United States        Office of
          Environmental Protection   Emergency and
          Agency           Remedial Response .
EPA/ROD/R03-93/177
March 1993
SEPA    Superfund
          Record of Decision:
          William Dick Lagoons, PA

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50272-101	
  REPORT DOCUMENTATION
           PAGE
1. REPORT NO.
EPA/ROD/R03-93/177
3. Recipient* * Accession No.
   Title and Subtitle
   SUPERFUND RECORD OF DECISION
   William Dick  Lagoons, PA
   Second Remedial Action  - Final
                                          5.  Report Date
                                                    03/31/93
7.  Authors)
                                          8.  Performing Organization Rept No.
9.   Performing Organization Nam* and Address
                                          10  Pro)** Tatk/Work Unit No.
                                                                     11. Contract(C)orGrant(G)No.

                                                                     (C)

                                                                     (G)
12. Sponsoring Organization Nam* and Address
   U.S.  Environmental Protection Agency
   401 M Street,  S.w.
   Washington, D.C.   20460
                                          13.  Type of Report a Period Covered

                                             800/800
                                          14.
15. Supplementary Notes
                   PB94-963906
16. Abstract (Limit: 200 words)

  The 4.4-acre William Dick Lagoons  site is an inactive waste disposal site located in
  West Cain Township,  Chester County,  Pennsylvania.   Land use in  the area is
  predominantly residential, with a  sparse population density.  The majority of  residents
  in the vicinity of the site use private wells as their drinking water supply.   The site
  is located near Birch Run, a tributary of the West  Branch of Brandywine- Creek,  which is
  used as  a water source for populations as far as Wilmington, Delaware.  From the late
  1950s until 1970, Mr.  William Dick used a series of onsite lagoons for the disposal of
  minor amounts  of chemical residuals and final rinse waters from the interior cleaning
  of tank  trailers owned by Chemical Leaman Tank Lines, Incorporated (CLTL).  These tank
  trailers were used to transport various chemical products using petroleum, latex,  and
  resins.   In 1971, Mr.  Dick, CLTL,  and the State reached an agreement to .close  the
  lagoons  after a violation of the Clean Streams Law  and a vandal-inflicted breach in one
  of the berms resulted in the discharge of approximately 300,000 gallons of wastewater
  into a nearby creek,  the death of  2,600 fish, and the closure of public water  supplies
  in the vicinity.  Any residual remaining in the bottom of the lagoons after drainage
  was buried by pushing the earthen  berms into the lagoons, filling them with soil,  and

  (See Attached Page)
17. Document Analysis     a. Descriptors
   Record of Decision - William Dick Lagoons,  PA
   Second Remedial Action -  Final
   Contaminated Medium: soil
   Key Contaminants:  VOCs  (PCE,  TCE), other  organics  (PAHs,  pesticides),  metals  (arsenic,
                       chromium)

   b.   Identifiers/Open-Ended Ti
   c.   COSATI Reid/Group
18. Availability Statement
                          19.  Security Class (This Report)
                                   None
                                                     20.  Security Class (This Pags)
                                                               None
         21. No. of Pages
                 82
                                                                              22.  Price
(See ANSt-Z39.1B)
                                   See Instructions on Reverse
                                                   OPTIONAL FORM 272 (4-77)
                                                   (Formerly NTO-35)
                                                   Department of Commerce

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EPA/ROD/R03-93/177
William Dick Lagoons, PA
Second Remedial Action - Final

Abstract  (Continued)

planting a vegetative cover on the surface.  In 1988, EPA sampled the former lagoon site
and collected well water samples from several surrounding residences.  These
investigations revealed elevated levels of numerous organic compounds in the soil.  In
1987, EPA required CLTL to install a fence around the site and point of entry.  A 1991 ROD
addressed final remedy for OU1 for the provision of an alternate water supply to more than
50 residences impacted by the site, carbon filtration units on homes where TCE
concentrations were above 5 ug/1, and also provided for an interim remedy for OU2
consisting of pumping and treatment of ground water and a hydrogeologic study.  In 1992,
CLTL also performed a soil vapor extraction/bioremediation treatability study  to
determine the feasibility of using this technology to remove contaminants from the onsite
soil.  This ROD addresses the 2.2 acres covered by the lagoons and the remaining 2.2
acres, which served as a burrow area for soil used to construct the compacted earthen
ridges or berros around the perimeter of the lagoons, as OU3.  The primary contaminants of
concern affecting the soil are VOCs, including PCE and TCE; other organics, including PAHs
and pesticides; and metals, including arsenic and chromium.

