supernatant
198
TREATMENT
-------
CHEMICAL TREATMENT OF IMPOUNDMENT
Two process schematics were prepared. One involved in situ
neutralization of the impoundment with the capability of polishing
prior to discharge to the sanitary sewer. The second provided
neutralization of the impoundment in a temporary facility con-
structed on site.
Bench scale tests conducted using 100 cm long and 1 cm inner
diameter tubes demonstrated that limestone slurry up to 35%
(w/w) sprayed over the surface of the impoundment to give a mean
dosage of 10 g/1 would result in uniform distribution of the
limestone with minimim mixing. Similar tests with Ca(OH)2 sug-
gested incomplete mixing.
Major equipment items were identified and costs allocated for in
situ neutralization and external neutralization. The most cost effec-
tive approach was the in situ neutralization with CaCO3 and
Ca(OH)2.
The selected approach involved bulk limestone deliveries of ap-
proximately 22 ton capacity. Specialized equipment to slurry
limestone at a concentration of 35% (w/w) CaCO3 in to dilution
tank was provided as illustrated in Figure 4. The slurry from the
dilution tank at 18% (w/w) was then pumped to a 100 ft distribu-
tion header utilizing flexible hose with a quick disconnect fitting. A
winch was used to move the distribution header across the im-
poundment in 100 ft swathes. The velocity was maintained at 1.5
ft/min.
TO DISTRIBUTION
SYSTEM
-1
OISTHBUTION WMP-^ 1
<_r
BULK SHIFMENT
1 // "--SLUfmr WSTER MMP
r~77
IMPOUNDMENT /I -I V
DILUTION TUK-S /
Figure 4
Lime Application Equipment
One thousand four hundred and thirty tons of limestone were ad-
ded to the impoundment over a period of two weeks. Visual obser-
vation indicated that the mixing of the impoundment due to injec-
tion velocity and wind provided good distribution of the limestone
throughout the impoundment.
Stoichiometric calculations indicated that 3.3 g CO2/1 would be
generated due to the limestone addition. Based on diffusion rates,3
the time for 90% of the CO2 generated to be released to the at-
mosphere was estimated to be 30 hr. Measurements at various
Figure 5
Effluent Polishing Facilities
points in the impoundment indicated that the pH rose steadily to
approximately 5 after five days with a clear supernatant observed.
Approximately a week after the final limestone additions, 220
tons of hydrated lime were added to the impoundment over a
period of five days. Although earlier laboratory tests with the 100
cm glass column indicated that lime did not mix as well as the
limestone, the high degree of mixing observed with limestone addi-
tion justified trying the same procedure with the hydrated lime. The
total amount of lime added resulted in a dosage of about 1.6 g/1.
When all the lime was added, the impoundment was uniformly at a
pH of approximately 11.5. Analysis of supernatant indicated that
lead and zinc concentrations were well below the sewer use limits.
The excess alkalinity was provided to neutralize expected subse-
quent discharges of acid waste from the processing plant.
Within a week of the final bulk lime addition, supernatant from
surface of the impoundment was pumped to a clarifier to remove
any suspended particles prior to discharge to the city sewer. The
system included for polishing the wastewater, if required, is shown
in Figure 5. The approved discharge was at an average rate of 180
gal/min. The discharge was discontinued during periods of rain
when the municipal treatment plant was close to its handling
capacity of 6 mgd. Typical effluent quality is presented in Table 8.
IMPOUNDMENT CLOSURE
As the impoundment was still actively treating the plant waste,
discharge to the sanitary sewers was in compliance with RCRA.
Final closure required that an approved Closure Plan be submitted
to the regulatory authorities at least 180 days prior to closure initia-
tion. As the waste treatment facilities were expected to be on line
during Aug. 1983, the Closure Plan was submitted to the regulatory
authorities in early Mar. 1983.
The projected timetable, presented as Figure 6, was submitted
with the Closure Plan. The actual timetable will be significantly af-
fected by weather conditions and regulatory action. At the time of
writing, the timetable is being met. However, indications are that
Table 8
Treated Impoundment Water Quality
Sample Date
Sample Site
Zn
Concentration (mg/1)
Pb Fe
Cr
April 4, 1983
April 4, 1983
April
-------
Groundwater Monitoring
Closure Plan Submlllal
Discharges to Impoundment
Equipment Delivery
ln~situ Neutralization
Water Level Reduction
Passive Dcwaterlnp.
Dellsling Petition
Grading and Compaction
Surface Reclamation
Certification of Closure
777%
177x1
V////A
X//////////////////777A
V/////////////////////1
Y77*
-t-
JFMAMJJASONDJFMAMJJ
1983 198<
Figure 6
Surface Impoundment Closure Timetable
Figure 1
Approximate Contours After Closure—Plan View
200 TREATMENT
-------
90S
994
992
990
a~ LIME MS40JC -
-EXISTING NATURAL ALLUVIAL O.OV3
996
906
994
992
990
960
90S
9*)
•M
984
EXISTING INTERNAL CLAY DUE
B LIME RESlBJt
Figure 8
Approximate Grade After Closure—Section View
additional residue samples will be required by the regulatory
authority prior to Closure Plan approval. This may delay
regulatory approval and thus move Final Closure into 1984.
The proposed Closure Plan results in a final grading plan
presented as Figure 7 and sections as illustrated in Figure 8. Use of
local clays for the cap will provide an environmentally sound
closure for the material present.
SUMMARY
A 33,000,000 gal. surface impoundment containing spent pickle
liquor and plating wastewater required treatment and aqueous
disposal. The combined use of a chemical equilibrium model and
bench scale tests made it possible to evaluate a combination of
chemicals within a short period of time. The required chemical
dosages and final pH conditions, as predicted by the computer pro-
gram, were in agreement with both bench scale tests and actual
treatment of the waste impoundment. The least cost chemical treat-
ment system consisted of limestone addition followed by hydrated
lime.
A specialized chemical slurry distribution system provided an ex-
cellent means of adding limestone and hydrated lime uniformly to
the impoundment. Effluent quality met sewer use limitations and
the aqueous disposal is continuing on schedule.
Final closure of the site will depend on regulatory review and ap-
proval. The projected final closure involves utilizing in situ passive
dewatering followed by the installation of a clay cap. The clay cap
will be graded and protected by top soil.
REFERENCES
1. Patterson, J.W., Wastewater Treatment Technology, Ann Arbor Sci-
ence, Ann Arbor, MI, 1970.
2. Westall, J.C., Zachary, J.L. and Morel, F.M.M., "MINEQL-A Com-
puter Program for the Calculation of Chemical Equilibrium Composi-
tion of Aqueous Systems," Technical Note No. 18, Department of Civil
Engineering, MIT, July 1976.
3. Stumm, W. and Morgan, J.J., Aquatic Chemistry: An Introduction
Emphasizing Chemical Equilibria in Natural Waters, Wiley-
Interscience, New York, 1970.
TREATMENT
201
-------
TREATABILITY OF HAZARDOUS WASTE LEACHATE
AT PUBLICLY OWNED TREATMENT WORKS
ROBERT D. GOLTZ
SALVATORE BADALAMENTI
ROBERT N. OGG
U.S. Environmental Protection Agency, Region II
New York, New York
INTRODUCTION
During the past three years, the control and cleanup of hazar-
dous waste landfills has become an environmental program priority
in the United States. One of the primary objectives of the program
has been to mitigate the effects of leachate from hazardous waste
landfills on ground and surface waters, especially those used as
drinking water supplies. One method being explored in USEPA
Region II is treatment of hazardous waste leachate in Publicly
Owned Treatment Works.
Since passage of the Clean Water Act in 1972, the Congress has
appropriated approximately $45 billion to construct new and
rehabilitate existing municipal sewer systems and treatment works
to provide a minimum of secondary treatment capability to ensure
attainment of water quality standards within the United States.
During the last 10 years, that effort has resulted in the construction
of plants, using federal, state and local funds, in many com-
munities. Frequently, however, those treatment systems are
hydraulically underutilized. Therefore, it appears prudent, where
possible, to utilize the excess capacity of Publicly Owned Treat-
ment Works (POTWs) to treat leachate from hazardous waste
landfills. Such an effort will increase the return on the public in-
vestment in the POTWs by providing new revenues while
simultaneously addressing the environmental priority of cleaning
up hazardous waste sites.
Because POTWs were generally designed to treat sewage, it is
critical to determine whether hazardous waste leachate can be safe-
ly treated before a full-scale addition is begun. Such a determina-
tion requires the performance of a treatability study.
In this paper, the authors present the results of two treatability
studies performed on leachate from the Lipari Landfill' in Pitman,
New Jersey and the Kin-Buc Landfill2 in Edison, New Jersey. Addi-
tionally, a general approach for conducting these types of studies is
discussed. As a result of this effort, the authors believe that treating
hazardous waste landfill leachate in POTWs will provide a cost-
effective solution for disposing of leachate from many hazardous
waste sites.
METHODS
The State of New Jersey has established the following guidelines
for conducting treatability studies:
•Sample Collection and Analysis
At least three samples of leachate must be taken, composited and
analyzed for conventional and priority pollutants. One 8 hr day-
time composite sample of the influent and effluent of the POTW
shall be analyzed in the same way.
•Inhibition
Using various dilutions of leachate and influent, either an acute
toxicity test or an oxygen uptake test shall be run to examine in-
hibitory effects of leachate on the activated sludge.
•Treatability
An influent (8 hr day-time composite) and leachate combination
shall be added to a stabilized bench-scale replicate of the activated
sludge treatment system. The dilution should provide for a safety
margin of five; that is, the fraction of leachate for the test shall be
at least five times the expected fraction of the final discharge. The
test shall be run for at least three days after the system is stabilized.
•Evaluation
The following tests shall be performed during the treatability
test:
(1) Sludge settling characteristics
(2) Mixed liquor suspended solids
(3) Oxygen uptake
(4) Treatment removal efficiency for conventional, selected or-
ganic compounds and metals
•Nitrification—Denitrification
If the POTW utilizes a nitrogenous treatment system, the
treatability tests and evaluation shall be replicated for the
nitrogenous and the carbonaceous systems.
•Discussion
In the report on this testing, the discussion should include: effect
of leachate on treatment system; need for pretreatment; effect of
pretreatment of leachate on treatability; calculation of pass
through and sludge contamination of pollutants of full-sized
system based on bench scale studies.
•Conclusions and Recommendations
As a result of conducting the study, it can be determined whether
or not the POTW should accept the leachate and any specific
pretreatment measures that may be required.
KIN-BUC LANDFILL STUDY
The Kin-Buc Landfill is located in Edison, New Jersey. From
1971 to 1976, it accepted approximately 70,000,000 gal of various
industrial and chemical waste. In 1979, an oily sheen, presumed to
be leachate from the landfill, was observed in a natural depression
near the toe of the landfill. Further investigation determined that
both an oily phase and aqueous phase leachate were flowing from
the landfill. The oily phase of the leachate contained high concen-
trations of polychlorinated biphenyls (PCBs) and the aqueous
phase contained other priority pollutants.
202
TREATMENT
-------
Since 1980, the USEPA has been collecting the oily phase
leachate while releasing the aqueous phase into a nearby creek
where it ultimately finds it way into the Raritan River. To alleviate
this situation, the USEPA developed a plan to collect the aqueous
phase, pretreat it, and discharge it to the Middlesex County Utility
Authority's (MCUA) POTW for treatment.
To determine specific pretreatment requirements for the
leachate, a treatability study was performed based on the New
Jersey Department of Environmental Protection guidelines. It was
calculated that a maximum of 10,000 gal/day of aqueous leachate
would have to be collected, pretreated and discharged to the
MCUA. Flow at the MCUA is estimated to be about 70 mgd with
an average flow between 80-85 mgd; the plant capacity is 120 mgd.
The biological treatment process of the plant utilizes pure oxygen.
A sample of the aqueous leachate was collected and analyzed.
The total petroleum hydrocarbon level was reduced by physical
separation to less than 100 mg/1, the pretreatment level required by
the New Jersey Department of Environmental Protection. This
sample was then analyzed for the 129 priority pollutants, seven con-
ventional pollutants and 24 non-conventional pollutants. The
pollutants that were found are shown on Table 1.
The aqueous phase leachate was subjected to an acute toxicity
test, an oxygen uptake study and a bench scale continuous ac-
tivated sludge treatability study.
There was no measurable effect of the Kin-Buc leachate even at
100% concentration as determined by final dissolved oxygen. The
oxygen uptake study demonstrated that greater than 2% by
volume of the Kin-Buc leachate has the potential to initially in-
hibit the unadapted MCUA activated sludge. Above 12.5% a
definite inhibition is apparent. Removal efficiencies of a bench
scale activated sludge system for the 129 priority pollutants that
were above detectable limits in the leachate and the accumulation
of these priority pollutants in the sludge generated by the system
are shown in Tables 2 and 3. As can be seen, the removal efficiency
for most compounds ranged from 95% to 99%. There also ap-
peared to be no accumulation of priority pollutants in the sludge
except for methylene chloride and bis (2-ethylhexyl) phthalate
which was probably due to the use of Tygon tubing.
Lipari Landfill Results
The Lipari Landfill is located in the Township of Pitman,
Gloucester County, New Jersey. From 1958-1971, the landfill ac-
cepted household wastes, liquid and semi-solid chemical wastes and
other industrial wastes and materials. Components of the hazar-
dous wastes dumped at the landfill have percolated into the
groundwater. Chemical contaminants have leached through the
embankments of two nearby streams.
Table 1
Analysis of Aqueous Kin-Buc Leachate
A) Priority Pollutants (GC/MS)
1) Purgeable Organics
Benzene
Chlorobenzene
1 ,2-Dichloroethane
1 , 1 -Dichloroethylene
Ethylbenzene
Methylene Chloride
Trichlorethylene
Toluene
Concentration
fno/n
lug/ U
2860
1390
1120
1530
243
1180
1040
5120
Non-Priority Pollutants in Purgeable Fraction
Acetone
Ethyl Acetate
Cyclopentane
Methyl Ethyl Ketone
Aklyl Ether
Total Xylenes
2) Acid Extractables
Phenol
1210
2220
884
1530
4750
393
(mg/1)
15.4
Non-Priority Pollutants in Acid Extractable Fraction
Cresol Isomer
Bensoic Acid
Phenyl Acetic Acid
Phenyl Proponic Acid
3) Base/Neutral Compounds
Diethylphthalate
Non-Priority Pollutants in Base/Neutral
Aniline
Anisol
Dimethyl Aniline Isomer
Alkyl Benzene Isomer
Methyl Benzylamide
Dichloroaniline Isomer
Quinoline or Isoquinoline
Alkylamine Isomer
4) Pesticides and PCB
Compounds were in concentrations below
detectable limits
4.23
29.1
53.3
20.9
(mg/1)
7.37
Fraction
0.50
1.27
3.68
1.57
11.4
0.41
2.79
15.2
(mg/1)
5) Metals
Antimony
Cadmium
Chromium (Total)
Copper
Lead
Mercury
Nickel
Zinc
B) Conventional Parameters
1) Analysis Parameters
BOD
COD
TOC
TSS
TDS
NH3
pH (units)
C) Non-conventional Parameters
1) Analysis Parameter
Color (units)
Nitrate-N
Nitrite-N
Total Organic Nitrogen
Oil and Grease
Total Phosphorus
Radioactivity
Sulfate
Sulfide
Sulfite
Surfactants
Aluminum
Boron
Cobalt
Iron
Magnesium
Manganese
Tin
Titanium
(mg/1)
0.535
0.012
0.439
0.06
0.108
0.0025
1.59
28.4
(mg/1)
18,000
15,200
940
1,860
2,048
44.8
5.8
mg/1
5,000
0.05
0.004
85
1,040
2.6
Insuff. sample
1,150
84.5
30
0.897
4.18
10.8
0.18
1,540
382
24.5
1.2
2.3
TREATMENT
203
-------
As part of USEPA's feasibility study, an examination of an alter-
native that includes collection and treatment of this leachate at the
Gloucester County Utilities Authority (GCUA) was conducted.
The GCUA treatment plant consists of primary clarification
followed by a "modified" contact stabilization activated sludge
process. After secondary clarification, the water is chlorinated and
discharged. The sludge is presently disposed of in a landfill, but
GCUA is considering composting of the sludge for application to
non-agricultural lands. The average flow rate is 14.5 mgd.
The treatability study examined the following:
•Pollutant removal
•Accumulation of pollutants in the sludge
•Release of volatiles into the air
•Inhibition screening study in accordance with the NJDEP guide-
lines
Two reactor vessels were used in the biotreatability study; Reac-
tor #1 represents a sewage to leachate ratio (by volume) of 100:1
which will reflect actual operations, and Reactor 02 represents a
sewage to leachate ratio of 20:1 which provides the safety margin of
five required by NJDEP.
Table 2
Kin-Bat: Purgeable Organic Constituent Analysis of Effluent Samples Treatability Testing
Compound
Benzene
Bronod ichlorone thane
Chloroform
1 ,1-Dichloroe thane
1 , 2-Dichloroethane
Ethylbenzene
Methylene Chloride
Toluene
1,1, 1-Tr ichloroe thane
Trichloroethylene
Total Xylenes
MCSV
Kin-Buc
Influent
10/25(ppb)
103
36.9
36.5
32.5
1240
10.4
689
132
8.0
4.5
24.0
Effluent
10/25-
10/26
(ppb)
ND
ND
ND
ND
ND
ND
10.7
ND
ND
ND
ND
%
Removal
10/25-
10/26
>99
>97
>97
>97
>99
>90
>98
>99
>87
>78
>95
MCSV
Kin-Buc
Influent
10/26(ppb)
112
31.4
32.4
30.2
1730
8.2
621
81.3
7.6
ND
18.6
Effluent
10/26-
10/27
(ppb)
ND
ND
ND
ND
ND
ND
5.3
ND
ND
ND
ND
%
Removal
10/26-
10/27
>99
>96
>96
>96
>99
>88
>99
>98
>87
—
>94
MCSV
Kin-Buc
Influent
10/27 (ppb)
106
30.7
30.7
31.5
1980
7.3
786
29.7
4.5
ND
12.4
Effluent
10/27-
10/28
(ppb)
ND
ND
ND
ND
ND
ND
4.1
ND
ND
ND
ND
%
Removal
10/27-
10/28
>99
>96
>96
>96
>99
>86
>99
>96
>78
—
>92
ND — Nondctcctable less than 1.0 ppb
Dales of Testing: 10/25, 10/26. 10/27
Table 2
Kin-Buc: Acid Extractable Organic Compound Constituent Analysis of Effluent Samples Treatability Testing
Compound
4-Chloro-3-Methyl-
phenol
2,4-Dinitrophenol
2-Methyl-4,6-
Dinitrophenol
Phenol
2,4, 6-Tr ichloro-
phenol
MCSV
Kin-Buc
Influent
10/25(ppb)
510
100
38
7850
210
Effluent
10/25-
10/26
(ppb)
ND
ND
ND
ND
ND
%
Removal
10/25-
10/26
>99
>99
>97
>99
>99
MCSV
Kin-Buc
Influent
10/26 (ppb)
ND
ND
53
9770
300
Effluent
10/26-
10/27
(ppb)
ND
ND
ND
ND
ND
%
Removal
10/26-
10/27
—
—
>98
>99
>99
MCSV
Kin-Buc
Influent
10/27 (ppb)
540
46.5
ND
8150
ND
Effluent
10/27-
10/28
(ppb)
ND
ND
ND
ND
ND
%
Removal
10/27-
10/28
>99
>97
—
>99
—
ND — NofKJctectable lew than 20 ppb
204
TREATMENT
-------
Table 2
Kin-Due: Base-Neutral Organic Compound Constituent Analysis of Effluent Samples Treatability Testing
Compound
Benzo( a ) Anthracene
Benzo ( a ) Pyrene
Bis ( 2-Ethylhexyl )
Phthalate
Butyl Benzyl
Phthalate
Di-n-Butylphthalate
1 , 2-Dichlorobenzene
Diethylphthalate
2 ,4-Dinitrotoluene
2 ,6-Dinitrotoluene
Hexachlorobutad iene
Hexachlorocyc lopent-
adiene
MCSA/
Kin-Buc
Influent
10/25 (ppb)
ND
ND
ND
58.9
ND
38.6
45.6
33.7
72.9
42.4
255
Effluent
10/25-
10/26
(ppb)
45.9
36.4
ND
ND
ND
ND
ND
ND
ND
ND
ND
%
Removal
10/25-
10/26
(in-
crease)
(in-
crease )
—
>98
—
>97
>97
>97
>98
>97
>99
MCSA/
Kin-Buc
Influent
10/26(ppb)
ND
ND
4890
48.5
ND
405
34.8
ND
ND
36.6
124
Effluent
10/26-
10/27
(ppb)
ND
ND
3900
ND
35.6
ND
ND
ND
ND
ND
ND
%
Removal
10/26-
10/27
—
—
20
>97
(in-
crease )
>99
>97
—
—
>97
>99
MCSA/
Kin-Buc
Influent
10/27 (ppb)
22.3
ND
ND
83.4
ND
40.8
38.8
25.7
45.8
43.8
229
Effluent
10/27-
10/28
(ppb)
ND
ND
4900
ND
ND
ND
ND
ND
ND
ND
ND
%
Removal
10/27-
10/28
>95
—
(in-
crease )
>98
—
>97
>97
>96
>98
>97
>99
ND — Nondetectable less than 20.0 ppb
Table 2
Kin-Buc: Selected Metal Constituent Analysis of Effluent Samples
Compound
Zinc
Chromium
Nickel
MCSA/
Kin-Buc
Influent
10/25(ppb)
4.90
0.075
0.054
Effluent
10/25-
10/26
(ppb)
1.58
0.028
0.043
%
Removal
10/25-
10/26
68
73
20
MCSA/
Kin-Buc
Influent
10/26(ppb)
3.44
0.069
0.049
Effluent
10/26-
10/27
(ppb)
2.99
0.036
0.044
%
Removal
10/26-
10/27
13
48
10
MCSA/
Kin-Buc
Influent
10/27(ppb)
6.63
0.083
0.060
Effluent
10/27-
10/28
(ppb)
2.77
0.043
0.060
%
Removal
10/27-
10/28
58
48
0
TREATMENT
205
-------
Table 3
Kin-Bnc: Purgeable Organic Compound Analysis of Sludge Samples
Compound
Chloroform
1,1-Dichloroethane
1,2-Dichloroethanc
Ethylbenzene
Methylene Chloride
Toluene
1,1,1-Trichloro-
ethane
Total Xylenes
Before Kn-Bac
Addition
10/25/S2
CoKtilration
0*/i)
118
12.9
25.6
8.8
ND
9.8
12.9
8.0
Dwtag Tmtabflity Testing
10/27/82 10/27/82 10/2I/S2
3:45 pm 6M pm 8:00 pm
18.9
19.2
18.3
7.8
ND
5.2
9.6
9.0
19.4
9.5
17.2
6.8
ND
4.8
9.3
5.2
12.3
10.9
10.6
3.8
5.9
2.41
11.4
ND
Kln-Bac: Add ExtracUble Organic Compound Analysis
of Sludge Samples
No compounds present above detectable limits (200 pg/1)
Kin-Buc: Base Neutral Organic Compound Constituent
Analysis of Sludge Samples
Bis(2-Ethylhe*yl) 6000 1710 3600 1600
Phthalate
Di-N-Butyl-
phthalate ND 330 ND ND
Kin-Buc: Pesticide and PCBs Organic Compound
Analysis of Sludge Samples
Aldrin 10.4 ND ND 1.3
Kin-Buc: Selected Metal Constituent Analysis of Sludge Samples
During Treatability Testing
Parameter
Zinc
Chromium
Nickel
Total Suspended
Solids
Before KJn-Boc
Addition
10/25/82
(mg/1)
47.8
0.596
0.176
4400
10/27/82 10/27/82 10/28/82
3:45 pm 6:35 pm 8:00 pm
(mg/1) (mg/1) (mg/1)
28.7 29.9 16.3
0.423 0.368 0.273
0.135 0.125 0.125
5000
4800
4560
Table 4
Llpari Water Quality Analyses*
Detection
Limit
Influent
Effluent
Percent
Removal
Expected
Percent
Removal
Mixed Liquid
Total
Sludge
Liquid
Phase
Total
Sludge
(mg/kg)
REACTOR II
COD (mg/L)
BOD, (mg/L)
Phenol
Benzene (pg/L)
Toluene (ug/L)
Ethyl-benzene (ug/L)
pMn xylene (ug/L)
o+Xylene (ug/L)
1,2-Dichloroethane (ug/L)
bis(chloroethayl)ether
(ug/L)
bis(chloroethoxy)ethane
(ug/L)
Copper (ug/L)
Iron (ug/L)
Manganese (ug/L)
Zinc (ug/L)
-
5
1
1
1
1
1
1
25
5
1
8
1
3
248(32)
157(10)
135(8)
11(13)
59(13)
1.5(13)
3.3(8)
1.5(8)
41.6(8)
174(8)
364(12)
6.4(9)
461(9)
4.5(9)
8.2(9)
28(31)
18(10)
<10(8)
<1(12)
<1(12)
92.3(8)
>86.5(11)
>96.6(11)
>42.7(4)
>58.4(8)
>50.7(4)
86.3(6)
>85.9(6)
>98.3(11)
-10.0(6)
71.4(9)
59.1(5)
8.4(9)
>90
>80
>80
>80
—
—
>60
>80
>50
<50
>80
<20
>60
NA
NA
<76.2(8)
-------
Table 4 (continued)
Detection
Limit
Influent
Effluent
Percent
Removal
Expected
Percent
Removal
Mixed Liquid
Total
Sludge
Liquid
Phase
Total
Sludge
(rog/kg)
REACTOR 12
COD (mg/L)
BOD, (rng/L)
Phenol
Benzene (pg/L)
Toluene (ug/L)
Ethyl-benzene (ug/L)
p-nn Xylene (ug/L)
o-Xylene (ug/L)
1 , 2-Dichlor oethane ( ug/L)
bis ( chloroethayl ) ether
(ug/L)
bis( chloroethoxy) ethane
(ug/L)
Copper (ug/L)
Iron (ug/L)
Manganese (ug/L)
Zinc (ug/L)
5
1
1
1
1
1
1
25
5
1
8
1
3
309(31)
184(10)
430(8)
65.3(11)
485(11)
7.6(11)
22(11)
11.5(11)
273(8)
1344(8)
1980(12)
8.0(9)
2265(9)
8.9(9)
15.5(9)
31(31)
17(10)
<8.1(10)
<1(10)
96.2(8)
>98.6(9)
>99.8(9)
>88.5(9)
>94.1(10)
>91.3(9)
79.6(8)
>97.1(8)
>99.8(11)
14.3(7)
84.7(9)
63.7(9)
-6.04(6)
>90
>80
>80
>80
—
—
>60
>80
>50
<50
>80
<20
>60
NA
NA
<152(8)
<2(10)
<8.8(10)
<1.4(10)
<1.3(9)
<1.1(10)
78.8(9)
<25.6(9)
<11.9(11)
<240(8)
45012(8)
157(8)
510(9)
NA
NA
<61.3(3)
<4.7(3)
<47.7(3)
<1(3)
<1.1(3)
<1(3)
41(4)
<25(3)
<28(5)
<2(4)
3498(4)
263(4)
11.5(4)
62.0
<0.82
3.6
0.57
0.53
0.45
32.2
10.4
4.8
97.9
18,372
64
208
A summary of the results of selected pollutants removed by the
system is shown in Table 4. In general, the organic removals were
consistent with expectations. However, the metal removals varied
widely.
The accumulation of the pollutants in the sludge are also noted in
Table 4. The concentrations of these substances do not exceed
any of the parameters listed in New Jersey's Sludge Quality
Assurance Regulations (Table 5). However, no regulations have
been established for the allowable concentrations of organic com-
pounds found in the Lipari ground water.
Results of the air quality monitoring during the reactor operation
are presented in Table 6. For the chemicals present in the Lipari
groundwater, no air concentrations exceeded the NIOSH-8 hour
Time Weighted Averages.
Inhibition screening tests were performed on composited
leachate samples. The objective of the tests was to determine if the
leachate would have an inhibiting effect on the activated sludge
process. The data indicated that only slight inhibition occurred at a
sewage to leachate ratio of 3:1. This inhibition, measured by a
decrease in the oxygen uptake rate, is not considered to be signifi-
cant.
CONCLUSIONS
The results of these two studies show that both the MCUA and
the GCUA POTWs are capable of treating the leachate from the
Table 5
State of New Jersey Sludge Quality Assurance Regulations
Contamination Indicators for Heavy Metals & Toxic Organic Compounds
Heavy Metals
Arsenic (total)
Cadmium (total)
Chromium (total)
Copper (total)
Lead (total)
Mercury
Nickel (total)
Zinc (total)
mg/kg
10
16
890
850
500
5
82
1,740
Toxic Organic
Compounds
Aldrin
Chlordane
Dieldrin
Endrin
Heptachlor
Heptachlor
exposide
Lindane
Methoxychlor
p.p-DDT
p,p'-DDE
Toxaphene
Polychlorinated
biphenyls (PCBs)
mg/kg
0.10
0.10
0.10
0.10
0.10
0.10
0.10
0.25
0.25
0.25
1.0
0.50
TREATMENT
207
-------
Table 6
N1OSH 8-Hour Time-Weighted Averages (TWA)1 for Chemicals in the
Leachate and Observed Emission Concentrations for Lipari Landfill
Compound
Benzene
Toluene
Ethylbenzene
m + p-Xylene
o-Xylene
Methylene chloride
1 ,2-Dichloroethane
bis(chloroethyl)-ether
1. OSHA Safely and Health
NIOSH 8-Hr
TWA (ppmv)
10
200
100
100
100
500
50
152
Manual; 29 CFR 1910,
Emission
Concentration
No Wind
(ppmv)
0.031
0.090
0.0031
0.0073
0.0035
0.405
0.537
0.0085
Revised November 7,
01. mph Wind
(ppmv)
0.00014
0.00038
0.000013
0.000031
0.000014
0.0017
0.0023
0.000036
1978. Reference (14)
Kin-Buc and Lipari landfills respectively. However, it is still the
prerogative of the POTW as to whether or not they will accept the
waste. Factors which the POTW must consider are the following:
•How much of the underutilized capacity does the POTW want to
be used by leachate? What is the anticipated future loading from
other sources in the POTW's service area?
•What additional cost would the POTW incur by accepting the
leachate? For example, are there any additional monitoring re-
quirements or are any process changes necessary to better accom-
modate the leachate?
•What pretreatment levels, if any, should be set for the leachate?
Are local pretreatment requirements being met?
•What is the public perception of the POTW treating the leachate?
Also, what are the POTW workers' perception? Air quality
studies alone may not allay people's fears.
Discharging to a POTW has the advantage of utilizing an existing
system that can effectively treat the waste and provides an alter-
native to creating another on-site treatment system with direct
discharge into a surface water and its associated operation and
maintenance cost.
REFERENCES
1. Radian Corporation; Draft Report of the "Treatability Study of Con-
taminated Groundwater From the Lipari Landfill, Pitman, N.J.,
Feb. 1983.
2. Princeton Aqua Science, "Treatability Study of Kin-Buc Landfill
Leachate", Dec. 1982.
208
TREATMENT
-------
COST EFFECTIVE TREATMENT OF PRIORITY POLLUTANT
COMPOUNDS WITH GRANULAR ACTIVATED CARBON
V.A. BRUNOTTS
L.R. EMERSON
E.N. REBIS
A.J. ROY
Calgon Corporation
Pittsburgh, Pennsylvania
INTRODUCTION
Carbon adsorption has played a key role in many wastewater
treatment installations in helping them meet their treatment objec-
tives. Based on a decade of experience, the authors discuss the ef-
fectiveness of activated carbon for the removal of a variety of
pollutants when utilized for treatment in a representative sample of
17 industrial projects. Data from 29 groundwater and spill control
applications will be presented to demonstrate the efficiency of car-
bon adsorption in this area of treatment. The cost effectiveness of
carbon adsorption, while accomplishing high removal efficiencies,
will also be discussed.
In light of new treatment challenges (groundwater contamina-
tion, for example) and future comprehensive priority pollutant
regulations, Calgon has developed a new technology for analyzing
contaminated water quickly. The newly developed Accelerated Col-
umn Test (ACT) has several advantages over conventional test
methods in addition to the speed with which it can be run. The ad-
vantages of the ACT will be discussed along with an example of
how the ACT correlates to current testing methods.
CARBON EFFICIENCY
During the past 10 years, granular activated carbon (GAC) has
been used to remove a wide variety of organic compounds from
many types of contaminated water. The wide diversity of applica-
tions is illustrated in Tables 1 and 2 which show the type of applica-
tion, major priority pollutants involved and project operating con-
ditions. In all, project operational data are presented for 17
industrial wastewater, 11 chemical spills and 18 groundwater ap-
plications.
The majority of applications employ dual adsorption units. Each
adsorber contains 20,000 Ib of granular activated carbon (GAC)
and operates under pressure in a downflow series mode. Series
operation provides for total exhaustion of the GAC in the lead bed
while the polish bed produces the required effluent quality.
Analytical monitoring data consisted of GC/MS characterization
of composite samples of adsorber influent and effluent. This
monitoring reflects the period between installation of fresh carbon
in the lead adsorber and the time of exhaustion for the organic
compound of interest. High percentage removals were observed in
all cases, regardless of the type or concentration of priority pollu-
tant present. Greater than 99% removal was achieved in a majority
of cases. Priority pollutants in these applications were typically
reduced to non-detectable levels (approximately 1 /tg/1).
When removal of other organic compounds (non-priority
pollutants) was not a treatment objective, the systems were not
operated to achieve low microgram per liter levels of these com-
pounds in the effluent.
A wide variety of organic compounds are present in the listed ap-
plications (Tables 1 and 2); the most common are aromatic and
halogenated solvents. Contaminants in both groups are removed
very well by the adsorption process. Solubility is a key parameter in
determining how well an organic compound will adsorb; low
solubilities are preferable for adsorption efficiency. Generally,
organic compounds which adsorb poorly are low molecular weight,
highly polar species such as methanol, formaldehyde or acetic acid.
High molecular weight highly branched aliphatics such as car-
bohydrates and proteins also adsorb poorly. A few of each group
are listed in Tables 1 and 2. Typically, the type of organic com-
pounds which do not adsorb well from water exhibit low toxicity
and can be discharged to a biological unit process for further
removal, if necessary.
Methylene chloride is one halogenated solvent present in fairly
high concentrations in a number of effluents. Because of its high
polarity and solubility, methylene chloride will break through a car-
bon bed earlier than most other priority pollutants. When methy-
lene chloride removal was not a specific requirement, this con-
taminant was allowed to opass into the effluent while other con-
taminants of more importance continued to adsorb on the lead
carbon adsorber. This is the case in Table 1, examples 2 and 12.
Another critical parameter in adsorption system design is contact
time, which is normally reported as empty bed contact time, as
computed by the ratio of adsorber volume to flow rate. The recom-
mended minimum contact time, 7.5 min for surface water treat-
ment, is adequate to assure no kinetic limitations to adsorption per-
formance. For wastewater applications, greater contact times are
sometimes needed. The projects listed have contact times ranging
from 12 min to 30 hr.
It is obvious that contact time must be critically evaluated for
each project. The new Accelerated Column Test, discussed later in
this paper, is a valuable tool for the evaluation of this parameter.
EXTRACTION/CONCENTRATION OF
ORGANIC COMPOUNDS
A prime benefit of adsorption is the ability of activated carbon to
concentrate organic compounds several thousand-fold from dilute
solutions (Table 3 and Figure 3). For highly contaminated streams,
organic compounds are concentrated 80 to 100 times. This adsorp-
tion characteristic is important in evaluating disposal costs of con-
taminated waters. Cleanup of contaminated waters through
adsorption, followed by transportation of the spend carbon to a
TREATMENT
209
-------
T»ble 1
Influent
Project
1
2
3
TVM Conwunds Cone.
WW TOC
Benzene
Toluene
Trimethylpyradine
Aniline
Benzonitrile
Phenol
Cresol
Dimethyl phenol
in Methylene Chloride
Dlchloroethylene
D1 ethyl Ether
Chloroform
Dlchloroe thane
Trlchloroe thane
Benzene
B1s(2-Chloroethyl) Ether
Benzole Add
TOC
WW Nltrophenol
Phenol
Chlorophenol
(•9/1)
440
.388
.290
.200
.460
.080
11
7.600
2.475
.013
.034
.207
5.080
.100
1.400
.008
2.240
.025
340
296
2.8
1.2
Dimethyl coumaranylmethylmethylcarbamate 2.4
Methyl phenol 21
Xylene ?•?
4
5
6
7
Ethylbenzene
1-Chloro 3-N1trobenzene
Nltrophenol
Acetophenone
Olchlorocyclobutane
TOC
WW Methylene Chloride
Chloroform
Trlchloroe thylene
Olmethylcoumaranylmethylcarbamate
Hydro xycuma rone
Methyl pro penyl phenol
Dlethylethanolamine
TOC
WW Methylene Chloride
Acetone
Hydroxymethyl pentanone
TOC
Mil Acetone
Methylene Chloride
Methyl ethyl Ketone
Tol uene
Methyl pentanone
Phenol
Dimethyl phenol
TOC
WW Butadiene
Chloroform
Methylchloropentane
Benzene
Toluene
Ethylbenzene
Napthalene
Flourene
Acenapthalene
Phenanthrene
Dimethyl phenol
Phenol
TOC
0.6
0.2
0.16
0.62
0.27
700
5.4
0.3
0.5
52.2
54.6
7.8
7.8
385
0.4
0.09
0.15
40
0.45
0.92
0.32
0.32
0.42
4
0.9
130
0.014
0.036
0.092
2.8
3.0
0.8
0.16
0.008
0.007
0.009
0.041
4.4
10
.„-„-, Contact
Effluent Q Annua1 , 6AC Tine
Cone, (ngyi) GPM Gal x 10° 1/1000 Gal (Min)
.002
N/D
N/D
N/D 30 6.5 40 330
N/D
.001
N/D
N/D
.013
N/D
N/D
754
'N/D 60 10.5 7.9 165
.011
N/D
N/D
.003
100
18
0.08
0.2
0.07
1.2 300 157 15 60
0.3
0.1
0.006
N/D
0.006
0.001
43
0.3
0.01
N/D
0.006 5 T.2 50 2000
0.01
N/D
0.005
7
0.2
0.01 270 140 0.6 37
0.04
20
0.14
N/D
0.002
N/D 40 20 25 250
N/D
N/D
N/D
5
0.002
0.025
0.002
0.6
0.3
N/D 1000 520 0.9 20
N/D
N/0
N/D
N/D
0.002
0.085
< 2
Pretreataent
Coagulation
Filtration
Sedimentation
Filtration
None
Coagulation
Bio-Treatment
Filtration
Coagulation
210
TREATMENT
-------
Table 1
Influent
Project Type Compounds Cone
8 WU Benzene
Toluene
Acrylonitrile
Dichloroethane
Thiophene
Benzonitrile
Styrene
Xylene
Pyrldine
Aniline
Phenol
Benzofuran
Cresol
Napthalene
Quinoline
Indole
Dimethyl phenol
TOC
9 WU TOC
Chloroform
Phenol
Dimethyl phenol
Trichlorophenol
Dichlorophenol
Isopropyl phenol
Arochlor 1242
10 WU Chlorotoluene
Xylene
Dimethylacetamide
Pyradine
Dichlorobenzene
Dimethylamiline
Isophorone
Dichlorobenzene
Chloroform
Butylalcohol
Benzene
Tetrachloroethylene
Toluene
Hethanol
Acetic Acid
TOC
11 WW TOC
Phenol
Nitrophenol
Chlorophenol
Methyl pyrolodone
Dimethyl Sulfone
Chlorocresol
Dimethyl acetami do
Acetone
Benzene
Toluene
Xylene
Hexyloxyethenol
Butoxy Ethoxy Ethanol
12 WU Phenol
Chlorocresol
Trichlorophenol
Isophorone
Napthalene
Ethylbenzene
Chlorobenzene
Toluene
Trichloroethylene
Trichlorethane
Chloroform
Methylene Chloride
TOC
13 WW Phenol
Cresol
Dimethyl phenol
Dichloroethane
Dichloropropane
Trichloroethylene
Tertbutyl Alcohol
Acetone
TOC
. (mg/1)
5.8
2.1
0.15
0.06
0.42
4.9
0.5
0.5
12.9
3.5
29
0.4
5.6
3.6
5.2
7.0
0.9
345
14
0.026
0.254
0.015
0.077
0.053
0.168
0.015
2
0.7
1.2
0.06
0.04
0.2
3.2
0.24
0.62
0.170
0.11
0.4
0.185
167
800
2000
1100
18
6.5
1.9
.62
.27
.30
.79
.42
0.22
0.065
0.2
10.9
2.9
8.9
0.7
0.08
0.3
0.036
0.1
0.04
1.6
1.4
1.3
0.6
10.3
3400
69
107
2.9
0.18
0.05
0.16
0.62
1.43
400
..,,. . n Annual /../•
Effluent Q fi 6AC
Cone, (mg/1) GPM Gal x 10° 1/1000 Gal
0.08
N/D
0.03
N/D
N/D
N/D
N/D
N/D
0.5 280 180 14
0.07
0.04
N/D
N/D
0.001
0.001
0.0004
N/D
70
4
0.006
0.002
0.002 200 126 0.6
N/D
N/D
0.016
N/D
N/D
N/D
0.4
N/D
N/D 40 10 50
N/D
N/D
N/D
0.005
0.105
N/D
N/D
N/D
150
800
1000
N/D
N/D
N/D
.32
.18
N/D 55 20 12
.56
.29
N/D
N/D
N/D
N/D
N/D
0.7
N/D
N/D
Of\A
• U*f
N/D
N/D 40 8.0 15
N/D
N/D
0.1
OT
. I
0.25
21.0
1000
N/D
N/D
N/D
N/D 175 90 16
N/D
0.01
0.32
0.31
Contact
Time
(Min) Pretreatment
71 Filtration
100 Sedimentation
Filtration
250 Precipitation
Coagulation
Filtration
180 Coagulation
Neutralization
Filtration
250 Coagulation
Ammonia Strip
Filtration
57 Equalization
Filtration
TREATMENT
211
-------
Table 1
Project Type
14 WW
IS WW *
16 WW
>7 WW
Leachate
Compounds
TOC
Phenol
Dimethyl phenol
Cresol
Tertbutyl phenol
Ethyl benzene
Xylene
Tetramethy 1 butyl phenol
Benzene
THoxane
Toluene
Formaldehyde
TOC
Dlchloroethylene
Trlchloroethylene
Tetrachloroethylene
Trlchlorobenzene
Alkyl Phthalate
P.CB
TOC
Methylbenzolcacld
Phenol
Benzole Acid
Benzene
Toluene
Chlorobenzene
Ethyl benzene
Xylene
Cresol
Chlorooctane
Butoxy Ethoxy Ethenol
Olphenylether
01ethylbenzam1de
Phenoxy Toluene
Butyl toluamlde
Dlallylphthalate
Phenoxybenzyl Alcohol
TOC
Phenol
Benzole Add
Chlorobenzolc Add
Dlchlorophenol
Dimethyl butadiene
Chlorotoluene
Benzaldehyde
Xylene
Toluene
Tetrachloroethylene
Influent
Cone. («g/1)
610
13.5
0.38
0.35
2.1
8.4
26.4
2.1
0.025
0.035
0.3
100
18
0.46
0.40
0.07
0.005
0.034
0.060
860
33
2.8
0.9
0.8
5.1
3.8
2.6
9.3
4.2
2.7
6.2
2.1
4.8
9.6
253
11.0
79.1
3100
47
79
35
2.9
7.8
26.3
3.5
7.1
7.1
17.1
Effluent Q
Cone. fug/I) GPH
320
0.12
N/D
N/D
N/D
0.016 70
0.07
0.002
N/D
0.004
N/D
100
7
0.12
0.031
N/D 100
N/D
0.014
N/D
245
0.71
0.3
N/D
0.3
2.1
1.0 7
0.3
0.7
N/D
0.035
0.5
0.035
1.1
0.1
63
0.011
12
250
1.2
1.8
1.5
N/D 40
N/D
N/D
N/D
N/D
N/D
N/D
Annual Contact
"nnu" 8 GAC Tine
Gal x 10° 1/1000 Gal (Mln) Pretreatnent
36 45 140 Sedimentation
52 1.6 100 Filtration
3.6 64 1400 011 Skin
Equalization
Filtration
20 40 250 None
* Carbon 1s land-filled and not reactivated
central reactivation facility, is almost always more cost effective
than transporting and handling bulk liquids for diposal. Com-
pounded with environmental and safety concerns of handling bulk
liquids, it is apparent that disposal of bulk liquids is not as desirable
as the reactivation or disposal of spent carbon.
Despite the variability of treatment requirements, the majority of
projects utilize adsorbers containing 20,000 Ib, the equivalent of
one full truckload (due to over-the-road weight limitations) of
granular activated carbon. The size of the adsorbers allows the car-
bon to be handled in bulk, thereby reducing freight expenses.
Spent carbon is removed from the treatment system when
organic contamination is detected in the system effluent. Carbon
removal is accomplished by using air pressure to automatically
transfer the carbon out of an adsorber as a slurry. The slurry is
directed to a waiting truck which transports the carbon to a central
reactivation center. The transfer is accomplished in a closed system
with no worker exposure to the spent carbon.
Costs
Several factors influence the costs of adsorption:
•The type of contaminants present
•Influent concentrations
•Flow rates
•Carbon (volume and type)
•Discharge requirements
•Urgency and duration of the project
The applications shown in Tables 1 and 2 range in flow from 5 to
1000 gal/min, in TOC concentrations from less than 1 mg/1 to 3400
mg/1 and in carbon utilization from 0.1 to 64 lb/1000 gal. In addi-
tion, a wide range of organic compounds is also encountered. Us-
ing this information, treatment economics are more clearly defined.
Adsorption costs per volume treated are illustrated by the shaded
area in Figure 1. The costs are all-inclusive, encompassing the car-
bon, adsorption equipment, reactivation and transportation. In
two applications in which the carbon is landfilled for disposal, the
cost of landfill disposal is included. At low concentrations (TOC
below 10 mg/1, as in the case of many groundwaters), adsorption
costs range from a few cents to about $3/1000 gal treated. At
higher concentrations, costs rise. TOC concentrations of 1000 mg/1
result in GAC treatment costs ranging from $6 to $35 per 1000 gal.
Low polarity, low solubility organic compounds have the lowest
unit costs in each case.
System economics can be viewed in another way by calculating
the $/lb of contaminant removed, as shown by the shaded area in
Figure 2. At TOC concentrations above 1000 mg/1, removal costs
are below $4/lb TOC removed for all the organic compounds
212
TREATMENT
-------
Table 2
Project
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
Type
Truck Spill
Rail Car
Spill
Rail Car
Spill
Rail Car
Spill
Chemical
Spill
Chemical
Spill
Chemical
Spill
Gasoline
Spill
Solvent
Spill
Gasoline
Tank
Leakage
Rail Car
Spill
Chemical
Solvents
Gasoline
Tank
Leakage
Chemical
Solvents
On-Site
Storage
Tanks
Chemical
Spill
Chemical
Spill
On-Site
Storage
Tanks
On-Site
Storage
Tanks
Chemical
Landfill
Landfill
Site
On-Site
Storage
Tanks
On-Site
Storage
Tanks
Compounds
Methylene Chloride
1 ,1 ,1-Trichloroethane
Phenol
Orthachl oro-Phenol
Phenol
Vinyl idine Chloride
Ethyl Aery late
Tetrachl oroethy 1 ene
Chloroform
Carbon Tetrachl oride
Trichloroethylene
Chloroform
Carbon Tetrachloride
Trichloroethylene
Tetrachl oroethy 1 ene
Benzene
Tetrachl oroethy 1 ene
Benzene
Toluene
Xylene
1 ,1 ,1-Trichloroethane
Trichloroethylene
Tetrachl oroethy 1 ene
Methyl T-Butyl Ether
Di-isopropyl Ether
Trichloroethylene
Chloroform
Trichloroethylene
Tetrachl oroethy 1 ene
Trichloroethylene
Di-isopropyl Ether
Trichloroethylene
CIS-1 ,2-Dichloroethylene
Trichloroethylene
CIS-1 ,2-Dichloroethylene
Trichloroethylene
Tetrachloroethylene
CIS-1 ,2-Dichloroethylene
Trichloroethylene
Tetrachl oroethy 1 ene
Chloroform
Trichloroethylene
Trichloroethylene
1 ,1 ,1-Trichloroethane
1 ,l-D1chloroethylene
TOC
Chloroform
Carbon Tetrachloride
Etc., Etc.
CIS,l-2-Dichloroethylene
Trichloroethylene
Tetrach 1 oroethy 1 ene
Methylene Chloride
1,1 ,1-Trichloroethane
Influent
Cone, (wj/1)
21
25
63
100
32-40
2-4
200
70
3-4
130-135
2-3
0.8
10.0
0.4
10-20
0.4
4.5
9-11
5-7
6-10
143
8.4
26
30-35
30-40
50-60
20
30-40
140-200
40-50
20-30
20-25
10-15
50
5
5
10
5
5
10
300-500
5-10
30-250
60-80
5-15
20
1.4
1.0
14.0
0.5
1.0
7.0
1.5
3.3
Effluent Q
Cone, (mg/1) GPM
< 0.001 20
< 0.001
< 0.001 80
< 0.001
< 0.01 173
< 0.01
< 0.001 100
< 0.001 40
< 0.001
< 0.001
< 0.001
< 0.001 180
< 0.001
< 0.001
< 0.001
< 0.001 95
< 0.001
< 0.1 5
Total
< 0.001 350
* 0.001
< 0.001
< 0.005 450
< 0.001
< 0.001
< 0.001 30
< 0.001 260
< 0.001
< 0.001 450
« 0.001
< 0.001 160
e 0.001
< 0.001 250
< 0.001 85
« 0.001
< 0.001
< 0.001 150
< 0.001
< 0.001
< .1 200
< 0.001
< 0.001 350
< 0.001 350
< 0.001
< 0.005 20
< 0.001
< 0.001
< 0.001
< 0.001 165
< 0.001
< 0.001
« 0.10 20
< 0.001
.„-.„! Contact
GAC Annua1 , TIM
0/1000 Gal Gal x 10b (Min)
3.9 10.4 534
5.8 41.5 201
2.1 875 TVT* 60
13.3 300 TVT* 52
11.6 20.7 262
2.8 93.3 58
1.9 49.2 112
< 1.01 2.6 214
.40 191.9 15
.62 233.3 12
7.7 15.6 160
0.21 131.4 21
0.10 233.3 12
0.32 82.9 35
0.38 129.6 42
0.25 44.1 121
0.25 77.8 70
1.19 103.7 26
0.16 181.4 30
<0.45 181.4 30
1.15 10.4 41
0.8 85.5 64
4.0 10.4 526
* TVT - TOTAL
Pretreatment
None
Filtration
None
Filtration
None
None
None
None
None
None
Air Strip
None
Air Strip
None
None
None
None
None
Filtration
Air Strip
None
Filtration
None
None
VOLUME TREATED
TREATMENT
213
-------
Table 2
Project Type
24 On-slte
Storage
Tanks
25 On-Slte
Storage
Tanks
26 On-S1te
Well
Storage
Tanks
27 Chemical
By-
Products
28 Hfg.
Residues
29 Leachate
Compounds
TMchloroethylene
Xylene
Isopropyl Alcohol
Acetone
1,1,1-Trlchloroe thane
1 ,2-D1chloroethylene
Xylene
CIS-l,2-D1chloroethylene
Trlchloroethylene
Tetrachl oroethy 1 ene
Dl-lsopropyl Methyl
Phosphonate
Dlchloropentadlene
DDT
TOC
1 ,3-Dichloropropane
Hexachloroe thane
Hexachlorobenzene
Hexachlorobutadlene
Influent
Cone, (mg/1)
3-8
.2-. 5
.2
.1
12
0.5
8.0
0.2
0.5
2.0
1.25
0.45
0.004
9.0
0.01
3
4
6
Annual Contact
Effluent Q GAC fi Time
Cone, (mg/1) 6PM 1/1000 Gal Gal x 10° (M1n)
< 0.001 30 1.54 15.6 36
< 0.001
< 0.01
< 0.01
< 0.005 200 1.0 103.7 52
< 0.001
* 0.001
< 0.001 150 0.75 77.8 70
< 0.001
< 0.001
< 0.05 175 0.70 90.7 30
< 0.01
O.0005 160 1.8 82.9 31
-
< 0.001
< 0.001 200 1.0 103.7 30
< 0.001
< 0.001
Pretreatment
None
None
None
Filtration
Filtration
1,000
100
1,000
100
10 -
10 20 30 40 50 60 70 80 90 100 110 120
Treatment Cost ($71000 Gallons Treated)
6 12 18 24 30
Treatment Cost ($/lb.TOC Removed)
Figure 1
Influent TOC Concentration vs. Treatment Cost (Gal treated)
Figure 2
Influent TOC Concentration vs. Treatment Cost (Ibs TOC removed)
214
TREATMENT
-------
listed. At lower concentrations, removal costs ranged from $6 to
$30/lb of TOC. In field applications, the economy of the successful
isolation of a concentrated point source can be readily seen. At
high concentrations, proportionally high percentage loadings are
possible. This reduces carbon usage and results in more favorable
treatment costs. The best way to determine treatment cost for a
particular stream is to test in a pilot plant.
ACCELERATED COLUMN TESTING
Once installed, the system must be effective in removing the con-
taminants and operate in a cost-effective manner. The key to
designing an operational adsorption system for a particular ap-
plication hinges on the validation testing done before installation.
Until now, necessary validation testing was often time consuming
and expensive. Extensive time consumption results from pilot
systems that totally simulate full-scale systems, therefore requiring
the same time period to saturate carbon as a full-scale system. In
the case of groundwaters, where systems can be on-line for months
or longer, feasibility testing time requirements limit the ability to
respond quickly to contamination emergencies.
Responding to a need for much shorter and accurate tests to ob-
tain design and predicted performance data, Calgon R&D
developed the Accelerated Column Test. The ACT is an improved
technique for testing carbon's ability to remove organic impurities;
it combines the speed of an isotherm with the accuracy of a pilot
column. The ACT can compress a month-long pilot study into a
few days, saving money and time, which can be a critical factor in
responding to spills or other emergencies.
Table 3
Concentration Factors
Project
1-3
1-5
1-10
1-11
1-16
1-17
2-1
2-4
2-5
2-7
2-21
2-22
2-38
TOC (mg/1)
700
40
2,000
400
18
3,100
45
200
200
4.9
20
8.5
9
lb/1000 Gal
15
0.6
50
16
1.6
40
3.9
13.3
11.6
1.9
1.15
0.8
1.1
Loading
mg/gm-
GAC
389
278
334
209
94
640
96.2
125.4
143.8
21.5
145.0
88.6
68.2
Loading
1/gm
Carbon
.555
6.95
.167
.52
5.2
.206
2.1
.627
.719
4.39
7.25
10.4
7.58
Concentra-
tion Factor
277
3,475
84
260
2,606
103
1,069
313
359
2,195
3,626
5,212
3,790
Table 4
Act Field Comparison
Field*
Conditions
ACT
Simulation
Influent Phenol
Concentration (mg/1)
Effluent Phenol
Concentration (mg/1)
Lbs/1000 Gallons
(Initial Breakthrough)
Lbs/1000 Gallons
(Saturation)
29
<1
16
14
mg/1
35.7
<1
12.5
10.7
mg/1
*The high variability of industrial waste influent is the primary reason for variability between ACT
simulation and field conditions.
1O,000
1,000
100
10
10
100 1,000
Influent TOC Concentration (mg/l)
10,000
Figure 3
Concentration Factor vs. Influent TOC Concentration
THREE WAY
VALVE
VENT
LIQUID
RESERVOIR
t UV CONTINUOUS MOMTORNM
2. TOC LOW LEVEL
X TOC HIGH LEVEL
4. CC FLAME KWIZATON
t. OC ELECTRON CAPTURE
DETECTION SYSTEM
100 r
Figure 4
Basic System
ACETOXIME/P-NITROPHENOL
1 FOOT BED DEPTH/7 GPM/FT1
ACCELERATED TEST VS11NCH COLUMN
% BREAKTHROUGH/
SO
25
ACETOXIME BREAKTHROUGH
ACT
___-1 INCH COLUMN
P-NITROraENOL BREAKTHROUGH
ACT
___ i1NCH COLUMN
JL
JL
20 40 60 80 100 120 140 160
VOLUME (LITERS)
Figure 5
Multicomponent Adsorption
180 200
TREATMENT
215
-------
The ACT generates data equivalent to a conventional laboratory
scale or field study, which can then be easily translated into a full-
scale design. Because only a few days are required to perform the
tests, problems with sample degradation or loss of volatile com-
ponents are eliminated. In fact, field validation of ACTs
demonstrates a degree of accuracy that is difficult to match with
any of the other more time-consuming methods.
Acceleration of the carbon adsorption cycle is achieved through
a scaling down of conventional column testing hardware. Except
for reduced scale, other components of the test system and the
overall system design are essentially identical to larger scale
laboratory or field evaluation systems (Figure 4). The technology
behind the ACT is based upon Calgon discoveries relating to the
basic kinetics of carbon adsorption. Using kinetic data, a
mathematical model of the column adsorption process was
developed. With this model, breakthrough curves for full-scale ad-
sorption systems are readily predicted from data generated by the
scaled-down column.
To confirm the validity of the ACT, a series of tests were con-
ducted comparing the ACT against a conventional 1 in. column for
the prediction of breakthrough for both strongly and weakly ad-
sorbed components. For the purpose of this test, a synthetic stream
containing acetoxime and paranitrophenol was prepared. The ac-
celerated test successfully predicted the performance of the 1 in.
column (Figure 5). This degree of correlation was maintained in 30
additional tests under a variety of operating parameters.
The ACT was also applied to several full-scale systems already in
operation. Actual operating data, compared to the ACT results,
are presented in Table 4. The influent phenol concentrations on the
full-scale system and ACT were 29 mg/I and 35.7 mg/1 respectively.
The ACT accurately predicted removal to less than 1 mg/1 phenol.
The close correlation with full-scale data shows that the ACT is a
valuable tool in predicting system performance; however, inherent
to the test is the small quantity of influent needed. This makes the
representativeness of the sample used critical to the accuracy of the
ACT results. Likewise, in systems where actual field operation has
highly variable influent characteristics, the ACT will predict the
performance corresponding to the influent characteristics of the
sample collected.
CONCLUSIONS
In summary, wastewater treatment is, and will continue to be, a
dominant concern for industries and municipalities. Granular ac-
tivated carbon is effective for removal of a broad range of con-
taminants over a variety of treatment conditions and concentra-
tions. Granular activated carbon treatment is cost-effective, mak-
ing this technology a viable alternative for point source, end-of-
pipe and groundwater treatment.
Finally, Calgon has introduced a quick, cost-effective Ac-
celerated Column Test to improve carbon system design and per-
formance prediction.
216
TREATMENf
-------
TREATMENT OF HAZARDOUS LANDFILL LEACHATES
UTILIZING IN-SITU MICROBIAL DEGRADATION
DAVID S. KOSSON
ROBERT C. AHLERT, Ph.D.
Department of Chemical and Biochemical Engineering
Rutgers University
Piscataway, New Jersey
INTRODUCTION
Industrial wastes have been frequently placed in landfills,
lagoons and uncontrolled dump sites, subsequently producing li-
quid residuals as the result of compaction, rainfall runoff and in-
filtration, and biodegradation. These liquids can leach from a
disposal site and contaminate underlying groundwater and adja-
cent surface waters.
Leachate management creates many dilemmas, both economic
and technical. These wastewaters are highly complex; composition
is site-specific and subject to seasonal variability. Treatment often
necessitates collection and transport of large volumes of hazardous
liquids, bulk oil and contaminated water, as well as waste con-
tainers, solid waste and soil. The potential for further dispersion of
hazardous substances in the environment is increased by the
cleanup process itself.
An in situ treatment process for treatment of aqueous landfill
leachates has been developed. Transport of hazardous materials is
avoided, offering safety and economic advantages. A combination
of physical, chemical and biological processes results in effective
ultimate disposal. Landfill leachate is pretreated to remove suspen-
sions, dispersed oil and heavy metals. Subsequently, treatment is
effected with a land based biological process. Utilizing aerobic and
anaerobic degradation processes associated with mixed microbial
populations, hazardous waste treatment is viewed as proceeding
either in the landfill structure or in a neighboring soil system.
RELATED RESEARCH
A viable in situ process must (1) operate within natural en-
vironmental temperature and precipitation fluctuations, (2) allow
for monitoring of treatment in progress and (3) provide an effective
pathway for safe ultimate disposal. Three primary studies of in situ
biodegradation of landfill leachates have been conducted. The first
study was conducted by Pohland.' His experimental system con-
sisted of four 3-ft diameter columns containing 10 ft of un-
shredded, compacted refuse covered with 2.5 ft of soil. Leachate
was collected from the base of the columns and recycled by means
of a distributor located at the interface between the soil and com-
pacted refuse. The refuse was domestic in origin and not of in-
dustrial character.
Refuse of the composition used by Pohland is more readily
biodegradable than the recalcitrant organics found in landfill
leachate of an industrial or hazardous nature. The effects of initial
sludge seeding and pH control on the rate of biological stabilization
of the refuse and resulting leachate were studied. Through analysis
of results over approximately three years, Pohland concluded that
recycling leachate helped to stabilize the refuse and leachate. Both
pH control, at approximately 7, and initial addition of sewage
sludge enhanced the rate of decrease of organic pollutants in the
leachate.
Tittlebaum2 conducted a second study using an experimental ap-
paratus similar to that of Pohland. Tittlebaum investigated the ef-
fects of refuse shredding on the rate of refuse and leachate organic
carbon (LOC) stabilization. The refuse had a composition com-
parable to that studied by Pohland. The effects of pH control,
nutrient control and initial sludge seeding were also considered.
After 514 days of operation, Tittlebaum concluded that refuse
shredding had little effect on the rate of stabilization. He also con-
cluded that nutrient control did not offer any advantage. However,
the refuse was readily biodegradable. Other conclusions were in
consonance with Pohland.
Another relevant study examined microbial degradation of
hazardous organic substances, resulting from spills, in soil
systems.' At a high octane gasoline spill in Whitemarsh Township,
Pennsylvania, stimulation of an indigenous microflora population
was utilized successfully to degrade the organics contaminating a
dolomite aquifier. Addition of nutrients and aeration stimulated
biodegradation of the gasoline residuals. Biodegradation required
approximately two years; data indicated approximately 95% of the
residual material was degraded.
PROCESS DESCRIPTION
The indigenous microflora of the soil or landfill is supplemented
through the addition of an inoculum of a mixed microbial popula-
tion derived from the secondary sludge of a municipal sewage treat-
ment facility. The microbial population is established in the soil
system through daily additions of an aqueous, nutrient-balanced,
glucose feed medium for ten days. Subsequent to the establishment
of the microbial population, daily additions of landfill leachate
with supplemental nutrients and glucose were distributed on the
surface. Prior to application, the leachate is pretreated using a lime
flocculation/recarbonation sequence developed by Slater.4
Natural selection is allowed to control the process as completely
as possible. Stratification results in response to chemical and
physical gradients that exist in the vertical profile of the treatment
zone. The principal gradient is in oxygen concentration. The ox-
ygen concentration is greatest at the surface, where diffusion from
ambient air drives the gradient. The oxygen concentration
diminishes with depth as it is depleted by aerobic respiration. This
leads to aerobic communities near the surface; anaerobic com-
munities dominate at greater depths. Other important gradients in-
TREATMENT
217
-------
elude available substrate and nutrients, pore water and
temperature. Competitive adsorption by the soil also creates an im-
portant gradient. Readily adsorbed components of the leachate will
be in greater concentration near the surface. Others will
predominate at greater depths.
EXPERIMENTAL DESIGN
Pilot-scale field demonstrations have been carried out with soil
filled, self-contained lysimeters (SCLs). The effective soil column
was 2 ft in diameter and 4 ft deep. A once-through configuration
has been employed.
The experiment was designed to evaluate the biochemical and
physical processes involved at a scale suited tcr simulation of field
conditions including soil type, permeability, cation exchange
capacity, moisture distribution, soil water activity, etc. Effluent
streams were collected continuously in entirety, under the vacuum
employed to balance capillary forces in the soil pore structures.
Thus, complete mass balances were possible. Two soil types, a
sandy loam and a clay loam (Table 1, have been evaluated at several
SO. <1 - S.AJ, Liu.
•—• InHuMt
tr--tL Effluent
(I In I Aru • ].«.)
48 60 68 189 128 148 160 11)8
TINC (MTS)
figure I • Influent end effluent Quantities
Figure 1
Influent and Effluent Quantities
le
1 1 1 1 1 \—•—r
28 48 68 SB 108 129 140 168 108
II* (MTS)
Figure 2
Influent and Effluent Quantities
feed dilutions and compositions. Leachate samples were obtained
from a USEPA designated "Superfund" site.
HYDRAULIC RESPONSE
Throughout the period of operation, influent was applied daily,
batchwise. The permeability of the soils varied considerably during
the experiment. Initially, there was considerable adsorption of in-
fluent by the soil as field status was established. After this period,
the original hydraulic loading target of 1 m/day was unreasonable.
A more workable hydraulic loading of approximately 0.5 in./day
was adopted.
When the permeability decreased significantly, it could usually
be increased by turning the top several inches of soil. Decreases
were probably the result of increased microbial growth in the
aerobic regions of the soil, near the surface. Suspending the ap-
plication of influent for short periods resulted in an increase in
permeability. On a larger scale, it would probably be advantageous
to turn the soil at regular intervals and to design excess capacity for
intermittent operation.
Small daily fluctuations of influent and effluent volumes most
likely resulted from the complex nature of the soil-water systems;'
see Figures 1 and 2. Long term decreases in permeability may be ac-
counted for by the increased mass of microflora. The three SCLs
containing clay loam displayed increasing permeability during ap-
proximately the first 100 days, as indicated by increasing influent
and effluent quantities. This is probably a result of a shift of the
sodium/calcium balance of the soil. The high concentration of
calcium ions in clarified leachate from lime flocculation pretreat-
ment can lead to soil aggregate formation, resulting in increased
permeability.6-7 Very small differences between influent and ef-
fluent quantities are the result of evaporation and variations in field
status. Maintaining uniform packing was difficult at times. Initial-
ly, continued settling of soil frequently allowed influent to pass
along relatively few pathways. When channeling occurred, the top
few inches, sometimes more, of soil were loosened and repacked.
Eventually channeling was eliminated, although it did reoccur
periodically. Periodic episodes probably resulted from cyclic drying
and saturation of the soil, inherent with batchwise influent addi-
tions. On a larger scale, channeling should not present difficulty.
Table 1
Soil Composition In Lysimeter Tests
Parameter
Designation
Sand (%)
Silt (%)
Clay (%)
Organic Carbon (%)
Total Nitrogen (%)
C.E.C. (meq/100 gin)
PH
Total Metals (mg/kg)
Cadmium
Chromium
Copper
Lead
Nickel
Zinc
Metals soluble in 0.1 N HC1
(mg/kg)
Cadmium
Copper
Iron
Lead
Nickel
Zinc
Glacial Till
Clay loam
35
37
28
1.34
0.12
6.9
5.54
1.0
6.2
12
10
19
70
0.10
0.49
40
1.2
0.3
3.2
Alluvlam
Sandy loam
59
24
17
0.52
0.06
3.6
5.41
1.0
4.2
6.8
10
7.9
44
0.10
2.1
105
4.5
0.30
7.4
218
TREATMENT
-------
4500-
1250-
u
3
•j 750-
500-
250-
0 —
.
_J 1
1 20
1 '
40
r-
a
• \ '
80
Toul
1 1
1 . ' 1 ' 1 ' 1
100 ' 120 140 161
li
700
SCL I 1 - Sandy Loam
21000-
TIHC (DAYS)
Figure 3
Influent Organic Carbon
SCL I 1 - Sandy Loam
12000-
-, 1 • 1 • 1 P 1 1 1 P 1 I 1 I | *•
0 20 40 60 80 100 120 140 160 180
TIME (DAYS)
Figure 4
Influent Total Organic Carbon, Mass Basis—6 Day Average
TOTAL ORGANIC CARBON RESPONSE
Total organic carbon was monitored throughout the experiment.
During 161 days of operation, the influent TOC consisted of eight
regimes including the dextrose-only feed solution for the initial
development interval (Table 2 and Figure 3). Six leachate samples,
exhibiting considerable variability, were used (Table 3). Dilutions
with sparged potable water were used to maintain the desired in-
fluent TOC concentration.
Effluent TOC was measured on alternate days. Because of vary-
ing flow rates through the SCLs, TOC data was evaluated in two
forms. The first approach was a concentration basis, with typical
units of mg TOC/1. The second approach was a mass basis; this
meass quantity is the product of daily effluent (influent) quantity
and TOC concentration. On days when effluent TOC was not
measured, the concentration was approximated by linear interpola-
tion.
The effluent TOC was low, if not negligible, during operation
with type A influent for all SCLs. Transition to type B influent
300 -
• I • I • I • I • I • I < I ' I
' 20 40 60 80 100 120 140 160 ISO
TIME (DAYS)
Figure 5
Effluent Total Organic Carbon, Mass Basis—6 Day Average
„ set i s - city IOM
1 r T r 'i ' i ' i • i ' i ' i r
0 ?0 40 10 80 100 UO 140 160 180
TIHC (UTS)
Figure 6
Influent Total Organic Carbon, Mass Balance—6 Day Average
700-
SCL I 5 - Clay Loam
1
g 300 —
100-
I
80
120
I
160
100
TIME (DAYS)
Figure 7
Effluent Total Organic Carbon, Mass Basis—6 Day Average
180
TREATMENT
219
-------
Table 2
Feed Solution Composition, Field Experiments
Type Dates (Days)
A 6/15/82-6/24/82(01-10)
B 6/25/82-7/16/82(11-32)
C 7/1 7/82-8/04/82 (22-5 1 )
D 8/05/82-8/10/82 (52-57)
E 8/11/82-8/19/82(58-66)
F 8/20/82-9/16/82 (67-94)
G 9/17/82-11/05/82(95-144)
H 1 1/06/82-1 1/22/82 (145-161)
(NH4hSO4/Trace Element Solution contains:
50 g/l (NVUnSO* 10 g/l MgSOt ' 7H2O
50 mg/l FeCb • 6H2O 1000 mg/l MnSO4 • H2O
750 mg/l CaCl2
TOC GOC
(mg/l) (mg/l)
1050 1050
1100 210
230 210
510 210
4500 210
710 210
1010 210
930 210
Trace Elements
LOC Leachate Solution 1M K2HPO4
(mg/l) Vol %, * (ml/1) (ml/1)
0 - 25 25
890 6.6% EPA-04 5 5
20 6.6% EPA-05 5 5
300 100% EPA-05 12 6
4290 100% EPA-05A 12 6
500 100% EPA-06 33 18
800 4.5% EPA-07A 50 27
720 4.5% EPA-07B 50 27
All dilutions made with dcchlohnated (sparged) potable water.
Table 3
Leachate Characteristics
Parameter Raw Leachate
pH 5.6 - 6.0
COD 1000-36000*
TOC 300-18000
TDS 2100-28000
Turbidity 75-150 NTU
Color Brown
Conductivity 5000-3500 pu/cm
Na lO'-lO6
Fe IQMO5
Mg lOMO3
Ca 10M06
Pretreated Sample TOC
EPA-04 13500*
EPA-05 300
EPA-05A 4500
EPA-06 710
EPA-07A 18000
EPA-07B 16100
•All values reported in mg/l unless noted otherwise
+ This pH is adjusted to the desired value
Pretreated
Leachate
12 +
1000-36000
300-18000
0
Yellow
1-10
0-1
COD
35000
1000
1100
34900
36100
dicate net reductions in TOC of over 95%. SCLs 3 and 4 showed
net TOC reductions of approximately 90%. Lower reductions in
TOC were due to prolonged periods of channeling in these col-
umns.
DESIGN CONSIDERATIONS
Process designs must be developed on a site specific basis. The
parameters that control the extent of microbial degradation and the
depthof the aerobic and anaerobic zones are hydraulic loading,
organic carbon content, carbon-to-nitrogen-to-phosphorous ratios,
buffer strength, supplemental energy (carbon) source and optimum
pH. The process can be run once-through on an intermittent or on
a continuous basis. Intermittent operation permits recovery of the
aerobic bioslime zone during the intervals between flooding. The
process can be operated with intermittent or continuous recycle,
also. Recycle allows control of feed stream organic carbon concen-
tration, i.e., dilution and overall carbon conversion. Recycle to
zero effluent carbon concentrations appears feasible for a "closed"
site. Effluent "polishing" may be required prior to discharge.
REFERENCES
1. Pohland, F.G., "Sanitary Landfill Stabilization with Leachate Recycle
and Residual Treatment," USEPA Report No. EPA/600/275/043,
Environmental Protection Technology Series, 1975.
2. Tittlebaum, M.E., "Organic Carbon Content Stabilization Through
Landfill Leachate Recirculation," JWPCF. 54, 1982, 428-433.
3. Chapin, R.W., "Microbiological Degradation of Organic Hazardous
resulted in a delayed response in SCLs 1, 2, and 3 (sandy loam)
followed by an adaptation period. The response delay varied from
approximately 13 days (SCLs 1 and 2) to 19 days (SCL 3). The
adaptation period varied in duration from approximately 10 days
(SCL 2) to 25 days (SCL 1). Maximum effluent TOC was between
134 (SCL 2) and 278 mg TOC/1 (SCL 1) or 994 and 1764 mg
TOC/mVday. A second peak in effluent TOC from the SCLs
packed with the sandy loam was in response to type E influent.
SCLs 3, 4 and 5 (clay loam) did not exhibit response or adaptation
periods until after 60 to 80 days. Typical long-term influent and ef-
fluent TOCs on a mass basis are shown in Figures 4 through 7.
Integration under the curves of influent and effluent TOC on a
mass basis for SCL 1 and 2 (sandy loam) and 5 and 6 (clay loam) in-
Substances: A Review of the Art and Its Application to Soil and
Groundwater Decontamination at the Goose Farm Hazardous Waste
Site, Plumsted Township, New Jersey." USEPA Region II, Hazard
Response Branch, Technical Assistance Team, Aug. 1981, 1-3.
4. Slater, C.S., "Coagulation/Flocculation and Oxidation Processes for
Pretreatment of Wastewater," Progress Report under Cooperative
Agreement CR807805 with USEPA, 1982.
5. Brady, N.C., The Nature and Properties of Soils, 8th Edition, Mac-
millan Publishing Co., Inc., New York, 1974.
6. Carlile, B.L. and Phillips, J.A., "Evaluation of Soil Systems for Land
Disposal of Industrial and Municipal Effluents," Water Resources
Research Institute of the University of North Carolina, Report No. 118,
July 1976.
7. Bonn, H., McNeal, B., and O'Connor, G., Soil Chemistry, John Wiley
& Sons, New York, 1979.
220
TREATMENT
-------
IN SITU TREATMENT ALTERNATIVES AND
SITE ASSESSMENT
DONALD G. MILLER, JR.
Law Engineering Testing Company
Marietta, Georgia
INTRODUCTION
Remedial action alternatives at sites contaminated by waste
management practices should be evaluated on the basis of technical
feasibility, cost and long term effectiveness.' One set of alter-
natives, in situ treatment, is attractive because it can result in
minimal exposure and eliminate off-site transportation of the
waste. In situ treatment, however, is questionable with regard to
physical and chemical uniformity of treatment and long term
chemical stability. Experience with numerous projects has
demonstrated the need for adequate physical and chemical
characterization of the system to be treated.
In situ treatment as considered in this paper is restricted to the in-
troduction of chemicals into the subsurface, rendering con-
taminants less hazardous to the environment (Figure 1). The pro-
cess has also been referred to as neutralization/detoxification2 or
detoxification and stabilization.3
In this paper, the author addresses in situ treatment of inorganic
contaminants, primarily heavy metals, although similar concepts
and physical characteristic concerns may be applicable to in situ
biodegradation. In spite of demonstrations of physical feasibility
by full scale tests, current use is limited because of the concerns of
overall reliability and costs associated with demonstration and im-
plementation. An understanding of these concerns is necessary to
properly evaluate in situ treatment as an alternative.
BASIC APPROACH TO ASSESSMENT
The basic steps in assessment of in situ treatment are summarized
in Figure 2. Additional details regarding initial feasibility and cost
review, physical characterization and chemical characterization are
presented in the following sections.
Initial Feasibility and Cost Review
This initial evaluation is based on available data and is intended
as a "fatal flaw" screening. The projected costs of other conven-
tional alternatives are estimated to provide a basis for comparison.
A maximum dollar amount for in situ treatment is therefore
established. A conservative estimate (probable maximum cost) of
the in situ treatment system cost is then developed. If the available
dollar amount would allow construction of such a system, then the
next stage of assessment is appropriate. Otherwise, in situ treat-
ment need not be evaluated in further detail.
For example, the maximum projected costs of conventional
alternatives are normally associated with off-site treatment and
disposal. If a waste comprises a one acre area to a depth of 10 ft,
the costs might typically be estimated based on the excavation,
SURFACE APPLICATION
V
TTTT
SHALLOW TRENCHES
WELLS
/ \
Figure 1
Basic Concepts of Treatment Fluid Application
transportation and disposal costs, approximately $100/yd3. For
this example, this off-site disposal would be about $1.6 million.
For in situ treatment the site requires injection wells to a depth of
10 ft at a cost of $40/ft (including a distribution system) plus an ad-
ditional evaluation cost of $50,000 and an operation/maintenance
allowance of $100,000. Wells could be spaced on approximately 3.5
ft centers across the site without exceeding the $1.6 million cost for
off-site removal.
Experience indicates that such spacing should be adequate for
subsurface materials behaving hydraulically as sands and silts and
possibly adequate for some finer grained, lower permeability
materials. Assuming the site met these characteristics, it would then
be feasible to proceed with the physical and chemical characteriza-
tions required for in situ treatment.
IN SITU TREATMENT
221
-------
PHYSICAL CHARACTERIZATION
The physical characterization attempts to determine how the
treatment fluids will move into the mass of material to be treated.
The mass to be treated may be either unsaturated, saturated or
both. The key factors are the lateral and horizontal extent of
various waste and subsurface materials and their corresponding
hydraulic properties. These factors can be effectively evaluated by
an incremental characterization as summarized in Figure 3.
The initial model of fluid movement is an extention of the initial
feasibility and cost review and is based on available site informa-
tion or limited additional data gathering. Plan drawings and sub-
surface profiles summarizing the subsurface conditions are the
primary components of the model. Boundary conditions and ques-
tionable areas are thus defined.
INITIAL FEASIBILITY
AND COST REVIEW
PLANS FOR IMPLEMENTATION
Figure 2
Flow Chart of In Situ Alternative Assessment
There are several techniques including conventional soil borings,
test pits and geophysical surveys that can be used to determine the
uniformity of wastes and subsurface materials in both lateral and
horizontal extent. At a settling pond site, reconnaissance revealed
some harder, apparently cemented, layers near the surface of the
waste. The waste, covering several acres, was a byproduct of a
single process. At this site, the immediate question was whether or
not these harder layers were laterally continuous, which would cer-
tainly impede the vertical movement of treatment fluids.
A shallow seismic refraction survey was performed. The survey
revealed a simple two layer system of unsaturated waste materials
approximately 20 ft thick overlying saturated waste. The shallow
refraction survey did, however, reveal a localized subsurface
anomaly related to an earlier stage of pond construction.
The type of detailed testing necessary to confirm the hydraulic
characteristics of waste and subsurface materials depends on
whether the materials are saturated or unsaturated. The degree of
saturation can be determined on the basis of conventional
laboratory measurements or by field measurements (geophysical
logging in boreholes).
INITIAL MODEL REVIEW
FLUID MOVEMENT
VERIFICATION OF
UNIFORMITY
DETAILED TESTING TO CONFIRM
WASTE/SUBSURFACE
CHARACTERISTICS
PREDICTION OF
FLUID MOVEMENT
FULL SCALE TESTING
VERIFICATION OF TREATMENT
QUANTITES AND TIME
Figure 3
Flow Chart of Physical Characterization
Porosity, important for evaluation of flow in saturated and un-
saturated materials, can also be determined in the laboratory or in
the field. Comparisons of laboratory and field measurements for
degree of saturation and porosity for waste in a partially drained
impoundment are shown in Figure 4. The laboratory degree of
saturation was based on a weight-volume relationship for un-
disturbed sampled. The field degree of saturation was based on
geophysical logging (density, gamma ray and velocity logs). The
field measurements of porosity (based on compensated bulk densi-
ty logs) were generally higher than the laboratory measurements.
Compression of the waste material during sampling and extruding
in the laboratory most likely accounted for the lower laboratory
values of porosities. Note that these porosities of the waste are
much higher than the 10 to 60% typically expected for natural
soils.4
A key factor in predicting movement of treatment fluids is
saturated permeability (hydraulic conductivity). Field
measurements in specially constructed observation wells or
piezometers are generally thought to produce measurements most
representative of the in situ materials. However, except in the case
of specially constructed test facilities, the permeant commonly used
is water. Laboratory tests on undisturbed samples allow use of
various fluids for permeants and thus the potential for changes in
permeability due to chemical reactions can be more thoroughly
evaluated because of controlled conditions. Changes in permeabil-
ity (reductions being the worst case with respect to time and extent
of in situ treatment) due to in situ chemical reactions have not been
thoroughly evaluated and are one of the primary concerns with
respect to use of in situ treatment. With some wastes, however,
misleading results can be obtained in the laboratory due to distur-
bance and incomplete saturation.
222
IN SITU TREATMENT
-------
90
*
> 8O
n
Q
I
g
_»
70
• 0
SO
tt «z
81
if
7t
Cf
**
H. -^ x too*
77
Vv - VOLUME OF VOIDS IN SOIL MASS
V - TOTAL VOLUME OF SOIL MASS
IIS >3 !
PI ltd !
i<" tOK _|!
i^; s»< <2
>J3 "jt. J?
!& 3! !i
sss; si: si
«
U. LOOGI
1 TC«T Al
PK
I>
*t
100
to
*. •«
z
0
H
4
C
3
< "
(ft
n
CO
• A
AVO. AVO.
-
97
• 1
-
Vw
91
AVO.
• 7
S • -yy X 100%
Vw • VOLUME OP WATER tN SOIL MASS
Vv • VCLUMK OF VOIDS IN SOIL MASS
I ;
ii L
"FJ; <"
IS !°
Ok * uz
loE n =
0
2
5
§
j
<
u
>
O
y
o
Figure 4
Summaries of Laboratory and Field "to Saturation
and Porosity for Confidential Waste Site
cr-i
01 D
a
CP-l
CP-l
CL-I
CT-I O A O "-I
CT-4 O A O«T-«
CP-l
CL-S
CP-l
a
CP-4
a
Q MONITORING WELLS
(2-C SCREENED SECTION, 5' BELOW GROUND WATER)
A MONITORING WELL AND LYSIMETERS
(1 LYSIMETERS AT 3, «. * 10FT.)
O TENSIOMETER STRING
(4 TENSIOMETERS AT 2, I, I, 4 I IFT.)
NUMBER INSTALLED
POND SURFACE
"
GROUND WATER
-\
O
a
WELLS «
LYSIMETERS 8
TENSIOMETERS It
Figure 5
Full Scale Test Facility
IN SITU TREATMENT 223
-------
For saturated materials, the prediction of fluid movement time
and distance into the waste mass can be accomplished by use of the
relatively simple equations' involving hydraulic conductivity,
porosity and quantity injected. The use of more sophisticated com-
puter models' is generally required for unsaturated flow conditions.
The latter model should be calibrated by full scale tests.
The full scale test apparatus for a mass of partially saturated
waste is shown schematically in Figure 5. The monitoring wells (2
in. O.D. PVC with bentonite seal at groundwater level and
manufactured screen extending into the groundwater) were used to
monitor changes in groundwater levels and to allow sampling for
chemical analyses. The pressure vacuum lysimeters, utilizing suc-
tion of pore water through a porous cup, were used to obtain water
samples for chemical analyses from above the groundwater level.
The mercury manometer type tensiometers were used to measure
negative pore water pressure around a porous tip. Negative pore
water pressure values along with water characteristic data are input
to the unsaturated flow computer model.
Data from the full scale tests can then be used to verify the treat-
ment method, quantities of treatment fluids and treatment times.
In the field test described in the preceding paragraph, it was deter-
mined that the water content of the waste should be slightly less
than required for saturation to be efficient with respect to treat-
ment fluid mixing and displacement of pore water. Thus, the op-
timum level of pore water pressure (as monitored by tensiometers)
to achieve miscible displacement was approximately 200 mb. This
meant that using natural rainfall with periods of wetting and
drainage to advance the treatment fluids would be more desirable
than flooding or injection to treat the contaminated unsaturated
zone. In fact, according to the theory of miscible flow,7 maintain-
ing complete saturation would result in flow of treatment fluid and,
thus, treatment only through the larger pores in the waste mass.
CHEMICAL CHARACTERIZATION
The general steps in the chemical characterization for in situ
treatment are summarized in Figure 6. The initial definition simply
consists of a tentative selection of a treatment process. For in-
organic contaminants, this may consist of reduction (i.e., Cr(VI) to
Cr(III)) or neutralization and precipitation. Thus, analyses must be
made of concentrations of contaminants at the site. Initially,
analyses typically available for site characterization and proper
evaluation of any alternatives should suffice. Care must be taken,
however, to distinguish between tal and dissolved metallic consti-
tuents.
The vertical and horizontal distribution of contaminants must be
defined to determine whether the treatment is to be applied
uniformly across the site or directed toward somewhat isolated
"hot spots." Sites with inorganic contamination typically exhibit
increased specific conductance of the pore water. Therefore, con-
taminant zones become excellent targets for electrical resistivity
surveys. The general approach for such surveys is described by
White and Brandwein.'
At a site in the southeastern United States, a combination of
review of pre-construction topographic maps, conventional soil
borings and surface geophysical surveys identified previous, now
buried, drainage features which corresponded to zones of increased
permeability. These zones provided paths of preferential movement
of various heavy metals and salts. These preferential flow zones
then became the focus for potential in situ treatment.
At this site, with preferential flow zones, the contaminants in-
cluded Fe, Zn, Ni, Cd, Cr and Pb in concentrations ranging from
21,000 to 2 mg/1, respectively. The groundwater within the con-
taminated zones had a pH as low as 2.5. The in situ treatment alter-
natives included introduction of calcium hydroxide for neutraliza-
tion and precipitation of each metal as the hydroxide. Considering
the species and concentrations, it was estimated that up to about
0.5 Ib of lime would be required for treatment of each gallon of
contaminated groundwater. Although this amount would not have
been prohibitive, there were other questions such as the ability to
INITIAL DEFINITION
OF TREATMENT PROCESS
CONTAMINANT CONCENTRATION
AND DISTRIBUTION
EVALUATION OF
SUBSURFACE GEOCHEMISTRY
PREDICTION OF
FLUID MOVEMENT
CONFIRMATION OF
TREAMENT PROCESS
OUANTATIES AND TIME
ASSESSMENT OF
LONG TERM
TREATMENT STABILITY
Figure 6
Flow Chart of Chemical Characterization
inject and maintain the calcium hydroxide slurry. These questions
resulted in in situ treatment not being selected as an initial alter-
native but held as a possible method of treating isolated hot spots
instead of removal and off-site disposal/treatment.
The geochemical stability at a site is a factor which may not be
evaluated in a conventional site characterization but is quite rele-
vant with regard to in situ treatment of metals. The chemical
stability of chromium in the shallow subsurface, for example, is
primarily a function of pH and oxidation reduction potential
(ORP). For shallow groundwater systems, the normal tendency is
for Cr(HI) to be the stable species under acid conditions. The ap-
proximate relationships that should exist to keep chromium in the
non-hazardous Cr(III) state as opposed to Cr(VI) are as follows:1
For pH of
14
12
10
8
6
Keep ORP less than: (MY)
-00
-100
+ 100
+ 200
+ 400
Based on actual field pH and ORP measurements, conditions
have been found where the geochemical system is close to the
equilibrium border and Cr(VI) occurs.
For sites with marginal geochemical stability, in situ treatment
may be a viable alternative used alone or in conjunction with other
remedial alternatives. For example, at a shallow waste fill site, one
option was to use a one-time in situ chemical stabilization in com-
bination with a low permeability cover. The purpose of the in situ
chemical stabilization was to drive the geochemical equilibrium
toward Cr(III) stability.
Conceptually, such a stabilization could be accomplished by ap-
plying a liquid reducing agent (such as sodium thiosulfate) on the
224
IN SITU TREATMENT
-------
fill surface and forcing circulation through a series of shallow
pumped trenches to recirculate reductant in the fill area. This cir-
culating system would also provide a means of reducing the pH of
the system by adding acidic material with the reductant. The op-
timum pH would be about 6 where Cr(VI) formation could be
prevented and Cr(III) solubility is still quite low. The clay cover
should be applied as soon as possible after the stabilization process
to achieve optimum results.
CONCLUSIONS
In situ treatment is subject to questions regarding uniformity of
treatment and long term reliability. However, it may be cost com-
petitive with other remedial alternatives. It may very well have
future use with respect to providing barriers to prevent off-site
migration and to selectively treat "hot spots" in conjunction with
other techniques.
The barrier concept would be to create a zone that would provide
subsurface treatment of contaminants such that discharge beyond
the barrier would be at environmentally acceptable levels. Barrier
construction could involve a line of injection wells spaced to pro-
vide a continuous treatment zone or a trench with granular material
into which treatment fluids could be injected. Such barriers could
also be used in conjunction with other groundwater control and
recovery systems. Essential to the design and construction of these
barriers would be adequate physical and chemical characterization
of the waste/subsurface system.
REFERENCES
1. 47 CFR§300.68 (j)
2. Kufs, C., Rogoshewski, P., Repa, E. and Barkley, N., "Alternates to
Ground Water Pumping for Controlling Hazardous Waste Leachates,"
Proc. National Conference on Management of Uncontrolled Hazardous
Waste S/to,Nov. 1982, 146-149.
3. Sills, M.A., Struzzierv, J.J. and Silberman, P.T., "Evaluation of Re-
medial Treatment Detoxification and Stabilization Alternatives,"
Proc. National Conference on Management of Uncontrolled Hazard-
ous Waste Sites, Oct., 1980, 192-201.
4. Fetter, C.W., Applied Hydrogeology, Merrill Publishing Co., Colum-
bus, OH, 1982, 60-67.
5. Warner, D.L. and Lehr, J.H., "An Introduction to the Technology of
Subsurface Wastewater Injection," EPA 600/2-77-240, 104.
6. Nielson, D.R., et al., "Spatial Variability of Field Measured Soil
Water Properties," Hilgardia, 42, 1973, 215-260.
7. Biggar, J.W. and Nielson, D.R., "Miscible Displacement and Leach-
ing Phenomenon," in Irrigation of Agricultural Lands, edited by
R.M. Hagan, et al., American Society of Agronomy Monograph
No. 11, Madison, WI, 1967, 254-274.
8. White, R.M. and Brandwein, S.S., "Applications of Geophysics to
Hazardous Waste Investigations," Proc. National Conference on Man-
agement of Uncontrolled Hazardous Waste Sites, Nov. 1982, 91-93.
9. Hem, J.D., "Reactions of Metal Ions at Surfaces of Hydrous Iron
Oxides," Geochem. et Cosmochim Acta 41, 1977, 527-538.
IN SITU TREATMENT
225
-------
IN SITU TREATMENT TECHNIQUES
APPLICABLE TO LARGE QUANTITIES OF
HAZARDOUS WASTE CONTAMINATED SOILS
RONALD C. SIMS
Utah Water Research Laboratory
Utah State University
Logan, Utah
KATHLEEN WAGNER
JRB Associates
McLean, Virginia
INTRODUCTION
Uncontrolled disposal of hazardous wastes frequently results in
the production of large quantities of contaminated soils. It is often
cost prohibitive or impractical to excavate, haul and dispose of
these soils in an approved landfill. In situ treatment of these soils
was investigated in this project as an alternative. The approach to
treating soils is based on: (1) fundamental soil chemical, physical
and biological processes, (2) methods developed for land treatment
of industrial wastes and (3) hazardous waste land treatment
(HWLT) regulations recently promulgated in 40CFR, part 264,
1983. The goals of in situ management include treating con-
taminated soils until an acceptable level is achieved and protecting
groundwater and surface water resources without physically remov-
ing or isolating the contaminated soil from the contiguous environ-
ment.
TECHNICAL GUIDANCE MANUAL
The results of this paper study will be presented in a two-volume
manual titled, "In Situ Treatment Techniques Applicable to Large
Quantities of Hazardous Waste Contaminated Soils." The manual
is being developed by the authors, and in this paper they present its
projected contents. Volume one will contain flow charts, decision
trees, procedures and quantitative and qualitative criteria for deter-
mining treatment feasibility and selecting treatment processes and
combinations of processes. Characterization of site specific condi-
tions requires information concerning soil, site and waste
parameters in order to assess the behavior and fate of chemical-soil
interactions using qualitative and quantitative models. Based on
the results obtained, treatment needs can be identified and
prioritized with respect to: (1) potential migration to groundwater
and surface water and to the atmosphere, and (2) recalcitrance, tox-
icity and persistence in soil systems.
Specific in situ treatment options will be selected based on the
following factors:
•Waste characterization
•Matching of waste constituent properties and treatment tech-
niques
•Safety considerations
•Analysis of the suitability of soil for treatment
•Economic analysis
Waste characterization includes chemical class, concentration
and behavior in soil systems. Matrices will be developed to match
specific treatment techniques with waste constituents. Complex
wastes will be constructed from individual constituents present in
the wastes, and treatment techniques will be evaluated for in-
dividual constituents as well as complex wastes. Finally, verifica-
tion procedures to determine in situ treatment effectiveness will be
suggested. The verification procedures include: (1) groundwater
sampling, (2) soil core/soil pore sampling, and (3) monitoring of
soil macrostructure characteristics.
Volume two will contain specific information concerning in situ
treatment technologies and soil-waste interactions. A discussion
and summary of specific physical, biological, chemical and
photochemical treatment techniques applicable for in situ treat-
ment will be presented. For each treatment process, factors ad-
dressed will include the achievable level of treatment, secondary im-
pacts of using the treatment technique, monitoring treatment per-
formance, equipment needs and application methods and costs.
Combinations of processes into treatment trains will also be con-
sidered. The final section of volume two will contain specific infor-
mation concerning the characterization and evaluation of fun-
damental processes in soil-waste systems that affect the feasibility
and effectiveness of in situ treatment.
The two-volume manual will be prepared for engineers and
managers to select and apply in situ treatment technologies. Since
the majority of in situ treatment technologies presently available
for hazardous wastes have not been thoroughly field tested, this
manual will contain information on promising techniques based on
laboratory and field results with hazardous and nonhazardous
wastes. Also, the manual will provide a framework for incor-
porating new developments in technology. The document can be
used by on-scene coordinators, toxic waste managers, regulatory
agencies and researchers as it will provide a format for bridging the
gap between research and development and field applications of in
situ treatment techniques which are applicable to large quantities of
hazardous waste contaminated soils.
APPROACH FOR IN SITU TREATMENT
Elements that are believed to be essential in a comprehensive ap-
proach to an in situ treatment program are shown in Figures 1 and
2. Those elements related to the goals of in situ treatment are
shown in Figure 1: (1) reducing concentration of contaminants to
an acceptable level and (2) protection of public health through con-
trol of transport pathways (leaching, runoff and volatilization)
from terrestrial systems to the environment (groundwater, surface
water and atmosphere).
The steps required for efficiently and cost-effectively accom-
plishing the goals of in situ treatment are shown in Figure 2: (I)
characterization of the site-waste system, (2) problem definition
with respect to potential waste impact, (3) management of the site-
226
IN SITU TREATMENT
-------
GOALS OF IN SITU MANAGEMENT7""!
PROTECTION OF PUBLIC HEALTH AND ENVIRONMENT
TREATMENT OF WASTE CONSTITUENTS TO AN ACCEPTABLE LEVEL
GROUNOWATER
SURFACE WATER
ATMOSPHERE
[SOIL SYSTEM j
DEGRADATION
TRANSFORMATION
IMMOBILIZATION
Figure 1
Elements related to the goals of in situ treatment of hazardous wastes
SOIL SYSTEM
DEGRADATION
TRANSFORMATION
IMMOBILIZATION
NO EXOGENOUS AGENT
ADDITION
ADDITION OF EXOGENOUS
AGENT
MANAGEMENT OF SITE-WASTE SYSTEM
PROBLEM DEFINITION
t
ASSESSMENT OF SITE-WASTE SYSTEM
CHARACTERIZATION OF SITE-WASTE SYSTEM
Figure 2
Steps required for accomplishing in situ treatment
waste system and (4) soil treatment technique(s) selection and ap-
plication including addition of a treatment agent(s), or augmenta-
tion of natural processes, for example, through amendment addi-
tion, or a combination of both approaches.
Characterization of the Site-Waste System
Characterization and evaluation of the site-waste system is
necessary in order to select treatment techniques that are appropri-
ate and cost-effective. Each of these factors shown below will in-
fluence the selection and application of treatment techniques for in
situ treatment. This phase of the methodology includes the follow-
ing specific components:
•Assessment of site-waste-soil conditions
•Role of sorption in determining the fate of waste constituents
•Fate of constituents with respect to microbial processes in soil
•Potential chemical reactions in the soil-waste matrix
•Assessment of potential volatilization of waste constituents from
the soil-waste matrix
Specific site and soil characteristics which need to be identified
during site assessment for in situ treatment management are sum-
marized in Table 1. The first aspect of site assessment with respect
Table 1
Site and Soil Characteristics Identified as Important in In Situ Treatment
Site location/topography
Slope of site — degree and aspect
Soil, type and extent
Soil profile properties
depth
boundary characteristics
texture*
amount and type of coarse fragments
structure*
color
degree of mottling
presence of carbonates
bulk density*
cation exchange capacity*
clay content
type of clay
PH*
Eh*
surface area*
organic matter content*
nutrient status*
microbial activity*
Hydraulic properties and conditions
depth to impermeable layer or bedrock
depth to ground water,* including seasonal variations
infiltration rates*
permeability* (under saturated and a range of unsaturated conditions)
water holding capacity*
soil water characteristic curve
field capacity/permanent wilting point
flooding frequency
runoff potential*
aeration status*
Climatological factors
temperature*
wind velocity and direction
*Factors that may be managed to enhance soil treatment
to in situ treatment is to evaluate potential public health hazards
due to off-site migration of hazardous compounds to ground and
surface waters and transmission through air. The potential for
migration, along with characteristics of the waste and the surround-
ing environment, indicate the degree of hazard the site poses.
Secondly, the site must be evaluated in terms of its potential for
decreasing the degree of hazard through degradation, transforma-
tion and immobilization. Those site-soil conditions that may be
managed to enhance these soil processes are indicated in Table 1. A
third aspect of site characterization involves assessment of the site
with regard to actual execution of in situ treatment, for example,
trafficability of the soil.
Soil sorption is perhaps the most important soil-waste process af-
fecting the toxic and recalcitrant fractions of hazardous wastes.
The influence of soil sorption on the extent and rate of leaching and
also on biological decomposition of these fractions must be
understood and described in order to effectively use the sorption
reaction as part of treatment processes. The relationship between
immobilization of chemical constituents in soil systems, based on
soil chemical properties, and chemical class, based on chemical
structure, is summarized in Table 2. Generally, nonionic consti-
tuents of low water solubility and cationic constituents have low
mobilities with respect to leaching potential. Acidic constituents at
neutral and high pH values are most easily leached from soil
systems.
Understanding the relationship between soil water content and
extent of sorption of hazardous chemicals provides the hazardous
waste manager with a process for controlling potential release and
migration of constituents through leaching. One commonly used
isotherm that is used to describe the immobilization of organic con-
stituents in soils is the Freundlich isotherm:
IN SITU TREATMENT
227
-------
Leaching
Potential
Table!
Leaching Potential of Chemicals in Soil Systems
Chemical Class
Nonionic
Ionic
Water
Solubility
bask
cationk
acidic
high med low low pH neutral pH
low pH neutral pH
Low
Medium X
High X
S = K C1/n (1)
where K and n are constants,
S = amount of chemical associated with the solid phase, or the
solid phase concentration (weight of chemical per weight
of solid),
C = amount of chemical associated with the solution phase, or
the solution phase concentration (weight of chemical per
weight or volume solution).
The Freundlich isotherm relates the solid phase concentration to
the solution phase concentration at equilibrium conditions.
The linear isotherm is an important isotherm which can be ob-
tained from the Freundlich isotherm when N = 1. The linear iso-
therm may be expressed as:
S = kd C (2)
where kd is called the distribution coefficient. This form of the
isotherm has been used for relatively low concentration of
pesticides in soil systems.
The relationship between kd, soil water 9, and percent adsorption
of an organic chemical can be used to manage a soil system:
percent adsorbed = kd/(kd + 0) (3)
where 6 = soil moisture content (volume of water per weight of dry
soil, assuming density of water = 1.0 g per ml).
90
so
70
60
50
• 9-20%
» 9- 40X
e- eo%
• e- eon
» 20
DISTRIBUTION COEFFICIENT, Kd
30
Figure 3
Extent of sorption as a function of soil moisture and kd
The extent of sorption (percent adsorbed) as a function of soil
moisture content for different values of the distribution coefficient
is illustrated in Figure 3. Thus, careful control of soil water content
will determine, to a large extent, the relative immobilization of a
given set of chemical constituents identified at a remedial site. Op-
timization of cost effective and efficient treatment may require a
compromise between optimum soil moisture content for
biodegradation versus sorption. Implications for specific treatment
schemes will be discussed in the manual.
The organic carbon content of a soil appears to play a dominant
role in influencing the distribution coefficient (kd). Results from in-
vestigations of soil-hazardous and soil-nonhazardous organic in-
teractions suggest that soil organic matter plays the most important
role in adsorption of organic chemicals by soils.
The fate of metals (inorganic constituents) added to soil is con-
trolled by a complex and dynamic system of physical, chemical and
biological reactions. Metals, unlike many hazardous organic consti-
tuents, cannot be degraded or readily detoxified. Toxic metals
represent a long term threat in the soil environment. This threat can
be reduced considerably if the heavy metals can be permanently im-
mobilized by either chemical or physical methods.
The concentration ranges of inorganic constituents in soils found
at 436 field investigation team (FIT) sites are shown in Table 3.
Also listed are the natural background levels of these constituents
in uncontaminated soils. Barium, cobalt and vanadium concentra-
tions were within background levels.
Table 3
Content of Various Elements in Uncontaminated1
Contaminated (FIT Sites) Soils
and
Element
Sb
As
Ba
Be
B
Cd
Cr
Cu
Co
Pb
Hg
Mo
Ni
Se
Ag
V
Zn
F
Common Range for
Soils (ppm)
2-10
1-50
100-3,000
0.1-40
2-100
0.01-0.70
1-1,000
2-100
1-40
2-200
0.01-0.3
0.2-5
5-500
0.1-2
0.01-5
20-500
10-300
104,000
Range at FIT Sites
for Soils (ppm)
15*
0.02-11,700
0.02-0.2
2-38
0.3*
0.3-118,300
0.04-136,000
2.2-186,300
2.6*
0.16-466,000
0.04-83,200
322*
0.4-8.800
0.9-1.3
1.2-18
0.04-2
0.03-38,000
110,000*
•one site reporting concentration
Source: Ecology and Environment, Inc. Field Investigations of uncontrolled hazardous waste sites.
FIT Project, USEPA Contract #68-01-«056.
The chemistry of heavy metals in soils can be divided into two in-
terdependent but separate categories: (1) solution chemistry and (2)
interfacial chemistry. Factors affecting and controlling the
behavior of inorganic constituents in soil systems will be considered
in detail in the field guidance manual.
Microorganisms are highly effective in removing certain hazar-
dous organic constituents from soil systems. Organic chemical
decomposition in soil systems is a complex process which depends
upon organic substance properties, soil properties and environmen-
tal factors. The addition of exogenous toxic organic wastes to soil
systems greatly increases the complexity of soil metabolic pro-
cesses. This is partly because organisms are exposed to at least three
different types of chemicals: (1) readily consumable substrates, (2)
228
IN SITU TREATMENT
-------
02
c
"f 101
o>
X
01
o
10° =
10'
*— ACENAPHTHENE
e— ACENAPHTHYLENE
••— ACRIDINE
*— ANTHRACENE
O— BENZU) ANTHRACENE
«— BENZO(b)FLUORANTHENE
t— BENZO(k)FLUORANTHENE
*— BENZOUJPYRENE
a— CHRYSENE
«— DIBENZd. j) ACRIDINE
•»— DI BENZU. K) ANTHRACENE
*— 01BENZOFURAN
a— 01BENZOTHIOPHENE
«— FLUORENE
*— FLUORANTHENE
e~ NAPHTHALENE
*— PHENANTHRENE
•I PYRENE
10'1 10° 10' 102 103 \04 105
INITIAL CONCENTRATION (ug/g-dry wt.)
Figure 4
Rates of transformation of PNA compounds in soil
as a function of initial soil concentration
toxic constituents which may inhibit metabolic processes and (3)
non-readily consumable organics which may not be toxic, but
which do not serve as sources of carbon and energy for cellular
metabolism (cosubstrates).
Although results for degradation of hazardous waste consti-
tuents cannot be presented here in full, data are summarized for the
polynuclear aromatic (PNA) class of organic priority pollutants in
Figure 4. The data compiled by Sims and Overcash2 represent
results from the literature and from laboratory results. General
trends can be summarized as follows: (1) the initial rate of transfor-
mation increases with increasing initial soil concentration for a
given PNA compound, (2) the initial rate of transformation de-
creases with increasing number of fused benzene rings within the
class of PNA compounds.
Several classes of chemical contaminants are considered concern-
ing chemical-soil reactions and reactions resulting from addition of
treatment agents to soil-waste systems. Only the solvent class of
chemical contaminants is discussed here.
Available studies indicate that little information has been
generated concerning the leaching behavior or effects of nonaque-
ous or aqueous-non-aqueous mixtures in terrestrial systems.
However, assessment of hazardous waste sites has identified
numerous organic solvents present that are not present as trace con-
taminants in an aqueous solvent.
Several recent studies have indicated that organic materials will
react with clay minerals in soil systems to generally increase clay
permeability.3'4-5'6'7 Studies onthe effects of solvents on clay
permeability have been concerned with clay liner integrity in land-
fill sites. However, results from these studies have important im-
plications for large quantities of hazardous waste contaminated
soils, specifically with respect to soil structure and the effects of soil
structure on leaching potential.
The effects of organic solvents on clay permeability of one soil
having smecitite as the dominant clay mineral are presented in
Table 4. Smecitite clays were the most susceptible to permeability
changes by organic solvents. General classes of organics, including
acidic, basic, neutral polar and neutral nonpolar are included. It is
evident that most solvent organics increase permeability of clay
minerals in soil systems. It is not known, at present, how dilute
aqueous mixtures of organic solvents will affect the permeability of
soils.
Table 4
Effect of Organic Solvent in Clay Permeability4
Chemical
Class
Acid
Base
Neutral
Polar
Neutral
Nonpolar
*smectite clay
Solvent
Acetic acid
Aniline
Acetone
Ethylene
Glycol
Xylene
Heptane
Effect on
Permeability
decrease
increase
increase
increase
increase
increase
Comment
dissolution of clay
100 fold for Lufkin"1
10 fold for H.B.*
1000 fold for Lufkin
50 fold for H.B.
100 fold for Lufkin
4 fold for H.B.
1000 fold for Lufkin
100 fold for H.B.
similar to Xylene
Volume I of the manual will include the methodology for choos-
ing treatment techniques. Specific information needs and analysis
and endpoints obtained will be indicated with respect to: (1) char-
acterization of the site-waste-soil system, (2) assessment of the site-
waste system, (3) problem definition and (4) management of the
soil-waste-site system. Examples for using the methodology for
specific site-soil-waste combinations will be reported in the field
guidance manual.
Soil Treatment Technique(s) Selection and Application
Soil treatment is defined as a set of physical, chemical and/or
biological reactions, natural or induced, that accomplishes
degradation, transformation or immobilization of hazardous con-
stituents in the soil system. The endpoint is to achieve acceptable
levels of constituents in the soil solution.
Treatment involves two major approaches. A treatment agent
(physical, chemical or biological) may be added to the soil-waste
system to accomplish the objectives of treatment, or treatment may
be accomplished through the augmentation of natural processes in
the soil-waste system. Addition of an amendment to a soil-waste
system may cause an increase in the rate, effectiveness or extent of
natural processes.
Physical, chemical and biological treatment processes considered
for in situ treatment of hazardous waste contaminated soil are
characterized and organized for presentation and evaluation
according to the outline presented in Table 5.
A summary of variables that can be controlled in physical,
chemical and biological treatment processes for in situ treatment in-
cluding treatment agent addition and treatment augmentation, are
presented in Table 6.
Based upon the information presented concerning the behavior,
fate and reactions of chemical constituents in soil systems and treat-
ment options available for in situ treatment, a methodology is
presented for choosing specific techniques to match site-waste-soil
requirements. In order to determine cost effective, rational and ap-
IN SITU TREATMENT
229
-------
TtbleS
la Situ Treatment Processes for Hazardous Wastes
1. IDENTIFICATION
Process fundamentals
Information requirements
2. EVALUATION
Status of the technique
Feasibility and effectiveness
3. DESIGN
Management variables
Equipment needs
Application methods
4. COST ANALYSIS
Unit costs
Other costs
5. EXAMPLES AND SOURCES OF INFORMATION
propriate treatment techniques it is necessary to define the problem
within the context of the treatment endpoints.
ACKNOWLEDGMENT
This work was funded by the USEPA Municipal Environmental
Research Laboratory, Cincinnati, Ohio, under Contract
68-03-3113, task 41. The authors wish to acknowledge the
assistance and support of the project officer, Naomi Barkley. They
also wish to thank the project staff, Dr. Darwin Sorensen, co-
principal investigator, Dr. Jerry Jurinak, Dr. Dean Adams, Joan
McLean, Judith Sims, Ramzi Mahmood and the support staff at
the Utah Water Research Laboratory. The contributions of Dr.
Ryan Dupont, Utah Water Research Laboratory, are appreciated.
REFERENCES
1. Lindsay, W.L., Chemical Equilibria in Soils. John Wiley and Sons,
New York.
2. Sims, R.C. and Overcash, M.R., "Fate of Polynuclear Aromatic Com-
pounds (PNAs) in Soil-Plant Systems". Residue Reviews, 88, 1983,
1-68.
3. Buchanan, P.N., "Effect of Temperature and Adsorbed Water on
Permeability and Consolidation Characteristics of Sodium and Cal-
cium Montmorillonite." Ph.D. Dissertation, Texas A & M University,
College Station, Texas, 1964.
Table 6
Physical, Chemical and Biological Treatment Processes
Considered for In Situ Treatment
No
Exogenous
Agent
Exogenous
Agent
Addition
Btotogkal
moisture
modification
nutrient
addition
analog enrichment
pH adjustment
aeration
organic matter
addition
temperature
adjustment
microorganism
seeding
genetic strains
acclimated
strains
Chemical
moisture
modification
(oxidation/
reduction)
pH adjustment
(hydrolysis)
temperature
adjustment
oxidation
ozone
peroxides
reduction
sodium sutfide
calcium sulfide
sodium boro-
hydride
organic matter
precipitation
calcium oxide
chelation
Physical
moisture
modification
pH adjustment
sorption
activated
carbon
organic
matter
mineral
addition
Photochemical
moisture
modification
volatilization
photosensitized
sensitizers
dyes
4. Anderson, D.C. and Brown, K.W., "Organic Leachate Effects on the
Permeability of Clay Liners". Proc. of the Seventh Annual Research
Symposium, D.W. Schultz, ed., EPA-600/9-81-002b, 1981.
5. Anderson, D.C., Brown, K.W. and Green, J., "Organic Solvent Ef-
fects on the Permeability of Clay Soils". Land Disposal of Hazardous
Wastes. EPA-600/9-82-002, 1982.
6. Brown, K.W. and Anderson, D.C., "Effects of Organic Solvents on
the Permeability of Clay Soils." EPA-600/2-83-016, 1983.
7. Brown, K.W., Green, J. and Thomas, J., "The Influence of Selected
Organics Liquid on the Permeability of Clay Liners." In: D.W. Schultz
(ed.) Land Disposal, Incineration, and Treatment of Hazardous Waste.
In Press. 1983.
230
IN SITU TREATMENT
-------
IN SITU DETOXIFICATION OF HAZARDOUS WASTE
VINOD K. SRIVASTAVA, Ph.D.
SIROUS HAJI-DJAFARI, Ph.D.
D'Appolonia Waste Management Services, Inc.
Pittsburgh, Pennsylvania
INTRODUCTION
Uncontrolled disposal of hazardous wastes usually results in con-
tamination of soil and rock followed by groundwater contamina-
tion. The removal of contaminated ground and emplaced waste is
costly and often impractical. Open excavation requires careful
transportation of contaminated mixtures and disposal in a safe
landfill. An alternative to contaminated ground removal is in situ
treatment or detoxification.
In situ detoxification in this paper means "in-place" treatment
of waste, soil and fluid to reduce the contamination level to an ac-
ceptable one. In this process, contaminated materials remain in
place, while external additives are used to alter their physical
and/or chemical characteristics.
Although many of the fundamental concepts of in situ detox-
ification are known, and others are being studied at several
laboratories, the feasibility assessment has not been collectively
considered for different applications, mainly because these
technologies are either in the conceptual or early infancy stage.
Recently, the USEPA began a research program at the Municipal
Environmental Research Laboratory, Cincinnati, Ohio, to in-
vestigate in situ treatment of hazardous wastes. A literature search
has been conducted to identify the technologies that either exist or
have the potential for further investigation. The most common
technologies considered for in situ treatment include:
•Immobilization
•Biodegradation
•Neutralization
•Solvent Mining
•Oxidation-Reduction
One significant limitation of in situ treatment is that it is waste
specific. Heavy metals, pesticides, residues, organic solvents, in-
organic salts, explosives, etc., have their own chemical properties
and require different treatment. Proper identification of wastes
and their physical, chemical and toxicological properties is vitally
important to determine the best strategy planning for in situ treat-
ment to avoid undesirable reactions or production of additional un-
wanted toxic species. In the following paragraphs, the present and
promising in situ detoxification technologies are evaluated; this
evaluation is summarized in Tables 1 and 2.
In these tables, the applications of in situ detoxification
technologies for organic and inorganic contaminants are identified
and their applications are assessed with particular regard to their:
•Availability—Commercially developed, pilot plant or laboratory
scale
•Feasibility—Design, construct and operation feasibility
•Cost-Effectiveness—Design, construction and operational cost
•Advantages and Disadvantages—Unwanted chemical reactions or
end products
•Environmental Impact—Assess environmental hazards, spread of
contamination
•Safety of the Method—Personnel safety
The application of each technology for treatment of solid and li-
quid wastes is as follows.
IMMOBILIZATION
Immobilization or gelation is the fixation of toxic waste to render
it insoluble. The waste materials are immobilized in a normal earth
Mutated organisms have been shown to break down the complex
persistent pollutant 2-4T13'14 pesticides and organic solvents.15 Use
Contaminated Soils/Solids
A field conceptual design1 of placing polymerized ion exchange
resins around the waste was studied in the laboratory. Reduced
concentrations of phenols, cyanide and nickel were recorded as the
leachate passed through ion exchange barriers. Complexing of
trinitrotoluene (TNT) using surfactants2 failed due to poor results
and potent mutagenic end products.
In laboratory experiments, a 70% decrease in the mobility of
radioactive strontium3 was achieved using CaCO3 as a fixative
agent. Feasibility studies for in situ stabilization of low-level
radioactive waste were accomplished4 by encapsulating the waste,
using cement kiln dust, fly ash, synthetic ion exchange resins and
impervious liners.
Contaminated Water/Liquids
Conceptual design1 as described earlier is not feasible; however,
external fixation technologies are commercially available.'
Technology Assessment
The technology of encapsulating and treating of waste to make it
non-hazardous is commercially available.5 Some technologies are
applicable in the field. The cost is dependent on the technology,
processing methods and the chemicals used. The process of encap-
sulating is generally cheaper than placement of an ion exchange
barrier. The major costs may be the determination of the extent of
the contamination and installation of monitoring wells.
The environmental impact is dependent on the length of time the
waste remains immobilized and is usually minimal. The technology
is waste specific and often cannot be used in mixed waste systems.
The health hazards associated with the technology may be minimal.
IN SITU TREATMENT
231
-------
Table 1
Assessment of In Situ Detoxification Technologies Organic Wastes
TECHNOLOGY
CONTAMINANT
Hydrocarbon!
Oi 1 and Greaae
Organic Acid!
S. Conpounds
Alcohol!
Peroxide!
Halocarbons
PCB's and
Peat icides
Phenols
Ethers
Anni 1 ine
Amines
Pyr id ine!
Nitro Compound!
Aldehyde
Herbicide!
Solvent!
COMMENTS :
Available Technology
X - None
L - Lab Scale
P - Pilot Plant Scale
F - Field Scale
OXIDATION ""ERENCES
IMMOBILIZATON BIOOECRADATION NEUTRALIZATION SOLVENT MINING REDUCTION
F,6,D,c,Y
F,8,D,d,Y
F,6,D,c,Y
N,8,E,d,Z
N,8,E,d,Z
F,6,D,c,Y
L,4,E,b,Z
L,4.E,d,Z
L,4,E,d,Z
F,6,I),c,Y
F,5,N,d,Y N,8,E,d,Z
L,4,E,d,Z
F,4,2,c,Z
F,5.D.>.,Z
F,5,D,C,Z
L,3,B,a,X
F,4,0,c,Y
L^.E.d.Z
P,8,E,d,Z
F,6,D,c,Y
1 - None A Severe
2 Very Poor B Moderate
3 - Poor C Poor
4 Fair D None
5 Good E Unknown
6 Very Good
7 Excellent
8 Not Known
6
7
21
23
11
N.B.E.d.Z N,8,E,d,Z 2,54
22
12
13
14
1
N,8,E,d,Z N,8,E,d,Z 22,55,16,54
34
56
N,8,E,d,Z 31,57
57
N,8,E,d,Z 2,34
N.S.E.d.Z 10,34
13,14
15
21
Cost Effect iveneai Safety of Method
a - High X Unsafe
b - Medium Y - Safe
c - Low Z Unknown
d - Not Known
BIODEGRADATION
Biodegradation or microbial degradation is the process of plac-
ing waste in contact with specific microorganisms and providing the
necessary environment for growth to metabolize the toxic com-
ponents to nontoxic or less toxic species. Biodegradation processes
may be aerobic or anaerobic, depending on the microorganisms
and chemical species.
Contaminated Soil/Solids
The use of microbes for treatment of oil residues has been
reported in the early 1970s.6'7 Extensive research and mutation
techniques have resulted in specific microbes now commercially
available.8 The success of these microbes has been demonstrated
during the cleanup of oil contaminated beaches of Great Yar-
mouth, United Kingdom,9 and a California formaldehyde spill.10
Laboratory scale degradation of phenols and benzoic acids11'12 is
promising.
Mutated organisms have been shown to break down the complex
persistent pollutant 2-4T13-14 pesticides and organic solvents.15 Use
of thermophilic organisms in composting process has shown
degradation of complex compounds such as chlorophenols and
chlorobenzenes;16 insecticides diszonium, parathion and dieldrin;17
chlordane;18 grease and oils;19 crude oil;20 TNT and pulp and paper
mill wastes; and pharmaceutical wastes.21
Contaminated Water/Liquids
Microbial detoxification is comparatively easy in external
aqueous systems. Field applications of aerobic microorganisms at
Mobay and Exxon Chemical have shown degradation of con-
taminants in wastewater contaminated with oil, grease, petroleum
waste and various other organics.22'23 including ethers56 and
amines.57 Degradation of substituted phenols," halocarbons12 and
trace organics and polynucleated hydrocarbons has been shown in
laboratory studies. Biological treatment systems for groundwater
contaminated with benzene and phenol24 and other organic
pollutants58 are under development.
Inorganic metals cannot be metabolized by microbes; however,
biological reduction of ammonia25 and denitrification of nitrites**
have been achieved. Phosphorous has been found to concentrate in
microbial cells under aerobic conditions.
Technology Assessment
Aerobic treatment technology is available on a commercial scale
for certain contaminated liquids and soils. The need for oxygen and
water restricts the use of the technology to surface contamination,
especially for solid systems; however, the aqueous streams can also
be effectively treated with greater efficiency. The technology can be
applied in the field. Portable biological treatment systems are com-
mercially available.27
232
IN SITU TREATMENT
-------
Table 2
Assessment of In Situ Detoxification Technologies Inorganic Waste
CONTAMINANT
IMMOBILIZATON BIODEGRADATION NEUTRALIZATION SOLVENT MINING
METALS
Arsenic
Barium
Cadmium
Chromium
Lead
Mercury
Selenium
Silvr
Nickel
Copper
Aluminum
NONMETALS
Acids
Alkalies
Ammonia
Salts
Cyanide
Fluoride
Nitrates
Peroxides
COMMENTS :
Available Technology
N - None
L Lab Scale
P - Pilot Plant Scale
F Field Scale
Complexing
Agent for As,
Cd, Cr, Cu, Zn
P,5,E,d,Y
L,4,E,d,Z
L,4,E,d,Z
L 5 E d Y
Feas ibi 1 it y
1 None
2 Very Poor
3 Poor
4 Fair
5 Good
6 - Very Good
7 Excellent
8 Not Known
Metals
L,4,E,d,Z 52
53
P,5,E,d,Z 46
L,S,E,d,Z 50
L,R,E,d,Z 50
L,8,E,d,Z 50
P,5,D,Y 25
N,l,E,d,Z F,4,E,b,Z 1,35,52
N,8,E,d,Z 35
L,4,E,«,Z 26
3
Environmental Impact Cost Effective Safety of Method
A - Severe a High X Unsafe
B - Moderate b - Medium Y Safe
C - Poor c Low Z Unknown
D - None d - Not Known
E - Unknown
The cost of biological treatment is low compared to excavation
and disposal in secure landfills. The processing cost is low and
dependent on the type, scale of process and concentration of the
contaminants.
The environmental impact is very limited because the end pro-
ducts are usually gases, spent microbes and low concentrations of
undegraded products. Commercially available technology is limited
to aerobic microbes. Further research is needed to develop
anaerobic systems and "oligotroph" groups of microbes capable of
growing on low concentrations of substrates. There are no ap-
parent health hazards associated with this technology.
NEUTRALIZATION
Contaminated Soil/Solids
Chemical neutralizing agents can be injected into a waste with an
acidic or basic functional group to destroy or change the chemical
properties. Organic compounds with acidic functional groups, such
as carboxylic, sulphonic acids and phenols and alkaline groups such
as amines and aniline, can be neutralized either by alkali or acids.
Neutralizing solid wastes with poor reactivity may be a long and
continuous process.
Contaminated Water/Liquids
The chemical industry produces wastewaters with diverse ranges
of pHs. These waters can be neutralized to make them nonhazar-
dous. Petrochemical wastes27 containing alkylation, sulphonation
products and steel mill pickling liquors can be neutralized on
site.28-29 Metal finishing wastewaters containing sulphuric,
phosphoric and chromic acids and metal ions30 and plating wastes
containing cyanides can be treated with the appropriate neutraliz-
ing agents on site before disposal.
Technology Assessment
It appears that solid wastes cannot be effectively treated with this
technique; however, it is a commercially feasible technology for
wastewater and may be applied to liquid wastes in the field. The
treatment cost should be less than for excavation, incineration or
disposal in a secure landfill, dependent on the treatment process,
volume of the waste and nature of the contaminants.
The environmental impact can be variable, based on the process.
The waste-specific process restricts its use to known contaminants
and noncontainerized wastes. Health hazards associated with the
technology are uncertain.
SOLVENT MINING
In solution mining or soil flushing, a solvent is injected or flood-
ed over the waste disposal area or the area of contamination to
remove the hazardous chemical. The elutriate (flushing liquid) is
collected by impervious liners placed under the waste and brought
back to the surface, treated to remove the contaminants and rein-
jected. The concept.is similar to leachate generation under natural
conditions. The rate of contaminant migration is dependent on
several factors such as waste-solvent interaction, active functional
group, soil-contaminant interaction, attenuation properties of the
waste, etc.
IN SITU TREATMENT
233
-------
SOLVENT
IMPERVIOUS LINER
LEACHATE COLLECTION SYSTEM-
Figure 1
Schematic Design for In Situ Solution Mining
The conceptual design of such a system is shown in Figure 1.
Water is the most accepted cost-effective solvent without the wor-
ries of secondary contamination, although other polar solvents or
aqueous mixtures of solvents can be used in a two-step process as
shown in Figure 2. The first step involved in the process of solution
mining is the use of an organic polar solvent to produce elutriate.
The contaminant is separated from the elutriate and the solvent
recycled. The second step is similar to the first except that the con-
taminant is the polar organic solvent and the elutriate is water. The
process of solution mining is continued until all the polar solvent is
removed.
Contaminated Soil/Solids
Organic compounds with hydrophobic functional groups
become strongly attached to the soil and cannot be eluted with
water. Leaching of these compounds can be enhanced using
suitable polar organic solvents, mixtures of solvents or complexing
agents. Wastes with hydrophilic groups can be more easily eluted
with water. Dilute acids may serve as a solvent to flush certain basic
organics such as amines and aniline.31 Surfactants may be useful in
dissolving oil and grease.
Inorganic acids may be used to dissolve basic metals, oxides,
hydroxides and carbonates. Carbon dioxide with ammonia has
been used for leaching copper and nickel.32 Other complexing or
chelation agents commonly employed may be ammonia, am-
monium sulfate, citric acid, EDTA, thiourea, etc. Sodium has been
used to dissolve metallic aluminum and can be used for zinc, tin,
lead and other metals. The Goose Farm site, Plumsted Township,
New Jersey, is an example of the solution mining technology being
developed.33
Contaminated Water/Liquids
Solvent flushing for a liquid system is not applicable.
Technology Assessment
The technology is not available commercially, although research
and field trials are in progress, its feasibility, however, is good. The
cost of the system could be less than for excavation and physical
removal or incineration; chemical properties, quantity of waste,
type of solvent and placement of an impervious layer under the
waste will govern the cleanup cost. Additional costs will include the
installation of monitoring wells and an elutriate treatment system.
The technology is dependent on the fail-safe placement of the
liner and elutriate collection system. There is always uncertainty
with respect to adequate contact of buried waste to solvent systems.
The technology is not applicable to mixed or containerized wastes.
There should be no health hazards associated with the properly ap-
plied technology.
OXIDATION-REDUCTION
In oxidation-reduction systems, the valency-electrons of wastes
are changed to convert them into nontoxic or less toxic substances.
Laboratory studies have shown the oxidation of highly toxic
cyanide to less toxic cyanates and the reduction of Cr+6 to Cr+3, in-
dicating the potential exists for use of this technology.
STEP I
ELUTRIATE
CONTAMINANT REMOVAL
BY
SOLUTION MINING
SOLVENT
STEP 2
WATER AS SOLVENT
SOLVENT RECOVERY
BY
SOLUTION MINING
'ELUTRIATE
Figure 2
Concept for Two-Step In Situ Solution Mining Using Polar Solvent
Contaminated Soils/Solids
Unsaturated organics can generally be treated by oxidation-
reduction techniques. Hydrogen peroxide has been used to oxidize
aldehydes, dialkyl sulfides, dithionate nitrogen compounds,
phenols and sulfur compounds.34 Conceptual design and in situ
cyanide detoxification by oxidation with sodium hypochlorite have
been described35 in a hypothetical ten-acre disposal site by injecting
hypochlorite at different depths.
Chloralkali industries are reported to use chemical oxidative
techniques to remove mercury from ores as well as from wastes
with a 99% recovery. In situ treatment of chlorinated pesticides
utilizing an anaerobic ferrous-ferric-redox system3*-37 was reported
in laboratory studies.
Contaminated Water/Liquids
Liquid wastes are easily treated by external chemical oxidation-
reduction. Trace quantities of phenols,38 diquat and paraquat,39
organic sulfur compounds40 and formaldehyde38-40 have been ox-
idized in aqueous streams using potassium permanganate,
hydrogen peroxide, sodium or potassium hypochlorite. Reduced
concentrations of phenols, trichloroethylene41 and benzene were
reported in lake waters following ozone oxidation.
Chemical oxidation of soluble lead43 and the reduction of Cr*6
to Cr*3 using sulfur dioxide and sodium metabisulphite44-45 have
234
IN SITU TREATMENT
-------
Table 3
Status of In Situ Detoxification Technologies Organic Wastes
Existing Promising
Technology Technology
Solids or Liquids Solids Liquids
Hydrocarbons
including Oil and
Grease Biodegradation E E
Organic Acids U Biodegradation Biodegradation
Oxidation-Reduction
Sulfur Compounds U Solution Mining Oxidation-Reduction
Oxidation-Reduction
Alcohols Biodegradation E E
Peroxides U U U
Halocarbons U Biodegradation Biodegradation
PCB and Pesticides Biodegradation E E
Phenols Biodegradation Immobilization Oxidation-Reduction
Oxidation-Reduction
Ether Biodegradation Solution Mining U
Anilines, Amines Biodegradation Solution Mining Neutralization
Neutralization
Pyridines U U U
Other Nitro-
compounds U Immobilization U
Oxidation-Reduction
Aldehydes Biodegradation Oxidation-Reduction Oxidation-Reduction
Herbicides U Biodegradation Biodegradation
Solvents Biodegradation E E
Pharmaceutical Waste Biodegradation E E
COMMENTS:
Technology Status: U - Unknown/Uncertain; E = Potential for Expansion
been achieved. In situ reduction of Cr+6 to Cr+3 in Arizona well
water using minute quantities of reducing agents46 is an indication
of the potential for this technology.
Technology Assessment
There are no fully developed commercially available
technologies, although several concepts look promising and feas-
ible in the field. The technology is cost-effective compared to ex-
cavation, physical removal and disposal to secure landfills. Major
costs incurred will be governed by such factors as nature, quantity
of the waste and chemical costs.
The technology is waste specific and not applicable to mixed
waste systems and containerized waste. Danger exists that the pro-
cess may add additional contaminants to the system. There are no
apparent health hazards associated with this technology.
OTHER NOVEL TECHNIQUES
Laboratory experiments have shown an effective oxidation of
phenols and amines by enzyme horseradish peroxidase and
hydrogen peroxide.46 Ninety-nine percent of the PBB and kepone
in soil was destroyed when exposed to solar radiation in the
presence of tertiary amines.47 Adsorption of metals by cellulosic
materials, such as wood product wastes, showed some promising
results.48
CONCLUSIONS
In this paper, the available and promising in situ detoxification
technologies have been reviewed; their application, feasibility and
cost-effectiveness have been assessed. The status of these
technologies has been summarized in Tables 3 and 4 for organic
and inorganic wastes. In situ treatment has been used in the field on
a limited basis for sites with well-defined wastes, especially shallow
and small contamination, chemical spills, surface contamination
and shallow industrial impoundments. In reviewing these technolo-
gies, in situ biological or chemical waste treatment may be an at-
tractive alternative compared to the waste removal. The literature
search indicates that the in situ detoxification can be applied for
aqueous and solid wastes separately.
For aqueous waste streams, the biodegradation is most promis-
ing followed by neutralization and oxidation-reduction.
GV\T cr\i1 /cnliHc nr fiiiripd u/actpc thp cnliitinn minimi fnllowpH hv
rtji awii/ aijiiu.& \ji uuiicu wdoicbf LIIC oiiiLiMuii milling, lunuwcu \jy
immobilization, neutralization and oxidation-reduction, respec-
tively, provide promising technology for in situ detoxification.
Biodegradation techniques can be applied to soils where the con-
tamination is at the surface and oxygen is readily available. The
technique of solution mining for buried wastes seems to be the
alternative to excavation and disposal to a landfill. The major
drawback of the technology is its limitation for use in mixed waste
systems and containerized wastes. More research is needed at the
laboratory and pilot plant scale level to develop these technologies
commercially.
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Table 4
Status of In Situ Detoxification Technologies Inorganic Waste
Existing Promising
Technology Technology
Solids or Liquids Solids Liquids
METALS
Arsenic Immobilization U U
mmo iization U
Cadmium Immobilization U U
Chromium Immobilization U Reduction
Reduction
Lead Immobilization Reduction U
Mercury Immobilization U U
Selenium Immobilization U U
Silver Immobilization U U
Nickel Immobilization Immobilization U
Solution Mining
Copper Immobilization Solution Mining U
Aluminum Immobilization Solution Mining U
Zinc Immobilization Solution Mining U
NONMETALS
Acids Neutralization U U
Alkalies Neutralization U U
Ammonia Biodegradation E E
Salts U U U
Cyanides Immobilization Immobilization Oxidation
Oxidation
Fluorides Neutralization E E
Nitrates Biodegradation E E
Peroxides U U U
RADIOACTIVE
WASTES Immobilization E E
COMMENTS:
Technology Status: U = Unknown/Uncertain; E = Potential for Expansion
IN SITU TREATMENT
235
-------
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236
IN SITU TREATMENT
-------
ENGINEERING TECHNIQUES APPLIED IN DESIGN OF A TOE
DRAIN SYSTEM THROUGH STRAITS SCHIST FORMATIONS
BRIAN D. GILLEN
MICHAEL A. BARBARA
Fred C. Hart Associates, Inc.
New York, New York
INTRODUCTION
In this paper, the authors discuss the engineering concepts and
design parameters developed for a remedial leachate collection
trench drain constructed in glacial till and straits schist formations
surrounding a landfill located on a hill top. The site is presently
receiving municipal wastes. However, in the past the site received
industrial and potentially hazardous wastes. It is currently listed as
a top priority Superfund site in the State of Connecticut,
The landfill property consists of approximately 30 acres, of
which about 17 are the active fill. Located above a bedrock forma-
tion known as Straits Schist, the environmental issue is the route
and effect of leachate migrating from the site and discharging at the
perimeter to the west and north (Figure 1). A small portion of the
leachate may flow via a man-made ditch to a nearby brook.
Leachate and contaminated runoff from the fill have migrated to
an unnamed tributary and have caused some degree of contamina-
tion. Geologic and hydrologic investigations by Fred C. Hart
Associates, Inc., (FCHA) of New York, New York1 have indicated
that the underlying bedrock and compacted glacial till acts as an
impermeable barrier and causes leachate to migrate radially from
the site.
Upon the completion of their study, FCHA recommended a
course of action to eliminate the current problem with the leachate
and contaminated runoff. The plan called for construction of
trenches in both glacial till and the Straits Schist formation,
backfilling with till and gravel, covering the trenches with till and
sand, installing flexible drainage tubing and capping the completed
trench. In this paper, the authors discuss the engineering concepts
used in the design of the leachate collection system.
DEVELOPMENT OF DESIGN CONCEPT
Prior to the design of remedial activities to control leachate
emanating from this site, FCHA and others conducted various sur-
face, subsurface and groundwater investigations.1'2 The initial ac-
tivities included installation of four 2 in. diameter wells varying in
depth from 20 ft to 100 ft. The following subsections briefly
describe key elements of the FCHA site characterization study.
Drainage Patterns
Prior to the development of the landfill (i.e., natural conditions),
an area known as Huntington Hill was the division between two
major watersheds in the area: (1) the Long Meadow Pond Brook
Watershed and (2) the Spruce Brook Watershed, both of which are
part of the Naugatuck Regional Basin (Figure 1).
The development of the landfill has significantly influenced
drainage patterns.2 As the result of landfilling operations, it was
Figure 1
Site Specific Drainage Patterns
necessary to delineate the Spruce Brook Watershed into two sub-
watersheds (Figure 1).
The major portion of the landfill, approximately 19 acres, is still
part of the Long Meadow Pond Brook Watershed. Most surface
drainage is channeled through a drainage ditch located around the
southern and western perimeter of the landfill. This drainage ditch
channels this controlled runoff around the site into the unnamed
creek. The unnamed creek flows into Long Meadow Pond Brook
within the city limits of Naugatuck and eventually empties into the
Naugatuck River.
The eastern portion of the site, approximately 7 acres, drains as
uncontrolled runoff. Some surface runoff enters the heavily
wooded area to the east as intermittent streams and flows down the
steep slopes toward the Naugatuck River. Another portion of sur-
face runoff is channeled east across the access road at the base of
the landfill (Figure 1). Additionally, some direct storm runoff, not
related to the landfill, drains east down Hunters Mountain Road.
Flow Volume
To develop estimates of flow volumes generated from the site, a
water balance was prepared to calculate the total yearly quantities
of anticipated leachate generation. The methodology used in this
assessment was developed by Fenn et al.1
IN SITU TREATMENT
237
-------
Table 1
Water Balance for Laurel Park Landfill (In.)
TOTAL
Pet
Preclp
Cr/o
r/o
I
I-PET
hcg
NOTES:
LT Less than
^H Organic carbon fraction of total solids
• Percentages extrapolated from actual Laurel Park leachate concentrations as reported in Uie 2/83
etc. laboratory testing report.
1 Estimates developed from leachate characterization as reported in Handbook of Environmental
Coni/ol. Vol. II. unless noted.
2 Assumptions and overall formulation used in developing the components of the total volatile
solids are provided in Figure 3.
3 Primarily iron and aluminum.
Figure 2
Landfill Leachate
tCharactertzauon of Tolal Solids Based on FCHA Estimates')
In summary, total yearly percolation is expected to total 4 in./yr.
This is equivalent to a leachate generation rate over the 19 acre sur-
face area of the fill of approximately 2,000,000 gal/yr. This flow
would actually vary on a month to month basis, with flows
reaching 20,000 gal/day during peak months and with no ap-
preciable leachate generation during months of high
evapotranspiration (late spring).
Leachate Characterization
The proposed leachate collection system was designed to convey
wastes off-site for ultimate discharge and disposal into the 10 mgd
Naugatuck wastewater treatment plant (NTP) located approx-
imately 2 miles away. Prior to entering into an agreement to accept
leachate into the plant, NTP operating personnel requested infor-
mation on the composition of total organic carbon and metals.4
Laboratory analysis' of landfill leachate revealed that the
leachate had a total solids (TS) concentration of 11,000 mg/1 and a
total organic carbon concentration of 2030 mg/1 (Figure 2).
Estimates of other constituent concentrations were based on
published data extrapolated from various other sources' in cases
where laboratory analyses were not available. Approximately
18.5% of the total solids consisted of total organic carbon (Figure
2). The organic component of the leachate, commonly referred to
as total volatile solids, consisted primarily of carbon, oxygen,
hydrogen and small quantities of nutrients and halogens (usually
chlorine). The carbon molecule represented between 30 and 80% by
weight of the total volatile solids, depending on the refuse compo-
nent from which the leachate originated. For example, the ultimate
analysis listed below indicates a wide variability of carbon,
hydrogen, oxygen (CHO) formulas typical of differing organic
municipal refuse components.
REFUSE
COMPONENT ULTIMATE ANALYSIS (%)
Plastic
Maga-
zine
paper
C
78
37.90
H
9
4.95
O
13
38.
N
0.07
0.09
Inert
22.47
For the analysis shown in Figure 2, FCHA assumed an average
ultimate analysis of refuse as 50% carbon, 5% hydrogen and 45%
oxygen. Using this formula and measured total organic carbon con-
centrations in the leachate, FCHA estimated that the total volatile
solids equals approximately twice the total organic carbon concen-
trations or approximately 31% of the total solids concentrations.
Assumptions used in developing estimates of the constituent com-
ponents in the total volatile solids are shown in Figure 3. More than
99% of the volatile solids were expected to be partially degraded
238
IN SITU TREATMENT
-------
TOTAL VOLATILE
SOLIDS 37%
C>o Ho O4« (2)
Table 2
Estimated Metal Effluent Concentrations Due to Leachate Contributions
"CHIOH-1
-(HC-OH)J
_CHO J
(3)
co-con
MCO-COH'
UCO-COR*
L*1 J
-PROTEINS
(h-co-
Zinc
Barium
Lead
Chromium
Arsenic
Iron
Copper
(A)
Laurel Park
Landfill Leachate
(Max. Concent.
Observed)
-------
The proposed design objective is to effectively capture the
leachate in perimeter gravity toe drains and convey the leachate by
gravity to the NTP for treatment and disposal. The leachate collec-
tion system consists of two separate systems, referred to as the East
and West Trench Drains. A 6 in. rigid polyethylene (RPE) gravity
sewer pipe will collect flow from both the drains and transport the
leachate to the NTP.
Figure 5
East Toe Drain Section through Straits Schist
East Trench Drain
The East Trench Drain will consist of approximately 1,400 ft of 4
in. diameter perforated flexible polyethylene (PFPE) placed within
a gravel envelope. The perforated leachate collection pipe and
gravel will be installed in a trench varying in size from 10 to 60 ft2 in
cross-sectional area and will cut through rock along the south and
east sides of Huntington Hill along the toe of the landfill slope.
This installation will require the removal of 900 yd3 of Straits
Schist, 1,200 yd3 of unconsolidated till and the placement of 1,700
yd3 of gravel. The 1,000 ft long, 6 in. diameter RPE trunk line will
also be required to transport the leachate from the East Trench
Drain to the proposed 8 in. polyvinyl chloride (PVC) sewer trunk
drain to be installed under a separate contract.
A plan view of the site, the approximate location of the East
Trench Drain and a typical cross-sectional detail of the proposed
method of construction are shown in Figure 5. A trench varying in
depth from 4 to 22 ft will be cut into the Straits Schist unit along
portions of the southern and eastern portions of the site. The
trench will be located in or near areas of exposed rock and will cir-
cumvent the present fill areas and toe of slope. The drain pipes will
be 4 in. diameter, ABS pipe conforming with A.A.S.H.T.O. M-252
specification with nylon covering with 0.25 in. diameter holes.
A bedding of 1 to 1.25 in. gravel will be placed in the trenches
and around perforated pipes to provide uniform lateral support
and to also serve as a high permeability channel (i.e., French drain).
The gravel media, consisting of coarse material, will not enter and
clog the 0.25 in. diameter perforations of the pipe. As an additional
protection against clogging, the pipes will be factory-covered with a
plastic filter fabric to prevent fines from entering the pipe. The
fabric will have a weave that will match a U.S. Standard pore size
of 200.
The trench will be sealed with a layer of cushion sand to convey
leachate down the slope and into the trench. A 1 ft layer of recom-
pacted till will be placed over the sand to prevent surface runoff
from entering the gravel envelope and to contain leachate in the fill
so that it will drain into the toe drain. The sand/clay blanket will
be topped with one foot of cover material and seeded.
West Trench Drain
The West Trench Drain will consist of approximately 2,400 ft of
4 in. diameter PFPE pipe placed within a gravel envelope. The pipe
and gravel will also be installed in a trench varying in size from 10
to 40 ft2 in cross-sectional area excavated in till along the south,
west and north sides of the landfill at the toe of the landfill slope.
This installation will require the removal of 2,500 yd3 of uncon-
solidated till and the placement of the same amount of gravel.
A plan view of the site, the approximate location of the West
Trench Drain and a typical cross-sectional detail of the proposed
method of construction are shown in Figure 6. A trench drain
similar in design to the East Trench Drain will be constructed with
minor differences. The trench will be cut into unconsolidated till
along the western and northern portions of the site. The
permeability of this material varies, but FCHA soil investigations'
suggest that soil permeabilities are low, ranging from 10~5 cm/sec
to 10"' cm/sec. Excavated material from this and other locations
on site will be used to cover the West Trench. Gravel, filter fabric,
pipe and cushion sand will be employed in the same manner as used
in the East Trench. After completion of the rock excavation, the
trench will be cleaned and inspected for cracks in the schist. Two
coats (20 mils thick) of a high-build, flexible epoxy protective
coating will be applied to fractures which may occur in the schist
during construction.
The contract also provides for installation of nine manholes and
17 standard single connection cleanout assemblies, with case iron
frame and covers. These facilities will be installed at breaks in grade
or direction to allow for periodic cleaning and/or testing of the
pipe in the leachate collection system.
Figure 6
West Toe Drain Section through Unconsolidated Till
CONTRACTUAL CONSIDERATIONS, TECHNICAL
SPECIFICATIONS AND ENGINEER'S ESTIMATE
Contract drawings and specifications for this job were prepared
May 2, 1983 and submitted to the Connecticut Department of En-
vironmental Protection (CDEP) for review and approval. The
specifications contained a unit price contract format with estimated
quantities provided for bidding purposes. Each work item was
numbered for identification in the Contract Bid Proposal and
Technical Specifications. These items (Item 2.01 through 7) are
summarized in Table 3. Items 2.01 through 7.12 refer to "State of
Connecticut Department of Transportation 1980 Standard
Specifications for Roads and Incidental Construction (Form 812).
240
IN SITU TREATMENT
-------
Table 3
Contract Unit Price Items
Item 2.01
Item 2.05X
Item 2.06
Item 2.07AX
Item 2.07BX
Item2.12X
Item 3-PFPE
Item 4X
Item 5
Item 6X
Item 7
Clearing and Grubbing
Trench Excavation
Ditch Excavation
Embankment in Place
Borrow
Trimming Shoulders and Slopes/Preparing Fine Grade
Rigid Polyethylene (RPE) Sewer Pipe
Manholes
Connection to Existing Sewer Facilities
Single Connection Cleanout Assembly
Protective Coating
NOTE:
a. Item Nos. 2.01-2.12 above refer to the "State of Connecticut Department of Transportation
1980 Standard Specifications for Roads and Incidental Construction (Form 812)" as detailed
in Section 1(3)(1) of the Supplementary and Special Conditions.
b. "X" denotes sub-items.
The Engineer's Estimate prepared for the contract is summarized
in Table 4. The total cost of the project is $150,000 with $100,000
required for earthwork and rock excavation and $50,000 required
for installation of the toe drain and leachate collection system.
Earthwork includes excavation of an estimated 3,900 yd3 of earth
and solid wastes and 900 yd3 of rock-in-trench. Excavation of an
estimated 200 yd3 of material from runon and runoff control and
construction of embankments from excavated sand (2,300 yd3), till
(2,500 yd3) and selected borrow (gravel, 3900 yd3) are other
earthwork items. Preparing fine grade for 7,900 yd3 of till and sand
cover subgrades is a major component of the earthwork activities.
The leachate collection system includes placement of an
estimated 3,800 ft of 4 in. diameter PFPE under drains for leachate
collection, an estimated 1,000 ft of 6 in. RPE sewer pipes for
leachate transport, manholes for the toe drain and trunk sewer
lines, connections to existing sewer lines and single cleanout con-
nection assemblies.
Table 4
Engineer's Estimate
Item
2.01 BXA
2.05 XA
2.05 XB
2.06
2.07 AXA
AX8
AXC
2.07 BXA
BXB
BXC
2.12 XA
XB
XC
3-PFPE
3-RPE
4XA
5
6AX
7
Description Pay
• Unit
Estimated Unit
Quantity Price
Total
Cost
Clearing and Grubbing Lump Sui
Trench Excavation
Rock-ln-Trehcn Excavation
Ditch Excavation
Embankaent In Place - Sand
- Till
- Rock
Borrow - Sand
- Gravel
- Till
Preparing Fine Grade - Subgrade
- Top of Till
- Top of Sand
4" diameter Perforated Flexible
Polyethylene Pipe
6" Rigid Polyethylene Sewer Pipe
Manhole
Connection to Existing Sewer
Facility
Cleanout
Protective Coating
CY
CY
CY
CY
CV
CV
CV
CY
CV
SY
SY
SY
LF
LF
Each
Each
Each
Gallon
3,700 2
900 20
200 5
2,300 5
2,500 5
5
3,900 7
7,200 1
7,900 1
7,900 1
3,800 2
1,000 6
9 2
2 1,000
17 1,000
1 50 20
TOTAL:
Say:
7,400
18,000
1,000
11,500
12,500
27,300
7,200
7,900
7,900
7,600
6,000
18,000
2,000
17,000
1.000
UsT.Joo
$150,000
This project was approved for construction by the CDEP in Aug.
1983 and was bid in Sept. 1983. At the time this paper was being
prepared, bids were being reviewed by the owner. Once a contract
is negotiated, project completion dates specified in the contract
documents call for completion of this project one month subse-
quent to commencement of construction.
JUSTIFICATION FOR PROPOSED DESIGN
The proposed design should provide a highly effective system for
controlling leachate surface escape from the landfill site. The
design offers a number of specific advantages including the provi-
sion of:
•A toe drain system at the base of the fill (above impermeable
materials) for the complete site perimeter
•Excess capacity in the trench and perforated pipe collection sys-
tem (i.e., the 4 in. perforated pipe alone can handle flows up to
300,000 gal/day)
•Design redundancy in providing a perforated pipe and gravel
envelope collection system
•A low-cost, essentially maintenance free system utilizing gravity
flow for fluid transports and a filter fabric pipe wrap for solids
screening
•Maintenance facilities including manholes and single connection
cleanout assemblies for the collection system
•A structurally sound system (i.e., by emplacement of the system
in rock excavation or undisturbed till)
•Easy to install flexible perforated polyethylene drainage tubing
designed to withstand burial under 150 ft of compacted solid
waste
•Contract quality control provisions insuring that the leachate
collection system contains leachate within the toe drain system
The last item was provided in the contract specifications which
called for a minimum of one permeability and one compaction test
per acre to insure that recompacted glacial till materials used as
liner in the toe drain system have a permeability of at least 10"6
cm/sec and an optimum moisture content of 95% for subgrades
and 90% for till.
For rock in trench excavation activities, the specifications called
for placement of two coats (20 mils) of a high build flexible epoxy
protective coating to be applied at the discretion of the engineer to
fractures which may occur in the schist during construction.
REFERENCES
1. Fred C. Hart Associates, Inc., "Laurel Park Landfill Hydrogeological
Assessment," Feb. 1983.
2. Fuss & O'Neill, Inc., "Hydrogeologic Report, Laurel Park Landfill,"
Jan. 1983.
3. Fenn. D., et al., "Methodology Used in the Assessment of Leachate
Generation from Landfills," 1975.
4. Personal Communication Fred C. Hart Associates to the Naugatuck
Treatment Company, Mar. 1983.
5. Personal Communication Fred C. Hart Associates to the Naugatuck
Treatment Company, Mar. 1983.
6. Environmental Testing Corporation Laboratory Report, Feb. 1983.
7. Richard C. Bond, et al., Handbook of Environmental Control,
Vol. II, 1971.
8. Personal Communication Fred C. Hart Associates, Inc. to the Nauga-
tuck Treatment Company, Mar. 1983.
9. USEPA Report, EPA-600-8-8-082.
IN SITU TREATMENT
241
-------
BIO-RECLAMATION OF GROUND AND GROUNDWATER
CASE HISTORY
VIDYUT JHAVERI, Ph.D.
ALFRED J. MAZZACCA
Groundwater Decontamination Systems, Inc.
Waldwick, New Jersey
HISTORY
In Aug. 1975, contamination was observed in a small creek that
discharges into Allendale Brook in New Jersey. A storm sewer line
that discharges into the stream was a point source of pollution.
Data obtained in Nov. 1975 indicated the contamination was com-
ing from Biocraft Laboratories, Inc., a semi-synthetic penicillin
manufacturing plant located nearby. Biocraft's investigation
revealed a leak in an underground process line that carried a mix-
ture of methylene chloride, acetone, n-butyl alcohol and dimethyl
aniline. This mixture infiltrated into the storm sewer line in front of
the building which was the point source of contamination.
On Nov. 24, 1975, all underground lines were disconnected and
above ground lines installed. The investigation failed to determine
when the leak started. Based on daily tank inventory readings from
June 1972 when the plant started up, it was estimated that the
following amounts of substances may have leaked into the subsur-
face:
•Methylene chloride 181,500 Ib
•N-butyl alcohol 66,825 Ib
•Dimethyl aniline 26,300 Ib
•Acetone 10,890 Ib
SITE INVESTIGATION
Biocraft's plant is located on a 4.3 acre site in the northern sec-
tion of Bergen County, NJ (Figure 1). The property is relatively flat
with approximately 30% of the area paved or covered with
buildings, lO^o grass and the remaining 60% lightly forested
(Figure 2). Glacial till underlying the surface at a thickness of about
8 to 15 ft is a poorly sorted mixture of boulders, cobbles, pebbles,
sand, silt and clay.
