&EPA
           United States
           Environmental Protection
           Agency
           Risk Reduction Engineering
           Laboratory
           Cmcmnati'OH 45268
EPA/540/5-89/001 a
February 1989
           Superfund
Technology Evaluation
Report SITE Program
Demonstration Test,
           Solidification,
           Douglassville,
           Pennsylvania

           Volume I
SUPERFUND INNOVATIVE
TECHNOLOGY EVALUATION

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                                         EPA/540/5-89/001a
                                         February 1989
                  VOLUME  I
        TECHNOLOGY EVALUATION  REPORT
      SITE  PROGRAM  DEMONSTRATION TEST
            HAZCON  SOLIDIFICATION
        DOUGLASSVILLE,  PENNSYLVANIA

               Stephen  Sawyer
  Enviresponse, Inc., Livingston,  NJ 07039
       EERU  Contract No.  68-03-3255
            SITE Project  Manager
               Paul de  Percin
Superfund Technology  Demonstration  Division
   Risk Reduction  Engineering  Laboratory
            Cincinnati, OH  45268
   RISK REDUCTION  ENGINEERING  LABORATORY
     OFFICE OF RESEARCH  AND  DEVELOPMENT
    U.S.  ENVIRONMENTAL  PROTECTION AGENCY
           CINCINNATI,  OHIO  45268
                              U.S. Environmental Protection Agency
                              Region 5, Library (PL-12J)
                              77 West Jackson Boulevard, 12th Floor
                              Chicago, IL 60604-3590

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                             NOTICE


The Information Is this document has been funded by the U.S.
Environmental Protection Agency under Contract No.  68-03-3255
and the Superfund Innovative Technology Evaluation  (SITE)
Program.  It has been subjected to the Agency's peer review
and administrative review and it has been approved  for
publication as a USEPA document.  Mention of trade  names or
commercial products does not constitute an endorsement or
recommendation for use.

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                                    FOREWORD
     The Superfund Innovative Technology Evaluation (SITE) program was
authorized in the 1986 Superfund amendments.  The program is a joint effort
between EPA's Office of Research and Development and Office of Solid Waste
and Emergency Response.  The purpose of the program is to assist the develop-
ment of hazardous waste treatment technologies necessary to implement new
cleanup standards which require greater reliance on permanent remedies.
This is accomplished through technology demonstrations which are designed
to provide engineering and cost data on selected technologies.

     This project consists of an analysis of Hazcon's proprietary solidifi-
cation process and represents the second field demonstration in the SITE
program.  The technology demonstration took place at a former oil reprocessing
plant which comprises the Douglassville Superfund site.  The demonstration
effort was directed at obtaining information on the performance and cost of
the process for use in assessments at other sites.  Documentation will consist
of two reports.  This Technology Evaluation Report describes the field activities
and laboratory results.  An Applications Analysis will follow and provide an
interpretation of the data and conclusions on the results and potential
applicability of the technology.

     Additional copies of this report may be obtained at no charge from
EPA's Center for Environmental Research Information, 26 West Martin Luther
King Drive, Cincinnati, Ohio, 45268, using the EPA document number found on
the report's front cover.  Once this supply is exhausted, copies can be
purchased from the National Technical Information Service, Ravensworth
Bldg., Springfield, VA, 22161, (702) 487-4600.  Reference copies will be
available at EPA libraries in their Hazardous Waste Collection.  You can
also call the SITE Clearinghouse hotline at 1-800-424-9346 or 382-3000 in
Washington, D.C. to inquire about the availability of other reports.
                 / < Si.
Margaret M. Kelly, Actifig
Director, Office of Program
 Management and Technology
Alfred W. Lindsey, Acting Director
Office of Environmental Engineering
 and Technology Demonstration

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                           ABSTRACT

    The major objectives of the HAZCON Solidification SITE
Program Demonstration Test were to develop reliable
performance and cost information.   The demonstration occurred
at a 50-acre site of a former oil  reprocessing plant at
Douglassvi11e,  PA containing  a wide range of organic and heavy
metal  contaminants.   The HAZCON process mixes the hazardous
waste  material  with  cement, a proprietary additive called
Chloranan,  and  water.  The Chloranan is claimed to neutralize
the inhibiting  effect that organics normally have on the
hydration of cement.

    The technical criteria used to evaluate the effectiveness
of the HAZCON process were contaminant mobility, based on
leaching and permeability tests; and potential integrity of
solidified  soils, based on measurements of physical and
microstructural properties.

    Extensive sampling and analyses were performed showing 1)
the concentration of the organics  were the same in the
leachates of the untreated and treated soils, 2) heavy metals
reductions  were achieved, and 3) structural properties of the
solidified  cores were found to indicate good long-term
stability.

    Cost per ton of contaminated soil at the Demonstration
Test conditions was  determined at  approximately $205.
                               i v

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                       VOLUME  I CONTENTS*

                                                        Page
Foreword	    iii
Abstract	     iv
Figures	     vi
Tables	    vii
Acknowledgments 	     ix

1. Introduction 	     1
    1.1  Background	     1
    1.2  Program Objectives 	     2
    1.3  Technology Evaluation Criteria 	     3
    1.4  Description of Operations  	     4
    1.5  Project Organization 	     5
2. Summary of Results	     6
3. Process Design	    10
    3.1  Process Description  	    10
    3.2  Equipment Specifications 	    10
    3.3  Process Scheme	    10
4. Test Site Description	    14
    4.1  Site Characteristics	    14
    4.2  Site Contamination	    17
5. Field Activities 	    27
    5.1  Operations Plan	    27
    5.2  Operating Summary  	    35
    5.3  Problems and Deviations from	
           Demonstration Plan	    42
    5.4  Material Balance 	    46
6. Sampling and Analysis Program  	    48
    6.1  Sampling Locations 	    48
    6.2  Sampling Schedule  	    48
    6.3  Sample Recovery Procedures 	    49
    6.4  Analytical Procedures  	    51
    6.5  Physical Tests	    60
    6.6  Chemical Tests	    62
7. Analytical Results 	    67
    7.1  Plant Area Results	    67
    7.2  Overall Results	    77
    7.3  Data Quality Assurance	    91
8. Discussion of Results	    95
    8.1  Analytical Results 	    95
    8.2  Operations	105
    8.3  Meeting of SITE Program Objectives	107
9. Economics	109
    9.1  Introduction	109
    9.2  Cost Elements	   110
    9.3  Overall Cost Evaluation	116
References	   119

* Volume II contains four appendices:
    Operating Log Data; Sampling and Analytical Report; a
    Consultant's Report:  Characterization of HAZCON Samples
    by Scanning Electron Microscopy, Optical  Microscopy,  and
    X-ray Diffraction; and Data Reduction Calculations

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                            FIGURES
Number                                                Page
 3.1        Flow diagram	   12
 3.2        Equipment layout diagram  	   13
 4.1        Subsurface soil, air, and groundwater
            sampling locations, Douglassville Site,
            based on RI/FS	   16
 4.2        Demonstration test sampling layout  ...   20
 5.1        Screening operations  	   29
 5.2        Soil feeding the HAZCON MFU	   30
 5.3        Slurry sampling from the MFU	   31
 5.4        Slurry containment molds  	   32
 5.5        Burying the solidified blocks  	   33
 5.6        28-Day core sampling	   34
 6.1        Sampling scheme	   50
                               VI

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                            TABLES
Number                                                Page
 4.1        Results of Polychlorinated Biphenyls
              in Soil  Analysis	   21
 4.2        Results of Base Neutral/Acid Extractables
              in Soil  Analysis	   22
 4.3        Results of Volatile Organics in Soil
              Analysis	   23
 4.4        Results of Priority Pollutant Metals
              in Soil  Analysis	   25
 4.5        Results of Oil  and Grease in Soil
              Analysis	   26
 5.1        Summary of Program Sampling 	   36
 5.2        Summary of HAZCON MFU Operating
              Conditions	   47
 6.1        Pretreatment Analyses 	   54
 6.2        Posttreatment Analyses - 7 Days	   55
 6.3        Posttreatment Analyses - 28 Days  ....   56
 6.4        Minimum Detection Limits  	   58
 7.1        Demonstration Test Results - DSA  ....   68
 7.2        Demonstration Test Results - LAN  ....   70
 7.3        Demonstration Test Results - FSA  ....   72
 7.4        Demonstration Test Results - LFA  ....   74
 7.5        Demonstration Test Results - PFA  ....   76
 7.6        Demonstration Test Results - LAS  ....   78
 7.7        Physical Properties of Untreated Soils   .   80
 7.8        Physical Properties of Treated Soils  .   .   81
                              vii

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                      TABLES  (continued)
Number                                                Page
 7.9        Chemical  Analyses of Untreated Soils  .  .    83
 7.10       Concentration of Metals in TCLP
              Leachates	    86
 7.11       Base Neutral/Acid Extractables in
              TCLP Leachates	    87
 7.12       Volatiles in TCLP Leachates	    89
 9.1        Cost Element Breakdwon	112
 9.2        Estimated Cost	117
                              vi i i

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                        ACKNOWLEDGMENTS
This document was prepared under the Superfund Innovative
Technology Evaluation (SITE) Program by Enviresponse, Inc. for
the U.S. Environmental Protection Agency under Contract No.
68-03-3255.

Enviresponse, Inc. would like to thank Mr. Paul de Percin of
the EPA, the overall Douglassville Superfund Site Project
Manager, Mr. Victor Janosik of EPA Region III, and other
contributors from the EPA's Office of Research and
Development, Office of Solid Waste and Emergency Response, and
Region III Office.

In addition, we extend our appreciation to Mr. Timothy Smith
from HAZCON Engineering, Inc.; and contributors from Radian
Corporation, and Scientific Waste Strategies, Inc.
                               IX

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                           SECTION 1

                          INTRODUCTION

1.1  BACKGROUND

In response to the Superfund Amendments and Reauthorization
Act of 1986 (SARA), the Environmental Protection Agency's
Offices of Research and Development (ORD) and Solid Waste and
Emergency Response (OSWER) have established a formal program
to accelerate the development, demonstration, and use of new
or innovative technologies as alternatives to current
containment systems for hazardous wastes.  This new program is
called Superfund Innovative Technology Evaluation or SITE.

The major objective of a Demonstration Test Program is to
develop reliable cost and performance information on
innovative alternative technologies so that they can be
adequately considered in Superfund decision making.  Common
measurement, monitoring, and evaluation guidelines and
protocols were developed by ORD and used to collect the data
and information from the demonstration.

One technology, which was demonstrated at the Douglassville,
PA Superfund Site, is the HAZCON proprietary solidification
process.  The process involves the mixing of hazardous waste
material and cement with a patented nontoxic chemical (as
claimed by HAZCON) called Chloranan.  The Chloranan is claimed
to neutralize the inhibiting effect that organic contaminants
normally have on the crystallization of cement-based
materials.  For this treatment, the wastes are immobilized and
bound by encapsulation into a hardened, leach-resistant
concrete-1ike mass.

The Douglassville site, No. 102 on the National Priority List,
is located along the Schuylkill River in Berks County,
Pennsylvania.  The site is approximately 5 miles west of
Pottstown and 11 miles southeast of Reading.  This rural
50-acre oil recovery facility includes two large lagoons once
filled with oily sludge, an oily filter cake disposal area, an
oil drum storage area, an area where generated sludge was
landfarmed into the soil, and the plant processing area.

More than 250,000 cu yd of soil is contaminated with the
following constituents:

          Oil and grease
          Polychlorinated biphenyls (PCBs)
          Toluene
          Benzene
          Xylenes

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          Phenols
          Ethyl benzene
          Tetrachloroethylene
          Base neutral/acid extractables (BNAs)
          Polycyclic aromatic hydrocarbons (PAHs)
          Heavy  metals (primarily lead)

In 1941, Berks Associates,  Inc.  began waste oil  recycling
operations at the site.   Waste generated from this process was
stored in two lagoon areas  located in the northwest and
northeast quadrants.  In November of 1970, ten days of heavy
rain caused the  overflowing of the lagoons and the breaching
of safety dikes,  releasing  two to three  million  gallons of
oily sludge.

The broken dikes  were repaired and a federal  order was issued,
stating that no  more residual oil was to be stored in the
lagoons.  Federal and State actions were taken to dispose of
the remaining oily sludge.   Before this  action could be
carried out, tropical storm Agnes occurred in June of 1972 and
caused the Schuylkill River to overflow  its banks and inundate
the entire lagoon complex.   An estimated six  to  eight million
gallons of oily  sludge were released and carried downstream
for about 15 miles by floodwaters.  During cleanup after the
storm, the lagoons were  drained and backfilled.

Berks Associates, Inc. continued the oil recycling operations
until 1979 when  the owner determined that the corrections
mandated by the  Pennsylvania Department  of Environmental
Resources (PADER) were cost-prohibitive.  Operations then
turned to refining waste oils for use as fuel in industrial
boilers.  Beginning in 1979, oily waste  sludge from the new
recycling process was landfarmed in the  area  of  the old
western lagoon.   This practice was halted in  1981 when PADER
mandated operational corrections to the  landfarm
configuration.

From September 1979 to April 1982, Berks Associates, Inc.
allowed Reclamation Resources, Inc. to store  730 drums of
solvents and wastewaters on site.  PADER found that several of
these drums were  leaking onto the surface soil during storage,
and in April 1982, the drums were removed.  Plant activities
ceased in December 1985.

1.2  PROGRAM OBJECTIVES

The major objectives of this SITE Program, utilizing the
HAZCON solidification technology at the  Douglassvi11e
Superfund Site,  were to  determine the following:

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     1.    Ability of the stabilization/solidification
          technology to immobilize the site contaminants,
          primarily polychlorinated  biphenyls (PCBs),
          volatile organics, base neutral/acid extractables
          (BNAs), oil and grease, and heavy metals (primarily
          lead).

     2.    Effectiveness of the technology for treating soil
          with contaminant concentrations varying over the
          range 1-25% by wt. oil  and grease.

     3.    Performance and reliability of the process system.

     4.    Long-term stability and integrity of the solidified
          contaminated soi1 .

     5.    Costs for applying the  technology to commercial size
          or Superfund sites.

1.3  TECHNOLOGY EVALUATION CRITERIA

The following technical criteria  were used to evaluate the
effectiveness of the HAZCON  process for immobilizing the
contaminants in the soils at the  Douglassvi1le site:

     1.    Mobility of the contaminants:

          a.   Leachability  of the contaminants and oil  and
               grease before and  after treatment
          b.   Relative permeability of the treated and
               untreated soil

     2.    Integrity of the solidified soil mass:

          a.   Unconfined compressive strength
          b.   Macro properties
          c.   Microstructural changes

The above criteria were used to develop the sampling program
described in Section 6; an explanation is provided in the
following paragraphs.

The Teachability of the metals and organics should be reduced
due to binding within the cement  structure and also due  to the
reduced  surface area of a solidified sample.  Three
Teachability tests were performed: the Toxicity Characteristic
Leaching Procedure (TCLP), which  required grinding of the
solidified treated soil, and leaching tests MCC-1P and ANS
16.1,  which simulate the solidified condition that exist after
soil  treatment.

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Relative permeability is a measure of the rate of movement of
water passing through a soil  mass, thus an indication of the
quantity of water contacting  the contaminants in the treated
and untreated soil.  Typical  unconsolidated soils have a
permeability of 10  -10"-3 cm/sec.   A reduction to 10"'
cm/sec or less would indicate that the HAZCON process produced
a highly impermeable solidified mass.

Unconfined compressive strength is an indirect measure of the
interaction of the cement-based additive with the organics in
the soil.  A low compressive  strength may be indicative of
inhibition of the normal setting reactions.

Treated soil integrity is a qualitative factor related to
internal fracturing within the solidified mass, and measurable
by the ability to survive freeze/thaw and wet/dry weathering
cycles, and to maintain physical integrity over time.  Since
freeze/thaw and wet/dry weathering tests were performed on the
solidified soil samples, followed  by unconfined compressive
strength tests, some quantitative  measure was obtained on
long-term treated soil integrity.   In addition, a long-term
monitoring program exists to  provide input on the integrity of
the solidified blocks over a  five-year period.

Solidified hazardous wastes are multiphased materials whose
microstructure influences their leaching behavior and
long-term stability.  Since pozzolanic setting reactions are
complex, it is important to characterize the microstructure to
identify potential durability problems.  Small-scale
non-homogeneities or porosity could lead to degradation of
mechanical properties over time and allow the release of
contaminants.  Treated soil samples were characterized by
using scanning electron microscopy (SEM) and x-ray
diffraction.  These techniques provided information about
specimen porosity, uniformity and  degree of mixing, mineral
content, degree of hydration  of the cement, and the presence
of unaltered waste material.

1.4  DESCRIPTION OF OPERATIONS

Contaminated soils from six plant  areas were processed by the
HAZCON Mobile Field Blending  Unit  (MFU).  Sufficient feedstock
was utilized from five areas  to produce from each 5 cu yd of
treated soil and from the sixth area to produce 25 cu yd.  The
purpose of the latter extended run was to obtain information
on equipment reliability.  The six areas, whose locations are
shown in Figure 4.2, are defined as follows:

Drum Storage Area         DSA                 5 cu yds
Lagoon North              LAN                 5 cu yds
Filter Cake Storage       FSA                 5 cu yds
 Area
Landfarm Area             LFA                 5 cu yds
Plant Facility Area       PFA                 5 cu yds
Lagoon South              LAS                25 cu yds

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The process Involves the blending of the contaminated soil,
cement, water, and the proprietary additive Chloranan.  All
soil feedstocks were taken from the top 12 inches of soil,
with the exception of LAN, where the feed was excavated from a
depth of 1-2 feet.  The soil  then was screened to remove rocks
and debris greater than 3 inches in diameter.  Utilizing a
front-end loader, the soil was brought to the MFU where it was
fed to the waste bin hopper.   A cement feed hopper,
intermittently fed from an on-site cement truck, also was
mounted on the MFU.  Chloranan and water were provided from
tanks on a support vehicle.   The four components were blended
in a 9-in diameter mixing screw.  For the five shorter runs,
the blended slurry was fed to five 1-cu-yd wooden molds.  For
the extended run, the slurry was fed to two large pits, each
8 ft x 16 ft x 3 ft, and three 1-cu-yd molds.

During feedstock processing,  the excavation holes were
enlarged to accommodate burial of treated blocks that have
grown in size by approximately 100%.  Before the blocks for a
particular feedstock were buried, the hole was lined with
plastic to prevent seepage in of contaminated water, and a
1-ft layer of clean soil was deposited.  After the blocks were
placed in the excavation hole, additional clean soil was added
to cover the blocks.  Stakes were planted to identify the
location of each block.

Untreated soil samples from 12 parts of each feedstock were
collected and composited for analysis.  Slurry samples were
collected for analysis after 7 days of curing.  Finally, core
samples, after they had cured for more than 28 days  in the
field, were taken from the same blocks as the slurry samples.

1.5  PROJECT ORGANIZATION

For the SITE Program Demonstration a Cooperative Agreement was
signed between EPA and HAZCON, Inc.  HAZCON was responsible
for operating their equipment and providing the chemical
additives.  EPA, through its contractor, Enviresponse, Inc.,
prepared the Demonstration Plan, performed the test  site
preparation, arranged for the sampling and analyses, evaluated
the data, and prepared the Technology Evaluation Report.

Enviresponse utilized the services of Radian Corporation for
the sampling and analysis work.  Radian is headquartered in
Austin, TX, with additional  laboratory facilities in Perimeter
Park, NC and Sacramento, CA.   In addition, Enviresponse
employed Scientific Waste Strategies, Inc. (SWS) of  Baton
Rouge, LA both as consultant and to perform the
microstructural studies.  SWS consists of three Louisiana
State University professors with expertise in hazardous waste
treatment utilizing cement-based stabilization/solidification
processes.

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                           SECTION 2

                      SUMMARY OF  RESULTS
The program obtained a large amount of analytical  and
operating data and was able to meet the five objectives
described in Section 1.2.   A summary of the results,  which
respond to the program objectives,  are summarized  below.

    1.   The six plant areas offered a wide range  of feeds.
         The oil and grease levels  ranged from 1-25% by wt.,
         and polychlorinated biphenyls (PCBs)  were detected  up
         to 52 ppm by wt.   High concentrations of  lead (up to
         23,000 ppm by wt.) were measured along with lower
         levels of chromium and zinc.  Volatile organic
         concentrations in excess of 100 ppm by wt.  and
         semivolatiles, particularly phenols,  at soil
         concentrations in excess of 500 ppm by wt.,  were
         measured at FSA.   For the  other five areas the total
         concentration for volatile organics and semivolatiles
         combined was less than 100 ppm by wt.

    2.   The volume of the solidified soils upon treatment
         increased by approximately 120%, at feedstock
         moisture levels up to 25%, the maximum measured at
         the site.  HAZCON can reduce the volume increase by
         optimizing the quantity of additives.  However,  other
         physical and chemical properties of the treated soil
         may change.

    3.   The unconfined compressive strengths of the
         solidified cores ranged from 220-1570 ps1, and the
         values were inversely related to the level of oil and
         grease.  These are quite satisfactory levels from a
         structural strength viewpoint.

    4.   Permeabilities of the solidified soils were very low,
         10'8-10'9 cm/sec, which is well below the 10''
         cm/sec value that is considered in the hazardous
         waste disposal industry to be acceptable  for soil
         barrier 1i ners.

    5.   The weathering tests showed only small losses in
         weight for both the test specimens and controls,
         about  1% by wt.  Unconfined compressive strength
         tests  performed on the weathered test specimens and
         controls showed values equivalent to those obtained
         for the standard test specimens described in item 3.

    6.   The TCLP leaching tests of the  solidified soils

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indicated very low levels of metals,  volatiles, and
semivolatiles in the leachates.   Essentially all
values were below 1 ppm.

For the metals,  lead is the predominant component.
The leachate concentrations for  all  but DSA for
untreated soil was 20-50  mg/1.   For  treated soils
this was reduced below 100 ug/1.

For volatile organics, the leachate  concentrations
were primarily in the range of   50-1000 ug/1,  in both
the untreated and treated soils.

The leachate concentrations of  BNAs  were equivalent
for untreated and treated soils.   Various phenols
were the primary contaminant with concentrations
ranging as high  as 3-4 mg/1 for  FSA.

Oil and grease leachate concentrations were greater
for each of the  treated soils  compared to the
untreated soils.  The treated  soil  values were
typically 2-4 mg/1, for soil concentrations
approximately 40% of that of the  untreated soil,
while the untreated soil  was less than 2 mg/1.

Leaching tests ANS 16.1 and MCC-1P were each
performed on one treated  soil  sample  from each area
except DSA and LFA.  Experience  with  these tests on
hazardous wastes is limited.  Comparisons to the
treated soil TCLP results are  made,  but the
significance of  any differences  is unclear.  The
results from these leach  tests  are as follows:

o    Metals

         MCC-1P  produced  leachate concentrations
         greater than TCLP concentrations.  ANS 16.1
         results were comparable  to  the TCLP extracts
         from treated soil cores.
         Concentrations increased with time interval
         of leaching.

o    Volatile Organics (VOC)

         MCC-1P  leachates had  larger  VOC contents
         then ANS 16.1 leachates  and  were comparable
         to the  TCLP leachates.
         Discernible trends of  concentration versus
         leach time ( 3 to 28  days)  were not
         observed.

o    Base Neutral/Acid Extractables  (BNAs)

         MCC-1P  leachates had  greater BNA

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              concentrations than ANS 16.1 leachates and
              were comparable to TCLP leachates.
              Leachate concentrations for the phenols,  the
              predominant BNA in a few of the samples,
              appeared to increase with time (3 to 28
              days) in MCC-1P but not in ANS 16.1.

     These results showed that the concentrations of the
     various analytes in the leachates, from uncrushed
     core samples, are approximately equal to that from
     the TCLP leach test.  They also confirm the  trends
     seen from the TCLP leach test on contaminant
     mobility.

8.   Polychlorinated biphenyl concentrations in all
     leachates, whether for treated or untreated  soils,
     were below the detection limits of 1 ug/1.

9.   Microstructural analyses are proven methods  for
     understanding the mechanisms of structural
     degradation of soil, cements, and soil-cement
     mixtures and each of these with inorganic  and organic
     compounds.  However, there has been relatively few
     studies of the microstructure of complex waste/soil
     mixtures like those resulting from
     stabilization/solidification procedures.
     Consequently, in some cases, interpretation  of
     microstructural observations may be difficult.  The
     microstructural analyses showed the following:

          o   The contaminant immobilization appears to
              show that encapsulation is a major  part of
              the mechanism of solidification/
              stabilization.  This is supported by the
              facts that 1) brownish aggregates passed
              through the soil unchanged, and 2)  peaks  in
              the x-ray diffraction patterns for  both the
              soil and cores could not be identified with
              any expected minerals.
          o   The solidified soils and buried blocks (28-
              day), were very porous.
          o   The mixing of the four process components,
              soil, cement, Chloranan, and water, was not
              highly efficient.  Four factors support
              this:  1) brownish aggregates do  not
              disaggregate, 2) there is more than expected
              unhydrated cement, 3) there are globules  of
              dark colored material in the cores, and 4)
              there are many pores.