The selected remedial action for this site includes determining the extent of soil
contamination; excavating and treating approximately 24,000 yd^ of contaminated soil
onsite using thermal desorption; treating air emissions from the thermal desorption
process using a control system consisting of a fabric filter for particulate removal,  a
wet scrubber for acidic gas conversion, and a carbon adsorption system for capturing the
contaminants; managing and disposing of treatment residuals offsite; backfilling the
treated soil in excavated areas; placing either a vegetative soil cover or multi-layer cap
over the excavated areas; and implementing institutional controls, including deed
restrictions.  The estimated present worth cost for this remedial action ranges from
$7,800,000 to $9,300,000, which includes an estimated annual OSM cost of $20,000 for 30
years.

PERFORMANCE STANDARDS OR GOALS:

Chemical-specific soil cleanup goals are based on either RCRA LDRs or a health-based risk
level of 10~6 or less and include acenaphthene 31 mg/kg; anthracene 94 mg/kg;
benzo(a)pyrene 7,300 mg/kg; bis(2-ethylhexyl)phthalate 266 mg/kg; chlorobenzene 5.7 mg/kg;
chloroform 280 mg/kg; 4,4-DDE 7,250 mg/kg; 2,4-dichlorophenol 230 mg/kg; fluorene 49
mg/kg; fluoroanthrene 250 mg/kg; naphthalene 3,100 mg/kg; phenanthrene 94 mg/kg; PCE 1.2
mg/kg; 1,2,4-trichlorobenzene 61 mg/kg; and TCE 0.42 mg/kg.

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                        RECORD OP DECISION
                     WILLIAM OZCX LAGOONS SITE
                           DECLARATION
 SITE MAMS AND LOCATION

 William Dick Lagoons Site
 West Cain Township,  Chester County, Pennsylvania

 STATEMENT OF BASIS AND* PURPOSE

 This decision document presents  the selected remedial action for
 Operable Unit 3  of the William Dick Lagoons Site  ("Site"), in
 West Cain Township,  Pennsylvania, which was chosen  in accordance
 with the Comprehensive Environmental Response, Compensation, and
 Liability Act of 1980 (CERCLA),  as amended by the Superfund
 Amendments and Reauthorization Act of  1986 (SARA),  and, to the
 extent  practicable,  the National Oil and Hazardous  Substances
 Pollution Contingency Plan (NCP).  This decision  document
 explains the factual and legal basis for selecting  the remedy for
 Operable Unit 3  at this Site.  This decision is based on the
 Administrative Record for this site.

 The  Commonwealth of  Pennsylvania has evaluated and  commented on
 the  alternatives presented in  this Record of Decision and has
 initially agreed with the technical remedy selected.  The
 official position of the Commonwealth  of Pennsylvania will be
 documented in the Administrative Record for this  Site upon
 receipt.

 ASSESSMENT OF THE SITE

 Actual  or threatened releases  of hazardous substances from this
 Site, if not addressed by implementing the response action
 selected in this Record of Decision (ROD), may present an
 imminent and substantial endangerment  to public health, welfare,
 or the  environment.

 DESCRIPTION OF THE REMEDY

 The remedy described in this Record of Decision is  for Operable
 Unit 3  at the Site.   This remedy addresses the principal threat
 at the  Site.

 Operable Unit 1  at this Site involves  providing a water line to
protect residents from contaminated private veil  water,  operable
Unit 2  involves  an interim remediation of the groundwater which
 includes measures to.pump and  treat the groundwater and further
 investigation of the hydrogeology.  A  Record of Decision for
Operable Unit One and the interim groundwater remediation measure

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                                58

 for Operable Unit Two was issued  on  June  28,  1991.  A decision on
 the final groundwater remediation is intended for this Site at a
 later date.