The contaminated area covered approximately 1.75 acres (Figure
2). Permeability is highly variable throughout the till layer; ground-
water migrates at an average rate of 0.4 ft/day. The hydraulic con-
ductivity calculated from slug tests ranged from 0.02 to 36 gal/day
ft2 and hydraulic gradients ranged from 0.002 to 0.03 ft/ft. A
noticeable groundwater mound is present, corresponding to the
south and east ends of the black-topped areas. Groundwater flow
from the mound is omnidirectional (Figure 3).
Approximately 40 ft of semi-consolidated silt and fine sand
underlies the till layer. Visual inspection of the material in this
deposit suggested very low permeability. Brunswick Shale of the
Treassic Newark Group underlies the semi-consolidated layer for a
thickness of several hundred feet. The Brunswick formation is the
primary source of water supply aquifer for the area (Figure 4).
Figure 1
Location of Biocraft Laboratories, Waldwick, N.J.
REMOVAL AND DISPOSAL
On Jan. 21,1976, the first monitoring wells were installed and by
Nov., ten were completed. Removal and disposal of contaminated
groundwater from selected wells started in Jan. 1977 at a rate of
2500 gal/month. This was later increased to 10,000 gal/month due
to the installation of 12 in. pumping wells. The average cost of
disposal was $0.35/gal. Contamination levels fluctuated widely
during periods of high and low groundwater levels.
Estimates indicated it would take decades to clean up the site. In
Dec. 1978 the New Jersey Department of Environmental Protec-
tion (NJDEP) ordered Biocraft to accelerate the decontamination
process.
BIODEGRADATION
Aerobic biodegradation of acetone and n-butyl alcohol has
been known for a long time.1'2-3 When Biocraft started the in-
vestigation in July 1978, the toxicity and the biodegradability of
methylene chloride was questionable. Later published reports and
242
GROUNDWATER TREATMENT
-------
05
\ .' UNDERGROUND TAMK FARM
Figure 2
Configuration of Biocraft Site, Waldwick, N.J.
INDUSTRIAL PARK
-i-
'5
" Deep Well
\ 213.5
Biocraft's own studies showed that methylene chloride is
biodegradable."
Initial Study
Contaminated groundwater was inoculated with various soil
samples to find organisms that would biodegrade methylene
chloride. Samples of soil were obtained from the homes of Biocraft
employees and from the contaminated site. The study indicated the
soil sample from the contaminated site was most promising.
Shake Flask Study
A shake flask study using contaminated water as the sole carbon
source was done. Various mineral salt combinations were used to
obtain maximum cell mass. A medium composed of NH4NO3 100
mg; Na2HPO4.7H2O 40 mg: KH2PO4 100 mg., MgSO4.7H2O 20
mg., Na2CO3 100 mg., CaCl2 1 mg., MnSO4 2 mg., FESo4.7H2O
0.5 mg. per liter was satisfactory. However, an increase in
methylene chloride concentration required an increase in dibasic
phosphate to buffer the acid formed due to the oxidation of
methylene chloride.
A similar anerobic study was not successful.
Field Feasibility Study
In Dec. 1978, a pilot study in one of the monitoring wells
demonstrated the feasibility of a biostimulation program. Aeration
•'.o.
0-3 Feet.* Silt and Gravel
3-5 Feet.* Glacial Till and Stratified Drift
40 Feet.* Semiconsolidated Silt and Fine
Sand
60 Feet.* Brunswick Shale
•Formation Thickness
Figure 3
Water Table Configuration—1979
Figure 4
Geologic Column for the Biocraft Site
GROUNDWATER TREATMENT 243
-------
of the groundwater (temperature 12-14°Q in this well with a small
sparger and the subsequent addition of nutrients resulted in an in-
crease of bacteria from 1.8 x lOVml to 1.6 x Iff/ml in seven days.
The oxygen uptake rate increased from an initial value so low it
could not be measured to 10 mg/1 hr.
Batch Process Study
The batch study was carried in a Chemap 14 1 glass fermentor.
The fermentor contained 10 1 of contaminated groundwater;
mineral salts were added and air was sparged through a fritted glass
tube at 0.6 wm. The effluent air was passed through activated car-
bon. Biodegradation was determined by COD analysis and total
bacterial count (Figure 5).
ssoo--
33oo--
lioo--
--IO
--IO
--IOJ
--10-
--IO
Pilot Plant Study
A pilot plant study was carried out in 55 gal drums set on their
sides to approximate a biological treatment plant. The drums were
set up in series with one drum as the activating unit and the other
drum as the settling unit. The activating drum was charged with 170
1 of contaminated groundwater and inoculated with 10% inoculum
obtained from the experiments in the laboratory. Air was sparged
through porous alumina air diffusers at a rate of 0.4 1/min. Con-
taminated groundwater was fed into the activating unit at the rate
of 12 1/hr. The temperature was held at 20°C (±2°).
The effluent was pumped to the settling unit where the superna-
tant was pumped out and the settled biomass returned to the ac-
tivating unit. Pilot plant studies ran for approximately 17 days
(Figures 6, 6a, 6b). The pilot plant studies gave the basic informa-
tion for the design of the biological treatment plant.
-INFLUENT
1000--
-_. 6°°--
u
OJ
5
200- -
-EFFLUENT
8
DAYS
Figure 6
Pilot Plant Study
12
"T'T'1—I""1
16
Figure 5
Batch Process Study
On the eighth day, a large decrease in COD was noticed cor-
relating with a large increase in total count on the ninth day. The
first eight days were evidently an acclimation period for the
organisms. On the twelfth day the COD values leveled off in-
dicating the completion of the biodegradation. A similar experi-
ment was done using acclimated inoculum and the log phase was
reduced from eight days to two days. There were no significant dif-
ferences between treatment at 20 °C and 30°C.
Continuous Biodegradation Process
Two Chemap 14 1 fermentors were set up in series. One, used as
the biodegradation unit (activating unit) contained 12 1 of con-
taminated groundwater while the second was used as the settling
unit. A 19 1 reservoir was filled with contaminated groundwater,
and essential minerals were added. One line of a multi-channel
peristaltic pump was used to pump contaminated water into the ac-
tivating unit at the rate of 0.7 1/hr. The second line pumped treated
water from the activating unit into the settling unit, and a third
pumped supernatant from the settling unit to an effluent reservoir.
The continuous process had a 17 hr retention time.
After the first four days, the level of methylene chloride was be-
ing reduced by 85-95% (Table 1). However, acetone showed a
three- to seven-fold increase in concentration. Under aerobic condi-
tions, isopropyl alcohol (IPA) is transformed into acetone.5'6 An
investigation of the gas chromatograph found that the methylene
choride peak was hiding the isopropyl alcohol (IPA) peak. Later
data indicated IPA was less than 100 mg/1.
A similar experiment was run using water contaminated with
dimethyl aniline (DMA) with a 90% reduction in DMA.
500--
300.--
INFLUENT
5
Q
100-- —
Figure 6a
Pilot Plant Study
-INFLUENT
i—i r i i—i ' i' i "i
15
Figure 6b
Pilot Plant Study
244
GROUNDWATER TREATMENT
-------
Table 1
Level of Organic Contaminants in Continuous Laboratory Process (mg/1)
INFLUENT
EFFLUENT
Day
2
3
4
5
6
7
MeClJ Acetone BuOH COO MeCLj Acetone BuOH COD
9975
4571
4847
4690
5040
4725
4583
4448
29
20
21
43
48
78
79
147
1091
491
518
508
584
501
476
431
11939
6320
6360
6460
6460
6115
5933
6437
9045
3285
1943
719
707
818
891
227
64
73
143
43
20
32
34
57
893
303
81
ND
3
30
ND
6
11497
5287
1908
1113
518
1127
759
440
ND: Not detectable. Detection limit 1 mg/1
SITE DECONTAMINATION SYSTEM
The biostimulation-decontamination system consists of the fol-
lowing major components: (1) a groundwater collection system
down gradient of the contamination area, (2) a four-tank, dual
aerobic biological treatment system, (3) a series of in situ aeration
ells along teh path of groundwater flow, (4) effluent injection tren-
ches up gradient of the contaminated area and, (5) a control room.
The groundwater collection system consists of a trench about 80
ft long, 4 ft wide and 10 ft deep. Two slotted collection pipes were
placed on a gravel bed at the bottom of the trench, sloped toward
the center and connected to a central collection pumping well. The
trench was backfilled with washed stone, and then covered with 15
mil plastic sheet and backfilled with earth to grade.
The pumping wells were installed by digging an open hole about
4 ft by 6 ft by 10 ft deep. A 12 in. PVC slotted casing was installed
and the trench backfilled with washed stone. A sump pump with a
10 gal/min. capacity was installed in the wells.
Four stainless steel, insulated, non-roadable tank wagons have
been altered so that two 6,000 gal wagons could be used for the
biodegradation process and two 5,000 gal wagons for the settling
tanks (Figure 7).
The activating tank wagon contains steam line, recirculating line,
sludge return line, influent line, porous aluminum oxide air dif-
fusers with an average pore size of 60 microns, effluent line, vent
line leading to an activated carbon filter, drain lines, gauges and
temperature recorders.
The settling tank wagon contains steam line, sludge line, influent
line, effluent line, vent line leading to an activated carbon filter,
drain lines, gauges and temperature indicators.
Air is sparged into the liquid through air diffusers in each 5000
activating tank at a rate of 20 standard ftVmin.
There are two injection trenches 80 ft long, 4 ft wide and 10 ft
deep. They are lined on the bottom, sides, back and top with 15 mil
plastic sheet, so that the injected, treated water leaves at the front
of the trench. The bottom section of the liner is laid on 1 ft of sand
base and then covered with 0.5 ft of sand. The trenches are hand
filled with 2 in. of washed stone to a thickness of 5 ft. A 2 in.
recharge pipe is installed in the center of the trench. The vertical in-
let pipe ends in a "Y" connection. Two 20 ft slotted sections of 2
in. pipe are connected to the "Y." The trenches are backfilled with
2 in. stone to the surface. A 4 ft high manhole is installed over the
recharge pipe and the top section of plastic is covered to a height of
4 ft with the soil that was removed. Each trench has two monitoring
wells, one at each end of the trench. The wells can also be used for
flushing the system if required (Figure 8).
Nine air injection wells, 30 ft apart, are installed in the subsur-
face along the major pathway of the groundwater flow. Air is
injected into each well at a pressure of 4 Ib/in. The radius of in-
fluence of each air well is greater than 15 ft. The average ground-
water flow through the aerated zones is 0.4 ft/day. Groundwater
temperatures range from 10 to 12 °C providing adequate conditions
for in situ biodegradation as the nutrient-rich water passes through
the aerated zone.
The nutrient tanks, pumps, flow meters, temperature recorders
and etc. are located in a small control room for monitoring and rate
adjustments as required.
Figure 7
Above-Ground Biological Treatment System Design
Figure 8
Injection Trenches
Biological Treatment Plant Operation
On June 30, 1981, the above ground biological treatment system
was started. The intial treatment was a batch operation to develop
growth of the organisms. Each activating tank wagon containing
4,000 gal of contaminated water was inoculated with 50 gal of inoc-
culum from the pilot plant. A combination of mineral salts was
added, air was sparged at the rate of 50 ftVmin. gal and the
temperature maintained at 20 to 25 °C.
After one month, the entire system was operated continuously.
The influent to the activating tank was gradually increased to
match the recharge rate of the pumping wells. The air was gradually
reduced and nutrient concentration was adjusted.
At present, about 13,500 gal of water are being treated per day
with a retention time of 17 hr. Air is sparged at a rate of 20 ftVmin.
GROUNDWATER TREATMENT
245
-------
and temperature maintained at 20 to 25 °C. The effluent air is pass-
ed through an activated carbon filter and the treated water is
pumped to the settling tanks at a rate to maintain a balanced
system.
Solids from the settling tanks are recycled back to the activating
tank. The supernatant of the settling tank which is low in solids is
pumped into the injection trenches.
The system could effectively treat 20,000 gal of water per day
with a 12 hr retention time. However, the pumping wells will not
yield the required amount of water at a steady rate.
The range and average composition of the process influent and
effluent are given in Table 2 for the first 16 months of operation
(Aug. 1981-Dec. 1982) and for the following seven months of
operation. The average removal efficiency for contaminants is
shown below.
August 1981-December 1982
Substance
Isopropyl Alcohol (IPA)
Methylene Chloride (MeCy
Acetone
n-Butyl Alcohol (BuOH)
Dimethyl Aniline (DMA)
December 1981-June 1983
Substance
Isopropyl Alcohol (IP A)
Methylene Chloride (MeCy
Acetone
n-Butyl Alcohol (BuOH)
Dimethyl Aniline
Removal
Efficiency (%)
>98
>98
>88
>97
>64
Removal
Efficiency (%)
>99
>98
>97
>98
>93
Samples of the air space in the activating tanks based on 101 air
samples show methylene chloride concentrations in the range of
0.030 to 0.040 mg/1 or less than 1 % of the contained methylene
chloride.
The microorganisms isolated from the activating tank consisted
of the following: Pseudomonas (40%), Agrobacterium (40%) and
Arthrobacter (20%). These are naturally occurring soil organisms
that are known to use a wide variety of organics as a carbon source.
A laboratory study using a Gilsen Differential Respirometer has
shown that the above isolates can respire on one or more of the
following compounds—acetone, methylene chloride, n-butyl
alcohol and di-methylaniline. Typical data for Pseudomonas
isolate #28 respiring on methylene chloride are shown in Figure 9.
Experiments to show that methylene chloride adhering to the soil
is biodegraded were done by Umbreit at Rutgers University using
'*C labelled methylene chloride. A 0.5 in . diameter glass column
was constructed using four 1 ft glass sections. The column was
packed with soil taken to a depth of 4 ft. Radioactive methylene
2oo--
loo- -
^
-
cellswithCH2CI2
cells without
TIME-mins.
Figure 9
Oxidation of Methylene Chloride
chloride was added to the bottom 1 ft section and air was sparged
through the bottom of the column at approximately 6 ml/min. The
exit gases passed through a trap containing 0.1 N KOH solution
and then through a series of activated carbon traps. The ex-
periments were run in duplicate for a total of six to seven days per
run. One column contained uninoculated soil and the second col-
umn was inoculated with organisms from the settling tanks. The
results indicated a small conversion of methylene chloride to car-
bon dioxide ( 2.3%) in the uninoculated column but appreciable
conversion (56.1 %) in the inoculated column. Radioactivity could
not be measured accurately in the soil because the soil granules in-
terfered with the measurement of radioactivity. The larger percen-
tage of CO2 was found adhering to the soil. This was measured by
removing the CO2 with acid treatment and then measuring the
radioactivity. A large percentage of the methylene chloride was
unaccounted for (Table 3). This could represent methylene chloride
tightly adsorbed to the soil, conversion to some non-volatile in-
termediate or incorporation of the radioactive carbon into the cells.
Table 2
Full Scale Biological Treatment Process
Organic Influent and Organic Effluent (mg/1)
PERIOD AUGUST 1981 - DECEMBER 1982
INFLUENT
EFFLUENT
Range
Avg.
IPA
1 20-ND
52
HeCl2 Acetone BuOH DMA IPA MeCl2 Acetone BuOH DMA
203-30 113-12 129-8 115-3 1-ND 22-ND 31-ND 7-ND 77-ND
98 47 43 23 1 2.2 5.4 1.4 8.3
Range
Avg.
IPA
13-ND
6.3
PERIOD DECEMBER 1982 - JUNE 1983
MeCl2 Acetone jiuOH DMA IPA MeCl2
Acetone
250-11 120-20 92-3 23-1
58.5 38.8 19.1 2.9
0.002-ND 5.7-ND 5.0-ND
0.0 0.92 1.12
ND • NOT DETECTED (Detection limit 5 »cg per liter)
BuOH DMA
0.5-ND 1.0-ND
0.04 0.18
246
GROUNDWATER TREATMENT
-------
Performance Evaluation
The groundwater quality cleanup goals for the decontamination
program were directed by the New Jersey Department of En-
vironmental Protection in an Administrative Consent Order dated
Sept. 25, 1980. The acceptable water quality is shown in Table 4.
The biostimulation process implemented at the Biocraft site is
reducing pollutant concentrations in the ground and groundwater.
Chemical analyses of groundwater for selected pumping and
monitoring wells prior to the startup of the continuous process and
after two years of operation are shown in Table 5.
Pumping well #13 in the main collection trench has shown a
dramatic decrease in pollutants during the two-year operation.
Pumping wells #30 and #32A show a significant decrease in
Table 3
Soil Column Experiments—Labeled MeCh
Table 6
Levels of Contaminants in Monitoring Wells
Columns
Uninoculated
Methylene Chloride — in air 2.2%
Carbon Dioxide— in air 0. 1 %
Carbon Dioxide — in soil 2.3%
% = percent of added radioactivity found
Table 4
Acceptable Water Quality Parameters
BOD
COD
TOC
Chlorides
Acetone
n-Butyl Alcohol
Methylene Chloride
Inoculated
2.9%
0.1%
56.1%
6.0 mg/1
23.0 mg/1
18.0 mg/1
153. mg/1
100 /tg/1
lOOfig/1
8.0/tg/l
Table 5
Levels of Organic Contaminants in Monitoring and Pumping Wells
Date
6/1-4/81
5/23/83
6/30/83
6/1-4/81
5/23/83
6/30/83
6/1-4/81
6/26/83
6/1-4/81
6/30/83
6/1-4/81
5/23/83
6/30/83
6/1-4/81
5/23/83
6/30/83
6/1-4/81
5/23/83
6/30/83
Well
4A
4A
4A
25
25
25
26
26
31
31
P-13
P-13
P-13
P-30
P-30
P-30
P-32A
P-32A
P-32A
MeCl2
67
ND
ND
260
ND
ND
360
<8«
78
<10*
989
ND
ND
880
23.5
64
305
182
281
Acetone
67
ND
ND
40
ND
ND
5
ND
81
ND
24
ND
ND
82
17.0
23.8
105
60
131
BuOH
.
ND
ND
ND
ND
<22*
to
<42
56
ND
ND
37
ND
ND
33
ND
129
DMA
23
ND
ND
ND
ND
19
ND
354
ND
ND
69
ND
ND
208
ND
ND
COD
300
48
60
286
5
3
939
180
425
75
2455
82
30
1418
200
600
1711
890
1600
Period
April- July 82
July-October 82
October 82-
March 83
March-Hay 83
6/30/83
Hell
1
2
4A
9
23
25
10
20
24
42
6
1 1
1 2
14
17
19
29
4A
5
9
24
25
42
S
17
29
HeClj
NO
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
Acetone
ND
ND
ND
ND
NO
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
All values in mg/1
ND = Not Detected (detection limit is 5 /ig/1)
MeCli methylene chloride
BuOH
ND
ND
ND
ND
ND
ND
ND
HD
HD
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
DMA
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
NO
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
ND
COD
S3
32
60
150
35
153
99
31
17
20
30
10
10
12
19
127
70
48
114
17
10
15.4
3
30
2
80
TOC
12
2
14
39.2
2
40
20.2
1.4
3
2
3
2
1 .5
3
4.5
39.2
15.5
42
23
4
2.5
1.2
5.6
11
2.3
1 1
BOD5
14
8.6
24
44
5.1
4.2
36
3.6
8
3
7.5
4.2
5.0
7
1.4
43.2
70
59.9
42.0
7
4.7
5
0
6
1
11
BuOH n-butyl alcohol
DMA Dimethylaniline
COD chemical oxygen demand
All values in mg/1
ND = Not Detected (detection limit is 5 /ig/1)
* = Values given in /tg/1
MeCli methylene chloride
BuOH n-butyl alcohol
DMA Dimethylaniline
COD chemical oxygen demand
P pumping well
pollutants. It is believed that pockets of gross contamination are
being collected by these wells. The data strongly indicate a gross
reduction of contamination in ground and groundwater (Table 6).
This demonstrates that biostimulation can be successful not only in
relatively permeable but also in low permeable formations.
Based on COD values from a few monitoring wells, it is
estimated that the site should be clean by the end of 1984.
Project Cost
The total cost for the biostimulation project is tabulated below.
1. Research and development $453,399.
2. Hydrogeological design and construction 184,243.
3. Process plant design and construction 221,207.
Total $858,849
A literature search revealed little or no information on in situ
biodegradation of contaminants in the ground and groundwater by
recirculation. Therefore, the total amount of dollars spent includes
all aspects of the three individual costs. If the cost of the learning
curve is not considered, the projected cost at the Biocraft site would
be approximately $300,000.00.
Operating Cost
Based on treating 13,500 gal/day, the total operating cost in-
cluding utilities, nutrient cost, labor, maintenance and overhead is
$0.0165/gal. The total cost including amortization base on pro-
jected cost is $0.0358/gal over a three-year period.
REFERENCES
1. Levine, S. and Krampitz, L.O., "The Oxidation of Acetone by a Soil
Diphtheroid.", J. Bacterial., 64, 1952, 645-650.
2. Heinle, D.A. and Fuerst, R., "Acetone Utilization in Streptococcus
Pyogenes." Dev. Ind. Microbiol. 17, 1976, 253-263.
3. Heinle, D.A. and Fuerst, R., "Acetone Incorporation in Streptococ-
cus," Dev. Ind. Microbiol., 18, 1977, 557-563.
4. Brunner, Staub & Leisinger (1980), Appl. Environ. Microbiol 40(5V
950-958.
5. Muller (1931), Biochem. z. 238: 253-267.
6. Pabst and Brown, Dev. Ind. Microbiol, 9, 1968, 394-400.
GROUNDWATER TREATMENT
247
-------
A COMPUTER MODEL FOR OPTIMIZATION OF
GROUND WATER DECONTAMINATION
LOUIS J. BILELLO
MICHAEL H. DYBEVICK
Environmental Science and Engineering, Inc.
Gainesville, Florida
INTRODUCTION
Groundwater contamination can result from past industrial
waste disposal practices. Groundwater in shallow and deep aquifers
underlying a disposal area, as well as off-site water sources, may
contain traces or even significant concentrations of most of the
contaminants contained in materials disposed of in the landfill or
on the ground surrounding an industrial facility.
Treatment of the contaminated ground water may be required (1)
for removal of contaminants from drinking water aquifers or wells,
(2) to lower the ground water table to implement a remedial action,
or (3) to prevent further off-site contaminant migration.
Organic contaminants can either be volatile or non-volatile, with
the volatile contaminants most common because of their
widespread use as industrial solvents and their greater mobility
through soils. Inorganic contaminants, especially heavy metals,
may also be found in many contaminated ground waters.
Although not the only applicable technologies, air stripping and
carbon adsorption are the most common ones used to remove
organic contaminants. They are generally favored for the following
reasons:
•Most organic compounds can be, to some degree, removed by
either or a combination of both processes
•Very low concentrations of most organics found in contaminated
groundwater can be attained after treatment
•Limited, if any, pre-treatment is required for implementation of
either process
•Costs are generally less than for other applicable water treatment
processes
•Equipment is readily available either for purchase or lease from
several manufacturers
Usefulness of a Rapid Assessment Model
In the development of a remedial action plan or activity,
numerous alternatives maybe considered. Associated with the
evaluation of each alternative is the development and achievement
of acceptable response objectives. In many cases, criteria may not
be established for recommended contaminant levels for a particular
site or aquifer. This effort may require the consideration and
evaluation of several groundwater treatment scenarios. To
minimize the time required to perform each evaluation and the
overall alternatives analysis, the use of a model that performs both
a technical and economic assessment is essential.
To more efficiently develop and cost remedial action alter-
natives, Environmental Science and Engineering, Inc. (ESE) has
combined its expertise in groundwater treatment and cost estima-
tion to develop a model that determines the design and cost of an
optimum treatment system using air stripping and/or granular ac-
tivated carbon (GAC). The system design and cost components are
specific to the treatment of contaminated groundwater at remedial
action sites and, therefore, may not be representative of other ap-
plications for either of the processes.
In this paper, the authors discuss the methodology used in
developing the computer model and present several examples of its
application. The theoretical and cost assumptions used are included
with the results and conclusions based on these assumptions.
AIR STRIPPING TECHNOLOGY
Theory
Removal of volatile organics from water by air stripping in a
packed column is based on the transfer of the compound from the
liquid to the gaseous phase. To accomplish this, intimate contact
between the liquid and gas is essential. In a packed column, the
packing medium provides a high surface-area-to-volume ratio,
allowing a thin water film to be produced and exposed to air. Effi-
ciency is dependent on the type and size of the packing medium and
several other factors.
The amenability of an organic compound to be stripped from
water by air is determined by the equilibrium between the concen-
tration of the organic in the water phase and the concentration in
the air phase. For partially miscible organics at low concentrations,
these concentrations can be related by Henry's Law:
Px = H,WL
(1)
where Px = partial pressure on the contaminant in the air (atm)
H! = Henry's Law constant (atm-mVmole)
WL = concentration of the contaminant in the water
phase (moles/m3)
Determination of Henry's Law coefficients in this manner requires
costly laboratory analysis to determine the equilibrium relation-
ship.
If Henry's Law constants are not available for a contaminant
from the literature or from experimental data, an estimate can be
made using the following approximation:
1/H, = 16.04(Vp)(MW) (2)
2 TOl
where 1/H2 = partition coefficient
Vp = vapor pressure of the contaminant in water
(mm Hg)
MW = molecular weight of the contaminant
T = temperature (°K)
S = contaminant solubility in water (mg/1)
24S
GROUNDWAtER TREATMENT
-------
1/H2 is usually reported as dimensionless. Either form should be
calculated for each contaminant at the minimum anticipated
temperature of the groundwater. Temperature dependency of
Henry's Law constants follows the Van't Hoff relationship:
10 t-
log H = -AH°
RT
(3)
where - AH ° = enthalpy change due to the dissolution of the
compound in water
R = universal gas constant
T = absolute temperature
Units for the coefficients are dependent on the units of the Henry's
Law constant. The higher the value of the Henry's Law constant,
the greater the potential for a contaminant to be stripped. McCarty
et a/.1 presented a number of Henry's Law constants for common
organic compounds. McCarty indicated that compounds with
Henry's Law constants greater than 1.0 x 10 ~3 atm - mVmole were
amenable to stripping. The partition coefficient (1/H2) is the
minimum theoretical air-to-water ratio required to achieve an
equilibrium between the air and water phases for a specific con-
taminant.2
Air Stripper Design
The design of an air stripping tower can be estimated from the
Henry's Law coefficient, the maximum concentration of each con-
taminant, the desired contaminant concentration in the stripper ef-
fluent, and knowledge of the mass transfer coefficient for the
specific contaminant, packing medium and liquid loading rate on
the column. Mass transfer coefficients can be obtained from ex-
perimental studies or can be estimated from theoretical predictions.
Treybal3 reports that the mass transfer coefficients of two com-
pounds are related by the ratio of their molecular weights to the 0.3
power. Therefore, if the mass transfer coefficient for a specific set
of conditions is known for one compound, it can be estimated for a
second compound.
In the design of the air stripper, the liquid loading rate (lbH2O/ft2
of column area) affects the maximum air loading rate that can be
used. This limitation, termed flooding, is a physical constraint of
the packing medium. At flooding, passage of water downflow
through the column is restricted by the upcoming air. Generalized
flooding correlations are available for all packing media, as well as
specific correlations for the individual packing materials.
Once a liquid loading rate for a selected packing medium is deter-
mined, the mass transfer coefficients (KL) can be determined from
theoretical correlations* or from empirically determined coeffi-
cients.
Singley and Bilello5 described a linear relationship between the
mass transfer coefficient and the liquid Reynolds number for water
passing through a column. This relationship was determined from
experimental data using chloroform as the contaminant. The ex-
periments were conducted in a 15 in. diameter column containing 1
in. Super Intalox® saddles. The equation is as follows:
Re = 3.32eLQ
aAuL
(4)
where Re = Reynolds number
eL = liquid density (lb/ft3)
Q = liquid flow rate (gal/min)
a = surface area of the packing medium per cubic
foot of packed volume (ftVft3)
A = column cross-sectional area (ft2)
uL = liquid viscosity (cp)
The experimentally determined relationship between the mass
transfer coefficient (KL) and the Reynolds number for 1 in. Super
Intalox® saddles is presented in Figure 1.
s
o
£
1
I
1.0
0.10
0.01
SLOPE* • 0.7«
10
REYNOLDS NUMBER
100
Figure 1
Mass Transfer Coefficient versus Reynolds Number
for Super Intalox® Saddles
The packed depth for the medium is calculated using equations
similar to the following:
dm/dt = KL a LAACfL (5)
where dm/dt = weight of compound transferred per unit
time Otg/min)
K^a = overall mass transfer coefficient specific to the
_ ' compound and packing material (1/ftVmin)
A€L = 1°8 mean concentration driving force 0*8/1)
L = packing depth (ft)
A = column area (ft2)
The log mean driving force is defined as follows:
- (C
CE*)
In
CI - CI*
CE - CE*
(6)
where Cj = influent concentration of the organic compound
in water Oig/1)
Cj* = concentration of the organic compound in water
in equilibrium with the outlet air (/tg/1) de-
termined from the partition coefficient
CE* = concentration of the organic compound in water
in equilibrium with the inlet air (jtg/1), which
should be free of the organic contaminant
(CE* = 0)
Cg © effluent concentration of the organic compound
in water (/tg/1)
GRANULAR ACTIVATED CARBON (GAC)
TECHNOLOGY
GAC is an established, effective technology for the removal of
organic contaminants from water and wastewaters. Removal of
contaminants by GAC treatment depends on the type of carbon
used and the composition and concentration of the organics pre-
GROUNDWATER TREATMENT
249
-------
sent. In contaminated groundwater, several contaminants may be
present in a varying range of concentrations. The ability of GAC to
adsorb a specific contaminant depends on its relative concentration
and the contaminant mix. The limiting contaminant is the first
compound to appear above its objective concentration in the car-
bon column effluent. At the breakthrough of this contaminant, the
GAC in the adsorber should be replaced.
Determination of the limiting contaminant and the frequency of
carbon replacement is best accomplished through pilot studies or
dynamic bench-scale studies such as the Dynamic Mini Column
Adsorption Technique (DMCAT).' Pilot studies could be con-
ducted on-site, but are a major effort and cost. DMCAT studies
can be conducted quickly and inexpensively on a sample of the
water or a synthetic matrix.
Published isotherm data, although not in a dynamic system or
determined in a competitive matrix, can be used to obtain estimates
of carbon loading (Ib contaminant/lb of carbon), albeit for single
component systems.
Several carbon manufacturers and vendors provide adsorbers
and GAC. Spent GAC is replaced and hauled away for reactivation
or disposal. Generally, adsorber sizes are fixed with 20,000 to
40,000 Ib of GAC.
In addition to frequency of GAC replacement, contact time is
another design variable of interest. In service systems, as would
most often be used at remedial action sites, contact time would be
determined by both flow and the amount of GAC. Since the quan-
tity of GAC is fixed per adsorber, a minimum contact time would
be selected and the number of adsorbers chosen to meet this
minimum contact time.
DESIGN CONSIDERATIONS AND
ASSUMPTIONS USED IN THE MODEL
Air Stripper Design
A series of air-to-water ratios (volume of air/volume of water)
was investigated for each contaminant identified in a hypothetical
groundwater matrix. The minimum ratio considered was twice the
theoretical air requirements based on the partition coefficient. The
maximum ratio was the lesser of 250 or 8 times the theoretical air-
to-water ratio. Above an air-to-water ratio of 250, the pressure
drop becomes too high for efficient column operation. This limit
eliminated compounds with low partition coefficients from treat-
ment by air stripping.
For a given compound and flow rate, the diameter for each air-
to-water ratio was calculated so that the column pressure drop was
no greater than 0.5 in water per packed foot, as recommended by
most packing manufacturers. Parallel streams were considered
when calculated column diameters for single streams exceeded 14
ft. A design diameter equal to or larger than the calculated
diameter was chosen from a set of standard diameters.
The Reynolds number at the design diameter and flow rate was
calculated, and the mass transfer coefficient is recalculated at the
design Reynolds number according to the following (as discussed
by Singley and Bilello):'
KU = KLI (NRea/NRe,) 0.76 (7)
The packed column length necessary for the required removal ef-
ficiency was calculated by equations discussed by Kavanaugh and
Trussel.4 Maximum column height was limited to 36 ft, which
allows for 22 ft of packing depth, 5 ft of column for a wet well and
9 ft for internal support equipment clearance. When the calculated
packed height exceeded 22 ft, a series operation was specified. In all
cases, use of 1 in. Super Intalox® packing medium was assumed.
Air Stripper Cost
Capital
Costs for columns and internals (distributors and support plates)
were based on vendor quotes for carbon steel. Packing costs as-
sumed were $14/ft3 for quantities greater than 100 ft3 and $18/ft3
for lesser quantities.
Fans and pumps were chosen from a set of standard sizes provid-
ed by vendors. Where possible, a single fan was used to supply air
to all columns. One pump was assigned to each column.
Installed piping costs were included for 100 ft of carbon steel
pipe to supply the system and 50 ft of pipe for each column.
The subtotal of the above costs was used as a basis to calculate
installation costs at 20% and electrical and instrumentation costs at
13%. Duct work was assumed to add 100% of fan cost to total
direct costs.
Indirect costs were assigned as percentages of direct costs as
shown in Table 1.
Table 1
Indirect Cost Assumptions
Engineering — 15%
Contractor fee — 15%
Legal — 2%
Contingencies — 15%
It was assumed, for purposes of this paper, that control of air
emissions from the stripper is not necessary. In cases where the
emissions may cause a concern to the local residents or to workers,
control systems such as carbon cannisters would be used and their
cost included.
Operating Costs
Operating costs included electrical, maintenance, labor and ad-
ministration costs. Cost assumptions for each item are listed in
Table 2.
Table 2
Operating Cost Assumptions for Air Stripper
•Electrical costs were based on total pump and fan horsepower at
$0.06/kWh.
•Maintenance material costs were estimated at 4% of direct costs.
•Labor costs were assumed to be $12/hr for 1 hr per day times the
number of columns to the one-third power.
•Administration costs were estimated at 20% of labor costs.
Granular Activated Carbon
The basis for the GAC system designed was a leased, truck-
mounted, pre-engineered contractor containing 20,000 Ib of car-
bon. The package design does not have capability for backwashing.
When carbon usage is low, carbon replacement may be less fre-
quent than necessary to prevent unacceptable pressure drop. Under
such low usage conditions, a smaller charge may be necessary to
allow room for backwashing, possibly necessitating an additional
contactor to maintain the minimum empty-bed contact time
(EBCT). Only non-backwash operation was considered in this
analysis.
The package contactor was assumed to be 10 ft in diameter. A
reactivated carbon with a bulk density of 30 lb/ft3 was assumed.
Contactors were arranged in series and parallel to ensure a
hydraulic loading less than 6 gal/min. ft2 and an EBCT of at least
40 min.
For the examples presented in this paper, carbon usage rates were
based on isotherm data collected by Dobbs and Cohen.' Usage
rates determined from experimental studies can also be input. Ad-
sorption capacities were based on influent concentrations.
Granular Activated Carbon System Cost
The assumptions for GAC system capital, indirect and operating
costs are listed in Table 3.
250
GROUNDWATER TREATMENT
-------
Table 3
GAC System Cost Assumptions
CAPITAL COSTS:
•Contactors—A lease fee of $3,560 per contactor per month was used. A
setup fee of $3,100 per site was assumed; setup labor to be provided on-
site at 4 manhours per contactor at $12/hr.
•Site Preparation—$400 per contactor was allowed for a concrete pad.
•Pumps—Vendor lists of pump and driver costs were used.
INDIRECT COSTS (assigned as percentages of direct costs):
•Legal—2%
•Contractor fee—15%
•Contingencies—20%
OPERATING COSTS
•Electricity costs were based on rated driven horsepower and $0.06/kWh.
•Carbon costs were calculated from $0.70/lb carbon replaced.
•Operating labor was assigned at 1 hr per day times the square root of
the number of contactors, plus 1 hr per carbon change.
•Administration and supervision costs were estimated at 20% of operating
labor.
NOTE: Because the designs addressed in this paper are most appropriate for response to waste site
cleanup, no cost for land or working capital is included. Start-up costs are included in the installation
cost.
PROGRAM REQUIREMENTS
For the design programs, each compound is completely
characterized by a carbon adsorption capacity at influent concen-
tration, a mass transfer coefficient and a partition coefficient. All
parameters are specific to the temperature of interest. The waste
stream flow rate is the only other parameter needed to specify a
design.
The program is used to calculate the number of GAC contactors
necessary to maintain a minimum contact time of 40 min. and max-
imum hydraulic loading, the column diameter and the packed
length for air stripping. The ancillary equipment and costs
associated with each design configuration have been previously
discussed.
EXAMPLES OF PREDICTIVE MODEL
The example compounds (Table 4) chosen for this paper had par-
tition coefficients of 0.015 to 0.117 and Freundlich adsorption
parameters ranging from 2.6 to 132 for K (adsorbate/g carbon).
In general, compounds that are easily removed by air stripping
are not easily removed by carbon adsorption. The effects of this in-
verse relationship on the economics of removal are shown in
Figures 2 and 3. As more contaminant is removed from the water at
a given flow rate, the capitalcost of the stripper increases more
PLOW HATE - IM •»•
INFLUENT COMCCNTIUTKW • 14M <**
TOTAL FIMT-TEAP. COtT HAPTHALEMEJ
CAPTTAL COtT P4APTHAUNQ
TOTAL PHUT-TEAM COtT' (CHLOnOTOP.MI
CAPITAL COST ICMLOftoFOHU)
OPEMATWM COtT (NAPTHALENQ
OPCMTMO COtT tCHLOWOFOMHI
AIR STRIPPER EFFLUENT CONCENTRATION (ugfl)
Figure 2
Capital and Operating Costs for Air Stripper Systems
rapidly than the stripper operating cost. The operating cost of a
carbon system, however, increases as more contaminant is re-
moved, and the least cost remains fixed. For compounds (such as
naphthalene) that are more efficiently removed by GAC, the GAC
operating costs are also relatively constant when compared to total
cost.
=>
£
FLOW KATI - 100 «pn
EFFLUENT CONCENTRATION • 0.1 upA
TOTAL FIRST-YEAR COST
(CHLOROFORM)
OPERATING COST
(NAPTHALEHQ
1-i W.t 10M 1.000.0
CARBON CONTACTOR INFLUENT CONCENTRATION (ug/l)
Figure 3
Capital and Operating Costs for Carbon Systems
AIR STRIPPER EFFLUENT CONCENTRATION (ugfl)
CARBON CONTACTOR INFLUENT CONCENTRATION (ug/l)
Figure 4
Air Stripper and Carbon System Costs for Chloroform Removal
Comparisons of air stripping and GAC technologies for the ex-
ample compounds are presented in Figures 4 through 6. For
chloroform, the compound with the highest partition coefficient
considered in this paper, it is always less expensive to use air strip-
ping than to use GAC (Figure 4).
For bromoform, a compound with a higher carbon adsorbability
but lower partition coefficient than chloroform, it is almost always
as economical to use air stripping as it is to use GAC at a flow rate
of 100 gal/min. But at greater flow rates, the cost of leasing more
GAC contactors to maintain sufficient contact time increases more
rapidly than the cost of using a larger stripper column. Stripping
again becomes the more economical choice.
GROUNDWATER TREATMENT
251
-------
AIR STRIPPER EFFLUENT CONCENTRATION (ufl/t)
CARBON CONTACTOR INFLUENT CONCENTRATION lugfl)
Figure 5
Air Stripper and Carbon System Costs for Bromoform Removal
••»• Cf
' KAMON
AIR STRIPPER EFFLUENT CONCENTRATION (l>0/T)
CARBON CONTACTOR INFLUENT CONCENTRATION (ue/l)
Figure 6
Air Stripper and Carbon System Costs for Naphthalene Removal
For naphthalene, GAC is more economical at higher flow rates
than it is for bromoform, but stripping is still more economical at
flow rates above 300 gal/min.
In general, for compounds with partition coefficients lower than
naphthalene, it becomes impractical to use air stripping. The
necessary air-to-water ratio becomes so high that very large column
diameters are necessary, and hydraulic loading becomes so low that
adequate wetting of packing material may not occur. Carbon ad-
sorption is economical only for removing compounds for which air
stripping is impractical.
SUMMARY
The design and cost estimating methods used in this paper allow
two processes to be compared by specifying the waste stream flow
rate and three parameters for each compound: partition coeffi-
cient, mass transfer coefficient and carbon adsorption capacity.
For single-component waste streams, the most economical choice is
usually clear; for waste streams with several contaminants for
Table 4
Physical Properties of Compounds Investigated
Compound
Chloroform
Bromoform
Naphthalene
Molecular
Weight
119.4
252.8
128.2
Partition
Coeffic.*
0.117
0.026
0.015
Miss Transfer
Coefficient
(KL)t
(l/f|2-mln)
0.55
0.44
0.54
Freundllch
Parameters**
K" I/a
2.6 0.73
19.6 0.52
132 0.42
• Ratio of concentration in air to concentration in water at 20°C. Calculated from EPA (1979)'
solubility data.
t Based on experimental data for chloroform at NRe = 100; based on ratio of molecular weights
to 0.3 power for other compounds. From ESE (1981)' and Treybal (1968).'
••From Dobbs and Cohen (197_).'
tt Adsorptive capacity (mg/g carbon) at residual concentration of 1.0 mg/l.
which there are varying response objectives, several alternatives, in-
cluding combined technologies, may be evaluated quickly and on
an equivalent basis to determine the most effective system or the
most likely candidates for pilot study. In none of the cases
evaluated for this paper were the economics of a combined system
more favorable than a system using only one of the technologies.
REFERENCES
1. McCarty, P.L., Sutherland, K.H., Graydon, J. and Reinhard, M.,
"Volatile Organic Contaminants Removal by Air Stripping." Pre-
sented at: Seminar on Controlling Organics in Drinking Water. 99th
Annual National AWWA Conference, San Francisco, CA, 1979.
2. Love, O.T. and Eilers, R.G., "Treatment for the Control of Trichloro-
ethylene and Related Industrial Solvents in Drinking Water." USEPA,
Drinking Water Research Division, Cincinnati, OH, 1981.
3. Treyval, R.A., Mass Transfer Operations, McGraw Hill, New York,
1968.
4. Kavanaugh, M.C. and Trussell, R.R., "Design of Aeration Towers to
Strip Volatile Contaminants from Drinking Water," JAWWA, 72,
1980, 684-69 2.
5. Singley, J.E. and Bilello, L.J., "Advances in the Development of De-
sign Criteria for Packed Column Aeration." Submitted to JAWWA,
1981.
6. Beaudet, B.A., Bilello, L.J., Kellar, E.M. and Allan, H.J., "Removal
of Specific Organics from Wastewaters by Activated Carbon Adsorp-
tion: Evaluation of a Rapid Method for Determining Carbon Usage
Rates." 35th Industrial Waste Conference, Purdue University, La-
fayette, Ind., 1980, 381-391.
7. Dobbs, R.A. and Cohen, J.M., "Carbon Adsorption Isotherms for
Toxic Organics," EPA 600/8-80-023. USEPA, Office of Research
and Development, MERL, Wastewater Research Division, Cincinnati,
OH, 1980.
252
GROUNDWATER TREATMENT
-------
REMOVAL OF POLYNUCLEAR AROMATIC
HYDROCARBONS FROM CONTAMINATED GROUNDWATER
MICHAEL R. HARRIS
CH2M Hill, Inc.
Industrial Processes Division
Milwaukee, Wisconsin
MICHAEL J. HANSEL
Minnesota Pollution Control Agency
Division of Solid and Hazardous Waste
Roseville, Minnesota
BACKGROUND
Reilly Tar and Chemical Corporation operated a coal tar distilla-
tion and wood preserving plant in St. Louis Park, Minnesota, be-
tween 1918 and 1972. Reilly disposed of wastes from the operation
consisting of a mixture of many compounds, including a class of
organic compounds known as Polynuclear Aromatic Hydrocar-
bons (PAH), some of which are carcinogenic, in a network of
ditches that discharged to an adjacent wetland.
In 1932, the first St. Louis Park village well was constructed. The
well was shut down after several weeks of operation because of
complaints about odors attributed to phenol.
Throughout the 1960's and early 1970's, the Minnesota Depart-
ment of Health (MDH) and St. Louis Park monitored municipal,
commercial and industrial wells for phenol. In the mid 1970's, the
MDH and Minnesota Pollution Control Agency (MPCA) became
concerned about PAH compounds which are found in coal tar.
In 1975, MPCA conducted a study to assess the extent and
magnitude of the contamination. The study concluded that the soil
and shallow unconsolidated sandy aquifers near the old Reilly site
were seriously contaminated and were acting as a source of con-
taminants to deeper bedrock aquifers.
In May 1978, the MDH began analyses using High Performance
Liquid Chromatography. An investigation in St. Louis Park iden-
tified PAHs present in several municipal wells. These wells, located
approximately 1/4 to 1/2 mile north of the site, were subsequently
closed down in 1978. Other well closures occurred in 1979 and
1981. The well closures in St. Louis Park accounted for over 35%
of the city's water supply capacity.
In the fall of 1978, the USGS conducted a study of private wells
in the area and, in particular, the Reilly deep well (W23) which was
used as a source of cooling water for the plant. The USGS in-
vestigation revealed a down-hole flow of contaminated water from
shallow aquifers to the Prairie du Chein-Jordan aquifer. This flow,
estimated to be greater than 150 gpm, was stopped in 1978. In 1982,
the MPCA cleaned out the well and removed over 150 ft of coal tar-
like wastes and debris. W23 is now regarded as a major source of
contamination of the Prairie du Chein-Jordan aquifer.
All of the closed municipal wells draw from a water-bearing rock
layer, known as the Prairie du Chein-Jordan aquifer, between 250
and 510 ft below the land surface. Approximately 80"% of the
groundwater utilized in the Twin Cities is from this aquifer.
The Reilly site has been designated as the State of Minnesota's
highest priority Superfund site.
CURRENT STUDY
In August 1982, MPCA contracted with CH2M Hill to complete
an evaluation of groundwater treatment and potable water supply
alternatives for the City of St. Louis Park. During this study,
CH2M Hill conducted bench-scale tests using a number of water
treatment technologies. These tests were designed to determine the
efficiency of various technologies in removing PAHs and other coal
tar derivatives from groundwater. Pilot-scale tests on one
technology were also conducted. The ultimate purpose of this
testing program was to determine whether contaminated ground-
water could be cost effectively treated for discharge into St. Louis
Park's potable water distribution system.
Analytical Procedures
During preparation for this study, CH2M Hill considered the use
of several analytical techniques for measuring compounds in the in-
fluent and effluent from the bench- and pilot-scale test units. Based
on historical analyses and project goals, it was expected that raw
water would contain several thousand nanograms/liter (ng/1) of
PAH and other compounds and that "treated effluents" could
contain total concentrations as low as 10 to 100 ng/1 for the selected
target compounds.
In consultation with MPCA and EPA, it was agreed that target
compounds would include:
•20 polynuclear aromatic hydrocarbons (7 carcinogens, 13 "other"
PAH compounds)
•5 nitrogen heterocycles
•2 sulfur heterocycles
•1 oxygen heterocycle
•3 aromatic amines
•3 miscellaneous compounds (indene, biphenyl and 2,3-dihydro-
indene)
Historically, analyses of groundwater at the site had primarily
used HPLC techniques and Selective Ion Monitoring techniques us-
ing GC/MS. Both of these techniques achieve low nanogram/liter
detection limits, but results are limited to specific target com-
pounds.
The GC/MS method developed by CH2M Hill for the St. Louis
Park project is a modification of USEPA Method 625. The method
detection limits for the PAH compounds are 1000 to 3000 times
lower than those published for Method 625. The method has been
validated and detection limits determined in accordance with pro-
cedures published by USEPA in the December 1981 issue of En-
vironmental Science and Technology.
The method deviates from Method 625 in the following ways:
•a 21 sample is extracted
•The final volume of the extract is 20 jtl as compared to 1 ml in
Method 625
GROUNDWATER TREATMENT
253
-------
•The electron multiplier of the mass spectrometer is adjusted to
provide 8 to 10 times more sensitivity than normally required for
Method 625
•The method utilizes a high resolution narrow bore fused silica
capillary column for better resolution and sensitivity
•A mixture of five internal standards are mixed with the 1 ml ex-
tract of the sample just prior to further concentration of the ex-
tract to 20 ii\
The USEPA Method 610 HPLC technique has been conven-
tionally applied to water samples requiring trace PAH analyses.
The trace GC/MS method used for this studylias the following ad-
vantages over Method 610:
•The average method detection limit for all of the PAH parameters
is approximately 400 times lower than the average detection limit
of the parameters published for Method 610.
•The GC/MS detection limits are more or less uniform (1 to 2 ng/1)
whereas the detection limits published for Method 610 vary for
different compounds by more than 2 orders of magnitude.
•The method is validated for both the PAH parameters and a vari-
ety of nitrogen, oxygen and sulfur heterocycles.
•The mass spectrometer provides more compound specificity than
ultraviolet or fluorescence detection prescribed by the PHLC
procedure. Chromotographic resolution is not- required for de-
tection and quantification.
•The method provides the capability of additional characteriza-
tion of samples by tentative identification of non-target com-
pounds that appear in the chromatogram.
•The method specifies spiking of surrogates into each sample an-
alyzed. The surrogate data can be used to judge the validity of the
sample processing steps for each analysis.
•All raw GC/MS data is stored on magnetic tape for future recall
in case further data processing is required at some later date.
Selection of Technologies for Bench-Scale Test Work
CH2M Hill conducted a search of technical literature for infor-
mation to assess technologies which are applicable for the removal
of PAH and other coal tar derivative compounds from ground-
water. The search was conducted through both in-house technical
libraries and two computerized data bases. The search produced
about 280 sources, but only about 40 sources (see bibliography)
were directly relevant to the situation at St. Louis Park.
Information collected in the literature search was used to assess
the potential applicability of a wide variety of technologies and to
select those to be tested in bench-scale tests. Technologies selected
were:
•Adsorption Technologies
-granular activated carbon
-macroreticular resins
•Oxidation Technologies
-ozone/ultraviolet (O3/UV)
-hydrogen peroxide/ultraviolet (H2O2/UV)
-"A
-chlorine (C12)
-chlorine dioxide (C1O2)
-chlorine in combination with aeration, flocculation and filtration
BENCH-SCALE TESTING RESULTS
Water samples were obtained from one of the contaminated
municipal wells in St. Louis Park and shipped to CH2M Hill's
laboratory for bench-scale testing.
A 2-round bench testing program was designed. The first round
of testing was conducted under very conservative test conditions
(high dosages, long retention times, etc.) and was designed to
quickly determine which technologies could achieve compliance
with treatment "goals" established by the Minnesota Department
of Health:
MDH Treatment
PAH Category Goal
Carcinogenic PAHs, total 28 ng/1
All other PAHs, total 280 ng/1
The goal for carcinogenic PAHs is based on USEPA criteria.
The goal for "other" PAHs is based on concerns about synergistic
effects, and concerns that not all compounds have been tested for
carcinogenicity.
Round two testing was conducted only on technologies which
met the treatment goals in the first round tests and was designed to
identify required dosages, loading rates and retention times in
greater detail.
Granular Activated Carbon (GAC)
During round one testing, adsorption isotherms were developed
for five granular activated carbons:
•Westvaco Nuchar WV-G
•ICI HD 40 W
•Calgon Filtrasorb 300
•Ceca Groundwater
•Witco Witcarb
Three dosages were investigated for each adsorbent: 1 mg/1, 10
mg/1 and 25 mg/1. A blank was also run to evaluate the effect of the
test apparatus on water quality. The isotherm procedure consisted
of pulverizing and selectively screening the carbon (Nos. 200 and
400 sieves), measuring the desired dose into 21 of sample (pH =
7.0), contacting the adsorbent and water for 2 hr at SOT, filtering
and analyzing for PAH and other target compounds. Filtration was
done using millipore all glass filter apparatus and Selas silver metal
membranes (0.45 /*). The apparatus is shown in Figure 1.
Raw water and effluent data from the isotherm tests are shown in
Table 1.
Isotherm data for the GACs was plotted using the Freundlich
equation:
log X/M = log kf + J_log c (1)
n
where:
X/M = weight of adsorbed PAHs
weight of carbon
kf and n are constants
C = residual total PAH concentration
Adsorption isotherms for the five tested carbons for total
residual PAH concentrations (not corrected for blank results) are
shown in Figure 2. Although the performance of all five carbons
was similar, the Calgon and Westvaco carbons appeared to have
slightly higher adsorptive capacity.
Bench-scale column tests (Figure 3) were conducted during round
two testing. Based on the results of the isotherm tests, only the
Calgon and Westvaco carbons were tested in round two.
The objective of round two testing was to evaluate carbon per-
formance after 100 bed volumes (BV) of water were passed through
the column at a loading rate of 4 gpm/ft2. Because of time con-
straints, cost of sample shipment, analytical cost and long com-
puted breakthrough times, no attempt was made to run the bench-
scale columns to breakthrough or exhaustion.
Analytical data from the column tests are shown in Table 2. Due
to sample volume availability, the Calgon run was terminated after
70 BV of water were passed through the column. Both carbons
achieved high removals of PAH and other compounds. Because of
the limited run-time, no attempt was made to plot column
breakthrough curves.
Macroreticular Resin Adsorption
During round one testing, isotherm testing (same procedures as
GAC) was conducted with three macroreticular resins:
254
GROUNDWATER TREATMENT
-------
JO
§
Table 1
Carbon Isotherm Results
(Note: No value is shown for compounds found at less than detection limit)
o
?o
O
c
o
$
PARAMETER
(ALL VALUES IN ng/1)
PAH ('INDICATES CARCINOGENIC PAH)
NAPHTHALENE
1 -METHYIMAPHTHALEHE
2-METHYUUPHTHALENE
ACENAPHTHYLENE
ACENAPHTHENE
FLOOREHE
ANTHRACENE
PHENANTHRENE
PYRENE
FLUORANTHENE
Raw
Hat«r
37
103
23
1200
1900
1900
170
66
440
560
Isotbera
Blank
120
120
71
1200
1900
1900
150
61
380
490
Calqcii
48
110
60
790
1400
1000
56
35
140
190
Calgon Calgon
10 Mj/1 35 Mj/1
IS 13
13 5.4
19 10
21 .3
46 .5
17 .5
0.49
1.6 .0
1.0 .0
1.6 .0
Nucnai
1 MJ/1
44
76
29
960
1700
1300
88
37
150
190
Nuchar Nuchar
10 Mj/1 25 Mj/1
9.0 .8
5.6 .3
7.1 .6
24 .8
52 .0
30 .3
0.48 0.48
1.5 .0
1.5 .0
3.6 .0
IC1
39
130
55
970
1700
1300
80
36
190
250
IC1 ICI tBL*
10 M]/l 25 M/ 1/Mi/l
11 . «*
8.4 . «
8.9 . 33
4B . 1000
110 . 1800
33 . 1600
0.93 0 9 1 110
l.S . 48
2.0 . 200
3.5 . 370
10 Ml/1
14
16
10
137
366
150
4.3
3.0
7.9
11
35 Mj/1 1 Mj/1
9. 37
4. 84
7. 27
6. 1000
1 1600
12 16OO
0.49 130
2.6 53
1.6 340
3.6 430
10 Mi/1 25 Mi/1
17 8.9
36 4.8
13 8.7
240 19
440 37
250 16
9.0 1.0
5.6 3.0
38 3.0
36 2.0
PHENYIJUPHTHALENE
1 , 2 , 6 , 7-TETRAWDROPYRENE
BENZO ( a) ANTHRACENE*
9 , 1 0- BENZPHENAHTHHENE
CHHYSENE*
BDtZO fb*JO FLUORANTHENE*
BENZO(a)PYREHE*
tEHZO(e)PYRENE
BEHZO(;))FLDORAWTHBiE«
PERYLENE
RENZOIg,h,l)PERYLDtE
I»EK)(1,2,3-«1)PYRO4E"
0-PHEMY LEMEPYRENE
DIBEKZO (a , h) ANTHRACENE*
TOTAL CARCINOGENIC PAH'S
TUTAL "OTHKK" PAH'S
NITROGEN HETOBXYCLES
ACRIDINE
CAFBAIOLE
IHTOLE
PHEKAKTHRIDINE
OUIHOLINE
SULFUR HETEROCYCLES
BENZO (b)THIOPHEHE
DIBENZOTHIOPHENE
OXYGEN HETEROCYCLES
DIBEHZOFURAN
MISCELLANEOUS
BIPHEHYL
2,3-DIHYDROINDEHE
INDENE
AROMATIC MINES
ANILINE
1-AMIHOHAPHTHALENE
3-AHIHOBIPHENVL
12 6.5 — -- ~ 5.6 ~ — — " 1.7 6.9 — — 8.4 3.5
9.2 4.8 — — -- 3.5 ____ — -- a.o 5.1 — — 6.5 2.4 —
31.3 11.3 — — — 9.1 — — — -- 3.7 13.0 — — 14.9 4.» —
6400 6392 3819 135.7 42.7 4574 123.8 45. 3 494O 326.2 41.5 5367 619.1 61.3 5300 1063.6 101.4
19 8.4 — — 11 — — 7.7 — — 18 0.65 — 12 3.3
14 9.7 7.4 ~ — 4.8 0.58 — 6.6 — 1.6 9.0 0.57 — 10 3.0
490 460 360 30 3.6 370 23 4.6 380 32 3.8 410 1OO 14 420 ISO 22
1300 12OO 740 14 2.8 900 13 3.4 880 17 3.4 1000 77 4.2 1000 ISO 13
610 370 35O 10 2.9 400 9.3 3.5 390 10 2.2 4SO 5* S.4 SO2 95 9.3
1500 1200 1300 100 51 1300 130 26 1300 260 26 1400 430 8.2 110O 480 110
100 91 79 11 3.1 81 8.3 3.3 77 11 1.6 «0 24 5.1 71 » 6.4
M
z
H
-------
PUHSTJtttC PUMP
COOtMS tUUff ODCULATIOU
TAP HirfTEP TO WdTFJ?
DOnftt* MAGNETIC
A-TEFU>M STIR EkAffS
Figure 1
Apparatus for Isotherm Testing
•Rohm and Haas XAD-2
•Rohm and Haas XAD-4
•Dow XFS-4022
Analytical data from the resin isotherm tests are shown in Table
3. Since the resins achieved little or no PAH removal, no isotherm
plots were developed and no round two testing was conducted.
Chemical Oxidation Testing
All oxidation tests were conducted in a stainless steel reactor
vessel. The unit was 3 in. diameter by a 3 ft length. The vessel was
jacketed with copper tubing for temperature control and housed in
an insulated container. The reactor was equipped with a quartz
tube into which an ultraviolet light source could be placed. The
reactor was also equipped with a fritted glass diffuser through
which air or ozone could be injected. A sketch of the reactor is
shown in Figure 4.
All oxidation "effluents" were extracted immediately upon
withdrawal from the reactor vessel. All samples requiring filtration
COtUMN
CM
MOTE- ALL TUBIM3 IS VO.DL
6TAMLESS Srffl EXCEPT
AIPC31.UMWS FOB
6UBGE SUPPRESSES
\cra\c Mixep
j STA/WLESS sreei.^
FT/1WD POOf \
/
/
/
/
/
/
/
/
/
/
<
£
?
s
TO--
DBAIW
55 G^L. TEFLOW
UWEO DBUt/l
FMI
PUMP
Figure 3
Bench-Scale Carbon Column Apparatus
I 1 I t i I 7 » » I 1 1 i i » T III 1 lit
0 1000
100
10
100
RESIDUAL TOTAL PAH
1000 10000
CONCENTRATION, Nq/1
Figure 2
Total PAH Isotherm—All Carbons
256
GROUND\VAT£R TREATMENT
-------
Table 2
Carbon Adsorption Column Test Results
(Note: No value Is shown for compounds found at less than detection limit)
PARAMETER Km
(ALL VALUES IN ng/1) Hater
>rui 1
PAH (• INDICATES CAKCINOGENI
NAPHTHALENE 3]
Row
Hater
Drua 2
70
Raw
Hater
Dru» 3
38
Calgon
35BV
MID
6.4
Calgon
35BV
BOTTOM
9.7
Calgon
70BV
HID
11
Nuchar
3SBV
HID
12.0
Nuchar
3SBV
BOTTOM
13
Nuchar
70BV
HID
12
Nuchar
70BV
BOTTOM
11
Nuchar
85BV
BOTTOM
11
Kucha r
85BV
BOTTOM
13
Ngchar
100BV
HID
13
100BV
BOTTOM
14
1-METHYLNAPHTHALENt
2-HETHYLNAPHTHALENE
ACENAPIrTHYLENE
ACENAnnHENE
FLUORENE
ANTHRACENE
PHENANTHRENE
PVRENE
FLUORANTHENE
110
14
1200
2000
2100
160
77
400
520
120
41
1200
2100
2100
170
85
450
580
120
19
1200
2000
2600
170
81
370
490
2.3
5. 5
1.4
1.0
1.9
S.S
1.5
.1
.2
.9
.0
.0
4.0
7.1
7.8
16
13
1.6
2.7
3.3
1.4
1.5 1.4 1.1
1.3 1.3 2.6 2.5 1.2 3.0
2.3 1.2
2.4 1.5 1.4
3.2 2.7
6.8 6.0
1.6
FHENyLNAPHTHALEHE
1 , 2 ,6 , 7-TETRAHYDROPIREHE
BENZOIalAHTKRACENE* 11
9 , lO-BENZPHENANTHRENE
CHXVSENE* 11
BENZO (btk) FLUORANTHENE*
BENZOIalPYRENE*
BENZO (c)PYRENE
BQIZO 1] ) FLUORANTHENE*
PERILENE
BENZOIg,h,l)PER¥UME
INDENO(l,2,3-cd)PyRENE*
0-PHENYLENEPYRENI
DIBENZOIa.hlANTHRACENE*
TOTAL CARCINOGENIC PAH'S 22
TOTAL "OTHER" PAH'S 6613
NITROGEN HETEROCYCLES
ACRID1NE 17
CARBAZOLE 14
INDOLE
PHENANTHRIDINE
ODINOLINE 11
SULFUR HETEROCYCLES
BEMZOIblTHIOPIIEME 480
DIBEHZOTHIOPHENE
OXYGEN IIETEROCVCLES
DIBENZOFURAN 1300
MISCELLANEOUS
BIPHENYL 590
2,3-DlHTDROINDEHE 1700
INDENE 100
AROMATIC AMINES
ANILINE
1-AMIHONAPHTHALENE
2-AKINOBIPHENYL
39 8.7
28 7.7
57 16.4
6916 7088 16.6 32.8 66.5 29.4 28.J 27.3 26.1 25.2 28.1 24.6 22.7
19 11
17 11
13 11 1.3 1.5 1.0
480 500 1.1 3.3 4.4 1.1 1.0 1.0 1.0
1400 1200 2.1 7.2
1400 1900 4.8 14 23 3.3 2.7 3.1 3.4 4.4 4.6 4.2 3.3
91 99 1.7 3.4 3.8 2.9 2.2 1.8 2.3 3.2 3.5 2.8 2.7
VE-WT PIPE
COOUUQ KMTEP
CUTLET
FEED PIPE fWOTOSEO
KB Jv&TCW CPEBATIOU)
MATEO JACKET
fEWBE LEW<5TM)
PIFFUSEC'
Figure 4
Oxidation Reactor Vessel
GROUNDWATER TREATMENT
257
-------
Table 3
Carbon Isotherm Results
(Note: No raise Is shown for compounds fonnd at less than detection limit)
Rav
PARAMETER "at«r
PAH 1'IMDlCATfS CARCUCGEtn
HAPBTBM-PT 37
2-HETKTLHAPHTrlALEHt 25
ACENAPtfTHrLPIE 1200
ACtHAPHTHEHE 1900
(Tuonan: 190Q
ANTHmCEHE 170
mowmaam 6*
rtOORAHTHDIE 560
nirimjunmui.BlE
BEHZOIalANTHDACENE* 12
? , 10-BBIZPHDMrrHREflE
CHRYSENE* 9.2
BENZO U>lk) rUX)RANTHENE»
BENZOIalPYRENE*
BENZO ItOPlRENE
Dm
170
130
120
1400
2400
170
71
500
650
7.6
7.0
Dow Dow
10 aq/1 25 «g/l
160 170
120 120
120 110
2100 2100
150 160
59 65
470 480
600 620
5.7 8.1
7.0 7.5
XAD-2 XAD-2
1 M/l 10 -J/l
180 ISO
140 130
140 130
2000 1900
160 160
67 64
390 380
500 490
6.0 5.9
5.9 5.8
XAD-2
25 ../I
190
140
130
HOP
1700
160
64
380
500
7.8
XAD-4 XAD-4
1 M/l 10 M/l
190 180
140 130
140 130
UfiS 1MB
1900 1800
160 140
65 58
390 J90
510 380
7.5 11
5.5 5.4
XAD-4
25 ml
ISO
IIP
110
1900
HP
58
sop
6.»
6.3
PERTLIXE
BENZOta ,h . 1 ) PERYUME
lNDENO 30 uln 7
75 0V npocur* far full ruction tt
75 DV «xponm for full mctlon tl
75 trv •Bpomra for full ronctlan tl
75 0V nroosaim tor ful motion til
50 350 ol/Bln nlr flov
50 350 Bl/Bln Mrntlaa prior to Cl,
50 350 ol/oln oirntlon prior to Cl,
M/l FOCI,
75
50 350 ul/oln otrntlon prior to Cl(
75
50
•0
m
m
rooctlon
, ftaM 10
rooctloB
Ira* round tvu ««lld*u«i unttlut.
258
GROUNDWATER TREATMENT
-------
Table 5
Round One Oxidation Test Results
(Note: No value Is shown for compounds found at less than detection limit)
PARAMETER Raw
(ALL VALUES IN ng/1) Hater
Druai 1
3519-A
PAH (•INDICATES CARCINOGEN:
NAPHTHAkBiE 37
l-HETHYUUPHTHALENE 102
2-NETHYLNAPHTHAUKE 25
ACENAPirniYLENE 1200
ACENAPHTHDffi 1900
FLUORQ1E 1900
ANTHRACENE 170
PHENAMTHRBIE 66
PYHQTE «4fl
FUlnMNTHDie 560
PHDIYLNAPHTHALBIE
Ran
Hater
DruB 2
M-lll
180
HO
150
1200
2000
2100
160
68
450
590
HjOj/UV H,0,/UV
N-121 N-126.
8.0 18
4.4 6.0
5.2 1.4
4.8 1.6
4.9 3.7
21 2.1
1.9 1.0
4.1 1.1
11 1.6
Aer/Cl,
Aer. Aer, Cl, /Hoc. Aeration/
0,/uv 0,/uv rut. rut. mu. ci., ci,-i cio,
M-141 N-142 M-117 M-128 M-166 M-119 M-130 M-107
6.1 4.9 140 67 49 63 71 54
1.9 1.8 110 8.7 29 7.3 14 90
3.7 4.2 110 7.7 14 2.9 5.8 53
1160 810
1000 1700
1900 1700 1700 1800 18OO 1900
150 5.4
1.0 63 23 48 16 10 61
1.1 170 180
1.1 470 160 190 150 210 560
CIO,
N-114
70
100
53
1100
1000
1100
65
380
570
1.2.6. 7-TETRAlttDROPYRENE
BEMZOIalANTHRACEKE* 12
9 . in-BENZPHENAHTHRENE
CHHYSENE* 9.1
BENZO (b£k ) FLUORAHTHDIE*
12
11
6.8
4.7 8.1
3.5
6.5
BENZO la IPYRENE*
BEMZOlelPYREKE
BFWZO t 11 FLUORANTHENE*
PERYLENE
BENZO (u ,h , 1 ) PERYLENE
INDENO (1 , 2 , 1-cd) PYRIHE*
0-PHDnLQ(EPYRENE
DIBENZO(a,MANTHRACENE«
TOTAL CARCINOGENIC PAH'S 21.2
TOTAL "OTHER" PAH'S 6400
NITROGEN HETEROCtCLES
ACRIDINE 19
rjiRMZoLe )4
INDOLE
23
7038
27
18
—
65.4 3B.S
. — ».e — — — — 8.1
15.1 10.9 6571 1966.4 1115.4 1019.2 1150.8 5509
20 20
13 5.7
10
6538
11
PHENAHTHRIDIHE
OUINOLINE
SlimiD IICTFR«!YCIJS
BEN20lblTHIOPHENE 490
DIBENZOTHIOPHENE
480
6.6 2.1
460 250 450
510
OXYGEN HETEROCYCLES
OIBEMZOFURAN 1300
1300
18 1.8
2.9 1300 1200 1100 1100 1100 1200
1400
MISCELLANEOUS
BIPHENYL 610
2.3-DIHYDROINDENE 1500
INDENE 100
AROMATIC AMINES
570
1300
100
7.4 1.8
20 9.3
1.2 7.7
1.0 560 500 430 540 510 520
1.6 1.9 950 760 690 1100 1000 1200
79 50
610
1500
81
ANILINE
1-ArlINONAPHTHAUHE
2-AHINOBIPHEHYL ,
M-156
H-159
H-160
N-157
H-158
H-168
M-147
H-152
H-153
H-148
H-149
n-154
Test Conditions
Dosage
Oxldant •0/1
0 /UV 6.0
Oj/tnr i.j
0,/UV 1.1
0, 5.6
05 5.3
03 1.2
H,0,/UV i
H,o,/irv 2
»,<>, !
H,0, 5
Table 6
for Round Two Chemical Oxidation Tests
Reactor
TlBe pH TeBp °F Comments
60 Bin 7.0 50 UV exposure for full reaction tlBe
60 Bin 7.0 40 UV exposure for full reaction tlae
20 Bin 7.0 40 UV exposure for full reaction tlBe
60 Bin 7.0 50 No UV
20 Bin 7.0 50 No UV
20 Bin 7.0 40 No UV
60 Bin 7.0 50 UV exposure for full reaction tlBe
60 Bin 7.0 40 UV exposure for full reaction tlBe
20 Bin 7.0 40 UV exposure for full reaction tlBe
60 Bin 7.0 50 No UV
20 Bin 7.0 50 No UV
20 Bin 7.0 40 No UV
This test was conducted In drum sample fro* round two validation testing.
GROUNDWATER TREATMENT
259
-------
Table 7
Round 2 Oxidation Test Results
(Note: No value Is shown for compounds found it less thin detection limit)
PARAMETER
UU. VALUES 1H ng/ll
[
SAMP1.E NUMBER
PAH (•IMDICATfr ("ABTINOGEf
1-METHYLHAPHTHALENE .
2-HETHYLNAPhTHALENE
ACEHAPHTHENE
FLUORENE
ANTHRACENE
PHENANTHRENE
FLUORANTHD4E
1 i2j6j7-TETRAMYDROPYRENE
BENZO (a ) ANTHRACENE*
9 . 10-BENZPHENANTHRENE
CHRYSENE*
BD4ZO (bfcX 1 FLUORANTHENE*
CENZOIolPYRENE*
BENZO lelPYRENE
BENZO 1 i ) FLUORANTHENE*
PERYL£NE
BENZOIel.h.DPERYLENE
INDENO(l,2,3-ccJ)PYRENE*
0-PHENYLENEPYRENE
DIBENZOU.h) ANTHRACENE*
TOTAL CARCINOGENIC PAH'S
TOTAL "OTHER" PAH'S
NITROGEN HETEROCYCLES
ACRIDINE
CARBAZOLE
IHrmi.F.
PHENANTHRIDINt
OUINOLINE
SULFUR HETEROCYCLES
BENZO ILITHIOPHENE
DIBENZOTIUOPHENE
OXYGEN HETEROCYCLES
DIBtNZOFURAN
MISCELLANEOUS
BIPHENYL
2.3-DIHYDROINDENE
INDENE
AROMATIC AMINES
ANILINE
1-AMINONAPHTHALENE
2-AMINOBIPHENYL
Raw
Hater
)run 1
M-144
32
no
14
1200
2000
2100
160
77
400
520
11
11
22
6613
17
14
11
480
1300
590
1700
100
FU.W
Hater
DniB 2
M-155
70
120
41
1200
2100
2100
170
85
450
580
29
28
57
6916
19
17
13
480
1400
600
1400
91
Ozone Ozone
Raw 5 Bg/1 1 Bg/1
Hater 60 Bin. 60 Bin.
Dm» 3 »/UV W/UV
M-163 H-156 M-159
38 4.3 7.4
120 2.4
1200 1.0
2000 2.2 1.7
2600 6.8 3.2
170
81 1.0
370 1.4 1.5
490 5.5 2.0
8.7
7.7
16.4
7088 20.9 24.1
11
11
11
500 26
1200 23 2.6
610 2.1 1.3
1900 9.6 4.1
99 5.9 2.6
Ozone Ozone Ozone Ozone
1 Bg/1 5 Bg/1 5 Bg/1 1 Bg/1
20 Bin. 60 Bin. 20 mln. 20 Bin.
w/UV w/o UV w/o UV w/o UV
M-160 M-157 N-158 H-168
7.8 12 4.4 7.3
2.9 3.0 1.2 1.2
1.0
2.2 1.1 1.7 2.8
34 430 740 990
1.4 1.0 1.4 0.93
2.0 1.0 1.5 1.5
5.5 1.0 4.5
1.1 1.9
1.1 1.9
60.6 454.4 753.2 1011.93
1.0
1.4
7.4 1.1
42 425 660 780
10 240 350 390
37 250 390 640
2.6 5.1 3.4 4.3
H2°2 H2°2 H2°2
5 Bg/1 2 Bg/1 2 Bg/1
60 Bin. 60 Bin. 20 Bin
w/UV w/UV w/UV
M-147 H-152 M-153
4.9 13
1.8 10
2-8 8.2
7.0 1.1 14
14 3.9 79
22 4.5 74
1.3
1.0 5.6
2.0 15
9.6 3.5 36
—
52.6 25.5 256.1
1.4
2.3 43
15 5.1 93
6.2 2.2 27
8.2 110
1.7 3.4
H2°2
5 Bg/1
60 Bin.
w/o UV
M-148
55
100
980
1800
1900
140
70
390
490
8.5
8.5
17
5945
9.1
11
8.1
470
1200
540
1400
87
H2°2
5 ag/1
20 Bin.
v/o UV
H-149
55
100
1100
1800
2300
159
78
370
4BO
9.1
7.0
16.1
6456
14
11
8.0
450
1200
550
1300
84
H2°2
Test B
2 Bg/1
20 Bin.
v/o UV
H-154
50
no
JO
940
1500
1900
140
76
330
. 450
9T0
7.3
16.3
5516
11
11
7.4
480
1100
580
1400
88
were passed through a 0.45 micron silver metal membrane prior to
extraction. When air was used for reagent preparation (i.e., C1O2)
or for aeration, compressed air was passed through activated car-
bon and a molecular sieve to ensure a "clean" air source.
Round One Oxidation Testing
During round one testing, special emphasis was placed on com-
binations of aeration, chlorination, flocculation and filtration.
These unit operations are employed in the iron removal treatment
plants at St. Louis Park's municipal wells. Test conditions for
round one oxidation tests are given in Table 4 while analytical
results are shown in Table 5.
Ozone/UV and Hydrogen Peroxide/UV were the only two oxi-
dant systems tested which met the treatment goal of 280 ng/1 total
"other" PAHs. Significantly less oxidation was seen with chlorine,
chlorine dioxide and the aeration/filtration/flocculation options.
This trend was expected based on the standard oxidation potential
of the oxidants tested.
Round Two Oxidation Testing
Based on the results of the first round tests, O3/UV and H2O2/
UV were selected for round two testing.
Test conditions and analytical results are shown in Tables 6 and 7
respectively.
Ozone/UV
Ozone/UV achieved the treatment goals at all conditions tested.
Ozone by itself did not achieve comparable results.
Two GC/MS data files from the round two tests were chosen to
search for oxidation by-products. The data file for bench-scale
sample M-158 was searched first to determine what by-products
resulted from ozone treatment only. A number of compounds were
detected whch had mass spectral properties expected for oxidized
PAH compounds. The mass spectra were searched through the Na-
tional Bureau of Standards Mass Spectral library for tentative iden-
tification. All of the compounds could not be identified, but the
following list of compounds did give high computer calculated cor-
relations:
1. 2,3-Dihydro-lH-Indene-l-one
2. Fluorene-9-one
3. 5H-Phenanthridine-6-one
4. Dibenzothiophene-5-oxide (sulfoxide)
5. 9,10-Anthracenedione
6. 1,10-Phenanthrenedione
The data file for bench-scale sample M-159 was then searched for
these compounds plus any other that might be present from O /UV
oxidation. No oxidation by-products were detected in this file.
260
GROUNDWATER TREATMENT
-------
FLOW TOTALIZED
Figure 5
Schematic of GAC Pilot Testing Equipment
10.000. ,, _
".^ j»Et,iw!r&1:fi!'£tw«*;tio>i':. "•.
: : ) tpIALflM«eR"»XH*|- -']'.•:
I!iMJiIT]Ji|)tlJp|r
:-4:.:-l" ' :.||q
..,,,. ,,r :,,|!;i,
• r-TRCMMf NT PQAf-; i T :-
/ (TOTAL >"OTHER*MH1I
12,000 11,000
VOL PAUED (OALLONI)
The literature indicates that the oxidation of PAH compounds
produces a wide variety of carboxylic acid derivatives. The method
of analysis used in this study would not detect such compounds.
These compounds do not present significant public health concerns
at these levels.
H2O2/UV
H2O2/UV met the stated treatment goals at the higher dosages
and retention times tested, but failed to meet the treatment goal at
the lowest dosage and retention time tested. H2O2, by itself, failed
to meet the stated goal of 280 ng/1 for total "other" PAH.
PILOT-SCALE TESTING
All of the tested technologies achieved compliance with the 28
ng/1 treatment goal for carcinogenic PAH. Based on the results of
the bench testing program, however, only three technologies were
shown to be effective in removing PAH compounds to below the
treatment goal of 280 ng/1 total "other" PAH compounds. These
three technologies were:
•Granular Activated Carbon (GAC)
•Ozone/Ultraviolet
•Hydrogen Peroxide/Ultraviolet
An analysis of these three technologies concluded that GAC
would be the most cost-effective treatment for the raw water PAH
concentrations (about 7,000 ng/1) anticipated at the municipal well
in St. Louis Park. Although no test work was completed on water
with very high PAH concentrations, it is possible that O3/UV could
prove to be more cost-effective at higher raw water PAH concen-
trations.
To provide design criteria for a full-scale treatment system, a
GAC pilot plant was set up and operated in the pump station at one
of St. Louis Park's contaminated wells. Two GAC pilot trains were
operated parallel. Each train (Figure 5) consisted of four 4 in.
diameter by 4-ft high glass columns, operated in series. Each col-
umn contained approximately 3 ft of carbon. Calgon Filtrasorb 300
and Westvaco Nuchar WV-G were used, respectively in the two
pilot trains.
Since the pilot train containing Westvaco carbon experienced a
number of mechanical and operational problems during the pilot
study, the data collected from this unit have been excluded from
this paper.
The train containing Calgon carbon was operated for 42 days.
Average operational conditions are summarized as follows:
Paramater
Flow rate, gpm
Surface Loading Rate gpm/ft2
Contact time (empty bed basis), min
Column 1
Column 2
Column 3
Column 4
Total
Temperature (average) °C
Conductivity, umhos/cm
Dissolved Oxygen, mg/1
PH
Value
0.44
5.04
4.69
4.59
4.43
4.44
18.15
10
412
0
7.10-7.45
Figure 6
Breakthrough Profile Calgon Column Train
Influent effluent samples from each of the four columns were
obtained at regular intervals throughout the pilot testing period and
analyzed for all target compounds. Analytical work from the pilot
testing program is given in Tables 8 to 12.
A chronological plot of total PAH concentrations in pilot plant
influent and in the effluent from each of the four pilot columns is
shown in Figure 6. After passing through the first column, total
PAH concentrations were reduced to roughly 10 to 20 ng/1. Essen-
tially, no further removals occurred across the second, third and
fourth columns.
GROUNDWATER TREATMENT
261
-------
PAkAHETES
(ALL VALUES IS 1.9/11
ANALYSIS BY:
2/28/83
Table 8
Influent to Pilot Column Trains
2/26/83 3/12/83 3/12/83 3/20/83 3/20/83
4/1/83
" CH2H HILL CH2M HILL CH2M HILL CH2H HILL CH2H HILL CH2M HILL CH2M HILL
DAY Or PILOT TEST
ANALYTICAL EQUIFHENT
GCHS
PAN VINDICATES CARCINOGENIC PAH)
NAPHTHALENE
1-HETHYLNAPHTHALENE
36
ISO
35
170
31
160
29
160
30
110
30
110
32
120
32
130
34
150
1 -HETHYLNAPHTHALENE
ACENAPHTHYLENE
1300
ACEHAPHTHENE
1800
PHENANTI IRENE
FLUORANniENE
FHENY LNA PIITHALENE
1,2,6,7 -TCTRAHYDROPYREHE
BENZO lal ANTHRACENE*
9,10-BENZPHENANTHRENE
CHRVSENE*
BENZO(bik) FLUORANTHENE*
BENZOlalPVRENE*
BENZO(e)PYRENE
BENZO(})FLUORANTHENE*
PERYLENE
BENZO(a,h,1)PERYLENE
INDENO(l,2,3-cd)PYRENE*
0-PHENYLENEPYRENE
DIBENZO(a,M ANTHRACENE*
22.0
~22T6~
TOTAL CARCINOGENIC PAH'S
TOTAL "OTHER" PAH'S
NITROGEN HETEROCYCLES
15
PHENANTHRIDINE
OUINOLINE
SULFUR HETEROCYCLES
BENZO(b)THIOPHENE
"BOCT
~840~
DIBENZOTHIOPHENE
OXYGEN HETEROCYCLES
DIBENZOFURAN
MISCELLANEOUS
BIPHENYL
720
2,3-niHYDROINDENE
INDENE
"120"
~TI6~
AROMATIC AMINES
1-AMINONAPHTHALENE
l-AMINOBIPHENYL
Note: No value Is shown for compounds found at less than the detection Halt.
Although several additional compounds started appearing in ef-
fluent from the first column toward the end of the testing period,
there was no evidence of PAH breakthrough after 42 days of
operation. Although increased run time would have been desirable
to define carbon breakthrough and exhaustion characteristics, the
pilot test was terminated after 42 days.
Data collected in the pilot testing program were used to evaluate
GAC treatment of contaminated groundwater versus providing
alternative potable water supply alternatives for St. Louis Park.
Discussion of the analysis of alternatives is beyond the scope of this
paper.
SUMMARY
As part of a study for the MPCA, CH2M Hill developed a
GC/MS test protocol with an average method of detection limit of
1 to 2 ng/1 for a variety of PAH and other coal tar derivative com-
pounds.
Bench-scale and pilot-scale testing data are presented for a varie-
ty of water treatment technologies, illustrating the degree of treat-
ment achievable with each technology. Influent and effluent con-
centrations are reported for 34 PAH and other coal tar derivative
compounds.
Three of the technologies tested (GAC, O/UV and H2O2/UV)
achieved compliance with project specific treatment goals and pro-
vided effluent water quality adequate for use in a potable water
distribution system.
REFERENCES
1. Fochtman, E.G., "Biodegradation and Carbon Adsorption of Car-
cinogenic and Hazardous Organic Compounds," IIT Research Inst.,
Chicago, IL. Available from the National Technical Information
Service, Springfield, VA 22161 as PB81-171852.
2. Shuckrow, A.J., Pajak, A.P. and Osheka, J.W., "Concentration
Technologies for Hazardous Aqueous Waste Treatment," Touhill,
Shuckrow and Associates, Inc., Pittsburgh, PA. Available from the
National Technical Information Service, Springfield, VA 22161 as
PBS 1-150583.
3. Snoeyink, V.L., McCreary, J.J. and Murin, C.H., "Activated Carbon
Adsorption of Trace Organic Compounds," Illinois Univ. at Urbana-
Champaign. Dept. of Civil and Ceramic Engineering. Available from
the National Technical Information Service, Springfield VA 22161 as
PB-279253.
262
GROUNDWATER TREATMENT
-------
Table 9
Effluent from Calgon Column tt\
PARAMETER
(ALL VALUES IN ng/1)
DATE:
ANALYSIS BY:
DATE OF COLLECTION
2/20/83 2/24/83 2/28/83 3/4/83 3/8/83 3/12/83 3/16/83 3/20/83 3/26/83 4/1/83
CH2M HILL CH2M HILL CH2M HILL CH2H HILL CH2M HILL CH2M HILL CH2M HILL CH2M HILL CH2M HILL CH2M HILL
DAY OF PILOT TEST:
ANALYTICAL EQUIPMENT
PAH ('INDICATES CARCINOGENIC PAH)
NAPHTHALENE
1-METHYLNAPHTHALENE
2-METHYLNAPHTHALENE
ACENAPHTllYLENE
ACENAPHTHENE
FLUORENE
2 6 10 13 18 22 26 30 36 42
GCMS GCMS GCMS GCMS GCMS GCMS GCMS GCMS GCMS GCMS
4.2 21 3.9 5.5 4.4 5.8 11 4.5 2.6 3.B
1.2 1.2 2.1 1.2 1.7 1.2 1.3 1.9
2-0 2.7 2.6 5.0 2.9 3.4 2.8 2.2 2.4 3.1
2.0
2.5 2.2 4.8
1.4 2.6
ANTHRACENE
PHENANTHRENE
PYRENE
FLUORANTHENE
PHENYLNAPHTHALENF.
1,2,6, 7-TETRAHYDROPYRENE
1.4 1.4 1.4 1.9 1.5 1.0
1.4 1.5
1.5 3.3
BEN20 (a) ANTHRACENE*
9 , 10-BENZPHENANTHRENE
CHRYSENE*
BENZO (btk ) FLUORANTHENE*
BENZO (a) PYRENE*
BENZO(e)PYRENE
BENZO (j I FLUORANTHENE*
fLKfLtm
BENHO(g,h,ill'ERYLmE
INDENO ( 1 , 2 , 3 -cd ) PYRENE*
O-PHENYLENEPYRENE
DIBENZO (a, h] ANTHRACENE*
TOTAL CARCINOGENIC PAH'S
TOTAL "OTHER" PAH'S
—
7.4 23.7 7.7 14.0 7.0 12.3 19.7 14.9 8.2 21.5
NITROGEN HETEROCYCLES
ACRIDINE
CARBAZOLE
INDOLE
PHENANTHRIDINE
QUINOLINE
3.0 1.4 1.4 2.1 1.5 1.8 1.7
SULFUR HETEROCYCLES
BENZO (b)THIOPHENE
DIBENZOTUIOPHENE
1.1 1.1 1.1 1.2 2.9
OXYGEN HETEROCYCLES
DIBENZOFORAN
MISCELLANEOUS
BIPHENYL
2,3-DIHYDROINDENE
INDENE
1.3 1.4 1.3
3.8 3.6 3.5 3.3 5.5 5.8 7.8 12 14 22
1.0 3.1 1.0 1.8 2.6 1.8 2.5 3.5 4.5 3.7
AROMATIC AMINES
ANILINE
1-AMINONAPHTHALENE
1-AMINOBIPHENYL
Note: No value is shown for compounds found at less than the detection limit.
4. Sforzolini, G.S., Savino, A. and Monarca, S., "Decontamination of
Water Contaminated with Polycyclic Aromatic Hydrocarbons (PAH)
II. Action of Chlorine and Ozone on PAH Dissolved in Drinking
and River Water (Rough Draft)," Perugia Univ. (Italy). Inst. of Hy-
giene. Available from the National Technical Information Service,
Springfield, VA 22161 as ORNL-tr-2961.
5. Duvel, W.A. Jr. and Helfgott, T., "Removal of Wastewater Organics
by Reverse Osmosis," JWPCF47, 1975, 57-65.
6. Sorrell, R.K., Barss, H.J. and Reding, R., "Review of Occurrences
and Treatment of Polynuclear Aromatic Hydrocarbons in Water,"
Env. Int., 4, 1980, 245-254.
7. Murin, C.J. and Snoeyink, V.L., "Competitive Adsorption of 2, 4-
Dichlorophenol and 2, 4, 6-Trichlorophenol in the Nanomolar to
Micromolar Concentration Range," Env. Sci. Tech. 13, 1979, 305-311.
8. Suffet, I.H., Brenner, L., Coyle, J.T. and Cairo, P.R., "Evaluation of
the Capability of Granular Activated Carbon and Xad-2 Resin to Re-
move Trace Organics from Treated Drinking Water," Env. Sci. Tech.
12, 1978, 1315-1322.
9. Basu, D.K. and Saxena, J., "Monitoring of Polynuclear Aromatic
Hydrocarbons in Water Compounds with Polyurethane Foams,"
Env. Sci. Tech. 12, 1978, 791-795.
10. Chriswell, C.D., Ericson, R.L., Jun, G.A., Lee, K.W., Fritz, J.S.
and Svec, H.J., JAWWA 69, 1977, 669-674.
11. Zogorski, J.S. and Faust, S.D., "Operational Parameters for Opti-
mum Removal of Phenolic Compounds from Polluted Waters by
Columns of Activated Carbon," Water-1976, AICHE Symp. Ser 73,
No. 166, 1977, 54-65.
12. Baird, R., Carmona, L. and Jenkins, R.L., "Behavior of Benzidine
and Other Aromatic Amines in Aerobic Wastewater Treatment,"
JWPCF, 49, 1977, 1609-1615.
13. Harrison, R.M., Perry, R. and Wellings, R.A., "Chemical Kinetics of
Chlorination of Some Polynuclear Aromatic Hydrocarbons under
Conditions of Water Treatment Processes," Env. Sci. Tech., 10,
1976, 1156-1160.
14. Harrison, R.M., Perry, R. and Wellings, R.A., "Effect of Water
Chlorination upon Levels of Some Polynuclear Aromatic Hydro-
carbons in Water," Env. Sci. Tech., 10, 1976, 1151-1156.
15. Acheson, M.A., Harrison, R.M., Perry, R. and Wellings, R.A.,
"Factors affecting the extraction and Analysis of Polynuclear
Aromatic Hydrocarbons in Water," Water Res., 10, 1976, 207-212.
GROUNDWATER TREATMENT
263
-------
Table 10
Effluent from Calgon Column #2
PARAMETER
(ALL VALUC IN nq/1)
UATt:
ANALYSIS BY:
DATE OF COLLECTION
2/20/83 2/24/83 2/28/83 3/4/83 3/8/83 3/12/83 3/16/83 3/20/83 3/26/83 4/1/83
CH2H HILL CH2H HILL CH2M HILL CH2H HILL CH2M HILL CH2K HILL CH2M HILL OUM HILL CH2M HILL CH2M HILL
DAY OF PILOT TEST:
ANALYTICAL EQUIPMENT
GCMS
PAH ('INDICATES CABC1NOGENIC PAH I
HAPHTHALEHE
5.1
1 -METHY LNAPHTHALENE
1.3
2-HETHY LNAPHTHALENE
ACENAPHTHYLENE
ACENAPHTHENE
PHENANTHREHE
FLUORANTHENE
PHENY LNAPHTHALENE
1,2,6,7-TETRAHYDROPYRENE
BENZO (a) ANTHRACENE*
9,10-BENZPHEHANTHRENE
BENZO(bSk)FLUORANTHEHE*
BENZOIolPYRENE*
BENZO(e)PYRENE
BENZO I)) FLUORANTHENE*
PERYLENE
BENZO(9,h,l)PERYLENE
INDENO(1,2,3-cd)PYRENE*
0-PHENYLENEPYRENE
D1BEHZOla,h)ANTHRACENE*
TOTAL CARCINOGENIC PAH'S
TOTAL "OTHER" PAH'S
12.2
NITROGEN HETEROCYCLES
I'HENANTHRIDINE
QUINOLINE
SULFUR HETEROCYCLES
BENZOIblTHIOPHENE
DIBENZOTHIOPHENE
OXYGEN HETEROCYCLES
D1BENZOFUKAN
MISCELLANEOUS
2,3-DIHYDROINDENE
3.5
5.3
7.8
2.9
AROMATIC AMINES
1-AHINONAPHTHALENE
1-AMINOBIPHENYL
Note: No valume is shown tor compounds found at lu^s than the detection Unit.
16. Abrams, I.M., "Removal of organics from water by synthetic resinous
adsorbents," Water-1969, Chem. Eng. Prog. Symp. Ser., 65, No. 97
1969, 106-12.
17. Hindin E., Bennett, P.J. and Narayanan, S.S., "Organic compounds
removed by reverse osmosis," Water & Sewage Works, 116, 1969
466-70.
18. Van Vliet, B.M., Weber, W.J. Jr. and Hozumi, H., "Modeling and
Prediction of Specific Compound Adsorption by Activated Carbon
and Synthetic Adsorbents," Water Res., 14, 1980, 1719-1728.
19. Pringle, W., "Analysis of the Chemistry Associated with Ozonolysis
of Organic Pollutants Molecules in Water." Available from the Na-
tional Technical Information Service, Springfield, VA 22161 as PB81-
115651.
20. Gracf, W. and Nothhafft, O., "Chlorination of Drinking Water and
Benzopyrene," Arch. Hyg. Bakl., 147, 1963, 135-146.
21. Reichert, J.K., "Carcinogenic Substances in Water and Soil. XXI.
Quantitative Results on the Removal of Polycyclic Aromatic Com-
pounds from Drinking Water by Chlorine Dioxide Treatment," Arch.
Hvg. Bakl.. 152, 1968, 37-44.
22. Reichert, J.K., "Carcinogens in Water and Soil. XXIV. Removal of
Polycyclic Aromatic Compounds in Drinking Water Treatment with
Chlorine Dioxide: Identification of Previously Unknown Products of
the Reaction of 3,4-benzopyrene and Chlorine Dioxide," Arch. Hug.
Bakt., 152, 1968, 277-279.
23. Reichert, J.K., "Carcinogens in Water and Soil. XXIV. Removal of
Polycyclic Aromatic Compounds in the Treatment of Tap Water
with Chlorine Dioxide: Isolation and Identification of Products of the
Reaction with 3,4-benzopyrene," Arch. Hyg. Bakt., 152, 1968,
265-276.
24. Smith, J.O., McCall, R.B. and Chan, P.K., "Formation of Poly-
chlorinated Aromatic Compounds during Aqueous Chlorination,"
Env. Pollut., 14, 1977, 289-296.
25. Oyler, A.R., et al., "Determination of Aqueous Chlorination Re-
action Products of Polynuclear Aromatic Hydrocarbons by Reversed
Phase High Performance Liquid Chromatography-Oas Chromato-
graphy," Anal. Chem., 50, 1978, 837-842.
26. Carlson, R.M., et al., "Aqueous Chlorination Products of Polynu-
clear Aromatic Hydrocarbons," Water Chlorination: Envir. Imp**
and Health Effects, Proc. of Conf. on the Envir. Impact of Wate
Chlorination, 2nd Ed., Ann Arbor Sci., 1978, 59-65.
264 GROUNDWATER TREATMENT
-------
Table 11
Effluent from Calgon Column #3
Table 12
Effluent from Calgon Column #4
PARAMETER
(ALL VALUES IN ng/l)
2/20/83
3/20/83
ANALYSIS BY:
DAY OF PILOT TEST
ANALYTICAL EQUIPMENT
PAH ('INDICATES CARCINOGENIC PAH)
NAPHTHALENE
1-METHYLNAPHTHALENE
2-METHYLNAPHTHALENE
ACENAPHTHYLENE
ACENAPHTHENE
PHENANTHRENE
FLUORANTHENE
THENYLNAPHTHALENE
1,2,6,7-TETSAHYDROPYRENE
BEN20(a)ANTHRACENE*
9,10-BENZPHENANTHRENE
BENZO(bsk)FLUORANTHENE*
BENZOIalPYRENE*
BENZO(e)PYRENE
BENZO(3)FLUORANTHENE*
BENZO(g,h,i)PERYLENE
INDENO(l,2,3-cd)PYRENE*
0-PHENYLENEPYRENE
DIBENZO (a,h)ANTHRACENE*
TOTAL CARCINOGENIC PAH'S
TOTAL "OTHER" PAH'S
NITROGEN HETEROCYCLES
PHENANTHRIDINE
QUINOLINE
SULFUR HETEROCYCLES
BENZO (b)THIOPHENE
DIBENZOTHIOPHENE
OXYGEN HETEROCYCLES
DIBENZOFURAN
MISCELLANEOUS
2,3-DIHYDROINDENE
AROMATIC AMINES
1-AMINONAPHTHALENE
1-AMIIIOBIPHENYL
CH2B HILL CH2M HILL CH2M HILL
6.0
NuLe: Mo value is shown for compounds found at less than the detection limits.
PARAMETER
(ALL VALUES IB ng/l)
DATE:
ANALYSIS BY:
2/20/83 3/8/83 3/20/83
CH2M HILLCH2M HILLCH2M HILL
DAY OF PILOT TEST
ANALYTICAL EQUIPMENT
PAI1 ("INDICATES CARCINOGENIC PAH)
NAPHTHALENE
1-METHYLNAPHTHALENE
2-METHYLNAPHTHALENE
ACENAPHTHYLENE
ACENAPHTHENE
PHENANTHRENE
FLUORANTHENE
PHENY LNAPHTHALENE
1,2,6,7-TETRAHYDROPYRENE
BENZO(a)ANTHRACENE*
9,10-BENZPHENANTHRENE
BENZO(b£k)FLUORANTHENE*
BENZOIalPYRENE*
BENZOIelPYRENE
BENZO(j)FLUORANTHENE*
PERYLENE
BENZO(g,h,i)PERYLENE
INDENO(l,2,3-cd)PYRENE*
0-PHENYLENEPYRENE
DIBENZO(a,hlANTHRACENE*
TOTAL CARCINOGENIC PAH'S
TOTAL "OTHER" PAH'S
NITROGEN HETEROCYCLES
PHENANTHRIDINE
QUINOLINE
SULFUR HETEROCYCLES
BENZO(b)THIOPHENE
DIBENZOTHIOPHENE
OXYGEN HETEROCYCLES
DIBENZOFURAN
MISCELLANEOUS
BIPHENYL
2,3-DIHYDROINDENE
AROMATIC AMINES
1-AMINONAPHTHALENE
1-AMINOBIPHENYL
Note: No value is shown for compounds found at loss than the detection limit.
27. Personal communication, Dr. Bricks Leitis of Westgate Research,
Sept. 1982.
28. Lipowicz, M., "Rapid Oxidation Destroys Organics in Wastewater,"
Chem. Ens., 88, Nov. 1981, 40-41.
29. Chang, I.L., "Rapid Free Radical Oxidation of Organic Wastewater
by U.V./H2O2/Cavitation," 21st WEH Seminar, Grundlagen der
Desinfektion and Reingung von Wasse mittels Ultraviolet—Strah-
lung, March 1982.
30. "Study of Groundwater Contamination in St. Louis Park, Minne-
sota Final Report," Memorandum No. GR8-12, Eugene A. Hickok
and Associates, Nov., 1981.
31. Leitis, E., Zeff, J.D. and Smith, M.M., "Chemistry and Application
of Ozone and Ozone/UV Light for Water Reuse," U.S. Department
of Interior, Office of Water Research and Technology, OWRT14-34-
0001-9436, May 1981.
32. Basu, D.K. and Saxena, J., "Polynuclear Aromatic Hydrocarbons in
Selected U.S. Drinking Waters and Their Raw Water Sources," Env.
Sci. Tech., 12, 1978, 791-794.
33. Carlson, R.M., et al., "Facile Incorporation of Chlorine into Aro-
matic Systems During Aqueous Chlorination Processes," Env. Sci.
Tech., 9, 1975, 674-675.
34. Gabovich, R.D., et al., "Effect of Ozone and Chlorine on 3,4-Ben-
zopyrene during the Disinfection of Water," Gig. Naselennykh Mest,
8, 1969, 88-91 (Russ.).
35. Reichert, J., "Elimination of Carcinogenic Aromatic Polycyclic Com-
pounds in Drinking Water Treatment with Special Consideration of
Ozone," Gas-Wasserbach, 110, 1969, 477-482, (German).
36. H'nsitkii, A.P., et al., "Effect of Ozonation on Aromatic, Particu-
larly Carcinogenic, Hydrocarbons," Gig. Sanit., 33 (3), 1968, 8-11,
(Russ.).
37. Saxena, J., Basu, D.K. and Kozuchowski, J., "Method Development
and Monitoring of Polynuclear Aromatic Hydrocarbons in Selected
U.S. Waters," U.S. Dept. of Comm., PB-276635, Nov. 1977.
38. CH2M Hill, "Evaluation of Groundwater Treatment and Water Sup-
ply Alternatives for St. Louis Park, Minnesota" prepared for the
Minnesota Pollution Central Agency, July 1983.
GROUNDWATER TREATMENT
265
-------
MINED CAVITIES IN SALT-A LAND DISPOSAL ALTERNATIVE
MARK W. HOOPER
JAN N. GEISELMAN
Pakhoed USA Inc.
Houston, Texas
THOMAS E. NOEL
EMPAK Inc.
Houston, Texas
EXISTING TECHNOLOGY
By 1985, United States industry will generate approximately 48
million metric tons of hazardous waste. The USEPA estimates that
approximately 50% of this hazardous waste will be disposed of
through land storage/disposal (Figure 1). However, current
legislative trends are to limit land disposal, especially landfills.
This suggests that the use of treatment/detoxification, incinera-
tion, recovery and/or conservation must increase. This theoretical-
ly optimum situation glosses over two realities:
•That the generation of large volumes of inorganic sludges and
solids contaminated with trace amounts of hazardous materials
such as asbestos, heavy metals and organic compounds are inher-
ent in the manufacturing service, mining industries and many
treatment processes
•That the disposal problem associated with these sludges and solids
is not going to be handled by treatment, incineration, recovery
and/or conservation; instead, some form of land storage/disposal
will continue to be necessary.
California, which is currently reducing its dependence on land
disposal faster than any other industrialized state, has estimated
that only 75"% of the hazardous waste disposal in landfills could be
recycled, treated or destroyed.'
More importantly, ignored in this legislative crusade is the hazar-
dous waste that has been deposited in landfills and lagoons in the
past. This waste, amounting to several hundred million tons, must
ESTIMATED NATIONAL HAZARDOUS
WASTE DISPOSAL METHODS
1985
CD SURFACE IMPOUNDMENTS
CD LANDFILL
CD INCINERATION
B DEEPWELL INJECTION
mQ TREATMENT
E3 RECOVERY
266
Figure I
ULTIMATE DfSPOSAL
be multiplied by a factor to take into consideration the amount of
additional earth contaminated.
Landfills and lagoons operated by private industry account for
the majority of this stored volume because over 85% of the hazar-
dous waste has been historically handled on-site, within the
generating plant's boundaries. Only 15"% has been handled off-site
in commercial facilities.2
Private industry will be closing many of these older landfills and
lagoons in coming years because of recently enacted monitoring
regulations and the anticipation of additional restrictions. Similar-
ly, billions of dollars will be expended to handle the small fraction
of sites that have been abandoned. The cleanup of these problems
alone will take many years.
The current and projected state of technology calls for the ma-
jority of these hundreds of millions of tons of sludges, solids and
contaminated soils to either be covered with clay caps and sur-
rounded by grout curtains or be removed to other landfills. These
short-term solutions will probably fail due to leaching, erosion,
breaching, faulting, subsidence, flooding, construction, etc., dur-
ing our lifetime.
ALTERNATIVE TECHNOLOGY
A 1983 report3 prepared by the National Research Council of the
National Academy of Science, the National Academy of Engineer-
ing and the Institute of Medicine, contained the following conclu-
sion:
"To subsurface disposal areas that have considerabale potential
for the disposal of hazardous industrial wastes (both solid and
liquid) are salt domes and arid region's unsaturated zones."
The USEPA,4 in a Request For Proposal issued Mar. 12,1983 to
initiate preliminary activities relative to a salt cavity waste disposal
demonstration project, stated:
"The absolute containment and isolation of many hazardous in-
dustrial wastes is an economic and environmental necessity. Use
of underground salt mines for the long-term, controlled storage
of these wastes has been and is recommended by EPA for fur-
ther study as a possible solution to this pressing problem. Prom-
ising results of studies by EPA's Solid and Hazardous Waste
Research Division (SHWRD) and other agencies, as well as the
successful operation of such a facility in West Germany, indi-
cate a high likelihood of success for such a technology."
Salt deposits have been used for the safe, secure storage of hazar-
dous materials since 1941. Currently, solution-mined and dry-
mined cavities in salt deposits are used for the storage of hundreds
of millions of tons of liquid and gaseous products, hazardous waste
-------
STORAGE IN SALT
(IN TEXAS, LOUISIANA & MISSISSIPPI)
CURRENT STORAGE TOTAL VALUE OF
VOLUME STORED PRODUCT
(BARRELS)
635,000,000
Figure 2
(DOLLARS)
13,640,000,000
and nuclear waste. Salt domes in Texas, Louisiana and Mississippi
store over 600 million barrels of hazardous product worth approx-
imately $14 billion (Figure 2). One such dome is used for over 100
million barrels of chemicals and gaseous hydrocarbons. Another,
located beneath Houston, has been used for the storage of 12
million barrels of high pressure hydrocarbons for over 30 years. An
additional 93 million barrels of hazardous products are stored in
mined cavities in bedded salt deposits in the Northeast, Midwest
and Western United States.
In the United States and Holland, solution-mined cavities are be-
ing used for the disposal of caustic-chlorine manufacturing sludges
and drilling muds.9 In West Germany, salt cavities are used for
strategic crude oil stockpiles, natural gas storage, compressed air
energy storage (CAES), a nuclear waste repository and hazardous
waste storage. The Herfa Neurode potash/salt mine in West Ger-
many has been operated by a subsidiary of Kali und Salz AG for
almost 10 years as a repository for containerized hazardous waste.
Waste from the United States has been deposited there, including
kepone from the Hopewell, Virginia incident.
U.S. SALT DEPOSITS
O ROCK SALT IN SUBSURFACE
B SALT DOME BASINS
Figures
The technology for hazardous waste placement in solution-
mined and dry-mined salt cavities is well developed and proven.
This technology has been developed in dry salt mining over the past
100 years, in industrial brining operations over 100 years and in
hazardous product storage over 40 years. The same technology cur-
rently used for the safe and retrievable storage of hundreds of
millions of tons of hazardous material is readily applicable to
hazardous waste storage in the United States. The only thing miss-
ing has been economic incentive.
Research
Research into the characteristics of salt deposits and their use for
product, hazardous waste and nuclear waste repositories has been
exhaustive. A bibliography on the subject would involve several
thousand entries. Only a very small sampling is included in the
reference section of this paper. A major task in the USEPA RFP is
a literature review and research activity update.
SALT CHARACTERISTICS
Two factors account for the extensive use of salt as a storage
medium: (1) distribution and (2) characteristics. In the United
States, salt deposits exist in bedded or domal form in most of the
industrial regions of the country (Figure 3). More important,
however, are the characteristics of salt which makes it particulary
amendable to storage. Salt, underground and under pressure, is
plastic, strong and impermeable.
Plastic Behavior
Underground, and at the associated pressures and temperatures,
salt behaves as a semi-plastic. This phenomena has enabled salt to
evolve from deep salt beds into salt domes along the Gulf Coast.
These domes are immense mountains of solid salt up to 13 miles in
diameter that have risen from mother salt beds via plastic flow
through 5 to 10 miles of sedimentary overburden over the past 100
million years or so at rates averaging 1 in. every 100 years (Figure
4).
Figure 4
A more familiar example of salt's plasticity is the salt block used
by livestock. This block starts out in a form similar to crushed ice
cream salt before it is subjected to 2000 lb/m2 of pressure. The
result is a solid block—without using glue—all due to salt's plas-
ticity.
Strength
One of the more visible examples of salt's strength is in a room
and pillar salt mine where the salt pillars hold up millions of tons of
ceiling weight. A more impressive example was the 5 kiloton
nuclear detonation set off deep inside a salt dome in Mississippi.
The salt was strong enough to contain this blast and 3 subsequent
ones with no release of blast gases through the salt.
Impermeability
The in situ permeability of salt is zero due to salt's crystalline and
plastic structure.6 Product storage and dry mining operations pro-
vide examples of this characteristic. Gaseous hydrocarbons are
stored at pressures up to 4000 lb/in2 with no leakage of material
through the surrounding salt. Salt domes are surrounded by
brackish and brine aquifers with no leakage through the salt into
room and pillar salt mines located within the dome. In one salt
dome in Louisiana, the United States Government is storing 70
ULTIMATE DISPOSAL
267
-------
was the Vinton Salt Dome in Louisiana. How this site measured up
to the key siting criteria is shown in Table 2.
Table 2
Vinton Sail Dome Analysis
Figure 5
million barrels of crude oil in a converted salt mine adjacent to an
active room and pillar salt mine employing over 100 miners with no
leakage of oil into the mine.
PROJECT DESCRIPTION
Site Selection
EMPAK developed a computer model to optimize site selection,
as well as site speciic facility design, capital investment and
operating budgets, market volumes and rates and waste logistics.
The major criteria considered in site selection are listed in Table 1.
Table 1
Site Screening Criteria
Population Density/Proximity
Wetland Proximity
Floodplain Proximity
Highway Access
Barge Access
Depth to Salt
Priot Salt Dome Activity
Land/Dome Ownership
Market Proximity
Power Supply
Land Availability/Cost
Dome Configuration/Size
Brine Disposal Availability
Prior Area Activity
Sites coinciding with the major industrialized states have been
fully analyzed; however, the Gulf Coast region was selected for the
First repository because it coincided with the company's major
facilities and headquarters. After thorough analysis of the 250 or so
salt domes onshore in Texas, Louisiana, Mississippi and Alabama,
plus a few offshore salt domes, the Big Hill Salt Dome in Texas was
ranked number one. Unfortunately, the United States Government
initiated condemnation proceedings in 1982 to take the dome for
inclusion in the Strategic Petroleum Reserve. The number two site
Population Density/Prixunity
Wetland Proximity
Floodplain Proximity
Highway Access
Barge Access
Depth to Salt
Prior Salt Dome Activity
Land/Dome Ownership
Market Proximity
Power Supply
Land Availability/Cost
Dome Configuration/Size
Brine Disposal Availability
Prior Area Activity
Less than 30 people within 2 miles; Vinton
3V* miles (Pop: 3.600)
None involved in project
Site above 100 year floodplain
Immediate to interstate highway
Immediate to barge canal
Less than 1,000 ft
No sulfur mining, no brining, no storage,
no mining
Single owner for all project requirements
More than sufficient market in Louisiana
Immediate, adequate
Available, reasonable
Large enough for buffers and project
Existing
Ranching, farming, oil/gas production
Surface Facilities
Surface facilities at the Vinton Salt Dome site will include an of-
fice, laboratory, vacuum truck unloading pad, dumpster unloading
pad, barge unloading dock, interim storage tanks and neutraliza-
tion tanks. They will conform to standardized company design,
which includes:
•All waste stored and processed in steel, Fiberglass or concrete
tanks—no earthen impoundments
•All waste storage and processing areas fully concreted and sur-
rounded by a concrete dike
•All unloading areas fully concreted and curbed
•All toxic and odorous emission sources collected and handled by
emission control equipment
•All waste handling areas surrounded by monitoring wells
Subsurface Facilities
The configuration of a storage cavity varies considerably, depen-
ding on whether it is in bedded or domal salt, the depth of the salt
and the cavity and whether it is new construction for storage or
conversion of a brining cavity (or mine). A typical new construc-
tion product storage cavity might have a cylindrical configuration
with dimensions of 900 ft in height and 200 ft in diameter. A similar
design could be used for hazardous waste storage, but computer
optimization indicated that breaking the single large cavity into a
series of smaller cavities or a "string-of-pearls" was preferable
(Figure 5).
This string-of-pearls design has been used in gas storage in bed-
ded salt and has been tested for waste storage in domal salt in
Holland.9 Patents have been granted to others for use of the design
in storing nuclear waste, garbage and municipal sewage sludges.
EMPAK has applied for a patent for its use in hazardous waste
storage.
PROJECT ECONOMICS
The capital investment through the third year in the Vinton Salt
Dome Waste Storage Project, inclusive of permitting, surface
facilities and subsurface facilities, will be approximately $20 million
(1983 dollars). The investment after 20 years will exceed $100
million, the difference being the additional investment in storage
wells and cavities. The capacity of the facility at this investment
level will be approximately 200,000 metric tons per year.
Although a capital intensive activity, the concept remains highly
competitive with landfill technology (Table 3).
268
ULTIMATE DISPOSAL
-------
Table 3
Economic Comparison of Landfill vs. Salt Dome
Disposal of Hazardous Waste
Disposal
Method
Landfill
Salt Dome
Waste
Type
Sludges
Sludges
Ave.
Breakeven
Disposal Cost
Rate-$ BBL$ BBL
12.50
11.76
11.86
4.72
Incremental
Cost
$BBL
5.22
1.78
PROJECT SAFETY
The long history of hazardous material storage in salt is
characterized by safety and reliability. On a volume stored basis, it
has proven to be safer than steel, above ground tankage and
definitely more secure than landfills and lagoons. No one would en-
trust the security of $14 billion worth of product on the Gulf Coast
to a landfill or lagoon.
However, EMPAK has reviewed case histories of accidents in-
volving salt domes7 as well as conceptualized failure scenarios and
has developed design and operating precautions to offset each and
every one. A few of these are identified in Table 4.
Table 4
Design and Operating Safety Precautions
of a Salt Dome Storage Facility
Potential Problem
1. Accidentally drilling
into filled cavity
2. Cavern Stability
Safety Precaution(s)
a. Only EMPAK allowed to drill on salt
dome
b. No oil and gas well allowed to be drilled
within 100 ft of salt
c. 500 ft salt buffer zone on sides of salt
dome
a. Cavern design dimensions and
configuration
b. Initial cavities above 3,000 ft
c. Brine evacuation stability test period
d. Cavern pressurization, if necessary
EMPAK is confident that a hazardous waste repository in salt
can be designed and operated to:
•Result in lower levels of toxic substances released to the environ-
ment over its lifetime than those from either incineratioan or
treatment facilities
•Be safe and secure in perpetuity
EMPAK has taken out insurance binders on the proposed facility
that will provide for $100 million worth of Sudden and Accidental
as well as Non-Sudden and Accidental insurance coverage and has
agreed to include this coverage as a permit provision. Apparently,
the insurance carrier shares the firm's confidence as evidenced by
both the commitment itself and the quite reasonable premium.
PERMITS
In the highly sensitized environment of hazardous waste disposal
facility permitting, public relations is paramount. EMPAK began
working on this problem in 1981, long before settling on a specific
site. A salt dome brochure was published in Dec., 1981, and this
was incorporated into a site specific public information/media
packet produced in Jan., 1983. These are only two elements in the
overall public relations strategy for this project.
The opposition to the Vinton Salt Dome Project has embraced
the "not-in-my-backyard" syndrome and has focused on emo-
tional rather than technical or substantive issues. The key opposi-
tion leaders have sought to ban the use of salt domes for hazardous
waste storage on the grounds that they are unsafe, while totally ig-
noring the safe, secure examples of salt dome utilization in their
"backyard" in the form of high pressure gaseous hydrocarbon and
crude oil storage as well as 100 year old salt mines still going strong.
The federal and state permit applications for the Vinton Salt
Dome site were filed with the appropriate agencies in Mar. and
Apr., 1983. The permitting process will probably take two to three
years.
FUTURE OPERATIONS
Mined cavities in salt enjoy obvious technological and economic
superiority over landfills. This fact, combined with the reality that
significant volumes of hazardous sludges and solids must continue
to go to land disposal, will ultimately create an increasing demand
for this method in the United States as well as other industrialized
countries. With this in mind, EMPAK continues to pursue sites in
other states as well as Latin America and Europe.
REFERENCES
. "Alternatives to the Land Disposal of Hazardous Wastes," Gover-
nor's Office of Appropriate Technology, CA, 1981.
2. "Hazardous Waste Market-Handling, Storage & Disposal," Frost &
Sullivan, Inc., New York, NY, 1981.
3. "Management of Hazardous Industrial Wastes: Research and Develop-
ment Needs," National Materials Advisory Board, Commission on
Engineering and Technical Systems, National Research Council
(NMAB-398, Washington, D.C., 1983)
4. "Assessment of Current Status of Using Mined Space for Long-Term
Retention of Nonradioactive Hazardous Waste," RFP CI 83-0094,
USEPA, Cincinnati, OH, 1983.
5. Wassmann, Th. Hans, "Cavity Utilization in the Netherlands," Hen-
gelo, The Netherlands, 1983.
6. Halbouty, Michel T., Salt Domes Gulf Region, United States and Mex-
ico, Second Edition, Houston, TX, 1979.
7. Coates, O.K., et al., "Failure of Man-Made Cavities In Salt and Sur-
face Subsidence Due to Sulfur Mining" (Topical Report RSI-0131),
Prepared for Sandia Corporation by RE/SPEC, Inc. under DOE Con-
tract AT (29-l)-789, Albuquerque, NM, 1981.
ULTIMATE DISPOSAL
269
-------
SOLIDIFICATION AND THERMAL DEGRADATION OF TNT
WASTE SLUDGES USING ASPHALT ENCAPSULATION
ELLY K. TRIEGEL
JOSEPH R. KOLMER
Woodward-Clyde Consultants
Plymouth Meeting, Pennsylvania
DOUGLAS W. OUNANIAN
Foster-Miller Associates, Inc.
Waltham, Massachusetts
INTRODUCTION
Research is being conducted by the USEPA to investigate closure
methods for lagoons containing TNT wastes (pink water). Asphalt
encapsulation, combining heating and mixing, is one process be-
ing considered' for the treatment of a sludge containing trinitroto-
luene (TNT), hexahydro-l,3-5-trinitro-l,3,5-triazine (RDX) and
other nitroaromatics. The lagoon under investigation contains
approximately 365 mj of sludge with up to 56,700 mg/kg TNT,
3740 mg/kg RDX and lesser amounts of other nitroaromatics and
metals.
Asphalt encapsulation techniques, consisting of mixing heated
asphalt with the sludge material, are being considered as a treat-
ment option. Coating (or microencapsulation) of the sludge par-
ticles would improve the leachate quality and should act to re-
duce the reactivity of the explosive compounds by decreasing the
propagation pathway of any reactions in the explosive compounds.
Addition heating of the mixture should act to thermally degrade
the nitroaromatic and RDX compounds in the sludge.
Research to date has included:
•An evaluation of existing asphalt encapsulation techniques for
hazardous wastes
•An evaluation of alternative heating/mixing systems
•Review of the properties of various asphalt products which may be
used
•Laboratory experiments on the temperature and holding times
required for thermal breakdown of the various compounds
present in the sludge
•Preliminary design of a pilot mixer/heating system.
A synthetic sludge with physical properties similar to the actual
sludge will be used during the initial runs and during modifications
of the pilot system. Actual lagoon sludge will be used in the field
for the final testing.
Factors which are being evaluated include residence times re-
quired for both mixing and thermal breakdown, mobility of the
system, safety considerations, batch vs. continuous designs and
throughput rates. Previously developed asphalt encapsulation pro-
cedures which could be mobilized would require excessive process-
ing times and high capital costs for lagoons of this size. Use of
ancillary processes, such as dewatering, and necessity for predry-
ing of the sludge prior to encapsulation will also be evaluated.
This work is being funded by the USEPA-MERL.
SITE CONDITIONS
The pink water lagoon under study is approximately 3500 m2 in
area and has been in existence since the late 1960s. Field mea-
surements were made to determine the thicknesses and volumes of
the sludge and wastewater in the lagoon. At the time of measure-
ment, the water was approximately 1 m deep and the sludge volume
was estimated to be 365 m'. It was found that the greatest thick-
ness of sludge occurred very near the point of discharge of wastes
into the lagoon, indicating rapid settling of coarser particulates in
the water.
Concentration distributions of several of the sludge constituents
(tetryl, RDX and 2,4-Dinitrotoluene) were similar to the thickness
contours, indicating a possible association of these compounds
with the coarser particulates. The concentration of 2,4,6-TNT did
not vary in a systematic manner with the sludge depths indicating
a more uniform, non-size dependent distribution of the compound.
Chemical analyses of the ground water, lagoon water, sludge and
soils underlying the lagoons were performed to identify the con-
taminants present and to characterize certain parameters which
could affect the treatment process. These results are summarized
in Table 1. Three monitoring wells were installed in addition to
an existing well for long-term monitoring of the groundwater qual-
ity near the lagoon.
PROCESS SELECTION
Asphalt encapsulation was considered as a treatment technique
at the pink water lagoon since it has the potential to both
thermally degrade as well as encapsulate the explosive and nitro-
aromatic compounds in the sludge. Asphalt encapsulation in this
situation is the combining, heating and mixing of asphalt and a
waste material. It is not the coating of a monolithic block of waste
with asphalt.
Coating of waste particles with asphalt using twin-screw extrud-
ers has been used in the past, primarily for waste processing in
the nuclear industry.1'2 In this process, the asphalt and wastes are
heated and mixed in the extruder, which serves the dual purposes of
reducing waste particle size while mixing and coating the waste
thoroughly with the asphalt. Coating of the pink water sludge par-
ticles should also reduce reaction propagation pathways and en-
hance the safety of the design.
The temperature profile along the screws (several feet in length)
can be closely controlled. The residence time in each section of the
screw can be varied by changing the screw configuration and the
speed of rotation. Water and volatile organics are evaporated and
collected in a condenser system or removed under vacuum. The
process generally results in a substantial volume reduction due to
the removal of water, and the treated product is more resistant to
weathering and cracking.
A vendor was contacted to evaluate the costs and feasibility of
utilizing a twin-screw extruder as a mobile unit. Several factors
which were unique to this project but had not been critical in past
waste encapsulation systems using the twin-screw extruder /asphalt
system included: (1) the need for a mobile system, (2) demon-
stration of the safety aspects prior to implementation to allow pro-
tection for personnel working with potentially reactive material, (3)
heating requirements beyond those necessary to melt and mix the
asphalt in order to enhance thermal degradation of nitroaromatic
270
ULTIMATE DISPOSAL
-------
Table 1
Summary of Analytical Results, Pink Water Lagoon
Parameter
Pink Water
2,4,6-TNT
Tetryl
RDX
2,4-DNT
2,6-DNT
Nitrobenzene
1,3-Dini-
trobenzene
Moisture
PH
Reactivity
Sludge
200 to 56,700 ppm
41.8 to 2100 ppm
611 to 3740 ppm
.825 to 40.1 ppm
.106 to .901 ppm
1.090 to 9.14 ppm
.287 to 7.02 ppm
49% to 92%
7.1 to 7.5
No
Soil
Directly Beneath the Lagoon
(sample depth less than 0.5 m)
18.9 to 158 ppm
.04 to 19.6 ppm
35.7 to 91.6 ppm
.04 to .180 ppm
.04 to .173 ppm
.05 to 1.78 ppm
.04 to .29 ppm
17% to 21%
7.5 to 8.6
NA
Lagoon
Water
774 to 998 ppb
NA
19170 ppb
1.1 ppb
1.1 ppb
11 ppb
1.8 ppb
NA
7.69
NA
Groundwater
2900 to 6400 ppb
NA
NA
113 to 185 ppb
10 to 19.5 ppb
11 ppb
135 to 173 ppb
NA
5.63 to 5.64
NA
NA: not determined
% moisture = (g water/g sample) x 100
compounds and (4) possible extension of the system to treat larger
volumes of contaminated soils that may be located beneath the
lagoons.
These considerations were in addition to the normal constraints
of time required to process the wastes, costs of treatment, com-
patability of the wastes and asphalt, lack of undesirable by-
products and the suitability of the product in terms of stability and
leaching characteristics.
After a preliminary evaluation, it was concluded that: (1) a twin-
screw extruder which was small enough to be mobile would require
excessive (more than 1 year) throughput times for the pink water
lagoon sludge, and (2) the cost of the equipment (rental or
purchase) and the additional engineering time was too great for
closure of only one lagoon.
At this point, a feasibility study of alternative mixer systems was
initiated by Foster-Miller Associates, Inc. This study included an
evaluation of existing mixing equipment and asphaltic materials, an
outline of the major process steps and a heating experiment to de-
termine the breakdown temperature and holding time for the nitro-
aromatics and RDX in the pink water sludge.
SELECTION CRITERIA FOR
MIXERS AND ASPHALT TYPES
Since a wide range of both batch and continuous type mixing
candidates was available for consideration, evaluation criteria were
established to compare the relevant features:
'Degree of Mixing—Generally, how well does the equipment mix
materials when used in its normal operating range for a nominal
duration?
•Provisions for Loading/Discharging Materials—Does the mixer
have loading chutes, discharge gates?
•Field Worthiness—Is it able to withstand over-the-road vibration?
Resistance to elements as is? Ruggedness?
•Heat Capabilities'—Is the mixer equipped with a heat jacket, is it
a standard option or is a separate design required?
•Sludge Consistencies—Can it be loaded and used at all ranges of
sludge water content from slurry to dried mud?
•Portability—Can it be taken over-the-road in terms of weight
and size? Is it compact in design? Can it fit on one truck trailer?
•Cost—What is the cost including the driving power, motors,
pumps, etc?
•Overall Complexity—Can it be operated with minimum worker
training? Number of working parts? Does it require specialized
service technicians? Are replacement parts difficult to locate?
A number of different mixers was considered (Table 2). Some
types of mixers are similar and were considered as a group, i.e.,
vertical axis mixers. The mixers were then evaluated using the cri-
teria outlined above (Table 3).
In the mixer selection process, two mixers appeared to be super-
ior: the pug mill and the static mixer. Since neither of these two
has been used for this particular encapsulation process, it is diffi-
cult to compare their anticipated performance. However, each
has a few general advantages and disadvantages described as
follows:
Mixer Advantages
Pug mill 'Proven construction
worthy machinery
•High degree of mixing
•Minimal design
change for use
Static 'Inexpensive
•No moving parts
•Can be used to
transfer heat to
sludge
•Extremely compact,
portable
•Easy to simulate
on a pilot scale
Disadvantages
•Large, heavy
machinery
•Requires large power
drive
•More expensive
option
•Requires pump to
drive materials
through mixer
•Sharp increases in
asphalt viscosity
at cooler temperatures
may cause problems
•Greater design cost
As a part of the effort to identify mixing methods, a survey of
the common asphalt grades was investigated (Table 4). The infor-
mation most pertinent to mixing is the viscosity properties and flash
points of the asphalts. These parameters help identify mixing
energy requirements and safe operating temperatures.
PRELIMINARY DESIGN OF THE SYSTEM
The major steps of the proposed encapsulation process are
shown in Figure 1. The raw sludge would be transported from the
ULTIMATE DISPOSAL 271
-------
Table 2
Mixer Candidates
Mixer
Pug Mill
Dryer-Drum
Vertical
Axis
Horizontal
Axis
Extruder
Static
Industry Use
Base Stabilization (soil mixing),
Asphalt Paving Concretes,
Portland Cement Concretes
Portable Asphalt Concrete Plants
Chemical: Abrasive, Corrosives
Explosives, Concretes, Clays
Food, Chemical: Pastes,
Batter, Candy
Plastics, Food, Waste
Disposal.
Chemical Processing, Fibrous
Slurries, Explosives, Polymer
Mixing, Liquid-Liquid or
Liquid-Solid Mixing. Rubber,
Paint Mixing, Food Mixing
t
Type
Batch or
Continuous
Continuous
Batch
Batch
Continuous
Continuous
Options
Spray Bar (liquid
additions), Covers,
Intake/Discharge
Chutes, Heat Jacketing
Sealed drum, Bag House
Raw Material Storage
Conveyors, Asphalt
Tank
Muller & Plow Combinations,
Dust Cover, Liquid Metering
System, Renewable Pan
Liners
Mixing Elements: Ribbon,
Gate, Differential Screw.
Heat Jacketing
Heat Jacketing, Vapor
Collection, Remote
Controlling
Heat Jacketing
Table 3
Mixer Selection Matrix
MIXER
CRITERION
Degree of Mixing
Provision for Loading/
Discharging Materials
Field Worthiness
Heat Capabilities
Handles all Sludge
Consistencies
Portability
Cost
Overall Complexity
VERTICAL HORIZONTAL
PUG DRYER AXIS AXIS
MILL DRUM (PLANETARY, (RIBBON, GATE,
(STABILIZER) COUNTER-CURRENT DOUBLE-SCREW)
Mod-High Low
Exists Exists
Rugged Rugged
Heat Jacket
is Common Exists
Option
Cannot Use
Yes a Slurry
Yes Yes
Low Mod
Low Low
Mod-High ,
Requires
Design
Requires
Weather-
proofing
Requires
Addition
of Heat
Jacket
Yes
Mod-High
Requires
Design
Requires
Weather-
proofing
Heat Jacket
Available
for Some
Types
Yes
Trailer mounting Trailer mounting
req'd. Many are req'd. Many are
not practical not practical
to use in field to use in field
Mod
Mod
Mod
Mod
EXTRUDER STATIC
High Mod
Exists Requires
Design
Requires Requires
Weather- Weather-
proofing proofing
Requires
Addition
Exists of Heat
Jacket
Must Use
Yes a Slurry
Trailer Trailer
Mounting Mounting
Required Required
High Very Low
High Low
272
ULTIMATE DISPOSAL
-------
Table 4
Asphalt Types
Type
Blown Asphalt
(oxidized)
ASTM D312
Asphalt
Cement
ASTM D946
ASTM D3381
Penetration & Viscosity
Graded
Viscosity
Range
80-550
Centistokes
at 275°F
Uses
Steep Roofing, Pipe Coating
Under Sealing, Cavity Filling
Waterproofing
Plant-Made Asphalt Concrete
for Roads, Sidewalks, Parking
Lots, Dam Facings, Penetra-
tion Macadam.
Pure
Asphalt Use Temp
To C
100 135°
(min)
100 82°-176°
ASTM Minimum
Flash Point**
°C
225°
(min)
163°-238° (min)
Cutback Asphalt
Rapid
Medium curing
Slow
ASTM D2028, D2027
D2026
30-6000
Centistokes
at 140°F
Road Mixing of Asphalt Concretes.
Asphalt Penetration Applications.
Prime & Tack Coats Before Paving.
Stockpiled Patching Mixes.
50-80
57°-116°**
RC-27
MC-38°-66°
SC-66°-107°
Emulsified
Asphalts
Rapid
Medium setting
Slow
ASTM D977, D2397
20-100
Saybolt
Seconds
at 77°F
Seal Coating. Penetration Macadam.
Road Mixing of Asphalt Concretes.
Fine Aggregate or Soil Stabiliza-
tion. Cold or Hot Plant Mixing.
Patching Mixes.
55-65
Will Not
Flash
*Flash points of specific products may exceed the minimum required by ASTM for that category.
"Application temperature may exceed flash point. Caution must be exercised.
TableS
Concentrations of Nitroaromatics, Tetryl and RDX in Heated Sludge Samples (ppm, dry weight basis)
Sample No.
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
17 Dupl
Method
Blank
Temperature Holding
(°C) Time (min)
150°C 5
10
15
20
200°C 5
10
15
20
250°C 5
10
15
20
300°C 5
10
15
20
100°C 120
120
— —
2,4,6-TNT
39,750
62,690
31,210
31,670
15,850
7180
23,660
22,680
2300
3500
3240
1740
35
3.6
5.6
1.5
42,360
43,320
0.47
RDX
604
470
495
668
779
862
974
926
362
357
485
685
10
29
0.85
0.85
300
314
0.85
Tetryl
2730
5050
16,000
11,300
2780
390
5260
3220
4140
23
19
19
(b)
1
1
1
43,760
——
1
NB*
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
1,3-DNB*
0.55
0.55
0.55
13
14
29
13
13
20
19
27
26
3
0.55
0.55
0.55
0.55
0.55
0.55
2,6-DNT*
126
104
69
83
76
42
94
115
57
71
89
62
6.9
0.42
0.42
0.42
0.42
0.42
0.42
2,4-DNT*
209
190
194
190
151
154
206
235
86
106
137
117
7.5
0.48
0.48
0.48
33
37
0.48
1,3,5-TNB*
0.6
0.6
0.6
0.6
0.6
0.6
0.6
0.6
91
95
125
122
6.4
0.6
0.6
0.6
0.6
0.6
0.6
*NB = nitrobenzene
DNB = dinitrobenzene
DNT = trinitrotoluene
TNB = trinitrobenzene
ULTIMATE DISPOSAL
273
-------
OPTION
r—i
••J PHETH6ATUENTJ
,
I EVAPORATOR |
•*) /HEATER
I J
Figure 1
Sludge Encapsulation Process
pond through a classifier which could take the form of a screen or
grizzly to prevent oversize and foreign objects such as wood and
cobbles from entering the system. The material would then proceed
to pretreatment such as dewatering by filters, centrifuges or heat-
ing, or it could be deposited directly into a surge tank to await
feeding to the mixer. The advantages of heating or other forms of
pretreatment depend upon the mixing process chosen. The muck
feeder may be a weight conveyor, screw conveyor, batch weigh-
ing system or positive displacement pump. This ensures that the
sludge is added in correct proportions to the asphalt.
Heated asphalt would be fed into the blender/mixer separately
using a positive displacement, oil-type pump. The grade of asphalt
used would depend upon the mixing temperature chosen. Once the
sludge and heated asphalt have been combined satisfactorily, the
encapsulated material may require an additional step involving
heating for a longer interval to dewater and/or degrade com-
ponents of the TNT sludge. Alternatively, if the mixing method
itself provides sufficient time and temperature to degrade as well as
encapsulate the sludge, the material can be discharged to contain-
ers or pumped to a storage pit/pond.
The operating rate and mixer size were evaluated in order to
assess whether the sludge in the lagoon could be processed in a
reasonable time frame using a portable mixer. Assuming a use of
50% asphalt to 50% wet sludge, a total of 730 m1 would be pro-
cessed. Assuming a reasonable operating period of 24 days at 8 hr.
each, an average throughput of 0.075 m'/min of encapsulated
waste must be handled. This requires sludge and asphalt feed rates
of 0.038 m'/min. The amount of time required to achieve proper
mixing plus the additional time (if any) at the temperature that is
required to degrade the TNT is regarded as the system residence
time. The residence time identifies the mixer and/or detention tank
volume by the following computation.
Throughput (m Vmin) x Residence Time (min) = Tank Size (m!)
Residence Time
(min)
5
10
15
20
Mixer/Tank Size
(m')
0.38
0.75
1.13
1.51
It is readily apparent that a residence time in excess of 20 min
will require an unpractically large tank. In this case two options
are available: (1) operate at lower throughput or (2) consider the
energy retained by the encapsulated sludge after discharge. De-
pending upon the size of casting or briquette used, the encapsulated
sludge may maintain a high temperature for hours.
HEATING REQUIREMENTS
A laboratory evaluation was conducted to assess the temperature
and holding times required for breakdown of the nitroaromatics
and RDX in the sludge. This information is necessary to design the
mixer system and to determine if thermal degradation occurs at
temperatures below the flashpoint of available asphalts. Seven-
teen tests were conducted at four temperatures (150, 200, 250 and
300°C) and four residence times (5, 10, 15 and 20 min) plus one
sample heated for 2 hr at boiling (100°C).
For each test, 80 g of sludge were placed in a 250 ml erlen-
meyer flask. The flask was then placed in the preheated high temp-
erature oven set to the end temperature desired. Temperature of the
sludge was monitored throughout the test.
The samples of the heated sludge were sent to the laboratory for
analysis. The results are found in Table 5.
Although the sludge was homogenized prior to the heating exper-
iment, variations in the concentrations were observed. These varia-
tions have occurred in most of the work with these sludges and may
be due to the presence of small particles of nearly pure TNT or for-
eign materials (sand, waxes, etc.) which cannot be completely
homogenized. The results, however, do indicate that thermal de-
gradation of approximately 90% of the explosive and nitro-
aromatic compounds occurs at 250 °C.
The results presented here are based solely on the heating of the
sludge. Further testing will be required to determine whether
various types of asphalt in combination with the sludge result in
equally low levels of explosive and nitroaromatic compounds.
CONCLUSIONS
Asphalt encapsulation of pink water sludges using either a static
or pug mill mixer appears to be a potential alternative to encapsu-
lation by twin-screw extruders or other treatment techniques based
on a preliminary evaluation of available mixers. The use of these
mixers may reduce equipment costs and processing times for mobile
systems. Heating experiments of pink water sludge not yet encap-
sulated indicated a 90% reduction in the levels of explosive and
nitroaromatic compounds at a temperature of 250 °C.
Pilot scale testing of the encapsulation system will be conducted
prior to implementation in the field. The initial tests will use a syn-
thetic sludge with physical properties similar to the pink water
sludge. Modifications to the system and safety reviews will be com-
pleted prior to final pilot testing of the actual TNT-sludge. Addi-
tional laboratory tests on the asphalt-sludge mixture, perhaps
heated to temperatures between 250 °C and 300 °C, may also be re-
quired to assess the leaching characteristics of the final product.
REFERENCES
1. Doyle, R.D., "Use of an extruder/evaporator to stabilize and solidify
hazardous wastes," Chapter 4 in Toxic and Hazardous Waste Disposal,
Vol. I, R.B. Pojasek, ed., Ann Arbor Science Publ., Ann Arbor,
MI, 1979.
2. Malone, P. and Jones, L., Guide to the Disposal of Chemically Stabil-
ized and Solidified Wastes, USEPA, Cincinnati, OH, 1980.
3. Triegel, E.K. and Kolmer, J.R., Remedial action research: waste-
water lagoons, in Proc. 9th Annual Research Symposium: Land Dis-
posal, Incineration and Treatment of Hazardous Waste, USEPA,
Cincinnati, OH, 1983.
4. Wentsel, R.S., Sommerer, S. and Kitchens, J.F., Treatment of Ex-
plosives Contaminated Lagoon Sediment—Phase I: Literature Review
and Evaluation, USATHAMA, Edgewood, MD, 1981.
274
ULTIMATE DISPOSAL
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EVOLUTION OF PRACTICAL ON SITE
ABOVE GROUND CLOSURES
LARRY GRAYBILL
Rollins Environmental Services, Inc.
Houston, Texas
INTRODUCTION
The basic disposal method through the ages has been land burial.
Prior to industrial development, the waste was minimal in quantity
and the composition could easily be handled by the planetary
ecological system. The industrialization process began generating
more complex waste products and larger per capita quantities both
in the form of discarded refuse and by-products of manufacture.
The explosion in technology and the standard of living during the
past 100 years has taken place without an appreciation or awareness
of the problems associated with the land disposal of the tremen-
dous quantities of complex waste that was an integral part of the in-
dustrialization process.
Due to this lack of awareness, industrial waste was handled by
burial methods. As the quantities of both household refuse and in-
dustrial waste continued to grow, a crude land disposal industry
developed that generally handled both municipal and industrial
waste in the same facility. Disposal was primarily a transportation,
dumping and sometimes covering operation. On-site disposal was a
common practice and eliminated the transportation cost for the in-
dustrial waste producers. These practices were simply an extension
of a cultural "burial heritage" and were a normal response that
resulted from both a lack of awareness of the long term ecological
implications and the abundance of land resources in this country.
Since most wastes have been deposited in or on the land, most
hazardous waste generated since the industrialization process began
still exists. The waste is either present in the many thousands of
waste sites or has been discharged into the air and water.
RCRA Passed
Once the growing awareness of the problems associated with the
"open dumps" reached a sufficient level, the passage of the
Resource Conservation and Recovery Act (RCRA) of 1976 was
possible. RCRA began a new era for the hazardous waste disposal
industry. An attack was launched on open dumping and new ef-
forts were made to encourage waste volume reduction, recycling
and high technological approaches to the treatment or destruction
or hazardous waste.
The geotechnical-hydrogeological disciplines were the initial
disciplines looked to for safe solutions to the land disposal prob-
lem. With their help, specifications were developed for the loca-
tion, clay liner construction and monitoring of new designs for
secure landfills. It was believed that these secure landfills could
safely store hazardous wastes for the decades necessary for
biological degradation of the waste.
The new secure landfill technology was a major improvement
over the preceding era. However, based on the anticipated security,
low cost of operation and federal support, the land disposal
policies effectively eliminated the more costly higher technology ap-
proaches to resource recovery, volume reduction, treatment and
disposal. The economics favored land disposal by a significant
margin.
The complexity of the secure landfilling of the broad spectrum of
hazardous waste, including the organic compounds, was
underestimated. The real world comingling of organic and in-
organic waste did not fit the models used by the geotechnical-
hydrogeological disciplines in their design specifications for secure
landfill. Many land disposal firms could not be regulated or
depended on to operate the landfills properly. Actual operating ex-
perience at many hazardous waste landfills did not support the long
life expectancy of the early RCRA secure landfill specifications.
The early RCRA land disposal policy is now under intense re-
examination, and the role of secure landfills for disposal of organic
hazardous waste has been reduced or curtailed in many states. This
re-examination has now become a national issue with both USEPA
and congressional pressures moving toward major changes in our
land disposal policies in this country. The issue of organics and
secure landfill is a complex issue and beyond the scope of this
paper. The major point to note is that the present direction of both
state and national land disposal policies will result in major limita-
tions on the types and quantities of hazardous organic waste going
into secure landfills.
RCRA Chapter Two
A second new era in the evolution of hazardous waste disposal
practices is now beginning. Continued limitation of the land
disposal or organic hazardous waste is obvious. The proposed tax-
ing schemes for land disposal, pro-rated transportation taxes, taxes
on per unit waste generation, along with the increasing generator
liability-remediation risks associated with land disposal and many
other considerations point to basic changes in future waste disposal.
practices. Without going into detail, one can safely say that as the
relatively inexpensive landfilling of organics is curtailed or becomes
cost intensive on site waste volume reduction, resource recovery,
technical detoxification and disposal methods will become the
economical method of choice for ongoing waste streams.
CLOSURE DILEMMA
RCRA Chapter Two presents a dilemma for the closure of cur-
rently used hazardous waste sites according to the regulations of
Superfund and RCRA. The nature of the wastes stored in the
thousands of waste lagoons, impoundments, etc., does not allow
ULTIMATE DISPOSAL
275
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the use of traditional proven technological treatment approaches.
The wastes generally have been comingled. The physical properties
range from liquids and sludges to significant quantities of con-
taminated soil and groundwater. The broader the range of chemical
composition, the more limited the treatment options. Therefore,
the majority of this material will not fit into the present technical
treatment scenario.
The economics of the closure of large impoundments are also
prohibitive. Typical closure cost ranges are as follows:
COST ELEMENT COST ($/yd3)
Secure Landfill Disposal 50-100
Transportation 10-50
On-Site Handling 5-20
Site Restoration 5-20
70-190
The above costs do not include assessment and engineering. Use of
higher technological approaches for off-site or on-site methods
(slurry walls, sheet piling, etc.) often are significantly more expen-
sive than the above range. Based on the above cost, closure of a 30
acre impoundment with 15 ft of organic sludge waste could range
from $50,000,000 to $150,000,000.
The following key points illustrate the present dilemma being
faced in the cleanup of waste sites:
•Tremendous quantities of historic hazardous organic waste are
currently stored in an extremely large number of uncontrolled
waste sites
•The economic and technical reality of available closure options
prohibit most disposal options with the possible exception of se-
cure landfill
•The current direction of the U.S. land disposal policy could soon
eliminate secure landfill as an economically viable closure option
for the vast majority of historic organic waste sites
Therefore, it can realistically be assumed that under RCRA
Chapter Two little progress can be made toward addressing the
historic waste sites in this country without the development of a
new generation of on-site closure methods that provide a signifi-
cant increase in environmental security and can be implemented at
a fraction of the present closure costs.
ON-SITE CLOSURES
Economics and current waste disposal technology will not en-
courage the closure of the historic waste sites under RCRA Chapter
Two. Waste migration from the present uncontrolled storage con-
ditions is continually expanding the total volume of contaminated
materials through contamination of air, surface water, subsurface
soil and groundwater. As a result of these pressures, the state and
federal regulatory agencies are re-assessing site closure regulations.
Most closure methods are based on surface or subsurface con-
tainment barriers. The waste, however, continues to be exposed to
the same hydrodynamic environmental forces as in the case of
secure landfills but without the design advantages of secure land-
fills. Since they are located on all kinds of geological formations,
the integrity and useful life of the containment method can be ex-
pected to be much less than secure landfill.
The above ground closure method to be discussed in the remain-
ing sections of this paper has successfully addressed the problems
associated with typical containment approaches and can be ex-
ecuted at a fraction of the traditional closure methods. The above
ground approach differs from traditional containment methods in
the following ways:
•The above ground method utilizes high volume waste handling
techniques developed by waste disposal firms during the first
chapter of RCRA. Use of civil construction methods and special
pumping equipment allows the economical bulk handling, manip-
ulation and exhumation of waste at large hazardous waste sites.
•The above ground method uses waste solidification processes
that were also developed from operating experience during RCRA
Chapter One. The waste solidification processes allow the his-
toric waste to be compacted into a load bearing material.
•The solidification and bulk handling capability allows the use of
traditional civil engineering methods to design above ground
closures that effectively address the environmental hydrodynamic
forces operating against traditional landfills and on-site contain-
ments.
EVOLUTION AND DESIGN OF
THE ABOVE GROUND CLOSURE
The above ground concept can be used on old impoundments as
well as for the design of future secure landfills. This concept is an
example of the benefits that have resulted from the waste disposal
experience under the first chapter of RCRA. The high volume bulk
waste handling and solidification methods developed for new
secure landfill operation and the study of landfill failures provided
new insights into the design of safer, longer life hazardous waste
structures. This information along with actual field experience
from early closure work at older waste sites led to the following
observations:
•Organic waste impoundments exposed to the environment for
several years generally contain 20% to 30% solids. The solids and
liquids are unique to each system and are continually interacting
with the environment: rainfall, sunlight, wind, soils, climate,
etc. Water is present in various states (entrained, layers, natural
emulsions, suspensions, solutions, etc.).
•Organic waste sludge dewatering to levels much below 50% is
seldom possible.
•A pozzolanic reaction with portland cement or cement kiln flue
dust and the water present in the organic waste sludge will yield a
"soil like" load bearing material in approximately 75% of the
impoundments examined to date.
•The ability to convert organic waste sludges to a load bearing
"soil like" consistency allows the use of conventional earth mov-
ing equipment for the handling, placement and compaction of
waste.
•Civil engineering concepts can be applied to solidified waste ma-
terial for the design of stable above ground compacted and formed
shapes.
The basic advantage of an above ground compacted shape versus
below ground containment approaches is shown in Figure 1. In the
lift
ijlil
ABOVE GROUND CLOSURE
BELOW GROUND
LANDFILL
Figure 1
Hydrodynamic Comparison
276
ULTIMATEDISPOSAL
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IASS
TOPSOIL
IP ACTED CLAY
GRAVITY FEED
LEAK
DETECTION
SYSTEMS
GRAVITV FEED
INFILTRATE
DIVERSION
SYSTEM
UNCONTROLLED MEDIUM
COMPACTED CLAY
Figure 2
Schematic—Above Ground Closure Concept
below ground approach, the hydrodynamic forces of gravity and
water are constantly working against the integrity of the structure.
Because of these forces, landfills are designed with the assumption
that leachate (water that has leached through the waste) will be
generated; therefore, various liners and removal systems are incor-
porated to protect or minimize damage of the system by the
leachate. When failure occurs, the exit is to the uncontrolled soil-
groundwater medium. Since few current on-site containment land-
fills are able to incorporate the internal lining and leachate protec-
tive systems associated with landfills and the above ground closure
concept, they are certain to succumb to the natural hydrodynamic
pressures on the system.
The lag between failure and detection can be significant with
respect to both time and cost of remediation. Since detection of
failure in the below grade system is documented by contaminated
groundwater, serious environmental damage and waste volume ex-
pansion may occur prior to detection. Even when technical
remedial methods are available, costs of exhuming waste, below
grade site repair and addressing expanded contamination in the un-
controlled medium are very expensive.
The above ground illustration (Figure 1) shows how the natural
hydrodynamic pressures can be controlled and isolated from the
waste. Since the structure is above ground, its shape can be de-
signed to remove rainfall or permeate from the system. Again the
shape along with the design of internal conduits allows the use of
gravity to redirect any water that penetrates the structure. Since the
entire system is above ground, a leak detection system can also be
incorporated to monitor both the top and bottom liners.
Another illustration of how the leak detection system of the
above ground approach prevents both the time lag and substantial
contamination of the uncontrolled medium associated with the
failure of a below grade system is given in Figure 2.
2ND LINER
STRUCTURAL
SUPPORT
WALL FUNCTIONALITY
AREA: RUNOFF
COLLECTION LINER
DETECTION SYSTEM
MOTION SENSORS
STRESS MONITORS
GAS VENTS
BASE PAD
IMPERVIOUS LOAD-
BEARING MATERIAL
-Y
/
Failure of the above ground closure is the loss of integrity or a
leak in either the upper liner or the lower liner. The gravity feed in-
filtrate diversion system eliminates continual head pressure on the
upper liner and significantly lowers the probability of water break-
ing down or penetrating the upper liner. Should the upper liner be
damaged or fail, the water will leach through the waste to the inter-
nal detection system. Since the above ground system is designed to
have no leachate generation, any effluent from either leak detection
system is an immediate notice that failure has occurred.
Equally important to early detection and non-contamination of
the surroundings is the ease of remedial work on an above ground
structure. The structure is easily accessible from the top and sides.
Since initial failure will be in the top lining, corrective repairs can
be done quickly and economically. Simple design methods can be
incorporated in the leak detection system to pinpoint the sector
where failure has occurred. Contrast this to exhuming the waste
material of a below grade containment, locating and repairing the
failure and handling the contaminated soil and groundwater.
With proper maintenance, the integrity of the internal lining
system is the probable limit to the useful life of the above ground
system. The wet interface between the waste and liner typical of
most secure landfill designs can result in accelerated deterioration
of the liner. Therefore, a key concept in the above ground ap-
proach is the conversion of the waste to a dry compactable form
and the provision for a protective layer of sand or other construc-
tion medium between the solidified waste material and the liner.
By eliminating a wet interface or any contact with the waste, the
life of a synthetic or clay lining system could last indefinitely. Use
of high density polyethylene resins for power line insulation has
demonstrated extremely long life under the full range of exposure
to sun and climatic fluctuations. Since the above ground design
eliminates sunlight exposure, climatic fluctuation and contact with
the waste, the most severe pressure on the liner becomes the contact
with water in the diversion systems. Therefore, the lifetime of a
properly maintained above ground closure could be indefinite.
ECONOMICS OF ABOVE GROUND CLOSURES
Typical above ground closures can be installed for 25% to 50%
of the off-site alternative. The cost advantages result from:
•The elimination of transportation and disposal fees associated
with off-site disposal
•Conventional simple civil methods can be executed by a large
number of general construction firms as compared to specialty
slurry wall contractors, etc.
•High volume waste handling methods shorten project time. Ex-
humation and solidification rates of 1,000-3,000 ydVday are
easily attainable
GROUND COVER/CLIMATE APPROPRIATE MATERIAL
CLAY/PROTECTIVE MATERIAL CAP
SAND - INNER LINER PROTECTION LAYER
SURFACE RUNOFF PROTECTION
LAYER
INNER LINER WASTE
COMPATIBLE
SAND INNER LINER
PROTECTION LAYER
SOLIDIFIED-COMPACTED
LOAD-BEARING WASTE
GRAVITY FED LINER INTEGRITY
DETECTION SYSTEM
Figure 3
Rollins Environmental Vault
ULTIMATE DISPOSAL
277
-------
CONTAINMENT VAULT
Figure 4
Above Ground Closure—Hillside Site Adaptation
Project cost ranges from $25.00/yd3 for a land intensive design
with inexpensive on-site clay or a waste material requiring no
solidification (such as contaminated earth), to S100.00/yd3 for dif-
ficult to handle waste requiring solidification and construction of
land efficient concrete wall structures with extensive monitoring
and control systems. Obviously, the scale of operation also has a
significant impact on the project economics.
A high security, long-life design approach to the above ground
concept is shown in Figure 3. This schematic is of the Rollins En-
vironmental Vault (patent applied for) which incorporates all the
design features outlined earlier and provides for additional
monitoring and security for more difficult waste problems.
The ease in adapting specific site and waste considerations to an
above ground closure design is illustrated in Figures 4 and 5, which
are based on an actual project to accommodate up to 10,000 yd3 of
organic waste from a PCB lagoon closure. The concept, as il-
lustrated in Figure 3, was adapted to a hillside site with all struc-
tural components remaining above grade, thereby maintaining the
above ground advantages while maximizing the efficiency and
asthetics of site land use. Details of the separate systems for surface
water runoff, infiltrate diversion systems and leak detection
systems for both top and bottom liners are shown in Figures 6
and 7.