10.  The operations for the first five runs  (5 cu yd)
     required many startups due to unscheduled shutdowns
     caused primarily by plugging in the  soil feed screw.
                           8

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     In addition, the consistency of the slurry mix was
     quite variable, running the gamut from powdery to a
     very thin slurry.  However, physical property changes
     due to this variation were not observed.  For the
     extended time run (25 cu yd) at LAS, operation was
     more uniform, with only a few short-term outages.

11.   The economic analsyis was based on the 70% on-stream
     factor and a 300 Ib/min operating capacity observed for
     the HAZCON Mobile Field BLending Unit.   A cost of
     $205/ton was calculated during the Douglassville, Pa.
     demonstration.   The process is very intensive in labor
     and chemical additives,  with these items amounting to
     approximately 90% of the total costs.   Substantial cost
     reductions are expected with process and chemical
     optimization.

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                           SECTION 3

                         PROCESS DESIGN

3.1  PROCESS DESCRIPTION

HAZCON,  Inc.'s Mobile Field Blending Unit (MFU)  is a
continuous processing unit and operates as shown in the flow
diagram,  Figure 3.1.

Operating capacities, though governed by predetermined mix
ratios set in the laboratory,  are  variable up to 15 cu yd of
processed raw waste per operating  hour.  The MFU has no
external  utility requirements   other than a standard water
hookup and the attachment of a "quick connect" line from a
bulk cement carrier.

The MFU  accepted soil feedstock from a front-end loader to the
onboard  waste bin.   The soil was fed by a variable-speed
calibrated 8-in diameter feed  screw to the 9-in  diameter screw
blender.   Simultaneously, cement from a second MFU storage bin
was also  fed by a variable-speed screw feeder to the blender.
The water and Chloranan, from  auxiliary vehicle  tanks, were
pumped at controlled  capacities to the inlet of  the blender
for blending with the soil and cement.  The mixed slurry was
then fed  to containment molds  for  solidification into blocks.

Equipment calibration was performed each time a  new waste feed
matrix entered the MFU.  Calibration involved the
determination of the  waste feed rate by weight,  then setting
the cement and Chloranan rates at  appropriate ratios to the
contaminated soil.   Water was  added as required.

3.2  EQUIPMENT SPECIFICATIONS

Bin, tank, auger sizes, and component locations  are shown on
the attached equipment layout  diagram, Figure 3.2.

A separate bulk cement carrier was provided for  feeding to the
cement bin on the equipment trailer carrying the MFU.  A water
supply truck was provided for  process water and  for feeding
high pressure equipment decontamination water.  In addition,
Chloranan was supplied from a  tank on the auxiliary trailer
provided  by HAZCON.

Photographs of the equipment at various process  stages are
shown in  Figures 5.1-5.6.

3.3  PROCESS SCHEME

The following steps are illustrated in Figure 3.1.


                               10

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o    Waste material  was introduced to the system through the
     use of earth moving equipment.

o    The waste was moved through the process in a controlled
     flow, allowing  for precise measurement of the material.
     The contaminated soil  was fed to the mixer by a
     calibrated screw feeder.

o    Based upon these measurements,  blending ratios, which
     were predetermined by  HAZCON, were set on a time-weighted
     basis for both  the Chloranan and a pozzolanic material
     such as No.  1 Portland cement.

o    The pozzolanic  ingredient was stored in a hopper and then
     metered into the mix by a calibrated screw feeder.
     Typical waste-to-pozzolan ratios,  on a weight basis,
     range from 1:1  to 3:1.  For the test at the Doug!assvi11e
     site, a 1:1  ratio was  used.

o    Chloranan was stored in a holding  tank, then pumped into
     the mixing chamber.  Through precise control of the flow
     rate, ratios of waste  to  Chloranan can be accurately
     metered from a  10:1 to a  50:1 blend.  For the
     Demonstration Test, the ratio was  approximately 10:1.

o    After initial combination of the primary ingredients,
     water was added as necessary to achieve the most
     desirable slump on the mix, based  upon visual inspection
     by HAZCON.

o    For the three soil feeds  that were spiked with toluene
     the injection point was at the  inlet of the blending
     auger.

o    All additives were fed via pump or auger through a  mixing
     chamber to achieve a homogenous blend.

o    The resultant mass was extruded into either temporary or
     permanent molds.
                               11

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     POZZOLANIC
     ADDITIVE
                A
                        WATER
              ir*YT*nifci f\ \r  _
METERING.
 DEVICE]
                               BLENDING
                               PROCESS
                        TOLUENE |
     CHLORANAN
     ADDITIVE
TREATED
OUTPUT
Figure 3.1.   Flow diagram.
                              12

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                           SECTION 4

                     TEST SITE DESCRIPTION

4.1  SITE CHARACTERISTICS

The Doug!assville site is located in a rural  setting
surrounded by croplands and light residential  and industrial
development.   The Schuylkill  River borders the site to the
north and to  the east.  This  stretch of the river lies within
the boundaries designated by  the Pennsylvania  Scenic Rivers
Act of 1972 and  is a component of the Pennsylvania Scenic
Rivers System.  It is required that the quality and quantity
of the river  and adjacent waters be adequate  for recreation
and fish propagation.

EPA Region III sampling in April of 1982 found groundwater
contaminants  in  the oil reprocessing facility  drinking water
well.  These  contaminants included 1,2-trans-dichloroethylene,
trichloroethylene,and 1,1,1-trichloroethane.   Compounds such
as trichloroethylene and  benzene were found in an on-site
drainage swale.   Lead and PCBs were found in  on-site
sediments.

The two wastewater settling lagoons, located  on approximately
seven acres of the site,  were drained and backfilled after the
major flooding in 1972.  The  remaining oil and solvent-stained
surface soils in the oil  processing area and  the oily sludge
in the backfilled lagoons potentially may cause three major
environmental results:

    o    Contamination of groundwater aquifers through the
         migration and infiltration of hazardous substances

    o    Toxic effects to people and the environment through
         contact with contaminated surface water runoff or
         through consumption  of contaminated  groundwater

    o    Contaminant loading  of the Schuylkill River via
         surface water runoff, flooding, or groundwater
         di scharge

Understanding the geology at  the site is required to determine
the routes by which contaminants may migrate.   Geologic
features that influence the flow of groundwater in
unconsolidated materials  and  bedrock aquifers  are of concern.
The character and distribution of soil types  also is
significant in determining whether contaminants are retained
on site or are transmitted into the general environment.
                               14

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The Douglassville Superfund Site is situated in the Triassic
Lowland section of the Piedmont Province.  It includes a
Triassic section many thousands of feet thick.   The rocks
range from shales to coarse limestone conglomerates.
Groundwater flow is controlled by secondary permeability;
water flow takes place along joints, faults, and especially
bedding planes.  Transmissivity ranges from 500 to 1000
gallons per day per foot (gpd/ft).  The groundwater within the
area is of calcium bicarbonate type, ranging from moderately
hard to very hard.  Total dissolved solids are  about 300 ppm.

Groundwater and geological  investigations at the site were
obtained during a Remedial  Investigation/Feasibility Study
(RI/FS) [1], which consisted of drilling 25 boreholes at 13
locations.  At each of the 13 drill sites a deep and a shallow
well were completed so that groundwater in the  overburden and
the bedrock could be observed.  The deep wells  penetrated
40-50 feet below the surface and the shallow wells penetrated
10-20 feet.  In addition, test pits were excavated to obtain
additional subsurface data.  See Figure 4.1 for the locations
of these initial borings and excavations.  As of May 1988,
there is another RI/FS in progress.

Site geology generally consists of 10 to 20 feet of
overburden, made up of topsoil, alluvium, waste material, and
backfill material in overlying lagoon areas.  Underlying
bedrock is composed of red shale, siltstone, and some fine
sandstone.  Groundwater flows in a north to northeast
direction toward the Schuylkill River.  Transport through
groundwater is potentially the most significant mechanism of
contaminant migration at the Douglassville Superfund Site.

Water level data provide a picture of the groundwater regime.
Data were collected in August and September, 1984, and in
March and January, 1985.  Water levels in all wells generally
declined 3 to 4 feet over the September to January monitoring
interval, and rose between 0.5 and 2.4 feet by  March 1985.

Despite these fluctuations  in water levels, the highest
measured water level elevations indicate that the groundwater
may not reach the known lower depths of subsurface waste
materials.

Permeability of subsurface  materials affects the rate of
groundwater movement.  The  alluvial materials at the site
range in permeability from 1.8 x 10"^ centimeters/second
(cm/sec) to 1.3 x 10"z cm/sec.  This range represents
average values determined from five of the alluvial wells, and
is characteristic of fine to coarse-grained unconsolidated
material.
                               15

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Permeability values measured within the Triassic bedrock
differ greatly, supporting the theory of highly variable
permeability in a fracture-dominated aquifer flow system.
These values ranged from 2.8 x 10"1 to 5.2 x 10"b cm/sec.
The higher permeability value apparently reflects a high
fracture/joint flow conduit located centrally in the site,
beneath the former sludge lagoon area.  Other high
permeability values within the bedrock are found in the area
of the oil processing facility.   The lowest value appears to
be at the eastern area of the site.  The alluvial (overburden)
material was generally more transmissive of water than the
bedrock at each site.  The highest transmissivity was 6600
gpd/ft and the lowest in the siltstone and shale was 80
gpd/ft.

4.2  SITE CONTAMINATION

The Douglassvi11e Superfund Site covers approximately 50
acres.  Seven acres of the site  were formerly used as two
lagoons, Lagoon North (LAN) and  Lagoon South (LAS), to settle
wastewater sludge generated by the facility's oil recycling
process.  After the flood in 1972, both lagoons were drained
and backfilled.  One of the former lagoons, located in the
northwestern corner, is in an area where oil sludge was
landfarmed (LFA) from 1979 through 1981.  This area was
unsuccessfully used for agricultural purposes between 1981 and
1984.  The second lagoon was located in the northeastern
corner of the site.

Located in the southern portion  of the site are the recycling
facility and office buildings (southwest).  This is referred
to as the Plant Facility Area (PFA).  Just east of the PFA is
a one acre area filled about 6-8 ft deep with oily filter
sludge.  This is called the Filter Sludge Storage Area (FSA).
To the south, near the drainage  ditch, is an area that was
used for the storage of hundreds of drums of oil and oily
water.  This area is referred to as the Drum Storage Area
(DSA).  The drainage ditch flows into the Schuylkill River,
which borders the northern and eastern sections of the site.

Relevant environmental media, i.e., air, surface water,
surface soil, subsurface soil, soil screening, and
groundwater, were sampled and analyzed to chemically
characterize the site.

4.2.1  SURFACE SOIL

RI/FS data reveal that surface soil at the Douglassvi11e Site
is contaminated with PCBs, phthalate esters, polycyclic
aromatic hydrocarbons (PAHs), pesticides, various volatile
organics, and trace elements.


                              17

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PCBs were detected in 11 of 16 surface soil  samples.
Concentrations of PCBs generally ranged from 38 micrograms per
kilogram (ug/kg) to 24,000 ug/kg,  except for one location in
the filter cake storage area,  which had PCB  concentrations of
500,000 ug/kg.

PCBs were thus identified in soil  samples from most areas of
the site.  The known environmental  behavior  of the PCBs leads
to the conclusion that the occurrence of PCBs at these
locations is probably attributable  to direct deposition,
migration by erosion of contaminated soil particles,  and
possibly to spills or drum leakage.

Various phthalate esters were  identified in  9 of 16 surface
soil samples.   Concentrations  of these compounds ranged from
170 ug/kg to 9,100 ug/kg.

The phthalate  esters identified in  soil samples were  detected
in areas where wastes were deposited, i.e.,  the former lagoon
and landfarming areas, or where spills or leakage from drums
may have occurred.

PAHs were identified in 2 of 16 surface soil samples.
Concentrations of these compounds  ranged from 93 ug/kg to 260
ug/kg.  Thus,  the contamination with these compounds  is not
extensive.

Volatile organic substances were identified  in all surface
soil samples at concentrations ranging from  51 ug/kg  to 550
ug/kg.  Volatile contamination of  surface soil is not
extensive.

Of the trace elements identified in site soil, arsenic,
cadmium, chromium, lead, and mercury are of  concern because of
their known toxicity to human  and  environmental receptors.
Concentrations of these elements encountered in site  surface
soil are quite low, except for lead, which is as high  as
14,000 ppm.

4.2.2  SUBSURFACE SOILS

Subsurface soil samples were obtained from a number of the
test pits excavated at the site.  Subsurface soil
contamination  generally reflects the contamination detected in
surface soil samples, although higher concentrations  of
volatile contaminants were identified.  Test pits located in
the former northeastern lagoon area, the northwestern  area,
and the northeast corner of the production facility were
contaminated with lead, PCBs,  and  phthalate  esters.

Three potential migration routes for subsurface soil
contaminants have been identified:
                               18

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     o    Infiltration of contaminants into the water table

     o    Subsequent convection of contaminants with flowing
          groundwater

     o    Convection to the surface with volatilizing organic
          compounds or other generated gases

4.2.3  SOIL SCREENING SAMPLES

Soil  samples were taken in May of 1987 by Enviresponse Inc.
[2] to chemically characterize the six areas proposed as
feedstocks for the Demonstration Tests.   Their locations are
shown in Figure 4.2.  The samples were taken from the top 12
inches of soil, except at LAN where the  sample was taken at a
depth of 1-3 feet.  The feedstock location for the filter cake
storage area was subsequently changed due to the inability of
the filter cake to support the weight of the mechanical
equipment required for excavation and sampling.  The locations
selected were near the highest contamination levels reported
in the RI/FS.  Where comparisons of the  results to the RI/FS
could be made at the two lagoons and the oily filter cake
storage area, the results agreed with the RI/FS.  The results
are provided in Tables 4.1 - 4.5, showing that the
concentration levels of volatile organics, BNAs, and PCBs are
quite small, a few parts per million.  These values are
significantly less than the soil analyses taken during the
Demonstration Test, which showed VOC concentrations up to 150
ppm and BNAs up to 500 ppm by weight.

4.2.4  SUMMARY

Based on the operational history of the  site, as described in
the RI/FS, with the placement of wastes  in lagoons and sludge
impoundments, subsurface soil was expected to show the
greatest degree of chemical contamination and to represent the
largest potential source for contamination of groundwater at
the site.  The occurrence and distribution of organic and
inorganic substances confirmed the extensive contamination in
subsurface soil samples obtained from the sludge disposal
areas.
                              19

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 TABLE 4.1.  RESULTS OF POLYCHLORINATED BIPHENYLS IN SOIL ANALYSIS
                    .      Concentration             Concentration
Sample Designation^3'      Aroclor 1260              Aroclor 1248
                             (mg/kg)                   (mg/kg)
LAN
LFA
LAS
PFA
DSA
-------
     TABLE 4.2.  RESULTS OF BASE NEUTRAL/ACID EXTRACTABLES IN SOIL ANALYSIS
    BNA
DSA
FSA
SAMPLE DESIGNATION

LAN     LAS     LFA
PFA
NAPHTHALENE                     ND      ND
FLUORENE                        ND      ND
FLUORANTHENE                    ND      ND
PYRENE                          ND      ND
BIS (2-ETHYLHEXYL) PHTHALATE    ND      ND
BENZO (K) FLUORANTHENE          ND      ND
                 ND      ND      ND      ND
                 ND      ND      ND      ND
                 ND      ND      ND      ND
                 ND      ND      ND   [8.68]
                210*     ND   [9.62]     ND
                 ND      ND      ND   [10.2]
*  Sample concentrations reported in mg/kg of soil.

ND denotes not detected.  Bracketed values are approximate because the
concentration was below the level of quantification  (LOQ).
                               22

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          TABLE 4.3.  RESULTS OF VOLATILE ORGANICS IN SOIL ANALYSIS
        VOC
LFA
FSA
DSA
LAN
PFA
METHYLENE CHLORIDE               ND
1,1-DICHLOROETHENE               ND
1,1-DICHLOROETHANE               ND
TRANS-1,2-DICHLOROETHENE         ND
CHLOROFORM                       ND
1,2,-DICHLOROETHANE              ND
1,1,1-TRICHLOROETHANE            ND
CARBON TETRACHLORIDE             ND
BROMODICHLOROMETHANE             ND
1,2-DICHLOROPROPANE              ND
TRANS-1.3-DICHLOROPROPENE        ND
TRICHLOROETHENE                  ND
BENZENE                          ND
DIBROMOCHLOROMETHANE*            ND
1,1,2-TRICHLOROETHANE*           ND
CIS-1.3-DICHLOROPROPENE*         ND
BROMOFORM                        ND
1,1,2,2-TETRACHLOROETHANE*       ND
TETRACHLOROETHENE*               ND
TOLUENE                          ND
CHLOROBENZENE                    ND
ETHYL BENZENE                    ND
TOTAL XYLENES                    ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
         3800(a)    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
          ND       ND
          ND       ND
          ND       ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
         5600
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
        [700]
          ND
          ND
          ND
        [1200]
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
          ND
                                 (continued)

(a)  Sample concentrations reported in ug/kg  of soil.

* - Denotes co-eluting compounds.

ND denotes not detected.   Values in brackets  are below the limit of
quantification and considered approximate.
                              23

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                            TABLE 4.3 (continued)
        VOC                     LAS      LAS
METHYLENE CHLORIDE               ND       ND
1,1-DICHLOROETHENE               ND       ND
1,1-DICHLOROETHANE               ND       ND
TRANS-1.2-DICHLOROETHENE         ND       ND
CHLOROFORM                       ND       ND
1,2,-DICHLOROETHANE              ND       ND
1,1,1-TRICHLOROETHANE          [460]    [500]
CARBON TETRACHLORIDE            2900     2900
BROMODICHLOROMETHANE             ND       ND
1,2-DICHLOROPROPANE              ND       ND
TRANS-1.3-DICHLOROPROPENE        ND       ND
TRICHLOROETHENE                 3100     3500
BENZENE                          ND       ND
DIBROMOCHLOROMETHANE*            ND       ND
1,1,2-TRICHLOROETHANE*           ND       ND
CIS-1,3-DICHLOROPROPENE*         ND       ND
BROMOFORM                     [1400]   [2100]
1,1,2,2-TETRACHLOROETHANE*       ND       ND
TETRACHLOROETHENE*              4100     4600
TOLUENE                         4100     3000
CHLOROBENZENE                    ND       ND
ETHYL BENZENE                   2700     3500
TOTAL XYLENES                  12000    14000
                               24

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TABLE  4.4.   RESULTS  OF  PRIORITY  POLLUTANT  METALS  IN  SOIL  ANALYSIS
  HETAL              FSA         LFA        LAS         LAN         PFA         DSA
Hg
As
Se
Cd
Zn
Sb
Be
Ni
Pb
Cu
Tl
Cr
Ag
ND (5.0)
[52.]
ND (50.)
ND (5.0)
170.
300.
ND (0.5)
[8.3]
4900.
120.
ND (2.5)
[19.0]
ND (5.0)
ND (5.0)
ND (50.)
ND (50.)
ND (5.0)
870.
140.
[1.0]
29.
6500.
120.
ND (2.5)
40.
ND (5.0)
[13.]
ND (50.)
ND (50.)
ND (5.0)
760.
240.
[0.5]
31.
9400.
170.
ND (2.5)
99.
ND (5.0)
[12.]
[66.]
ND (50.)
ND (5.0)
250.
400.
[0.5]
19.
8300.
68.
ND (2.5)
120.
ND (5.0)
36.
[65.]
ND (50.)
[11.]
1800.
650.
[1.0]
75.
16000.
510.
ND (2.5)
130.
ND (5.0)
18.
[63.]
[82.]
ND (5.0)
98.
320.
ND (0.5)
36.
8600.
160.
ND (2.5)
64.
ND (5.0)
  Results in ug/gm (dry weight)

  ND denotes not detected.  Values in () represent detection limit.   [] denotes values below the lower limit
  of quantification (LOQ).
                                         25

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    TABLE 4.5.  RESULTS OF OIL AND GREASE IN SOIL ANALYSIS
      SAMPLE                               CONCENTRATION
                                             (ug/g)
      DSA                                     23,000  (a)
      FSA                                    317,000  (b)
      LAN                                    358,000
      LAS                                    126,000
      LFA                                     76,800
      PFA                                     54,200
(a)  denotes  average  of 5  analyses.

(b)  denotes  average  of 2  analyses.
                               26

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                           SECTION 5

                        FIELD ACTIVITIES

The plans for the Demonstration Test are described in section
5.1.   A summary of the actual  operations is described in
section 5.2.  The few operational  deviations from the
Demonstration Plan are discussed in Section 5.3, along with
some  additions to the analytical testing program that were
incorporated into the Program while at the site.

5.1 OPERATIONS PLAN

The overall  operating procedure started with excavating the
contaminated soil from the predesignated areas.   These areas
are illustrated on Figure 4.2.   The feedstock was taken from
the top 12 in, except at LAN where it was taken  1-3 feet below
the surface.  The soil then was screened to minus 3 in and
transferred  to the HAZCON unit by a front-end loader, with a 2
1/4 cu yd bucket.  Two 12-part composite samples were taken
from  the bucket.   The soil then was ready for feeding into the
HAZCON Modified Field Blending Unit (MFU).

Before the start  of each run,  the soil, cement,  and additive
feed  systems were calibrated and set to the proper rates.
During the actual test, equipment operating data was taken.

During operation, slurry samples were taken in a long handled
stainless steel pot.  Since five 1-cu-yd molds were to be
filled on all but the LAS run,  samples were to be taken for
blocks 1, 3, and  5 (deviations occurred - see section 5.2).
Figure 6.1 shows  the planned sampling scheme.

Soil  excavations  and soil sizing were performed  on the same
day that the soil was processed in the MFU.  This was done to
minimize loss of  organic volatiles.

While the soil was being processed and cured, the excavation
was enlarged to accept the cured blocks, with each pit at a
depth of 4-5 feet.  A nonporous plastic liner was placed in
the pit covering  the entire bottom and sides, and a 12-inch
layer of clean fill was deposited on top of the  liner.  The
solidified blocks were returned to the respective excavation
holes 48-96  hours after treatment, and then the  entire
excavation area was back-filled with clean soil  and
identification stakes were placed over each block.  The excess
contaminated soil was spread in the immediate area, but well
outside the  lined excavation zone.

After curing for  28+ days, core samples were taken from the
same  blocks  from  which the slurry samples were collected, so
that  a known batch of slurry could be tracked.  It is the

                               27

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intent of the Long Term Monitoring Plan to sample the
surrounding clean soil  to obtain a measurement of contaminants
that may be leaching from the solidified blocks.

For the 25-cu-yd test,  the three excavation holes for the
treatment slurry were not located where the feedstock was
taken.  Since wooden molds (8 ftx!6 ft) had to be fabricated
and installed in the excavated holes to contain the slurry,
the three excavation holes were dug to the northeast (Lagoon
South) of the soil feedstock location two to three days before
the test.  The contaminated soil from the excavation holes was
spread to the east of the excavation holes but still in LAS.

It had been anticipated that either two or three  feedstocks
per day would be processed.  Between each feedstock treatment,
the HAZCON MFU would be moved to the decontamination area at
the northwest end of Lagoon South.  The blending  equipment
would be flushed with high pressure water that would be
allowed to drain onto the ground.  Care would be  taken to
prevent the decontamination water from contaminating the
Lagoon South feedstock.  It was expected that the actual
processing of each 5-cu-yd feedstock batch at the MFU would
take 30-60 minutes.  However, due to some minor operational
problems only two feedstocks could be processed in a day.
This is discussed in Section 5.3.

The 25-cu-yd test, originally intended to use feed from the
Filter Cake Storage Area, but subsequently taken  from Lagoon
South, provided a more extended test run.  For this test, the
MFU was relocated closer to the feedstock source, near the
decontamination area, as shown in Figure 4.2.  The product
slurry (except for three 1-cu-yd blocks) was returned directly
to the excavation by a cement pump discharging through a 4-in
diameter hose, both provided by HAZCON, Inc.  The product feed
rate was about the same as for the 5 cu yd tests.

Allowing 1 day for setup and 1 day for demobilization, the
entire operational test period was expected to be 5 days.
Actually the operation lasted 4 days.  However, HAZCON
demobilized on the last operating day, and the total test
program time at Douglassvi11e, exclusive of site  preparation
which included burying and covering the test blocks, was 5
days as planned.

Photographs from the operation and sampling work are shown  in
Figures 5.1-5.6.