 The remedy selected for Operable  Unit 3 will  reduce the
 concentrations of hazardous  substances in the Site soils so that
 leaching of contaminants into  the groundwater will be minimized.
 Reduction of the volatile organic compounds and semi-volatile
 organic compounds in the soils is necessary in order the
 groundwater will not continue  to  be  impacted  above acceptable
 levels.  In addition,  the installation of a vegetative soil cover
 or multi-layer cap will prevent the  surrounding community from
 exposure to Site-related contaminants through inhalation,
 ingestion,  and dermal contact.

 The selected remedy includes the  following major components:

        1.  Determination of extent of soil contamination.

        2.  Excavation of contaminated soils and treatment of
           contaminated soils in an on-site thermal desorption
           unit.

        3.  Treatment of air emissions from the thermal desorption
           unit.

        4.  Management and off-site disposal of treatment residuals
           and wastewaters.

        5.  Backfilling of treated  soils in the excavated areas and
           placement of a vegetative  soil  cover or multi-layer cap
           over such areas.

        6.  Operation and maintenance  ("O&M") of the vegetative
           soil cover or multi-layer  cap.

        7.  Institutional controls  in  the fora  of deed
           restrictions.

DECLARATION  OF STATUTORY DBTBRMIMATIOITS

The selected remedy is protective of human health and the
environment,  complies  with Federal and State  requirements that
are legally  applicable or relevant and appropriate to the
remedial action,  and is cost-effective.   This remedy utilizes
permanent  solutions and alternative  treatment technologies to the
maximum extent practicable,  and satisfies the statutory
preference for remedies that employ  treatments that reduce
toxicity, mobility,  or volume  as  a principal  element.

Subsequent actions are planned to more fully  address the threats
posed by the groundwater at  this  Site.

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Because this remedy may result in hazardous substances remaining
on-site above health-based levels, a review will be conducted
within five years after the start of this remedial action to
ensure that the remedy continues to provide adequate protection
of human health and the environment.
Stanley LT Laskowski                    Date
Acting Regional Administrator
Region III

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                     WILLIAM DICK LAGOONS SITE
                        RECORD OF DECISION
                          OPERABLE UNIT  3
                      SOURCE OF  CONTAMINATION

                         TABLE OF CONTENTS

 I.  Site Name,  Location,  and Description	   i

 II.  Site History and Enforcement Activity  	 ...   i

 III.  Highlights  of  Community Participation 	   7

 IV.  Scope and  Role  of Operable  Unit 3	   8

 V.   Summary  of Site Characteristics	   9

 VI.  Summary  of Site Risks	    12

 VII.  Description of Alternatives 	    21
      Alternative 1:  NO ACTION	    23
      Alternative 2:  CAPPING 	    24
      Alternative 3:  SOIL VAPOR  EXTRACTION/BIOREMEDIATION
                     WITH MULTI-LAYER CAP                       25
      Alternative 4:  THERMAL DESORPTION  WITH VEGETATIVE SOIL
                     COVER OR MULTI-LAYER CAP	27
      Alternative 5:  INCINERATION WITH VEGETATIVE SOIL
                     COVER	   30

 VIII. Summary  of the Comparative Analysis  of Alternatives  .  .  31
      A. Overall  Protection   	  31
      B. Compliance  with  Applicable or Relevant and
        Appropriate Requirements (ARARs)   	    31
      C. Long-Term Effectiveness and Permanence:	   37
      D. Reduction of toxicity,  mobility, or volume of the
        contaminants through treatment: 	  38
      E. Short Term  Effectiveness:	  .  39
      F. Implementability 	  39
     G. Cost	40
     H. State Acceptance: 	  <40
      I. Community Acceptance:	40

IX.  Selected Remedy and  Performance Standards  .......  41

X.   Statutory Determinations 	  49
     A. Protection  of Human Health and  the Environment  ...  49
     B. Compliance with ARARs	50
          l.  Chemical-Specific ARARs  	  50
          2.  Location-Specific ARARs  	  50
          3.  Action-Specific ARARs	50
     C. Cost-Effectiveness   	  53

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     D. Utilization of Permanent Solutions and
        Alternative Treatment Technologies or Resource
        Recovery Technologies to the Maximum Extent
        Practicable	54
     E. Preference for Treatment as a Principle Element  ...  54

XI.  Documentation of Significant Changes	   54


APPENDIX A- RESPONSIVENESS SUMMARY
APPENDIX B- ADMINISTRATIVE RECORD INDEX
APPENDIX C- AIR EMISSIONS MODELS AND RISK ASSESSMENT FOR
            EXCAVATION
APPENDIX D.- RISK ASSESSMENT DATA