The project detailed in Figures 4 through 7 was estimated to cost
$70-$80/yd3 for a solidified PCB sludge. This cost included:
•Detailed site assessment and evaluation
•Detailed engineering design
•Preparation, submittal and USEPA approval of closure plan
•Groundwater monitoring system for new facility
•Project execution of all construction, waste placement, closure
and landscaping of the site
The off-site disposal alternative excluding site restoration was
approximately $192/yd3 of waste transported to a PCB approved
landfill.
FUTURE RECOVERY AND TREATMENT OPTIONS
Most land disposal and containment options are, at best, long
term storage as opposed to true disposal. Present treatment and
recovery methods do not exist for the large comingled waste masses
present in older impoundments. The above ground closure method
is the only land disposal or storage method that approaches a 100%
level of containment security over a very long period. Performance
of routine maintenance should allow the structures to last in-
definitely.
Future access for recovery or treatment of the waste is a signifi-
cant advantage, especially if individual cells are used to isolate
specific waste materials that have not been comingled with a broad
spectrum of other wastes. For example, specific biological
organisms are being developed for specific wastes such as 2,4,5-T,
dioxin wastes, etc. These organisms are very specific in their ability
to detoxify certain chemicals. The preservation of specific wastes
will be a major benefit for future biological treatment.
Comingling of waste also compounds the resource recovery
problem. Closure of two large waste impoundments resulted in the
landfilling of 5,000,000 Ib of manganese from a 90,000 yd3 organic
waste lagoon and over $1,000,000.00 worth of mercury from a
14,000 yd3 lagoon. The comingling of these valuable raw materials
in a large landfill compounds or eliminates future recovery options.
Who knows the value of these rare metals 50 years from now. Had
these waste materials been segregated in an above ground cell, the
opportunity for future treatment and recovery options would be
much more attractive.
ABOVE GROUND VAULT SCHEME
" >" ,'(! I P-, <
Compacted Clay Base & Compacted Clay Cap
1. A minimum thickness of 3.0 (1 is required for the in-place, compacted clay base and clay cap.
2. Cla> Soils forming the cap and base will be placed in lifts not greater than 9 in. loose thickness.
The clay will be compacted to a unit dty weight of at least 95 percent of the maximum dry density
indicated by ASTM D-698, the Standard Proctor Compaction Test.
.1 Clay Soils used for the base and cap will have the following properties:
-• liquid limn greater than 30
•a plastiaiy index greater than 15
-the percentage of material passing a No. 200 mesh sieve greater than 30
-an in-plice permeabilit> not greater than 1.0 - ' cm/sec when compacted.
Leachate Collection System
1. The leachate collector system will consist of well-compacted, well-graded, free-draining gravel.
2. The collector system will have a minimum thickness of at least 1.0 ft.
Sand Drainage Blankets
1. The drainage blankets will consist of well-compacted, free-draining sand.
2. The drainage blankets will have a minimum thickness of 6 in.
Synthetic Liner
The synthetic membrane liner will have the following properties:
-a minimum thickness of 30 mils
-chemically compatible with Compacted fill
-a permeability of not more than IxlO-' cm/sec.
Figure 5
Above Ground Closure—Hillside Section Details
278
ULTIMATE DISPOSAL
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Sand-filled
Cinder Uiocks
or Sand it.uts
Synthetic Liner
Reinforrr-d
ConcreU- «.ill
DRAINAGE MONITORING DETAIL
(i 1 ? 1 Fec-l
Figure 6
Above Ground Closure—Detection System Details
SUMMARY
In summary, the above ground closure method offers the follow-
ing advantages over conventional surface and subsurface ap-
proaches:
•There is essentially zero risk of contaminating the uncontrolled
medium of soil and groundwater because the entire system is
above ground, with buffer zones and failure detection systems
between the waste and groundwater
•Easier access for maintenance
•Top, walls and all effluent can be visually inspected
•Provides opportunity to detect any errant leachate prior to
groundwater contamination
•Provides easy access for future manipulation of the waste for re-
source recovery and new treatment methodology
•Versatility—the above ground cells can be used over low and
high water tables and over clay and non-clay substrata
•Their design is in harmony with environmental, hydrodynamic
pressure; therefore, no leachate collection system is necessary
for pumping leachate up from the bottom of a landfill
•Rick of groundwater contamination is reduced in the event of
geological action such as fault slippage, slumping or any other
massive earth movement. Remedial action is easier, quicker and
less costly
The above advantages, along with the long-term security,
economics and widespread application make the above ground
closure approach a powerful new tool for addressing many of the
pressing hazardous waste problems in this country.
REFERENCES
1. Miller, D.W., (Ed.), "Waste Disposal Practices and Their Effects on
Ground Water." USEPA, Report No. E.P.A.-660/2-74-001, Final
Report to Congress, 1977.
2. "Notice of Proposed Changes in Regulations of the Department of
Health Services Regarding Hazardous Waste Land Disposal Re-
strictions (R-32-82)." Department of Health Services, State of Cali-
fornia.
3. For detailed review of solidification materials and processes, see
Toxic and Hazardous Waste Disposal, Volume 2, "Options for Sta-
bilization/Solidification". R.B. Pojasek, Ed., Ann Arbor Science
Publishers, Ann Arbor, MI, 1981.
4. Morrison, Allen, "Can Clay Liners Prevent Migration of Toxic
Leachate?" Civil Engineering, ASCE, July 1981, 60-63.
5. Landreth, R.E., Project Officer. "Design and Construction of Covers
for Solid Waste Landfills". EPA-600/2-79-165, August 1979.
6. Haxo, H.E., Jr., "Effects of Liner Materials of Long-Term Exposure
in Waste Environments". Paper read at 8th Annual Research Sum-
posium, Land Disposal, Incineration and Treatment of Hazardous
Waste, USEPA, Ft. Mitchell, KY, Mar. 1982.
7. Julien, P.A., "Land Burial of Hazardous Wastes in Clay-Lined Land-
fills in Illinois: A Permanent Economic Solution?" Paper presented
at 1981 Annual Meeting of American Geographers, San Francisco,
CA.
8. Water budget models, or, water balance models, are generally cov-
ered in climate, engineering, and hydrology texts. For detailed ex-
planation, see: Thornthwaite, C.W. and Mather, J.R., The Water
Balance, 1955. Volume 3, Number 1, Publications in Climatology,
Centerton, NJ, and J.R. Mather, The Climatic Water Budget in
Environmental Analysis. Lexington Books, D.C. Heath and Com-
pany, Lexington, MA, 1978.
9. Carter, D.B., et al.. Applications of the Water Budget in Physical
Geography. Publications in Climatology, Centerton, NJ, 24, 1973,
and J.R. Mather, Climatology: Fundamentals and Applications,
McGraw-Hill, New York, 1974.
10. Brown, K.W. Landfills of the Future. Paper available from Soil and
Crop Science Department, Texas A & M University, College Station,
TX.
TOP-OF-SLOPE DRAINAGE DETAIL
Figure 7
Above Ground Closure—Surface Water Diversion Details
ULTIMATE DISPOSAL
279
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SAFETY PLAN FOR CONSTRUCTION OF REMEDIAL ACTIONS
DONNA LYNN BAREIS, Ph.D.
Science Applications, Inc.
McLean, Virginia
LARY R. COOK
GENE A. PARKS
U.S. Army Corps of Engineers
Washington, D.C.
INTRODUCTION
The USEPA and the Army Corps of Engineers have an inter-
agency agreement for the Corps of Engineers to manage Super-
fund design and construction contracts and provide other technical
assistance as requested in support of remedial action at hazardous
waste sites. The Corps of Engineers primary responsibilities under
this agreement take place when the USEPA has determined that
Federal cleanup is appropriate (as opposed to remedial measures
managed by states or private entities), and the USEPA has selected
the remedial alternative to be implemented. The Corps then con-
tracts for actual design and construction work and serves as the
contract manager, reviewing designs and monitoring construction.
A detailed description of the Corps of Engineers management
plan and contracting processes for these activities was presented
last year at the Third National Conference on Management of
Uncontrolled Hazardous Waste Sites.1
A crucial part of successful remedial actions is insuring ade-
quate safety and health precautions to protect both on-site em-
ployees and off-site populations. Construction of remedial meas-
ures often involves extensive physical disturbance of hazardous
material; this creates hazards in addition to those normally encoun-
tered in site investigations. Another factor increasing the likeli-
hood of a serious accident during construction activities involving
hazardous waste is that construction workers often lack the special-
ized training given to site investigation teams. For these and other
reasons, it became evident that existing safety manuals written to
cover hazardous waste site investigations2 would not be directly
applicable to construction activities. Therefore, the Corps of En-
gineers has developed guidelines for design contractors to prepare
site-specific construction safety plans.
CORPS USE OF THE SAFETY PLAN
FOR SUPERFUND SITES
Safety planning is considered an integral part of the remedial
action design process. Corps guidance to design contractors in-
cludes the safety plan presented here and a sample construction
contract specification containing minimum safety and health re-
quirements at hazardous waste sites. The design contractor pre-
pares a site-specific safety plan by using the information he has on
the site and the nature of the remedial action in order to address
all the topics in the outline. The design contractor also expands
the construction contract specifications to include additional occu-
pational health and safety requirements (identified in the safety
plan) that will be the responsibility of the construction contrac-
tor. Both the site-specific safety plan and the contract specifica-
tions are reviewed by Corps' industrial hygienists and occupational
health specialists.
From a health and safety viewpoint, the site-specific safety plan
is slightly more comprehensive than the construction contract
specifications. The safety plan outlines Federal, State, local and
contractor organizational responsibilities for implementation of the
safety requirements, whereas the contract specifications contain
only those elements which are the responsibility of the construc-
tion contractor. The construction contractor prepares an Acci-
dent Prevention Plan which describes his methods for meeting the
contract safety requirements. The net effect of all these documents
is that all on-site personnel during construction must comply with
the provisions of both the site specific safety plan and the Corps of
Engineers. "Safety and Health Requirements Manual", a manual
which covers standard safety practices on all construction pro-
jects.1
Each of the next 11 sections is devoted to a major element in
the Corps of Engineers Safety Plan. The plan is in outline form,
so each section will begin with an element of the outline followed
by a brief narrative discussion of the components of that element.
THE SAFETY PLAN
Background
A listing of chemicals identified at the site and a discussion of
the safety and health implications of each, to include acute,
chronic and delayed effects (mutagenicity, carcinogenicity, terato-
genicity, sensitization reactions), radioactivity, flammability and
explosibility. A fact sheet shall be prepared in layman's language
outlining possible adverse consequences of working on the site if
proper safety procedures are not observed or if protective equip-
ment fails or is worn improperly.
The first section amounts to a summary of what is known about
the chemicals at a particular site. The Corps of Engineers recog-
nizes that in at least some, and probably most, instances this list
will be incomplete. The prepared safety plan should not just ex-
plain the extent of the knowledge available; it should also indicate
the amount of ignorance or uncertainty which exists concerning the
possible hazards.
Site investigations and a review of the site history will normally
identify major components of the hazardous waste present. Iden-
tification of safety problems (explosivity, flammability) associated
with these compounds is critically important. Such hazards are too
often neglected because of a preoccupation with toxic effects.
Whenever possible, the health effects discussed should be limited
to those supported by data which have been critically reviewed.
280
SITE SAFETY
-------
The "fact sheet" prepared under this section is later used as part
of the training given to all on-site personnel. It should supplement
the NIOSH Worker Bulletin on "Hazardous Waste Sites and Haz-
ardous Substance Emergencies" which was prepared to provide
preliminary guidance to protect the health of hazardous waste
workers.4
Site Location
•Vicinity Map
•Perimeter identification
•Existing geographic features, public utilities and/or private im-
provements
•Security measures
This general information on the site geography is obviously not
just related to health and safety, but it is necessary in order to pre-
pare the site layout and determine where it is most critical to mon-
itor possible migration of contaminants off site. Some examples
of the pertinent information to be obtained are: (1) the location
of the nearest residence of development; (2) whether or not a school
or playground is nearby; (3) potential for contaminant runoff into
a body of water; and (4) possible contamination of food crops. The
usual necessary security measures consist of restricting public
access to the site through guards and fencing. The purpose of
security precautions is primarily to protect public health and safety
in addition to preventing interference with the construction opera-
tions.
Site Layout
Every work site will have three basic areas—Exclusion, Contam-
ination Reduction and Support. The Exclusion Area will be divided
into up to three zones as determined by the degree of hazard pres-
ent. A maximum of three zones exists because Zone D may not be
included if there is a requirement for Zone A. When established
standards or adequate site information are not available, a mini-
mum of Zone B will be established. All items listed in Paragraph
A & B below will be displayed on a site map.
A. Determination of areas
1. Exclusion Area. Criteria for determining zones are listed be-
low. Protective equipment may be specified for workers in
the Exclusion Area on the basis of location or operation or
both.
a. Zone A. Maximum respiratory, skin and eye protection
is required.
(1) Where atmospheres have the potential to be immed-
iately dangerous to life and health (IDLH)
(2) Atmospheric sampling indicates concentrations cap-
able of being absorbed through the skin or eyes in
toxic quantities or atmospheric concentrations of
corrosives exist which could destroy skin.
(3) Skin contact with extremely hazardous substances
(known or suspected to be on site) is possible.
b. Zone B. Maximum respiratory protection required and
low probability of skin contact.
(1) Where atmospheric concentration of contaminant is
known and the concentration of contaminants is
greater than the protection factor for air purifying
respirators or atmosphere is oxygen deficient (less
than 19.5% oxygen).
(2) Contaminants absorbed through or toxic to skin are
not present.
(3) Safeguards preclude splashing of contaminant on the
skin or in eyes of individuals.
c. ZoneC.
(1) Air contaminant levels are being monitored and do
not exceed the protection factors of air purifying
respirators.
(2) The contaminants have good warning properties.
(3) The contaminants are not known to be absorbed
through or to be toxic to the skin.
(4) A reliable history of prior entry exists without acute
or chronic effects on personnel.
d. Zone D. Can only be included inside the Exclusion Area
if there is no Zone A or requirement for Level A pro-
tective equipment, and if there is no requirement for
Zone B or Level B protection other than a restricted
area with an oxygen deficient atmosphere.
(1) No known airborne hazards present and there is lit-
tle or no potential for release of an airborne con-
taminant.
(2) Work function precludes splashing.
2. Contamination Reduction Area. Provides area to prevent
the transfer of contaminants from the Exclusion Area to the
Support area, including personnel showers, change rooms,
equipment decontamination.
3. Support Area. The outer area, considered to be clear of
contamination, including vehicle parking, administrative
areas, etc.
B. Access to existing roadways and any associated problems with
access and egress to the site.
The Corps of Engineers has adopted the plan and terminology
for a site layout which has been standardized and promulgated by
the USPEA Environmental Response Team in Edison, NJ; these
USEPA recommendations have been distributed as the "Interim
Standard Operating Safety Guides".5 A "Zone" inside the Exclu-
sion Area does not have to be a geographic area; it is also possible
to classify a particular job or work operation as "Zone B". When-
ever possible (and it usually is not), zone classifications should be
based on the amounts and types of atmospheric contaminants
present using good industrial hygiene practices and established
standards such as the current threshold limit values (TLVs) for
occupational exposure.6 In the absence of sufficient information to
use such standards, zone classifications can be made on the basis
of total gas/vapor readings as initially suggested by Turpin of the
USEPA Environmental Response Team7 and subsequently pub-
lished in the "Interim Standard Operating Safety Guides". These
criteria are:
Zone/Level A: 500-1000 ppm above background
Zone/Level B: 5-500 ppm above background
Zone/Level C: 0-5 ppm above background
The zone designation determines the level of personal protective
equipment to be worn; a description of each level follows in the
next section.
Personnel Protection—Personal Protective Equipment
Personal protective equipment for each zone and area will be
determined. Protective gloves, boots and suits shall be of material
resistant to the chemicals present on the specific site. All respira-
tory protective equipment must be approved by NIOSH or MSHA.
1. Level A Protection. Required in Zone A.
a. Positive-pressure demand type, air-supplied breathing
apparatus
b. Fully encapsulating suit
c. Outer and inner gloves (both chemical-resistant)
d. Steel toe and shank boots
e. Hard hat (under suit)
f. Options as required:
(1) Coveralls
(2) Long cotton underwear
(3) Disposable protective suit, gloves and boots, worn
fully encapsulating suit
2. Level B. Protection. Required in Zone B.
a. Positive pressure demand, air-supplied breathing appa-
ratus
b. Chemical-resistant clothing, long sleeves, one or two
pieces, requirement for hood to be determined
c. Outer and inner gloves (both chemical-resistant)
d. Steel toe and shank boots
e. Hard hat
SITE SAFETY
281
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f. Options as required:
(1) Coveralls
(2) Disposable outer boots
3. Level C Protection. Required in Zone C.
a. Full-face piece, air-purifying, canister-equipped respir-
ator
b. Chemical-resistant clothing, long sleeves, one or two
pieces, requirement for hood to be determined
c. Gloves
d. Steel toe and shank boots
e. Hard hat
f. Options as required:
(1) Coveralls
(2) Inner chemical-resistant gloves
(3) Disposable outer boots
(4) Escape mask
4. Level D Protection. Required in Zone D and in the Con-
tamination Reduction Area
a. Coveralls
b. Leather or chemical-resistant boots or shoes, steel toe
and shank
c. Hard hat
d. Options as required:
(1) Gloves
(2) Disposable outer boots
(3) Safety glasses or chemical splash goggles
(4) Escape mask or respirator
Three levels of personal protective equipment are based on those
in the USEPA "Interim Standard Operating Safety Guides", but
there are a few differences, two of which are notable. First, a
hard hat is always required on a construction project; it is not an
option. The second difference is that a requirement for supplied
air does not necessarily dictate use of a self-contained breathing
apparatus (SCBA). Positive pressure manifold-type air line systems
may also be acceptable under some circumstances if the use of such
a system will facilitate the construction operations and not create
additional safety hazards.
Fortunately, a requirement for Level A equipment is extremely
rare (the only example on a Corps project to date was for entry
into a buried tank), and Level B has not had to be used extensive-
ly. Hard labor is difficult in Level B and nearly impossible in Level
A. When feasible, the first priority during any remedial action at
a hazardous waste site should be to control or eliminate major
hazards in order to reduce subsequent requirements for personal
protective equipment.
Personnel Protection—Medical Surveillance
Establishment of medical requirements and special tests for
chemical exposure, if available. Frequency of exams and tests will
be specified.
1. Preemployment medical examinations
2. Periodic medical examinations
3. Pretermination medical examinations
C. Work-rest scheduled for each level of protective equipment
considering the expected climate.
D. Heat or cold stress monitoring requirements and procedures.
The purpose of this section is to identify any additional med-
ical tests and examinations which may be required over and above
the minimal requirements in the Corps of Engineers guide specif-
ication and "Medical Surveillance Handbook."1 The minimal re-
quirements include a medical examination and certification as to
fitness for employment on the job prior to participation in on-site
operations, at the conclusion of the work, and/or at 12-month
intervals during the progress of the operations. The examinations
must include: medical history, work history, vital signs, physical
examination of all major organ systems, audiogram, vision screen-
ing, chest X-ray (normally only once every four years), EKG for
individuals over 35, CBC with differential, blood chemistry screen-
SMAC 23 test survey, urinalysis and a pulmonary function test
that includes Force Expiratory Capacity at 1 sec (FEV10) and
Forced Vital Capacity (FVC). Depending on the site and work
operations to be performed, some additional tests commonly rec-
ommended are: full SMAC series (SMA 32), blood and/or urine
heavy metals, an exercise stress test and EKG and blood cholines-
terase activity. During the course of the project, any employee who
has a time-loss illness or injury must be certified fit to return to
work by a physician before resuming his duties.
The requirements for personal protective equipment may create
heat stress. Heat stress symptoms may occur at any level of protec-
tion, but they are especially common in Levels A and B. The safe-
ty plan should consider the expected climate and suggest monitor-
ing ambient temperature and employee heat stress (pulse, body
temperature and water loss) above a certain ambient temperature.
Corps construction contractors are usually provided with the Army
guidelines for personnel wearing a military M3 lexicological suit (a
two-piece, hooded, butyl rubber suit).
Ambient Temperature
Above 90 degrees F
85-90 degrees F
80-85 degrees F
70-80 degrees F
60-70 degrees F
50-60 degrees F
30-50 degrees F
Below 30 degrees F
Maximum Wearing Time, (hr)
1/4
Vi
1
Contractors should develop their own work-rest schedules for
Levels A, B and C, using this information for guidance.
Contaminant Monitoring
Identification of specific methods, frequency and locations.
When available, NIOSH approved methods must be used.
A. Personnel Monitoring (breathing zone samples)
1. High hazard operations
2. Hazardous site areas or zones
B. Area Monitoring
1. Atmospheric concentrations of contaminants
2. Oxygen' content
3. Explosive atmospheres
4. Radioactivity (primarily beta and gamma emissions)
Construction work operations which involve handling of haz-
ardous waste require continuous contaminant monitoring using
direct-reading field instruments. Site conditions may change rapid-
ly as a result of construction activity; excavation may bring haz-
ardous wastes to the surface, drums may be accidentally ruptured
and tanks may accumulate explosive concentrations of vapors
when emptied. Continuous monitoring indicates when the level of
personnel protection needs to be adjusted, or when an area of the
site must be evacuated. Contaminant monitoring is usually accom-
plished using organic vapor analyzers or photoionization detectors,
but these devices are not sufficient at sites where hydrogen cya-
nide or hydrogen sulfide could be generated. Drawer tubes should
be used to detect these compounds.
Air monitoring stations for collection of air samples for subse-
quent analysis should also be provided in addition to portable
direct-reading equipment. This serves two purposes. First, ab-
normally high readings on the field instruments can be confirmed
and the nature of the principal contaminants identified. Although
the results are obtained later, it is still a useful check to determine
if appropriate action was taken, the likely nature of future inci-
dents and whether or not personnel need to be examined for symp-
toms of chemical exposure. The second purpose is monitoring of
the site perimeter to insure that off-site populations are not ad-
versely affected by construction activities.
282
SITE SAFETY
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Decontamination
A. Personnel decontamination procedures
B. Equipment decontamination procedures
C. "Scrap" decontamination procedures
The extent of the decontamination necessary for personnel and
equipment is highly site-specific. For personnel, the extent of de-
contamination increases as the level of protection increases. Per-
sonnel assisting in decontamination should be in the next lower
level of protection from the person being decontaminated. Basic
elements of a personnel decontamination station include an equip-
ment drop area, solutions for outer garment washdown and rinse, a
place to remove outer clothing for additional decontamination or
disposal, a place to remove respiratory protection devices and,
finally, an area to remove remaining clothing for laundering or dis-
posal before entering the shower.' Initial equipment drop and outer
garment washdown occurs just inside the Exclusion Area; the re-
maining operations are in the Contamination Reduction Area,
located in a place which is normally upwind of the Exclusion Areas.
Decontamination of trucks and other construction equipment
can involve simply washing down the tires and undercarriage or
can require steam cleaning or sand blasting. In truly extreme cases,
equipment may be buried on site. The minimum Corps of Engi-
neers requirements for an equipment decontamination facility are
a high pressure wash area for equipment and vehicles and a steam
180°F hot water for use after the mud and/or dirt has been cleaned
from the equipment. Equipment maintenance requiring contact
with ground soil must be done in a special "clean area" set aside
for that purpose. Before removing equipment from the site at the
conclusion of the project, fluids and filters should be changed and
the old materials should be disposed of as hazardous waste.
All wash water used for personnel or equipment decontamina-
tion must be contained and collected in a segregated system for
subsequent treatment and disposal as hazardous waste.
Prevention of Contamination Spread
Identification of specific methods, frequency and location for
monitoring. USEPA approved methods should be used where ap-
plicable.
A. Waste water
B. Soil
C. Groundwater/Surface water
D. Meteorological Monitoring
Spills or releases of hazardous materials are not merely poss-
ible, but probable during construction activities, requiring special
attention to specific spill control procedures. As mentioned in the
previous section, waste water is segregated for disposal as haz-
ardous waste. Liquid spills can be controlled by adsorbent ma-
terials kept close to active work areas. Both the adsorbent and
surrounding soil are contained for subsequent disposal. Erosion
and storm water run-off control measures are a part of the remed-
ial action design in order to prevent contaminant migration dur-
ing construction.
Continuous meteorological monitoring is required during all
Corps remedial actions at hazardous waste sites. This determines
the downwind locations for air monitoring stations and also the
likely dispersion of airborne contaminants in case of a hazardous
substance release. Other kinds of environmental monitoring involv-
ing off-site migration of contaminants (particularly groundwater
monitoring) are not normally part of Corps Superfund construc-
tion activities; at most sites the USEPA provides for this under a
separate contract.
Communications
A. Communications on site compatible with protection equip-
ment used
B. Communications with on call emergency equipment
Two-way radio communications are needed to link all active
work areas with the office and support areas. Two-way radios
should also be provided to all personnel wearing Level A or Level
B protective equipment. Although radio communication with local
emergency response organizations (fire and police departments,
ambulance service, hospital) can be arranged if desired, it is usual-
ly sufficient to post the necessary phone numbers next to all pro-
ject phones and be certain that someone near a phone has radio
contact with the rest of the site at all times.
Emergency Procedures
Establishment of protocols and equipment necessary for emer-
gency response procedures for occurrence of A through E below in
each of the site areas and zones.
A. Chemical Exposure
B. Personal Injury
C. Potential or actual fire or explosion (including criteria for
determining a hazard exists)
D. Environmental accident
1. Spill control procedures
2. Information resources for emergency response
3. Reporting requirements
E. Radiation
1. Criteria for determining hazard
2. Regulatory agency requirements
F. Identification of local and state emergency response personnel
required on standby to support activities on site (fire depart-
ment, police, hospital and emergency room, others).
1. Level of expertise available
2. Emergency and personal protective equipment available
3. Training required for emergency personnel supporting site
operations
G. Definition of interfaces between the contractor, Corps repre-
sentative, and USEPA On-Scene Coordinator for implemen-
tation of the USEPA Community Protection Plan. The Com-
munity Protection Plan shall be a part of the Site Specific
Safety Plan in order to insure adequate contingency planning
has been done by all Federal, State and local agencies in-
volved.
Contingency planning to cover possible emergencies on site must
consider all kinds of accidents whether or not they are related to
hazardous materials. Basic factors to consider are: (1) criteria for
determining an emergency exists; (2) specific procedures to con-
trol or abate the hazard, or prevent injury; and (3) who to call
for help or information. This information should be written down
and conspicuously posted in convenient locations.
One of the major problems which must be addressed is the hand-
ling of ill or injured persons inside the Exclusion Area. An on-site
employee with a current first aid certification (and wearing appro-
priate protective gear) should administer immediate treatment and
determine if the employee can be moved and go through decon-
tamination. A handbook of first aid protocols for chemical ex-
posures has recently been published as an Army Field Manual;10
a copy of this book is on-site at all Corps of Engineers Super-
fund remedial actions. Emergency medical care support must be
prearranged with a convenient medical facility. The staff at that
facility should be aware of the potential medical emergencies and
be advised that the patient's clothing and skin might be contam-
inated with specific chemicals.
An extremely important part of emergency planning is making
the necessary arrangements with off-site emergency response per-
sonnel to provide support upon request when on-site employees
can not handle the crisis alone. It is not sufficient just to make sure
the phone numbers are correct for the police department, fire
department, ambulance company and poison control center. Other
issues must be addressed such as whether or not the fire depart-
ment has the training, equipment and materials to fight chemical
fires and determining who can and will supply personal protective
equipment for emergency personnel. It may be necessary to train
and equip some local departments that will be supporting site
operations.
SITE SAFETY
283
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Each site should be carefully evaluated to determine if a cata-
strophic accident requiring evacuation of local residents could
occur. Actual evacuation planning is usually done by a state or
local agency, and it should be coordinated with the USEPA
Regional Office as well as the construction contractor and other
government representatives, as appropriate. All parties involved
in evacuation planning for community protection should realize
that an evacuation, or even the act of planning one, presents an
enormous public relations problem which could interfere with con-
struction of remedial measures.
Training
Personnel will have either formal training or prior on-the-job
training for those tasks they are assigned to perform. All un-
familiar operations will be rehearsed prior to performing the ac-
tual procedure. Additionally, an on-site orientation session must
be developed covering the following subjects as a minimum.
A. Health effects and hazards of the chemicals identified or sus-
pected to be on site. The basis for this discussion will be the
background information and fact sheet prepared under Sec-
tion I.
B. Personnel Protection
1. Use, care and fitting of personnel protective equipment
2. Necessity for personnel protection, effectiveness and lim-
itations of equipment
C. Decontamination Procedures
D. Prohibitions in areas and zones
1. Site layout
2. Procedures for entry and exit of areas and zones
3. Use of lunch, break and shower facilities
E. Emergency procedures as identified in Section IX
F. Medical requirements, necessity for medical examinations and
specific tests
Before proceeding with any construction operations at a haz-
ardous waste site, all on-site personnel (contractor, subcontractor
and government) should receive site orientation training to famil-
iarize them with the hazards present, specific equipment to be
used, special work procedures and prohibitions required, and what
to do in an emergency. This orientation should supplement, not
replace, prior training in handling hazardous materials and use of
protective gear. It is important that site workers have both a heal-
thy degree of respect for the hazards and confidence in their abil-
ity to work safely. Experience has demonstrated that this confi-
dence is usually not developed during a single training session.
During the construction project, regular periodic safety sessions
should be held to review problem areas and also call attention to
special hazards associated with each phase of work or change in
operations.
CONCLUSION
The outline of a site safety plan which has been presented here
should not be regarded as final or totally comprehensive. The
Corps of Engineers expects revisions as Corps personnel gain ex-
perience with hazardous waste remedial actions. Most importantly,
the Corps welcomes comments and suggestions from other haz-
ardous waste experts in order to improve Corps guidance for in-
suring safe implementation of remedial measures.
ACKNOWLEDGEMENTS
The authors wish to thank Dr. Stephen Dorrler, Dr. Joseph La-
Fornara and Rodney Turpin of the USEPA Environmental Re-
sponse Team, and Noel Urban, James Ballif, Dr. George Schloss-
nagle, John Geiglein, John Dezan and Frank Bizzoco of the U.S.
Army Corps of Engineers for their helpful comments and dis-
cussions during the development of this plan.
The views expressed here are those of the authors and do not
necessarily represent those of the Army Corps of Engineers or the
Department of the Army.
REFERENCES
1. Gay, F.T., Urban, N.W. and Ballif, J.D., "U.S. Army Corps of En-
gineers Role in Remedial Response", Proc. National Conference on
Management of Uncontrolled Hazardous Waste Sites, 1982,414-417.
2. USEPA, "Safety Manual for Hazardous Waste Site Investigations",
Office of Occupational Health and Safety, and the National Enforce-
ment Investigation Center. Denver, CO, Draft 1979.
3. U.S. Army Corps of Engineers, "Safety and Health Requirements
Manual", EM 385-1-1 with Change 1 (1 Dec 81), Office of the Chief
of Engineers, Washington, DC, Apr. 1981.
4. NIOSH Worker Bulletin, "Hazardous Waste Sites and Hazardous
Substance Emergencies", DHHS (NIOSH) Publication No. 82-115,
Cincinnati, OH, 1982.
5. USEPA, "Interim Standard Operating Safety Guides", Office of
Emergency and Remedial Response, Hazardous Response Support
Division, Washington, DC. Revised Sept. 1982.
6. ACGIH, "TLVs-Threshold Limit Values for Chemical Substances in
Work Air", ISBN: 0-936712-39-2, Cincinnati, OH, Adopted by
ACGIH for 1982. Revised annually.
7. Turpin, R.D., "Initial Site Personnel Protection Levels Based on Total
Vapor Readings", Proc. National Conference on Management of
Uncontrolled Hazardous Waste Sites, 1981,277-279.
8. U.S. Army Corps of Engineers. "Medical Surveillance Handbook",
EP 385-1-58, Office of the Chief of Engineers, Washington, DC, 1981.
9. Gallagher, G.A., "TAT/FIT Health and Safety Program for Haz-
ardous Waste Site Investigation", Proc. National Conference on
Management of Uncontrolled Hazardous Waste Sites, 1980,85-90.
10. Stutz, D.R., Ricks, R.C., and Olsen, M.F., "Hazardous Materials
Injuries—A Handbook for Pre-Hospital Care", FM 8-500, Office of
the Surgeon General, Department of the Army, Washington, DC.
Copyright by Bradford Communications Corporation, Greenbelt,
MD 1982.
284
SITE SAFETY
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HEALTH AND SAFETY CONSIDERATIONS:
SUPERFUND HAZARDOUS WASTE SITES
KATHLEEN S. ROOS
PATRICIA A. SCOFIELD
Rockwell International
Environmental Monitoring & Services Center
Newbury Park, California
INTRODUCTION
The Superfund program has added a new dimension to the
science as well as potential legal ramifications resulting from pro-
viding health and safety protection for the worker and general pub-
lic. The Occupational Safety and Health Administration (OSHA)
has primarily concentrated on employee health and safety in the in-
dustrial setting. However, the Superfund program has illustrated
the need and growing concern for field health and safety. The haz-
ardous materials cleanup employee can be exposed to toxic and
hazardous substances that may or may not be identified, and the
potential health effects of exposure to these substances may not be
known. Hence, Health and Safety considerations must be oriented
toward the "prevention" of exposures and impacts, rather than
toward "after-the-fact" emergency actions. Having a Health and
Safety Program oriented toward "prevention" of exposures will
hopefully reduce the potential, if not the magnitude, of employee
and general public legal actions.
The OSHA General Industry Standards (29 CFR 1910) are gen-
erally applicable to a wide range of "normal" industrial opera-
tions but are limited in their applicability to field operations as
well as to the number and type of chemical substances regulated.
However, the Occupational Safety and Health Act of 1970 broadly
defines employer duties and responsibilities. These duties require
the employer to provide a place of employment free from "recog-
nized hazards." Section 5(1 )(A) of the Act gives the OSHA the
authority to require safe working conditions in any place of em-
ployment. Failure of an employer to comply with the "recognized
hazard" duty could result in a citation or notice of violation and,
if established, the imposition of a penalty. Therefore, one must be
concerned not only with potential legal actions from employees and
the general public, but also from regulatory agencies.
To protect a party, both government and contractor, from lit-
igation incurred by the loss of health or safety, the party must
demonstrate best professional judgment in preventing any harm to
workers or public. Prevention is the key to protection from legal
action. To prevent harm to the worker and the public, a thor-
oughly reviewed Health and Safety Program and effective man-
agement and enforcement of the program are essential.
A health and safety program consists of many elements including
a Health and Safety (H&S) Plan for worker safety and contin-
gency planning for public safety. Other elements include the devel-
opment of a medical surveillance and training program for per-
sonnel. The objective of any health and safety program is to estab-
lish and assure safe procedures and practices throughout the organ-
ization for investigation and cleanup of a site. Safety responsibil-
ities must be incorporated into the site management roles to ensure
the protection of all those involved. The plan is not complete until
it has undergone review and is finally executed by the office in
charge. In any health and safety program, tradeoffs must be con-
sidered and operational efficiency and expediency of work bal-
anced with ultimate protection of workers and the public. An H&S
program can only minimize, but never eliminate, all risks inherent
in cleanup.
The effective management of a hazardous waste site remedial
and cleanup action requires a realistic health and safety program
for both on-site personnel and for the general public. The 'Love
Canal" situation has affected public perception of what is con-
sidered dangerous. Prevention and containment should be the is-
sues addressed in the Community Relations Plan and considered by
first line managers to assure the public that their health and safe-
ty are continuously addressed. The public must believe that the
problem is contained and that the responsible parties will prevent
any harm from coming to them.
In this paper, the authors discuss methods that are available to
responsible parties to demonstrate best professional judgment to
protect public and worker safety and health.
HEALTH AND SAFETY PLAN
The prime contractor to the USEPA and/or the Corps of En-
gineers is responsible for development and implementation of the
H&S plan for the hazardous waste site. However, the USEPA or
Corps of Engineers must approve the plan. To provide assistance
to the contractor for H&S plan development, both federal agen-
cies have issued draft guidelines for health and safety at spill, re-
moval and remedial action-sites.7'8
The primary objective of a H&S plan is to establish, prior to
work start, work safety guidelines, requirements and procedures.
The plan must address the two types of potential exposures—acute
and chronic. Acute exposures are often of short duration and may
result from splashes or sudden high concentrations of toxic con-
taminants. Chronic exposures generally occur over longer periods
of time and often from low concentrations of toxic contaminants.
Chronic exposures at hazardous waste sites represent significant
problems. Acute exposure may also increase due to activities such
as sampling and handling of containers due to splashes, mists,
gases or particulate releases.
The health and safety plan must account for site specific con-
ditions but be flexible to cover unanticipated hazards. Unlike in-
dustrial exposures, workers at hazardous waste sites may be ex-
SITE SAFETY
285
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posed to unknown quantities and types of chemical substances.
Chemical substances existing at Superfund sites may be combus-
tible, explosive, corrosive, reactive, toxic, biologically active or any
combination of these characteristics. Due to the unknown nature of
the sites, all possible realistic scenarios in plan development must
be evaluated.
Additional factors that must be addressed in H&S plan develop-
ment include:
•Site and work descriptions
•Role definition for responsible parties
•Hazard analysis-definition of contamination type, levels and
zones
•Operational safety procedures
•Appropriate protection and decontamination levels
•Training and education requirements
•Emergency procedures
•Medical surveillance program
•Recordkeeping procedures
The plan must be site specific. Site description may include dia-
grams of locations of waste containing drums, sampling stations
and exploratory boreholes or trenches. It may also describe the
proximity of the hazardous waste site to groundwater or surface
water supplies, demographic population distribution and other
characteristics that impact the investigative, removal or remedial
actions. The plan should also outline the proposed work activities
and procedures. For example, the plan should specify that work ac-
tivities include field investigations and collection of environmental
samples of soil, groundwater and surface water.
The role of responsible parties is of paramount importance in
health and safety planning. Specifying responsibilities of the gov-
ernmental agencies, contractors and employees helps to highlight
potential gaps in the plan and safety procedures as well as dictates
who does what, when and where. Delineation of responsibilities
may have a significant impact on future legal actions. For example,
it is the responsibility of the USEPA to approve all aspects of the
contractor health and safety program and any procedures per-
formed by the contractors or state agency and work zones. The
contractor is responsible for implementation of all health and
safety procedures, providing safe hazardous waste site conditions,
designation of a safety officer and establishing on-site work zones.
The employee responsibilities include understanding all safety
operations and decontamination procedures and utilizing protec-
tive equipment required for various work zones. The plan must
state these responsibilities and describe how they will be imple-
mented.
A hazard analysis or assessment must be conducted for the haz-
ardous waste site to determine where hazards are likely to exist,
what type and amount of chemical contaminant substance are in-
volved, what area would most likely be adversely affected and the
probability of hazardous material incidents. Hazard analysis is
essential for both H&S planning and contingency planning. The
hazard analysis helps to decide the types of safe operating pro-
cedures, emergency actions, equipment needs and medical screen-
ing and training requirements.
The plan must define safe operating procedures and work prac-
tices. These procedures are intended to provide uniform instruc-
tions for accomplishing a specific task in a manner that protects
the worker. These procedures may cover various activities at the
hazardous waste site, such as site control and entry. As an example,
for site entry the following safe operating procedures may apply1:
•Entrance and exit must be planned and emergency escape routes
delineated. Warning signals for site evacuation must be estab-
lished.
•Personnel on-site must use the "buddy" system when wearing
respiratory protective equipment.
•Communications using radios or other means must be maintained
among initial entry members at all times. Emergency communica-
tions should be prearranged in case of radio failure, necessity for
e%acuation of site or other reasons.
•Personnel and equipment in the contaminated area should be min-
imized, consistent with effective site operations.
•Work areas for various operational activities must be established.
The plan for the hazardous waste site must also define appro-
priate protection level and site control, otherwise known as decon-
tamination levels. The USEPA and the Corps of Engineers have
established four levels (A, B, C, and D) that correspond with per-
sonal protective equipment needed for specific types and concen-
trations of contaminants. The protection levels A, B, C and D are
briefly described as follows:
LEVEL A requires the highest level of respiratory, skin and eye
protection and often corresponds to the exclusion zone (area of
potential contamination).
LEVEL B is selected when the highest level of respiratory pro-
tection is needed, but a lesser level of skin protection is suffic-
ient. Level B protection is the minimum level recommended on
initial site entries until the hazards are further defined.
LEVEL C is selected when the type of airborne substances are
known and the criteria for air purifying respirators are met.
LEVEL D is selected when there are no respiratory or skin haz-
ards. A work uniform may be worn which provides minimal pro-
tection.
Site control or decontamination procedures must be delineated
and followed. Even when protective clothing, respirators and good
work practices are utilized, contamination may occur. Harmful
materials can be transferred into clean areas, exposing unprotected
personnel. To prevent such occurrences, methods to reduce con-
tamination and decontamination procedures must be developed
and be contaminant specific. Defined procedures and their execu-
tion must be enforceable.
Decontamination procedures are often based on worst-case
situations. Specific conditions at the hazardous waste site that
should be evaluated include: type of contaminant(s), amount of
contamination, levels of protection required and type of protec-
tive clothing worn. Decontamination procedures must also identify
use and possible reuse of protective gear, on-site and off-site clean-
ing methods, disposal methods for gear and contaminated wash
water and specific wet/dry decontamination procedures.
Areas of contamination reduction must also be determined. An
example of a contamination reduction zone layout is shown in
Figure 1. An area within the contamination reduction zone is desig-
nated the Contamination Reduction Corridor (CRC). The size of
the corridor depends on the number of stations required in the
decontamination procedures, overall dimensions of work con-
trol zones and the amount of space available at the site.
Training and education requirements for personnel should be
outlined in the plan. The primary topics that should be addressed
include: (1) H&S program organization and structure, (2) safe
operating procedures, (3) emergency procedures, (4) protection
levels and personal protective equipment use, (5) safe field equip-
ment use, e.g., construction, and (6) decontamination procedures.
For a detailed discussion on training program requirements refer
to the subsection on the H&S Training program.
The emphasis of the H&S program as well as investigative,
removal and remedial actions must be oriented toward "preven-
tion", especially as these relate to liability considerations. How-
ever, procedures must be established to handle emergency situa-
tions. In this case, if one is liable but can prove everything pos-
sible was done to remedy the situation, one may suffer less in the
legal action. Emergency planning procedures should include notif-
ication requirements, telephone roster of key individuals and emer-
gency response groups, emergency decontamination procedures,
rescue techniques, first aid procedures and the itemization and
location of emergency equipment and supplies, e.g., eye wash and
shower areas. It should also include emergency evacuation and
transport routes.
The establishment of a medical surveillance program is another
element of the plan. The medical surveillance program consists of
two components: medical screening and emergency medical care
286
SITE SAFETY
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HEAVY EQUIPMENT
DECONTAMINATION
AKEA
EXCLUSION
ZONE
BIT
»ATH
CONTAMINATION
REDUCTION
ZONE
ill
3 U S
hi
!? iu W
SUPPORT
ZONE
Figure 1.
Contamination Reduction Zone Layout
and treatment. The plan must dictate specific responsibilities of
the physician, contractor and employee, and type of examinations
and treatment procedures.
Recordkeeping procedures, though listed last, are by no means
of least importance. Delineation of recordkeeping procedures is
essential, especially as it related to liabilities. Recordkeeping pro-
cedures should be required for all aspects of the H&S program.
OSHA has established both general and specific requirements for
maintaining medical training surveillance records. The OSHA Gen-
eral Industry Standards, Title 29, Section 1910.20 states that "each
employer who makes, maintains, or has access to employee ex-
posure records or employee medical records shall preserve these
records." Recordkeeping requirements for 29 CFR 1910, Subpart
Z, Toxic and Hazardous Substances are more specific. For ex-
ample, the medical records for workers who work with benzi-
dine must be maintained for the duration of the employee's em-
ployment. Upon termination, records or notarized true copies
must be forwarded to the OSHA Director. Recordkeeping is also
important to validate that training requirements were satisfied.
Maintenance of records, whether legally required or not, may
greatly reduce the impact of any possible legal actions.
Preparation of a hazardous waste site H&S plan requires the
input from groups with varied responsibilities. These groups may
include contractors, hospitals and local agencies such as the police,
fire and health departments. It should never be assumed that these
groups are prepared for emergency situations emanating from a
hazardous waste site. In the case of E&E's cleanup of General
Disposal, the H&S plan required input from USEPA, Region IX,
the USEPA Environmental Response Team, USCG Strike Team,
LA County Sheriff's Department, City of Santa Fe Springs Fire
Department, Department of Health Services, prime & subcontrac-
tors and E&E.'
The groups that may be involved in H&S actions should be
contacted prior to work start, and the possible hazards outlined
and protocols arranged. A copy of the reviewed and approved
health & safety plan should be made available to all personnel and
agencies which may be involved in a hazardous waste site cleanup
or resultant emergency situation. A plan distribution list should be
developed so that any revisions or updates to the plan will be sent to
these groups.
MEDICAL SURVEILLANCE PROGRAM
Hazardous materials cleanup personnel can be exposed to condi-
tions that are atypical of normal occupational exposures. There-
fore, special attention should be given when developing medical
surveillance programs for this type of worker. The team member
can be exposed to thousands of toxic chemicals that may or may
not be identified and the potential health effects of exposure to
these chemicals or mixtures of the chemical may not be known.
Some other differences between the normal worker and the
response team member are as follows:
•Usually the response team member's exposure to hazardous sub-
stances is relatively short in duration and primarily dependent on
the length of the cleanup operation.
•Industrial exposures are controlled by engineering and industrial
hygiene practices. However, the response team member's source
of protection from exposure to hazardous substances is usually
proper work practices and proper utilization of personal protec-
tive equipment, e.g., gloves, respirators, coveralls, chemical
suits, boots, etc.
•Generally, industrial exposures evolve from known substances
and sources, whereas the response team member may be exposed
to substances that are unknown in type, quantity and concentra-
tion, as well as combinations of substances.
With these differences between the normal industrial worker and
the hazardous waste cleanup team member, a medical surveillance
program should be established to meet the following objectives:"
•Preassignment health screening of all employees who will be di-
rectly engaged in hazardous waste investigations, removal and/or
remedial actions.
•Support of the health of employees assigned to hazardous waste
investigations
•Evaluation and care of individuals with work-related exposures,
injuries or illness
•Monitoring of workers' health for evidence of work-related health
effects and their suitability for further assignments in this field
To safeguard the health of response personnel, a medical sur-
veillance program must be developed, established and maintained.
A physician experienced in occupational medicine and the effects
of toxic industrial substances should develop and be involved in
maintenance of the medical surveillance program. An experienced
physician not only helps to ensure the protection of on-site workers
health, but also helps to protect the employer from legal action.
Two components of a medical surveillance program are medical
screening and emergency treatment. Medical screening generally
consists of preplacement, periodic and termination examinations.
These examinations establish an individual's state of health, base-
line physiological data and ability to use personal protective equip-
ment. Medical screening also provides for special medical exam-
inations, usually as periodic examinations, in evaluating known
or suspected exposure to toxic substances. Emergency treatment,
on the other hand, is medical care given when possible overex-
posure to toxic substances or injuries occur due to accidents or
physical problems. In the event of emergency treatment, specific
emergency care provisions should have already been delineated.
For the purposes of this report, the authors will focus on medical
screening provisions.
MEDICAL SCREENING—EXAMINATIONS
As mentioned previously, medical screening usually consists of
three main examinations—preplacement or baseline, periodic and
termination. Preplacement or baseline examinations serve an essen-
tial function in medical surveillance by providing a historical record
of previous exposures, information on the state of health prior to
joining the team and a baseline for comparison with later health
SITE SAFETY
287
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examinations. Preplacement examinations are used to ensure that
workers are physically able to use personal protective equipment
as specified by Occupational Safety and Health Administration
Standards, 29CFR1910, Part 134. Preplacement examinations also
serve to document preexisting conditions and exposures prior to
new job assignment, thus establishing a point of reference in case
of future legal actions.
Periodic examinations can be used as a tool to detect incipient
disease, physiological changes and evidence of absorption of toxic
agents. It is important to consider periodic examinations in terms
of what is legally required, what is recommended by official agen-
cies such as the USEPA and the National Institute for Occupation-
al Safety and Health (NIOSH) and what has persuasive medical
justification. The periodic examination is similar to the preplace-
ment examination, i.e., occupational/medical history, physical
exam and biological monitoring; however, emphasis is oriented
toward followup studies on possible exposures that had occurred
since the previous examination. Periodic examinations can contrib-
ute to early diagnosis and treatment of the individual and may
identify common factors in a group, thereby enhancing the value of
preventive programs. Periodic examination can also be used as a
tool to determine whether the individual should be removed from
the work environment if it is indicated that his/her health may be
adversely affected.
Examinations at the termination of employment or job assign-
ment are desirable since they can be used to document the health
status at the end of employment and provide evidence of any
changes that occurred during the job assignment or employment
period. This does not rule out the possibility that effects may show
up at a later date. For example, asbestosis can progress years after
the last exposure to asbestos dust, and cancer from a chemical car-
cinogen may not appear for decades. The termination examina-
tion would be very similar to the preplacement examination, al-
though special tests may be required if occupational exposures had
occurred during the work period that the employee had been work-
ing at a hazardous waste cleanup site.
MEDICAL SCREENING—SURVEILLANCE ELEMENTS
Each of these examinations—preplacement, periodic and term-
ination, consists of occupational and medical history, physical
examination and biological monitoring elements. Each of these
elements is described below.
Occupational/Medical History
The occupational and medical history information obtained
from the employee assists the examining physician in perform-
ing an examination of appropriate scope. Examples of occupa-
tional and medical history parameters of interest may include:
•Job-related illnesses or injuries
•Types of substances handled at work
•Personal habits, e.g., smoking, alcohol and drug consumption
•Medication history
•Allergies
•Immunizations, vaccines and antitoxins
The USEPA strongly recommends that a medical and occupa-
tional history form similar to the one that USEPA developed be
used. The USEPA feels that "standard" medical history forms are
too sketchy, especially in terms of occupational history exposure.
Physical Examinations
A physician or medical advisory board responsible for medical
screening should determine the content and methods required for
the physical examination. Examples of physical parameters that
are typically evaluated include: basic physiological parameters
such as vision, tonometry, hearing, height and weight; respira-
tory parameters such as pulmonary function analysis and chest
and back X-rays; cardiac parameters—electrocardiogram and
blood pressure; and a physical examination. The physical exami-
nation may include skin inspection, reflex evaluation and a chest
examination. The USEPA recommends that the physical exam-
ination be recorded on a standard form such as government stand-
ard Form 88. Although the physician may have similar forms, all
work places are urged to adopt this standard form to achieve uni-
formity.
Biological Monitoring
Industrial chemicals that might cause systemic effects are often
transported by the blood systems, metabolized by enzymes and
excreted by the body. In an effort to measure exposure(s) to in-
dustrial chemicals, biological monitoring is often a logical ap-
proach. The USEPA recommends that each individual should re-
ceive a basic panel of blood counts and chemistries to evaluate
blood-forming, kidney, liver and endocrine/metabolic functions.
The following blood tests are considered to be the minimum de-
sired:'
•White blood and differential cell count
•Hemoglobin and/or hematocrit
•Albumin, globulin, and total protein
•Total bilirubin
•Serum glutamic oxalacetic transaminase (SCOT)
•Lactic dehydrogenase (LDH)
•Alkaline phosphatase
•Calcium
•Creatinine
•Urea nitrogen
•Phosphorus
•Cholesterol
•Glucose
•Uric acid
The USEPA also recommends that each employee have a rou-
tine urinalysis that consists of the following tests:'
•Specific gravity
•pH
•Microscopic examination
•Protein
Workers who are significantly exposed to certain designated ma-
terials may require special procedures in addition to the basic panel
of tests. Examples of special tests that may be requested due to ex-
posure to specific hazardous substances are as follows:4-6
•Lead—Lead analysis in blood or urine, neurologic exam
•Acrylonitrile—Proctosigmoidoscopy and fecal blood
•Vinyl chloride—SGOT, Serum Glutamic Phosphoric Transam-
inase (SGPT) and Alkaline Phosphate
•Asbestos—Sputum cytology
•Mercury—Mercury in blood or urine, neurologic exam
•Organophosphate pesticides—Blood cholinesterase
The physician should determine who is in need of special tests
after reviewing the occupational and medical forms and after con-
sulting with supervisors and/or medical monitoring coordinators
and health and safety designers. Provisions should be made for re-
peating tests when necessary.
Participants in this medical surveillance program should be ad-
vised that these examinations are not a direct substitute for "gen-
eral checkups" or other periodic examinations designed to monitor
or promote general health. The occupational medical surveillance
program is designed to screen for evidence of adverse effects of
occupational exposure, particularly exposure to toxic substances.
The examinations do not provide a comprehensive health evalua-
tion; neither do they provide significant screening for many of the
common nonoccupational chronic disorders.
HEALTH AND SAFETY TRAINING PROGRAM
The prime contractor is responsible for developing, implement-
ing and maintaining a training program for cleanup personnel.
The prime contractor must also insure that the subcontractors have
a comparable training program for their employees. Due to these
specified requirements, the contractor must develop a training pro-
gram that is comprehensive and effective. A training program can
288
SITE SAFETY
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be considered a "preventive" measure since it allows, if conducted
properly, the employee : (1) to understand the hazardous aspects
of the work; (2) to be aware of the regulations and rules of con-
duct specific to on-site activities; (3) to understand and be com-
fortable with safe operating procedures, work practices and emer-
gency actions; and (4) to increase confidence because he/she knows
what to do and how to act in emergencies in a safe, effective man-
ner. Therefore, the training program as a "preventive" measure, if
implemented and enforced, will help to reduce employee injury,
illnesses and accidents, thus decreasing the likelihood of worker
compensation claims and suits and other legal actions.
Currently, the USEPA and the Corps of Engineers recommend
at least 16 hours of practical and theoretical instruction for haz-
ardous waste cleanup personnel. They also recommend that re-
fresher training courses be conducted for at least two hours an-
nually. Training requirements, as defined in the OSHA General In-
dustry Standards, are oriented toward specific chemical substance
requirements (Subpart Z), respirator usage (29 CFR 1910.134) and
for activities, such as truck operations (29 CFR 1910.178). As
stated, the OSHA standards specify training and indoctrination
program requirements for employees working with toxic and haz-
ardous substances (29 CFR 1910.1000-1046). According to these
regulations, the employee should receive a training program that
includes the following elements:
•The nature of the toxic or carcinogenic hazards of the chemical
substances in question; this includes local and systemic toxicity.
•The specific nature of the operation involving the toxic or haz-
ardous substance which could result in exposure.
•The purpose for and application of the medical surveillance pro-
gram including, as appropriate, methods of self-examination.
•The purpose for and application of decontamination procedures
and purposes.
•The purpose for and significance of emergency practices and pro-
cedures.
•The employer's specific role in emergency procedures.
•Specific information to aid the employee in recognition and eval-
uation of conditions and situations which may result in the release
of the toxic and hazardous substances.
•The purpose for and application of specific first aid procedures
and practices.
•Specific emergency procedures should be prescribed and posted.
The employees must be familiar with the terms and rehearsed
(drilled) in this application.
•Review of these elements at the employee's first training program
and annually thereafter.
These training elements, though specific for OSHA designated
toxic and hazardous substances, are also key elements of the train-
ing program for hazardous waste sites. However, additional ele-
ments are also recommended for hazardous waste sites. These in-
clude:
•The proper use of field sampling and laboratory equipment; this
includes work tools, sampling equipment and decontamination of
tools.
•The purpose and proper use of personal protective gear such as
the fitting and use of respirators and personal protective apparel
and the use of Self-Contained Breathing Apparatus (SCBA).
•The general structure of the Health and Safety program, includ-
ing responsibilities, and general rules of conduct at the hazardous
waste site.
•The identification of contamination areas and level of protection
and protective gear required.
•The implementation of safe operating procedures and work prac-
tices; this includes rules for site entry and exit, site control pro-
cedures and work limitations.
Effective personnel training programs, as developed and imple-
mented by the prime contractor, should address not only safety and
welfare of the cleanup personnel, but must also inform all person-
nel about the waste site hazards, and train all personnel via spill
drills prior to site investigation and cleanup. Initial and refresher
training courses are essential and should be documented to help re-
duce not only employee illness, injuries and accidents, but also re-
sultant worker compensation claims, suits and other legal actions.
CONCLUSIONS
The nature of liability cannot be adequately addressed in a pres-
entation of this nature, nor at this time, since legalities and prec-
edence have not been set. However, it may be useful to point out
some steps which can be taken to protect responsible parties from
possible litigation.
•Document that the health and safety program was enforced.
•All procedures should be documented and approved by appro-
priate officials.
•Multiple experienced groups should be involved in preparing
health and safety and contingency plans, especially the Fire De-
partment and USEPA.
•Use only experienced and trained personnel for any projects.
•Do not always take the "cheapest" route; it may be expensive
in the end.
•Investigate limitations of protective equipment and assure that
it is protective against chemical substances and any combinations
found on-site.
•Use only certified and guaranteed equipment meeting all approved
OSHA, MSHA and/or NIOSH safety approval for personnel
standards.
•Construction activities require trained equipment operators and
support personnel. This requires a different, yet defined, safety
procedures guideline, e.g., the operation of heavy equipment is
dangerous in and of itself. Assure that all subcontractor personnel
meet safety training requirements.
•All procedures should be referenced and/or support specialists
kept on call.
•Alternative operating procedures should be available to on-site
personnel, if possible.
•Contingency plans should address realistic scenarios. All agen-
cies and/or groups involved in a release scenario should be de-
briefed prior to work start.
•All data must be documented with strict QA/QC procedures;
strict chain-of-custody protocol must be followed in every aspect.
•Health and safety responsibilities should be integrated into man-
agement roles. Chain-of-command with inherent responsibilities
must be well defined.
•Safe operating procedures must be posted and enforced. Penal-
ties for failure to follow these procedures should be enforced.
•One party (OSC) must have ultimate authority to make decisions.
•Reference material, including codes and publications such as
NFPA, OSHA, NIOSH, EPA, NIOSH/CHRIS and CMA's
CHEMTREC, should be available for emergencies as well as for
use in development of the Health and Safety Program.
•The training program should be approved by the appropriate
agency and all on-site personnel should be required to attend. A
method of judging understanding of the course should be met.
•The medical surveillance program must be approved by appro-
priate officials. The physican and industrial hygienist must also
be approved by appropriate officials, and their responsibilities
completely understood.
•Laboratories selected for medical screening analysis and sample
analysis should be reputable, certified and experienced.
•All contractors must secure adequate insurance to protect employ-
ees and themselves.
•Employees want to know that the employer is concerned with their
future health as well as on the job health. Increased morale,
productivity and favorable workmen's compensation insurance
ratings may result with a health and safety program designed with
the employee and public of prime concern.
•Have all phases of operation available to all personnel in written
form and posted.
•Assure that all personnel are familiar with safe operating pro-
cedures.
SITE SAFETY
289
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•Assure that all personnel are trained in anticipation of hazards,
equipment operation, safety practices, hygiene, emergency pro-
cedures, communications and decontamination procedures.
•Assure that all required protection—respirators, SCBA, etc., is
available on-site and be worn by all supervisors and workers in
specific zones.
•Written instructions must be prepared in advance.
•Operation and safety procedures are based on best available
knowledge, operational principles and technical guidance. Docu-
ment this information.
•Operation and safety procedures should be field tested, reviewed
and revised continuously.
•These procedures must be understandable, feasible and appro-
priate without sacrificing safety
•All personnel must have copies and be briefed on the use of the
Health and Safety plan.
•Response personnel must be trained and undergo refresher
courses.
•The prime contractor must also ensure that his subcontractors
meet the demands of the established H&S program. The contrac-
tor should also determine that the appropriate health and safety
requirements have been estimated in the subcontractor cost.
REFERENCES
1. Buecker, D.A. and Bradford, 1982. "Safety and Air Monitoring
Considerations at the Cleanup of a Hazardous Waste Site" Proc.
of the Third National Conference on the Management of Uncon-
trolled Hazardous Waste Sites, 1982.
2. Federal Emergency Management Agency. Planning Guide and Check-
list for Hazardous Materials Contingency Plans, FEMA, July, 1982.
3. Camp, Dresser, and McKee. Remedial Response Activities Zone I
Uncontrolled Hazardous Waste Sites, Health and Safety Guidelines
for Cutoff Wall Construction LIPARI Landfill, NJ, Work Assign-
ment No. 2-1-21 (Draft), 1982.
4. Galley, L.J. and Cralley, L.V. "Theory and Rationale of Indus-
trial Hygiene Practices", Patty's Industrial Hygiene and Toxicol-
ogy, Volume III, John Wiley and Son, New York, 1979.
5. OSHA (29 CFR 1910). General Industry—Occupational Safety and
Health Standards, GPO, Washington, D.C., 1979.
6. Proctor, N.H. and Hughes, J.P. Chemical Hazards of the Work-
place, J.B. Lippincott Co, Philadelphia, 1978.
7. U.S. Army Corps of Engineers. Safety and Health Requirements
Manual, EM-385-1-1, 1982.
8. USEPA OERR. Interim Standard Operating Safety and Health
Guides, Sept. Hazardous Response Support Division, Edison, NJ,
1982.
9. USEPA. Medical Monitoring Program, EPA Monitoring Guide-
lines, Poison Control Centers. 1980.
10. USEPA. Office of Water and Hazardous Materials, Quality Criteria
for Water, Washington, 1976.
11. Woodward and Clyde Consultants, Inc. Hazardous Waste Health
and Safety Manual, Unpublished document, 1982.
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SITE SAFETY
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DUAL-PURPOSE FTIR: QUALITATIVE ANALYTICAL
SCREENING TOOL AND QUANTITATIVE SITE MONITOR
AN EXTENDED ABSTRACT
KURT W. EASTMAN
Analect Instruments
Utica, New York
As the analysis of toxic materials has become increasingly im-
portant due to imposition of governmental constraints, technolo-
gies and methodology for evaluating dangerous substances have
concomitantly developed. Since the advent of computerized FTIR
technology, rapid and sensitive measurements of chemical species
have been achieved in laboratory investigations. However, the true
benefits of FTIR methodology are realizable in field situations
requiring speed, accuracy and continuous surveillance of noxious
fumes. Monitoring exposures of workers engaged in cleanup of
Analytical
Scraaning
Parsonnel
Safety
hazardous waste storage locations presents a prime example of such
a field application.
Consider the flow chart in Figure 1 which involves preliminary
sampling of several quadrants of a storage facility prior to com-
mencement of cleanup activities. A given sample may exist in gel,
liquid or gaseous state. Various sampling accessories are required
for cells, while low concentrations of gases need long pathlengths
for high sensitivity. Any of these accessories is mountable in the
EVM-60 FTIR spectrometer, which displays capabilities for both
qualitative screening and personnel safety monitoring.
A large sample compartment containing dual analytical beams
provides this flexibility. Transmission cells, thin films, crystal
smears, attenuated total reflectance (ATR) and cylindrical flow
through ATR measurements are performed using easily inter-
changeable accessories in one beam. The other beam is dedicated
to serving the long path gas cell for analytical work and auto-
mated monitoring. In this fashion, gel and liquid samples are
evaluated using the utility beam, while vapor samples are analyzed
with the dedicated beam.
For semi-quantitative or gross leak detection, site administra-
tors may prefer a general identification technique. The procedure
involves monitoring absorbing frequencies for functional groups of
interest (e.g., alcohol, ketone, cyanide). In cases requiring more
accurate data, a specific identification method can be employed.
Spectral subtraction and computer search programs aid in isolating
major toxic species. Several computer data bases exist for both
liquid and gas phases. Additionally, users with no special skills
may be able to identify chemicals from resultant spectra after per-
forming accurate subtractions of interferences.
Upon ascertaining the identities of the hazardous compounds
and interfering components, analytical frequencies for all com-
ponents are selected based on band intensities and positions (Fig-
ure 2). A calibration matrix (Figure 3) is devised by measuring the
Measurement Point
Left
Right End
LOCAL BASELINE
Reference
FIXED REFERENCE
Figure 1
EVM-60 flow scheme for hazardous substance classification and monitoring
Figure 2
Mapping region for measurement
SITE SAFETY
291
-------
absorption of all chemicals at each chosen frequency. Stations for
monitoring are then entered into the analyzer program. Automated
data collection for TWA exposure levels are then initiated,
followed by report generation and printout (Figure 4).
In the event of additional unknowns entering the monitored
quadrant, the user diverges from the cycling routine to perform
supplemental investigatory work using the appropriate analytical
beam. Additional compounds can be incorporated into the analy-
tical matrix to achieve a maximum of ten components. Matrices
and station sequences are alterable to meet each imminent situa-
tion. Remote locations are accessible with the analyzer since its
ruggedized optical bench allows transportability.
RAW-DATA UATHIK
Region 1 Region 2 R«01on 3 Region 4 fleoton 5
Component I 075075 E-02 0.15421 £-04 0.4 r062 E-04 -0.4SOg5 E-04 -0.26300 E-04
Component 2 0.10S70E-04 0.50323 E-02 O.S3072E-03 0.26950 E-03 0.32054 E-03
Component 3 0.05497 E-04 017051 E-03 0.532 IS E-02 0023g3E-03 0.01273 E-04
Component 4 -0.T7750 E-04 0.17705 E-03 0.50350 E-03 O.S8400 E-02 0.12004 E-03
Components 0.73240 E-04 0.37007 E-04 0.43024 E-03 -0 00 14 1 E-04
Calculated time-weighted average (TWA) exposure assuming each person
was in the sampled areas a predesisnaled amount of time, was exposed
to average concentration, and used no respirator.
LOCATION:
TWA Exposure for Tetrahydro Furan 04/21/83 08:02:1 1
r E-OI
INVERSE MATRIX
Region I Region 2 eglon 3 Region 4 Region 5
Component 1 0.13322
Components -0.10002 E 01 -0
Component 4 0 10040 £01 -0
Component ft -0.47220 E 00 -0
.401 13 E 00
.10530 E 01
JOB CLASS
Worker «* 1
Worker *2
Driver •> 1
Driver *2
DAY
16.3 PPB
16.4 PPB
32.3 PPB
26.6 PPB
Sample Collector 3.33 PPB
AFT
2.04 PPM
2.06 PPM
2.54 PPM
2.70 PPM
2.83 PPM
EVE
9.21 PPM
9.30 PPM
1 1.6 PPM
12.1 PPM
1 1.9 PPM
TWA Exposure for Methylene Chloride 04/21/83 08:02:22
JOB CLASS
Worker * 1
Worker *2
Driver «*1
Driver *2
DAY
3.97 PPB
4.01 PPB
7.87 PPB
6.48 PPB
Sample Collector 0.81 PPB
AFT
1.15 PPM
1.16 PPM
1.44 PPM
1.53 PPM
1.60 PPM
EVE
2.32 PPM
2.34 PPM
2.72 PPM
2.79 PPM
2.85 PPM
Figure 3
Calibration matrix for a five component mixture
Figure 4
Twenty-four hour TWA values for job classes of interest
292
SITE SAFETY
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OFF-SITE ASSESSMENT OF AIR EMISSIONS FROM
HAZARDOUS WASTE DISPOSAL FACILITIES
CHARLES E. SCHMIDT, Ph.D.
M.W. ELTGROTH, Ph.D.
Radian Corporation
Austin, Texas
INTRODUCTION
The assessment of the air emissions from hazardous waste
facilities can involve the use of several monitoring and measure-
ment approaches and modeling methodologies. Often both on-site
and off-site measurements are needed to fully characterize gaseous
emissions from these facilities. These data, when modeled, provide
assessment of the atmospheric contaminant gas releases as well as a
predictive tool for exposure assessment studies and remedial action
design.
In this paper, the authors describe a method of characterizing at-
mospheric gas emissions from hazardous waste facilities. In order
to satisfy the assessment objective, ambient monitoring and emis-
sion measurement techniques are employed. As shown in Figure 1,
both techniques generate data (i.e., downwind concentration data
and source emissions data) that can be used to satisfy program ob-
jectives. These data are used as collected and processed or used as
input to modeling studies for waste site assessment. Note that in-
direct emission measurement techniques involve modeling to
generate useful data where ambient monitoring and direct emis-
sions measurements do not.
The following components of the approach are discussed:
•Design of ambient monitoring system, on site and off site
•Source-receptor modeling
•Design of emission source measurement techniques
•Receptor-source modeling
Data are presented from field investigations at a hazardous waste
landfill where both ambient monitoring and source measurements
were performed. Results from source-receptor and receptor-source
modeling demonstrate the utility of the assessment approach. Ap-
plications and limitations of the approach are discussed.
METHODS AND MATERIALS
Ambient Monitoring
The ambient monitoring portion of an assessment program (on
site and/or off site) should provide: upwind or background air
quality data, micrometeorological data base, an air quality data
base characterizing the site emissions and monitoring for uncertain-
ty estimates. The design of the ambient monitoring program must
provide the information identified as satisfying the program objec-
tives. The design of site specific monitoring strategies includes the
selection of: tracer species/parameters for monitoring, analytical
methods and instrumentation, monitoring site locations, quality
control/quality assurance procedures and data reduction/evalua-
tion procedures. The tracer species selected depend on the type of
materials disposed of at the facility. Often this selection is influenc-
ed by state-of-the-art monitoring capabilities. The meteorological
parameters selected to characterize the micrometeorology of the
site are determined by the modeling input requirements. Standard
analytical methods and EPA approved instrumentation for
monitoring should be used for detection methods, where possible.
Unfortunately, these applications usually involve noncriteria con-
taminants and standard methods and approved instrumentation are
not available. Thus, investigation for the best available scientific
approach is required.
Assistance, however, is available for the selection of monitoring
site locations. Guidelines published by the USEPA Office of Air
Quality Planning and Standards describe the proper site location
procedure and requirements for air quality and meteorological sta-
tions. USEPA also recommends the use of modeling for site selec-
tion (USEPA industrial source complex dispersion model 1979,
DOWNWIND
CONCENTRATION
DATA
INDIRECT
MEASUREMENT
METEOROLOGICAL
MODELING
DIRECT
MEASUREMENT
SOURCE EMISSIONS INFORMATION
I
Satlslfy Program Objectives
Figure 1
Data generated from ambient monitoring and emission measurements
USEPA single source model 1977). Quality control procedures
described in the USEPA Interim Guidelines and Specifications for
Preparing Quality Assurance Project Plans provide the design
work for the program quality assurance. Data reduction and
evaluation are dependent upon the type of data collected, computer
storage and transducer capabilities and model hardware com-
patibilities.
The monitors and sensors used for these studies and their
specifications are listed in Table 1. Air quality upwind and down-
wind of the site during these experiments was monitored for SO2,
THC and odor. Odor was assessed using trained odor experts
and/or GC analysis. Meteorological monitoring consisted of wind
SITE SAFETY
293
-------
speed and wind direction. All monitors were operated continuously
during the studies according to recommended operating pro-
cedures. All data were recorded on stripchart recorders.
Source-Receptor Modeling
As used in this paper, source-receptor modeling means using a
model to determine source characteristics from measurements
made at receptor sites. Source-receptor modeling requires that the
model go back in time from when the measurements were taken to
when the effluent was emitted from the source.
This type of modeling usually utilizes a Lagrangian technique
which assumes there are one or more homogeneous separate air
parcels whose identity can always be known. The receptor
measurements are assumed to take place in a single air parcel at dif-
ferent times post emission. Thus, the major effects (such as diffu-
sion) are modeled in reverse.
Table 1
Description of Monitors/Sensors
SO2
THC
Wind Wind
Speed Direction
Manufacturer
Model
Technique
Precision
Sensitivity
Response Time
Range
Power Supply
Service Life
Weight
InterScan
Portable
Analyzer
Electro-
chemical Cell
10%
0.05 ppm
1 sec
0-1 ppm
1 Mercury Cell
4 Aklaline
Cells
2 NiCad Cells
8hr
14 Ib
Century
Systems
OVA-1
GC/FID
10% for STD
Analyses
1 ppmv
(methane)
1 sec
1-10,000 ppm
1-100,000 ppm
Logarithmic
DC
8hr
8 Ib
Metone
010
Chopper/
Counter
1%
0.6 mph
0-50 mph
AC/DC
DC-5
days
DNA
Metone
020
Potentio-
metric
\%
0.6 mph
0-540°
AC/DC
DC-5 days
DNA
A major problem with this type of model is that each measure-
ment will predict different source characteristics because of the in-
accuracies of the model. No model considers each process affecting
the concentrations of some effluent to a sufficient degree to make
these discrepancies insignificant. Because of this, interpretation of
the results can be difficult when there are multiple receptor points
at which measurements are made.
A variation of the source-receptor modeling is to alternate the
source term until the overall error between predicted and measured
concentrations is minimized. This technique usually requires
several user iterations rather than having a model decide for itself
how many and what source assumptions should be made.
In general, source-receptor modeling requires at least multiple
measurement values separated in space and time. Also required are
wind speed/direction and stability. From these basic requirements
other parameters may be required depending on the sophistication
and completeness of the model.
A Gaussian puff model was used as the source-receptor model. A
Gaussian puff model assumes that the emissions from a source can
be divided into a series of puffs that, when superimposed, depict
the actual plume. A Gaussian puff model is usually less demanding
than other models on computer resources and could be used on a
small computer. However, this type of model also has some severe
limitations.
The most severe limitation of a Gaussian puff model is that
material in the puff is assumed to be distributed in a Gaussian man-
ner. Deformation of a puff due to terrain or non-uniform wind
field is not allowed. Due to the assumption of a Gaussian distribu-
tion, horizontal dispersion parameters (
-------
used as a source-receptor model. It is usually a time-consuming ef-
fort, however, to change the source term often enough to deter-
mine which source term gives a minimum error to receptor
measurements.
The minimum input requirements for a receptor-source model
are a source term, wind direction/speed and stability. These re-
quirements can increase dramatically for the more sophisticated
models. Some receptor-source models also can use terrain defini-
tion, chemical mechanisms and multiple wind measurement sites.
An Eulerian grid model was used as the receptor-source model.
An Eulerian grid model is the most realistic type of atmospheric
computer model available. However, this type of model can require
large computer resources. An Eulerian grid model assumes the at-
mosphere is subdivided horizontally and vertically into boxes.
These boxes, in principle, can be any size. Advection and diffusion
is then allowed to occur between the boxes. In addition, chemistry
and other processes besides advection/diffusion can easily be
allowed in an Eulerian model.
Radian has a state-of-the-art Eulerian model called MAGIC
(Multi-Scale Aerosol and Gas Impact Calculation). MAGIC was
developed by merging three existing, validated models previously
developed by Radian scientists. The model allows for advection,
diffusion, multiple sources in complex terrain, any user-supplied
chemistry and particle dynamics. It is fully optionalized so that
calculations not required are bypassed, thus saving both computer
storage and calculation time.
One of the advantages of MAGIC is the model's flexibility. The
physical characteristics of the area being modeled are input to the
model, grid-by-grid, and not assumed. At present, secondary pro-
ducts of the emissions are not of concern. If, at a later date this is
not the case, MAGIC has the capability of handling almost any
user-supplied chemical mechanism. Particle dynamics are also in-
cluded in MAGIC to allow for considering deposition pattern of
fugitive dust during any site disturbance.1
Model Inputs
Both of these assessment approaches were employed to assess the
air emissions from a hazardous waste site under different condi-
tions. Source emission measurements were conducted on site under
disturbed waste conditions. Simultaneous upwind and downwind
air quality and meteorological monitoring was conducted. The
tracer species observed included SO2, benzene and odor.
Portions of air monitoring and source measurement data cor-
relating to site conditions were selected and validated and used to
satisfy specific program objectives via modeling. From these data,
representative test cases were selected and used to demonstrate the
effectiveness of this assessment approach. The input data used for
the assessment modeling (source-receptor, receptor-source) are
given in Table 2.
RESULTS
The results from the receptor-source modeling of the disturbed
waste test case is given in Table 4. Shown here is a comparison of
the predicted downwind SO2, THC and odor levels at the down-
wind distance where actual monitoring of these species was ob-
served and reported. The odor estimate was based on use of the
quantitation of an ambient air sample and calculation of the odor
level using odor/species concentration correlations provided by
TRC consultants. It appears that the receptor-source modeling
simulates the situation very well.
The result from the source-receptor modeling (conducted by
TRC) provided an odor source term used for further predictive
assessment (via receptor-source modeling). In this application, an
odor term was difficult to measure but convenient to estimate from
downwind odor observations. The odor term estimated was an
ED50 rating of 400,000. The odor source term modeled here was
comparable to other measured odor emissions at this site at other
locations. This odor source was in turn used for downwind odor
level prediction via receptor-source modeling and then compared to
Table 3
Modeling Inputs
Source-Receptor (MAGIC Model)
Stability - Class "D"
Wind Speed - 4 mph
Wind Direction - 270 °
Complex Site Terrain
Disturbed Waste Area - 100m2
SO2 Emission Rate - 3.2 x 106 (/ig/m2min)
THC Emission Rate - 1.1 x 105 (/«g/m2min)
Receptor-Source (ODORAR Model)
Stability - Class "B"
Wind Speed - 3 mph
Wind Direction - 230°
Disturbed Waste Area - 14m2
Odor Monitoring Observations
Receptor 1, 137 meters downwind - 500 D/T*
Receptor 2, 213 meters downwind - 240 T/D
Receptor 3, 411 meters downwind - <190>50 D/T
•D/T = Dilution to Threshold Value
Table 4
Comparisons of Measured Downwind Parameters
with MAGIC Predicted Values
Parameter Measured
Maximum So2 O.lOppm
Ratio of downwind to back-
ground hydrocarbons 3.4
ED50 (assumed THT) 74
•Steady-state emission estimate
MAGIC
Predicted*
0.11 ppm
3.4
67
observed odor levels during site testing. These observed and
predicted odor levels agreed well.
Other applications of this approach for assessment of air emis-
sions from the landfill included:
•Undisturbed site emission measurements and prediction of down-
wind gas species concentration (validated with air quality moni-
toring data)
•Disturbed site emission measurements under different conditions
and prediction of downwind gas species concentration at different
downwind distances (validated with air quality monitoring data)
•Estimate of emission control effectiveness using measured source
data (validated with air quality monitoring data)
•Verification of source emission measurement data modeling emis-
sions using off-site air quality data and meteorological data.
CONCLUSIONS
The assessment approach described for assessing the air emis-
sions from waste sites/facilities has been shown to be very valuable
in site characterization. The approach provides for a validation of
predicted levels of gas or emissions source terms by employing com-
plementing sampling and modeling techniques. The approach is ap-
plicable to a variety of assessment programs and can be used to pro-
vide data useful in hazardous waste management design work.
REFERENCES
1. Schmidt, C.E. and Balfour, W.D., "Direct Gas Emission Techniques
and the Utilization of Emissions Data from Hazardous Waste Sites,"
presented at the Environmental Engineering Division Conference
July 1983.
2. Schmidt, C.E., Balfour, W.D., and Cox, R.D., "Sampling Techniques
for Emissions Measurement at Hazardous Waste Sites," Proc. Na-
tional Conference on Management of Uncontrolled Waste Sites
Nov. 1982.
SITE SAFETY
295
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CLEAN-UP OF SHOPE'S LANDFILL, GIRARD, PA.
ROBERT D. MUTCH, JR.
JAMES DAIGLER
Wehran Engineering Corporation
Middletown, New York
JAMES H. CLARKE, Ph.D.
AWARE Corporation
Nashville, Tennessee
INTRODUCTION
Mel Shope began dumping refuse and industrial waste at the
rear of his property in the late 1950s. Most of the material came
from the Lord Corporation of Erie, Pennsylvania, where Mel
Shope was employed in the Maintenance Department. The waste
dumped at the site consisted of scrap rubber, paper, wooden
pallets, cement, oils, solvents, acids and caustics. Following a fire
in 1971, all solvent disposal at the site ceased.
The landfill was closed in 1979 after having blanketed an area of
about 4.5 acres (Figure 1). Very evident leachate problems at the
landfill prompted the Pennsylvania Department of Environmental
Resources to initiate discussions with Mel Shope and the Lord
Corporation. Lord Corporation, recognizing its role as generator
of virtually all of the wastes in the landfill, accepted responsibility
for investigation and remediation of the landfill.
HYDROGEOLOGIC INVESTIGATION
A hydrogeologic investigation was begun in 1979 with the in-
stallation of six monitoring wells in the immediate vicinity of the
landfill. After contamination was found in the wells, another
series of wells was constructed further downgradient of the landfill.
All the wells were constructed as well clusters, with two or three
wells at each site screened at different intervals in the subsurface.
The early hydrogeologic work was undertaken by Dr. Samuel
Harrison of Allegheny College. Eleven well clusters were con-
structed, making a total of 37 individual wells at the site. The loca-
tions of the wells are depicted in Figure 2. Analyses of the ground-
water samples from the monitoring network revealed significant
levels of vinyl chloride monomer, MIBK, MEK, acetone, 4-methyl-
2 pentanol, methylene chloride, 1,2-dichloroethylene, benzene,
toluene and xylene.
Wehran Engineering Corporation was retained by Lord Corpor-
ation in Jan. 1981, to complete the hydrogeologic investigations
begun by Dr. Harrison and to develop a remedial program for
the landfill. Understanding the role of a landfill within its hydro-
geologic surroundings is vital to conceptualization and design of
remedial measures. A final investigative plan was designed to fill
in several critical data gaps requisite to design of a remedial pro-
gram. A key area where information was lacking was the hydro-
geologic condition of the landfill.
A specific question of concern was to what extent (if any) the
basal portions of the landfill intersected the groundwater table.
The investigative program called for four borings within the land-
fill which were to be completed as small diameter piezometers.
In addition to providing hydrogeologic information, the piezo-
meters would also permit direct sampling of leachate within or
beneath the landfill.
A second focal point of the investigation was a low permeability
clay strata at a depth beneath the landfill. The landfill sits atop 20
to 30 ft of glacial outwash deposits of highly variable and lenticu-
lar lithology. The glacial outwash grades into lower permeability
glaciolacustrine and glacial till deposits at depth. The water table
is very close to the surface in the area. Several borings were pro-
posed to investigate the depth, nature and continuity of that strata.
It was anticipated that this strata could play a pivotal role in the
remedial program. A series of exploratory test pits was also exca-
vated around the landfill perimeter. The purpose was to further de-
fine the surficial hydrogeologic conditions and to assess the stabil-
ity of the soils under excavation, thus providing insight in the selec-
tion of subsequent remedial techniques. An additional well cluster
was also proposed. Well Cluster 12 was constructed approximately
300 ft downgradient of Well 3 (Figure 1), which appeared to coin-
cide with the main axis of the plume.
Figure 1
Aerial photograph of Shope's Landfill and its surrounding!
296
REMEDIAL RESPONSE
-------
MALE l» FEET
Figure 2
Site plan
A particularly important objective of the investigation was the
development of a water balance for the landfill. A quantitative
assessment and tabulation of all mechanisms of leachate genera-
tion in a landfill forms the cornerstone of the remedial action selec-
tion process. In the case of Shope's Landfill, the water balance
was quite simple. Two mechanisms of moisture infiltration and
resulting leachate generation from the landfill were identified.
These were the infiltration of precipitation through the landfill
surface and the flow of groundwater through the basal portions
of the landfill.
The amount of precipitation percolating into the landfill was
calculated employing the USEPA water balance method.' This
technique takes into account climatic, soil, slope and vegetative
considerations in the estimation of percolation. The extent of
groundwater inflow to the landfill was estimated by means of
Darcy's Law and was based upon the observed extent of the land-
fill/groundwater table intersection. Discharge mechanisms were
not specifically quantified, although two mechanisms were ob-
vious: (1) surface seepage of leachate, and (2) discharge to ground-
water. The results of the landfill water balance are presented in
Table 1.
Table 1
Mechanisms of Leachate Generation
Est. Rate of Leachate
Generation in a Typical
Climatic Year
Mechanism (Gal/day)
Infiltration of Precipitation
Inflow of Groundwater
Total
3,500
500
4,000
The evaluation of previous analyses of groundwater led to sev-
eral conclusions. First, the well sampling procedures were insuffic-
iently stringent to prevent cross-contamination and to assure collec-
tion of truly representative samples. Second, previous analyses
had focused solely upon organic contamination instead of under-
taking a more balanced program of priority organic pollutants,
heavy metals and other indicators of groundwater quality. This
deficiency, coupled with the sampling inconsistencies, made con-
fident interpretation of groundwater conditions impossible.
In order to overcome this problem, a program for future samp-
ling, designed to assure representative sampling, was established.
A revised analytical program was also proposed which consisted of
analysis for 11 halogenated organics, eight non-halogenated or-
ganics, eight heavy metals and six indicators of groundwater qual-
ity (i.e., chlorides, conductance, etc.). Also called for were a Total
Volatile Organic scan (TVO) and a Total Volatile Halogenated
Organic scan (TVHO). These less expensive surrogate parameters
were added in hopes of performing them in leiu of GC identifica-
tion and quantification of each organic species of concern.
The results of the analyses permitted, for the first time, delin-
eation of the extent of the landfill-derived plume of contamina-
tion. The plume was found to cover an area of eight acres, in-
cluding that portion beneath the landfill. Those parameters most
useful in identifying the extent of the plume were chlorides, spe-
cific conductance and total volatile priority pollutants. Chlorides
and volatile organics are particularly mobile in most groundwater
systems, and their presence is often indicative of the leading edge
of the plume.
Mass loadings of the contaminants of concern entering the
groundwater and surface water regions of the area were calcu-
lated using the average concentrations detected in the leachate
and the estimated hydraulic flux through the landfill. The mass
loadings for pre-remedial action conditions during an average cli-
matic year are given in Table 2.
Table 2
Existing Conditions at Shope's Landfill
Parameter
Total Dissolved Solids
Chloride
Chemical Oxygen Demand
Chromium, Total
Lead
TVO
THVO
1 ,2-Dichloroethylene
1 , 1 -Dichloroethylene
Acetone
MEK
MIBK
Toluene
Xylene
Average Concentration
in Leachate
(mg/1)
2,533
590
3,360
0.25
0.10
129,000
89,900
893
18,852
1,131
386
13,980
1,313
2,340
Mass Loading
(Ibs/day)
84
19.5
111
0.0083
0.0034
4.3
3.0
0.030
0.63
0.038
0.013
0.46
0.044
0.078
REMEDIAL PROGRAM OBJECTIVES
A particularly critical hurdle in the remediation process, due to
the emotion and controversy created, is the determination of the
acceptable degree of pollution abatement. Professionals con-
fronted with this decision find it necessary to balance concerns
for the environment and public health with the realities and lim-
itations of available funding and the effectiveness of available en-
gineering options. This difficult decision is made much more troub-
lesome by the uncertainties and paucity of information or stand-
ards on the toxicities of organic chemicals and resultant risks to
public health.
Notwithstanding the lexicological uncertainties, the goals for
the remedial program must be set in as tangible a form as possible.
For example, the goal of maintenance of potable groundwater
quality at some key point, such as the property line, is often used.
This standard is often established as a combination of the In-
terim Primary Drinking Water Standards and a more arbitrary
standard for volatile organics. New Jersey sets an active level of 100
ug/1 for total volatile priority pollutants, with a level of 50 jig/1
for any single volatile priority pollutant. Although this type of
standard clearly does not differentiate between the variable toxici-
ties of the priority volatile organics, it is an attempt to deal with
the problem in a practical way. In a case where all or a portion of
REMEDIAL RESPONSE
297
-------
Table 3
Evaluation of Remedial Action Alternatives
Shope's Landfill
Alternative
(1)
Anticipated
Degree of
Abatement
Alternative I - No Action
Alternative 2 - Regrading; Surface Water Diversion;
Cover; Revegetatlon
Alternative 3 - Impermeable Cap
Alternative 4 - Impermeable Cap; Southern Cut-Off
Wall
Alternative 5 - Circumferential Collection
System; Leachate Treatment
Alternative 6 - Circumferential Collection
System; Southern Cut-Off Wall; Leachate
Treatment
Alternative 7 - Circumferential Cut-Off
Wall and Collection System; Leachate
-0-
44%
87.5%
99+%
99+%
99+%
(1)
Estimated
Construction Cost
In Dollars
(3)
Estimated
Operational Costs;
30-yr Duration;
(Present Worth)
In Dollars
-0-
100,000
200,000
250,000
150,000
200,000
188,600
207,460
207,460
207,460
2,751,674
2,434,826
(4)
Estimated
Total Cost
In Dollars
(2) + (3)
188,600
307,460
407,460
457,460
2,901,674
2,634,826
Cost Per 1,000 Gal.
of Leachate Managed
In $/1000 Gallons
1000(4)
(1) x 43,890,000
N/A
IS.92
10.61
10.42
66.11
60.03
Treatment
Alternative 8 - Alternative 6; Impermeable Cap
Alternative 9 - Alternative 7; Impermeable Cap
Alternative 10 - Exhumation
99+% 225,000
99+% 350,000
99+% 375,000
99+% 12,500,000
1,484,282
850,586
229,564
-0-
1,709,282
1,200,586
604,564
12,500,000
38.94
27.35
13.77
284.80
the leachate discharge from a waste site enters an adjacent surface
water body, a similar standard can be established with respect to
surface water quality.
Once the environmental or public health goals are set, it is then
possible to work toward a definition of the level of abatement
required at the waste disposal site. This environmental modeling
can be performed using simple linear solute transport models or
more sophisticated two or three dimensional solute transport mod-
els, if warranted. Input data to the model can be derived from
literature or laboratory studies in the case of relatively simple or
"first-cut" modeling efforts. If better estimates are needed, field
measurements of key input parameters can be provided.
The objective of the modeling is to define the maximum dis-
charge of contaminants from the landfill into the groundwater or
surface water beyond which the prescribed performance goals can-
not be attained. The discharge can be expressed as a quantita-
tive discharge of the contaminants of concern (i.e., 0.1 Ib/day of
TCE). The discharge can also be expressed in terms of a percent
abatement by comparison to existing rates of discharge (i.e., if
there was initially a discharge of 2 Ib/day of total volatile prior-
ity pollutants, a reduction to 0.1 Ib/day would be a 95% decrease).
The goals for the actual waste site remediation having been thus
established, the land disposal engineer's task is relatively simple—
to evaluate and design a remedial program which meets the dis-
charge goals. Since there will typically be numerous ways to
achieve the prescribed discharge goal, a series of alternatives is
evaluated in terms of the costs of implementation and long-term
monitoring and maintenance costs. The most cost-effective alterna-
tive is then selected and ultimately designed and implemented.
At Shope's Landfill, the groundwater quality had already been
degraded beyond potable water standards several hundred feet past
the property line. The objective established for the remedial ac-
tion plan at Shope's Landfill was that the existing plume of ground-
water contamination not expand to the point of adversely im-
pacting groundwater supplies. This objective was translated into
performance goals for the remedial action plan in consideration of
the proximity of water supply sources and the relative mobility of
the contaminants of concern within the aquifer.
It was decided that the remedial action program for Shope's
Landfill should result in more than a 99% abatement of leachate
contaminants discharged. The attainment of this goal would per-
mit the ultimate dissipation of the plume within the aquifer as
the aquifer's natural attenuating mechanisms became dominant.
The plan also embodied a comprehensive monitoring program to
verify this hypothesis over time.
EVALUATION OF REMEDIAL ALTERNATIVES
Ten alternatives for remediation of Shope's Landfill were con-
sidered, although three were dismissed since they failed to achieve
the requisite 99+% abatement goal. The alternatives listed in
Table 3 ranged from "No Action" to excavation of the landfill
and subsequent off-site disposal of the exhumed material. The re-
maining alternatives considered to be capable of meeting the pre-
scribed performance goals, consisted of combinations of upgrad-
ient (southern) or circumferential cutoffs, leachate collection sys-
tems and low permeability final cover (capping).
In each case, except Alternative 1, the remedial plan also in-
volved removal of drums lying on the surface or encountered in
construction activities and removal of standing pools of leachate.
These costs are not reflected in Table 3. Construction costs for the
alternatives under consideration (Alternatives 4 through 10) varied
from $250,000 for Alternative 4 to $12,500,000 for Alternative 10.
Alternative 10 was omitted from further consideration due to the
unreasonable costs, thereby setting the upper limit of the con-
struction costs at $375,000.
The annual operating and maintenance costs for each alterna-
tive were also evaluated. A uniform period of 30 years was em-
ployed to calculate the present worth value of the annual costs.
The interest rate over the 30 years was assumed to be 10°7o. Annual
operating costs were assumed to remain constant. Although it is
likely that the operation and maintenance period would be longer
than 30 years for each alternative, the effect of longer time periods
of total present worth costs is nominal. Total costs are then cal-
culated as the sum of the construction costs and the present worth
value of the 30 years of operational and maintenance expenditures.
The last column of Table 3 presents the costs in terms of the cost
298
REMEDIAL RESPONSE
-------
per 1,000 gallons of leachate managed over the 30 year period.
Leachate management is considered to include leachate preven-
tion as well as leachate collection and treatment.
The impermeable cap and upgradient (southern) cut-off wall
alternative was selected since it achieved the prescribed degree of
abatement at the least cost.
REMEDIAL ACTION PLAN
The selected remedial program, Alternative 4, encompasses a
number of individual remedial components. The principle objec-
tive of the plan is the virtual elimination of recharge to the land-
fill, which is accomplished by the combination of the imperme-
able cap and the upgradient cut-off wall. The plan's major com-
ponents are:
1. Removal and off-site disposal of drums from the landfill sur-
face and those encountered in regrading of the fill's side-
slopes
2. Removal of standing pools of leachate and site drainage facil-
ities
3. Surface water diversion and site drainage facilities
4. An impermeable final cover (cap)
5. An upgradient (southern) cut-off wall
6. A short- and long-term monitoring program
Several of these components warrant further discussion with
respect to their engineering design.
Final Cover (Capping)
The final cover or "cap" of the landfill was designed with the
intent to cut off virtually all recharge to the landfill. Consequent-
ly, the cap was designed, where feasible, as a composite cap in-
corporating both compacted clay and a geomembrane. Extensive
regrading was required in preparation for the placement of the
cap. Regrading involved both trimming back the nearly vertical
sideslopes along some sides of the landfill and placement of up to
6 ft of clean fill on top of the landfill to bring the subgrade slope
to at least 4"%. The top of the fill was essentially flat prior to re-
grading.
Two final cover designs were uSed. The majprity of the land-
fill was capped with a composite cap consisting of (in ascending
order): 12 in. of compacted clay with a maximum permeability of
1 x 10~6 cm/sec, a 20 mil PVC membrane and 18 in. of soil capable
of supporting begetation. Where the slope of the prepared surface
exceeded 25%, a modified final cover was specified consisting of
(in ascending order) 18 in. of compacted clay with a maximum
permeability of 1 x 10~7 cm/sec followed by 18 in. of soil capable
of supporting vegetation. This latter cover design constituted only
15% of the cap, being localized to the particularly steep northern
and western sideslopes.
Subsurface Cut-Off Wall
The design of an effective cut-off wall in a relatively complex
hydrogeologic setting, such as that of Shope's Landfill, must be
founded upon a predictive model capable of quantitatively assess-
ing the effectiveness of various designs. In this case, the assess-
ment was performed by flow net analyses. A flow net is a graphical
representation of a groundwater flow system consisting of an inter-
secting and interrelated network of equipotential lines and flow
lines.2 The objective of the flow net analysis was to depict and
quantify flow beneath the wall and also to predict the position of
the post-construction phreatic surface (groundwater table) be-
neath the landfill, downgradient of the cut-off wall.
The flow net analysis revealed that the combination of the sub-
surface cut-off wall and the impervious cap should result in a
marked decline in the phreatic surface (groundwater table) beneath
the landfill. This decline should be approximately 6 ft immediate-
ly downgradient of the cut-off wall, about 4.5 ft, 100 ft downgrad-
ient of the cut-off wall and approximately 2 ft, 200 ft downggrad-
ient. At either end of the cut-off wall, boundary effects will re-
duce this decline to some extent. The combined effect of the cut-
off wall and the impervious cap should be, therefore, to decrease
the phreatic surface within the fill to such an extent that the inter-
section of the phreatic surface and the base of the landfill is min-
imized or eliminated. Accordingly, leachate generation attributable
to groundwater flow through the waste should be virtually elim-
inated in keeping with the overall objective of the remedial action
plan.
REMEDIAL PLAN IMPLEMENTATION
Initial remedial efforts involved characterization and removal of
exposed drums and regrading of the site, particularly the landfill
itself. Waste deposition at the landfill resulted in a majority of the
edges of the landfill being very steep and, in some areas, essen-
tially vertical. The deteriorated and loosely packed nature of the
drums and waste materials resulted in dense growths of vines,
bushes and small trees through the slopes. The engineering design
called for reduction of the slopes by the removal of drums and veg-
etative growth and regrading to allow the placement of the final
compacted clay, geomembrane and topsoil cover.
Since the simple task of clearing and grubbing was to occur in
close proximity to drums known to contain toxic and flammable
substances, constant monitoring of the air, continual observation
and supervision of the laborers and the presence of the fully
equipped safety equipment trailer near the work were considered
essential to the safe performance of the work. Special training of
the newly hired workers was required to familiarize them with the
use and care of respirators, self-contained breathing apparatus
and fire extinguishing equipment and methods. Additionally, a pul-
monary and respiratory physical check-up was required for all
personnel to be involved with the drum removal.
A soil erosion and sedimentation plan was implemented, in-
volving construction of channels around the perimeter of the land-
fill and a large sedimentation basin. All runoff was to be routed to
the sediment basin prior to sampling to ascertain its acceptability
for discharge. Every effort was made to prevent the entry of leach-
ate to the stormwater retention basin. Intermediate collection
ponds, solely for leachate containment, were constructed at areas
of visible seepage. All collected leachate was pumped from the
collection basins to specially lined tank trucks for transport to ap-
proved treatment facilities. When the seepage problem was min-
imized by placement of the cap, the intermediate ponds were filled
with compacted soils.
Prior to construction, a comprehensive soils investigation had
been conducted to locate a borrow pit which could supply the
quantity and quality of clay necessary for the cap. More than 20
sites, mostly active borrow pits, were investigated; only two sites
were found acceptable.
Compaction of the clay was initially accomplished with a static,
two-behind, sheepsfoot roller. However, after compaction control
testing with a nuclear densometer (used to correlate achieved field
moisture and density to laboratory permeabilities) indicated that
this equipment did not obtain the required densities, a smooth
drum vibratory two-behind roller was brought to the job. The
sheepsfoot and smooth drum roller were then used in conjunction
with each other. The sheepsfoot roller provided the kneading ac-
tion important in achieving low soil permeability and knitting of
subsequent lifts (used before and after the smooth drum roller),
and the smooth drum vibratory roller providing the high densities
and smooth surfaces for subsequent PCV membrane placement.
Approximately 4 acres of 20 mil PVC membrane were placed
over the compacted clay. Panels up to 400 ft x 50 ft were used to
minimize the required field seaming. During the warm, early
autumn, seaming and placement of the PVC membrane were rou-
tine and relatively simple tasks. However, as colder weather accom-
panied by persistent rain and snow set in, special techniques had to
be developed to correctly place and seam the membrane.
Rainwater collecting on top of the geomembrane severely ham-
pered the seaming operation. This often had to be controlled by
actually constructing small soil dams on top of the membrane to
REMEDIAL RESPONSE
299
-------
keep water away from the seams and by supporting the seam from
below with cardboard to provide a firm, dry base on which to seam
the sheets.
Cold weather also created a problem for the solvents used to
bond adjacent sheets of PVC. Methods of warming the membrane
and the solvents included the use of kerosene "torpedo" heaters
and electric hair dryers. These instruments not only heat but also
dry the membrane and allow seaming to proceed effectively in
moderately cold and wet conditions. The liner was then covered
with soil. This operation was accomplished by pushing the soil out
over the geomembrane, being careful to always maintain a min-
imum of 18 in. of soil beneath the bulldozer.
Prior to construction of the slurry trench cut-off wall, a work
platform was built to provide a relatively flat working surface.
Existing grades along the slurry trench outline were approximate-
ly 8 to 10%. The top of the work platform was constructed to pro-
vide a slope of 2%—steep for slurry trench construction, but ac-
ceptable. Two smaller slurry mixing and holding ponds were con-
structed adjacent to the water supply and storage ponds. Soil of a
specified gradation was trucked to the site for mixing with ben-
tonite slurry to produce a trench backfill capable of meeting the
1 x 10~7 cm/sec permeability specification.
The bentonite-soil backfill mix was also subjected to a search
and laboratory investigation. Samples of the soil, bentonite and
mixing water were shipped to a soils lab for testing of the design
mix and preparation of field quality control data. Following com-
pletion of the slurry trench cut-off wall, the cap was "keyed" into
the top of the wall.
GROUNDWATER MONITORING
The groundwater monitoring program, aimed at assessing the
effectiveness of the remedial measures, was designed to maximize
cost-effectiveness while still ensuring a thorough understanding of
the fate and distribution of contaminants within the plume. This
was achieved through a judicious selection of both sampling points
and chemical parameters. The overall program incorporated the
following approach:
•Use of indicators such as specific conductivity, chloride ion con-
centration and total volatile organics to delineate the areal and
vertical extent of the plume
•Analysis for specific organic constituents and heavy metals to
evaluate character and distribution of contaminants within the
plume
Those chemicals which were present in high concentrations and
had the highest mobilities, together with the indicators used to de-
lineate the plume were selected for long-term monitoring. Moni-
toring results will be interpreted annually as part of an assessment
of the effectiveness of the remedial program. A summary report of
the post-construction monitoring will be prepared at the end of five
years.
REFERENCES
1. Fenn, D. and Hanley, K.J., "Use of the Water Balance Method for
Predicting Leachate from Sanitary Landfills," Washington, USEPA/
OSWP, 1973.
2. Cedergren, H.R., Seepage, Drainage, and Flow Nets, John Wiley &
Sons, New York, 1967.
300 REMEDIAL RESPONSE
-------
APPROACH TOWARDS ESTABLISHING INTERIM
HAZARDOUS WASTE CLEANUP CRITERIA
RICHARD A. DIME, Ph.D.
MARWAN M. SADAT, Ph.D.
JORGE BERKOWITZ, Ph.D.
New Jersey Department of Environmental Protection
Hazardous Site Migration Administration
Trenton, New Jersey
INTRODUCTION
There is great concern among scientists, academicians and the
general public about chemicals in the environment and their human
health implications. In the past decade, numerous legislation has
been passed and implemented to control the indiscriminate release
of chemicals into the ground, the water, the atmosphere and work
place environments. Legislation has been adopted to regulate the
disposal of chemical wastes and to rectify the situations created by
poor waste disposal techniques used in the past. With the estab-
lishment of Superfund, the enormous task of remediating uncon-
trolled hazardous waste sites is beginning, however, guidelines to
direct cleanup activities are not available.
The Federal government, through the USEPA, is mandated to
develop methods and criteria for determining the appropriate ex-
tent of removal, remedy and other measures to remediate haz-
ardous waste sites as described in the "Comprehensive Environ-
mental Response Compensation and Liability Act of 1980". To
date, these guidelines have not been forthcoming and the absence
of such criteria make remediation efforts quite difficult. Regula-
tory agencies are forced to rely on intuition and judgement,
rather than good science. Further, regulatory agencies are placed in
a position of entering into consent agreements with private parties
(a) causing industry to embark on remediation without precise
knowledge of the objectives or their extent and (b) causing regu-
latory agencies and industry to enter into cleanup agreements with-
out defined goals causing criticism at later dates.
New Jersey has a critical hazardous waste problem. The State
has generated funds and is acquiring staff power to tackle the
tremendous problem of uncontrolled hazardous waste sites within
its borders. As the State can not wait for the federal government to
establish hazardous waste cleanup criteria, the N.J. Department of
Environmental Protection (NJDEP) is in the process of develop-
ing interim guidelines. It is the mission of the NJDEP to "formu-
late comprehensive policies for the conservation of natural re-
sources of the State, the promotion of environmental protection
and the prevention of pollution throughout the State" (NJSA
13:l-D-9). The State of New Jersey has several legislative mandates
which adopt an anti-degradation policy in environmental protec-
tion and this coupled with the protection of human health are the
premises upon which these guidelines are being developed.
GENERAL CONSIDERATIONS
This Report summarizes NJDEP's approach to setting interim
guidelines, the classification system employed, criteria for place-
ment of chemicals into the classification system, chemicals to be
classified and methodology to be used to establish acceptable
contaminant levels at remediated sites. Guidelines could be es-
tablished (1) on a site specific basis according to existing or poten-
tial land uses, proximity to populated areas or proximity to en-
vironmentally sensitive areas (i.e., wildlife refuses), or (2) based
on site hydrogeological characteristics (i.e., depth to aquifer, soil
type, potential for erosion), or (3) which would be applied to all
sites regardless of site characteristics or locations.
The development of site-specific guidelines seems to be a never
ending task as the number of guidelines to be developed would
depend on the number of sites to be remediated. The formula-
tion of one set of guidelines to be applied to all sites is somewhat
more straightforward, yet, may be questionable in value. A work-
able approach is a combination of the two. The guidelines cur-
rently being developed by NJDEP are general in scope and are to
be modified based on specific site characteristics. This appears to
be the only realistic approach toward developing guidelines to
protect man and the environment while not needlessly spending
tremendous sums of money and time during remediation efforts.
CLASSIFICATION SCHEME
A variety of chemical classification schemes can be found in the
scientific literature. The European Economic Community uses a
numerical hazard ranking scheme to classify new chemicals con-
sidered for production. The chemicals are placed into categories
(black, white, gray) depending on the number generated by the
ranking scheme. An alternative is to establish broad categories
based on selected parameters (i.e., carcinogen, noncarcinogen),
followed by placement of the chemicals of interest into the appro-
priate categories. Either approach would yield a workable system
for classifying chemical hazards and each is likely to yield sim-
ilar results. NJDEP has established broad categories into which
chemicals of interest will be placed.
Chemicals to be Included in Remedial
Action Guidelines
The number of chemicals known is tremendous and to include all
these chemicals into the Hazardous Waste Cleanup Criteria is an
impossible task. Accordingly, NJDEP decided to incorporate into
the following interim guidelines: (1) known human carcinogens,
(2) suspected human carcinogens (known animal carcinogens),
(3) compounds (and metabolites) recognized as being toxic to man
and/or biota, (4) compounds resistant to decomposition in the
environment (persistent), and (5) any priority pollutants not in-
cluded above since these are currently regulated.
REMEDIAL RESPONSE
301
-------
Class
I
II
III
TV
V
VI
VII
VIII
DC
Known Human Carcinogens
Suspected Human Carginogens
Extremely Toxic Chemical:
(LD»50mg/kg)
Very Toxic Chemicals
(LD» 50-500 mg/kg)
Moderately Toxic Chemicals— (Persistent and
(LDjo 500 mg/kg) Degradable)
Metals
Figure 1
Proposed Chemical Classification Scheme
Chemicals will be added or deleted from the guidelines as re-
quired and when justified.
Chemical Classification System
Chemicals will be placed in one of ten categories (Figure 1).
Placement into the classification scheme is based on the toxicol-
ogy, environmental chemistry and environmental fate of the chem-
ical. The system is devised to differentiate carcinogens from non-
carcinogens, and persistent compounds from degradable com-
pounds. The utilization of such an approach allows for the es-
tablishment of realistic contaminate levels which would be accep-
table after remediation. For example, PCBs and benzene, both
human carcinogens, would fall into different categories with the
acceptable levels for PCBs being more stringent than for benzene
since PCBs are resistent to degradation in the environment.
A chemical must meet a majority of the criteria listed to be
placed into a particular category described below. A few examples
of chemicals which clearly fall into each category are provided
in Table 1.
I. KNOWN HUMAN CARCINOGENS—PERSISTENT
All chemicals that:
(a) have been shown via epidemiology or isolated case reports to
cause cancer in humans. A chemical is considered a known car-
cinogen when a solid link between exposure and cancer in
humans is well documented. If the results of a study are ques-
tionable due to exposure to multiple chemicals or lifestyle, such
as smoking, the study is considered inadequate to establish
human carcinogenicity and these chemicals would be placed in
III or IV.
(b) are resistant to metabolism by aquatic and terrestrial biota
and microorganisms.
(c) are resistant to environmental hydrolysis and photolysis.
(d) exhibit the tendency to bioaccumulate.
II. KNOWN HUMAN CARCINOGENS—DEGRADABLE
All chemicals that:
(a) have been shown via epidemiology or isolated case reports to
cause cancer in humans (I(a)).
(b) are susceptible to environmental hydrolysis, photolysis and/or
biological decomposition.
III. SUSPECTED HUMAN CARCINOGENS—PERSISTENT
All compounds that:
(a) have been shown to initiate malignant neoplasms in at least
one species of laboratory animals regardless of route of admin-
istration of test chemical.
(b) are resistant to metabolism by aquatic and terrestrial biota
and microorganism';
(c) are resistant to environmental hydrolysis and photolysis.
(d) exhibit the tendency to bioaccumulate.
IV. SUSPECTED HUMAN CARCINOGENS—DEGRADABLE
All compounds that:
(a) have been shown to initiate malignant neoplasms in at least one
species of laboratory animals, regardless of route of administra-
tion.
(b) are susceptible to environmental hydrolysis, photolysis and/or
biological decomposition.
V. EXTREMELY TOXIC CHEMICALS—PERSISTENT
All compounds that:
(a) exhibit LDM values less than SO mg/kg in standard laboratory
animals or aquatic species.
(b) are resistant to metabolism by aquatic and terrestrial biota and
microorganisms.
(c) are resistant to environmental hydrolysis and photolysis.
(d) exhibit the tendency to bioaccumulate.
VI. EXTREMELY TOXIC CHEMICALS—DEGRADABLE
All compounds that:
(a) exhibit LD50 values less than SOmg/kg in standard laboratory
animals or aquatic species.
(b) are susceptible to environmental hydrolysis, photolysis and/or
biological decomposition.
Table 1
I. Known Human Carcinogens-Persistent
II. Known Human Carcinogens-Degradable
III. Suspected Human Carcinogens-Persistent
IV. Suspected Human Carcinogens-Degradable
V. Extremely Toxic-Persistent
VI. Extremely Toxic-Degradable
VII. Very Toxic-Persistent
VIII. Very Toxic-Degradable
IX. Moderately Toxic Chemicals
Persistent and Degradable
X. Metals
PCBs
benzene
dimethyl sulfate
amitrole
kepone
lindane
mirex
Toxaphene
TCDD
dibromochloropropane
dimethyl carbamoyl
nitrosoamines
endosulfan
endrin
endrin aldehyde
nitrophenol
Acrolein
1,2 dichlorobenzene
1,2,4 trichlorobenzene
higher chlorinated benzenes
nitrophenols
phenol
hexachlorocyclopentadiene
1,1,1 -Trichloroethane
1,2-dichloropropane
1,3-dichloropropane
methyl chloride
methyl bromide
dichloroethylene
isophorone
phthlates (non-carcinogenic)
2-4 dimethylphenol
antimony
copper
mercury
selenium
thallium
zinc
302
REMEDIAL RESPONSE
-------
VII. VERY TOXIC CHEMICALS—PERSISTENT
All compounds that:
(a) exhibit LDJO values of 50-500 mg/kg in standard laboratory
animals or aquatic species.
(b) are resistant to metabolism by aquatic and terrestrial biota and
microorganisms.
(c) are resistant to environmental hydrolysis and photolysis.
(d) exhibit the tendency to bioaccumulate.
VIII. VERY TOXIC CHEMICALS—DEGRADABLE
All compounds that:
(a) exhibit LD50 values of 50-500 mg/kg in standard laboratory
animals.
(b) are susceptible to environmental hydrolysis, photolysis and/or
biological decomposition.
IX. MODERATELY TOXIC CHEMICALS-
PERSISTENT OR DEGRADABLE
All compounds that exhibit LD50 values greater than 500 mg/kg
in standard laboratory animals and aquatic species regardless of
their behavior in the environment.
X. METALS
Any noncarcinogenic metal (on priority pollutant list) will be
placed into this category.
Information on carcinogenicity is obtained from the Second
Annual Report on Carcinogens (NTP), I ARC monographs and
EPA-CAG Reports. Toxicology and aquatic toxicology data is ob-
tained from the Registry of Toxic Effects of Chemical Substances
(RTECS), Toxicology Data Bank (TDB), the Handbook of Toxic
and Hazardous Chemicals and the Merck Index. Oral LD50 data for
the most sensitive species reported will be used. When no oral
LD50 data are available, data from other routes of administration
will be used. If no toxicity data are available quantitative structure
activity relationships will be used, if appropriate, or toxicity will be
predicted based on scientific judgement inferred from closely re-
lated structural analogs.
Sources for environmental chemistry and fate information will
be obtained from the Water-related Environmental Fate of 129
Priority Pollutants—Volumes I and II, and from other available
scientific literature. When data are lacking, established physical-
chemical relationships or good scientific judgement inferred from
structural analogs will be used to estimate the desired parameters.
Establishment of Acceptable Contaminant
Levels at Remediated Sites
Acceptable contaminant levels in soils, ground water and land
(surface) runoff entering into rivers or estuarine environments for
remediated sites will be established. These levels will be based on
the protection of human health and on the NJDEP's policy of non-
degradation of the environment:
SOILS
The acceptable residual contaminant level on soils will be based
on the potential of the compound to migrate into groundwater and
the potential for adverse health effects from direct contact with soil
(after remediation). An appropriate model incorporating soil
adsorption/desorption coefficients, water solubility and soil char-
acteristics will be used to assess the potential for groundwater
contamination.
GROUNDWATER
Groundwater will be viewed as a potential source of drinking
water. When setting acceptable levels, all degradation processes
other than chemical hydrolysis will be considered unimportant.
Available Water Quality Criteria and suggested no adverse re-
sponse levels (SNARLs) will be used when available.
LAND (SURFACE) RUNOFF
Surface water receiving land runoff from remediated hazardous
waste sites will be viewed as a possible source of drinking water,
commercial fisheries and shellfish resource, recreational area,
and/or ecological habitat. Acceptable contaminant levels in land
runoff will be set so none of the above uses would be disrupted.
The establishment of acceptable contaminant levels in soils,
groundwater and land (surface) runoff is a complicated task requir-
ing a thorough knowledge of the chemical and physical properties
of each chemical (or class of chemicals) for which acceptable con-
taminant levels are desired. The NJDEP is actively reviewing avail-
able data which will allow the formulation of acceptable contam-
inant levels. Although it would be premature to propose such lev-
els at this time, generalizations about acceptable levels can be
made.
Acceptable levels for known human carcinogens will be more
stringent than noncarcinogens. Within each group, acceptable lev-
els for persistent compounds will be more stringent than for de-
gradable compounds. Levels in groundwater will be more stringent
than those for surface waters since more dissipation processes
are likely to prevail in the latter.
SUMMARY
The State of New Jersey, through the Department of Environ-
mental Protection, is formulating interinxguidelines for use during
hazardous site remediation based on the protection of human
health and a policy of non-degradation of the environment. Al-
though not yet complete, the approach taken by NJDEP is being
presented for review and comment by scientists and policy makers.
NJDEP welcomes comments to help achieve the goal of establish-
ing scientifically justifiable guidelines for use in hazardous site
remediation. It is hoped that the effort of NJDEP coupled with
comments by interested individuals will produce guidelines that
will enable the State to remediate hazardous waste sites in a manner
that will protect man and the environment without spending large
sums of money and time needlessly.
REMEDIAL RESPONSE
303
-------
TRAINING RESOURCES FOR SUPERFUND
BENJAMIN TAYLOR, Ph.D.
GEORGE W. SCHLOSSNAGLE, Ph.D.
NOEL URBAN
Office of the Chief of Engineers
Washington, D.C.
INTRODUCTION
In 1980, Congress passed, and the President signed, enabling
legislation establishing the Comprehensive Environmental Re-
sponse Compensation and Liability Act (CERCLA) better known
as Superfund. The intent of the Superfund program was to estab-
lish a means by which former hazardous waste sites could be more
effectively cleaned-up or controlled. The USEPA was assigned
overall responsibility for management of the Superfund program,
and in 1982 the USEPA and the Army Corps of Engineers signed
an interagency agreement. Under this agreement, USEPA assigns
to the Corps responsibility for providing technical assistance and
supervision of engineering design and construction for Federal lead
remedial actions.
An important aspect which had to be considered by the USEPA
and Corps, as well as private contractors involved in Superfund
activities, was the training of personnel. A review of available re-
sources for training showed that, generally, training specifically
geared to Superfund was very limited. Most of the available train-
ing resources were devoted to emergency response measures and
spill control techniques. In most cases actual remedial action (for
example, site cleanup) was not considered.
This picture is changing somewhat as the need for training in
Superfund related activities increases. Closer review of many of the
courses devoted to emergency response training indicated that, in
many instances, some of the material was also relevant to remed-
ial action. In fact, some organizations offering training have
started to include some discussion of remedial actions.
Table 1
Superfund Training Resources—Governmental
AGENCY
MISI. Fin righting Acid.
CM Iciponie Brinch
CON mi I
Cout Guird Mir. Sftr. Sen.
USD* Old. Seh.
Amy Log lit. Mgwt. Ctr.
DoD (JMPTC)
Nit. Nln« Kith. 1 Sftr. Acid.
FEMA (Kit. Bur. Trn. Ctr.)
FEXA [N.t. Fir* Acid.)
Fll. St. Fir* Colllgt
Mil. Dipt, or Tinn.
CoD Army Corpj Engs.
Dlv. of Ifcer . Srva.
Ohio St. Fin Mirih. Off.
KIOSH (Dlv. of Trn. t Manpower Dev
OSHA (Trn. tnit.)
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Nebr iki Fir* Aginey
Mont ni Oept. of Mil, Affilrs
HI»I Sch. Trins, Ngnt.
At S . Off of Dier. Sr»J.
ADDRESS
59 Horsepond M.. Sudbury. NA. 01776
Edison Ub. Edison. N.J.. 04*37
6 Penn. Ctr. Plata. PMle. PA. 1910*
Torktown, VA, 23690
11th 4 Independence Av... Wish. D.C. 20250
DRXMC-A*, Ft. Lee. VA. 21801
Aberdeen P.O., MD. 21005
P.O. Bo i 1166. Beckley WV. 25401
1(825 S. S*ton Av«.. Dmltsburg, MD, 21727
16425 S. Seton A*i.. Bmltsburg. MO, 21727
1501 S.W. Broeduey. Ocili. FL. 32670
3011 Sldeo Dr., Nishvllle. TN. 3T20«
P.O. Bo i 1600, Huntsvllle. AL, 35807
B5 Still CipHol. St. Piul. MN. 55155
8895 E. Main St. fteynoldsburg. OH »30«8
)
«"6T6 Colwbll Pkvy.. Clnn.. OH. 15226
1555 TUes Dr.. DCS PI lines. 11. 60018
6500 S. HicArthur Blvd.. Okls City, OK 73125
3721 W. Cumin*, Lincoln. HE, 6852*
Dlsistir ind Ener. Srvs. Dlv., Helens, NT
NSPDM. Oaklind Amy Bist, Oaklind, CA 9*625
P.O. Bo i 758, Conw.y, AK, 72032
PHOME CONTACT
Stephen Coin (617) **3-"926
Thomu VU (513) 6M-7537
H. «. Rhoids (215) 977-1560
(Mr. Jin Townliy (202' *26-62A6
Dr. Ednund Fulkcr (202' <*7-207T
*tglitrir'i Offloi («0») 73»-337(
nsl* M. Clirk (301) 27H.f1n5
Jin Sohiwlti (30«) 255-0* 51
Bitty Funn (202) 2R7-'902
•ogtr Unihin (301) M7-6771
Mr. Stirk (90*) 732-0526
Dr. Krwiir (615) 7*1-5141
Jmes Willis (202) 495-5032
Hick Moluton i 612) 296-0*59
Ron Ryin (61* 86«-5510
Oonni Wiligi (513) 64*-8225
Frink Wilsh (202) 376-2001
David Coodnan («05) 686-*82*
Viyni Mclaughlin («02) 171-2403
Ed Swell Jh («06) «*9.303«
Ms. Cannon (901) 872-5706
Ut Collard (501) 37*-1201
SUBJECT
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TAPES 4
MANUALS
T«s
V*S
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Tei
No
Tas
Yis
Tts
Tas
Tas
Tas
No
No
Tas
Tas
Tas
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NO
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Tas
COST
No
Tai
Tas
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1. Hulth ind Sifity
2. Pirionil Protection
J. ffc*rgencr S»lf-Hilp leieui
«. leiplntory Protection
1. Vehicle Uie it Kanrdoul Sltei
SUBJECT AIEAS
6. Usi of Field EqulpMnt
7. Monitoring
4. Contingency Planning
9. Swpllnf Techniquel
10. Handling. Storing and Transport
11. Orientation
12. feployia 41ghti and •eiponslbllltln
13. DMrianer/Dmtdlal Maniganint Prof"*
1*. Mmulng lestrlete't Ionia
304
REMEDIAL RESPONSE
-------
Table 2
Superfund Training Resources—Private Associations
AGENCY
ASME (Professional Dev. Dept.)
C«nter for Prof. Adv.
H«t. H«t. Ctrl. Inst.
N.E. Haz. Waste Com.
Cntr. for En. end Env. Mgmt.
Chen. Manufacturer's Assoc.
Government Institutes
Gov. Defuse Coll. 4 Clip. Assoe.
Hit. Hit. Advisory Council
Amer. Ind. Hyg. Assoe. (I.C.E.)
ADDRESS
315 E. «7th St. M.T.. N.T. 10017
P.O. Bo i 864. E. Brunswick. M.J. 08816
P.O. Boi 1085. Alpha. N.J. 08865
Hughes Just. Corep.. Trenton, N.J., OA625
P.O. Boi 536. Fairfax. VA. 22030
2501 M St. N.V.. Wash.. O.C. 20037
P.O. Boi 1096, Rockvllle. MO. 20850
5101 Dtioh Ave.. Silver Spring. HO 20902
1100 17th St., N.W., Vash.r D.C. 20036
175 Wolf Ledges Ptrvy, Akron. OH 44311
Hit. Sfty Council (Sfty. Trn. Inst.}
' FW ». Michigan Ave.. Chicago. II. 60611
PHONE CONTACT
Robert Ferry (212) 705-7743
Edith Webb (201) 249-1400
Mr. Bollokl (215) 258-7015
Robert Roblllard (609) 984-6374
Water Pearee (703) 250-5400
Carl UallU (202) 887-1257
Martin Heavner (301) 251-9250
Lanny Hlokman (301) 583-2898
Julia Selbert (202) 223-1271
J. 1. Contl (216) 762-7294
Director (312) 527-4800
SUBJECT
AREA*
1-1*
1-3,7.10.13
1-3,8,10.13
1.9 i 13
B. 10-13
6*9
11
1-10 A 13-14
11
1-1,7 » 12
10
TAPES i
MANUALS
No
No
Yea
Yes
Yes
Yes
No
Yes
No
No
No
COST
Yes
Yes
Yes
No
Yes
Yes
Yes
Yes
Yes
Yes
Yes
Health and Safety
Personal Protection
Emergency Self-Help Rescue
Respiratory Protection
Vehicle Use at Hazardous Sites
SUBJECT AREAS
6. Use of Field Equipment
7. Monitoring
8. Contingency Planning
9. Sampling Techniques
10. Handling, Storing and Transport
11. Orientation
12. Fnployee Rights and Responsibilities
13. Emergency/Remedial Management Program
1*. Managing Restricted Zones
Table 3
Superfund Training Resources—Firms
AGENCY
Env. Haz. Mgmt. Inst.
J. T. Baker Chem. Co.
ITS Corporation
Lion Technology, Inc.
DuPont * Co. (Fin. i Fab. Dept.)
Haz. Hat. Ctrl. Reach. Inst.
Hailna Corporation
Phoenli Sfty. Aasoc.
Trans. Skills Prog.. Inc.
ENSAFE
Gov. Srvs. Inst.
D. W. Ryckman & Assocs.. Inc.
ADDRESS
283, 15 Pleasant St., Portsmouth^ NH^ 03801
222 Red School Ln., PMlllpsburg, NJ, 08865
823 E. Gate Dr.. Mt. Laurel. NJ, 08051
P.O. Drawer 700, LaFayette, NJ, 07818
Barley Hill Plaza, Wilmington, DE, 19JJ98
9300 Colunbla Rd.^ Silver Spring, MD, 20910
7315 Wisconsin Ave., Bethesda, MD, 20811
P.O. Box 515 Phoenlivllle, PA, 19160
320 W. Main St., Kutztowrij PA, 19530
P.O. Box 31207, Memphis, TN. 38131
P.O. Box 5212. Sprlnghlll, FL. 33526
115 W. Wisconsin Ave.j^Neena^ WI, 51916
2208 Welsch Indust. Ct., St. Louis, MO, 63111
PHONE CONTACT
Kevin Soles (603) 136-3950
Robert Outer (201) 859-2151
Charles Lay (609) 231-2600
William Taggert (201) 383-OBOO
Stewart Harrison (302) 999-2390
Beverly Vilcoff (301) 587-9390
Mark Moreln (301) 652-6366
Anthony Fuscaldo (215) 935-1770
Linda Baver (215) 683-5098
Wendell ICnlght (901) 372-7962
Gary J. Gorman (901) 683-8553
Kevin Lehner (111) 722-2818
Jeff Peters (311) 569-0991
SUBJECT
AREAS
1A6.7 * 10
8^10,11 & 12
1.11 & 13-11
1.2.1-R * 10-11
10
1.2,6.7,8,9,10
11 & 13
1-1,6-10,* 13-1*
8.10.11 * 12
1.8.10.11 * 13
10
1t2,1 * 10
1-1.6-8.10.12-1-
FAPES *
ANIIALS
No
No
Yes
Yes
Yes
Yes
No
No
Yes
No
Yes
Yes
NO
COST
Yes
Yes
Yes
Yes
Yes
Yes
Yes
Yes
Yes
Yes
Yes
Yes
Yes
1. Health and Safety
2. Personal Protection
3. Emergency Self-Help Rescue
1. Respiratory Protection
5. Vehicle Use at Hazardous Sites
SUBJECT AREAS
6. Use of Field Equipment
7. Monitoring
8. Contingency Planning
9. Sampling Techniques
10. Handling, Storing and Transport
11. Orientation
12. Employee Rights and Responsibilities
13. Emergency/Remedial Management Program
11. Managing Restricted Zones
In this paper, the authors review some of the training resources
currently available which may be useful to those involved in Super-
fund activities. This material should only be used as a guide to re-
sources and is intended only as a reference source. The intent here
is only to offer a resource which includes those sources we are
aware of and is not an endorsement of anyone's product. Many
courses related to aspects of Superfund are continually being devel-
oped, and others are being revised as the training needs dictate;
therefore, it is important for the reader to keep abreast of changes.
SUPERFUND TRAINING COURSES
A survey of available training courses covering various aspects
of Superfund activities is presented in Tables 1-4. The offerings
have been separated into four categories indicating those services
offered by: governmental agencies (Table 1); private associations
(Table 2); private firms (Table 3); and educational institutions
(Table 4). In each case, the name of a contact person and the major
subject areas covered have been included.
Information about the existence of videotapes and other course
materials which may be available for purchase has also been in-
cluded. For some of the resources shown (especially government
sponsored ones) the sessions are free or the cost is nominal. How-
ever, for many of the other resources the cost varies widely de-
pending on the offering. Since the exact cost of such services may
not be accurate at the time of inquiry, only the fact that the re-
source is available free or for a fee has been included. One area
not covered specifically in the Tables, but which is implicit in most
of the course offerings, is the regulatory requirements under Super-
fund. In compiling the data for Tables 1-4, it was usually found
that the agency sponsoring the course does cover the regulatory re-
quirements for the specific areas covered. The reader should con-
tact the person listed to obtain more details regarding course des-
cription and content.
OTHER RESOURCES
There are other areas of training which may be useful to those
involved in Superfund programs. Some of these areas include train-
ing in the use of computerized information systems, and training
on how to interpret and use the information and data contained
in reference books and manuals. In the following section on LINE
REMEDIAL RESPONSE
305
-------
Table 4
Superfund Training Resources—Educational Institutions
AGENCT
Rutgers U. (Dept. En*. Scl.)
Dal. St. Fire Sett.
Jnlv. of Delaware Oct. of Civ. Eng.)
Johns Hopkins (Sch. of Hyu. I P. A.)
Jnl» of Cln. (Inst. of En*, nth.)
•at. Spill Ctrl. Sch.
Tex. AtHU. Sr>. (Eng. Eit. Srv.) F.E.
Mlverslty of Teias
low* St. U. (Fir* Sr». Eit.)
Colorado Tm Inat.
Jnly. of Cal. (H. Oee. nth. Ctr.) '
Ire 3r». Tm.
ADDRESS
Cook College. New Brunswick. NJ, 08903
Rte. 2. P.O. Boi 166. Dover. OF.. 19901
Of f of Cont. Ed.. Newark. OE, 19711
615 N. Wolfe St., Baltimore. MD. 21205
3223 Eden Are.. Clnolnatl. OH. 45267
6300 Oeean Dr., Corpus Chrlstl. TX 78112
Drawer. College St».. TX 778*3
Cont. Eng. Studies. Austin. TX 78712
A«es. IA. 50011
1001 E. 62nd Ave.. Denver. CO, 60216
Berkeley. CA, 9*720
COM for Voo. Ed.. Olynpla. WA, 98504
PHONE CONTACT
Vleent Dtgregorlo (201) 932-9571
touts Anablll (302) 736-4773
Dr. C. P. Huan* (302) 738-2741
Dr. Jacqueline Corn (301) 955-33*3
Dr. Raymond Susklnd (513) 872-5701
George OBerholtzer (512) 991-8692
David White (713) 845-7A41/341H
Dr. Nell Armstrong (512) 471-1711
Keith Royer (515) 294-6817
Walter DeFreeee (303) 2R9-*891
Dr. Robert Spear (415) 642-1681
Edward Prendergast (206) 753-5679
SIIBJF.CT
AREAS
1-10 4 13-14
1-6.8-10 A, 1*
10
1.7-9. 12 * 1*
1-10 t 12-1*
1.2.7.8.10.1141;
10 4 14
10
1-4.6 4 10
1.Z.5.8.10.1141J
1-10 4 12-1*
1.2.5-10 4 13
TAPES 4
«ANUAL3
Ha
TM
No
No
No
Kb
NO
No
T«s
T«s
Tta
Tes
COST
111
111
In
111
hi
T.;
hi
hi
to
'II
111
ll
Health and Safety
Personal Protection
Emergency Self-Help Rescue
Respiratory Protection
Vehicle Use at Hazardous Sites
SUBJECT AREAS
6. Use of Field Equipment
7. Monitoring
8. Contingency Planning
9. Sarapllng Techniques
10. Handling. Storing and Transport
11. Orientation
12. feployea »lghts end ResponslbllUlei
13. Emergency/Remedial HanaKtawnt Profrai
1*. Manning Restricted Zone*
DATA BASES, and the succeeding section, BOOKS AND
MANUALS, some of the current resources available in these areas
are presented. The attempt has not been to prepare an exhaustive
list of these resources but rather to specify some items which are
available and which may be useful to those with Superfund respon-
sibilities at all levels. Many of the training courses presently avail-
able have sections devoted to an introduction to computer re-
sources as well as books and manuals applicable for Superfund
planning and implementation. Much of the training on computer-
ized systems, however, is supplied by the vendors of such systems.
It is up to the purchaser to shop for the best deal.
ON-LINE DATA BASES
There are several vendors supplying a variety of on-line com-
puter searchable records which may be used by those responsible
for all aspects of Superfund activities. A list of vendors and their
database services is given in Table 5. Vendors such as Lockheed
and SDC have quite comprehensive offerings which span a wide
variety of database systems. Most vendors charge the user an initial
fee for the necessary log on passwords and start-up fees. Once the
user has acquired access to a system, charges are incurred with use
of the system depending upon the specific cost of the database used
and the telephone connect time to the system.
Most vendors offer training courses and user manuals as a part
of their start-up fees and it is incumbent upon the user to take ad-
vantage of these services to learn the proper use of the system.
Each system has its own computer language and cost, and the data
format may vary widely for the same database among vendors. In
order to limit the time and cost of using a system, it is important
that the user make inquiries of several vendors to compare costs
of the systems offered.
BOOKS AND MANUALS
Everyone involved in Superfund activities should be aware of the
many books and manuals available. These references contain a
variety of information which can be used by those involved at all
levels of Superfund planning and implementation. An integral
part of many of the training courses listed in this paper is training in
the use and understanding of reference materials. Many of these
references contain physical and chemical data about hazardous
substances. Others contain information about lexicological prop-
erties and health and safety data of a variety of commonly used
industrial chemicals.
The reader should note that in most instances the edition and
year of publication have been omitted from the listed references;
the reason for this omission is that these resources are constantly
updated and revised. It is incumbent upon the reader to acquire
the most current references available. The list presented is incom-
plete and is intended only as a guide to the kinds of information
available. There are some references which should be considered a
minimum requirement; these include:
•Physical, Chemical and Biological data
•Health and Safety information
•Hazard assessment and emergency response information
•Sampling and Analysis methods
Several organizations such as the American Conference of Gov-
ernment Industrial Hygienists (ACGIH) and the American Indus-
trial Hygiene Association'(AIHA) publish a variety of pamphlets
and manuals. The address for the ACGIH Publication Office is
6500 Glenway Avenue, Building D-5, Cincinnati, OH 45211
(Phone 513/661-7881). References from the ACGIH include:
•"Air Sampling Instruments for Evaluation of Atmospheric Con-
taminants".
•"Documentation of the Threshold Limit Values (TLV)". The
address for the (AIHA) is 475 Wolf Ledges Parkway, Akron,
OH 44311 (Phone 216/762-7294) and some of the publications
obtainable include:
•"Basic Industrial Hygiene"
•"Direct Reading Colorimetric Indicator Tubes Manual"
•"Manual of Recommended Practice for Combustible Gas Indi-
cators and Portable, Direct Reading Hydrocarbon Detectors"
•"Respiratory Protective Devices Manual"
•"Hygiene Guide"
The National Institute for Occupational Safety and Health
(NIOSH) and the Occupational Safety and Health Administra-
tion (OSHA) also publish several useful handbooks and pamph-
lets. These documents may be purchased from the U.S. Govern-
ment Printing Office (GPO), Washington, DC 20402 (Phone 202/
783-3238). Some of the publications available include:
•"The Industrial Environment"
•"Occupational Health Guidelines for Chemical Hazards"
•"Registry of Toxic Effects of Chemical Substances"
•"Pocket Guide to Chemical Hazards"
The USEPA publishes a variety of methods manuals for the
sampling and analysis of hazardous materials. Some of these man-
uals can be invaluable to those considering water treatment and
analysis methods. Some of these references are:
306
REMEDIAL RESPONSE
-------
Tables
Environmental Chemical Computerized Data Bases
Dn-Llne Data Bases
MTIONAL LIBRARY OF
(EDICINE - MEDLARS
Avllnt
Cancerllt
Cancer proj
Chenllne
Ned line
led 66 - 70
Med 71 - 7*
led 75 - 76
Med 77 - 79
Foxllne
roxback 65 - 73
Poxback 7* - 78
toxicology Data Bank
BTECS
EH IS
HATREHS
NEDS
SAROAD
STORE!
NPDES
Chemical
Information
X
X
X
OSHA HEALTH DATA
SYSTEM
OHDS
NAWDEX
LOCKHEAD INFORMATION
SYSTEMS - DIALOG
Agrloeola
Air Pollution Tech.
Infer. Center
Aquatle Sciences and
Fisheries Abstracts
Health Effects
and
Toilcologlcal
Information
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
Environmental
Information
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
Manufacturing
Uses and
Economic
Information
X
X
Disposal
Information
X
X
X
X
X
i
X
X
X
X
Comments
Bibliographic and review data for
non-print materials In health
sciences.
Covers all aspects of cancer
literature: Includes books In
addition to standard sources.
Ongoing research funded during the
most recent three fiscal years:
overlaps with SSIC data base.
Chemical dictionary file: does not
give structural formula: provides
locator Information to MKDLARS data
bases and TSCA Inventory.
Excellent source of blomedlcal/
health effects material: Indexes
Index Medlcus plus special list
journals .
Back files of Medllne
Back files of Medllne
Back files of Medllne
Back files of Medllne
Good for toxlcologlcal and environ-
mental data: many duplicates within
system.
Back files of Toxllne - not search-
able on line.
Rack files of Toxllne
Limited number of chemicals: very
comprehensive dictionary file; lacks
Information on new chemicals.
Registry of toxic effects of
chemical substances, provided by
MIOSH. containing over 10.000
toxlcologleal measurements.
Synonyms In RETECS differ from those
in Chemllne
estimates of II. S. pollutant
emissions for previous years.
Provides data for making pollutant
trend predictions.
Emissions data on pollutants not
regulated hy the Primary Ambient Air
Standards. Included data can he
used for modeling.
Emissions data on the oollutants for
which there are Primary Ambient Air
Standards are collected 'ran about
7S,OflO point sources and T.200 area
sources. Include data on ftTC Code.
and such modeling parameters as
stack height and diameter, emissions
rate . and temperature .
Ambient air quality data 'rom over
»,000 active air monitoring sites
across the country. Uses modeling
to permit evaluation of air quality
data.
Oata on water quality across the
country collected in connection with
•L 02-WO.
Information on the quality and
quantity of discharges which have
been permitted under the National
Discharge Permit Program for all
point source discharges Into '1. X.
waters .
Monitoring data of exposure to toxic
substances.
Water monitoring data from federal
state, and local programs.
Index of data Is available by
location and pollutant category.
Good general agricultural Informa-
tion source.
Good source for air pollution
Information. Contains some emission
data. Closed file to 1978.
Some water pollution data but mostly
Overlaps the MF.OLINE file. Good for
searching 1969-1977 data on-line.
REMEDIAL RESPONSE
307
-------
TableS
Environmental Chemical Computerized Data Bases (cont'd)
ta-LlM Data Bases
CA Abstracts Search
Chemical
Information
X
CAI Abstracts
Chem Industry notes
Chemname X
Chemsearch X
Chemsls X
Chemical Regulation
•nd Guidelines System
(cues)
Clalma/U. S. Patents X
Clalms/Chem X
Claim/Class X
SYSTEMS DEVELOPMENT CORP. -
)RBIT
Chemcon and
Chem 7071
FSIA
Pa per chen
P/C Newa
Rlngdoo
Safety
Titus
Waterllft
VPI
IIH/EPA - CIS
CNHR
CRYST
CTCP
FRSS
MSSS
OHM-TADS
POSH
RTECS
TSC»PP
WDROP
X
X
X
X
I
I
X
X
Health Effects
and
Tbilcologleal
Information
X
X
X
I
I
X
T
Environmental
Information
X
X
X
X
«
K
I
(
Manufacturing
Uses and
Reonomle
Information
X
X
X
X
X
1
»
Y.
t
X
t
<
T
Msposal
Information
X
X
X
X
X
X
t
T
t
X
»
«
«
t
T.
Comments
Information.
Deals primarily with applied
agriculture.
Information.
substructure searching via
nomenclature .
Chemical dictionary file - or moat
recently cited substances in CA
Search .
Chemical dictionary file or ohemle.il
substances cited only once during
C. I. period.
Guide to II. S. federal government
regulatory material relating to
control of chemical substances.
Patent and use data.
Patent and use data.
Dictionary file enhances retrieval
In the two files listed above.
Overlaps CA search.
food science and teehnoloav data
base.
Uses Information: paoer Industry.
Business and economic Information In
the petroleum industry.
Pharmaceutical Information.
Information on industrial and
occupational safety: environmental
and ecological safety.
Covers uses and biological and
environmental Information on
petroleum Industry.
International coverage of energy.
biochemistry, environment.
pollution, analytical chemistry and
health Information concerning vater.
Patent specifications.
Carbon 11 Nuclear Magnetic "esourct
Search Systems provide Information
for compounds hearing specific
spectral characteristics.
"rolvde access to the Cambridge T.
rav Cryatallographte tta *ase of
37,0?* structures.
CTCP permits searching of common
commercial products hv identifying
the product or its constituents.
•Hie toiteltv of the products in Ct»
will also he available.
"rovlrtes access to up-to-date Infor-
mation on regulatlona, rules.
atandards and guidelines Involving
chemical aubstances.
•<*S.S permits search for maas
spectral data. Oata baae Include!
spectra of 13."" eompeunda.
OHH-TUDS data base Includes a «l*e
variety of physical, chemical.
biological, toileologlcal and
commercial data on these matarlall,
with emphasis placed on their
deleterious effects on water
qualllty. lip to 126 different
fields of Information are maintain*
for more than 1.000 ehemteala.
Permits searching or data eollaeMi
by Joint Committee on Bowler
mr«Vactlon Standarda. 11.000
substances contained in data bate.
Including organles. Inorganics,
minerals and alloVR.
*ee previous listing.
lant and production range or
chemical reported under T*C»-
ntstrlbutlon teglatry of Organic
Pollui-.ant! eontalna data on drlrttN
and other types or water, date aa4
location or water sample, onmeoiavl
Identity, analytical method use".
concentration detected, and
reference to published result"-
308
REMEDIAL RESPONSE
-------
Table 5
Environmental Chemical Computerized Data Bases (cont'd)
On-Llne Data Bases
EPA ON-LINE
SYSTEMS
Aeronetrlo and
Emission System
( AEROS)
Chemical
Information
Health Effects
and
Toxlcologlcal
Information
Environmental
Information
X
Manufacturing
Uses and
Economic
Information
Disposal
Information
X
Comments
Comprehensive data system use to
collect, store, and analyze air
pollution data. Provides concise
standarlzed reports on various
aspects of air pollution. SAHOAO,
HATRFHS, mm. and PHIS are all part
of the A^ROS system.
•"Biological Field and Laboratory Methods for Measuring the
Quality of Surface Water and Effluents" (EPA 670/4-73-001)
•"USEPA Solid Waste Manual, Test Methods for Evaluating
Solid Waste, Physical/Chemical Methods" (SW-846)
•"Handbook for Analytical Quality Control in Water and Waste-
water Laboratories" (EPA 600/4-79-019)
•"Methods of Chemical Analysis of Water and Wastes" (EPA
600/4-79-020)
•"Procedures Manual for Groundwater Monitoring at Solid
Wastes Disposal Facilities".
The address for these publications is USEPA Office of Re-
search and Development, Publications- (CERI), Cincinnati, OH
45268 (Phone 513/684-7562). The reader should also make in-
quiries at CERI about the numerous technical papers and mono-
graphs prepared by the agency covering a wide variety of spe-
cific topics which may be relevant to Superfund activities. Many
of these monographs and technical reports cover such subjects as
site entry and control as well as site monitoring and construc-
tion techniques.
References containing basic physical, chemical and biological
data include the following:
•Chemistry of Hazardous Materials, E. Meyer, Prentice-Hall,
Box 500 Engjewood Cliffs, NJ 07632 (Phone 201/592-2000)
•The Condensed Chemical Dictionary, G. Hawley, Van Nos-
trand Reinhold Co., New York, NY 10020 (Phone 212/265-8700)
•CRC Handbook of Chemistry and Physics, CRC Press, 2000
Corporate Blvd., N.W., Boca Raton, FL 33431 (Phone 305/
994-0555 Ext. 330)
•Dangerous Properties of Industrial Materials, N. Irving Sax, Van
Nostrand Reinhold Co., New York, NY 10020 (Phone 212/265-
8700)
•Fire Protection Guide to Hazardous Materials, National Fire
Protection Association, Batterymarch Park, Quincy, MA 02269
(Phone 617/328-9290)
•The Merck Index, Merck and Co., Inc. P.O. Box 2000 Rahway,
NJ 07065 (Phone 201/574-5403)
Most of these references are quite comprehensive in their cov-
erage of the chemicals referenced; however, the reader should be
aware that no reference contains all of the chemicals which may be
present at a site, so some preliminary scanning of the reference ma-
terials or inquiry to the publishers should be made to assure pur-
chasing the appropriate references for one's purposes.
Several other books are devoted specifically to safety and first-
aid measures. Again, the reader should peruse several reference
sources in this area to obtain the one most appropriate for present
and projected Superfund needs. Three such resources are:
•Best's Safety Directory, A.M. Best Company Inc., Ambest Road,
Oldwick, NJ 08858 (Phone 201/439-2200)
•CRC Handbook of Laboratory Safety, N.V. Steere, 2000 Corp-
orate Blvd., N.W., CRC Press, Boca Raton, FL 33431 (Phone
305/994-0555 Ext. 330)
•National Safety Council Safety Sheets, National Safety Council,
444 North Michigan Ave., Chicago, IL 60611 (Phone 312/527-
4800)
CONCLUSIONS
The list of training courses, databases, books and other re-
sources contained in this paper is representative of some of the re-
sources currently available. In many instances, a specific course or
other resource only covers a portion of the training requirements
of an organization. Many of the resources listed are used primarily
by emergency response groups and, only recently, has a portion of
the courses, books and manuals been devoted to Superfund. There-
fore, it is incumbent upon those seeking training in Superfund re-
lated areas to review as much of the available training informa-
tion as possible.
There are some organizations which will organize training
courses to suit the specific needs and objectives of a hiring group.
These courses are usually more expensive in terms of initial cost;
however, this may be the most cost effective way of training a
large group of workers at one time.
Another approach to training was developed by the U.S. Corps
of Engineers. After reviewing the available offerings for training
and discovering that most of these resources were devoted to emer-
gency response rather than remedial action, the Corps developed
its own Superfund Overview Course. This course was specifically
designed to meet the needs of Corps personnel involved in Super-
fund activities and addresses the design and construction activities
at Federal lead Superfund sites. This course is not available to the
general public; however, it does indicate that other organizations
interested in Superfund involvement may find it more advan-
tageous to pool together specific resources to train their personnel.
It is advisable that those interested in Superfund training shop
around and make inquiries of several suppliers to achieve the most
cost effective use of training dollars.
REFERENCES
1. The information for Tables 1-4 was taken from "Hazardous Ma-
terials Response Training" draft report prepared for USEPA by Booz-
Allen & Hamilton, Inc.
2. The list of data bases contained in Table 5 were kindly supplied by
the Hazardous Materials Technical Center (HMTC), P.O. Box 8168,
Rockville, MD. 20856-8168.
REMEDIAL RESPONSE
309
-------
SITE SECURITY AND WASTE REMOVAL ACTIVITIES
AT AN ABANDONED HAZARDOUS WASTE SITE
MICHAEL A. BARBARA
THOMAS J. MORAHAN
Fred C. Hart Associates
New York, New York
ROBERT W. TEETS
Cooper Industries
Houston, Texas
SUE HISTORY
The Osborne landfill is located in Pine Township, Pennsyl-
vania just east of the Borough of Grove City (Figure 1) in an area
known for its coal mining and steel related industries. The land-
fill is located in an abandoned coal strip mine about IS acres in
size. Upon abandonment, the mine filled with water and was sub-
sequently used as a dump for a variety of industrial and domestic
wastes including foundry sand. The foundry sand filled almost
three-quarters of the stripped area. In addition, scrap metal and
drums containing potentially hazardous materials were also dis-
posed of there.
The site was evaluated by USEPA using the MITRE Hazard
Ranking System. Because of its proximity to the water supply wells
of Grove City, the Osbome site was ranked as one of the top 50
Superfund Sites in the nation.
At that time, USEPA identified a number of suspected gener-
ators and haulers possibly responsible for the waste problems at
the Osborne Landfill. Cooper Bessemer, a local foundry and
subsidiary of Cooper Industries of Houston, Texas, was named as
one Of several suspected generators. Cooper, a long time resident
and major employer in Grove City, maintained that, for the safety
and well being of area residents, it would undertake the task of
investigating the problems associated with the Osborne site.
Cooper retained Fred C. Hart Associates, Inc., (FCHA) a New
York based environmental consulting firm, to provide technical
assistance in the investigation of the Osborne Landfill.
Cooper and FCHA, working closely with the Pennsylvania De-
partment of Environmental Resources (PADER) and USEPA,
developed a phased approach to the investigation. In this paper,
the authors discuss the problems encountered at the site and trace
the steps performed in the implementation of the initial remedial
measures and site security.
INITIAL CONDITIONS
Initial site conditions were not conducive to performing a de-
tailed investigation of the site. An unknown number of 55 gal
drums were scattered about the site. These drums may have con-
tained potentially hazardous materials. Many were crushed, rusted
or bulged and were in no condition to be safety handled. In addi-
tion, areas of contaminated soil were found.
These problems were compounded by unrestricted public access.
After the landfill stopped accepting wastes in the late 1970s, un-
restricted access afforded an excellent motivation for the illegal
dumping of wastes. Three ponds located on-site were extremely
dangerous to children.
The unknown characteristics of the wastes and the proximity
of large surface water and groundwater impoundments made a
comprehensive site investigation imperative.
Since the degree of hazard posed by the site conditions pro-
hibited appropriate investigatory work, a site security program was
recommended. This program was designed to restrict access and
reduce liability while rendering the surface of the landfill safe for
personnel implementing the site investigation.
A 6 ft high 3,740 ft chain link fence was constructed around the
site including a newly found contaminated area. Appropriate warn-
ing signs were also erected.
DRUM INVENTORY
In order to plan for the ultimate disposal of the wastes, FCHA
gathered information from outside sources, performed a waste
(drum) inventory and then sampled. The waste inventory was de-
signed to identify the number, locations, types, conditions and
possible contents of drums scattered on site. A standard form was
developed and utilized throughout the study. The site was divided
into ten distinct areas (Figure 2) which contained drums. These
areas were referred to as "clusters". Within each cluster, drums
were consecutively numbered.
Each drum was then recorded on a log form with its number,
condition, possible contents and label information. Each cluster
was extensively photographed. The data gathered during the in-
ventory were then fed into computers for future use. Found were
433 drums, of which 75 were full and sealed. Of the 75 sealed
drums, approximately 20% were selected for sampling. Each drum
was chosen for sampling based on its location, accessibility and
condition.
FCHA designed and fabricated a remote drum opener to en-
sure the safety of the sampling crew. This opener consisted of a
pneumatic impact wrench mounted on a support stand. A tempor-
ary explosion shield was erected around each drum as it was
opened. The device was operated with an SCBA air tank from a
distance of 100 ft.
Upon opening, each drum was checked with an Organic Vapor
Analyzer (OVA) and an explosimeter to characterize the materials
inside the drum. An "Action Level" was set at 50 ppm of organic
vapor. Drums exceeding the 50 ppm level required level "B" (Self
Contained Breathing Apparatus). All other drums were sampled in
level "C" (Cartridge respirators).
Each sample was collected with a glass drum thief. Samples
were analyzed for PCBs, fuel value and RCRA characteristics in-
cluding ignitability, corrosivity, reactivity, metals and pesticides/
310
REMEDIAL RESPONSE
-------
CONTOUR INTERVAL 10 FEET
NATIONAL GEODETIC VERTICAL DATUM OF 1929
Figure 1
Site Location Map
herbicides. Parameters were chosen based on requirements for the
proper manifesting and disposal of the waste.
The results of the selected drum analyses were crucial to de-
termine the level of protection necessary for site security work
efforts as well as to anticipate the approximate cost of this task.
Chemical analyses of the 17 liquid drum samples and three soil/
solid samples are presented in Table I. Of particular importance
was the fact that no PCB compounds were detected in any of the
liquid samples.
In general, the contents of the drums contained low levels of
RCRA metals (barium, cadmium, chromium and lead), had some
fuel value and, with only one exception, had pHs within the RCRA
non-corrosive limits of 2-12.5. Three of the samples did have flash
points below 60 °C, however.
WASTE REMOVAL
A detailed scope of work for the removal of the wastes, drums
and contaminated soils was developed by FCHA and issued with a
form of contract in an RFP on June 23, 1983. The scope of work
called for the restaging and sampling (where appropriate) of all
drums visible on the surface of the Osborne Landfill. This was
taken to include all drums floating on the surfaces of the three
ponds. The contractor was required to restage all drums on plastic
covered, bermed areas for sampling. Leaking or weak drums were
to be overpacked, as required. In addition, areas of obvious soil
contamination beneath leaking drums were to be excavated and
restaged in a separate area. All drums and contaminated soils were
to be analyzed, and the contractor was required to submit a formal
waste disposal plan prior to removal of any materials from the site.