Information was logged in a notebook to report the sampling
operations and the overall operations at the site.  This
included the following:

    o    Notes on daily preparations of HAZCON and EPA

    o    Problems
                               28

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33

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Figure 5.6.   28-day core sampling.
                             34

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     o    Health and Safety related procedures,  meetings, and
          concerns

     o    Chronology and summary of daily activities.  This
          includes check-in and check-out of all  personnel

     o    Sampling logs of Sampling and Analysis  contractor

     o    Weather conditions

     o    Li st of vi si tors

5.2  OPERATING SUMMARY

Work at the Douglassvi11e site commenced on October 5 and was
completed on October 20, 1987.  The Demonstration Tests
occurred on October 13-16, 1987.  The six working days before
the actual  tests involved site preparation and equipment
setup, and  the two working days after completion  of the
Demonstration Test were used to return the Douglassvi11e site
to the Pre-Demonstration Test condition.  Highlights of the
site preparation, operation, and posttreatment sampling are
described below.  A summary of the sampling program appears in
Table 5.1.

5.2.1  SITE PREPARATION

October 5-9 -- During this week, prior to the Demonstration
Test, the site was prepared.  This included the  following:

     o    Clear area of vegetation to Lagoon South and Drum
          Storage.

     o    Set up mobile equipment and tools to prepare site
          and assist Demonstration Test operations.

     o    Laying a gravel road to and preparing  a 50x50 ft
          area at Lagoon South to provide an equipment
          decontamination area.  Also provide an  area for
          HAZCON to set up their equipment for the 25-cu-yd
          run on Lagoon South feedstock.

     o    Set up trailer and personnel sanitary  facilities.

     o    Obtain diesel generator to power trailer and area
          1ighti ng.

     o    Build an observation platform next to  the trailer
          for visitors  to witness the operations.

     o    Obtain water  supply truck to be used for process
          water supply  and equipment decontamination.

     o    Stake out exact areas to be sampled during Program.


                               35

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               TABLE: 5.1.   SUMMARY OF  PROGRAM SAMPLING
Sampling
Date location
10/13/87 DSA




10/14/87 LAN
10/14/87 FSA
10/15/87 LFA
10/15/87 PFA



10/16/87 LAS
Test Blocks Time, hrs
Produced Sampled Start/stop Comments
4 1,3 1430/1815 Losing daylight -
last block cancelled
by consent of HAZCON/
EPA. Toluene
injected.
5 1,3,5 1136/1201
5 1,3,5 1645/1703
5 1,3,5 1059/1144 Toluene injected
4 1,2,3 1617/1817 Fifth block cancelled
due to loss of
daylight. Toluene
injected.
5 SM2, LM1 1309/1645 Extended time run
LM 2A, Produced three - 1 cu
*
LM 2B. yd blocks plus two -
LM 2C 12 cu yd blocks
* Three samples taken from final 12 cu yd block poured.
                                            36

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5.2.2  OPERATIONS

October 12 -- Day 1 was utilized by Enviresponse for final
site preparations before commencement of testing.  HAZCON,
Inc. and Radian Corporation, the Sampling and Analytical
contractor, arrived and started their preparations.  The tasks
of the various parties included:

     o    Setting up of the HAZCON Mobile Field Blending Unit.

     o    Sampling equipment and documentation preparation by
          Radi an.

     o    Providing electricity to the trailer and Radian's
          mobi1e field vehi cle .

     o    Setting up the health and safety equipment,
          including the personnel  decontamination area.

     o    Taking undisturbed soil  samples at the Drum Storage
          Area.

     o    Initiating construction  of wooden forms to contain
          treated soil slurry  for  the 25 cu yd run at Lagoon
          South.

October 13 -- The following highlights in chronological order
the activities of Day 2 of the Demonstration Test.

0800-0900  Detailed Health and Safety meetings took place with
           all the on-site contractors.

0900-1200  Radian collected undisturbed  (with Shelby tubes)
           soils from LAN, LFA, and PFA.

0930-1000  HAZCON made preparations for  a preliminary 1 cu yd
           trial run to check  out  all aspects of their system
           from feeding soil to decontamination.

1030-1200  HAZCON preliminary  test performed.

1200-1300  Grubbed at Drum Storage Area  and checked for
           volatile organics with  HNU meter.

1300-1400  Excavated and screened  feedstock from DSA.

1430-1700  Started feed to HAZCON  MFU.  Feed screw jammed
           almost immediately.  Problem  was probably due to a
           buildup of dry soil in  soil auger feedscrew that
           caked and displaced the auger.  Chloranan feed line
           also ruptured.  HAZCON  unit was disconnected and
           flushed clear at decontamination area.  Future runs
           added water at the  auger through the top of the bin
           to facilitate the soil  flow.

                               37

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1715-1815  Restarted DSA 5 cu yd run.   Soil  feed screw jammed
           almost immediately,  but  it  was  flushed clean in 5
           minutes.   Chloranan  feed lines  ruptured four
           times.  First product for sample  block 1  at 1735
           hours.  Operations erratic  after  commencement.
           Samples taken while  block 1 being poured.
           Operations at time of slurry samples  unstable.
           Pouring of block 2 smooth.   Pouring of block 3  was
           very erratic, as feed screw plugged again  and
           Chloranan lines disconnected again.  Samples taken
           from block 3.  The final block  for this run was No
           4,  with the slurry feed  quite dry at  the  start  and
           quite wet near the end of filling.  Toluene was
           added at  a constant  rate throughout the run at
           approximately 19 ml/min  even though slurry
           production was variable.

1815       The run,  based upon  the  agreement between  EPA and
           HAZCON, was stopped  before  a fifth block  could  be
           poured due to the need for  more feedstock  and a
           lack of daylight.  Time  was still needed  by HAZCON
           to  decontaminate their equipment  before total
           darkness.

October 14 --  The following highlights in  chronological order
Day 3 of the Demonstration Test.
0800
A short health and safety meeting was held.
0815-1000  HAZCON installed a new water pump for better
           control  of water addition and fixed the Chloranan
           feed line.

0830-0930  Undisturbed soil samples taken at LAS and FSA.
0930-1030
1136
1142
Lagoon North contaminated soil
screened.
excavated and
Started Demonstration Test on Lagoon North soil
which is very black in appearance.   First block
took 6 minutes with slurry very thick.  Some loss
in Chloranan flow at the beginning  of the block.
Slurry sample taken at 1139 hrs.   Feed hopper kept
only partially ful1.

Started slurry flow to mold 2, and  it was very
wet.  After 2 minutes the process unit had to be
shut down for one minute.  After restart, the
slurry was thick, then turned watery again.
                               38

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1146       Started slurry flow to mold 3.   Except for one
           brief stop,  mold was filled with very wet cement
           siurry.

1152       Started slurry to mode 4.   Consistency was judged
           by  El to be  good relative  to normal  concrete
           consistency.  Slurry flow  stopped for one minute at
           1154 hrs.   Sampled at beginning of block.
           Restarted  and consistency  remained good.

1157       /Started slurry to mold 5 and sampled immediately.
           ^Stopped at 1158 hrs for one minute,  then  completed
           "block.   Consistency ranged from watery to good.

1201       Test completed.


1500-1530  Excavated  Filter Storage Area (sludge too sticky to
           screen).  Cement and soil  feed  calibrated.

1645       Started filling mold 1 of  FSA.   Slurry consistency
           very thick.   First sample  taken.  Slurry  color
           quite black.

1649       Started filling mold 2.  Slurry rate high.  Slurry
           quite wet  and grayish in color.

1652       Started filling mold 3.  Slurry better consistency
           but still  periods of being watery.  Slurry sample
           taken.   Color is gray.  The wooden block  frame
           partly  failed, and some slurry  was lost,  less than
           1 cu ft.

1656       Started filling mold 4.  Slurry started very wet,
           but halfway  through became thick, dry, and black in
           color.

1659-1703  Started filling mold 5.  Slurry became wet almost
           immediately.  Sample taken early in  filling of
           mold.
October 15 -- The following highlights in chronological order
Day 4 of the Demonstration Test.

0900-1000  Landfarm feedstock excavated and screened.

1028-1056  Calibration of soil,  cement, Chloranan, and toluene
           feeds.

1059       Started filling of mold 1.   Slurry started very dry
           but then was adjusted  to a  good consistency.
           Slurry sample then was taken.   Toluene feed rate 18

                              39

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           ml/min.   Toluene feed lost  for almost 30 seconds
           during filling of mold.

1105       Started  filling of mold  2.   Slurry started with
           good consistency.  Production stopped at 1106 for
           30 seconds.   Slurry then ran very wet for 3
           minutes.   System ran out of cement and was shut
           down for  11  minutes.  Test  resumed with slurry
           starting  very dry and then  becoming of satisfactory
           consi stency.

1120       Started  filling of mold  3.   Consistency of slurry
           started  well  and sample  taken.  After 3 1/2
           minutes,  slurry became so dry that water was added
           directly  to  the block.  Production stopped.

1129       Started  filling of mold  4.   Consistency started
           well.   After two minutes production stopped for
           almost 2  minutes so waste can be tamped down in
           bin.  After  2 1/2 more minutes (1136) production
           stopped  to wait for additional feedstock, which
           arrived  at 1138 hrs.  Production resumed.

1139-1144  Started  filling of mold  5.   Consistency of slurry
           was good  throughout.  Samples were taken.

1400-1500  Plant  facility area feedstock was excavated and
           screened.

1617-1650  Started  filling of mold  1.   Toluene addition was
           made at  17 ml/min.  Sample  taken after 1 1/2
           minutes.   After 3 minutes,  the auger was obstructed
           and unit  stopped with only  half of first block
           filled.   HAZCON flushed  unit out at decontamination
           area.   Feedstock discarded  - new feed potentially
           lower  in  organics obtained.

1802       Filling  of mold 1 continued without further
           recalibration of processing unit.

1805       Started  filling of mold  2.   Sample taken.
           Operation smooth with good  consistency of product.

1810       Started  filling of mold  3.   Production interrupted
           for 30 seconds due to problem in blending auger.
           Sample taken.

1817       Started  filling of mold  4.   Filled half of the mold
           and shut down, 2 minutes.  There was a problem in
           soil feed.  Fourth block completed.  Due to time,
           fifth  block cancelled by agreement of EPA and
           HAZCON.
                               40

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October 16
0800-1300  Excavating and screening feed from Lagoon South.
           Excavation holes for treated slurry had been
           previously prepared, and a wooden containment mold
           had been installed in a different area of LAS.
           HAZCON relocated their equipment to the LAS
           decontamination area.
1154-1220  HAZCON calibrates equipment.
1309       Operations began for LAS feed.
1315       Slurry reached first block.  Consistency good.
1320       Started filling of mold 2.  Sample taken.
           Consistency good.
1325       Started filling of mold 3.  Consistency good.
1330       Started filling first hole.
1333       Cement hopper refilled - no lost operation time.
1336       One minute interruption in operation.  Second load
           of feedstock started.
1348       Sample taken.
1401       One minute interruption in operation waiting for
           feed.  Third front-end loader feedstock started.
1414       Six minute interruption while cement hopper
           refilled.
1435       Cement hopper refilled.
1448       Filling of hole 1 complete.  Block for DSA placed
           in its hole and covered with backfill and staked.
           Pipe moved to second hole.
1508       Operation resumes to 2nd hole.
1513       Operation interrupted for 7 minutes waiting for
           soil feedstock.  Start fourth load of feed.
1525       Sample taken.  Consistency of product good.
1536       Three minute interruption due to jamming of
           blending auger.
1550       Fifth load of waste soil started.
1624       Sixth load of waste soil started.
                               41

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1625       Three minute interruption due to jamming of
           blending auger.

1635       Sample taken.

1645       Run completed.   HAZCON and Radian cleaned and
           packed up to leave site.

October 19-20 -- All blocks from LAS, PFA,  LFA,  LAN, and FSA
placed in excavations,  backfilled with clean soil,  and staked
for identification.  Site  was then returned to
Pre-Demonstration Test  conditions.

5.2.3  POSTTREATMENT SAMPLING

Sampling of cured blocks  commenced the week of November 16.  A
series of 3-in and 1.8-in  cores were taken  from the blocks to
be consistent with the  slurry feed samples.  Core sampling
started midday on 11/17/87  at LFA.  Blocks  1,  5,  and 3 were
sampled in that order.

On November 18, LFA was completed, and sampling at  LAS
commenced, with the first  large excavation  hole.   Sampling at
Lagoon South continued  next at the second large excavation
hole where two sets of  samples plus  a duplicate were
collected.  On November 19, core sampling was  done  at the
second large excavation;  LAS sampling was conducted with block
2.  Sampling at LAN on  block 4 began on the afternoon of the
19th.  Samples from block  1 were also taken.  Work  on November
20 commenced with the completion of  sampling at LAN, block 5.
Cores from the Plant Facility Area commenced with block 1.
Sampling was then discontinued for the weekend.   The weekend
was very cold and windy causing some freezing  of the wet clean
soi1 backfi11.

On Monday morning, November 23, sampling at the Plant Facility
Area commenced with  the  completion  of sampling of  block 1.
Blocks 2 and 3 were sampled and the  drill rig  was moved to the
Drum Storage Area.  Block  1 was sampled before darkness halted
operations.  On November  24 the DSA  was completed and the
final area, FSA, was started with block 5.   All  the blocks in
FSA were "soft" and some  difficulty  was encountered in
obtaining sufficiently  large core pieces to perform the
laboratory analyses, particularly for FSA-3.  However, a full
set of laboratory analyses on the cores from this block was
possi ble.

5.3  PROBLEMS AND DEVIATIONS FROM DEMONSTRATION PLAN

This section describes  changes in the Demonstration Test that
have occurred since the approval of the Quality Assurance
Project Plan and the final  issue of the Demonstration Plan.
Field operational problems are described.


                               42

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5.3.1  FIELD OPERATION PROBLEMS

Major problems were not encountered during the Demonstration
test.  Two runs per day of the 5-cu-yd test areas were
possible,  although the hope for three-run capability proved
not to be  practical.  Accumulation of minor unexpected
difficulties extended the duration of each test.   Some of
these difficulties were as follows:

     o     The shallow depth,  12 inches or less,  of the
           contamination in all areas except LAN, required
           added time to collect the feedstock.

     o     The soil feedstock jammed the feed auger on the
           HAZCON unit many times.  On two occasions, this
           required the complete flushing of the  process unit
           at the decontamination area, which resulted in up
           to 2-3 hours in delay.

     As a  result of these minor delays, the 25-cu-yd extended
     duration test was not performed until Friday, October
     16.  So although the entire Demonstration Test was
     completed in 5 days as planned, including mobilization
     and demobilization, the actual testing period spanned
     four  days instead of three.

5.3.2  SAMPLING AND ANALYSIS CHANGES

Changes in the Sampling and Analysis program occurred in the
field, based upon discussions with Radian Corporation and
observations of the operation.  These changes, primarily
additions, are listed below with an explanation.

     o     Access to the Filter Sludge Storage Area was very
           limited due to the inability of the filter cake to
           support the weight of the mechanical  equipment.
           For this reason LAS material was used  for the
           extended run instead of FSA.  In addition, the feed
           for FSA was taken at the SE corner of  the area, not
           in the area that the preliminary screening samples
           were taken.  As a result of changing  the feedstock,
           the HAZCON MFU for the 25-cu-yd run was relocated
           to the northwest edge of LAS instead  of an area
           west of the filter cake.

     o     All of the 25-cu-yd treated soil, except for the
           three 1-cu-yd blocks, was pumped into  two
           excavations instead of three.  Due to  the practical
           convenience of constructing the forms  to contain
           the slurry using standard size 4x8-ft  sheeting, the
           excavations were larger than originally planned.
           Therefore, instead of three excavations of 9 cu yd
           each, only two were needed, each filled with 10-12
           cu yd of treated slurry.  The third excavation

                               43

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hole prepared,  the one furthest to the south,
contains only the three 1-cu-yd blocks.

The baseline laboratory formulations (without
Chloranan) were performed in duplicate for two
contaminated soil feedstocks,  LAN and FSA, instead
of the originally planned one,  which although  not
defined, would  have been FSA.   Physical  tests  were
performed after 9 and 28 days  to conform to the
field samples.

The seven-day physical testing  was performed over a
variable time frame.   This was  mainly due to the
fact that the samples were taken over a  four-day
period and they did not return  to the laboratory
until 8 days after the first samples (DSA) were
taken.  Unconfined compressive  strength  was
performed after 8-10  days.  The permeability tests
were performed  2-12 weeks after collection.  This
was due to laboratory difficulties that  had to be
overcome.

Untreated soil  samples were taken by scoop from the
front-end loaders used to transport the  screened
feedstock to the HAZCON unit.   Shovels and triers
were not necessary to obtain representative
samples.

Slurry samples  were taken in a  1-liter stainless
steel dipper.  This was not clearly defined in the
Demonstration Plan.

Constant head permeability measurements  were made
on undisturbed  soil collected  in Shelby  tubes, not
on remolded samples,  as specified by ASTM D2434.

The toluene injection rate was  about 25-50% higher
than planned.  This was due to  lower process feed
rates being used than anticipated, and to the  fact
that the minimum pumping rate  for the toluene  pump
was 17-18 ml/min, which is too  high for  the reduced
feed rate.

Six EP Tox leaching tests were  performed on
untreated Filter Cake and Lagoon North feedstocks
for priority pollutant metals  only.  This addition
provides some comparative data  on EP Tox and TCLP
for metals.

Slurry  samples  were not always  taken at  the 1/10,
5/10, and 9/10  time frames of a run.  This would
have been equivalent  to blocks  1, 3, and 5.  Due to
some of the minor difficulties  in operation that

                   44

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HAZCON encountered, this had to be adjusted for the
Drum Storage Area (blocks 1, 3, 4 - no block 5),
Plant Facility Area (blocks 1,  2, and 3), and
Lagoon North (blocks 1,  4,  and  5).  The 28-day
samples were taken from appropriate blocks to
conform with the slurry samples.

Some practical adjustments  were made to the ANS
16.1 multiple extraction leaching procedure to
reduce the complexity and costs and be more
practical for use on hazardous  wastes.  The time
frames for leaching were reduced  to 5 intervals
over a 28-day period as compared  to the nuclear
industry test of 10 time frames over an 89-day
period.  They were conducted at 1, 3, 7,  14, and 28
days.  In addition, the container rinses, which are
expected to be clean, were  saved, but not
analyzed.  This leaching procedure was developed
for testing of low radioactive  level nuclear
material and there is no definitive criteria in its
application to hazardous wastes.   This is based
upon verbal contact with the procedure developers
at Oak Ridge National Laboratory.

The quality of No. 1 Portland cement was  checked by
measuring its compressive strength after  7 and 28
days, not by chemical analysis  as previously
stated.  ASTM C150-85 was used  as a basis.

The process water was also  added  to the analyses
performed.  The water was analyzed for pH, TOC,
suspended and dissolved solids, and standard water
chemistry anlons and cations.  This analysis was
added so that all the feed  streams to the process,
except HAZCON's proprietary additive, would be
defined.

Screening of the FSA feedstock  to remove  material
greater than 3 inches was not possible due to the
stickiness of the feedstock.  It  was not  expected
to encounter any rocks or large objects in this
feed.  Feed problems due to oversized material were
not encountered.

Because the field schedule  made it impractical,
soil pH was measured at Radian's  laboratory, not at
Douglassville as originally intended.

Unconfined compressive strength tests were
performed after the weathering  tests, which is a
program addition.
                   45

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     o     Additional  deviations from the approved QAPP are
           described in Radian Corporation's report in
           Appendix B,  pages 22-23.

5.4  MATERIAL BALANCE

Six test runs were performed using contaminated soil  feed from
six plant site locations.   The first five tests,  DSA,  LAN,
FSA,  LFA, and PFA, fed  sufficient soil  to produce
approximately 5 cu yd  of slurry products.  These  were  fed to
1-cu  yd wooden molds to cure for a time period of 48-96 hours,
sufficient time so that they could be unmolded, moved, and
buried.  The sixth feed stock, from LAS,  produced
approximately 22 cu yd  (original intent 25-30 cu  yd)  to test
longer-term operability of the HAZCON MFU.  The parameters and
material balance for each  test are shown  in Table 5.2.  The
operating rates were taken from HAZCON's  Calibration  and
Monitoring Work Sheets, copies of which are included  in
Appendix A.

For LFA, PFA, and DSA  one  front-end loader load (bucket filled
level  to the rim is ~  2 1/4 cu yd) of soil plus cement, water,
and Chloranan produced  3 1/2 to 4 cu yd of slurry mix.  For
LAN and FSA, one soil  load was sufficient to fill five slurry
molds.  Although loose  soil from the screening operation was
used,  with a bulk density  less than the undisturbed or treated
soil  sample values reported in Section  6.0, the volume of
treated slurry would be expected to more  than double  that of
the loose soil.  Therefore, producing 4.0 to 5.0  cu yd of
slurry appears proper.   In addition, the  number of blocks
produced tends to agree with the total  weight of  the  four
feeds.  Exact volume measurements of each cube was not
performed.  However, most  of the molds  (39" x 39" x 32") were
filled to about 2-4 inches from the top,  which is a volume of
approximately 0.95 cu  yd.
                               46

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          TABLE 5.2.   SUMMARY OF HAZCON MFU OPERATING CONDITIONS
Soil Feed, lb/min (b)
Cement, lb/min
Chloranan, Ib/min
Water, lb/min
Total Feed Addition, lb/min

Total Soil, Ib
Total Cement, Ib
Total Chloranan, Ib
Total Water, Ib
Total Weight, Ib
Bulk Density, Ib/cu ft6
  (slurry core)
Total Volume, cu yd (d)

Cement/Soil Ratio
Chloranan/Soil Ratio
Water/Soil Ratio
Soil-to-Total Feed Ratio
Number of 1-cu-yd blocks (c)

Operating Time, minutes'3'
  (based upon chronology)
                              DAS
 3.6
        LAN

        210
        212
        16.7
        _88_
        527
       FSA
       LFA     PFA
               224
               228
               20.0
               551
4.2
4.5
5.2
3.5
15.9    21.5
       18.4
       29.3
       22.6
               LAS

               178
               183
               21.1
                98
               480
4765
4860
450
1810
11885
122
4478
4521
360
1890
11249
100
4308
4418
225
2450
11401
94
6570
6688
585
2316
16159
115
4891
4982
387
1832
12092
129
19385
19928
2295
10659
52267(d)
106
18.3
1.02
0.094
0.38
0.40
4
1.01
0.080
0.42
0.40
5
1.03
0.052
0.57
0.38
5
1.02
0.089
0.35
0.41
5
1.02
0.079
0.38
0.40
<4
1.03
0.119
0.55
0.37
--
       170
Notes:

(a)   A comparison of operating time from the chronology versus time to
      process total cement and Chloranan at measured rates agree for the
      five 5-cu yd test.  For LAS, the chronology indicated that the total
      operating time was - 170 minutes.  On this basis, the total cement
      and soil consumption, if at a 1:1 ratio, is low by about 20%.  If the
      soil calibration rate held then the cement rate tailed off about
      35%.  For the Chloranan, if the run time was 170 minutes, then the
      average feed rate  was 13.5 Ibs/min with a Chloranan to soil feed
      ratio, assuming the soil feed was maintained,  of 0.076 by wt.

(b)   Quantity of soil is determined by calibration before the run started
      and its ratio to the cement during calibration.  Cement is measured
      through a bag counter.  Chloranan is measured by level change in a
      tank.  Water is measured by flow totalizer plus supplementary water
      by tank level change.

(c)   The 1-cu-yd molds were filled to within 2-4 inches of the top, which
      is about 0.95 cu yds.

(d)   Based upon HAZCON Monitoring Work Sheets
                               47

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                               SECTION 6

                SAMPLING AND ANALYTICAL PROGRAM

6.1  SAMPLING LOCATIONS

Soil feedstocks for the Demonstration Test were drawn from six
areas.  The sources of the contamination  were the result of
different plant operations.  The  locations, using Figure 4.2
as a reference, are as follows:

    Lagoon North (LAN) - 380 feet NNE of  MW 11-1
    Lagoon South (LAS) - 100 feet SSE of  MW 3-2
    Plant Facility (PFA) - 60 feet N of MW 10-2
    Filter Cake Storage (FSA) - SE corner about 50 ft west of
    N-S road
    Drum Storage (DSA) - 60 feet  SSE of incinerator stack
    Landfarm (LFA)- 60 feet east  of MW 11-1

Sampling locations were based upon results from the RI/FS
report performed by NUS Corp.

The lagoons were for many years sludge storage areas from the
waste oil reprocessing plant operations.   Most of the organics
were washed away in the floods of 1970 and 1972, and the
lagoons were subsequently backfilled with clean soil.  The
contamination at the processing plant and drum storage areas
is the result of spills.  The filter sludge area contains a
piled oil sludge filter cake.  Oily sludge from the oil
reprocessing operations was tilled into the soil from 1979 to
1981 producing the landfarm area.

The screening samples, as discussed in section 4.2.6, helped
define the feedstock locations.  At Lagoon North, the highly
contaminated soils were 1 to 3 feet below the surface.  At the
other five locations, the contamination was at the surface.
The depth to which the feed was excavated was closely
monitored to minimize the use of relatively clean soil.