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 I. Sit* Name, Location and Description

      The William Dick Lagoons Site is located in West Cain
 Township, Chester County,  Pennsylvania approximately 3.5 miles
.south-southeast of the Village of Honey Brook.   The 4.4 acre site
 is located within a larger 105-acre parcel of land and is
 situated in a rural wooded setting on the crest of a small ridge
 known as the Baron Hills.   It is accessible via Telegraph Road,
 at approximately 2,500 feet west of Sandy Hill  Road (see Figure
 1).   The nearest residence is located, roughly 300 feet to the
 north and approximately thirty homes are within 1000 feet of the
 Site.  Figures 1 and 5 provide a perspective of the site setting
 relative to proximal residencies.

    •; The site currently appears as a sparsely vegetated field
 behind several residences  located on the south  side of Telegraph
 Read. The site is obscured from view by both the surrounding
 trees and its position at  the crest of a hill.   Land use
 surrounding the site is primarily residential,  with a generally
 sparse population density.  Housing development in West Cain
 Township is progressing relatively quickly and  several new homes
 have been built since the  commencement of site  remedial
 investigative activities.   The majority of the  residences are
 single family dwellings with private wells and  onsite septic
 systems.   Several trailer  parks and a campground exist within the
 vicinity of the site and two separate automobile junkyards are
 located just north of the  site.

      Much of the area extending outward from the near-site
residences is actively farmed.  Important crops include corn,
wheat,  oats,  soy beans and hay.  Dairy cattle are also raised
within the surrounding countryside.

      Two  other Superfund sites are located within five miles of
the site.   The Blosenski Landfill is located approximately 1.7
miles to  the southeast and the Welsh Road Landfill is roughly 5
miles to  the northwest.

II. site  History and Enforcement Activities

      Waste disposal activities at the site were conducted by its
former owner,  Mr.  William  Dick, in the late 1950s through May
1970.   Originally,  the Site consisted of three  unlined earthen
lagoons or ponds that were used for the disposal of wastewater.
The lagoons covered approximately 2.2 acres of  the 4.4 acre Site;
the remaining 2.2  acres served as a borrow area for soil used to
construct the compacted earthen ridges or barns around the
perimeter of the lagoons (see Figure 2).

      The  lagoons were used to dispose of final  rinse waters from
the interior cleaning of tank trailers owned by Chemical Leaman
Tank  Lines,  Incorporated ("CLTL").   Trichloroethylene (TCE) was
used  to clean out  the tank trailers.   In addition, minor amounts
of residual  chemical products were occasionally disposed of in

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 the lagoons.   The tank trailers were used  for  transporting
 petroleum products,  latex,  and resins.   Following the rinsing and
 cleaning of the tank trailers at CLTL's  Downingtown, Pennsylvania
 facility,  the rinse  water was delivered  to the lagoons by tanker
 approximately every  three days for disposal.   The information
 currently available  to EPA  indicates that  all  disposal activities
 at the Site were completed  prior to the  effective date of the
 regulations implementing the Resource Conservation and Recovery
 Act,  November 19,  1980.

      On April 26,  1970,  37  wild geese were shot at the site by
 the district game protector for humane reasons.  The birds'
 feathers were coated with waste after the  birds descended onto
 the lagoons.   In May 1970,  the Pennsylvania Department of Health
 (PADH)  notified Mr.  William Dick that the  discharge from the
 lagoons to underground waters was a violation  of the Clean
 Streams Law,  the Act of June 22, 1937, P.L. 1987, as amended and
 ordered the lagoons  closed.  On June 7,  1970,  vandals allegedly
 caused a breach in the berm of the second  lagoon, resulting in
 the release of an estimated 300,000 gallons of wastewater that
 moved into Birch Run,  a tributary of the West  Branch of
 Brandywine Creek.  The discharge caused  the death of more than
 2,600 fish and the closure  of public water supplies which used
 the creek  as  a water source as far downstream  as Wilmington,
 Delaware.   Mr.  William Dick was notified by PADH that the
 discharge  into the into Birch Run violated the Clean Streams Law.
 A  complaint was filed by the Commonwealth  of Pennsylvania in the
 Court of Common Pleas,  Dauphin County, Pennsylvania (Number 3072
 Equity Docket,  No.345 C.D.  1970)