Five firms were invited to bid on the project.
A site visit was held on June 28 to familiarize the bidders with
the conditions of the site and answer any questions relating to the
implementation of the scope of work. Representatives of four of
the five firms visited the site and submitted proposals on July 7,
1983. Of these responses, two were deemed non-responsive to the
terms of the RFP. The choice between the remaining two bidders
was made on the contractors' preliminary waste disposal plan, per-
sonnel safety plans, compliance with the terms and schedules de-
REMEDIAL RESPONSE
311
-------
Table 1
Chemical Analysis of Selected Drams at the Osborne Site Parameters
Ignitability Corrosivit
Fuel
DRUM Value (Flash Point
NUMBER (BTU/lb) in °C) (pH)
B14
119
J32
05
J45
B53
B4
H22
G36
B91
G50
G42
F17
A2
G33
143
Jl
AREA B SOIL
AREA G SOIL
G31 (SOLID)
RCRA ALERT
LEVEL
13741 ** 6.5
19892 49 9.5
18232
*
19631
13890
19275
19741
17243
19295
*
19453
19449
19101
13429
A
—
3.0
5.4
3.7
7.0
3.7
2.9
5.7
5.2
13.8
3.7
5.7
2.7
8.2
9.6
5.4
— 5.5
— 6
— 5.6
<60°C pH H2 or
y PCB Aroclors
1242
mgAg
ItlO
H10
11250
H250
ItlO
mo
ItlO
ItlO
ItlO
ItlO
ItlO
ItlO
ItlO
mo
mo
mo
m
—
—
—
1254
•gAg
mo
mo
mo
H250
mo
mo
mo
mo
mo
mo
mo
mo
mo
mo
mo
mo
HI
—
—
—
D004/
1260 Arsenic
mg/kg
mo
mo
mo
H250
mo
mo
mo
mo
mo
mo
mo
mo
mo
mo
mo
mo
HI
—
—
—
mg/kg
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 2
HO. 5
HO. 5
HO. 5
HO. 5
5
RCRA METALS
(EPA Hazardous Waste number/parameter)
D005/ Dfl06/ DuO?/
Barium Cadniun Chromium
ng/kg mg/kg
7
HO. 2
HO. 2
HO. 2
HO. 2
5
H5
1
0.4
HO. 8
0.9
HO. 2
H5
H5
7
2
H5.0
H5.0
H5.0
H5.0
100
HO. 8
HO. 8
HO. 8
HO. 8
HO. 8
2.6
HO. 8
1.2
HO. 8
HO. 8
HO. 8
HO. 8
HO. 8
HO. 8
0.9
HO. 8
HO. 8
HO. 8
HO. 8
HO. 8
1
ng/kg
0.4
HO. 2
2
HO. 2
HO. 2
HO. 2
HI
HO. 2
HO. 2
0.6
HO. 4
HO. 2
HI
HI
0.2
0.5
Hl.O
ltl.0
Hl.O
Hl.O
5
0008/ D009/ DOW
Lead Mercury Selenium
mg/kg
30
20
It2
H2
20
15
H2
8.7
4.5
4.5
H4
H2
H2
2
H2
7.7
H2.0
H2.0
6.0
H2.0
5
mg/kg
HO. 09
HO. 07
HO. 08
HO. 09
HO. 002
HO. 002
HO. 002
HO. 08
HO. 09
HO. 08
HO.l
HO. 08
HO. 002
HO. 002
HO. 008
HO. 09
0.004
HO. 002
0.003
0.002
0.2
mg/kg
HO.l
HO.l
HO.l
HO.l
HO.l
HO.l
HO. 2
HO.l
HO.l
HO.l
HO.l
HO.l
HO. 2
HO. 2
HO.l
HO.l
HO. 5
HO. 5
HO. 5
HO. 5
1
D011/
Silver
•gAg '
0.9
HO. Z
HO. 2
0.7
HO. 2
HO. 2
HO. 5
HO. 2
0.4
HO. 2
HO. 4
HO. 2
HO. 5
HO. 5
0.9
0.5
HO. 2
HO. 2
HO. 2
HO. 2
5
It
gt
No Analysis
Not ignitable
Flash Point Over 60°C
less than
greater than
pH gt!2.5
-. — ONIO
Figure 2
Drum Cluster Boundary at the Osborne Landfill
lineated in the RFP and price. Using these criteria, Fondessy
Enterprises, Inc./Associated Chemical and Environmental Services
(ACES) of Oregon, Ohio was selected to perform the work.
Following an oral presentation, a unit price contract was nego-
tiated and signed by representatives of Cooper and Fondessy.
ACES' personnel mobilized their equipment on-site on July 25,
1983. Security personnel were retained to limit access 24 hours a
day for the duration of the cleanup. A field office trailer and de-
contamination/personnel safety trailer was also set up. After a
safety meeting, cleanup operations commenced on the morning of
July 26.
Level "D" protection was required for all personnel entering the
site. Personnel involved with the supervision and handling of the
drums were required to utilize Level "C" (cartridge respirator)
protection whenever wastes were handled. Periodic checks of site
condition were made by the safety officer using an OVA. Within
five days, approximately 630 drums (460 of which were empty)
restaged and 45 yd' of soil were evacuated. Each drum contain-
ing liquid was sampled for manifest requirements. One composite
soil sample was also collected.
ACES formally submitted their Waste Disposal Plan to repre-
sentatives of Cooper, FCHA, PADER and USEPA on Aug. 5,
1983. The plan specified the packaging, transportation and ulti-
mate disposition of the wastes collected. Removal of the wastes
commenced on Aug. 9. The nonaqueous waste was pumped into a
tanker truck and utilized for fuel blending by Deleware Con-
tainer Corp., Coatsville, PA. The drums containing aqueous solu-
tions were also transported to Delaware Container, solidified and
trucked to Fondessy's secure landfill in Ohio. All contaminated
soils and solids were transported in lined dump trucks for disposal
at the Fondessy site. All empty drums were crushed, using a
front-end loader, and transported to the Fondessy facility in box
vans.
A final inspection of the surface cleanup was made by Cooper
personnel on Aug. 12,1983.
312 REMEDIAL RESPONSE
-------
STATUS OF REM/FIT EPA CONTRACTS
PAUL F. NADEAU
U.S. Environmental Protection Agency
Office of Emergency and Remedial Response
Washington, D.C.
WILLIAM T. DEHN
CH2M Hill
Reston, Virginia
PAUL GOLDSTEIN
NUS Corporation
Arlington, Virginia
INTRODUCTION
The Comprehensive Environmental Response, Compensation
and Liability Act of 1980, commonly called Superfund, established
a dual-phase program for responding to environmental problems
caused by hazardous substances. The "emergency program"
focuses on situations where a prompt response is needed to prevent
harm to public health or welfare or the environment. Emergency
actions generally focus on controlling the immediate threat. The
"remedial program," on the other hand, is aimed at investigating
problem hazardous waste sites and providing cost-effective solu-
tions to these problems. In this paper, the authors discuss only the
"remedial" portion of the program.
On Sept. 30, 1982, the USEPA awarded two 2-year contracts,
each with two 1-year options, to investigate and plan for the
cleanup of hazardous waste sites in the United States. The contract
for USEPA Regions I through IV, in the amount of $75 million,
was awarded to NUS Corporation of Gaithersburg, Maryland.
NUS is supported by Dynamac Corporation of Rockville,
Maryland in the area of personnel health and safety, and Brown &
Root Development Inc. of Houston, Texas for engineering and
conceptual designs. The contract for USEPA Regions V through
X, in the amount of $89 million, was awarded to CH2M Hill of
Reston, Virginia. Ecology and Environment of Buffalo, New York
provides field investigation support to CH2M Hill.
The purpose of this paper is to identify the various elements of
the REM/FIT contract (the acronym, REM/FIT, is composed of
REM, which stands for Remedial Planning, and FIT, which stands
for Field Investigation Teams), to discuss their present status and
accomplishments and to describe contractor's activities on two
typical projects.
ELEMENTS OF THE REM/FIT PROGRAM
Organization
Each REM/FIT contractor maintains a Zone Program Manage-
ment Office (ZPMO) in the Washington, D.C. metropolitan area
for managing the overall programs and providing liaison with
USEPA headquarters. The ZPMO also provides all support ser-
vices such as health and safety, training, quality control/assurance,
community relations, cost control and scheduling, forecasting,
maintenance of records and equipment and direction of all subcon-
tracting activities.
The heart of the program is the FIT and REM human resources.
A FIT team resides in each of the 10 USEPA Regional offices to in-
vestigate sites and determine their hazard potential. High ranking
sites are then considered for placement on the National Priorities
List (NPL). A total of 228 positions are currently authorized and
staffed on a full-time basis to support these activities.
CH2M Hill and NUS also maintain one or more Remedial Plan-
ning (REM PLNG) centers in selected permanent operating offices.
These centers are responsible for the engineering activities of REM.
Staff members from these and other firm offices serve as Site Pro-
ject Managers (SPMs). Project team members are assigned from a
variety of disciplines depending on the needs of the project.
FIT Activities
A FIT is a fully dedicated, multi-disciplinary unit ranging in size
from 13 to 40 people. Over 70% of the team members are profes-
sionals with a variety of college degrees and experience. The teams
are responsible for performing the preliminary investigative ac-
tivities at sites to characterize the threat to public health and en-
vironment. Specific steps in the investigative process are shown on
HAZARD
RANKING
SYSTEM
Figure 1
FIT Overview
REMEDIAL RESPONSE
313
-------
Figure 1 and described below:
•Site Discovery is an initial survey of sites to confirm their existence
and location, to eliminate duplication on site lists, to make an
initial determination of the types of contaminant and industrial
waste categories and to define potential adverse impacts.
•Preliminary Assessment is a survey to characterize in a preliminary
fashion the hazardous substances present, potential pollutant dis-
persal pathways, the population and resources which might be
affected, facility management practices and the potential respon-
sible parties. The purpose of the assessment phase is to examine
the list of potential hazardous waste sites contained in the Agency
inventory (approximately 16,000) to determine if a site merits
further action.
•Site Inspection is intended to better define the extent of the prob-
lem at a site and provide a data base sufficient to determine the
next action (i.e., emergency response, enforcement and/or re-
medial response). A site inspection usually provides data ade-
quate to apply the USEPA Hazard Ranking System. Also, initial
enforcement measures may be supported with these data. To ac-
complish these objectives, site specific data on the hazardous
substances present, pollutant dispersal pathways, types of re-
ceptors and site management practices are gathered.
•USEPA's Hazard Ranking System (HRS) model is used to rank
each site relative to other sites nationwide employing the data
collected during a site inspection. The HRS model handles five
pathways of exposure: groundwater, surface water, air, direct
contact and fire and explosion. Pathway scores for groundwater,
surface water and air are combined and sites receiving the highest
total scores can be placed on the National Priorities List (NPL).
Pathway scores for fire and explosion and direct contact are used
as indicators for emergency action. In June 1983, 419 sites were
proposed for inclusion on the NPL.
The teams spend most of their time in field related activities.
Projects are scheduled in accordance with FIT regional work plans.
Team personnel are fully trained in health and safety and in field
activities such as opening containers and sampling groundwater, air
and soil. In addition to performing the activities just described, the
teams provide support to enforcement activities.
Remedial Activities
Once the site in on the NPL, it is a candidate for remedial action.
The REM portion of the contracts contains level-of-effort hours
and subcontract pool dollars to develop and implement a long-term
remedy which is consistent with a permanent solution to a hazar-
dous site. A variety of trained professionals ranging from chemical,
sanitary and civil engineers, chemists, biologists, geologists,
hydrogeologists and public health specialists are employed as
needed. The sequence of activities is shown on Figure 2, and the
key steps are described below:
•Remedial Action Master Plan (RAMP) is a planning-level effort
to compile existing data, to map out the activities needed to
clean up the site (with time and cost schedules) and to specifically
define the first remedial activity recommended for the site.
•Initial Remedial Measures (IRMs) may be taken at a site to miti-
gate a situation which poses a significant threat to the public or
environment. Examples of IRMs include staging or off-site re-
moval and disposal of drums, installing a security fence around a
site, on-site draining control and providing temporary alternate
water supplies.
•Remedial Investigation is a field-oriented effort to collect suf-
ficient data to permit the development and evaluation of remedial
response alternatives for a hazardous site. The remedial investi-
gation also assesses the need for IRMs to remedy any immediate
hazards.
•Feasibility Study develops the cost-effective solution for a site.
It involves selection of a number of remedial alternatives; initial
screening of the alterantives based on cost, environmental ef-
fects and engineering feasibility to indicate which alternatives
warrant further evaluation; performance of a detailed cost, en-
vironmental and engineering analysis; public review and comment
on the alternative remedies considered; and selection of the most
cost-effective solution for a site. A conceptual design is prepared
to define the selection solution.
•Design is the preparation of bid documents to allow cost-compe-
titive selection of a construction contractor to implement the
selected solution. This is done primarily under the auspices of
the States or the U.S. Army Corps of Engineers.
•Implementation is the process by which the actual site cleanup
occurs, again done primarily by the States or the Corps of
Engineers.
The Remedial Investigation (RI) and the Feasibility Study (FS)
are the primary activities of the REM/FIT contractors. A detailed
work plan is prepared for each project. Although shown as sequen-
tial steps on the flow diagram, it is essential that the investigation
and feasibility study be closely coordinated. This is done to target
the scope of the investigation to provide the data needed to assess
potentially feasible alternatives. The objective is to reduce the costs
and shorten the tune schedules for completion of the studies and
selection of the remedy.
REM/FIT PROGRAM STATUS
AND ACCOMPLISHMENTS
The two REM/FIT zone contractors have been operational since
Oct. 1, 1982. Despite a three month mobilization period, they have
already worked on over 650 hazardous waste sites through the end
of June 1983. They have also involved over 190 subcontractors in
the program.
EPA LEAD PROJECT
Corp* of Engr$.
IMPLEMENTATION |
Figure 2
Remedial Planning Flow Diagram
FIT Activities
The 10 regional Teams have focused their effort in performing
preliminary assessments and site inspections. Since the inception of
the two contracts, 1,716 assessments and 452 inspections have been
completed, increasing program-wide totals to over 6,570
assessments and 1,760 inspections. The ability of the Teams to per-
form assessments and inspections has been hampered somewhat by
other high priority projects, particularly in support of enforce-
ment. The following summaries are intended to illustrate the types
of projects typically assigned to the FIT.
*The Regional FIT spent over 7,000 person-hours at the Seymour
Recycling Corp. site in Indiana monitoring site safety, operating an
on-site treatment facility, supervising the installation of monitoring
wells, sampling the wells and sampling over 100 drums per month.
^•FIT personnal in Regions II and VII have been extensively in-
volved in sampling soils suspected of containing dioxin. Cort-
314
REMEDIAL RESPONSE
-------
effective and safe sampling and personnel protection procedure
were developed for these activities.
^ Another FIT team designed and fabricated a down-hole sampler
for studying in situ emissions of organic vapors during drilling
operations. When hooked up to a Photo-Vac unit, the sampler pro-
vides real-time data on potential organic vapor releases from the
soil and groundwater. Immediate or real-time data allow the field
scientist to be more selective about where to take samples down-
hole. These samples are then sent to a laboratory for confirmation
of the field data. The technique saves time, sampling collection and
analysis costs and provides an early indication of the order of
magnitude of the subsurface problem.
^•Around-the-clock sampling was carried out by the Region X
team for six consecutive days during an aquifer pump test at the
Lakewood Water District site in Washington. The data obtained
from a continuous three-day sampling during both drawdown and
aquifer recovery enables a hydrogeologist to determine the aquifer
characteristics and any change in contaminants entering the
aquifer. While tedious and time consuming, the technique has
proven itself in practice to be worthwhile.
^•Special techniques for sampling mining and wood preservative
wastes are in use in Regions VII and X.
^•The Revion IV FIT provided an electromagnetometer and
magnetometer survey on a landfill in Alabama on a restricted time
schedule in support of a criminal investigation.
^•Immediately following a warehouse five in Canton, Mississippi,
a Region IV FIT sampling team found and removed several boxes
of sodium cyanide among auto and plumbing parts. This swift ac-
tion removed a danger to the neighborhood.
*-In Oct. 1982, eight of 45 wells sampled in Perdido, Alabama,
were found to be contaminated with benzene. The wells were con-
demned, forcing the residents to use drinking water from mobile
tanks. Through the use of resistivity testing and geophysical well
logging, the FIT provided information that determined the extent
and degree of the contamination. This was done with minimum
disruption to the residents.
REM Activities
REM activities were started on 222 of the 419 sites on the Na-
tional Priorities List from Oct. 1, 1982 through June 30, 1983.
Specific activities include 186 RAMPs, 9 IRM projects, 26 remedial
investigations and 25 feasibility studies. Several projects were also
initiated to support enforcement related activities. The following
summaries illustrate typical remedial activities. In addition, de-
tailed project summaries for two sites are provided at the end of the
paper.
^•Focused feasibility studies were developed to assess the cost ef-
fectiveness of permanent relocation for the Minker Stout site in Im-
perial, Missouri, which was contaminated with dioxin and for the
Mountain View Mobile Home Estates in Globe, Arizona, which
was contaminated with asbestos.
^•A feasibility study for the Outboard Marine Corp. site,
Waukegan, Illinois, involved dredging the sediments in the harbor
contaminated with PCBs.
^•For the Chem-Dyne site in Hamilton, Ohio, an initial remedial
measure was authorized to relocate a power line to enable the
cleanup contractor to drain, dismantle and remove several bulk
storage tanks.
^•The design of a carbon system was necessary for the removal of
trichloroethylene and other organic solvents from groundwater for
the New Brighton/Arden Hills site in Minnesota.
^•A special catamaran-style vessel was designed and built to
facilitate sampling on a waste oil and wastewater lagoon at the
Bridgeport Rental and Oil Services Site in Gloucester, New Jersey.
^•Advanced geophysical techniques are being employed to deter-
mine the locations and attitudes of bedrock fractures under the
Krysowaty Farm Site in Somerset County, New Jersey, where bulk
and containerized liquid chemical wastes were dumped in a remote
ravine and threaten potable water supplies.
^•Two computer models are incorporated in the remedial investiga-
tion for the New Bedford Harbor Site in Massachusetts. One in-
volves the food chain uptake, particularly for lobsters and other
shellfish, and the second addresses the movement of contaminated
sediments by ocean currents.
Subcontracting Activities
The two contracts contain a total of $60 million in subcontract-
ing funds over the four-year period of performance for other firms
to assist in the REM/FIT work. Goals have been established to
award 30% of the funds to Small Business Enterprises (SBE) and
10% to Socially and Economically Disadvantaged Business Enter-
prises (SDBE) such as minority and women-owned firms. In addi-
tion, preference is given to firms located in Labor Surplus Areas
(high unemployment areas) (LSA).
As of June 30, 1983, the program is far ahead of its goals. Over
60% of the subcontract funds committed have gone to SBEs and
24% to SDBEs. In addition, 22% of the subcontracts have been
awarded to LSA firms. A more detailed summary is provided in
Table 1.
Principal services that are subcontracted include engineering,
field services (well drilling, sampling, land and aerial surveys, etc.),
computer services, data and records research, community relations,
construction and expert testimony. Examples include subcontracts
for expert testimony about potential environmental impacts of a
specific chemical upon groundwater in support of USEPA enforce-
ment activities, basic ordering agreements for engineering services
for the preparation of RAMPs and RI/FS projects, soil sampling
for dioxin, well drilling for groundwater contamination and air
monitoring.
To date, over 750 firms have filed qualifications and experience
statements with the prime firms. Opportunities still exist for addi-
tional firms to express their interest in serving as a subcontractor.
For this purpose, any interested firm should contact the subcon-
tracts administrators of the two prime firms.
Table 1
REM/FIT Subcontract Activities (6/30/83)
Total
SDBE
SBE
LSA
No. of
Contracts
Amounts
195 41 131 35
$7,599,630 $1,844,271 $4,589,901 $1,635,381
EXAMPLE REMEDIAL PROJECTS
Two projects have been selected to illustrate the scope of ac-
tivities performed under REM/FIT. 'One project, decontamination
of Municipal Water Well 12A in Tacoma, Washington, involves
the installation of a treatment facility and has advanced to the
operational phase. The other project involves building demolition
and on-site containment measures at the Silresim Chemical Corp.
site in Lowell, Massachusetts. Planning for an initial remedial
measure has been completed and implementation is ready to begin.
In Apr. 1982, USEPA, with contract support from Black and
Veatch, Inc., began an investigation of the extent and nature of the
contamination found in Well 12A. The results indicated that there
was a dispersed underground plume of organic solvent contamina-
tion. The highest concentrations, reaching into the /ig/1 range, were
immediately to the northeast of Well 12A. Identifying the specific
source(s) of contamination was not in the scope of this initial
assignment but is being addressed in a subsequent assignment.
Decontamination of Municipal Water Well
The South Tacoma Channel site, which lies within the Puget
Sound's Commencement Bay area, includes an area of approx-
imately 10 mi2 throughout a heavy industrial and commercial area
(Figure 3).
REMEDIAL RESPONSE
315
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• EXISTING CITY WATER WELLS
•CALI IH 'IIT
Concentration
Figure 3
Existing City Water Wells
Although there are several areas of concern within the South
Tacoma Channel itself, the first problem to be addressed was the
contamination of the City of Tacoma drinking water wells with
chlorinated organic solvents. These solvents were first detected in
Well 12A in Sept. 1981. At that time, the city, in cooperation with
the Washington State Department of Social and Health Services,
voluntarily removed the well from service.
Well 12A is one of 13 wells in Tacoma's largest municipal well
field and is located nearest to and immediately southwest of the
general area suspected of being the source of contamination
(Figure 3). Groundwater hydrology studies have indicated that
when Well 12A and the other municipal wells are in operation, the
hydraulic gradient runs from the contamination source area toward
Well 12A and the entire well field. An ever-increasing plume of
contamination was expected to spread throughout the well field
unless some remedial action was taken.
Historically, during July, August and September, the 13 wells in
the field have supplied as much as 30% of Tacoma's water. Total
capacity of the well field is 45 mgd. The closing of several major in-
dustrial plants due to economic conditions during 1982, coupled
with abnormally abundant surface-water supplies, reduced summer
demand. Consequently, the majority of the 13 wells were not re-
quired during 1982. However, the reopening of industrial plants in
1983 indicated that water from the well field would be required.
Because the contamination source was unknown, USEPA asked
CH2M Hill to perform a focused, or fast-track feasibility study
during Jan. 1983, to determine the most feasible and cost-effective
remedial action that would (1) prevent the spread of further con-
tamination into the well field and (2) supply Tacoma with enough
water to meet anticipated peak summer demands.
CH2M Hill first determined that an alternative supply of water
for the city was unavailable. Further, CH2M Hill found that Well
12A, being nearest to the contamination source area, could be
pumped at or near its maximum capacity and could effectively
serve as a blocking or barrier well. If Well 12A were not pumped
and the other wells in the field were, concentrations of pollutants at
the other wells could be expected to increase gradually as the con-
taminated plume was pulled farther into the well field. However, if
the water from Well 12A were brought to the surface, it would have
to be treated either for comsumptive use or discharge.
Design
Well 12A was contaminated with:
Contaminant
1,1,2,2-tetrachloroethane 17 to 300
1,2-transdichloroethylene 30 to 100
trichloroethylene 54 to 130
tetrachloroethylene 1.6 to 5.4
Based on an analysis of groundwater hydrology, the maximum
contamination detected to the northeast of Well 12A and the an-
ticipated effects of aquifer dilution, CH2M Hill selected an influent
level concentration of 1,000 /tg/1 of total chlorinated hydrocarbons
for the design of the treatment system.
The minimum acceptable blocking flow rate for Well 12A was
determined to be 2,000 gpm. However, maximum blocking effect
could be achieved if the well were operated at its maximum possible
flow rate of 3,500 gpm. Because the city indicated that it probably
would make maximum use of Well 12A to meet peak water
demands, CH2M Hill established a design flow rate of 3,500 gpm.
Alternatives Analysis
CH2M Hill screened several treatment alternatives and discarded
them as not feasible. Conventional treatment processes such as
coagulation and sedimentation, softening, filtration and chlorina-
tion cannot control volatile organics. Ozone has been used in
laboratory and pilot studies but with only limited success. The
technologies worthy of consideration, therefore, included aeration
and adsorption on granular activated carbon.
Two types of aeration are generally used: diffused aeration
systems which bubble air through the water and air stripping towers
in which water cascades down the tower through a porous medium
while air is forced upwards, countercurrent to the water. Air strip-
ping towers are generally more efficient and cost-effective than dif-
fused aeration systems.
Volatile organics also can be adsorbed with granular activated
carbon. However, laboratory-scale pilot tests found that for the
contaminants in Well 12A, removal efficiencies were significantly
less than those given for forced air stripping. CH2M Hill recom-
mended that the cost-effective technology for the removal of the
volatile organic contaminants at Well 12A was forced air stripping
in a packed tower system.
System Design
A preliminary review of the data suggested that 1,1,2,2-tetra-
chloroethane was the most difficult of the contaminants to remove.
Removal of volatile contaminants is a function of their volatility as
measured by the Henry's Law coefficient. To put this problem into
perspective, the coefficient for the most common volatile organic
hydrocarbon, trichloroethylene, is 290 atmospheres and that for
1,1,2,2-tetrachloroethane is 11 atmospheres. Thus, if 1,1,2,2-tetra-
chloroethane can be removed to acceptable levels, the other volatile
contaminants should be more than adequately removed.
A series of laboratory-scale pilot tests verified the removal effi-
ciency of the compounds and determined if there were any interac-
tions among the compounds that would interfere with their
removal. The results of the pilot testing compared favorably with
those reported in the literature and, as predicted, 1,1,2,2-tetra-
chloroethane dictated the overall removal efficiency.
Full-scale air stripping towers were designed from the pilot plant
data. The design was then analyzed to determine the optimum
number and size of towers and the overall contaminant removal ef-
ficiency, per tower, that could be anticipated.
The cost-effectiveness curve for a 3,500-gpm tower system i»
shown in Figure 4. It is cost-effective to consider going from four to
five towers in terms of the percent removal of 1,1,2,2-tetrachloro-
ethane versus cost. Beyond five towers, the curve breaks sharply
upward.
This treatment system will achieve approximately 90% removal
of the major contaminant. This removal level, considering further
316
REMEDIAL RESPONSE
-------
dilution of the Well 12A discharge with other well discharges prior
to mixing in the city distribution system, is sufficient to meet the
applicable health standards recommended by the Washington
Department of Social and Health Services.
As designed, each of the five 12-ft-diameter forced air stripping
towers contains 21 ft of 1 in. plastic saddle packing. The height of
each tower, with stack, is approximately 50 ft. The 60 hp blowers
force 29,000 ftVmin of air through each tower. The treatment
system's effect on surrounding air quality is insignificant. Com-
puter modeling indicates that the maximum ground level concen-
trations of volatile organics due to the air stripping towers are
several orders of magnitude less than current recommended stan-
dards.
Contracting
Overall responsibility for construction, testing and startup of the
facilities was assigned to CH2M Hill. This was done to maintain
continuity on the project and to meet the very short startup date of
July 1, 1983. Five subcontracts were developed for procurement
and construction. The first four, awarded during March and April
1983, covered the five fiberglass towers, the tower packing
material, fan (blower) units and prefabricated piping. A single, on-
site construction contract, also awarded in April, was developed to
NOTE: NUMBERS SHOWN NEAR DATA POINTS INDICATE
THE NUMBER Of 12 FT. DIAMETER TOWERS REQUIRED.
EACH WITH 21 FT. OF PACKING.
I REMOVAL . I.I.:.] TETRACHIOROETHANE
Figure 4
Forced Air-Stripping Towers/Cost vs. Removal
assign all coordination and site construction responsibility to an ex-
perienced contractor.
Each subcontractor was selected through a bidding process in
which from four to eight qualified firms were asked to prepare
fixed price bids on the subcontract package. This included defined
scope of work, schedule and contract terms. Overall, 30 firms were
given the opportunity to bid on this work.
Firms which could meet the project's time schedule with the
lowest fixed price bid were selected. The total bidding, evaluation,
award and approval process took one month. USEPA received all
proposed subcontracts before they were signed. All five subcon-
tracts were awarded to small business firms and three, amounting
to about two-thirds of the total dollar amount, went to minority
and women-owned firms.
The estimated cost at completion of these subcontracts and the
associated construction management services is approximately
$850,000 compared to the $920,000 originally authorized by
USEPA.
Construction
The subcontractors started as soon as USEPA approved the con-
tracts. Shop fabrication of the fiberglass towers started on Mar. 30,
and all five towers were delivered within 11 weeks. About 14,000 ft3
of tower packing material was delivered by truck starting in mid-
April and continuing into early July. The fan units and piping also
arrived on-site to be assembled by the construction contractor as
his work progressed. The site contractor's work involved the
following:
•Site preparation, including moving some existing facilities
•Trenching to install piping for the system
•Forming and pouring 3000 ft3 of concrete for the tower and fan
base pads
•Construction of an effluent diversion valving system in a buried
vault
•Erection of the towers; installation of the packing material
•Mounting and connecting the fans, motors and noise abatement
silencers
•Fabrication and installation of piping valves
•Installation of electrical controls and wiring
Two photographs of the construction in progress are shown in
Figures 5 and 6. Each tower is 12 ft in diameter and 50 ft high.
When mounted in place, each fan unit stands about 9 ft high. Well
water is distributed to the towers by a 24 in. piping header. An 8 in.
pipe then carries the water to the inlet distributors of each tower.
At the base of each tower a large 10 in. water trap in the discharge
piping prevents air leakage from the tower into the water system.
Construction was essentially completed before major summer
demands on the system occurred and the system was tested and
placed into operation. The fast-track schedule, consisting of in-
vestigation, design and construction, took less than four months.
This was less than one-third of the normal schedule for such a pro-
ject.
Operation
At this point, responsibility for the facility has been turned over
to the City's Water Division. Tacoma will operate the well and the
treatment towers any time its water demand requires use of the well
field. The pumping of Well 12A will block the spread of con-
tamination to other wells and will contribute to the cleanup of the
contaminated aquifer. Depending on the measured quality of the
treated water from the system, Tacoma may direct it into either a
reservoir for use in the water system or to the storm drain system.
At this time, it is not clear how long the system will be needed on
well 12A. USEPA is aggressively proceeding with additional ac-
tivities to locate and quantify the source of contamination, so that
measures can be taken to permanently correct the situation. In the
meantime, the Tacoma well 12A towers are operating evidence of
USEPA's commitment to the protection of public health and
welfare from uncontrolled toxic materials.
Cleanup of Silresim Chemical Waste Site
The Silresim Chemical Corporation in Lowell, approximately 10
miles north of Boston, occupies approximately 15 acres of land in
an area that includes numerous small businesses and one-story
buildings (Figure 7). Figures 8 and 9 are photographs of existing
conditions.
Prior to going out of business in Dec. 1977, Silresim processed
industrial waste. It was the largest corporation of its type in New
England. Federal and state environmental agencies placed certain
conditions on continued operations at the plant which the company
could not meet. As a result, the build-up of the number of barrels
containing waste material reached dangerous proportions.
Ultimately, 23,000 drums of toxic chemicals and industrial solid
waste were removed over a two-year period (1980-1981).
An estimated 6,000 gal of toxic chemicals have seeped into the
ground as a result of ruptured drums. Principal contaminants iden-
ified at the site are listed in Table 2.
Several investigations conducted at Silresim indicate that:
•Surface drainage is generally to the west-northwest toward River
Meadow Brook
•Groundwater is contaminated near the site. The plume is 50 ft
deep and covers an area 1,000 ft (north-south) by 800 ft (east-
west)
•Groundwater flow is generally to the north with an estimated
velocity of 16 ft/yr
•Approximately 6,000 gal of volatile organic compounds have
contaminated the site; approximately 8% is dissolved in the
groundwater and 92% is contained in soil
REMEDIAL RESPONSE
317
-------
Figure 5
Three Towers in Place
Figure 6
Five Towers in Place
•Maximum levels of volatile organics exceed 1000 ppm in the soil
at the 5 to 10 ft depths and 100 pg/1 in the groundwater at a depth
of 15 ft
•Surface and subsurface soil contamination extends beyond the
site boundaries
•Volatilization to the atmosphere and transport by groundwater
are the major contaminant pathways
With this information, USEPA asked NUS Corporation to
prepare a Remedial Action Master Plan. The RAMP called for In-
itial Remedial Measures (IRM) to protect humans from contact
with contaminated soils. Also, the RAMP recommended that the
on-site facilities be dismantled.
Initial Remedial Measures
The USEPA authorized an IRM for the Silresim Site in June
1983. the work consisted of dismantling and disposing of selected
buildings and tanks, followed by installation of a temporary clay
cap, a gas collection and treatment system and surface drainage.
The project is aimed at preventing air emissions and contaminated
surface runoff from leaving the site and minimizing the infiltration
of rainwater through the contaminated soils. A remedial investiga-
tions/feasibility study will be performed concurrent with the IRM
to select the final remedy for the site. This study will address both
on-site conditions and off-site contamination, primarily con-
taminated groundwater.
NUS began the planning for the IRM in May 1983, so that the
remedy could be completed during the 1983 construction season.
The subcontractor procurement process was started and pre-
qualified subcontractors were provided with requests for bids to
conduct the first phase of the IRM. The initial subcontract for
dismantling the building and tanks was awarded, and a second sub-
contract for construction of the cap is scheduled for award during
Sept.
Engineering Design for Dismantling
On-Site Facilities
An engineering design and bid specifications were needed for
dismantling the faculties. The objective of the design was to
Table 2
Chemkab Detected at Stlrate, 1M2
VotatUe OrgMks
dichloromethane
1,1 -dichloroethylene
1,2-transdichloroethylene
1,1-dichloroethane
chloroform
1,2-dichloroethane
1,1,1 -trichloroethane
1,2-dichloropropane
trichloroethylene
benzene
1,1,2-trichloroethane
tetrachloroethylene
1,1,2,2-tetrachloroethane
toluene
chlorobenzene
ethylbenzene
trichlorofluoromethane
ityrene
dimethyl formamide
tetrahylfonnamide
tetrahydrofuran
dimethylsulfide
Pesticides
lindane
2,4-dichlorophenoxyacetic
acid (2,4-D)
2,4,5-trichlorophenoxypropionic
acid (2,4,5-TP)
PCBs
Arochlor 1016
Arochlor 1248
CHUMD fTONC
(iT-OMC HM-.
UK CWMf • r THC«
TO» eouwci
Figure 7
Site Map — Silresim Chemical Corp., Lowell, MA
318
REMEDIAL RESPONSE
-------
Figure 8
Existing Buildings
Figure 9
Existing Tanks
minimize the potential for disturbing surface soils and the possibil-
ity of direct contact with soils. This was accomplished by covering
the site with a base course of crushed stone during removal of the
numberous buildings and storage tanks from the site. The stone
will serve as a protective barrier from contact with the soil, will
eliminate the potential for disturbing surface soil, and will serve as
the base course for the impermeable cap to be installed at the site.
The engineering design also specifies the use of dismantling
techniques rather than demolition. The use of blasting is pro-
hibited. Concrete will be broken by using drills and an expandable
grout instead of wrecking balls and jackhammers. Concrete
footings and slabs will be left in place to avoid disturbing the soil.
The use of cutting torches will be minimized and closely monitored.
All dismantled facilities, except the buildings, will be decon-
taminated, cleaned and removed from the site. The buildings
located on-site also will be removed, although they do not require
decontamination. The NUS site management team will monitor the
decontamination process to ensure compliance with the specifica-
tions.
Engineering Design for Sealing
The surface of the site and adjacent off-site areas will be sealed
with a temporary impermeable cap. The cap will:
•Limit direct contact exposure to the contaminated surface soils
•Prevent contamination of surface runoff
•Reduce contamination of the groundwater by eliminating infil-
tration through the contaminated soils
•Reduce odors emanating from the site
The cap will be compatible with the base course material placed
on the site for dismantling. Also, the cap will be compatible with a
permanent capping alternative if capping is included as a final
remedial action. Finally the cap will be constructed with cost-
effective materials that will provide the required protection and
have the potential for being part of a permanent system.
A gas-venting system is required since natural and biologically
derived gases will be generated in the contaminated soils beneath
the cap. The venting system is designed to allow surface monitoring
of the gases after installation of the cap. The design also provides
for directing the gases to a central location for treatment if air
monitoring indicates treatment is required.
Finally, the cap design includes a storm water runoff collection
and diversion system. The system includes grading and revegeta-
tion, draining ways and a retention basin. The storm runoff collec-
tion and diversion system will use the existing right-of-way for a
public storm sewer that passes adjacent to the site and discharges to
Meadow Brook. The design requires safe discharge of a 100 yr
storm.
Other IRM Activities
A testing program will be conducted to determine what objects
exist beneath the surface and if they should be removed. This is be-
ing done based upon reports from local residents that containers
may have been buried at the site. A survey was conducted with a
metal-detecting instrument, which had a depth of penetration of
approximately 3 ft. This survey identified areas with unexplained
anomalous readings. Since metal drums are a commonly used
method of containment, NUS will use a two-phase exploration pro-
gram to locate metallic and non-metallic subsurface containers.
The first phase will be a magnetometer survey, while the second
phase will involve the excavation of exploratory test pits.
The test pits will be used to check areas identified as possibly
containing buried objects. The specification requires that a rubber-
tired backhoe equipped with a nonsparking bucket be used to
minimize disturbance of surface soil and to prevent sparks. Con-
tinuous air monitoring will be required during excavation. If buried
drums containing chemicals are encountered, their position will be
marked for removal under separate contract. Excavations that do
not encounter buried objects will be backfilled with the excavated
soils in accordance with specifications.
Neighborhood Contingency Plans
The need for relocation of the local population is considered
unlikely. The dismantling and sealing of the site will be conducted
in a manner to minimize disturbance to the surface soils, and to
"dismantle" rather than "demolish" the facilities. However, as a
precautionary measure, NUS and several federal, state and local
government agencies are preparing standby plans for emergencies.
Plan details include arrangement for broadcast of emergency infor-
mation on radio, television and police loud-speaker. Specific plans
have also been prepared for transportation, area security and tem-
porary shelter should relocation become necessary.
CONTRIBUTORS
Tacoma Well 12A project writeup prepared by R. Schilling, Site
Project Manager and R. Rosain, Assistant Project Manager of
CH2M Hill.
Silresim Chemical Waste project writeup prepared by Patrick
Falbey, Project Manager and George Gardner, Project Engineer of
NUS Corp.
Initial draft of remaining material prepared by James R.
Woglom, former Zone II Program Manager for CH2M Hill.
REMEDIAL RESPONSE
319
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EXPEDITIOUS COMPLETION: A FORGOTTEN GOAL
JAMES C. SCOTT
ROBERT B. PEARCE
Black & Veatch
Detroit, Michigan
INTRODUCTION
In Oct. 1981, a paper' was presented at this conference on the
Berlin & Farro Liquid Incinerator, a hazardous waste site near
Flint, MI. Black & Veatch was appointed Receiver by the Gen-
esee County Circuit Court in Sept. 1980. Initially, the firm's
assignment was to act as manager of the cleanup activities. How-
ever, the role soon evolved into one of providing evaluation and
technical recommendations to the judge.
In 1981, the site was declared a hazardous emergency by the
Governor. Since 1981, Berlin & Farro has moved to first on the
priority ranking of hazardous waste sites in the State of Michigan.
The State Legislature appropriated additional monies for site clean-
up. A cooperative agreement between the State and USEPA was
executed. Superfund monies were granted for immediate waste
removal and continuing investigation. The court intervened and
provided direction for specific action. In spite of these apparently
positive actions, only limited cleanup has been accomplished.
The first Formal Administrative Complaint in this case was filed
against Berlin & Farro Liquid Incineration by the State of Mich-
igan in 1973. A suit was initiated against the firm in 1979. There
is repeated reference in the court orders to the need for "expe-
ditious" action or completion. Random House dictionary indi-
cates that expeditious is "characterized by promptness" and that
prompt means "done...without delay."
CONTRIBUTING FACTORS
Numerous factors are responsible for the cleanup delays. While
the items to be discussed here are project specific, they are rep-
resentative of the types of factors that are likely to be encountered
in many hazardous waste cleanup projects. Awareness of these
problems may provide a basis for initiating mitigative measures if
similar difficulties are anticipated in other projects.
Bureaucratic Encumbrances
In 1981, the authors reported' that responsibility for directing
actions at this site had been transferred from one State agency to
another. Responsibility was subsequently reversed again. Struggle
within the State agencies for ultimate jurisdiction and authority
was conspicuous and appears to have caused significant delays in
the cleanup. Not only were inter-agency disagreements evident,
but intra-agency disputes developed as well. The role of the Re-
ceiver was to assist the judge in understanding the technical issues
and arguments in this chaotic period. Even though State agencies
should have provided unbiased opinions to the court, many ex-
amples of poor analysis and incomplete planning by the State
agencies were found.
In 1983, there were several major public administration changes
which markedly affected this project. A new governor was elected
for the first time in 14 years, thus creating changes in major de-
partment heads. In addition, a new judge was elected to the circuit
court. With these changes came the delays resulting from the need
for familiarization. There were also changes in direction as a re-
sult of new opinions.
During a court hearing in Aug. 1983, another bureaucratic
difficulty became apparent. Under the cooperative agreement be-
tween the State and USEPA, the State had been designated the
lead agency. USEPA, however, indicated that this relationship was
only effective during periods of normal remedial activities. In in-
stances where emergency funding and actions are provided,
USEPA advised that they claim total control over the emergency
work and any portions of the site effected by their activities. In a
situation where the State court has repeatedly announced its con-
tinuing jurisdiction, the conflict is obvious.
Technical Opinion
In Apr. 1983, a court hearing was held, resulting in a major
change in direction in cleanup activities. This hearing was orig-
inally scheduled to provide a basis for reporting progress in the
cleanup but evolved into a forum for debate of the announced in-
tention of the State agencies to defer cleanup activities until the
fall of 1983. The decision to delay had been reached by the new
governor on the basis of advice received from his staff. However,
the State agencies were now cross-defendants in the lawsuit and
were called upon by the Court to justify their decision.
The hearing started early one Saturday morning, was interrupted
only briefly for a lunch break and continued until 10:00 p.m.
The majority of the testimony during this long hearing came from
technical representatives of State and federal agencies. The testi-
mony was particularly interesting in three respects: (1) the extent
to which the witnesses disagreed, (2) the extent to which witnesses
were willing to rely on assumed or statistical projections and (3)
the ultra-conservative nature of some of the underlying technical
assumptions.
Controversy on the issue of continuing or deferring cleanup had
arisen as a result of fears that the impending warm weather would
aggravate the emission of volatile hazardous materials from the
site. Representatives from departments commonly associated in
remedial and response activities tended to favor continued clean-
up and believed that appropriate controls could be exercised to
allow safe and expeditious completion of the work in warm
weather. Representatives from agencies more commonly associated
320
REMEDIAL RESPONSE
-------
with evaluative activities and standard setting tended to favor con-
tinued observation and study rather than continued cleanup.
Blind faith in historical information provided a lighthearted
moment. One witness testified that the current warm dry trend
would continue for at least five days. The witness was so con-
vinced of the accuracy of the projections that they stated all of
their predictions were going to occur with nearly 100% certainty.
Later that evening, the authors had great difficulty in finding their
way home due to an intense storm which blanketed the Flint area
with 6 to 8 in. of snow. The authors jokingly concluded that since
the weather predictions had been so accurate, the remaining pre-
dictions made during the hearing were likely to all come true.
The impractical nature of some of the technical opinions and
recommended controls were a further impediment to the cleanup.
Based on hearsay, there was concern that both cyanide and acids
might be present in the materials on the site in sufficient quan-
tities to provide a reaction and emission of cyanide gas. Staff from
the State had carefully modeled the area and assumed a worse case
scenario in which violent reaction occurred, weather conditions
were least advantageous and emissions at the boundary resulted.
Not only did it appear that great confidence was being placed in a
model which was generated from an assumed and empirical base,
but the allowable cyanide exposure levels at the boundary were also
unbelievably conservative. The allowable exposure had been set at
a level many times lower than the exposure levels that are accep-
table for cyanide gas in an industrial working space.
The variety of testimony made it evident that the new governor
must have found it extremely difficult to evaluate the question of
continued remedial action. The opportunity for in-depth question-
ing at the prolonged hearing and the wide variety of witnesses re-
sulted in a different conclusion being drawn by the Court; so much
so that the Court appointed a special Administrator to direct the
cleanup activities and instructed the Administrator on the goals to
be achieved. However, even this direct intervention has not re-
sulted in achievement of the intended goal.
Legal Constraints
In 1981, the authors reported1 that legal constraints were en-
cumbering progress. The bankruptcy of Berlin & Farro had re-
sulted in a temporary restraining order being imposed by the fed-
eral bankruptcy court which stopped cleanup activities. Owner-
ship of a portion of the site by another party interfered with the
right to access and enforcement. As these legal difficulties were
overcome, it appears the State agencies failed to use the judicial
process to its maximum advantage. Having obtained the ability to
proceed, the State agencies failed to follow the agreed upon plans
for remedial action. This failure prompted intervention and caused
the State agencies to become defendants in the lawsuit. This legal
maneuvering significantly delayed the cleanup work.
Contracting
The State agencies divided the remedial action at the site into a
variety of individual contractual elements, i.e., fencing, sludge re-
moval, liquid and tank removal, drum removal, hydrogeologic
study, etc. Efforts were made to contract the work for each element
by solicitation of separate competitive proposals. Ideally, such an
approach should bring specialists to bear on each area of need, but
it also carries with it the need for extensive coordination. In reality,
the multiple contract approach appears to have fostered confusion,
higher costs, lack of federal support and time delavs.
Broad general contracts are intended to place the responsibility
for cost control and subcontractor coordination with a contrac-
tor that is experienced and successful in these types of activities.
Broad general contracts also allow the administrative effort to be
focused on a single company and provide a better opportunity for
responding to changes in the work as it is performed. The authors
believe such an approach would have benefitted this project.
It appears that both the State and federal agencies favor the seg-
mented approach. While the segmented approach provides an
opportunity for a more exact evaluation of specific items of work
and of specific funding actions, it greatly delays the cleanup. In
this case, a specific contract was expanded in scope to expedite
completion of the work. USEPA has now indicated that the addi-
tional work will not be eligible for federal funds due to the lack of
competitive solicitation of bids. State funds have been exhausted
and effective remedial action has been brought to a standstill.
Availability of Funds
In 1981, the authors stated1 that "Money has and will continue
to be the key issue." Nothing that has happened in the past two
years suggests that this will change. The State has expended over
$4 million in the cleanup process. The USEPA has made some con-
tributions, but appears to seek every opportunity to avoid doing so.
USEPA funds are, of course, limited and USEPA has asserted
that one of its primary objectives is maintaining the ability to
achieve cost recovery from industry. Any activity which might
jeopardize this opportunity is apparently not acceptable to
USEPA.
CONCLUSIONS
One of the conclusions drawn in the 1981 paper1 was:
"A realistic assessment should be made at the onset regarding
desired results and the time for accomplishment. Wasted effort
and lost time will otherwise result."
Unfortunately, this basic concept has not been followed at
Berlin & Farro. It is obvious that a realistic assessment has never
been made, cleanup has not occurred and considerable wasted
effort has resulted.
As Receiver, the authors' firm continually calls attention to the
need to overcome this deficiency, but the contributing factors dis-
cussed above have prevented this from occurring.
The Berlin & Farro site cleanup is a task which, if properly
planned, should have taken only a few months for implementa-
tion. After more than two years, the cleanup is only half com-
pleted. It is now being suggested that the final cost of cleanup at
Berlin & Farro will be more than double the funds expended to
date. Along with these high costs, and in many instances contrib-
uting to them, are associated delays in completion of the work.
Public dissatisfaction with the repeated and extended delays has
been pronounced to the point that a state representative, a town-
ship supervisor and private citizens have brought suit against agen-
cies of the State of Michigan for failure to achieve a solution. This
caused some agencies which initiated action as plaintiffs to become
cross-defendants. Further, the Court pre-empted the decision mak-
ing authority of the State agencies and directed remedial action.
The authors believe the Receiver, as a non-adversarial tech-
nical adviser to the Court, has played an effective role in assist-
ing the Court in its efforts. Improved cooperation between State
and federal agencies and continuity in their objectives would have
further improved the results. Administrative changes such as the
utilization of a broad general contract would also have worked to
advantage.
The Court and the public have sound reason for calling for
"expeditious completion." From a contractual standpoint, it re-
duces cost. From an environmental standpoint, it increases bene-
fit. From a political standpoint, it provides public satisfaction.
The nation's approach to cleanup activities must be modified if it
is to fulfill this demand for timely results.
REFERENCES
1. Scott, J.C. and Pearce, R.B., "Forced Cleanup: A Police Action or a
Moral Judgement," Proc. Second National Conference on Manage-
ment of Uncontrolled Hazardous Waste Sites, Oct. 1981, Washing-
ton, D.C.255-258.
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HAZARDOUS WASTES WORKER HEALTH
AND SAFETY GUIDELINES
LYNN P. WALLACE, Ph.D.
WILLIAM F. MARTIN
Department of Health and Human Services
Public Health Service
Centers for Disease Control
National Institute for Occupational Safety and Health
Cincinnati, Ohio
INTRODUCTION
Man has been faced with waste problems since he threw away the
first food scraps, bones and used clothing. These were not very
hazardous to his health except for sanitation and nuisance. As man
has left agriculture and become involved in commercial and indus-
trial pursuits, workers have increasingly encountered materials that
affected their health and safety. The mining of mercury ore (cinne-
bar) in Roman times is one recorded example of a recognized haz-
ard for which worker protection was attempted.' As more and
more man-made or synthetic materials have been developed and
utilized, the exposure of workers to materials that are or can be
hazardous to health and safety has greatly increased. The science
and art of Industrial Hygiene has emerged over the years with the
express purpose of protecting workers who handle or are exposed
to materials or conditions that are hazardous or unsafe.
Unfortunately, while efforts were being made to improve work
conditions and reduce work exposures, very little was done to con-
trol the disposal of hazardous materials. Incidents such as "Love
Canal" and "Valley of the Drums" focused the attention of Con-
gress and the public on problems of hazardous waste disposal and
precipitated action to correct these problems. Public Law 94-580,
The Resource Conservation and Recovery Act of 1976 (RCRA),
and Public Law 95-510, The Comprehensive Environmental Re-
sponse, Compensation and Liability Act of 1980 (CERCLA or
Superfund) were two very important legislative actions passed to
prevent future disposal problems and to remedy past disposal prac-
tices.
These two pieces of legislation have had a profound effect on
the number of workers that are or can be exposed to hazardous
materials. It is estimated that up to 40,000 workers2 may be in-
volved in cleaning the estimated 30,000 abandoned sites' in the
United States that contain hazardous wastes. These numbers are
in addition to the workers involved with hazardous wastes at ap-
proved disposal sites. To this estimate must be added the workers
of other industrialized nations who will also be handling hazardous
wastes throughout the world.
Transportation accidents involving hazardous materials could
expose police, firemen, transportation employees and even entire
neighborhoods during efforts to contain and cleanup these mater-
ials. The total number of such accidents and persons who may be
exposed is anyone's guess, but it could happen anywhere that
trucks, trains, barges, airplanes and pipelines carry hazardous
materials.
Not only are many workers involved in the actual handling or
cleanup of hazardous wastes, but workers are also directly in-
volved in determining the extent or severity of the problems. Other
workers at neighboring facilities may not even be aware that there is
a potential for exposure. It is important to remember that each in-
dividual in this country has a legislated right to a safe work-
place.4
As a vital part of its studies of occupational environments and
worker health, the National Institute for Occupational Safety and
Health (NIOSH) has a long history of involvement in the study of
hazardous materials and their effects on workers. NIOSH has
developed and recommended standards for good workplace prac-
tices for government, industry and labor. NIOSH has also pro-
vided recommendations for specific problems through technical re-
ports, health hazard evaluations and health and safety guides for
both employers and employees. NIOSH has established an en-
viable record of accomplishments in worker protection and con-
tinues to be actively involved in health and safety considerations
for workers throughout the workforce.
It is not surprising that the majority of the chemicals studied by
NIOSH in the past have been identified by USEPA as those of
greatest concern at hazardous waste sites or during emergency ac-
tions. This experience with toxic materials and work environ-
ments was a very important reason that NIOSH was given spe-
cific responsibilities under the CERCLA-Superfund legislation5
for hazardous waste worker health and safety. These Superfund
responsibilities have expanded many on-going NIOSH research ac-
tivities that probe the interactions between worker and hazardous
work environments and have initiated other necessary investiga-
tions.
INTERAGENCY AGREEMENTS
Two Interagency Agreements between the Department of Health
and Human Services (DHHS) and USEPA have been enacted to
accomplish these responsibilities. These agreements outline the
scope of occupational health and safety activities and provide the
funding for their implementation. The two major activities are:
(1) to develop comprehensive guidelines for worker health and
safety and (2) to provide scientific support and training. In this
paper, the authors discuss the first of these two activities.
Comprehensive Guidance Manual
Comprehensive guidelines were developed under a Memorandum
of Understanding (MOU) signed on Dec. 18, 1980, by USEPA,
the Occupational Safety and Health Administration (OSHA), the
U.S. Coast Guard (USCG) and NIOSH. The four agencies, with
322
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NIOSH as lead, agreed to jointly develop a "Comprehensive
Guidance Manual" to be used by field supervisors and govern-
ment authorities.
Because of differences in anticipated user groups, including the
state and local bureaucracies that regulate such groups, it was de-
cided to present the guidelines in two separate volumes. Even
though they would be similar in outline and content, each vol-
ume had significant differences and was designed for a different
audience. Volume One deals with cleanup operations at remedial
sites where hazardous wastes are known to exist and where clean-
up will be undertaken. Volume Two deals with worker protec-
tion during accidental releases of hazardous substances and haz-
ardous waste emergencies.
The purpose of the two-volume "Comprehensive Guidance
Manual" is to provide consistent, sound and detailed occupa-
tional health and safety technical information to all those in-
volved in the management, cleanup, treatment and disposal of
hazardous waste. The Manual is designed for use by many agen-
cies: Federal, State and local government; emergency response
groups at all levels; cleanup crews; unions and employee groups;
and other public interest groups or individuals. The primary users,
however, will be those responsible for the management and super-
vision of workers involved in the cleanup and control of hazardous
waste.
NIOSH has completed the first drafts of the two volumes and
has submitted them to USEPA, OSHA and the USCG for review.
The Comprehensive Guidance Manual will be distributed to each
State and local control agency as soon as it is completed. This
paper will discuss only the contents of Volume I which deals with
cleanup operations at remedial sites.
CLEANUP OPERATIONS MANUAL
The Manual is divided into four sections, and a very large appen-
dix of technical information. Section "A" introduces the Manual
and contains its purpose and historical background. It defines the
waste disposal problem, the intended audience and outlines the
scope and Manual format. Section "B" discusses information
gathering processes and techniques from pre-entry to post closure
monitoring. This section is concerned with how to obtain the neces-
sary data to determine the extent of any hazards. Section "C"
covers information evaluation and hazard assessment procedures.
This section is designed to guide in evaluating the significance of
the data that are collected. Section "D" contains hazard control
programs including recommended administrative practices, work
practices, personal protective equipment, decontamination pro-
cedures, engineering controls, training requirements and medical
surveillance protocols. This section tells what should be done to
control or eliminate hazards to workers. The appendices contain a
variety of useful references and decision-making data that are use-
ful but encumbered the main sections of the Manual.
The Manual is a current state-of-the-art document and should be
a valuable tool to all who are involved in hazardous waste ac-
tivities. It contains guidelines and recommendations from which
standard operating procedures can be developed for state agencies
or specific sites. It is designed to be updated as additional in-
vestigative tools are developed or as the state-of-the-art improves.
The entire contents of this Manual would be too extensive to
cover in a short presentation such as this. Some of the interesting
aspects of the Manual are presented to give a flavor of what is
contained therein and to "spark" reader's interest.
It is not the intent of the guidance Manual to repeat basic in-
dustrial hygiene or toxicological information that could be found in
standard textbooks but rather to emphasize those techniques, prob-
lems and considerations that are unique at hazardous waste sites.
The guidance Manual discusses advantages and disadvantages of
various screening, sampling and monitoring techniques and makes
recommendations as to which may be best suited to a particular
circumstance or operation. Detailed information on methods, pro-
cedures, mathematical models and sampling strategies is contained
in the appendices. Guidance is given for monitoring and eval-
uating chemical hazards, physical hazards, safety hazards and
biological hazards that pertain to remedial actions.
The main premise of the Manual is that accurate information is
needed from which to assess the risks involved and make intelli-
gent decisions regarding worker protection. While this is not news
to those involved in hazardous waste activities, many decisions may
currently be based on inaccurate or insufficient information.
Selecting Worker Protection Levels
Many of the current methods for selecting worker protection
levels have developed as work has progressed and experience has
accumulated. When an individual approaches an unknown and
potentially hazardous environment, caution must indeed be taken.
Every effort must be extended to obtain pertinent information
from existing sources before physically entering a site. Experience
to date, however, consistently indicates lower levels of measured
contaminants than was anticipated. This would suggest that, in
most cases, lower levels of protection could therefore be required.
Because of the unknown elements or the uncertainty of many
situations, there is an extreme reluctance to lower levels of pro-
tection even when the collected data indicate that it is safe to do so.
It is certainly proper for first entry personnel to be over-pro-
tected until actual levels of contamination are determined. To con-
tinue to utilize extra protection when the data do not warrant it or
because insufficient data have been collected from which to make
intelligent decisions is an irresponsible action on the part of de-
cision makers. In addition, practice has led to increased opera-
tional costs and in some cases has actually contributed to occupa-
tional health and safety problems.
The conservative approach is taken mainly to protect workers
against exposure to chemical hazards. This becomes the overriding
hazard consideration and other hazards, such as physical or safety
hazards, may not be given proper consideration. If inn attempts to
protect against chemicals a worker suffers heat exhaustion, or is
run over by a piece of heavy equipment because his visibility was
restricted, or suffers back strain, or is severely cut or crushed,
has the worker's health and safety been adequately protected?
The conservative approach is often the correct method, but some-
times the productivity of the workers is unnecessarily restricted or
worker stress is excessive because the approach is too conserva-
tive for actual conditions. If a worker is injured by practices that
are supposed to protect him, these practices become a false form
of worker protection. Worker protection practices should be com-
mensurate with the hazards. This implies that the hazards must be
defined. Accurate information on existing or suspected hazards
must be obtained in order to properly define the hazard. The cost
of obtaining needed information prior to decision-making may be
considerably less than the cost of remedial actions based on in-
accurate or incomplete information.
IDLH LEVELS
The most important first task is to identify any conditions or
situations that may be immediately dangerous to life or health
(IDHL). This, of course, includes all such situations and not just
those associated with toxic chemicals. Monitoring for or identify-
ing IDLH situations must continue throughout the entire remedial
action at each site. One of the most effective methods to identify
many IDLH situations is to screen for explosive atmospheres, am-
bient air with insufficient oxygen to sustain life, air mixtures con-
taining volatile organics that may be toxic and particulates or non-
organic substances that may be toxic. When the screening indi-
cates a problem, more specific sampling should then take place to
properly define the problem.
The current procedure at many sites is to measure the levels of
volatile organics with an organic vapor analyzer (OVA) or an HNU
Photoionizer and determine the needed levels of protection based
on the obtained readings. The authors have learned that volatile
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organics, although almost always present in low concentrations,
are only one of several classes of materials that will be encountered.
Additionally, paniculate material, in the form of organic, non-
volatile organic or particulate-bound compounds may also be re-
sponsible for a large fraction of the overall chemical exposures
that might be encountered on or near a hazardous waste site.6
These and other contaminants may be missed by using only the
HNU or OVA instruments.
SDRITS
To help fill the gap and provide needed information for proper
decision-making, NIOSH developed a Simultaneous Direct Read-
ing Indicator Tube System (SDRITS) which concurrently draws
air through ten separate colorimetric direct reading detection
tubes.7 This device enables field personnel to complete the ten tube
scKening protocol suggested by Schneider with greatly reduced
sampling time.' The SDRITS was developed to detect the type
and extent of unconfined dangerous chemicals or their reaction by-
products, due to interaction with water, each other or fire and is
sufficiently sensitive to avoid acutely dangerous conditions. The
identification is limited to definition of various substance groups,
such as acid reacting substances, amines and alcohols. Substances
not included in the Schneider scheme (such as hydrogen cyanide
and hydrogen sulfide) can also be rapidly detected, either by de-
ployment of a second sampling device or by serial screening us-
ing a single device.'
By screening with a combination of the OVA, HNU, SDRITS
and other devices such as explosion meters and oxygen level in-
dicators, vital information can be obtained which will help inves-
tigators determine what specific additional sampling is required for
materials that are suspected or indicated to be present. The level
or levels of protection can then be set commensurate with the
actual problem or problems and not based on partial or perhaps in-
correct information. Using these screening devices and then samp-
ling or monitoring with more accurate instruments (gas chrom-
atograph and spectrometer, for example) that can detect actual
levels of specific contaminants is a preferred method of determin-
ing the actual hazard and more accurately assessing the risk.
PHYSICAL HAZARDS
Most of the lost work time at hazardous waste sites to date has
been from injuries due to physical hazards and not from ex-
posure to chemicals or toxic substances. Slips, trips and falls along
with back strains and cuts and abrasions are reported as the lead-
ing causes of workers being absent from work. All of the causes
for this phenomena may never be known, but it is postulated that
the loss of vision and agility from wearing protective clothing is a
contributing factor. The presence of sharp objects, unlevel ground,
improperly stacked barrels, deteriorated buildings and unstable
materials are all contributors to these accidents.
The problems of working in protective clothing and equipment
have additional ramifications. Excess water vapor inside masks and
facepieces can cause fogging and severely reduce vision. The nature
of many facepieces restricts the range of vision, especially per-
ipheral vision. The ability to communicate is reduced while wear-
ing a mask or hood. Thick gloves can severely reduce the manual
dexterity required to do certain tasks. Special boots or boot covers
can increase clumsiness and contribute to slips, trips and falls.
Bulky clothing can easily catch on protruding objects. The bulk
and weight of air tanks, hoses and controls carried for air supply
can both get in the way and increase fatigue. The ability to freely
or quickly exit during emergencies is often reduced.
Heat Stress
Another and perhaps more significant cause of lost or unpro-
ductive time is caused by conditions which produce heat stress. The
very nature of personal protective clothing and equipment causes
other problems for workers who must use them. Materials are
selected which will provide a barrier of protection for the worker by
keeping liquids, vapors, fumes and smoke from reaching the body.
These same barriers prevent body generated liquids and vapors
from escaping. This can be particularly devastating when workers
are subjected to ambient conditions which exacerbate this prob-
lem. Simply put, the body is designed to dissipate heat by sweat-
ing and evaporation. If the sweat is not allowed to evaporate be-
cause of a combination of impermeable clothing and hot, humid,
ambient conditions, the body cannot get rid of its excess heat.
When hard manual work such as lifting, pulling, shoveling, etc., is
required, additional stresses are placed on the workers and addi-
tional heat must be dissipated. As heat builds up in the body, it
causes a variety of strains leading to heat exhaustion and possible
heat stroke which can be fatal.
Add to these heat and work stress related problems the psycho-
logical stress of being surrounded by unknown toxic materials or
the claustrophobic impact of being enclosed in a fully encap-
sulated suit with increased breathing requirements due to a pro-
tective respirator, and the concerns for worker safety and health
are significantly increased.
When workers are grossly uncomfortable wearing protective
equipment while doing hard manual labor in hot humid con-
ditions, their reaction is to remove the protective equipment when
it may be unsafe to do so or to refuse to wear it. Unfortunately,
these same hot conditions usually increase the volatility of many
toxic materials and their ambient concentrations increase. To re-
move the protective equipment when toxic concentrations may be
the highest seems folly indeed, but when the temperature becomes
unbearably hot the temptation is great.
Working in protective clothing and wearing respirators can place
additional stress on the lungs and heart. Workers who have lung or
heart conditions should not be allowed to wear this equipment if
it could cause damage to their vital organs. Medical screening of
workers and supervision to determine if these workers can handle
the stress of wearing protective equipment is vital to their safety
and health. Consequently, some people should not be permitted
at hazardous waste operations if they cannot wear the special
clothing and equipment required for their protection. The sec-
tions on heat stress and medical monitoring should be very use-
ful to all who are concerned with worker protection.
If workers are required to wear excess protective equipment or
higher levels of protection simply because those in charge are not
willing to properly sample or monitor in order to specify the cor-
rect level of protection comensurate with the actual (not supposed)
conditions, then those in charge must accept responsibility for the
heat stress and other problems caused by wearing such equipment.
Where the protective equipment is required because of actual haz-
ards, then work schedules must be altered to provide the needed
rest and cool-down periods for worker health and safety. Physical
hazards that produce the slips, trips and falls must be removed.
Mechanical handling of heavy or contaminated objects must be in-
stituted. Engineered controls must be implemented and proper de-
contamination procedures must be followed. The cost for adjust-
ing to these conditions is certainly justified.
PERSONAL PROTECTIVE EQUIPMENT
One particular section on the selection, use and limitations of
personal protective equipment (PPE) should prove very useful. The
schemes suggested are perhaps different than existing USEPA lev-
els of protection in that respiratory tract protection is separate
from skin or body protection rather than being combined into a
level of protection. This scheme is based on the potential entry to
the body of toxic materials by either skin absorption or respira-
tory tract absorption and levels of protection are separately selected
commensurate with the separate problems.
The basic criteria for selection of PPE are as'follows:
•The characteristics of the substance (toxic, explosive, corrosive,
concentration, physical state, length of exposure, permissible ex-
posure limits)
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REMEDIAL RESPONSE
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•The work task to be performed (expected work duration, type of
work, level of physical effort, proximity to exposure)
•The protective equipment function (respiratory skin, face and
eye, foot, head, hearing, entry and fall)
•The environment (temperature, humidity, wind, effects on both
the worker and the PPE selected)
•Human Factors (susceptability to stress, weight of equipment,
physical fitness, acclimatization, age, medical history)
These factors all combine to select the final criteria:
•Protective ensemble (correct combinations of protective equip-
ment to satisfy the previous criteria)
The main point is that several factors must be simultaneously
considered in PPE selection. Different levels of protection may be
required for different jobs or for different locations on-site. It is
not an arbitrary "well let's specify level for everyone on site B to-
day" type of an approach if one truly has the total health and
safety of each worker as his objective.
The Manual contains a large section on the recognition, evalua-
tion and control of physical and safety hazards. This information
is in tabular form and contains the applicable regulations pertain-
ing to the hazards listed. The Manual also contains an extensive
site safety checklist. Both of these items should be very useful to
those concerned with remedial actions at hazardous waste sites.
Basic administrative and program requirements for proper site
control, work practices, emergency controls and safeguards, emer-
gency medical care, health surveillance and medical screening are
covered in the Manual. Because it was observed at some sites that
the highest levels of airborne contamination were measured in the
mobile laboratory and not where the remedial work was proceed-
ing, a section on health and safety controls for mobile labora-
tories is included.
APPENDED INFORMATION
The appendices contain sources of occupational health and safe-
ty data and information and describe the advantages and disad-
vantages of various computerized information systems as they
apply to remedial actions and hazardous substances incidents.
NIH/USEPA Chemical Information Systems, CHEMTREC, Na-
tional Response Center, Hazardous Materials Emergency Re-
sponse, MEDlars, Toxline, Library of Medicine and Orbit are some
of the computerized systems discussed. CHRIS Manual Informa-
tion, Hygienic Guide Series, NFPA Data Sheets, OHM-TADS File
listings and sample formats, RTECS, WDROP, FRSS, CTCP and
TSCAPP are other systems that are discussed.
The appendices also contain a sample Occupational Health and
Safety Program, Guidelines for Selection of Personal Protective
Equipment, more detailed decontamination procedures, a sample
Occupational Health Checklist for Hazardous Waste Sites, a Data
Book on Chemical Hazards, Mathematical models used in air
sampling strategies, sampling procedures and information on use
of available equipment.
CONCLUSION
The Manual is comprehensive and the appendices are volum-
inous but together they contain valuable information which will
benefit the intended users. The appendices are separately bound
from the main Manual in order to reduce the actual volume but
still be available as reference material. The Manuals are state-of-
the-art and are designed to be updated as additional informa-
tion becomes available. The authors invite their use and solicit
correctional information to make them more useful and accurate.
REFERENCES
1. Herrick, R. "Dangerous Properties of Industrial Materials". Sax,
N.I., Ed; Van Nostrand: New York, 1979, 1-3.
2. Robinson, D.M. and Scott, D.M. "NIOSH Program Plan for Haz-
ardous Waste" NIOSH program concept memorandum, Appendix II.
July 13, 1981, NIOSH, Cincinnati, Ohio.
3. Public Law 96-510, "The Comprehensive Environmental Response,
Compensation, and Liability Act of 1980", 96 Congress, HR 2020,
Dec. 11, 1980 (Legislation History, paage 6120).
4. Public Law 91-596, "Occupational Safety and Health Act of 1970", 91
Congress, S. 2193, Dec. 29, 1970.
5. Public Law 96-510, "The Comprehensive Environmental Response,
Compensation, and Liability Act of 1980", 96 Congress, HR 2020,
Dec. 11, 1980, Sec 104(i), 111 (c)(6), 301 (f).
6. Geraci, C.L. Jr. and Costello, R.H. "Qualitative Screening of Air-
borne Containments at a Hazardous Waste Site", Proc. of The Amer-
ican Industrial Hygiene Association and American Conference of Gov-
ernmental Industrial Hygienists Hazardous Waste Symposium, May
1983. Philadelphia, Pa.
7. King, M.V., Eller, P.M. and Costello, R.J. "A Qualitative Sampling
Device for Use at Hazardous Waste Sites". Proc. of The American
Industrial Hygiene Association and American Conference of Gov-
ernmental Industrial Hygienists Hazardous Waste Symposium, May
1983. Philadelphia, Pa.
8. Schneider, D. "The Draeger Gas Detection Kit, Draeger Review 46,
(1980), 5-12.
9. King, M.V., Eller, P.M. and Costello, R.J. "A Qualitative Sampling
Device for Use at Hazardous Waste Sites". Proc. of The American
Industrial Hygiene Association and American Conference of Gov-
ernmental Industrial Hygienists Hazardous Waste Symposium, May
1983. Philadelphia, Pa.
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NAVY MANAGEMENT OF ABANDONED
HAZARDOUS WASTE SITES
LT. (jg) LILY-ANN OPENSHAW, CEC, USN
ELIZABETH B. LUECKER
CDR. JOHN P. COLLINS, Ph.D., CEC, USN
Naval Facilities Engineering Command
Port Hueneme, California
BACKGROUND
The Navy Assessment and Control of Installation Pollutants
(NACIP) program began in 1980 as part of the Department of
Defense (DOD) Installation Restoration program. DOD initiated
hazardous waste site investigations in 1975, five years before the
Comprehensive Environmental Response, Compensation and Li-
ability Act (CERCLA) of 1980.' In this paper, the Naval Energy
and Environmental Support Activity (NEESA), NACIP program
executive manager, reviews techniques in site discovery, risk assess-
ment, site sampling and site restoration.
The NACIP program uses three levels of assessment in screen-
ing hazardous waste sites. Phase I, the Initial Assessment Study
(IAS), identifies where hazardous wastes were disposed and which
of these sites have potential problems. Phase II, the Confirmation
Study, investigates these sites and verifies those with definite con-
tamination. Phase III, the Corrective Measures Study, determines
the most effective way to control contaminant migration and pro-
vides site restoration.
Based on the presence of heavy industrial operations, past in-
discriminate disposal of hazardous wastes and local ground or sur-
face water used for agricultural or potable supplies, the Navy
scheduled 79 bases for study in the 5-year NACIP program. For a
consistent approach in the study of all Navy sites, NEESA, a
specialized consulting group within the Navy, conducts the Phase
1 effort. After the Phase I study has been completed at a naval
base, six regional Engineering Field Divisions of the Naval Facil-
ities Engineering Command conduct the site specific Phase II and
III efforts.
Initial Assessment Study
NEESA assigns a team of scientists and engineers to each In-
itial Assessment Study. The team collects and evaluates informa-
tion on past naval base industrial operations. Information ob-
tained may identify hazardous waste sites on the base. The study
includes a review of archival and base records, interviews with
base personnel and an on-site survey.
The IAS begins with records searches at various national and
regional government agencies for a complete history of the naval
base. More specific information needed to assess likely contam-
ination sources is found in the naval base's files. In most cases,
the type of detailed information needed for the IAS will not be
found in records. Base records on waste disposal were often lost,
destroyed or not kept. Shops were concerned with keeping track of
products—not wastes.
For these reasons, the most important part of the IAS is the time
spent interviewing long-term employees or retirees about past oper-
ations, especially past waste disposal. Although interview tech-
nique is as important to the success of the study as technical exper-
tise, it is the most difficult skill to master for the IAS team. Scien-
tists and engineers ask exacting questions and expect immediate
and complete answers. Inexperienced team members can become
frustrated with this approach. In interviews, the NACIP program
managers stress a patient, personal approach to win the worker's
confidence.
Interviews lead the IAS team to the majority of the sites un-
covered during a study. The team then inspects the sites for signs of
contamination, such as stressed vegetation or ground stains, and
reviews local hydrogeology. If the waste disposed of, or spilled, has
a high soil attenuation such as PCBs or DDT, the team may take a
mixed grab sample of the area.
With information compiled and assimilated from records
searches, interviews, observations and these few samples, the team
evaluates each site. If the team determines the possibility exists for
a site to endanger human health or the environment, a Phase II
Confirmation Study will be recommended in the IAS. This Con-
firmation Study may call for extensive sampling such as vertical
and horizontal sampling grids and monitoring wells to determine
the existence and amount of contamination.
Ranking Models
To determine the need for and priority of Phase II efforts,
NEESA developed a ranking model to score sites. This model
makes it possible to compare sites containing different wastes,
ranging from pesticides to plating wastes, and located in different
hydrogeologic areas, ranging from arctic tundra to South Pacific
island jungles. This decision process standardizes the type of in-
formation documented on each site and is known as the Confirma-
tion Study Ranking System (CSRS).
The first step of the CSRS is a flowchart that eliminates innoc-
uous sites from further consideration. This flowchart ensures that
all important characteristics of a site are considered before the site
is labeled innocuous. Aspects of a site reviewed in the flowchart
include the type and amount of waste, type and condition of con-
tainment (if any), hydrogeology conducive to migration, degrada-
tion of the waste and possible receptors such as humans and en-
dangered species.
Step two of the CSRS is the Confirmation Study Ranking Model
(CSRM) which objectively ranks sites needing further study. Fund-
ing priorities for further site investigations can be effectively es-
tablished in this step. The CSRM incorporates three major areas of
concern at a site: receptors of possible contaminants, potential mi-
gration pathways and characteristics of the wastes. The receptors
category subscore includes items such as nearby population, crit-
ical environments for endangered species, land use and surface and
groundwater uses.
The pathways category subscore is based on analytical evidence
of contamination or the highest of one of three potential pathways
of migration. These migration pathways consider factors such as
soil permeability, rainfall intensity, net precipitation, distance to
326
REMEDIAL RESPONSE
-------
nearest surface water body and depth to groundwater. The waste
characteristics category subscore includes waste quantity, acute and
chronic toxicity, persistency, solubility, years since site closure and
similar items. The factors considered in each of the three categor-
ies are listed in Table 3. Once computed, the three category sub-
scores are then incorporated in a multiplicative model to produce
an overall score for the site.3
As previously mentioned, most of the important information on
the various sites is obtained through interviews with long time per-
sonnel. In many cases, due to the uncertainty of the corporate
memory involved, this information is only available in orders of
magnitude. Because of this uncertainty, the interviewers only ask
questions about location of, dates of use of and quantities of waste
at a site. Other information the model uses is readily available from
the literature,4'5 other records and field observations.
Scores for a CSRS model may range from 0 to 100; 0 being an
innocuous site such as a construction rubble disposal area, 100
being the worst possible site. The highest recorded score so far is
64, where the three categories of receptors, pathways and waste
characteristics combined to produce a significant environmental
concern. As this range of scores shows, sites within a naval base,
across the country and throughout the Navy are being success-
fully compared with the use of this model. This range of scores
can be seen in Figure 1.
Category
Table 1
Factors Considered in the CSRM
Rating Factor
Receptors -Population within 1000 ft of site
-Distance to nearest down gradient well
-Land use/zoning within 1 mile radius
-Distance to reservation boundary
-Critical Environments within 1 mile radius
-Water quality/use of nearest surface water body
-Groundwater use of the aquifer of concern
-Population served by surface water supply within 3
miles downstream
-Population served by groundwater supply within 3
miles
Pathways -Direct Evidence of Contamination or potential for
1—Surface Water Migration, or
-Distance to nearest down gradient surface water
-Net precipitation
-Surface erosion
-Soil permeability
-Rainfall intensity
2—Flooding, or
-Floodplain
3—Groundwater Migration Potential
-Depth to groundwater
Net precipitation
-Soil permeability
Subsurface flows
Direct access to groundwater
Waste
Characteristics -Waste Quantity
-Acute Toxicity
-Chronic Toxicity
-Persistency
-Flammability
-Reactivity
-Incompatibility
-Corrosiveness
-Solubility
-Bioaccumulation
-Physical State
-Years site was in use
-Years since site closed
An important aspect of funding and cleanup priorities not con-
sidered in the CSRM is public opinion. The cleanup of abandoned
hazardous waste sites is a high visibility program and the Navy a
high visibility organization. Public opinion may demand further
action at sites that do not pose as much of a potential hazard
as others. Funding priorities may then be adjusted to incorporate
these other considerations.
Findings
In the past three years, the Navy has completed Initial Assess-
ment Studies at 35 naval bases and has investigated over 700
sites. When an IAS team undertakes a study, it examines all
disposal, storage and spill sites, ranging from the unquestionably
innocuous—rubble dumps, to the potentially hazardous—indus-
trial waste landfills. Over two-thirds of the sites identified have
proved to be innocuous. Because the Navy's highest potential
problem bases, those with heavy industrial operations such as ship-
yards and air rework facilities, were studied first, the future per-
centage of innocuous sites should increase. In the past three years
this projection has proven accurate: in FY1981, 65% of the sites;
in FY1982, 69% of the sites; and to date in FY1983, 78% of the
sites investigated required no further action.
CASE STUDIES
During each study, several potentially contaminated sites are
usually identified that require further sampling and minor correc-
tive action. The Navy has initiated Phase II, Confirmation Study,
and Phase III, Corrective Measures Study, at several naval bases.
In order to discuss the general trends of the NACIP program in
site sampling during Confirmation Study and in site restoration
during Corrective Measures Study, several case studies are pre-
sented. The sites described represent four typical sites recom-
mended for further action in the IAS: (1) a POL (petroleum,
oils, and lubricants) disposal area, (2) a landfill, (3) a PCB site
and (4) a blasting grit pile. The sites also represent the three most
frequent courses of action taken after the IAS.
POL Disposal Areas
POL disposal areas may include surface spills and underground
spills of POL (petroleum, oils and lubricants), POL sludge dis-
posal pits and other similar areas. The range of risk assessment
scores given for these sites is shown in Figure 2. The site that will be
Waste
Management
-Waste Containment
25 35 45
CSRM SCORES
Figure 1
CSRM Score Range for all Sites
REMEDIAL RESPONSE
327
-------
25
CSRM SCORE
Figure 2
CSRM Score Range for POL Disposal Sites
BVERflGE SCORE . 25 ~]
25 35
CSRM SCORE
Figure 3
CSRM Score Range for Landfills
discussed was a series of oily sludge disposal pits located on top of
an old landfill.
Between 1944 and 1976, oil sludges were disposed of in three un-
lined earthen pits. Two of the pits were filled and covered in 1956,
and the third was emptied and covered in 1976. Portions of the area
have since been used as a parking lot. Exact locations of the pits
were found on historical aerial photos from the National Archives.
The na\ al base is located on a peninsula bordered by a large river
and marshes. Local soils consist of a mixture of fine sand, silts
and gray clay extending to a depth of about 50 ft. Due to the
peninsula's level terrain and soil composition, the IAS team geolo-
gist predicted the movement of trapped subsurface oil on the sur-
face groundsater would closely follow surface water drainage pat-
terns.
As expected, several longtime employees reported oil seepage in
the adjacent marsh areas and nearby river banks during heavy
rains. Because of these reports, the IAS team dug some post holes
and observed approximately 1 ft of oil floating on the shallow
ground water in the area of the sludge pits.6
The detrimental impact of oil on aquatic ecosystems has been
well documented.7'8-9'10 This impact and the evidence of a waste oil
plume migrating toward surface water bodies gave the site a CSRM
score of 26. The LAS team recommended a Confirmation Study to
determine the concentrations and movement of the oils. First, to
define the real extent of the oil contamination, two options were
proposed. _
Option 1 involved mapping the area using shallow borings on a
grid system throughout the area. Borings would be visually in-
spected for oil, then checked with a portable gas chromatograph
(GC) for hydrocarbons from oily residues.
Option 2 involved the use of geophysical methods such as ground
penetrating radar (GPR) and a non-contact terrain conductivity
meter to map the area. A few soil borings would be required for
verification and calibration purposes. GPR data could help the
team evaluate the thickness and location of the liquid oil layer in
the ground. A hand held auger and the portable GC would be used
to map out the extent of the oily residues in the soil.6
Option 1 was chosen because geophysical methods were used
during the IAS to try to define the oil lens, but the heterogeneity
of the soils and the presence of buried conductors prevented in-
terpretation of the data. Eighty-seven shallow borings were drilled
to determine the extent of subsurface oil. Six additional borings
were drilled along the river to determine the extent of oil migra-
tion to the river. Although the use of a portable GC had been
recommended, the GC was not used because visual and odor tests
would detect the levels of oils that could potentially migrate.
Results of the borings identified an oil body approximately 600
ft by 50 ft by 2-4 in. deep in the southwestern portion of the oil
sludge area. East of the oil body, an area of oily residue was also
identified." The location of the oil body was adjacent to the areas
of the marsh where oil seepage had been reported.
Results of the sampling showed that the slow contaminant migra-
tion was due to a combination of the low soil permeability, the low
hydraulic gradient and the high viscosity of the waste oils. Perme-
abilities of the surficial soils were calculated as 1 x 10"6 cm/sec,
and the hydraulic gradient was 4.5 x 10"3.
The Confirmation Study report concluded that, although an oil
body existed and oil movement was occurring, the migration was
slow. Therefore, immediate corrective measures, such as soil exca-
vation, were not needed. Instead, the report recommended two al-
ternative collection systems to prevent further migration.
The first collection system consisted of ditches, infiltration
galleries or a combination of these placed around the oil body. The
drains would be pumped so oil could be separated from the water
and recycled. The recycled water would be used to recharge the
shallow groundwater system to speed up the oil recovery process.
The second collection system consisted of a drainage ditch along
the southwestern edge of the oil body. The ditch would be dammed
at the downstream end. A bypass pipe would be installed at the
base of the dam to divert the water into a storm sewer. Periodical-
ly, naval base personnel would pump the ditch to remove the top oil
layer.
The system installed followed the design of the second alterna-
tive because there was no need to expedite oil recovery. A drain-
age ditch dug for an adjacent road conveniently intercepted the
subsurface oil body and was used in the collection system. Samp-
ling, followed by a corrective measure such as this collection sys-
tem, is a typical course of action at sites investigated.
Landfills
Sanitary landfills were the central depository for all waste ma-
terials on naval bases as in every region of the country. Liquid
wastes were generally drummed, and combustible products were
REMEDIAL RESPONSE
-------
burned. Trenches were sometimes used, but usually wastes were
dumped on the ground and covered with fill material. Because of
the varied industrial wastes present, landfills are often the high
scoring sites for a naval base (Figure 3).
The sanitary landfill described in this case study was used from
the 1930s until 1973 to dispose of solid wastes generated by a ship-
yard. Shipyards must provide all the services required to maintain
the U.S. Navy fleet of ships: manufacturing, alterations, overhaul
and repair. As a result, the landfill received large quantities of solid
and hazardous wastes including waste solvents, paints, paint
sludges, asbestos, metal plating sludges, mercury, PCBs, industrial
liquid wastes (organic and inorganic chemicals) and construction
rubble. In 1973, the landfill was closed and capped with a clay
layer. Since that time, solid wastes have been ahuled off-base under
contract.
The shipyard is located on a natural peninsula developed with fill
and bounded by a brackish river and a main tributary creek. The
landfill lies in the marsh near the headwaters of the tributary creek.
Surface sediments extend downward 45 ft to an underlying clay
formation. As groundwater moves slowly through fine grained silts
and clays, it is mineralized due to the proximity of the brackish
river and the use of river and creek bed sediments for fill. No
potential exists for using shallow groundwaters for potable sup-
plies, since dissolved solid levels naturally exceed USEPA drinking
water standards. The deep potable aquifer is artesian and is sep-
arated from the shallow aquifer by 200 ft of relatively impermeable
calcareous clay.
From this initial' geologic assessment and waste characteriza-
tion, the landfill received a relatively high CSRM score of 31. Thus,
the IAS team recommended a Confirmation Study to determine
the lateral migration potential of contaminants. Specifically, the
program would evaluate subsurface stratigraphy, permeability, pie-
zometry and local groundwater quality.
The groundwater monitoring program was to be conducted in
two phases: verification and characterization. The verification
would consist of collecting one sample from each monitoring well
over the saturated zone. The sampling parameters selected were
based on suspect contaminants in the landfill: heavy metals, cya-
nides, oil and grease or petroleum hydrocarbons, PCBs and prior-
ity pollutant volatile organic compounds.
If contaminants were present in well samples, then further samp-
ling in the characterization phase was recommended to develop a
vertical profile of contaminant concentration and define contami-
nant migration paths.6
In the Confirmation Study, 13 monitoring wells were installed at
different depths around the landfill perimeter. Data collected dur-
ing well installation confirmed previous hydrogeologic assess-
ments. The surficial sediments had a low permeability and a
low hydraulic gradient. In addition, an upward hydraulic gradi-
ent existed between the deep aquifer and the surficial deposits.
Initial sampling of the shallow aquifer showed a mineralized con-
tent with levels of dissolved solids above USEPA drinking water
standards.
The chemical analyses of water samples collected from monitor-
ing wells along the edge of the landfill detected the presence of low
levels of barium from paint pigments and coatings, flouride, iron,
pentachlorphenol from wood preservatives, bis-2-ethylhexyl phtha-
late, chloroform, dibromochloromethane, chlorobenzene and vinyl
chloride. Water from the upper calcareous clay formation was
analyzed for volatile organic compounds; none were detected.''
For the contaminants present in the shallow groundwater, the
rates of migration toward the creek and river were calculated at 1 to
2 ft/yr. At these slow rates, many of the contaminants would like-
ly be attentuated in the soil and would never reach the surface
waters. Those contaminants that might reach the creek or river
would end up in brackish mineralized waters subject to discharges
from heavy industry upstream. In other words, the low levels of
contaminants that might reach the waters would not significantly
affect the existing water quality.
Alternatives for preventing leachate migration considered, but
not recommended, included the installation of an impermeable bar-
rier around the landfill and the installation of a groundwater collec-
tion system around the landfill to intercept the leachate for treat-
ment. To date in the NACIP program, corrective measures such
as these have not been warranted because the Navy has found few
instances where contaminants contributed from abandoned land-
fills are significantly affecting the surface water quality. Conse-
quently, as at many sites investigated, no further action other than
continued monitoring was recommended.''
25 35
CSRM SCORES
Figure 4
CSRM Score Range for PCB Sites
PCB Sites
Other typical sites are those with possible polychlorinated bi-
phenyls (PCBs) contamination. An extremely stable compound,
PCBs are resistant to biodegradation and thermal destruction.12 As
a result, PCBs were widely used in dielectric fluid until the late
1960s. Unfortunately PCBs, as a chlorinated organic, are also
bioaccumulative and pose a potential threat to human health.12
This case study involves a location with three PCBs sites; two
transformer leaks or spills dating to the mid-1960s and one trans-
former storage yard used until 1976. These sites were discovered
during interviews with electrical shop personnel.
The above sites were located in a coastal plain area on the sandy
soil of a peninsula adjacent to the ocean. Grab samples were taken
at these three sites during the IAS on site visit. The two spills did
not show significant quantities of PCBs; however, the oily sludge
on the surface of the old transformer storage area had more than
70,000 ppm Archlor 1260, as well as other PCBs and chlorinated
hydrocarbons. Due to this evidence of contamination, the storage
yard was recommended for a Confirmation Study."
The PCBs storage yard was also ranked using the CSRM. As
mentioned before, this site is located on the coast on sandy soil
and has a high groundwater table. However, the corner of the stor-
age yard that was used for transformer and capacitor storage is
paved with asphalt. The entire storage area, currently used for sand
and gravel storage for road beds and foundations, is fenced and
locked. The yard is fairly isolated, with only public works shops
nearby and no occupied buildings adjacent to the site. Because of
these factors, the CSRM score was a 26. PCBs sites uncovered dur-
ing lASs so far can be compared to each other as shown in figure 4.
REMEDIAL RESPONSE
329
-------
In the case of this storage yard, the Engineering Field Division
and the naval base decided to go immediately to cleanup, rather
than the further testing of a Confirmation Study. The asphalt area
was scraped and all visible stains in the area were removed and
placed in drums. The area was then retested for PCBs and was
found to be uncontaminated to the limits required by regulations."
The three drums of collected material were then sent to a secure
landfill.
This immediate cleanup action, while not necessarily typical of
PCBs sites, is typical of one of the three main types of action taken
at a potentially contaminated site uncovered during an IAS. Be-
cause of the simplicity of the proposed cleanup and the known exis-
tence of the contaminant, the expense of a Confirmation Study
may be simply bypassed and corrective measures immediately
undertaken. In other cases, as at the following site, corrective
measures may be immediately started due to a potential health haz-
ard.
Blasting Grit Pile
Another typical site at industrial naval bases contains spent blast-
ing grit. When ships or aircraft are overhauled, they must be
painted. Old paint is sandblasted off, producing large quantities
of spent blasting grit which contains paint particles. The grit itself
can be sand, glass beads, metallic slags or walnut hulls.
In this case, the spent metallic slag grit was used to fill a low
area behind a Navy housing complex. Thirteen years later, large
areas of grit were still exposed and children played in the sand
piles. The site was located adjacent to a creek on clayey sandy
soil.
This site was discovered on the last day of the on site visit.
Samples of the grit were taken within the next week. Analyses of
these samples showed high concentrations of lead, copper and zinc.
However, the samples did pass the EP toxicity test and, thus, were
not classified as a hazardous waste. The concern here was the possi-
bility of the paint particles containing the heavy metals becoming
airborne. The particles could then be inhaled and pose a potential
health hazard. The paint particles and grit could also be ingested
by children playing in the piles. Shortly after receiving results of
the sampling, the naval base started cleanup, which consisted of
leveling the pile, covering with clean fill and seeding."
This immediate cleanup is not necessarily typical of sandblast
grit sites. In many cases the grit has already been covered and,
as indicated above, is not considered a hazardous waste. This
site, then, is typical of sites where corrective measures are immed-
iately undertaken due to a potential health hazard.
Discussion
The four sites discussed represent typical sites found, and also
characterize the three most frequent courses of action taken, after
the IAS. A Confirmation Study of sampling and well monitor-
ing followed by corrective measures may be done, as was the case
with the POL sludge pit.
In other cases, such as the landfill, results of a Confirma-
tion Study conclude that, due to the low levels of contaminants
found and their minimal impact on present surface and ground-
water quality, no further action is required other than continued
monitoring. In the third case, corrective measures may be immed-
iately implemented due to cost, as at the PCB storage yard, or due
to possible health hazards, as at the grit pile, when a surficial
sample has shown the presence of a specific contaminant.
CONCLUSIONS
The three year old NACIP program continues to be a challenge
for the Navy scientists and engineers involved. One of the most
important, and hard to master, skills of site discovery is an effec-
tive interview technique. When effective interviewing is combined
with inspections of a site and information from records searches,
the IAS team can determine the need for further action with the
help of the Confirmation Study Ranking System. Using the Con-
firmation Study Ranking Model scores, the Navy can then com-
pare sties studied and set funding priorities for further action.
A review of completed Confirmation Studies and Corrective
Measures Studies shows further action at sites has typically
followed one of three courses: extensive sampling with restora-
tion or cleanup, extensive sampling with no further action other
than continued monitoring and immediate cleanup. As proven by
the case studies, the Navy is prepared to expediently resolve any
serious contamination problems that may arise.
With the Installation Restoration Program, DOD has shown in-
itiative in searching for abandoned hazardous waste sites. The
Navy, in support of this program, developed expertise in the fields
of hydrogeology, biology, chemistry, toxicology and engineering as
shown by the design and use of the CSRM. By anticipating rather
than reacting to problems associated with abandoned hazardous
waste sites, the Navy can propose sound engineering and cost effec-
tive solutions for these sites. In this way, the Navy will continue
to ensure the safety of naval base populations and surrounding
communities.
ACKNOWLEDGEMENTS
The authors thank their colleague Dr. Richard J. Watts for
his technical assistance with and critical review of this manuscript.
REFERENCES
1. Comprehensive Environmental Response, Compensation, and Liabil-
ity Act of 1980, Public Law 96-510, as amended.
2. Office of the Chief of Naval Operations, Department of the Navy,
Environmental Protection and Natural Resources Manual, OP-
NAVINST 5091.1, 26 May 1983.
3. Collins, J.P. and Luecker, E.B., "Decision Strategies for Evaluating
Abandoned Hazardous Waste Sites," Proc. Hazardous Materials
Management Conference, July 1983, in press.
4. National Fire Prevention Association, Fire Protection Guide on Haz-
ardous Materials, seventh edition, 1979.
5. Sax, N. Irving, Dangerous Properties of Industrial Materials, fifth
edition, Van Nostrand Rheinhold, New York, 1979.
6. Environmental Science and Engineering, Inc., Initial Assessment Study
of Naval Base Charleston, Charleston, S.C., NEESA-007, prepared
for Naval Energy and Environmental Support Activity, Naval Facil-
ities Engineering Command, May 1983.
7. Connell, D.W. and Miller, G.J. "Petroleum Hydrocarbons in Aquatic
Ecosystems—Behavior and Effects of Sublethal Concentrations,"
Critical Reviews In Environmental Control, 11, 1981, 37-105.
8. Gonsoulin, F. et al., "Fate and Effects of Heavy Fuel Spills on
Georgia Salt Marsh," Marine Environmental Resources, 5, 1981,125.
9. Griffiths, R.P. et al., "Long Term Effects of Crude Oil on Uptake
and Respiration of Glucose and Glutamate in Arctic and Subarctic
Marine Sediments," AppliedEnvir. Micro. 42, 1981, 792.
10. Knapp, A.H. and Williams, P.J., "Experimental Studies to Determine
the Fate of Petroleum Hydrocarbons from Refinery Effluent on an
Estuarine System," Environ. Sci. Tech., 16, 1982, 1.
11. Geraghty and Miller, Inc., Confirmation Study, Assessment of Poten-
tial Oil and Hazardous Waste Contamination of Soil and Ground
Water at Charleston Naval Shipyard, Charleston, S. C., prepared for
Southern Division, Naval Facilities Engineering Command, Oct. 1982.
12. Lloyd, J.W. et al., "Polychlorinated Biphenyls," J. of Occupational
Medicine, 18, Feb. 1976.
13. Naval Energy and Environmental Support Activity, Naval Facilities
Engineering Command, Initial Assessment Study of Naval Air Station
Pensacola, Pensacola, Florida, NEESA 13-015, June 1983.
14. United States Environmental Protection Agency, 40 Consolidated
Federal Register (CFR) 761, "Polychlorinated 'fiiphenyls (PCBs)
Manufacturing, Processing, Distribution in Commerce and Use Pro-
hibitions," as amended.
15. Water and Air Research, Inc., Initial Assessment Study of Norfolk
Naval Shipyard, Portsmouth, Virginia, NEESA, 13-010, prepared for
Naval Energy and Environmental Support Activity, Naval Facilities
Engineering Command, March 1983.
330
REMEDIAL RESPONSE
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COAL TAR CONTAINMENT & CLEANUP
PLATTSBURGH, NEW YORK
STEWART N. THOMPSON
ANTHONY S. BURGESS, Ph.D.
Acres American Incorporated
Buffalo, New York
DENNIS O'DEA
New York State Electric & Gas Corp.
Binghamton, New York
INTRODUCTION
A gas generating plant was operated along the banks of the
Saranac River in the City of Plattsburgh, New York, from 1896 to
1960. Coal tar, a by-product of the gasification process, was inter-
mittently disposed of in unlined ponds adjacent to the river.
Throughout the years, the coal tar has migrated through the
substrata resulting in periodic coal tar release into the river.
Acres American Incorporated (Acres), Buffalo, New York, was
retained in 1979 to:
•Identify the extent of coal tar contamination
•Define the physical and chemical properties of the contaminant
•Define the mode of contaminant transport
•Define and assess the corrective remedial alternatives
•Perform final design
•Provide construction supervision and management
The work was undertaken in a multi-phase approach from 1979
to 1982. In this paper, the authors discuss the site investigation,
remedial alternatives and final design and construction undertaken
at the site.
ASSESSMENT OF THE PROBLEM
Site Description
The site covers an area of approximately 11 acres and lies within
the City of Plattsburgh on the south bank of the Saranac River
(Figure 1). Topography falls gently in steps from approximate
Elevation 125 to 130 ft Mean Sea Level (MSL) along the south edge
of the site to 102 to 107 ft MSL along the Saranac River banks.
Apart from a narrow band of trees and bushes adjacent to the
river, most of the site has been cleared and filled. A 24 in diameter
concrete sanitary sewer crosses the site with invert elevations bet-
ween 107.4 ft and 110.3 ft. An active transmission line owned by
the Plattsburgh Municipal Lighting District crosses the site along
the south bank of the river (Figure 1).
After the decommissioning of the plant in 1960, the coal tar
ponds were filled with random material and covered with layers of
cinders and ash. Large portions of the site to the west and north
have been filled and regraded at various times during and post plant
operation. No maps or drawings could be found showing the
original site contours, nor do any records exist regarding the
amount and times of coal tar disposal into the unlined ponds.
Site Geology and Hydrology
A total of 53 boreholes were drilled during a three-phase site in-
vestigation to define the site geology, hydrology and area of con-
Figure 1
General Site Plan
lamination (Figure 1). All borings were drilled vertically using
either a hollow stem auger or 4 in ID rotary drill with casing. Stan-
dard split-spoon samples were continuously taken in the uncon-
solidated overburden, with several borings drilled into the underly-
ing bedrock. In addition, three test pits were excavated on site to
obtain additional information regarding stratigraphy and to collect
bulk samples of the coal tar and soil for laboratory testing.
Nineteen standpipe piezometers were installed in selected
boreholes to monitor ground water levels across the site. In situ fall-
ing and constant head permeability tests were performed in selected
borings to define subsurface permeabilities.
As a result of this investigation, three soil units were delineated.
From ground surface to bedrock they are:
•Sand and Fill
Fill—dark brown to black cinders and ash with traces of gravel,
sand, coal, wood and brick fragment; medium dense to dense.
Sand—medium brown to yellow brown; fine-grained with traces
of salt and gravel; loose to medium dense.
•Sand and Gravel
Dark brown to black; fine-to-coarse-grained sand and gravel;
loose to medium dense.
CASE HISTORIES
331
-------
•Till
Medium gray silt and fine sand with some medium-to-coarse-
grained sand and gravel; extremely dense.
The top of the till unit was readily identifiable during subsurface
drilling because of its extremely dense and impervious nature. Con-
tours of the top of the till layer are shown in Figure 2. Bedrock is a
dark gray to black, hard, competent, fine-grained limestone.
Figure 2
Till Surface Contour Map
Coal tar contamination was found over most of the site. Con-
tours of the maximum elevation of coal tar are shown in Figure 3
with a plot of equal thickness (isopachs) of contaminated soils
shown in Figure 4. Maximum thickness of contaminated soils was
found to be 13 ft beneath the original coal tar ponds. The investiga-
tion indicated that the coal tar was more dense than the ground-
water and formed a separate phase. The direction of coal tar move-
ment was controlled by the dense impermeable (
-------
LEOEN.,
t::X?\ FINE SANO AND FILL •£• OKOUMMATEII LEVEL
[23 5*NI> •"• OUAVEL -4£- mvra LEVEL
.. COAL TA> m«> ^
HORIZONTAL SCALE
0 «0 >0 FEET
124 NOTE . SECTION LOCATIONS
SHOWN ON FIGURE I.
Figure 5
Geologic Sections, A-A, B-B and C-C
Figure 6
Groundwater Surface Contour Map
to dissolve the coal tar. The acetone was then boiled off leaving the
coal tar fraction behind, from which the percentage of coal tar was
determined. The second test procedure employed using xylene for
water extraction. Under this procedure, the contaminated samples
were mixed with xylene and heated. The water was then extracted
and the weight of the remaining solids determined.
These tests showed that the tar content (percent dry weight)
ranged from 0% for an uncontaminated sample to a high of 9.6%,
with an average content of approximately 1.5%. Water content for
the same samples ranged from 4.9% to 35.9% with an average of
14%. These results show that the majority of contaminated soils on
the site contain only about 1.5% coal tar by weight, which means
that the soil is unsaturated with respect to coal tar. To further
quantify this finding, a series of laboratory model tests were under-
taken to simulate the sequence of events that has taken place at the
site. These events involved:
•Pre-coal tar disposal with a groundwater saturated strata
•Displacement of all, or part of, the groundwater by coal tar with
simulated flow of coal tar through the strata
•Removal of the coal tar source and re-establishment of the natural
groundwater flow
Table 1
Chemical Analyses—Heavy Metals
Sample
Al
Ba
Ca Cd
Cr
Cu Fe
Mg (1n Na HI Pb Sb
Se
Stage I Total Lcachaole Salts In Tar/SotT Samples
0.07 0.9 3 <0.3 <0.05 27 <0.05 0.12 0.2 0.4 <0.04 6.3 3.9 0.3 6.7 0.15 0.9 <0.4 <0.5
BH-6 SSI9
16.0' - 18.0'
BII-8 SSI6
10.0' -11.0' 0.07 0.7 2 <0.3 <0.05 27 <0.05 0.3 0.3 0.4 <0.04 8.4 3.4 0.7 6.3 0.1 1.0 <0.4 <0. 5
<1.0
<1.0
Stage II Total teachable Salts In Coal Tar
Tar of BH-6 <0.04 <0. 5 <0. 5 <0. 3 <0.05
Tar of BII-8 <0.04 <0.5 <0.5 <0.3 <0.05
River Tar 0.06 <0. 5 <0. 5 <0. 3 <0.05 8 <0.05 <0. 1
<0.05 <0. 1 <0.05 0.2 <0.04 1.0 3.0 1.2 4.5 0.1
<0.05 <0.1 <0.05 0.2 <0.04 3.0 3.2 1.0 4.5 0.1
Stage 111 Total Salts In Coal Tar
Tar of BH-6 0.6 25 1.0 <0.3 0.1
Tar of DH-8 0.8 15 1.0 <0.3 0.1
River Tar 1.3 30 4 <0.3 0.2
44 <0.05 5.0
67 <0.05 7.0
70 <0.05 12.0
0.1 0.3 <0.04 3.0 2.4 1.1 3.6 0.15
1.2 5 <0.04 2.0 7.0 7.5 5.0 6.0
0.7 7 <0.04 3.5 8.0 6.6 5.0 3.7
5.0 2 <0.04 3.0 7.0 4.5 4.0 5.3
<0.2 <0.4
<0.2 <0.4
0.4 <0.4
2.0 <0.4
2.9 <0.4
2.0 <0.4
<0. 5
<0.5
<0. 5
2.0
2.5
3.0
<1.0
<1.0
<1.0
<2.0 <1.0 0.3
<2.0 <1.0 0.2
<2.0 <1.0 1.0
<2.0 <1.0 0.4
<2.0 <1.0 0.4
<2.0 <1.0 31
<2.0 <1.0 i;
<2.0 <1.0 14
HOTE: ALL RESULTS ARE GIVEN AS HICROCRAHS PER CRAM IT MATERIAL TESTED
CASE HISTORIES
333
-------
Table 2
Chemical Analyses—Salt and Organics
SAMPLE pH Cl CN KJL-N NH3-N N03-N PHENOLS SULFIDE COD TOC Si 02
Stage I Total Leachable Salts
BH-6 SS »9 7.4 17.3 <1 0
16.0'-18.0'
BH-8 SS*6 7.8 20.0 <1 0
lO.O'-ll.O'
Stage II Total Leachable Salts
TAR of 4.5 — <1 <0
BH-6
TAR of 4.5 — <1 <0
BH-8
TAR from 4.6 34.4 <1 0
river
Stage III Total Salts in Coal
TAR — -- <1 0
BH-6
TAR -- - <1 0
BH-8
TAR from -- 34.4 <1 1
river
NOTE: ALL RESULTS ARE GIVEN AS
DRY
SAMPLE DESCRIPTION DENSITY
(PCF)
Compaction Test #1 127.7
(composite sample
of sand/gravel )
Perm/Retention Test »1 130.7
(composite sample
of sand/gravel )
Perm/Retention Test 12 118.1
(sand/gravel/tar
from Test Pit 79-T1 )
Compaction Test 12 129.9
(clean sand/gravel
from Test Pit 79-T3)
Perm/Retention Test 13 130.4
in Tar/soil Samples
.5 <0.1 10 0.3 <0.1 627 206 15
.4 <0.1 13 0.15 <0.1 870 310 12
in Coal Tar
.1 <0.1 <5 0.17 <0.1 2490 900
.1 <0.1 <5 0.13 <0.4 2460 850
.3 <0.1 <5 4.0 <0.1 2650 935
Tar
.4 -- <5 15
.4 --
-------
Table 4
Coal Tar Retention Tests
Sample Sample
No. Description
1 Composite sample of
sand/gravel from
split spoon
sample
2 Sand/gravel sample
w/coal tar from
Test Pit 79-T1
Coal Tar
Retained
1.38
Water
Retained
Remarks
8.35 Sample Hushed
w/water under
slight head &
allowed to drain.
1.96 9.7 (Prior to testing)
5.9 7.6 Sample taken
after completion of
Permeability Test
w/coal tar. Not
flushed or allowed
to drain.
3 Clean sand/gravel 1.29 8.74 Sample Hushed
from Test Pit w/water under
79-T3 slight head &
allowed to drain.
NOTE: All retention tests were run on samples immediately following completion of Permeability
Tests with coal tar.
perties allowed the tar to migrate as an independent phase to the
groundwater regime. With continued disposal, the coal tar moved
relatively rapidly down gradient along the top of the impervious till
layer into the river. Once dumping stopped, the rate of migration
gradually decreased.
It is believed that the majority of coal tar presently on site is prin-
cipally being retained within the pores and matrix structure of the
soil grains, and that the mechanism causing the tar migration today
is different from that when the ponds were in operation. Although
difficult to quantify, the mechanism causing tar migration today is
most likely influenced by one or more factors, including seasonal
groundwater fluctuations causing changes in pore water pressure,
increased ground and groundwater temperature during summer
causing the tar to become more mobile due to decreased surface
tension and viscosity and increased river flow causing a flushing of
the contaminants from the soil.
ALTERNATIVE REMEDIAL SCHEMES
Using the principal criteria that all further coal tar contamination
into the Saranac.River must be stopped, eight alternative remedial
concepts were evaluated. These included:
1. Excavation and replacement of contaminated soil.
2. On-site isolation of contaminated soil by slurry walls, sheet
piping, etc.
3. Grouting of soils and consolidation of contaminated materials
in place.
4. Interception and treatment of coal tar plume.
5. Chemical immobilization of contaminated soils.
6. Biodegradation of coal tar.
7. Tertiary injection wells and recovery of coal tar.
8. Rerouting of the Saranac River.
Each alternative was evaluated for its technical feasibility,
method of implementation, impacts and costs. Those alternatives
that were considered technically unsuitable, or were beyond the ex-
isting state-of-the-art, were eliminated from further consideration.
Of the eight alternatives, 1, 2 and 4 appeared the most viable. The
excessive costs and problems associated with alternative 1 and 4
made the concept of on-site isolation the most acceptable for fur-
ther consideration.
ALTERNATIVE SELECTION & FINAL DESIGN
A number of alternative on-site isolation concepts were
evaluated. The various design alternatives had to take into con-
sideration multi-land-ownership, underground and surface utilities
and contaminated riverbed sediments. Working closely in associa-
tion with the New York State Department of Environmental Con-
servation (NYSDEC), a list of design criteria was developed. These
were:
•Elimination of all further coal tar contamination into the river
•Insurance of the long-term integrity of the remedial method
In addition to the above criteria, a list of desirable attributes were
addressed in the alternative evaluation. These included:
•Minimal cost
•No discharge of contaminants from the site during construction
•Potential future use of site
•Minimize long-term maintenance
Based on the above, a total of 4 on-site isolation concepts were
developed. These were:
Construction of a single cut-off wall along the riverbank
2. Complete isolation of the main ponds with the construction of
slurry wall and impervious cap in addition to the construction
of a cut-off wall along the river
3. Alternative 2 with the addition of river cleanup
4. Total site isolation by the construction of a slurry wall and im-
pervious cap
The advantages, disadvantages and costs of each of the alter-
natives were carefully evaluated and presented to the NYSDEC and
property owners. It was agreed that Alternative 3, Isolation of the
main ponds and construction of a cut-off wall along the river with
excavation and replacement of the most contaminated riverbank
and bed material, best met the criteria.
Due to the delays in obtaining contracts and access, the work was
done in two construction seasons. Phase I, undertaken in the fall of
1981, involved the installation of 735 ft of a soil bentonite slurry
wall around the main pond area and capping it with a temporary
20-mil polyvinyl chloride (PVC) liner (Figures 7 and 8). It was
estimated that approximately 80% of the on-site coal tar was en-
capsulated within this cell, The wall was keyed into the underlying
dense impervious till. Slurry wall depths ranged from 13 to 20 ft. A
well was placed within the cell to monitor the effectiveness of isola-
tion.
®
/ EXIST. .. ; I
• i /SUB-srArioN '
Figure 7
Phase I Construction
CASE HISTORIES
335
-------
t „.-
^
IE«*0
P•~~. [j SAKO AND CRUSHCD STOMt
| "i#>'-J COMTAMINATED S
•nu.
CLAY
*- MOUMMUTn LIVCL
-^- MfVCJt LCVCL
MQMBMTM. SCALE
0 15 3OFECT
Figure 10
Section A-A, Phase II Construction
336
CASE HISTORIES
-------
To prevent groundwater buildup that could result in uncon-
trolled breaching of the wall, a groundwater collection system con-
sisting of 6-in. perforated drain pipe was placed 2 ft below and 10 ft
upgradient of the cement-bentonite slurry wall. The drain pipe
discharges into a precast manhole. A discharge line was cut through
the cement bentonite to the river (Figure 9).
Finally, a soil bentonite cut-off wall was placed around the re-
mainder of the spoils material. The spoils were graded and capped
with a permanent 36 mil Hypalon liner. The liner was covered with
6 in. of sand, topsoiled and seeded. Site work was completed in
September 1982.
POST CONSTRUCTION MONITORING
& SITE RESTRICTIONS
A groundwater and river monitoring program was implemented
to supplement river water quality studies being performed by the
NYSDEC. Samples were obtained monthly and analyzed by an in-
dependent certified laboratory for total phenols and naphthalene.
Both of these compounds were identified during the initial site in-
vestigation (see Tables 1 and 2). Under expected field conditions,
phenols would show the behavior of compounds soluble in water
and naphthalene the response of those lighter fractions of coal tar
that are immiscible in water.
During the initial nine months of monitoring, all 28 samples ob-
tained upstream and downstream of the rehabilitated river bed and
bank sections showed no measurable concentrations of phenols or
naphthalene (
-------
EMERGENCY REMOVAL ACTION AT THE
BANKRUPT CRYSTAL CHEMICAL PLANT
HOUSTON, TEXAS
E. WALLACE COOPER
U.S. Environmental Protection Agency
Emergency Response Branch
Dallas, Texas
LOCATION AND PHYSICAL DESCRIPTION
The Crystal Chemical Plant is located on a five-acre tract in ex-
treme western Houston adjacent to Westchase, a fast growing
development of multistory office buildings and shopping centers.
The plant was constructed in 1968 and started producing mono-
sodium methylarsenate (MSMA) and disodium methylarsenate
(DSMA). Arsenic trioxide (ASjOj), one of the most toxic forms of
arsenic, was the chief component in these herbicides. The site is
adjacent to a major flood control drainage ditch which empties into
Brays Bayou. Brays Bayou flows in an easterly direction through
the city of Houston and has its confluence with the Houston Ship
Channel in the Port of Houston.
When the plant was constructed, it was in a rather remote area;
however, urban growth has reached and surrounded the site. A
pipe company and lumber yard are located to the north and east,
respectively. A private elementary school is located one block to the
south, a large apartment complex one block northwest and a resi-
dential area two blocks southwest. Several large office buildings
have been constructed recently about one-half mile northeast of the
site.
INITIAL SITUATION
Operations at the plant were conducted with little or no regard
for maintenance, safety and environmental protection. Spills inside
and outside the build;ngs, holes in the roofs of buildings and gen-
erally i-eavy rainfall' -ised the entire site to become contaminated
withari.ji;;.
The Texas Ueparuntnt of Water Resources (TDWR) had mon-
itored the plant for several years. After determining that any re-
lease from the site was hazardous, due to the high arsenic concen-
tration, they issued a "No Discharge Order" for the entire site.
Action taken at the site as a result of this order prevented large
quantities of arsenic laden rainfall runoff from leaving the site.
Crystal Cehmical Company constructed a dike around the perim-
eter of the plant to contain all spills and precipitation. Three large
pits and several sumps were constructed to hold the contaminated
liquid, and spray evaporation systems were installed in the pits to
help evaporate the liquid. Additionally, a gas-fired evaporator was
installed to increase the volume that could be evaporated. Some of
the contaminated liquid was periodically trucked offsite and dis-
posed of by injection into a State approved commercial injection
well.
A flooded to semi-flooded condition existed at the plant most of
the time. The floor of the process buildings was covered with 6 to
8 in. of contaminated liquid due to corrosion holes in the metal
roof. Removal and/or disposal of the contaminated liquid from
inside the buildings and the plant grounds was an ongoing prob-
lem for several years.
Efforts for site cleanup and compliance were being exerted by
USEPA, State and county agencies. There was $112,000.00 in
USEPA penalties pending against the company.
Operations continued under adverse conditions until mid-Sept.
1981, when unusually heavy rains flooded the entire site and
created a serious potential for overflowing the dikes. At this time
the TDWR ordered the company to remove the contaminated
liquid to prevent an offsite discharge. The company responded by
saying it was beyond their financial capability to remove that much
liquid and subsequently filed for bankruptcy. As the State had no
emergency funds to cover the situation, the TDWR requested that
an emergency removal action be initiated by USEPA under Super-
fund.
RESPONSE ORGANIZATION
The USEPA initiated an emergency removal action on Sunday,
Sept. 20, 1981. A meeting was called at the site with the plant man-
ager, USEPA contractor, TDWR representative and USEPA On-
Scene Coordinator. The decision was made to dewater the site in
Phase I as the entire site was inundated with an estimated 1,000,000
gal of contaminated liquid that would have to be removed before
any additional work could be undertaken.
Twenty 7,500 gal stainless steel tank trucks were obtained to
transport the liquid approximately 40 miles to a State approved in-
jection well. On-site pumps and two rented pumps were positioned
so that four transports could be loaded simultaneously. Liquid re-
moval operations were conducted on a 24-hour basis for seven
days. A total of 815,000 gal of liquid was removed in that time
and it contained an average arsenic concentration of 20,000 mg/1.
After all liquid was removed from the site, it was found that most
of the area outside the buildings was covered with mud. In order to
determine what areas contained concrete, it was necessary to probe
most of the site and prepare a plat delineating the concrete from
the exposed soil. From the plat it was determined that approx-
imately one-half the site (2 Vi acres) was covered with concrete and
the remaining one-half consisted of pits, sumps and exposed soil.
Next, it was decided that Phase II would consist of removing one
foot of the contaminated top soil from the exposed areas to use to
backfill the pits and sumps. When this was accomplished, the sur-
face would be leveled and covered with a sheet of six-mil plastic.
This was to be covered with 6 to 12 in. of clean clay to be brought
on site. This clay cap would be graded for proper drainage and
338
CASE HISTORIES
-------
seeded for erosion control. Work commenced on Phase II, Oct. 6,
1981.
Periodic heavy rainfall continued to be a problem. Aside from
having to haul off many additional loads of contaminated liquid,
it made working conditions almost impossible at times. There were
no periods between rains adequate to dry the site. Heavy equip-
ment would bog down in the mud, and leveling and clay capping
were impossible. It was necessary to use powdered lime to dry and
stabilize the soil so the work could be accomplished. A total of 425
tons of lime was used during Phase II operations. This stabilized
the sludge in the pits as well as the muddy soil so it could be leveled
with heavy equipment and clay capped. Continued rain required
the building of dikes to keep the clean areas separated from the
contaminated areas. Rain falling on the clay capped areas was
allowed to run offsite, but that falling on the contaminated area
had to be contained and transported offsite for disposal.
Three-fourths of the site was clay capped and Phase II was com-
pleted on Nov. 8, 1981. The southwest one-fourth of the site con-
tained the process buildings, process equipment and storage tanks,
all of which were contaminated. No work could be accomplished
in this area until the Trustee in Bankruptcy sold the equipment and
tanks, and they were removed. The equipment was sold in Feb.
1982, removal operations commenced in May and were completed
in Sept.
In August 1982, the Trustee in Bankruptcy entered into a con-
tract to have the seven metal buildings removed from the site. This
work began in Sept. and was completed in Dec. During the removal
of equipment and buildings, some of the clay capped area was dam-
aged and had to be reworked. After the last building was removed,
the southwest one-fourth of the site was stabilized and clay capped,
and necessary repairs were made to other areas. Inclement weather
delayed work, and it was not until Feb. 20, 1983, that the final cap-
ping and grading were completed. A total of 1,700,000 gal of con-
taminated liquid was removed from the site.
PROBLEMS ENCOUNTERED
A significant problem and delay occurred in conjunction with the
sale and removal of the equipment and buildings arranged by the
Trustee in Bankruptcy. The OSC had no control over the timing
of third party operations arranged by the Trustee. This caused
numerous delays, considerable frustration and additional expense
in planning and scheduling work for USEPA contractors.
Process Buildings
The general condition of the three process buildings presented a
critical problem prior to their dismantling. The metal roofs were
so corroded and deteriorated that approximately 85-90% of all
precipitation falling on the roofs ran inside the buildings. The water
became contaminated as soon as it fell on the floor and had to be
trucked away for disposal. It was determined that any roof repairs
that could be made at a modest cost would be very cost effective.
Considerable savings would result from decreasing the amount of
contaminated water to be removed.
The chief problem to overcome was not the repairs, but how to
safely put workers on the roof to make the repairs. None of the
metal building contractors that wer? contacted would attempt the
repairs because the roofs were so weak. Even the beams were cor-
roded to the point that some were broken.
A system was devised using a safety cable attached to the build-
ing corners of the tallest building and stretched along the roof.
Workers wearing parachute harnesses with a safety line attached to
the cable could then get onto the roof. They also used a set of criss-
crossed boards to distribute the weight over a broad area. The large
holes and gutters were repaired, and this significantly reduced the
amount of rainfall entering the buildings. This effort reduced the
number of truckloads of contaminated liquid to be removed and
resulted in a substantial cost saving.
Binary Chemical Reactions
Possible binary reactions resulting from the mixing or spilling of
chemicals stored on-site presented a substantial threat to the health
and safety of the workers and residents in the immediate area.
Safety considerations commanded the highest priority and dic-
tated the removal of these chemicals prior to removing the tanks.
The chemicals were ranked according to the priority of their re-
moval, taking into account physical state (gases ranked first), po-
tential for binary reactions, toxicity and tank location. The follow-
ing list contains the chemicals found at the site listed in the priority
of removal:
Methyl Chloride—gas, stored as liquid under pressure. Methyl
chloride will react with aluminum and other active metals (mg, K,
Na). It will react with oxidizing materials (hydrogen, peroxide)
giving off phosgene (a very toxic gas). It may react with a strong
acid, such as sulfuric. The methyl chloride is in the same section
of the plant as the storage for arsenic trioxide, sodium arsenite,
sodium hydroxide, sulfuric acid and hydrogen peroxide. Methyl
chloride is a dangerous gas and therefore ranked as the highest
priority.
Sulfur Dioxide—gas, stored as liquid under pressure. It will react
with water or steam to form sulfurous acid. Sulfur dioxide is stored
near tanks of TEA, cacodylic acid, other suspected arsenic com-
pounds and rayon caustic. It is a gas and therefore ranked very
high.
Sulfuric Acid—liquid, assumed 98% pure. Sulfuric acid can com-
bine with any arsenic compound, releasing arsine (a very toxic gas).
Contact with methyl chloride may liberate phosgene. Sulfuric acid
will react with sodium hydroxide or water in an exothermic reac-
tion. Contact with active metals (zinc, iron, magnesium, etc.) will
generate explosive hydrogen. The acid tank is next to the hydrogen
peroxide tank and near the arsenic trioxide, sodium arsenite and
sodium hydroxide. The sulfuric acid can combine with many chem-
icals stored nearby, releasing dangerous gases. This is ranked as the
third priority.
Hydrogen Peroxide—liquid, oxidizing agent, assumed to be at
least 90% HjC^. Contact with organic materials (diesel fuel) will
cause explosive oxidation reaction. Concentrated hydrogen per-
oxide can explosively decompose, especially when it is contami-
nated with metals or metal salts. It was located next to the sulfuric
acid tank and near the tanks of: arsenic trioxide, sodium arsen-
ite, sodium hydroxide and methyl chloride. Its potential for explo-
sive reactions ranked its as the next priority.
Toluene—liquid, will react with strong oxidizing agents (hydrogen
peroxide). It was located near the napthylamine storage. Toluene's
flammability gives it the next priority.
Beta-napthylamine—solid, is not dangerously reactive. It may re-
act with hydrogen peroxide or sulfuric acid. It was stored near the
toluene. It is very toxic and should be removed after the toluene
because of its high toxicity.
Diesel Fuel—liquid, will react with hydrogen peroxide. It was
located near the office building. The danger of fire gave removal of
diesel fuel the next priority.
Sodium Arsenite—solid, will react with sulfuric acid to produce
arsine gas. It will also react with sodium hydroxide. It was located
near arsenic trioxide, sodium hydroxide, methyl chloride, hydrogen
peroxide and sulfuric acid.
Arsenic Trioxide—solid, will react with sulfuric acid to produce
arsine gas. It will also react with sodium hydroxide. It was located
near the sodium arsenite, sodium hydroxide, methyl chloride,
hydrogen peroxide and sulfuric acid.
Sodium Hydroxide—solid, may be stored as water solution. It will
react exothermally with acid or water. The storage tank was lo-
cated near the arsenic trioxide, sodium arsenate, methyl chloride,
sulfuric acid and hydrogen peroxide. Its corrosiveness and reac-
tivity gave it the next priority.
Mono or Di-sodium Methane Arsenate-Cacodylic Acid—liquids,
arsenic compounds may react with sulfuric acid to produce arsine.
CASE HISTORIES
339
-------
They were contained in numerous tanks located throughout the
facility.
Cyclohexanone—liquid. It is moderately flammable and will burn
when in contact with strong oxidents such as hydrogen peroxide. It
was stored near the napthylamine storage.
Triethanolamine (TEA)—liquid. It is slightly flammable and may
burn in contact with hydrogen peroxide or sulfuric acid. It was
stored near the sulfur dioxide tank.
Dinitrophenol—liquid. Explosion hazard when heated. Moderately
flammable. It was stored inside Process Building C.
TANK AND EQUIPMENT REMOVAL
All tank and equipment sold by the Bankruptcy Trustee had to
be decontaminated before removal from the site. Approximately
75 railcar and truck loads of equipment were hauled to other
plants, and about 25 truck loads of contaminated junk were hauled
to a state approved chemical landfill for disposal.
As each area was cleared, it would be stabilized and clay capped.
Diversionary dikes would be constructed to separate the clean from
the contaminated areas.
DRAINAGE
Accumulation of rainfall and site drainage was a serious prob-
lem. At first, there was no drainage from the site because all ac-
cumulated liquid was contaminated and had to be trucked away.
As each area was clay capped, runoff from that particular area
could be released, but it required diversionary structures to sep-
arate the clean from the contaminated areas and containment of
the contaminated liquid.
Eventually, the entire site was capped with a clay cover overly-
ing a sheet of polyethylene. The cap was graded to a low-angle
slope for drainage of precipitation. Approximately 60% of the site
drains toward the concrete driveway in the center of the site and
there was no outlet for this run-off except allowing it to exit the
property at the north fence on the west side of the driveway. This
caused the run-off to move across the unpaved section of the access
road west of the gate and enter a roadside ditch on the north side.
It caused the road to be muddy and soft most of the time.
On the east side of the entrance gate there is an inlet to a buried
storm drain, but the concrete driveway blocks drainage in that di-
rection. Consideration was given to breaking a section of the drive-
way and laying a drain pipe from the west side to the east side
and then repairing the concrete drive. Upon closer investigation,
it was determined that the concrete was approximately 18 in. thick.
Breaking out a trench would be a very labor intensive undertak-
ing and would have the driveway closed for an undetermined time.
This was not a desirable solution as equipment was being re-
moved and dump trucks were hauling in clay. Closing the drive-
way for any extended time would virtually shut down the entire
operation.
The OSC had knowledge of water jet equipment designed to
clean out storm sewers. This system uses high pressure water jets
to dislodge sand and trash and flush it out of the pipe. A water-
jet device is secured to a flexible high pressure hose and inserted
into the line. The device has two jets that point forward to dig into
the material, two jets on the side (one on either side) at 90° angles
to serve as reamers to widen the opening, and four jets at the rear,
set at 45 ° angles. These rear jets flush the material back from the
digging operation and out of the pipe; they also furnish the force
to drive the device forward.
The company was contacted to see if the device would dig a tun-
nel under the concrete driveway, a distance of about 40 ft, so an 8
in. drain pipe could be inserted. The company representative said
the device was designed to work inside pipe and therefore the direc-
tion of digging could not be controlled as the device was mounted
on a flexible hose.
It was proposed to the company that an 8 in. pipe be placed in
the ditch on the east side, by the storm drain inlet. Then place the
west end of the 8 in. pipe against the soil underneath the driveway,
aim the pipe in the desired direction and let the jetting device dig
out the end of the pipe. It was further suggested that a 10 ft sec-
tion of rigid steel pipe be inserted between the jetting device and
the flexible hose. This rigid pipe would limit the amount of devia-
tion that the jetting device could take. This proposal was accepted
by the company and the next day work was commenced. As the
device would dig and ream a few inches, the 8 in. drain pipe was
forced into the tunnel. The excavated material was washed out the
east end of the pipe.
This system worked with few problems, and the 8 in. drain pipe
was installed under the driveway without closing it to traffic. This
pipe now carries all run-off from the ditch on the west side of the
driveway directly to the underground storm drain.
EROSION CONTROL
Establishing a Vegetation Cover
After the north half of the site (about 2 acres) was capped and
proper drainage established, Bermuda grass was planted. Bermuda
was chosen because of the thick mat it forms on the surface and
the dense root system it develops to a depth of about 12 in. Bulk
seed was purchased and applied with a small broadcast spreader.
Since the clay contained very few nutrients, the area was fertil-
ized after the seed germinated.
In order to speed growth during the favorable growing season, it
was necessary to establish a watering system. The only water source
on site was a water well on the south side of the property. On-
site material was collected for water lines. Steel pipe previously
used for steam lines and PVC pipe previously used for overhead
electrical conduit was fabricated into water lines. Faucets were in-
stalled along these lines and the grass was watered with garden
hoses and sprinklers. A good stand of Bermuda developed.
Gravel Berms
A major concern associated with the integrity of the clay cap was
the control of erosion. The cap itself is essentially clay, and a veg-
etative growth has been established for two reasons. First, the vege-
tation will tend to prevent washouts or erosion on the surface and
secondly, the root system will help to hold the soil together and
prevent any trenches from forming. The site was graded to a gentle
slope in most areas so the runoff would be as uniform as possible
and prevent a large volume of runoff from occurring at any one
place. A concrete curb runs along the south and west sides of the
site at the fence line and the clay cap is slightly higher than the
curb. However, as the ground level of the site was built up higher
than surrounding ground, it created a steeper slope at the east and
north fence line and along the driveway inside the plant. To min-
imize the possibility of trenches forming along these steeper slopes
where the velocity of run-off would be increased, it was decided to
install gravel berms along the ridge where the slope is increased.
The berms were constructed by placing a mound of 1 '/i in. size
gravel about 18 in. wide and approximately 8 in. high along the
crest of the slope change. This would cause the run-off from the
broad gradual sloped area to accumulate behind the berm and de-
crease its velocity significantly. Then, the run-off would trickle
through the gravel over a wide area and migrate down the steeper
slope. Along the north and east fence, the run-off then leaves the
site. Along the driveway, the run-off would enter a drainage ditch
constructed along the west side of the driveway and enter a storm
drain just east of the north gate and be carried directly to the large
drainage ditch.
The berm and drainage ditch along the driveway and the benns
along the north and east fence were constructed in June 1982 and
worked well during the remainder of the emergency removal
action.
REMOVAL OF ARSENIC TRIOXIDE
When the plant was operating, arsenic trioxide, in a dry-powder
form similar to wheat flour, was delivered in railroad hopper cars.
340
CASE HISTORIES
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It was unloaded into an elevated storage tank with a capacity of
130,000 Ib. During the initial evaluation, the plant manager re-
ported that the storage tank was empty. There were, however,
three hopper cars containing various amounts of arsenic trioxide,
and arrangements were made for them to be removed. At that time
it was thought that the only remaining pure arsenic trioxide on
site was that portion that had been spilled during normal unload-
ing operations.
The storage tank was the last piece of equipment to be removed.
While making preparations for its removal, it was discovered that
the tank was 3/4 full (later determined to contain 99,000 Ib.) of
arsenic trioxide. The tank was owned by one of the equipment pur-
chasers, but the product was the property of the Bankruptcy Court.
The Trustee in Bankruptcy sold the product to a metal process-
ing company, and arrangements were made for the cleanup con-
tractor to transfer it to 55-gal drums and deliver the drums to the
purchaser.
This operation was evaluated as probably the most difficult and
dangerous to be conducted. Not only was the handling of the ma-
terial dangerous, but the condition of the tank was an unknown.
Several of the other tanks cracked or broke apart when they were
moved, and there was no reason to believe that this tank would not
be a problem. A large vibrator was attached to the bottom of the
tank, and it would be necessary to use the vibrator to get the ma-
terial to flow out the bottom. An auger was attached to the vibra-
tor, and this would also have to be used in the operation. As all
electric lines had already been removed, it was necessary to run
temporary lines to these two pieces of equipment. Both the vibrator
and auger were found to be in working condition.
A flexible hose was attached to the end of the auger and run
through a hole in the roof of the adjacent building. Inside the
building, a 16 ft x 16 ft room was constructed and covered with
plastic for dust control. The flexible hose delivered the product
through the roof of the room and into 55 gal drums. A vacuum
truck was used to continuously pull air from the room and pass it
through bag filters. A total of 133 plastic-lined drums were filled
with arsenic trioxide. Each drum weighed approximately 800 Ib.
The drums were placed on a roller platform before filling. When
filled, they were sealed and pushed outside the room on the rollers.
A forklift then moved each drum to another building where it
was washed off and then loaded onto a transport trailer outside the
building.
All personnel involved in this operation were equipped with fully
encapsulated, Level A, protective equipment. Before commencing
the transfer, all phases of the operation were checked, and a com-
plete practice run was conducted. Aside from a preliminary prob-
lem of getting the product to flow out of the tank, the operation
was a complete success.
In the event the tank had ruptured or arsenic trioxide was
spilled in any way, a fire truck was standing by. It was equipped
with a water cannon that could spray any dust cloud that might
form.
The Harris County Pollution Control Department conducted a
continuous air monitoring survey throughout this operation. One
upwind and two downwind stations were used. Chemical analyses
showed only background concentrations in these samples.
All nearby businesses had been alerted for possible evacuation
in the event a problem developed. The operation was conducted
on a Friday, Saturday and Sunday. Since school officials decided
that it would not be feasible to evacuate 200 small children in case
of an emergency, the school was closed Friday.
The all-clear signal was given at approximately 3:30 p.m. on
Sunday.
SAFETY AND COMMUNITY RELATIONS
A safety plan and Community Relations Plan were prepared.
However, coordinating the work and safety of several contractors
on scene at one time proved to be a problem. One equipment
purchaser had nine employees, a crane, a large fork-lift loader and
several trucks. The other equipment purchaser had ten employees,
a crane and several trucks on-site at the same time. Additional
damage was done to the roofs of the process buildings by the
cranes, and several clay capped areas were damaged by operating
equipment in the removal process. The water lines were broken
several times as were the safety showers and eyewash fountains.
All these damages necessitated repairs at USEPA's expense.
The purchaser of the metal buildings utilized as many as twelve
employees, two cranes and several trucks. He would remove a
building, or parts of one or two buildings, and then not come back
for several days. Extended periods of ideal weather would elapse
with no activity, and when the crew returned, it was frequently at
a time of inclement weather. Working under these conditions
caused additional damage to the site and the delay created a need to
remove more contaminated water after rains. After the OSC had
made numerous unsuccessful attempts to get the purchaser to pur-
sue the removal of buildings in a prudent manner, it became neces-
sary for the Bankruptcy Trustee to establish a cut-off date for this
operation.
While dismantling one of the process buildings, an employee
was using a cutting torch in an area where no fires were permitted.
Sparks and molten metal fragments ignited an area saturated with
dinitrophenol. The ensuing fire created a large plume of yellow
and black smoke. Houston police closed a major street due to poor
visibility and evacuated workers from a nearby construction site for
fear of toxic fumes. The Houston Fire Department responded with
more than adequate equipment; five firetrucks and an ambulance.
This incident caused a serious community relations problem and
probably destroyed the goodwill that USEPA had established to
this point.
However, in accordance with the Community Relations Plan, a
meeting was held with concerned citizens, media and parents of
children attending the nearby elementary school. The USEPA,
State and County representatives gave explanations, answered
questions and assured those present that third party contractors
and their employees would be closely supervised. This event and
succeeding events caused the OSC to inform the purchaser and
his employees that any additional violations of safety and/or site
protection instructions would result in USEPA's obtaining a court
order for their removal from the site by a U.S. Marshal.
This group completed their removal operation on Dec. 2, 1982,
but left a significant amount of trash which had to be removed
and disposed of at USEPA's expense.
CONCLUSIONS
Much of the work was conducted on week-ends and days run-
ning longer than eight hours. Even though this time frame re-
quired paying labor time-and-one-half, it proved to be cost-effec-
tive in getting work accomplished when working conditions were
good. As each area was clay capped, it reduced the amount of
water to be hauled out after a rain. The clay capping method of
covering was effective in presenting a discharge of contaminated
run-off.
The use of lime to stabilize the sludge created an additional bene-
fit, as it converted some of the arsenic to calcium arsenate, which
is less soluble in water.
All work was completed on Feb. 20, 1983. The duration of the
removal was 519 days. USEPA work consisted of 138 days (26.6%
of the time) while the balance of the time, 381 days (73.4%), was
consumed by waiting on decisions of the Bankruptcy Trustee,
waiting on and monitoring third party contractors and delays
caused by inclement weather.
The total expenditure from Superfund for this project was
$761,798.53. A cost-recovery action was filed by USEPA in the
Bankruptcy Court to establish a primary claim against the assets of
the bankrupt estate. This issue was settled out of court in favor of
USEPA.
The State has assumed the lead role in conducting a feasibility
study to determine what remedial action should be undertaken.
CASE HISTORIES
341
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THE CASE STORY OF THE BT-KEMI DUMPSITE
PETER SOLYOM
Swedish Environmental Research Institutet (IVL)
Stockholm, Sweden
INTRODUCTION
Sweden's chemical industry is, in comparison with the United
States' chemical industry, rather small. The structure of it is, how-
ever, similar to that in the U.S. A number of the Swedish chem-
ical companies also have subsidiary companies in the U.S., and
some of them are not unknown in connection with hazardous waste
sites.
Hazardous waste management in Sweden is regulated by a 1975
decree. The law defines hazardous waste and contains regulations
on the obligation for information, transport, final disposal and
export of hazardous wastes. Detailed regulations for application of
the law are issued by the Swedish Environmental Protection Board.
The number of known hazardous waste disposal sites in Sweden
is limited. An inventory of municipal waste disposal sites, with
specific regard to the inclusion of hazardous wastes, is in pro-
gress. The BT-Kemi dumpsite is at present the only major clean-
up activity in Sweden.
DESCRIPTION OF BT-KEMI
BT-Kemi was a chemical company which produced herbicides,
mainly phenoxy acids, involving chlorination and condensation re-
actions of phenol and cresol. Production took place from 1965 to
1977 in a former sugar mill in southern Sweden. The wastewater
from the production was, for a number of years, collected in hold-
ing ponds on the mill area. Some of the solid wastes from produc-
tion were buried, as the company claimed, after "careful purifi-
cation", in the same area. As the factory did not have any dis-
charge, the company claimed that biological degradation took
place in the holding ponds and evaporation from the ponds kept
the water in balance.
Very soon after the start of production, signs of pollution were
observed.
In the fall of 1975, about 200 drums were excavated. The chem-
ical analysis of their contents revealed high concentrations of chlor-
ophenols and phenoxy acids. During the summer of 1977 more
Figure 1
The BT-Kemi Area
342
CASE HISTORIES
-------
drums were dug up. A total of about 600 drums, many degraded
by corrosion and leaking into the ground, was found. Investiga-
tions by the Swedish Environmental Protection Board showed that
highly polluted water was being discharged into the nearby river at
the same time.
As a consequence of disobedience of environmental legislation,
the presence of highly toxic chemicals (for example di-nitro-sec-
butyl phenol, DNBP, in addition to the above mentioned chem-
icals) and the suspicion of the presence of 2,3,7,8-TCDD, the fac-
tory was closed down by the authorities.
At this time, the responsibility for the cleanup of the BT-Kemi
area was taken over by the County Administration. The Admin-
istration commissioned the Swedish Environmental Research In-
stitute (IVL) to investigate:
•Measures against contamination of groundwater and the river
•Contamination of wastewater in the holding ponds
•Contaminated soil
•Highly contaminated wastes stored in drums and tanks
•Residual chemicals in the factory
•Contamination of factory building and processing equipment
The investigations should result in recommendations for meas-
ures against pollution, recommendations for destruction tech-
niques for different wastes, information about the quantities of
different wastes and cost assessment for technically feasible
destruction alternatives.
INVESTIGATIONS
Risk Assessment
The site plan of the area is shown in Figure 1. The area is about
100,000 m2 and is divided by a railway.
The factory building, holding tanks for chemicals, etc., are on
the southern part. The holding ponds and the dumpsite are on the
northern part. The area is bordered by a small river. Numerous
sewers and pipes of varying dimensions and quality were found
beneath the factory area. A risk assessment of health and environ-
mental effects was performed.
One hundred seven wells, selected by the health authorities and
located in the vicinity of the BT-area and along the river down-
stream of the area, were sampled and analyzed. The choice of the
wells was in many cases based on geographical and topographic
conditions, but public concern and fear had to be considered.
The samples were analyzed for phenoxy acids, chlorophenols
and cresols and DNBP. The determinations were carried out by
means of gas chromatography (GC). Six different phenoxy acids
(including 2,4-D and 2,4,5-T), five chlorinated phenols (di, tri-,
tetra- and pentachlorophenols) and DNBP were determined with a
sensitivity of 0.01 to 0.2 jig/1, depending on the determined chem-
ical. Ten of the 107 wells showed contamination by some of the
chemicals occurring at BT-Kemi. Only four wells were directly in-
fluenced by the contaminated river. The level of contamination was
in the range of 0.2 to 3 jtg/1.
According to the evaluation of medical and lexicological ex-
pertise, this degree of contamination did not pose any risk to
public health. Moreover, a health investigation of the inhabitants
near BT-Kemi, conducted by the County Administration, did not
detect symptoms attributable to the activities of BT-Kemi. Never-
theless, secondary effects, such as social and psychological effects,
were notable.
The risk assessment from the environmental viewpoint was per-
formed by chemical analysis of river water both up and down-
stream of the dumpsite. The river was sampled at four points up-
stream and four points downstream of the area.
The chemical analysis showed an increase of the phenoxy acid
content by a factor of 5 to 25 depending on the rainfall in the area.
The increased concentration of herbicides caused serious damage to
market gardens downstream of BT-Kemi where river water was
used for irrigation.
It was shown that the dumpsite and the piping beneath the area
were leaking contaminants into the river.
Protection of the River
In order to establish the conditions at the dumpsite relative to
the content, amount, extension and migration of contaminants,
geological, hydrogeological and chemical investigations were per-
formed.
The geological investigation included determination of soil struc-
ture by screw drill sampling at 140 bore holes down to firm clay
(2-12 m) and separation of different types of earth layers. About
250 earth samples were collected for chemical analysis. The
position of firm clay between the bore holes was determined by a
refractometric seismological method.
The hydrogeological study, conducted by observation of the
movement of the groundwater table in 33 pipes, showed the exis-
tence of four aquifers in the area depending on the presence of
different earth layers with varied high and low permeabilities.
Chemical analysis of the groundwater revealed that the two upper
aquifers were contaminated.
From the combined results of the geological, hydrogeological
and chemical investigations, it could be concluded, that:
•Wastes were deposited in three main areas
•The area contained about 150,000 m3 of earth with contam-
ination ranging from 0 to more than 500 ppm phenoxy acids,
chlorophenols and DNBP from the surface to between 2 to 6 m in
depth
•The maximum seepage rate from the area was 7.5 mVhr
•The area had to be shielded in order to protect the river
These conclusions led to the immediate construction of sunken
wells, a drainage system around the area, collection of drainage
water in holding ponds, a bentonite shield outside of the drainage
system and a safety dike toward the river.
The bentonite shield was constructed down to firm clay by us-
ing two different techniques. The shield along the river and at the
west side of the dumpsite was placed by first excavating a slit about
0.6 m wide. The slit was filled continuously during the excava-
tion with a 10% bentonite slurry in order to protect it from
collapse. Finally, the slit was filled with a mixture of bentonite,
sand and water.
Toward the east, the shield was constructed by injection of a
15% bentonite slurry through a number of perforated pipes at the
same time. The separate injections formed an interconnected, tight
shield down to firm clay.
The contamination of the river by leakage from the dumpsite
ceased after the completion of the described measures.
The Treatment of Drainage Water
The drainage water, which at this stage was collected in the
holding pond, consisted of leachate from the deposited wastes and
other liquid wastes pumped to the pond from different parts of
the factory. As the BT-company installed, while still in produc-
tion, an activated carbon (AC) treatment plant, it was obvious
that it should be further tested for treatment purposes.
Although different treatment alternatives, such as chemical floc-
culation, extraction with solvents, direct biological treatment, etc.
were tested under laboratory conditions, the AC-treatment proved
to be the most successful.
The efficiency of the AC-treatment was very high. The con-
centrations of 190 mg/1 of phenoxy acids and 12 mg/1 chloro-
phenols were reduced on an average to less than 0.1 and 0.01 mg/1.
Seven tons of activated carbon eliminated 1 ton of phenoxy acids
and chlorophenols. The costs of the AC-treatment amounted to
about 2.20/m3 pounds of drainage water.
However, the treated water still contained organic matter which
measured as 200 mg/1 BOD. The treated water was, therefore, dis-
charged to a municipal biological treatment plant prior to dis-
charge to receiving water.
The Treatment of Wastes
The wastes in the area consisted of liquid and solid wastes from
the factory and contaminated earth from the dumpsite. As men-
CASE HISTORIES
343
-------
tioned previously, certain liquid wastes with lower concentrations
of phenoxy acids and chlorophenols (less than 500 mg/1) were
either pumped to the holding pond at the dumpsite or directly to
the AC-plant.
Destruction of the more concentrated liquid wastes by incinera-
tion in a cement kiln was tried. The incineration was successful and
the costs were calculated to be about $100 per ton.
The destruction of solid wastes, including the contaminated
earth, was more complicated. Possibilities of composting, inciner-
ation and leaching were investigated.
Composting was tested under laboratory conditions. In order to
obtain satisfactory results, the waste had te be mixed with bark
and digested municipal sludge in the proportion of 1:1:0.5 (by
volume). Eighty to ninety <7o removal of the chemicals, with the
exception of 2,4,5-tri-chlorophenol, was achieved after about 1
month.
The most suitable composting technique was performed in aer-
ated strings with suction of the air. The exhaust air had to be
treated in a humic filter in order to avoid odor problems. The
costs ot the composting were estimated to be about $10 per ton
of waste.
The incineration of solid wastes was not possible in Sweden at
that time (1978). The investigation showed, however, that existing
cement kilns could be supplemented with a pre-kiln operated at
low temperature, 400-500°C, for volatilization of the chlorinated
substances from the solid wastes. The volatilized gases would be
incinerated in the cement kiln. This alternative was never utilized.
Incineration facilities were available abroad (France, Germany,
U.K.) and the destruction costs were given at that time (1978) as
about $250 per ton waste.
The possibility of leaching the contaminants from the earth and
solid waste was evaluated using data from the previous geological
and hydrogeological investigations and laboratory tests conducted
with contaminated earth with varying permeabilities. The findings
showed that phenoxy acids and chlorophenols were leachable. The
best results were obtained by forced leaching through an infiltra-
tion ditch. If performed, the leachate would be directed through
the drainage system and treated by activated carbon adsorption.
SUGGESTED CLEANUP ALTERNATIVES
The purpose of the cleanup was to remove the contamination
from the area. Based on the results of the investigations, the clean-
up would preferably be performed by leaching of the contam-
inants and by AC-treatment of the leachates. The AC-treatment
would continue until the concentration of contaminants in the
drainage water decreased to less than 0.5 mg/1, the limit set by the
authorities. After that period, the drainage water would be dis-
charged directly to biological treatment.
The wastes on the dumpsite could roughly be divided in three
groups, based on the degree of contamination:
1. Low contamination (less than 50 ppm), about 130,000 m3
2. Medium contamination (50-500 ppm), about 15,000 m3
3. High contamination (more than 500 ppm); about 2,000 m3
Eight theoretically possible cleanup alternatives were considered.
All included natural and forced leaching and some kind of special
treatment of medium and highly contaminated wastes. Only three
of the alternatives were realistic regarding time and cost aspects.
These alternatives are given in table 1:
Table 1
Cleanup Alternatives
Alternative Waste group Duration, Cost, million
1 2 3 years USS
Forced leaching -•-( + ) 5-6
Forced leaching + + 3
composing + +
Forced leaching •+• + 3
composting +
incineration +
2.5
2.5
3.5
The County Administration chose forced leaching as the most
suitable alternative because of the risk of smell with composting.
Additional suggestions included the transfer of certain wastes, for
instance parts of the deposition on the factory site and the remains
of the demolished factory (about 2,800 tons), to the dumpsite. The
cleanup of the BT-dumpsite was authorized by the Swedish Gov-
ernment in June 1978 and started immediately.
CLEANUP ACTIVITIES 1978-1983
Since 1978, the dumpsite has been treated through forced leach-
ing and the drainage water purified by AC-adsorption. The leach-
ing was performed with AC-treated drainage water and some-
times with some additional river water. During heavy rainfall, when
the holding capacity of the pond was not sufficient, surplus quan-
tities of purified water were discharged into the municipal sewer.
The recirculation of water was high, but an average of 50,000 m!
per year had to be discharged.
Since 1978, about 5 to 6 tons of phenoxy acids and 0.5 to 0.6
tons of chlorinated phenols have been removed from the dump-
site by leaching and AC-treatment. The efficiency of the AC-treat-
ment was controlled by chemical analysis of weekly composite
samples. The efficiency and adsorption capacity of the activated
carbon was approximately the same as during the test period in
1977. As the AC-plant and the activated carbon were leased from
Chemviron Corp., the activated carbon was replaced every fourth
month. Each exhausted activated carbon batch (about 9 tons)
was sampled and analyzed especially for TCDD before shipment
for regeneration.
The TCDD content was always under detection limit. The regen-
eration was performed in the U.K. About 110 tons of activated car-
bon were used until the AC-treatment was stopped in Nov. 1982.
The AC-treatment of drainage water was run without problems
during the first two years. Increasing pressure drops through the
AC units, which consisted of a sand filter and two carbon filters
in series, were observed in spite of normal back flushing routines.
The main part of the clogging was located in the first carbon
filter.
Microbiological investigations showed a massive growth of bac-
teria. Bacteria were absent during the first two years because of
the high toxicity of the drainage water. The isolated bacteria from
the carbon filter were capable of metabolizing phenoxy acids and
chlorophenols.
In September 1981, the organic content of the drainage water
was about 10 mg/1. The direct discharge limit of 0.5 mg/1 had not
been achieved. The treatability of the drainage water without AC-
treatment was stopped. The direct discharge of untreated water
did not influence the efficiency of the biological treatment plant
since the hazardous waste site flow only comprised 1 to 2% of the
total flow.
In Nov. 1982, when the AC-treatment was finally stopped, the
organic content of the drainage water was approximately 0.9 mg/1.
The municipality which operates the biological treatment plant and
is responsible for the sewer, charges the County Administration
$1.20 m! for treating the drainage water. This amounts to about
$60,000 per year. The County Administration commissioned IVL
to investigate the possibility of directly discharging the untreated
drainage water to the river, which is the natural recipient of the
dumpsite area.
These investigations included tests of biodegradability, bio-
accumulation, acute and subacute toxicity toward aquatic organ-
isms and growth of aquatic and higher plants. The tests were
conducted with a number of drainage water samples under differ-
ent weather conditions and with river water for dilution.
The biodegradation of the organic components was slow at the
bacterial densities present in the river water. Some of the com-
ponents were nondegradable and showed a potential for bioaccum-
ulation. Toxic effects on fish, daphnia and algae were eliminated
at dilutions of 50:1. Elimination of growth inhibition of higher
plants demanded dilutions of drainage water by 2,000 to 5,000
344
CASE HISTORIES
-------
times. Considering the volumes of drainage water discharged and
the flow variation of the river throughout the year, these dilu-
tions could not be achieved. No direct discharge of drainage water
was therefore possible.
The heavily concentrated solid and liquid wastes were stored
for a number of years awaiting final destruction. After long nego-
tiations, the wastes were transported abroad for incineration. Both
solid and liquid wastes had to be repacked in order to meet trans-
port regulations for toxic chemicals. The liquid wastes, amounting
to about 300 m3, were pumped into railway tanks. The solid wastes
(about 45 m3) were packed into 60 or 200 kg drums according to
the instructions of different destruction companies in Europe.
About 3.5 m3 of wastes are still at the BT-area. These are
dioxine-containing production residures which never were depos-
ited in the dumpsite. There are presently no facilities in Europe
willing to undertake the destruction of these wastes.
SUMMARY
The historical background, the initial investigations and the
cleanup of the BT-Kemi dumpsite have been described.
The activities demanded the expertise of many disciplines, both
managerial and scientific. Besides project management, IVL sup-
plied experts in chemistry, biology, geology, treatment technology,
toxicology, ecology, etc., from its own organization. Medical and
health aspects were covered by the County Administration.
As many problems in connection with the cleanup were new, a
certain amount of research had to be undertaken, especially in the
treatment of liquid and solid wastes.
An unexpected, but very important, part of the work was within
the information field. The inhabitants of the municipality near
BT-Kemi had to be informed about the activities carried out and
the results of different investigations. The cleanup activities would
not have been possible without the confidence of environmental
groups in the area and in the country.
The cleanup limits set by the authorities were severe, depending
partly on the actions of environmental groups.
IVL predicted that the contamination limit would be achieved
within five to six years. Now, six years after the cleanup started,
the concentration of drainage water in the holding pond is approx-
imately 0.5 mg/1, equal to the limit set by the authorities. The
effluent of the dumpsite can now be regarded as an ordinary
industrial effluent. The forced leaching of the dumpsite has to be
continued in order to prevent breakthrough of contaminated
groundwater to the river. It is very difficult to predict how long this
activity must go on.