6.2  SAMPLING SCHEDULE

The Demonstration Test Plan  [3] called for soil samples to be
taken during three time frames.  These were:

    Pretreatment -  Samples of feedstock were taken just prior
    to feeding the holding bin on the HAZCON MFU

    Treated Slurry - Treated slurry samples were taken at the
    outlet of the processing unit, the blending auger.
    Laboratory analyses were scheduled to be initiated after
    approximately seven days of curing.  Due to the long time

                               48

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     required to perform the permeability analyses, many of
     these tests occurred after 28 days.

     Solidified Soil - The solidified soil blocks, returned to
     their excavation sites, were sampled a little more than
     28 days after treatment.

Samples from the solidified blocks and the surrounding soil
will be taken periodically to monitor the solidified block
integrity over a five-year time span.  All the pretreatment
and treated slurry samples were collected at the time of
testing, in October 1987.  Solidified soil samples were bored
out of the solidified blocks during the third week in
November, 1987.  The initial long-term samples will be taken
in July of 1988.

6.3  SAMPLE RECOVERY PROCEDURES

The Sampling and Analysis contractor (S&A), Radian
Corporation, collected samples of the following:  contaminated
soil prior to treatment, treated slurry as it exited the
mobile processing unit, and 28-day-old solidified treated soil
(see Figure 6.1).

6.3.1  PRETREATMENT

Minimally disturbed contaminated soil samples were collected
for bulk density and permeability measurements.  The S&A
sampling crew went to the area designated for a given test
before excavation started and obtained the scheduled number of
cores using a 3-inch Shelby tube.  The depth of the cores
depended upon the estimated depth of contamination in the area
being sampled.  The cores were sealed by covering the ends of
the Shelby tube with aluminum foil and sealed with tape.  If
needed to assure core integrity during shipping, inert
material (plastic packing foam or clean sand) was added to the
portions of the tube not filled with the core.

Contaminated soils for the other tests were collected either
from a composite pile at the excavation site or from the earth
moving equipment, as it was transferred to the mobile
processing unit.  Scoops were used to obtain the samples.
Individual soil portions were taken from different parts of
the composite pile or from the material in the earth moving
equipment so that several parts of the source contaminated
soil were represented.  The individual portions that were
obtained each time the scoop was dipped into the soil were
placed into a stainless steel container.

Once all individual portions were collected, the contents of
the container were mixed by hand and the mixture transferred
to individual labeled sample jars.


                               49

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               5 CU YD TESTS
    COMPOSITE
     SAMPLES
                                        NA
                                        NA
  PROCESS PRODUCT        1 CU YD
       SLURRY        SOLIDIFIED BLOCKS
       (7 Days)             (28 Days)
             D:  Duplicate     NA: Not analyzed


             --- Duplicate performed for Lagoon North only
               25 CU YD TEST
1
2
3
4
5

NA
1
NA
Block 1
2
3
Holel
D

D
2
2
2

   COMPOSITE
    SAMPLES
PROCESS PRODUCT
     SLURRY
     (7 Days)
Figure  6.1.  Sampling scheme
SOLIDIFIED BLOCKS
  3 Small-2 Large
     (28 Days)
                         50

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6.3.2  TREATED SLURRY

The treated slurry was collected at the discharge point of the
HAZCON mobile processing unit.  Grab samples were taken during
the beginning, mid-portion, and end of a treatment run.  The
grab samples were taken using a stainless steel dipper.  The
pan part of the dipper had a capacity of 1000 ml, and the
handle was approximately 3 feet long.  The dipper had the
advantage that the person collecting the sample was farther
from the waste stream.  Samples were packed into cylindrical
cardboard molds immediately after they were collected.  The
cardboard cylinders were placed in individual sealable plastic
bags.  The glass jars were sealed by screwing on a
Teflon-lined lid.  A containment vessel (shallow pan) was
required at the point the treated slurry was transferred from
the dipper to the sample containers.

6.3.3  SOLIDIFIED SOIL

After approximately 28 days, samples of solidified soil were
collected using a rotary rig with core barrel.  The outside
diameters for the cores were 7 cm for unconfined compressive
strength and permeability tests and 4.5 cm for wet/dry,
freeze/thaw and leaching tests.  Cores were removed from the
core barrel and sealed in aluminum foil to prevent moisture
loss.  Packing and shipping methods were chosen to minimize
disturbance to the cores.

Cores were removed from the solidified blocks in a pattern
designed to obtain solidified material that was representive
of each block.

6.4  ANALYTICAL PROCEDURES

Soil samples were collected before treatment and after
processing.  Processed soil samples were analyzed both after
approximately 9-12 days of curing and after 28+ days.
Significant changes in treated material were not anticipated
after four weeks.

Samples were taken to directly relate the feedstock properties
with both the HAZCON process unit product slurry and the
corresponding buried posttreatment blocks.  The criteria for
when and how the samples were to be taken is shown in Figure
6.1 and described in Sections 6.4.1 through 6.4.4 below.

6.4.1  BASE CASE

     o    Clean soil backfill plus cement formulations,
          without Chloranan, were prepared in triplicate in
          the laboratory and many of the physical properties
          were checked (moisture, bulk density, compressive

                               51

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          strength,  and permeability),  as a baseline against
          the results from the contaminated soil  tests.   These
          tests were performed nominally after 7  and 28+
          days.  Only one permeability  on each formulation was
          performed  after 28 days.

          The same as above except  filter cake was used
          instead of clean soil.

          The same as above except  sludge from Lagoon North
          was used.

          Samples of clean soil,  cement, and water were  taken
          for analyses.  The clean  soil  was analyzed for TOC,
          PCBs, and  lead.  The cement was checked for
          compressive strength after 7  and 28 days to confirm
          that it was a typical  No.  1 Portland cement.   The
          water was  analyzed for  pH, TOC, suspended solids,
          and standard water chemistry  anions and cations.
6.4.2  PRETREATMENT SOIL
          Two composite soil  samples were prepared for each of
          the five 5-cu-yd feedstocks.   The composites were
          prepared by taking  soil  scoops from twelve locations
          within the feed pile.

          The first soil  composite was  mixed and split into
          three parts,  two for analysis and one held in
          reserve.  The second soil  composite,  taken
          completely independent of the first,  was analyzed as
          fol1ows:

               For Lagoon North, the composite  was split into
               two parts.  One part was analyzed completely
               and the  second part for  key component
               properties such as  oil and grease, moisture,
               bulk density,  pH, and lead content.

               For the  three  feedstocks spiked  with toluene at
               the mixing auger, laboratory spiking was
               performed, equal  to the  concentration level
               measured in the 7-day treated samples, before
               running  the  TCLP test.

               For the  other  four  areas producing 5 cu yd of
               treated  soil,  the second composite was not
               divided  and was analyzed for only the key
               component properties.

          Four composite feed samples were taken at Lagoon
          South over the approximate three hour duration of
          the test.  One of the composite feeds was divided
          into two parts with the  second part analyzed for the
          key component properties only.
                               52

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6.4.3  SLURRY SAMPLES (NOMINAL 7 DAYS)

     o    For the 5 cu yd tests, three separate sample sets
          were taken.  The time frames targeted were
          approximately a tenth, a half,  and nine tenths into
          the total run time.  However,  for LAN, samples were
          taken for slurry producing blocks 1,  4, and 5; DSA
          blocks 1 and 3; and PFA blocks  1, 2,  and 3.

     o    For the 25 cu yd test, four sets of samples were
          taken over the three hour operating time frame.  A
          duplicate sample set was taken  during the second
          sampling period and was held in reserve.

6.4.4  POSTTREATMENT SAMPLES (28 DAYS)   »

     o    For the 5 cu yd tests the treated material was
          poured into five 1-cu yd molds, which after partial
          curing were buried in the excavation.  Samples were
          taken to conform to the blocks  from which the slurry
          samples were taken.

     o    For the 25 cu yd extended run  test, the first three
          cu yds were fed into 1 cu yd molds and the remaining
          slurry into two 12 cu yd excavation pits.  Sample
          sets were taken from the second 1-cu-yd block, plus
          one from the first and two from the second 12-cu-yd
          blocks (see Figure 5.1).  A duplicate sample set was
          taken from the first sample of  the second large
          block and held in reserve.

The tests, with analytical procedures performed for each
pretreatment sample, are shown in Table  6.1.  Seven-day
posttreatment sample analyses are defined in Table 6.2, and
the 28+ day posttreatment analyses are defined  in Table 6.3.

Due to the anticipated low level of contaminants (particularly
volatile organics) in the soil, toluene  was injected into
three of the five 1 cu yd feedstocks.  The injection of 125
ppm toluene, which is typical of total volatile concentration
found at Superfund sites, was added to facilitate volatiles
measurement in the leachates from the three low-contaminant
feedstocks, DSA, PFA, and LFA.  The intent of this injection
was to have one volatile organic that could be  readily
followed from untreated soil to treated  soil to leachates (of
untreated and treated soils).  The minimum detection limits
for the compounds being analyzed in soil  and water are
provided in Table 6.4.  In many samples,  due to the relative
concentrations of the contaminants, higher detection limits
were used.

All samples were carefully taken and kept in sealed containers
at a reduced temperature to prevent loss  of volatiles,
particularly when toluene was injected.
                               53

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                 TABLE  6.1   PRETREATMENT ANALYSES
   Test Type
 Procedure^)
Grain Size


PH

Moi sture

Bulk Density



Oil and Grease



Total Organic Carbon
Priority Pollutant Metals
  (Sb, As,  Be, Cd, Cr, Cu,
   Pb, Hg,  Ni, Se, Ag, Th, Zn)
Total PCBs in Soil

Permeabi1i ty
Leaching - PCBs,
  Priority Pollutant Metals,
  VOC, BNA, and Oil and Grease
  in leachate
Selected Volatile Organics - Soil

Selected Base Neutral/Acid
Extractable Organics

Microstructural Examination(a)
ASTM D422-63 (reapproved
1972)

SW 846-9045

ASTM D2216-80

American Society of Agronomy
- Methods of Soil Analysis,
p.375

Standard Method 503D -
American Public Health
Associ ation

Waikley-Black or combustion
alternative

Digestion and Atomic
Absorption  or Inductive
Coupled Plasma Atomic
Emission Spectroscopy -
SW-846; Digestion - SW-3050,
SW-7471; Analysis (ICPAES)  -
SW-6010, (AA) SW-7060,
SW-7421, SW-7740, SW-7841,
(AA-Mercury) SW-7471

SW846, Method 8080

Constant Head - ASTM
D-2434-68 (reapproved 1974)

EP TCLP - Federal Register
11/7/86, Vol. 51, No. 216,
Appendix 1,  part 268; EPA
608
Metals - same as above
VOC  - SW-8240; BNA SW-8270
Oil  & Grease - APHA SM-503D

SW846, Method 5030, 8240

SW846, Method 3540, 8270
X-ray Diffraction and
Scanning Electron Microscope
 (a)  One sample only from each location.
 (b)  A brief description of each procedure is provided  in
    Secti ons 6.5 and 6.6.
                               54

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          TABLE  6.2   POSTTREATMENT  ANALYSES  -  SEVEN  DAYS
Test Type
     Procedure
Bulk Density



Moi sture

Unconfined Compresslve Strength

Permeabi1ity

Leaching
  PCBs, Volatile*, Toluene, BNA,
  and Oil  and Grease
Toluene in Soil
Test Methods for Sol id
Waste Characterization
(TMSWC) - Section 2

TMSWC - Section 4

ASTM D-2166

TMSWC - Section 13

TCLP - Federal Register,
11/7/86,  Vol.51, No.216,
Appendix  1, Part 268;
PCB - EPA-608
VOC - Method SW-8240
BNA - Method SW-8270; Oil
and Grease APHA SM-502

SW846 Method 8240
                               55

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           TABLE 6.3  POSTTREATMENT ANALYSES - 28 DAYS
   Test Type
   Procedure(e)
Moi sture
Bulk Density

Unconfirmed Compressive
  Strength(c)

Wet/Dry Weathering Test(c)

Freeze/Thaw Weathering Test(c)

Permeability (Falling Head)

Leaching - PCBs, VOC, Toluene,
  BNAs, Oil and Grease
Priority Pollutant Metals(a)
  (Pb, Cr, N1, Zn, Cu, Cd)
Test Methods for Solidified
Waste Characterization
(TMSWC) Section 4

TMSWC - Section 2

ASTM D-2166


TMSWC - Section 12

TMSWC - Section 11

TMSWC - Section 13

EP TCLP - Fed Reg.,
11/7/86,
Vol. 51, No. 216, Appendix
1, Part 268 + EPA 608-PCB;
VOC - SW846 Method 8240;
BNA Method 8270;
Oil & Grease - APHA SM-502

Atomic Absorption and
Inductively Coupled Plasma
Atomic Emission
Spectroscopy - SW-846
Methods SW-7060, SW-7421,
SW-6010

MCC-lP-Static Leach Test(b)
- Matrix B, 40°C
(Materials Characterization
Center) - metals same as
for TCLP
                           (continued)
                               56

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                      TABLE  6.3   (continued)
   Test Type                            Procedure
.	{	

                                     
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TABLE 6.4.   MINIMUM DETECTION LIMITS
Chemi
Pri or













Base








Volat








PCBs


cal
ity Pollutant Metals
Arseni c
Antimony
Beryl 1 i urn
Cadmi urn
Chromi urn
Copper
Lead
Mercury
Nickel
Sel enium
Silver
Thai 1 i um
Zinc
Neutral/Acid Extractables
Naphthal ene
Fl uorene
Fl uoranthene
Pyrene
Bis(2-ethylhexyl)
phthal ate
Benzo-(k)-fl uoranthene
Phenol s
i 1 es-Organics
Tol uene
Benzene
Xyl enes
Ethyl benzene
Tetrachloroethene
Trichl oroethene
1 , 2-Di chl oroethane
Carbon Tetrachl ori de

Aroclor 1260
Aroclor 1248
In Water
ug/1 iter

4
6
1
3
9
10
50
0.2
20
2
10
3
6

20
20
20
20

20
20
20

10
10
10
10
10
10
10
10

1
0.5
In Soil
ppm by wt.

< 50
<100
< 0.5
5
< 20
< 50
5
5
< 5
50
5
2.5
< 50

0.7
0.7
0.7
0.7

0.7
0.7
0.7

0.010
0.010
0.010
0.010
0.010
0.010
0.010
0.010

0.040
0.020
                58

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The purposes of the various pretreatment analyses are many.
Grain size, pH, moisture, and bulk density define basic soil
characteristics.  Bulk density will  define volume changes that
occur to the soil  during remediations.   Oil and grease and
total organic carbon are both measures  of organics in the soil
being treated that may impact on the
stabilization/solidification process.  In many technologies
that are cement-based, organics inhibit the cement hydration
reactions.  Analyses for priority pollutant metals,  PCBs, base
neutral/acid extractables,  and volatile organics in  all the
samples determine  the contaminant levels of the soils being
processed.  The permeability and leaching tests provide
baseline data on physical mechanisms such as contaminant
mobility that should change dramatically with the soil
treatment.

Posttreatment analyses characterize the treated soil.
Moisture and bulk  density analyses provide treated soil
property information.  The  unconfined compressive strength
(UCS) provides a measure of the uniformity of the product mix
and the impact of  oil and grease concentrations.  High
strengths indicate a more uniform soil  and additive  mix (due
to the cement microstructure produced)  and provide maximum
benefits, such as  durability.  An inability to tie up the
organics, (organics exist at concentrations of up to 25% by
weight), would significantly reduce unconfined compressive
strength.  Other factors that affect UCS are cement-to-soil
ratio, mixing efficiency, soil characteristics, other
pozzolans, and moisture quantity.  (These parameters were not
varied to check their impact for this Program.)  The x-ray
diffraction and scanning electron microscopic examinations
provide additional information on the integrity of the
solidified soil, and may provide qualitative information on
the potential durability of the soil blocks.  The wet/dry and
freeze/thaw weathering tests provide an indication of the life
expectancy of the  solidified material when under repeated
extremes in cyclic exposure (12) to moisture and temperature
cycles.

Two special leach  tests were included for the 28-day treated
soil that simulate the material as it would exist in a
solidified mass; they were  the MCC-1P (Static Leach  Test) and
the ANS 16.1 (Multiple Extraction Leach Test).  Both of these
tests were developed for use with low-level radioactive wastes
for the nuclear industry, but have been modified for use with
hazardous wastes.   Since the standard TCLP procedure requires
grinding of the solidified  mass, it may have represented a
more severe leaching condition.

6.4.5,  RANGE OF TESTING

The range of contaminant testing on which the HAZCON
technology was demonstrated were limited to the contamination
and soil characteristics existing at the Douglassvi11e site.

                               59

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The primary variables investigated in the Demonstration Test
were:

     o    Particle size,  moisture content,  and contaminant
          levels in the soil  from the six locations

     o    Grease and oil  content

     o    Volatiles and BNAs  including 3 feedstocks where 125
          ppm by wt. toluene  was added

     o    PCBs

     p    Lead

6.5  PHYSICAL TESTS

The physical tests described  below were used to analyze the
soil and leachate samples during this SITE Program.

ASTM D 422-63:  Grain Size Analysis

This method covers the quantitative determination of the
distribution of particle sizes in soils.  The distribution of
particle sizes larger than 75 urn (retained on the No. 200
sieve) is determined by sieving, while the distribution of
particle sizes smaller than 75 urn is determined by a
sedimentation process using a hydrometer to secure the
necessary data.

SW846 Method 9045:  Soil pH

The pH of a sample was determined electrometrically using
either a glass electrode in combination with a reference
potential or a combination electrode.  In soil samples, pH
will be determined by preparing a slurry using equal volumes
of  soil and deionized water and measuring the pH of the
decanted liquid.

ASTM D 2216-80:  Water Content (Moisture)

ASTM Method D 2216 was used to determine the water content of
untreated soil samples.  Moisture is determined by measuring
the mass of water removed by drying the sample to a constant
mass at 110 ±5°C.

TMSWC-4;  Water Content (Moisture) - Solid Cores

The  sample  is ground to pass an ASTM No. 10 sieve.  The mass
of  the sample is measured before and after drying  in an oven
maintained  at 60 ±3°C.  The dry weight must be a constant
weight (mass change of less than 0.03 g in 4 hours).  The wet
sample mass is divided into the difference of the wet sample
mass minus  the dry  sample mass.
                               60

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Bulk Density

Bulk density was determined using the method described in
Methods of Soil  Analysis.  American Society of Agronomy,  1965.
The mass of the  samples were calculated by difference using a
top loading balance.  The  dimensions of the specimen (cube or
cylinder) are measured using a 30-cm ruler having a precision
of ±1 mm.  The bulk density is calculated by dividing the
volume into the  mass.

APHA 503D:  Oil  and Grease

Method 503D is a modification of the Soxhlet extraction
method, which is suitable  for sludges.  Magnesium sulfate
monohydrate is combined with the sludge to remove water  (as
MgS04 x 7HoO).  After drying, the oil and grease is
extracted in a Soxhlet apparatus with trichlorof1uoromethane
and measured gravimetrically.

Total Organic Carbon

Inorganic carbon is removed by sulfurous acid treatment  and
the remaining organic carbon analyzed by dry combustion.   Dry
combustion will  be carried out using a Perkin Elmer 240C
elemental (C, H, N) analyzer with a thermal conductivity
detector.

ASTM D 2434:  Permeability Coefficient-Constant Head

Permeability coefficient is determined by a constant head
method for determining the laminar flowrate of water through
granular soils.   This procedure is limited to disturbed
granular soils containing  not more than 10 percent soil
passing the 75 micrometer  (No. 200) sieve.  For this project,
measurements were made on  minimally disturbed soils samples
collected in Shelby Tubes  when the bulk density samples  were
taken.

TMSWC-13:  Permeability Coefficient-Falling Head-Solid Cores

This test was carried out  on the solidified 7- and 28-day core
samples.  A cylindrical sample 7.62x7.62 cm was used.
Permeability is  determined using a triaxial cell measuring
changes of water volume over time under controlled conditions
of temperature and pressure.

ASTM 1633;  Unconfined Compressive Strength Test

This test method covers the determination of the unconfined
compressive strength of molded soil-cement cylinders using
strain-controlled application of the axial load.
                               61

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TMSWC-12:   Wet/Dry Weathering Test

This test  was performed using two 4.5x7.4 cm cylindrical  core
specimens  of solidified wastes.   It was carried out in
conjunction with TMSWC Method 4.0, Water Content.   One of the
specimens  was used as the test specimen, the other as the
control.

Two solidified test samples were compared by weight
difference.  One sample,  the control,  was placed in a humidity
chamber,  and the other was dried in a  vacuum oven  at 60 £3°C
for 24 ±1  hours.  The sample specimen  then was cooled in  a
desiccator, and 230 ml of water was added to each  sample.  The
sample and control then were placed in the humidity chamber
for 24 hours.  This was repeated 11 times, with the weight
loss being recorded each  time.

TMSWC-11;   Freeze/Thaw Test

This test  was performed using two 4.5x7.4 cm cylindrical  core
specimens  of solidified waste.  The test was carried out  in
conjunction with the water content determination.   One of the
two specimens was used as a control.  The test specimen was
placed in  a freezer at -20 i3°C for 24 +1 hours.  Water was
then added to the frozen  specimen and  control  and  maintained
at 22 ±3°C for 24 ±1 hours.  The process was repeated 11
additional times, with relative weight loss calculated after
each cycle.

6.6  CHEMICAL TESTS

The chemical tests described below were used to analyze the
soil and leachate samples during this  SITE Program.

Toxicitv Characteristics  Leaching Procedure (TCLP)

The TCLP is designed to determine the  mobility of both organic
and inorganic contaminants present in  liquid,  solid, and
multiphase wastes.  For wastes comprised of solids, the
particle size of the waste is reduced  and analytes are
extracted  for 18 hours with an acetic  acid solution.  The
extract is then separated from the solid phase and analyzed
for VOC, BNA, Priority Pollutant Metals, PCBs, and oil and
grease.  This procedure was developed  to measure a wider
variety of contaminants including volatile organics, than  is
measured by EP Toxicity.

MCC-1P:  Modified Static Leach Test

The static leach test establishes the  maximum credible
concentrations of elements in a quasi-static groundwater
regime that has been  in contact with a  stabilized waste.   The
samples are kept as solid cores to simulate an in situ
condition.  For this  project, 28-day cylinders were used  from

                               62

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the core barrel  drilling.  Four test specimens for each test
were leached with organic-free ultra pure water,  at 40°C for
four varying time periods up to 28 days.   Leachates then were
analyzed for all  contaminants.

ANS 16.1;  Leach  Test

The intact samples, cut from the solid cores,  were leached
using ultra pure  water.  The sample specimen is placed in
fresh leachates  at five different time intervals, with the
total leaching time being 28 days.  This  differs  from TCLP and
MCC-1P,  where each of four specimens is placed in its own
leachate and held there for varying time  frames up to 28
days.  Therefore, five leachates were analyzed for the organic
and inorganic contaminants.

EP Toxicitv

This extraction  procedure is specified by the  United States
Environmental Protection Agency to classify solid waste as
hazardous (or not) according to the characteristic of "EP
Toxicity."  The  solid cores are crushed and agitated for 24
hours with the pH controlled at 5.0.  This test specifies only
eight metals and  six pesticides and herbicides to be measured
in the extract.

SW846 Method 3510:  Liquid-Liquid Extraction

Method 3510 is a  procedure for isolating  organic  compounds
from aqueous samples.  A measured volume  of sample is serially
extracted with methylene chloride using a separatory funnel.
The extract is dried, concentrated, and,  as necessary,
exchanged into a  solvent compatible with  the cleanup or
determinative step to be used.

SW846 Method 3540:  Soxhlet Extraction

Method 3540 is a  procedure for extracting nonvolatile and
semivolatile organic compounds from solids such as soils,
sludges, and wastes.  The solid sample is mixed with anhydrous
sodium sulfate and placed in an extraction thimble.  Extract
then is  dried, concentrated, and, as necessary, exchanged with
a solvent compatible with the cleanup or  determinative step
being employed.

SW846 Method 5030;  Purge-and-Trao

Method 5030 describes sample preparation  and extraction for
the analysis of  volatile organics by a purge-and-trap
procedure.  An inert gas is bubbled through the solution at
ambient  temperature, and the volatile compounds are
transferred from  the aqueous to the vapor phase.   The vapor is
swept through a  sorbent column where the  volatile components

                               63

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are adsorbed.   After purging is  completed,  the  sorbent  column
is heated and  back-flushed with  inert  gas  to  desorb the
components onto a gas chromatographic  column.

EPA Method 8240:  Gas Chromatograohv/Mass  Soectrometrv  (GC/MS
for Volatile Organics

Method 8240 is a GC/MS procedure used  to determine the
concentration  of volatile organic compounds in  a variety of
solid waste matrices.  Method 8240 can be  used  to quantify
most volatile  organic compounds  that have  boiling points below
200°C and that are insoluble or  slightly soluble in water.
These include  low-molecular-weight halogenated  hydrocarbons,
aromatic, nitriles, ketones, acetates, acrylates, ethers,  and
sulfides.  The volatile compounds are  introduced into the  GC
by the purge-and-trap method; detection is by mass
spectrometer.

EPA Method 8270:  GC/MS for Semivolatile Organics

Method 8270 is a capillary column procedure used to determine
the concentration of semivolatile organic  compounds in  sample
extracts.  Method 8270 can be used to  quantify  most neutral,
acidic, and basic organic compounds that are  soluble in
methylene chloride, including polynuclear  aromatic
hydrocarbons,  chlorinated hydrocarbons and pesticides,
phthalate esters, organophosphate esters,  nitrosamines,
haloethers, aldehydes, ethers, ketones, anilines, pyridines,
quinolines, aromatic nitro compounds,  and  phenols.

SW846 Method 8080:  GC/ECD for PCBs

Method 8080 provides gas chromatographic conditions for the
detection of PCBs.  Prior to analysis, samples  are subject to
appropriate extraction procedures.  Samples are  injected  into
the GC using the solvent flush technique.   Compounds in the  GC
effluent are detected by an electron capture  detector  (ECD).

SW836 Method 680:  GC/MS for PCBs

Method 680 covers determination of pesticides and
polychlorinated biphenyls (PCBs)  in waters, soils, and
sediments by gas chromatography/mass spectrometry  (GC/MS).   It
is applicable to samples containing single congeners or to
samples containing complex mixtures, such as  Aroclors.
Polychlorinated biphenyls (PCBs)  are identified  and measured
as isomer groups by levels of chlorination.

SW846 Method 3050:  Acid Digestion for Metals

Method 3050 is  an acid digestion  procedure used  to prepare
sediments, sludges, and  soil samples for analysis  by flame or
furnace Atomic Absorption (AA) spectroscopy,  or  for analysis

                              64

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by Inductively coupled plasma atomic emissions spectroscopy
(ICPES).  A representative sample is digested in HNOo and
HoOo.  The digestate is then refluxed with either NH03
or RC1.

SW846 Method 3010;  Acid Digestion for Metals

Method 3010 is a digestion procedure used to prepare samples
for analysis by flame AA and ICPES.  The sample is mixed with
HNOo and allowed to reflux in a covered Griffin breaker
followed by refluxing with HC1 .

SW846 Method 3020:  Acid Digestion for Metals

Method 3020 is a digestion procedure used to prepare samples
for analysis by graphite furnace AA spectroscopy.  The sample
is mixed with HN03 and allowed to reflux in a covered
Griffin breaker.  The digestate is then diluted to achieve a
reconstituted sample containing 3% by volume HN03.

SW846 Method 6010:  Metals bv ICPES

Method 6010 describes the simultaneous, or sequential,
determination of elements using ICPES.  The method measures
element-emitted light by optical spectrometry.  Samples are
nebulized, and the resulting aerosol is transported to the
plasma torch.  Element-specific atomic-line emissions spectra
are produced, which are dispersed by a grating spectrometer
and monitored for intensity by photomultiplier tubes.

SW846 Methods 7060/7421/7740/7841:  Furnace AA

Methods 7060, 7421, 7740, and 7841 are graphite furnace atomic
absorption techniques approved for determination of arsenic,
lead, selenium, and thallium, respectively.  Following sample
digestion, an aliquot of sample is placed in a graphite tube
in the furnace, evaporated to dryness, charred, and atomized.
The metal atoms to be measured are placed in the light path of
an atomic spectrophotometer.

SW846 Method 7470/7471:  Mercury bv Cold Vapor Atomic
Absorption fCVAA)

Method 7470 is a cold-vapor atomic absorption procedure for
determining the concentration of mercury in mobility-procedure
extractions.  Method 7471 is prescribed for solid and sludge-
type wastes.  Sample preparation is specified in each method.
Following dissolution, mercury in the sample is reduced to the
elemental state and aerated from solution in a closed system.
The mercury vapor passes through a cell positioned in the
light path of an atomic absorption spectrophotometer.


                               65

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6.6.1  Contaminant Definitions

Priority Pollutant Metals

Thirteen priority pollutant metals have been specified to be
of particular environmental concern by the United States
Environmental Protection Agency.  The metals are antimony,
arsenic, beryllium, cadmium, chromium, copper,  lead, mercury,
nickel, selenium, silver, thallium, and zinc.  Six of these
metals were found in measurable concentrations  in contaminated
soils from the Douglassvi1le site.  To conserve resources,
only the six metals found at the site were analyzed for in
many of the samples tested.  The six metals found were
cadmium, chromium, copper,  lead, nickel, and zinc.

Base Neutral/Acid Exractables (BNA)

Semivolatile organic compounds are prepared for analysis by
extraction either into a base-neutral (BN) extract or an
acidic  (A) extract.  Examples of BNAs include phenol,
naphthalene, and phthalates.

Volatile Organic Carbon  (VOC)

Volatile organic compounds are determined by purging volatiles
from the sample tested.  Examples  include toluene,
tetrachloroethene, xylenes, trichloroethene, and ethyl
benzene.

Polvchlorinated Biohenvls  (PCBs)

Polychlorinated biphenyls  are a group of related isomers of
chlorinated organic compounds characterized by having 1 to  10
chlorine atoms substituted on the  biphenyl group.
                               66

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                           SECTION 7

                      ANALYTICAL  RESULTS
In each of the following subsections,  the results are first
presented by plant area and then on an overall  basis across
the six plant areas.   In the overall  results presentation, the
analytical data are divided into three parts:   1) physical
results, such as permeability,  moisture content,  unconfined
compressive strength, etc., 2)  chemical analyses  of the soils
and leachates, and 3) microstructural  studies  based upon x-ray
diffraction and microscopic analyses.   The data quality is
discussed in Section  7.3.

A discussion and interpretation of the results  are presented
in Section 8.  The full details of the physical and chemical
laboratory analyses are provided in Appendix B, and the
microstructural study in Appendix C.

7.1  PLANT AREA RESULTS

The results by plant  area  are presented in the  following
subsections:

7.1.1  DRUM STORAGE AREA

The results of the physical and chemical  analyses for the Drum
Storage Area are summarized in  Table  7.1.  Highlights of these
results are as follows:

o   The bulk density  of the undisturbed soil increased from
    1.23 g/ml to almost 2.0 g/ml upon  treatment.

o   The permeability  was reduced by the treatment process from
    0.57 to 2.3xlO~9  cm/sec.

o   The unconfined compressive  strength was in  excess of 1000
    psi, with the average  of the 7-day cores,  1447 psi, being
    greater than the  average of the 28-day cores, 1113 psi.

o   Volatiles were not detected in the untreated  soil.  After
    toluene injection, the solidified  cores (28-day) indicated
    only 1.35 ppm by  wt. toluene, which is only about 3% of
    that injected.  TCLP leaching test results  showed
    equivalent levels of toluene in the untreated and treated
    soil leachates.  For the untreated soil TCLP  test only,
    toluene was added to the sample to be leached at a dosage
    level equivalent  to that actually  measured  in the
    solidified 7-day  cores.
                               67

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           TABLE 7.1.   DEMONSTRATION TEST  RESULTS -  DSA
Physical Tests
                                Untreated Soil      Treated soil
Parameter                                       7 day          28 day
Moisture content, %
pH
Bulk Density, g/ml (Ibs/ft )
Oil and Grease, %
Total organic carbon, %
Permeability, cm/sec
Unconfined compressive strength.
11.8
6.41
1.23 (76.8)
1.0
4.9
0.57
psi -
14.2
-
1.95 (121.5)
-
.
1.6x10'9(a)
1447
14.8
-
1.99 (124
0.54
.
2.3x!0"9
1113


.0)




Chemical  Tests

                        Soils, pan by wt.                      TCLP extracts,  mg/l
Parameter
Total VOC
Toluene(c>
Total BNA
Phthalates
Phenols
Metals - Pb
Total PCBs
Oi 1 and grease, X
Untreated
NO
ND
12.15
12.15
ND
3230
1.2
1.0
7-day(b) 28-day
1.35 1.32
1.35 1.24
ND
ND
ND
830
-
0.54
Untreated
0.915
0.915
ND
ND
ND
1.500
ND
ND
7-day
0.384
0.380
0.05
ND
0.04
0.015
ND
0.63
28-day
0.376
0.370
ND
ND
ND
0.007
ND
4.3
 (a)   This 7-day value is calculated based on a test value at 28+ days of curing.
 (b)   Only VOC tests were performed on 7-day cores.
 (c)   Toluene injected into treated slurry.
 ND    Not detected
                                                68

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    The feed soil  contained about 12 ppm by wt.  BNA,
    essentially only phthalates.   The treated soil  did
    show any phthalates nor did any of the leachates.
       not
    The lead content in the soil  was 3230 ppm by wt.   The
    results from the leachate analyses showed decreasing
    extraction concentrations from untreated soil  to  28-day
    cores.
    The PCB level  in the soil  was 1  ppm by wt.
    detected in the leachates.
PCBs were not
o   The oil  and grease content of the soil  was 1.0%.   The
    concentrations measured in the treated  cores,  based upon a
    material  balance, are consistent.  Leachate results showed
    increasing quantities,  from undetected  in untreated soil
    to 4.3 mg/1 in the 28-day cores.

7.1.2  LAGOON NORTH

The results  of the physical and chemical  analyses  for Lagoon
North are summarized in Table 7.2.  Highlights of  these
results are  as follows:

o   The bulk density of the undisturbed soil  increased upon
    treatment from 1.4 to 1.6 g/ml.

o   The permeability was reduced by  the treatment  process from
    l.SxlO"3 to less than 3.6xlO~9 cm/sec.

o   The unconfined compressive strength was approximately 430
    psi after 7 days and 520 psi after 28 days of  curing.

o   Total volatiles in the soil was  measured  as 2.41  ppm by
    wt. with equivalent values measured in  the treated soil
    samples.   The TCLP leaching tests, for  untreated  and
    treated  soil samples, gave equivalent leachate
    concentrations, all under 50 ug/1 .  The special leach
    tests, ANS 16.1 and MCC-1P did not detect any  volatiles in
    the leachates.

o   The feed soil contained nearly 21 ppm by  wt. BNA  with the
    phthalates predominant.  After treatment  the phthalates
    were not detected, but high levels of phenols  were
    measured.  The concentration of  BNAs  in the leachates,
    whether  treated or untreated, was about 1 ppm  by  wt,
    virtually all phenols.   The results from  the MCC-1P leach
    test were equivalent to the TCLP results  and showed higher
    concentrations of BNAs than ANS  16.1  leachate  results by a
    factor of two.

o   The lead content in the soil was 9200 ppm by wt.  and in
    the TCLP leachate, just below 32 mg/1.   After  soil
    solidification and 7 days of curing,  the  concentration  in
    the leachates was reduced to near detection limits of
    approximately 0.005 mg/1.  The concentration in the ANS

                               69

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             TABLE  7.2.    DEMONSTRATION TEST  RESULTS  -  LAN
Physical Tests
                                                                           Base case:
Parameter
Moisture content, X
PH
Bulk Density, g/ml (Ibs/ft )
Oil and Grease, %
Total organic carbon, %
Permeability, cm/sec
Unconfined compressive strength.
Untreated Soil
17.6
3.69
1.4 (87.3)
16.5
23.0
1.8x10'3
psi -
Treated soi I
7-day
20.1
.
1.61 (100.3)
-
.
1.7x10'9(a)
427
28-day
17.2
-
1.59 (99.1)
7.54
-
3.6x10-9
-------
    16.1 leachates were 0.01-0.05 mg/1  and for MCC-1P 0.07 to
    0.11 rng/1.   In both special  leach tests,  the concentration
    in the extracts increased with time.

o   The PCB content of the soil  was 51  ppm by wt.   PCBs were
    not detected in any leachates.

o   The oil and grease level  in  the untreated soil  was 16.5%
    by wt. and  in the 28 day  cores, 7.54%.  The concentration
    measurements for the treated cores,  based upon  a material
    balance,  are consistent.   The concentration in  the TCLP
    leachates for untreated soil was approximately  1 mg/1 and
    slightly  greater in the treated soil  leachates, ranging
    from 2-4  mg/1.

o   The physical properties of the base  case  samples, prepare.d
    in Radian's laboratory without Chloranan, after 28 days of
    curing were similar to the HAZCON treated material, except
    that the  permeability was greater by  a factor  of
    approximately ten.

7.1.3  FILTER CAKE STORAGE AREA

The results of  the physical and  chemical  analyses  for the
Filter Cake Storage Area are  summarized  in Table 7.3.
Highlights of these results are  as follows:

o   The bulk  density of the undisturbed  and  untreated soil was
    1.6 g/ml  and appears to decrease by  5% after treatment.
    Cores prepared in the laboratory without  Chloranan were
    15% lower in bulk density than the  undisturbed  soil
    sample.
    The permeability of the treated soil,  taken as a slurry in
    the field (7-day),.was 4.5xlO~9 cm/sec and for the 28-
    day cores,  8.4x10"° cm/sec.   The laboratory sample,
    without Chloranan,  was 3.2x10"° cm/sec.
    The unconfined compressive strength after 28 days of
    curing was 219 ps1.  The samples without Chloranan, from
    the base case study,  averaged 38 psi.

    The total  volatiles in the soil  was 150 ppm by wt.  with
    the treated core values lower.   The TCLP extracts for
    treated and untreated soils were 0.71-1.03 mg/1.  The
    leachate concentrations from the MCC-1P leach test  were
    equivalent to those of TCLP and  greater than for ANS 16.1
    by a factor of two.

    The filter cake contained about  500 ppm by wt BNA with
    most of it being phenols.  Upon  leaching, whether the soil
    was treated or untreated, the leachate contained 2.7-3.8
    mg/1 phenols, with the phthalates and  naphthalene at
    detection  limits.   The treated  soil showed a sharp
    decrease in phthalates.  In these samples more naphthalene

                               71

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                TABLE  7.3.   DEMONSTRATION TEST RESULTS -  FSA
Physical Tests
                                                                          Base case:
Parameter
Moisture content, X
PH
Bulk Density, g/ml (Ibs/ft )
Oil and Grease, X
Total organic carbon, X
Permeability, cm/sec
Unconfined compress ive strength.
Untreated Soil
24.7
2.56
1.60 (99.7)
25.3
27.5
(a)
psi -
Treated
7-day
24.7
-
1.51 (94.
-
-
4.5x10"9
238
soil
28-day
22.1
-
1) 1.51 (94.1)
9.54
.
8.4x10"8
219
Soil +
cement
28.9
-
1.36 (84.7)
-
.
3.2x10"8
38
Chemical Tests
Parameter
    Soils, pern by wt.
Untreated     7-day
28-day
       TCLP extracts, mg/l
Untreated     7-day     28-day
Total VOC
Toluene
Total BNA
Phthalates
Phenols
Naphthalene
Metals - Pb
Total PCBs
Oil and grease, X
150
26
534
14.2
405
115
22600
40
25.3
113.3 105.3
20.7 19
368.9
1.3
126.8
216.7
10300
-
9.45
1.03
0.25
2.86
ND
2.81
0.05
17.9
ND
3.7
0.71
0.22
3.91
ND
3.85
0.06
0.07
ND
4.1
0.74
0.23
2.78
0.01
2.72
0.06
0.41
ND
10.4
(a)   Could not be measured
(b)   Solidified FSA soil, without the use of Chloranan, after 28 days of curing
ND    Not  detected
                                                 72

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    was observed than all the phenols.  The leachate
    concentrations from MCC-1P were equivalent to the TCLP
    leachates and greater than those from ANS 16.1.

o   The lead content in the soil was about 2.3% by wt.  The
    28-day treated soil TCLP leachates averaged 0.4 mg/1,  with
    the 7-day values less than 0.1 mg/1.  The MCC-1P leach
    test extracts contained equivalent amounts of lead and the
    concentrations in ANS 16.1 extracts were less, in the
    range of 0.05-0.47 mg/1.

o   The PCBs in the untreated soil were 40 ppm by wt, but  they
    were not detected in the leachates.

o   The oil and grease content in the untreated soil was 25.3%
    and 9.45% by wt in the treated soil, which is consistent
    on a material balance basis.  The leachate results ranged
    from 4.1-10.4 mg/1, with the treated soil samples slightly
    higher in oil and grease.  The special leach tests'
    leachate concentrations were the same as in the TCLP
    extracts.

7.1.4  LANDFARM AREA

The results of the physical and chemical analyses for the
Landfarm Area are summarized in Table 7.4.  Highlights of
these results are as follows:

o   The bulk density of the untreated and undisturbed soil was
    1.68 g/ml and increased after solidification to 1.86 g/ml.

o   The permeability of the soil.upon treatment in the HAZCON
    process decreased from 2xlO~z to 4.5xlO"9 cm/sec.

o   The unconfined compressive strength of the cores was
    approximately 945 psi after both 7 and 28 days of curing.

o   The total volatiles in the soil was below detection
    limits.  Analysis of the 28-day cores showed that about
    40% of the toluene spike remained with the treated soil.
    TCLP leachate results showed a VOC concentration (toluene
    only) of 0.37 mg/1.

o   The LFA soil contained about 37 ppm BNA, with this being
    predominantly phthalates with some naphthalene.  The TCLP
    leachates, for both the treated and untreated soils, were
    near the detection limits of each component of 10 ug/1 .

o   The lead content in the untreated soil was 1.37% by wt.
    The TCLP leachate, after the soil was treated, had a
    concentration of 0.05 mg/1 as compared to the untreated
    soil leachate of 27.7 mg/1.

o   The PCBs in the soil were 10 ppm by wt.  PCBs were not
    detected in any of the leachates.


                               73

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              TABLE  7.4.   DEMONSTRATION  TEST RESULTS -  LFA
Physical  Tests
Parameter
                                Untreated Soil
                                                    Treated soil
                                                7-day         28-day
                                                  1.84 (114.6)    1.86 (115.9)
Moisture content, %                 16.7           17.0           15.1
pH                                  4.57
Bulk Density,  g/ml (lbs/ft3)         1.68 (104.6)
Oil and Grease, %                    4.3
Total organic  carbon, %              8.9
Permeability,  cm/sec                 2x10"2         4.5x10"9      4.5x10"
Unconfined compressive strength, psi  -              947           945
Chemical Tests
Parameter
                           Soils,  ppm by  wt.
                      Untreated     7 day
28-day
       TCLP  extracts, mg/l
Untreated     7-day     28-day
Total VOC
Toluene(a)
Total BNA
Phthalates
Phenols
Metals - Pb
Total PCBs
Oi 1 and grease, %
NO
ND
36.7
33.5
ND
13700
10
4.3
12.1 24.7
12.1 23.7
ND
ND
ND
1860
-
1.53
0.21
0.21
0.01
0.01
ND
27.7
ND
2.0
0.21
0.21
0.05
0.01
0.03
0.04
ND
2.8
0.37
0.37
0.10
0.02
0.08
0.05
ND
1.9
 (a)   Toluene injected  into treated slurry at  a  target concentration equivalent to 125 ppm
      by wt. in the untreated soil.
 (b)   Values vary from  0.13 to 28 ppm; averaged  lower two values.
 ND    Not detected
                                                 74

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o   The oil  and grease level  in the untreated soil  was 4.3% by
    wt.  The treated soil  content,  after correcting for the
    addition of cement,  water,  and  Chloranan, was consistent
    with the untreated soil.   The TCLP leachates for treated
    and untreated soil samples  were both about 2 mg/1 .

7.1.5  PLANT FACILITY AREA

The results  of the physical and chemical analyses for  the
Plant Facility Area are  summarized  in Table 7.5.  Highlights
of these results are as  follows:

o   The bulk density of  undisturbed soil increases  from 1.73
    mg/1 to  2.02 mg/1 after solidification.
                                                      p
o   The permeability of  the untreated soil  was 7.7x10   .
    The treated soil had values ranging from 1.2xlO"a  to
    2.5xlO'10 cm/sec.

o   The unconfined compressive  strength reached 1574 psi  after
    28 days.

o   The total volatiles  in the  untreated soil was 0.42 ppm.
    However, the 28 day  cores showed approximately  23  ppm
    volatiles with approximately 18 ppm being injected
    toluene.  The VOC concentrations in the TCLP extracts, for
    both the untreated and treated  soil samples, were  in  the
    approximate range of 0.7-1.0 mg/1.  The VOC concentrations
    in the leachate from both special leach tests were less
    than the TCLP values by a factor of 5-10.

o   The PFA  soil contained approximately 18 ppm by  wt  BNA,
    phthalates and naphthalene.  The values for the leachate
    concentrations in untreated and treated soils were less
    than 0.11 mg/1.  The leachates  for MCC-1P and ANS  16.1
    were comparable to the TCLP extracts.

o   The lead content in  the soil was approximately  0.8%.   The
    TCLP leachates, after treatment, showed a concentration of
    0.01 mg/1.  This is  equivalent  to the leachates from  ANS
    16.1,  but significantly less than those of MCC-1P  where
    the leachate concentrations were higher, as high as 0.7
    mg/1 for the 14-day  leaching interval.

o   The PCBs in the soil totaled 34 ppm by wt.  PCBs were not
    detected in any of the leachates.

o   The oil  and grease content  of the soil  was 4.5% by wt.
    The concentration in the treated cores averaged 2.1%  by
    wt., which is consistent for a  material balance.  The TCLP
    leachate results ranged from 0.4 to 3.5 mg/1, with the
    leachate concentrations of  the  treated soil slightly
    greater.  The oil and grease concentrations for ANS 16.1
    and MCC-1P ranged from undetected to 1.7 mg/1.


                               75

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           TABLE  7.5.   DEMONSTRATION TEST  RESULTS -  PFA
Physical Tests
                              Untreated SoiI        Treated soil
Parameter                                       7-day          28-day
Moisture content, %
pH
Bulk Density, g/ml (lbs/ft3)
Oil and Grease, %
Total organic carbon, %
Permeabi 1 i ty, cm/see
Unconfined compressive strength,
6.6
7.00
1.73 (108.0)
4.5
7.5
7.7x10"2
psi -
11.6
-
2.07 (129.0)
-
-
1.2x10-8(a)
1435
10.0
-
2.02
-
-


(125.8)


1.2x10-8(b>
1574

Chemical  Tests

                           Soils, ppm by wt.                   TCLP extracts, mg/l
Parameter             Untreated     7-day    28-day    Untreated     7-day     28-day
Total VOC
Toluene
-------
7.1.6  LAGOON SOUTH

The results of the physical and chemical analyses for Lagoon
South are summarized in Table 7.6.  Highlights of these
results are as follows:

o   The bulk density of the undisturbed soil  sample increases
    from 1.59 g/ml to 1.74 g/ml after being treated in the
    HAZCON process.

o   The permeability of the soil  was reduced  from l.BxlO"5
    to 2.2xlO~9 cm/sec after soil  treatment.

o   The unconfined compressive strength was approximately 890
    psi for both the 7- and 28-day core samples.

o   The total volatiles in the untreated soil  was 6.5 ppm by
    wt.  The concentrations appear to be the  same after soil
    treatment.  The VOC concentrations of the TCLP extracts
    were equivalent, in the range  of 0.03-0.11 mg/1.   For the
    special leach tests, extract  concentrations were  lower,
    being close to the detection  limits of 0.01 mg/1.

o   The LAS untreated soil samples showed only phthalates as
    the BNA at a concentration of  34.2 ppm by wt.  However, in
    the 28-day cores, phenols, and naphthalene exist  and are
    the predominant compounds.  The TCLP leachate
    concentrations were greater for the treated soil, with the
    primary compounds being phenols.  The MCC-1P leachate
    concentrations were equivalent to the TCLP extracts and
    greater than for ANS 16.1.

o   The lead content in the soil  was 1.49% by wt.  The
    untreated soil TCLP leachate  was 52 mg/1,  but after
    treatment this was reduced to  0.05 mg/1,  which is
    approximately equal to the maximum leachate concentrations
    for ANS 16.1,  The leachates  for MCC-1P were in the range
    of 0.3-0.5 mg/1 for all the time intervals.

o   The PCB concentration  in the  soil was 52  ppm by wt.  PCBs
    were not detected in any leachates.

o   The untreated soil contained  7.82% oil and grease.  The
    treated soil values were very  erratic, ranging from 0.06%
    to 4.25% by wt.  A material balance could not be
    confirmed.  The leachates concentrations  for untreated and
    treated soils were 0.6 mg/1 and approximately 2.1 mg/1,
    respectively.