The costs of the cleanup including investigations, research, treat-
ment and disposal, amount to about $6 to $7 million U.S. The
annual costs of operating the leaching system and paying the
charges for treatment of the leachate are estimated to be $100,000.
The costs are being paid by the taxpayers of Sweden through the
Swedish Government.
CASE HISTORIES
345
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INVESTIGATION OF SUBSURFACE DISCHARGE
FROM A METAL FINISHING INDUSTRY
GEORGE W. LEE, JR.
RICHARD D. JONES
G. DAVID KNOWLES
SCOTT J. ADAMOWSKI
O'Brien & Gere Engineers, Inc.
Syracuse, New York
INTRODUCTION
In Aug. 1981, the New York State Department of Environmental
Conservation (NYSDEC) issued an order to a metal finishing and
manufacturing facility indicating alleged violations of Article 17 of
the Environmental Conservation Law (ECL). The order stated that
the facility had a permitted point source discharge into the ground-
waters of the State, the discharge was located approximately
1000 ft from a Town water supply well and the Town well had been
tested and determined to contain 1,1,1-trichloroethane (which had
been handled, stored or otherwise utilized by the metal finishing
and manufacturing facility). It ordered that a hydrogeologkal in-
vestigation should be conducted.
The order stipulated that the hydrogeological study must pro-
vide information relative to the metal finishing and manufac-
turing facility and include the following:
1. A statement indicating the property affected by the discharge
and the extent to which the party controlling the discharge is
responsible for any contamination present
2. A hydrogeologic analysis of the affected aquifer, including re-
sults of a drilling and sampling program
3. A determination of direction and rate of flow of both the dis-
charge and natural groundwater
4. An evaluation of adverse effects of the discharge on aquifers,
potable water supplies or other surface or groundwater of the
State.
5. An evaluation of the underlying strata's ability to attenuate
potential pollutants such that best usage of groundwaters is
maintained
In Oct. 1981, O'Brien & Gere Engineers, Inc. was authorized to
perform the hydrogeological investigation and prepare a report
which would address the concerns of the order. The investiga-
tion was divided into five categories:
•Background research and gathering of available data
•Field investigation
•Evaluation of data
• Development of remedial alternatives
•Additional work
AVAILABLE DATA
Prior to the initiation of a field investigation, pertinent data was
obtained to aid in the selection of investigative techniques which
could be used. All previous analytical results obtained by NYS-
DEC, the New York State Department of Health (NYSDOH) and
other sources were located, obtained and reviewed. An understand-
ing of the manufacturing operation, the subsurface disposal
mechanism, the nature of the chemical in question, the quanti-
ties used and the effects of the chemical on man and the environ-
ment were also acquired in order to execute a safe, thorough and
effective field investigative program.
The metal finishing and manufacturing facility began operation
in Nov. 1977, and ceased operation in Dec. 1980; there are no plans
to resume manufacturing operations at the location.
The manufacturing operation at the facility consisted of cleaning
stainless steel and non-stainless metal products. The cleaning was
accomplished utilizing a mechanized conveyor system, with a
separate conveyor utilized for the washing and rinsing of the metal
products prior to the assembly of the component parts. Clean-
ing consisted of the metal products passing through a degreas-
ing tank, where a mist of 1,1,1-trichloroethane was sprayed onto
the metal surface. The parts were then submerged in a bath of
1,1,1-trichloroethane, where contact with the degreaser was main-
tained for a period of time to remove residual cutting oil and
other contaminants attached to the metal. Following degreasing,
the metal products were washed and rinsed. Wastewater from the
washing and rinsing operation was discharged along with other
waters, primarily from restrooms and process cooling waters, to the
subsurface disposal system.
The facility was issued a NYSDEC State Pollutant Discharge
Elimination System (SPDES) discharge permit which became effec-
tive in Aug. 1979. This discharge permit authorized a discharge
into the receiving groundwaters, tributary to a major river, at a
1,1,1-trichloroethane concentration not to exceed 0.05 mg/1.
Based upon the contamination evidenced by analytical results of
NYSDEC, NYSDOH and others, it was alleged that the facility
had exceeded its permit limitations. To examine this allegation, a
materials mass balance was performed.
The mass balance evaluation was based upon purchasing
records, interviews with available facility personnel and the docu-
mentation of sizes and ratings of various pieces of equipment.
Chemical purchase and recycle records provided an indication of
the amount of 1,1,1-trichloroethane which was purchased and the
amount which was returned to vendors. The difference between
the amount purchased and the amount returned was considered to
be the amount which was utilized during processing. Of this
amount, some portion had been released to the atmosphere
through volatilization, with the remainder being attributed to
effluent discharge to the subsurface waste disposal system.
The subsurface waste disposal system for the facility was con-
structed in early 1979. The system was designed as a leach field,
with a total leach field area 72 ft x 100 ft. Based upon SPDES per-
346
CASE HISTORIES
-------
mit issued and the plant's water use records, it was calculated that
the allowable mass of 1,1,1-trichloroethane which could have been
legally discharged to the subsurface disposal system over the course
of the facility operation was 10.4 Ib.
Volatilization calculations were performed based upon physical
characteristics of the 1,1,1-trichloroethane, conditions of operation
including temperature, surface area of chemical exposure, sizes of
exhaust fans and vents and operating times and on chemical pur-
chasing records. From this information, the estimated amount of
1,1,1-trichloroethane which was discharged to the subsurface dis-
posal system, and hence, potentially to the groundwater system,
was calculated by difference to be 2200 Ib.
This figure was checked by a calculation of the total pounds of
1,1,1-trichloroethane leaving the facility, utilizing the facility's
water use records and an estimate of the discharge concentra-
tion. This concentration was based on the limited data available,
but generated a reasonable result, indicating the estimate to be rep-
resentative of actual conditions.
This estimate supported previous groundwater analyses per-
formed by NYSDEC, NYSDOH and others which showed elevated
levels of 1,1,1-trichloroethane in samples from the Town well and
nearby residential wells. The mass balance evaluation then served
to support the premise that the 1,1,1-trichloroethane was in fact
in the groundwater and may have originated from the metal fin-
ishing and manufacturing firm.
This presented a bonafide concern on the part of the regulatory
agencies and municipalities involved, since 1,1,1-trichloroethane,
although not considered a carcinogen, has been considered a poten-
tial risk to humans by the USEPA based on the limited toxicologi-
cal data that exist.1
A computer based literature search was performed to locate the
available sources of information;2"10 specifically to determine the
environmental fate of the 1,1,1-trichloroethane. Several documents
were obtained which outlined the potential fate mechanisms con-
sisting of sorption, biodegradation and bioaccumulation, hydrol-
ysis and oxidation. From these documents, it was determined that
the 1,1,1-trichloroethane in the groundwater was not readily adap-
table to any of these mechanisms, and, therefore, would likely re-
main in the environment if not removed from a subsurface loca-
tion.
Based upon the above, it became imperative that the field inves-
tigation begin; to further document the existence of the chemical in
the groundwaters, to define the limits of the affected area and to
address the concerns and develop responses to the issues raised in
the consent order.
FIELD INVESTIGATION
The field investigation was conducted from Nov. 1981 to June
1982, and included:
•Drilling of test borings to determine the underlying soil profile and
aquifer lithology
•Installation of groundwater monitoring wells to establish hy-
draulic heads within the aquifer, to determine groundwater flow
rates and direction and to establish the distribution and concen-
tration of 1,1,1-trichloroethane, if detected, migrating from the
site
•Collection and analysis of surface water, sediment and residential
groundwater samples to ascertain if 1,1,1-trichloroethane had
migrated beyond the property of the metal finishing and manu-
facturing facility
•Performance of aquifer pump tests in order to measure the trans-
missivity and specific yield of the aquifer in question
•Topographic survey to determine the location and elevation of the
significant features at the facility
The first phase of the field investigatory work included the in-
stallation of a total of 11 groundwater monitoring wells between
Nov. 1981 and May 1982. These groundwater monitoring wells
served to establish a contour map of hydraulic heads, the flow rate
and direction of groundwater movement and to provide informa-
tion regarding the geology of the site. They also provided sampling
points from which representative samples of the groundwater could
be withdrawn.
The monitoring wells were installed using a Central Mine Equip-
ment 3-1/4 in. inside diameter hollow stem auger with a stainless
steel well screen integrated into the bottom 5 ft. section. This uni-
que approach to drilling enabled the collection and analyses of
groundwater samples at various depths during the drilling process
so that the permanent stainless steel well screen could be placed in
the vertical zone which had the greatest apparent contamination.
The technique utilized the screened auger as the lead auger, with
groundwater samples collected at the screened elevation through
the auger's hollow stem.
The successful implementation of this technique required rapid
(24 hr) laboratory turnaround time so that groundwater monitor-
ing wells could be installed with screens placed at the desired eleva-
tions on the day following sample collection.
All groundwater monitoring wells were constructed of 2 in. out-
side diameter stainless steel well screen and riser pipe. Stainless steel
was used to ensure that there would be no analytical interference,
as could be the case were standard polyvinyl chloride (PVC) screens
and risers used.
Well nests were constructed in several borings where two stain-
less steel well screens and stainless steel riser pipes were installed.
The well screen to be installed at the lower elevation was placed
first at the selected depth, and Silica sand was placed around the
well screen to an elevation just above the top of the well screen.
Auger cuttings were then placed in the boring to the lower eleva-
tion where the upper well screen was to be placed. Nesting of wells
provided for the monitoring of upper and lower aquifer zones so
that the location having the greatest contamination could be de-
termined.
Following installation, all wells were developed by removing at
least three well volumes of water from each well. Exact elevations
of all groundwater monitoring wells were established, and upon
sufficient recovery, groundwater surface elevations were recorded.
The ground elevation at each of the groundwater monitoring wells
was also established using USGS datum, as determined from a top-
ographical survey.
During installation, it was imperative that equipment which
would be used between boreholes, including all augers, split spoons
samplers and miscellaneous tools used in the installation of ground-
water monitoring wells, be thoroughly cleaned by washing with
soap and water, a rinse with hexane and a final rinse with distilled
water. The equipment was then dried under a heat lamp prior to
reuse. This cleaning and rinsing process was conducted to prevent
cross-contamination of the borings by the equipment.
During drilling operations and the installation of groundwater
monitoring wells, a safety protocol was implemented to protect
the workers. The safety equipment available for use as necessary
included:
•Protective goggles
•Rubber gloves
•Rubber boots
•Acid-resistant suits
•Hard hat(s)
•Dual carbon filter respirators
Groundwater samples were obtained from the monitoring wells
periodically to evaluate the characteristics of the groundwater
and to document variations in 1,1,1-trichloroethane concentrations
with time. Residential well samples were also obtained from nearby
homes and businesses to aid in the definition of the limits of con-
tamination.
The next phase of the work consisted of drilling four soil borings
into the previously described subsurface disposal area. The purpose
of installing these borings was to obtain an undisturbed soil sample
beneath the leach field. Soil samples were then analyzed to deter-
mine if a reservoir of 1,1,1-trichloroethane resided in the soils
beneath the leach field. The test borings were completed using
CASE HISTORIES
347
-------
LOCATION OF SEDIMENT SAMPLE
TEST 0OPJNG
APPROXIMATE PHOPEHTY LtIC LOCATION
Figure 1
Site plan including locations of wells, test borings and sampling locations.
conventional hollow-stem augers, with split spoon samples ob-
tained continuously from the groundwater table. Equipment was
cleaned in the previously mentioned manner to eliminate contam-
ination between boreholes.
Finally, sediment samples and surface water samples were
obtained from a lagoon adjacent to the facility. Sediment samples
were obtained by driving Lexan tubing into the sediment and ex-
tracting the tubing to retrieve sediment cores. These core samples
were analyzed for 1,1,1-trichloroethane to ascertain whether or not
the chemical had migrated to the soils beneath the lagoon.
All sampling was performed in accordance with standardized
sampling protocols. Samples were collected utilizing methods that
minimized cross contamination, placed in laboratory cleaned glass
containers and placed on ice for preservation during transport to
the laboratory. During groundwater, soil, surface water and sedi-
ment sampling, the previously listed safety equipment was utilized;
rubber gloves were disposed of after each sample was collected to
avoid any possible cross-contamination of samples.
In addition to the groundwater monitoring wells previously
identified, a 4 in. diameter PVC well was also installed. PVC was
utilized in the construction of this well, since the well's primary
function was as a pumping well from which aquifer characteris-
tics could be identified.
Two pump tests were performed to determine aquifer character-
istics during June of 1982. The pump test data were useful in inter-
preting aquifer coefficients including transmissivity, hydraulic con-
ductivity, specific yield and the radius of the cone of depression.
Information such as this is used as an aid in estimating the rate
at which the groundwater can flow, the degree of contamination
which could be intercepted by a well or well system and the length
of time which would be required for the natural restoration of the
aquifer. The information could also be used to estimate the maxi-
mum rate at which the aquifer could effectively be pumped as an
active method of aquifer restoration.
Last, a topographic survey of the facility was performed to
establish elevations and locations of groundwater monitoring wells
and soil borings as well as other significant land features (Figure
1). The results of the investigation were presented as a hydrogeo-
logical report to the client and all involved regulatory agencies in
Aug. 1982.
RESULTS OF FIELD INVESTIGATION
As a result of the field investigation, it was determined that the
metal finishing and manufacturing facility had exceeded the
SPDES permit for 1,1,1-trichloroethane. This conclusion was
based upon the results of groundwater samples obtained from the
monitoring wells installed as part of the investigation and the ma-
terial mass balance evaluations as previously discussed.
Data from each well were plotted on a base map to present all
1,1,1-trichloroethane concentrations detected. This identified a
plume of contaminant which appeared to have originated at the
discharge point of the facility and extended to the locations shown
on Figure 2.
348
CASE HISTORIES
-------
mvert
LOCATION OF 3URACE SAMPLE
TEST BORING
CROUNOWATER FLOW LMC
GROUNOWATER CONTOUR LINE
Figure 2
Results of field investigation under static (non-pumping) conditions.
During the course of the groundwater sampling and monitoring
program, it became evident that the concentrations of 1,1,1-trich-
lorethane detected in the groundwater were decreasing in the direc-
tion of the Town well. This trend was to be expected since there had
been no additional sources of wastewater since the facility closed
in 1980. When the Town well, which is approximately 1000 ft from
the discharge location, was operational, the well was expected to
have created a cone of depression that extended such that the dis-
charge location would have been within the radius of influence of
the well. This created a situation in which the well pumping in-.
creased the water table gradient and accelerated the flow of
groundwater to the well, drawing the 1,1,1-trichloroethane with the
water. Following shut down of the well, this situation ceased and
concentrations approaching the well began to diminish.
The analytical results of the soil boring samples from the sub-
surface disposal system contained no residual 1,1,1-trichloroethane
concentration. This was verified by data obtained during the
previously mentioned literature search which produced docu-
ments stating that the 1,1,1-trichloroethane is not attenuable by
most soils. This finding was documented by conducting a soil iso-
therm experiment utilizing actual soil and groundwater obtained
from the site (Table 1).
It was concluded that the 1,1,1-trichloroethane had entered the
groundwater in the same direction and at the same rate as the
groundwater toward a nearby river. Samples of the river water were
analyzed and found not to contain concentrations of 1,1,1-trich-
loroethane. This natural boundary and the groundwater monitor-
ing wells and residential wells sampled serve to define the extent of
the contamination, with the groundwater monitoring wells also
providing sufficient data to calculate the direction and rate of
movement of the groundwater. In general, the hydrogeologic in-
vestigation produced results which could be used to address the
concerns of the order and provide a basis for the development of
remedial alternatives.
DEVELOPMENT OF REMEDIAL ALTERNATIVES
The field work and hydrogeological investigation provided
engineers with sufficient data to formulate a list of remedial altern-
atives which would provide the town with a potable water supply
and, if required by NYSDEC, restore the aquifer to a condition
where levels of 1,1,1-trichloroethane would be essentially non-
existent.
The USEPA has developed a Suggested No Adverse Response
Level (SNARL) for 1,1,1-trichloroethane. Since the chemical is not
considered a carcinogen, the taste and odor threshold range of
0.3 to 0.5 mg/1 is considered by the USEPA as the limiting concen-
tration to protect the aesthetic value of drinking water and to pro-
tect the public health. The municipality and regulatory agencies
involved were not satisfied with this level. To date, New York
State has not developed groundwater standards for 1,1,1-trichloro-
ethane. The state has, however, developed guidelines which suggest
a limit of 50 ug/1 range. It was, therefore, anticipated that any
CASE HISTORIES
349
-------
treatment alternative to yield potable water would have to produce
an effluent that would meet this latter limit.
To attain the required removals, current technology for the elim-
ination of VHOs from drinking water"-12-13 suggests the use of:
•Granular activated carbon (GAQ
•Powdered activated carbon (PAQ
•Aeration
•Ion exchange resins
•Ozonation or chemical oxidation
As another alternative, the location of an alternate water supply
was explored. This measure could alleviate the burden of treating
the aquifer to the extremely low levels of 5-10 ug/1 and possibly,
pending regulatory approval and future monitoring results, elim-
inate treatment of the aquifer completely.
Treatment of the existing aquifer to remove the 1,1,1-trichloro-
ethane from the groundwater provides three distinct advantages:
•Restores water supply to Town
•Cleans up the aquifer
•Can be taken of f-line when monitoring data warrants
Table 1
Soil Isotherm Experiment
Soil1
Quantity
(gm)
Groundwater
Quantity
(ml)
Delonlzed
Water Quantity
(ml)
Concentration of
1,1,1-trichloroethane
Jg/l
1.02
0
0.50
1.03
2.04
10.00
0
3002
300
300
300
300
300
0
0
0
0
0
1
520
500
480
520
520
I. Wet wcighl basis.
2. pH of groundwater sample was 6.8.
Table 1—Results of soil isotherm performed utilizing actual groundwater and soil obtained at the
site.
The major drawback to treatment is that the treated water would
be pumped into the existing water distribution system causing
public concern. With this in mind, an alternative which combines
the location of an alternate water supply and the restoration of
the aquifer (if required by regulatory agencies) was proposed.
This alternative offers the potential for increasing the 5 »ig/l
1,1,1-trichloroethane limitation since the treated groundwater
would be discharged to a nearby river. It is anticipated that in this
instance only the 50 >ig/l limitation developed in the state guide-
lines would have to be met.
Based upon the above, it appeared that treatment of the ground-
water, whether it be to a potable level (5 ug/1) or to a level suitable
for discharge to the nearby river (50 )ig/l), was a feasible alterna-
tive. Further investigation was appropriate.
Prior to selection of a treatment scheme, criteria for per-
formance in addition to effluent stipulations had to be addressed.
Characteristics considered favorable in the selection of a treatment
plan included:
•Minimal capital and installation cost
•Minimal operational and maintenance costs
•System portability
•Proven design
•Ease of implementation
•Technical feasibility
Powdered activated carbon, ion exchange resins and ozona-
tion/chemical oxidation were eliminated since they did not meet
all the desired performance criteria. The remaining alternatives,
GAC and aeration, appeared to be the most favorable. A draw-
ing depicting the treatment scheme using either technique is shown
as Figure 3.
The use of activated carbon is a well recognized and field proven
method for removal of volatile organic chemicals from drinking
water supplies. The incorporation of the activated carbon as a
GAC unit makes the system portable and implementation relative-
ly quick and easy. For short term applications, many vendors
offer "rental" services which include certain operational and main-
tenance items in their fee. If the duration of use can be determined,
these can be relatively inexpensive and worry free systems com-
pared to the outright purchase and operation of a GAC unit.
Carbon regeneration, constituting high operational and main-
tenance costs, is considered the major disadvantage.
Aeration, or air stripping, is a liquid-gas mass transfer opera-
tion in which the volatiles are stripped out of the liquid by a
counter-current air stream, are transferred to the air stream and
are discharged or recovered, leaving the purified effluent. This
technique has been widely used in the chemical industry and in
other industrial applications for many years but only recently has
been applied to the treatment of contaminated drinking water
supplies.
Capital and installation costs of aeration systems are slightly
lower than for the GAC, while operational and maintenance costs
are considerably lower since there are no material regeneration
costs.
In lieu of treatment to a potable level or treatment to a level
suitable for river discharge, the concept of locating a new water
supply is an appropriate alternative. This alternative is the least
capital intense, providing the contaminated aquifer does not have
to be restored, and eliminates the public apprehension associated
with pumping the contaminated groundwater directly to the water
distribution system following treatment.
Should it be determined that the contaminated aquifer requires
treatment, the cost advantage held by this alternative disappears,
leaving only the advantage of public acceptance.
To date, an accepted remedial alternative has not been agreed
upon. It is anticipated that, since the monitoring program pro-
duced evidence of contaminant reduction, the aquifer will flush
itself clean over time.
Based upon this premise, a new water supply could be located
and utilized by the municipality while the aquifer is regularly mon-
itored to document the anticipated decline of 1,1,1-trichloroethane.
In the event it is determined that an active treatment system must
be applied to the aquifer, further evaluation leading to design of
an aeration or other appropriate system will be initiated.
ADDITIONAL WORK
With the problem defined and remedial alternatives identified,
there remains only the further development of the most viable
alternative. As previously mentioned, the location of a new Town
water supply is currently being investigated. Alternatives being
considered include the purchase of water from a nearby munici-
pality and the pumping of water from the river and treating to a
potable level.
Figure 3
Remedial scheme in the event aquifer restoration is required.
350
CASE HISTORIES
-------
Additionally, work is currently being undertaken by hydrogeol-
ogists with the aid of computer modeling to simulate groundwater
flow characteristics under various natural and pumping conditions.
The modeling effort will assist in predicting the effectiveness of
the aquifer's natural cleansing ability and thereby identify whether
or not treatment of the contaminated aquifer is needed.
SUMMARY
An order was issued to a metal finishing and manufacturing
facility in Aug. 1981. The document required that a complete
hydrogeological investigation pertaining to the subsurface dis-
charge of 1,1,1-trichloroethane which allegedly migrated through
the groundwater system to a nearby Town water supply well be
performed.
O'Brien & Gere Engineers, Inc. was authorized to perform the
investigation which included the installation of groundwater mon-
itoring wells, soil and groundwater sampling and research oriented
work to confirm or refute the allegations and to address the con-
cerns of the consent order. It was found that the metal finishing
and manufacturing facility was responsible for the contamination
and that remedial work was in order. Alternatives were developed
and evaluated. The work completed to date indicates that the
development of a new water supply, with the possible treatment
of the groundwater aquifer, is the most reasonable remedial altern-
ative. Investigations are ongoing to determine the level of treat-
ment, if any, required for the clean up of the groundwater aquifer.
REFERENCES
1. USEPA Office of Drinking Water "SNARLS" Program, SNARL For
1,1,1-Trichloroethane, Washington, D.C., May 1980.
2. Pearson, C.R. and McConnel, G., "Chlorinated C, and €2 Hydro-
carbons in the Marine Environment," Proc. Roy. Soc., London B.
189,1975, 305-322.
3. Patterson, J.W. and Kodukala, P.S., Chem. Engr. Prog., 77, Apr.
1981,45-48.
5. Boughman, G.L. and Lasister, R.R., "Prediction of Environmental
Pollutant Concentration in Estimating the Hazard of Chemical Sub-
stances to Aquatic Life," ASTM, STP. 657, J. Cairns, Jr., K.L. Dick-
son, A.W. Maki, Eds. ASTM, 1978, 33-54.
6. Dilling, W.L., Teferiller, N.E. and Kallos, G.J., Evaporation Rates
and Reactivities of Methylene Chloride, Chloroform, 1,1,1-Trichloro-
ethylene, Trichloroethylene, Tetrachloroethylene and Other Chlor-
inated Compounds in Dilute Aqueous Solution, Env. Sci. Tech. 9,
1975,833-838.
7. Tabak, H.H., Quave, S.A., Mashni, C.I. and Barth, E.F., "Biode-
gradability Studies with Organic Priority Pollutant Compounds,"
JWPCF, 53, 1981, 1503-1518.
8. Thorn, N.S. and Agg, A.R., "The Breakdown of Synthetic Organic
Compounds in Biological Processes," Proc. Royal Soc. London B
198,1975, 347-357.
9. Land, R.R., et. al., "Introductory Study of Biodegradation of the
Chlorinated Methane, Ethane and Ethene Compounds," Presented at
the AWWA Annual Meeting, St. Louis, MO, June 1981.
10. Colwell, R.R. and Sayler, G.S., "Microbial Degradation of Industrial
Chemicals," Water Pollution Microbiology, R. Mitchell, Ed., John
Wiley & Sons, New York, 1978.
11. EPA Treatability Manual Vol. 1. Treatability Data, USEPA 600/8-
80-042A-July 1980.
12. Controlling Pollution from the Manufacturing and Coating of Metal
Products, Solvent Metal Cleaning, Air Pollution Control, 11, USEPA
625/3-77-009, May 1977.
13. Petura, J.A., "Trichloroethylene and Methyl Chloroform in Ground-
water: A Problem Assessment," JAWWA, 1981, 200-205.
CASE HISTORIES
351
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A DUAL PURPOSE CLEANUP AT A SUPERFUND SITE
WILLIAM R. ADAMS, JR.
Perkins Jordan, Inc.
Reading, Massachusetts
JAMES S. ATWELL
B.C. Jordan Company
Portland, Maine
OVERVIEW
In this paper, the authors discuss the successful results gen-
erated by cooperative efforts between two state agencies, one faced
with the need to construct a highway over a Superfund site and
another responsible for the cleanup of that site. Also addressed
are the engineering consultant's assessment of remedial alterna-
tives and subsequent selection of the most cost-effective and en-
vironmentally sound solution to the problem posed by the con-
struction. The hazardous waste site is the Pine Street Canal site in
Burlington, Vermont, which was designated as Vermont's priority
Superfund site because of its proximity to both business and resi-
dential areas and because of its location adjacent to Lake Cham-
plain—the city's source of drinking water.
PROJECT HISTORY
Over a decade ago, after studies had determined the need and a
route had been selected, the Vermont Agency of Transportation
(AOT) and the city of Burlington entered into an agreement to
construct a connector from Interstate 89 to downtown Burlington.
The AOT began preliminary engineering and made cost estimates
for budget purposes. The only practical and readily available right
of way for this road crossed an area adjacent to a wetland of Lake
Champlain, a large beautiful lake bordered by the states of Ver-
mont and New York and the Province of Quebec. However, the
seemingly logical choice of this location was complicated by a
major obstacle—a hazardous waste area was located approximate-
ly on the centerline of the selected route.
Between the years of 1908 and 1966 a coal gasification plant
was operated in the Burlington area, and the byproducts of the
gasification process, which included coal tars, coal oils and sludges,
were disposed of in the low areas on and adjacent to this site.
Visual observation and a history of oil seeps and discharges to
the barge canal leading to the lake prompted a review of the prob-
lem by the USEPA under the provisions of Superfund. Prelim-
inary investigations by the Vermont Agency of Environmental
Conservation (AEC) and the USEPA determined that substantial
quantities of coal tars, oils and sludges were buried at the site.
The question was whether or not this area could be feasibly util-
ized for highway construction and, if it could, how the proposed
construction could be accomplished within the relatively short
timetable established by AOT. There was no doubt that the am-
bitious construction schedule established by AOT would not mesh
with the long and tedious timetable of the Superfund process.
STATE AGENCY COOPERATIVE EFFORTS
As is the case with most highway transportation agencies, the
AOT is staffed with extremely knowledgeable, dedicated and per-
sistent professionals. They had agreed with the City to construct
this road and, after learning of the hazardous waste problem, be-
gan to search for innovative ways to fulfill their commitment. AOT
engineers recognized the ramifications of constructing a highway
over a Superfund site, but instead of abandoning the project or
attempting to find another location, the AOT decided to see if a
satisfactory solution would be found to allow highway construc-
AOT officials began to look for a solution that would meet cri-
teria for good highway construction and be environmentally sound
and acceptable. At this time a course was set which would be
followed throughout the project—one of cooperation with other
involved agencies rather than confrontation. Instead of confront-
ing AEC, the AOT decided to make them a partner in determin-
ing the proper solution. Senior officials from the AOT met senior
AEC officials and established a friendly and cooperative working
arrangement which has continued throughout the project and has
carried through to their staffs.
AOT officials made it clear at the outset that, while the construc-
tion of the road across this area and the established time schedule
were of great importance, environmental responsibilities would not
be sacrificed. They believed, and later convinced AEC, that they
could accomplish their construction program in an environmental-
ly sound manner.
The meeting with the top officials of both departments pro-
duced an agreement on how the project should proceed and the
responsibilities of the two departments. In essence, the AOT agreed
to do whatever was necessary to produce an environmentally ac-
ceptable solution. They agreed to fund the necessary field investi-
gation and feasibility study to determine an acceptable solution
and requested AEC and its environmental staff to provide the
technical direction and approval for the required environmental
studies. The AEC agreed to accept this invitation to serve as tech-
nical consultant to AOT and to review, comment upon and
approve work plans, methods and solutions. AEC also agreed to
be the State's sole contact with the USEPA for the project and
assisted AOT in the preparation of an RFP for the required site
investigation and feasibility study.
Throughout the process, the technical decisions for this haz-
ardous waste work were made by AEC staff. The AOT accepted
these decisions at face value. AEC staff also became the only State
contact with the USEPA, with the exception of one meeting at
which AOT outlined its goals and schedule. This agreement of
one state agency, namely AEC, working with and for the AOT,
greatly accelerated conduct of the study and the decision-mak-
ing processes.
The two agencies realized that both were working for the same
public. They were able to put aside petty differences, which fre-
352
CASE HISTORIES
-------
quently drive similar agencies apart, and provide the joint lead-
ership necessary to produce an innovative, cost-effective solution
which would not only allow construction of the road, but provide
a suitable site cleanup.
With the agreements and understanding between AOT and AEC
in place, the State was ready to investigate the site and determine
whether or not a cost-effective solution could be found to allow the
planned construction.
In addition to the AEC and the AOT, which were the principal
agencies, both the USEPA and the Federal Highway Adminis-
tration were brought into the process and have played key roles in
the project. The USEPA has provided services through its FIT
contractors and technical consultation and review.
The Federal Highway Administration has reviewed the road con-
struction and the remedial action program and is allowing remedial
action costs to be included in the funding of the roadway con-
struction when the activity is an integral part of the roadway con-
struction.
FHA funding is possible because:
•The remedial action—groundwater extraction to accelerate con-
solidation of the peat and provide a more stable road base—
is designed to be an integral part of the roadway construction.
•The estimated cost of roadway construction, including the remed-
ial action, is less than the initial cost estimates for the road which
were made assuming conventional construction methods without
any special provisions for waste handling.
With the basic agreements concerning responsibility and funding
in place, AOT made the decision to proceed and requested AEC
to prepare an RFP to study the area. The work requested took ad-
vantage of the preliminary studies and extensive soil investiga-
tions already completed by AOT. It also provided that AOT drill
crews would perform additional drilling. The State requested the
following program, which Perkins Jordan, Inc. was retained to
provide:
•A review of the regulations and requirements that might bear on
this project
•An analysis of the liabilities connected with the proposed exca-
vation, treatment and disposal of this material
•A strategy to ensure close coordination among the various regu-
lating agencies and other interested parties
•Advice and guidance in the selection of boring locations
•Assistance in establishing the extent of contamination and degree
of hazard of material encountered
•Determination of feasible alternative solutions and their esti-
mated costs
•Determination of what, if any, safety requirements should be
followed in the design, construction and disposal activities
•Development of any monitoring program necessary during or
after construction.
During the course of this work it became apparent to Jordan that
additional hydrogeologic data were necessary to properly determine
the most cost-effective remedial alternative for the Pine Street
Canal site. The contract was amended to provide this work.
THE CONSULTANT'S STUDY
Hydrogeologic data revealed that 10 to 12 ft of silty fill material
overlie 10 to 15 ft of very permeable peat on top of 50 to 60 ft of
silt. The mobile contaminants were mainly found in the peat. Con-
taminants which had entered the silt were found to be relatively
stable and immobile.
The groundwater table was generally at a shallow depth and
dropped from east to west. It was also determined that there was
an upward gradient from the bedrock through the silt, as well as
horizontal movement toward the canal. The peat was about 100
times more permeable than either the overlying fill or underlying
silt and, hence, acted as a drain for the area.
After the study, Jordan listed five remedial alternatives:
•Excavation and solidification or stabilization
•Excavation and offsite land farming
•Excavation and disposal at a licensed hazardous waste disposal
facility
•Slurry trench containment
•Groundwater collection and treatment
The first three alternatives were quickly eliminated from further
consideration because of the potential adverse environmental im-
pact and the cost involved in the excavation and disposal or treat-
ment of up to 240,000 yd3 of contaminated soil. It was also de-
termined that excavation of this volatile material could create po-
tential health problems for nearby residents. The alternative of
constructing a slurry wall received additional study but was later
dismissed because of the required 17,000 yd3 of excavation neces-
sary to build the wall and the excavation/disposal problems just
mentioned. It was also determined that upward seepage gradients
in the groundwater would require long-term pumping and treat-
ment. There were also some questions as to the long-term in-
tegrity of a slurry wall.
GROUNDWATER COLLECTION AND
TREATMENT ALTERNATIVE SELECTED
The remaining alternative of groundwater collection and treat-
ment was thoroughly investigated. Jordan determined that a com-
bination of preloading and pumping of groundwater would accom-
plish two significant purposes. First, most mobile contaminants
were included in the peat and the groundwater surrounding it.
Pumping and treating this groundwater would remove large quan-
tities of contaminants in an environmentally acceptable manner.
Second, dewatering of the peat, combined with the controlled pre-
loading of the roadway, would bring about compaction in a period
of two years equivalent to 30 years naturally. Through laboratory
testing of the peat, Jordan determined that the combination of
groundwater extraction and controlled placement of the roadway
base would provide a stable base and reduce roadway maintenance.
The groundwater treatment facility could be of modest size since
the flows would be carefully controlled by the amount of surcharge
placed on the area and the rate of pumping. As a result, after two
years of operation, it will be possible to discontinue the pumping
and treatment and to construct the road. It is anticipated that
further pumping and treatment will not be required.
Because this solution is innovative and is based upon some com-
plex calculations, the AEC has requested, and the AOT has agreed,
to keep the groundwater extraction equipment and the treatment
facility itself in place after highway construction to provide treat-
ment if oil seepage continues after the two year consolidation
period.
CONCLUSIONS
The unusual features of this project are that two state agencies,
who often have diverse goals, joined together to embrace a cost-
effective solution which meets the goals of both agencies. The two
agencies brought their equivalent federal agencies into the project,
and the cooperation of the four agencies has allowed a highway to
be constructed and a hazardous waste site to be corrected in a
single effort. Their cooperation has been outstanding.
The second feature is that Jordan, following a careful study and
evaluation of the site hydrogeology and contaminant location and
mobility, was able to utilize the age-old concept of dewatering to
accomplish contaminant removal with the bonus of constructing a
stable highway. The estimated cost for this remedy is no greater
than what had been originally estimated to excavate what was then
believed to be uncontaminated peat and to replace it with granular
material. The chosen solution will give AOT its highway within
budget and on schedule, and give AEC an accelerated, cost-effec-
tive site cleanup.
CASE HISTORIES
353
-------
REMEDIAL ACTIVITIES AT
THE MIAMI DRUM SITE, FLORIDA
VERNON B. MYERS, Ph.D.
Florida Department of Environmental Regulation
Tallahassee, Florida
SITE DESCRIPTION
Miami Drum Services is an inactive drum recycling facility
located in western Miami in Dade County, Florida. The site is 0.5
hectares in area and is located in a predominantly industrial area.
The facility operated for approximately 15 years before litigation
forced it to cease operation in June 1981. As many as 5,000 drums
of various chemical waste materials were observed on the site while
the company was operating. Drums were washed with a caustic
cleaning solution which, along with drum residues containing in-
dustrial solvents, acids and heavy metals, was disposed of on-site
and eventually saturated the surface soils.
The Biscayne Aquifer is approximately 1 m below the natural
ground surface at this site. This aquifer is the only source of fresh
water utilized for the drinking water supply of two million in-
habitants of Dade County. It is a highly permeable unconfined
shallow aquifer composed of limestone and sandstone which
underlies the entire county. At the site, the base of the aquifer is ap-
proximately 28 m below the natural ground surface. The natural
groundwater flow is horizontal and eastward at a velocity of about
2 ft/day. Recharge to the aquifer is from rain entering vertically
over the entire area.
The locations of the Miami Drum site and nearby major public
well fields are shown in Figure 1. The Medley wellfield is situated
only 230 m west of this site, and the Miami Springs-Preston
wellfields are located about 1,500 m southeast of the site.
The withdrawal rate from the Miami Springs-Preston wellfields
ranges from about 75 mgd during the rainy season to nearly 150
mgd during the dry season. Medley wellfield is used during dry
periods when the Miami Springs-Preston wellfields are threatened
by saltwater encroachment from the sea. Medley has a pumping
capacity of 50 mgd.
In spite of the excellent hydrologic characteristics of the Biscayne
Aquifer, the withdrawal of about 150 mgd of water from the Miami
Springs-Preston wellfields causes a cone of depression about 3 m
deep. The Miami Drum site is within this cone of depression and
within the 100-day travel time from the well fields. During
withdrawal from the Medley wellfield, there is another cone of
depression around this well field, but smaller in extent than the one
from the Miami Springs-Preston wellfields.
PAST INVESTIGATIONS
Analytical results given in Table 1 indicated that the soil and
water below the Miami Drum site were contaminated.' These
results were based on samples collected to a maximum depth of 3
m. The soils showed high concentrations of phenols, heavy metals,
oil and grease and pesticides. The water from the top few feet of the
Biscayne Aquifer at the site showed high concentrations of
phenols, oil and grease, cyanide and volatile organic compounds.
Maximum allowable concentrations for several heavy metals in
groundwater and in public drinking water supplies were exceeded in
the on-site wells at the site.2
Miami Spring!
Well Field
(23 Well
Figure 1
Location of Miami Drum Site and public wellfields
In late 1981, the Florida Department of Environmental Regula-
tion contracted with Technos, Inc. to determine the extent of
groundwater pollution associated with the site. Geophysical data
from Electromagnetics (EM) and Ground Penetrating Radar
354
CASE HISTORIES
-------
Table 1
Contaminants in Shallow Groundwater and Soil at the Miami Drum Site
Parameter
Concentration (/tg/1)
In Water
378
839
12.4
959
22,500
3.2
220
170
310
170
210
945,000
1,200
In Soil
19,200
8,170
695,000
154,600
153,000
48,000
44,200
31,300,000
1,1-dichloroethane
Cis-1, 2-dichlorethylene
Chloroform
Trichlorethylene
Phenols
Mercury
Lead
Cadmium
Chromium
Arsenic
Nickel
Oil and Grease
Cyanide
Dieldrin — 18,000
Lindane — 140
Wingerter Laboratories, Inc. (1981) — Maximum levels found at site prior to cleanup.
(GPR) were used to selectively position groundwater wells for
direct sampling of suspected contaminated areas around the site.
The EM results showed a significant conductivity anomaly coinci-
dent with the site.3 The conductivity anomaly provided evidence of
a strong plume-like trend to the southeast in the direction of
groundwater flow and toward the Miami Springs-Preston wellfield.
Several less significant conductivity lobes were also detected west
and north of the site toward the Medley wellfield. Groundwater
sampling levels detected significant volatile organic contamination
levels below the site (Table 2).
CONTAMINATED SOILS CLEANUP
In 1981, the Dade County Department of Transportation pur-
chased several hectares in the area around Miami Drum, including
the site itself, as the location for a maintenance facility for its rapid
transit system. When the county learned that it had purchased the
Miami Drum site, it decided to undertake remedial cleanup of sur-
face material and to apply for reimbursement under Superfund.
In Dec. 1981, the USEPA contracted with Ecology & Environ-
ment, Inc. to determine the most feasible method of dealing with
surface contamination at the Miami Drum Services site. The most
cost-effective approach was determined to be soil excavation with
off-site disposal." Dade County took the lead for the surface soil
cleanup. The question soon arose as to the extent of surface
cleanup necessary to protect the aquifer. Dade County sought ad-
vice and guidance from the USEPA and the Florida Department of
Environmental Regulation in determining the appropriate level of
cleanup and prepared a protocol for the cleanup action.
Table 2
Shallow Groundwater Analyses at Miami Drum Site
Contaminant
Chlorobenzene
1,1 dichloroethane
1,3 dichlorobenzene
1,4 dichlorobenzene
Tetrachloroethylene
Trichloroethylene
cis 1 ,2 dichloroethane
Concentration
0.3 m
3.3
44.4
25.7
26.6
5.7
5.8
17.9
0*8/1)
3m
14.0
39.7
5.9
4.5
4.1
5.6
13.3
Technos, Inc. (1983). Maximum levels found in monitoring wells prior to cleanup.
It was jointly decided to stabilize the site by excavation of highly
contaminated soils and any associated groundwater based upon
laboratory work and best engineering and scientific judgment. The
intent of this protocol was to excavate soils showing concentrations
in excess of the 10 times "minimum criteria" for groundwater
unless it was determined during the excavation process that soils
almost meeting these criteria could be left in place without posing a
threat to the public health and welfare. This judgment was made
based upon daily field observations and analytical results.
Soil borings were initially collected and analyzed at 29 locations
within the site. Soil borings at 0.3, 0.6, 2 and 3 m depths were
analyzed for oil and grease, PCBs, heavy metals and pesticides.
During the time Miami Drum Services was in operation, certain
low-lying areas on the property received the runoff from the drum
washing operations. Additional core samples were taken from these
areas to determine the extent and level of hazardous materials that
might be concentrated there.
Thirty-four core samples were collected from the site at various
depths to a maximum of 3 m. These soil samples were initially
analyzed for: oil and grease, selenium, PCBs, silver, arsenic, en-
drin, cadmium, methoxychlor, chromium, toxaphene, lead, 2,4-D,
mercury and 2,4,5-TP (Silvex). The initial excavation conducted
during the cleanup activities was based upon the following criteria:
•Excavation of soils obviously contaminated as indicated by the
total metal analyses
•Visual observations of soil coring showing highly colored, oily
deposits
•Known locations of deep pits that had received contaminated
runoff during the time Miami Drum Services was in operation.
This initial excavation occurred in the northwest portion of the
property in an area 45 m by 45 m. This area was excavated to a
depth of 0.75 m. Core samples obtained in contaminated locations
indicated the need to remove soils to depths of 2.5 to 3 m in some
areas; visual observation of the site confirmed this need. Additional
soils were removed in these areas up to a depth of 3 m. Forty-one
selected core samples were submitted for analysis of the following
EP toxicity parameters: arsenic, mercury, barium, silver, cad-
miium, selenium, chromium, PCBs, lead, oil and grease.
After completion of the analytical program, the contractor was
directed to conduct final excavations on the site based upon soils
with parameter values significantly higher than 10 times the State's
"minimum criteria" for groundwater based on EP toxicity
analyses. At this point in the cleanup activities, engineering and
scientific judgment played key roles in determining the final degree
of excavation to be accomplished on the site.
The levels of mercury found in EP extraction analyses were
slightly higher than the "minimum criteria" standard of 1.4 /tg/1.
All the mercury values indicated, however, were the same order of
magnitude as the standard. Visual observation of the core samples
at these depths gave no indication that these soils contained the oily
deposits or the high color exhibited by the contaminated soils ob-
tained from other locations within the property. Based upon this
information, it was decided to leave in place the soils displaying
slightly elevated mercury values. A total of 7335 m3 of hazardous
debris and soil was excavated from the Miami Drum site. These
materials were placed in Visqueen-lined trucks and transported to
the authorized hazardous waste disposal site operated by Chemical
Waste Management, Inc., in Emelle, Alabama.
In addition to the excavation operations, 2,460,000 1 of exposed
groundwater were treated prior to recharge to the Biscayne
Aquifer. Unit processes employed in the water treatment are shown
in Table 3.
GROUNDWATER INVESTIGATION
Groundwater contamination at the Miami Drum site was not ad-
dressed by the surface remedial actions. In 1982, USEPA funded a
remedial investigation/feasibility study designed to examine the
vertical and horizontal extent of the migration of hazardous
substances from the Miami Drum site.
CASE HISTORIES
355
-------
The Florida Department of Environmental Regulation (DER)
was the lead agency in this phase of the project. In Apr., 1983, the
Department contracted with the U.S. Geological Survey (USGS) to
drill monitoring wells at the site. A dual-well reverse air circulation
drilling method was used. This method offers several advantages
over standard mud rotary or standard air rotary methods: (1) ac-
curate and "clean sampling" of geologic formations; (2) observa-
tion of water yield as bit passes various lithologies; (3) indication of
gross water quality profile; and (4) no loss of circulation in caver-
nous zones. The information provides a good characterization of
the permeability variation of the aquifer, the geologic composition
of the aquifer and a general water quality profile for selecting zones
in which to install finished observation wells. Furthermore, the for-
mation and water are not contaminated with drilling muds.
A geological test well was drilled to the top of the confining layer
of the aquifer (55 m). A geological log was made of the test well,
and preliminary results were used to determine the depth of the
other monitoring wells. Seven monitoring wells were subsequently
drilled at the site in three clusters (Figure 3). Cluster MD-1 was
located directly east of the site with a well 3 m deep and a well 14 m
deep. Cluster MD-2 was south of the site with a well 3 m deep, one
14 m deep and one 27 m deep. Cluster MD-3 was located west of
the site with a well 14 m deep and one 27 m deep.
Table 3
Water Treatment System
Unit Process
Acidification of water
Caustic addition
Aeration
Sand filtration
Carbon nitration
Purpose/Function
Break up emulsions and skim off resultant
floating oil/grease layer
Convert heavy metal ionic species to non-
soluble hydroxide forms
Oxidation of organic compounds, purging
of volatile organic compounds
Removal of suspended paniculate matter
Adsorption of residual organic compounds
Monitor wells were 7.5 cm diameter, black, steel-cased, gravel-
packed and sealed from the bottom of the casing to the land surface
with cement grout. The wells were developed until samples were
free from turbidity and the conductivity had stabilized. The wells
were finished approximately 0.6 m above land surface and capped
with locking caps.
Prior to drilling, all drill pipes, casings and bits were decon-
taminated by sandblasting and steam cleaning. No grease of any
type was used on the drilling tools and bits. The wells were sampled
by USGS in accordance with the Department's Sampling Protocol.'
The 129 priority pollutants tested for included: metals, her-
bicides, pesticides, PCBs, volatile organic compounds, acid extrac-
table organic compounds and base/neutral extractable organic
compounds. Samples were analyzed by both USGS and the State
DER for quality assurance purposes.
Preliminary results of analyses are listed in Table 4. No metals,
acid or base/neutral extractable organic compounds were found
above detection limits. However, several volatile organic com-
pounds and the pesticide Kelthane were found.
The volatile organic compounds included: 1,1 dichloroethane,
chlorobenzene, chloroethane, chloroethene, ethyl benzene and 1,1
dichloroethene. Chloroethene (vinyl chloride) is a known human
carcinogen; ethyl benzene, 1,1 dichloroethene, 1,1 dichloroethane
and chlorobenzene are suspected carcinogens.'
The volatile organic compounds were found in greatest concen-
tration in the deeper wells, at 13 and 27 m depth. Verification of
these results will occur when the USGS analytical data are
available. The preliminary results of USEPA's Biscayne Aquifer
r
MD-3*
• MD-1
MO-2*
Figure 2
Location of Monitoring Well Clusters
Table 4
Miami Drum Groundwater Data
Welb
Depths (m)
CONTAMINANTS
+ 1,1 Dichloroethane
+ Chlorobenzene
Chloroethane
•Chloroethene (vinyl chloride)
+ Ethyl benzene
+ 1,1 Dichloroethene
VOC's
Kelthane
1A
2.4
IB
13
2A
2.4
2B
13
2C
23
3A
13.7
38
23
CONCENTRATION (/ij/1)
2.6
—
—
...
--
2.6
1.5
7.7
3.4
136
3.8
—
_
150.9
1.8
—
—
4.3
—
_-
._
4.3
0.8
4.4
2.6
44
2.9
5.2
—
59.1
1.2
9.5
5.8
6.7
2.0
—
._
25.8
1.8
9.1
_
128
38
—
7.7
264.7
.„
3.5
—
84
II
_
—
98
0.2
+ Suspected carcinogens (NCI test underway)
•Known carcinogens (W.H.O.)
FDER data (May, 1983)
Table 5
Biscayne Aquifer Groundwater Data in the Vicinity
of the Miami Drum Site
Welb
Depth (m)
CONTAMINANTS
I.I Dichloroethane
Chlorobenzene
Chloroethene
1,1 Dichloroethene
1 ,2 Dichloroethene
Toluene
Metbylbutylketonc
USEPA Data (November, 1982)
CIB
15.5
CIC
30.8
CJA
5.5
CONCENTRATIONS Of /!)
5
6.8
130
—
12
—
14
5
110
2
26
._
-
-
-
-
—
_
t>
356
CASE HISTORIES
-------
Study also found similar volatile organic compounds in this area of
Dade County (Table 5).' Again, the greatest concentrations of
volatile organics were found in the deeper wells. The preliminary
results of this study and other data from the area confirm the
presence of contamination of the Biscayne Aquifer.2'3 This con-
tamination appears to extend to the west and south of the Miami
Drum site. These data are in agreement with the regional directions
of groundwater movement and the specific effects of wellfield
pumping in the area.
Levels of volatile organic compounds in the groundwater under
this site were significant enough to warrant a feasiability study. The
non-threshold limits for carcinogens and the proximity of two ma-
jor potable water wellfields makes the assessment of water treat-
ment alternatives imperative. The feasibility study may be part of
the USEPA's general feasibility study for the Biscayne Aquifer
sites. A decision will be made in the summer of 1983 on the scope of
the feasibility study.
REFERENCES
1. Wingerter Laboratories, Inc., "Miami Drum Data Report." 1981.
2. Florida Administrative Code. "Chapters 17-3 and 17-22." 1983.
3. Technos, Inc., "Geophysical and Hydrogeological Investigation of the
Miami Drum Site." 1983.
4. Ecology and Environment, Inc. "The Feasibility of abating the Source
of Groundwater Pollution at Miami Drum Services, Dade County,
Florida." 1981.
5. Florida Department of Environmental Regulation. "Standard Operat-
ing Procedure Manual for Handling and Collection of Groundwater
and Surface Water Samples." 1982.
6. Kool, H.J., Van Kreijl, C.F., and Zoeteman, B.C.J., "Toxicology
Assessment of Organic Compounds in Drinking Water." CRC Critical
Reviews in Environmental Control, 12, 1982, 307-359.
7. U.S. Environmental Protection Agency "Draft—Biscayne Aquifer/
Dade County, Phase II Report." 1983.
CASE HISTORIES
357
-------
PRICE LANDFILL:
INTERIM AND LONG-TERM REMEDIAL ACTIONS
JAMES R. WALLACE
Camp Dresser & McKee, Inc.
Boston, Massachusetts
SALVATORE BADALAMENTI
ROBERT N. OGG
U.S. Environmental Protection Agency, Region II
New York, New York
INTRODUCTION
The Price Landfill site near Atlantic City, New Jersey, is an in-
active landfill that operated from the mid-1960s to the mid-1970s.
Initially, it served as a sand and gravel pit, but when the con-
tents had been excavated to within approximately 2 ft of the
groundwater level, gravel operations ceased. At that time the site
began receiving private and municipal wastes. For approximate-
ly 18 months, the landfill reportedly received liquid industrial
wastes, both in 55-gal drums and bulk liquids that were poured
directly onto the ground. Landfill operations ceased in the mid-
1970s, and at that time the landfill was covered with sand and
gravel.
The site is located on a coastal plain and the area is generally
flat. The soil is mainly sandy and has a high permeability. The area
is underlain by two primary aquifers: (1) the Cohansey Sands
Aquifer, and (2) the Kirkwood Aquifer. Both are aquifers used
for private and public drinking water supplies. The Cohansey and
Kirkwood aquifers are divided by a thick clay layer that prevents
the transfer of water between them. The Cohansey is divided into
two zones, an upper and lower zone, that are both used for drink-
ing water. The two zones are divided by a thin, possibly discon-
tinuous layer of clay that retards, but probably does not prevent,
the movement from one level to the other.
Groundwater generally flows northeast and east toward the
ocean. Between the site and the ocean lie a number of privately
owned drinking wells and the Atlantic City Municipal Utilities
Authority (ACMUA) wellfield, which supplies drinking water to
Atlantic City.
The USEPA, State of New Jersey and local agencies have all
conducted sampling programs to determine the characteristics and
movement of the contaminant plume. The plume contains pollu-
tants such as benzene, 1,2-dichloroethane, toluene, vinyl chlor-
ide, phenol and bis (2-ethylhexyl) phthalate as well as several heavy
metals. Several private wells in the area of the landfill have been
closed, and the residents connected to the New Jersey Water Com-
pany (NJWCo) supply system. There is strong evidence that the
plume is moving toward the ACMUA wellfield.
OBJECTIVES
There are two major objectives, a short term and a long term, to
be addressed in evaluating this site. Atlantic City has a seasonal
variation in the drinking water demand, and the demand increases
significantly in the summer. Because residents were in imminent
danger, the short-term objective was to ensure a safe and ade-
quate supply of drinking water to Atlantic City for the summer of
1982 and until a long-term remedial action could be in place. The
long-term objective is to eliminate or mitigate any adverse effects
that contamination from the landfill will produce on the ACMUA
wellfield, on the NJWCo wells or on private wells in the area.
SHORT-TERM REMEDIAL ACTION
Contaminant Movement
The area between the landfill site and the ACMUA wellfield
contains approximately 60 wells where the water quality has been
periodically sampled over the past few years. In addition, private
wells in the area were sampled. The available data were entered
into a computer and sorted by contaminant, concentration, loca-
tion and sampling data in an effort to quantify the behavior of
the contaminant movement through the groundwater in this area.
Data analysis indicated the following major aspects of the con-
taminant movement:
•Contaminants generally move east and east-northeast from the
landfill site.
•High concentrations of benzene and toluene are noted in the top
50 ft of the upper Cohansey Aquifer immediately downstream
of the landfill site. These organics are known to be biodegrad-
able, particularly in sandy aquifers, and it appears that they may
be breaking down because they are not measured in high concen-
trations as the distance from the source increases.
•Several other, similarly non-conservative, contaminants were
noted in the region within 0.3 miles from the landfill. Highest
concentrations were typically noted in the immediate vicinity of
the landfill, as expected, and they decreased significantly with
distance. In addition, concentrations decreased with depth. Little
contamination was noted below the 50 ft depth at monitoring
wells.
•The contaminant 1,2-trans-dichloroethylene has also been de-
tected, almost reaching the production well AC-13.
The approximate locations of the production wells are shown in
Figure 1. Insufficient field data exist to precisely determine the
rate of movement of the specific contaminants. A three dimen-
sional groundwater model was developed to predict the general
movement of the entire contaminant plume. This model used total
volatile organics as an indicator of groundwater contamination.
The following points relating to the potential contamination of the
ACMUA wellfield can be noted:
•Based upon modeling efforts, well AC-13 lies just beyond the
fringe of the contaminated plume, and it should not be returned
to service without wellhead treatment.
•Wells AC-2 and AC-4A, located in the upper zone, are likely to
be impacted within one to three years.
•Of the lower Cohansey wells, well AC-9 is nearest the plume,
which is presently lying in the upper Cohansey. It is likely that
this plume will overlay the location of well AC-9 in one to three
years. Based on the reported clay permeabilities, we estimate that
it would take approximately 10 years for a contaminant to pene-
trate the clay layer that lies between the upper and lower Cohan-
sey. Unless a hole exists in this clay layer, no immediate threat
to well AC-9 exists, provided that the well casing is properly
sealed.
358
CASE HISTORIES
-------
;KS> ,. '• i ' '.'.'•'!''.j;;Vv""^N
Vs. * Ahsornn I".-... •'_'.' .','•'."''- ' . >>
'• IACMUAUATER SUPPLY WAI'MCNI, PLANT
' ••".•• "
•Well AC-9 can be expected to be reached by the plume in one to
three years. As with well AC-9, no immediate threat to this well
exists, providing its casing is properly installed.
•All other wells should not be impacted by the plume in the next
few years; these other wells are not threatened, unless some other
contamination is present that has not been detected.
Short-Term Modifications
Before the summer of 1982, several actions were taken to en-
sure a safe supply of water until long-term remedial actions were
evaluated.
A water conservation program was initiated by Atlantic City.
This program was very successful, and the anticipated peak de-
mand during the summer of 1982 of 20 mgd. was never reached.
The actual peak demands were approximately 15 mgd.
Piping and structural modifications were installed at two
ACMUA production wells to accommodate portable, truck-
mounted, granular activated carbon adsorption units. These units
could be used for well-head treatment in the event that contamina-
tion reached the upper Cohansey wells located near the water treat-
ment plant. After well-head treatment, the water would be treated
in the ACMUA plant.
An interconnecting pipe was installed to allow Atlantic City to
receive water from the NJWCo distribution system. This water
would be added directly to the ACMUA clearwell and could be
used to augment ACMUA treatment capabilities.
Plant piping modifications were installed to allow the ACMUA
to bypass the water treatment plant with the Kirkwood Aquifer
supplies if the plant's hydraulic capacity became a limiting factor
in supplying sufficient quantities of water to Atlantic City. The
raw water quality of the Kirkwood Aquifer is sufficient to allow
discharge directly into the clearwell for chlorination only.
LONG-TERM REMEDIAL ACTION
Alternatives
Using the results of the three dimensional groundwater model-
ing of the contaminated plume, several long-term alternatives were
Figure 1
Well Location Map
Price Landfill
evaluated for feasibility, performance, cost and environmental ef-
fects. These alternatives were divided into one of two main cate-
gories.
One category of alternatives includes the containment and treat-
ment of the groundwater plume. Treatment options were evaluated
as well as the various methods of discharging the treated water.
For example, the treated effluent could be discharged to the
groundwater, a surface water body, or, after little or no pretreat-
ment, to a municipal wastewater treatment plant.
The other category of alternatives would not include cleanup of
the plume; rather, it would relocate or provide alternatives for
downstream receptors. Under this category, various combinations
of water supply options were investigated for Atlantic City. One of
the options is to relocate the entire ACMUA wellfield to an area
north of the surface water reservoirs. The environmental effects
on private well users in the area and on the NJWCo wells are also
a concern.
Treatment Criteria
At the time of this study, the USEPA had not established min-
imum response criteria to be used in the evaluation of remedial
actions at uncontrolled hazardous waste sites, like Price Land-
fill. Additionally, safe drinking water standards have not been
established for most of the contaminants at the site. The USEPA
and the NJDEP developed the following criteria to be used in eval-
uating the remedial action alternatives for Price Landfill.
The treated plume could be recharged into a contaminated por-
tion of the aquifer, provided the discharge was part of an overall
treatment system. Treatment of the plume was considered com-
plete when the level of volatile organic compounds in the ground-
water at the extraction pumping site reached 100 /tg/1. Con-
currently, monitoring wells must be placed downstream of the
pump site to ensure that the entire plurne is captured. The num-
ber and location of the monitoring wells would be determined
during the final design prior to applying for any required permits.
The treated plume could be recharged into an uncontaminated
portion of the aquifer if the level of volatile organic compounds
was at or below 100 /tg/1.
CASE HISTORIES
359
-------
The significant concentration of volatile organics in the plume
(benzene, chlorobenzene, toluene, ethylbenzene, 1,2 dichloroeth-
ane, chloroform, methylene chloride, etc.) must be reduced for
discharge into a surface water. Based on pilot studies, conven-
tional air stripping treatment should produce an effluent with a
volatile organic concentration of less than 100 /tg/1, which is the
concentration specified by the NJDEP for the protection of pub-
lic health. Therefore, an effluent with a volatile organics concen-
tration limit of 100 /ig/1, in conjunction with a total organic car-
bon limit of 50 mg/1 for correlation purposes, was designated as a
substitute for BOD5 for the oxygen demand limitation. Petroleum
hydrocarbons and pH were limited to the standards of 15 mg/1
maximum and 6 to 9 range, respectively.
Pilot Plant Studies
To determine the treatability of the contaminated groundwater,
a pilot plant was set up at a monitoring well to evaluate the unit
processes of air stripping and granular activated carbon. The air to
water ratio was 80:1, with a total carbon depth of approximately 8
ft and an empty bed carbon contact time of 20 min. The results of
the pilot study (Table 1) were favorable, and this type of a treat-
ment system was considered viable for the plume treatment alterna-
tives.
Evaluation of Alternatives
Originally, 17 different alternatives, including the no-action al-
ternative, were considered for the long-term remedial action at
Price Landfill. A preliminary evaluation was conducted to elim-
inate those alternatives that may have been redundant or might
have significant technical or health related limitations.
Ten alternatives were evaluated using a present worth cost
analyses of both capital and operating and maintenance costs. In
addition, we also conducted non-cost analyses of reliability, feasi-
bility of implementation, operation and maintenance considera-
tions, environmental considerations and safety. The results of the
costs analyses are shown on Table 2, and the results of the non-
cost analyses are shown on Table 3.
Recommendations
When the cost, non-cost and environmental evaluations are
all considered, Alternative 13 and Alternative 14b give the best re-
sults. Alternative 13 involves relocating 13.5 mgd of ACMUA
water supply capacity north of the reservoir with a 2 mgd plume
abatement well. Alternative 14b involves relocating 13.5 mgd north
Table 1
Water Quality Analysis—Pilot Plant Study
EPA
COMPOUNO(S) DETECTED
EPA
DETECTION
LIMIT
ug/1
PRELIMINARY
-DATE OF SAMPLING
SAMPLING
2-5-82 4-15-82 4-Z1-B2 4-22-82 4-30-82 5-5-8? 5-12-67 5-18-82 5-Z5-BZ
INFL EFF INFL EFF INFL EFF INFL EFF INFL EFF INFL EFF I NFL EFF INFL EFF 1NFL EFF
65 A phenol
18 B bis (2-chloroethyl) etherlO
L'5 B 1,2-dlchlorobenzene
26 B 1,3-dlchlorobenzene
27 B 1,4-dlchlorobenzene
54 B Isophorone
66 B bis (2-ethy(henyl)phtha- 10
late
69 B dl-n-octyl phthai ate
4 V benzene
7 V chlorobenzene
10 V 1,2-dlchloroethane
11 V 1,1,1-trlchloroethane
13 V 1,1-dlchloroethane
38 V ethylbenzene
86 V toluene
88 V vinyl chloride
tetrahydroFuran
dlethylether
dllsopropylether
102P alpha-BHC
111P PCB-1260
Aluminum
Chromium
Barium
Beryllium
Cadmium
Cobalt
Copper
'Iron (rrg/1)
Lead
Nickel
Manganese
Zinc
Boron
Vanadium
•Calcium
-------
Table 2
Price Landfill*Summary
Present Worth Analysis
Alternative
2 RELOCATE 13.5 HGD IN ICIRKWOOO
"• WELLS ON THE MAINLAND
3 RELOCATE 13.5 NGO IN LOWER
COHANSEV WELLS NORTH OF
RESERVOIR
7 WELLHEAD CARBON AND AIR
STRIPPING TREATMENT
8a RELOCATE 6 MGD NORTH OF
RESERVOIR IN LOWER COHANSEV
7 HGD PLUHE ABATEMENT AND
TREATMENT
Rh RELOCATE 6 HGD NORTH OF
RESERVOIR IN LOWER COHANSEV
2 MGD PLUHE ABATEMENT AND
TREATMENT
10 SAME AS 84 WITH SLURRY WALL
AROUND LANDFILL SITE AND
TREATMENT
12 SLURRY WALL AROUND LANDFILL
SITE WITH EXTRACTION PUMPING
AND TREATMENT
13 RELOCATE 13.S HGD NORTH OF
RESERVOIR -
2 HGO PLUME ABATEMENT AND
TREATHENT
14a RELOCATE 13.5 HGD NORTH
OF RESERVOIR -
SLURRY WALL AROUND LANDFILL
SITE WITH EXTRACTION PUMPING
14b SAME AS 141 WITH 2 HGD
PLUHE ABATEMENT AND
TREATMENT
Nott: Actull mlntenince pumping wll
In th< slurry xill will list
for in extended period of time
it rtlltlvtly loo pimping riti.
For rtlitlvt cost co«P!rlson purposes
only - I 5 ytir duritlon It i higher
rite his been used.
Capital
Costs
4, ISO. 000
S. 070. 000
6.440.000
16.850.000
7. OSS, 000
20.22S.OOO
7,985,000
9.675.000
13. OSS. 000
I3.oeo.ooo
Annual
O&M
Costs
0
0
3.250.000
3.277,000'
967.000"
947.000
3.277.000'
(0)"
947,000'
(0)"
947.000
947,1)00-
0"
947.000
Present Worth
25 Year
4.168.000
5,039, ODD
35 .997 .ODD
25.092,000
15,620.000
25,253.000
9,111,000
18. 232,000
13.279.000
21.617,000
50 Year
4, 185.000
5.154.000
36.088.000
28,717,000
16.792.000
25,427.000
9,111,000
20,022.000
13,496,000
23,407.000
yeirs 1 thru 5
•fter ycir 5
of the reservoir, a 2 mgd plume abatement well and a slurry wall
around the landfill site. Both alternatives provide:
•An adequate drinking water supply for Atlantic City that should
not be affected by the plume from Price Landfill
•Positive measures to control and remove the contaminated plume
•Positive measures to control the source at Price Landfill
Several factors were considered when the final comparison of al-
ternatives was made. First, about 10 private residences are near
the plume and are not connected to a public water supply. If
the plume is not controlled and treated, about 100 to 200 private
residences could be affected. Second, the New Jersey Water Com-
pany's Well 3 is within a mile to the south of Price Landfill. If the
plume is controlled, it may impact this well in the future. And
third, this study and the groundwater model only addressed the
single source of contamination from the Price Landfill. It is be-
lieved there may be other sources of contamination in the area.
These sources may change the contamination patterns in the aqui-
fer, and the recommended action should account for the possi-
bility of other contaminant sources.
The possibility of treating the contaminated plume at the Atlan-
tic County (ACUA) wastewater treatment plant should be inves-
tigated. If treatability tests conducted on the waste show that the
ACUA plant can accept the waste, then the disposal charge would
be between $1100 and $1300 /mg, provided that the BOD/SS of
the waste is less than 250 mg/1. The net effect would be a decrease
of $2,000,000 in capital costs for the on-site treatment plant, but
the annual operating costs would essentially not change. A treat-
ability study will be conducted to determine if the contaminated
groundwater can be accepted at the ACUA treatment plant.
The final decision concerning the long-term remedial action for
the Price Landfill site will be made by the USEPA, and the
NJDEP, with public comments taken into consideration.
Table 3
Non-Cost Evaluation Criteria Matrix
ALTERNATIVES
10 - NO ACTION
11 . REPLACE LOST SUPPLIES
WITH (1RKUOOO WELLS
1) • REPLACE LOST SUPPLIES
WITH COHANSEY WELLS
17 . WELL HEAD TREATMENT
181- RELOCATE WELLS NORTH
OF RESERVOIR WITH 7 HGD
ABATEMENT PUMPING
lit- RELOCATE WELLS NORTH
OF RESERVOIR WITH 2 HGD
ABATEMENT PUMPING
•10- RELOCATE WELLS NORTH
OF RESERVOIR WITH 7 HGO
ABATEMENT PUMPING AND
SlURRY WALL
112- SLURRY WALL AND CAP
LANDFILL SITE
113- REPLACE LOST SUPPLIES
WITH COKANSEV WELLS
NORTH OF RESERVOIR WITH
2 HGD ABATEMENT PUMPING
I14i- RELOCATE WELLS NORTH
OF RESERVOIR WITH
SLURRY WALL
I14H-RELOCATE WELLS NORTH
OF RESERVOIR WITH
SLURRY WALL AND 2 HGD
ABATEHENT PUMPING
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0 I LEGEND: •! SIGNIFICANT ADVANTAGE OVER
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-1 DISTINCT DISADVANTAGE
COMPARED TO OTHER ALTERNATIVES
CASE HISTORIES
361
-------
THE APPLICATION OF COMPUTER MODELS TO THE
EVALUATION OF HAZARDOUS WASTE MANAGEMENT
OPTIONS FOR UNCONTROLLED HAZARDOUS WASTE SITES
ROSALIE T. MATTHEWS
Matthews Consulting & Construction, Inc.
Silver Spring, Maryland
INTRODUCTION
A model should provide the user with assistance in: (1) avoiding
the unnecessary expenditure of funds; (2) mitigating the expen-
diture of funds; and (3) providing a foundation for requesting addi-
tional funding if necessary. In this regard, model utilization is ap-
propriate in considering hazardous waste management options,
either by an individual generating facility or by a regulatory agency
developing a multiple facility hazardous waste management plan.
The former may be an uncontrolled hazardous waste site from
which hazardous materials may be generated on a continual or
sporadic basis. Uncontrolled hazardous waste management sites
may also be encompassed in a hazardous waste management
regional plan.
Hazardous wastes sites can be administered according to
statutory distinctions as delineated by the Resource Conservation
and Recovery Act, or as defined by a host of other federal and state
laws addressing the production and disposal of toxic materials or
primary pollutants. However, the generation and disposition of
hazardous wastes occurred in many instances prior to the establish-
ment of these statutory distinctions. Hazardous wastes can be pro-
duced by product development, storage and delivery; by product
obsolescence or aging; or by the storage, treatment and disposal of
discarded materials. A model user need not distinguish statutorily
the facility or site to be addressed. A site, controlled or otherwise
described, can be considered in a model depending upon the needs
of the model user. A model user must be able to provide the site
specific data required by the particular model in order to consider
the economic evaluation of management options encompassing
that particular site.
Models can be advantageous in evaluating options which concur-
rently manage waste streams from different type facilities and sites.
For example, a generator may be responsible for managing produc-
tion wastes, spill cleanup residues, wastes emanating from a closed
landfill and for the removal of wastes placed in an off-site disposal
facility. Depending upon the capabilities and capacity of the
model(s) employed, the generator may consider options addressing
one or several of these waste streams. Model utilization by a
generator will be explored first and will be followed by a discussion
of generation of a regional hazardous waste management plan via
model utilization.
ECONOMIC EVALUATION OF
OPTIONS FOR GENERATORS
The Michigan Department of Commerce developed several
methodologies in order to determine whether or not hazardous
waste generating industries in the region would select resource
recovery. The Department's efforts included development of tech-
niques to project the economic effects of hazardous waste re-
quirements and to assess the potential for resource recovery. These
techniques were applied to three industries selected on the basis of
regional economic importance, employment and potential for
waste stream recovery. The selected industries were steel manu-
facturing, paint manufacturing and electroplating. The first step,
establishment of criteria for generator selection, addresses the size
and concentration of the industry in the region, waste stream
volume and disposal methods employed and the impacts of the
RCRA in the region. Consequently, the application of the criteria
to other regions may result in the selection of other industries.
Paint Industry
The next step in the analysis process entails the characterization
of the nature of the industry selected (location, size, product
development and delivery) and its particular economic condition
and constraints. Approximately 30% of the paint manufacturing
industry is located in the Great Lakes Basin region. Of the 540
plants, approximately 19% employ fewer than 50 individuals while
9% employ over 100. Total employment is approximately 25,000.
Overall, the number of paint manufacturing plants has been
decreasing since the 1960's. This decrease is based on increasingly
restrictive fire and nuisance regulations rather than environmental
requirements. In addition, aging proprietorships have contributed
to the decline. The paint manufacturing industry generally ex-
periences difficulty in passing on the costs of hazardous waste
management. Historically, the industry has not been able to pass
on increases in raw material costs; consequently, profits after taxes
as a per cent of sales are less than half of those for all manufactur-
ing industries. The high level of product substitution (e.g.,
wallpaper, plastics, glass and paneling) is a major reason for this
constraint.
The paint manufacturing industry currently utilizes recovery,
treatment and disposal including secure landfill. Overall, the paint
manufacturing industry generates 112 primary pollutants that are
regulated as hazardous wastes under RCRA. Total waste genera-
tion in the region is 41,060 tons annually.
Electroplating
The electroplating industry encompasses motor vehicle, elec-
tronic component manufacture, blast furnace and steel mill opera-
tion, radio and television equipment and screw machine produc-
tion. The industry is composed of predominantly small enterprise*.
362
COST
-------
Approximately half of the electroplating industry is located in the
Great Lakes Basin region with 40% of all plants in Michigan, Ohio,
Illinois and Pennsylvania.
This industry generates approximately 80,000 metric tonnes of
hazardous wastes per year in the region. The generated wastes vary
in nature and composition and include water treatment sludges,
process wastes, degreaser sludges, salt precipitates and metal clean-
ing wastes.
Steel Industry
The steel industry is predominantly comprised of large firms with
high employment levels depending upon market requirements. Ap-
proximately 60% of all steel plants are located in this region and are
concentrated in Pennsylvania, Ohio, Illinois and Indiana. In this
region, the steel industry generates substantial volumes of hazar-
dous wastes. Projected generation volumes for 1983 in metric ton-
nes, dry weight are: sludge, 996,000; dust, 300,000; scale,
1,000,000; and pickle liquor, 167,000. Recovery of ferric chloride,
hydrochloric acid and ferric oxide from waste pickle liquors is cur-
rently underway.
Trade association reports cite the steel industry's difficulty in
capital accumulation which is aggravated by environmental control
costs. The American Iron and Steel Institute estimates that en-
vironmental control costs account for approximately 18% of the
industry's total capital requirements. Of that amount, approx-
imately 16% of costs are associated with solid waste management
including hazardous waste management.
Discussion
In sum, the Michigan Department of Commerce identified three
industries (steel, paint manufacturing and electroplating) that were
(1) concentrated in the Great Lakes Basin region; (2) responsible
for substantial employment in the region; (3) experiencing cost con-
straints in either cost pass-through or capital accumulation; (4) pay-
ing for increasingly more expensive disposal options; and (5)
generating significant volumes of hazardous wastes of varying
nature.
Waste Management Costs
A review of the total monetary costs of hazardous waste manage-
ment regulations is the next step in the economic analysis process.
The cost of storage, treatment and disposal is a concern for those
responsible for the disposition of wastes generated by removal of
wastes from non-process sources as well as from on-going produc-
tion activities.
The first question addressed was whether or not costs, such as
closure and post-closure costs and liability insurance requirements,
were uniform for all types of treatment, storage and disposal
facilities (TSDF). The Department estimated that such costs
associated with land disposal and deep well injection should be dif-
ferent than those for incineration and treatment facilities. The lat-
ter need only meet closure and liability insurance requirements.
Data accumulated supported the prediction that costs for closure
and post-closure for an average (200 acres) landfill would be ap-
proximately $2.5M and $75,000 for liability insurance coverage;
costs for closure and post-closure for deep well injection facilities
would be $2M and $60,000 for liability insurance coverage. Closure
costs for incineration facilities ranged from $10,000 to $200,000
and $50,000 for liability insurance coverage. The accumulation of
these data may be applicable in a generic approach to developing
model scenarios.
The relationship between regulatory costs and the tons per day of
hazardous wastes handled by the TSDF was not demonstrated.
However, closure and post-closure costs were determined to be af-
fected by the size of the facility. The insurance carrier's estimation
of risk determined the cost of liability coverage.
In order to determine charges to firms utilizing TSDFs, operators
of the latter were requested to estimate costs not only of closure,
post-closure and insurance, but also annual paperwork costs, addi-
tional annual costs of personnel (field and administrative), cost for
emergency equipment and other annual payments, if required. The
anticipated incremental cost of compliance per gallon was deter-
mined for each disposal option of average .size for that option.
Table 1
Disposal Option Costs per Gallon—Pre- and Posl-RCRA
Disposal
Option
Deep well
injection
Landfill
Incineration
Treatment
INCREMENTAL COST OF COMPLIANCE
Pre-RCRA Anticipated Actual Posl-RCRA
Charge
26*
40«
43«
1C
8«
2«
3«
3t
4
-------
wastestream; interest rate; steam cost per million BTU; time be-
tween anion regeneration; time between cation regeneration; tax
incentive; and water cost.
The waste streams included chromium, cyanide and acid-alkali.
The waste processes considered are chromium reduction, cyanide
oxidation, physical/chemical treatment, sludge dewatering and
storage.
The disposal options considered are conventional treatment
without any flow reduction, conventional treatment with flow
reduction, incorporation of ion exchange process for metal
recovery, incorporation of an evaporative process for metal
recovery, and incorporation of electrodialysis for metal recovery.
The 12 cases considered are shown in Table 2.
Table 2
List of Cases, Hazardous Waste Treatment
Alternative Analysis Model
Case
Disposal
Trans-
Costs/gal porta-
1
2
$ .25
.25
lion/
miles
100
100
CRFi*
Interest
Rate %
Years
metal
CFRj*
Interest
Rate %
Years
and treatment chemical costs are
doubled
3
4
5
6
7
8
9
10
11
.50
.50
3.00
.25
.25
.25
.25
.25
.25
25
500
75
100
100
100
100
100
100
15
15
15
20
10
20
20
20
20
20
total
7
12
10
10
10
20
15
10
10
20
annual costs of wastewater treat-
12
.25
100
ment—10% resource recovery credit
investment tax credit based on 25% of
total capital costs for plants with resource
recovery
*CRF| Capital Recovery Factor, conventional treatment methods
••CRF2 Capital Recovery Factor, resource recovery processes
The Hazardous Waste Treatment Alternative Analysis Model
was applied to 24 facilities in the Cleveland, Ohio and Milwaukee,
Wisconsin areas. These facilities had varying input values for
wastewater flows, metal values within waste streams, potential for
flow reduction and waste streams generated. The results of the
model application are shown in Table 3.
The following conditions were shown to have a positive impact
on the utilization of resource recovery by electroplating facilities:
(1) rapid increase in plating metal costs and treatment chemical
costs as compared to other costs; (2) rapid increase in waste
disposal costs in comparison to other costs; (3) favorable difference
in financing resource recovery equipment; and (4) substantial in
vestment tax credit deductable from total capital costs upon in-
stallation of resource recovery equipment.
Conditions which had little or no positive effect on resource
recovery selection were: (1) unfavorable difference in financing
resource recovery equipment; (2) implementing a modest resource
recovery credit; and (3) an increase in the price of disposal offset by
a decrease in distance to the disposal site.
PRODUCTION OF AN OPTIMAL
HAZARDOUS WASTE MANAGEMENT PLAN
The Resource Recovery Planning Model (RRPlan) developed by
the National Bureau of Standards, U.S. Department of Commerce
and Edward B. Berman Associates, Inc., can be utilized to: (1) gen-
erate an optimal solid waste management plan; (2) evaluate a
specified plan for its technical and economic feasibility; and (3)
provide guidance in reaching a decision by completing a series of
what-if questions. The RRPlan provides the user with a configura-
tion of facility locations, process to be employed at each location
and outputs at each facility; transportation network and costs;
direction of tonnages through the network to assigned facilities
with residue to disposal sites or secondary markets; and total
system costs including cost per ton throughput at each faculty and
cost per ton disposed.
The user can direct the model to select an option which (1) mini-
mizes the lifetime costs of the regional plan; (2) minimizes the
lifetime discounted costs of the regional plan; (3) maximizes the net
energy balance of the regional plan; (4) considers a weighted
cost/energy composite; and (5) considers a specified regional plan.
Source separation options can be exercised to provide the user with
the means to assess the trade-offs in the cost of material sorting at a
source versus a centralized location, or between the recovery of the
material versus its energy value.
Table 3
Number of Plants Utilizing Resource Recovery
Under Each Case and the Average Cost
Case No.
1
2
3
4
5
6
7
8
9
10
11
12
No. of Plants
2
12
4
5
11
9
3
2
9
5
4
9
Average Cost
$141,763
81,826
101,924
104,900
79,732
82,774
142,182
171,338
91,721
88,426
145,068
83,763
The RRPlan model user supplies basic information on: trans-
portation distance and costs; facility construction, operation and
maintenance costs; labor costs; disposal costs and capacity
availability; and market information. While this model is data-
intensive, the user will find that similar data is required for utiliza-
tion of other models such as the Hazardous Waste Treatment
Alternative Analysis Model and, hence, the effort can be produc-
tive and helpful in assuring data consistency. In order to facilitate
data acquisition, worksheets have been developed. A worksheet for
site data requires information on:
1. a. Name of this site .
b. Number of this site _
2. Depth of tracing requested.
3. Location of this site
4. Incoming commodity
Site preparation information:
a. Cost category for site preparation
b. Total site preparation costs
c. Energy category for site preparation
d. Total energy required for site preparation
6. Capacity considerations:
a. Is the site capacitated?
b. Is landfill possible at the site?
The magnitude of the data to be acquired as well as the overall
dimensions of the source-transport-process-market solution fe
shown in Table 4.
RRPlan employs a fixed charge linear programming algorithm
with a forcing procedure in order to assure that the model passe
over an area of temporarily increasing cost in the solution domain
to find the true optimum or preferred regional plan. The model
sites and sizes solid waste processing facilities by firfl appro*
364
COST
-------
Table 4
Allowable Number of Key Variables
Key Variable
Waste sources
Sites
Processes*
Segments per process
Output coefficients**
Site-process combinations
Landfillst
Markets*
Segments per market
Transportation activities
Min. Value
1
1
2
1
0
1
0
0
1
1
Max. Value
60
50
30
3
7
80
30
30
5.
300
•First process in municipal solid waste plan must be a new transfer station
"By-products of processing
fThere must be at least one landfill for each location at which a land-using process is offered
{There must be at least one market if source separation is offered
imating non-linearities in the capital and operating cost functions
with up to three linear segments. Each segment has a fixed charge
(intercept), and incremental cost associated with increased process-
ing activities (slope). The assumption is made that only site-specific
or site-process specific cost functions have fixed charges. The cost
functions associated with transportation activities (e.g., source-to-
site shipments) consist only of variable costs.
In summary, RRPlan provides the user with a preferred regional
plan encompassing a complete characterization of each component
(sources, sites, processes, transport routes and markets), or an
evaluation of a specified regional plan. The model user can com-
pare the costs of the optimum to the specified (constrained) solu-
tion in order to ascertain the premium imposed.
SUMMARY
The Hazardous Waste Treatment Alternative Analysis Model
determines the optimum economic hazardous waste management
option for an individual hazardous waste generating facility. In
contrast, RRPlan determines an optimal regional solid waste
management plan encompassing multiple facilities which generate,
process and receive both marketable and non-marketable residuals.
Models, such as those discussed herein, may be helpful in achieving
a hazardous waste management program addressing all phases of
waste generation and disposition which provide for the minimiza-
tion of costs to the generator while maximizing the efficient use of
existing or planned environmentally acceptable management op-
tions. For example, models can be directed to address not only the
technical feasibility of waste consolidation regardless of source, but
also the economic advantages. Models cannot change the facts but
may be employed to arrange them in a comprehensive fashion so
that various parties can communicate in an orderly process.
Under Section 3006 of RCRA, states are developing statewide
hazardous waste management plans which must provide for the
management of wastes generated, stored, treated and disposed of
within the state. State programs must also support the tracking of
hazardous wastes via the manifest system. Under Section 3012 of
RCRA, each state will undertake an effort to compile, publish and
provide to the USEPA an inventory of sites in which hazardous
wastes have at any time been stored or disposed.
Models may be useful tools in achieving these administrative and
planning requirements. The data accumulated under Section 3006
of RCRA and compiled under Section 3012 of RCRA can be util-
ized to fulfill model data requirements. Models, such as the
RRPlan, may be used to assist the state regulatory agencies in
developing intra- and inter-state hazardous waste management net-
works. This model may be used in tandem with other models, such
as the Hazardous Waste Management Treatment Alternative
Analysis Model, to provide a common foundation for discussion of
specific regulatory requirements or cleanup activities with in-
terested parties. The interested parties and the regulatory agency
can concurrently consider actions which not only meet statutory
goals but also are affordable least cost options.
Model utilization may enhance the discussion of the concept of
developing a degree of hazard program. Waste characterizations
and management options serve as the foundation to any degree of
hazard program. Waste management options include a full range of
selections from waste reduction techniques (source segregation or
separation, process modification, end-product substituting and
material recovery/recycling); combination of pretreatment
methods; to final disposition (deep well injection, landfilling and
ocean disposal).
An integrated degree of hazard approach, according to the Of-
fice of Technology Assessment, includes:
•Consideration of degrees of hazard and risk in relation to waste
and management practices
•Assessment of the potential to reduce either the amount or hazard
level of hazardous waste through the use of appropriate tech-
nology
•Development of effective designs for monitoring strategies at all
types of facilities
•A means for addressing severe public opposition to siting of new
hazardous waste facilities by providing a technically sound basis
for evaluating management proposals.
However, technical and administrative development should be
accompanied by economic analysis. Should the total regulatory
costs of compliance (such as those cited in the Hazardous Waste
Treatment Alternative Analysis Model) remain level while the
volume of hazardous wastes received by selected management op-
tions be reduced under a specific degree of hazard approach, then
unwelcomed distortions in disposal practices may occur. The latter
may include the proliferation of uncontrolled sites rather than the
reduction or elimination of such options. Models can be utilized to
predict and, thereby, perhaps forestall such an outcome.
REFERENCES
1. Michigan Department of Commerce, "Hazardous Waste Management
in the Great Lakes Region: Opportunities for Economic Development
and Resource1 Recovery," U.S. Department of Commerce, Washington,
D.C., September 1982.
2. Chapman, R.E. and Herman, E.B., "The Resource Recovery Plan-
ning Model: A New Tool for Solid Waste Management," U.S. De-
partment of Commerce, Washington, D.C., July 1983.
3. Office of Technology Assessment, "Technologies and Management
Strategies for Hazardous Waste Control," Washington, D.C., March
1983.
COST
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THE IMPACT OF LIMITED COMPETITION
ON REMOVAL PROJECT COST BUDGETS
GREGORY A. VANDERLAAN
United States Environmental Protection Agency
Chicago, Illinois
INTRODUCTION
As an administrative funding category developed under the
authority of the Comprehensive Environmental Response Com-
pensation and Liability Act of 1980 (CERCLA), planned removals
have been used primarily to achieve a necessary level of cleanup at
sites not on the National Priorities List.1 Planned removals are
funded and administered through the immediate removal pro-
visions of CERCLA and, because they are categorized as "re-
movals", their scope and duration are limited according to the
terms of the statute itself.1 Current USEPA policy requires that
states contribute funds toward the costs associated with project im-
plementation.
Early in the CERCLA program development, it was important
to have a funding mechanism available that allowed the Agency
to address uncontrolled sites that were neither on the National
Priorities List (NPL) nor emergencies requiring immediate action.
As administrative policies change and the program matures, it is
becoming increasingly clear that an additional benefit associated
with planned removals has been the limited procurement process.
Generally, conditions at these sites provide USEPA with enough
time to undertake a limited procurement process which normally
requires 45 to 90 days to complete (a full scale competitive pro-
curement may take 6 to 9 months to complete).
The procurement process associated with a planned removal
allows for a limited level of competition. Theoretically, the intro-
duction of competition will result in lower costs for those aspects
of cleanup involving onsite, transportation and disposal activities.
When the concept of limited competition was first introduced,
there appeared to be a noticeable decrease in project costs3; how-
ever, no evaluation has been performed to demonstrate the ac-
tual impact the process has on project costs.
During 1982, USEPA Region V completed a number of immed-
iate and planned removal projects. The range of activities under-
taken at selected projects allows a comparison to be made of the
costs incurred under either an immediate or planned removal ac-
tion. Specific categories for comparison have been identified to in-
clude contaminated soil, crushed drums, aqueous waste and waste
liquids disposal. Unit prices for these categories have been devel-
oped by evaluating their respective disposal costs. A comparison of
these unit prices provides the basis for evaluation of costs so that
a general assessment can be made regarding expected cost savings
associated with planned removals.
BACKGROUND
Early in 1983, cost summaries were prepared for selected sites
in Region V where immediate or planned removal projects had
been completed.4 The cost data summarized in this report involved
the sites listed below.
Immediate Removals
Anaconda Road Site, Akron, Ohio.
There was the abandonment in a highly populated area of Akron
of two stationary holding tanks containing flammable organic
materials and one tank truck trailer containing flammable organ-
ic materials with a corrosive water layer. Analyses of samples taken
from the tanks indicated that the material was flammable and cor-
rosive. An immediate removal action was necessary to prevent
immediate and significant risk to the affected population from
potential contamination of a drinking water supply and potential
for a fire at the site.
Chem Dyne Site, Hamilton, Ohio.
The company failed to meet a court ordered waste reduction
schedule, was closed and placed in the control of a court appointed
receiver to utilize corporate assets to achieve site cleanup. The com-
pany was used as a waste transfer and storage facility and handled
a wide variety of wastes including pesticides, chlorinated com-
pounds, polychlorinated biphenyls (PCBs), acids and solvents.
Previous spills from the site had resulted in massive fish kills in a
nearby river. An immediate removal was necessary to prevent
future discharges to this river and stabilize several bulk storage
vessels.
Isanti Sites, Isanti, Minnesota.
Four separate problem locations developed as a result of the
local operations of a solvent recycling business. Drums stored in
semi-trailers on the site surface and more than 800 buried drums all
contained product grade solvents. Three of the four sites were in
close proximity to a National Wild and Scenic River. Preliminary
sampling indicated groundwater flow was toward the river. Because
many of the surface storage areas were directly adjacent to resi-
dences, an immediate removal was necessary to prevent the threat
of fire, explosion or contact with those who lived nearby.
Planned Removals
Midco I Site, Gary, Indiana.
Several thousand drums containing materials such as paint
sludge, solvents, acids, caustics and cyanides were left on-site sub-
sequent to a fire that halted reclaiming and recycling operations.
The site was located in a lowland area adjacent to wetlands and
366
COST
-------
commercial establishments. During intense storms, a nearby resi-
dential area was often inundated with flood waters including run-
off from the site. Preliminary studies of the area indicated con-
tamination of surface water, groundwater and soils. A planned re-
moval Nvas necessary to remove the drums and contaminated soils
based on the threat of fire and explosion, human contact and run-
off into nearby wetlands.
Laskin/Poplar Waste Oil, Jefferson, Ohio.
The site was an abandoned waste oil recovery operation with
ponds and bulk storage vessels containing high levels of PCBs and
lesser amounts of phenols and other organic solvents. The storage
vessels and ponds posed a threat of contaminated overflow and
leachate to Cemetary Creek adjacent to the site. This creek is a
tributary of the Grand River which is a drinking water source for
Astabula County. A planned removal was necessary to eliminate
the threat posed by the storage vessels and large lagoons containing
PCB-contaminated waste oil.
COST CATEGORIES
Common tasks on which to base development of cost categories
for purposes of comparison were more difficult to identify than
anticipated. The scope of activities necessary to complete the de-
fined tasks for the projects discussed above varied considerably.
Their diversity, however, is representative of any given group of
sites in the industrial regions of the country.
Because the cost data were not consistent from one site to the
next, a comparative analysis for total project costs incurred was
not possible. Instead, several common activities were identified for
more than one site and, in some cases, for immediate and planned
removals. Common tasks and the site where they were undertaken
are shown in Table 1. A review of these data indicates that each
category of activity is broad and very general, so much so that addi-
tional detail must be sought in order to make a valid comparison of
their respective costs.
Prominent factors that ostensibly affect a unitized disposal cost
for any of the categories of activities shown in Table 1, are con-
taminants, contaminant concentration and amount of material.
The major contaminants found within these general categories and
descriptions of the ultimate method of disposal are shown in Table
2.
Upon closely examining the specific waste characteristics asso-
ciated with the categories of activities, it becomes clear that there
are few commonalities on which to base a fair comparison. Of the
six categories in Table 1, four can be considered as having had sim-
ilar disposal approaches. These four categories represent activities
conducted at immediate and planned removal projects. The unit
price for the specific disposal method used for each site and the
highest concentration of notable contaminants are given in Table 3.
For two of these categories, the planned removal project incurred
considerably less cost on a unit basis. The unit prices shown in
Table 3 are for disposal costs only. They include no personnel, ma-
terials or transportation costs incurred by contractors at the sites
under discussion.
In the crushed drum category for Midco I, the residual materials
remaining in many of the drums required classification of that
waste stream as a hazardous waste. This is a provision of the Re-
source Conservation and Recovery Act regulations under 40 CFR
261.7.s The crushed drums at Isanti, however, were suspected of
PCB contamination. Although PCB is not a regulated substance
under RCRA and, therefore, not subject to the waste residuals
provisions of 40 CFR 261.7, disposal of PCB articles is governed
under regulations promulgated pursuant to the Toxic Substances
Control Act.6 These regulations required the crushed drums from
Isanti to be disposed of as PCB articles.
The category of contaminated soils also shows a considerable
unit price cost difference between an immediate and planned re-
moval project. The disposal option employed for these projects
Table 1
Common Tasks Associated with Immediate and Planned Removals
CrnM
Dnm
SWf«
Wnu
Oi
Anaconda. (1)
Akron, Ohio
Cham Dyn«, (1)
Hamilton, Ohio
laantl. (1)
Isanti County.
Minn. iota
Laikln'a. (P)
JaHanon. Ohio
Mldco 1. (P)
Gary, Indiana
•
•
•
•
•
•
•
•
•
•
•
•
•
•
•
(IMmmedlete Remove!
(P)-Plenned Remove)
Table!
Activity Categories and Methods of Disposal
MAJOR
CONTAMINANTS
DISPOSAL/
TREATMENT
WASTE OIL
Cham Dyne. (1)
Hamilton, Ohio
Laskin's. (P)
Jefferson, Ohio
Pesticide and
Solvents
Polychlorinatad
Biphenyls (PCB)
Lead
Incineration
Incineration
CRUSHED DRUMS
Isanti, (1)
leant) County Minn
Midco I,(P)
Gary. Indiana
PCB Residuals
Residuals
Landfill
Landfill
CONTAMINATED SOIL
Anaconda, (t)
Akron, Ohio
Midco 1, (P)
Gary, Indiana
Cyanide
Lead and PCB
Landfill
Landfill
LIQUIDS
Anaconda, (1)
Akron, Ohio
Ishanti, (1)
Isanti County, Minn
Midco 1, (PI
Gary, Indiana
Cyanide,
Low Flash
Chlorinated Solvents
Non-Chlorineted
Solvent*
Waste Solvents
Treatment
Recycle
Incineration
AQUEOUS WASTES
Cham-Dyne, (1)
Hamilton. Ohio
Laskin's, (P)
Jefferson, Ohio
Midco 1, (P)
Gary, Indiana
Pesticides, PCB
PCB. Phenols
Metals, Flourides
Carbon
Adsorption
Carbon
Adsorption
Treatment/
Landfill
SLUDGES
Anaconda, (1)
Akron, Ohio
Cham-Dyne, (1)
Hamilton, Ohio
Isanti, (1)
Isanti, County.
Cyanide,
Low Flash
Pesticides
PCB
Solvents
Paint Wastes
Treatment and
Landfill
Landfill
Treatment/
Incineration
COST
367
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was landfilling. While there was no prominent contaminant anal-
agous to cyanide found in the Midco I soils, soils from both Isanti
and Midco I were classified as hazardous under the provisions of
40 CFR 261.3. That is, a material becomes hazardous if contam-
inated by a listed waste or any mixture of a listed waste.
Table 3
Unit Price for Certain Activity Categories
CONTAMINANT
CONCENTRATION
Crushad
Druma
Contaminated
Soils
Aquaoua
Wastal
Liquid!
(Wast*
Solvants)
Isanti (1)
Midco 1. (P)
Anaconda. (1)
Midco 1. |P)
Cham
Dyna. H)
Laskin-s, |P)
Midco 1. (P)
Anaconda. ID
(•ami, |l)
Midco 1. IP)
11S yards3
•.MOyard3
3» yards3
7,220 y»rd.3
35,837
Billons
430.OOO
gallons
131,300
gallons
2,737
gallons
3.200
gallons
1.SOO
gallons
PCB
Rnidu.ll
Cy»nid«
303 ppm
La»d 1170 ppm
PCB 12 ppm
Chlordana 416 ppm
Tohrana 4300 ppm
PCB SS ppb
Phanols 1 1 ppm
Mstals ^ 5 ppm
Flourlda 23« ppm
Cyanlda and
Low Flash
Chlorlnatod
Wast* Solvants
Wasta Solvents
•47-58/yard
• 17.02/yard3
S40.OO/ysrd3
• 17.O2/yard3
M.SO/gallon
•O.IS/gallon
•0^7/gallon
•0.90/gallon
•0.145/gallon
•0-27/gallon
The aqueous phase category shown in Table 3 compares water
treatment activities at three sites. The need for water treatment
at these sites was satisfied through immediate removal contracting
provisions. The contaminants of concern and their concentrations
vary considerably. The treatment system used at Laskin is owned
by USEPA and operated by a contractor under a cost plus fixed
fee type contract.
The final category compared in Table 3 addresses disposal of
liquids at two immediate removal projects and one planned re-
moval. Although the methods of treatment are not directly com-
parable, the costs associated with them provide an insight into the
effect that recycling could have on overall project costs.
COST COMPARISONS
In order to determine the effectiveness of limited competition
on removal project cost budgets, it was necessary to review the past
costs incurred at both immediate and planned removal projects.
This review was necessary so that an accurate basis of comparison
could be developed. General task categories were first developed
for activities common to more than one site. A detailed review was
then undertaken for site specific information associated with that
particular project to determine if those specifics could have af-
fected the cost. When this activity was completed, it was concluded
that the most accurate basis for a project by project comparison
would be disposal cost. Other cost centers, such as equipment,
labor and material, were found to be highly site specific and
such specificity would preclude an accurate comparison.
It came as no surprise to discover the diversity of disposal op-
tions used during cleanup operations. This diversity is directly pro-
portional to that associated with waste materials on site. Type of
waste or material contaminant and its concentration appeared to be
a major factor in determining disposal option and price. From the
four categories in Table 3 that were subjected to the detailed re-
view, only contaminated soils could legitimately be used as a valid
basis of comparison.
It is interesting to note the prices paid in the three other cate-
gories in order to highlight the prominent cost factors associated
with that particular disposal option. In the crushed drum category,
unit prices were developed for Isanti, an immediate removal, and
Midco I, a planned removal. Part of the waste stream from Midco
possibly could have been handled under the residual provisions of
RCRA. However, due to economies associated with labor, equip-
ment and transportation, all shipments were chosen to be mani-
fested as a hazardous waste. The crushed drums from the Isanti
site contained PCB contaminated liquids prior to pumping. Be-
cause of this, they had to be handled and disposed of according to
regulatory procedures under the Toxic Substances Control Act (40
CFR 761). As a result of compliance with this requirement, the
price difference between crushed drum disposal costs for Isanti and
Midco cannot be compared for the purposes of determining the
impact of limited competition. The three fold increase in cost can
possibly be explained on the basis of disposal requirements asso-
ciated with PCB articles.
The aqueous phase category compares three projects that re-
quired treatment of contaminated water found on site either before
cleanup started or after cleanup was underway. The Chem-Dyne
effort involved transport of materials to the contractor's carbon
adsorption treatment unit to remove high levels of solvents and
pesticides from water before discharging to the local sanitary sewer
system. This was done under an emergency contract and included
sand filtration prior to adsorption.
At Midco I, run-off water generated from storms was collected
and transported to the contractor's treatment system where it was
subjected to a series of physical treatment processes including pH
adjustment and clarification to remove metals and florides. Solids
were thickened, solidified and placed in a hazardous waste land-
fill. Treated water was discharged to the local sanitary sewer sys-
tem. Although Midco I was contracted through limited compe-
tition, this aspect of work was performed under a special emer-
gency contract.
The treatment activities at Laskin involved use of the USEPA's
mobile carbon adsorption system to remove PCB and phenols from
ponded water. The water was filtered, treated and discharged to
a nearby stream according to state established standards. Solids
generated during filtration were removed with the system; spent
carbon was left on-site.
These three projects and the costs generated for this category of
work also cannot be compared fairly for the purpose of determin-
ing the impact of limited competition on overall project budget.
The unit price at Laskin, a planned removal, reflects the use of a
system that is subsidized by government funding for operations
and maintenance costs. Personnel costs are also subsidized through
a long term government contract. The costs associated with the
two immediate projects, Chem-Dyne and Midco I, reflect consider-
ably different treatment schemes for widely divergent waste
streams. The cost associated with the Midco I project most likely
reflects a very advantageous government negotiating position. This
cost could have been higher if the Agency and contractor had not
already been involved together, undertaking other cleanup activ-
ities at the site. The author believes this allowed the USEPA to
negotiate very effectively a fair price for the immediate removal
work associated with storm water run-off at the Midco I site.
In the liquid waste category, direct and fair cost comparisons
could not be made between immediate and planned removals.
Nevertheless, the information in Table 3 does give one an idea of
the potential cost impact associated with the recycling alternative to
disposal. The material from Isanti was "disposed of by being sub-
jected to a recycling process. The cost of this effort, performed
under an immediate removal time and materials contract, was al-
most half of that associated with the incineration alternative used
at Midco I. The incineration alternative used at Midco I was pro-
cured through the limited competitive process associated with
planned removals. The contaminated liquid waste stream at Ana-
conda involved a treatment scheme to reduce the cyanide and in-
crease the flash point. As in other unit costs categories, this process
could not be compared to Isanti or Midco I because of the obvious
dissimilarities in waste stream and treatment process.
The contaminated soils category provides data on which to make
an accurate unit cost comparison. The contaminated soils from
both projects were loaded and iandfilled in bulk and manifested as
368
COST
-------
a hazardous waste solid, not otherwise specified. Costs associated
with the cyanide contaminated soild from Anaconda were approx-
imately two and one-half times those for the lead and PCB con-
taminated soils from Midco I. The author is reluctant, however,
to attribute this entire cost differential to limited competition.
Although there were no special handling or treatment provisions
necessary to minimize the reactivity of the cyanide contaminated
soils, the landfill operator may have perceived additional long term
risks associated with this material, requiring purchase of special in-
surance provisions. Another explanation for at least part of the
cost differential may be due to the quantities involved. The quan-
tity of material shipped from Midco I was considerably greater
than that shipped from Anaconda. Basing unit prices on quantity
is a common practice in the waste disposal industry.
CONCLUSIONS
Based on the above review of the immediate and planned re-
moval projects completed in Region 5, it is difficult to make a
definitive statement regarding the impact of limited competition
on removal project cost budgets. Activity categories, types and
amounts of waste materials, characteristics of waste materials and
disposal options vary considerably from one site to the next. Al-
though the limited data generated during this effort do not provide
conclusive results regarding cost savings associated with planned
removals, they do indicate, in general, that planned removals can
be more cost effective. This cost effectiveness can be attributed in
large part to the additional time provided to contractors for
project planning. The data supplied in this paper mdicates_that_
limited competitive procurement efforts will yield lower costs for
work categories addressing similar waste streams under time and
materials contracts than those projects where there is no compe-
tition.
Additional comparative work needs to be done to better assess
the impact of limited procurement in the removal program. More
projects should be reviewed to identify waste categories, character-
istics and disposal approaches^ A greater data base would provide
for a valid comparison of costs from one project to the next. With
more valid comparisons, better assessments could be made in re-
gard to the value and importance of the planned removal and lim-
ited competitive procurement process.
REFERENCES
1. 40CFR300.
2. 94 STAT. 2767-2811.
3. Vanderlaan, G.A. "A Fast Track Approach to Impact Assessment at
Uncontrolled Hazardous Waste Sites", Proc., Second National Con-
ference on Management of Uncontrolled Hazardous Waste Sites, Oct.
1981,348.
4. Rutter, A. J. "Cost Summaries For Region 5 Remedial Response Branch
Superfund Projects For 1982" unpublished.
5. 40CFR261.
6. 40CFR761.
COST
369
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REMEDIAL ACTION MANAGEMENT AND COST ANALYSIS
JAMES D. WERNER
EDWARD J. YANG, Ph.D.
ERIC NAGLE
Environmental Law Institute
Washington, D.C.
INTRODUCTION
Superfund presents a classic economic and management dilemma
—how to clean up the seemingly unlimited number of problem haz-
ardous waste sites using limited resources. Congress" recognition
of this dilemma is reflected in the Comprehensive Environmental
Response, Compensation and Liability Act of 1980, by the specific
statutory requirement for selection of the most "cost-effective"
remedial alternative at Superfund sites. Cost effectiveness, as out-
lined in section 300.68, subpart F of the National Contingency
Plan, does not mean that public health concerns should be sub-
ordinated but rather that the least cost alternative should be selec-
ted from among adequately effective options.
However, carrying out this mandate for cost effective remedies
requires first, that accurate cost information be available for es-
timating the relative costs of remedial atlernatives and second,
that this information be used to implement the remedial alterna-
tive as efficiently as possible through effective planning and man-
agement. To help provide this information to the EPA's Super-
fund remedial action program, the Environmental Law Institute
(ELI) performed detailed case studies on remedial actions at 23
hazardous waste sites across the United States.
This study is the most comprehensive compilation of actual ex-
penditure data for remedial actions that has been performed to
date. For 16 of the 23 case studies, ELI worked in conjunction
with JRB Associates, which compiled the technical information
at the sites. This paper summarizes the findings on the costs, the
planning and the management of the cleanups at these sites.
METHODS AND MATERIALS
Site Selection
The following information sources were used to find potential
uncontrolled hazardous waste sites for case study consideration:
•1981 SCS Engineers Survey
•USEPA Hazardous Material Incident Reports
•USEPA Regional Offices
•State lists of hazardous substances spills responses
•Remedial contractors
•Trade Associations
•Professional contacts
From these sources, 23 sites were selected using the following
criteria:
•Data availability
•Useful remedial technology
•Post-1975
•Remedial actions completed
About 385 sites were considered for study at which some remed-
ial action, or in some cases, spill response, had occurred or was
planned. In practice, the availability of data was the most com-
mon limiting factor. For this reason, the sites may not be repre-
sentative of the universe of existing uncontrolled hazardous waste
sites and their remedial costs.
Approximately equal numbers of private and government fi-
nanced remedial actions were chosen at 12 and 11 sites, respec-
tively. The variety of remedial technologies included cut-off walls,
subsurface drains, solidification, excavation and groundwater ex-
traction, treatment (physical, chemical and biological) and reinjec-
tion.
Data Collection
Data were generally collected in three stages:
1. Interview preparation
2. On-site interview and file search
3. Follow-up and refinement
After obtaining permission to study a site, preliminary informa-
tion was obtained to prepare for the site visit. This information
helped confirm the utility of the available information, generate
useful questions and organize the component tasks and aspects of
the remedial projects.
Interviews and file searches during the site visit were the primary
sources of cost and decision making information. All invoices,
memoranda, letters, proposals, contracts, consent decrees and
pleadings were photocopied. This information was typically sup-
plemented by extensive discussions with responsible personnel and
a site tour. These sources were invaluable in providing perspec-
tive to the large volume of file material.
The last phase of the data collection process was the site visit
follow-up to refine and verify the data. Again, site contacts were
helpful in organizing related tasks and specifying what activities
were or were not included in a contractors invoices as well as de-
tailing decision making processes.
Categorization of Data
The data base resulting from this search consists primarily of
three forms:
1. Invoices
2. Reports and correspondence
3. Interview notes
Cost data were divided into functional categories by two primary
means and supplemented with a variety of sources. The categor-
ization method depended on the type of the data available from
the source. The first method was the aggregation and summing
370
COST
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of specific costs on invoices to determine the cost for a general
operation such as slurry wall construction. All costs related to a
particular task were totalled to derive the cost of the operation.
Component costs of the total are described and dissected in the
text of the particular case study. Unit costs for items like dis-
posal or slurry mixture were multiplied with the volumes given in
as-built engineering reports to double check the numbers.
The second method was the correlation of weekly invoice sum-
maries of general cost categories with the activity occurring dur-
ing that period to estimate the cost of an operation. Weekly in-
voice summaries were often categorized by items such as labor,
equipment, transportation and disposal. These categories were
broken down according to the operation to which its function
contributed and the proportion of the weekly total used for that
operation. For example, excavation might have been performed
for 100% of a given week, and 50% of the labor and 30% of the
equipment were devoted to this operation, with the remainder
devoted to analytical work. The cost would be further broken down
if the daily reports showed that transportation and disposal oc-
curred during two of the seven days included on the invoice for
which X% labor and equipment were used for loading and
analysis.
These invoice based methods were supplemented with other
sources such as interviews, reports, correspondence and contracts.
When aggregating specific invoice items, particular items were
sometimes explained by references to file material or the site con-
tacts. The breakdowns of general invoice summaries according to
daily reports were often refined by interviewing or correspond- (
ing by mail with site contacts about the execution and timetable
for particular operations. In-house costs were estimated, when
available, by totalling company time sheets for the appropriate
project. In-house private party costs were the most difficult cost
to obtain, usually because of the lack of available records.
Planning and management information sources varied widely.
For many sites, agency correspondence provided most of the in-
formation. For private site responses, the agency correspondence
often included justifications for decisions. For government
responses, decision making information was usually obtained
through interviews. Court documents, such as consent decrees,
provided another important source of data on planning and man-
agement. At virtually all sites, follow-up phone calls were neces-
sary for gathering supplemental decision making information.
Memoranda to files were perhaps the most useful, but least com-
mon, source of planning and management data.
RESULTS
Costs
The results of the research on remedial action costs of the 23
remedial actions were organized and explained in two ways. First,
the cost of remedial work at each site was given, and categorized
according to component tasks. A complete explanation of the costs
is given in each case study in a cost section that corresponds to
the technology and planning and management sections. Second,
costs of similar remedial technologies at different sites were com-
pared with comparable construction-engineering manual estimates
calculated by SCS Engineers in 1980.
The frequency distribution of the total costs of the remedial ac-
tions at the 23 case study sites, ranging from $23,000 to $10.3
million, is shown (Figure 1). In Table 1 the total costs of the first
four of the 23 case study sites are given in alphabetical order.
Also given are the problems, the response and a quantification of
the response. The year of the expenditure is given but was not
found to significantly affect costs since they were all performed
relatively recently. The mean total cost per site was $1.4 million.
Seventeen of the 23 case study responses cost between $200,000
and $2 million.
However, these costs for total site costs, as well as the costs for
specific technologies, are not necessarily representative of the costs
that should be expected in the universe of hazardous waste sites for
four reasons.
First, the remedial work is not necessarily completed. Some
sites were studied because of useful isolated preliminary tasks. At
some sites the need and funding source for future site work re-
mained unclear.
Second, some hidden or in-house costs were excluded. Despite
attempts to include these costs, all costs were not necessarily doc-
umented. For example, private parties often did not record in-
house labor, equipment and overhead costs; and government
actions usually did not include administrative costs. These limita-
tions also prevented any conclusions about the relative cost-effec-
tiveness of private vs. public responses.
Third, costs for case study responses were incurred in a period of
dynamic conditions in the remedial actions contracting market. In-
creased economies of scale and increased government expertise
tended to decrease costs in the more recent remedial actions, while
RCRA regulations and privatization of research and development
have worked to increase costs during the same period.
Finally, the site selection procedure did not attempt to assemble
a group of 23 sites that were statistically representative of the range
of site types and costs, which are themselves still unknown. How-
ever, the exclusionary site selection criteria that affected the lower
end of the cost spectrum were probably less significant than those
affecting the upper end. For example, the average total response
cost may be an underestimate because the site selection procedure
excluded most CERCLA-funded sites, which are generally the
largest uncontrolled hazardous waste sites in the country. Also,
more costly sites tend to involve litigation that rendered them un-
available for study.
The costs for four of the technologies analyzed in the case stud-
ies are summarized briefly below. These are not suggested as de-
rived average costs for any of the technologies, but merely as the
costs for four of the technologies analyzed in the case studies.
Ideally, the number of data points would have been allowed to
approach infinity, but the availability of data was limited because
of the small number of remedial actions that have been undertaken
and that were available for study. Also, these costs inconsistently
included related costs, such as grading for capping, because the
invoices were totalled for the entire unit of operation.
ft >'
I:
;-*!.« Billion
S.D.- » 1.1 Billion
TOTAL COST OF SITE HESKMSE (In Millions I)
Figure 1
Distribution of Total Site Costs
Capping
Capping cost data for three of the case study sites are summar-
ized in Table 2. These response unit costs are supplemented with
significant descriptors, and compared with the SCS estimate. These
COST
371
-------
Table 1
Total Cost by Site (4 of 23 sites)
Site Haj»e
ABOBTBOiia
lite A.
AaooTBoaa
lite 1.
ABOBTBOUa
Site C.
ABoayBoua
110 D.
DBU
ixa
1MO
1M1
1M1
Probleia/Rtek
pesticide/
fertilizer
pooh leaked
CB»
aolventV
hBTMdcc-fw
hex. chromium
«H.f"
eoliUmlimtloil
•olmnU, iw,
•w eomjUBlmUoB
Prieury RespanM
TochBolcflo
dbpcwl,
cut-off ma
BDwface or»l«
(w treatment
•utarfec* drab
|>w treatment
Hteurte* c»lB/
Kntln,
Modepxktkai
QwnUiy
l_liw"l
t.OTm'
II. lonf
4-6 BI deep
UO.MOlpl
Tim lore
4 • deep
l,M*lpd
SMMlpd ,
1
Total Slla
Con
lll.J
•IIUOB
$lU.nT
«U,*M
WJI.1M
gw = ground water
sw = surrace water
Ipd = liters per day
Table 2
Capping Costs
Sltl Kane
Anonrmu
Slt« A.
AoonyBoue
511. 1.
AnonyBoue
Slt« C.
"SCS CatlBate"
Date
ltd
i9«i
1961
I960
I960
Cap Katerlal
clay
gravel/
bentonlte-aoll
eephalt
da?
bltwlnoue
concrete
TMckncR*
6 Inchce
(0.1S .)
4 IncKcs
(0.15 .)/
4-n Incltee
(0.1-0.2 •)
(fc>
1 foot
(0.1 •) (a)
9 Inchei
(O.OS .)
Coverage
(b)
1M.ODO (t2
(U.«9) >Z>
13S.OOO (I2
(12. MJ •*)
100.000 ft1
(292. Ul «2)
595,95) (t2
(55.JM . )
Unit Cost
Jl.tVft2
($17. 55/.')
51. I)/ It'
($12. M/.2)
1.1J/ It2
($12. 26/.2)
io.nl ft2
(S10.23/.!)
$0.61 - O.M/ft2
(St.M-9.Ot/B2)
(a) Reported thickness in proposed design
(b) Data not available
costs include capital but not operation and maintenanrccosts. The
capping costs found at the case study sites were relatively similar,
ranging from $0.95-1.63/ft2 ($10.23-17.55/mJ). The range of costs
estimated by SCS was lower than at any case study sites. These
costs are of limited comparability, however, because of the various
designs of the caps, these variations are useful in considering signif-
icant cost factors.
These factors included:
A. Material Variations
(1) Cap Material
(a) Bentonite/clay
(b) Asphalt
(2) Related material
(1) Top gravel
(2) Gravel bed
(3) Curbs
(4) Topsoil and seeding
B. Dimensional Variations
(1) Thickness
(2) Area Covered
The cost data were inadequate to determine an average cost for a
particular cap type or to quantify the effect of a particular cost
factor, but some patterns and absence of patterns were suggested.
Among material costs, the type of cap material (bentonite/clay vs.
asphalt) may have been less significant than the costs for related
materials such as gravel and curbing. This is suggested by the sim-
ilar costs for the two caps at site 2. The dimensional variations,
such as thickness and the area covered, may explain the lower unit
costs for the SCS estimate since the hypothetical cap used in the
estimate was much larger, resulting in significant economies of
scale.
Cut-off Walls
Cut-off wall costs for five case study sites are summarized in
Table 3. The wall size and basic composition are also given, along
with the comparable SCS estimate. These costs include capital but
not operation and maintenance costs. Unit costs for the case study
site cut-off walls ranged from $0.21-$29.59/ft2, but, excluding the
extremes, they ranged from $1.42-$14/ft2. The entire range esti-
mated by SCS for a hypothetical cut-off wall was lower than the
Table 3
Summary of Cut-off Wall Costs (a)
Site Hue
AnonjTBOu* Site A
AnonJTMHi* Site A
AnOBjnMHia Site 1
AnonrBou* site C
AAOByBeue Site D
AwnrBMU site I
•scs
EetlBate"
(c) 4 (e)
Dete
1950
19S2
19SO
19S1
191}
19*0
19SO
Cut-off Well Tr»e
A5FDUI (()
ASTDUI (f)
ASrEMII (f)
ecntonite
elvrry
local clajr
local clay COB-
pacced In llfta
bentonlta
Blurry
SUe (depth underlined)
2.000 I 17 I 0.13 ft-M.OOOtt2
(510 I 5 S 0.02} B - 3.159 B2)
2,929 I 17 I 0.13 (t-»9.»J* ft2
(993 I i * 0.021 B - t.«7l B2)
l.ttl I 10 X 1 It - 14,450 ft2
(447 I j > 0.3 B - 1.341 B2)
618 I 17 I 1ft - ll.Olt ft'
(191.4 S 5.2 I 0.3 B - 1023 B')
2.745 I 14.3 I lft-39.490 •< fc
HA (b)
2.306 I 41 I 3.2 feet -
110. Ml Tc2
(720 I 15 I 1 B - 10. (00 B2)
Expendltttra
J23I.OOO
$974.274
$13.000
$316.0007}/B>)
»14/ft2
WJO/B?)
t>.tO/ft>
(S41/B2)
II9.M/IC2
(319/B2)(d)
$1.42/ft»
U5.11/B>)
*0.21/ft2
($2.2t/B2
$4. 21-7. 34 /It2
(a) Cosls arc of limited comparability; sec text.
(b) Repotted to be 2 feet thick by design drawings.
(c) Based on Means "Building Construction Cost Data: 1983"
(d) Includes excavating the trench, transporting and disposing of contaminated soil.
(e) Total capital costs.
(0 Asphalt, sand, concrete, water emulsion.
372
COST
-------
mean found at the case study sites. The range of costs largely re-
flects the wide variation in the cut-off wall types.
The two most significant factors affecting costs were the wall
type and the disposal of the contaminated trench material. The
ASPE MIX walls cost significantly more than standard clay cut-
off walls, but their low permeability, demonstrated in bench scale
tests, was required by the government agencies overseeing the
clean-up. At one site, the cut-off wall was constructed within-the
contaminated area, and, hence, the trench material required dis-
posal in an engineered landfill.
Excavation, transportation and disposal—Because of the large
amount of data for excavation, transportation and disposal, only
the ranges found for these costs are summarized in Table 4. The
costs of RCRA hazardous waste were separated from the TSCA
hazardous PCB waste because of the widely differing costs and
regulatory programs. The cost of excavating the waste (without
transportation or disposal) ranged from $8-146/yd3. Transporta-
tion costs were relatively similar at $0.13-0.28 ton/mile. The costs
for disposal ranged from $5/tonne (metric ton) at a USEPA sub-
sidized landfarming operation to $277/tonne for incineration of
highly contaminated PCB oil. Most RCRA hazardous waste dis-
posal costs were about $100/tonne. No significant differences were
found between disposal costs for bulk and containerized wastes.
Other factors affecting these costs were:
I. Technical
A. Excavation or On-site Transfer
1. Excavation depth
2. Site surface characteristics
3. Waste explosivity
4. Material-liquid/solid/drums
5. Waste quantity
B. Transportation
1. Distance to disposal facility
2. Accessibility to road
3. Material-liquid vs. solid
4. Waste quantity
C. Disposal
1. PCB
a. Concentration-over/under 500 ppm
b. Material-solid vs. liquid
2. Non-PCB RCRA Hazardous
a. Solid vs. liquid
b. Aqueous vs. organic
II.Non-Technical
A. Community relations
B. Interstate relations
C. Inflation and regulatory factors.
Table 4
Range of Costs for Excavation, Transportation and Disposal
Excavation
Transportation
Disposal
non-PCB H.W.
PCB
TOTAL
SlO/m1
$0.08/tonne/km
$10/tonne
(landfarming)
$212/tonne
(engineered
landfill)
$57/mJ
$119/m!
$0.18/tonne/km
$93/tonne
(engineered landfill)
$277/tonne
(incineration)
$335/m'
Water Treatment
Finally, costs for water treatment at eight of the 23 case study
sites are summarized and compared with the comparable SCS es-
timate in Table 5. These costs include either: operation and main-
tenance costs for permanent systems constructed on-site; labor,
material and rental costs for temporary on-site systems; prices
charged by the contractors for water sent to commercial industrial
waste treatment plants; or the prices charged by publicly owned
treatment works for accepting wastewater. Capital costs were ex-
cluded from this summary because they are not consistently applic-
able and because of the uncertainty about the length of the opera-
tional lifetimes for amortization purposes. Operation and main-
tenance costs ranged from 6-20% of capital costs.
Probably the most important factor affecting the unit costs
found for treating a given volume of waste was total volume of
waste treated. Systems with large capacities were able to take ad-
vantage of their greater economies of scale. For example, at site
1 only 1,000-1,500 gal/month of water were treated; whereas at
site 8, about 3.5 mg of water/month were treated.
Other factors found to affect these costs:
A. Technical Factors
1. Nature and degree of contamination
a. Treatability
b. Solubility
c. Concentration
d. Diversity of contaminants
2. Variations in type of treatment processes selected
a. Carbon
b. Biological
c. Physicochemical secondary treatment (POTW)
d. Other individual treatments (e.g., air stripping, fabric
filtering)
3. Variations among particular processes
a. Level of treatment
b. On-site/off-site
c. Efficiency
d. Treatment system capacity
e. Collection limitations
f. Climate
B. Non-technical Factors
1. POTW rate system
2. Use of existing system
3. Rental vs. purchase of treatment system
4. Market competition by treatment contractors
5. Inflation
Planning and Management
The five most significant factors regarding the planning and
management of the remedial actions were found to be:
•The basis for initiation of the response
•Public interaction with the response
•The basis for the extent of response
•The role of federal and state statutes in the execution of the re-
sponse
•Methods for selecting and retaining contractors
The reasons for initiating the responses were significant because
(1) if they were perceived as emergencies, the choice of technolo-
gies was significantly limited, and (2) clear identification of the
nature and extent of the risk was found to provide a firm basis for
designing a response strategy.
About half of the responses were initially reported to the author-
ities by local citizens. Public attention was usually focused on in-
itiating a response, rather than on particular aspects of the re-
sponse. Public interaction with the cleanup was found to be very
limited. At one site, however, citizen opposition blocked five
initial proposals for disposal of contaminated material. At an-
other site, though, the local media focused attention on the large
amount of money and time being spent on what was perceived as
just a minor spill.
Perhaps the most important aspect of planning and management
of the case study responses regarded the decisions about the extent
of the responses. At every case study site the general goal was to
eliminate the threat to public health and the environment, but spe-
COST
373
-------
Tables
Contaminated Water Treatment Cost (a)
Sic* K*»e
Aaoajntous
Site A
Anonyanus
Site B
Aaonysous
Sice C
Anonyanus
Site D
Anonyaous
Site E
Anonymous
Site r
Anonymous
Site C
Anonysious
Site H
"SCS estimate"
Date
19*1
19*2
1980
1979
1983
1982
1979
1982
1980
Treatnent
Technology
On-alte advanced oil/
vater separator
Off-site Cowereial
Treatment
On-site carbon t
clarification, air
•ttipping
On-slte carbon, pea
gravel/lie*
filtration
On-alte
Biodegradation
Off-lite
POTW (c)
Off-lite
POTW (c)
On-alte
Granular Activated
Carbon (reverie
pulae)
On-lite
"Chemical,
biological and/or
physical"
Primary
Contaminant
rct/oii
Cyanide
•Ixed aolvents,
PCS
Pentachloropheno]
(PCP)
•ethylene
chloride,
butanol,
acetone
hexavalent
chromium
Pesticides
(atracine,
alachlor)
Pestlcldea
(DBCP)
"contaminant"
Quantity Treated
1,000-1.500 gallons
(3.785-5678 I)/ month
9.425 gallons
(35,674 1)
7.C x 10* gallons
(2.9 x 10' 1)
over 6 Month period
t x 10* gallons
(8 x 10s 1)
ever 1 Month period
13,680 gallons
(51,779 l)/day
273,000 gallons
(1.03 x 106 1)
9 x 107 gallons
(3.4 x 10* 1)
over 5 »nth period
1.5-2.6 x 108 gallons
(6.8-9.8 x 108 l)/year
4.3 x 10 gallons
(1.6 x IflS 1 )/year
Expenditure
54.167/month
$12.724
52-3
•llllon
$200.000-
350,000
$226.53/day
$2,275
$50.169
$133.320-
370,800/year
$51,900-
94,340/year
Unit Coat
52.70-4.6/gal
($0.73-1.10/1)
$1.35/gallon
($0.036/1)
$0.26-0.40/gal(b
($0.068-0.10/1)
$0.10-0.18/gal
(50. 026-0. 048/
1)
50.0165/gal
($0.0044/1)
50.008/g.llon
($0.002/1)
$0.00056/gallon
($0.00015/1)
50.0005-0.0011/
gallon
$0.00013-
0.00029/1)
50.0012-
0.0022/gal.
($0.00032-
0.00058/1)
(a) Operation and maintenance, or rental cost
(b) Includes ground water recovery cost
(c) Publicity Owned Treatment Works
cifically defining that goal took many different forms. First, the
goals were chosen in three major ways: through judicial or ad-
ministrative processes, by voluntary agreement between agencies
and a private party, or within the government agency undertaking
the response.
The second issue studied in the planning and management of the
case study responses was the specific cleanup goals chosen. The
sources and types of the standards varied widely at the case study
sites. Sources of the standards were important because they de-
termined how clearly and precisely the standards were expressed
and how justifiable or defensible the standards would be if called
into question. Emergency cleanups were often terminated when the
threat of fire or explosion was eliminated. These emergency ac-
tions, which were virtually all government responses, were made
through a "best professional judgement" approach rather than
relying on preexisting standards. Though, in three emergency re-
sponses, the Coast Guard and/or the USEPA established specific
physicochemical cleanup goals for themselves.
Remedial actions goals were generally more thoroughly con-
sidered. However, for remedial actions at eight of the case study
sites, best professional judgement was used to establish a cleanup
standard. These judgements ranged from a visual notion of what
constituted clean soil, to the determination of an ad hoc group of
lexicologists and public health scientists who drew upon labora-
tory and epidemiological studies. Preexisting standards, such as
landfill design criteria and NPDES discharge requirements, also
served as benchmarks for cleanups. At only two of the 23 sites was
the contaminant level required to be brought to a given level. At
most sites, plume spread had to be halted and/or reversed, and
drawn off water had to be treated to acceptable pretreatment or
surface water standards. The plume control periods were all in-
determinant. Specific groundwater cleanup goals were determined
at one site from three sources: (l)Suggested No Adverse Response
Levels developed by the National Academy of Sciences; (2) Allow-
able Daily Intake for pesticides set by the World Health Organ-
ization; and (3) extrapolation from crop tolerances levels estab-
lished by the USEPA. At other sites, states used "Action Levels"
or "Levels of Concern", set by the health department, to deter-
mine cleanup requirements for soil or reinjected treatment effluent.
Most of the case study responses were affected by laws govern-
ing hazardous substances or law protecting water resources, but
not by laws governing air quality, although air pollution was often
a significant concern. The three major ways laws affected clean-
ups were: (1) they provided government agencies with the author-
ity and/or funding to initiate responses and provided funding for
the work (section 311k of the Federal Water Pollution Control
Act and state spill funds); (2) they provided the basis for gov-
ernment authorities to prompt private parties to undertake clean-
ups (section 7003 of the Resource Conservation and Recovery
Act, the Toxic Substances Control Act and the Federal Water
Pollution Control Act); and (3) they contained design or per-
formance standards that were used as standards for determining
the extent of response (discharge requirements in the California
Administrative Code for land disposal facilities, NPDES).
Two major contracting issues were studied—contractor selec-
tion methods and contract types. Private parties usually used bid-
ding procedures slightly more often, and allowed subcontracting
much less often, than government agencies. Three major contract
types were used at the case study sites: lump sum, unit price and
time and materials. Private parties used lump sum contracts, with
change orders, more often than time and materials, while govern-
ment agencies had the opposite pattern. However, these general-
izations should be tempered with the fact that 10 out of 11 gov-
ernment responses were considered to be emergency responses.
Preference for unit price contracts which involved, for example,
charging a given unit price for a square foot of cut-off wall, or a
cubic yard of sludge removal, was equally divided between the pri-
vate and government responses.
374
COST
-------
CONCLUSIONS
The case study method was an extremely effective method for
deriving useful lessons from previous remedial actions at haz-
ardous waste sites. Important findings of the research include cost
accounting procedures, contracting techniques and the importance
of determining the extent of response as a management tool.
The accounting procedures used at the case study sites were
found to vary widely. The research suggested that the most useful
way of recording costs is to aggregate the costs according to task. In
this way, it is possible to clearly determine exactly what a slurry
wall cost in terms of a bottom line number useful for decision
making. This method contrasts with the site-wide multiple task
equipment/materials/labor breakdowns found at many sites. This
information would be most useful in a Response Summary Report
which also contains a clear summary of events and significant de-
cisions.
The most useful contracting method seemed to be the unit price
form. This contract offers not only the cost control advantage of
lump sum contracts, but also provides the flexibility of time and
materials contracts that is needed for the typically uncertain situa-
tions at hazardous waste sites. Lump sum contracts, by contrast,
prompt contractors to protect themselves against these uncertain-
ties with explicit or hidden contingency allowances. Time and ma-
terials contracts are subject to abuse in drawn-out projects.
Finally, although the sources and use of standards varied wide-
ly at the case study sites, some type of clear end point goal seemed
necessary for all sites. Planning and management of the cleanup
seemed to be more efficient and effective when some goal was set
before committing significant resources. These goals may have
been altered as the work proceeded, but setting of some justifiable
goal helped organize the cleanup operation by serving as a focus for
the various tasks.
Many of these findings, made elsewhere, have resulted in the
planning process in Feasibility Studies and, hence, serve to rein-
force ongoing programs. Future revisions of the National Contin-
gency Plan may draw upon these early lessons to improve the
guidance given to future cleanups. An objective, open appraisal of
past cleanups should continue in order to avoid reinventing the
wheel in efficiently managing remedial actions at hazardous waste
sites.
ACKNOWLEDGEMENTS
This paper is based on research performed to the USEPA Office
of Research and Development and Cooperative Agreement R-
8059200-10. The authors wish to express their sincere thanks to
Douglas Ammon and Richard L. Stanford of the USEPA for their
sage guidance.
REFERENCES
1. Environmental Law Institute/JRB Associates. "Survey and Case Stud-
ies of Remedial Actions at Hazardous Waste Sites." For USEPA Office
of Research and Development, Final Draft, Apr. 1983.
2. SCS Engineers, "Costs of Remedial Response Actions at Uncontrolled
Hazardous Waste Sites," for USEPA Office of Research and Devel-
opment, Apr. 1981.
COST
375
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COSTS OF REMEDIAL ACTIONS AT UNCONTROLLED
HAZARDOUS WASTE SITES—IMPACTS OF WORKER
HEALTH AND SAFETY CONSIDERATIONS
JAMES J. WALSH
JOHN M. LIPPITT
M. SCOTT
SCS Engineers
Covington, Kentucky
INTRODUCTION
In December 1980, the U.S. Congress passed legislation entitled
"The Comprehensive Environmental Response, Compensation
and Liability Act." This Act provides the USEPA with the legis-
lative mandate and the money to assist in the elimination of public
health hazards posed by uncontrolled hazardous waste sites. Sec-
tion 105 of the Superfund legislation requires the USEPA to in-
vestigate the costs of remedial/cleanup actions at uncontrolled
waste sites. Specifically, Item 2 of Section 105 requires the devel-
opment of cost ranges for various types of remedial actions.
Responsibility for implementing Superfund actions and response
to uncontrolled hazardous waste sites rests primarily with the
USEPA Office of Emergency and Remedial Response (OERR). At
the request of OERR, the USEPA Office of Research and Devel-
opment (ORD) has been conducting research on the costs of re-
medial actions to fulfill the requirements of Section 105. In sup-
port of these activities, several studies have been conducted to
evaluate the types of remedial actions and associated costs applic-
able to Superfund sites (i.e., sites for which Superfund monies have
been allocated) and other hazardous waste sites.
In these studies, costs associated with health and safety of work-
ers were either not included or not uniformly identifiable as sep-
arate cost items. As a result, the project presented in this paper was
designed to specifically address the additional costs of protecting
worker health and safety on a hazardous waste site. These costs do
not include costs associated with addressing concerns of the public
health and safety in the vicinity around an uncontrolled hazardous
waste site. However, the controls and costs associated with pro-
tection of workers on the site should reflect much, if not all, of the
additional costs of protecting the public in areas removed from the
source of contamination (i.e., the hazardous waste site itself).
The objectives of this project were:
•Identify categories of health and safety costs
•Collect and compile health and safety cost estimates and deter-
mine a range of costs which can be encountered on hazardous
waste sites
•Calculate percentage incremental health and safety cost adjust-
ment factors
•Identify factors which impact health and safety costs and should
be considered for future study and evaluation
STUDY DESIGN AND APPROACH
Initial data collection was based on reviews of case studies, bid
documents for Superfund sites and a telephone survey of firms and
regulatory agencies. After reviewing available data and the sum-
maries of the telephone survey, it was determined that health and
safety costs could not be readily identified. Normal accounting
practices did not distinguish many health and safety costs. Such
costs were routinely incorporated into general categories such as
labor rates, equipment O&M costs and overhead expenditures.
In addition, extensive analysis of cost data from existing sites was
viewed by many contractors as extremely sensitive due to compet-
itive and proprietary considerations.
On the other hand, most of the contacts felt that general dis-
cussions of costs would be of little value because of site specific
considerations which impact on the overall costs and particularly
health and safety costs. As a result, it was concluded that realistic,
but ficticious, hazardous waste site scenarios would provide the
best format for providing and evaluating cost estimates for remed-
ial action unit operations. In fact, several of the contacts indicated
they felt it was the only reasonable approach.
From previous studies and case history reports, 28 discrete
remedial action activities (hereafter referred to as remedial action
unit operations) were identified (Table 1). The basis of classifica-
tion was the media that the remedial actions control: surface
water, groundwater, subsurface gas and waste. Nine of these are
classified as surface water controls, eight as groundwater controls,
three as gas migration controls and eight as waste controls.
Ten health and safety cost components were identified based on
literature reviews, previous site observations, discussions with field
personnel from state and federal regulatory officials and discus-
sions with cleanup contractors (Table 2).
In providing cost estimates, contractors were requested not to
address costs of transportation and disposal. This approach was
taken due to the amount of information available on transporta-
tion and disposal costs and to minimize the amount of cost esti-
mations required of the contractors responding to the scenarios. A
separate telephone survey was conducted involving 11 transporta-
tion firms to identify current ranges of transportation costs fw
hazardous waste.
Disposal cost estimates were obtained from the 1981 update of
the USEPA report entitled, "Review of Activities of Major Firms
Involved in Commercial Hazardous Waste Management Indus-
try."1 Since transportation and disposal costs are often included
as separate line item costs, separation of these costs in the scenartol
is consistent with normal contractor procedures.
TELEPHONE SURVEY
An extensive telephone survey was made to identify available
sources of data on health and safety costs. The survey included:
376
COST
-------
Table 1
Remedial Action Unit Operations
SURFACE WATER CONTROLS
Surface Sealing with Synthetic Membrane
Surface Sealing with Clay
Surface Sealing with Asphalt
Surface Sealing with Fly Ash
Revegetation
Contour Grading
Surface Water Diversion Structures
Basins and Ponds
Dikes and Berms
GROUNDWATER CONTROLS
Well Point System
Deep Well System
Drain System
Injection System
Bentonite Slurry Trenches
Grout Curtain
Sheet Piling Cutoff
Grout Bottom Sealing
GAS MIGRATION CONTROLS
Passive Trench Vents
Passive Trench Barriers
Active Gas Extraction Wells
WASTE CONTROLS
Chemical Injection
Chemical Fixation
Excavation
Leachate Recirculation
Treatment of Contaminated Water
Drum Processing
Bulk Tank Processing
Transformer Processing
Table 2
Health and Safety Cost Component Categories
Decontamination
Emergency Preparedness
Hazard Assessment
Insurance
Manpower Inefficiencies
Medical Services/Surveillance
Personal Protection
Personnel Training
Record Keeping
Site Security
•Forty-seven firms with experience in remedial action responses
on hazardous waste sites
•Eleven state and federal regulatory agency representatives in-
volved with management and/or assessment of hazardous waste
site cleanup operations
•Eight military contacts involved in the management and/or assess-
ment of military hazardous waste sites
•Six consulting firms that have conducted studies concerned with
remedial actions on hazardous waste sites
•Three research oriented institutions involved in hazardous waste
management research activities
Each telephone interview was recorded on a written telephone
summary report, evaluated and rated based on the following four
general criteria:
1. Amount of experience in assessment and management of remed-
ial actions on hazardous waste sites
2. The variety of experiences with types of sites and/or remedial
actions
3. Access to available data
4. Willingness to cooperate in providing data and discussing cost
allocations
HAZARDOUS WASTE SITE COSTING SCENARIOS
Six hazardous waste site scenarios were developed to be repre-
sentative of three basic types of sites:
•Subsurface Burial
•Surface Impoundments
•Above-Grade Storage
Whenever possible, these scenarios were developed based on ac-
tual cleanup operations either completed, in progress or planned
for the future. This approach was adopted to ensure that the
scenarios would reflect realistic site conditions while providing a
means of controlling site variables which could impact cost esti-
mates. .
Each scenario was composed of a number of distinct unit oper-
ations. The combination of the unit operations represented a com-
plete remedial action program for each hypothetical site. Site char-
acteristics (e.g., size, topography, hydrology, weather, etc.) were
defined for each scenario to provide a detailed profile on the site.
Similarly, the characteristics of the wastes present on each site were
defined so that the degree-of-hazard conditions could be deter-
mined for each unit operation.
The degree-of-hazard conditions described represented con-
ditions which parallel four levels of personal protection recom-
mended in the Interim Standard Operating Safety Guides devel-
oped by the Office of Emergency and Remedial Response, Haz-
ardous Response Support Division, USEPA.2 A brief description
of the conditions associated with the four levels of personal pro-
tection (designated as Levels A, B, C and D in order of decreas-
ing degree-of-hazard conditions) is given in Table 3. Contractors
were instructed to utilize the recommended guides in determin-
ing the level of personal protection required.
Contractors providing cost estimates were instructed to provide
cost estimates for each unit operation under the conditions set forth
in the scenario and costs representative of conducting the same ac-
tivity if the hazardous wastes were not on-site (i.e., base construc-
tion costs). In order to identify the relative impact of variations in
degree-of-hazard conditions, contractors were also instructed to
provide cost estimates based on three other modifications of hazard
conditions which were also specified. The modifications were based
only on variations of waste characteristics while all other site con-
ditions and activities remained constant.
One additional factor which may significantly impact health and
safety costs is ambient temperature. To identify the relative impact
of temperature, contractors were instructed to provide an estimate
of the cost variations of the total scenario, health and safety costs
estimated for each of the four degree-of-hazard conditions. The
cost estimate variations were based on the costs under the range
of temperatures given in the scenario and two additional temper-
ature ranges. The result was an estimate of total scenario health
and safetyjiosts under the four degree-of-hazard conditions for
low K 0°C), normal (0-18 °C) and high (18-38 °C) ambient tem-
perature ranges. The relative temperature ranges included wind
chill considerations.
Table 3
Conditions Associated with Levels of Personal Protection
Level A—requires full encapsulation and protection from any body con-
tact or exposure to materials (i.e., toxic by inhalation and skin absorp-
tion).
Level B—requires self-contained breathing apparatus (SCBA), and cutan-
eous or percutaneous exposure to unprotected areas of the body (i.e.,
neck and back of head) is within acceptable exposure standards (i.e., below
harmful concentrations).
Level C—hazardous constituents known; protection required for low level
concentrations in air; exposure of unprotected body areas (i.e., head, face,
and neck) is not harmful.
Level D—no identified hazard present, but conditions are monitored and
minimal safety equipment is available.
COST
377
-------
The selection of contractors to respond to the scenarios was
based on the following criteria:
•Their relative rating provided from the evaluation of the tele-
phone survey results
•A match of their previous experience with sites similar to one or
more of the scenarios
•The availability of personnel routinely involved in cost estima-
tion and familiar with health and safety requirements on a haz-
ardous waste site
•Project funding limitations for payment of subcontractors (i.e.,
site cleanup contractors) to provide cost estimates
The final selection included seven hazardous waste cleanup con-
tractors responsible for one to three scenarios apiece. Each scenario
was assigned to two different contractors for cost estimation.
A questionnaire was also sent to the contractors providing cost
estimates. The questionnaire was designed to identify differences
in approaches to health and safety considerations which impact
costs. The purpose of requesting the information was to provide
additional information to assist in determining probable reasons
for cost variations anticipated. In addition, contractors were re-
quested to comment on other considerations or differences, if
any, that they considered significant.
TRANSPORTATION COST SURVEY
Initial literature search and review was based on: (1) in-house
library sources and (2) the USEPA Library in the Environmental
Research Center in Cincinnati, OH. The available literature did
not specifically address transportation costs for hazardous waste
cleanup sites. Very little current data (1980 to 1982) were avail-
able for hazardous materials transportation costs. Additional
efforts were made to identify cost information from current
studies. Unfortunately, none of the data were available.
In order to obtain current cost data, a telephone survey of trans-
portation companies and services was conducted. A tele-
phone interview questionnaire was developed for data collection
from companies contacted. Eleven companies were contacted. The
six responses obtained can be divided into three major groups:
1. Companies concentrating or specializing in transportation of
hazardous wastes
2. Companies whose main interests and efforts involve general
freight and commodities and only limited involvement in haz-
ardous waste transportation
3. Waste disposal and treatment companies who provide trans-
portation services for their customers
Two responses were obtained from companies in each category.
RESULTS
Responses to Scenarios
Eleven completed remedial action costing scenarios were re-
turned. Two contractors could not provide the requested cost es-
timates within the required time period due to conflicting work
schedules. As a result, cost estimates for Scenario 5 were provided
by only one contractor. The remaining Scenarios 1, 2, 3, 4 and 6
were estimated by two contractors apiece.
The original cost estimates were reviewed and modifications were
made (e.g., assigning travel and per diem costs to base construc-
tion costs instead of health and safety costs, correction of cal-
culation errors, etc.). Additional information was requested, as
necessary, to reallocate costs to uniformly cover the health and
safety cost component items. Modifications were reviewed with the
respective contractors. Cost estimates were provided for the four
degree-of-hazard conditions which were established in the scenar-
ios. The degree-of-hazard conditions were identified as Levels
A, B, C and D which indicate maximum level of personal protec-
tion required based on the information given in the scenario in-
formation/instruction packets sent to the contractors. The degree-
of-hazard condition designated Level A as the worst case, while
Level D is the least hazardous condition.
In Scenario 2, costs were only requested for Level C conditions
which were considered sufficient for worker protection for hand-
Table 4
Range of Health and Safety Costs per Unit*
Unit Operation
Surface Water Controls:
Surface Seal - Synthetic Membrane
Surface Seal - Clay
Re vegetation*
Contour Grading
Surface Water Diversion
Basins and Ponds
Dikes and Berms
Ground Water Controls:
Well Point Systeo
Drain System
Bentonite Slurry Trench
Waste Controls:
Che»1cal FUatlon (Solidification)
Eicavation of Wastes/Contaminated Soil
Treatment of Contaminated Water
OruM Processing
Bulk Tank Processing
Transformer Processing
Unit of
Measure
.2
sj yd
sq yd
ha
acre
•3
cu yd
.5
cu yd
.3
cu yd
•^
cu yd
•2
sq yd
•3
cu yd
«3
cu yd
.3
c^ yd
cu yd
I/day
gpd
208 1 (55
gal) drum
30,280 1
(8.000 gal)
tanks
Transformer
Base Construction
Costs Per Unit
S14.41-S19.eS
S17.24-S23.SO
$2.74
$2.29
$6,372-$124.000l
SZ.S49-S49.600
S2.9S-S5.76
S2.22-S4.40
S1.91-S16.05"
$1.46-$12.2B
$4.52-$8.S3
$3.46-$6.S2
$12.78-$1S.96
S9.78-S12.21
$133
$111
S38.87-S49.22
$29.72-$37.63
$50.96
$38.97
$25.06-5147.33
S19.16-$112.63
$3.10-5324.41
$2.37-5248.08
S0.09-S14.31
SO. 35-553. 49
$36.18-$630.89
51.222-54.032
S2IO-S3M
Level D
Sl.l3-$3.99
$1.35-$4.77
$0.26
$0.22
$340-565.115
$136-$26,046
$0.38- $2. 10
$0.29-$1,61
S0.23-S9.13
$0.17-$6.99
$0.41-$3.4S
$0.31 -$2.64
S0.84-S14.68
S0.65-S11.23
$11.70
$9.78
S3.31-S22.99
$2.53-$17.58
$4.46
$3.41
$2.75-S46.62
$2.10-$35.64
S14.S2-S112.10
S11.I1-S8S.72
S0.01-SS.3S
S0.03-S20.27
S51.94-S928.42
S1.047-S4.162
Health and Safety Costs Per UnU
level C
$2.06-54.63
$2.46-55.53
SO. 52
SO .43
$1,215-573,342
$486-$29.337
S0.73-S2.66
$O.Se-$2.03
$0. 38-S10.72
$0.29-$8.20
$0.93-$4.60
$0.71-53.52
$2.6S-$19.94
S2.03-S1S.26
$19.63
$16.41
$6.17-$29.75
$4.72-$22.75
$6.97
$5.33
S4.12-$60.97
$3.15-546.61
SS.90-S246.42
$4. 51 -$188. 44
$0.01-$5.44
$0.05- $20. 59
$69.63-51.165.63
$1.926-55.560
$48.57-51 .196
Level B
S2.41-S5.49
S2.88-S6.S6
$0.66
$0.55
$1,215-574,940
S486-S29.976
S0.96-S3.02
S0.73-$2.31
$0.46-512.34
S0.3S-S9.44
$1.28- $5. 22
$0.98-53.99
$3.04-520.91
S2.33-S16.00
$24.06
$20.12
$7.51-532.46
S5.74-S24.82
$16.40
$12.54
S4.29-S70.04
S3.28-SS3.S4
524.70-5169.38
$18.88-5129.53
S0.02-S6.14
S0.06-S23.22
$88.89-$! .402. 86
t5.670-t6.9S8
Level Ik
S2.48-S5.93
S2.97-S7.09
$0.74
$0.62
S1.215-S78.637
S486-S31 ,455
S0.97-S3.70
S0.75-S2.83
SO. 47-513. 34
S0.36-S10.20
S1.S9-$S.S8
$1.21 -$4.27
S3. 35-523. 31
S2.57-SI7.83
$31.34
$26.20
SI0.60-S34.06
$S.IO-S26.04
$18.24
$13.94
54 .64-580. 38
S3.55-S6I.4S
$28.99-SI98.02
S22.I7-S1S1.43
S0.02-t6.97
S0.08-S26.37
S102.68-tl.690.07
$8.354-58,434
*Cost ranges arc not adjusted for economy of scale or regional variations.
t Range includes cosi estimates from one contractor which were significantly higher than the others.
fA, composite of base construction costs for revegetation from previous SCS report [3J yields a range of S3,974-$ 18,079 per ha (SI ,603-57,300 per acre).
••Costs from previous SCS report [3] yield cost ranges of JI.75-S3.63 perm' (S1.34-S2.78 percuyd) for surf ace water diversion base construction.
378
COST
-------
Table 5
Incremental Health and Safety Costs—Range of Percentage Adjustments Over Base Construction Costs
Unit Operation
Level D
Degree-of-Hazard Conditions
Level C
Level B
Level A
Surface Water Control s:
1. Surface Sealing Synthetic
2. Surface Sealing Clay
3. Surface Sealing Asphalt
4. Surface Sealing Fly Ash
5. Revegetation
6. Contour Grading
Membrane
7. Surface Water Diversion Structures
8. Basins and Ponds
9. Dikes and Berms
Ground Water Controls:
1. Well Point System
2. Deep Well System
3. Drain System
4. Injection System
5. Bentonite Slurry Trench
6. Grout Curtain
7. Sheet Piling Cutoff
8. Grout Bottom Sealing
Gas Migration Controls:
1. Passive Trench Vents
2. Passive Trench Barriers
3. Active Gas Extraction Systems
Waste Controls:
1. Chemical Fixation (Solidification)
2. Chemical Injection
3. Excavation of Wastes/Contaminated Soil
4. Leachate Recirculation
5. Treatment of Contaminated Water
6. Drum Processing
7. Bulk Tank Processing
8. Transformer Processing
8-20%
9%
5-53%
9-45%
12-57%
9-40%
7-92%
10%
9-47%
9%
11-32%
32-545%
11-38%
32-166%
86-103%
14-24%
19%
12-59%
17-57%
20-67%
21-54%
21-125%
17%
16-60%
14%
16-41%
44-613%
11-38%
75-192%
138-158%
23-36 %
17-28%
24%
13-60%
22-65%
24-77%
28-61%
24-131%
21%
19-66%
32%
17-48%
50-785%
22-43%
50-277%
173-464%
17-30%
27%
14-63%
24-80%
25-83%
35-65%
26-146%
28%
27-69%
36%
19-55%
58-1990%
22-49%
58-353%
209-690%
ling PCBs. The scenario was included because of the number of
sites and public concern involving electrical equipment containing
PCBs and the special requirements established for PCBs by the
Toxic Substances Control Act (TSCA).
The contractor's cost estimates were compiled and evaluated,
then used to calculate a cost per unit range for each remedial action
unit operation. Cost per unit calculations were made for health
and safety costs at the four degree-of-hazard conditions and for
base construction costs (Table 4). A percentage incremental cost
factor was calculated by dividing the health and safety costs per
unit for each of the degree-of-hazard conditions by the costs per
unit calculated for the base construction costs. The resulting per-
cent range of incremental health and safety cost adjustment fac-
tors are presented in Table 5.
Estimates for those remedial action unit operations not costed as
part of the six cost scenarios can be calculated based on a com-
parison of potential worker exposures while conducting remedial
action unit operations. The types of activities which determine the
potential for worker exposures were identified for each of the 28
remedial action unit operations and are presented in Table 6.
The estimated impacts of temperature on remedial action costs
are summarized in Table 7. The original estimates did provide
costs for each unit operation, but the specific component costs
which contractors considered temperature sensitive and the amount
of the impact were not identified. Therefore, revisions of original
cost estimates, after review of data and follow-up telephone con-
tacts, prevented direct modification of individual unit operations.
However, general indications of temperature impacts can be drawn
from the data provided. The percent variations were based on in-
creases above base construction costs estimated for the moderate
0 to 18°C range. As shown in Table 7, base construction costs
and health and safety increased with higher or lower temper-
atures. Use of an average variation (Table 8) would enable general
estimate adjustments relative to the impact of anticipated seasonal
or climatic temperature differences.
Transportation and Disposal Costs
The costs of transportation of hazardous wastes varies widely
with respect to specific jobs and the type of company employed
to transport the wastes. In addition, the lack of standardized rates
can result in even more variation depending on the amount of com-
petition for a given job. The ranges obtained from this survey
should reflect cost for most of the hazardous waste transporta-
tion but will not reflect unusual costs associated with some sites.
Rates can be based on costs per mile, cost per unit measure (i.e.,
volume and/or weight of cargo) or cost per hour. A cost per mile
rate assumes full use of vehicle load capacity. Economies of scale
will apply to cost per mile and cost per unit measure rates. This is
true for mileage rates because the cost effectiveness of operation
is greater when the ratio of time on the road increases over the
down time spent for mobilizing, loading and unloading.
When rates are based on cost per unit measure, the cost per unit
will decrease as load capacity is approached since the cost of trans-
porting (i.e., costs previously identified) is divided among more
units. Hourly rates normally are applied to short hauls (due to the
increase in percentage of down time), jobs which involve indef-
inite loading and unloading periods and for additional costs of de-
tention times exceeding the time allocated (included in the cost per
mile or cost per unit measure rates). The ranges of rates obtained
during the survey are shown in Table 9. Costs provided by one
of the general freight transporters give an indication of the impact
of distance on rates and are shown in Table 10.
The disposal costs used for this project (Table 11) were obtained
from a USEPA publication "Review of Activities of Major Firms
COST
379
-------
Tablet
Activities Which Impact Potential Worker Exposures While
Conducting Remedial Actions on Hazardous Waste Sites
Unit Operation
Surface Water Controls:
1. Surface Sealing - Synthetic Membrane
2. Surface Sealing Clay
3. Surface Sealing - Asphalt
4. Surface Sealing - Fly Ash
5. Revegetation
6. Contour Grading
7. Surface Water Diversion Structures
8. Basins and Ponds
9. Dikes and Berms
Ground Water Controls:
1. Well Point System
2. Deep Well System
3. Drain System
4. Injection System
5. Bentonite Slurry Trench
6. Grout Curtain
7. Sheet Piling Cutoff
8. Grout Bottom Sealing
t/i
5
VI
5
Ifl
(5s
o-
+>
>
tj
X
LU
•
•
•
•
•
•
•
•
ID
t» f-
y "S
en 4}
c 3 o>
l_ *fl ••—
* (/)
CT CT> in
= S £ fe
»— C i— Q.
U C71 Li_
Q C 0
-•- "D 4-»
- > C
§•«-«! W»
t- O>
._ Q en i-
4-> C 3
(J -O -i- */l
OJ C T3 O
••-) n
«
u
X
Unit Operation ">
Gas Migration Controls:
1. Passive Trench Vents •
2. Passive Trench Barriers •
3. Active Gas Extraction Systems •
Waste Controls:
1. Chemical Fixation (Solidification) •
2. Chemical Injection
3. Excavation of Wastes/Contaminated Soil •
4. Leachate Recirculation
5. Treatment of Contaminated Water
6. Drum Processing 0
7. Bulk Tank Processing o
8. Transformer Processing o
M
S
VI
CTIM
= »
L. VI
0 i—
"5
01 01
•ES .£
t— C •—
t- 0» U.
a c
••- -o
- > c
§T "
Jt
•*- o at
<-> c
u -a ••-
OJ C TO
•O (D 10
C U-
*-i o
•
*
*
*
*
•
«
I
en
C
*n
«/»
Oi
U
o
1_
e;
?
c
•o
c
5
X
V
u
S!
o
0
0
*
VI
fe
£
«
>
o
**
(A
3
VI
&
X
ul
1
*
*
1
*
1
*
I
•
• Denotes applicability.
o Denotes applicability 1f done 1n contaminated area.
Table 7
Impact of Temperature on Remedial Action Costs
ContTKtor-
Scmirlo
11-1
1-2
III-2
II-)
IV-3
III-4
IV-4
l»-5
III-6
*-6
TBWKrtture
™
0-18-
18-38-
co-
0-18-
18-38-
CO-
0-18-
18-38-
CO-
0-18-
18-38*
CO-
0-18-
18r38-
CO-
o-is-
18-38-
co-
0-18-
18-38-
CO-
0-18-
18-38-
CO-
0-18-
18-38*
CO*
0-18-
18-38-
CO-
0-18-
18-38-
CO-
32-65-
65-100*
C32-
32-65-
65-100-
C32-
32-65-
65-100-
C32-
32-65-
65-100-
C32-
32-65-
65-100-
C32-
32-65-
65-100-
C32-
32-65-
65-100-
C32-
32-65-
65-100-
C32-
32-65-
65-100-
C32'
32-65-
65-100-
C32-
32-65-
65-100-
C32-
U«1 0
»
542.921
5S4.633
553.980
181.993
272.990
242.051
~
z
239.184
263.102
318.115
83.909
85.036
84.923
1.083.950
1.104.892
1.140.992
152.055
154.267
•126.037
121.434
123.564
•118.746
374.846
188.812
384.098
17,283
17.283
1 7 .283
I
186
190
189
35
52
46
"
--
225
248
299
35
35
35
30
31
32
8
B
4
9
9
34
48
49
49
11
11
11
n
Le«1 C
632.693
702.569
651.717
215.083
322,625
286.060
96.212
139,694
132.142
1.847.859
1 .999,002
1.976,913
282.672
310.939
375,954
121.689
123.741
123.536
2,586,279
2.690,078
2,732.903
276.819
284.368
•232.442
191,175
194.504
•167,207
461,192
482.787
456,403
26.275
28.139
28.139
ETtTTSr
216
240
223
41
62
55
29
43
40
146
345
341
266
293
354
50
51
51
72
75
76
14
15
57
14
14
48
59
61
58
17
18
18
Uvel 8
843.502
1 .067.258
898.484
248,173
372.259
300.070
~
E
326,160
358.776
433.792
136.845
139.921
139.653
4.840.374
5.326. 286
5.315,501
322.347
351.174
•258.518
380.581
409.655
•213,120
459.778
536 .855
486.169
28.584
33.239
33,239
288
364
307
47
71
63
--
--
307
338
408
56
58
57
135
149
149
17
18
64
28
X
61
58
72
62
18
21
21
L«v«l
1.132.788
1.406.375
1.203.433
281 .262
421 ,893
374.078
— +
E
369.648
406.613
491 .632
151.865
160.677
157.851
S. 632. 91 3
6.440.973
6.185.373
341.186
374,881
•281 ,424
432,941
467,512
•258.411
490,210
598,652
S13.582
31,094
39,908
39,908
A
387
480
411
54
81
71
~
--
348
383
463
47
66
65
157
180
17)
18
19
70
32
J4
74
62
76
65
20
25
25
Base Construction
292.636
300.156
299.069
523.763
654,704
591 ,852
326.905
346,818
382,466
579,239
608.201
637.163
106,293
116.922
12O.111
243.044
253,927
251 .044
3.578.0)4
3,805,192
4,145.229
1.946.303
1.9S6.7S9
407,841
1.364,876
1.379.281
•349,836
787,426
820.592
814.315
159.005
161.915
161.915
100
102
102
100
12S
113
100
106
117
109
105
110
100
110
11)
100
104
101
100
IOC
116
100
101
101
100
101
101
100
104
10)
100
192
101
' Partial costs excluding unit opcritlo
* Mot 4v«lUbte since this Scenario Z •
considered Infe«itb1» «t lower tc*>p«r«turt
• only «wltc«bU to («rwJ priced *t) Level C.
Note: Pvrctnttgef provided «r* reUtlw to bit* construction costs for 0-18"C temperature r*no4-
380
COST
-------
Table 8
Average Percent Cost Variations due to Temperature
Tenperature Ranqes
°C 'F
0-18° 32-65°
18-38° 65-100°
<0° <32°
Base
Construction
100
106
107
Level
Health 1
Safety
65
70
78
D
Total*
165
176
185
Level
Health 1
Safety
84
111
120
C
Total*
1B4
217
227
Lev
health 1
Safety
106
125
132
el B
Total*
206
255
239
Level A
Health 1
Safety
125
149
157
Total*
225
255
264
• Totll • Health I Safety Costi Plus Base Construction Costs.
Table 9
Ranges of Transportation Costs by Type of Transporter
Type of Transporter
Rates
($/km)
Treatment, Storage, and Disposal Facilities
Providing Service to Customers
General Freight Transportation Companies
Which May Haul Hazardous Wastes on Request
Hazardous Waste Transportation Companies
Specializing in Hazardous Wastes
$0.75-$2.57
$0.75-$3.73
$1.99-$2.60
•Range based on 320 to 1,609 km (200 to 1,000 miles) distance for one-way shipment at $3/220.5
kg (100 IDS).
Table 10
Rate Schedules for Various Distances and Geographic Locations
Distance
(km)
370
560
740
1,110
1,480
1,850
2*,630
East of the
Mississippi
$1.62
1.34
1.16
0.96
0.86
0.81 +
0.81
Destination Rates*
One-Way
West of the
Mississippi
$1.78
1.51
1.34
1.15
1.05
1.00
0.90+
Round
Trip
$1.27
1.01
0.86
0.74+
0.74
0.74
,0.24
*Rates quoted in dollars per km.
+ Minimum rate-remains constant for all distances above that shown.
in the Commercial Hazardous Waste Management Industry: 1981
Update", SW-894-1. As indicated in the table, the data were based
on interviews conducted in May 1980 and Feb. 1982. The assump-
tions made to convert estimates to $/wet metric tons (WMT), when
conversion factor estimates were not available, were reported to be:
•Volumes in gallons were converted to WMT assuming the waste
density was that of water (i.e., 8.34 Ib/gal or 0.0037 WMT/gal)
•Cubic yards were converted to WMT on the assumption of den-
sity equal to water at 62.4 lb/ft3 or 0.76 WMT/yd'
•Volumes disposed of in landfills were assumed to be bulk ma-
terials unless drum and bulk distribution was stated
•Capacity reported in acres was converted to WMT by assuming
available capacity of 430,000 ftVacre or a disposal capacity of
12,100WMT/acre
CONCLUSIONS
Cost-effectiveness evaluations of Superfund expenditures require
consideration of additional costs of protecting workers' health and
safety. Unfortunately, not much cost data have been available con-
cerning health and safety considerations. This study represents part
of the effort to identify and estimate costs associated with protec-
tion of worker health and safety. Although the findings and results
of this project cannot be considered the final answer, they will en-
able site management and planning personnel to generalize health
and safety cost impacts.
Several factors which impact cost were identified but not
addressed within the scope of this project. These include:
•Scale Economies
•Regional Differences
•Management Policies and Procedures
•Type and Size of Company
Previous studies have shown scale economies and regional var-
iations to be significant in construction costs. It would be reason-
able to assume similar impacts on health and safety costs. How-
ever, it was not possible to quantify the impact of these factors
based on the existing data.
During the course of this project, differences in the management
procedures and policies were identified which impacted the cost es-
timates provided. Currently, there are no regulatory standards
which are uniformly enforced on hazardous waste sites. There-
fore, the impact of safety management policies and procedures of
individual contractors can significantly impact health and safety
costs. In addition, the emphasis placed by a given contractor on the
use of equipment versus manpower to accomplish the tasks re-
quired can also impact the health and safety costs due to the differ-
ences in the exposure potential for workers operating machinery
versus workers directly handling containers and/or contaminated
materials.
The type and size of companies involved will impact their abil-
ity to make most efficient use of equipment and personnel. Large
companies with deep resources and a backlog of work projects
can coordinate the use of equipment and personnel among projects
to be more cost-efficient. However, smaller companies or specialty
firms with smaller resources and fewer projects may incur higher
costs in order to maintain a qualified staff and cover overhead ex-
penses of idle equipment. Use of the data from this report should
include evaluation of possible impacts of these factors.
The primary result of this report is a means to adjust remedial
action cost estimates to reflect additional costs of health and safe-
ty considerations. This may involve adding these health and safety
costs to engineering study cost estimates based on standard con-
struction cost estimates or adjusting cost estimates from actual
sites. Adjustments made will reflect the costs associated with varia-
tions in the degree-of-hazard conditions on the site being evaluated.
Additional applications may include:
•Calculation of costs for various applications of unit operations.
For example, the cost of constructing a drain system for leach-
ate collection could be evaluated for on-site versus off-site loca-
tions. The added costs for increasing the intercept area off-site
could be compared with the added costs of worker safety and
health considerations for a smaller system installed in the contam-
inated areas on-site.
•Planning of site assessment activities prior to initiation of remed-
ial action activities. The worst degree-of-hazard condition which
COST
381
-------
Table 11
Comparison of Hazardous Waste Management Quoted Prices for all Firms in 1980 and for Nine Major Firms in 1981*
Price
Type of Waste
Landfill
Management Type or Form of Waste
Drum
Bulk
1980
$25-$35 $/55 gal drum
$40-$50/ton
1981
$35-$50/55 gal drum
$50-$75/ton
^/Metric Ton
1980
$120-$168
$44-$55
1961
$168-$240
$55-$83
Land Treatment
All
$0.02-$0.09/gal
$0.02-$0.09/gal
$5-$24
$5-$24
Incineration
Chemical Treatment
Resource Recovery
Deep Well Injection
Transportation
Relatively clean liquids, high
Btu value
Liquids
Solids, heavily toxic liquids
Acids/Alkalines
Cyanides, heavy metals, highly
toxic wastes
All
Oily wastewaters
Toxic rinse waters
$0.20-$0.90/gal
$0.20-$0.90/gal
$1.25-$2.50/gal
$0.06-$0.30/gal
$0.20-$2.00/gal
$0.19-$0.80/gal
$0.06-$0.15/gal
S0.50-$1.00/gal
$(0.05) -$0.20/gal
$0.20-$0.90/gal '
$1.50-$3.00/gal
$0.08-$0.35/gal
$0.25-$3.00/gal
$0.25-$1.00/gal
$0.06-$0.15/gal
$0.50-$1.00/gal
$0.15/ton mile
$53-$237
$53-$237
$330-$660
$16-$79
$53-$528
$50-$211
$16-$40
$132-$264
$(13)*-$53
$53-$237
$395-$791
$21 -$92
$66-1791
$66-$264
$16-$40
$132-$264
•Interviews were conducted in May of 1980 and Feb. of 1982.
-I- Some cement kilns and light aggregate manufacturers are now paying for wastes.
SOURCE: U.S. Environmental Protection Agency. "Review of Activities of Major Firms in the Commercial Hazardous Waste Management Industry: 1981 Update". SW-894.1. May 1982.
is anticipated, based on available information, would determine
the cost of worker health and safety protection which would be
provided. The potential savings of reduced health and safety costs
for less hazardous conditions could be calculated. The cost-
effectiveness evaluation of conducting more detailed site char-
acterization and waste stream identifications to define degree-
of-hazard conditions could then include consideration of potential
savings if conducted prior to initiation of remedial actions.
ACKNOWLEDGEMENTS
The project discussed in this paper was performed under USEPA
Contract No. 68-03-3028, Directive of Work No. 14. The authors
would like to thank the USEPA Project Monitors, D. Ammon
and D. Sanning of the USEPA Municipal Environmental Research
Laboratory, Solid and Hazardous Waste Research Division in
Cincinnati, Ohio.
DISCLAIMER
The information and data presented in this paper do not neces-
sarily reflect the views and policy of the USEPA. This paper was
based on the Draft Final Report—Costs of Remedial Actions at
Uncontrolled Hazardous Waste Sites— Worker Health and Safety
Considerations which is currently in the USEPA peer review
process.
REFERENCES
1. "Review of Activities of Major Firms Involved in the Commercial
Hazardous Waste Management Industry: 1981 Update," SW-894.1,
USEPA, Washington, D.C., May 1982.
2. "Interim Standard Operating Safety Guides", USEPA Office of Emer-
gency and Remedial Response, Hazardous Response Support Division,
Edison, N.J., Sept. 1982.
3. "Remedial Actions at Hazardous Waste Sites: Survey and Case Stud-
ies," EPA 430/9-81-05 SW-910. Oil and Special Materials Control
Division, USEPA, Washington, D.C. Jan. 1981.
382
COST
-------
PUBLIC AWARENESS PROGRAMS
GEORGE M. FELL
Chem-Technics Inc.
Rolling Meadows, Illinois
INTRODUCTION
Public awareness of waste disposal grows daily as issues and con-
tinuing revelations unfold across the country adding emphasis and
credence to continue the public "hue and cry." The public's senti-
ments were captured by Shakespeare in King John: "Oppressed
with wrongs and therefore full of fears." For despite new and far-
reaching legislation, including public participation, many Amer-
icans perceive that the risks to their health and safety are still too
great.
What those who would and do operate under the new guidelines
have found is a polarized public who will, under no circumstance,
tolerate waste disposal activities in or adjacent to their community.
Those charged with implementing the new standards are now call-
ing for public education programs. In a confrontational atmos-
phere in which industry, legislators and regulatory agencies have
lost the credibility and the confidence of the public, can one be
so presumptuous as to imply that it is the public who must be edu-
cated? What is needed and sought by the public is the opportun-
ity to discuss the issues as equals. A surgeon will approach his
patient with respect for human nature, expertise notwithstanding.
To be on the receiving end of subjective logic is not conducive to
allaying one's fears.
Consider the average citizen's position. The new regulations
have not eased the financial burden if one feels that he has been
exposed to or impaired by a waste disposal activity. Certainly the
grounds for restitution are more clearly defined. However, legal
fees, expert witnesses and medical expenses are costly and time-
consuming even if the citizen is fortunate enough to find a law
firm that will take the case on a contingency basis and if there is a
medical policy in effect that provides maximum benefits. Is it any
wonder, then, that, upon learning that a company intends to con-
struct a waste disposal facility, a community bans together to stop
its development and urges that it be put "somewhere else."
As many of you know, "somewhere else" meets with the same
reception. Equally, current facilities will soon compound the crisis
by reaching capacity. Knowing that, it is doubly important to in-
stitute frank and open discussions with the public as equals. The
name given to such programs is immaterial. It is essential that these
programs be implemented, even if initially unsuccessful, for they
can create a cadre of people from all walks of life and divergent
views who, through their own scrutiny, will agree that waste dis-
posal as an industrial activity can be conducted safely and with-
out stigma to the host community or its citizens. Such a group,
C.A.R.E.S.—Committee for the Advancement of Responsible En-
vironmental Solutions, has emerged in Illinois. They reflect what is
intrinsic in American society. Indeed, Thomas Jefferson must
have had such people and problems as the nation now faces in
mind when he stated: "I know of no safe depository of the ulti-
mate forms of society but the people themselves; and if we think
them not enlightened enough to exercise their control with a whole-
some discretion, the remedy is not to take it from them, but to
inform their discretion." So, it is with these thoughts in mind, that
the following remarks are offered.
PUBLIC RELATIONS PROGRAM
Developing a compatible relationship between a company pro-
posing to locate a waste facility, the elected officials of the host
community and its citizens requires sensitivity, skill, timing and
respect. All parties must acknowledge that a company seeking to
locate a facility has a vast number of basic business and logistical
evaluations to undertake: road network, utilities, rate structure,
land costs, applicability to the market to be served and regulatory
environmental needs. Factors such as these are normally conducted
within the confines of the company, not in the public forum, since
there may be a whole series of commercial reasons for rejecting a
potential location.
However, once a location has been chosen, it is critical that
everyone in the community has access to the same information
simultaneously. Informational material must be in plain language
with an introduction that provides an explanation for choosing
that location, the background work that has already been com-
pleted, any discussions that have taken place and who was party
to those discussions. This is a key factor in assuring the public
that there have been no clandestine arrangements other than pro-
prietary activities up to this point in time.
Other information that should be provided includes the site loca-
tion, the type of facility that is proposed (including its operating
life), the types of materials to be handled and the industrial source
(geographic location: local, state or regional).
Additional information might include statutory review pro-
cedures, the time frame and how it will dictate construction and
operational start-up of the facility, the company's policy in either
staying within the mandatory time frame or staggering its applica-
tions to provide additional public discussion, the name of the per-
son within the company responsible for responding to the public in-
quiry and where that person can be reached.
The public also needs to have a history of the company and its
past experience or rationale for considering that it has or will ob-
tain the necessary experience in the activity proposed.
PUBLIC PARTICIPATION
383
-------
There should be a summary listing the various elected representa-
tives (Federal, State, County, Municipal) by name, address and
telephone number for citizen contact. Regulatory agencies from
which information may be secured, and names of individuals to
whom representations might be made should be listed. Local chap-
ters of national environmental organizations and other public
action groups where a citizen might get a different perspective
might also be included in the information. Conclude by listing
detailed or technical data that will become available as part of the
statutory application. All of the above information should be con-
tained in a handy reference-size brochure.
Perhaps the most difficult task is a simultaneous release of in-
formation without offending either side. Experience has suggested
that a mass mailing to every household in the host community
coinciding the delivery date with a press conference (radio, tele-
vision and print) with time set aside for reporters to conduct
followup interviews, is very effective. Thought should also be given
to regional media, as well, because of interest from communities
adjacent to the host community.
Presentations to local and county officials should be followed by
more extensive written material and technical data for their pro-
fessional staffs. This should include adjacent communities with
special emphasis on the facets that are of particular importance
such as transportation routes and emergency response plans in the
event of an accident. It is particularly important to recognize
that elected officials and their staff will bear the brunt of citizen
complaints and requests for information, and every effort must be
made to insure that they have access to information generated by
independent sources. If information is derived solely from the
company, it is suspect.
It is vitally important to maintain candor with the media, to keep
them apprised of questions that are being raised and the com-
pany's response and its rationale for the response. Above all,
presentations and meetings with community residents must be
conducted in a non-threatening atmosphere and in surroundings
that are conducive to discussion such as private homes, schools or
church halls.
A company must recognize that the issues they will have to face
are not all centered upon environmental regulations. Questions
will arise on such matters as Federal and State highway and vehicle
construction. Indeed, the very fundamentals of engineering and
construction will be called into question.
Risk Assessment
Perhaps the most difficult areas of questioning will focus on the
highly specialized fields of epidemiology, toxicology and risk
assessment. The latter, quite frankly, places a value on human life
and welfare. When an individual is confronted with that knowl-
edge, insuring peace of mind becomes much more difficult. Point-
ing out that an individual is already covered by actuary tables on
just about every insurance or medical policy issued to him is not
much comfort either. It is a chilling thought to consider one's own
mortality: everyone else is mortal except one's self. How is it
possible to weigh possibility against probability when one's chil-
dren are at stake? As companies such as the Ford Motor Com-
pany with its Pinto problem or the Johns-Manville reorganiza-
tion under Chapter Eleven on the asbestos-related claims have
found, risk assessment and cost benefit analysis take their toll, not
only in financial terms, but also in their public images. One must
ponder which of the existing disposal companies could not find
themselves in a similar situation.
The cornerstone for developing a relationship with the host com-
munity is the intent to the company. For better or worse, the pub-
lic will judge the company on its past performance. And while no
company brandishes a stainless record, past practices must be
acknowledged. Public confidence will depend, too, on the reliabil-
ity and sincerity of the company spokesperson, who should be
senior or executive-level management. Continuity of the spokes-
person and assured public access is essential to the credibility and
the intent of the company.
PUBLIC PARTICIPATION
Public participation in hazardous waste issues, more than in
any other, is one in which a citizen must collaborate with his
neighbor. Many in industry, regulatory agencies and the media see
the public as the protagonist, and in many community-oriented
groups this has been true. However, this role has been forced upon
the public because it has had to deal with the aftermath of un-
scrupulous practices rather than acting as a full participant. An
informed citizen, given all the facts, scientific or otherwise, can
be a vitally important participant.
The importance of this lies in the urgency of the current situa-
tion: landfills are rapidly filling up, and implementing alternative
technology takes time. How can the public be expected to partic-
ipate in an evenhanded and expeditous manner when it is con-
stantly bombarded with revelations resulting in lengthy investi-
gation, litigation and resolution by the judiciary? Taxpayers and
consumers know this is costly. How, then, can the public have faith
in the system that put it at risk in the first place?
Benjamin Franklin had some excellent advice about this: "In the
affairs of this world people are saved not by faith, but the want of
it."
Waste disposal is an issue that can divide families, friends and
community leaders; it is an issue that one cannot and should not
ignore. One cannot accept another's perfunctory position.
What should be the public's level of participation? If a waste
disposal facility is proposed for a community, its residents should
know that under recent Federal, State and local regulations a facil-
ity would not be approved if it did not technically meet or exceed
the standards established for its construction, operation and clos-
ing at the end of its useful life. However, these reviews are under-
taken between experts, and the public is aware that people do make
mistakes. So what if there is a fire or a truck turns over and spills
it contents? Accidents do happen. Will poisonous fumes or liquids
escape into the air and water? How do the experts know that they
will not? Whom would one contact with a complaint? If residents
are affected, who pays and how quickly? What about property
values during operation and, particularly, after the facility is
closed? These are just a sample of questions that spring to mind
when one learns of a proposal to site a facility in the community.
Finally, one cannot forget the stigma of "Garbage City U.S.A."
in playing host to "state-of-the-art" technology. Is it that, or just
a variation on the shell game—now you see it, later you may have
to eat or drink it! These are questions to which one can and should
solicit answers, assurances and explanations.
Information
A request for information from a company usually results in
presentation of an enormous amount of written material contain-
ing expert testimony with terms and expressions akin to a new
language. How does one phrase and pose questions without
appearing foolish? When attending a public meeting and being
faced with opposing factions who are hostile, how does one raise
concerns without becoming the target of community fury and
scorn?
Collect information made available by the company, local,
County and State officials; watch for articles in the local and
regional newspaper, on radio and on television. Use them to ans-
wer questions—they are "only a phone call away." This is an ex-
cellent way of getting citizens' views heard, and the professional
staffs of these organizations, particularly the media, are skilled in
sifting through comments and determining the core of the ques-
tions.
Be particularly careful of petitions and telephone canvassing
unless there is an opportunity to study the questions and ask for
clarification. Stock or carefully-worded phrases do not always re-
384
PUBLlt PARTICIPATION
-------
flect^ or address the concerns one may have, and they are often
used to reflect an opinion that is not held by the popular majority.
Sometimes a response to a question is covered by certain regula-
tions such as the control of liquids and fumes escaping from the
facility. Request a copy of the regulation or a plain language ex-
planation of it. If a plain language document is provided, there
will be a disclaimer such as, "This document does not include com-
plete or verbatim quotations from Federal, State or local regula-
tions or hearings. References made to them are to summarize
pertinent aspects for general information only, etc., etc." This is
not a company or agency trying to dodge issues at the public's
expense but is rather a liability requirement to protect the research-
er who produced the material, which is, after all, an interpreta-
tion and not the actual document. The important factor is that one
then has the knowledge of the applicable regulation and the in-
formation from which to form an opinion.
Quite often a regulation calls for specific equipment to be used.
Ask where it is currently in use and, if it is at a local company,
ascertain what their experience has been from friends or asso-
ciates who may work there. In this manner it is possible to gain
firsthand knowledge from a known and trusted source. Without
doubt, collaboration with one's neighbors will open up a whole
area of practical experience, since many of the principles that will
be employed at a waste disposal facility have their roots in estab-
lished manufacturing, construction and engineering tenets.
Insurance
Ask about insurance and what level of coverage is provided.
Next to government regulations and statute, an insurance company
can be the best protector of health and welfare. They always
attempt to minimize their risks and, in addition to the experts they
have on staff, they have access to information on a whole range of
actual documented experience in equipment, chemical compatabil-
ity and health safety. Inquire if an insurance representative will
attend a neighborhood meeting. They like to chat and they are a
friendly bunch! Find out how the community can be kept advised
if there is a change either in the policy or the insurance company.
Everyone knows, for example, that a bad driving record will result
in a loss of policy or, at best, lower coverage and higher premiums.
These considerations are often overlooked by citizens who should
be aware that an insurance company's critique and ongoing review
is every bit as rigorous as a regulatory agency's.
PAST PROBLEMS
There have been a number of tragic chapters written about the
inadequacy of the waste disposal industry, and the remainder of
the story has yet to be written. However, many facets, including
citizen awareness and new and more stringent regulations, will pro-
hibit these issues from arising again. To insure that they do not,
requires citizen participation in discussions with regulatory person-
nel, elected officials and the companies that will operate the facil-
ities. These discussions should be frank and non-hostile, for noth-
ing can be gained if fear and anger prevail. Father a few neighbors
together in a home, club or church hall, and invite a company
representative to talk with community residents—not at them or
above them. In this manner they will come to know a person, not
an entity that is lost behind a corporate or agency image that has
no form or substance other than in legal terms. It is the public's
trust and understanding that is sought, ana the public must grant
it, albeit carefully, if waste disposal is to be accomplished as it
must. For despite the notoriety the waste disposal industry has
gained, citizens do have a contribution to make in reviewing pro-
posals: it would be unfortunate if the only contribution is through
enmity, perfidy and cynicism.
CONCLUSIONS
To summarize, public awareness and participation is long over-
due in the area of waste disposal. It is a public health service that
has as vital an impact upon society as the medical profession and
the food and pharmaceutical industries. They come from similar
beginnings to reach the prominence they enjoy today, because the
public accepts their high standards as a fundamental requirement.
This was not achieved by simply implementing more stringent legis-
lation, but by the practitioners in their fields striving for stand-
ards greater than the minimum required by law. Such internal self-
discipline has brought its own rewards of public confidence and
trust. When there has been a breach in these standards, it has been
recognized by the public for what it was, an isolated incident that
was not necessarily a breach of credibility in an entire profession
or industry.
Likewise, all those associated with waste disposal activities
must try to provide more information, better access to decision-
makers and greater time so that the public believes that it has had
an opportunity to weigh the alternatives. As workers, shareholders,
consumers or taxpayers, they will ultimately pay the bill. A pru-
dent person, from whatever point of interest or involvement, must
admit that ideas and knowledge improve with sharing.
It would appear that the only arbiter acceptable to all parties
at this time is the judiciary who render decisions on the spirit or
intent as well as on the letter of the law. A program of awareness or
participation that addresses the issues in substance will have cred-
ibility in their decision-making. This will then earn the respect of
the majority of the public. However, this is not a long term solu-
tion: in fact, it is one of last resort, for it will still pit the clear-
eyed objectivity and logic of the expert against the ordinary person
feeling ill at ease and threatened because he does not know how
best to prepare for his own or his children's future.
Perhaps the most fitting closing is to quote E.F. Schumacher's
SMALL IS BEA UTIFUL: Economics As If People Mattered:
"Out of the whole Christian tradition, there is perhaps no body
of teaching which is more relevant and appropriate to the modern
predicament than the marvelously subtle and realistic doctrines of
the Four Cardinal Virtues—prudentia, justitia, fortitude, and
temperantia."
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INSTITUTIONAL CHALLENGES OF THE SUPERFUND
COMMUNITY RELATIONS PROGRAM
ANTHONY M. DIECIDUE
DAPHNE GEMMILL
U.S. Environmental Protection Agency
Washington, D.C.
EDWIN BERK
ICF Incorporated
Washington, D.C.
INTRODUCTION
With nearly three years experience in implementing the Super-
fund program, response to hazardous waste site problems contin-
ues to be one of America's most emotionally sensitive public issues.
Within the past year alone, several major controversies surround-
ing sites across the nation have intensified the frustration citizens
are expressing about these problems.
The USEPA, having the primary responsibility for administer-
ing the Superfund program, has established a community rela-
tions program that, under its policy, recognizes and requires cit-
izen involvement as an integral part of every Superfund-fmanced
action. Although USEPA established the final policy and guide-
lines for conducting community relations programs on May 9,
1983, institutional challenges remain to be overcome if these pro-
grams are to be successful.
In this paper, the authors discuss the evolution USEPA's Super-
fund Community Relations Policy has undergone while the Agency
has attempted to educate citizens about hazardous waste site prob-
lems they are facing and to involve them during response actions
to correct these problems. The authors also discuss institutional
challenges that have arisen in the past three years, as well as ones
likely to be encountered in the future. These challenges will need to
be overcome if technical solutions to hazardous waste site problems
are to be successful and supported by the public.
HAS THE SUPERFUND COMMUNITY
RELATIONS POLICY CHANGED?
In Nov. 1981, the newly formed Office of Emergency and
Remedial Response issued a Superfund community relations pol-
icy and guidance document whose purpose was to provide guide-
lines for implementing community relations programs for Super-
fund-financed remedial actions and removal actions lasting longer
than a few days. The document provided USEPA's regional offices
with the necessary flexibility to conduct community relations pro-
grams tailored to each specific Superfund site. The only require-
ment was for the preparation of a community relations plan. These
plans are to enable community relations activities to be integrated
into the technical responses at Superfund sites to ensure that the
community has a voice in these actions.
In Mar. 1982 and May 1983, additional refinements to the policy
were issued. The basic intent of the 1981 policy, however, is as rele-
vant today as it was when first issued.
Program Objectives
Each Superfund community relations program is directed toward
the following objectives:
•To gather information about the community in which a site or
incident is located. A community relations program provides a
vehicle for exchanges between USEPA, the state, the public, and
local government. It enables USEPA and state staff to identify cit-
izen leaders, public concerns and a site's social and political his-
tory. Sometimes it can also yield technical data useful in plan-
ning a solution to the site's problem—or information useful in an
enforcement case against a responsible party.
•To inform the public of planned or ongoing actions. The pro-
gram should inform the public of the nature of the environmental
problem, the remedies under consideration and the progress al-
ready made.
•To give the public the opportunity to comment on and provide
input to technical site decisions. The program should enable cit-
izens to understand and comment on decisions that will have long-
term effects on their community. Any course of action stands a
greater chance of public acceptance if citizens have been involved
in its planning.
•To focus and resolve controversy. Conflict has been unavoidable
in some circumstances, but it can be constructive if it brings into
the open alternative viewpoints based upon solid reasons for crit-
icism or dissent. An effective community relations program chan-
nels conflict into a forum where it can serve a useful purpose.
When such opposition has already arisen, a concerted attempt to
communicate with and involve all parties can help reduce tension.
The program, therefore, continues to encourage two-way com-
munication between communities and government.
In meeting these objectives, five general principles must be
stressed.
•The community relations effort at a particular site must be tail-
ored to the distinctive and individual characteristics of the site and
surrounding community.
•The design of a community relations program for a site should
take into account both the technical complexity of the problem
and the level of citizen concern. A more intensive program is re-
quired for situations that are either technically complicated or
have generated a high level of citizen concern.
•Open and honest community relations planning is essential to an
effective Superfund response. The key to proper planning is 8
thorough knowledge of a particular community's concerns at a
site and the schedule for technical action.
•In most cases, small-scale, informal communication techniques
should be used rather than large scale, formal techniques (such
as public hearings).
•Finally, adequate opportunity must be given for the public to
comment on proposed remedial cleanup actions prior to final
USEPA decision-making.
386
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Program Implementation
As noted above, the only firm requirement for a site com-
munity relations program is the preparation of a plan in advance of
initiating site activities. A community relations plan is really a
management tool which outlines the specific communications activ-
ities to be used during a Superfund response and how these activ-
ities will be integrated with the technical work to be performed.
The plan must include an assessment of community interests and
concerns. These assessments are based on discussions with local
officials, civic leaders and residents living in the vicinity of the site.
The assessments enable those responsible for conducting the
response action to gauge concerns and determine the level of com-
munity interaction necessary during the response. Each plan must
contain the following elements:
•A background and history of community involvement at the site,
which in most cases can be extracted from the assessment
•The specific objectives of the community relations program for
each particular site being addressed
•The community relations techniques to be used to meet these
specific objectives, including periodic progress reports on site
work being performed and reports on upcoming activities
•A workplan and schedule
•A budget and staffing plan
•A list of names and addresses of affected and interested groups
and individuals, USEPA, other federal and state technical and
community relations officials
An important aspect of these plans is that they are evolving
documents, revised at each stage of the process—from the remedial
investigation and feasibility study through design and construction
of the solution. At the conclusion of each stage (e.g., after a
feasibility study and after a construction) a responsiveness sum-
mary is prepared. This summary includes a list of the community
relations activities conducted, an account of the issues that arose
and an explanation of how citizen concerns were dealt with during
the response.
Administering the Community Relations Program
USEPA headquarters will continue to be responsible for na-
tional management of the program including policy development,
review of community relations plans and overall monitoring and
evaluation. Headquarters also continues to provide informational
materials on Superfund and overall management of contractors
providing support to site-specific response actions. A permanent
community relations staff has also been established at headquart-
ers, enabling the program to provide the needed supervision to
make community relations in Superfund a success.
The USEPA regional offices continue to be responsible for
development, implementation and revision of community relations
plans (in conformance with the policy) during federal lead response
actions. The regions also continue to supervise contractors provid-
ing community relations support as well as coordinating their activ-
ities with states.
The states continue to be responsible for development, imple-
mentation and revision of community relations plans (also in con-
formance with this policy) when they have the lead during response
actions. They are also responsible for hiring their own support
contractors, if necessary, and for coordinating their activities with
the Region.
Community Relations Policy Additions
In May 1983, two new elements were introduced to the com-
munity relations program. With three years of experience imple-
menting community relations programs at Superfund sites, the
Office of Emergency and Remedial Response recognized the need
to stress community relations during emergency actions. Until
recently, press and community briefings, informational meetings
and on-site information offices—in other words, one-way com-
munication—had been the recommended techniques. A short com-
munity relations plan (or profile) must now be prepared. This re-
quirement is intended to ensure that two-way communication is
now carried out during emergency actions lasting longer than a
few days.
The major addition to the policy, however, is the requirement
that the public be given a three week comment period to review
feasibility studies prior to selection of a site remedy. This require-
ment, together with other community relations activities, enables
the Superfund community relations program requirements to be
functionally equivalent to National Environmental Policy Act
(NEPA) public participation requirements.
Emphasis on Community Discussions
While the initial policy suggested the use of interviews as a basis
for establishing communication with citizens and developing com-
munity relations plans, this technique was not emphasized. The
purpose of these interviews with citizens and local officials is to
accurately identify local concerns and major issues. These dis-
cussions provide USEPA regional staff with valuable background
information necessary to fully understand the site history from the
community's perspective, to identify citizens, officials and organ-
ized groups expressing concern and to evaluate the level and nature
of these concerns.
It has become increasingly clear to those individuals conduct-
ing community relations programs that this information is indis-
pensible in preparing community relations plans. Information de-
rived from these discussions is also proving to be a required pre-
requisite to successful community relations efforts at sites. There-
fore, as of May 1983, local discussions have become the founda-
tion for community relations planning at each site.
HOW IS USEPA ENSURING THAT
THE POLICY IS CARRIED OUT?
USEPA's Superfund community relations policy is a head-
quarters office product. Programs are implemented, however, by
the regional offices or by state governments when they have the
lead in a response action.
Requirements for implementing the program, as noted, have
been kept to a minimum. This enables regional offices and states
to tailor their efforts to the distinctive characteristics of the site
and surrounding community, while remaining free from too many
bureaucratic requirements. In consequence, however, headquarters
staff have found it difficult to keep track of whether commun-
ity relations programs were being developed for Superfund
responses and, even if so, whether any of the activities planned
were being conducted. Furthermore, a headquarters review team's
visit of regional offices over the past year, although confirming the
soundness of a flexible approach, found that the commitment to
the program differed from region to region.
Additional Procedures
In response to this problem, the policy changes outlined above
have been implemented and new procedures have been devel-
oped to permit better program oversight and accountability at
headquarters. Some of the major improvements include:
•Formal procedures have been outlined detailing the specific
responsibilities and timetables for meeting internal community
relations requirements. These procedures give headquarters, reg-
ions and states for the first time a specific understanding of how
the community relations process must take place.
•USEPA headquarters has also developed a tracking system for
community relations activities at sites. This system provides com-
munity relations staff and management with site specific informa-
tion about whether or not planned activities have occurred and
when events are scheduled, including changes or modifications
when conditions warrant.
•An interim final version of the community relations handbook—
Community Relations in Superfund—A Handbook—is also now
available. This handbook supplements the policy and incorpor-
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ates the program's background material and detailed procedural
guidance into one complete document.
These management and procedural changes should also strength-
en coordination between USEPA headquarters, regional Super-
fund offices and state offices. The desired result should be a well
defined and administered system of community relations that re-
flects the Agency's commitment to the program.
WHAT INSTITUTIONAL CHALLENGES REMAIN?
The Superfund program has witnessed a steady growth in iden-
tifying sites that appear to present a significant risk to public
health and the environment. USEPA's National Priorities List
(NPL) has grown from 115 sites in Oct. 1981, to a total of 546 sites,
final and proposed, in Sept. 1983. The environmental commun-
ity, meanwhile, has begun to organize. Various environmental
groups are conducting regional meetings on community organ-
izing. The Environmental Defense Fund (EDF) has even issued a
handbook, Dumpsite Cleanup: A Citizen Guide to Superfund.
An aware public can only mean an increase in the amount of com-
munity interaction for the Agency in the next few years. Several
barriers to an effective community relations program must still be
overcome.
Better Understanding Still Required
USEPA's efforts at identifying uncontrolled hazardous waste
site problems do not necessarily correlate to its ability to respond
quickly to the problem. Furthermore, inclusion of a site on the
NPL does not mean that USEPA will undertake a response ac-
tion, nor does it establish timetables for response. Public educa-
tion on the complexities of the problem and the various avenues
of response to be considered will help prevent the development
of unrealistic public expectations for the program. Areas where
further public understanding is most pressingly needed are as
follows:
•Why listing of a site on the NPL does not bring immediate clean-
up. The public needs to understand that initial listing of a site on
the NPL is intended only to guide USEPA in determining which
sites warrant further investigation and to help set priorities for
possible funding. Information collected to qualify sites for the
priorities list is not sufficient to determine the appropriate rem-
edy for a particular site.
•Why additional studies are required to select an appropriate
remedy. The public must understand that after a site has been in-
cluded on the NPL, USEPA will conduct further, more detailed
studies. USEPA relies on these studies to determine what re-
sponse, if any, is appropriate. Public understanding is also essen-
tial on how decisions on the type and extent of remedial action
are made, especially as they relate to cost-effectiveness, fund-
balancing and other statutory and regulatory requirements.
•Why various response and enforcement actions are considered.
Given the limited resources available in the Hazardous Substance
Response Trust Fund, USEPA must carefully decide between two
avenues on a site-by-site basis: whether to take enforcement ac-
tion or to proveed directly with Fund-financed cleanup and seek
recovery of response costs afterward. The public needs to under-
stand how these determinations are made and the factors influ-
encing them.
Dedication of Resources
Most of the funds expended so far for sites on the NPL have
been for remedial investigations and feasibility studies. Sites with
these activities now underway will begin to enter the cleanup stages
in the near future. In the Superfund program, citizen involvement
peaks when long-term cleanup proposals are announced. The ac-
tual cleanup actions selected are frequently the source of actual or
perceived significant personal inconveniences and potential im-
pacts to nearby residences.
USEPA and state staff responsible for carrying out commun-
ity relations programs must be aware of and be ready for an in-
tensification of their efforts. This will continue to be a critical and
challenging task as more and more sites begin to receive funding.
USEPA's Regional office and state resources—already overly taxed
in some cases—may be insufficient to meet an increase in the
demands upon community relations programs. To counter these re-
source limitations, contractor support will be required. Additional
USEPA and state staff may also be required.
Interagency Involvement
As the Superfund program gains maturity and experience, addi-
tional government agencies—the Army Corps of Engineers, the
Federal Emergency Management Agency, the Department of
Health and Human Services—will have increased roles and respon-
sibilities. This division of responsibilities, although a partnership,
will make it difficult to ensure that the government "speaks with
one voice". USEPA will need to work closely with these agencies
in order to maintain coordination and consistency toward their
individual technical and community relations efforts. If these
agencies are perceived as being uncoordinated and conflicting, it is
only natural that citizens will question their ability to solve site
problems.
CONCLUSIONS
It has been an unfortunate history of the Superfund program
that controversial issues surrounding sites have received the major
public, political and media attention. There is no doubt that the
program will live out most of its life in a "fishbowl."
Community relations programs taking place now and in the
future will need to keep communities well informed and provide
some local role in decision-making. The results should be to pre-
vent misunderstandings, unrealistic expectations and needless frus-
trations. In turn, there should be greater local acceptance of re-
sponse actions that are intended to protect the health of citizens in
the community, their welfare and their environment.
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HOW ONSITE ASSESSMENTS CAN HELP ACHIEVE
SUCCESSFUL SITE CLEANUP
NANCY R. TUOR
NANCY J. JERRICK
CH2M Hill
Portland, Oregon
INTRODUCTION
The cleanup of hazardous work sites can be highly controversial.
The reasons for this may not be readily apparent, because no one is
really for hazardous waste. However, some points of controversy
are readily apparent. What is an unacceptable hazard to one per-
son, may be a livelihood to another. What seems to require im-
mediate action may take years, during which time the people who
are involved with the site may become increasingly frustrated and
angry.
Finally, there are those points of controversy and conflict that
may not be apparent at all until they are actively investigated—or
until it is too late. In this paper, the authors discuss the use of on-
site assessments or interviews in gaining a full understanding of the
participants and issues that may surround a hazardous waste site
and show why that understanding is important in arriving at prac-
ticable, cost-effective cleanup solutions.
THE NEED TO KNOW
The establishment of community relations programs for all
Superfund hazardous waste sites is a requirement based on two
fundamental premises. The first is that people who are affected by
the release of hazardous substances have a right to know the atten-
dant risks, the actions that are being taken and the possible solu-
tions to the problem. The second premise is that technical adequacy
alone does not ensure that a cleanup solution can be successfully
implemented. The involvement, understanding and cooperation of
the public affected is essential in arriving at acceptable solutions.
The American public has become increasingly knowledgeable
about both the technical and political aspects of hazardous waste
sites. Information is readily available to them from the media, from
technical experts and from environmental and public interest
groups. At the same time, the perception of governmental inaction
or obstruction has grown. As a result, people increasingly both
want and have the ability to know what is being done in situations
that directly affect them. They are becoming more actively in-
volved, and they are becoming less and less tolerate of apparent
unilateral decisions by governmental agencies.
Effective, two-way communication can help avoid the adver-
sarial positions that have sometimes arisen between the public and
responsible agencies. It can help establish a mutual sense of
credibility and responsibility, which is particularly important in
highly complex situations.
If public distrust exists, any governmental decision or solution is
likely to be viewed with suspicion. Technical information may be
disbelieved, and matters of judgment may be especially challenged
if the public has no confidence in the decision-makers. The ongoing
exchange of information does not guarantee that all parties will
agree at all times. However, it does offer a greater opportunity for
arriving at a mutually satisfactory resolution of the problem.
Listening to the public and responding appropriately is an
achievable alternative to the conflicts, legal actions and costly
delays that occur when people feel there is no other recourse.
THE USE OF ON-SITE ASSESSMENTS
In order to establish and maintain effective communication
among the various parties connected with a site, several com-
ponents of a community relations program must be determined:
•With whom to communicate
•How to communicate
•What concerns and issues need to be addressed
This information can be derived by conducting on-site
assessments: personal discussions with involved or potentially in-
volved parties and an evaluation of their concerns, perceptions and
information needs.
Personal contact can be very different from the more usual
"bureaucratic" contacts by letter or announcement. It allows two-
way communication and affords an opportunity to ask questions
and offer opinions. If the interviews are handled openly and with
sensitivity, they can create a sense of trust and can begin a dialogue
that will continue throughout the project. Personal interviews with
people who live in the area and who are familiar with its history and
nature can often reveal information that cannot be obtained other-
wise.
With Whom to Communicate
The parties likely to be concerned with a hazardous waste site
may include the following:*
•Neighbors
•Local and state agencies (utilities, natural resources, planning,
health departments, etc.)
•Local, state and Federal elected officials or staff (mayor, coun-
cil, county commissioners, state and Federal legislators)
•Local representatives of business, industry or labor (unions,
Chamber of Commerce, real estate groups)
•Local civic groups (League of Women Voters, church groups,
neighborhood associations)
•Environmental groups (Sierra Club, Izaak Walton League, re-
gional or state-wide groups)
•Based on draft Community Relations Handbook. Prepared for USEPA by ICF, 1983.
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•Ad hoc groups organized because of site issues
•Health organizations (American Cancer Society, Lung Associa-
tion)
•Media representatives
Some of these groups may already be known and can be contacted
for initial on-site interviews. However, others may not yet be iden-
tified and may be first discovered during the course of a site visit.
At a fairly controversial site in Michigan, the responsible agency
was aware of one community group that was well organized, vocal
and actively pursuing political and media contacts. From their con-
versations with people in the community, the interviewers became
aware that another faction in the community did not agree with this
viewpoint but had been reluctant to express opposition to the first
group. The interviewer was able to talk with representatives of this
group and to determine their concerns and needs. The community
relations program was, therefore, designed to reflect the needs of
both parties; this in turn could help avoid problems that would oc-
cur if all sides were not understood and addressed.
Site visits can also help identify targets of communication that
may not yet exist. Interviews may reveal that few people are con-
cerned or even aware of a problem. However, these discussions
may also indicate that people will be interested in a site if they learn
more about it or if it will affect them in the future.
One site in Arizona could potentially affect thousands of people
if investigations reveal further contamination. Although current in-
terest is limited, it could increase dramatically. An understanding
of the potentially affected community was important in designing a
community relations program that includes information dissemina-
tion to the general public and a means for the public to make in-
quiries and receive further information. This can prevent the
misunderstanding and distrust that arise when people learn too lit-
tle about the situation, too late.
How to Communicate
As these examples indicate, the methods by which information is
exchanged must be appropriate to the situation. Site assessments
can help identify the communications techniques that should be in-
corporated into a community relations program. This point is il-
lustrated by an assessment of a small community in Iowa where a
number of farmers live in the vicinity of leaking pesticide con-
tainers. The responsible agencies believed that community concern
was moderate and that active involvement was not likely to occur.
Interviews revealed otherwise.
Both the neighboring farmers and local officials expressed in-
tense concern. However, they felt they were viewed by governmen-
tal agencies as "ignorant farmers" and that their opinions and
needs were, therefore, not being heeded. They also believed that
their only recourse was through political pressure and were
prepared to take whatever action was necessary. While community
representatives were in contact with an agency staff member and
perceived him to be responsive and credible, they believed that
agency policy was to give them only partial information.
The discussions revealed that the amount and kind of informa-
tion being disseminated was not sufficient to meet these people's
needs. They desired a more extensive explanation of the technical
issues,the decisions that were being made and the circumstances
that were responsible for delays. Once these needs were deter-
mined, the agency was able to establish an information format and
schedule that was appropriate to this particular community.
The media is one of the most influential means of disseminating
information. Familiarity with the local media and with local
perceptions of the media is important. Agencies that were involved
with a site in Arizona were concerned that media coverage was in-
accurate and sensationalized. As a result, citizens were confused
and alarmed about possible health impacts. Because the media
would be the most effective means of educating the public, an
evaluation of its performance was essential. The community rela-
tions program in this case included distributing fact sheets and pro-
viding full information to the media to promote accurate, com-
prehensive coverage.
In a small community in the state of Washington, a local agency
has been involved with a site for several years. It has established a
credible, thorough community relations program through com-
munity meetings, telephone calls and personal visits to people living
near the site. Superfund involvement may change the lead in the
cleanup process to a state agency. Because the site assessment deter-
mined the extreme effectiveness of the local agency, however, it
was recommended that the local agency staff person remain as the
primary contact with the citizens. It was also determined that the
means of communication remain the same; even though telephone
calls and visits are time-consuming, they are most appropriate to
the community involved.
CONCERNS AND ISSUES
All of the foregoing examples indicate the kinds of concerns and
issues that can be revealed during site assessments. A number of
other points are also instructive. As discussed in USEPA's Com-
munity Relations Handbook for Superfund, the severity of the risk
associated with the site is not in itself indicative of public reaction.
Sites that have a significant potential for hazardous release often
generate very little public concern, while sites with a low risk factor
can often generate a vocal public response. Discussed in the hand-
book are a number of apparent reasons for this disparity including
perceived public health risks, the role of the waste generator in the
local economy and perceived loss of property value. After com-
pleting over 60 site assessments in the last nine months, the authors
would like to add two additional factors that seem to strongly im-
pact a community's response to site activities—speed of response
and "lightning rod" effect.
Speed of Response
It is becoming increasingly apparent that slow governmental
response to a perceived problem is a major factor in local reaction
to site cleanup. Numerous examples exist of citizen complaints that
occurred over a ten-year period before site closure and/or cleanup
commenced. In these instances residents have formed hardened
animosity and distrust toward local and state officials for their
perceived lack of action. To residents who believe themselves at
risk, the fact that local government was constrained by limited
authority and money is not important. What is important is that
they believe the agencies were not responsive to their concerns and
had little regard for the potential risk that affected the community.
Once such an aura of distrust exists, it is very difficult to
establish effective two-way communication. If local residents feel
they have been ignored in the past, they are likely to feel that at-
tempts to communicate with them are half-hearted and less than
totally candid. If this situation exists and is not corrected, the pro-
mise of achieving a cleanup plan that can be implemented is
substantially lessened. Personal interviews have proven to be a key
factor in determining when such a situation exists. As would be ex-
pected, the agencies affected are often relucant to admit that rela-
tions with local residents are strained. In fact, program staff may
not even be aware of the situation if it relates to past activities in
which they were not involved.
Successful interviews, which allow local residents an opportunity
to share their concerns, can help to "clear the air" and establish a
more positive future working relationship. The information gained
from these interviews can help determine which governmental
agencies are viewed as credible sources and what kind of informa-
tion the residents need in order to understand the alternative
cleanup options.
On a more positive note, if local and state governmental response
has been quick and effective, residents often believe the problem it
in good hands and are willing to wait for final governmental action.
This was the case in a northern California community where mine
waste runoff has caused major fish kills. The area draws many
tourists and sports fishermen; thus the fish kills caused widespread
390
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alarm. However, state regulatory action and lawsuits over the past
eight years have convinced the community that the government is
doing what it can to resolve the problem. All residents interviewed
indicated a high level of trust in the agency involved and said that
media coverage was sufficient to keep them informed. This is much
different from communities characterized by distrust of the respon-
sible governmental agencies.
"Lightning Rod" Effect
Recent media coverage of national events surrounding the
USEPA has heightened local awareness of the Superfund program.
It has also guaranteed press coverage of the most mundane ac-
tivities if they are associated with Superfund. Thus, public meetings
or other events associated with site remedial activities often become
a "lightning rod" for community dissatisfaction that has little to
do with the actual site.
Past planning and zoning issue, local taxes, sewer and water
questions or just plain dislike of a public official can quickly take
over the public forum. While some may argue this provides a
worthwhile local catharsis, it leaves those seriously concerned
about site cleanup without a forum.
For example, residents adjacent to an Arizona site asked the
USEPA to forego further public meetings because, as the residents
put it, they had turned into a "media circus of local demagogues
and people running for office." The solution in this instance was a
series of small meetings between USEPA officials and local
residents in their homes. Information exchange was far more pro-
ductive and even the most reluctant residents felt comfortable ask-
ing the questions that were on their minds.
A critical element in the assessment process is, then, a determina-
tion of peripheral issues that could impact community response to
remedial actions. This is not meant as an attempt to dig up the local
"dirt," but rather as an assessment of overriding local concerns
that may have an impact on the effectiveness of various com-
munication techniques.
CONCLUSIONS
Information needs will continue to vary from community to
community based on cultural patterns, local political systems and
the history and people surrounding each site. If effective two-way
communication is to be achieved,- it must be based on an understan-
ding of the local community and its specific information needs.
Community relations activities that fail to recognize these basic dif-
ferences will cause problems, rather than resolving them.
As the American public becomes more technically and politically
sophisticated, it is increasingly important to provide it with the in-
formation needed to review governmental decisions. The present
visibility of the Superfund program and the intense public reaction
engendered by the hazardous waste issue make good communica-
tion even more critical. Site assessments provide the information
needed to design effective communication programs.
Whether it be Superfund cleanup or licensing of a new facility,
intense public reaction can potentially halt future action. An effec-
tive two-way communication/education program may be the only
thing that stands between success and failure. There is no better
way to determine what kind of information people need than to ask
them. While this technique alone cannot ensure success, success
may be very difficult to achieve without it.
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WHY GOVERNMENT AND INDUSTRY HAVE FAILED AT
PUBLIC PARTICIPATION PROGRAMS AT SUPERFUND SITES
LOIS MARIE GIBBS
Citizens Clearinghouse for Hazardous Wastes, Inc.
Arlington, Virginia
DEVELOPING GOOD WORKING RELATIONSHIPS
The first important step in any program is to develop good work-
ing relationships between all parties involved. However, developing
good working relationships between a community faced with a
toxic waste problem, industry and government has been a difficult
task. Experience has shown that the approaches used in the past
have failed. To make matters worse, no one is actively attempt-
ing to change the existing methods to take advantage of the lessons
learned.
There will never be a good public participation program imple-
mented in this country if government and industry are not willing
to treat affected or potentially affected community people as
equals, rather than as obstacles to be dealt with. Clearly, changes
need to be made if a cohesive working relationship is to be devel-
oped. One way to define those changes is to look at what went
wrong in the past and then to define what needs to be done in the
future. To accomplish this, the following comments are examples
of problems that the author has seen in the course of her travels
and personal experiences and suggested recommendations to elim-
inate these problems in the future.
ALL COMMUNITIES MUST HAVE A
PUBLIC PARTICIPATION PROGRAM
The first change that needs to be made is to have a Public Partic-
ipation Program for all communities that will have any involve-
ment with hazardous waste. USEPA's present policy to provide
only a program in areas where citizens are organized is simply ask-
ing for trouble. The message this policy sends out is "organize
and raise hell and you'll have input—sit back, behave yourselves
and you'll be ignored." The very nature of this policy is designed
to force people into an adversarial role. Once a relationship begins
poorly, it is difficult, if not impossible, to build trust.
If a community is not organized, it does not mean it is not in-
terested. Rather, the public probably does not know what is hap-
pening or what to do about it. If there is no public participation
program—and, as a consequence, little or no information locally
on the issue—how can anyone expect local residents to become in-
terested or voice concern?
In most cases, the local people do not know or fail to understand
what is happening until the first truck comes down the street. It is
at this point that the community begins to organize. One of the first
responses is outrage, followed by mistrust, as they generally be-
lieve that government and industry tried to deceive them.
The end result is an immediate adversarial relationship between
the community and industry and government. This problem usually
haunts government and industry representatives throughout the
project. It is also an easy, uncomplicated problem to resolve. All
that needs to be done is to implement a public participation pro-
gram at every site where an action is planned.
INVOLVEMENT FROM THE START
The local people must be involved as soon as the field investi-
gators arrive on-site. Too often, citizens are informed of a planned
action after it has already been decided upon. Thus, the residents
have no say about what needs to be done or where or how it is to be
carried out. Consequently, they become angry, scared, confused
and once again feel a loss of control over their own destinies.
"Public Participation" as currently practiced by USEPA at
Superfund sites is not designed to involve the public in any real
decisions that need to be made but rather to give the public care-
fully selected portions of information. The USEPA seems to care
more about maintaining control of data and information than shar-
ing what is known with a community. Why does USEPA do this?
One can only imagine what thoughts lurk in the minds of a Wash-
ington bureaucrat, but here are several suggestions:
•People are generally technically ignorant and will not understand
•USEPA makes the decisions—it is their money!
•USEPA cannot answer the questions that arise
•Scientists and society have no easy answers to what it means to
have 25 ug/1 benzene in the drinking water
Perhaps the last suggestion is the driving force behind all the
others. As experts, most scientists and bureaucrats cannot admit
their failings in not having answers to the questions posed to them.
As has been expressed by many government officials, "we cannot
release these data until we have a good answer or response to the
questions they will raise." So what happens? Data are withheld,
people find out about them and distrust ensues, further alienating
the public rather than building open lines of communication.
Past history has shown this lack of concern for true public par-
ticipation to be very damaging and extremely expensive for the
parties involved. For example, it is not unusual for USEPA to de-
fine, in isolation from a community, a cleanup action with a tight
timetable based on engineering or economic consideration. The
local people hear about the plan through the media and request
(from USEPA or the state agency involved) a copy of the planned
actions. Note that I say planned actions, not proposed, as the de-
cisions have already been made.
In response to this request from the community, USEPA, not
realizing or thinking about what they are sending or to whom, re-
leases a 500-page technical document. The local people now must
392
PUBLIC PARTICIPATION
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attempt to read and understand this technical report (which might
as well be written in Greek), become overwhelmed, more fright-
ened than ever and unsure of what to do. Their choices are (1)
trust USEPA—a difficult task, considering recent Congressional
findings, (2) hire an expert to review the document for them—also
an unlikely event because of the cost and the lack of knowledge
about whom to hire or (3) file a lawsuit to stop the work, to give
them more time and the opportunity to develop a mechanism for
input on the planned actions. A lawsuit is usually what occurs.
All of this is expensive and embarrassing to both government
and industry. A construction season can be lost and the adverse
publicity can create tremendous public relations problems for in-
dustry, government and elected officials. Such a lawsuit also stim-
ulates other legal actions against one or all of the parties involved.
The early involvement of citizens is also very important in
settlements with responsible parties before they are finalized. If
the local people are not involved in the decisions made in respon-
sible party settlements, they will immediately question the settle-
ment and possibly accuse USEPA and the other parties of ex-
cessive cooperation with the industry at the expense of public in-
terest. This is especially true now after the recent Congressional
investigations.
Many, if not all, of these problems can be avoided or minimized
if people are involved from the first step. Trust, good working
relations and cooperation can and must be established from the be-
ginning, since it is almost impossible to establish these after the
damage has already been done.
CITIZEN INVOLVEMENT MUST BE MORE THAN TOKEN
The local people must have a meaningful voice in the decisions
made regarding a site in their community. The community and its
future belong to the local people, their families and their neigh-
bors. They no more want government/industry to define their
futures without consulting them, than you want me to define yours.
Consultation does not mean being informed after the decisions
are made. The current practice of news conferences and releases,
distributing fact sheets and holding informational meetings with
little or no substantive information being exchanged is not serious
public participation; and the public recognizes this. Yet these ac-
tivities comprise the main thrust of the "Public Participation"
programs implemented across the country. Not only are these
token steps not serious, but the manner in which they are carried
out further alienates the public rather than building open lines of
communications.
News Releases. News releases of actions or changes in the planned
actions are always given to the media before community leaders
obtain them. Consequently, the media calls local people who are
unprepared to comment. Therefore, local people immediately be-
come angry, feeling that they are not being kept informed, and they
naturally lash out at whoever released the press statement. Local
leaders do not like to look or feel that they are uninformed. So,
releasing a story without notifying key community people first is
asking for bad press.
The second problem is releasing impact information on Friday
afternoon. This is especially true of health-related information.
Too many times, people have heard on Friday that they may be ex-
posed to lethal chemicals or that a health problem was clearly doc-
umented in their community. There is nowhere for these now-
scared and panicky people to go or call for information on what
this all means to their families. Instead, they must sit all weekend,
upset and uncertain, and wait until Monday morning for explana-
tions. This type of action not only closes most doors to commun-
ications but is also unnecessarily cruel to already suffering fam-
ilies. If such a release must be made, I firmly believe that waiting
until Monday will not change the release's value.
Fact Sheets. Fact sheets are useful tools to help explain what is
planned, how it will be done and other activities at the site. How-
ever, too much weight is given to the effectiveness of fact sheets.
They serve as a good tool in a meaningful dialogue but not as a
substitute for meeting face-to-face and seriously discussing the
issues or actions.
Public Meetings. Public meetings are an essential part of a public
participation program for several reasons. First, they provide a
mechanism for shy, quiet people and the elderly to hear what is
happening and the issues. These people will not meet face-to-face
with industry or government because of their own shyness or dis-
abilities. Therefore, without a public meeting, these more fragile
citizens could end up closed off in their homes, uninformed and
needlessly frightened and confused about the happenings around
them.
The second reason is that this type of meeting usually brings
out all issues from all sides. In this way, local people can have a
better understanding of who's recommending what and why. Too
often, people hear only part of the story and thus can not make a
fair and educated decision. A public meeting not only provides the
mechanism for bringing out the issues, but also serves as a forum
for asking questions and for benefitting from questions raised by
others.
The third reason for public meetings is to provide additional
information to the field investigators. No one knows more about
the community than the people who live and work there. Many
times in the past, the local residents were able to supply valuable
information to the investigating teams who reached out to the
community at a public meeting.
However, in the past, public meetings have often proved to be
unproductive, uninformative and, at times, completely out of con-
trol. There are reasons for these problems and possible ways to
correct them:
(1) Involving local citizens from the beginning will stop people
from walking into the meeting angry and ready to criticize.
(2) People who attend an informational meeting expect informa-
tion. I have attended hundreds of informational meetings
where no new information was provided. This lack of informa-
tion sometimes resulted from the meeting getting out of con-
trol, but the majority of times it was intentional. Informa-
tion was too often withheld from the affected people because
the policy decisions has not yet been made or because there
were negotiations going on with the responsible parties and it
could hurt the legal actions.
There are also those individuals who enjoy playing power games
with local residents. I overheard two separate conversations where
the officials sponsoring the meetings, in both instances, were brag-
ging in a bar about how successful they were because they did
not "give anything away." They were actually congratulating each
other on successful meetings. The mindset of such individuals is
hardly the proper attitude for conducting a public meeting!
Providing local people with all the available information is not
only fair, but it's also the only way to ensure a good working
relationship. Once the residents discover something has been kept
from them, the trust and rapport will be lost.
The language and terms used by those presenting the informa-
tion must be at the level of education and understanding of the
community. Too often, information is presented to communities in
either technical jargon or so simplified as to be insulting. For ex-
ample, explaining the security of a complete containment system as
having "a clay cap with a permeability of 10~7, the hydraulic pres-
sure created beneath the site by existing soil structures and the
leachate collection system, with its on-site treatment capabilities,
nothing will leak" cannot be understood by the lay person.
An example at the other extreme, from Love Canal, was the ex-
planation of how the Love Canal leaked. An engineer explained
that the Canal was like a bath tub full of water. "When you put a
fat lady in the tub, it overflows; that's what happened here."
Needless to say, the heavier women in the audience were not
pleased with this analogy.
The last language problem that I feel needs to be addressed is the
use of "in-house" lingo. This includes the use of initials instead of
PUBLIC PARTICIPATION
393
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names and terms used within a given profession. The use of in-
itials is completely confusing and the use of esoteric terms is
totally inappropriate. For example, a health official was ap-
proached by a woman who had recently had a miscarriage. Not
realizing what he was saying, the official kept referring to this
woman's miscarriage as "fetal wastage." Halfway through the
conversation, she became very upset and pointed out to the offic-
ial that her definition of wastage was something you flush down the
drain or put out on the street each week—not an innocent baby.
Her expression of anger and emotion was contagious and many
other people became upset over other things. A once peaceful room
was turned into the scene of an emotional confrontation.
Careful planning and serious "thinking before speaking" could
avoid many of these language barriers. Moreover, people who be-
come involved in the issue at hand quickly become educated on var-
ious aspects of the problem. Therefore, one should not underes-
timate their ability to understand and comprehend what's happen-
ing and why.
COMMUNITIES NEED TO HAVE THEIR OWN EXPERTS
There is absolutely no reason to believe that either industry or
government will look out for the primary interests of the commun-
ity. Everyone involved at a problem site has a vested interest. The
residents are concerned about the health of their families, industry
is concerned about potential lawsuits and USEPA is concerned
about politics and protecting the interests of major corporations.
One of the most significant gaps in the past and present public
participation program is the lack of funds to provide a way for cit-
izens to hire their own experts to review a proposed plan. A pro-
gram designed to sincerely involve lay people who can have an edu-
cated and articulate voice in the decision-making process must in-
clude a way for citizens to consult with qualified professionals of
their own choosing to help critique the plans. Without these pro-
fessionals, a real public participation program will never exist.
Communities faced with a problem usually are not financially
able to hire their own experts, and donated services are min-
imal. Without some qualified person the community can trust, who
can say that the project is safe, few communities would accept any
plan. However, since they lack the expertise, they are unable to ar-
ticulate why they think it is not a good plan and end up speaking
from emotion rather than fact.
Would you, for example, buy a house tomorrow, simply accept-
ing the seller's and the real estate agent's word that the house was
structurally sound and termite-free? The answer is no. You would
bring in someone you trust to check out the house, not because
you thought there was something wrong with the house or felt that
you were being lied to but to protect your interests. It is no differ-
ent for people living near a waste site. They want to protect their
interests, too.
At Love Canal, the local organization was provided with the re-
sources to hire its own expert. This person proved to be very help-
ful in explaining to residents what was going on and why. Because
the actions were explained and approved by the group's expert,
no one objected to the plan. This person also served as a valuable
resource person at professional meetings where a resident's pres-
ence might have made the other experts uneasy or created com-
munications problems.
The small amount of funding that it would take to provide this
invaluable resource to local communities could eliminate a large
amount of future problems.
CONCLUSIONS
The problems of the past public participation efforts show the
way to future solutions. Rather than force residents into the role of
uninformed children who have no say—and no right to have a
say—in what their "parents," played by government and in-
dustry, decide, we suggest that those in charge of uncontrolled
hazardous waste site cleanups:
•Provide the means for residents to hire their own experts
•Involve residents from the very start
•Never try to deceive communities by presenting plans when the
decisions have already been made as though you really wanted
their input
•Be sensitive to the various mistakes that can set up walls to com-
munications.
Sensitivity is something we all have to learn, usually the hard
way through experience. Communities have to learn it all the time,
since they are usually forced to learn the bureaucrats' and indus-
try representatives' language and ways of thinking just to com-
municate. It is the housewives, farmers, blue collar workers and
others who have had to reach out by learning new jargon and new
scientific information. We'd like you to learn some new things
about communicating, too. It's not hard. We've done it and so can
you.
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PUBLIC PARTICIPATION
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THE ROLE OF REMOVAL ACTIONS AT UNCONTROLLED
HAZARDOUS WASTE SITES: CASE STUDIES
JOANNE WYMAN, Ph.D.
JANN DULLER
Booz, Allen & Hamilton, Inc.
Washington, D.C.
CHERYL HAWKINS
STEVE HEARE
U.S. Environmental Protection Agency
Office of Emergency and Remedial Response
Washington, D.C.
INTRODUCTION
The Comprehensive Environmental Response, Compensation
and Liability Act of 1980 establishes a program of Federally
financed response to actual or threatened releases of hazardous
substances at uncontrolled waste sites. Under this program, two
types of responses are authorized: remedial action and removal ac-
tion.
Remedial action is defined in CERCLA as a "permanent rem-
edy." Generally, this type of response requires lengthy, compre-
hensive cleanup activities with an estimated average cost per site
of $6.5 million. The National Priorities List (NPL), which USEPA
published pursuant to section 105 of CERCLA, identifies the high-
est priority releases at uncontrolled sites nationwide and, thus,
the most likely candidates for remedial action. Removal actions,
by contrast, are short-term responses designed to provide prompt
relief from urgent threats at both NPL and non-NPL sites.
The USEPA1 has adopted procedures for selecting and conduct-
ing the type of Superfund response most suitable for the release.
The remedial portion of the program, because of its visibility and
the magnitude of its resources, has attracted considerable public
attention. The purpose of the authors in writing this paper, there-
fore, is to give potential response participants a more informed
understanding of the role of removal actions in Superfund. Spe-
cific topics addressed are: selecting a removal response, processing
the removal request, requesting and approving ceiling increases,
requesting and approving exemptions to the six month and
$1,000,000 limits and negotiating state participation. Information
on operating procedures was derived from USEPA's removal pro-
gram guidance, and case study data were taken from the Agency's
Removal Tracking System.
SELECTING A REMOVAL RESPONSE
The Oil and Hazardous Substances National Contingency Plan
(40 CFR 300, NCP)2 establishes the framework for selecting a
CERCLA-financed response. Under this framework, removals fall
into two categories—immediate and planned—and procedures for
evaluating the urgency of the threat and the alternative cleanup
techniques lead to selection of an appropriate response. If the
risk to human life, health and the environment is immediate and
significant, an immediate removal is the appropriate response re-
gardless of whether the release is at a listed or unlisted site. A
planned removal may be appropriate either to continue response
actions following completion of an immediate removal or to take
action at an unlisted site when threats at that site are too urgent
to await ranking and listing. Both types of removals cannot exceed
$1,000,000 or six months without special approval.
Immediate Removals
USEPA initiates an immediate removal when a preliminary
assessment3 of a release unequivocably supports the need for emer-
gency action to protect human life, health and the environment.
Indicators of immediate and significant risk are: human, animal or
food chain exposure to acutely toxic substances, contamination of
a drinking water supply, fire or explosion and similarly acute
situations.4
In some cases, the urgency of threats from releases are so sig-
nificant that USEPA can make a decision at once to proceed with
an immediate removal. For example, the Agency authorized an
immediate removal to contain and remove toxic substances and
contaminated materials within hours of an explosion at the Plasti-
fax plant in Mississippi last year. That explosion killed two peo-
ple and injured 64 others. It also left pools of liquid chemicals
and contaminated water in concentrations potent enough to eat
through a firefighter's boots. Additionally, rain threatened to dis-
perse the contaminants off-site. The site later was added to the
NPL and is eligible for future remedial action.
On occasion, even when a release appears to pose a significant
and imminent threat, USEPA may seek outside opinions on the ex-
tent of contamination and the efficacy of proposed response
activities before making a final decision on an immediate removal
request. For example, in the case of six asbestos-contaminated
sites in the Northeast, USEPA asked the Center for Disease Con-
trol to prepare a health advisory and to assist the Agency in assess-
ing the urgency of the threats and determining the appropriate type
and method of response. The CDC study confirmed the need for
an immediate removal, and USEPA approved the action shortly
thereafter.
Planned Removals
If the preliminary assessment has ruled out an immediate re-
moval but indicated a need for a different type of CERCLA
response, USEPA continues to investigate the release. Releases at
sites already on the NPL may be referred for remedial action.
Other releases at unlisted sites may be candidates either for hazard
ranking and eventual listing or for planned removals. Considera-
tion of a planned removal action may occur in three different
situations.
One such circumstance may arise after USEPA has determined
an incident does not meet the NCP criteria for an immediate
RISK/DECISION ANALYSIS 395
-------
removal request. For example, the Agency decided that an aban-
doned landfill, which had been used for industrial waste disposal
for many years and was located in a remote area of Pennsylvania,
did not pose imminent threats to public health and welfare and
thus did not warrant an immediate removal. A more thorough
review of the site, with consideration to the presence of priority
pollutants and migration of contaminants to groundwater, resulted
in USEPA's decision that the action met the NCP criteria for a
planned removal.
In other instances, such as the Triangle Chemical site in Texas, a
planned removal may be an appropriate follow-on to an immediate
removal. Releases from hundreds of leaking drums at that unse-
cured site had contaminated the surrounding soil heavily and were
linked to several fishkills. Further, the Agency's investigation
showed that nearby residents were removing materials from the
site, thus exposing themselves to significant risk of direct contact
with highly corrosive substances. Consequently, USEPA author-
ized an immediate removal to secure the site by constructing a
fence until mitigative action could be undertaken. Since Triangle
Chemical still posed significant direct contact, groundwater and
environmental threats, but was not on the NPL, USEPA decided
to undertake a planned removal in order to remove and dispose
of the drums and contaminated soil. The site subsequently was
added to the NPL and now is eligible for remedial action.
A former solvent reprocessing facility in Texas provides an
example of the third situation in which a planned removal be-
comes the selected course of action—that is, in response to a spe-
cific request for a planned removal to mitigate threats at a site
not on the NPL. This unsecured site, containing 24 deteriorated
storage tanks and littered with leaking drums, posed direct con-
tact, fire and explosion risks as well as surface and groundwater
contamination threats. USEPA approved a planned removal action
to treat and discharge the contaminated wastewater, remove and
dispose of the drums and tank contents and encapsulate contam-
inated soil and sludges.
APPROVING THE REMOVAL REQUEST
In order to manage Superfund resources prudently and to pro-
mote consistent removal decisions, USEPA has adopted operating
procedures for the packaging, processing and approval of removal
requests. Removals must be approved by either the Assistant
Administrator (AA), Office of Solid Waste and Emergency Re-
sponse (OSWER) in Headquarters, or the Regional Administra-
tors (RAs) in accordance with USEPA's Delegations Manual and
operating guidelines. Since May 1983, RAs have had authority to
approve the majority of immediate removals for which the expendi-
ture or extramural (procurement) funds are not expected to exceed
$250,000. More costly immediate removals require the approval of
the AA, OSWER as do all planned removals.
Regional Approval of Immediate Removals
A recent case involving an abandoned rubber and plastics facil-
ity, located in a populous area of a Pennsylvania town, is typical
of an immediate removal approved by a Regional Administrator.
A power substation located on the site was vandalized, resulting
in an uncontrolled release of PCBs. Several schools and a neigh-
borhood park lie within 1500 ft of the facility, and children were
seen playing on the site. The Regional Administrator approved an
immediate removal to dispose of the transformers and contam-
inated soil and to incinerate PCB-contaminated liquids.
Headquarters Approval of Immediate and Planned Removals
An immediate removal action in the Pacific Islands is represen-
tative of the types of actions requiring the approval of the AA,
OSWER. This complex case involves 32 separate sites, some of
which are on the NPL, located on Guam as well as various other
islands in the Pacific Trust Territories. These sites contain PCBs,
pesticides, acids, bases and organic solvents; more than half are
unsecured and easily accessible. Deteriorating site conditions,
documented instances of direct contact and the high potential for
food chain and drinking water contamination indicated that
immediate removal action was required. Because of the expected
high cost of response, dictated in large part by the lack of an
approved disposal site in the Pacific Territories and the shortage of
adequate storage sites on the islands, the proposed action was
referred to Headquarters. Following a review of the Immediate
Removal Request (known informally as the ten-point document)
prepared by the Region, the removal was approved by the AA,
OSWER.
The AA, OSWER also may require Headquarters approval for
certain types of immediate removals regardless of their costs. Pro-
posed immediate removals at dioxin-contaminated sites in
Missouri, for example, have been referred to Headquarters for
approval so that actions taken are consistent with the Agency's
dioxin strategy now under development.
In addition, the AA, OSWER acts on all requests for planned
removals. Unlike immediate removal requests, each request for a
planned removal must include a letter from the Governor or other
designated individual of the state in which the proposed removal is
to take place. Under Section 300.67 of the NCP, the letter must
describe the nature and extent of the release, the actions taken or
underway at the site and the proposed planned removal. The
letter also must include assurances that the state will pay its pre-
scribed share of the costs. In accordance with Agency procedures,
the Regional staff include this letter in the formal planned removal
request package they prepare and submit to Headquarters.
REQUESTING AND APPROVING CEILING INCREASES
Throughout the removal action, response costs are tracked for
several purposes: to promote sound financial management, to en-
sure that the $1 million statutory limit is not exceeded unknow-
ingly and to support potential cost recovery actions. Tracking
begins with the establishment of an initial project ceiling at the
time the response is approved. As the response proceeds, the On-
Scene Coordinator (OSC) may find that costs are likely to exceed
the initial ceiling if the actual extent of the release or threat is
greater than anticipated (e.g., a bulldozer uncovers several hun-
dred buried drums). Consequently, USEPA has established pro-
cedures for requesting and approving ceiling increases.
All requests for ceiling increases for planned removals must be
submitted to Headquarters for approval. Ceiling increase requests
for immediate removals also must be referred to Headquarters if
additional funding requirements will raise the project ceiling above
the $250,000 limit established by delegation. Requests to increase
the project ceiling, typically sent by the OSC to Headquarters in
the form of a pollution report (or POLREP), must document the
reason for and the amount of additional funds requested.
The Crystal Chemical site in Texas, now on the NPL, illustrates
the type of circumstances in which a removal action requires a
ceiling increase. In this case, response personnel could not com-
plete the clay cap until a buyer was found to purchase and remove
equipment left at the site. Heavy rains damaged the cap before it
could be completed, forming pools of arsenic-contaminated water.
Remaining contract money then had to be used to remove the
contaminated water. The OSC submitted a written request for,
and Headquarters approved, a ceiling increase to repair the cap and
complete it once the equipment had been moved.
EXEMPTIONS TO THE STATUTORY COST
AND DURATION LIMITS
Section 104(c)(l) of CERCLA limits all removal actions to six
months or $1 million except in prescribed circumstances. Pro-
cedures for calculating and tracking duration and cost and for
submitting requests are designed to ensure that the limits are not
exceeded unknowingly and that response work is not disrupted.
All exemptions require the approval of the AA, OSWER and
each request must document that the statutory criteria for exemp-
tions are met. These criteria are: continued-response actions are
immediately required to prevent, limit or mitigate an emergency;
there is an immediate risk to public health or welfare or the en-
3%
RISK/DECISION ANALYSIS
-------
vironment; and such assistance will not otherwise be provided on a
timely basis.
Site conditions at a bankrupt recycling facility in Indiana illus-
trate the type of situation for which USEPA may approve an excep-
tion to the six-month limit. Following a fire at this site, USEPA
conducted limited immediate removal activities to prevent severely
contaminated surface water from migrating off-site. Site conditions
continued to deteriorate, however, because flammables were stored
haphazardly and because runoff was contaminating a nearby lake
used for recreational fishing. USEPA identified a planned removal
as the best form of mitigative action, because timely private party
cleanup appeared unlikely and the site was not on the NPL. Before
approving the planned removal, however, the Agency first had to
approve an exemption to the statutory time limit because more
than six months had elapsed since the start of the immediate re-
moval.
Cleanup activities at the Western Processing facility in Wash-
ington illustrate a removal action justifying an exemption from the
$1 million limit. USEPA initiated an immediate removal at this
NPL site to stabilize it until a remedial action could be under-
taken for long-term cleanup. Cost estimates for conducting the
immediate removal were based upon the premise that most ma-
terials could be sent to local recyclers or other potential users.
Unfortunately, many materials were found to be contaminated or
to contain chemicals that were unsuitable for recycling, necessi-
tating additional funds for hazardous wastes disposal. Since this
funding would raise the project ceiling above $1 million, USEPA
had to approve an exemption from the statutory ceiling to enable
the OSC to dispose of the wastes and complete the removal action.
NEGOTIATING STATE PARTICIPATION
The NCP and USEPA policy require that states at a minimum
make three assurances for removals: (1) cost sharing, (2) opera-
tion and maintenance (O&M) and, (3) off-site disposal. The state's
share of costs is at least 50% for immediate removals at publicly
owned NPL sites and for planned removals at publicly owned sites
and 10% for planned removals at privately owned sites. Cost shar-
ing is not required for immediate removals at privately owned or
non-NPL sites. The O&M requirement for both types of removals
is that states must pay 100% of the cost, starting no later than
six months after the removal begins. If off-site disposal is neces-
sary, states must assure the availability of a properly permitted
facility with the capacity to accept the type and quantity of the
removed substance.
Beyond these requirements, states and their localities may under-
take specific removal activities. The legal instruments USEPA
uses to document a state's role in removals are Letter Contracts,
Cooperative Agreements (CAs) and Superfund State Contracts
(SSCs). Under current policy, Letter Contracts for procurement are
suitable only for immediate removals, while CAs and SSCs are
used only for planned removals.
Letter Contracts
Since Dec. 1981, OSCs have had the authority under CERCLA
to procure emergency response services from states and localities
on a non-competitive basis. The mechanism for doing so is the
"Letter Contract for State or Local Response to Emergency
Hazardous Substance Release," a standard form designed to min-
imize negotiation and avoid delays in response initiation. A Letter
Contract is a preliminary contractual mechanism that must be
definitized within a certain period. While the Letter Contract
itself cannot exceed $50,000, the definitized contract can be for any
amount approved by USEPA's procurement office.
Between Dec. 1981 and Aug. 1983, OSCs had used the Letter
Contract in six incidents. These Letter Contracts were designed
to take advantage of state and local familiarity with local con-
ditions and availability for rapid response. For example, the Letter
Contract between USEPA and Cattaraugus County, NY, illus-
trates the types of immediate removal response services localities
can provide effectively because of their knowledge of and prox-
imity to local problems. In this case, Cattaraugus County had
taken the lead in investigating and seeking relief for drinking water
wells contaminated with trichloroethylene. Because of its active
role and willingness to take long-term responsibility for operations,
the County Department of Health received a Letter Contract to
purchase, install and operate individual carbon filtration units for
16 wells. Consistent with USEPA's O&M policy, the County
accepted responsibility for maintenance after the expiration of the
six month statutory limit on removal actions.
Cooperative Agreements
A Cooperative Agreement is an assistance award and is the
mechanism used whenever a state leads a response action. Since
current policy is for USEPA to lead all immediate removals, the
mechanism applies only to planned removals. As of Aug. 1983,
USEPA had awarded only one planned removal Cooperative
Agreement, for cleanup of several residences and a commercial
facility contaminated by radium. The State of Ohio elected to lead
this planned removal, which included removal of contaminated soil
and materials, transporting them to a disposal facility in Wash-
ington and backfilling and landscaping excavated areas.
Superfund State Contracts
In the remaining planned removal cases to date, USEPA has
led the response action, therefore using SSCs to obtain state
assurances. Typically, negotiation of the SSC begins while the
Region is preparing the planned removal request and procure-
ment package and continues throughout the processing of those
documents. The significant feature of SSCs for planned removals
is that they allow states to meet their cost share obligation by
providing specified response services. In the case of a solvent re-
covery facility, located in a populous residential and commercial
area of North Carolina, the- state provided a project coordinator,
personnel to assist the OSC with technical tasks and community
relations and a variety of services supporting the planned removal.
CONCLUSIONS
The 14 cases discussed here have illustrated the principal de-
cision procedures in USEPA's Superfund removal program in
effect during late FY83. These procedures have been developed in
keeping with Agency experience as the program has matured. Some
changes may be expected in the future, however, as the Agency
continues to refine procedures to expedite removal responses to
threats at uncontrolled waste sites.
REFERENCES
1. Executive Order 12216 (Aug. 14, 1981) delegates Superfund authorities
to various Federal departments and agencies, including USEPA. This
paper focuses solely on the USEPA-administered activities.
2. Federal Register, 47, July 16, 1982, 31180-31242.
3. See 40 CFR 300.64 for preliminary assessment requirements.
4. See 40 CFR 300.65 "Phase III—Immediate Removal."
RISK/DECISION ANALYSIS
397
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RISKS, COSTS AND PUBLIC POLICY:
DETERMINING ACCEPTABLE CLEANUP LEVELS
J. O'NEILL COLLINS, J.D.
PHILIP C. LeCLARE, Ph.D.
Chas. T. Main, Inc.
Boston, Massachusetts
INTRODUCTION
Super fund1 legislation is designed to provide a governmental
mechanism to correct or mitigate the threat of a hazardous sub-
stance that may present an imminent and substantial danger to the
public health or welfare.2 The extent of remedy or the degree of
mitigation is to be determined by the selection of the most cost-
effective remedial alternative.' Cost-effectiveness is defined in the
National Oil and Hazardous Substances Pollution Contingency
Plan (the Superfund regulations) as the lowest cost alternative that
is technologically feasible and reliable and which provides ade-
quate protection of public health, welfare and the environment.4
Key issues for public policy decisions in the Superfund mandate
arise under the questions of imminent and substantial danger to
public health—how dangerous is "substantial" and what level of
mitigation provides "adequate" protection of public health, wel-
fare and the environment? The principal guidance Congress pro-
vided was that the choice of the degree of the cleanup should in-
clude some consideration of how much Superfund money is avail-
able and the need for immediate action at other sites.5
In this paper, the authors review what happens when decisions
on cleanup options are based on cost-effectiveness considerations
without risk assessment, what happens when risk assessment is
undertaken without a full review of opportunities for risk man-
agement and how risk management requires the establishment of a
specified acceptable level of risk. Finally, the authors propose an
initial approach for identifying a level of acceptable risk.
RISK ASSESSMENT
In the context of hazardous waste site remedial action programs,
the authors refer to risk assessment as the estimation of the
frequency of occurrence of some adverse effect on human health
as a consequence of exposure to toxic levels of chemicals.
The approach taken to estimate risk is to determine the dose of
a chemical to an individual or population through one or more en-
vironmental pathways and then to compare the dose to a unit risk
or potency derived for the specific chemical in question. While this
may sound straightforward, the data needed to perform a risk
assessment may be difficult to obtain. For example, these data
must include:
•Identification and quantification of all the waste constituents, if
only to determine the most potent or the most likely indicators in
environmental media
•Stability of the wastes—are they biodegradeable, subject to chem-
ical reactions, or photodecomposition? At what rates?
•Ability to migrate through or from the media—are the chemicals
soluble or insoluble, volatile, strongly sorbed on soils and sed-
iments, transported in runoff or leachate, biologically available to
plants, etc.
•Identification of the rates at which the materials migrate to air,
water, land and biological materials.
•The behavior of the chemicals in ecosystems and the potential for
bioaccumulation in food chains.
•The concentrations of chemicals to which people are exposed and
the resultant dose from this exposure.
•The toxic effects of the chemicals to humans for the modes of ex-
posure (inhalation, ingestion, direct contact) at the doses
involved.
Each of these items must not only be determined for each chem-
ical, but also will probably have to be determined at a more pre-
cise level than allowed by currently available data. That is, one may
need information on the sorbtion of a chemical by highly organic
soils or soil high in clay minerals and one may need information
on the bioaccumulation of the chemical in a particular food crop or
fish species.
Perhaps the most serious deficiency is a lack of human toxico-
logical data for all the chemicals encountered at a wide range of
predicted doses and dose rates. The USEPA has sponsored work
such as the Multi-Media Environmental Goals (MMEG) program
to develop acceptable ambient concentrations of toxic materials.
The USEPA's Carcinogen Assessment Group (CAG) and Environ-
mental Criteria and Assessment Office (ECAO) have both been
active in evaluating epidemiological and laboratory animal studies
to provide carcinogenic potency and potency slope estimates.
While it is understood that more health related data are needed,
one can still benefit from the use of health risk assessments. Two
case studies are presented for sites where there are some lexico-
logical data for the chemicals of concern.
SITE A
Site A is an abandoned hazardous waste site, inactive for 15
years. Sources of contamination include a number of lagoons,
drums with various chemical wastes, SO acres of contaminated
soil and two contaminated wetland areas.
This site is located in a rural area with 25 residences within
1/3 mile and a population of 1,000 people within a mile. Con-
siderable future residential development is planned for the area
within 1 or 2 miles of the site.
Sampling of the lagoons, site soils and surface and ground water
found a relatively large number of USEPA Priority Pollutants in-
398
RISK/QECISION ANALYSIS
-------
eluding: Methylene chloride, PCBs, trichloroethylene, benzene,
chloroform, arsenic, phenols and other chemical contaminants.
Wells providing domestic water at Site A were sampled at the tap
and analyzed. A number of metals and several organic compounds
were identified at or near the detection limit. However, methy-
lene chloride, a suspected human carcinogen, was measured at con-
centrations as high as 1.24 mg/1.
The USEPA's water quality criterion for halomethanes includ-
ing methylene chloride is stated in terms of incremental increase
in lifetime cancer risk. A concentration 0.19 jig/1 has an incre-
mental cancer risk of one in a million. If one assumes, as did
USEPA in deriving this criterion, that people (the 1,000 residents
within a mile of Site A) drink water at a rate of 2 I/day and have
a mass of 70 kg, they will experience an increased lifetime can-
cer risk of 1 in 150. Their increased annual cancer risk from this
single chemical would be on the order of 1 in 10,000.
In order to reduce the increased lifetime cancer risk from 1 in
150 to 1 in a million, the present methylene chloride concentra-
tion must be reduced by a factor of 1,240 -nO.19 or about 6,500. If
the premise that methylene chloride causes cancer is accepted, then
the value of the potency could be high or low by an order of magni-
tude (e.g., 1 in 15 or 1 in 1,500 increased lifetime cancer risk) and
not alter the conclusion that there is a substantial health risk. A re-
duction of the current methylene chloride concentration by a factor
of 650 or 65,000 would be required to reduce the cancer risk from
that one chemical to water quality criterion levels. Or, alternatively,
water source substitution would be recommended.
A complete risk assessment for this site would have to evaluate
other chemicals and exposure pathways and would require addi-
tional information of the type described previously. But even with
the limited data available, it can be concluded that an immed-
iate change in drinking water supply would be prudent. Such a
recommendation was not made in the feasibility study, apparently
because specific health risks were not quantified.
Instead, a cost-effectiveness approach which compared remedial
action costs to indicators of effectiveness was utilized at Site A. The
overall cost-effectiveness rating of a remedial action option was the
product of the sum of cost and the sum of non-cost items. There
were two categories of cost: construction costs and operation and
maintenance costs. Eleven categories of effectiveness were defined.
The effectiveness indicators used at the abandoned waste site are
presented in Table 1.
Costs were given a relative ranking from 1 (least expensive) to 5
(most expensive). Effectiveness measures were generally ranked as
to their ability to achieve the stated goal on the same scale as cost
with 1 being no action and 5 being completely effective action.
The study compared and rated action options for four discrete
phrases: source removal or isolation, groundwater aquifer man-
agement, groundwater end use management and site restoration.
The most cost-effective options identified within each phase were
combined into ten remedial action plans which were then ranked as
to their overall cost effectiveness.
The feasibility study at Site A recommended: (1) removal of the
sources of pollution ($5.5 million); (2) provision of alternate water
supplies ($0.5 million), (3) no groundwater cleanup and (4) addi-
tional sampling and analysis for one of the affected wetland areas
to determine whether a no action option would be cost-effective.
(Data costs of $100,000 versus cleanup costs of $4.5 million.)
Table 1
Effectiveness Indicators
Level of Cleanup or Isolation
Feasibility
Reliability
Ease of Implementation
Time to Achieve Cleanup
Attendant On-site Impacts
Attendant Off-site Impacts
Remoteness to Nearby Residents
Site Usability
Groundwater Usability
Surface Water Usability
The most cost-effective measure defined for groundwater aquifer
management at this site was "no action but monitor" at a yearly
cost of $100,000. The second ranked measure—and only half as
cost-effective as no action—was passive collection of groundwater
and discharge to a municipal sewer at a cost of $500,000. Tie-in to a
municipal water supply at a cost of $170,000 and new wells in the
deep aquifer at a cost of $250,000 would supplement these two
alternatives, respectively. Additionally, other source specific
measures proposed to be taken at the site would remove or isolate
the sources of methylene chloride from the groundwater so that in
time the levels of contamination would be reduced as a result of
recharge and plume migration (dilution). These additional actions
would bring total site remedial costs to about $6 million.
The feasibility study did not include risk assessments. Instead, it
spoke in qualitative terms such as "trace", "low" or "high"
levels of contamination. Using a relative assessment of costs and
benefits, most reviewers would come to the same conclusion as did
the feasibility study. However, a risk assessment approach, at least
in the area of the provision of alternate water supply, would have
modified the recommended remedial action to include immediate
provision of an alternate water supply, regardless of the fact that
municipal water would be provided in the future.
SITEB
Site B is Times Beach, Missouri, located on the Meramac
River 15 to 20 miles southwest of St. Louis. Times Beach is, or
was, a suburban community of 800 families with a total popula-
tion of approximately 1,700 and with 700 to 800 commercial and
residential structures worth approximately $33 million. In the early
1970s the Times Beach roads were sprayed with waste oil contain-
ing 2,3,7,8-tetrachlorodibenzo-p-dioxin ("TCDD" or "dioxin").
The community is located in a flood hazard area. Sampling after
a Dec. 1982 flood detected dioxin levels in several yards that
ranged between 1 and 5 parts ppb. Sample locations on streets,
street shoulders and ditches showed dioxin levels up to 100 ppb.
The Center for Disease Control (CDC) has determined that 1 ppb
of TCDD was detrimental to public health and that people should
be disassociated from the hazard.
Since soils are considered the primary source of dioxin, the
principal exposure pathways to be considered are dermal contact
and uptake, inhalation of suspended dust and direct ingestion of
contaminated soil. It has been suggested that a child playing in the
dirt of a yard could ingest a significant quantity of dioxin.
The CAG has estimated the carcinogenic potency of dioxin
which is equivalent to 8.5 x 105 per mg/kg day. (This, incidentally,
is the highest carcinogenic potency value determined thus far by
CAG). If one assumes that a child weighing 7 kg were to eat one
gram of dirt each day, it would have an intake of 10~6 to 5 x 10~6
mg/day. If one further assumes that the dose rate remains constant
over the lifetime of the person—which is highly unlikely—one com-
putes a range of increased cancer risk of 1 in 8 to 10 in 16. Even if
the risk of increased cancer were computed for a three year time
span—the estimated number of years a child might directly ingest
dioxin contaminated soil—increased risk of cancer would be on the
range of 1 in 200 to 1 in 40. If CDC's risk assessment produced
even remotely similar values, there's no question as to why it
recommended removing people from the source of exposure.
At Times Beach, the USEPA's remedial action decisions were
based on the Center for Disease Control's health risk determina-
tion that a soil concentration of 1 ppb of dioxin was an unaccep-
table level of exposure in residential areas. No in depth risk assess-
ment of options was undertaken; nor was a detailed cost-effec-
tiveness feasibility study made.
In assessing remedial action options, the USEPA found that be-
cause the area was flood prone, dioxin levels of 1 ppb could be ex-
pected in residential areas after every flood.' USEPA found that
the costs for soil excavation and its off-site disposal would be con-
sidered too high, basically because of the transportation costs.
The possibility of capping the highly contaminated areas was dis-
RISK/DECISION ANALYSIS
399
-------
carded as too unreliable. The option of removing all the soil and
temporarily containing it in Times Beach, although identified
among "temporary alternatives that may be available," was dis-
carded because of the "flood prone" nature of the area.' Whether
this last option could have been implemented at a cost below $33
million was unknown at the time of the relocation decision. No
detailed risk assessments were made for any of the options. Perm-
anent population relocation was judged the most reliable remedial
action to assure adequate protection of public health. It was con-
sidered cost effective because it was judged a necessary component
of any remedial action program undertaken.
RISK MANAGEMENT
Risk management is defined as: "the evaluation of alternative
regulatory options and selecting among them."1 On the one hand,
risk management decisions that rely on the cost-effectiveness rank-
ing of options, as done at Site A, without health risk assessments
cannot assure protection of public health. On the other hand, the
use of a risk assessment approach to identify unacceptable risks but
not to identify potentially acceptable levels of risk, leads to the
situation as in Times Beach where the only governmental choice
can be to take the lowest risk option. The proposition is put for-
ward that without an identified and quantified level of acceptable
risk, risk management decisions remain essentially qualitative de-
cisions regardless of the degree of cost-effectiveness or risk assess-
ment input.
In an effort to alter the practice of making risk management
decisions on a purely qualitative basis, the hypothesis is offered
that if a commonly acceptable risk event can be found wherein
most people feel secure, then the risk level of that event would iden-
tify an "acceptable" risk. The concept is offered to stimulate dis-
cussion and provide direction for future work. A preliminary
search for such an acceptable risk is given below.
Crouch and Wilson, in their book Risk/Benefit Analysis,'' pre-
sent some tables of commonplace risks of death in the United
States derived from the Bureau of Census, the National Safety
Council, the Department of Agriculture and the Bureau of Mines.
A summary table of some of the representative risks is presented
in Table 2. The risks shown are the average risk found for the 20
to 25 years of data reviewed.
Home accidents and the service and government occupational
accident categories from the risk table appear to offer promise for
defining an acceptable risk level. Would people feel safe if you
could promise to make them as safe as an upper income individ-
ual at home during his or her least risk prone years or as safe as a
bureaucrat sitting at a desk? These seem relatively secure environ-
ments. What is the risk level? The assumption is made that these
examples define a risk event for which most people would be will-
ing to say: "Protect me to that level and I should feel quite se-
cure; at least, I would not want major government programs to re-
quire additional expensive safety measures."
The best available surrogate indicator found for an upper middle
class population in their least risk prone years was that population
group in the 30-50 years age bracket with at least 16 years of educa-
tion. Data were obtained for this population group and home ac-
cidents in New York State. Similar data could not be found for
government workers.
In 1980, the New York population 30 to 50 years old with 16 or
more years of education totalled 450,000 for those outside of the
five boroughs of Manhattan. (Data for the five New York City
boroughs were not available.) Accidental home deaths among this
age and education bracket totaled 14. The annual risk of death was
1 in 31,000 or 3.2 x 10~5. The risk is 3 times safer than the na-
tional average accidental home facility risk of 1 in 10,000. The risk
reduces life expectancy by about 10 hours.
Table 2
Common Risks of Accidental Death
Occupation, Activity
or Risk Event*
Manufacturing
Service and Government
Agriculture
Construction
Mining and Quarrying
Motor Vehicle Accident
Home Accidents
Tornadoes
Lightning
Annual Risk
8.2x10-'
l.OxlO-4
6.0 xlO-4
6.1x10-*
9.5xlO-4
2.4xlO-«
l.lxlO-4
6xlO-7
5x10-'
•Crouch, -E.A.C. and Wilson, R.. 1982. Risk/Benefit Analysis. Cambridge, Massachusetts:
Ballinger Publishing Company.
The question then becomes: "Is a 1 in 30,000 or even 1 in 50,000
increased risk of death an acceptable risk?"
If the external environment were as safe as living in an upper in-
come house, most people would feel secure. Most people would
not perceive the need for expenditures of money to reduce this risk
unless the cost were relatively low. The authors propose this this
level of risk demonstrates an acceptable level of risk. Such an iden-
tifiable acceptable level should be used in comparing risks under
remedial action options for hazardous waste sites. Certainly, more
work needs to be done in identifying comparable risk events.
Study needs to be undertaken on how to assess relative life risks
(e.g., risks at home versus environmental risks versus occupational
or transportation risks, etc.).
CONCLUSIONS
The authors have reviewed what happens when decisions on
cleanup options are based on cost-effectiveness considerations
without risk assessment, what happens when risk assessment is
undertaken without a full review of opportunities for risk manage-
ment and how risk management needs the establishment of a spec-
ified acceptable level of risk. Finally, the authors have proposed
the beginnings of an approach for identifying a level of acceptable
risk.
The issues raised are not new issues. But addressing them will
help bring perspective to the basic questions of how risks, costs
and public policy should be factored into Superfund decisions.
REFERENCES
1. The Comprehensive Environmental Response, Compensation and
Liability Act of 1980, (CERCLA or Superfund) Pub. L. 96-510, 94
Stat. 2767; 42 LISC 9601, et. seq.
2. CERCLA, supra. Section 104(a)(l).
3. CERCLA, supra, Section 104(c)(4).
4. National Oil and Hazardous Substances Pollution Contingency Plan,
40 CFR 300, Section 300.680).
5. CERCLA, supra. Section 104(c)(4).
6. Hedeman, W.N., Jr., Director, USEPA Office of Emergency and
Remedial Response to the Administrator, USEPA, "Authorization to
Proceed with Permanent Relocation at Times Beach, Missouri—Action
Memorandum," Feb. 21, 1983.
7. Ibid., p. 5.
8. National Research Council, Risk Assessment In the Federal Govern-
ment: Managing the Process. Washington, D.C. National Academy
Press, 1983.
9. Crouch, E.A.C. and Wilson, R., Risk/Benefit Analysis. Ballenger
Publishing Company, Cambridge, MA., 1982.
400
RISK/DECISION ANALYSIS
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COMPARATIVE RISK ASSESSMENT:
A TOOL FOR REMEDIAL ACTION PLANNING
JOSEPH V. RODRICKS, Ph.D.
Environ Corporation
Washington, D.C.
INTRODUCTION
One of the principal objectives of remedial actions at hazardous
waste sites is to ensure that residual concentrations of substances
present in the environment following such actions will not pose a
significant threat to human health. It also seems desirable that the
objective of health protection is achieved in the most cost-effective
manner. The author's purpose in writing this paper is to suggest a
health evaluation process consistent with these objectives and to
describe the data that must be available to perform the required
evaluation.
In the paper, the author also provides guidance on the methods
to be used to assess the relative merits of alternative remedial action
plans according to the degree of health protection they yield. His
premise is that the most appropriate measure of effectiveness is the
degree of health protection achieved.
The Evaluation Process
Regardless of the context in which it is performed, evaluation of
the health consequences of chemical exposures consists of two
discrete steps. The first includes a determination of the likelihood
that a toxic injury or adverse effects will result from various condi-
tions of exposure to a hazardous substance. The second step re-
quires a judgment regarding the conditions of exposure under
which the likelihood of adverse effects is sufficiently small to pro-
tect health. Although this evaluation process has not been rigor-
ously applied to operation of remedial action at hazardous waste
sites, there is extensive experience from the evaluation of other
types of chemical exposures that can be relied upon in the formula-
tion of an approach appropriate to the objectives of the remedial
action program.1'2
Thus, the methodologies described in this paper are, at least in
their essential components, drawn directly from those that have
been in use for many years to evaluate air and water contaminants,
pesticides, food additives and occupational agents. However, none
of the methods used for these other categories of substances can be
taken without modification and be directly applied to environmen-
tal residues of substances remaining after remedial action at a
hazardous waste site. The evaluation process described in this
paper incorporates the necessary modifications and briefly explains
their bases.
The first step in the evaluation process requires several types of
data and analysis. Information must be available on the likely
residual concentrations of contaminants in each of the environmen-
tal media to which human populations will be exposed following
each of the remedial action alternatives proposed for a given site.
This information can be used to estimate a critical measure of
health effects: the daily human intake of residual contaminants
from all media. This measure will be referred to as the daily human
dose (DHD). Completion of the first step of the analysis also re-
quires information on the toxic properties of contaminants and a
means to assess the likelihood of adverse effects at the DHD pro-
jected for each remedial action alternative.
DEFINING PUBLIC HEALTH GOALS
FOR REMEDIAL ACTION
Measures of Health Damage
Data are available from experimental studies and from studies in
exposed human populations to show that many substances present
at hazardous waste sites are capable of causing various types of
health injury. Some forms of injury are relatively mild and usually
disappear after exposure ceases. Other forms can be quite severe
and can sometimes be life-threatening; many of these forms of in-
jury are progressive and do not disappear even if exposure ceases.
And, of course, other forms fall between these two extremes. For
any form of toxic injury, the extent and severity of health damage
increases as exposure to the toxic agent increases. A description of
the relation between exposure and injury is the critical element in
the health evaluation process.
Evaluation of data for purposes of characterizing the toxic at-
tributes of chemical substances and the exposure-response relation-
ship requires experts in the science of toxicology. Such data come in
a wide variety of forms and can vary widely in quality and the ex-
tent to which they can be applied in exposure situations not iden-
tical to those in which they were developed. Fortunately, most of
the substances likely to be found at hazardous waste sites have
already been subject to the necessary expert evaluation, usually in
connection with their regulation in other situations. These expert
evaluations of toxicity data can form the basis for the evaluation
process to be used in connection with remedial action planning, al-
though results of these analyses in other contexts cannot be directly
applied to the present task.
Substances that Are Not Carcinogenic
A threshold dose is the amount of a substance minimally
necessary to produce an adverse effect. For most substances, a
threshold in experimental animals can be approximated by the "no
observable adverse effect level" (NOAEL). The NOAEL is the
maximum experimental dose at which no toxic effects are observed.
The experimental NOAEL cannot, however, be taken directly as
the human threshold dose. It is known that thresholds vary among
RISK/DECISION ANALYSIS
401
-------
individuals and that the variability in the human population is
much greater than it is for small populations of experimental sub-
jects.1'2 For this reason, and also to compensate for inadequacies in
the toxicity data and to adjust for differences between the condi-
tions of exposure under which toxicity data were collected (usually
animals under controlled conditions) and the conditions under
which they will be used (humans under vastly different conditions),
it has become common practice to divide the experimental NOAEL
by an uncertainty factor to estimate the dose considered tolerable
for the general human population. The magnitude of the uncertain-
ty factor varies and is a function of the data available on a specific
substance.3
For purposes of the scheme described in this paper, the accep-
table human intake derived by this procedure will be called the ac-
ceptable daily intake for the general population (ADI). This term
has long been used to describe acceptable intakes of food and color
additives and pesticide residues.
The tolerable human dose estimated by this procedure (ADI) is
not a dividing line between "safe" and "unsafe" exposures. In
fact, there is no way to identify such a dividing line. It should rather
be thought of as an estimate of the dose that is likely to be low
enough to prevent health damage in most members of the general
population under most circumstances, but which has to be further
adjusted depending upon specific circumstances. In the case of con-
taminants at hazardous waste sites, additional safety factors may
have to be incorporated to take into account circumstances at a
site.* Moreover, because individuals near hazardous waste sites
may be simultaneously exposed through air and water and perhaps
soil, the specific acceptable intakes through each of these media
will have to be established so that the total human intake from all
media does not exceed the acceptable intake.
For these reasons, and because the cost-effectiveness of remedial
action plans will be site-dependent, acceptable intakes of
substances remaining in various media after remedial action at
hazardous waste sites will vary from site to site, even though the
general methodology of health evaluation will be the same for all
sites.
Carcinogens
Carcinogens, many of which appear to lack definable thresholds,
are evaluated somewhat differently from threshold agents.1>2'4 The
evaluation consists first of making an explicit determination of risk
as a function of dose. Risk is the probability that cancer will be pro-
duced and thus takes values from zero to one. The application of
current methods of risk assessment will yield an estimate of risk as a
function of dose. This is usually expressed as the risk for each unit
of dose: unit carcinogenic risk (UCR). The risk at a specific dose
can then be easily estimated by multiplying the UCR by the dose.
The decision on tolerable intakes then rests on a policy determina-
tion of the risk thought to be tolerable at a specific site.
Although carcinogens may pose risks at all finite exposure levels,
there is a wide range of very low risks usually considered to be of
negligible health consequence. Moreover, the methods now used to
estimate carcinogenic risk yield upper bounds on risk and it can
reasonably be assumed that the actual risk will be lower, and
perhaps very much lower, than the estimated risk.4 In any event,
because there is no sharp division between tolerable and intolerable
risks, the residual risk from carcinogens can vary from site to site
depending on local circumstances. Thus, as in the case of non-
carcinogens and for many of the same reasons, residual acceptable
environmental concentrations at different sites will vary even
though the methods used to arrive at these concentrations will be
uniformly applied at all sites.
•There may be circumstances in which the ADI derived for the general population may be un-
necessarily Icm Thus, healthy worker populations may be able to tolerate higher doses than the
genera! population
Steps in the Evaluation Process
Given this background, the major steps in the evaluation process
can be summarized as follows:
•For each substance to be individually evaluated,}: determine the
DHD resulting from each alternative remedial action plan.
•For each substance, consult the toxicity and carcinogenicity data
and identify the ADI and the UCR.
•For each substance, adjust the ADI to suit the specific cir-
cumstances at the site.
•The adjusted ADI will be termed the site-specific acceptable daily
intake (SADI).
•For each substance perform the following:
(1) Compare DHD to the SADI
(2) For carcinogens, multiply the DHD times the UCR to cal-
culate risk
•Eliminate all remedial action alternatives in which any one of
the following conditions holds for any single substance:
(1) DHD exceed SADI
(2) Carcinogenic risk exceeds a given level which has been de-
termined to be tolerable
•Evaluate all the remaining remedial action alternatives and iden-
tify the alterative that achieves, at lowest cost, the maximum
difference between:
(1) DHD and SADI
(2) Calculated carcinogenic risk and the selected tolerable car-
cinogenic risk.
tit will be shown in later sections of this paper that, while the number and identity of substance! pre-
sent at the site need to be known, only a selected few of these will have to be Individually evaluated.
SELECTION OF SUBSTANCES FOR EVALUATION
Hazardous waste sites contain many substances and it is imprac-
tical to perform health evaluations on all of those present. Rather,
evaluations will be conducted on selected substances and the results
of these then generalized to the entire collection of substances pre-
sent at a site and likely to continue entering the surrounding en-
vironment following remedial action.
Because the only practical approach is the selective one, there is a
risk that the likely extent of health damage predicted by the
methods presented here will be underestimated. The only practical
adjustment for this possibility is the addition of safety factors, tne
magnitude of which depend on the number of substances present
and any knowledge of specific interactions among these substances
that might exacerbate their effects.
In most circumstances it is probably not practical to select more
than a few individual substances for evaluation. This determination
will have to be site-specific and will have to be made after the
following preliminary information is gathered:
•The total number of substances present
•The quantity of each
•The likelihood of their escape from the site and their stability in
the environment
•Their lexicological characteristics
Generally, those substances whose chemical identities are well-
defined, which are present in large amounts, which are likely to
escape into the environment and persist there and which have at
least moderate toxicity should be selected for full evaluation. In
some cases, substances displaying these attributes but which IK
present in relatively small amounts should be selected if their tox-
icities are high. Specific decision rules for selecting substances for
evaluation can be devised based on these principles.
EXPOSURE ANALYSIS: ESTIMATION OF DHD
The application of various environmental modeling technique*
will produce estimates of the concentrations of each of the
substances selected for evaluation in air, water and soil in regiOOl
where human contact is expected to occur at the time remedial «•
402
RISK/DECISION ANALYSIS
-------
tion is taken and in the years following such action. These estimates
will have to be produced for each alternative remedial action plan.
These residual environmental concentrations are the starting point
for the calculation of DHD. Although a discussion of the en-
vironmental modeling techniques is beyond the scope of this paper,
they have been extensively used and their limitations are well
understood.5'6
Environmental Concentrations
To be useful for the health evaluation, the environmental con-
centrations produced by modeling exercise will be estimated in
various media at the likely point of human contact. These concen-
trations can be used to estimate the DHD.
Human Dose: Defining Routes of Exposure
The medium in which a substance is present will determine the
route of human exposure, i.e., the route by which the DHD will be
received. Substances present in water may be ingested. Con-
taminated water may also lead to inhalation exposure when water is
used for cooking or showering, although this exposure route is like-
ly to be minor unless the contaminant is poorly water soluble and
highly volatile. Further ingestion may occur if fish are present in
contaminated water and used as food. Substances present in air
because of volatilization in the environment (outside the home) will
be inhaled. Substances present in soil may be adsorbed through the
skin if there is direct contact with soil, this route may be especially
important for children. Substances in soil may also be taken in by
plants; human exposure could result if these plants are used as food
or if these plants are fed to livestock, the various products of which
are used as food (meat, milk, eggs).5'6
Some of these routes of exposure may be important and others
may not; moreover, the relative importance of the various routes
will depend on circumstances at a specific site. For example, sites
near areas where there is extensive farming or commercial or
recreational fishing will display quite different exposure route pro-
files than those near heavily populated areas.
It is for these reasons that the health evaluator must work closely
with the environmental modeler to identify populations at potential
risk and the various routes by which they may be exposed. In many
circumstances the exposure modeler may not be able to predict ex-
posure in quantitative terms but may, nevertheless, be able to
demonstrate that a particular route of exposure is likely to occur.
Such circumstances should always be recorded, because it may be
necessary to incorporate additional safety factors to compensate
for lack of certainty in these areas.
Human Dose: Identifying Populations at Risk
One of the critical factors in health evaluation is the nature of the
population at risk. The ADI and the UCR will be determined on the
assumption that it is the general population that is to be protected
rather than any special subpopulation (e.g., healthy adult workers).
It is expected that in most circumstances populations at potential
risk from hazardous waste sites will be the general population and
that no special subgroups will be present and require special atten-
tion. Moreover, because it is the individual that is to be protected,
it will not be necessary to collect information on the size of the
populations at potential risk. This is probably the appropriate
choice, since it will generally not be possible to predict population
changes many years into the future.
There may, however, be circumstances in which unusual toxic
properties of certain substances may put certain subpopulations at
especially high risk. For each substance to be evaluated, it is,
therefore, essential to consult the toxicological data to determine
whether any such special circumstances might exist and whether it
is, therefore, necessary to make a special effort to determine if
there are unusually high proportions of individuals at special risk
among the general population present near a specific site.1'7
Subpopulations at high potential risk because of unusually high
exposure will be taken into account because the exposure model is
designed to yield estimates of concentrations for such groups.
Human Dose: Estimation of Intake (DHD)
Dose is the amount of a substance taken into the body per unit of
body weight per unit of time. The usual expression of dose is
mg/kg body weight/day. To calculate the DHD for each substance,
the dose obtained by each route of exposure is first calculated, and
then the total dose is obtained by adding the route-specific doses.
There will be some substances for which it is inappropriate to add
doses from different routes because the toxic properties of the
substance depend on the route of exposure. A full understanding of
the toxicity is necessary to decide when it is appropriate to combine
exposures from several routes.
The method for calculating dose depends on the route of ex-
posure. For example, to calculate dose from ingestion of a drinking
water contaminant, it is necessary to know the concentration of the
substance in water, the volume of water consumed each day, the
fraction of the substance present in water that is absorbed through
the walls of the gastrointestinal tract and the weight of the person
consuming the water. For substances that are inhaled or that pass
through the skin, different factors (e.g., breathing rates, skin
penetration rates, etc.) determine dose.
There are various methods available to calculate dose for each of
the three routes of exposure. These methods are based on certain
assumptions and data that have long been used in various USEPA
programs and in the programs of the federal health agencies.5'6 The
formulas assume knowledge of environmental concentrations
(mg/J. for water; mg/m' for air; and mg/kg for soil and for food).
The DHD is expressed in units of mg/kg body weight/day.
HEALTH EVALUATION
ADI and UCR
It will be necessary to have available toxicity profiles of the
substances to be evaluated. The NOAELs, directly available from
experimental data or estimated therefrom, are divided by uncer-
tainty factors to estimate the ADI. The UCR is obtained for car-
cinogens by application of certain mathematical models to car-
cinogenicity dose-response data. Expert toxicologists are required
to perform the necessary data analyses.
The units for these measures of toxicity are mg/kg body weight/
day for the ADI and risk for a dose of one (1) mg/kg body weight/
day for the UCR. For a few substances, the form of toxicity
depends on the route of exposure (e.g., dusts in nickel refineries
cause lung cancer when inhaled but nickel and its compounds do
not appear to display this form of toxicity when ingested). The tox-
icity profiles should note such circumstances, should specify the
route(s) of exposure for which a given ADI or UCR can be con-
sidered appropriate and the routes for which they would be con-
sidered inappropriate.
SADI and Tolerable Carcinogenic Risk
For carcinogens, the dose considered tolerable for exposures
resulting from a given hazardous waste site is a function of the
magnitude of risk that is considered tolerable given the relative
costs of achieving various levels of risk. A maximum lifetime risk
goal of 1 in 1,000,000 is chosen as the starting point for the analysis
presented here, although other low risk levels could be selected.
The relative costs of various remedial options are considered in
relation to how much they reduce risk below this level. Thus, the
goal is to ensure that the risk be below 1 in 1,000,000. The methods
for making this evaluation are presented in the next subsection.
For non-carcinogens, the minimum goal is the site-specific accep-
table intake (SADI) which is either equal to or less than the ADI.
The SADI is derived by dividing the ADI by various safety factors.
The conditions present at a specific site determine the magnitude of
the safety factors.
Perhaps the most important factor in determining the need for
and the magnitude of safety factors is the number of substances
present at a site other than those that have been evaluated. The
potential for interactions having adverse health consequences in-
RISK/DECISION ANALYSIS
403
-------
creases as the number of substances to which individuals may be ex-
posed increases. A systematic means for determining the magnitude
of safety factors is needed to compensate for this uncertainty in the
analysis.
There may be additional factors, such as the presence of specially
sensitive subpopulations, that require the further addition of safety
factors at specific sites. The SADI is then derived for each
substance at each site.
Finally, there may be sites at which two or more carcinogens are
present. In such cases, the maximum tolerable risk of 1 in 1,000,000
will be ensured only if the risk produced by each carcinogen is less
than the maximum and the total produced by all carcinogens is
equal to or less than 1 in 1,000,000. In the absence of other infor-
mation, it might be assumed that the risks from carcinogens are ad-
ditive.
Evaluation of Alternative Remedial Action Plans
Organization of Data
The data have now been assembled to permit determination of
the relative degree of protection offered by each of the remedial ac-
tion plans under consideration. For each alternative plan, the
following comparisons are made:
•For each substance, the quantitative relationship between DHD
and SADI
•For each carcinogen, multiply the DHD by the UCR to calculate
the risk. Add the risks for all carcinogens evaluated and calculate
the total carcinogenic risk.
Elimination of Inadequate Action Plans
Any remedial action plan that does not meet the following
criteria should be eliminated from consideration:
•DHD greater than SADI or
•Total carcinogenic risk greater than 1 in 1,000,000.
The criterion of maximum achieveable health protection at
lowest cost requires consideration of the relative degrees of health
protection offered by alternative plans. As the evaluation scheme
has been designed, this determination is relatively straightforward,
at least in concept, and can be summarized as follows:
Remedial action plans that result in the greatest numerical
difference between SADI and DHD and between the total
carcinogenic risk and a risk of 1 in 1,000,000 provide the
greatest degree of protection.
Because several different substances are ordinarily evaluated,
and because the numerical differences will be substance-specific,
estimation of differences for the total collection of substances is
complex and requires a means of integrating such differences.
However, such schemes can be developed, based on the principle
stated above, to rank remedial action plans according to the degree
of health protection they afford. This ranking can then be used as a
basis for determining which plans offer the greatest protection at
the lowest cost.
CONCLUSIONS
In the interest of presenting a practical guide to incorporating a
public health analysis into remedial action planning, the imperfec-
tions and uncertainties in the proposed scheme have been ignored.
However, these imperfections and uncertainties are not much
greater in the context described here than they are in other areas of
environmental risk assessments.
It is better to use an imperfect scheme for the public health
evaluation process than to make remedial action decisions without
explicit regard to the degree of public health protection being
achieved. Use of the proposed scheme will not only permit the
remedial action planner to state that the most cost-effective
scheme—as judged by the best available assessment
technology—has been found for a specific site, but also that the
public health has been adequately considered in advance of action.
If the latter is not done, it will be very difficult to substantiate the
view that a chosen remedial plan is truly protective of the public
health.
REFERENCES
1. National Academy of Sciences, "Drinking Water and Health." Vol. 3.
Safe Drinking Water Commission, National Academy Press, Wash-
ington, D.C. 1980.
2. Food Safety Council, "Quantitative Risk Assessment," Food Cosmet,
Toxicol. 18, 1980,711-734.
3. Calabrese, E., Principles of Animal Extrapolation, John Wiley & Sons,
New York, 1983, 529-566.
4. National Academy of Sciences, "Risk Assessment in the Federal Gov-
ernment: Managing the Process," National Academy Press, Washing-
ton, D.C. 1983.
5. Baughman, G.L. and Burno, L.A., "Transport and transportation of
chemicals: a perspective," The Handbook of Environmental Chem-
istry. Vol. 2. Part A. Hutzinger, A. (ed.) Springer-Verlag, New York,
1982.
6. Jenni, E.A., Ed., Chemical Modeling in Aqueous Systems. ACS Sym-
posium Services, No. 93. American Chemical Society, Washington,
D.C. 1979.
7. Interagency Regulatory Liaison Group, "Scientific basis for identifi-
cation of potential carcinogens and estimation of risks," J. Nat. Cancer
Inst., 63, 1979, 241-268.
404
RISK/DECISION ANALYSIS
-------
RISK ACCEPTABILITY FOR HANDLING, ANALYSIS AND
DISPOSAL OF DIOXIN IN A LABORATORY
CHIA SHUN SHIH, Ph.D.
University of Texas at San Antonio
San Antonio, Texas
INTRODUCTION
Dioxin contamination and cleanup has become one of the most
volatile and controversial issues in the Missouri-Kansas area. This is
due both to the toxicity of the dioxin and its widespread contamina-
tion in over 60 different locations. In addition to pollution of the
environment, there is also the potential risk to laboratory personnel
and the surrounding community near the center which is handling
and processing the dioxin samples.
In this paper, the author focuses on a method of estimating the
risks and the evaluation of risk acceptability for laboratory person-
nel, co-workers and the surrounding community involved in hand-
ling and analyzing TCDD samples received from contaminated
areas. The method, based on Revealed Preference techniques as
originally proposed by Rowe1 has been utilized with some modifica-
tions.
RISK ACCEPTABILITY
Risk Acceptability is concerned with the determination of the
specific level of safety measures required by the affected society for
specific risk situations. In this case, the risk situation is the TCDD
sample process and analysis at a regional sample processing and
analysis laboratory.
To develop a range of potential risk situations, laboratory pro-
cedures followed were those used by USEPA laboratories and their
contractors, beginning with sample packaging in the field and con-
tinuing through the final disposal of the TCDD sample residue. In
addition, it was assumed that the laboratory was located in a
populated office/residential complex. The basic risk elements in-
cluded the following key steps of the risk pathways (Figure 1):
•Sample packing in the field
•Trans-shipment of packaged sample
•Pre-analysis storage
•Sample cataloguing or inventory
•Extraction and cleaning of the sample in the laboratory
•Concentration and digestion for 2,3,7,8-TCDD
•GC/MS sample preparation
•Intra-laboratory transport of the prepared concentrates of dioxin
•GC/MS analysis
•Data log-in for the computer
•Disposal of the residue of sample and wastewater
•Contamination of the air in the building and to the surrounding
community
RISK ESTIMATIONS
To prepare for the risk estimation analysis, a series of alternative
risk scenarios was developed (Figure 2). In developing the risk
scenarios, alternative risk occurrence pathways and exposure situa-
tions for the laboratory personnel, the co-workers in the building
and the surrounding communities were considered.
To illustrate the risk relationship between potential hazards and
events that may result from contamination to laboratory personnel,
co-workers located in the same building and the surrounding
populace, a fault tree was constructed.
Contamination pathways for the dioxin may include one or more
independent pathways. This is clearly delineated by the separate
pathway columns in the fault tree. The hierarchy of the fault tree
structure is established by the horizontal levels in the fault tree.
The mathematical relationship quantifying the probability of
dioxin contamination during its sample analysis was developed
based on the accompanying fault tree and the assigned probability
values of specific events as designated by the alpha-numeric
variables printed next to the event in the fault tree. The fault tree
formula is as follows:
P(T)
WHERE
P(A2)
P(A2)+P(A+)+Any combination of
(A2.B2.C2 . . .G2)
• P(A2a)[P(A2al/A2a+P(A2a2/A2a)]
+P(A2b)P(A2bl/A2b)
+P(A2c)[P(A2cl/A2c)+P(A2c2/A2c)]
+P(A2c)P(A2cl/A2c) P(A2c2/A2cl)
P(A+) = P(B2)+P(B+)
3
P(B2) = P(B2a)= p(B2ai/B2a)
+P(B2b) ^=1 P(B2bi/B2b)
+P(B2c) ^=1P(B2ci/B2c)
P(B+) = P(C2)+P(C+)
P(C2a)j P(C2ai/C2a)
P(C2) +P(C2bVT(C2bl/C2b)
+P(C2c) =P(C2ci/C2c)
P(C+) = P(D2)+P(D+)
P(C2) = P(D2a) 1L1P(D2ai/D2a)
+P(D2b) P(D2bl/D2b)
+P(D2c) P(D2cl/D2c)
RISK/DECISION ANALYSIS
405
-------
P(D-t-) - P(E2) + P(E+)
P(E2) • P(E2a) I . P(E2ai/E2a)
+P(E2b) P\E2b /E2b)
2
+P(E2c) fml P(E2cl/E2c)
P(E+) - P(F2)+P(F+)
P(F2) - P(F2a) £ml P(F2al/F2a)
+P(F2b) fml P(F2bi/F2b)
+P(F2c) P(F2cl/F2c)
P(F + ) - P(G2a)
+P(G2b)
+P(G2c)
P(G2ai/G2a)
1 P(G2bi/G2b)
P(G2ci/G2c)
The variables used to define specific events are consistent with
the designation of tree branches in the event tree (Figure 2). For in-
stance, A2 designates the event of contamination due to the sample
packaging and A2a designates the event of contamination caused
by the contaminated vermiculite and/or plastic bags used in the
packing. The only unique events included in the fault tree analysis
are those events associated with the final consequences of the diox-
in contamination such as events A2cl or A2c2.
Based on this fault tree analysis, the probability of occurrence
for each of the potential dioxin contamination scenarios during its
routine through the processing laboratory was evaluated. However,
as historical data which can be directly utilized to provide a basis
for such assessments is almost non-existent for most of the events,
many of the values given for each of the individual events are based
primarily on subjective judgments. Others are based on the values
used for similar situations in the chemical industry.
Rationale for Assessing Probability Values
With few exceptions, most of the TCDD samples are in solid
form. Because of the TCDD's low solubility and high adhesion to
soil particles, it is not likely to be separated from the soil in any
media. Meanwhile, the undeniable facts do suggest that TCDD is
Sample Packaging
on Site
Trans-shipment of
Packaged Samples
Sample Cataloguing
and Inventory
Extraction & Cleaninc
for Dioxin
Concentration
Digestion for
Dioxin
Intra-Lab
Transport
of Concentrate
Temporary Storage
To Storage •*-
Sample
Residue
Disposal
To Air
I
A1r
Emission
f
GC/MS Sample
Preparation
Intra-Lab
Transport
of Syringes
GC/MS
Analysis
Computer Data
Incut
Hastewater
Discharge
To Sewer
Figure 1
Elements of Risk for Dioxin Analysis
406
RISK/DECISION ANALYSIS
-------
FAULT TREE
T: Contamination
A2: ContaalMted
Packaging,
GO
\
O
w
o
GO
>— i
O
00
So
h2c: Sample
Damage
A2cl: Con-
taalaated
Venlcullte
A2c2: Cont-
amloatin to
Worker*
-------
»*™^Q
Figure 2
Event Tree for Risk Scenarios (1/4)
Figure 2
Event Tree for Risk Scenarios (2/4)
408 RISK/DECISION ANALYSIS
-------
GC/MS
Analysts
Figure 2
Event Tree for Risk Scenarios (3/4)
Alr/Bater
Discharge
Contamination to Voluntary Ubrkcn
Contamination to Iftvoluntan
Co-Workers
Contamination to IndlvlduaU In
ttw Surroundlnf Comwiltv
Cont«AlMlton to th« CnvlroMwnt
Contf«ln«tlon to
Voluntary Worker*
loA to
Involuntary Co-vork*r»
Contamination to lndtvl~
dualt In th«
Surrounding Comnunlty
Contanlnatlon to th*
Environment
Contamination to
Voluntary Worker*
Contamination to
Involuntary Co-Workeri
Contamination to Indivi-
duals In the
Surrounding Comnunlty
Contamination to the
Environment
Contamination to
Voluntary Worken
Contamination to
Involuntary Co-Workers
Contamination to Indivi-
duals In the
Surrounding Community
Contamination to the
Environment
Figure 2
Event Tree for Risk Scenarios (4/4)
RISK/DECISION ANALYSIS
409
-------
quite persistent in its existence, and it appears unlikely to be
degraded by itself. Therefore, the TCDD contamination to any ex-
posed person will generally result from inhalation, ingestion or ab-
sorption through the skin.
Potential Routes of Contamination
Inhalation
TCDD contaminated dust and TCDD vapors generated during
the sample analysis procedure may accumulate in the air through
the existing air circulation systems. Levels would be higher than
those occurring where there is much better ventilation.
Direct Ingestion
Dust which settles on food or dirt on hands and is then trans-
ferred to the mouth could be ingested. This route would be of par-
ticular concern where non-voluntary co-workers, without the
knowledge of specific spills or contamination, are involved.
However, exposure that occurs via this route may vary considerably
among individuals depending on their behavior regarding protec-
tion of food, washing of hands, etc. The judgmental value of prob-
ability placed upon this direct ingestion route is very shaky and its
accuracy can be seriously questioned.
Absorption through the Skin
Dust which settles on exposed skin and direct contact with the
dirt provides opportunities for TCDD to be absorbed through the
skin. However, this route for exposure in the laboratory is affected
by the following considerations:
•Most of the skin area of the lab personnel is covered by clothing
•The contact time, if any, may be very short
•TCDD cannot pass through the skin unless it is removed from the
dust particles. Consequently, this route may be considered mini-
mal when compared with all of the other possibilities
Other Potential Exposures
•Direct contact with TCDD when it is concentrated in the solvents
•Inhalation of fumes of TCDD while it is being extracted, digested
and concentrated
•Direct contact of TCDD by non-workers or involuntary co-
workers because of improper handling of the sample residues or
the pre-inventory samples
In view of all the potential routes of the various TCDD exposure
pathways, the air transport route would probably cause the highest
or the most severe exposure levels.
Estimation of TCDD Concentrations in the Air
Though laboratory and personnel movement play an important
role, for this exercise the following are utilized: dust levels inside
the laboratory building are generally low; the activity of people in-
side and outside the restricted rooms is moderate, causing
minimum air turbulence or physical agitation of the dirt and subse-
quent escape of the dirt from the central area; the building is well
ventilated, with the supply air intake point located downstream
along the prevailing wind of the exhaust point of the returning air;
and the ventilation could create some recycling of the exhaust air
and accumulation of the contaminated dust particles.
The TCDD levels in the soil were found to range from 70 to 200
ppb. It was assumed that the total dust levels ranged from 0.4 to 1.0
mg/m3. Assuming the TCDD levels in the dust particles are the
same as in the soil, the concentration of TCDD in the air = TCDD
concentration in soil x total particulate concentration in air = 3 x
10-" to 2 x 10-7 mg/m3.
The low vapor pressure of TCDD has been widely assumed to in-
dicate that very little TCDD would evaporate from contaminated
soil. However, many investigators are now discovering that low
vapor pressure compounds which also have low water solubility
evaporate more readily from soil, thus TCDD may have an en-
hanced ventilation rate from the samples, particularly after it has
been cleaned, extracted, digested and concentrated. For these
reasons, it was assumed that the vapor pressure of TCDD may be
much higher than 10~6 mm of mercury. All these facts suggest that
TCDD vapors could cause exposure inside the poorly ventilated
rooms.
Table 1
Estimate of Probability Values
P{A2a) • 10"3
P(A2al/A2a) •
P(A2a2/A2a) •
P(A2b) • 10'6
P(A2bl/A2b) •
P(A2c) • 10'6
P(A2cl/A2c) •
P(A2c2/A2c)
P(A2c2/A2cl) •
P(B2a) • ID"4
P(B2al/B2a) •
P(B2a2/B2a) •
P(B2a3/B2a) •
P(B2b) • ID'5
P(B2bl/B2b) -
P(B2b2/B2b) •
-10-5
0.1
o.oi-
o.i-
-10-8
o.i-
• n.
• 0.1
10-2-
10-2
10-3
10-2
10-3
0.01
• io-4
0.01
0.01
m- in-4
-o.oi
• 10-3
-10-3
•io-4
-10-3
-io-4
P(B2c) • 10'4
P(B2cl/B2c) -
P(B2c2/B2c) »
P(C2a) * 10'4
P(C2al/C2a) -
P(C2a2/C2a) -
P(C2b) ' lO"6
P(C2bl/C2b) •
P(C2c) • 10'6
P(C2cl/C2c) -
P(C2e2/C2c) •
P(C2c3/C2c) •
P(C2c4/C2c) -
P(02a) • 10'4
P(02al/D2a) -
P(D2a2/D2a) •
P(02b) • 1 -3
10-5
10-2-
io-4-
io-6
lo-1-
10-2-
-10-7
10-3-
-10-7
10-3-
io-4-
10-6-
10-7-
io-6
10-'-
io-3-
lO-5
io-4
IO-6
10-3
10-4
io-4
10-5
ID"6
io-7
10-8
1
10-3
iir*
P(D2bl/02b) '
P(D2c) « ID'3
P(D2cl/D2c) *
P(E2a) « ID'4
P(E2al/E2a) •
P(E2a2/E2a) •
P(E2a3/E2a) •
P(E2b) • 10-2
P(E2bl/E2b) •
P(E2c) - ID'2
P(E2cl/E2c) •
P(E2cl/E2c) •
P(F2a) • ID'3
P(F2al/F2a) •
P(F2a2/F2a) •
P(F2a3/F2a) -
10-3-
io-4
10-2-
io-6
10'1-
10-2-
io-4
10-3
10-2
ID'3
10"4 -lO-5
-10-3
10'1 -10-3
-io-3
io-1 -
lO'1-
-lo-4
ID'2-
lo-1-
10-3-
ID'2
ID'2
P(F2b) • ID'5
P(F2bl/F2b) •
P(F2bR/F?b)
P(F2c) - 10'4
P(F2c1/F2c) •
P(G2a) - 10'1
P(G2al/G2a) •
PG2a2/G2a) •
P(G2b) • 10"3
P(G2bl/G2b) •
P(G2b2/G2b) -
P(G2b3/G2b) •
-ID'6
10-2-
ID'3
« in-3 - io"4
-io-s
10-2-
-10-2
io-3-
10-3
io-4
io"4- io'6
-ID'5
10-3-
10-5-
10"6 -
io-4
ID'6
io-7
P(G2c) • ID'5- 10-6
10-3
ID'3
io-4
P(G2cl/G2c) •
P(G2c2/G2c) •
P(G2c3/G2c) •
, lO"3 -
, 10*5 .
' 10"6 -
io-4
ID'*
io-7
410
RISK/DECISION ANALYSIS
-------
The toxicity of the TCDD to animals is fairly well documented;
extrapolation of these effects to humans is unknown. Consequent-
ly, the risk ratios of TCDD to human health cannot be quantified.
Therefore, it is assumed that its risk ratio is in the range of 200 to
300, which is the same as the worst ratios for vinyl chloride.
Estimates of the probability values are based on the in-
vestigators' perception of the likelihood of occurrence of the events
in consideration and should lean toward the conservative side.
Conditional probability values following each of the key events are
also based on the investigators' judgments. In order to compensate
for the uncertainties of these judgmental values, a fairly liberal
range is given for each of the probability values. A subsequent sen-
sitivity analysis for selected events should be conducted to assess
the resultant probability of the contamination to both lab person-
nel and the community and the sensitivity of the various assumed
values.
RISK ACCEPTABILITY
In order to assess the acceptability of the risk associated with the
dioxin laboratory analyses for both the laboratory personnel direct-
ly and indirectly involved and for the surrounding community,
basic characteristics of the risk in terms of the probability of occur-
rence and the potential consequent to both individuals and the
society must be analyzed in detail. First, the basic characteristics of
the risk must be defined and delineated. Second, the incremental
risk acceptance value for each of the risks identified in terms of risk
referent shall be developed. Finally, the objective risk value com-
puted, based on the potential consequence, should be compared
with the risk referent value to determine the acceptability of the
current practice.
Based on the risk classification as outlined in Table 2, the risks
associated with the dioxin laboratory analysis can be characterized
as immediate statistical accidents and categorized as follows:
•Risk for the laboratory personnel specifically assigned to the di-
oxin analysis: ordinary voluntary risk.
•Risk for the co-workers located in the same building: ordinary
voluntary regulated risk.
•Risk for the surrounding community of the USEPA Region VII
laboratory: ordinary involuntary risk.
The procedures to be followed for the determination of risk ac-
ceptability for the TCDD processing centers are:
•Develop an appropriate risk classification scheme.
•Determine the risk reference value for each class of risk encoun-
tered in the dioxin analysis procedures
•Compute risk referents for each class of risk
•Compare the estimated risk from fault tree analysis with the risk
referent values
In view of the risks confronted by different sectors of population
in the laboratory and its surroundings, appropriate risk classifica-
tions developed for each sector of the population are summarized
in Table 3. The dioxin analysis is essentially a typical man-
originated, ordinary event. However, since the reliability and
statistical validity of existing data characterizing various conse-
quences of the dioxin exposure accidents are absent, only piecemeal
information covering personal injuries and immobility could be
collected and reviewed. Thus, the risk reference value characteriz-
ing the personal injury in terms of health effects per year is the only
consequence included in the risk acceptability evaluation as shown
in Table 3. In fact, based on limited data, personal injury seems to
be the only visible and pronounced consequence due to dioxin ex-
posure being reported so far.
Table 3
Summary of Risk References for Dioxin Exposure in Laboratory
Type of Risk
Personal injury or
immobility for laboratory
workers
Personal injury or
immobility for co-workers
in the laboratory
Personal injury to the
population in local
community
Risk Classification
Voluntary, ordinary
man originated
ordinary regulated
voluntary man
originated
ordinary involuntary,
man originated
Risk Reference
(rath. Eff./Yr.)
3 x 10-1
6x 10-2
3x 10-5
Table 2
Risk References for Immediate Statistical Accidents
Ilik
Cluilfleielon
naturally
Occurring!
Catai tropic i
Ordinary)
"an Trigger*!
Cataitrophic-
Involuntary
Volulntary
Ordinary
Involuntary
Voluntary
'egulated
Voluntary
ratallttaa
far
Tear
1 z 10
7 X 10
Han Originated
Cataatrophic-
tnvoluntary
Voluntary
>*julatad
Voluntary
Ordinary-
Involuntary
Voluntary
Itgulated
Voluntary
1
2
j
S
1
1
x
x
X
X
X
>
10"7
10"'
10"5
10~*
10"4
10"4
I * 10 '
4 x 10"°
1 x 10"!
1 x 10 J
2 x 10"*
COA««qU«IlC«>
•••1th Affacts Prop. Daug* Reduction of
$/P«r Lif« Span
Year f««r (Y««r*)
S x 10
4 x 10*
S x 10"'
2.x 10"s
-5
1 x 10
} x 10
« x 10"'
C x 10"2
i x io:6
4 xlO 6
0.02
3
2 x 10-'
.4
1
200
JO
O.I
1 x 10
0.2
,-J
1 x 10"
4 x 10"
( x 10
1 x 10
0.1
0.1
C x 10"
3 x 10
Source: Rowe, W., An Anatomy of Risk, John Wiley & Sons, New York, 1977.
OBTAINING RISK REFERENT VALUES:
These risk reference values are estimated directly from historical
and societal risk data that are analogous to the situations and con-
sequences involved in dioxin analysis. Transforming the risk
reference values into appropriate risk referents requires the follow-
ing four steps:
•Determine the appropriate risk proportionality factor (Fl) which
incorporates the societal attitude due to its expectations associated
with the degree of voluntarism of the affected population.
•Determine the appropriate risk proportionality derating factor
(F2) which discounts the existing societal risk acceptable level
due to the indirect benefit/cost balance considerations for the di-
oxin exposure via laboratory analysis (Table 4).
•Develop and quantify the risk controllability factor (F3) which
characterizes the basic control approach, the degree of control,
the state of implementation and the judgment of control effective-
ness (Table 5).
•Determine the referent using the factors derived in the above
three steps by the formula:
risk referent = (risk reference) x Fl x F2 x F2
These factors are subjective.
The first two factors address the inherent propensity of effected
populations to take risks and also incorporates the additional deci-
sion dimension of indirect benefits/cost balance. This
acknowledges the tendency of people to accept higher levels of risk
when the potential benefits far outweigh the potential costs. On the
other hand, people may become increasingly risk aversive when the
potential benefits are likely to be offset by the costs.
RISK/DECISION ANALYSIS
411
-------
The risk proportionality and its derating factors, as determined
for different sectors of populations, are shown in Table 4. Though
not to the same degree, the controllability factor is also found to be
varied due to the target population, as shown in Table 5.
Incorporating all the factors determined above, the appropriate
risk referents for different affected population sectors are derived
as shown in Table 6.
Table 4
Risk Proportionality and Risk Proportionality Derating Factor
Factor
Proportionality Factor
Derating Factor
Laboratory Worker
Co-Worker in the Building
Surrounding Community
Value
1.0
0.2
0.1
0.1
Table 5
Controlability Factor
Control
Approach Control
Laboratory Worker 1.0 1.0
Co-Workers in the
Building 0.5 1.0
Surrounding
Degree of State of
Control
Implementa. Effectiveness
0.5 1.0
Community
0.3
0.3
0.5
0.1
1.0
0.5
Table 6
Risk Referents and Estimated Maximum Risks
Population
Sector
USEPA Lab
Personnel
USEPA Co-
Workers in the
Same Building
Surrounding
Community
Risk
Reference
3 x 10-1
6x 10-2
3 x 10-5
Risk
Reference
3x 10-2
1.5 x 10-3
1.4 x 10-8
Est. Max.
Risk
3.2 x 10-3
1.2 x 10-3
1.1 x 10-6
RESULTS
On the basis of the above judgments and limited data, the risk
referent values versus the estimated v???s???c??? the risks for both
laboratory workers and their co-workers in USEPA are considered
to be acceptable. On the other hand, the risks for the surrounding
community may be marginally acceptable.
Sensitivity
All the values shown in Table 6 are based on a very conservative
judgment for the occurrence of all potential accidents described in
the fault tree. A difference of magnitude in the order of two to
three may still be within the range of cumulative errors. Thus, in
reality, the risk estimated for the community may be too high and it
is therefore considered to be marginally acceptable.
For the facility considered, the sensitivity analysis for selected
fault events indicates that with minimum modification of sample
inventory, disposal procedures and paniculate air filters, the risk to
the community could be significantly reduced.
Specifically, the modifications are:
•Collect all liquid wastes from the dioxin analysis laboratory and
release it into the sewer only after its concentration of dioxin has
been confirmed to be below the allowable level.
•Install efficient filters for the air exhaust system of the analytical
laboratories used for dioxin.
•Institute and maintain an organized and strict procedure for the
disposal and inventory of sample residues.
Based on the investigators' analysis, the above modifications
would reduce the risk to the community to 1.1 x 108 which is well
within the acceptable level. In addition, maximum estimated risk
for the co-workers may be lowered from 1.2 x 103 to 2.1 x 104 which
is well below the acceptable level of 1.5 x 103.
CONCLUSIONS
Risk assessment for the potential hazards to lab workers, co-
workers in the same building and the surrounding community due
to the handling and analysis of dioxin samples [TCDD] can be con-
ducted based on some piecemeal information characterizing the
consequences and the conservative judgments of the investigators.
However, with a built-in cushion of error allowance, it may be con-
cluded that:
•The risk to both laboratory workers and their co-workers in the
building is acceptable.
•The risk to the surrounding community may be considered mar-
ginally acceptable. However, with minimal modifications to the
facility and to practices, the risk can be acceptable.
REFERENCES
. Rowe, W. An Anatomy of Risk, John Wiley & Sons, New York, 1977.
2. Shih, C.S. and Ess, T., "Perspectives of Risk Assessment for Haz-
ardous Waste Management,-- Proc., Third National Conference on
Uncontrolled Hazardous Waste Sites, Washington, D.C., November
1982, 408-413.
3. Veseley, W., et at.. Fault Tree Handbook, U.S. Nuclear Regulatory
Commission, NURGC-0492, 1981.
412
RISK/DECISION ANALYSIS
-------
MANAGEMENT PLAN FOR HAZARDOUS WASTE
SITE CLEANUPS IN NEW JERSEY
MARWAN M. SADAT, Ph.D.
MICHELE MATEO
ANTHONY FARRO
New Jersey Department of Environmental Protection
Trenton, New Jersey
INTRODUCTION
This Management Plan for hazardous waste site mitigation has
been prepared by the Department of Environmental Protection
(DEP), Division of Waste Management, of the State of New
Jersey, for the period of 1983-1986. The purpose of the plan is to
develop a systematic approach to remedial action at hazardous
waste* sites, to coordinate cleanup and enforcement actions and to
identify future funding needs and sources.
There are a total of 106 hazardous waste sites identified in the
plan (Table 1). These include: 65 sites on the National Priorities
List (NPL) issued by the USEPA on Dec. 20, 1982 and eligible for
Federal Superfund monies and 41 sites which were not included on
the NPL. Thirty-four drum dump sites listed in the draft plan ap-
proved by USEPA on Apr. 11, 1983, were cleaned up in 1983.
Those sites not on the NPL will be addressed through New Jersey's
Spill Compensation Fund and Hazardous Discharge Fund as were
the recently cleaned up sites. While cleanup projects are expected to
be initiated within the period of the plan, completion of cleanups at
all scheduled sites will be a seven- to eight-year effort with some
sites requiring maintenance for many years beyond that time.
As additional sites are approved for Superfund status or as other
sites requiring priority status are identified, the list will be changed
accordingly. For example, in response to the discovery of chemical
contamination with dioxin at some industrial sites, four sites**
have recently been added. These discoveries were made as a result
of systematic investigations conducted by a special Dioxin Task
Force instituted by DEP, and stringent precautions are being taken
to limit human and environmental exposure to the chemical at these
sites. To date, sampling and analyses have been conducted at 11
sites and cleanup has begun in several areas.
The plan also lists the 68 hazardous waste sites (Table 2) with
over 10,000 drums cleaned up by DEP since 1980 at a cost of ap-
proximately $3 million. Including the $26 million spent on cleanup
of Chemical Control in Elizabeth and $6 million on Goose Farm in
Plumsted Township, the state's cost for remedial work at these 70
hazardous waste sites is over $35 million to date.
The plan represents the culmination of a review process which
started with an original list of sites ranked by DEP and USEPA ac-
cording to the Federal Hazard Ranking System (HRS). This system
* "Hazardous waste" is being used here as a generic term to include discharges of all hazardous
materials which pose a threat to public health or the environment.
"Blue Spruce International, Inc.; Chemical Insecticide Corporation, Diamond Alkali/Diamond
Shamrock Corporation and Givaudan Corporation.
HAZARDOUS WASTE DUMP SITES
• Superfund Sites
A Non-Supeifund Sites
Drum Dump Sites
August, 1983
Figure 1
Hazardous Waste Dump Sites
STATE PROGRAMS
413
-------
Table 1
Sites Included In Management Plan/1983-1986
Site Name
Albert Steel
American Cyanamid*
A.O. Polymer'
Arky Property
Asbestos Dump*
Ashland Company
Barrier Chemical Industry!
Beachwood/Berkeley Wells*
Blue Spruce international Inc.
Bog Creek Farm't
Borne Chemical
Brick Township Landfill*
Bridgeport Rental & Oil
Service* t
Burnt Fly Bog't
Buzby Brothers Landfill t
Caldwell Trucking Co.*
Cheesequake State Park
Chemical Control Corp.*
Chemical Insecticide Corp.
Chemsol, Inc.*
Chipman Chemical
Combe-Fill North Landfill*
Combe-Fill South Landfill*
Cooper Road?
CPS/Madison Industries*
Delilah Road Landfill*
(aka Price's Landfill Site #4)
Denzer & Schafer X-Ray Co.*
Diamond Alkali Co.
D'Imperio Property* t
Dover Municipal Well #4*
Duane Marine
Duck Island Landfill
Ellis Property*
Evor-Phillips*
Fairlawn Wellfield*
T. Fiore Demolition t
Friedman Property* t
Frontage Roadi
OEMS Landfill* t
Oivaudan Corp.
Goose Farm*
Green Acres Landfill}
Hercules, Inc.*
Horseshoe Road Dump)
Ideal Cooperage
Imperial Oil/Champion
Chemical*
Jackson Twp. Landfill't
JIS Landfill't
Kearny Drum Dumps
(Nos. l-5)t
Kin-Buc Landfill*!
King of Prussia Landfill*
Kit Enterprises
Koppers Company
Kramer Sanitary Landfill*
Krysowaly Fann't
Lang Property* t
Lipari Landfill* t
Municipality
Newark
Bridgewater Twp
Bound Brook Boro
Sparta Twp
Marlboro Twp
Passaic Twp
Woodbridge Twp
Vernon Twp
Berkeley Twp
Bound Brook
Howell Twp
Elizabeth City
Brick Twp
Logan Twp
Marlboro Twp
Voorhees Twp
Fairfield Twp
Old Bridge Twp
Elizabeth City
Edison Twp
Piscataway Twp
Middlesex Boro
Mount Olive Twp
Chester Twp/
Washington Twp
Voorhees Twp
Old Bridge Twp
Egg Harbor Twp
Berkeley Twp
Newark City
Hamilton Twp
Dover Twp
Perth Amboy City
Hamilton Twp
Evesham Twp
Old Bridge Twp
Fairlawn Boro
Newark City
Upper Freehold Twp
Newark City
Gloucester Twp
Clifton
Plumsted Twp
Frelinghuysen Twp
Greenwich Twp
Sayreville Boro
Jersey City
Marlboro Twp
Jackson Twp
Monroe Twp
Keamy
Edison Twp
Winslow Twp
Elizabeth City
Kearny Town
Mantua Twp
Hillsborough Twp
Pemberton Twp
Mantua Twp
County
Essex
Somerset
Sussex
Monmouth
Morris
Middlesex
Sussex
Ocean
Somerset
Monmouth
Union
Ocean
Gloucester
Monmouth
Camden
Essex
Middlesex
Union
Middlesex
Middlesex
Middlesex
Morris
Morris
Camden
Middlesex
Atlantic
Ocean
Essex
Atlantic
Morris
Middlesex
Mercer
Burlington
Middlesex
Bergen
Essex
Monmouth
Essex
Camden
Passaic
Ocean
Warren
Gloucester
Middlesex
Hudson
Monmouth
Ocean
Middlesex
Hudson
Middlesex
Camden
Union
Hudson
Gloucester
Somerset
Burlington
Gloucester
Site Name
Lone Pine Landfill* t
Manchester Twp Mile
Marker 28
Manheim Ave. Dump Site*
Maywood Chemical*
Metaltec/Aerosystems*
Minsei Kogyo Shojit
kk America, Inc.
Mirex Dump
Mobil Chemical
Monroe Twp Landfill*
Montgomery Twp Housing
Development*
Myers Property* t
N.L. Industries*
Pepe Field*
Perth Amboy PCB Case
Pijak Farm't
PJP Landfill*
Price's Landfill't
(Nos. 1,2,3)
Quanta Resources
Reich Farm*
Renora, tnc.'t
Ringwood Boro Landfill/
Mines*
Rockaway Borough Wellfield*
Rockaway Township Wells*
Rocky Hill Municipal Well*
Roebling Steel Company*
Roosevelt Drive-In t
Sayreville Landfill*
Sayreville Pesticide Dumpt
Scientific Chemical Processing*
Seaview Square Mall/M & T
Delisa Landfill*
Sharkey's Farm Landfill*
South Brunswick Landfill*
Spence Farm*t
Storer Dumpt
Swope Oil and Chemical* t
Syncon Resins*
Tabernacle Site!