7.2  OVERALL RESULTS

7.2.1  PHYSICAL TEST RESULTS
                               77

-------
            TABLE  7.6.   DEMONSTRATION TEST  RESULTS  -  LAS
Physical Tests
Parameter
                             Untreated Soil
                            Treated soil
                         7-day         28-day
Moisture content, %
pH
Bulk Density, g/ml (lbs/ft3)
Oi 1 and Grease, %
Total organic carbon, %
Permeability, cm/sec
Unconfined compressive strength,
11.9
4.11
1.59 (99.1)
7.82
14.3
1.5x10~5
psi -
16.3
-
1.70 (105.9)
-
-
2.4x10"9
894
15.8
-
1.74 (108
-
-
2.2x10"9
889


.4)




Chemical Tests
Parameter
     Soi Is. ppm by wt.
Untreated     7-day
                                           28-day
      TCLP extracts, mg/l
Untreated     7-day     28-day
Total VOC
Toluene
Total BNA
Phthalates
Phenols
Naphthalene
Metals - Pb
Total PCBs
Oil and grease, X
6.5
0.3
39.6
34.2
ND
5.4
14900
52
7.82
6.29 7.20
0.79 1.78
15.7
2.15
6.70
4.55
3200
.
1.67
0.05
0.01
0.01
NO
ND
0.01
52.6
ND
0.6
0.02
0.02
0.47
ND
0.47
ND
0.13
ND
2.55
0.11
0.05
0.73
0.08
0.65
ND
0.05
ND
1.6
(a)   Results very erratic from 0.06 to 4.25X.
                                               78

-------
The results of the physical  tests,  the full  details of which
are in Appendix B, are summarized in Tables  7.7 and 7.8.  An
overview of the individual  plant area results are presented
below:

7.2.1.1  UNTREATED SOIL

o   The soil  pH ranged from 2.5 for FSA to 7.0 for PFA.

o   The particle size distribution  shows that PFA had the
    coarsest  and DSA the finest soil.  For most samples except
    PFA, 30-60% by wt. of the soil  was finer than 200 mesh (74
    microns).

o   The average of three samples for the undisturbed soil bulk
    density ranged from 1.23 g/ml for DSA to 1.73 mg/ml for
    PFA.

o   The oil and grease (O&G) in the soil ranged from 1.02% to
    25.3% by  wt.  The Total  Organic Carbon (TOC) ranged from
    4.9% to 27.3% by wt.  The highest values for both were for
    FSA, the  lowest for DSA.

o   The permeability analyses for the feedstock ranged from
    0.57 cm/sec for DSA to 1.5xlO"b cm/sec for LAS.  The FSA
    samples were too impermeable to measure.

7.2.1.2  TREATED SOIL - 7 AND 28 DAYS

The averaged  results of the 7-day and 28-day samples are
presented in  Table 7.8.  The results can be  summarized as
follows:

o   The bulk  density ranged from 1.51 g/ml (94.2 Ib/cu ft) for
    FSA to 2.02 g/ml (125.8 Ib/cu ft) for PFA.  The values are
    approximately the same at 7 and 28 days  and are 10-20%
    greater than for the undisturbed, untreated soil.  The
    largest Increase in bulk density 1s for  PFA, and FSA had a
    bulk density decrease of about  5%.

o   The moisture content ranged from 11.6% for PFA to 24.7%
    for FSA at 7 days.  At 28 days  the range was 10.0% for PFA
    to 22.1%  for FSA.

o   The unconfined compressive strength ranged from 238 psi
    for FSA to 1446 psi for DSA at  7 days.  At 28 days it
    ranged from 219 psi for FSA to  1574 psi  for PFA.  These
    values are the same order of magnitude at both 7 and 28
    days.

o   The permeability ranged for the Z-day cores from 1.6 x
    10'y cm/sec for DSA to 4.5 x 10"y cm/sec for FSA and
    LFA.  At  28 days it ranged from 8.4xlO"B cm/sec to
    1.8xlO"y  cm/sec for FSA and DSA, respectively.  This
    compares  to 10"1 to 10"b cm/sec for untreated soils.


                               79

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o   The wet/dry and freeze/thaw weathering tests showed small
    weight losses (0.5-1.5%)  at the end of the 12-cycle test
    for the test specimens and their controls.  Unconfined
    compressive strength tests performed after the final
    weathering cycle showed no loss in UCS compared to the
    unweathered samples.

o   Both field- and laboratory-cured samples were used to
    evaluate the effectiveness of the HAZCON process during
    the Demonstration test.  The laboratory formulations  were
    prepared using cement with clean soil, FSA and LAN soils
    without Chloranan.   For bulk density and moisture, the
    values were close to field-processed soils.   For
    uncorifined compressive strength (UCS) FSA was reduced to
    27 psi at 7 days and 38 psi at 28 days.  For LAN the  UCS
    values were 373 psi at 7  days and 539 psi at 28 days.
    These latter values are comparable to the field-treated
    samples.  In comparison,  the clean soil produced the
    highest unconfined  compressive strength of 2000 psi.   The
    permeabilities of the laboratory-formulated  samples were
    in the range of 3.8xlO"8  for LAN to 5.9xlO~9 for clean
    soil and cement.  The values are equivalent  to the field
    results for FSA but a factor of about ten greater for LAN.

It should be noted that due to the difficulties  and time
required to perform the permeability tests, these tests were
run anywhere from 6 to  15 weeks after the soils  were treated.

7.2.?.  CHEMICAL ANALYSES

7.2.2.1  UNTREATED SOIL ANALYSES

The results of the untreated  soil analyses are reported in
Appendix B and summarized in  Table 7.9.  They can be
highlighted as follows:

o   Oil and grease ranged from 1.0% by wt. for DSA to 25.3% by
    wt. for FSA.  The oil and grease levels in the 28-day
    treated cores were  about  40% of the untreated soils as
    would be anticipated from the material balances.

o   Total PCBs ranged from 1.2 ppm for DSA to 52 ppm by wt.
    for LAS.  Most of the PCBs were Aroclor 1260.  However,
    Aroclor 1248 was measured at 19 ppm by wt. in PFA and 25
    ppm by wt. in LAS.   In the other areas, Aroclor 1248 was
    below detection limits of 20 parts per billion by wt.
    Aroclor 1260 was measured in all six plant areas.  These
    values are greater than those reported in the screening
    study, whose samples were collected in May 1987 and are
    reported in Table 4.1.

o   The thirteen priority pollutant metals were analyzed for
    in the untreated soil.  Lead is the predominant metal
    contaminant.  Five other metals of measurable
    concentration were analyzed  for in the 28-day cores  and
    leachates.  These other metals are chromium, nickel,

                               82

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    cadmium,  copper,  and zinc.   The average of the analyses in
    the six areas shows that lead exists in concentrations
    from 0.3% to 2.3% by wt.  Chromium,  nickel,  and cadmium
    exist at  concentration levels of less than 100 ppm by wt.
    with cadmium the  least.   Copper and  zinc are at
    concentrations of a few  hundred ppm  by wt.  These overall
    levels agree with the values obtained from the screening
    samples.

o   Analyses  for BNA  showed  that all areas contained
    phthalates,  primarily di-n-butylphthalate and
    bis(2-ethylhexyl)phthalate.   Total  phthalate
    concentrations up to 34  ppm  by wt.  in LAS were measured.
    Phenols were also abundant,  with total concentrations over
    400 ppm measured  in the  FSA.  Naphthalene also was
    detected  in  the soil in  all  areas except DSA and LAN with
    concentrations over 100  ppm  by wt.  at FSA.
    Bis(2-ethylhexyl)phthalate was the  primary semivolatile
    detected  in  the screening samples.

o   Volatiles were not detected  in the  soil samples at DSA and
    LFA.  The primary volatiles  detected were toluene, xylene,
    trichloroethene,  tetrachloroethene,  and ethyl benzene.
    Some samples also contained  1,1,1-trichloroethane and
    trans-1,2-dichloroethene.  The maximum volatiles, based
    upon multiple sample averaging, were measured at FSA with
    up to 14  ppm by wt. trichloroethene, 6 ppm
    tetrachloroethene, 26 ppm toluene,  and 91 ppm xylenes.
    The area  with the second largest quantity of volatiles is
    LAS with  maximum  sample  values primarily in  the range for
    each component of 0.3-3.7 ppm by wt.  Toluene was injected
    into the  slurry samples  exiting the  HAZCON unit for DSA,
    LFA, and  PFA, to  produce an  equivalent concentration in
    the feed  soil of  approximately 125  ppm by wt.
    Concentrations of the Injected toluene in the 7-day core
    samples ranged from 1.3  ppm  by wt.  in DSA to 12 ppm in
    LFA.  The toluene in the 28-day core samples ranged from a
    minimum at DSA of 1.3 ppm by wt. to  a maximum at LFA of 24
    ppm by wt.

7.2.2.2  LEACHATE ANALYSES

Results of the leachate analyses, for which data reduction
calculations  are provided in Appendix D, are highlighted as
fol1ows:

o   The TCLP  leachates of the six feedstock soils showed very
    low oil and grease.  For each area,  the treated soil
    leachate  concentrations  were greater than for untreated
    soil leachates, even though  the untreated soil
    concentrations are greater on average by a factor of 2.5.
    The values were from below the detection limits (0.2 mg/1)
    for DSA to 3.7 mg/1 at  FSA.   The leachate results for the
    7-  and 28-day cores appear higher than the untreated soil,
    ranging from 0.6 ppm by wt.  for DSA to 4.1 ppm  for LAN and

                              84

-------
FSA at 7 days, and 1.6 to 10.4 ppm by wt. for LAS and FSA,
respectively at 28 days.

PCBs were not detected in any leachate, whether the soil
was treated or untreated.

The 7- and 28-day TCLP leachates for metals showed that
the quantity of metals in the treated soil  leachates (see
Table 7.10) is well  below that for untreated soils.   For
the 7- day and 28- day cores leachates, except for lead,
all the metal concentration levels were near or below
detection limits.  The lead concentrations  were close to
detection limits, at levels of about 2-90 ug/liter except
for FSA, where the concentration ranged from 7-950 ug/1,
averaging 400 ug/1.   For the untreated soils, chromium and
copper were below detection limits and cadmium and nickel
were near the detection limits.   The lead concentration
ranged from 1.5 mg/1 for DSA to  52.6 mg/1 for LAS.  For
zinc, the values ranged from 0.7 mg/1 for DSA to 23.0 mg/1
for FSA.  The solidification process reduced the lead
concentration by a factor of ajjout 500 to 1000.  TCLP data
on the 28-day cores  were equivalent to the  7-day cores.

The leachate concentrations from ANS 16.1 were generally
equivalent to those  of TCLP, while those of MCC-1P were
greater by a factor  of 5-10.  The leachate  concentrations
increased with increased leaching time for  both tests.

For the BNAs, very significant reductions in
concentrations were  obtained between the soil and the TCLP
leachates of the untreated, 7-,  and 28-day  cores.  The
phthalates, as a group, for all  leachates were reduced to
approximately their  detection limit of 0.010 mg/1.  This
may be because the phthalates concentrations were very
significantly reduced from the untreated soils to the
treated soils.  For  the phenols, measurable quantities in
the leachates were observed.  For FSA, where the soil
samples contained about 400 ppm  by wt, leachate
concentrations of 3-4 mg/1 were  measured.  In each area,
concentrations in the untreated  soil, 7-day, and 28-day
core leachates were  approximately the same, even though
the concentrations in the cores  were less than one-half
that in the untreated soil.  The same trend existed for
naphthalene, except  at lower concentrations.  Table 7.11
provides a summary of the leachate concentrations.

The special leach tests, performed only on  28 day cores,
provided results that showed that the leachate
concentrations from  MCC-1P were  equivalent  to TCLP
leachates, but greater than for  ANS 16.1.  For the ANS
16.1 leachates, concentration did not appear to be a
function of leaching time.  However, for MCC-1P the phenol
concentrations in the extracts increased with time,  but
the phthalates and naphthalene did not.
                          85

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      TABLE  7.10.   CONCENTRATION  OF  METALS  IN  TCLP  LEACHATES
                                                         *
                             Metal Concentration -  mg/liter

Soil  Location       Pb         Cr           Ni          Cd          Cu          Zn
Soil
DSA
LAN
FSA
LFA
PFA
LAS

1.5
31.8
17.9
27.7
22.4
52.6

<0.008
<0.008
0.27
<0.008
<0.008
<0.008

0.02
0.07
0.11
0.06
0.05
0.07

<0.004
0.02
0.13
0.03
0.01
0.04

<0.03
<0.03
<0.3
<0.08
<0.03
0.13

0.07
1.1
23.0
6.7
1.4
4.8
7-Day Cores
    DSA            0.015    <0.07       <0.15       <0.04       <0.06        <0.02
    LAN           <0.002    <0.07       <0.15       <0.04       <0.06        <0.02
    FSA            0.07      0.02       <0.008      <0.003      <0.03         0.02
    LFA            0.04     <0.07        0.15       <0.04       <0.06         0.04
    PFA            0.01     <0.07        0.15       <0.04       <0.06        <0.02
    LAS            0.14     <0.008      <0.008      <0.003      <0.05         0.04

28-Day Cores
DSA
LAN
FSA
LFA
PFA
LAS
0.007
0.005
0.400
0.050
0.011
0.051
<0.007
0.007
<0.070
0.009
<0.007
0.015
0.020
<0.015
<0.15
0.015
<0.015
0.025
<0.004
<0.004
<0.040
<0.004
<0.004
<0.004
0.023
0.010
<0.060
0.080
0.027
0.055
0.037
0.017
0.037
0.013
0.030
0.258
            Where  the symbol < is used,  indicates values below detection limits of
            quantity shown.  The detection  limits vary between metals and from
            analysis to analysis.

            Where  2 of 3 values were above  detection limits,  three  values were averaged
            assuming the one below detection  limits is zero.   If  only one of three values
            are above detection limits,  the results are reported  as below detection
            Iimits.
                                                   86

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          TABLE 7.11
     BASE NEUTRAL/ACID EXTRACTABLES
     IN TCLP LEACHATES
BNA
OSA
    Concentration -  ug/1

LAN     FSA     LFA      PFA
LAS
Untreated Soil

  phthalates       ND      10      ND     10      10      NO
  phenols          ND    1010    2810     ND      ND      ND
  naphthalene      ND      ND      50     ND      ND      10

7-Dav Cores

  phthalates       ND      30      ND     10      20      ND
  phenols          40    1310    3850     30      50     470
  naphthalene      15      ND      60     10      20      ND

28-Dav Cores

  phthalates       ND      10      10     20      30      80
  phenols          ND    1440    2720     80      80     650
  naphthalene      ND      ND      60     ND      ND      ND
ND - Not Detected
                               87

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o   For the volatile organics,  the primary compounds detected
    were trichloroethene,  tetrachloroethene,  xylenes,  ethyl
    benzene,  and toluene.   During the Demonstration Test
    operations,  toluene was injected into the slurry mix zone
    of the HAZCON MFU for  DSA,  LFA and PFA as described
    earlier.   For the TCLP leach tests on the untreated soils,
    toluene was  added to the soil at approximately the same
    concentrations as measured  in the 7-day cores.  In the
    TCLP leachates for untreated soils for DSA,  LFA, and PFA,
    toluene concentrations were quite high, 900-5100 ug/1.
    For FSA,  where the feedstock averaged 26  ppm by wt.
    toluene,  the soil leachate  averaged 230 ug/1 toluene.   The
    other primary volatile organics, trichloroethene,
    tetrachloroethene, ethyl benzene, and xylenes were greatly
    reduced in the untreated soil leachates.

    The results  of the 7-day and 28-day core  leachates are
    similar in magnitude to the untreated soil,  even though
    the core concentrations are less than one half of the
    untreated soil.  See Table  7.12 for a comparison of the
    average key  volatile organic components in the TCLP
    1eachates.

    The results  of the two special leach tests showed that the
    leachate concentrations were approximately equal.   They
    were lower by about a  factor of 2 compared to TCLP
    extracts.  VOC concentrations did not appear to increase
    with increased leaching time intervals.

o   Extraction Procedure Toxicity (EP Tox) tests were
    performed on 28-day cores for metals only, for LAN and
    FSA.  For LAN, the leachate metals were predominantly lead
    (Pb) and averaged 0.02 mg/1 for cores averaging
    approximately 0.3% Pb  by wt.  For FSA, where the cores
    contained 1.0% by wt.  lead, the leachate concentrations
    averaged 0.21 mg/1.  These values appear to be larger for
    LAN and less for FSA than the TCLP results.

7.2.2.3  WATER CHEMISTRY

An analysis of the process water, supplied by truck from the
local   fire department, was performed.  The water was low  in
dissolved solids, 340 mg/1, and very low in suspended  solids,
1 mg/1, with a pH of 8.05.  The primary cations detected were
calcium, magnesium,  sodium, and silicon.  Two of  the primary
anions detected were sulfate and chloride at concentration
levels of 35 mg/1.   Details of the water chemistry  analyses
are provided in Appendix B, Tables A-50 and A-51.

7.2.3  MICROSTRUCTURAL STUDIES

Analyses of the untreated  soil and  28-day core  samples were
performed on a microstructural scale.  All analyses were
performed more than  three  months  after soil processing.   All

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          TABLE  7.12.   VOLATILES  IN  TCLP  LEACHATES^
Volatile Organic
     Concentrations - ug/l

DSA      LAN     PSA       LFA
                                     PFA
                                              LAS
Untreated Soil
Toluene
Xylenes
Trichloroethene
Tetrachloroethene
Ethyl benzene
7 Day Cores
Toluene
Xylenes
Trichloroethene
Tetrachloroethene
Ethyl benzene
28 Day Cores
Toluene
Xylenes
Trichloroethene
Tetrachloroethene
Ethyl benzene

915
< 50
< 20
< 40
< 70

380
3.5
< 10
< 20
< 40

370
6
< 9
< 6
< 3

10
7
2.4
< 4
< 7

< 6
6
< 2
< 4
< 7

40
8
2
3
2

245
525
165
19
80

220
340
105
11
60

230
330
100
20
60

5100
< 230
< 95
< 210
< 360

210
5
< 2
< 4
< 7

370
< 6
< 9
< 6
2

1100(b)
< 180
< 76
< 160
< 290 <

350 <
20
< 5 <
< 10 <
< 20 <

670
170
< 9
< 6
< 3

10
35
8
5
7

15
15
5
10
20

50
40
8
10
4
     (a)  < indicates  less than detection limits.  Within one sampling area, the
         detection limit may change between samples.   For these,  the highest
         detection limit is shown.
     (b)  Two values <60 and 2200 ug/l.
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samples were studied by scanning electron microscopy (SEM),
x-ray diffraction (XRD),  and optical  microscopy (OM) .   Energy
dispersive x-ray spectrometry (EDXRA) was also performed on
selected samples.  The type of information to be obtained from
each test is:

o   X-ray diffractometry  - crystalline structure of the soil
    and hydration products

o   Energy dispersive x-ray spectrometry - elemental analysis,
    i.e., calcium,  aluminum

o   Microscopy - characterizes crystal appearance,  porosity,
    fractures, and the presence of unaltered soil/waste
    material

The detailed report with  photographs and x-ray diffraction
patterns is included in Appendix C.

The results can be summarized as follows:

o   The untreated soils consist of quartz and clay minerals,
    illite, and in some cases kaolinite.  The filter storage
    area feed was low in  quartz, as would be expected.

o   The solidified samples show crystals of portlandite,
    ettringite, calcium silicates, calcium aluminate,  and
    sometimes gypsum.

o   Abundant pores of various sizes and shapes could be seen
    in all core samples.   Some of the pores include trapped
    air bubbles.  Large cracks also are seen in some of the
    pores.

o   Unhydrated tricalcium silicate was seen in all  core
    samples.  In some cases dicalcium silicate was observed,
    particularly for FSA.

o   Several peaks in each x-ray diffraction pattern could not
    be identified, as known minerals, but were seen both in
    the soil and core samples.  These peaks are likely to be
    the organics.

o   Mixing does not appear to be completely efficient.

o   The cores contain unaltered brownish aggregates that were
    also observed in the untreated soil.

The interpretation of the above observations is presented  in
section 8.1.3.
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7.3  DATA QUALITY ASSURANCE

In Section 7 of the approved Quality Assurance Project Plan
(QAPP), it was indicated that various Quality Control  (QC)
samples would be taken to control  and/or assess data quality.
These are:

o   QC check samples - standard samples of known analyte
    concentration.

o   Laboratory Blanks - deionized  water taken through  sample
    preparation steps.

o   Field blanks -  clean soil samples brought to the field and
    then analyzed in the laboratory to check for field
    contami nati ons.

o   Spiked samples  - samples were  spiked with either known
    contaminants or surrogate standards to confirm analytical
    recoveries and  thus accuracy of the analyses.   Duplicates
    on the spiked samples were also performed.

o   Duplicate samples - duplicate  samples from the field were
    collected and analyzed to confirm soil sample  data.

To verify that correct sampling procedures were used,  EPA sent
a Quality Assurance (QA) team to the field to observe  Radian
Corporation's sampling procedures.   In addition, QA teams went
to Radian's laboratories both in Austin, TX and Sacramento, CA
to observe and correct, if necessary, procedures being used in
the laboratory.  The audits found  Radian's work satisfactory.

The detailed QA/QC  results reported on Radian procedures is
provided in Appendix B.  Overall the QA/QC data indicated that
the measurement data are acceptable and defensible.

The purpose of the  QA/QC program was to fulfill two related
purposes :

o   An organized frame work for sampling and analytical
    efforts.

o   To control data quality within  preestablished  limits to
    ensure that it  was adequate to  achieve the objectives of
    the program.

The following is a  brief summary of the QA analyses:

o   Soil samples

       Blanks--For  metals, the blanks showed levels the  same
       as in uncontaminated soil.   PCBs were not detected in
       the reagent  blank.  Methylene chloride, toluene,
       acetone, and three other VOCs were detected in  the

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   reagent blanks.   Methylene  chloride  is  probably  a
   laboratory contaminant.   Only  toluene  of these  six  was
   considered in the VOC analyses,  and  some errors  in
   these values may exist.   Toluene was  only one  of five
   VOCs looked at for reporting  VOC data.

   Spiked sample results — All  the metals  recoveries and
   almost all the VOC and PCB  recoveries  were within  the
   acceptance range.

   Duplicate sample results--Matrix spike  duplicates  for
   metals showed excellent  repeatability,  with a
   coefficient of variation (CV)  less  than 5%.
   Repeatability for VOCs was  also  acceptable, with a  CV
   of 50%.  The repeatability  for PCBs,  which had  a CV
   within 10%, was  acceptable;  50% is  the  maximum
   acceptable CV.  The repeatabi1itity  for O&G was  good,
   with almost all  CV less  than  5%, but  wide variations in
   sample homogeneity was observed.

Soil  sample leachates

   Blanks — Only acetone was detected in  two samples near
   the detection limits of 5 ug/1 and  was  probably  due to
   laboratory contamination.  Metals and  PCBs were  not
   detected in the  blanks.

   Spiked samples — Matrix spike  recoveries of lead  were
   high; therefore, results for  Pb may  be  biased  slightly
   high.  The recovery of the  other metals was within  the
   acceptable target range of  80-120%  of the theoretical
   value.  Volatile organic matrix and  surrogate  spikes
   were all within  the acceptance criteria.  For  PCBs  the
   surrogate spike  recovery of the samples was below
   acceptance limits; therefore  the detection limits of
   these compounds   (measured by  Method  680) could  be
   slightly greater than the laboratory reported.   PCBs
   were not found in any leachates.

-  Duplicate sampl es —Resul ts  for VOC  and O&G all  met
   acceptance criteria.  Duplicates for untreated metals
   samples were not performed,  but duplicates for metals
   in treated samples showed very low  CVs.

Slurry samples  (7-day cores)

   Blanks —No analytes were detected in the reagent
   blanks.

   Spiked samples —Matrix and  surrogate spike recoveries
   were within  the  acceptance  limits.   Recovery of toluene
   was above the acceptance limits, but impact on the
   overall results  should not  be significant.
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       Duplicate samples--Duplicate samples  analyzed for VOC
       by Method 8240 were within accuracy acceptance limits.

o   Slurry sample leachates

       Blanks — No metals or PCBs were detected.   Acetone was
       detected in some of the  blanks,  but since this is not a
       field contaminant and the levels were so  low, the
       effect on the results is negligible.

       Spike samples--Metals recoveries for  the  nine samples
       were all acceptable.  Matrix spike and surrogate spike
       recoveries for five VOCs were good although a few
       examples of deviation from the acceptance range were
       noted.  For PCBs the recoveries  were  low, indicating
       detection limits may be  higher than reported.  However,
       no PCBs were detected in the leachates.

       Duplicates--Al1  metals and volatile organics met the
       acceptance criteria on coefficient of variation.

o   Core samples and core sample leachates

       Blanks--Chromiurn, lead,  copper,  and zinc  were detected
       in reagent blanks.  However, review of the field data
       shows that the low levels of the analytes make these
       values insignificant.  Eight VOCs were detected in 1 or
       2 of 10 laboratory reagent blanks; therefore low levels
       of those compounds must  be reviewed with  some suspicion
       since toluene, xylene, and ethyl benzene, three of the
       five measurable components of VOCs, are  included.  PCBs
       were not detected in the blank.   Some phthalates were
       detected, but may be laboratory  contaminants.

       Spiked samples — Ten spiked samples for metals were all
       within acceptance limits of 80-120%.   Eight spiked
       samples for VOC were performed and virtually all
       results were within acceptance limits.  All BNA spikes
       met acceptance limits.