Toms River Chemical Co.*
U.S. Radium Site*
Universal Oil Products*
Vineland State School*
White Chemical Company
Williams Property *t
Woodland Twp Dump *
Woodland Twp Dump Ifl
Municipality
Freehold Twp
Manchester Twp
Galloway Twp
Maywood Twp/
Rochelle Park Boro
Franklin Boro
Woodland Twp
Sayreville Boro
Carteret Boro
Monroe Twp
Montgomery Twp
Franklin Twp
OldmansTwp
Boonton Town
Perth Amboy City
Plumsted Twp
Jersey City
Egg Harbor Twp/
PleasantvUle City
Edgewater
Dover Twp
Edison Twp
Ringwood Boro
Rockaway Boro
Rockaway Twp
Rocky Hill Boro
Florence Twp
Jersey City
Sayreville Boro
Sayreville Boro
Carlstadt Boro
Ocean Twp
Parsippany-Troy Hills
Twp
S. Brunswick Twp
Plumsted Twp
Marlboro Twp
Pennsauken Twp
Kearny Town
Tabernacle Twp
Dover Twp
Orange City
E. Rutherford Boro
Vineland City
Bayonne City
Middle Twp
Woodland Twp
Woodland Twp
County
Monmouth
Ocean
Atlantic
Bergen
Sussex
Burlington
Middlesex
Middlesex
Middlesex
Somerset
Hunterdon
Salem
Morris
Middlesex
Ocean
Hudson
Atlantic
Bergen
Ocean
Middlesex
Passaic
Morris
Morris
Somerset
Burlington
Hudson
Middlesex
Middlesex
Bergen
Monmouth
Morris
Middlesex
Ocean
Monmouth
Camden
Hudson
Burlington
Ocean
Essex
Bergen
Cumberland
Hudson
Cape May
Burlington
Burlington
•Superfund sites included on the proposed National Priorities Lut of 12/20/82
tSites includes on the Hazardous Discharge Bond Act effective 1/6/82
(Drum Dump Sites
414
STATE PROGRAMS
-------
Table 2
Completed Small (Surface) Drum Dump Cleanups
From 1980 to the Present
Site Name
AUoway Township
Altman Street Drum Dump
Atlantic Development Stage II
A-Z Chemical*
Barnegat Light Boro DPW*
Barone Barrel & Drum Co.
Bayonne DPW*
Bayonne Landfill Drums
Bjomlass Kennels*
Black River Area*
Blue Spruce/Tifa
Boro Garage Route 47
Bubenick Property
Burlington Avenue*
Camden Fire Department*
Carlstadt DPW*
Clinton Place
Cohawkin Road*
Columbus Avenue*
Communipaw Avenue*
Thomas A. Cook
Creekturn Ceramics*
DOT*
DOT Yard*
Doughty Road*
Dover DPW*
314 East Fourth St.
El Cid Contracting Corp.
Ellis Property*t
(Drum Removal)
Emerald Trail*
Fish Road
Franklin Mines
Fulton Street
Glassboro Lab Pack Co.
Gold Leaf Trucking
Gordon Services
Harleigh Cemetery*
17 Horizon Boulevard
Jackson DPW*
Jersey City Department of
Public Works Rte 440
Kurtz Residence*
Lab Reagents
Liberty State Park
Madison Circle
Manchester DWP*
Mikropul*
Murray Hill Parkway*
Nash Property*
Newark Stamp & Dye
NJ Turnpike Mile Market 16.7
North Bergen/Keystone Steel
North Hook Road
Northern Fines
Oldham Road
Paterson DPW*
Pleasant Grove Road*
Rahway River Park*
Reimer Street*
Ringwood/West Milford
Township
County
Alloway
Rutherford
Sayreville
New Brunswick
Barnegat
Paterson
Bayonne
Bayonne
Montville
Chester
Bound Brook
Clayton
Piscataway
Delanco
Camden City
Carstadt
Newark
E. Greenwich
Roselle
Jersey City
Newark
Hainesport
Wall Twp
Logan Twp
Egg Harbor Twp
Dover Twp
Plainfield
Howell Twp
Evesham
Bridgewater
Jackson Twp
Franklin
Paterson
Glassboro
Sewaren
Jersey City
Camden City
South Hackensack
Jackson Twp
Jersey City
Woodstown
Burlington
Jersey City
East Rutherford
Manchester
Garwood
E. Rutherford
Buena
Newark
Mantua
North Bergen
Bayonne
Franklin
Wayne
Paterson
Long Valley
Rahway
Mount Holly
Ringwood/West Milford
Salem
Bergen
Middlesex
Middlesex
Ocean
Passaic
Hudson
Hudson
Morris
Morris
Somerset
Gloucester
Middlesex
Burlington
Camden
Bergen
Essex
Gloucester
Union
Hudson
Essex
Burlington
Monmouth
Gloucester
Atlantic
Ocean
Union
Monmouth
Burlington
Somerset
Ocean
Sussex
Passaic
Gloucester
Middlesex
Hudson
Camden
Bergen
Ocean
Hudson
Salem
Burlington
Hudson
Bergen
Ocean
Union
Bergen
Atlantic
Essex
Gloucester
Hudson
Hudson
Sussex
Passaic
Passaic
Morris
Union
Burlington
Passaic
Site Name
Rt. 1-95 Trailer
Samson Tank
South Amboy Water Works*
610 South Thirteenth St.
Swoco
Union Twp. DPW*
Venice Boulevard*
Victoria Lane*
Wilson Farm (Surface
Cleanup Only)
•Cleanups conducted in April 1983
Township
Jackson
Jersey City
S. Amboy
Newark
Hillsboro
Union Twp
Buena Twp
Hackettstown
Plumsted Twp.
County
Ocean
Hudson
Middlesex
Essex
Somerset
Union
Atlantic
Warren
Ocean
Figure 2
Completed Surface Cleanups from 1980 through August 1983
STATE PROGRAMS
415
-------
Table 3
Cleanup Work Schedule
SITE NA*
(in Buc Luruirm
Burnt flf Bog
Lone Pine Landfill
Friedman Property
D'lmnerlo Property
Brld|teport Rental
Oil Service
GEHS Landrlll
Pljak Farm
Spence Far*
Goose Fan*
Chenlcal Control
Price's Landrill
Prlce'n Landfill I
Price' a Landrlll II,
III and IV
Perth Amboy PCB i:os«-
Kramer Landrlll
Combe- rill North
Landfill
Swop* Oil • Chemical
Bog Creek Farn
LI par 1 Landfill
Hockaway Boro
Uelirield
Retch Far*
Combe- Mil South
Landfill
Falrlawn Tup.
WelUleld
Sharkey's Fam
Landfill
Beacnwood/Berkeley
Valirield
Syncon Realns
Kryaowaty Fan
Caldwell Trucking
Brick Township
Landfill
Scientific Chemtral
Processing
Duck lit am]
Landfill
Universal Oil
Products
ftlngwood Boro
Landflll/Hlnes
Woodland Top.
Dump Ho. 11
Haywood Chemical
Barrier Che*lcal
Industry
FEASIBILITY
4th quarter
Completed
Completed
Completed
3rd quarter
Cnapleted
3rd quarter
3rd quarter
3rd quarter
Ird quarter
3rd quarter
4l.h quarter
Completed
4th quarter
4th quarter
4th quarter
4th quarter
4th quarter
4th quarter
STUDY
of '83
of
of
of
of
of
of
of
of
of
of
of
of
of
Completed ISWI
1st quarter of
1st quarter
lat quarter
1st quarter
lat quarter
lat quarter
lat quarter
2nd quarter
2nd quarter
2nd quarter
2nd quarter
2nd quarter
2nd quarter
2nd quarter
3rd quarter
3rd quarter
3rd quarter
3rd quarter
of
of
of
of
of
of
of
of
of
of
of
of
of
of
of
of
of
•B3
•83
•83
•83
•83
•83
•83
•83
•BJ
•83
•83
•83
•83
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
•84
2nd
4th
lat
3rd
3rd
DESIGN
quarter
quarter
quarter
quarter
quarter
Couple ted
2nd quarter
1st
3rd
3rd
3rd
3rd
3rd
1st
2nd
2nd
4lh
4th
3rd
4th
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
of
of
or
or
or
of
or
or
or
or
or
of
of
or
of
of
of
of
or
Completed (SW)
3rd quarter of
1st
lat
1st
1st
1st
1st
2nd
2nd
2nd
2nd
2nd
2nJ
2nd
1st
1st
1st
3rd
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
quarter
or
of
or
or
or
of
of
or
or
or
or
or
or-
or
or
or
or
'84
•83
•84
•84
•84
•84
'85
'84
•84
•84
•83
•84
•84
•85
•85
•84
•84
•84
•84
•85
•85
•85
•85
•85
•85
•05
•85
•85
•85
•85
'85
•85
85
•86
•86
•86
•85
TREATteNT/REMOVAL
ongoing (141
4th quarter or '84
1st quarter or
2nd quarter or
2nd quarter of
4th quarter of
3rd quarter or
Completed IIA)
4th quarter or
Completed (IA)
2nd quarter or
3rd quarter of
3rd quarter of
3rd quarter of
4th quarter or
2nd quarter of
4th quarter or
4th quarter of
3rd quarter or
2nd quarter or
3rd quarter or
3rd quarter or
4th quarter or
4th quarter or
2nd quarter or
3rd quarter or
Completed (IA)
Completed ISWI
4th quarter or
4th quarter or
4th quarter or
4th quarter or
1st quarter or
'ith quarter of
lat quarter of
3rd quarter of
1st quarter of
4th quarter of
2nd quarter or
2nd quarter or
2nd quarter of
2nd quarter or
2nd quarter or
2nd quarter or
2nd quarter or
2nd quarter or
2nd quarter of
2nd quarter or
•85
•85
•85
•83 (IA)
•85
•84
•85
•85
•85
•85
•83 (IA)
•85
•83 IIA)
•84
•86
•84 (IA)
•86
•83 (IA)
•80
•85
•85
•85
•86
'85
•85
•85
•86
•85
•86
•83 (IA)
•86
•83 IIA)
'86
•86
•86
•86
•86
•86
•88
•88
•88
•86
LEAP"
EPA/OP
DEP
EPA
DEP
EPA
EPA
DEP
DEP
DEP
DEP
EPA
EPA
EPA
DEP
EPA
DEP
EPA
EPA
EPA
DEP
EPA
DEP
DF.P
DEP
DEP
DEP
EPA
DP.P/RP
DEP/HP
F.PA/RP
DEP
DEP/RP
EPA
DEP
EPA
DEP
FUNDING SOURCE**
RP
SF
SF
SF
SF
SF
SF
SF
SF
SF
SF
SF
SF
NS
SF
SF
SF
SF
SF
SF
SF
SF
SF
SF
SF
SF
SF
RP
RP
RP
NS
RP
SF
NS
SF
NS
416
STATE PROGRAMS
-------
Table 3 (continued)
SITE NAME FEASIBILITY STUDY
Metal lec/Aerosystens 3rd quarter of '84
Lang Property 4th quarter of '84
Manchester Tup. /Mile tth quater of '84
Marker 128
King of Prussia Landfill 4th quarter of '84
Ideal Cooperage 4th quarter of '84
Toms Diver Chemical Irst quarter of '8S
Rockauay Twp. Wells 1st quarter of '85
Chemsol, Inc. 1st quarter of 'B*>
Imperial Oil /Chanplon 2nd quarter of '85
Chemical
Dover Tup. 2nd quarter of '85
Municipal Well 14
Roebllng Steel 2nd quarter of '85
Company
Vlneland State 3rd quarter of '85
School
Williams Property 3rd quarter of -85
Renora, inc. 3rd quarter of '85
Denier H Schafer 3rd quarter of '85
X-Ray Co.
Hercules, Inc. 4th quarter of '85
Arky Property 4th 'tunr'.er of '85
Asbestos Dump/ 4i.h .|Uvler of '85
Mllllngton
Chlpman Chemical 4th quarter of 'B5
Rocky Hill Municipal 4th quarter of '85
Well
Montgomery Twp. 1st quarter of '86
Housing Development
Ashland Chemical \st quarter of '86
Sayrevllle Landfill is( quarter of'H6
Evor-I'hllllps i3t quarter of '86
Mannheim Ave. 1st quarter of '86
Dump .Site
Ellis Property
?nd quarter of '86
?nd quarter of '86
Pepe Field 2nd quarter of '86
Seavlew Square Mall/ 3rd quarter of '86
M t T Dellsa Landfill
Buzby Bros. Ird quarter of '86
Landfill
A.O. Polymer Ird quarter of '86
PJP Landfill 'ith quarter of '86
Horseshoe Road Dumps 4th quarter of '86
Horseshoe Road Dump
Sayrevllle Pesticide
Koppers Co. ^th quarter of '86
Woodland Dump 4th quarter of '86
No. 12
EPA Environmental Protection Agency
'RP Responsible Party
SF Superfund
NS Non-Superfund Sources of fund Ings. In
case of responsible parties. It la expe
that such parlies will finance clean-up
though the site may be on the National
List.
DESIGN
2nd quarter of '85
4th quarter of '85
4th quarter of '85
4th quarter of '85
3rd quarter of '85
3rd quarter of '86
1st quarter of '86
1st quarter of '86
2nd quarter of '66
2nd quarter of '86
1st quarter of '86
3rd quarter of '86
3rd quarter of '86
2nd quarter, of '86
3rd quarter of '86
4th quarter of '86
4th quarter of '86
4th quarter of '86
4th quarter of '86
4th quarter of '86
1st quarter of '87
1st quarter of '87
4th quarter of '86
1st quarter of '87
1st quarter of '87
1st quarter of '87
1st. quarter uf '87
1st quarter of '87
2nd quarter of '87
3rd quarter of '87
2nd quarter of '87
4th quarter of '87
4th quarter of '87
4th quarter of '87
ctlon (IA)
(SW>
the
cted
, even "NOTEi
Priorities
TREATMENT/REMOVAL LEAD FUNDING SOURCES
1st quarter of '86 DEP/RP
4th quarter of '86 EPA
4th quarter of 86 DEP
4th quarter of '86 EPA
2nd quarter of -86 DEP
4th quarter of '87 DEP/np
1st quarter of '87 DEP
1st quarter of '87 DEV/HP
1st quarter of '87 DEP/RP
1st quarter of '87 ngp
4th quarter of '86 DEP
3rd quarter of '87 DEP
3rd quarter of "87 DEP
1st quarter of '87 DEP/RP
2nd quarter of '87 DEP/np
3rd quarter of '87 EPA/RP
3rd quarter of '87 DEP/RP
3rd quarter of '87 EPA
3rd quarter of '87 DEP/RP
3rd quarter of '87 DEP
4th quarter of '87 EPA
4th quarter of '87 EPA
3rd quarter of '87 DEP
4th quarter of '87 DEP
1st quarter of '88 DEP
1st quarter of '88 DEP
Completed (IAI DEP
4th quarter of '87
4th quarter of '83I1A) EPA
4th quarter of '87
4th quarter of "87 DEP
1st quarter of '88 EPA
2nd quarter of '88 DEP
1st quarter of '88 DEP
2nd quarter of '88 DEP
3rd quarter of '88 DEP
4th quarter of 'SB DEP
4th quarter of '88 PEP
Interim Action
Slurry Wall
Dates Indicate project Initiation.
A "Completed" alte Indicate* work hue been
initiated or completed.
RP
SF
NS
SF
NS
np
SF
RP
RP
SF
SF
SF
SF
RP
RP
RP
(IS
SF
NS
SF
SF
SF
NS
SF
SF
SF
SF
SF
SF
SF
NS
SF
SF
SF
NS
NS
STATE PROGRAMS
417
-------
Table 4
Drum Damp Cleanup Work Schedule
Site Nmme
Storcr Dump*
Minsei Kogyo Shoji*
kk America
Frontage Road
Kearny Dumps (Nos. 1-5)
Tabernacle Site
Cooper Road
Green Acres Landfill
Staging*
Sampling
3rd qtr. of '83
4th qlr. of '83
4th qtr. of '83
4th qtr. of '83
1st qtr. of '84
1st qtr. of '84
1st qtr. of '84
Dram Removal &
Disposal
4th qtr. of '83
1st qtr. of '84
1st qtr. of '84
1st qtr. of '84
2nd qtr. of '84
2nd qtr. of '84
2nd qtr. of '84
•Cleanup expected to be conducted by responsible party.
NOTE: Dates indicate project initiation
Table S
Sites Currently Not Scheduled for Cleanup Action
Albert Steel
American Cyanamid*
Blue Spruce
Borne Chemical
Cheesequake State Park
Chemical Insecticide
CPS/Madison Industries*
Duane Marine
T. Fiore Demolition t
Givaudan
Jackson Township Landfill* t
tSites included on the Hazardous Discharge Bond Act
•Sites included on the proposed National Priority List
JIS Landfill*!
Kit Enterprises
Mirex Dump
Mobil Chemical
Monroe Township Landfill*
N.L. Industries*
Quanta Resources Corporation
Roosevelt Drive-Int
South Brunswick Landfill*
White Chemical Company
Table 6
Sites to be Scheduled/Rescheduled Following USEPA Evaluation and
Ranking for the National Priority List
Chemical teaman
Cooper Road*
Delilah Road*
DeRewal Chemical Company
Diamond Alkali
Ewan Property
Florence Land Recontouring Inc.
W.R. Grace and Company
Hopkins Farm
L & D Landfill
Minsei Kogyo Shoji, kk America*
•Currently in work schedules C or D
Nascolite Corporation
Radiation Technology
Shieldalloy Corporation
Tabernacle Drum Dump*
Upper Deerfield Two Sanitary Landfill
Ventron Velsicol
Vineland Chemical Company
Wilson Farm (Residual Cleanup)
Woodland Twp Route 72 Dump*
Woodland Twp Route 532 Dump*
Table 7
Estimated Costs for Projects Scheduled for Cleanup
1983 1984 19*5 1986
Feasibility Study $ 6,224,000 $ 7,700,000 $ 4,450,000 S 4,100,000
Design* $ 2,850,000 $10,064,440 $ 2,655,000 $ 4,685,000
Treatment/
Removal $13,743,000 $67,276,000 $47,894,000 $60,050,000
Total Costs $22,817,000 $85,040,440 $54,999,000 $68,835,000
Total 1983-1986 $231.691,440.00
•Aclual deiign costs presented, if knovn. Estimated design costs equal 10^ of project treatment/
remcnal COM*
is based on potential danger to public health and the environment
and takes into account surface and groundwater pollution as well
as releases of hazardous chemicals into the atmosphere. Emerging
from this list were 93 sites which, when further screened, were
reduced to 72 for submission to USEPA based on information
available at the time. Of these, 17 sites received high priority ap-
proval in mid-1982. In Dec. 1982, USEPA identified a total of 65
New Jersey sites which are eligible for Superfund monies. DEP will
continue to evaluate sites which are not now eligible for Superfund
assistance, and some of these sites have been included in the plan.
Currently, 21 sites are being evaluated by USEPA for Superfund
status (Table 6).
Cleanup Ponding
The three major stages of a hazardous waste site cleanup pro-
cedure are: (1) a feasibility study to determine the extent of the
problem and to recommend remedial alternatives; (2) an engineer-
ing design of the selected remedial action to mitigate the problem;
and (3) the remedial action or actual physical cleanup process, in-
cluding treatment and/or removal. The Federal Superfund pro-
gram provides 100% of feasibility study and engineering design
costs and up to 90% of remedial costs for eligible hazardous waste
sites, with the state providing the remainder of the monies from
either the New Jersey Spill Compensation Fund or the $100 million
Hazardous Discharge Fund approved by voters in November 1981.
Because of this funding mechanism, New Jersey will need the full
cooperation and assistance of the USEPA, both in Region II in
New York City, and from headquarters in Washington. In some
cases, DEP will have responsibility for cleanup programs while in
others, USEPA will take the lead.
To date, the state has entered into contracts/cooperative
agreements with the USEPA for remedial action at 15 sites. In ad-
dition, 11 signings for the initiation of feasibility studies are an-
ticipated in the fall of 1983, and amendments to six of the 15 ex-
isting contracts/cooperative agreements for engineering design and
remedial actions are expected in 1983.
The actions proposed in the plan are currently estimated to cost
approximately $232 million (Table 7), although this amount could
increase substantially depending upon further findings and con-
tractor bids. Estimated costs do not include long-term maintenance
costs, such as groundwater pumping and treatment, which may be
required at some sites. In order to estimate project duration and
cost, the sites included in the plan were considered on the basis of
the anticipated soil and groundwater contamination. The most dif-
ficult, and thus most costly, sites are those exhibiting extensive soil
and groundwater contamination and requiring complex and
lengthy procedures for cleanup.
SCHEDULING METHODOLOGY
DEP has developed a methodology for scheduling cleanup ac-
tivities at both Superfund and non-Superfund sites. This system
provides a means of tracking progress in cleanup operations.
Sites included on the proposed National Priorities List (NPL)
(Superfund sites) were considered to represent the greatest potential
hazard to public health and/or the environment. The sites included
on the NPL where remedial action had previously been projected
for initiation were scheduled first (e.g., Burnt Fly Bog, Bridgeport
Rental and Oil Services, etc.) (Table 3). All other NPL sites were
scheduled in order of the Hazard Ranking System (HRS) score at a
rate of approximately one per month.
Sites not included on the NPL, such as the Hazardous Discharge
Bond Act sites, were introduced into the schedule concurrently
with those remedial actions proposed as an USEPA lead site and in
order of their HRS scores. This reflects the additional manpower
available at DEP when USEPA has the lead for a remedial action
and will provide for more timely cleanup of those sites not eligible
for Superfund monies. All 27 Bond Act sites were included on the
plan.
418
STATE PROGRAMS
-------
me 11 sites categorized as drum dumps were scheduled separ-
ately (Table 4) because operations at these sites differ from those at
other sites in the plan. It is expected that these surface drum dump
cleanups can be cleaned up more rapidly than remedial action at
other more complex sites. According to Superfund regulations,
responsible parties are liable for cleanup costs. Accordingly, most
sites currently not scheduled primarily because of their responsible
party enforcement status are shown in Table 5.
DISCUSSION
The cleanup of hazardous waste sites is an extremely complex
undertaking. The scheduling of remedial actions is dependent upon
many variables such as enforcement status, identification of addi-
tional sites having higher priorities, information altering the
relative potential public and environmental hazards of sites
previously identified, as well as a Federal/State cooperative effort.
Thus, the schedule is not static and will be subject to continued
revision.
Additions, deletions or other schedule changes will be made
every six months in compliance with USEPA's "Guidance for Up-
dating the National Priorities List". Annual public hearings will be
held on these changes as well as in compliance with P.L. 1982,
c.202, N.J.S.A. 58:10-23.15 (Assembly Bill 285) enacted in Dec.
1982. This law requires the DEP to prepare a Master List of all the
known hazardous discharge sites in the State and a ranking of the
sites based on criteria recommended by the Hazardous Waste
Advisory Council pursuant to P.L. 1983, c.222, N.J.S.A. 58:10-
23.20, (Assembly Bill 1255) enacted on June 27,1983.
The DEP will continue its program of identification and ranking
of hazardous waste sites in New Jersey. The Hazardous Site Master
List developed by the Department now consists of over 900 sites
known or suspected to contain hazardous substances. Most of these
sites are still to be evaluated. Although the task is enormous, the
state is committed to a vigorous program of cleanup operations at
hazardous waste sites in order to protect public health and the en-
vironment.
STATE PROGRAMS
419
-------
THE DEVELOPMENT OF THE MASSACHUSETTS
CONTINGENCY PLAN FOR THE STATE SUPERFUND
YEE CHO
Massachusetts Department of Environmental Quality Engineering
Division of Hazardous Waste
Boston, Massachusetts
INTRODUCTION
The passage of the Massachusetts "Superfund Bill" in March
1983 gives the Commonwealth extensive enforcement powers in
the management of uncontrolled hazardous waste sites and estab-
lishes a $25 million fund for the tasks ahead. The three most im-
portant objectives of the new law are:
•To encourage the prevention of releases of oil and hazardous
materials (including hazardous waste)
•To ensure that individuals responsible for releases pay the full
cost of cleanup
•To facilitate the cleanup of releases of oil and hazardous ma-
terials when responsible parties fail to cleanup
The fund is to be used by the Commonwealth when all enforce-
ment avenues have been exhausted for the cleanup of spills and
releases of oil and hazardous materials (including hazardous waste
sites) and for the Commonwealth's share of the federal "Super-
fund" cost-match.
Central to the implementation of the new law is a Massachu-
setts contingency plan covering both emergency response and
remedial actions. The plan will serve as a standard operating pro-
cedure for response to chemical releases and will include emergency
contacts, decision making and site assessment guidance; it will also
establish a method for the priority ranking of Massachusetts
sites for enforcement or cleanup action. A discussion draft of the
plan should be completed in the fall of 1983.
BACKGROUND
A program for the Commonwealth's abandoned hazardous
waste sites emerged with the publication of a list of potential and
actual (confirmed) abandoned sites by the Department of Environ-
mental Quality Engineering in late 1980. This list was compiled
from information in the Eckhardt report,' the Department's files
especially in the water related programs and the Surface Impound-
ment Assessment2 study completed by the state government. Over
300 potential hazardous waste sites were evaluated in the process.
Enforcement actions against responsible parties in conjunction
with the State Attorney General's Office were pursued as part of
the assessment and investigation at the confirmed sites. Almost to
75% of the contamination at the confirmed sites has been resolved
or addressed by the responsible parties. The state's enforcement
authorities, however, were limited. In some instances, there were
no incentives for responsible parties to undertake remedial actions
at the contaminated sites themselves.
Approximately 25% of the contaminated sites have required
public funds for cleanup. The sources of the state funds for these
sites have been from site specific legislative appropriations and
from a $5 million budget appropriation for cleanup known as
the Capital Outlay Budget of 1979. The single most costly aban-
doned hazardous waste site cleanup undertaken by the Common-
wealth has been the Silresim site in Lowell, MA., a five acre chem-
ical reclamation facility abandoned in Jan. 1978. Approximately
one million gallons of hazardous material in drum and bulk stor-
age were left. The state also had funded approximately half a dozen
additional sites for remedial actions.
In 1982, the need for stronger enforcement tools and funding
was obvious. The 1979 cleanup budget was inadequate and nearly
exhausted. Site activities under the Comprehensive Environmental
Response, Compensation and Liability Act of 1980 were sched-
uled, but the state could obtain federal assistance only if the cost
was shared. There were already 50 confirmed sites requiring re-
medial action; new sites were being discovered and added to this
list; 170 sites from the CERCLA notifiers* list were compiled. This
potential list of sites to be addressed is not yet complete.
THE MASSACHUSETTS SUPERFUND ACT
On Mar. 24, 1983, Governor Michael S. Dukakis signed the
new "Massachusetts Oil and Hazardous Materials Release Preven-
tion and Response Act." This Act (Chapter 7 of the Acts of
1983) greatly expanded the Department of Environmental Quality
Engineering's (DEQE's) authority to protect citizens and the en-
vironment from hazardous substances. The law encourages the pre-
vention of releases of oil and hazardous materials, ensures that
individuals responsible for releases pay the full cost of cleanup and
provides funds and authority for cleanup when those responsible
fail to take appropriate action or cannot be identified.
The statute generally constitutes a state counterpart of the 1980
federal "Comprehensive Environmental Response, Compensation,
and Liability Act" (CERCLA). The new Act aims to correct some
deficiencies in previous state legislation:
•Existing funding was inadequate to assure state match for all fed-
eral Superfund projects in Massachusetts and the Common-
wealth's ability to respond to anticipated major hazardous ma-
terials emergencies in the near future.
•Existing enabling legislation did not give Massachusetts sufficient
authority to respond to all types of emergencies involving oil and
hazardous materials. Prior to the Act, DEQE could only respond
to releases and threats of release of oil and hazardous materials
when an impact on water quality could be demonstrated.
General Enabling Authority
The Act adds to the General Laws a new Chapter 21E which pro-
vides DEQE with wide-ranging authority to deal with emergency
situations:
420
STATE PROGRAMS
-------
•DEQE may take a wide range of actions necessary to content
with releases and threats of release of oil and hazardous ma-
terials.
•Immediate notification to DEQE is required when there is a re-
lease or threat of release of oil or hazardous material.
•There are provisions to prevent, to the extent possible, the Com-
monwealth from assuming the full costs and responsibilities for
cleanup.
Specifically, the new Act expands the categories of people who
are potentially liable to both the Commonwealth for repayment
of DEQE response costs and to other people for damage to or loss
of real or personal property. Subject to narrowly-drawn defenses
and limitations, responsible people are strictly liable, jointly and
severally. Individuals responsible for a release or threat of release
for which the state incurs cleanup costs are strictly liable for up to
three times the state's costs. The law establishes a five-year statute
of limitations for actions brought to recover costs. The law im-
poses a lien on property owned by anyone who may be liable for
cleanup costs. The Superfund lien would take priority over all
previously recorded mortgages.
Implementation
In implementing the new Act, DEQE faces a complex set of
issues and many responsibilities. The Department must develop
and implement several sets of plans, regulations and procedures in
the near future. Implementation procedures must be flexible to
allow DEQE to respond to problems raised by unique sites and
situations and by ever-changing technology. The major program
elements include the Massachusetts contingency plan, the release
notification regulations, civil and criminal penalties for violations
of the new law of $25,000 per violation per day with the potential
for five years imprisonment for individuals and administrative ac-
tions to remedy situations for the DEQE.
The DEQE is to prepare a Massachusetts contingency plan
covering both emergency response and remedial actions. The plan
will include standard operating procedures for responses to re-
leases (decision making and site assessment guidance) and a method
for the ranking of Massachusetts sites for cleanup action. The
statute also gives DEQE authority to respond to releases before the
contingency plan has been developed.
The new law further gives DEQE authority to regulate activ-
ities when necessary to prevent releases of hazardous materials.
The requirements are intended to avert the likelihood of releases
and to enable quick response should releases occur.
Funding
The new law establishes a $25 million general obligation fund
for state cleanup actions. It also specifies that funds received as
fines and penalties under the Act, as well as funds recovered from
cleanup actions, shall be applied to payment of debt service on
short and long-term borrowing under the loan fund.
The Commonwealth must apply recovered funds to the General
Fund to offset debt service payments on bonds used to cover the
$25 million appropriation. The difference between costs recovered
for state response actions and the annual outlays for debt service
will be collected by fees imposed on hazardous waste transport-
ers. Fee levels will be reviewed annually. '
Special Commission
A special legislative study commission is established to determine
the adequacy of existing liability provisions, including liability for
third-party personal injury. The commission, which is composed
of members of legislature and gubernatorial appointees, is to sub-
mit its findings and recommendations by Dec. 1983.
DEVELOPMENT OF THE MASSACHUSETTS
CONTINGENCY PLAN
The DEQE under the Massachusetts Superfund Act is required
to prepare a contingency plan to deal with remedial actions and
emergency response. This plan should comply with and comple-
ment the National Contingency Plan (NCP) adopted by the
USEPA. The plan, however, is not required to follow the na-
tional plan.
Prior to initiating the process to develop the plan, the Depart-
ment should be organized on three major levels. First, it must
examine and mobilize the resources and personnel needed to under-
take the project. Second, the Department should be able to pro-
vide the administrative leadership and support necessary for the
plan to be expeditiously and successfully developed. And third, the
Department needs to decide the basis by which the plan will be
developed.
Resources and Advisory Committee
The first part of the process, identifying and organizing the re-
sources, is crucial. Without question, staff are required to coor-
dinate and implement the development of the plan. The staff
should be identified and mobilized early on in the process.
After mobilizing the resources, administrative commitment to
the completion of the tasks is important for continuous pro-
gress throughout the plan development phase. A six month time
schedule for completion of a draft contingency plan is possible
given the full support and commitment of resources, personnel
and leadership.
A document which would be the cornerstone for response ac-
tions under the State Superfund Act demands the expertise of a
multidisciplinary team consisting of site response and waste man-
agers, engineers, scientists, health specialists and lawyers. This
team can be assembled into an advisory committee for the initial
phases of the plan development process. The membership in this
advisory committee should have basic knowledge of the scope of
the National Contingency Plan as adopted by the USEPA, the
nature of hazardous materials response, the complexities of aban-
doned site response and the intricate interplay of public agencies in
both the same and different levels of government. The member-
ship should include representatives from the different sectors of the
community: academia, industry, environmental and public interest
groups, government and citizens.
To be immediately effective, the rules and roles of this com-
mittee should be well defined prior to its assemblage. The rules
on resolving issues on divergent viewpoints within the member-
ship need to be detailed. The resolution can take the form of a
majority vote of the entire membership, majority vote of the mem-
bers present, consensus of the entire membership, etc.
The role of an advisory committee should be exactly defined.
The committee can serve as a sounding board on the contents of
the draft plan prior to its release to the public for general com-
ments and input. The committee can provide expertise on different
sections of the plan. It would not be necessary, however, for the
committee's opinion to be binding. The Department can retain the
decision making process throughout the plan development phases.
An advisory committee is an option for the development of the
plan for Massachusetts. Its value, however, should not be over-
looked. The Department has successfully employed an advisory
committee in the development of other regulations.
Basis and Guidance
The State Superfund Act is the counterpart to the federal Super-
fund legislation. Unequivocally, the National Contingency Plan,
especially as it addresses abandoned site response, provides the
basis for the development of the Massachusetts Contingency Plan.
The operating procedures (i.e., contingency plan equivalents) of
other states with similar superfund programs and concerns should
provide valuable guidance to the development of the Common-
wealth's plan.
The contents of the National Contingency Plan offer a starting
point for discussions for the Commonwealth's plan. The Depart-
ment will have to decide what features of the NCP to include and
exclude in the Massachusetts Contingency Plan (MCP). The basic
STATE PROGRAMS
421
-------
subject categories will most likely be similar to the NCP, but the
levels and types of details within each subject category will prob-
ably vary. These subject categories include site discovery, site
assessment, remedial action and site orioritization.
In developing the plan, the Department will endeavor to review
published comments on the NCP. It will be important for the De-
partment to be aware of the concerns different groups have raised
about the NCP. This review would furnish a perspective and basis
for the Department to make its decisions on adopting any parts of
the NCP for its own plan.
The approaches that other states have taken in their state Super-
fund programs have been useful in the development of the MCP.
A review of California's experience with their two year old pro-
gram has been valuable. Their approach t6 site prioritization is in-
triguing. They employed a slightly revised version of the USEPA's
Hazard Ranking System (HRS) to prioritize their sites for remed-
ial action. Their revisions reflect similar concerns that DEQE has
about the federal ranking model. Prioritizing sites for spending the
state Superfund monies in an integral part of the Massachusetts
Contingency Plan.
Major Issue
Before the contingency plan becomes final, there will be num-
erous issues that must be resolved. The one major issue that will
consistently come up throughout the development process centers
around what subject matters and what levels of detail the MCP
should consist of. The issue is if certain issues should be addressed
only generally in the MCP and specifically in the Department
policy guidance, which would be separate from, but consistent
with, the MCP.
There will probably not be much disagreement with the basic
subject categories listed above. The discussions will focus on the
level of details and guidance to be incorporated within the subject
categories. A paucity of details would permit the Department more
flexibility in the implementation of the state Superfund response.
It would not confine the Department in responding to problems
that are fairly dynamic. It, however, may not define the Depart-
ment's response action sufficiently for the public to be assured that
the response level and action are sufficient.
A more defined and detailed operating procedures document
could limit the Department's response action. It could mean a rigid
response process that would be difficult to implement without
hindering progress on the remedial actions. The technologies in
abandoned hazardous waste site response are new and constantly
changing. Discoveries and improvements are frequent in this field.
Detailed procedures could ignore this significant parameter.
Other Issues
The numerous issues involved in the development of the plan
cannot be fully addressed in this paper. There will be issues that can
examine the practicality of a five year spending plan, the process
by which CERCLA sites are handled relative to the state Super-
fund priorities and the inter-relationship of the CERCLA program
with the state program. Issues relative to the entire abandoned site
response process will be raised; there will be discussions on aban-
doned site discovery attempts, site assessment procedures and
policies and remedial action alternatives. Fund-balancing criteria,
the "how clean is clean?" question and operation and mainten-
ance after the remedial action will not be ignored. Deliberations
over health and safety requirements for personnel, community rela-
tions, cost recovery and site prioritization can also be included.
Site Prioritization
A process to rank and prioritize the abandoned hazardous waste
sites in the state can lead the discussion. This process would deter-
mine the priorities by which the Department would spend the state
Superfund monies for investigation and cleanup. The discussions
would focus first on whether a mathematical ranking system based
upon the physical conditions at each site is appropriate and ac-
ceptable. The advantages of a mathematical model rest on its in-
herent attempt to be objective. A mathematical model would pro-
vide the fairest means to prioritize a large number of sites. The
prioritization system would be sheltered from the influence of
politics.
An alternative to a mathematical model can be a system based
on "best engineering judgments". This system would, of course, be
more subjective.
If the decision is made to employ a mathematical model, the next
problem would be which mathematical model to adopt. There is al-
ways the Hazard Ranking System (HRS) adopted by CERCLA.
Using that system would avoid lengthy discussions and justifica-
tion arguments for the existence of two priority lists—USEPA's
list and the Department's list. Another advantage of using the HRS
is that the ranking can be readily used for nomination as a
CERCLA site.
The disadvantage of using the HRS would initially rest on its in-
adequacy to address the unique conditions and problems in the
Commonwealth. The HRS was established for gross ranking of all
sites nationwide and not for relative ranking of a small number of
sites (relative to the number of sites nationwide).
If the HRS is not adopted, then one of the Department's op-
tions would be to develop a new model to consider the unique-
ness of Massachusetts. Another option would be to take USEPA's
model and revise it slightly to more closely meet the Department's
needs and interests. Nevertheless, selecting the ranking system for
the prioritization of Massachusetts hazardous waste sites will be a
challenge and will be an important decision.
CONCLUSIONS
The potential impact of the Commonwealth's Superfund legis-
lation has not yet been realized. It will undoubtedly be extensive,
markedly aftering the Commonwealth's approach to the manage-
ment of abandoned hazardous waste sites. It will be an added com-
plexity to the lives of many people—people engaged in real or per-
sonal property transactions: bankers, brokers, lawyers, insurance
firms. It will invite industries and those involved in handling haz-
ardous materials to learn the science and economies of release and
spill prevention.
Strong enforcement tools with a triple damage clause are a major
part of this legislation. The $25 million fund for remedial action is
available to support the enforcement strategies. The Massachu-
setts Contingency Plan will be the blueprint for abandoned site
response clearly establishing, for the first time, the rules, pro-
cedures and guidance for responding to abandoned sites in the
Commonwealth. It will provide standardized and structured pro-
cesses for the abandoned site program and the beginning of a
strong abandoned site management program for the Common-
wealth.
Twenty-five million dollars is not a large sum of money for this
activity, but it is a beginning. The Massachusetts Contingency Plan
will be the cornerstone in the implementation of the state Super-
fund program. A state Superfund legislation guided by an oper-
ating standards document, such as a contingency plan, and com-
plemented by the federal Superfund program is the key founda-
tion for a comprehensive, progressive and successful abandoned
hazardous waste site program.
REFERENCES
1. "Eckhardt Report", U.S. Congressional Committee on Interstate and
Foreign Commerce, Oct. 1979.
2. "Surface Waste Impoundments in Massachusetts", Massachusetts
Department of Environmental Quality Engineering, Nov. 1983.
422
STATE PROGRAMS
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STATE OF TEXAS SUPERFUND PROGRAM AND
REVIEW OF TWO SPECIFIC SITES
JAMES W. TREMBLAY
Lockwood, Andrews & Newman, Inc.
Houston, Texas
J. CHRIS LIPPE
Texas Department of Water Resources
Austin, Texas
INTRODUCTION
The State of Texas is managing its Superfund efforts through
an aggressive program including awarding contracts to Lockwood,
Andrews & Newman, Inc., for remedial action at two sites in
Houston. These two sites, French Limited and Sikes Disposal Pits,
are located within a half mile of each other approximately 20 miles
northeast of downtown Houston near the town of Crosby.
In this paper, the authors describe the Texas Superfund pro-
gram along with the recent activities at these two sites. Develop-
ment of work plan protocols, results of field activities and con-
clusions are covered.
TEXAS SUPERFUND PROGRAM
The State of Texas has had an aggressive solid waste program
since enactment of the Texas Solid Waste Disposal Act in 1969.
In fact, the waste shipping manifest and reporting system devel-
oped under the Texas program became the model upon which the
current national system is based. However, until passage of the
Comprehensive Environmental Response, Compensation, and
Liability Act (CERCLA) and state legislation establishing the Texas
Disposal Facility Response Fund in April of 1981, the state did
not have a means of cleaning up abandoned hazardous waste
sites.
In February of 1982, the Governor of Texas designated the
Texas Department of Water Resources (TDWR) as the agency
with authority to develop and manage the Superfund program.
Because of the strong solid waste program already in existence
and the early passage of legislation providing for 10% match-
ing state funds, Texas has become one of the leading states in the
Superfund program.
Priority List Sites
The TDWR identified 20 candidate sites to the USEPA in April
1981. Twelve of the original 20 sites had sufficient existing data
to rank under the National Hazard Ranking System (HRS) for
submission to USEPA. Of those 12, 8 sites scored high enough to
be included on the National Priority List and thus were eligible
for remedial action funding under Superfund. Six of these sites,
including the Sikes Disposal Pits and French Limited Sites, are
in the Houston area.
Staffing
The total Superfund staff at TDWR consists of nine people
including the Superfund unit manager, four project officers, a
candidate site investigations project officer, an accountant, a
public affairs officer and a technical assistant. The four staff
members designated as project officers are responsible for two
sites each. It appears that the current ratio of two sites per project
officer is a reasonable level, at least for the site investigation and
feasibility study phases of projects.
Federal Funding
More than $2,500,000 has been awarded TDWR under cooper-
ative agreements with USEPA for remedial investigations and feas-
ibility studies. The Sikes Disposal Pits Site Investigation has a
grant budget of $500,000 and the French Limited Site Investiga-
tion and Feasibility Study has a total grant budget of $467,000.
Remedial Action Consultant Selection
The Sikes Disposal Pits Site Investigation and the French Lim-
ited Site Investigation and Feasibility Study were advertised in the
Texas Register on July 27, 1982, requesting proposals for these
projects from qualified consultants. Following a site visit for inter-
ested consultants in mid-August, proposals were submitted on
Aug. 31 and Sept. 10 for French Limited and Sikes, respectively.
Nineteen proposals were received for French Limited and 23 for the
Sikes project.
A panel of four TDWR staff independently reviewed and scored
the proposals using a prepared scoring form. This form elabor-
ated on the general evaluation criteria of: (1) company qualifica-
tions, (2) personnel qualifications, (3) technical approach and (4)
management plan. Following the proposal scoring and ranking, the
top three ranking firms (or proposal teams) were invited to make
presentations.
The outcome of this procedure was that the firm of Lockwood,
Andrews & Newnam, Inc. (LAN) and their subconsultants, En-
vironmental Science and Engineering, Inc. (ESE) and Harding
Lawson Associates (HLA) were selected to enter into contract
negotiations .with TDWR in late November. Contracts for both
Sikes and French Limited were signed on Jan. 17, 1983, and
formal notice to proceed was granted to LAN. HLA was respon-
sible for all geotechnical aspects of the site studies; ESE accom-
plished all environmental sampling and analyses. LAN was respon-
sible for overall project management and the feasibility study.
The time requirement for subsequent Superfund project con-
sultant procurement (from request for proposals to contract sign-
ing) has been reduced to approximately three months as compared
to the six months required for the initial projects. The longer time
requirements on earlier projects, such as Sikes and French, are
attributed to program development. During this early procure-
STATE PROGRAMS
423
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merit period, methods and procedures had to be developed, the
request for proposals, scoring forms and contracts were orig-
inated and numerous legal decisions had to be made.
SITE BACKGROUND
The French Limited and Sikes Disposal Pits are located in close
proximity to one another near Crosby, Texas (Figure 1). French
is approximately 22 acres in size and Sikes is approximately 25
acres. The French site has a single 8-acre unlined pit, while Sikes
has one unlined main waste pit and several small unlined pits
(Figure 2). Both sites are located within the floodplain of the San
Jacinto River. On at least three occasions in the last 15 years, the
sites have been inundated by flood waters from the San Jacinto
River. The Sikes site is ranked 30th and French 25th on the Na-
tional Priority list.
Both sites operated during the 1960s. Petrochemical industry
wastes deposited at the French site are believed to have been
brought to the site in bulk form. During the six-year period end-
ing in 1972, approximately 600,000 barrels of industrial wastes
were received at French. The disposal operation at French was
granted a permit in 1970 with special conditions relative to on-
site controls of the wastes. Less than one year later, the state can-
celled the permit at French for failure to comply with special per-
mit conditions.
The Sikes site reportedly operated for approximately six years,
ending disposal operations in 1967 when Mr. Sikes died. Bulk and
drummed petrochemical industry wastes were disposed at Sikes.
The Sikes operation was never permitted.
Major concerns for offsite contamination were for: (1) ground-
water contamination and (2) potential transportation of sludges
and contaminated surface water offsite. The Riverdale subdivision
(approximately 50 to 60 homes) is located less than one-quarter
mile southwest of the disposal pit at French. Some of these homes
depend on the shallow wells for a water supply.
MtLES 10
HOUSTON
INTERCONTINENTAL
AIRPORT
LAKE HOUSTON
FRENCH
SAN JACNTO
RIVER
Figure 1
General Location of Sites
In the 1979 flooding of the sites, the pits overflowed. Sludges
were deposited in areas adjacent to the pit on French, while
sludges from the main pit on Sikes were transported across a large
(10 to 15 acres) low-lying area east of the main pit and off the
Sikes property. (Figure 2). Lack of maintenance had allowed con-
tainment levees to deteriorate and be breached by the flooding.
SAMPLING
Both state and federal sampling were conducted at various times
between 1971 and 1981. Sampling at French was more extensive
Figure 2
French and Sikes Sites
and revealed that the sludges, soils, surface and groundwaters
were contaminated with heavy metals and chlorinated organics,
including polychlorinated biphenyls (PCBs), benzene, chloroform,
carbon tetrachloride, trichloroethylene and vinyl chloride. Samp-
ling of shallow groundwaters in the vicinity of French in 1981
showed that a variety of organic compounds were present. The
limited preliminary sampling at Sikes in mid-1981 indicated the
presence in the waste pits of phenolic compounds, xylene, ben-
zene, toluene and other organics.
SITE GEOLOGY/HYDROGEOLOGY
The shallow aquifer beneath the sites resides in a broad sandy
aquifer believed to be relatively permeable. Some residences in the
vicinity of the sites depend on this shallow aquifer for drinking
water. In the 1970s, numerous complaints of tastes and odors in
the drinking water were reported. In 1979 the Harris County
Pollution Board reported marked improvement in the overall qual-
ity of the shallow groundwaters in the site vicinity.
OBJECTIVES
The scope of the studies at the French and Sikes sites was de-
fined as follows:
•French: Conduct a remedial investigation and a feasibility study
•Sikes: Conduct a remedial investigation only
The remedial investigation at each site was to characterize the
site in terms of wastes present, magnitude and extent of contam-
ination, rate and direction of any waste migration, target recep-
tors, site geology and hydrogeology.
The feasibility study at French was designed to develop and
evaluate alternative remedial measures considering economic fac-
tors, environmental impacts, regulatory constraints and timeliness
of completion.
FIELD PROGRAM PROTOCOL
The overall objectives of the field studies at both sites were to
characterize the sites with respect to contamination and waste
migration potential. A separate protocol for each site was devel-
oped. These protocols were subsequently refined in separate work
plans for each site. The rationale used in selecting sampling sites
at each site is described below.
Soil Borings/Groundwater and Surface Water Sediment Sampling
The planned soil borings, installation of wells and groundwater/
surface water and sediment sampling were developed to character-
ize the site waters and subsurface soils from both a physical and
chemical viewpoint. Both shallow and deep wells were planned,
chemical analyses were outlined and physical testing of the sub-
424
STATE PROGRAMS
-------
surface soils was outlined. The general locations of groundwater
samples is shown in Figure 3.
Surface water samples were requested to define the levels of
surface water contamination on and around the sites. These sur-
face water sites were divided into three categories: ponds/pits,
drainageways and the main river channel. Sediment samples were
planned to characterize the on-site and off-site sediment deposits.
The location of surface water and sediment samples is shown in
Figure 4.
Air, Soil, Biota, Core and Waste Sampling
The environmental sampling protocols developed for each site
included air, soil, biota, core and waste sampling. The location
of these samples is shown in Figure 5.
At the beginning of the field work at each site, a field recon-
naissance was developed. As indicated, ambient air sampling was
to be accomplished.
CROSBY
8
Figure 3
French and Sikes Soil Borings and Groundwater Samples
FRENCH
/•^ SIKES . J,
fe;p £*M
Figure 4
French and Sikes Surface and Sediment Samples
Figure 5
French and Sikes Soil, Biological and Core Sampling
Soils sampling was planned only for French. Previous flooding
had left waste sludge residue on the site outside the waste pit and
possibly beyond the site boundaries. In mid-1982, USEPA re-
moved some of these sludges and placed them back into the waste
pit. The objective of the soils sampling was to determine the levels
and quantities of soil contamination off-site.
Biological samples were planned for each site. The samples
collected at French were for three off-site composite fish specimens
to determine if metals and PCBs could be found in indigenous
fish. The Sikes biological samples consisted of nine benthos
samples from the nearby bayou/river network. The object of the
Sikes samples was to determine if nearby aquatic ecosystems were
being stressed by contaminants from the site.
During the 1979 flooding, sludge wastes were transported out-
side the Sikes main waste pit dikes and across a low-lying area,
approximately 10 to 15 acres, east of the site. The objective of the
15 core samples was to obtain initial physical and chemical char-
acterization of these sludges. Estimates of sludge volume would be
made.
Ten waste samples were planned for Sikes to cover representative
samples of waste materials found outside the waste pits such as
containerized wastes, other small waste pits, etc.
Hydrogeology
The planned hydrogeological studies at both sites included soil
borings, development of monitoring wells, groundwater level meas-
urements, field permeability tests and physical soil analyses. In
addition, geophysical tests were planned for Sikes.
Groundwater level measurements were planned at each site us-
ing existing and newly drilled wells. Weekly readings were planned
to collect data on changes in groundwater gradient so that ground-
water flow direction could be determined. Slug tests were pro-
grammed to determine the permeability of the aquifer.
Geophysical tests proposed for the Sikes site included ground
penetrating radar, electrical resistivity and electrical borehole log-
ging. Use of geophysical techniques at French was not planned
because the site inspection indicated that the subsurface contam-
inants were probably so dispersed that they could not be detected
using geophysical techniques. Additionally, there was no evidence
of wastes being buried at French.
Ground penetrating radar was planned for use at Sikes to de-
tect the presence of buried drums and to determine the thickness
and continuity of sand and clay layers underlying the site. Elec-
trical resistivity profiling and sounding was planned to evaluate the
STATE PROGRAMS
425
-------
extent of a contaminant plume and to correlate stratigraphy. Elec-
trical borehole logging was planned for both sites to obtain a de-
tailed view of the stratigraphy.
PROJECT DELAYS
The Sikes family, consisting of the widow of the former site
operator, her two sons and two grandsons, was residing in the
central area of the site, virtually surrounded by waste disposal
areas. The family's relocation was based on a need to protect their
health and safety as well as to reduce the possibility of interfer-
ence by the family with the investigation crews.
TDWR had earlier established an excellent rapport with the
family. Nevertheless, the family was reluctant to relocate for the
duration of the survey. The eldest son would agree to move and
then reverse his decision later. Many of his concerns seemed to
stem from a fear of his family losing its property. Their owner-
ship had been established several years earlier under squatters'
rights.
TDWR was finally able to get the family to agree to move into
two new mobile homes furnished by the Federal Emergency Man-
agement Agency (FEMA). The agreement assured the family that
they could remain on their property as the mobile homes would be
located in an uncontaminated corner of the site. This created
further problems since the entire site is within the 100 year flood-
plain of the San Jacinto River and there is a county ordinance
against issuing building permits within the floodplain.
Negotiations between LAN and county officials culminated in
the special hearing and the granting of the special permit. The
family relocation then went without incident. The family was sat-
isfied, their safety was assured and investigation crews were un-
encumbered by their presence.
Initial field work at French was delayed by four weeks. Initial
field activities (soil borings) at Sikes were begun on May 9, a delay
of approximately ten weeks from the original schedule. Environ-
mental sampling at Sikes was to begin on May 23. However,
between May 21 and May 25 the San Jacinto River flooded and
both the Sikes and French sites were inundated.
FLOOD RESPONSE
The flooding of the sites in late May resulted in a one-week de-
lay of Sikes field work. This incident did afford a unique oppor-
tunity to make first hand observations of effects and flow patterns
of flood waters.
The San Jacinto River flooded as a result of extremely heavy
rainfall at a time when Lake Houston's water elevation was very
high. The River reportedly left its banks from May 21-25. Flood
water elevations near the sites peaked on May 24. Most areas on
Sikes were under 6 to 8 ft of water. French was under 4 to 6 ft
of water. Flood waters receded by the afternoon of May 25.
LAN made aerial observations of the flooding on May 23. Flood
waters covered both sites. All waste pits on Sikes and the French
pit were inundated. Surface reconnaissance of both sites was
accomplished by LAN and ESE in boats on May 23 and 24.
This unexpected event presented an opportunity to observe the
flood flow patterns and better understand the possible spread of
contamination caused by earlier flooding of the sites. Some float-
ing sludge from the French pit was transported out of the pit dur-
ing the flood. This was cleaned up as an emergency response by
USEPA during the first week of June.
REMEDIAL INVESTIGATION RESULTS
Because of the delays encountered, the results of the field in-
vestigations at Sikes are not yet available. The results of the French
remedial investigation are presented below.
Groundwater
The French Limited site is located in the middle of a filled ox-
bow lake/channel of the San Jacinto River (Figure 6). As uncon-
fined aquifer (sand layer) underlies the site. Prevailing water levels
in the main pit at the French Limited site were about 10.6 ft above
main sea level during April 1983 (Figure 7). These readings are at
approximately the same elevation as the shallow groundwater table
in the immediate area of the main pit.
The shallow aquifer is anticipated to have a slight overall grad-
ient (approximately 0.001) toward the San Jacinto River. Over
short distances, this gradient could be somewhat higher because
of various land features. Shallow groundwater flow away from the
main pit is estimated to be approximately 20 ft per year, prob-
ably in a radial direction with the shallow contaminant plume elon-
gated to the south-southwest and the north-northwest.
Figure 6
Oxbow Lake Location
Figure?
French Site Groundwater Elevations
The shallow groundwater immediately south of the site con-
tained benzene (180 /tg/1), toluene (67 /tg/1), methylene chloride
(74 /tg/1), carbon tetrachloride (44 /tg/1), 1,1-dichloroethane (130
/ig/1), 1,2-dichloroethane (440 /tg/1), trans-1, 2-dichloroethane
(180 /tg/1), tetrachloroethene (910 /tg/1), phenol (32 /tg/1), naph-
thalene (150 /tg/1) and a variety of other organic compounds
(primarily volatile in nature). Many of these levels are substantial-
ly above the recommended 10~s incremental cancer risk criteria
established for human health protection.
The other shallow wells at greater distances south of the French
Limited site were analyzed for indicator parameters (TOC, TOX,
pH and conductivity) of contamination. Traces of contamination
may be due to landfills south of Gulf Pump Road. Samples from
426
STATE PROGRAMS
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two residential wells in the Riverdale Subdivision were free of con-
tamination.
A deep water-bearing zone was found in a sand formation
approximately 125 ft beneath the site. An aquitard of lower perme-
ability clays and sandy clays separates the upper and lower
aquifers. The deep aquifer exhibited a pH of 9.2, and water in the
aquitard has a pH of 7.6 to 7.8. In contrast, the shallow aquifer
exhibited pH in the range of 5.4 to 7.1. The deep aquifer had a
TOCof4.8Mg/I.
Sludges/Sediments
All floating oily residues at the French Limited site were removed
by USEPA emergency response efforts during 1982 and 1983.
A deposit of sludges on the floor of the main pit was identified
using sub-bottom profiling geophysical techniques. The depth of
this sludge deposit is 0.8 to 3 ft (Figure 8). The entire pit contains
about 210,000 ft3 of sludge and contaminated sediments contain-
ing a variety of organic compounds including naphthalene (0.24%
by weight dry), phenanthrene (0.18%), polychlorinated biphenyls
(507 ppm), phenols (22.9 ppm) and several other base/neutral frac-
tion class compounds. Sludges in the main pit contained total ex-
tractable organics (TOE) ranging from 0.78 to 9.26%.
Between the main pit and U.S. Highway 90 the sludges had TOEs
as high as 9.14% by weight on a wet basis. Soils from the same
area had TOE values between 3.7 and 31.3%. The chemistry of
these sludges is similar to those in the main pit.
The highly soluble, solvent chemicals (benzene, toluene, methy-
lene chloride and others) contained in the sludges and sediments of
the main pit have the highest potential for migration into and con-
tamination of the groundwater and surface water environment.
Surface Waters
Surface waters in the main pit had concentrations of volatile
organic compounds (benzene, vinyl chloride, chloroform and
others) between 2 and 4 /tg/1. One pesticide, Lindane, was found
in the main pit at a concentration of 0.003 /ig/1. The depth of the
main pit averaged 10.6 ft during a survey in April 1983 and con-
tained an estimated 24,500,000 gal of water.
Surface waters outside the main pit contained Lindane at 0.045
/tg/1 in the lake south of Gulf Pump Road and at 0.005 /*g/l in
the slough north of the pit. The slough also had a TOC of 35.7
LEGEND:
SLUDGE DEPTH
f 3 FT DEPTH
fg IS FT DEPTH
^ 1,0 FT DEPTH
F] 25 FT. DEPTH
Figure 8
Sub-Bottom Profile
The surface waters overlying the heavily contaminated sludges
in the main pit were found to contain trade (/ig/1) levels of vola-
tile organic chemicals. Many of the non- volatile organic com-
pounds found in the sludges and sediments were either not found
or were detected at low levels in the overlying waters. Thus, only
low transport rates from the sludges into the overlying waters are
occurring.
Surface Soils
A soil sample off-site south of Gulf Pump Road had a TOE
value of 1,230 ppm and total organic halogen (TOX) of 140 ppm.
Another soil sample off-site north of U.S. Highway 90 contained
lower levels of these indicators (TOE-421 ppm and TOX-17.2
ppm).
This contamination is believed to be the result of past flood
events at the French Limited site. The landfills and dumps along
Gulf Pump Road may also have made a contribution. The areal
extent of this contamination beyond the sampling areas is not
known.
Fish Tissues
Three fish tissue samples from the "fishing hole" beneath the
U.S. Highway 90 bridge north of the site contained PCBs rang-
ing from 18 to 194 ppb. These levels are well below the FDA 5,000
ppb PCB limit.
CONCLUSIONS
The State of Texas Superfund Program, as administered by
TDWR, is aggressively pursuing solutions to the State's aban-
doned hazardous waste sites. Although unexpected problems have
developed during the administration of some of the projects, such
as the relocation problem with the Sikes family and the flooding
at both the French and Sikes sites, TDWR and the consultants have
worked together to minimize their impact on schedules and
budgets.
Detailed protocols for site work were developed in separate site
work plans. Such detail proved to be very useful as only minor
adjustments of the work plan were required. Separate work plans
for each site were based on extensive review of all existing data
and consisted of detailed rationale for all field efforts and assess-
ment of the site hydrology/hydrogeology.
This preplanning is essential to the successful completion of a
Remedial Investigation study. The thorough review of all avail-
able background data prior to developing a work plan can reduce
field sampling changes and ensure that the final results will sup-
port the follow-on Feasibility Study.
Based on this specific data on French and the general physical
observations made at Sikes to date, follow-on remedial actions
are warranted. Feasibility studies at both sites should be carried to
completion.
STATE PROGRAMS
427
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THE STATES AND EPA: AN EVOLVING
PARTNERSHIP UNDER SUPERFUND
JAN WINE
Hazardous Site Control Division
U.S. Environmental Protection Agency
Washington, D.C.
HEATHER BURNS
Booz, Allen & Hamilton, Inc.
Washington, D.C.
INTRODUCTION
The Superfund program, administered by the USEPA, has the
ambitious mission of responding to releases of hazardous materials
and pollutants in order to safeguard the public health, welfare and
the environment. A fund of $1.6 billion was authorized under
the Comprehensive Environmental, Response Compensation and
Liability Act of 1980 (CERCLA) to finance this activity.
In passing CERCLA, Congress recognized that success was
possible only if many parties shared responsibilities. Most critical
was a joint role for the Federal government and the states. The
purpose of this paper is to examine how USEPA and the states
have shared responsibilities since the program's inception and how
recent Superfund policies and directions signal a more extensive
and flexible role in the future.
In this paper, the authors address only one aspect of the Super-
fund program: remedial response. This includes both planning for
and actual implementation of the final remedial action. Relation-
ships between USEPA and the states in conducting other responses
under Superfund, namely immediate or planned removals, differ
somewhat and are not discussed here.
THE PARTNERSHIP TO DATE:
SHARED RESPONSIBILITIES
Participation of the states in the Superfund program is not only
encouraged by USEPA, but also required by CERCLA. Specific-
ally, states have the following three responsibilities as part of
Superfund remedial actions:
•They must assure for adequate operation and maintenance of
remedial measures at the site after a prescribed time
•They must assure the long term availability of a facility for the
disposal of wastes
•They must contribute a share of costs in certain circumstances
At a minimum, state participation under the program is limited
to providing these three assurances, and in such cases, USEPA re-
tains primary responsibility for managing site cleanup. The option
for significantly greater involvement is open to states, however,
including assumption of full management responsibility for the
remedial action. Many states have assumed these expanded duties.
The factors a state must consider in deciding the role to be taken
and a description of the specific implications of that decision are
discussed below.
The Decision of Lead Responsibility
The decision of lead management responsibility is a complex
one. In weighing the possibility of a lead role, a state must consider
the adequacy of its legal authority and resources and its ability to
mobilize those resources in the prescribed time frame.
Legal Authority
States must provide explicit documentation from the Governor
or Attorney General that they have full legal authority to admin-
ister and manage CERCLA funded response actions. They must
be able to undertake responses, receive funds from USEPA and
obligate monies to other governmental agencies or private con-
tractors. They also must have the authority to enter into contracts.
If legal authority is clearly insufficient or impossible to obtain
expeditiously, states may opt to have USEPA manage the remed-
ial response. The importance of expeditious action should be
stressed, since it can take on special significance in certain circum-
stances. In Colorado, for example, the legislature must approve
each Superfund remedial activity before the state can assume lead-
ership. Since the legislature's schedule does not always coincide
with the needs for remedial site cleanup, the initiation of cleanup
at a site can be delayed.
Resources
States must also consider the availability of staff and monetary
resources as they determine their preferred management position.
It must be clear that state technical and management personnel,
as well as the systems to support them, are sufficient to meet the
exacting demands of the site cleanup.
Hazardous waste response is a massive undertaking involving
million dollar budgets, technical oversight of cleanup activities and
strict reporting of accomplishments and progress. Engineering
costs for cleanup alone can range from hundreds of thousands to
millions of dollars. (Containment of hazardous materials at one site
in California has been under way for five years and planned costs
already exceed $12 million). Even beyond these costs are those
associated with the management of the cleanup effort. These typic-
ally average 10 to 12% of actual site cleanup and pose a consider-
able extra demand for state management personnel.
States typically find that their internal resources are insuffic-
ient to manage and conduct the response. Many prefer to augment
state staff with outside contractor support to ensure an adequate
level of resources. Contractors are used in this way not only for
remedial design and construction, but also for overall management
of the response as well.
Time
Closely related to the issue of resources is another important
consideration of the states in determining their management role:
their ability to respond in the necessary time frame. Many states,
relying on their current staff and their established procedures to
acquire contractual support, can respond quickly even to time crit-
428
STATE PROGRAMS
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ical "emergency" releases. It is not always possible, however, for
the state to quickly plan, organize and procure necessary contrac-
tual support. For example, the option of relying on contractors to
augment state staff may be viable only if states can obtain such sup-
port within the time frame dictated by the hazardous waste re-
lease. Thus, lack of existing state personnel, compounded by
lengthy procurement procedures, may preclude a state from assum-
ing prime management authority.
Implications of the Leadership Decision
The decision of Federal or state lead for a remedial action has
far-reaching consequences. It directly affects the specific manage-
ment duties and responsibilities assumed by each party, the legal
instrument that is signed to formalize the relationship and the
manner in which funds are provided.
Management Responsibilities
By assuming the lead role for a remedial action, the state assumes
primary management responsibility for all phases of the cleanup
from planning through construction. The specific responsibilities
of different states vary under the terms and conditions established
with USEPA, but the state will generally accomplish the following
activities:
•Plan the entire remedial action, which includes developing a
schedule and setting the level of effort, milestones and specific
remedial actions to be undertaken. The workplan is a funda-
mental component of the cooperative agreement between the state
and USEPA.
•Obtain necessary staff support for both overall management and
engineering response at the site. As mentioned earlier, such sup-
port may be drawn from existing state rosters or may be obtained
through private contractors. If contractors are utilized, the state
must initiate the procurement process, issue a request for pro-
posal, screen all candidates and select final contractors.
•Monitor progress at the site and report on progress. Because of
the magnitude of expenditures and the complexity of the technical
response, rigorous management is essential. Quarterly reports on
progress must be submitted to USEPA. Included must be: item-
ized expenditures by task and activity, totals of labor and costs
incurred since the last report, estimated completion of work com-
pleted for each activity and estimated variances in cost and time
expected at project completion.
•Select individuals to prepare and implement a community rela-
tions plan. To effectively accomplish site cleanup, the public must
be involved in the decision-making process. To this end, a com-
munity relations assessment is undertaken to evaluate the history
of community involvement and the concerns or issues associated
with problems at the site. A community relations plan is devel-
oped to initiate formal and consistent contact with interested in-
dividuals and citizens' groups. The communications techniques
used for one site are not necessarily applicable for all sites, but
each plan should establish a repository for technical informa-
tion and a mechanism for advising citizens living near the site of
work to be conducted by either the state or USEPA. A three-
week public comment period is required once the feasibility study
is complete and before a final response action is chosen.
•Prepare safety and quality assurance project plans. The state must
also assume responsibility for developing a plan to ensure the
safety of both personnel working at the site and residents nearby.
The objectives of the plan must be clearly stated and specific pre-
cautions must be detailed, i.e., mandatory training of site work-
ers. The plan governs the actions of state as well as contractor
personnel. In addition to the safety plan, the state must also
assure the quality of environmental samples taken. A plan must
be written to specify procedures for sampling, documenting chain
of custody and labelling sample materials.
In cases where USEPA assumes the lead for a remedial action,
Agency staff take on responsibility for the activities noted above.
With the exception of quarterly reporting, all functions are basical-
ly the same.
The Legal Instrument Binding the Two Parties
The decision of a state as opposed to a Federal lead for remed-
ial actions at a site also determines the sort of legal instrument that
will be utilized to formalize each party's responsibilities. Two sep-
arate types of instruments are used: the cooperative agreement,
which is employed if the state assumes the lead, and the Super-
fund state contract (SSC) which is signed when USEPA retains
management responsibility. The SSC, it should be noted, is not a
traditional procurement contract, but rather a binding agreement
that authorizes the USEPA to proceed with remedial response ac-
tivities within state borders.
Contracts and cooperative agreements have basic similarities:
they are both legally binding instruments that assign responsibil-
ities to the state and USEPA, they both allow the transfer of funds
and they both are instruments for obtaining required assurances.
Each provides for the different management roles discussed earlier
in this paper.
Despite these similarities, however, the detail and scope of these
vehicles differ. While both contain work plans assigning specific
responsibilities, the cooperative agreement plan is more specific
and identifies particular tasks, dates for completion and level of
effort. It ensures the allowability of all costs incurred so the states
may receive full compensation for tasks they undertake. Such de-
tails are excluded from an SSC, since the costs of management are
incurred by the federal government.
Funding Mechanisms
Regardless of the assignment of lead responsibility, the USEPA
provides funds equivalent to the total cost of cleanup exclusive of
the state's cost share. Methods of transfer and overall responsibil-
ity for financial management differ, however, depending on
whether the state or EPA leads the action.
Most significant is the difference in the flow of funds. If the
states take the lead, the USEPA prefers to transfer funds to the
state via an already established letter of credit. Conversely, if EPA
takes the lead for cleanup, the flow of funds is reversed, as the
state pays its share of costs of EPA via the Superfund state agree-
ment.
Upon transfer of dollars, the state assumes responsibility for
establishing and operating the cleanup budget, pays contractors
directly from this budget, and reimburses its own agency and
offices for expenses incurred. Under this arrangement the state has
direct control over its outlays setting its pace in accordance with
the state budget cycle. If USEPA leads the action, separate pay-
ments of cost share are required according to a payment schedule
agreed to by USEPA and the state. Specific terms of such schedules
vary from case to case.
THE FUTURE PARTNERSHIP: MORE FLEXIBLE
STATE PARTICIPATION
So far, states and USEPA have shared responsibilities for re-
medial site response and management over the course of the Super-
fund program. In many cases, states have assumed major respon-
sibility for managing the overall cleanup effort; in other situa-
tions, state involvement has been more limited and has included
such activities as providing mandatory cost shares, secondary con-
tractor oversight and participating in community relations activ-
ities.
USEPA has long recognized that state participation is critical to
program success and that a maximum level of involvement should
be encouraged. Policies have been revised to ease administrative
requirements and to lessen the financial burden on state budgets.
These trends, together with the program's ongoing decentraliza-
tion, suggest a more flexible relationship with USEPA in the
future.
STATE PROGRAMS
429
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Program Decentralization
For the first two years of the program, states dealt extensive-
ly with USEPA Headquarters and the regions, but ultimate de-
cision-making authority resided in Washington. Thus, officials in
the states worked closely with USEPA regional personnel, who
monitored and guided site cleanups and reviewed draft coopera-
tive agreements and SSCs. States also worked with Headquarters
personnel, receiving policy direction and guidance on procedures.
In addition, final approval of cooperative agreements and con-
tracts was given at the Headquarters level.
As the program has developed, more and more responsibilities
have been delegated to the regions. This shift is expected to re-
duce the number of USEPA personnel with whom states inter-
act, sharpen lines of authority and bring the administration of the
program physically closer to the states and to the conduct of site
activities. The hope is that decision-making will be expedited and
that, as a result, USEPA as well as state-led remedial actions will
be more timely and responsive.
Relaxed State Cost Share Requirements
Recent Agency policy has emphasized the need for planning at a
greater number of sites to fully assess the requirements for subse-
quent remedial action. To lessen state expenses of an expanded
planning function, USEPA has set policy to reduce state require-
ments for sharing these costs. Thus, states are no longer required
to pay part of the costs of planning and investigation at privately
owned sites.
Further, at publicly owned sites they need not pay for planning
until (and only if) USEPA and the states decide that a Superfund
financed remedial action is appropriate. Such action might be pre-
cluded, for example, if a responsible party came forward to finance
the cleanup. In that case, of if for some other reason subsequent
Superfund activity were not undertaken, the states would incur no
planning costs. The intent of this policy is to encourage state partic-
ipation in remedial planning.
Provisions for Multi-Site Planning Cooperative Agreements
Yet another direction taken by USEPA to encourage state par-
ticipation with minimum strain on state resources is the proposed
development of multi-site planning cooperative agreements. These
agreements would cover state administrative planning activities at
more than one site and fund program activities that support the
state's assumption of the full program. Activities might include the
preparation of Superfund state contracts and review of Remedial
Action Master Plans. This policy recognizes that states should re-
ceive compensation for the expense of planning for and undertak-
ing the management of the Superfund program.
More Flexible Superfund Contracts
Administrative requirements of Superfund contracts have also
been relaxed under recent policy since the state is no longer re-
quired to cost share during remedial planning. Thus, lengthy pro-
cedures to develop SSCs for such planning activities have been
eliminated. To expedite site cleanup, the state and USEPA now
simply agree that a remedial investigation and feasibility study are
needed. The state also identifies a project officer and an individual
who will participate in community relations activities. USEPA es-
timates that as much as three months may be saved by this ex-
pedited procedure. A full SSC is still required once a remedial
action is initiated to provide state assurances and a mechanism for
cost share.
CONCLUSIONS
The changes in policy noted above suggest a significant evolving
program direction: greater state involvement with less administra-
tive and financial burden. The Agency's intent is to further en-
courage states to expand the roles they have already assumed under
Superfund and to work closely with USEPA to accomplish effec-
tive hazardous waste cleanup.
430
STATE PROGRAMS
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MINIMIZING LIABILITY EXPOSURE WHEN
CONTRACTING HAZARDOUS WASTE SERVICES
JOHN C. ROBBINS
EMPAK Services Group
Pennsauken, New Jersey
INTRODUCTION
Involvement with hazardous waste subjects generators and their
commercial hazardous waste service contractors to liability from
a number of sources, including:
•Property damage
•Impairment of environmental rights and amenities
•Bodily injury
•Intangibles such as impairment of corporate image
These sources of liability have frequently involved the use of in-
competent contractors by generators of hazardous wastes. In this
paper, the author deals specifically with how hazardous waste gen-
erators can minimize their liability of exposure when using out-
side service organizations during hazardous waste remedial action
activities.
"Remedial action", as used in this paper, refers to activities
such as waste removal, transport, detoxification, etc., which are
not normally performed on a routine basis. These activities can be
scheduled, such as a lagoon closure, Superfund site cleanup or
building decontamination, or unscheduled, such as a spill cleanup.
"Generators" refer to those who either produced, used, owned or
otherwise could be traced to the waste in question.'
BACKGROUND
The trend in environmental enforcement is toward criminal
prosecution of individuals. The imposition of criminal liability is
usually derived from various federal and state statutes. However,
there are recent cases where general criminal statutes such as con-
spiracy or fraud have been used to prosecute corporate officials.
Insulating oneself from liability by hiding behind the nameless
corporation is no longer possible, as illustrated by the USEPA's
RCRA and Consolidated Permit regulations which require the
signature of responsible individuals on permit applications, waste
manifests, etc.
Civil liability in the hazardous waste field seems to be in an
uncertain, but definitely expanding, state of flux. Civil liability has
traditionally been used in environmental damage cases as a means
for the federal and state governments to proceed against the gener-
ator with the most financial resources.
Personal lawsuits from third parties have traditionally been re-
lated to nuisance and negligence. But now there are a number of
1. At hazardous waste conferences, there invariably is an argument over whether liability passes
along with title to wastes. A broad definition of "generator" is used because-(l) this is an evolving
area of law and (2) there have been some extreme examples under so-called "joint-and-several
liability", such as generators of non-hazardous wastes, which were commingled with hazardous
waste, having been brought into a suit.
other theories of laws being developed which increase the individ-
ual's exposure to liability.2 These include liability imposed by:
•Increased risk or future harm
•Mental distress
•Intentional infliction of mental distress
Moreover, generators of hazardous waste have more than just a
moral obligation to protect the environment; individual corpor-
ate officials can be held liable for environmental damage as part
of a presently unclear, but evolving, case law.
The purpose of this paper is to point out to generators of waste
that it is in their own personal interest, as well as their company's
interest, to pay careful attention to the selection of, and contrac-
tual arrangements with, hazardous waste service organizations.
CONTRACTOR QUALIFICATIONS
There are organizations available for generators to contract
services ranging from such seemingly trivial tasks as transporting
metal sludges to such obviously dangerous tasks as detonating gas
cylinders containing highly toxic materials. The one thing all these
services have in common is that they involve risk of environmental
damage. As such, they subject the contracting party to liability.
The following represent minimal contractor qualifications which
should be considered by generators:
Financial Resources
A key element in minimizing risk when contracting hazardous
waste services is assurance that the contractor has sufficient finan-
cial resources to undertake correction of any environmental dam-
age resulting from action involving the generator's waste.
If the contractor could be potentially deficient in financial re-
sources, then the generator should be sure to include contractual
requirements such as insurance, performance bonds, etc.
Performance Record
The hazardous waste service contractor should have a proven
record in performing hazardous waste cleanup and disposal.
While this may seem obvious, it is an area which is often taken
for granted. For example, many of the major service companies
claim to be able to handle just about any problem that a gener-
ator might have while, in fact, a subcontractor is used for many
services. While there is nothing wrong with using subcontractors,
2. For an excellent synopsis of recent trends in civil liability for environmental damages, the
reader is referred to Individual Civil and Criminal Liability for Environmental Damages, 1982, by
the Hartford Steam Boiler Inspection and Insurance Co., Hartford, CT.
LEGAL LIABILITY
431
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risk exposure could increase if they do not have adequate per-
formance records. At the very least, contractors should indicate
what subcontractors may be used and provide assurance that they
are qualified and reputable (e.g., not on USEPA's listing of barred
companies).
Medical Surveillance Program
The contractor should have a medical surveillance program for
personnel involved in the direct handling and/or exposure to toxic
materials. The goal of the program is to demonstrate and correct
any job related injury or condition. While some would argue that
such a program can be a "smoking gun", it only seems right that
everything possible be done to protect the health and safety of em-
ployees. Medical surveillance programs typically should involve
most of the following:
•Medical history
•Annual general physical to assess person's capability of working
in respiratory protection equipment
•Blood and urine laboratory tests to assess status of kidney, liver
and nervous system
•Other laboratory tests for known contaminants to which the per-
son has been exposed (serum lead, PCB, pesticide screen)
The more comprehensive programs established by some contrac-
tors include EKGs, chest x-rays, frozen specimen storage and other
special procedures.
Attitude Toward Fixed-Priced Contracts
Most people have heard of at least one instance of gross cost
overruns on hazardous waste cleanup projects performed on a time
and materials basis. Obviously, there are many situations such as
emergency responses and excavations of unknown materials where
it is not possible to obtain a fixed-price contract. Nevertheless, the
contractor should at least be willing to try to establish a fixed price
for as much of the project as possible. If a contractor is unwill-
ing to do this, one should ask himself whether he and/or his con-
tractor know enough about the problem to proceed cost effec-
tively and safely.
Disposal of Wastes
The contractor should specify exactly where he intends to dis-
pose of any wastes, should that be part of his responsibility. If one
has any doubts, set up an escrow account to provide an incentive
to dispose at the agreed upon facility. Ideally, wastes should be
sent to a facility with an approved Part B, RCRA application,
not to a facility with just a RCRA "interim status" permit, un-
less the facility has been audited to one's own satisfaction.
The contractor should be willing to become the generator and
not just the handler, transporter or disposer, of any wastes to be
removed. While this does not necessarily reduce one's liability, it
tends to increase the contractor's liability, providing an indirect in-
centive to perform properly.
There may also be some reduction in risk exposure if wastes can
be sent directly to a facility where wastes become essentially "non-
traceable". Such facilities generally include incinerators, injec-
tion wells and liquid treatment facilities. The "traceability" of
wastes can become more important if one contracts to someone
who will broker his wastes to a third party. In this instance, one
should insist upon a certificate of disposal showing the ultimate
fate of wastes.
CONTRACT REQUIREMENTS
When attempting to contract for less environmental risk ex-
posure, the following can be considered:
Insurance
Most general Liability insurance coverage excludes environmental
damage. Hence, it is important to require a hazardous waste
service contractor to carry more than just comprehensive general
liability insurance. Furthermore, the process of acquiring environ-
mental risk insurance with a recognized carrier can itself reduce en-
vironmental risk exposure. This is a result of the insurance carrier's
own evaluation of the insured's potential liability.
The amount of insurance coverage required would vary with the
amount of risk involved in a specific project. Insurance coverage
is generally available in the following amounts, which are also
recommended as minimum coverage for any contractor with his
own disposal facility:
Comprehensive General $5 to 10 million per occurrence
Liability
Sudden Release Environment $5 to 10 million per occurrence
Impairment Liability
Non-sudden Release $5 to 10 million per occurrence
Environment
Impairment Liability
Surety Bonds
The furnishing of surety bonds by the hazardous waste services
contractor is a further guarantee of the faithful performance of
the contract and the payment of bills for labor and materials. For
the bonds to have meaning, they must be obligated by a reputable
financial institution.
There are normally up to three types of bonds used: (1) bid
bonds, (2) performance bonds and, (3) payment bonds. The bid
bond is usually required only on government competitive-bid con-
tracts to assure that bids have been submitted in good faith. The
performance bond guarantees that the contractor will carry out a
contract in accordance with its terms. The requirement of a per-
formance bond is commonly used in service and construction
contracts. The payment bond simply insures that the contractor
will pay his bills incurred under a contract, rendering the owner
harmless from claims filed after completion of work.
Surety bonds only minimize financial risk exposure and then
only in the amount of the bond. Any contract inadequacies, en-
vironmental risks, etc., are not covered. Nevertheless, the use of
surety bonds offers some direct financial protection as well as in-
direct protection by eliminating unqualified contractors from the
hazardous waste service industry.
Confidentiality Requirements
It is often appropriate to protect information on products,
processes, customers, etc. In many firms, secrecy agreements are
a routine requirement for contractors; the added dimension of
public sensitivity to toxic wastes can make confidentiality even
more important when dealing with hazardous waste service con-
tractors.
SUMMARY
Liability exposure from hazardous waste service projects can be
significant. Because of a possible trend toward individuals being
held liable for environmental damage, it is important for gener-
ators to take steps to ensure that their hazardous waste service
contractors are well qualified.
The generator should insist on minimal contractor requirements
for financial resources, performance record and medical surveil-
lance program. In addition, generators should insist on fixed-price
contracts whenever possible. Of paramount importance is obtain-
ing assurances that disposal of any wastes be clearly agreed upon,
and that such disposal represents the alternative with the least
possible risk exposure which is economically feasible.
Contractual means of minimizing liability exposure include re-
quirements for general and environmental liability insurance, per-
formance bonds and secrecy agreements.
432
LEGAl LIABILITY
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LEGAL MECHANISMS FOR DEFINING
APPROPRIATE EXTENT OF REMEDIAL ACTION
RANDY M. MOTT, ESQUIRE
Breed, Abbot & Morgan
Washington. D.C.
INTRODUCTION
Most private parties identified by federal and state agencies as
"responsible parties" in connection with hazardous waste site in-
vestigations will actively seek settlement of the case. The reasons
for preferring settlement to litigation are obvious as is the pub-
lic's interest in supplementing CERCLA and state funds with size-
able private funding. A key issue in settling cases and in defining
the amount of financial resources necessary for remedial activities,
is the appropriate extent of cleanup.
The principal problem in negotiating a conclusion to a hazardous
waste case is how to resolve the uncertainty over the nature and
extent of remedial action needed at the site. It is useful to view this
as a problem of assigning the uncertainty over the scope of relief
necessary; where remedial activity cannot be defined with pre-
cision, how can a settlement resolve the obligations of the defen-
dants?
This uncertainty is invariably aggravated by the problem of deter-
mining the appropriate extent of remedy, even when the facts are
known. The question, "how clean is clean?" exists, not because of
a lack of data, but rather due to the political difficulties of defin-
ing acceptable or tolerable levels of risk. Completion of the most
extensive site monitoring and feasibility studies will not reduce the
intrinsic necessity of balancing cost and risk. Even where such de-
tailed information is available on a hazardous waste site, the parties
must still face the politically delicate job of defining the appro-
priate degree of remedial activity and, hence, the scope of the de-
fendant's obligation.
This inherent political problem has now been amplified into a
crisis that threatens to severely constrict the ability of private fund-
ing for remedial activities. Reeling from political wounds, USEPA
is rapidly becoming incapable of the kind of sensitive and careful
weighing of risks and costs that is crucial to effectively reach a
consensus on remedial actions. This immediate, and hopefully
temporary, state of affairs has an overwhelming influence on the
types of mechanisms used to settle remedial uncertainties and on
the levels of contamination deemed tolerable as a result of "clean-
up" operations.
This paper is based on a review of several dozen hazardous waste
settlement agreements, consent decrees and court judgments. The
mechanisms used in these settlements to achieve what lawyers call
"respose" will be classified and critically reviewed.
OVERVIEW
The focus of this paper is on the means used in the agreements
to define the scope of a company's obligations where it is obli-
gated to do more than pay a fixed cash amount. The viability of the
settlement process in any case depends upon finding a mutually
agreeable method of "turning off" the financial commitment
placed on the company. The open-ended provision requiring a de-
fendant to do everything that is "necessary" remains highly sus-
pect. In the current political climate, this type of provision has
been resurrected since it shifts the total burden of uncertainty over
the scope of remedial action onto the company.
A variety of other provisions have been used in addition to the
blind vow to do all that is "necessary." These provisions range
from the most simple cash "buy-out" to an environmentally-based
performance standard. Creative and flexible methods of dealing
with the uncertainty implicit in defining the extent of remedial ac-
tivities are critical to the successful resolution of most cases.
Where the parties can reasonably identify the risks intended to
be addressed by the remedy, it seems imperative that more care-
fully worded provisions be used to define the activities agreed upon
to reduce those risks. Settlements which contain some numerical
objective that adequately reflects cost-risk balancing are obviously
preferable to commitments to do whatever is "necessary" or "ap-
proved by USEPA." Because actual risk from a hazardous waste
site depends so heavily upon site conditions unique to each situa-
tion, these performance standards need to be viewed on an ad hoc
basis to avoid regulatory overkill. Pollutant fate and transport
mechanisms present at a particular site and the number and type of
"receptors" are the principal determinants of relative risk. These
factors defy generalization since they depend on site location, geol-
ogy, climate and hydrological conditions.
Where site-specific numerical objectives or environmental per-
formance standards based on specific risk assessment cannot be
agreed upon, the parties may be compelled to settle on the basis of
remedial plans to be developed by the company and submitted to
USEPA and the court. A crucial consideration, in that event, is
what happens if the parties disagree. Provisions that make
USEPA's position binding unless it is "arbitrary and capricious"
pose very serious problems for settling defendants.
If an agreement is not actually a "settlement," but ends up
only specifying the procedures to resolve a dispute, provisions
surrendering the defendant company's normal evidentiary and sub-
stantive rights should be avoided wherever possible.
THE CASH "BUY-OUT"
By far the most preferable settlement from the defendant's view
is the cash "buy-out," shorthand for a complete release of gov-
ernment claims in exchange for payment of a specified cash
LEGAL LIABILITY
433
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amount. The controversial "buy-out" announced in the Seymour
Recycling case involved 24 generators paying $7.7 million in ex-
change for a full release from surface or groundwater cleanup
claims. Other generators not privy to the settlement remained sub-
ject to claims by the government, a key factor in the willingness of
the government to accept the arrangement. This situation simply
shifts the uncertainty over final cleanup costs onto the nonsettling
defendants. If all defendants were privy to the agreement, such a
buy-out would place the burden of this uncertainty on the govern-
ment which has generally espoused, since Seymour, that it will
not accept the burden of uncertainty. See also United States v.
Wade, 3 CHEM. & RAD. WASTE LIT. REP. 566 (E.D. Pa.,
1981), (where the settling defendants received a release in exchange
for a fixed monetary contribution).
Cash buy-outs, where a nonsettling party is not available, typic-
ally lack the finality obtained by the settling defendants in Wade.
In United States v. Duracell, the defendants created a $500,000
cleanup fund for removal activities subject to the Government's
right:
"to bring a subsequent action for injunctive or similar relief con-
cerning the site including, but not limited to, an action seeking
additional funds for work contemplated by or of the type con-
templated by this Degree and seeking rehabilitation of Beech
Creek." 1 HAZ. WASTE LIT. REP. 1817, 1822 (M.D. Tenn.
1982).
In summary, cash buy-outs have depended not only on the abil-
ity to provide reasonable dollar estimates of remedial action cost,
but also upon the presence of nonsettling defendants who will be
relied upon by the government to provide any additional con-
tingency funding.
OBLIGATION TO CONDUCT ACTIVITIES
Perhaps the most common form of settlement in owner-oper-
ator cases—especially where wastes are present on the defendant's
premises—is an agreement to undertake a list of activities. For
instance, the Inmont agreement provided that the completion of
the described activities is "acceptable to USEPA as constituting
cleanup of the site...." 1 HAZ. WASTE LIT. REP. 1824(1982).
Similarly, the consent judgment announced in United States v.
Velsicol Chemical Corp., Civil No. 82-10303 (E.D. Mich., Con-
sent Judgment, Nov. 18, 1982), involved detailed plans and pro-
cedures for disposal of Velsicol's wastes at three Michigan sites.
The Velsicol settlement involves a minimum of uncertainty to the
parties by the use of detailed remedial plans and limited dispute
resolution clauses. In United States v. American Ecological Re-
cycle Research Corp., Civil No. 80-A-811 (D. Colo., Consent De-
cree, Aug. 15, 1981), the defendants agreed to segregate drums on
site by waste type, to repackage leaking drums and to provide ade-
quate fire protection, site security and a closure plan. Any chem-
icals creating an "imminent hazard" are to be removed from the
site to another approved by EPA. While the American Ecological
list of activities seems finite, the consent decree contains a blanket
removal obligation left to USEPA's unguided discretion.
The "Bluff Road" consent decree in United States v. South
Carolina Recycling and Disposal, Inc. Civil No. 80-1274-6 (D.
S.C., March 23, 1982), contains another example of an activity-
based obligation. One defendant agreed to the "cleanup of a por-
tion of the surface of the Bluff Road site" and others contrib-
uted funding—all in exchange for a release of surface cleanup
claims. The release specifically excluded claims for "contamina-
tion of groundwater (including drinking water supplies), surface
suit contamination which is threatening to contaminate ground-
water and off-site surface water contamination...." Nonsettling
waste generators were subsequently sued by the United States.
The consent decree in United States v. Energy Systems Com-
pany, Civil No. 81-1-006 (W.D. Ark., 1981), involves a complete
release once all of the defendant's obligations have been completed
to the United States' satisfaction. The obligations undertaken in-
volve cleanup of a drum storage site and upgrading of lagoons on
site and bulk waste storage under predefined programs, implemen-
tation of a fire control plan, removal of tetraethyl lead residues
and several other programs. 1 HAZ. WASTE LIT. REP. 481-
486 (1981). Each activity was defined in an accompanying appen-
dix.
The state-initiated consent judgment in Kelley v. Cast Forge Inc.,
File No. 77-3724-CE (Mich. Or. Ct., Livingston County, Con-
sent Judgment, June 19, 1981), is another variation of this type of
agreement. Cast Forge agreed to implement a cleanup plan in-
volving removal of PCB-contaminated material including specified
soils and sediments. Once completed, the activities are stipulated
to be sufficient to bring the company into compliance. See also,
Kelley v. Hooker Chemicals & Plastic Corp., File No. 79-22878-
CE (Mich. Cir. Ct., Ingham County, Consent Judgment, October
30, 1979), (obligations defined by on-site activities at the Montague
Michigan site).
In West Virginia v. Allied Corp., Civil No. 81-C-554N (W. Va.
Cir. Ct., Marshall County, Consent Decree, Oct. 22, 1981), the
defendant agreed to "initiate corrective measures to prevent
further migration of contaminants in the groundwater." 1 HAZ.
WASTE LIT. REP. 1967, 1968 (1982). The program described in
the decree envisions long-term pumping of the groundwater suffic-
ient to change the normal water table contours. Compliance with
the terms of the decree is measured by the absence of an "off-
site gradient." This obligation to counterpump is to last for 20
years and may be augmented by such "corrective measures as are
necessary to prevent further migration. ..."Id.
Many of these types of settlements do not involve definitive
terms concerning the defendant's obligation; however, provisions
limiting the stipulated relief to specified activities have obvious ad-
vantages to defendants. The use of designated activities as a settle-
ment device should be seriously explored by the parties, particularly
in combination with environmental performance standards.
ENVIRONMENTAL PERFORMANCE STANDARDS
The stipulation of environmental performance standards pro-
vides an even more objective obligation. Numerical objectives that
define actionable levels of a pollutant under the remedial program
help eliminate future disputes.
The drawback to numerical standards is the assumption by many
that USEPA's water quality criteria goals should be utilized for
this purpose. If the criteria number is used at all, it should only be
at the point of the "receptor."1 There is a tendency for agency
staff to use these numbers as a priori groundwater goals. See
United States v. Chemcentral/Detroil Corp., 6 CHEM & RAD.
WASTE LIT. REP. 298 (E.D. Mich. 1983) (Appendix D and E).
The applicability of criteria concentration levels cannot be assumed
by the parties without site specific risk assessment.
If environmental fate and transport mechanisms are taken into
account in developing a cogent, site-specific risk assessment, then
numerical objectives may present a workable method of determin-
ing the appropriate extent of remedy. If the critical "receptors"
can be defined, the application of an objective standard provides
some protection to both parties. Contrast In the Matter of the
Receiver of the Water and Wastewater Technical School, Inc.,
No. 82-H-033 (USEPA Administrative Order, Aug. 16, 1982),
(monitoring site "until such time as the hazard is eliminated")
and United States v. American Ecological Recycle, Civil No. 80-A-
811 (D. Colo., Consent Decree, Aug. 15, 1981), removal of all
wastes that "are creating or may create an imminent and substan-
tial endangerment to health and the environment").
The good example of the use of environmental performance
standards appears in United States v. Spectron, Inc., Civil No.
HM-80-1552 (D. Md., Settlement Decree, Mar. 25, 1982). In
format, Spectron involves the obligation to undertake specified
activities, such as site security and abatement of ongoing poten-
tial discharges as well as groundwater corrective action. A detailed
groundwater monitoring program is defined (Para. IV.C.), in con-
trast to the generalized obligation to conduct a hydrology study
434
LEGAL LIABILITY
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contained in many settlements. Ongoing surface water monitoring
is limited to four years after the termination of the groundwater
program. Para. IV.D. The most ambitious obligation is the pump-
ing and "decontamination" of the groundwater. Spectron calls for
a system that "will prevent migration of substantially all the con-
taminated groundwater to the creek...." Para. IV.E.2.b., de-
fined by sampling for fifteen specific organic chemicals at spe-
cified detection limits. A maximum obligation of six years from
commencement of the decontamination system is set out, with peri-
odic ability to terminate groundwater pumping and treatment
keyed to the concentrations in the Creek.
The Spectron agreement provides a useful conceptual method
for identifying the environmental concerns and meeting them by
specific commitments. The use of performance-based goals
throughout the agreement should allow for more predictable obli-
gations assumed by the defendant and more definitive protection
of the public. See also United States v. Solvent Recovery Service
of New England, Inc., 5 CHEM. & RAD. WASTE LIT. REP.
899 (D. Conn. 1983).
REQUISITE REMEDIAL TECHNOLOGY
The leading example of "requisite remedial technology's" use
in a settlement agreement is United States v. Hooker Chemical &
Plastics Corp., Civil No. 79-989 (W.D. N.Y., Stipulation and
Judgment Approving Settlement Agreement, Jan. 19, 1981) (Hyde
Park) 1 CHEM. & RADIATION WASTE LIT. REP. 691 (1981).
The key provisions in the Hyde Park agreement which encom-
pass "requisite remedial technology" are fairly short:
(a) "The containment, monitoring and maintenance programs
described in this Judgment have been designed, and have as
a goal, to protect against endangerment to human health
and the environment in the Hyde Park-Bloody Run Area
Utilizing Requisite Remedial Technology to achieve the pur-
poses set forth in this Judgment.
(b) "In determining whether a Remedial Technology is 'Req-
uisite,' consideration shall be given by the parties to the
following factors: the nature of the endangerment to human
health and the environment which the Remedial Technology
is designed to address; the extent to which application of the
Remedial Technology would reduce such endangerment to
human health or the environment or would otherwise bene-
fit human health or the environment; and the economic costs
required to apply the Remedial Technology...." 1 CHEM.
& RADIATION WASTE LIT. REP. 696.
This provision obviously does little to define what the defen-
dant's obligation actually entails. It is interesting that cost is used
apparently to balance the benefits achievable by a particular
remedy.
The most discussed provision of Hyde Park's "Requisite Remed-
ial Technology" is the dispute resolution mechanism. This pro-
vision reportedly requires the company to show that the use of a
particular remedy is "arbitrary and capricious" before the court
may tamper with the government's preferred remedy. Yet, the re-
strictive standard of review only applies to the cost balancing de-
termination. The company may still challenge a remedy as "un-
necessary to satisfy the goal [of protection of human health and
the environment]," and the burden of proof apparently will not
shift to the company.
The court described the Requisite Remedial Technology
("RRT") concept as "enormously flexible...with adequate safe-
guards... [that make] it a viable, workable solution to the prob-
lem...." 1 CHEM. & RADIATION WASTE LIT. REP. 2,419
(1982). On the ambiguity of RRT, the court found:
"The term RRT is necessarily loosely defined, because at this
time, it is impossible for any party or nonparty to know what
methodology will be appropriate and will be most successful in
halting the leaching process." Id.
Thus, the concept does little more than embellish the notion that
the defendant will do whatever is "necessary." See also United
States v. Occidental Petroleum Corp., Civil No. S-79-989 MLS
(E.D. Cal., Stipulation and Judgment Approving Settlement, Feb.
6, 1981) (court determination of "Requisite Remedial Technology"
based on "all relevant factors").
OPEN-ENDED COMMITMENTS
Several agreements have been signed which basically commit the
defendant to do whatever is "necessary." Trends in recent ad-
ministrative orders by USEPA suggest that this type of general-
ized obligation will be used routinely in unilateral orders as well.
Some examples of an open-ended commitment illustrate the ten-
dency of USEPA and the Justice Department to shift the burden of
uncertainty entirely to the defendant. In United States v. Wau-
kesha County, Civil No. 80-C-1070 (E.D. Wise., Consent Decree,
filed Dec. 1, 1980), any soil or surface water sample above 10 ;tg/l
of 2,4,5-T or trichlorophenol triggered an obligation to submit a
cleanup plan to USEPA. The scope of the plan is vague:
"The Defendant shall then formulate a plan which will result in
removal or containment of the 2,4,5-T and any dioxin found,
in a manner which will eliminate any imminent and substantial
endangerment to the public health and/or the environment
caused by its presence." Para. VILA.
The decree simply provides that the plan will be implemented upon
USEPA's approval. The agency's discretion seems virtually ab-
solute.
The agreement in United States v. W.R. Grace & Co., Civil No.
80-748-C (D. Mass., Final Decree, Oct. 21, 1980), contained a sim-
ilar broad obligation. Government authority under that decree re-
quires that "[a]ll plans, programs, and proposed actions...shall be
subject to the approval of the federal government parties" to the
decree. Para. IV. One of the plans called for requires "an en-
gineering report for aquifer cleanup and restoration to a fully use-
able condition...." Para. XII.A. Disputes over the relief proposed
will be reviewed by the court in light of "the reasonableness in all
the circumstances of the relief requested...." Para. XIII.C.
Reasonableness is defined rather broadly:
"[A] remedial action shall be deemed reasonable if it is neces-
sary or appropriate, under all the circumstances to remedy pollu-
tion for which W.R. Grace is responsible."
In United States v. Gulf Coast Lead, Civil No. 80-1127 (M.D.
Fla., consent decree,) the defendant was directed to prepare a re-
medial plan "necessary to successfully isolate and contain haz-
ardous contaminants in the shallow groundwater and possibly
deeper groundwater and soil beneath the GCL site attributable
to GCL plant operations...." The defendant is further obliged to
revise the plan to reflect USEPA comments unless it establishes by
"clear and convincing evidence that its Plan of Study or the Re-
medial Plan will successfully isolate and contain hazardous con-
taminants on or beneath the GCL site...." Obviously, the defen-
dant in this situation has been placed in a difficult position to
argue cost-effectiveness of the relief, not to mention cost-bene-
fit considerations. See also United States v. Laskin, Civil No. C79-
7594 (N.D. Ohio, Consent Decree, 1980), (remedial plans to in-
clude "any reasonable modifications made by USEPA.")
The type of commitments undertaken in these agreements gen-
erally require USEPA approval and provide for restricted judicial
review of disagreements or for no specific review procedure at all.
A superior method of resolving disputes concerning the "reason-
ableness" ' of a remedial plan is discussed below.
PLANS SUBJECT TO COURT APPROVAL OR CHALLENGE
In some situations, it may be impossible to agree to do more than
study a site and propose a remedial plan. As discussed above, how-
ever, this type of undertaking can begin to "box in" a company
by making USEPA or state determinations either a prerequisite
or presumptively valid. A superior procedure for private parties
follows the first steps, but then allows a full de novo review by
the courts in the event of disputes. This is a right that defendants
LEGAL LIABILITY
435
-------
should not lightly relinquish and a procedure that remains the best
means of adjudicating factual controversies.
The type of flexibility that should be sought by defendants is
illustrated by In the Matter of Stauffer Chemical Co., Docket No.
82-1070 (USEPA, May 25, 1982) 1 HAZ. WASTE LIT. REP. 2595
(1982) (the Woburn, Mass. site). This administrative agreement,
made under CERCLA Section 106 and RCRA Section 7003, com-
mits the company to an "investigative study" which includes a site
sampling program and development of a "Recommended Remed-
ial Action." The procedure in the event of disagreement over the
scope of the remedial proposal is as follows:
"If, within sixty (60) days after receipt of USEPA and DEQE's
disapproval..., the parties are unable to agree on a Recom-
mended Remedial Action and if Stauffer has complied with all
preceding paragraphs of this Consent Order, Stauffer's obliga-
tions regarding this Consent Order shall be satisfied in full and
Stauffer shall have no further commitment regarding this Con-
sent Order, nor shall Stauffer be released from liability....
USEPA and DEQE retain all rights to require such further ac-
tion as they deem necessary, including the issuance of further
orders or the seeking of judicial recourse."
Similarly, other agreements have provided for full review by the
court in the event that the parties cannot reach a consensus on the
remedial plan proposed by the defendant. See In the Matter of
FMC Corp., No. 8371021282 (NYDEC, Order of Consent, Feb.
17, 1982) 1 HAZ. WASTE LIT. REP. 2176, 2179 (1982); United
States v. Vertac Chemical Corp., No. LR-C-80-109 (E.D. Ark.,
Consent Decree, Jan. 18, 1982). These arrangements do not sur-
render the government's legal right to proceed nor do they prema-
turely shift the uncertainty of appropriate relief onto the defen-
dants.
CONCLUSION
The various methods used in settlements to date have dealt with
the appropriate extent of a defendant's remedial action by several
broad approaches. Seeking a finite and reasonable ceiling on the
company's obligation should be the key objective of defense coun-
sel in settlement negotiations. The advisability of any specific
model for determining the scope of the defendant's obligations
hinges on site specific factors.
FOOTNOTES
1. Even use at the receptor point could be inconsistent with the statutory
provisions of CERCLA where the abatement cost to reduce the level
at the receptor was wildly disproportionate to the threat presented by
exceedence of the criteria. See CERCLA Sections 104(c)(4) and 101
(24); 47 Fed. Reg. 31217 (1982) (Preamble to NCP) (discussing "cost-
effectiveness" and effective "mitigation"). Inherent in this formula-
tion is the need to examine mitigative measures that address the sub-
stantive potential threat from a site as well as measures that remove
potential threats regardless of their costs or the severity of the threat.
That this statutorily-mandated process would lead to a nonquantitive
but thorough review of relative costs, benefits and risks was the spe-
cific intent of Congress. Sponsors of the legislation clearly assumed
that "cost-benefit considerations [will be taken] into account...in de-
termining whether and when action should be taken at all" at a par-
ticular site. Colloquium between Senator Helms and Senator Stafford,
126 Cong. REC. S15.007 (Nov. 24,1980).
436
LEGAL LIABILITY
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LIABILITIES AT COMMON LAW FOR
GROUNDWATER CONTAMINATION
EDWARD I. SELIG, ESQUIRE
DiCara, Selig & Holt
Boston, Massachusetts and Washington, D.C.
INTRODUCTION
The scope of this paper can be illustrated by a simple example.
Suppose that an industrial firm deposited hazardous process wastes
on the ground some years ago. By leaching or leaking, contam-
inants from that waste pile went below ground, entered an aqui-
fer and eventually reached a well field some distance away. Health
authorities ordered the contaminated wells to be shut down. The
owners of these wells, and certain individuals who claim to have
consumed contaminated water from them, bring suit against the
industrial firm, alleging destruction of their water supply and in-
juries to their health.
The complaint demands both compensation for the personal and
property injuries suffered by the plaintiffs and an injunction
ordering the defendant to take whatever action may be neces-
sary to correct or eliminate the cause. In addition to physical causes
and effects linking defendant's waste disposal to injuries suffered
by plaintiffs, the complaint alleges that the defendant should be
held liable because he knew of the risks he was creating by dis-
posing of his wastes, because he failed to exercise reasonable care
in disposing of them or because their disposal was an abnormally
dangerous activity which he undertook entirely at his own risk for
any harmful consequences.
Whether won or lost on the merits,1 such a case illustrates the
three main functions or goals of the common law system of rights
and remedies known as tort law: (1) to compensate persons who
have sustained loss or harm as the result of another's conduct;
(2) to place the cost of that compensation on those who, in jus-
tice, ought to bear it, but only on such persons; and (3) to pre-
vent future losses and harms.2 For centuries, this system of law has
been and still is being developed more or less independently by
the courts in cases alleging injury to persons or property as a re-
sult of risk-taking activity including—for present purposes—ac-
tivities that expose other people to environmental hazards.
Tort liabilities, as they appear in the environmental (or any
other) field, need to be distinguished from penalties, injunctions
and cost recoveries authorized by statute against violators of
statutorily established standards and regulations. The latter are of
critical importance to environmental protection, but limitations of
space and time prevent their being addressed here. This paper is
concerned with how the common law of torts applies to redress in-
juries to persons or property via groundwater contamination that
has resulted from faulty storage or disposal of hazardous wastes.
TORT ACTIONS AT COMMON LAW
In general, tort liability is based upon conduct that creates an
unreasonable or unacceptable risk of harm. Such conduct may be
intentional, negligent or so inherently risky that the defendant will
be held liable even without fault for any harm that ensues. In
nearly all such cases, the cardinal question is whether the loss or
injury suffered by the plaintiff will be allowed to remain where it
fell or will be shifted back to the defendant, primarily in the form
of compensatory damages, i.e., monetary recompense to be paid by
defendant to plaintiff. The principal elements of tort law may now
be briefly summarized, with particular reference to the paradigm
case outlined above.
Conduct of Defendant
The requisite intent need not involve any motive to inflict harm
upon the plaintiff. In most cases, intent can be inferred from con-
duct undertaken by an actor who clearly foresees its consequences.
The law presumes that one intends the natural and probable
consequences of one's acts in the light of surrounding circum-
stances of which one must be aware.
Suppose, for example, that in the paradigm case, the company
had been forewarned by a consultant that land disposal of its
wastes could eventually jeopardize the aquifer. Since defendant
knew the risk he was taking when he acted in spite of that advice,
he can be deemed to have inflicted an intentional injury on the
plaintiff when the risk materialized.
It is even clearer that he commits an intentional tort if he per-
sists in the harmful activity or fails to control its effects after learn-
ing of the actual harm it has begun to cause.3 It is true, however,
that intent will be difficult to show in most cases involving re-
leases of hazardous waste or other chemicals, especially where the
causative activity occurred some time ago when its effects could
not have been reasonably foreseen in the light of the scientific and
technological knowledge existing at that time.
Negligence is the second major behavioral basis for tort liability.
As enunciated through centuries of judicial case law, negligence is
a breach of duty to conform to the required standard of care for
protection of others against unreasonable risks of harm. This is
the standard that a prudent person in the defendant's position
would have observed, considering the risk his activity creates.
And such a risk is deemed unreasonable when the foreseeable
probability and gravity of the harm outweighs the burden to the
actor of alternative conduct that would have prevented the harm.
For example, in the paradigm case, the plaintiff might be able to
prove that other industries comparable to the defendant disposed
of their wastes by safer means at the same time the defendant was
putting his on the ground. Cases are not difficult to find in which
courts have held industrial enterprises liable for personal injury
and property damage as a result of negligent releases of hazardous
waste and other contaminants to the environment."
LEGAL LIABILITY
437
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Finally—and most important in the current trend of tort liability
—a standard of strict liability may be imposed upon defendants
who undertake activities of an ultrahazardous or abnormally
dangerous nature. This is liability without fault, imputed to the
defendant even though he acted neither negligently nor intention-
ally with respect to the consequences of his action. "One who
carries on abnormally dangerous activity is subject to liability for
harm to person, land or chattels of another resulting from the
activity, although he has exercised the utmost care to prevent the
harm.'" An activity may be deemed abnormally dangerous if it
involves a high degree of risk, or if the gravity of harm that may
result from it is likely to be great though the risk is small. The
context in which the activity is carried on is relevant to this determ-
ination: i.e., whether the activity is not a matter of common
usage, or is inappropriate to the locale or is not of substantial
value to the community.
Whether particular conduct is "abnormally dangerous" for
purposes of strict liability is a question of law for the courts to
decide, and courts have not been reluctant to impose strict liabil-
ity for injuries caused by the release of toxic chemicals to the en-
vironment.' For example, strict liability was imposed on a com-
pany for costs of cleaning up waste residues that had leached from
the company's processing plant into a local stream, even though
the court found that defendant's conduct "was reasonable in light
of the state of knowledge as it then existed."7
Activities giving rise to strict liability may be socially useful, but
they are so dangerous or unusually risky that the law requires
them to be carried on at the actor's peril. In fact, cases involving
strict liability should be viewed "as special instances of manda-
tory insurance against particular designated risks imposed as a mat-
ter of policy irrespective of fault."1 The rationale is that defen-
dants who engage in such activities are best able to insure against
the risks they pose, to allocate the costs of insurance by passing
them on to consumers of their products and to reduce or warn
against the dangers. In particular, it has been suggested that strict
liability will force generators, disposers and other managers of haz-
ardous wastes to develop and employ the safest and most effic-
ient practices that ingenuity can invent and money can buy.'
Suppose (to complicate the paradigm case) that the wastes were
deposited on the ground by a disposal firm to which generators
had shipped them from many miles away and that the hazardous
chemicals in the waste can be traced back further to manufac-
turers of materials used by the generators. How far back up the
chain of successive sellers and buyers is the plaintiff entitled to go
in search of responsible defendants? A plaintiff may decide to go
all the way back and sue the manufacturer of the original ma-
terial, even though the latter lacked knowledge or control of the
disposal practice because he was at two removes from the disposer
and at one from the generator.
The most promising theory on which to sustain such a suit is that
a manufacturer may be held liable for failing to give adequate
warning of the inherent dangers of his product, including the
dangers that arise from failing to handle or dispose of it properly.'"
One who sells any product "in a defective condition and unrea-
sonably dangerous to the user or consumer or to his property" is
subject to strict product liability for physical harm thereby caused
to the ultimate user or consumer, and the defect may consist pre-
cisely "in the failure to warn or to provide adequate directions
for use."" A manufacturer knows more about his product and
can supply more information concerning its dangers than those
who subsequently handle and dispose of it.
But what constitutes adequate warning should depend on how
much the manufacturer can be expected to have known at the time
he sold the product, not on any more sophisticated, recently
acquired appreciation of dangers posed by improper management
of hazardous waste. This could be an important distinction in cases
where the relevant sales took place years before the injury became
manifest. In fact, similar discrepancies may arise in the law of
negligence with respect to evolving standards of care and in the law
of strict liability with respect to evolving perceptions of what
activities are abnormally dangerous. Moreover, manufacturers
might be entitled to assume that their customers will properly dis-
pose of any waste generated in the use of their products, even
without explicit directions or warnings. It remains to be seen how
successful plaintiffs will be in suing original manufacturers for
damages caused by improper waste disposal.
It is another question whether a generator who ships hazardous
wastes offsite for disposal will be held liable in tort" for their
escape from transportation or disposal facilities. Generators who
operate outside the manifest system established under RCRA will
probably be held liable for such releases, along with the trans-
porter or disposer, since failure to comply with applicable regula-
tions is prima facie evidence of negligence or culpable intent. It
will be a harder case if the shipment of waste offsite occurred a
number of years ago and was lawful at that time, when the only
legal requirement may have been to entrust the wastes to a licensed
transporter. Was the generator negligent back then in having failed
to foresee and forestall the risks of careless transportation or
improper disposal? Or should he be held strictly liable on the
theory that, even back then, the shipment of his particular waste
off-site would have been perceived to be an abnormally dangerous
activity? These are relevant questions that the courts have yet to
resolve in such cases.
Current waste-handling practices may also give rise to hard cases.
Suppose that an accident occurs in transportation or disposal
despite the fact that the generator selected his transporter and
disposer with great care and complied with all applicable RCRA
requirements. Will the generator nonetheless be held liable in tort
for releases of hazardous wastes from sites or facilities over which
he could exercise no control? Even if the shipment of hazardous
wastes off-site for disposal were to be considered an abnormally
dangerous activity, their mishandling by an independent third party
may be a supervening cause that delimits the scope of the genera-
tor's strict liability." There is some precedent, moreover, for not
considering the disposal of hazardous waste as an abnormally
dangerous activity, insofar as relatively simple precautions (such
as lining the disposal pit or providing leachate collection systems)
could be taken to ensure safe disposal." The scope of the gen-
erator's liability in tort for off-site releases of hazardous waste will
no doubt be hotly contested under state law."
Compound and Extended Liability
In most cases of injury caused by groundwater contamina-
tion, there are several potentially responsible parties. The law not
only anticipates and recognizes this multiplicity, but also extends
the range of possible defendants beyond those who can be shown
to have caused or contributed directly to the injury by disposing
of their wastes upon the ground.
Suppose that a landowner's wells are contaminated by discharges
from one or more of three leaking sites and that the landowner
sues all three site owners for loss of his water supply. In such a case,
it may be difficult to prove that the pollution was caused by re-
leases from any particular site or to assess the degree to which each
of them contributed to the harm. But the plaintiff may be relieved
of such burdens of proof under the rule of joint and several lia-
bility. When the harm complained of is "indivisible", i.e., when
there is no rational basis for calculating the proportional liability
shares of multiple defendants, this rule allows the plaintiff to
recover all his damages from any one defendant.' •
Although in most jurisdictions the defendant who actually paid
the plaintiff has a right to seek "contribution" from his OHle-
fendants in a separate action, his ability to obtain any money from
them may depend on whether they are solvent. In other words, the
rule has the effect of shifting the risk of non-recovery from platar
tiff to defendant.
In contrast, damages will be severally apportioned by the court
when the harm complained of is deemed to be "divisible" to
accordance with some rational principal." Under these circum-
438
LEGAL LIABILITY
-------
stances, the plaintiff bears the risk that one or another defendant
will be unable to satisfy the judgment against him, for when the
rule of joint and several liability does not govern disposition of a
case, no defendant may be forced to pay more than his appor-
tioned share of liability. The trend in environmental case law, how-
ever, favors application of joint and several liability in most cir-
cumstances where a solvent defendant can be found who contrib-
uted significantly to the plaintiff's injury.
There are also rules of vicarious liability under which indirectly
responsible parties may be required to pay damages. For example,
a parent company may be held strictly liable for the environ-
mental torts of its subsidiary, where the parent exercises or is in a
position to exercise control over the activities of the latter (as
though overlapping officers and directors).'8 Nor will a parent
corporation succeed in insulating itself from tort liability by creat-
ing a shell of a subsidiary for that purpose. In such cases, courts
can be expected to "pierce the corporate veil."" For analogous
reasons, if company B acquires the assets of company A and con-
tinues the same line of business, B may be held liable for the
environmental torts of A on a theory of continuing enterprise
liability;20 a principal may be held liable for the tort of his inde-
pendent contractor in the course of performing an abnormally
dangerous activity (such as hazardous waste management) for
which the principal had hired him; and a lessor may become
liable for the tort of his lessee upon reversion of the property to
the lessor.
Corporate officers may bear vicarious liability for the environ-
mental torts of subordinate employees. The law of negligence sup-
plies the usual standard for determining liability in such cases:
"If the defendant's general responsibility has been delegated
with due care to some responsible subordinate or subordinates,
he is not himself personally at fault and liable for the negligent
performance of this responsibility unless he personally knows
or personally should know of its non-performance or mal-
performance and has nevertheless failed to cure the risk of
harm."21
Those who directly supervise the handling of hazardous wastes
will be expected to exercise a high degree of care in controlling
and monitoring performance by their subordinate employees. In
the upper echelons of corporate management, practical necessity
requires the application of a somewhat more flexible standard. In
general, top executives and directors are entitled to rely on the
competence and integrity of their subordinates "until something
occurs to put them on suspicion that something is wrong. If this
occurs and goes unheeded, then liability of the directors might well
follow...."" Moreover, a corporate supervisor or officer cannot
escape liability by pleading ignorance of facts he ought to know in
the course of discharging his corporate duties. "... [ W] here the duty
to know exists, ignorance resulting from a neglected official duty
creates the same liability as actual knowledge....""
Damages
Tort law is concerned not only with conduct giving rise to liabil-
ity, but also with the resulting injuries and the means of redress-
ing them for the benefit of injured plaintiffs. Where personal
injury is alleged—as when a plaintiff claims that his health has
been impaired by ingestion of contaminated water—compensa-
tory money damages may be recovered for such items as cost of
medical care or monitoring, estimated income loss as a result of
physical disability and a surcharge for plaintiff's "pain and suffer-
ing." In attempting to restore the plaintiff to his pre-injury con-
dition so far as it is possible to do so with money, the law assumes
that both economic and noneconomic losses are capable of being
translated into dollars.
Harm to property, such as land and appurtenant groundwater
rights, may also be compensable and can be measured by the
difference between the value of the property before and after the
'«, by the reasonable costs of repairing and restoring it, by its
value at the time it was irrevocably converted to the defendant's
own use or by the cost of obtaining a substitute (such as an alterna-
tive source of water supply). Private or common property re-
sources damaged by releases of hazardous wastes might include
aquifers, fisheries and crops for whose loss a dollar value can be
calculated.
Private and Public Nuisance
Suits at common law may also seek "equitable" remedies, such
as an injunction ordering defendant to cease or control his in-
jurious activity, or even to reverse its harmful effects. In environ-
mental litigation, the widest range of equitable remedies appears
in actions brought under the common law of nuisance, a category
of tort that focuses not so much upon the conduct of the defendant
as upon its consequences for the plaintiff.
A private nuisance is a substantial and unreasonable interference
with the use and enjoyment of an interest in land. A public
nuisance is an unreasonable interference with a right common to
the general public, such as the right to a clean municipal water
supply.
When hazardous wastes have been released to the environment,
equitable remedies in a nuisance action may be directed not only to
current and continuing activity of the defendant (should he be
allowed, under any circumstances, to go on discharging hazardous
wastes?), but also to present consequences of discontinued activity,
such as existing or threatened pollution of an aquifer from a leach-
ate plume originating at the defendant's facility. The defendant
might be required to control the plume by whatever means and at
whatever costs are necessary, to buy out land-use and groundwater
withdrawal rights from adjacent landowners and to monitor the
health of potentially injured populations.
Some outer limits of injunctive relief in litigation over haz-
ardous wastes may already have been reached in the Wilsonville
case,24 where a chemical landfill that had been fully permitted by
both the USEPA and the Illinois EPA was nonetheless enjoined
as a common law nuisance and required to close down, primarily
because of the possibility that hazardous waste might one day
escape from the site and cause substantial future harm. The order
in this case required the defendant not only to cease operations
but also to exhume the buried wastes and to reclaim the site. There
was evidence that the site was not ideal because of an abandoned
mine that had already caused considerable subsidence in the vicin-
ity, but the risks posed by use of the site had been considered and
found acceptable by the permit-issuing authorities on the basis of
information concerning groundwater, soil permeabilities, sub-
sidence and other relevant conditions. The order of the court, how-
ever, rested not upon the likelihood of harm but upon its magni-
tude if it were ever to materialize. In other words, defendant was
ordered to shut down "even though the feared harm was uncer-
tain as to occurrence and, in any event, unlikely to occur until the
distant future."25
Several important lessons can be learned from the Wilsonville
case: (1) a site for disposal of hazardous waste may be enjoined as
a prospective nuisance if it poses a small likelihood of causing
substantial future harm; (2) a court may hold, as this one did, that
"a site's dangers outweigh its utility," despite the urgent need for
new and expanded capacity to dispose of hazardous waste; and (3)
the fact that all necessary permits have been issued for a facility by
state and federal authorities will not bar a court from ordering it
to be closed down if there is evidence suggesting that more rigorous
standards of site selection might have been applied by the adminis-
tering agencies in considering whether to issue those permits.
This last point should be emphasized. Unless a statute makes it
clear that administrative regulations and permits are to preempt the
common law on the subject, "courts are reluctant to embrace the
concept of legalized nuisance...[a]nd are not inclined to relinquish
sweeping powers to correct technological and land use abuses
unless legislatures unmistakeably dictate the terms of surrender."26
Without such overriding action of the legislature, courts are re-
LEGAL LIABILITY
439
-------
luctant "to accept evidence of compliance with an administrative
...permit as answering fully an inquiry under nuisance law.""
In fact, federal environmental statutes typically aver that they
are intended to establish only minimum requirements for pollution
control and not to preclude a state from establishing stricter ones
of its own with respect to the same subject matter. For example,
§3009 of RCRA provides that federal regulations for hazardous
waste management shall not "be construed to prohibit any State or
political subdivision thereof from imposing any requirements, in-
cluding those of site selection, which are more stringent than those
imposed by such regulations." So far as federal law is considered,
more stringent requirement could be imposed by either the legisla-
ture or the courts of a state. And as a matter of state law, state
courts are usually authorized to exercise their own judgment in
nuisance cases unless the state legislature has expressed an inten-
tion to preempt the field.
Critique of Common Law Actions
For various reasons, plaintiffs may have difficulty recovering
damages in tort actions at common law. Litigation is costly, time-
consuming and uncertain in outcome. Moreover, where personal
injuries are alleged from releases of hazardous waste, plaintiffs
may confront several peculiarly difficult obstacles to recovery.
To begin with, a plaintiff may have suffered too small or too
uncertain an injury to attract competent counsel on a contingent
fee basis. This problem can sometimes be overcome through "class
actions" where numerous persons who claim to have suffered
similar injuries are joined as plaintiffs against a single defendant
or group of defendants. Such actions may arise, for example,
where many people have used a contaminated water supply. By
aggregating their claims through class certification, the plaintiffs
can seek together a total sum in damages that is large enough to
warrant expensive resort to judicial process. However, class ac-
tions can generally be brought only where common questions of
law or fact predominate over questions affecting only individual
members of the class in a particular case.21
A second difficulty may be a lapse of a relatively long time be-
tween the escape of hazardous wastes from a disposal site, their
migration into plaintiff's water supply and the manifestation of
injury to plaintiff from consuming the contaminated water.
Plaintiff's action may be barred by expiration of the Statute of
Limitations, which sets a deadline on the filing of suit after
"injury" occurs—a difficult problem when injury is not suddenly
inflicted but gradually accrued. Or in the long latency period be-
tween cause and effect, defendant may have gone out of business
and critical witnesses disappeared. In fact, it may not even be
possible to find and identify a responsible defendant whom the
plaintiff can sue.
Moreover, in cases arising from exposure to hazardous waste,
scientific uncertainties may make it difficult for plaintiff to meet
the stringent standards of proof by which causation in tort is de-
termined. There are two focal points of factual uncertainty in many
of these cases: the pathway from the alleged site of release to the
victim's property or person, and (in cases alleging personal injury)
the effects of personal exposure to the contaminant.
"...[B]ecause of the lack of scientific certainty, and the several
years lag time between waste release and damage, it is extremely
difficult to establish the causal link. To establish causation,
the plaintiff must isolate the harm-causing chemical, trace the
pathway from the site to the victim, and prove medically that
the chemical caused the injury or disease. This difficulty is ex-
acerbated by other factors, such as the possibility of natural
processes in the soil affecting its composition, the spread of
leachate, the presence of more than one disposal site which
may have caused the damage, mixture of chemicals at the dis-
posal site, and subsequent exposure of the plaintiff to other
synergistic hazards which may have added to his injury. Per-
haps the most difficult element of causation in a personal in-
jury action is proving that a certain toxic substance caused a
certain disease. The determination that X chemical caused Y
disease is hindered by scientific complications in the evalua-
tion of the experimental data, use of statistical reports, extrap-
olation of animal testing to persons, and evaluation of low-
level exposure.""
Another commentator has observed:
"In the case of chemicals which present a risk of cancer, the
concentrations above which drinking water is considered to be
'contaminated' are typically levels at which the risk of getting
cancer is very low — approximately one-in-a-million lifetime
risk. Where the plaintiffs have been exposed to such a small
added risk of cancer, it should be virtually impossible to show
that any particular case of cancer occurring among users of the
water supply is attributable to chemical contamination— as
opposed to any of the plethora of other factors that can result
in cancer."30
For all the foregoing reasons, it is fashionable these days to crit-
icize tort actions at common law as an inadequate vehicle for re-
dressing injuries caused by releases of hazardous wastes to the
environment. Such criticism is largely justified. On the other hand,
as indicated by the rapidly growing number of reported judicial
opinions in this field, tort liability has been repeatedly imposed
upon defendants who were responsible for the mishandling of haz-
ardous wastes, especially where the plaintiff could make just
enough of a case to get to a sympathetic jury or could prove
damage to property, an easier undertaking than proof of injury
to personal health.
Moreover, the difficulties of proving causation are not neces-
sarily a deficiency of tort law. It may be that alleged injuries
from hazardous waste exposures have been overstated and ought
not to be accepted as facts giving rise to substantial monetary re-
coveries unless the plaintiff can prove his case by a clear preponder-
ance of the evidence in a court of law. In this connection, it should
be noted that courts are not likely to be overwhelmed by statis-
tical evidence from the environmental and health sciences, includ-
ing epidemiology. What is generally demanded in tort litigation is
proof linking the particular injuries suffered by the plaintiff at bar
with the activities of the particular defendant. This insistence on
particular proof may change with the passage of time, but tort
liability will seldom be determined by offers of statistical proof
unless rules of evidence are modified to that effect by statute.
Whatever the shortcomings may be of tort action in this field,
well publicized cases in which plaintiffs have recovered substan-
tial damages have begun to put industrial enterprises on their guard
against mismanagement of hazardous waste and have given them
every incentive to limit damage when it is discovered at uncon-
trolled sites. Tort liability is now and will remain a major incen-
tive for proper waste management, even beyond the minimum
standards established by regulatory law.
REFERENCES
1. In order to secure recovery, plaintiff must, of course, meet the burden
of proof on the factual allegations of his complaint. Even if plain-
tiff does or could prove his case, however, he may still lose because of
procedural bars, such as the statute of limitations (which sets a time
limit for bringing suit after the injury occurs), or because of affirm-
ative defenses such as contributory negligence, consent or assumption
of the risk.
2. E. Kionka, Torts in a Nutshell 6 (1977) [hereinafter cited as Kionka].
3. See, e.g., Ewell v. Petro Processors of Louisiana, Inc., 364 So. 2d
604 (La. App. 1978), cert, den., 366 So. 2d 575 (1979), in which de-
fendant Ethyl Corporation was required to share in cleanup costs from
a leak in an off-site disposal facility since the corporation continued
to ship hazardous wastes to the site after it acquired knowledge that
the site was leaking.
4. Ewell v. Petro Processors of Louisiana, Inc., supra note 3
from disposal facilities to adjacent property and navigable waters);
Ballantine v. Public Service Corp., 91 A. 95 (N.J. 1914) (leakage of
industrial waste into groundwater used by plaintiff to make its beerjf
Hagy v. Allied Chemical and Dye Corp., 122 Cal. App. 2d 361, 265
440
LEGAL LIABILITY
-------
P.2d 86 (1953) (injury to larynx of auto passenger driving through
sulfuric acid smog emitted from a factory); Reynolds Metals Co. v.
Yturbide, 258 F.2d 321 (9th Cir. 1958), cert, den., 358 U.S. 840 (1958)
(fluoride poisoning from aluminum plant emissions).
5. Restatement (Second) of Torts, §519 (1976).
6. Such cases have involved, for example, discharges from landfills, as
in Ortega Cabrera v. Municipality of Bayamon, 562 F.2d 91 (1st Cir.
1977); and discharges from industrial facilities, as in Cities Service
Co. v. State of Florida, 312 So. 2d 799 (Fla. Dist. Ct. App. 1975) and
Department of Transportation v. PSC Resources, Inc., 15 Env't Rep.
Cas. 1053 (Sup. Ct. N. J. 1980).
7. State of New Jersey Department of Environmental Protection v.
Ventron Corp., Nos. C-2996-75, C-1954-77, C-l 110-78 (N.J. Superior
Court, Trial Division, Aug. 27, 1979); modified and remanded, A-
1395-79; A-1432-79; A-1446-79; A-1545-79 (N.J. Superior Court,
Appellate Division, Dec. 9, 1981). The same principles of liability
enunciated in public nuisance cases brought by government agencies,
such as the Ventron case (and other cited in these footnotes), will also
be found to apply in private tort litigation based on similar sets of
facts.
8. E. Kionka, supra note 2, at 36.
9. Note, Strict Liability for Generators, Transporters and Disposers of
Hazardous Waste, 64 Minn. L. Rev. 949, 968 (1980).
10. Thus, the government has named Monsanto, a manufacturer of PCBs,
as co-defendant in a suit brought against an industrial user of that
chemical from whose plant it was discharged into Lake Michigan.
United States v. Outboard Marine Corp., Civ. No. 78C-1004 (E.D.
111., filed July 21, 1980). The complaint alleges that Monsanto failed
to warn adequately of the dangers inherent in the use of hydraulic
fluids containing PCB in an open hydraulic system. Another example
isMcKeever v. Shell Oil Co., Civ. No. 77-1128 (Sup. Ct. Cal., filed
Sept. 8, 1980), in which well owners and users sued manufacturers of
a pesticide, DBCP, that leached into groundwater after being applied
to crops, allegedly causing widespread groundwater contamination.
11. E. Kionka, supra note 2, at 268.
12. See the discussion in Section II.A below of generators' liability under
Section 107 of the Superfund Act.
13. See, for example, Ewell v. Petro Processors of Louisiana, Inc., supra
note 3, in which generators/customers of a disposal facility were not
held strictly liable because the leakage was "caused" by the facility
owner. The issue in such a case concerns the responsible or so-called
"proximate" cause, which is "essentially a question of duty—was the
defendant under a duty to protect this particular plaintiff against the
particular event which injured him or the consequences of that event?"
See E. Kionka, supra note 2, at 88. "Fairness dictates that it liability
is strict, at least the risk must be consciously assumed...in strict liabil-
ity cases unforeseeable intervening cause is a defense." Id. at 48.
The question would be, then, whether leakage from a RCRA-per-
mitted disposal facility is within the foreseeable scope of the risk
assumed by the generator/customer.
14. Ewell v. Petro Processors of Louisiana, Inc., supra note 3.
15. When hazardous wastes were released from the site of a bankrupt
company, the State of Michigan sued the generator/customers on the
theory that they had a "duty to the public...to dispose of their waste
products without threatening the public health and safety or its even
more precious natural resources." Kelly v. Ankersen, Civ. No. 77-
151279-CE (Michigan Cir. Ct., filed Feb. 19, 1977). This case was
settled before trial by agreement of the generators to remove their
wastes from the site.
16. See Michie v. Great Lakes Steel Division, National Steel Corpora-
tion, 495 F.2d 213, 217 (6th Cir. 1974), citing Cooley on Torts, and
holding that multiple defendants, emitters of air pollutants, could be
held jointly and severally liable for numerous individual injuries that
plaintiffs consequently suffered when the pollutants from their respec-
tive sources mixed in the air so that their effects in causing the par-
ticular injuries were impossible to analyze. See also Borel v, Fibre-
board Corp., 493 F.2d 1076 (5th Cir. 1973), where a group of asbestos
insulation manufacturers who supplied an insulation contractor were
held jointly and severally liable to an employee of the contractor who
got asbestosis, since each defendant contributed to the totality of
exposure that created the disease. See also Hall v. E.I. DePont de
Nemours and Co., 345 F. Supp. 353 (E.D.N.Y. 1972), holding a group
of explosives manufacturers jointly liable in a products liability case
on the ground that the individual manufacturer of the explosive caus-
ing the injury could not be determined.
17. In Sindell v. Abbot Laboratories, 163 Cal. Rptr. 132, 160 P.2d 924,
cert, den., 101 S. Ct. 285 (1980), plaintiff alleged that her cancer was
caused by her mother's having taken the drug DBS, but plaintiff could
not prove which company manufactured the particular supply of the
drug so taken. The court held that damages could be apportioned
among all the defendant manufacturers according to their relative
market shares.
18. Department of Transportation v. PSC Resources, Inc., 15 Env't Rep.
Cas. 1053 (Sup. Ct. N.J. 1980); State of New Jersey Department of
Environmental Protection v. Ventron Corp., supra note 7.
19. United States v. Ira S. Bushey & Sons, Inc., 363 F. Supp. 110 (D. Vt.
1973), 487 F.2d 1393 (2d Cir. 1973), cert, den., 417 U.S. 976 (1974).
20. Cyr v. B. Offen & Co., 501 F.2d 1145 (1st Cir. 1974); Ray v. Alad
Corp., 19 Cal. 3d22, 560P.2d3, 136 Cal. Rptr. 574(1977).
21. Canter v. Koehring Co., 283 So. 2d 716, 721, quoted with approval
in Shaefer v. D & J Produce, Inc., 62 Ohio App. 2d 53, 403 N.E.2d
1015(1978).
22. Graham v. Allis-Chambers Manufacturing Co., 41 Del. Ch. 78, 188
A.2d 125, 130(1963).
23. Preston-Thomas Construction v. Central Leasing Corp. 518 P.2d
1125 (Okla. 1973).
24. Village of Witsonville v. SCA Services, Inc., 396 N.E. 2d 552 (1979).
The decision and order of the Illinois Appellate Court for the Fourth
District in this case, printed at 13 Env't Rep. Cas. 1908-1821, was up-
held on May 22, 1981 by the Supreme Court of Illinois.
25. Id. at 1818.
26. W. Rodgers, Handbook on Environmental Law 138 (1977).
27. Id. at 141.
28. "Applying this test, the district in the Three Mile Island litigation
held that it would certify the plaintiffs' economic claims, as well as
claims from medical monitoring of the possible latent consequences
of low-level exposures...." Zener, Stakes High in Civil Suit for Waste
Damages, Legal Times of Washington, Dec. 22, 1980, at 17.
29. Meyer, Compensating Hazardous Waste Victims, 11 Envtl. L. 689,
714 (Spring 1981).
30. Zener, supra note 28, at 2. Faced with this difficulty, plaintiffs in the
Three Mile Island suits are demanding that defendants be ordered to
provide periodic medical examinations to persons who may have
been exposed to low-level cancer risk as a result of the TMI accident.
It remains to be seen whether this novel type of relief will be decreed
by the court or be incorporated in any out-of-court settlement by the
parties. "The difficulty with this theory of damages is that periodic
medical examinations are useful to detect illnesses that may result from
a wide variety of causes; it is not at all obvious that the defendant
who may have contributed to a slight increase in one of those causes
should underwrite the entire range of benefits that these examina-
tions provide." Id.
LEGAL LIABILITY
441
-------
COMPENSATING THE THIRD PARTY FOR A
SUPERFUND CLEANUP FAILURE
JULIE C. BECKER
DAVID VAN SLYKE
Booz, Allen & Hamilton, Inc.
Washington, D.C.
INTRODUCTION
Under the authority of the Comprehensive Environmental Re-
sponse, Compensation, and Liability Act of 1980,' the USEPA
has been taking actions to clean up the nation's worst hazardous
waste sites. Estimates of the total number of hazardous waste
sites in the United States range up to a high of 50,000.' Thus far,
however, CERCLA action has been taken only for the most seri-
ously polluted sites.
Three basic approaches to site cleanup are currently being used:
•A USEPA-led cleanup completed by the U.S. Army Corps of
Engineers or a private contractor
•A state-led cleanup, under a Cooperative Agreement, completed
by a private contractor
•A voluntary responsible party cleanup action completed by a pri-
vate contractor or, in a "cash out" type of arrangement, by the
Army Corps of Engineers or a contractor hired by the USEPA.
Despite the variety of approaches available to the USEPA, the
policies and procedures for cleanup of hazardous waste sites are
only beginning to emerge. In a few cases, the USEPA has paid for
the relocation of residents living near a hazardous waste site. Clear-
ly, however, relocation will not always be a feasible or cost-effec-
tive alternative, and many of the priority sites will need to be
cleaned up while people continue to live and work in the vicinity.
This situation results in important questions regarding government
and contractor liability to a third party for a removal or remedial
action failure, questions that the authors begin to address in this
paper.
Remedial action may fail for a number of reasons. It may be
the result of negligent or faulty design or construction, inadequate
investigation into the problems at the site or intentional acts or
omissions to act by the contractor. For example, the site may be-
come contaminated again by wastes that the contractor knowingly
left on the site or that the USEPA or the contractor negligently
failed to locate. Contamination may also occur because structures
designed by the USEPA or the state and installed by the contractor
began to leak.
The only mechanism currently available to private parties who
seek redress for this problem is a common law cause of action
against the USEPA, the state or the cleanup contractor. The
answer to the question of who will ultimately be liable for a remed-
ial action failure, however, depends on a combination of factors
including the party or parties responsible for undertaking the clean-
up (design and/or construction) and the cause of the remedial
action failure. Of course, indemnification agreements between the
parties involved in the cleanup may shift the liability.
THE FEDERAL APPROACH
TO LIABILITY AND INDEMNIFICATION
The Federal government may be held liable in several different
situations for injuries caused by remedial action failure. Common
law tort theories may be invoked, in certain circumstances,1 against
a Federal agency. In addition, the Federal kgovernment may be
held liable if an indemnification arrangement has been created
between a government contractor and a Federal agency.
Under the various common law theories, the USEPA and/or
the Army Corps of Engineers may be held liable for faulty de-
sign or construction of a remedial cleanup project.4 Third party
recovery under any of the tort theories, however, is not at all guar-
anteed. A 1972 Report of the Commission on Government Pro-
curement, for example, sets forth several criticisms of the Federal
government's response to catastrophic accidents occurring in
connection with Government programs. The Commission reports
that victims often have the burden of proving the cause of injury.1
For those whose injuries result from Superfund cleanup activities,
such burdens may be insurmountable. The action or inaction of a
contractor which caused a release of chemicals must be pinpointed
and the link between post and cleanup chemical exposure and
injury must be proved. The result can be years of trial prepara-
tion and significant expense to the plaintiff.'
The USEPA, as an indemnitor, may also be held liable for the
negligent acts of its contractors. The Agency has adopted a policy
of indemnifying Superfund contractors for any uninsurable liabil-
ity.' According to the USEPA Office of General Counsel, indem-
nification is necessary because the insurance industry does not
offer affordable long-term insurance coverage for Superfund sites,
and contractors have expressed reluctance to bid on remedial ac-
tions unless such an arrangement is available.' Under this pro-
cedure, if a contractor is found liable for personal injury or
property damage resulting from cleanup activities, and the injury
or damage is not (and was not required to be) insured for by the
contractor, the United States will pay the victim on behalf of the
contractor.
It would seem, therefore, that Federal indemnification would
allow a third party to recover for injuries or damages resulting
from the acts of USEPA contractors. However, several serious
obstacles still must be overcome. First, under the USEPA in-
demnification procedures, a third party harmed by remedial action
failure must bring a successful legal action against the contrac-
tor before he can recover from the Agency. This invokes all the
problems inherent in obtaining a judgment based on a common law
cause of action. Another barrier to recovery from a governmental
442
LEGAL LIABILITY
-------
indemnitor is the USEPA's inability to indemnify a contractor for
liability resulting from a willfully negligent act. While the courts
do allow indemnification for negligence, public policy considera-
tions have led them to prohibit indemnification in cases arising
out of the willful misconduct of a contractor.'
To illustrate the problem suppose the USEPA contracts to have
wastes removed from a Superfund site and the contractor know-
ingly buries several hundred newly discovered barrels of highly
toxic chemicals in an unsecured area, contrary to the site cleanup
plan. Suppose, in addition, that the contractor has gone bankrupt
since completing the remedial action and residents living near the
site begin to experience health difficulties. Since the contractor
was willfully negligent, the government is prohibited from paying
damages proved by the residents. Additionally, the contractor's in-
solvency means that the residents will not have a party from which
to recover.
A final problem with the Federal scheme is the uncertainty re-
garding the availability of funds for indemnification. The limi-
tations imposed by the Anti-Deficiency Act, together with the
"sunset" provisions of CERCLA, may prevent even a successful
third party from enforcing a judgement.
The Anti-Deficiency Act, which governs Federal indemnifica-
tion, prohibits an agency from "entering obligations in excess of
funds available."10 Recovery by victims of a major incident will,
therefore, be limited to whatever funds remain in the CERCLA
Trust Fund at the tune that judgement is entered against the con-
tractor. In this situation, the third party would also be prohibited
from recovering from general revenue or from the USEPA budget
unless Congress passes a special appropriation.''
An additional factor here is the CERCLA "sunset" provisions
that automatically terminate the taxing power of the Fund in
1985 unless the Act is reauthorized.12 Should the Act's taxing
power lapse and the Fund be drawn down by the costs of con-
tinuing response actions, the victim's ability to recover becomes
even more uncertain. A major lawsuit can take years to proceed
through filing of claims, discovery and trial. In addition, remedial
action failure may not become apparent until years after the com-
pletion of clean-up operations, at which time the Trust Fund
may be depleted.
The Federal Government's approach is designed for the benefit
of the government and its contractors but does little to assure that
third parties will recover. Any one of the factors discussed above
(common law burdens of proof, Federal government limitations
on indemnification, contractor insolvency, the Anti-Deficiency
Act and the Superfund sunset provisions) could serve as a barrier to
recovery. In short, there are no guarantees that a decade after
site cleanup either the contractor or the Federal government will
be available as financially viable defendants.
THE STATE'S APPROACH TO
LIABILITY AND INDEMNIFICATION
In the event that the hazardous waste site cleanup is undertaken
by a state under a Cooperative Agreement with the USEPA, the
state is a potential defendant in a suit for injuries suffered due
to failure of a site cleanup. However, the third party plaintiff may
also find recovery from a state or state-hired Superfund contractor
problematic. Contractor's indemnification agreements, common
law doctrines and Federal constitutional law all tend to protect a
state government from lawsuits and do little to aid the individual
living or working near a former CERCLA site.
State Indemnification Agreements
States conducting remedial actions, in contrast to the USEPA,
generally have chosen not to indemnify contractors. Instead, state
indemnification schemes are designed to protect states from liabil-
ity for the acts of their agents. Both New Jersey and California,
for example, require Superfund contractors to indemnify the state
against liability to third parties. Several other states are consider-
ing similar contract requirements.'3
In contrast, the State of Michigan uses a partial indemnifica-
tion scheme in which the state may be held liable for a design-re-
lated failure but not for a construction-related failure.14 This
scheme may result in several problems for the third party. For
example, the steps involving the removal of waste from a site are
part of a "construction" and the complete responsibility of the
Michigan contractor. But if a contractor has become insolvent, the
residents will not have a viable party from which to recover.
Design-related failure of a remedial action designed by the
USEPA but implemented by the state also poses a problem, as
Michigan only agrees to indemnify contractors if the project has
been designed by the state. Since the USEPA designed the remed-
ial action, the state could not be held liable based on the faulty
design. In addition, the USEPA has concluded that, under the
Grant Regulations governing Cooperative Agreements, only the
state and its contractors can be held liable should a cleanup oper-
ation fail.15 Nor could the third party sue the contractor, whose
only responsibility was construction of the remedial project.
State Government Immunity
Even in states which do not require the contractor to provide
indemnification, the state may otherwise be protected from liabil-
ity. The doctrine of sovereign immunity and the Eleventh Amend-
ment to the Federal Constitution can be a bar to recovery for the
plaintiff suing for failure of a state-supervised remedial action.
The Eleventh Amendment and Supreme Court decisions inter-
preting it," protect a state from being sued in Federal court by
citizens of that state or any other state unless consent is implic-
itly or explicitly given. Although a third party still has the option
of suing in state court, states generally have stricter discovery
rules, a less experienced bench and lower jury awards. They are,
therefore, a less desirable forum. While many states do have
statutes consenting to be sued in specific situations, few accept gen-
eral tort liability. In a state that maintains its Eleventh Amend-
ment immunity, therefore, the plaintiff must sue the contractor
directly and hope that the contractor is still in existence and has
the financial resources to allow a recovery sufficient to compen-
sate for the injury suffered.
An additional barrier to suit against a state is the common law
doctrine of sovereign immunity. Based on the ancient English tenet
that "the King can do no wrong," it is intended today to protect
the state from burdensome interference with its governmental
(versus proprietary) functions." Whether a state-run cleanup of an
abandoned hazardous waste site is a "governmental" or "pro-
prietary" function has not yet been determined by any court.
However, given the purpose of the cleanup (the welfare of the
citizens of the state) the governmental nature of the action is rea-
sonably clear and, absent consent, suit would likely_be barred.
To Illustrate the problem of governmental immunity, consider
the following example. A remedial action failure occurs following
a state supervised cleanup operation. In a state that has not waived
its Eleventh Amendment immunity for general tort liability, a suit
in Federal court against the state would be barred. The Federal
forum would also not be available for a suit against the contrac-
tor unless diversity or Federal question jurisdiction could be
established.18 If, upon bringing suit in the less desirable state court
forum, the site cleanup is determined to be a governmental func-
tion, suit against the state would likely be dismissed under the
doctrine of sovereign immunity. A suit against the Superfund con-
tractor in state court would generally be the last resort of the
injured resident. However, even if the plaintiff(s) could afford the
time and expense of a trial and is able to show causation, recov-
ery will depend on the solvency of the contractor and the extent and
applicability of its insurance coverage.
PROPOSED SOLUTIONS AND RECOMMENDATIONS
A single, uniform approach to state and Federal response in the
event of a remedial action failure is clearly needed. The approach
should be designed to maximize competition among contractors
LEGAL LIABILITY
443
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while allowing the public to recover for personal injuries. Ideally,
this program will include the following elements:
•An administrative process for direct victim compensation
•Preservation of existing common law remedies
•Financial responsibility requirements for Superfund contractors
The first two points are addressed in a broader sense in the recent
CERCLA section 301(c) report to Congress on victim compensa-
tion." The authors' recommendations for these three elements,
discussed below, are focused strictly on the issue of compensa-
tion for Superfund cleanup failures.
Recommendation 1: Establish a Federal Administrative Process
for Direct Victim Compensation
The Commission on Government Procurement recommends that
the Federal Government provide more prompt financial assistance
to victims of disasters caused by Federal activities. In proposing
"the creation of a speedy and effective" administrative remedy,
the Superfund Section 301(e) Study Group reaches a similar con-
clusion."
The administrative system that we propose would have the
following elements:
•A Federally managed victim compensation review board to review
claims of individuals allegedly injured by Superfund cleanup
failures
•An administrative process for verifying and reviewing claims
•A level of proof that recognizes the latency and randomness of
chronic hazardous waste injuries
•A finite (12 month) period of time for agency review of the claim
•A ceiling on the recovery amount per episode
Each of these elements has some precedent in Federal disaster
relief programs or other Federal law, as described below.
The Teton Dam Act" authorized the Secretary of the Interior or
his designee to investigate claims and make compensation for dam-
ages arising out of the failure of the Teton Dam. The regulations
promulgated under the Act set up an administrative review system
to "investigate, consider, ascertain, adjust and settle" any claims
made." Similarly, the Texas City Disaster Relief Act" authorized
the Secretary of the Army or his designee to investigate and settle
claims against the United States resulting from the death, personal
injury and property damage associated with the explosion and fires
in the Texas City dock incident. In addition, Administrators of
Federal agencies have been given the authority to settle general
tort claims."
Under the Teton Dam Act and the Texas City Disaster Relief
Act, once the injured party presented his or her claim, the sole
responsibility of the administrative review system was to determine
three items:
•Whether the losses sustained resulted from the incident
•The amounts to be paid
•The person entitled to receive the award
The system proposed here would set up a review board to make
awards based using the same criteria.
The basic problem encountered in applying that system to a
Superfund cleanup failure scenario, however, is the uncertainty in
determining that the injuries in fact resulted from the failure of the
cleanup. To alleviate that problem, the authors propose a system
that would compensate those persons who suffer injuries from ex-
posure to toxic chemicals from hazardous waste sites but would not
require victims to prove that their specific injuries had been
caused by a CERCLA cleanup failure. The system would compen-
sate victims of a hazardous waste cleanup failure according to the
exposure received by each. The exposure received could be de-
termined according to each victim's location during and following
the cleanup.
Contrary to available common law remedies, only proof of ex-
posure, not proof of causation would be required. The review
board analyzing these claims would be charged with determining
which of the diseases or other injuries were sufficiently related to
the type of particular exposures experienced to warrant compen-
sation.
For example, anyone who had lived within a certain radius of
the site for a certain period of time during or after the cleanup
would be entitled to full compensation if their particular injury
was determined to be sufficiently related to the exposure exper-
ienced, even though the exposure could not be isolated as the
cause. This system is somewhat imperfect because it would also
compensate those persons living near the site during the cleanup
whose injuries may have originated from problems caused by the
original waste site, rather than the cleanup failure. Nevertheless,
the administrative system would avoid the need to select the proper
party or parties responsible for the release, and the relaxed stand-
ards of proof would help to assure residents that the government
will take ultimate responsibility for its activities.
The proposed system would also require the review board to
determine the validity of the claim and the award amount within
one year of presenting the claim. Similarly, the Teton Dam Act re-
quired the Secretary of the Interior to determine awards within
one year after the claim was filed. The Texas City Disaster Relief
Act imposed like requirements upon the Secretary of the Army.
To limit the ultimate liability of the Federal government, ceil-
ings could be established based on the type and extent of the claims.
The Price-Anderson Act," which sets a limit of $560 million per
accident, might serve as a model for the establishment of a ceiling.
In the alternative, Congress could set a limit for each claimant.
Both the Teton Dam Act and the Texas City Disaster Relief Act
establish limits on the amount an individual may claim.
Experience with these statutes indicates that the public may view
a ceiling on compensation as an indication that they will not be
fully compensated for hazardous waste injuries. When balanced
against the delay and costs of a trial and the problem of proving
causation, however, an administrative remedy that nevertheless in-
cludes a limitation on total government liability becomes more
attractive. In addition, as discussed below, the opportunity to pur-
sue traditional legal remedies is not foreclosed.
Recommendation 2: Preservation of Existing
Common Law Remedies
The administrative program outlined above is not intended to be
the exclusive remedy for the victim of a hazardous waste cleanup
failure. The existing common law tort remedies should also be
available, and victims should be able to bring direct civil actions
against parties who have allegedly injured them." This scheme is
similar to that recommended by the Section 301 (e) Study Group in
its "Tier II" system.
To alleviate one of the critical problems in traditional toxic torts
litigation, the Federal legislation creating the proposed system
should also adopt a statute of limitations that employs the "dis-
covery rule" and that preempts any state statute of limitation for-
bidding the maintenance of an action prior to three years follow-
ing discovery of an injury."
Recommendation 3: Financial Responsibility
Requirements for Superfund Contractors
To help ensure that Superfund cleanup contractors are reliable
and financially able to compensate injured parties for at least a
portion of the damage that might result from a CERCLA cleanup
failure, the USEPA may require a contractor to prove financial
viability or maintain some type of extended financial protection
such as pre-paid long term insurance. The Price-Anderson Act,
for example, requires Nuclear Regulatory Commission licensees
to maintain financial protection in "the amount of liability in-
surance available from private sources."2'
This approach has also been applied to hazardous waste disposal
in the Resource Conservation and Recovery Act, which requires
disposal facility operators to obtain $6 million of liability cover-
age." Similar provisions are found in Section 108 of Superfund,
which requires operators of vessels being used to transport haz-
ardous wastes to present evidence of financial responsibility
amounting to a minimum of $5 million in coverage. This section
also authorizes the President to establish financial responsibility
444
LEGAL LIABILITY
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requirements for closure of an approved hazardous waste facility.30
By imposing financial responsibility requirements on Superfund
contractors, the government would be better able to ensure re-
covery to those who suffer personal injuries and/or property
damage resulting from a remedial action failure.
CONCLUSION
Toxic torts are receiving much attention in Congress.3' If one
of the bills now being considered is adopted, it should include
some provision for hazardous waste cleanup failure, such as the
program the authors have suggested.
To implement the above recommendations, Congress would
need to devise a system for resolving claims, establish reasonable
ceilings on recovery, develop some means to assure contractor
solvency and make other basic decisions regarding how best to
compensate the victim of a removal or remedial action failure.