       Duplicate samples--Results for metals and VOC were very
       good, within a CV of 10%.

       BNA analyses — The high results for phthalates levels in
       blanks and low naphthalene in the matrix  spikes may
       provide cause for suspicion.  However, phthalates are a
       common laboratory contaminant and low levels in field
       samples may be an error.  An interlaboratory
       performance audit by Radian also left suspicions on the
       phthalates results.  The spiked  sample results for
       phenols met acceptance criteria.

From the above results for blanks, spikes, and  duplicates, the
chemical analyses should be acceptable.  The primary purpose
of the analyses is to observe changes and orders of magnitude

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of the values before and after the HAZCON treatment.   The
deviations noted above should have an insignificant impact.

The physical  tests,  moisture, bulk density,  and unconfined
compressive strength were performed in triplicate for each
sample collected.  The other physical tests,  permeability,
particles size,  and  pH,  were performed only  once on each
sample.  Permeability is the most important  parameter of the
tests performed  once.  The results showed all  the treated soil
permeabilities were  in the 10"° to 10"9 cm/sec range,
which is very low.  Exact numerical values and differences
between samples  is less  important than the observed
consistency of the order of magnitude results.

The QAPP did not include any protocols for the microstructural
analyses, which  were performed by Scientific  Waste
Strategies.  Since these results are only intended to be
qualitative and  no attempt was made to quantify, the trends
reported should  be valid.
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                           SECTION 8

                     DISCUSSION OF RESULTS
The analytical results summarized in Section 7.0, are
discussed and evaluated in Section 8.1. Operating procedures,
a chronology of which is presented in Section 5.2 for the
HAZCON Demonstration Test, are evaluated in Section 8.2

8.1  ANALYTICAL RESULTS

The analytical data consist of physical test results of
untreated soil, treated soil after a nominal 7-day curing
period, and essentially fully cured samples, which were
analyzed more than 28 days after treatment.  The discussion of
the analytical results can be further subdivided into the
fol1owi ng:

o   Physical tests
o   Chemical analysis - primarily soil composition and
    leachate results
o   Microstructural analyses
o   Overall evaluation

8.1.1  PHYSICAL TESTS

The physical tests on the soil and cores consisted of the
fol1 owing:

o   Free moisture - untreated, 7-day, 28-day
o   Undisturbed bulk density - untreated, 7-day, 28-day
o   Particle size distribution - untreated
o   Permeability - untreated, 7-day, 28-day
o   Unconfined compressive strength - 7-day, 28-day
o   Total organic carbon - untreated
o   Oil and grease - untreated, 28-day
o   pH - untreated soil
o   Wet/dry weathering - 28-day
o   Freeze/thaw weathering - 28-day
o   Unconfined compressive strength after weathering - 28-day

8.1.1.1  BULK DENSITY

The treated soil density was about 10-20% greater on average
than  the undisturbed untreated soils.  The bulk density test
for all samples was performed in triplicate.  In general,
except for the untreated soil in DSA, the individual area
results were in tight bands, with a bulk density greater than
1.4 mg/1 particularly for the treated soils.  For FSA, the
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treated soil  results were 5% lower than the untreated soil
results.  Results of the microstructural  analysis presented in
Section 7.2.3 indicate a very porous structure for all  the  7-
and 28-day cores, which may account in part for the relatively
small  bulk density increases.

The bulk density did not change between 7 and 28 days;  the
change occurred entirely in the initial 7-day period.  Density
decreased with higher oil and grease content, both for  the
untreated and treated soils.  Since the soil  represents only
about  40% of the total weight of the mix of soil, cement,
water, and Chloranan, and the bulk density increase is  10-20%,
the volume of the treated soil more than doubles.
Calculations for volume increase for each plant area is
provided in Appendix D.

The laboratory-prepared solidified formulations on soils from
LAN and FSA,  without the use of Chloranan, showed a lower bulk
density than the field samples, particularly for FSA.  For  FSA
the bulk density was reduced from 1.51 to 1.36 mg/1.  Two
possible contributory causes may be the lack of Chloranan or
the higher moisture content.

8.1.1.2  FREE MOISTURE

The water addition during processing was not tightly
controlled or adjusted for moisture in the feed.  The water
was adjusted by HAZCON based upon visual  observation of the
slump of the concrete mix.  Based upon the material balances
shown in Table 5.2, the total water added per run is the
correct order of magnitude, 40% by wt. of cement.  Comparing
the untreated soil with 7-day treated soil showed an increase
in free moisture content.  Comparing the 7-day material to
28-day showed that, except for DSA, the moisture content
decreased by about 10-15%.  This is probably due to the
continuation of the cement hydration reactions, which would
reduce free moisture  (drying at 60°C).  It appears that the
hydration reactions are 60-80% complete at 7 days, with DSA
and LAS close to 100% complete.

8.1.1.3  PERMEABILITY

The permeabilities of the treated soils were very low,
primarily in the range of 10"8 to 10"9 cm/sec.  This
compares to undisturbed soil permeabilities  of about 10"1 to
10"z  cm/sec, except LAS, which was near 10"5 cm/sec.
Calculations for the  permeability reduction  factors  are
provided in Appendix  D.  The permeability for the laboratory
formulations without  the use of Chloranan were a factor of  10
greater than field cores for LAN and  equivalent to the field
cores for FSA.  The untreated  filter  sludge  was  impermeable,
and the scheduled  tests could  not be  performed.  In  general,
for stabilization/ solidification processes, 10"' cm/sec is


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considered impermeable.  The design of soil  barrier liners for
waste disposal sites target permeabilities of 10"' cm/sec or
less.  The permeability for the two laboratory formulations on
LAN and FSA, without the use of Chloranan, provided results
that were a factor of 10 greater for LAN and equivalent for
FSA to the field cores.  There were not any  differences
between the nominal 7- and 28-day core sample permeabilities.
This is due to the fact that the 7-day as well as the 28-day
permeability tests were run after curing for 30+ days.  The
permeability measurements were very time-consuming, and
difficulties were encountered in performing  the analyses.
Therefore, they could not be performed in the time frame
originally planned.  Tables A-14 and A-23 in Appendix B
provide all the permeability results and the dates on which
the tests were performed.

8.1.1.4  UNCONFINED COMPRESSIVE STRENGTH

The unconfined compressive strength test, which for each
sample was performed in triplicate, produced individual values
that ranged from about 100 psi for FSA to above 2200 psi for
DSA.  Based upon the averages of the three tests, the range
was from 220 psi at FSA to 1570 psi at PFA,  both at 28 days.
In general, compressive strength was markedly lower with
increased oil and grease (O&G).  The average of triplicate
tests at 28 days for the two highest oil and grease areas was
about 220 psi for FSA (25.3% O&G) and 520 psi for LAN (16.5%
O&G).

Decreasing pH with increased O&G is believed to be a result of
the oil and grease concentrations and not a  factor in the
unconfined compressive strengths.  The soil  particle size
distribution may influence core strengths, but insufficient
data exists to confirm.  In addition, with the exception of
PFA, which was a litter coarser, the particle size
distributions were equivalent.

Although it was expected that the 28-day sample tests would
give higher strengths, this was not evident  from the results.
The free water levels discussed above indicate that the cement
hydration reactions were still proceeding, which should have
resulted in increased strengths.  It appears that LAN and PFA
did increase  in strength, but that the others either decreased
or remained unchanged.  An explanation for this unexpected
lack of strength increase is not available.

For the laboratory formulation tests on FSA and LAN, definite
increases in  strength between 7- and 28-day cores of 30-50%
were observed.  These formulations for LAN obtained 7- and
28-day core strengths comparable to the field blocks.
However, for  FSA, the field blocks were many times stronger.
This seems to confirm that the Chloranan helped the
solidification process.  At lower oil and grease levels, the
effect of Chloranan may be less significant.


                               97

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8.1.1.5  OIL AND GREASE

Oil  and grease levels ranged from about one percent by weight
for  DSA to 25% for FSA.  Typically the total  organic carbon
(TOC) level  is about 4-5% greater than the level  of O&G,  which
is as expected.   The values for O&G reported  for  the screening
samples are  consistently greater than for the feedstocks  used
in the Program.   This probably can be explained by the method
of obtaining each feedstock for the Demonstration Test,  where
a backhoe was used; some less-contaminated soil was excavated
along with the more-contaminated soils.  For  the  screening
samples,  the most contaminated area in each plant location was
targeted  and only a 40 Ib sample was collected.

8.1.1.6  pH

In general,  the  feedstocks were acidic, except for PFA.
Values as low as a pH = 2.4 were obtained for FSA samples.
There is  some trend toward lower pH values with increased oil
and  grease levels.  However, the original source  of the
contamination would also have an impact,  not  just the
quantity.

8.1.1.7  PARTICLE SIZE

Particle  size distributions on the untreated  soils were  also
measured, except for FSA, which was too sticky for the
screening analyses.  Basically the soils  are  fine, with  about
half the  soil by weight finer than 200 mesh (74 micron).   PFA
was  somewhat coarser than the other soils.

8.1.1.8  WEATHERING

The  two weathering tests, wet/dry and freeze/thaw, are twelve-
cycle tests, measuring weight loss relative to a  control
specimen.  The control specimen is maintained at  72°F in  a
moisture  chamber, when the test specimens are dried or frozen
for  24 hrs.   Both samples then are inserted into  water and
placed in the moisture chamber for 24 hrs.  The results  of
samples from each site location for the wet/dry tests indicate
that the  weight  loss of the test specimens is only slightly
greater than for the control.  However, the loss  differentials
during the freeze/thaw tests appear to be larger.  All weight
losses were  about one percent for both the specimens and
control s.

Unconfined compressive strengths on both  the  test and control
specimens were run.  The results for the  test samples show
that compressive strength was not lost in either the test
specimens or controls.

8.1.1.9  OTHER OBSERVATIONS

Significant  variations in physical properties of the soil

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between each composite within a soil  area were noted.  For
example, oil and grease at LAS ranged from 6.1% to 8.6% and
for LAN from 14% to 18%.  Moisture levels were also somewhat
variable at FSA, LAS,  and LFA.  This  means that individual
grab samples within a  given feedstock are even more variable.
Thus,  physical  test results on untreated soil  based on average
feed properties may not be directly related to the 7-day and
28-day core sample results, which are based more on localized
properties of the solidified soil samples.  Although it is
believed that the overall results are representative for each
plant  area, individual distortions in the data do exist.

In addition, significant variations even within a sample,
split  spoon or  core,  probably exist.   Many of the leaching
tests  (see Appendix D) showed a larger weight of an analyte or
organics group  existed in the leachate than in the solid.
Also,  consistent material balances for the lead and organic
analytes between treated and untreated soil could not be
obtained from the data.  Only for total  oil and grease was
there  a consistency in the concentrations before and after
treatment.  However,  due to the large amount of data
available, definitive  trends in the results exist.  Therefore,
the results obtained  are still valid.

The laboratory  formulations were prepared without Chloranan,
similar to the  method  concrete is typically blended.  For  FSA,
the UCS test values were about one-tenth of those for samples
collected in the field.  In addition, the bulk density was
lower  by almost 10%.   Results for the other laboratory
prepared samples were  equivalent to the  field prepared and
cured  samples.   Thus,  Chloranan improved the physical
properties of a treated soil where the oil and grease levels
were high, about 25%  by wt in the untreated soil.

A grab sample of the  process water showed low suspended and
dissolved solids, with a pH of 8.05.   This water should not
impact the process or  any of the laboratory analyses.

8.1.2   CHEMICAL ANALYSES

The chemical analyses  consist of the  following:

    o     Untreated and treated soil compositions
    o     TCLP leachate analyses
    o     Special leach test analyses

A discussion of the results highlighted  in Section 7.2.2
fol1ows.

8.1.2.1  SOIL COMPOSITION

The composition of the untreated soil was basically as
expected.  The  oil and grease values  were a little low

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compared to the values anticipated based upon the screening
samples and the RI/FS prepared by NUS Corporation for EPA
Region III.  This probably is due to the inclusion of
less-contaminated soil around and below the targeted soil and
to the general  variability within each area.   Samples having
the maximum oil and grease in each of the six plant areas were
targeted for the screening samples.

The PCB concentration levels, with averaged values up to 52
ppm at LAS, were higher than originally anticipated based upon
the RI/FS and screening samples,  which were at less than 25
ppm.  The two Aroclors detected were the same as measured in
the screening samples, but both were at higher concentrations.

The results for the priority pollutant metals were as
expected.  Lead was the major contaminant with concentrations
up to 2.3% by wt. measured.  After reviewing  the soil
analyses, only the major metal contaminants were carried
forward to analyze in the 28-day cores and leachates.  These
were chromium,  nickel, zinc, copper, and cadmium.  In general
the levels of contamination in the soil agreed with those
obtained during the screening tests.

The results for the base neutral/acid extractable (BNAs)
showed primarily phthalates, phenols, and naphthalene.
Phenols differ from other BNAs in that they have greater
solubility in water and therefore, may be more readily
Teachable.  Other BNAs reported in the RI/FS  but not detected
in the screening analyses, such as fluorene,  pyrene, and
f1uoranthene, were only occasionally detected in these
analyses.  The phenols were not checked for on the screening
samples.  Phthalate concentrations in the 28-day core samples
(ND to 2.15 mg/kg) were very low compared to  the untreated
soil (12.15 to 34.2 mg/kg).  This may be caused by
base-catalyzed hydrolysis reactions, which is a reasonable
possibility, or possibly other reactions caused by the
Chioranan.

The volatiles  in the  FSA samples were considerably greater
than anticipated, averaging 150 ppm by wt.  It had not been
expected to observe volatile levels above 30 ppm for any of
the plant areas.  The screening test results showed LAS  to
have the highest concentration of volatiles,  with much less
reported for any of the other plant areas.  For LFA, PFA, and
DSA, toluene was injected into the slurry mix to produce a
final concentration of 125 ppm by wt., based upon the feed
soil.  The maximum value reported in the core samples was 24
ppm in 28-day  cores at LFA, with values down to  1 ppm.   Since
the soil  is only 40%  of the total core weight, this maximum
value is equivalent to 60 ppm on a soil weight basis.
Therefore, the majority of the toluene was lost.  This
indicates  that the toluene either vaporized off  in the HAZCON
mixing screw,  possibly due to poor injection or  improper

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mixing, or during sample preparation in the pulverization
step, or both.  However, sufficient toluene remained to
provide valuable information for leaching test analyses.

Attempts to relate VOC and BNA component concentrations before
and after solidification were not successful.   There was such
variability in the grab samples that in some cases it appeared
that concentrations were greater in the cores  than in the
untreated soil.  However, for oil and grease,  approximate
material balances could be obtained; see Tables 7.1-7.6.

8.1.2.2  TCLP LEACHATE ANALYSES

Oil and grease in the leachates from the untreated soils were
near the detection limit of 0.2 ppm by wt.  in  the range of
<0.2 ppm at DSA to 3.7 ppm at FSA.   These results are lower
for each plant area than for the 7- and 28-day core leachates,
where the results were in the range of 1-10 ppm by wt.  (mostly
2-4 ppm by wt.) .  Since these values are all so close to the
detection limits for the laboratory procedure, it may not be
proper to differentiate between them.  However, it is also
possible that the treatment process tended  to  agglomerate the
oil and grease and after crushing the solid core for
performing the leach test, some O&G globules were released
into the leachate.  The leachate concentrations for the
special leach tests were less than  for TCLP.  Also, the oil
and grease concentrations in the treated cores are about 40%
of these of the untreated soils.

The immobilizing of the priority pollutant  metals was
accomplished by the solidification.  Except for lead and zinc,
virtually all the metals were reduced to their detection
limits in water.  For lead the values were  just above
detection limits, ranging up to 400 ug/1, which is well below
regulatory levels of about 5 ppm by wt.  However, lead  was the
predominant metal contaminant with  measured soil
concentrations ranging from 0.3 to  2.3% by  wt., so the  lead
reduction was dramatic.

Except for phenols, the BNAs (semivolati1e  organics) were
reduced to near their detection limits of 10 ug/1 in the
leachates of both untreated and treated soil samples.  This is
a reduction of more than one thousandfold,  compared to  the
contaminated soil.  However, the phenols were  not reduced to
the same extent.  For LAN and FSA,  with concentrations  in the
soil or cores ranging from 5-400 ppm by wt., the reduction
factor is of the order of 10-100.  For FSA, TCLP leachate
concentrations of 3-4 mg/1 were observed for both treated and
untreated soils.  Therefore, the HAZCON process did not appear
to reduce the Teachability of phenols.  Results of the  MCC-1P
and ANS 16.1 leach tests provided equivalent results.  In
addition, the quantity of phenols in the leachate increased
with time.
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The volatiles in the leachates ranged from 100 to 1000
micrograms per liter (for the higher soil  and core
concentrations).  These are reduction factors of about 100 on
average compared to the soil.  However,  the concentrations in
the untreated soil, 7-, and 28-day core  leachates are
approximately the same.  Therefore,  at least in the
concentration range investigated,  up to  150 ppm by wt. (FSA),
the solidification did not appear  to impact the leachate
results.  The results of the special leach tests showed
leachate concentrations less than  for TCLP leachates, and the
concentrations did not appear to be  time-dependent.

Calculations for total VOCs, toluene, total BNAs, phenols, and
lead showed in many instances, except for  lead, greater
quantities of the analyte(s) in the  leachate than in the
soil.   This indicates that great variability in the
concentration of these analytes may  exist  within a given
sample.  Concentrations in the test  specimens used for the
three  leach tests were possibly much greater than in the
material used for determining concentration levels in the
total  samples.  This could also account  for, in some cases,
the greater migration potential (leaching  potential) of the
organic analytes in the treated soil compared to that in the
untreated soil,  even though average  concentrations of the
analytes in the  cores are less than  one-half those in the
untreated soil.   However, since many leaching analyses have
been performed,  the general observations for organics, that
the leachate concentrations for the  treated soils are about
the same as the  untreated soil, is valid.

The special leach tests, MCC-1P and  ANS  16.1, were performed
on one sample set taken from 28-day  cores  for LAN, FSA, PFA,
and LAS.  In general, for a given  time frame, the results from
MCC-1P were greater than from ANS  16.1,  which may be due to
MCC-1P being performed at 40°C vs. ambient conditions for
ANS 16.1.

The MCC-1P leachate concentrations for VOC and BNAs were
equivalent to TCLP extracts.  For  lead the values were greater
and increased with leach time.  For  oil  and grease, the TCLP,
MCC-1P, and ANS  16.1 leachate concentrations appear equal.

A brief comparison test between EP Tox and TCLP for metals was
performed on samples from LAN and  FSA.  The results for EP Tox
were greater for LAN and about the same  for FSA.  This is
expected for basic solutions  (these  leachates are basic due to
the cement components).

8.1.2.3  SPECIAL LEACH TEST ANALYSES

Leach tests ANS  16.1 and MCC-1P were two procedures originally
developed for the  nuclear  industry for the leaching of low
level  radioactive  wastes, but have been  applied with
modifications to hazardous wastes.  These tests utilized solid

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cores simulating the solidified wastes,  as  compared to TCLP
and EP Tox where the solid cores are first  ground to a
powder.  MCC-1P simulates a relatively static groundwater
flow, with the samples in contact with one  leachate for time
periods of 3,  7, 14, and 28 days at a temperature of 40°C.
ANS 16.1 simulates a moving groundwater  regime with the solid
core specimen  placed in a new fresh leachate, so that the
boundary concentrations of the analytes  are kept below
saturation level.   Samples are collected after 1, 3, 7, 14
days with the  total  leach time being 28  days. A diffusion
coefficient might  then be calculated.

It should be noted that experience with  these tests on
hazardous wastes is  limited.  Comparisons to the treated soil
TCLP results have  been made, but the significance of the
differences is unclear.  Some differences would be expected
due to the diverse ratios of solid to extract used in each
test.  The nature  of these two procedures,  that of simulating
leaching from  a solidified mass, makes it illogical to perform
these tests on untreated soils.  Therefore, the results of
these tests are compared to the treated  soil TCLP tests only.

It was anticipated that TCLP would be the most severe leaching
test, providing the  highest contaminant  concentrations in the
extracts.  However,  the extract concentrations for the metals
for MCC-1P were greater than for TCLP, 0.3-0.7 mg/1 versus
0.01-0.06 mg/1, and  approximately equivalent for VOCs, BNAs,
and oil and grease.   This indicates that at least for the
28-day cores from  the HAZCON process the increased surface
area for leaching  for the TCLP test is balanced by the
increased time and temperature of MCC-1P.  The differences
between MCC-1P and ANS 16.1 extracts may be due to the higher
leaching temperature, 40°C versus 22°C.

Since the leaching times range from 1 to 28 days in these
tests, the effect  of time was reviewed.   For the organics,
time did not appear  to be related to leachate concentrations
except for phenols in the MCC-1P test.  Since phenols are
soluble in water,  this is not unexpected.  The concentration
of lead appears to increase with time for both leach tests,
although the trend for MCC-1P is less definitive.

8.1.3  MICROSTRUCTURAL STUDIES

Microstructural and  microchemical analyses  are proven methods
for understanding  the mechanisms of structural degradation  in
materials similar  to those in this Demonstration Test.  The
literature is  replete with examples of SEN  and XRD analyses of
soils, cement, soil-cement mixtures, and each of these mixed
with various inorganic and organic compounds.  However, there
have been relatively few studies of the  microstructure of
complex waste/soil mixtures like those resulting from
stabilization/solidification procedures.  Consequently, in

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some cases interpretation of microstructural  observations may
be difficult.  The microstructual  report is intended to be
complete in its reporting,  yet conservative in its
conclusions.   Many observations will  become more useful as the
understanding of stabilization/solidification technologies
improve.

A discussion  of the results presented in Section 7.2.3
fol1ows:

o   The two predominant clays seen in the samples, illite and
    kaolinite, are nonexpandable clays.   Therefore,  the
    organic compounds in the soil  will  not be adsorbed within
    the layers of the clay minerals.   Any organics adsorbed
    will be on the outside surface and  therefore will  be more
    loosely held.

o   The crystalline phases seen in the  core samples,
    portlandite, ettringite, calcium silicates,  calcium
    aluminate, and gypsum,  are the principal  components of
    Portland  cement.  Portlandite  and ettringite are the major
    hydration phases of portland cement.  Thus,  the  major
    bonding agent is portland cement, and SEM observations
    agree with this conclusion.

o   An abundance of pores of all sizes  and shapes were
    observed  in the core samples.   Some  of the pores were due
    to trapped air bubbles.  The high concentration  of the
    pores may be due to incomplete mixing.  Crystals of
    portlandite, calcium aluminate hydrate, and  ettringite
    grew into these pores.   These  crystals are thus  more
    easily accessible to percolating water.

o   The quantities of unhydrated tricalcium silicate and
    dicalcium silicate were much greater than usually observed
    in hydrated portland cement with moderate water-to-cement
    ratios.  The water-to-cement ratio  of 0.4, typical of
    cement, is used in the processing operation.  The high
    concentration of unhydrated silicates could  result from
    inefficient mixing, resulting  in insufficient water
    transported to these grains.

o   Mixing does not appear to be highly efficient.  Among the
    facts indicating this are:  1) the  brownish  aggregates do
    not undergo disaggregation 2)  there  are significant
    amounts of unhydrated Portland cement clinker in the
    samples,  3) there are globules of dark colored material  in
    the core samples visible to the naked eye, and 4) there
    are many pores, including air bubbles.

o   Two factors suggest that soil  components passed through
    the process unchanged.  They are the presence in the cores
    of apparently unaltered brownish aggregates  and peaks in


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    the x-ray diffraction pattern for both the soil  and the
    cores, which could not be identified with any expected
    mineral constituents of the soil.

In summary, some of the waste in the soil appears to pass
through the process unaltered, and thus, it appears  that
encapsulation is a major part of the mechanism of
solidification/stabilization.  In addition, the mixing
operation is not highly efficient, resulting in incomplete
hydration of the cement and high porosity.

8.2  OPERATIONS

For the 5-cu-yd test runs, HAZCON utilized four people to
operate the unit.  Their functions were as follows:

    o    1 man - add feed soil and water to feed hopper
    o    2 men - move and watch slurry mixer, smooth surface
         of blocks, and control Chloranan flow
    o    1 man - at the control panel and supervise  operations

In addition, EPA provided support services to excavate the
feedstock, screen it, and bring it to the HAZCON MFU.  The
soil was brought to the unit in a 2 1/4 cu yd (soil  level to
surface of bucket) front-end loader, which fed it very slowly
to the feed hopper at approximately the rate the MFU processed
it.  Therefore, at least two support people were required full
time to provide feed to the HAZCON unit.  Also a cement supply
truck with operator/driver was on hand full time.  For the
25-cu-yd run, three additional people were required  to operate
the cement pump and control the feed to the large pits.

Some operating difficulties were encountered in all  of the
runs, causing down times on the order of one minute  to two
hours.  The shutdown periods related to momentary screw
pluggages due to lack of water, oversized feedstock  (stones
greater than 3 inches), interruptions of Chloranan feed, or
emptying of the cement feed hopper, which required refilling
from a supply truck.  For two runs, DSA and PFA, only four
blocks were prepared due to a combination of lack of daylight,
need for more feed, and operating difficulties.  On  two
occasions the soil feed screw jammed so badly that the MFU had
to be brought to the decontamination area for a complete clean
out.  Direct addition of water by hose to the feed screw
facilitated the movement of the soil and reduced the
likelihood of jamming.  This was a water feed stream that was
not measured directly by the in-line flowmeter.  Only
approximate consumptions could be provided.

In generally observing the operations, the consistency of the
slurry was quite variable due to variations in water
feedrate.  The consistency of the mixed product varied from a
very thin slurry to almost a dry powder.  In addition, the

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variability of the slurry mix may have prevented the Chloranan
from achieving its fully claimed benefit in counteracting the
presence of organics.  As indicated in Section 8.1.3,  if
insufficient water is provided,  components of the cement, such
as the tricalcium silicate was incompletely hydrate, as
observed in the x-ray diffraction analyses.  This will  result
in a weaker and less durable block, as compared to a block
from fully mixed components.

A review of the material balances shows that for the 5-cu-yd
runs, the total mass of the blocks was consistent with  the
calibrated rates for cement and  soil  adjusting for outage
time.  Material balances also indicate the following:

o   The soil was only 40% of the total weight of the blocks.
o   The cement-to-feed ratio was approximately 1:1.
o   The Chioranan-to-feed ratio  on a  weight basis ranged from
    0.05 to 0.09, which is less  than  the target value  of 0.1.
    The lowest value was for FSA.  No apparent reduction in
    physical properties were observed.
o   The water-to-feed ratio was  approximately 0.4 on a  weight
    basis, which is appropriate  for concrete preparation.
o   The volume of undisturbed feedstock to produce the  5 cu yd
    of slurry to fill the five 1-cu-yd molds was approximately
    2 cu yd.  (The front-end loader held 2 1/4 cu yd,  filled
    level to the top of the bucket, which produced 4 to 5
    blocks.)  The approximate bulk density of the screened
    soil after transporting to the unit was about 20-30% less
    than in the undisturbed samples analyzed and reported in
    Tables 7.1-7.6.

For the extended length run at LAS, approximately 22-24 cu yd
of slurry was produced to fill the three 1-cu-yd molds  and the
two large excavations.  The excavations were 8x16 ft and were
filled to a depth of 2-2 1/4 ft.  As  shown in Table 5.1,
approximately 52,300 Ibs of the  total feed (soil + cement +
Chloranan + water) was used.  However, based upon the  bulk
density of solidified soil of 1.7 g/ml (106 lbs/ft3),  for
the total weight processed only  about 18 cu yd of slurry would
have been produced.  Therefore,  it appears that 10,000-15,000
Ib more total feed material was  processed.  Since the  cement
and water rates are constantly measured and the soil is based
upon the initial calibration, it is quite likely that  the
missing mass, compared to the HAZCON  Monitoring Worksheet, is
contaminated soil.  Six front-end loader loads of soil  were
processed, which is approximately 13-14 cu yd.  If the
screened feed soil had a bulk density of 1.2-1.3 g/ml  (75-80
lb/ftj), this would indicate a total  soil usage of about
30,000 Ib, which is over 10,000  Ib greater than that recorded
on the HAZCON Monitoring Worksheet, thus providing sufficient
feed to fill the pits.

Also shown on the Monitoring Worksheet, two-thirds of the
cement was used before starting  the slurry flow to the second

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large pit; this value should have been only slightly more than
50%.  This ratio tended to be confirmed by the fact that 130
of a total of 255 gallons of Chloranan was used only 10
minutes after the second large pit was started.

Based upon this reasoning, the overall ratio of cement-to-soil
was about 2:3 and probably even lower for the second large
pit.  In addition, the Chioranan-to-soi1  feed rate is about
0.08 versus that listed in Table 5.2, 0.119, which is based
upon the HAZCON Monitoring Worksheet.  It does not appear that
any loss in physical  properties resulted  from this apparent
reduction in cement feed.  (See Appendix  B, Table A-14.)

8.3  MEETING OF SITE PROGRAM OBJECTIVES

Information relating to each of the program objectives in
Section 1.2 was obtained.  This information can be summarized
as follows:

o   Immobilization of site contaminants — The priority
    pollutant metals were very satisfactorily immobilized,
    with leachate concentrations reduced  to below 0.1 ug/1 for
    soils containing metals up to 23,000  mg/kg.  Untreated
    soil extract concentrations were typically 20 to 50 mg/1.
    Immobilization of organics, VOCs, BNAs, and PCBs was not
    observed.  TCLP leachate concentrations for organics in
    untreated and treated soils were approximately equal.
    This occurred even though, on average, the treated soil
    composition is lower in contaminants, due to the addition
    of cement, water, and Chloranan.

o   Technology effectiveness as a function of oil and grease
    concentrations—The soil samples taken were in the range
    of 1-25% by wt. oil and grease (O&G).  Higher O&G soils
    tended to have more VOCs and BNAs.  Greater VOCs and
    phenols (BNA components) led to higher leachate
    concentrations.  The most direct impact of higher O&G is
    reduced unconfined compressive strength.  In addition,
    FSA, which had the greatest O&G content, appeared to have
    a slightly greater permeability than  the other test
    samples.

o   System performance—The operational performance of the
    system was erratic, with many short and long shutdowns.
    The system shutdowns ranged from 1-2  minutes up to 2-3
    hours.  Many shutdowns occurred for each soil feedstock.
    The slurry consistency was quite variable, ranging from a
    powdery mix to a very thin slurry.  However, for the
    extended duration run, operation outages were less and the
    consistency of the product slurry improved.  The impact of
    consistency on physical or chemical properties of the
    solidified blocks was not observed.
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Long-term integrity--Measurements  of long-term integrity
of the solidified  masses cannot be directly performed.
However,  indications  of potential  difficulties could be
inferred  from the  microstructural  analyses.  These
observations showed a porous structure,  with incomplete
cement hydration and  organic globules existing in the
solidified cores.

Remediation costs--Remediation costs were prepared based
upon using HAZCON's MFU and the operating conditions used
for the Demonstration Test.  The results showed that the
cleanup cost was $205 per ton of contaminated soil under
the ground rules defined.
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                           SECTION 9

                           ECONOMICS
9.1   INTRODUCTION

A cost analysis addresses two main categories,  capital  costs
and operating and maintenance costs.

Capital  costs include both depreciable and nondepreciable cost
elements.   Depreciable costs include  direct costs for site
development, capital equipment,  and equipment installation as
well as  indirect costs for engineering services prior to unit
construction, such as feasibility studies and consultant
costs, administrative tasks such as permitting, construction
overhead and fee, and contingencies.   Nondepreciable costs
include  start-up costs including operator training,  trial or
test run expenses, and working capital.   Operating and
maintenance costs include variable, semivariable and fixed
cost elements.   Variable operating cost  elements include raw
materials,  utilities, and residual water disposal costs.
Semivariable costs include unit  labor and maintenance costs,
and laboratory  analyses.  Fixed  costs include depreciation,
insurance,  and  taxes.

The above  cost  element breakdown, however, is based  upon a
permanently sited hazardous waste cleanup device.  The  HAZCON
MFU as employed at the Douglassvi11e  Superfund  site  is  a
transportable unit that will not be installed at a fixed
site.  Thus, it assumes some different cost elements that will
impact on  a cost analysis from the more  frequently encountered
permanent  installations.

In general, the cost for a transportable hazardous waste
remediation facility falls into  three categories:  capital
costs including all  costs that can be amortized over the
service  life of the  unit; mobilization/demobilization costs
associated  with start-up and shutdown at a given site,  that
can be amortized over the duration at the site; and  operating
cost to  operate and  maintain the system.  Capital costs can be
subdivided  into direct, indirect, and nondepreciable cost
elements.   Mobilization/demobilization costs can be  accrued as
semivariable operating and maintenance costs.  Operating costs
include  variable utility and raw material costs, semivariable
labor and  maintenance costs, and fixed costs such as
depreciation, insurance, and taxes.

In addition, for a mobile unit,  several  capital cost elements
defined  for the permanently sited unit should be redefined
into a different cost element category.   These  include  the
direct costs for site development and the direct costs  for

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engineering studies,  which on a site-specific basis become
mobilization/demobilization costs.   These factors are not
included here because of the complexity of the analysis and
planning in this area.   Total site  cleanup is the
responsibility of others,  with the  HAZCON technology used for
only part of the total  remediation.

Based on the above,  an  overall cost  element breakdown, as
illustrated in Table  9.1,  can be developed.

9.2  COST ELEMENTS

A detailed discussion of each of the cost elements defined in
Table 9.1 is provided in the following subsections.  Since
this cost analysis is being prepared based upon the
Demonstration Test,  the cost to process each ton of
contaminated soil will  be  distorted  to a greater value.  Cost
projections for a commercial installation will be included in
the Applications Analysis  Report.   In addition, not every
expense that might be encountered  in a site cleanup is
included.  Items such as permitting  and site preparation were
omitted due to their  complexity to  predict costs.

9.2.1  CAPITAL COSTS

9.2.1.1  DIRECT COSTS

Equipment Fabrication/Construction  and/or Purchase --

The costs for the design,  engineering, materials and equipment
procurement, fabrication and installation of the HAZCON MFU
(including vehicle),  are included  as direct costs.  The costs
include all the subsystems and components installed but do not
include the costs of the vehicles  for the transport of the
accessory equipment,  described in  Section 3.2.  Waste
preparation equipment is not included as it can be assumed to
be rented or provided by the site-responsible party.
Pretreatment or posttreatment of the soil is assumed not to be
required.  For the items calculated  as a fraction of direct
costs, the total of the HAZCON MFU  and associated tanks,
pumps, etc., is the capital cost value used.

The capital cost value of the MFU was provided by HAZCON and
is $100,000.  It is assumed that the equipment has a 10 yr
life.  In addition, storage bins or tanks for cement,
Chloranan, and fuel are required,  as well as an air blower for
transferring cement,  pumps for the  liquid, and associated
piping and controls.   This was assumed to be an $80,000 cost
to the project, whether the equipment was purchased new or
used or it was sold or discarded at project completion.  These
factors are site specific and major variations could occur
between sites.
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9.2.1.2  INDIRECT COSTS

Administrative/Permitting --

Administrative costs associated with regulatory compliance
issues could be numerous and varied.  The costs that are being
accrued under this cost element are directed to the overall
non-site-related regulatory activities in establishing federal
and state permit requirements,  preparing initial  permit
applications, and supporting permit application information
throughout the permit issuance  process.   Once the final
permits are issued, recordkeeping,  inspection,  survey response
to permitting agencies, and additional reporting  activities
may be required.  These costs include the preparation of
technical support data, sampling/analysis,  and  quality
assurance project plans by in-house engineering personnel,
RCRA/TSCA permit forms (if applicable);  time, travel, and per
diem for consultant and in-house staff interfacing with
Federal EPA officials; and in-house administrative and
clerical staff.  For the cost estimates  developed in this
analysis, these factors are not included.

For this cost analysis, administration costs are  taken as 10%
of direct costs (HAZCON MFU and tanks, pumps, etc.) on an
annual basis.  It includes office expenses  such as supplies,
telephones, reproduction equipment, and  furniture, but not
salaries (included elsewhere).

Contingency --

A contingency cost, approximating 10% of the direct capital
cost on an annual basis, is allowed for  unforeseen or poorly
defined cost definitions.  For  the  HAZCON process this is a
minor factor.

9.2.1.3   NONDEPRECIABLE COSTS

Operations Procedures/Training  --

In order to ensure the safe, economical, and efficient
operation of the unit, the creation of operating  procedures
and a program to train operators is necessary.   Costs that may
accrue include:  preparation of a unit health/safety and
operating manual, development and implementation  of an
operator training program, equipment decontamination
procedures, and reporting procedures.  These documents must be
site-specific.  They can be related to basic documents, the
preparation costs for which can be  amortized over the life of
the equipment.
                              Ill

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               TABLE  9.1.   COST  ELEMENT  BREAKDOWN
CAPITAL COST

  Direct

     o  Equipment Fabrication/Construction or Purchase

  Indirect

     o  Administrative/Permitting
     o  Contingency

  Nondepreciable

     o  Operations Procedures/Training
     o  Initial Start-up/Shakedown
     o  Working Capital

OPERATING & MAINTENANCE COSTS

  Variable

     o  Raw Materials - Cement
     o  Fuel
     o  Power
     o  Water
     o  Chemicals - Chloranan

  Semi vari able

     o  Labor
     o  Maintenance
     o  Equipment Rentals and Consumables
     o  Analytical Services
     o  Mobilization/Demobilization

           Site Preparation/Logistics
           Transportation/Setup
           On-Site Checkout
           Working Capital
           Decontamination/Demobilization

  Fixed

     o  Depreciation
     o  Insurance
     o  Taxes
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It was assumed that three days of training would be required
for all  HAZCON personnel, site support personnel,  health and
safety officer,  and sampling technician.   The cost includes
salaries and living expenses.   These are  the only  costs
included in this category.

Initial  Start-up/Shakedown  --

After the unit is brought to a site it must be initially
started  and  operated to check out the mechanical  and
technical integrity of the  equipment and  its controls.   This
cost is  assumed as part of  site mobilization.

Working  Capital  --

Although the unit is a transportable system, it will  require a
supply of maintenance materials attributable to a
nondepreciable capital cost.  Maintenance materials account
for approximately one-half  of  the total  maintenance cost,  and
3-month  inventories are usually maintained.  This  cost  as  used
in Table 9.2 is assumed as  10% of maintenance costs.

9.2.2  OPERATING & MAINTENANCE COSTS

9.2.2.1   VARIABLE COSTS

Variable operating cost elements for this unit include  fuel,
power, water, chemicals, and process waste disposal.   They are
defined  as variable operating  cost elements because they can
usually  be expressed in terms  of dol1ars-per-unit  flow  of  soil
treated  and as such, these  costs are more or less  proportional
to overall facility utilization during specific site
operations.  It is also assumed for the tabulation of costs
that there are no process waste byproducts.

Fuel --

The fuel requirement for the unit includes diesel  fuel  to
power the vehicle part of the  MFU.  In addition, fuel is used
for supporting vehicles - backhoe, front-end loader,  etc.   It
is estimated by HAZCON that their equipment will consume 4
gph.  It is assumed that the supporting equipment  consumes an
additional 4 gph.  The cost of diesel  fuel is about $1.00/gal.

Power --

The power requirement for the  unit includes the electrical
requirements for the trailers, sampling equipment, auxiliary
lighting, etc.  It is assumed  that the daily average  power
consumption is 5 kw with the cost of electricity $0.04/kwhr.

Water --

Water use is based upon the water content of the feedstock to

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bring the cement-like final  slurry to about 20% by wt.  water.
In addition,  some water is used for decontamination.   The
total average water usage rate is 14 gpm at a cost of $0.80
per 1000 gal Ions.

Chemi cals - -

The HAZCON proprietary additive is Chloranan, which inhibits
the effects organics have on the solidification of cement.  It
is utilized in a ratio to the contaminated soil of 1:10.
HAZCON indicates the delivered cost for cement is $50/ton and
Chloranan is  $3.00/gal (Chloranan density is 9.0 Ibs/gal).

Decontamination Water --

If the unit is not operated  24 hours per day, the unit needs
to be cleaned with high pressure water or steam to prevent
plugging.  Costs will accrue for the containment and  disposal
of this waste stream.  An additional 10% water consumption was
assumed.

9.2.2.2  SEMIVARIABLE COSTS

Labor --

Operating costs for personnel for the HAZCON unit is  based
upon 3 shifts per day, 21 shifts per week and totals  17
people; this  includes 12  process operators, 4 supervisors, and
1 overall coordinator.  In addition, there are support
personnel for operating the  contaminated soil moving
equipment, a  site safety  and health office, the project
manager, office personnel, and a part-time sampling
technician.  This totals  21  people.

The labor and living expenses for the HAZCON personnel  was
provided by HAZCON.  These costs range form $17.50/hr to
$50/hr for salaries with  overhead and $85/day for expenses.
The support personnel costs  were based upon actual costs
Incurred by EPA/Env1response for the Demonstration Test.
Salaries with overhead range from $20 to $60/hr with  living
expenses (except local hires) at $120/day.

Maintenance --

Maintenance materials and labor costs are extremely difficult
to estimate and cannot be predicted as functions of a few
simple waste  and facility design characteristics because  a
myriad of site-specific factors can dramatically affect
maintenance requirements.  Annual maintenance cost will be
assumed as 10% of capital cost.

Analyses --

In order to ensure that the unit is operating efficiently  and

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meeting environmental standards, a program for continuously
analyzing waste feed and treated solids is required.
Initially sample sets will be taken daily, and less often as
operation efficiency improves, approximately once per week.
based upon the expected need to perform many of the laboratory
tests described for the Demonstration Test, the cost of a
sample set is estimated to be $5000.

Mobilization/Demobilization --

As discussed in Section 9.1, the following costs will accrue
to the HAZCON unit at each specific site.   The costs are site-
specific and may vary widely depending on  the nature and
location of the site.  They include site preparation/
logistics, transportation/set-up,  construction supervision,
on-site checkout, site-specific permitting/engineering
services, working capital, and decontamination/
demobilization.  Site preparation  is assumed to be by others
and no costs are included.  The other costs listed above are
included elsewhere.  It is assumed that mobilization is three
days of salaries plus living expenses for  all personnel.

Site Preparation/Logistics -- The  costs associated with site
preparation/logistics include advanced planning and
management, detailed site design and development, auxiliary
and temporary equipment and facilities, water conditioning,
emergency and safety equipment, and site staff support.  Soil
excavation, feedstock preparation, and feed handling costs are
also included.  This may be performed by other than HAZCON,
but still comprises part of the site remediation costs.  Due
to the temporary and transient nature of the setup at
Douglassvi11e, the costs incurred  by EPA for the test are not
directly used because they would be misleading.  Costs for
advanced planning, detailed site design and development, and
water conditioning if needed, are  assumed  to be part of the
site prime contractor's expenses,  and are  not included.

Transportation/Set-Up --  The cost of transportation and
set-up includes disassembly of the unit at its presen*
location and transport to a new location.   The HAZCON unit is
integral with the vehicle automotive function.  Auxiliary
process equipment is transported on separate flatbed trucks.
The costs for transporting the unit to the Douglassvi11e site
are not included.

On-site Checkout --  Once the unit has been set up, it is
necessary to shakedown the system  to ensure that no damage
occurred as a result of disassembly, transport, and
reassembly.  This cost is shown as initial startup and is
assumed to be 10% of direct costs  calculated on an annual
basis.
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Working Capital  -- Fuel  inventory,  Chloranan,  and cement
storage facilities will  exist at each site,  and as such are
semivariable operating costs specific to the site-specific
mobilization/demobilization cost element breakdown.   It is
assumed that all these raw material  items will  be fully
consumed and therefore,  no additional charge to the  project is
added.  The storage facilities for  these materials are
included as part of the  direct capital  costs.

Decentamination/Demobilization -- With  the completion of
activities at a specific site, the  unit must be decontaminated
and demobilized before  being transported to its next
location.  Costs that will accrue to this cost  element include
field labor and supervision, decontamination equipment and
materials, utilities, security, health/safety activities, and
site staff support.  The demobilization costs included are
based upon three days for all personnel.

9.3  OVERALL COST EVALUATION

A primary purpose of this economic  analysis is  to estimate
costs for a commercial-size remediation.  It was assumed for
this analyses that part  of the Douglassvi11e site would be
remediated.  Due to the  short-term  nature of the Demonstration
Test and the fact that labor and chemical costs dominate the
remediation costs, actual costs for the test were not directly
used.  However, since HAZCON used a small-scale, continuous,
commercial unit, the capacity, on-stream factor, and chemical
usage during the Demonstration Test was the starting basis  for
a commercial cleanup estimate.  The results of the analysis
are presented in Table 9.2.

The results of  the analysis show that the cost per ton of soil
processed is $206.   In comparison to the costs of a future
commercial unit, which would be larger, have an improved
on-stream factor and probably use less chemicals, the cost  per
ton of soil processed is very high.  The lower values can be
obtained based  upon  HAZCON's recommendations for reducing
chemical consumptions 25-50% for attaining an on-stream  factor
of 90%,  and for use  of a new 2300 Ib/min batch processing unit
and might reduce these costs by 50%.  This type of analysis
will be  included in  the Applications Analysis Report.  Since  a
70% on-stream factor with  high chemical consumption was
actually seen at Douglassvi11e, PA,  the costs for this level
of operating efficiency were calculated.  It should be noted
that not all the expenses  encountered in a site cleanup  are
included, such  as  site preparation  and  permitting.

As can be seen  from  the results, 90% of the costs consist of
raw materials  (cement and  Chloranan) and labor.
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                   TABLE  9.2.   ESTIMATED  COST
CAPITAL COST

     Pi rect
       Equipment Costs, $                       100,000
       Chemical Storage, $/ton                     2.25

     Indirect.  $/ton
       Administration (10% Direct Costs)           0.32
       Contingency (10% Direct Costs)              0.32

     Nondepreciable. $/ton
       Operator Training (3 days)                  0.84
       Working  Capital

OPERATING AND MAINTENANCE COSTS

     Variable,  $/ton
       Cement                                     50.00
       Chloranan                                  66.67
       Fuel ($1.00/gal-diesel)                     1.29
       Electricity ($0.04/kwhr)                    0.03
       Water ($0.80/1000 gal)                      0.08

     Semivariable. $/ton
       Salaries and Living Expenses               64.70
       Equipment Rentals and Consumables          10.36
       Analytical Services                         6.50
       Maintenance (10% Direct Costs)              0.32
       Mobilization/Demobilization                 1.66

     HAZCON and Support Fixed
       Site Preparations
       Insurance and Taxes (10% Direct Costs)      0.32
       Depreciation (10 yrs.)                      0.18

       TOTALS,  $/ton                             205.84
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                       TABLE 9.2. NOTES

1.   The demonstrated HAZCON MFU capacity is 300 Ib/min.

2.   It is assumed that 35,400 tons  of soil  at the
    Doug!assvi11e site was processed.  This value derives from
    continuously  operating the  demonstrated unit for 6 months
    at an on-stream factor of 90%.   The actual  on-stream
    factor used  was 70%.

3.   Utilities Consumption Estimates
    1,200 max installed KVA
    Water - 14  gpm
    Diesel Fuel  - 8 gph

4.   Chemical  Consumption
    Cement    -  1:1 to contaminated  soil
    Chloranan -  1:10 to contaminated soil

5.   Labor Estimate - 4 shifts per week - includes overhead
    HAZCON -  1  Manager, $50/hr; 4 Shift Supervisors, $35/hr;
               12 Operators, $17.50/hour;  10% OT
    Support Personnel  - 1 Manager,  $50/hr;  4 Shift
                        Supervisors, $45/hr; 12 Operators,
                        $40/hr; 10% OT
    Others -  1  SSHO, $50/hr; 1  Project Manager, $60/hr;
             Laboratory Technician  (part-time), $40/hr;  Office
             Manager,  $40/hr; Secretary, $20/hr
    Living Expenses (motel, food, car rentals,  etc.) -
             HAZCON, $85/D; Support Personnel - Managers and
             Supervisors  $120/D,  Operator  - local - no charge;
             Others -  $120/0

6.   Rental and  Consumable Supplies
    Health and  Safety consumables and instruments - $450/D

         Office  space, office supplies, portable sanitary
         faci1i ti es -  $50/day
         Sampling Materials - $40/set
         Heavy  Equipment  Rental - front-end loaders, backhoes,
         steam  cleaner, drill rig,  etc. -  $1000/day

7.   Site preparation costs, since it would  be so interrelated
    with the  overall planning and costs of  the Prime
    Contractor  for the entire site,  are not included.

8.   The costs taken as a  fraction of capital and maintenance
    costs are prorated to the actual time  on site.

9.   Operator  training assumes 3 days of training for HAZCON
    operators,  site preparation operators,  the Health and
    Safety Officer, and sample technician.
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                           REFERENCES
1.  Remedial Investigation  Report/Feasibility Study of
    Alternatives, Berks Associates  -  Douglassvi1le Disposal
    Site - Union Township,  Berks  County,  PA., EPA Work
    Assignment No. 59-3651,  Contract  No.  68-01-6699, June
    1986.  Prepared by NUS  Corporation  for  Region III.

2.  Letter Report, S. Sawyer  to  P.  de Percin, Laboratory
    Analyses of Screening Samples,  July 6,  1987.

3.  Demonstration Plan - HAZCON/Douglassvi11e SITE Program,
    August 31, 1987, EERU Contract  No.  68-32-3255.  Submitted
    to P. de Percin, EPA HWERL,  Cincinnati,  Ohio, August 31,
    1987.
                             «U.S. GOVERNMENT PRINTING OFFICE:! 9 89 -6 its-16 3^7066
                              119

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