This paper, however, is not intended to be a definitive answer
to the problem of third party recovery. It is clear, nonetheless,
that hazardous waste cleanup operations pose a serious threat to
those living or working nearby and that the common law and state
and federal indemnification schemes currently fail to provide ade-
quate assurance that the public will be compensated for personal
injuries or property damage resulting from such activities. A more
direct compensation scheme would help to provide a quicker, more
predictable mechanism for third party compensation.
REFERENCES
1. 42 U.S.C. 9601 etseq. (1980).
2. Preliminary Assessment of Cleanup Costs for National Hazardous
Waste Problems, USEPA Office of Solid Waste, Fred C. Hart Assoc.,
EPA Contract No. 685-01-5063, 1979.
3. The Federal Tort Claims Act, 28 U.S.C.§§1346(b), 1402, 2401, 2671-
2680, is a limited waiver of sovereign immunity, allowing liability to
be incurred, under certain circumstances, for the negligence of Fed-
eral government employees or agents.
4. Section 107(d) of Superfund appears to protect the Federal Govern-
ment and its contractors from liability. However, in the opinion of the
USEPA Office of General Counsel, Section 107(d) probably does not
protect EPA or its contractors from private rights of action under
ordinary tort principles. Nantkes, Donnell L., "Indemnification of
Superfund Contractors," Internal USEPA Memorandum, June 26,
1981.
5. Report of the Commission on Government Procurement, 4, Dec.
1972, 99-104.
6. For further discussion on the difficulty of invoking common law
remedies in hazardous waste cases, see Comment, "Hazardous Waste
Liability and Compensation: Old Solutions, New Solutions, No Solu-
tions," 14 Conn L. Rev. 307 (1982).
7. See, Nantkes, supra. Note 4.
8. See, Nantkes, supra. Note 4.
9. Globus v. Law Research Service, Inc., 418 F.2d 1276, 1288 (2d Cir.
1969), cert, denied, 397 U.S. 913 (1970); Stamford Board of Educa-
tion v. Stamford Education Assoc., 697 F.2d 70 (2d Cir. 1982).
10. 31 U.S.C. §665 (a) (1974).
11. 54Comp. Gen. 824, 826-27(1975).
12. 42 U.S.C. §963l(b)(2) (1980); 26 U.S.C. §§ 461 l(d),4661(c) (1980).
13. Sanders, D.E., Sweeney, F. and Hillenbrand, E., "Protection from
Long-Term Liability as a Result of Superfund Remedial Actions,"
Proc. of the National Conference on Management of Uncontrolled
Hazardous Waste Sites, Nov. 1982, 46M62.
14. Id.
15. Id.
16. See, e.g., Parden v. Terminal K. of Alabama State Docks Dept.,
377 U.S. 184, reh. denied, 377 U.S. 299 (1964).
17. While the doctrine is currently in judicial disfavor, most states have
enacted legislation to retain some form of sovereign immunity. For a
more complete discussion, see Prosser, Torts §131 (4th ed. 1971).
18. 28 U.S.C. §1331 (1980) (Federal question jurisdiction); 28 U.S.C.
§1332 (1976) (diversity jurisdiction).
19. Senate Comm. on Environment and Public Works, Inquiries and
Damages from Hazardous Wastes—Analysis and Improvement of
Legal Remedies—A Report by the Section 301(e) Study Group, S.
Doc. No. 12, 97th Cong., 2nd Sess. (1982).
20. The 301(e) study group proposed a two part system. Tier I, an admin-
istrative system, is based on the use of rebuttable presumptions to
prove causation. Tier II keeps intact the traditional common law
remedies.
21. Pub L. No. 94-400, 90Stat.l211 (1976).
22. 43 C.F.R. §419(1977).
23. Pub. L. No. 84-378, 69 Stat.707 (1955).
24. 28 U.S.C. §§2672, 2675 (1966).
25. Pub. L. No. 85-256, 71 Stat. 576 (1957) (current version at 42 U.S.C.
§§2012(i), 2014(j), (m), (p), (q), (t), (w), 2210 (1970 & Supp. V 1975)).
26. Similar to the procedures instituted in the National Swine Flu Immuni-
zation Program of 1976, claims should be presented to the adminis-
trative review board before a legal action is brought. See, 42 U.S.C.
§247(b) (1976). See also, 28 U.S.C. §2672 (1966) (Administrative
adjustment of claims under the Federal Tort Claims Act).
27. SeeH.R. 2330, 98th Cong., 1st Sess. (1983).
28. 42 U.S.C. §2210(b) (Supp. V 1975).
29. 40 C.F.R. §264.147(b), as revised in 47 Fed. Reg. 16554 (April 16,
1982).
30. 42 U.S.C. §9601, 9608(a) and (b) (1980).
31. See, e.g., S. 917, 98th Cong., 1st Sess. (1983); S. 945, 98th Cong.,
1st Sess. (1983); H.R. 2482, 98th Cong., 1st Sess. (1983); H.R. 2330,
98th Cong., 1st Sess. (1983); H.R. 2582, 98th Cong., 1st Sess. (1983).
LEGAL LIABILITY
445
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INDICATOR METHODS FOR POST-CLOSURE
MONITORING OF GROUND WATERS
IHORLYSYJ
Rockwell International Corporation
Environmental Monitoring & Services Center
Newbury Park, California
INTRODUCTION
In order to assure protection of groundwater from contamina-
tion by leachates from hazardous waste disposal facilities, the
USEPA has issued two regulations: 40CFR264 and 40CFR265
covering both legal responsibilities and technical requirements for
such protection. Specifically, these regulations require owners and
operators of waste disposal facilities to design and implement either
detection or implementation programs.
Detection programs are used at facilities where existence of con-
tamination is unknown, while assessment programs are directed
at facilities where groundwater contamination is known to have
occurred due to the operation of the waste disposal facility. The
detection program is, in essence, a diagnostic measure, while the
assessment program quantifies the degree of damage done to
groundwaters. In this paper, the author addresses the first topic,
that is the detection of groundwater contamination. The discussion
applies equally to monitoring of operating interim status facilities
and required monitoring during long post-closure periods.
TECHNICAL SCOPE
The technical scope of monitoring requirements is defined in
Subpart F of both regulations. This subpart specifically addresses
technical aspects of groundwater monitoring in the context of the
subject regulations. The regulations address three distinct sets of
tests associated with determining groundwater quality:
1. Parameters characterizing the suitability of the water as drink-
ing water
2. Parameters used to characterize groundwater quality
3. Parameters used as indicators of groundwater contamination
In the first group of parameters (drinking water suitability),
one finds a number of metals which are known as toxicants
(arsenic, barium, cadmium, chromium, lead, mercury, selenium
and silver); two anions (nitrate and flouride); and a number of
pesticides (Endrin, Lindane, Methoxychlor, Toxaphene, 2.-4D,
2,4,5-TP Silvex). Additionally, water is monitored for its radio-
logical characteristics (radium, gross alpha and gross beta radia-
tion) as well as coliform bacteria.
In the second group (general water quality parameters), there
are two anions (chloride and sulfate), three metals (sodium, iron
and manganese) and one organic compound (phenol).
The third group (indicator parameters of groundwater contam-
ination) comprises four general water characteristics( pH, specific
conductance, Total Organic Carbon (TOC) and Total Organic
Halogen (TOX). These four indicator parameters reflect changes
in the organic and inorganic make-up of groundwater and are
used to detect any effect of facility operation on groundwater qual-
ity. The indicator approach to monitoring groundwater contam-
ination is based on measurement of changes in respective values
of pH, specific conductance, TOC and TOX, since all ground-
waters possess some nominal values in each category. To be effec-
tive as a tool of monitoring and detection, the indicator approach
presupposes that changes and fluctuations in the pH, specific
conductance, TOC and TOX induced by natural phenomena in
groundwater are minimal and insignificant, and that the magnitude
of such naturally induced fluctuations can be compensated for and
statistically differentiated from changes induced by intrusions of
hazardous and toxic species from waste disposal facilities.
INDICATOR PARAMETERS
The basis for indicator parameter selection is a belief that signif-
icant discharges from hazardous waste management facilities to
the groundwater will often result in an observable change in at
least one of the four selected indicators: pH, specific conductance,
TOC and TOX. It is further believed that there is a small probabil-
ity that major discharge could occur without significant change in
at least one of the four indicators in groundwater samples. The
conceptual approach to design of indicator monitoring protocol is
based on responsiveness to a large number of largely undefine-
able sets of chemical compounds at unspecified concentration
levels which can be classed in general terms: ionic, nonionic, organ-
ic, inorganic and suspended or dissolved in groundwater.
As described in the "Groundwater Monitoring Guidance for
Owners and Operators of Interim Status Facilities",1 pH and spe-
cific conductance were chosen for monitoring of inorganic con-
stituents because they satisfy all basic requirements for being ac-
ceptable test procedures, and there are no alternative inorganic
indicators that can provide equivalent information value. The pH
affects solubility and mobility of many toxic constituents of waste
and determines the rate and outcome of chemical reactions the
pollutant will undergo. Specific conductance is a numerical ex-
pression of the summation of contributions from all ions present in
a solution. Since such a measurement is an additive property, it is
useful as an indicator parameter because it can determine effec-
tively all ions simultaneously.
TOC was chosen as an indicator parameter for organics be-
cause of its widespread use, acceptability as an effective test pro-
cedure and general applicability to all types of organic contam-
ination. It is one of the few parameters that provides a broad
description of the organic content of water and is replacing chem-
ical oxygen demand (COD) in groundwater analysis. TOC pro-
vides a more direct expression of organic content than COD, is
more sensitive and is a less difficult procedure.
TOX was selected to measure only those organic compounds
containing halogens. Despite the somewhat more limited use of
TOX, it is included among the four indicators in view of the rela-
tively large amount of hazardous wastes which may contain halo-
genated hydrocarbons and the higher degree of toxicity usually
associated with these compounds.
It must be recognized that the proposed approach of indicator
parameter monitoring is based on measuring changes in various
relevant parameters and presupposes that such changes deriving
from natural phenomena will be statistically insignificant, while
parameter changes deriving from intrusions of hazardous and/or
toxic substances will be statistically significant. Because of the
largely statistical justification of the technological validity of the
proposed approach, the regulations devote significant amounts of
importance to statistical analysis. It is postulated that the owner or
operator of a facility must perform a statistical analysis of the
concentrations or values of indicator parameters as determined
from the sampling and analysis of required monitoring weUs.
Specifically, the Section 265.92(c)(2) on sampling and analysis re-
446
POST-CLOSURE
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quires mat tne initial background mean and variance for each in-
dicator parameter be determined by pooling the replicate meas-
urements for the respective parameter concentrations in samples
obtained from the upgradient well(s) during the first year. Repli-
cate analyses are not required for downgradient wells during the
first year.
After the first year of monitoring, the owner or operator is re-
quired to analyze for and calculate the mean and variance of each
indicator parameter (i.e., pH, Specific Conductance, TOC and
TOX), based on at least four replicate measurements on each
sample, for each well in the monitoring system. Results for each
indicator parameter from each sampling event (for each and every
well in the monitoring system) must be compared with the initial
background mean (i.e., that established for the upgradient well(s)
during the first year). The "Student's t" test at the 0.01 level of
significance must be used to determine statistically significant in-
creases over the initial background values.
The approach to indicator monitoring for detection of hazardous
and toxic wastes intrusion into groundwater as proposed by the
EPA is practical and based on sound theoretical considerations;
however, physical evidence in a form of supportive data must be
developed to support this concept. The critical element of the pro-
posed scheme is degree and magnitude of background fluctuations
of selected parameters (pH, specific conductance, TOC and TOX)
induced by natural phenomena and independent of any intrusions
of hazardous waste that might or might not have taken place.
To satisfy a need for such supportive evidence, the USEPA is
conducting an effort to determine background groundwater qual-
ity data for indicator parameters from interim status facilities
across the country in order to establish distribution of concentra-
tions or values of these parameters over a period of time. With this
information on actual fluctuations in the chemical content of
groundwaters, the USEPA will be able to determine the number of
facilities for which the specified statistical compensation procedure
is appropriate and to further identify alternative data evaluation
and comparison procedures for those situations where the pro-
cedures specified in Regulation 265.93 may not be appropriate.
A principal component of this evaluation will be an estimate of
the "false positive" and "false negative" probabilities for various
statistical procedures in various circumstances of groundwater var-
iability over time.
This ongoing effort will most likely result in amendments to
the USEPA regulations regarding monitoring of groundwater (sub-
part F) and revisions in related documents.
In instances where it is currently known that applicability of the
indicator monitoring approach is unacceptable on technical
grounds, the USEPA suggests use of alternative groundwater mon-
itoring schemes. Specifically, it is stated that: "If an owner or
operator assumes (or knows) that groundwater monitoring of indi-
cator parameters...would show statistically significant increases...
he may install, operate and maintain an alternate groundwater
monitoring system (other than the one described in 265.91 and
265.92)."
This paper addresses potential technical approaches to such al-
ternative indicator parameter monitoring.
DIFFERENTIATING INDICATOR METHODS
The proposed USEPA methods for indicator parameter moni-
toring of groundwater are nondifferentiating, i.e., the methods
cannot discriminate between fluctuations in specific parameters
induced by the natural phenomena and those produced by the in-
trusions of hazardous and/or toxic wastes into groundwater. Such
nondifferentiating methods are applicable only to the situations
where normal fluctuations in background chemistry of ground-
water are minimal and statistically insignificant. They cannot be
used effectively in any other instances.
In situations where normal background fluctuations in the chem-
istry of groundwater are significant, an indicator method must be
capable of differentiating between fluctuations induced by the
normal natural process and those produced by hazardous waste in-
trusions. The theoretical and practical technological capabilities
for such a differentiation do exist at this time.
First, the theoretical aspects of this problem will be considered.
The normal and natural organic background content of unpolluted
waters derives mainly from biomass activity and decomposition
and decay of vegetable matter. In a series of classic studies, Birge
and Juday2 established almost a half a century ago that natural
organics found in lakes are composed largely of carbohydrates,
proteins and lipids. Additional supportive evidence was developed
in the early seventies using the pyrographic method of analysis
by Lysyj.3 These studies disclosed that while the quantitatively
organic content of natural waters fluctuates from source to source
and season to season, it remains similar in qualitative terms. Prin-
cipal classes present in all cases examined were found to be carbo-
hydrates, proteins and lipids.
Unlike the organic matter derived from natural sources in water,
the organic matter found in hazardous waste is largely of man-
made origin and is chemically significantly different from that of
natural origin.
In hazardous wastes, one finds a predominance of hydrocarbons
(both aliphatic and aromatic), halogen compounds, pesticides,
ketones, aldehydes, substituted aromatic compounds and a variety
of specialty chemicals.
Consequently, there exists a significant qualitative differential
between organics found naturally in the groundwater and those
found in hazardous wastes. Because of this fact, differentiation
between types of organic matter to be found in contaminated
groundwater is possible using the theory of multicomponent pat-
tern recognition and differentiation.
This theory postulates that matter of discrete composition can
be characterized qualitatively and defined quantitatively by con-
sidering the overall pattern formed by the individual components
of such composition. For example, in natural waters contaminated
by the intrusion of leachates from a hazardous waste site, one can
expect to find a number of organic compounds contributed by
hazardous waste and a number of organic compounds derived from
natural sources. The overall patterns formed by each of two such
compositions of matter will be different and, when developed by
physical means, should be differentiable by application of suitable
mathematical techniques.
In most cases where pollution of groundwater took place, the
subset of organic matter derived from natural sources will be de-
finable, while subset or organic matter derived from intruding
hazardous waste will be undefinable. The overall effect will be dis-
tortion in a definable pattern of natural organic background of a
given water source. Such a pattern distortion will signify that pollu-
tion of groundwater by man-made chemicals took place. In situa-
tions where the nature of intruding hazardous waste is known or
suspected, the system could be calibrated for both subsets of
naturally derived organics, and the subset of organics derived from
a hazardous waste source and both multicomponent compositions
could be treated quantitatively. The quantitative fluctuations in
the background organic content of a given source of groundwater
will not have a detrimental effect on such determination, since
qualitatively the pattern produced by such organics will remain
essentially the same.
Pyrographic Analysis
The physical means for making such a water sample examina-
tion exist. A pyrographic method of analysis developed in the
early seventies under USEPA sponsorship has been successfully
used for gross characterization of unpolluted surface water in the
southeast part of the United States, as well as for detection and
characterization of waste discharges into such waters."
Briefly, the pyrographic method of analysis, as applied to water
analysis, is a multidimensional technique. It permits definition of
both the magnitude and the nature of the phenomena being ob-
served and, as such, is quite suitable as a method for determina-
POST-CLOSURE
447
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tion of hazardous waste intrusions in instances when significant
fluctuations in the background chemistry of groundwater are
known to take place.
Two principal dimensions of the pyrographic method are:
1. Intensity of the signal
2. Pattern of the signal
The intensity of the signal relates to concentration, while the
pattern of the signal relates to the qualitative nature of the material
being analyzed. For example, the natural organic content of sur-
face water could change by orders of magnitude between winter
and summer months in a temperate climatic zone. When such
waters are analyzed, this change will be reflected in the intensity
of pyrographic peaks, but not in the patterns themselves. The ratio
or proportion of peaks will remain constant, since similar organic
matter (derived from biomass activity) is being analyzed, and only
the amount or quantity of produced matter is being changed.
Consequently, programs reflecting different levels of naturally
derived organic matter will be of different intensity, but constant
in pattern. When external pollutants are introduced into such
water, both the peak intensity and the peak pattern will change
since, in this case, we are analyzing a sum of two dissimilar com-
positions. It is this two-dimensional capability of pyrographic
methodology that provides a basis for differentiation between
compositional fluctuations attributable to natural phenomena and
compositional fluctuations produced by external events.
There are a number of mathematical and statistical approaches
available for handling and interpretation of pyrographic data. A
tailor-made approach could be developed for meeting the require-
ments.
A visual examination of pyrographic patterns provides the sim-
plest form of detection of the presence of hazardous waste (or
other man-made pollutant) in natural water. If no pollution (in-
trusion of hazardous waste) took place in groundwater, the pyro-
graphic pattern will match that produced by analysis of unpolluted
water. If ground or surface water has been contaminated by man-
made organic matter, the pyrographic pattern will be distorted
and the ratios and magnitudes of the peaks will be different from
those of natural unpolluted waters.
The next step in the sophistication of pyrographic data handling
is to calibrate the pyrographic instrument in terms of principal
classes of organic matter found in unpolluted waters: carbohy-
drates, proteins and lipids, and then subtract patterns produced by
those three classes of organic matter from the overall (total) pat-
tern produced by water sample analysis. Where there is no intru-
sion of hazardous substances and the only contributions to the
pyrographic pattern are made by naturally derived organic matter,
mathematical manipulation of the data will produce a blank, i.e.,
a calibrated pattern will be subtracted from the pattern of analyzed
water, and no peaks will appear on the graph. Where organic mat-
ter of a man-made nature is to be found in a water sample con-
taining natural organic background of carbohydrates, proteins and
lipids, mathematical manipulation of data will remove natural
organic contributions to the pattern, and much of the pattern will
consist only of contributions from man-made sources. The pro-
duced pattern will signify intrusions of hazardous substances into
groundwater. It could be further interpreted in qualitative and
quantitative terms.
Where the nature of the chemical waste present at a given haz-
ardous waste site is known and a sample of such is available for
calibration, a complete qualitative and quantitative analysis of
organic matter in a water sample is possible. The instrumental sys-
tem is calibrated in the usual manner for carbohydrates, proteins
and lipids and additionally calibrated for one or more suspected
hazardous waste compositions. After the analysis is performed, the
concentrations of natural organics and contaminants are computed
using calibration constants in the mathematical logic.
The instrumentation hardware used for performance of pyro-
graphic analysis is relatively simple. The system consists of a spe-
cially designed injector which provides for a uniform and consis-
tent mode of introducing a water sample into a pyrolysis tube.
The pyrolysis tube is made of nickel and is filled with nickel shots.
It is usually maintained at a temperature of 600 °C in an appro-
priate heating mantle. The effluent from the pyrolysis tube enters
the gas chromatographic column where, produced by pyrolysis,
molecular fragments are separated and then detected by the hydro-
gen flame ionization detector. The compressed gases required for
the system operation are high purity hydrogen, nitrogen and oxy-
gen. The signals produced as a result of pyrographic analysis are
amplified by an electometer and recorded either in analog or dig-
ital form. An Apple II microprocessor was used for storage of
mathematical logic, calibration constants and computation of re-
sults.
DISCUSSION
The indicator parameters monitoring approach to detection of
hazardous waste intrusions into groundwater is theoretically sound
and practical in terms of operational requirements. It is designed
to detect complex chemical compositions of an undefined nature in
a water matrix. The selected parameters (pH, specific conductance,
TOC and TOX) represent well established methodologies, with
on-the-shelf equipment available. The procedural steps are simple
and can be performed by personnel with minimal technical train-
ing. The alternative approach of detailed chemical analysis for
over 300 hazardous chemical species designated under RCRA Reg-
ulations is neither operationally practical, nor economically feas-
ible.
While these considerations lead to the selection of an indicator
parameter approach in monitoring groundwater, the limitations of
the specified techniques cannot be overlooked. The techniques,
as proposed, are suitable only in a limited way in situations where
natural fluctuation in the background chemistry of groundwater is
minimal and statistically insignificant. There will be many instances
where this is not the case, and differential approaches to detec-
tion of toxic intrusions into groundwater must be explored.
At this time, it appears that the differentiating approach to de-
tection of contaminants in groundwater offers the best technical
avenue in situations where natural fluctuations in the chemistry of
groundwater are significant. Such an approach can provide the
means for differentiation between fluctuating natural organic back-
ground of water and organic matter intruding from hazardous
waste sites. Use of multicomponent pattern recognition and the
differentiation theory in conjunction with pyrographic analysis
for organic content of water samples makes such a task possible.
The theoretical foundation and proven instrumental hardware,
mathematical logic for data handling and computer processing
methodology for data reduction exist.' The principal problem with
the use of this approach is that the general public is largely unfamil-
iar with this methodology, and that the multicomponent pattern
recognition and differentiation is conceptually more complex than
conventional analysis for pH, TOC or TOX.
In order to develop practical means for indicator parameter
monitoring in the groundwater, which fluctuates significantly in
its chemical content, a practical demonstration of proposed
method capabilities must be performed in the real-life scenario of
the hazardous waste site environment.
REFERENCES
1. "Groundwater Monitoring Guidance for Owners and Operators of
Interim Status Facilities", USEPA, Washington, D.C. 1982.
2. Birge, E.D., and Juday, C., Ecological Monographs, 4, No. 9, 1930,
63.
3. "Pyrographic Gross Characterization of Waste Contaminants", EPA-
R2-73-227, USEPA, Washington, D.C., 1973.
4. Lysyj, I., "Pyrographic Analysis of Waste Waters", Env. Sci. Tech.,
5,1974,31.
5. Lysyj, I., Newton, P.R., and Taylor, W.J., "Instrumental—Com-
puter System for Analysis of Multicomponent Organic Mixtures",
Analytic Chemistry, 43, 1971, 1277.
448
POST-CLOSURE
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POST-CLOSURE MONITORING RESEARCH NEEDS
FOR HAZARDOUS WASTE DISPOSAL SITES
JOHN D. KOUTSANDREAS
U.S. Environmental Protection Agency
Office of Monitoring Systems and Quality Assurance
Washington, D.C.
PETER J. MAVRAGANIS
WILLIAM A. BAILEY, Ph.D.
SRA Technologies, Inc.
Arlington, Virginia
INTRODUCTION
Monitoring is the most important aspect for compliance assess-
ment of hazardous waste land disposal facilities. A recent work-
shop revealed that monitoring systems should be in place at a facil-
ity prior to the initiation of operations, continue throughout its
operational life and remain on through the post-closure period for
as long as public health and the environment is at risk. In Super-
fund sites subjected to remedial action, this same type of monitor-
ing program is applicable. The importance of monitoring haz-
ardous wastes facilities created a demand to develop improved
monitoring systems capable of delivering accurate quality-assured
data over long periods as cost effectively as possible.
Post-closure monitoring is concerned principally with long term
monitoring for groundwater protection. This requires that a sys-
tems approach toward monitoring be employed consisting of an
adequate mix of monitoring technologies throughout the monitor-
ing period. These technologies must employ measurement methods
designed to provide the quality of data necessary to assure that
the risk of groundwater contamination is minimized. Thus, for
post-closure monitoring to be effective it is essential that sufficient
data be acquired during site characterization to provide the con-
tinuum of data required to determine the status of a site and the
risk to public health and the environment.
With this in mind, the USEPA's Office of Research and Devel-
opment, Office of Monitoring Systems and Quality Assurance has
embarked on a monitoring research task which will provide guide-
lines for post-closure monitoring of hazardous waste facilities. As
part of this task, a report was recently completed which identifies
monitoring research needed to provide the essential data discussed
above. The gaps in current monitoring technology were identified
and research actions designed to fill those gaps were developed.
RESEARCH NEEDS FOR RCRA
LAND DISPOSAL MONITORING
This workshop also revealed the need for long-term monitoring
at hazardous waste disposal facilities. It was established that mon-
itoring systems should be designed and installed prior to the oper-
ational use of the facility.
For sites that have been abandoned and subsequently subjected
to remedial action, many of the same types of monitoring would
pertain to the facility. As a result, these monitoring techniques
will be discussed and, where possible, examples will be given.
Although most of the current research conducted in this area
focuses on in situ groundwater monitoring, there is concern that
the research program should actually be addressing groundwater
protection monitoring. Consequently, this paper also presents
recommendations on research tasks that will help to implement
programs that will lead to early detection of contaminants through
monitoring before these pollutants reach the groundwater. These
tasks are identified primarily in the vadose zone (unsaturated zone)
monitoring, geophysical/geochemical and remote sensing research
areas. As toxic gases emanating from landfill sites may escape to
the ambient air, research into air emissions is also included in this
paper.
Specific research topics and general research areas concerning
monitoring can be grouped into six general areas:
1. Groundwater Monitoring in the Saturated Zone
a. Sampling Procedures
b. Network Design for Groundwater Monitoring
2. Vadose Zone Monitoring
3. Indicator Parameters and Hazardous Constituents
4. Advanced Monitoring Methods
a. Geophysical/Geochemical
b. Remote Sensing
c. Groundwater Tracers
d. Leachate Collection Systems Monitoring
5. Statistical Methods
6. Air Emission Monitoring
Groundwater Monitoring in the Saturated Zone
A number of issues have been identified as saturated zone
groundwater sampling and analysis problems needing additional re-
search. These issues can be grouped into the following general
topics:
1. Groundwater Sampling Procedures
•Well drilling methods
•Well casing and completion methods
•Well flushing sample preparation (e.g., filtering), and quality
assurance
2. Groundwater Monitoring Well Network Design
Sampling Procedures
The need for continuing research into improved methods for
sampling groundwater is based on concerns about sample validity
and the cost-effectiveness of available procedures.
Collection of a groundwater sample involves several steps: drill-
ing and casing the hole; placing the appropriate well screens and
sealing materials; pumping the well to purge it of standing water
and introduced contaminants; collecting, preparing and preserving
the sample; and transporting the sample to the laboratory for
POST-CLOSURE
449
-------
analysis. To ensure that the sample is representative and unadul-
terated, the ability of currently available techniques to collect a
groundwater sample without adding or removing trace contam-
inants should be assessed. Candidate materials should be evaluated
through laboratory tests to determine their suitability for sampling
system components. Based on their suitability, the recommended
components should be evaluated through actual field tests and
guidance materials prepared.
Compliance monitoring is accomplished by direct sampling of
groundwater. This implies that appropriate equipment and tech-
niques are currently available to perform each step of the process.
Although some information is available on these topics, little data
exist on the effects of different types of equipment and construc-
tion materials on trace concentrations in groundwater samples.
For example, PVC pipe is commonly used to case the wells, as well
as (at depths greater than 25 ft) water supply pumps with graphite,
plastic or steel impellers to purge wells and collect samples. It is
known that these materials can alter the concentrations of trace
metals, trace organics and halogenated organics in groundwater
samples, but little quantitative information about the magnitude of
these effects is available. The only currently available alternative
is the use of Teflon or stainless steel well sets for casing and screen-
ing. However, these materials are many times more expensive than
PVC pipe and, at present, there are insufficient data available to
ensure that the materials are adequate for the intended purpose.
Groundwater Monitoring Well Network Design
Implicit in the requirement for groundwater monitoring is the
assurance that the upgradient and downgradient monitoring wells
are placed, constructed and operated to provide a high probability
of detecting leachate plumes escaping through facility liners. Two
basic groundwater hydrology issues affect the ability to specify
compliance monitoring well networks: perched aquifers and con-
tinuous well pumping.
A hydrogeological situation that affects the ability to specify de-
tection and compliance monitoring well networks is the presence
and extent of low permeability lenses of earth materials beneath
disposal facilities. Such lenses can create perched water zones
above the "permanent" uppermost aquifer. These lenses may in-
tercept a contaminant plume before it reaches the permanent
uppermost aquifer. If the presence and extent of such lenses are
not specifically known, and if only the permanent uppermost
aquifer is monitored, an existing contaminant plume may go unde-
tected.
Therefore, the technology to adequately define the presence and
extent of such low permeability lenses should be evaluated. Well
number and locations as well as sampling procedures (e.g., fre-
quency and collection methodology) necessary to ensure ground-
water protection should be addressed.
Continuous pumping of downgradient wells has been suggested
as a means of ensuring plume interception. The Agency recog-
nizes that the use of continuously pumping wells will increase the
radius of influence of the wells and may allow the use of fewer wells
than would be needed for intermittent sampling. However, con-
tinuous pumping may also cause artificial dilution of contami-
nants, thus yielding measurements of artificially low concentra-
tions.
Vadose Zone (Unsaturated) Monitoring
The Agency initially considered requiring that monitoring sys-
tems be installed beneath landfills, surface impoundments and
waste piles in the vadose zone. However, the technical feasibility
and reliability of such systems was not sufficiently proven to be in-
cluded in the regulatory program. The potential of vadose zone
monitoring as an "early warning system" to detect leakage before
the leachate reaches the aquifer is being seriously evaluated. If
feasible, such early detection could allow speedy remedial action
that could significantly reduce the costs of corrective action.
Some literature on vadose zone sampling already exists.1-2
Equipment, including suction-cup lysimeters, geophysical tech-
niques and soil sampling techniques, has the potential for provid-
ing valuable data for detecting and determining the migration of
hazardous wastes in the subsurface. Research is needed to labor-
atory test and field demonstrate the application range of selected
monitoring devices. The monitoring devices for this application
appear to include both direct and indirect monitoring techniques
such as those mentioned above and salinity sensors, tensiometers,
neutron probes and electrical resistivity networks placed under
waste units.
Indicator Parameters and Hazardous Constituents
The current groundwater regulatory program distinguishes be-
tween two groups of parameters: indicator parameters and haz-
ardous constituents. Indicator parameters are measured during the
detection monitoring phase and may include specific conductance,
total organic carbon (TOC) and total organic halogen (TOX),
Hazardous constituents are measured during the compliance mon-
itoring phase. They include all of the 387 constituents identified in
Appendix VIII of 40 CFR Part 261, unless the USEPA Regional
Administrator excludes specific constituents.
Factors that must be considered when specifying the parameters
or constituents to be monitored include:
•Mobility, stability and persistence of waste constituents or their
reaction products in the unsaturated zone beneath the facility
•Detectability of indicator parameters, waste constituents and re-
action products in groundwater
•Concentrations or values and coefficients of variation in pro-
posed monitoring parameters or constituents in the groundwater
background
Research is required to provide answers to such basic questions
as:
•What are the correlations observed at actual sites of ground-
water contamination between the indicator parameters and haz-
ardous constituents of interest?
•What are the seasonal variations expected from natural causes in
groundwater parameters such as specific conductance, total or-
ganic carbon and total organic halogen?
•What classes of hazardous constituents will not be detected by the
indicator parameters?
•What kinds of indicator parameters or other field monitoring
methods can be used to identify these "missed" classes of haz-
ardous constituents?
•For given types of wastes, what are appropriate sets of indicator
parameters and under what conditions are they reliable?
•How redundant is the information obtained from different indi-
cator parameters?
Currently, for the Appendix VIII compounds, there are insuffic-
ient quality-assured laboratory analytical techniques available for
monitoring all of these compounds. Research is needed in the
following areas:
•Development of quality-assured analytical techniques for Appen-
dix VIII compounds
•Determination of whether the number of Appendix VIII com-
pounds should be reduced or expanded based on latest data from
hazardous waste site investigations including Consent Decree and
Superfund.
Advanced Monitoring Methods
Implicit in the requirements for groundwater monitoring at land
disposal facilities are the assumptions that well networks can be de-
signed at a reasonable cost and will ensure detection of leachates
leaking through the liners into groundwater. Monitoring wells are
quite expensive and, without a large number of wells at each facil-
ity, escaped leachates may go undetected. Also implicit in the re-
quirements for groundwater monitoring is the assumption that geo-
logic stratigraphy and the site hydrogeology are well known or can
450
POST-CLOSURE
-------
be readily ascertained at each site. Groundwater piezometric head
gradients and the direction and speed of groundwater flow are es-
pecially important. With the drilling of sufficient holes, this re-
quirement may be achievable. However, advanced methods offer a
means of reducing the costs involved in monitoring and in char-
acterizing the subsurface prior to remedial action and in placement
of the well network.
Geophysical/Geochemical Techniques
Surface Methods—Leak detection systems installed in landfills
and surface impoundments with double-liners allow the operator
to forego detection monitoring of groundwater. The only such leak
detection systems addressed in the regulations involve leachate
collection systems installed in the space between the two liners.
Certainly such systems can be installed and the technology exists to
build them, but the double-liner construction presents an ideal
geometry for electrical sensing methods which, in many cases,
would be more sensitive than leachate collection and would have a
much faster response. Automation of these electrical systems is en-
tirely feasible. To date, the only studies of advanced leak detec-
tion systems have dealt with simple resistivity tests on single-liner
site designs and microseismic detection schemes intended to pick
up audible noise of liquids moving through soil.
One of the most promising such methods appears to be repre-
sented by the four-electrode resistivity system.3 Another method
which appears to have considerable potential in leak detection ap-
plications is the electromagnetic conductivity survey.4'5Surface
geophysical techniques can also be used to look for conductive
leachate plumes which might otherwise go undetected by the mon-
itoring wells.
Another technique with promise for monitoring landfill and sur-
face impoundment liner leakage employs fiber optics. Laser-in-
duced fluorescence spectroscopy covering fiber optic cables has re-
cently become both technologically and economically feasible.
Many hydrocarbons of interest have fluorescence signatures. For
many other substances without fluorescence signatures (for ex-
ample, chloride ions), the reaction of the substance of interest with
a fiber coating or other substrate can produce a unique reaction
product that does fluoresce. Devices capable of detecting non-
fluorescing substances or measuring physical parameters such as
temperature have been dubbed optrodes (to indicate the optical
analog of ion-specific electrodes). Remote Fiber Fluorimetry (RFF)
apparatus and techniques are currently under development. The
feasibility of detecting dissolved organics has been demonstrated;
optrodes for detection and measurement of chlorides, chlorinated
hydrocarbons and other substances are under development. The
measurement of temperature, pH, redox potential, water level and
even groundwater flow rates and directions appears to be feas-
ible. Such RFF methods could provide rapid analysis and could
prove cost-effective since they would require limited manpower.
They would also be a convenient adjunct to leachate collection
systems. Further research is needed to test the suitability of apply-
ing RFF techniques.
Downhole Methods—Downhole geophysical/geochemical meth-
ods can be used to ensure that monitoring wells are completed
(screened) in the right vertical range, as well as to give good in-
dications of the subsurface lithology and considerable information
on the chemical quality of groundwater. These methods can also
yield information about the direction and speed of groundwater
flow, which is essential to the design and operation of ground-
water monitoring networks.
Limited work in the application of surface/geophysical tech-
niques to hazardous waste site monitoring has been done, but no
systematic exploration of their use in monitoring programs is avail-
able. The petroleum exploration field has used a variety of down-
hole logging equipment in large-diameter, uncased holes, but there
is no literature on the use of such methods in the monitoring of haz-
ardous waste sites.
Remote Sensing
The use of remote sensing as a long-term monitoring tool at
hazardous waste landfills has been demonstrated and should be in-
vestigated further. The use of multispectral scanners, spectroradio-
meters, thermal scanners and cameras using special filters and films
can result in the detection of spectral changes in vegetation stressed
by hazardous leachates. Remote sensing with infrared equipment
would also be particularly applicable during the post-closure period
to monitor for leakage due to cap failure. Spectral changes in
stressed vegetation can give a clear indication of the location of the
leak and the direction of the leakage flow. Guidance documents
should be prepared on when and how to use various sensors under
various climatic and geographic conditions.
Groundwater Tracers
Present regulations require the use of synthetic or clay liners
under landfills and surface impoundments. When liner leaks occur,
it is difficult to undertake remedial action unless the locations of a
leak can be determined. It is often difficult to establish that the
contamination detected is coming from the disposal facility and did
not result from some other source, such as an inadvertent spill or
accidental well contamination from sampling equipment. Thus,
a means of identifying both the contaminants resulting from liner
leakage and the specific area of the leak is needed.
One means of finding the leak and resultant contaminants if the
placement of easily identified, soluble, non-degradable non-toxic
tracer compounds above specific sections of liner during liner in-
stallation. A rupture of the liner would release the tracer along with
the contaminants. The presence of the tracer would indicate that
liner leakage has occurred and is the contaminant source. Exam-
ination of the particular tracer compound would thus pinpoint the
area or areas of leakage.
The trivalent rare earth compounds are outstanding candidates
for such tracer applications. They are of low toxicity and can be
detected in extremely low concentrations (ug/1 and lower) in com-
plex chemicalmatrices (such as contaminated groundwater) by us-
ing neutron activation analyses. An initial screening of rare earths
and other potential tracers should be conducted and followed up
by pilot and field testing of selected compounds to evaluate prob-
lems related to transport, recovery and analyses of the tracers.
Leachate Collection System Monitoring
The RCRA Land Disposal Regulations do not currently require
backup monitoring of the leachate collection system. How does
one know that the collection system will survive and operate after
the site is closed? If no leachates can be pumped out of the sys-
tem, there is no way of determining whether leachates are no longer
being produced or whether the collection system has failed.6
Research is required on renovation and long-term maintenance
of leachate collection systems and on backup systems in case of
failure. Innovative approaches to long-term monitoring of the per-
formance of leachate collection systems should be investigated.
Statistical Methods
Statistical methods are an important element of the Land Dis-
posal Regulations because the decision to implement a compliance
monitoring program is based on finding a significant increase in
indicator parameter values or concentrations of primary haz-
ardous constituents (PHCs) over background levels. The process
will specify a sampling program, a statistical comparison procedure
and a level of significance at which the test will be conducted. The
USEPA has proposed some basic statistical procedures which jnay
be replaced with alternative methods. The applicability of existing
statistical procedures for monitoring hazardous waste facilities
needs further study. Currently used statistical procedures assume
that monitoring data are generally normally distributed. However,
this may not be the case, and there is a possibility of obtaining a
POST-CLOSURE
451
-------
wide range of variations depending upon The specific PHCs and a
log-normal distribution.
A larger data base on the temporal and spatial variability of
groundwater quality, particularly that of Appendix VIII constit-
uents, is needed to better understand when observed parameter
concentrations may be attributable to natural variabilities rather
than to landfill leachate.
Key questions relating to statistical methods are:
•What statistical procedures are appropriate for interpreting
groundwater monitoring data and under what conditions?
•What are the potential consequences of not meeting assumptions
of random samples, normal distributions, independent means and
variances and equal variances (homoscedasticity)?
•What transformations of monitoring data should be used and un-
der what conditions?
•What is the power (ability to reject a false hypothesis) of different
statistical tests in groundwater monitoring programs?
•What new developments in statistical methods might be appro-
priate for groundwater monitoring data?
•What are the major sources of variance in groundwater monitor-
ing data (e.g., unexplained error, analytical variability, sampling
variability, true variability in groundwater quality)?
These issues, as they relate to monitoring of hazardous waste
facilities under the regulations, are currently being addressed by the
USEPA. The need in this area is to field test the refined statistical
procedures that are being developed in order to verify their applic-
ability.
Air Emissions Monitoring
The USEPA had considered the possible need for air emissions
monitoring at land disposal facilities but concluded that insuffic-
ient air emissions information was available to justify such a regula-
tory requirement at the present time. Several investigators have re-
cently reported on methods used in monitoring air emissions at
Superfund sites in papers from the Third National Conference on
Management of Uncontrolled Hazardous Waste Sites .7>8>9 Air emis-
sions can be a serious concern at certain classes of land disposal
and land treatment facilities.
The USEPA is currently assessing the problem of toxic air emis-
sions from hazardous waste treatment, storage and disposal facil-
ities. This effort is directed toward providing the documentation
necessary to establish the need for air emissions regulation and
monitoring requirements. Needs in this area include documenting
state-of-the-art techniques for measuring emission rates from land
disposal sites, identifying adsorbent materials suitable for ambient
air monitoring, determining the migration potential of toxic gases
in the unsaturated zone and providing quality assurance for am-
bient air monitoring techniques.
ACKNOWLEDGEMENTS
The efforts of Ms. Kim Smith of SRA Technologies were instru-
mental in the development of the final report. In addition, the
monitoring R&D needs presented are also based on the results of
a peer review of the draft document, which culminated in a work-
ing meeting held in Arlington, Virginia on Feb. 24, 1983. OMSQA
would like to thank the following people for their participation in
and/or contribution to this effort:
Philip Malone, Norman Francingues and James Crabtree
U.S. Army Corps of Engineers, Waterways Experiment Station,
Vicksburg, MS
Stephen Ragone
Office of Hazardous Waste Hydrology, U.S. Geological Survey,
Reston, VA
Richard C. Kibler
HQ U.S. Air Force LEEV, Boiling AFB, Washington, DC
Major Stephen TerMaath
U.S. Air Force Engineering and Services Center, Tyndall Air Force
Base, FL
Eileen Riley-Wiedow
U.S. Army Toxic and Hazardous Materials Agency, Aberdeen, MD
Roy Evans and Leslie McMillion
USEPA, Environmental Monitoring Systems Laboratory, Las
Vegas, NV
Jerry Thornhill
USEPA, R.S. Kerr Environmental Research Laboratory, Ada, OK
William Budde
USEPA, Environmental Monitoring and Support Laboratory,
Cincinnati, OH
Jack McGinnity
USEPA, Office of Air Quality Planning and Standards, Research
Triangle Park, NC
Barret Benson
USEPA, National Enforcement Investigations Center, Denver, CO
Basil Constantelos
USEPA, Waste Management Division, Region V, Chicago, IL
David Mowday
USEPA, Office of Technical and Scientific Assistance, Region
IX, San Francisco, CA
John Warren
USEPA, Statistical Policy Staff, OPRM, Washington, DC
Richard Allan, George Dixon, Mike Flynn, David Freidman,
Seong Hwang, Lawrence Greenfeld, and Burnell Vincent
USEPA, Office of Solid Waste, Washington, DC
Robert Clemens
USEPA, Office of Waste Programs Enforcement, Washington, DC
William Lacy, Robert Holmes and Darwin Wright
USEPA, Office of Research and Development, Office of Monitor-
ing Systems and Quality Assurance, Washington, DC
This project was conducted under EPA Contract No. 68-02-
3778, John D. Koutsandreas, Project Officer.
REFERENCES
1. Wilson, L.G., Monitoring in the Vadose Zone: A Review of Technical
Elements and Methods, USEPA, 600/7-80-134, 1980.
2. Everett, L.G., Hoylman, E.W. and Wilson, L.G., Vadose Zone Mon-
itoring for Hazardous Waste Sites, Final Draft, EPA Contract No.
68-03-3090, Kaman Tempo, Santa Barbara, CA., 1980.
3. Peters, W.R., Shultz, D.W. and Duff, R.M., "Electrical Resistivity
Techniques for Locating Liner Leaks," in Proc. of Third National
Conference on Management of Uncontrolled Hazardous Waste Sites,
Nov. 1982,31-35.
4. White, R.M. and Brandwein, S.S., "Application of Geophysics to
Hazardous Waste Site Investigations," in Proc. of Third National
Conference on Management of Uncontrolled Hazardous Waste Sites,
Nov. 1982,91-93.
5. Evans, R.B., "Currently Available Geophysical Methods for Use in
Hazardous Waste Site Investigations," in Risk Assessment at Haz-
ardous Waste Sites, ACS Symposium #204, F.A. Long and G.E.
Schweitzer, Editors, Washington, D.C., 1982,93-115.
6. Morrison, A., "USEPA's New Land Disposal Rules—A Closer Look",
Civil Engineering, 53, Jan. 1983,440-49.
7. Astle, A.D., Duffee, R.A. and Stankunas, A.R., "Estimating Vapor
and Odor Emission Rates from Hazardous Waste Sites," in Proc.
Third National Conference on Management of Uncontrolled Hazardous
Waste Sites, Nov. 1982, 326-330.
8. Murphy, B.L., "Air Modeling and Monitoring for Site Excavation,"
in Proc. Third National Conference on Management of Uncontrolled
Hazardous Waste Sites, Nov. 1982, 331-333.
9. Schmidt, C.E., Balfour, W.D. and Cox, R.D., "Sampling Tech-
niques for Emissions Measurement at Hazardous Waste Sites," in
Proc. Third National Conference on Management of Uncontrolled
Hazardous Waste Sites, Nov. 1982, 334-339.
452
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FAILURE PREDICTIONS FOR THE POST-CLOSURE
LIABILITY TRUST FUND ANALYSIS
GAYNOR W. DAWSON
C.JOE ENGLISH
PETER GUERRERO
Battelle Pacific Northwest Laboratory
Richland, Washington
INTRODUCTION
With passage of the Comprehensive Environmental Response
Compensation and Liability Act (CERCLA) of 1980, Congress
created two funds to assist in the restoration of areas contaminated
with hazardous wastes. In addition to the better known "Super-
fund" which helps cover the cost of remedial action at abandoned
or uncontrolled hazardous waste sites, Congress mandated the
Post-Closure Liability Trust Fund (PCLTF). The latter fund is
designed to cover the cost of post-closure maintenance, monitoring
and remedial action for sites closed under the Resource Conserva-
tion and Recovery Act (RCRA) regulations. To be eligible, these
sites must have displayed no evidence of contaminant migration
over a five-year post-closure period during which they were
monitored according to the RCRA permit conditions. Upon accep-
tance into the fund coverage by USEPA, the federal government
accepts responsibility for remedial action costs, liability claims and
all monitoring and maintenance costs above those required for
post-closure procedures under the permit.
When the fund was created, Congress chose to finance the
PCLTF by imposing a tax on hazardous wastes. An arbitrary ceil-
ing value of $200 million was placed on the fund. It was mandated
that whenever the fund balance exceeded the ceiling in the previous
year, the tax would be discontinued for that year. Since the fund
can be invested to generate income, it is possible that it will sustain
itself. On the other hand, if demands are high, it is also possible
that the fund will be insufficient to meet the demands placed on it
in any given year. In order to determine the adequacy of the ceiling
value of $200 million, Congress charged USEPA with preparing a
report by Dec. 1983 which would identify required changes in fund-
ing base or the ceiling level to assure fund availability.
USEPA chose to construct that report on the basis of a coupled
economic and geohydrologic model. The latter would predict when
and how various representative facilities will fail while the former
would estimate what the subsequent demands would be on the
fund. The following paper describes the failure prediction module
of the overall model.
GENERAL STRUCTURE
The failure/exposure preduction elements of the module are
designed within the framework illustrated in Figure 1. In essence,
the functional nodes rely on user supplied data, correlation data
held within captive data banks, programmed analytical constructs
for predicting continuous events (e.g., leachate movement) and
Monte Carlo simulations to predict discrete probabilistic events
(e.g., rainfall patterns). The individual algorithms employed, data
sources ana assumptions made to render the module operable are
discussed for each structural component.
MODULE INPUTS
At the initiation of a simulation, the user supplies a base set of
input information. This is supplemented by internally generated
values to create the required suite of data outlined in Table 1. For
inputs supplied by the user, default values have been programmed
into the module and can be utilized whenever the user does not sup-
ply a preferred value. Some inputs are self-explanatory, others are
discussed with respect to their use and the default value, when ap-
propriate.
The type of site is required to define the potential source term.
Specifically, the site must be characterized by:
•Number of layers
•Thickness of each layer (in cm)
•Field capacity of each layer (cm/cm)
•Saturation for each layer (cm/cm)
•Probability that synthetic liners/caps will fail in any given month
•Probability that synthetic liner/cap will be punctured during in-
stallation
The first four characteristics are either supplied by the user or
obtained from an internal data base. To perform the latter option,
the user must identify the site as one of several standard designs
considered by the module. The final two characteristics must be put
in by the user. Default values are 0.25 for synthetic membrane
liners, 0.05 for synthetic membrane covers and 0.00 for asphalt
and concrete liners and covers. These values are based upon limited
data reporting actual landfill failures and should be revised over
time to reflect changes in both the data base and landfill construc-
tion practices as available. An identifier for each layer is assigned to
designate the material type: waste-1, sand-2, clay-3, synthetic (e.g.,
plastic, asphalt, concrete)-4 and soil-5. A separate identifier is used
to denote the presence of a leachate collection system which would
prevent upper layers from becoming saturated.
If all data are not available tor a given site, the design is specified
from a previous module in the overall model on the basis of pro-
bability functions for seven prototypes such as that illustrated in
Figure 2. If this approach is taken, the thickness of each layer can
be specified independently. Clay lined and capped landfills, with or
without leachate collection systems, are the most common site
types selected. Permeability properties for each layer are accounted
for as noted in the narrative on water movement simulation. While
the seven prototype designs are for landfills, land farms and im-
poundments can also be evaluated by inputing the proper design
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453
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Figure 1
Relationship of Components in Failure Prediction Module
dimensions and characteristics at closure. These sites are not
modeled during operation since major modifications in waste
characteristics will occur before these facilities can be closed. The
latitude and longitude are input to specify the location of the site.
This allows data to be withdrawn from the national data base from
the appropriate region of the country thus insuring proper con-
sideration of site-specific features.
USEPA wastes codes must be specified for the wastes expected at
a given site. While the code designation provides no input directly
applicable to subsequent analyses, it does identify a discrete waste
type which offers entry to an internal data base. This can subse-
quently specify toxic constituents of concern and their properties
which will affect transport and fate.
Dates of opening and closure are specified to indicate: (1) when
the face is first opened and, therefore, allowed to collect precipita-
tion, (2) how long the face is open and (3) when the cap is em-
placed. The date when post-closure care is terminated is equated
with the time when leachate collection is terminated and erosion
may proceed unabated. This assumption may be changed by the
user to reflect the fact that leachate collection may cease when the
cap is emplaced. Leachate generation and migration will begin
when the site opens as will the aging process for any synthetic
liners. Waters of infiltration will accumulate at a faster rate while
the site is in operation because of the lack of a low permeability
cap. After closure, the cap will be in place and infiltration will be
reduced. Leachate migration can be substantial during operation.
Hence, it must be tracked from the opening date. If a breach occurs
prior to closure, the site may not qualify for the PCLTF. At a
minimum, some form of repair will be required. All breaches are of
direct interest to the analysis.
The length of run is specified by the user upon activating the
model. This is the period of time following closure that the model
will check for breaches. Simulation will stop at a date equal to the
sum of latest closing date and the length of run.
The probability of liner failure refers to the density function to
be employed in determining when a synthetic membrane liner is
likely to fail through natural degradation. This is separate from the
probability of improper installation or puncturing during site
operation (failure at time zero). It addresses the finite life of a prop-
erly installed membrane due to chemical degradation and natural
Table 1
Standard Inputs Required by the Failure Prediction Module
User Inputs Needed at the Start of a Run:
•Number of sites
•Number of Monte Carlo replications
•Base year (i.e., the time origin for the run [e.g. 1982])
•Starting "random" number seed(s)
Variables that the User Can Rest at the Start of a Run include:
•The probability that a synthetic cover fails at time zero
•The probability that a synthetic liner fails during a given month
•The probability that a synthetic cover fails during a goven month
•The probability that a synthetic liner fails at time zero
•The amount of water which defines a breach when the monitoring is
done inside the site
For Each Site or Facility the User Must Define the Following:
•The site type (If the user picks one of the standard site types, then the
thickness, field capacity, saturation, starting water content, probabili-
ties of synthetic liner failure, number of layers, type of layers [e.g., clay,
sand, etc.] and drainage are obtained from an internal site data base. If
the user does not pick one of these standard types, he must supply his
own values). Field capacity refers to the amount of moisture a medium
will hold before the water begins to leak into the next lower layer. Starting
water content refers to the amount of moisture in the layer to begin with.
•Latitude and longitude
•Number of wastes in the site and an EPA waste code for each waste
•Date opened and closed
•Date when post-closure care ceases
•Date on which study ends for this site
•Type of waste package (drum or sludge)
•Width
•Length
•Distance to the monitoring well (which will be set to zero if monitoring is
to be done at the site boundary)
The Computer Will Supply All Other Variables. The User, However, Can
Overrule the Computer and Supply Alternative Values for the Following:
•Seepage velocity range—velocity range of the aquifer, speed at which the
water is moving
•Distance to the drinking well and/or surface water
•Choose to use the Blaney-Criddle Method over the Thornthwaite
Method to characterize evapotranspiration (if the user does this, he must
also supply all the parameters needed by the Blaney-Criddle Method)
•Runoff coefficients—the fraction of precipitation which runs off the
surface rather than infiltrates into the soil
•Erosion
•Effective porosity range—the range of values defining pore or void space
in the soil; this is the space between soil particles through which soil
moisture can flow
•Range of depth to groundwater range
•Field capacity of the top soil
•Random number seeds for the climate calculations
•Water quality of the uppermost aquifer
•Aquifer thickness
forces. The user may specify a value for this probability or may
choose to rely on the programmed default values.
Internally Held Inputs
In addition to inputs supplied by the user, the module requires
waste and geography specific inputs to conduct the analysis. These
are held in a data base internal to the module itself.
Waste Specific Data
The USEPA waste identifier codes specify the waste type or
source. For the analysis required here, information is needed on the
constituents in those wastes and their properties with respect to
transport and fate in the environment. As a consequence, a data
base has been generated to provide the desired inputs on a call-up
basis.
For each waste code, toxic constituents were identified for the
purposes of subsequent modeling of breaches. For each of the
above constituents, data were compiled on solubility, drinking
454
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LANDFILL DESIGN - TYPE 1
VEGETATED TOP COVER:
DEPTH AT LEAST in". 3-51 SLOPE,
PLANTED TO MINIMIZE EROSION;
FOR SLOPE GREATER THAN St. EROSION
CAN BE NO MORE THAN ] TONS/ACRE-YEAR
2. MIDDLE DRAINAGE LAYER: 12*. OVERLAIN BY .
GRANULAR OR SYNTHETIC FABRIC FILTER. /
SATURATED HYDRAULIC CONDUCTIVITY OF/
LAYER MUST BE AT LEAST UT^cm/sec ' ,
3. SYNTHETIC MEMBRANE: AT LEAST 20 mil' f
«. RECOMPACTED SOIL (CLAY): AT LEAST M"
5. WASTE •
6. DRAINAGE LAYER: SAME SPECIFICATIONS AS
7. LEACHATE DETECTION. COLLECTION, AND REMOVAL
SYSTEM: MUST KEEP LEACHATE DEPTH BELOW
«. SYNTHETIC LINER: AT LEAST 30 mil
Figure 2
Prototype Landfill Design—Type 1
water or priority pollutant criteria levels, detection limits, octanol-
water partition coefficients* (organics) and Kd values!
(inorganics). With respect to toxicity criteria based on car-
cinogenesis, the 10~6 risk level value was used. (The 10~6 risk level
is defined as the concentration at which exposure over a lifetime
would result in one additional case of cancer in 106 people.) The
above physical constants are found in the "Background Document-
Listing of Hazardous Wastes," Nov. 14, 1980, and its reference
material: Dawson, G.S., C.J. English and S.E. Petty. "Physical-
Chemical Properties of Hazardous Waste Constituents," USEPA,
Mar. 5, 1980 (unpublished).
*An octanol-water partition coefficient represents the degree to which a chemicai will distribute itself
between water and octanol when shaken in a mixture of the two. It is used as a measure of a
chemical's affinity for water as opposed to organic fluids.
f 'Kd" is a parameter used to represent the distribution of a chemical between the soil and water in a
given location at equilibrium, i.e.,
Kd = concentration in soil
concentration in water
Average detection limits of 10/tg/l for organics and 20 /ig/1 for
inorganics were obtained from USEPA's "Guidelines Establishing
Test Procedures for the Analysis of Pollutants; Proposed Regula-
tions," (FederalRegister, 69464-69575, Dec. 3, 1979).
In addition, data are entered on the taste and odor threshold, the
total dissolved solids (TDSQ and total organic carbon (TOC) levels
associated with all constituents in a waste to denote when indicator
parameter or organoleptic properties will lead to detection of
leakage in monitoring or potable wells.
The detection of a breach is based on arrival of mobile species at
the point of detection. Detection may constitute discovery of
positive values during monitoring or the impairment of taste and
odor. Therefore, the most important constituent(s) in each waste
will be the "early arrival" contaminant(s), i.e., those constituents
which will first arrive at the monitoring or potable well in detec-
table or toxic concentrations. Recognizing this, (a) representative
chemical(s) were identified for each waste. This was accomplished
by comparison of solubility, detection limit, toxicity criteria and
data on interactions with soil (attenuation).
For consideration of breaches defined by arrival of detectable
levels, the ratio of the solubility (S) and the detection limit (DL)
were derived (S/DL) to indicate how much dilution and attenuation
is necessary for each constituent before leachate will not produce a
detectable level at the monitoring well (it is assumed that all consti-
tuents are leached from the site at their water solubility). Detection
may be by analyses, by taste and odor or by indicator parameter.
Similarly for breaches defined by toxicity considerations, the ratio
of the solutility (S) and toxicity criteria (TC) were derived (S/TC)
to indicate the level of dilution and attentuation necessary to pre-
vent a toxic level from occurring at the monitoring well.
For organic chemicals, the octanol-water partition coefficient (P)
is converted into Koc** using the Karichhoff relation (log Koc =
0.02 + 0.94 log P), which is subsequently employed to calculate a
Kd (soil-water partition coefficient) for organic contaminants
assuming an average soil organic content of 2%. Kds are fed direct-
ly to subsequent modeling algorithms to designate soil attenuation.
The Kd value is specified to indicate soil attenuation for inorganic
constituents. No degradation is accounted for in the transport
model. It is assumed that groundwater is abiotic (i.e., has no active
biological community as a result of filtration of bacteria by the soil
and potential toxicity of leachate) and, therefore, does not subject
contaminants to biodegradation. Photodegradation (decomposi-
tion sponsored by the presence of light, e.g., sunlight) is also
eliminated in groundwater systems. Hydrolysis and chemical oxida-
tion may still occur but since the worst case scenario is of primary
interest, degradation is not considered.
**"Kod" is the distribution coefficient adjusted to the organic carbon content of the soil.
Koc = concentration in soil organic carbon
' concentration in water
For each waste code, the values [Log (S/DL) - Log (Kd)] and
[Log (S/TC) - log (Kd)] were calculated for each constituent. The
constituents yielding the highest values were designated the "early
arrival" contaminants for use in subsequent analyses since they
display the greatest speed in moving through the environment.
Therefore, the one or two constituents with the highest value are
employed to designate the properties of a given waste type. For a
site receiving more than one waste, the values are compared be-
tween wastes and the constituents with the greatest speed employed
for subsequent modeling. In essence, this process distills the model-
ing effort to one of following the "early arrival" chemicals. For in-
dicator parameters, the sum of all constituents' solubilities are
employed.
In addition, wastes are characterized by the number of com-
pound classes present and the total organic content. The compound
classes of constituents in the waste are designated as inorganic,
polar organic and non-polar organic to assist in predictint liner
failure. Synthetic liners are often only effective for a single class of
POST-CLOSURE
455
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chemical. Therefore, synthetic liner life is shortened when more
than one category of chemicals is present. In addition, it has been
reported that clay liners become more permeable when exposed to
organic chemicals.' Therefore, in sites receiving these materials, a
permeability change of two orders of magnitude is applied.
Geography Specific Data
Site specific data on environmental factors are housed in the Na-
tional Data Base. This information file contains pertinent
hydrogeological, geological and meteorological data registered by
longitude and latitude. In this way, when a given site is identified by
its geographic coordinates, the model can access the National Data
Base to determine the appropriate environmental input data.
Specific parameters included in this data base are listed in Table 2.
Table 2
Inputs Included in the National Data Base
Temperature Profile (°C)—monthly mean and standard deviation
Precipitation Profile (cm/mo)—monthly mean and standard deviation
Depth to Groundwater (cm)
Gradient/Porosity (dimensionless)
Hydraulic Conductivity (cm/sec)
Distance to the Drinking Well or Surface Water (cm)
Overburden Field Capacity (cm/cm)
Erosion Loss (cm/mo)
Runoff Coefficient (dimensionless)
Aquifer Water Quality (/ig/1)
Aquifer Thickness
A reference file was added as an additional element in the
geography specific data base. This cross-referened file identifies the
FIPS code (Federal Information Processing System Code) county
and latitude and longitude for the county seat of all counties. This
was necessary to register the erosion loss data which was identified
by FIPS code. The cross reference was retained on the data base to
facilitate addition of new data not registered by latitude and
longitude. It can also be utilized to locate sites when only the coun-
ty or FIPS code is given.
RELATIONSHIPS AND FUNCTIONS
The failure prediction is carried out through a number of rela-
tions and functions as provided by the elements or submodules
described as Weather Simulation, Baseline Analysis, Site Data File
and Water Movement Simulation in Figure 1.
The Weather Simulation is accomplished utilizing a random
draw or Monte Carlo Technique. The ranges of average monthly
temperature and precipitation are used to create a normal distribu-
tion of probable occurrence. A pseudo-random number generator
program is then employed to select a value for each month of the
simulation method. This is done for each of the primary weather
stations in the U.S. The program package utilizes a congruential
method, the entire weather pattern for a simulation can be retained
by putting the starting draw number in memory. (A congruential
method is one in which each successive number is generated by ap-
plying an algorithm to the preceding number. As such, given the
same starting number, an identical series can be generated.) In this
way, the same weather pattern is simulated for all sites in the prox-
imity of any given weather station. The output from the weather
simulation is ultimately employed to calculate monthly precipita-
tion and evapotranspiration losses at a site.
The Baseline Analysis element is an integration point wherein all
pertinent input points are assembled for a given site. In addition to
data supplied by the user and data drawn from the waste and na-
tional data bases, the baseline element provides the starting water
content.
Water content during the operation is determined by assuming
that all infiltration during the operational period enters the system
(i.e., no plants are present to cause evapotranspiration, evapora-
tion is minor). Water is then distributed throughout the layers of
the site in a manner described in the section on water movement
simulation.
The Site Data File is merely a locus wherein the integrated and
calculated data in puts from the Baseline Analysis are stored for a
given site. The site file acts as a tailored data bank for each site
while subsequent analyses are performed.
The Water Movement Simulation submodule is the heart of the
breach scenario development mechanism. Basically, this unit
models the infiltration of precipitation and subsequent migration
of leachate to the point of detection. Because of the random nature
of initiating and contributing events, the simulation relies on
Monte Carlo techniques. This process begins with the submodule
accounting for uncertainties in the seepage velocities and dispersion
values by drawing values from density curves. These values are used
for the rest of a 50-yr (or more) simulation.
Having established the initial conditions at a site by either:
•Reading values in from the data base
•Letting the user define the value
•Making a stochastic decision (described above)
the program simulates water movement over time. It begins this
process with the output from the weather simulation. Having this
information, the program can now account for the water balance in
the surface layer, in each month, in the following way:
•The thickness of the layer is first reduced by an amount indicating
monthly erosion loss if post-closure monitoring is no longer ac-
tive. Erosion loss is based on user specified values when avail-
able. If specific loss data are not employed, generalized data for
each of the seven prototype designs are taken. Lacking either of
these, the state average value is employed from the National Data
Base. In all cases, once post-closure care is terminated, erosion
losses are accounted for by subtraction of a given amount each
month.
•The amount of raw infiltration (precipitation-runoff) is calculated
using a runoff coefficient from the National Data Base.
•The potential evapotranspiration is calculated using either the
Thornthwaite or Blaney-Criddle Method.10 The choice of method
is dependent on the site's geographic location. If the soil cover has
been eroded away, then the evapotranspiration is considered
negligible because of the subsequent lack of vegetation.
•The amount of water in the cover layer is reduced if the potential
evapotranspiration exceeds the raw infiltration.
If there is a net movement of water into the cover layer beyond
its field capacity, the water percolates into the layers below. Like
the cover material, the underlying layers exhibit a certain capacity
to hold water. In other words, once the field capacity of any layer is
reached, it passes any water it receives to the layer below. The rela-
tion is depicted conceptually in Figure 3. The water balance ap-
proach taken there is analogous to viewing each layer as a bucket
with a finite capacity to hold water. The inflows and outflows of
water are calculated at each step. When the bucket is full, it
overflows into the next bucket (the underlying layer). This process
continues until a bucket with a detection site (monitoring well) or
potable use (potable well or surface water) is encountered. At that
time, a breach event is recorded.
This approach implicitly assumes that the rate at which the layers
can accept water is large enough that, within a time step (i.e., a
month), it can accept all the water "offered" to it. This is not
necessarily a good assumption for either the clay liners or synthetic
layers. Thus, extra consideration is made for these layers. First an
estimate for the hydraulic conductivity as a function of water con-
tent is found. The driving force moving the water downward (head
gradient) is taken as the distance between the mid-point of the two
layers. With these values, an estimate of the total amount of water
which the clay can accept in a month's time can be found. If this
amount is less than the "offered" amount, then the smaller
456
POST-CLOSURE
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amount is accepted into the clay layer and the rest is redistributed in
the layer(s) above the clay. If a synthetic layer is intact, it causes the
same redistribution of water except that no water is allowed to pass
through the synthetic layer. If an active leachate collection system is
present, all water in excess of the field capacity for the layer that is
not passed by the next lower layer is assumed to be removed by the
collection system.
At the end of a simulated year's time, the submodule has an
estimate of the volume of water, if any, which has passed through
the site for every month of the simulated eyar. Running sums of the
total amount of leachate and of the total volume of water collected
in the leachate collection system are kept. The latter can be divided
by run time to estimate leachate treatment requirements. If the
total amount of water is less than a critical value (defined below),
then the calculation goes on to the next year with no calculation
made for travel time to the monitoring well. This is because it is
assumed that the leachate contaminant is held in the intervening
layers between the waste layer and the water table. Until these
layers are saturated with contaminants, no significant movement of
waste into the saturated zone will occur. However, if this critical
value has been exceeded, the waste enters the groundwater system
and dilution effects and travel time to both the monitoring well and
the point of potable use are calculated.
The hydrologic transport model is composed of:
•Landfill Leachate Source Model
(1) The landfill site is assumed to be a two-dimensional leachate
source to the unsaturated soil column beneath the site; ap-
proximate dimensions of the site are obtained from the input
site type.
(2) The leachate discharge (concentration and flux) is assumed to
be uniformly distributed over the site at any instant in time;
however, the discharge varies with time according to the mois-
ture infiltration of the site. Attenuation due to retention on
soils in the unsaturated zone is considered at this point.
•Saturated Zone Transport Model
(1) The leachate plume from the unsaturated zone acts as a two-
dimensional horizontal area source on the water table sur-
face to the saturzed zone; it is assumed the water flux from the
unsaturated zone is insignificant compared to the water flux
in the saturated zone. Thus, only contaminant particles are
released to the saturated zone.
(2) The leachate plume moves through the saturated zone ac-
cording to a constant value seepage velocity and dispersion co-
efficient influenced by geochemical retardation of flow and
the dispersion model's attenuation in the system.
(3) The transport equation is given by
3C ,VX,3C
=
Failure of synthetic liners and covers is determined by Monte
Carlo simulation using a probability distribution curve which varies
over time. In other words, the probability of rupture increases with
the age of the liners. These are: (1) failure due to improper installa-
tion, and (2) failure due to "aging." Failure due to improper in-
stallation will be calculated using the user inputed probability of
improper installation. Failure will then occur at randomly selected
sites (based on this probability) beginning at the opening date for
liners or the closing date for covers. Failure due to aging is com-
plicated by the lack of any data with which to calculate expected
lifetimes. Current USEPA publications describing the behavior and
performance of synthetic liners do not contain sufficient data to ac-
curately predict liner life.4'5'7 An average lifetime of 25 years for
synthetic liners and 50 years for synthetic covers is assumed by the
module unless overriden by user supplied values. This is based on
expected values for pond liner life reported by Lee6 and on the
20-25 year guarantees that many synthetic manufacturers offer for
their products. Liners are expected to age faster than covers
because of interactions with wastes. It has been observed that waste
incompatibility will lead to increased aging of liners. To account
for this, waste constituents are classified as polar organics, non-
polar organics, or acids, caustics and salts. If more than one of
these waste types is present at a site, it is assumed that the liner will
age twice as fast as those exposed to a single constituent type. If
erosion has removed soil over a cover, it is assumed that the cover
will then age at double the normal rate.
A potential failure mode for clay liners is intrusion by plants and
animals. Work is presently being conducted by Battelle Pacific
Northwest Laboratories concerning plant and animal intrustion in-
to waste burial grounds. Preliminary results were reviewed as well
as results of Hakoson and Gladney.3 It was concluded that, while
plant root intrusion to the depths of the waste cover was possible,
the effect on permeability would probably be small. The main con-
cern with plant intrusion appears to be with uptake of wastes rather
than increased permeability. Therefore, it was decided to ignore
plant intrusion. Preliminary work regarding animal intrusion
shows that this may have a significant effect if the cover is shallow
enough to be in the burrowing zone of animals. Based on
preliminary results, it is assumed that animal intrusion will affect
10% of the site area. Using data presented by Moore and Ali8 and
assuming that the effects of animal intrusions are similar to crack-
ing, the chance of cover failure will be increased by a factor of two
following animal intrusion.
Research being performed at Texas A&M University has shown
that organic leachates may have a significant effect on the
permeability of clay liners. Based on results presented by Ander-
son, Brown and Green,1 the model increases the permeability of
clay liners by two orders of magnitude if organic wastes are present
in leachate.
where C - C)x,y,z,t) - leachate concentration at position
(x,y,z) at time t
Vx = seepage velocity of water (x-direction)
Dx = dispersion coefficient of water (x-direction)
R = geochemical retardation coefficient of the leachate
This is expressed in a simple three-dimensional hydrologic
transport model that monitors four fronts: (1) change in
background indicator parameter (TDS for inorganics, TOC for
organics) concentrations, (2) the detectable concentration of the
first arrival detectable constituent, (3) the toxic concentration of
the first arrival toxic constituent and (4) the taste and odor concen-
tration of the first arrival constituent. Initial concentrations are
assumed to be at the constituent's solubility level. Dilution and at-
tenuation are accounted for during movement through the soil col-
umn and the aquifer. The initial point of detection is assumed to be
the monitoring well which is located at the downflow perimeter of
the site.
EVAPOTRANSPIRATI ON
PRECIPITATION
—- RUNOFF
| INFLOW 1 • PRECIPITATION - EVAPOTRANSPIRATION - RUNOFF
| INFLOW 2 =
INFLOW 1
FIELD CAPACITY 1
Figure 3
Conceptual Model of Water Balance Calculation
OUTPUT
The output from each simulation is the probable timing and type
of breach for a given site. Replicate runs are made for each site to
generate a probability value for each type of event for each site.
Seven breaches are included:
Breach 1—Indicator parameters arrive at monitoring well
POST-CLOSURE
457
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1
X
X
X
X
X
X
X
2
X
X
X
X
X
X
X
3
X
X
X
X
X
X
X
4
X
X
X
X
X
X
X
5
X
X
X
X
X
X
X
6
X
X
X
X
X
X
X
7
X
X
X
X
X
X
X
Breach 2—Detection levels for specific contaminants arrive at
monitoring well
Breach 3—Toxic levels for specific contaminants arrive at moni-
toring well
Breach 4—Taste and odor threshold arrives at potable well/
surface water
Breach 5—Detection levels for specific contaminants arrive at
potable well/surface water
Breach 6—Toxic levels for specific contaminants arrive at pot-
able well/surface water
Breach 7—Infiltration backs up and overflows
Site Type
Event
Type
1
2
3
4
5
6
7
Figure 4
Example Breach Probability Table
This information creates a breach probability table, Figure 4,
which is passed on to subsequent modules to determine the con-
comitant financial demands that would be put on the PCLFT.
DISCUSSION
At this time, the model does not account for acute disruptive
events such as earthquakes and extreme storms. Review of causes
of hazardous waste mismanagement damage cases showed that
these are probably very minor causes of discharges from hazardous
waste facilities.2
No special provisions have been made for entry of surface im-
poundments or land treatment facilities in the model. It is assumed
that, when closed, these facilities will be treated as landfills if
hazardous residuals remain. If residuals do not remain, no signifi-
cant breach scenarios are evident. Hence, the landfill model will
suffice as long as the user provides information on the site design,
the moisture content at closing and the nature of the waste.
No special provisions have been made for sites receiving correc-
tive actions. It is assumed that once corrective actions are specified,
the site can be reentered in the system. As currently envisioned, cor-
rective action will consist of two elements: cap/liner repair and
withdrawal of contaminated groundwater (counterpumping).
When cap/liner repair is undertaken, the site should be reentered
in the simulation as a new site with a design that reflects the repair
work. Functionally, the user must specify the new design. The
model would then reenter the site and complete the simulation. The
default value is to return to the original design for the site.
Withdrawal wells require slightly different treatment. The model
is too simple to accommodate well fields to withdraw contaminated
water for treatment. However, the effects of withdrawal would not
be all that dissimilar to activation of a leachate control system, i.e.,
termination of all uncontrolled contaminated flows through the
liner during the period of pumping. The user must specify how long
pumping will be performed. The default value is set as a period
equivalent to the time it took for the breach to be discovered in the
first place. This is somewhat analagous to the new regulations set-
ting the compliance period equal to the period of operation for a
given site. However, it is still a source of inaccuracy. There is no
hysteresis effect in such systems. Desorption may well take much
longer than the original adsorption onto soils depending on pump-
ing rates and the contaminates involved. A second area of concern
is the residual contamination in the unsaturated zone. Flushing the
aquifer does not impact this zone. Hence, a source of concentration
would remain below the liners which would effectively accelerate
movement of subsequent breaches compared to how the model
would simulate the post-remedial action period. The effect is prob-
ably small, but it does constitute an inaccuracy.
The model is currently being exercised to provide quantitative
output on probable failure modes and consequences for RCRA
sites in the future. This will have implications for future landfill
regulatory programs as well as the adequacy of the PCLTF.
REFERENCES
1. Anderson, D., Brown, K.W. and Green, J., "Effect of Organic Fluids
on the Permeability of Clay Soil Liners," Proc. of the Eighth Annual
Symposium on Land Disposal of Hazardous Wastes, 1982.
2. Fred C. Hart Associates. Assessment of Hazardous Waste Misman-
agement Damage Case Histories, Draft, Prepared for USEPA Under
Contract 68-01-6474, 1981.
3. Hakonson, T.E. and Gladney, E.S., Biological Intrusion of Low
Level-Waste Trench Covers, LA-UR-81-2972, Los Alamos National
Laboratory, New Mexico, 1981.
4. Haxo, H.E., "Effects of Liner Materials of Long-Term Exposure in
Waste Environments," Proc. of the Eighth Annual Research Sym-
posium of Land Disposal: Hazardous Waste, EPA-600/9-82-002,
EPA, Cincinnati, Ohio, 1982, 191-211.
5. Haxo, H.E., "Durability of Liner Materials for Hazardous Waste
Disposal Facilities," Proc. of the Seventh Annual Research Sympos-
ium on Land Disposal: Hazardous Waste, EPA-600/9-81-0026, EPA,
Cincinnati, Ohio, 1982, 140-156.
6. Lee, J., "Selecting Membrane Pond Liners," Pollut. Engi., 6, (1),
1974, 33-40.
7. Matrecon, Inc., Lining of Waste Impoundment and Disposal Facili-
ties, SW-870, USEPA, Washington, D.C. 1980.
8. Moore, C.A. and Ali, E.M., "Permeability of Cracked Clay Liners,"
Proc. of the Eighth Annual Symposium on Land Disposal of Haz-
ardous Wastes, 1982.
9. Neely, W.B., Chemicals in the Environment, Marcel Dekker, New
York, 1980.
10. Thornthwaite, C.W. and Mather, J.R., "Instructions and Tables for
Computing Potential Evapotranspiration and the Water Balance,"
Publications in Climatology. Laboratory of Climatology, Drexel In-
stitute of Technology, 3, 1957, 185-311.
458
POST-CLOSURE
-------
SUPERFUND AND RCRA CLOSURE/POST-CLOSURE:
AN ILLINOIS PERSPECTIVE
ROBERT G. KUYKENDALL
Land Pollution Control Division
Illinois Environmental Protection Agency
INTRODUCTION
At the present time, state regulatory agencies have gained ex-
perience in the area of facility closure and post closure. Addi-
tionally, extensive activity has occurred in the cleanup of uncon-
trolled hazardous waste sites under both State and Superfund aus-
pices. There are opportunities and problems in both areas.
Illinois' experience thus far has shown that technical and legal
problems quickly come to the forefront. Some facilities which had
interim status under RCRA have ceased their hazardous waste
operations but may continue to have hazardous wastes on-site
needing cleanup. Other facilities have gone bankrupt or have been
abandoned without having financial instruments accessible to the
State Agency. An operating facility with an inactive area (no in-
terim status) is listed as a Superfund site and wishes to close out
the inactive area. Sanitary landfills did and continue to receive
quantities of hazardous wastes, although somewhat reduced by the
small generator requirements. Each of these presents a different
set of circumstances that must be dealt with from technical, legal
and public confidence perspectives.
The closure/post-closure and financial requirements under
RCRA are powerful tools in the prevention of future uncontrolled
hazardous waste sites. An additional operative incentive is a com-
pany's potential liability under CERCLA.
The closure/post-closure requirements are found in 40 CFR
Part 264-265 Subpart G. The purpose of these regulations is "...to
ensure that all hazardous waste facilities are closed in a manner
that: (1) minimizes the need for post-closure maintenance, and
(2) controls, minimizes, or eliminates, to the extent necessary to
protect human health and the environment, post-closure escape of
waste, leachate contaminated rainfall, or waste decomposition pro-
ducts to ground or surface waters, and the atmosphere." The cur-
rent post-closure care period (maintenance and monitoring disposal
sites) is 30 years. In some instances this may be adequate and in
others totally inadequate.
Access to viable financial instruments in conjunction with proper
closure and post-closure care should prevent the development of
many future Superfund sites such as presently exist.
CURRENT STATUS
The current national assessment by USEPA that most compa-
nies do not have approved closure/post-closure plans or valid and
adequate financial instruments in place is correct. This situation
must be changed if future Superfund sites are to be prevented
and the public's trust in the regulatory process restored. Aggres-
sive enforcement by USEPA and states should mitigate this level
of non-compliance in FY 84.
Starting with the RCRA Part A notification process in Nov.
1980 and continuing to the present time with Part B permit call-
in, many firms have dropped out of the RCRA regulatory scheme.
Many facilities filed protective notifications or misunderstood the
intent of RCRA Sec. 3010. More recently, companies have decided
to cease their hazardous waste management activities and have
chosen not to pursue a Part B permit application. The dropout rate
is approximately 40% of the Part B permits called in by USEPA.
What has happened to the hazardous wastes that were stored,
treated or disposed at these facilities since Nov. 1980? In many
instances no financial instruments, closure or post-closure docu-
ments have been submitted. Such facilities are prime targets for in-
vestigation and enforcement.
Two Illinois hazardous waste land disposal facilities ceased re-
ceipt of hazardous wastes on or before Jan. 26, 1983. In one in-
stance, groundwater contamination is present and will require
proper closure and post-closure care and monitoring or, if the
situation worsens, possible exhumation given the contaminants and
local geological characteristics. The other land disposal site has
ceased receipt of hazardous waste but not non-hazardous wastes.
This site will supposedly be in a state of suspended animation for a
few years until market conditions improve. The State has inade-
quate financial instruments on file, and further action is being
taken to ensure compliance with the closure/post-closure require-
ments. Litigation may be necessary, but that is less costly to all
parties than use of Superfund.
ABANDONED SITE
A more vivid example which illustrates several issues is a case in-
volving a hazardous waste treatment company near Chicago which
went bankrupt and abandoned its site last fall. Approximately
100,000 gal of water and oil based hazardous and non-hazardous
wastes were left behind in tanks, drums and tank trucks. Neither
closure/post-closure plans nor financial instruments were on file
with the State which could have provided funds for the abatement
of the situation. Literally, the state was responsible for a vandal-
ized abandoned problem site in a residential area. Subsequent
cleanup action by USEPA and Illinois required the expenditure of
more than $60,000 from Superfund and the State Hazardous Waste
Fund.
OPERATING SITE
Illinois finds itself in the midst of a complex situation in which
an operating chemical company has interim status for the manufac-
turing area but has an inactive series of lagoons which it is closing
out. This inactive area is on the National Priorities List and
POST-CLOSURE
459
-------
groundwater problems exist. Financial instruments are in place.
However, the dilemma is whether a RCRA authorized action
should be required for an inactive and unpermitted sub-unit for
closure or a consent agreement should be used as the appropriate
instrument.
Since the proposed close out of the inactive lagoons is primar-
ily an action to address the CERCLA listing, the consent agree-
ment may be preferable. Questions arise as to the appropriate
cleanup level for groundwater contaminants and the length of the
post-closure period. The implementation of the consent agree-
ment does not, on the surface, provide a means of getting the facil-
ity off the NPL because no "cleanup" has been completed. An
additional complicating matter is that two deep injection wells are
operated on the facility and will need an Underground Injec-
tion Control (UIC) permit under the Safe Drinking Water Act.
The wells have been used to dewater several of the lagoons prior to
their stabilization. Does the consent agreement need to account for
this prior action?
ILLINOIS COMPLIANCE STATUS
At the present time, 32 closure/post-closures have been sub-
mitted to IEPA for approval. Fifteen have been approved; two
were rejected; and five need additional information. Four plans
have been withdrawn for further work at the Agency's suggestion,
and six are under review. Twenty-eight of the plans received were
from generators with on-site hazardous waste management activ-
ities.
In the area of financial assurance, approximately 380 facilities
are required to file with IEPA. Three hundred twenty-nine facil-
ities have filed with the State. This was only after 200 enforce-
ment letters were sent to the Companies' Presidents or Chairmen
of the Board. Only 30% of the filings are adequate at this time.
Forty-three companies have filed on liability insurance but have
filed no documents to guarantee closure costs. Many companies do
not appear to be updating their instruments yearly. Nearly 40% of
the filings so far are generators storing on-site for more than 90
days. Aggressive action will continue in this area to bring about
compliance by all subject facilities.
CONCLUSION
Although most of lEPA's attention is focused on Superfund and
hazardous waste site issues, the author believes that the area of
solid waste landfills (Subtitle D) should not be overlooked. As the
reader is aware, many Superfund and ERRIS sites are abandoned
sanitary landfills where hazardous wastes were historically dis-
posed or are presently operating sites where small generator ex-
emption level wastes are being disposed. Illinois is addressing this
issue by having the small generator cut-off level at 100 kg/mo.
and with the passage of legislation requiring closure and post-clos-
ure liability coverage for all Illinois sanitary landfills. This may not
be the final answer but it is a step in the right direction.
Both the USEPA and States must pay greater attention to com-
pliance with RCRA closure/post-closure and financial assurance
requirements in order to prevent future Superfund sites from devel-
oping and requiring expenditure of public funds. Regulatory agen-
cies are still on a "learning curve" in the implementation of
RCRA, and many activities still require trial and error approaches.
460
POST-CLOSURE
-------
1983 EXHIBITORS
AGES Corporation 1604
1151 S. Trooper Road
Norristown 215-666-7404
PA 19403
Full service engineering firm with a
range of technical disciplines including
environmental engineering, ground and
surface water hydrology, soils
engineering, geology, and laboratory
facilities.
Aerial Data Reduction 1701
p. 0. Box 557
Pennsauken, 609-663-7200
NJ 08110
Aerial Data Reduction, Inc., is a
privately owned photogrammetric service
firm organized in April, 1970, to offer
professional services in the field of
aerial photography, photo interpretation,
and stereo-photogrammetric mapping for
consulting engineers, and surveyors,
planners, government, and industry as
well as other related disciplines having
need for precision photogrammetric
services. ADR also has branch offices in
Hevron, CT., Richmond, VA. , and E.
Providence, HI.
Analect Instruments
1231 Hart Street
Otica, NY 13502
#1203
315-797-4449
Analect1 s EVM-60 refractively scanning
FTIR gas monitoring system provides
rapid, real-time analysis for a maximum
of ten gases from twenty locations.
Alarm capabilities and time-weighted
average computation ensure immediate and
long term site safety for personnel. A
ruggedized optical bench allows
installation in mobile laboratories for
on-site analysis of liquids, gels, and
gas phase samples.
Analytical Instrument 1203
Development
Route 41 & Newark Road 215-268-3181
Avondale, PA 19311
Analytical Instrument Development
manufactures portable instrumentation for
the determination of trace organic
materials in the environment. The Model
511 portable gas chromatograph with
electron capture detection for PCB's in
soil will be on exhibit. In addition
AID'S new Model 590 GC/OVM for total
organic vapors (OVM) or specific
materials (GO in air will be shown.
Other AID instruments for on-site organic
measurements at waste sites will also be
displayed.
At-Sea Incineration 1612 & 614
1930 North Fleet Street
Elizabeth 201-354-9100
NJ 07201
At-Sea Incineration Inc., offers
America's first fully integrated ocean
incineration system for destroying
hazardous wastes. The American-built ASI
incinerator ships meet the highest
standards of safety and efficiency.
Orders are now being accepted for ASI's
comprehensive collection, land transport,
marine transfer and waste destruction
service. At-Sea Incineration, Inc. AN
AMERICAN SOLUTION TO ONE OF AMERICA'S
TOUGHEST PROBLEMS.
Biospherics Incorporated
4928 Wyaconda Road
Rockville, MD 20852
1710
301-770-7700
#311 & 313
CECOS International, Inc.
2321 Kenmore Avenue
Buffalo, NY 14207 716-873-4200
Hazardous waste treatment and disposal of
hazardous, toxic and industrial wastes.
CH2M HILL, Inc. 1416
1941 Roland Clark Place
Reston, VA 22091 703-620-5200
Founded in 1946, CH2M HILL is one of the
largest engineering consulting firms in
the United States with a staff of over
2,000 men and women. We provide
comprehensive study, design and
construction management services for
technological systems that include water,
waste mangement, agriculture, energy,
industry, transportation, and civil
engineering. Our name is an abbreviation
for the firm of Cornell, Rowland, Hayes
and Merryfield, which merged with Clair
A. Hill s Associates to form CH2M HILL.
California Analytical #906
Laboratories, Inc.
5895 Power Inn Road 916-381-5105
Sacramento, CA 95824
CAL Labs' staff (4 PhD and 23 BS/MS level
chemists) and equipment (6 GC/MS, 15 GC,
2 AA, 1 ICP) occupy 16,000 ft
laboratory in Sacramento, CA. CAL Labs
performs analyses of hazardous wastes for
federal and state regulatory agencies as
well as for private and industrial
clients. CAL Labs now operates a
Finnigan 8222 high resolution GC/MS
system, particulary useful for TCDD
measurements.
Case International Company 1504
P. 0. Box 40
Roselle, IL 60172 312-625-1250
Case International Company is a specialty
geotechnical contractor. Operating
nationwide, Case specializes in the
installation of slurry cut off walls for
ground water control and containment.
Case has installed several large slurry
cut off walls in hazardous waste
environments, including the first
"Superfund Slurry Wall" in Nashua, New
Hampshire. Stop by the booth and pick up
a complimentary copy of the Case Slurry
Wall Technical Information Review, a
thirty-seven page booklet.
Clement Associates, Inc. 1805
1515 Wilson Boulevard
Arlington, VA 22209 703-276-7700
Clement Associates, Inc., is a scientific
and engineering consulting firm assisting
clients in solving environmental
problems. Clement does work in and
performs environmental audits, risk
assessments and risk management,
litigation support, permit applications
development, toxicology and pathological
research.
Controls for Environmental 1900
Pollution, Inc.
P. 0. Box 5351 505-982-9841
Santa Fe, NM 87502
Controls for Environmental Pollution,
Inc. (CEP) is a national environmental
consulting and analytical firm. In
addition to offering a complete
environmental consulting service, the
company maintains a nationally certified
state-of-the-art laboratory. CEP
specializes in hazardous waste management
programs, radiochemistry, environmental
monitoring programs and AQUATRACE, an
advanced tracer technology.
Crosby & Overton, Inc. 1308
1610 W. 17th Street
Long Beach, CA 90813 213-432-5445
Crosby & Overston, Inc., is a heavy duty
industrial marine and environmental
cleanup contractor. Since 1950, Crosby &
Overton has provided superior emergency
response and planned remedial cleanup
activities involving oil and hazardous
chemical substances in all environmental
media. A full range of services have
been provided to all levels of
governmental agencies and all types of
industry. Branch locations are in
California, Oregon and Washington.
Additional field operations are conducted
in eight other western states.
Crown Zellerbach
Geotextile Fabrics
One Bush St., Rm. 1303
San Francisco, CA 94104
#800
415-951-5060
D'Appolonia Waste #620 S 621
Management Services
10 Duff Road 412-243-3200
Pittsburgh, PA 15235
D'Appolonia will be exhibiting its
engineering, scientific and construction
services. These services cover a wide
range of activities including: siting
studies, hydrogeologic investigations and
contaminant transport studies, design and
construction of waste management
facilities and cleanup of formerly
utilized hazardous waste sites.
Dames & Moore
6 Commerce Drive
Cranford, NJ 07016
*713
201-272-8300
EXHIBITOR LIST 461
-------
Delaware Container Co., 11211
Inc.
M. llth Ave. & Valley Rd. 215-383-6600
Coatesville, PA 19320
Delaware Container Company, Inc., is
basically a transfer, treatment, and
disposal company for hazadous wste.
Delaware Container provides and maintains
its own transportation program and
on-site laboratory. It completes on-site
solidification and stabiliization
procedures. The company also offers
reuse, recycling, and recovery programs
as well as emergency response and
remedial action designs. Delaware
Container is a turn-key operation which
supplies a full line of services from
initial sampling to final disposal.
E. c. Jordan Company 1400
P. O. Box 7050
Portland, ME 04112 207-775-5401
Solid and hazardous waste management
servics provided to industry and
government agencies include geophysical
and geohydrological investigations,
record searches, chemical
characterization, contamination risk
assessment, identification and evaluation
of remedial action alternatives and
implementation plans at hazardous waste
sites. Hazardous waste TSD facilities
are developed from initial planning
stages, through site selection and
investigation, design permit application
and construction management.
E. I. du Pont de Nemours 1709
Tech Lab (D), Chambers Hks
Deepwater, NJ 08023 609-299-8098
Wastewater treatment service.
EAL Corporation 1708
2030 Wright Avenue
Richmond, CA 94804 415-235-2633
EAL Corporation, formerly LFE
Environmental, provides consulting and
analytical services in the technical
fields of environmental science,
occupational health and safety, and
nuclear science. EAL's exhibit shows how
industry and government agencies, as well
as the consulting engineering profession
can utilize EAL's services to suppport
their hazardous waste programs.
EHPAK, Inc. 1714
2000 West Loop South
Suite 1800 713-623-0000
Houston, TX 77027
EMPAK, Inc., offers deep well injection,
waste water treatment, and remedial
action on-site cleanup to disposal
customers, as well as, complete rail car
cleaning services. EMPAK Disposal and
Cleaning facilities are located on the
Houston ship channel in Deer Park, Texas,
readily accessible by truck, rail, and
marine vessels. EMPAK1s Field Service
office is located in Pennsauken, NJ
609-665-6886.
ENRAC Division 11207
Chemical Haste Management
3003 Butterfield Road 312-654-8800
Oak Brook, IL 60521
The ENRAC Division of Chemical Waste
Management, Inc., serves waste generators
and regulatory agencies in the cleanup of
hazardous waste sites. ENRAC's network
of analytical laboratories,
transportation vehicles,
treatment/disposal facilities combined
with past experience support its
capability to handle situations from
emergency spills to complex, large scale
remedial action.
The Earth Technology »410
Corporation
3777 Long Beach Blvd. 213-595-6611
Long Beach, CA 90807
The Earth Technology Corporation provides
hydrogeology, geology, geotechnical
engineering, geochemical, geophysics,
modeling (hydrologic, geochemical) and
environmental consulting services that
focus on defining and mitigating sources
of existing or potential ground-water
contamination from hazardous materials.
The firm offers unique in-situ subsurface
profiling, sampling (gas, liquid, soil)
and monitoring capabilities using the
Electronic Cone Penetrometer (CPT).
Ecological Analysts, Inc. 1902
15 Loveton Circle
Sparks, MD 21152 301-771-4950
Ecological Analysts, Inc. (EA) is an
independent, nationwide,
multidisciplinary environmental
consulting firm of 200 professionals.
Major hazardous waste program areas at EA
include analytical chemistry engineering,
hydrology and geological sciences, and
environmental health sciences. Our GC/MS
lab and corporate QA/QC program provide
reliable, high-quality data to EA staff
who are designing landfills, engineering
solutions to effluent and process waste
problems, testing and analyzing
groundwater quality, and assessing the
health impacts of hazardous and toxic
wastes.
Ecology & Environment, 1811 & 910
Inc.
P. 0. Box D 716-632-4491
Buffalo, NY 14225
Ecology and Environment provides
consulting and analytical services for
all phases of emergency spill response
and cleanup. Similar services are
provided for waste site evaluation and
remedial action. Risk analyses on public
and employee health and the environment
are offered in conjunction with these
services.
Engineering-Science 1705 & 707
57 Executive Park South
Suite 590 404-325-0770
Atlanta, GA 30329
Engineering-Science is an international
environmental engineering firm offering
full services in hazardous solid waste
management, remedial design and
implementation, air pollution services,
wastewater treatment, hydrological
studies, and laboratory analyses.
Through offices in major cities.
Engineering Science provides services to
clients in the government, military and
private sectors.
Environmental Science and 1315 & 316
Engineering, Inc.
Box ESE 904-332-3318
Gainesville, PL 32602
ESE, a full service multidisciplinary
environmental engineering firm, has
performed work at more than 120 hazardous
waste sites including 15 CERCLA NCP
sites. Capabilities include remedial
investigations, feasibility studies,
QA/QC plans, safety and health planning
and monitoring, community relations,
analytical services, and expert witness
testimony.
Environmental Testing 11205
and Certification Corp.
284 Raritan Center Pkwy. 201-225-6711
Edison, NJ 08837
Environmental Testing and Certification
Corporation (ETC) tests wastes and
groundwater; helps maintain required
shipment, treatment and disposal records)
and prepares monitoring reports that are
required by laws affecting both solid and
hazardous wastes. ETC tailors its
services to specific needs. For example,
Student's t-Test, pollutants trends,
waste shipment histories by generator,
transporter and by treatment or disposal
site and method.
GAI Consultants, Inc. 1602
570 Beatty Road
Monroeville, PA 15146 412-856-6400
GAI Consultants, Inc., provides
engineering consulting services in the
areas of identification, control, and
remedial activities for industrial and
hazardous waste sites. Over 120
engineers, geologists, and environmental'
specialists are on staff to serve
generators, transporters, disposers and
regulatory agencies.
GCA/Technology Division
213 Burlington Road
Bedford, MA 01730
1809
617-275-5444
GCA/Technology Division, with a staff of
250, offers a wide range of hazardous
materials services including field
investigation, laboratory analysis and
engineering evaluation and design.
Engineering experience Includes
hydrogeological evaluations, RCRA Part B
permit assistance, evaluation of
hazardous waste control and disposal
technologies. All services are backed by
a comprehensive quality control system.
GEO-CON, Inc. 1716
P. 0. Box 17380
Pittsburgh, PA 15235 412-244-8200
Specializing in geotechnical
construction, GEO-CON, Inc., exhibits the
Slurry Cutoff Wall technique for
underground pollution control as well as
grouting and related work.
Geo-Physi-Con, Inc. 1908
12860 West Cedar Drive
Suite 201 303-987-9307
Lakewood, CO 80228
Geo-Physi-Con, Inc., provides the full
range of engineering geophysical service!
and also undertakes research and
development projects. Our services
include electrical and electromagnetic
surveys, gravity, seismic refraction,
magnetics, and ground penetrating radar
for hazardous waste site investigation
and monitoring.
Geonics Limited »615
1745 Meyerside Drive, 18
Mississauga, Ontario 416-676-9580
Canada L5T 1C5
Geophysical electromagnetic meters.
462
EXHIBITOR LIST
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Colder Associates 1703
5125 Peachtree Road
Atlanta, GA 30341 404-458-9686
Golder Associates, an international
consulting engineering firm, has been
responsible for the geotechnical,
geohydrochemical and hydrogeological
aspects of many new and existing waste
disposal facilities including siting,
design, permit assistance, and
construction inspection. The present
worldwide staff exceeds 400 members
including approxmately 300 professionals,
located in the United States, the United
Kingdom, Canada, the Caribbean, and
Australia.
Greenhorne s O'Mara, Inc. |617
9001 Edmonston Road
Greenbelt, MD 20770 301-982-2800
Greenhorne & O'Mara, Inc., is a
nationally recognized consulting firm of
engineers, scientists, photogrammetrists,
and other professionals providing
hazardous waste management services. Our
experience includes treatability studies
design reports, design and construction
review, risk analysis, process
instrumentation control and design, life
cycle cost studies, facilities start-up
and performance evaluations, and remote
sensing capabilities. Greenhorne &
O'Mara provides hazardous waste
management consulting services for
numerous governmental, industrial and
private clients.
Groundwater 1622
Decontamination Systems
12 Industrial Park 201-796-6938
Waldwick, NJ 07463
Introducing Groundwater Decontamination
Systems (GDS), the unique new system for
soil and groundwater decontamination.
Groundwater Decontamination Systems Inc.
eliminates hydrocarbon and halogenated
hydrocrbon contaminants from the
groundwater and from the soil through a
process of accelerated bio-degradation by
micro-organisms existing in the
contaminated soil. Patent awarded.
Gulf Oil Chemicals Company
P. 0. Box 3766
Houston, TX 77253
1801
713-754-2436
Drums for storage and transportation of
hazardous materials; HOPE plastic resins
for manufacture of synthetic liners for
landfills, containment ponds or waste
piles; large diameter pipe systems for
transportation of hazardous liquid
wastes.
Gundle Lining Systems, 1807
Inc.
1340 E. Richey Road 713-443-8564
Houston, TX 77073
Gundle Lining Systems, Inc., is a
manufacturer of high density polyethylene
(HOPE) sheeting in thicknesses ranging
from 20 mil to 100 mil and widths of 22.5
feet. These flexible membrane liners are
used for applications pertaining to
environmental protection such as dams,
reservoirs, hazardous and nonhazardous
waste containments.
HMD Systems, Inc. #406
160 Charlemont Street
Newton, MA 02161 617-964-6690
Model 301 gas chromatograph - A portable
version of the 301 with DC power/gas
supply option provides field
investigation capabilities. This G.C. can
be equipped with both photoionization
detector and FID detector which provides
field confirmation of unknown species.
Model PI-101 hazardous waste detector
provides immediate indication of the
presence of potential toxic chemicals,
even at sub ppm levels, and gives a
breakdown of existing compounds when used
with three available probes.
Harmon Engineering and 1110-113
Testing, Inc.
Auburn Industrial Park 205-821-9250
Auburn, AL 36830
Harmon Engineering & Testing (HE&T) will
demonstrate a mobile laboratory equipped
to perform testing necessary at hazardous
waste remedial action sites. The GC/MS
system, along with support
instrumentation, can provide on-site
waste analyses for PCBs, organic
solvents, cyanide, phenols, heavy metals
and related hazardous compounds. HE&T
will also provide an exhibition
describing their hazardous waste
management program which includes
industrial hygiene consultation (HE&T is
an AIHA accredited firm), site
assessments, engineering and removal
activities.
HazTech
3300 Marjan Drive, N.E.
Atlanta, GA 30340
#307
404-451-5772
HazTech will provide speciality
engineering and field operations services
to: private industry, architects and
engineering firms; hazardous waste
treatment, storage, disposal and cleanup
contractors; and federal, state, and
municipal governments. Specific
operational capabilities include: site
cleanup, contaminated water treatment,
borehole drilling, and well installation.
ICOS #717
4 West Fifty-Eighth Street
New York, NY 10019 212-688-9216
In-Situ, Inc.
209 Grand Avenue
Laramie, WY 82070
#1209
307-742-8213
In-Situ, Inc., is a hydrologic
instrumentation and software company. We
are exhibiting the SE-200 Hydrologic
Analysis System. This is a
computer-automated field hydrologic
analysis system that monitors and records
water levels in a maximum of 10 wells
simultaneously. The system also prints a
preliminary report in the field that
includes graphs of time drawn curves.
Also on exhibit is the SE-1000, a solid
state simple channel monitor for
long-term monitoring of wells. It is
compact, weathertight and contains a
long-life battery pack. Extensive
software available from In-Situ includes
programs for surface and groundwater,
restoration programs, and oil and gas
software.
Industrial Marine Service, t202
Inc.
1301 Marsh Street, Box 177804-543-5718
Norfolk, VA 23501
Hazardous material and oil spill
contractor.
International Minerals & #802
Chemical Corporation
421 East Hawley Street 312-566-2600
Mundelein, IL 60060
IMC produces sodium bentonite products
for civil engineering applications;
slurry trenching, irrigation trenches,
cut-off walls, pond sealing, sewage
lagoons, earthen dams and sanitary
landfills.
JRB Associates #403
8400 Westpark Drive
McLean, VA 22102 703-821-4886
JRB is pleased to demonstrate its
experience and expertise in the
management of hazardous wastes including
site investigations, RCRA "Part B" Permit
applications, chemical industry studies,
technology evaluation for hazardous spill
clean up and site remediation.
Additional services include environmental
audits, expert witness testimony and
regulatory development.
K-V Associates #205
P. 0. Box 574
Falmouth, MA 02541 617-540-0561
K-V Associates, Inc., manufactures
groundwater equipment for the oil
industry, hazardous waste contractors,
civil engineers, and environmental
consultants. These include groundwater
flowmeters, leachate detectors, and
miniature portable well point samplers.
The flowmeters allow rapid determination
of direction and rate of groundwater and
gasoline product flow.
K. W. Brown and Associates #603
707 Texas Avenue South
Suite 202D 409-693-8716
College Station, TX 77840
K. W. Brown and Associates is a
consulting firm specializing in
soil-related aspects of environmental
problems and issues. Areas of expertise
include both hazardous and nonhazardous
waste disposal, land treatment, advanced
landfill designs, in place closure of
surface impoundments, clay line-waste
compatability testing and cleanup
assessment of chemical spills.
Law Engineering Testing f513
Company
1140 Hammond Drive 404-396-8000
Atlanta, GA 30328
Law Engineering is an established
environmental consulting firm with
extensive experience in contamination
investigations and remediation studies.
Law has gained valuable knowledge of
regional and local geology/hydrology near
many existing hazardous waste sites.
Years of experience with hazardous waste
make Law Engineering a credible firm to
help solve contamination problems.
Marine Pollution Control
8631 West Jefferson Avenue
Detroit, MI 48209
#500 & 502
313-849-2333
Mead CompuChem #616
P. 0. Box 12652
Research Triangle Park, 919-549-8263
NC 27709
Mead CompuChem combines sophisticated
GC/MS (gas chromatography/mass
spectrometry) technology with
computer-based systems to deliver high
EXHIBITOR LIST 463
-------
quality GC/MS analytical testing services
including the analysis of low level
organics. Inorganic analysis is also
available by AA and ICAP. Analyses can
be performed on a variety of sample
matrices including air, water, soil,
tissue and hazardous waste for both
clinical and environmental needs.
Med-Tox Associates, Inc. »305
4020 Birch Street
Suite 202 714-851-1028
Newport Beach, CA 92660
Med-Tox Associates, Inc., is an
environmental health consulting and
managemnt company. Med-Tox provides
expertise in the field of hazardous waste
management, environemntal toxicilogy,
industrial hygiene, and occupational
medicine. Hazardous waste services
include: environmental testing, site
investigations, regulatory compliance,
personal monitoring, and overall
management of waste cleanup operations.
ModuTank, Inc. (520
29-24 40th Avenue
Long Island City, 212-392-1112
NY 11101
ModuTank provides low cost, above-ground,
bolt-together tanks in a wide range of
sizes and capacities for virtually all
liquid holding needs; as well as
secondary containment dikes and linings
for storage pond. Also standard
"off-the-shelf" products and custom
designs are available.
NIB/EPA Chemical 1306
Information System
CSC, P. 0. Box 2227 703-237-1333
Falls Church, VA 22042
The NIH/EPA Chemical Information System
is a collection of scientific, emergency
response and regulatory data bases
available world-wide via Telenet or
Tymnet, 24 hours a day, 365 days a year.
This system allows for structure,
substructure and full or partial name
searching for over 250,000 unique
chemical substance and 800,000 synonyms
or trade names.
NUS Corporation 1413 & 415
910 Clopper Road
Gaithersburg, MD 20878 301-258-1299
NUS offers complete hazardous waste
management and RCRA-related services.
The exhibit presents NUS1 consulting,
engineering, analytical, and earth
sciences capabilities, including site
assessement and groundwater monitoring,
chemical waste management, remedial
action services, and sophisticated
laboratory facilities. Our computerized
Real-Time Emergency Assessment System and
NUS1 High Integrity Container for
hazardous and radioactive wastes are also
displayed.
National Library of 1818
Medicine
8600 Rockville Pike 301-496-1131
Bethesda, MD 20209
The National Library of Medicine Chemical
and Toxicological files are online,
interactive retrieval services in
toxicology maintained by the Specialized
Information Services Division of the
National Library of Medicine. The files
include TDB (Toxicology Data Bank), RTECS
(Registry of Toxic Effects of Chemical
Substances), TOXLINE (Toxicology
Information Online), and CHEMLINE
(Chemical Dictionary Online).
New York Testing M02
Laboratories, Inc.
75 Urban Avenue 516-334-7770
Westbury, NY 11590
New York Testing Laboratories, Inc.
provides management and analysis of
hazardous wastes to the RCRA
requirements, including the screening of
priority pollutants, ignitability,
corrosivity, reactivity and EP toxicity
tests. Other allied services include
NPDES and SPDES compliance testing,
bioassay, bioaccumulation and toxicity
studies, and complete organic and
inorganic analysis of sediment,
wastewater and sludge samples.
0. H. Materials Co. 1312
P. 0. Box 551
Findlay, OH 45840 419-423-3526
0. H. Materials provides on-site
treatment of a variety of environmental
hazards. Previous work for public and
private sector clients has included:
hazardous waste site cleanup, groundwater
recovery and cleanup, radiological
cleanup, carbon filtration, consulting,
site assessment biological degradation,
emergency response and complete
analytical services.
Occupational Health 1404
Services, Inc.
515 Madison Avenue 212-752-4530
New York, NY 10023
Occupational Health Services, Inc., is a
subsidiary of P. W. Communications, Inc.,
a leading international medical
communications corporation. OHS, Inc.,
provides HA2ARDLINE an online,
interactional database designed to
provide occupational/environmental
specialists with the most current
regulatory and risk assessment
information on hazardous substances.
Also online availability is ENVIRONMENTAL
HEALTH NEWS which provides late breaking
news items as they happen from government
regulatory agencies on related court
decisions, emergency occurrences, toxics
research and other events.
Oil Recovery Systems, Inc. 1405
299 Second Avenue
Needham, MA 02194 617-449-5222
Oil Recovery Systems/Groundwater
Technology offers the entire solution to
groundwater contamination by
cost-effectively incorporating
experienced hydrogeologists, local
service, and proven innovative equipment.
We provide laboratory analysis,
scavenger systems, water table depression
pumps, water purification and air
stripping systems, samplers, and
monitoring equipment.
Palco Linings, Inc. 1200
P. 0. Box 526
South Plainfield, NJ 07080201-753-6262
Palco Linings, Inc., has been involved in
the seepage control industry for over 20
years. The Company has fabricated more
than 100 million square feet of flexible
membrance lining in a wide diversity of
over 1500 projects. Palco manufactures a
variety of standard and custom linings.
Technical assistance and turn-key
installations are also provided. For
international and west coast customers
call 714-898-0867, or write to P. 0. Box
919, Stanton, CA 90680
Photovac Incorporated 1506
Unit 2, 134 Doncaster Ave.
Thornhill, Ontario 416-881-8225
Canada L3T 1L3
Photovac Incorporated cordially invites
all attendees to stop by the booth to
learn how the following chronograph, data
analyzer and air monitoring system can
help your company in hazardous waste
control: Photovac 10A10 Portable
Photoionization Gas Chromotograph,
Photovac P1500 Portable Chromotograph
Controller Data Analyzer, Photovac
A-4000/S-9000 Area Air Monitoring System.
QED Environmental Systems, 1702 « 704
Inc.
P. O. Box 7209 313-995-2547
Ann Arbor, MI 48107
The original Well Wizard™ dedicated
groundwater sampling system is designed
for two-inch and larger monitoring wells.
A line of portable, fully pneumatic,
automatic and widely adjustable cycle
controller is available to operate the
system. The system, available in both
PVC and teflon, sharply reduces the
purging and sampling time requirements
while simultaneously improving sample
integrity.
R. E. Wright Associates 1600
3240 Schoolhouse Road
Middletown, PA 17057 717-944-5501
R. E. Wright Associates, Inc., is an
applied groundwater consulting firm
employing professional scientists in the
fields of hydrogeology, geochemistry,
engineering geology, soil science,
aquatic biology, and geophysics. Wright
Associates also provides consulting
services for the manufacture, use, and
disposal of hazardous materials to State
and Federal environmental agencies.
REACT 1517
P. 0. Box 27310
St. Louis, MO 63141 800-325-1398
REACT environmental crisis engineers
offer nationwide 24-hour emergency
response for hazardous material
accidents; environmental crisis
engineering for the containment and
control of hazardous waste sites; and
consulting engineering, including
industrial hygiene, RCRA compliance
audits, SPCC plan preparation and
chemical hazard analysis and evaluation
of health effects from chemical exposure.
REMIC Corporation
726 Middleton Run Road
Elkhart, IN 46516
1207
219-295-1806
U'nI-COM , the two-way hands-free
communications headset for increasing
personal safety and communications
efficiency in industrial, commercial,
professional operations and cleanup of
hazardous waste and material situations.
— voice controlled and cordless.
^nl-BASE for supervisors. Alert-COH
„, the new personal alert safety system
for use in all personal hazardous
situations.
464 EXHIBITOR LIST
-------
Radecca, Inc. 1606
P. 0. Box 9948
Austin, TX 78766 512-454-1420
Radecca sorbents find application to
water treatment and to waste and soil
stabilization. Radecca's KLENSORB fills a
long existing need for an economic and
effective means of treating water
contaminated with organics and
particularly oil. LOCKSORB provides
significantly lower costs in the
solidification/stabilization of hazardous
waste; LOCKSORB also retards leaching of
most organics from the stabilized waste.
Radian Corporation
p. 0. Box 9948
Austin, TX 78766
#715
512-454-4797
1214
Residuals Management
Technology, Inc.
1406 E. Washington Avenue 608-255-2134
Madison, WI 53703
Consultants in industrial, solid and
hazardous waste management. Specialties
include: landfill selection, design, and
construction management; waste
characterization and analysis;
environmental audits; air and water
pollution control engineering;
hydrogeologic investigation and
monitoring; regulatory permit analysis;
resource recovery; environmental
mediation; water and waste laboratory
analysis; and leaching tests.
Resources Technology 1601
Services, Inc.
6 Berkeley Road 215-687-4592
Devon, PA 19333
Resource Technology Services, Inc., is a
full service hazardous waste organization
dedicated to the environmentally sound,
cost-effective disposal of chemical
wastes. RTS offers a complete range of
services including transportation,
storage, consulting, remedial action,
emergency response and the handling and
disposal of highly reactive and shock
sensitive materials.
Rockwell International 1804 & 806
2421 W. Hillcrest Drive
Newbury Park, CA 91320 805-498-6771
Rockwell has the technological base,
engineering expertise and extensive
environmental program experience
necessary to address all phases of waste
management problems. Offices are located
in Newbury Park, CA; Denver, CO; Chapel
Hill, NC; and Washington, DC.
Rollins Environmental 1401
Services, Inc.
One Rollins Plaza 302-429-2767
Wilmington, DE 19899
the nation's first and most experienced
hazardous waste management company,
Rollins continues to lead in the
development and application of
state-of-the-art technologies and
services. From consultation to
destruction, Rollins offers a complete
spectrum of hazardous waste management
options at regional facilities located in
industrialized areas of the country.
Because hazardous waste management is our
only business, we have the skilled
personnel, equipment and technical
expertise to provide the most
cost-effective treatment, disposal and
remedial services possible.
Roy P. Boston, Inc. 1514
Weston Way
West Chester, PA 19335 215-692-3030
Roy F. Weston, Inc. provides
comprehensive environmental energy
management services on an international
scale. WESTON1s management and
technological expertise is applied in the
areas of: air resources management;
water supply; wastewater; geosciences;
environmental management; resource
development/recovery; technology
management; land use; energy management;
hazardous waste management; and solid
waste management.
SCA Chemical 1808 & 810
Services, Inc.
5 Middlesex Avenue 617-367-8300
Somerville, MA 02145
SCA is a total service company geared to
meet all the needs of hazardous waste or
PCB generators. We presently provide
transformer decommissioning and
decontamination, PCB capacitor disposal
by EPA approved secure chemical landfill,
transportation with total liability
protection, and analysis and consultation
on PCB situations or remedial activities.
SCA's Chicago incinerator has passed all
technical requirements to incinerate
PCBs. We expect to receive our PCB
permit from the Environmental Protection
Agency in September, 1983.
SCS Engineers 1407
4014 Long Beach Blvd.
Long Beach, CA 90807 213-426-9544
SCS Engineers provides consulting and
engineering services to the waste
management industry and government
agencies. The company's staff
capabilities include all engineering
disciplines, complimented by geologists,
soil specialists, chemists, and
biologists. Principal work areas include
landfill/landfarm design, hydrogeologic
investigations, permitting/EIS, landfill
gas, incineration, SPCC, expert testimony
and risk management.
SMC Martin, Inc. #521
Box 859
Valley Forge, PA 19482 215-265-2700
SMC Martin provides civil, chemical,
design engineering services in addition
to geochemical, geophysics,
hydrogeologic, geologic and soils
capabilities to industrial, governmental,
and judicial clients in hazardous waste
assessment and remediation.
SRW Associates, Inc. #412
2793 Noblestown Road
Pittsburgh, PA 15205 412-921-0321
SRW Associates, Inc., is a geotechnical
and environmental engineering firm
specializing in waste management and
waste engineering for industry. Services
include design, permitting, ground water
monitoring, planning, site investigation,
site closure, soil laboratory testing,
liner compatibility testing, and Part B
applications.
Safety First Industries, #210
Inc.
161 Thorn Hill Road 412-776-2900
Warrendale, PA 15086
Safety First Industries is a manufacturer
of safety and firefighting equipment,
distributing the I.L.C. Dover Totally
Encapsulating Chemical Suit available
with optional aluminizing Kevlar cover
flash suit.
Safeware, Inc. #712
3838 Ironwood Place
Landover, MD 20785 301-322-2800
Products for the safety and protection of
people.
Schlegel Lining #211
Technology, Inc.
P. 0. Box 7730 409-273-3066
The Woodlands, TX 77380
Manufactures and installs lining systems
of SCHLEGEL sheet, a high density
polyethylene liner in single pieces, 34'
wide and up to 900' long, and thicknesses
of 60, 80, 100 mils. The liner is seamed
with an extrusion welding process.
Schlegel is the only company in the
lining industry offering single-source
responsibility for system.
Slurry Systems #700
7100 Industrial Avenue
Gary, IN 46406 312-721-9797
Slurry Systems presents VIBRATED BEAM
slurry cut off wall technology, specially
formulatd slurries and ASPEMIX
resistant to most aggressive chemicals,
and MANPOWER with technical 'know-how1
and hands-on experience providing a
successful approach for toxic waste
containment.
Soletanche & Rodio, Inc. #201
1340 Old Chain Bridge Road
McLean, VA 22101 703-821-6727
Soletanche and Rodio, Inc., provides
specialty underground construction
techniques for seepage control and waste
isolation including: soil bentonite and
cement bentonite slurry wall cutoffs, and
all types of soil and rock grouting.
Stablex-Reutter, Inc. #904
P. O. Box 499
Camden, NJ 08101 609-541-6700
Stablex-Reutter, Inc., is a consulting
environmental laboratory specializing in
analysis and characterization of
industrial process waste streams.
Stablex-Reutter's expertise encompasses a
variety of analytical protocols
including: RCRA testing; priority
pollutants analysis; waste
characterization for manifests; chemical
analysis of raw wastes; field sampling of
drums, spills, tanks; and studies of
industrial wastes treatment.
Stokes Division/ #803
Pennwalt Corporation
3 Parkway 215-587-7618
Philadelphia, PA 19102
The Stokes Vacuum Solid Recovery System
is a compact, highly efficient rotary
drying unit that captures 90-95% of spent
solvents from a wide range of slurry and
sludges. With the Stokes Recovery
System, it is possible to reduce the
residual solvent in the waste to less
than 1% which greatly reduces the
environmental problems connected with
their disposal.
TRC Environmental #101 109
Consultants, Inc.
800 Connecticut Blvd. 203-289-8631
East Hartford, CT 06108
TRC Environmental Consultants, Inc., is
headquartered in East Hartfod,
Connecticut, with offices in Denver,
Colorado, and Washington, D.C. TRC
EXHIBITOR LIST 465
-------
specializes in innovative solutions to
air, water,and hazardous pollution
problems. Services in hazardous waste
include determination of contaminated
migration, evaluation and design of
remedial actions, waste management
engineering preparation of RCRA Part B
permit application site audits, and real
timejionitoring of toxic pollutants using
TAGA , a mobile MS/MS system owned by
TRC Advanced Analytics Inc.
Technos, Inc. 1414
3333 NW 21st Street
Miami, FL 33142 305-634-4507
Technos Inc., specializes in site
investigation at hazardous waste sites
utilizing their state-of-the-art systems
approach for optimum cost-effective
results.
Triangle Resources 1812
Industries
P. 0. Box 370 301-953-9583
Laurel, MD 20707
Operating from RCRA-permitted facilities
in Maryland, North Carolina and
Tennessee, TRI is a 90-person service
company offering (1) hazardous waste
packaging, transport and disposal; (2)
remedial action cleanup; (3) 24-hour
emergency response; (4) safety training;
(5) safety supplies and packaging
materials; and (6) regulatory compliance
programs.
Trofe Incineration, Inc. 1706
Pine Road
Mt. Laurel, NJ 08054 609-235-3030
Trofe has incineration systems for solid
and liquid wastes, hazardous or
nonhazadous including waste heat recovery
and co-generation capabilities.
US Array Corps of Engineers 1310
P. 0. Box 103
Downtown Station 402-221-7317
Omaha, NE 68101
The U. S. Army Corps of Engineers and the
U. S. EPA have joined forces to clean up
Federal Lead hazardous waste sites under
the Superfund Program. The booth will be
manned by Corps' personnel to assist
architect-engineer firms and construction
contractors take advantage of work
available to them under Superfund through
the Corps of Engineers.
US Ecology, Inc. 1301
P. 0. Box 7246
Louisville, KY 40207 502-426-7160
US Ecology operates low-level radioactive
disposal landfills in Washington and
Nevada, and chemical disposal landfills
in Nevada and Texas. The company is
affiliated with chemical waste
incinerator facilities in Kentucky and
treatment facilities in Illinois and
Tennessee. Other services include
disposal of solid PCB materials,
engineering services, laboratory
services, and seminars.
US Environmental 1501 - 507
Protection Agency
Raritan Depot 201-321-6677
Edison, NJ 08837
The USEPA has been actively involved at
all levels of hazardous waste management
with the investigation, categorization,
response activities and remedial actions
at hundreds of uncontrolled hazardous
waste sites. This display exhibits
products for the protection of response
personnel, and provides information on
current Superfund activities, the latest
response equipment for site
investigation, research and development
for long term remedial action and EPA's
mobile treatment systems.
US Geological Survey 11102-1106
27 Butternut Way
Sterling, VA 22092 703-860-6162
U.S. Geological Survey research
concerning hydro-geologic considerations
for safe disposal of hazardous wastes.
Watersaver Company, Inc. 1512
P. O. Box 16465
Denver, CO 80216 303-623-4111
Watersaver Company is involved in the
fabrication of flexible membrane liners,
both reinforced and unreinforced.
Specializing in PVC, CPE, and HYPALON for
solid waste landfills, surface
impoundments, and hazardous waste
containment.
Wehran Engineering 1215
Corporation
666 East Main Street 914-343-0660
Middletown, NY 10940
Wehran, a multidisciplinary firm
specializing in the field of waste
management, provides engineering and
scientific services from offices located
in the northeast and midwest. With 15
years of hands-on experience in all
facets of land disposal engineering -
from waste sampling exhumation to
subsurface cut-off walls and impermeable
caps our staff of 150 has earned a
national reputation as a leader in the
practical application of innovative
technology to solid and hazardous waste
disposal.
Westbay Instruments Ltd. 1814
507 E. Third Steet
North Vancouver, B.C. 604-984-4215
Canada V7L 1G4
Westbay Instruments Ltd. - Designers and
manufacturers of the MP System, a modular
multi-ported groundwater instrumentation
system for pressure measurements and
groundwater sampling. Components include
plastic or stainless steel casing and
couplings, inflatable or mechanical
packers and pneumatic or electric
pressure probes and sampling probes.
Weston Geophysical 1515
Corporation
P. 0. Box 550 617-366-9191
Westhorough, MA 01581
Weston Geophysical Corporation has
provided integrated multidisciplinary
geophysical and geological consulting
services on over 1,000 projects since its
founding in 1957. We specialize in
state-of-the-art, non-destructive
geophysical techniques which when
combined with our geologic expertise
enable acquisition and interpretation of
data necessary for preliminary, remedial
and feasibility investigations. Weston
has recently adapted Vertical Seismic
Profiling, an oil industry technique, to
the evaluation of the destribution and
hydrolic conductivity of fracture zones
for analyzing contaminant flow pathways.
World Information Systems 1408
P. 0. Box 535
Cambridge, MA 02238 617-491-5000
Zimpro, Inc. 1300 « 302
Military Road
Rothschild, WI 54474 715-359-7211
Zimpro Inc., provides wet air oxidaton
systems, PACT units, furnaces, rapid sand
filters for hazardous and toxic
wastewater treatment. Package units are
available for groundwater and leachate
treatment. Zimpro has more than 35 units
operating on HTW in the field. Complete
laboratory, pilot plant, design, and
operation services are available as
required. The company is based in
Wisconsin, and is a subsidiary of
Sterling Drug Inc.
466 EXHIBITOR LIST
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PMOMTIES LIST AND PROPOSED UPDATE SITES
UNITED STATES
SITE NAME/LOCATION
ALASKA (10)
ALABAMA (04)
Mowbray Engineering Co., Greenville
Perdido Ground Water Contamination, Perdido
Triana-Tennessee River (formerly Triana
(Redstone) Arsenal), Limestone/Morgan
Counties
Ciba-Geigy Corp. (Mclntosh Plant), Mclntosh
Olin Corp. (Mclntosh Plant), Mclntosh
Stauffer Chemical Co. (Cold Creek Plant)
Bucks
Stauffer Chemical Co. (Lemoyne Plant), Axis
ARKANSAS (06)
Cecil Lindsey, Newport
Crittenden County Landfill8, Marion
Frit Industries, Walnut Ridge
Gurley Pit, Edmondson
Industrial Waste Control, Fort Smith
Mid-South Wood Products, Mena
Vertac, Inc., Jacksonville
AMERICAN SOMOA (09)
Taputimu Farm*, Island of Tutuila
ARIZONA (09)
Indian Bend Wash Area, Scottsdale-Tempe-
Phoenix
Kingman Airport Industrial AreaP, Kingman
Litchfield Airport Area, Goodyear/Avondale
Mountain View Mobile Home Estates*,
(formerly Globe), Globe
19th Avenue Landfill, Phoenix
Tuscon Airport Area, Tucson
CALIFORNIA (09)
Aerojet General Corp., Rancho Cordova
Celtor Chemical Works, Hoopa
Coast Wood Preserving, Ukiah
Iron Mountain Mine, Redding
Jibboom Junkyard, Sacramento
Liquid Gold Oil Corp., Richmond
MGM Brakes, Cloverdale
McCoIl, Fullerton
Purity Oil Sales, Inc., Malaga
Selma Treating Co., Selma
Stringfellow*, Glen Avon Heights
Atlas Asbestos Mine, Fresno County
Coalinga Asbestos Mine, Coalinga
NPL Update Total
406 133 546t
3
X
X
X
6
X
X
X
X
X
X
1
X
X
X
X
X
X
11
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
— 1
— 5
19
X
X
t Includes seven sites proposed in Dec. 1982 on which rulemaking is pending.
* Designated as State's top priority.
c Not included because site was cleaned up.
P Rulemaking pending.
s Not included because proposed score was revised.
I Not included because no longer designated as State's top priority.
(00) EPA Regions
NPL Update Total
Del Norte County Pesticide Storage Area,
Crescent City X
Koppers Co., Inc. (Oroville Plant), Oroville X
San Gabriel Valley (Area 1), El Monte X
San Gabriel Valley (Area 2), Baldwin
Park Area X
San Gabriel Valley (Area 3), Alhambra X
San Gabriel Valley (Area 4), La Puente X
NORTHERN MARIANA ISLANDS (09)
PCB Warehouse, Saipan
COLORADO (08) 6 3
California Gulch, Leadville X
Central City-Clear Creak, Idaho Springs X
Denver Radium, Denver X
Marshall Landfill*, Boulder County X
Sand Creek Industrial, Commerce City X
Woodbury Chemical Co., Commerce City X
Broderick Wood Products, Denver , X
Lincoln Park, Canon City X
Lowry Landfill, Arapahoe County X
CONNECTICUT (01) 4 2
Beacon Heights Landfill, Beacon Falls X
Laurel Park, Inc. (formerly Laurel Park
Landfill), Naugatuck Borough X
Solvents Recovery Service of New England
Southington X
Yaworski Waste Lagoon, Canterbury X
Kellogg-Deering Well Field, Norwalk X
Old Southington Landfill, Southington X
DISTRICT OF COLUMBIA (03) — —
DELAWARE (03) 8 1
Army Creek Landfill (formerly Delaware
Sand & Gravel—Llangollen Army Creek
Landfills), New Castle County X
Delaware City PVC Plant (formerly Stauffer
Chemical Co.), Delaware City X
Delaware Sand & Gravel Landfill (formerly
Delaware Sandd & Gravel—Llangollen
Army Creek Landfills), New Castle County X
Harvey & Knott Drum, Inc., Kirkwood X
New Castle Spill (formerly Tris Spill), New
Castle County X
New Castle Steel, New Castle County X
Tybouts Corner Landfill*, New Castle County X
Wildcat Landfill, Dover X
Old Brine Sludge Landfill, Delaware City X
FLORIDA (04) 25
Alpha Chemical Corp., Galloway X
American Creosote Works, Pensacola X
Brown Wood Preserving, Live Oak X
Coleman-Evans Wood Preserving Co.,
Whitehouse x
Davie Landfill (formerly Broward County
Solid Waste Disposal Facility), Davie X
Florida Steel Corp., Indiantown X
Gold Coast Oil Corp., Miami X
29
NATIONAL PRIORITIES LIST
467
-------
Hollingsworth Solderless Terminal Co.,
Fort Lauderdale
Kassauf Kimerling Battery (formerly Timber
Lake Battery Disposal), Tampa
Miami Drum Services (formerly a part of
Biscayne Aquifer), Miami
Munisport Landfill, North Miami
Northwest 58th Street Landfill (formerly a
part of Biscayne Aquifer), Hialeah
Parramore Surplus, Mount Pleasant
Pickettville Road Landfill, Jacksonville
Pioneer Sand Co., Warrington
Reeves Southeastern Galvanizing Corp., Tampa
Sapp Battery Salvage, Cottondale
Schuylkil) Metals Corp., Plant City
Sherwood Medical Industries, Deland
62nd Street Dump, Tampa
Taylor Road Landfill, Seffner
Tower Chemical Co., Clermont
Varsol Spill (formerly a part of
Biscayne Aquifer), Miami
Whitehouse Oil Pits, Whitehouse
Zellwood Ground Water Contamination,
Zellwood
Cabot/Koppers, Gainesville
Hipps Road Landfill, Duval County
Pepper Steel & Alloys, Inc., Medley
Tri-City Oil Conservationist, Inc., Temple
Terrace
GEORGIA (04)
Hercules 009 Landfill, Brunswick
Monsanto Corp. (Augusta Plant), Augusta
Olin Corp. (Areas 1, 2 & 4), Augusta
Powersville, Peach County
GUAM (09)
Ordot Landfill*, Ordot
HAWAII (09)
IOWA (07)
Aidex Corp.", Council Bluffs
Des Moines TCE (formerly DICO),
Des Moines
Labounty, Charles City
IDAHO (10)
Arrcom (Drexler Enterprises), Rathdrum
Bunker Hill Mining & Metallurgical,
Smelterville
Flynn Lumber Co.s, Caldwell
Pacific Hide & Fur Recycling Co., Pocatello
Union Pacific Railroad Co., Pocatello
ILLINOIS (05)
A & F Materials Reclaiming, Inc., Greenup
Acme Solvent Reclaiming, Inc.,Morristown
Belvidere Municipal Landfill, Belvidere
Byron Salvage Yard, Byron
Cross Brothers Pail Recycling, Pembrook Twp
Galesburg/Koppers, Galesburg
Johns-Manville Corp., Waukegan
Lasalle Electric Utilities, La Salle
Outboard Marine Corp.*, Waukegan
Velsicol Chemical Corp. (Marshall Plant),
Marshall
Wauconda Sand & Gravel, Wauconda
NPL Update Total
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
1
X
3
X
X
X
2
X
11
X
X
X
X
X
X
X
X
X
X
X
X
X
X
4 4
X
X
X
X
— 1
X
X
— 11
NPL Update Total
INDIANA (OS) 12 5 17
Envirochem Corp., Zionsville X
Fisher Calo, LaPorte X
Lake Sandy Jo (M&M Landfill), Gary X
Lemon Lane Landfill, Bloomington X
Main Street Well Field, Elkhart X
Marion (Bragg) Dump, Marion X
Midco I, Gary X
Neal's Landfill, Bloomington X
Ninth Avenue Dump, Gary X
Parrot Road Dump9, Seymour
Seymour Recycling Corp.*, Seymour X
Wayne Waste Oil, Columbia City X
Wedzeb Enterprises, Inc., Lebanon X
American Chemical Service, Griffith X
Bennett Stone Quarry, Bloomington X
Northside Sanitary Landfill, Zionsville X
Poer Farm, Hancock County X
Reilly Tar & Chemical Corp., Indianapolis X
KANSAS (07) 4—4
Arkansas City Dump*, Arkansas City X
Cherokee County (formerly TAR Creek),
Cherokee County X
Doepke Disposal (Holliday), Johnson County X
Johns' Sludge Pond, Wichita X
KENTUCKY (04) 6—6
A.L. Taylor (Valley of the Drums)*, Brooks X
AircoP, Calvert
B.F. Goodrich, Calvert City X
Distler Brickyard, West Point X
Distler Farm, Jefferson County X
Lee's Lane Landfill, Louisville X
Newport Dump, Newport X
LOUISIANA (06) 3 1 4
Bayou Bonfouca, Slidell X
Bayou SorrelP, Bayou Sorrel
Cleve Reber, Sorrento X
Old Inger Oil Refinery*, Darrow X
Petro-Processors, Scotlandville
MASSACHUSETTS (01) 14
Baird & McGuire, Holbrook X
Cannon Engineering Corp. (CEC),
Bridgewater X
Charles George Reclamation Trust Landfill,
Tyngsborough X
Groveland Wells, Groveland X
Hocomonco Pond, Westborough X
Industri-Plex 128 (formerly Mark Phillip
Trust), Woburn X
New Bedford*, New Bedford X
Nyanza Chemical Waste Dump, Ashland X
PSC Resources, Palmer x
Plymouth Harbor/Cannon Engineering Corp.,
Plymouth x
Re-Solve, Inc., Dartmouth x
Silresim Chemical Corp., Lowell x
W.R. Grace & Co., Inc. (Acton Plant),
Acton x
Wells G4H, Woburn X
Iron Horse Park, Billerica
Sullivan's Ledge, New Bedford
X
2
16
468
NATIONAL PRIORITIES LIST
-------
MARYLAND (03)
Limestone Road, Cumberland
Middletown Road Dump, Annapolis
Sand, Gravel & Stone, Elkton
MAINE (01)
F. O'Connor Site, Augusta
McKin Co., Gray
Pinette's Salvage Yard, Washburn
Saco Tannery Waste Pits, Saco
Winthrop Landfill, Winthrop
MICHIGAN (05)
Anderson Development Co., Adrian
Auto Ion Chemicals, Inc., Kalamazoo
Berlin & Farro, Swartz Creek
Butterworth No. 2 Landfill, Grand Rapids
Cemetery Dump, Rose Center
Cbarlevoix Municipal Well, Charlevoix
Chem Central, Wyoming Twp
Qare Water SupplyP, Clare
Cliff /Dow Dump, Marquette
Duell & Gardner Landfill, Dal ton Twp
ElectrovoiceP, Buchanan
Forest Waste Products, Otisville
G&H Landfill, Utica
Grand Traverse Overall Supply Co.,
Greilickville
Gratiot County Golf Coursec, St. Louis
Gratiot County Landfill*, St. Louis
Hedblum Industries, Oscoda
Ionia City Landfill, Ionia
K & L Avenue Landfill, Oshtemo Twp
Kentwood Landfill, Kent wood
Liquid Disposal, Inc., Utica
Littlefield Township DumpP, Oden
Mason County Landfill, Pere Marquette Twp
McGraw Edison Corp., Albion
Northernaire Plating, Cadillac
Novaco Industries, Temperance
Organic Chemicals, Inc., Grandville
Ossineke Ground Water Contamination,
Ossineke
Ott/Story/Cordova Chemical Co., Dalton Twp
Packaging Corp. of America, Filer City
Petoskey Municipal Well Field, Petoskey
Rasmussen's Dump, Green Oak Twp
Rose Township Dump, Rose Twp
SCA Independent Landfill, Muskegon Heights
Shiawassee River, Howell
Southwest Ottawa County Landfill, Park Twp
Sparta Landfill, Sparta Twp
Spartan Chemical Co., Wyoming
Spiegelberg Landfill, Green Oak Twp
Springfield Township Dump, Davisburg
Tar Lake, Mancelona Twp
U.S. Aviex, Howard Twp
Velsicol Chemical Corp. (St. Louis Plant),
St. Louis
Verona Well Field, Butler Creek
Wash King Laundry, Pleasant Plains
Township
Whitehall Well FieldP, Whitehall
Burrows Sanitation, Hartford
Metamora Landfill, Metamora
Sturgis Municipal Wells, Sturgis
NPL Update Total
3 - 3
X
X
X
5
X
X
X
X
X
41
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
— 5
44
X
X
X
NPL Update Total
MINNESOTA (05) 10 13 23
Burlington Northern, Brainerd/Baxter X
FMC Corp. (Fridley Plant), Fridley X
Koppers Coke, St. Paul X
Lehillier/Mankato, Lehillier/Mankato X
NL Industries/Taracorp/Golden Auto,
St. Louis Park X
New Brighton/Arden Hills, New Brighton X
Oakdale Dump, Oakdale X
Reilly Tar & Chemical Corp.*, St. Louis Park X
South Andover (formerly Andover Sites),
Andover X
Waste Disposal Engineering, Andover X
Arrowhead Refinery Co., Hermantown X
Boise Cascade/Onan/Medtronics, Fridley X
General Mills/Henkel Corp., Minneapolis X
Joslyn Manufacturing & Supply Co., Brooklyn
Center X
MacGillis & Gibbs Co./Bell Lumber & Pole
Co., New Brighton X
Morris Arsenic Dump, Morris X
Nutting Truck & Caster Co., Faribault X
Perham Arsenic, Perham X
St. Louis River, St. Louis County X
St. Regis Paper Co., Cass Lake X
Union Scrap, Minneapolis X
Washington County Landfill, Lake Elmo X
Whittaker Corp., Minneapolis X
MISSOURI (07) 6 1 7
Ellisville*, Ellisville X
Fulbright Landfill, Springfield X
Minker/Stout/Romaine Creek (formerly
Arena 2: Fills 1 & 2), Imperial X
Shenandoah Stables (formerly Arena 1:
Shenandoah Stables), Moscow Mills X
Syntex Facility, Verona X
Times Beach, Times Beach X
Quail Run Mobile Manor, Gray Summit X
MISSISSIPPI (04) — 1 1
Plastifax, Inc.1, Gulfport
Flowood*, Flowood X
MONTANA (08) 4 1 5
Anaconda Smelter, Anaconda X
Libby Ground Water Contamination, Libby X
Mill town Reservoir Sediments, Milltown X
Silver Bow Creek, Silver Bow/Deer Lodge
Counties X
East Helena Smelter, East Helena X
NORTH CAROLINA (04) 3—3
Chemtronics, Inc., Swannanoa X
Martin Marietta, Sodyedo, Inc., Charlotte X
PCB Spills*, 210 Miles of Roads X
NORTH DAKOTA (08) 1 — 1
Arsenic Trioxide*, Southeastern X
NEBRASKA (07) — — —
Phillips Chemical Co.s, Beatrice
NEW HAMPSHIRE (01) 7 3 10
Auburn Road Landfill, Londonderry X
Dover Municipal Landfill, Dover X
Keefe Environmental Services (KES), Epping X
NATIONAL PRIORITIES LIST
469
-------
Ottati & Gogs/Kingston Steel Drum, Kingston
Somersworth Sanitary Landfill, Somersworth
Sylvester", Nashua
Tinkham Garage, Londonderry
Kearsage Metallurgical Corp., Conway
Savage Municipal Water Supply, Milford
South Municipal Water Supply Well,
Peterborough
NEW JERSEY (02)
A.O. Polymer, Sparta Twp
American Cyanamid Co., Bound Brook
Asbestos Dump, Millington
Beachwood/Berkley Wells, Berkley Twp
Bog Creek Farm, Howell Twp
Brick Township Landfill, Brick Twp
Bridgeport Rental & Oil Services, Bridgeport
Burnt Fly Bog, Marlboro Twp
Caldwell Trucking Co., Fairfield
Chemical Control, Elizabeth
Chemsol, Inc., Piscataway
Combe Fill North Landfill, Mount Olive Twp
Combe Fill South Landfill, Mount Olive Twp
CPS/Madison Industries, Old Bridge Twp
D'lmperio Property, Hamilton Twp
Denzer & Schafer X-Ray Co., Bayville
Dover Municipal Well 4, Dover Twp
Ellis Property, Evesham Twp
Evor Phillips Leasing, Old Bridge Twp
Fair Lawn Well Field, Fair Lawn
Friedman Property (formerly Upper Freehold
Site), Upper Freehold Twp
Gems Landfill, Gloucester Twp
Goose Farm, Plumstead Twp
Helen Kramer Landfill, Mantua Twp
Hercules, Inc. (Gibbstown Plant), Gibbstown
Imperial Oil Co., Inc./Champion Chemicals
(formerly Imperial Oil Co., Inc.),
Morgan ville
JIS Landfill, Jamesburg/South Brunswick Twp
Jackson Township Landfill, Jackson Twp
Kin-Buc Landfill, Edison Twp
King of Prussia, Winslow Twp
Krysowaty Farm, Hillsborough
Lang Property, Pemberton Twp
Lipari Landfill, Pitman
Lone Pine Landfill, Freehold Twp
MAT Delisa Landfill, Asbury Park
Mannheim Avenue Dump, Galloway Twp
May wood Chemical Co., Maywood/Rochelle
Park
Metaltec/Aerosystems, Monroe Twp
Monroe Township Landfill, Monroe Twp
Montgomery Township Housing Development
Montgomery Twp
Myers Property, Franklin Twp
NL Industries, Pedricktown
PJP Landfill, Jersey City
Pepe Field, Boonton
Pijak Farm, Plumstead Twp
Price Landfill*, Pleasantville
Reich Farms, Pleasant Plains
Renora, Inc., Edison Twp
Ringwood Mines/Landfill, Ringwood Borough
Rockaway Borough Well Field, Rockaway Twp
NPL Update Total
X
X
X
X
X
X
65
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
20 85
NPL Update Total
Rockaway Township Wells, Rockaway X
Rocky Hill Municipal Wen, Rocky Hill
Borough X
Roebling Steel Co., Florence X
Sayreville Landfill, Sayreville X
Scientific Chemical Processing, Inc., Carlstadt X
Sharkey Landfill, Parsippany/Troy Hills X
South Brunswick Landfill, South Brunswick X
Spence Farm, Plumstead Twp X
Swope Oil & Chemical Co., Pennsauken X
Syncon Resins, South Kearny X
Toms River Chemical, Toms River X
U.S. Radium Corp., Orange X
Universal Oil Products (Chemical Division),
East Rutherford X
Vineland State School, Vineland X
Williams Property, Swainton X
Chemical Leaman Tank Liners, Inc.,
Bridgeport X
Cooper Road, Voorhees Twp X
De Rewal Chemical Co., Kingwood Twp X
Delilah Road, Egg Harbor Twp X
Diamond Alkali Co., Newark X
Ewan Property, Shamong Twp X
Florence Land Recontouring, Inc., Landfill,
Florence Twp X
Hopkins Farm, Plumstead Twp X
Landfill & Development Co., Mount Holly X
Nascolite Corp., Millville X
Radiation Technology, Inc., Rockaway Twp X
Shieldalloy Corp., Newfield Borough X
Tabernacle Drum Dump, Tabernacle Twp X
Upper Deerfield Township Sanitary Landfill,
Upper Deerfield Twp X
Ventron/Velsicol, Woodridge Borough X
Vineland Chemical Co., Inc., Vineland X
W.R. Grace & Co., Inc. (Wayne Plant),
Wayne Twp X
Wilson Farm, Plumstead Twp X
Woodland Route 532 Dump, Woodland Twp X
Woodland Route 72 Dump, Woodland Twp X
NEW MEXICO (06) 4
AT & SF/Clovis, Clovis X
Homestake Mining Co., Milan X
South Valley*, Albuquerque X
United Nuclear Corp., Church Rock X
NEVADA (09) —
NEW YORK (02) 27
American Thermostt Co., South Cairo X
Batavia Landfill, Batavia X
Brewster Well Field, Putnam County X
Facet Enterprises, Inc., Elmira X
Fulton Terminals, Fulton X
GE Moreau, South Glens Falls X
Hooker (Hyde Park), Niagara Falls X
Hooker (102nd Street), Niagara Falls X
Hooker (S-Area), Niagara Falls X
Kentucky Avenue Well Field, Horseheads X
Love Canal, Niagara Falls X
Lndlow Sand & Gravel, Clayville X
Marathon Battery Corp., Cold Springs X
Mercury Refining, Inc., Colonie X
— 4
29
470
NATIONAL PRIORITIES LIST
-------
Niagara County Refuse, Wheatfield
Old Bethpage Landfill, Oyster Bay
Olean Well Field, Olean
Pollution Abatement Services (PAS)*, Oswego
Port Washington Landfill, Port Washington
Ramapo Landfill, Ramapo
Sinclair Refinery, Wellsville
Solvent Savers, Lincklaen
Syosset Landfill, Oyster Bay
Vestal Water Supply Well 1-1, Vestal
Vestal Water Supply Well 4-2, Vestal
(formerly one site)
Wide Beach Development, Brant
York Oil Co., Moria
General Motors/Central Foundry Division,
Massena
Hudson River PCBs, Hudson River
OHIO (05)
Allied Chemical & Ironton Coke, Ironton
Arcanum Iron & Metal, Darke County
Big D Campground, Kingsville
Bowers Landfill, Circleville
Buckeye Reclamation, St. Clairsville
Chem-Dyne*, Hamilton
Coshocton Landfill, Franklin Twp
E.H. Schilling Landfill, Hamilton Twp
Fields Brook, Ashtabula
Fultz Landfill, Jackson Twp
Luskin/Poplar Oil Co. (formerly Poplar Oil
Co.), Jefferson Twp
Nease Chemical, Salem
New Lyme Landfill, New Lyme
Old Mill (formerly Rock Creek/Jack Webb),
Rock Creek
Pristine, Inc., Reading
Skinner Landfill, West Chester
Summit National, Deerfield Township
Van Dale Junkyard3, Marietta
Zanesville Well Field, Zanesville
Miami County Incinerator, Troy
Powell Road Landfill, Dayton
South Point Plant, South Point
United Scrap Lead Co., Inc., Troy
OKLAHOMA (06)
Hardage/Criner, Criner
Tar Creek (Ottawa County), Ottawa County
Compass Industries, Tulsa
Sand Springs Petrochemical Complex,
Sand Springs
OREGON (10)
Gould, Inc., Portland
Teledyne Wah Chang (Albany), Albany
United Chrome Products, Inc., Corvalis
PENNSYLVANIA (03)
Blosenski Landfill, West Cain Twp
Brodhead Creek, Stoudsburg
Bruin Lagoon, Bruin Borough
Centre County Kepone, State College Borough
Craig Farm Drum, Parker
Douglassville Disposal, Douglassville
Drake Chemical, Lock Haven
NFL Update Total
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
18
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
2
X
X
2
X
X
30
X
X
X
X
X
X
X
22
X
X
X
X
X
X
1
39
NPL Update Total
Enterprise Avenue, Philadelphia X
Fischer & Porter Co., Warminster X
Havertown PCP, Haverford X
Heleva Landfill, North Whitehall Twp X
Hranica Landfill, Buffalo Twp X
Kimberton, Kimberton Borough X
Lackawanna Refuse, Old Forge Borough X
Lehigh Electric & Engineering Co., Old Forge
Borough X
Llndane Dump, Harrison Twp X
Lord-Shope Landfill, Girard Twp X
Malvern TCE, Malvern X
McAdoo Associates*, McAdoo Borough/Kline
Twp X
Metal Banks, Philadelphia X
Meyers Landfill, Eagleville X
Old City of York Landfill, Seven Valleys X
Osborne Landfill, Grove City X
Palmerton Zinc Pile, Palmerton X
Presque Isle, Erie X
Resin Disposal, Jefferson Borough X
Stanley Kessler, King of Prussia X
Voortman Farm, Upper Saucon Twp X
Wade (ABM) (formerly ABM-Wade), Chester X
Westline, Westline X
Berks Sand Pit, Longswamp Twp X
Dorney Road Landfill, Upper MacungieTwp X
East Mount Zion, Springettsbury Twp X
Henderson Road, Upper Merion Twp X
Mill Creek Dump, Erie X
Industrial Lane, Williams Twp X
Taylor Borough Dump, Taylor Borough X
Tysons Dump, Upper Merion Twp X
Walsh Landfill, Honeybrook Twp X
PUERTO RICO (02) 538
Barceloneta Landfill, Florida Afuera X
Frontera Creek, Rio Abajo X
GE Wiring Devices, Juana Diaz X
Juncos Landfill, Juncos X
RCA Del Caribe, Barceloneta X
Fibers Public Supply Wells, Jobos X
Upjohn Facility, Barceloneta X
Vega Alta Public Supply Wells, Vega Alta X
RHODE ISLAND (01) 6—6
Davis Liquid Waste, Smithfield X
Landfill & Resource Recovery, Inc. (L & RR),
North Smithfield X
Peterson-Puritan, Inc., Lincoln/Cumberland X
Picillo Farm*, Coventry X
Stamina Mills, Inc. (formerly Forestdale-
Stamina Mills, Inc.), North Smithfield X
Western Sand & Grave), Burrillville X
SOUTH CAROLINA (04) 3 7 10
Carolawn, Inc., Fort Lawn X
SCRDI Bluff Road*, Columbia X
SCRDI Dixiana, Cayce X
Geiger (C&M Oil), Rantoules X
Independent Nail Co., Beaufort X
Kalama Specialty Chemicals, Beaufort X
Koppers Co., Inc. (Florence Plant), Florence X
Leonard Chemical Co., Inc., Rock Hill X
NATIONAL PRIORITIES LIST
471
-------
Palmetto Wood Preserving, Dixianna
Wamchem, Inc., Burton
SOUTH DAKOTA (08)
Whitewood Creek*, Whitewood
TENNESSEE (04)
Amnlcola Dump, Chattanooga
Gallaway Pits, Gallaway
Lewisburg Dump, Lewisburg
Murray-Ohio Damp, Lawrenceburg
North Hollywood Dump*, Memphis
Velsicol Chemical Corp. (Hardeman County),
Toone
TRUST TERRITORIES (09)
PCB Wastes*, Trust Territory of the
Pacific Islands
TEXAS (06)
Bio-Ecology Systems, Inc., Grand Prairie
Crystal Chemical Co., Houston
French, Ltd., Crosby
Harris (Farley Street), Houston
Highlands Acid Pit, Highlands
Motco, Inc.*, La Marque
Slkes Disposal Pits, Crosby
Triangle Chemical Co., Bridge City
Geneva Industries (Fuhrmann Energy Corp.),
Houston
Pig Road, New Waverly
United Creosoting Co., Conroe
UTAH (08)
Rose Park Sludge Pit*, Salt Lake City
VIRGINIA (04)
Cbisman Creek, York County
Matthews Electroplating*, Roanoke County
Saltville Waste Disposal Ponds, Saltville
U.S. Titanium, Piney River
VIRGIN ISLANDS (02)
VERMONT (01)
Old Springfield Landfill, Springfield
Pine Street Canal*, Burlington
WASHINGTON (10)
Colbert Landfill, Colbert
Commencement Bay, Near Shore/Tideflats,
Pierce County
NFL UpUte Total
X
X
1
X
6
X
X
X
X
X
X
1 —
8 3
X
X
X
X
X
X
X
X
X
X
X
1 —
X
— 1
4
X
X
X
X
2
X
X
10
X
— 6
11
— 4
— 2
14
NPL Update Total
Commencement Bay, South Tacoma Channel,
Tacoma X
FMC Corp. (Yakima), Yakima X
Frontier Hard Chrome, Inc., Vancouver X
Harbor Island (Lead), Seattle X
Kaiser Aluminum (Mead Works), Mead X
Lake wood, Lakewood X
Pesticide Lab (Yakima), Yakima X
Western Processing Co., Inc., Kent X
American Lake Gardens, Tacoma X
Greenacres Landfill, Spokane County X
Queen City Farms, Maple Valley X
Rosch Property, Roy X
WISCONSIN (05) — 20 20
City Disposal Corp Landfill, Dunn X
Delavan Municipal Well No. 4, Delavan X
Eau Claire Municipal Well Field, Eau Claire
City X
Janesville Ash Beds, Janesville X
Janesville Old Landfill, Janesville X
Kohler Co. Landfill, Sheboygan X
Lauer I Sanitary Landfill, Menomonee Falls X
Lemberger Transport & Recycling, Inc.,
Franklin Twp X
Master Disposal Service, Inc., Landfill,
Brookfield X
Mid-State Disposal, Inc. Landfill, Cleveland
Twp X
Moss-American (Kerr-McGee Oil Co.),
Milwaukee X
Muskego Sanitary Landfill, Muskego X
Northern Engraving Co., Sparta X
Oconomowoc Electroplating Co., Inc.,
Ashippin X
Omega Hills North Landfill, Germantown X
Onalaska Municipal Landfill, Onalaska X
Schmalz Dump, Harrison X
Scrap Processing Co., Inc., Medford X
Waste Research & Reclamation Co., Eau Claire X
Wheeler Pit, La Prairie Twp X
WEST VIRGINIA (03) 4—4
Fike Chemical, Inc., Nitro X
Follansbee, Follansbee X
Leetown Pesticide, Leetown X
West Virginia Ordance*, Point Pleasant X
WYOMING (08) 1 — 1
Baxter/Union Pacific Tie Treating, Laramie X
472
NATIONAL PRIORITIES LIST
------- |