           In  early 1971, per the agreement reached with PADH
 under the  aforementioned complaint, CLTL and William Dick began
 work  to close the lagoons.  This activity  included the addition
 of  alum to -the lagoon wastewater, and spray irrigation of the
 ntreated"  wastewater into the woods adjacent to the lagoons.
 Settled residue remaining in the bottom  of the lagoons was buried
 by  pushing the earthen b«rms into the lagoons. The lagoons were
 completely filled in with soil and a vegetative cover planted on
 the surface.

      In April 1985,  under the authority  of the Comprehensive
 Environmental Response,  Compensation, and  Liability Act  (CERCLA)
 of  1980, an EPA contractor  performed a sit* sampling inspection
 of  the  former lagoon sit* and collected  well water samples from
 several surrounding  residences.  This inspection was conducted in
 response to a 1981 CERCLA notification to  EPA  by CLTL which
 indicated  that the former lagoons may contain  hazardous
 substances.   During  the inspection, elevated levels of numerous
 organic compounds  were detected in the soil samples collected
 from the former lagoon area.  A few site-related compounds also
were found in two residential wells.

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      In May 1987,  additional sampling of 28 residential veils  by
 EPA's Technical Assistance Team (TAT)  found TCE to be the most
 prevalent organic  compound, at the highest concentration,  in
 groundwater.   This, volatile organic compound (VOC),  a suspected
 carcinogen and common industrial solvent,  was detected in two
 spring-fed water supplies and five wells.   Following the
 completion of these follow-up evaluations,  the Site  was listed in
 July 1987 on the National Priorities List  (NPL)  of hazardous
 waste sites eligible for cleanup under Superfund.

      On July 20, 1987,  EPA informed CLTL of its potential
 responsibility regarding contamination at  the site by issuing  a
 special notice letter.   On January 27, 1988,  EPA and CLTL entered
 into an Administrative  Order on Consent ("1988 Removal Order")
 which required CLTL to  install a fence around the site, conduct
 at  least yearly monitoring of residential  wells (more frequent
 monitoring in some cases),  and install point-of-entry treatment
 systems for home well water exceeding Maximum contaminant  Levels
 (MCLs).   The fence was  installed at the site in February 1988.
 The sampling and treatment unit requirements of the  Consent Order
 will continue to be in  effect until the waterline is constructed
 and is operating at the affected and potentially affected
 residences.   At that time,  the treatment units will  be removed
 from the residences and CLTL will discontinue the residential
 well monitoring.

      CLTL has supplied  bottled water to all homes (approximately
 34)  in which  TCE levels between 0 to 5 parts per billion (ppb)
 were detected in residential wells.   The company has supplied
 bottled water under its own initiative; CLTL is not  required to
 do  so by EPA.   To  date,  CLTL has installed point-of-entry carbon
 filtration units in the twelve homes where TCE concentrations  in
 well  water exceed  EPA's MCL of 5 ppb.

      On  September  14, 1988,  CLTL and EPA signed a second
 Administrative Order on Consent,  requiring that a Remedial
 Investigation/Feasibility Study (RI/FS) be conducted.  CLTL .
 obtained the  services of Environmental Resources Management
 ("ERM")  for this work.   The RI began in December 1988 and
 progressed throughout the Spring and Summer of 1989.  Based upon
 data  gaps  identified by both EPA and ERM,  a second shorter phase
 of RI work was initiated in October 1989.   An interim RI report
 was submitted to EPA in December 1989.  After EPA comments, a
more detailed draft RI  report,  along with  a draft FS report and
 Risk Assessment (RA), ware  submitted for EPA review  on March 8,
 1990.  Following receipt of EPA comments,  a Preliminary Final
 RI/RA/FS was  submitted  by CLTL on September 6, 1990.

     On  September  24, 1990,  EPA informed the Rohm &  Haas Company
 of Philadelphia, Pennsylvania of its potential responsibility
regarding contamination at  the site by issuing a general notice
 letter  .  This notification was based on information received  on

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 the  company's past involvement at the site through interviews
 with former  CLTL employees.  Specifically, CLTL hauled Rohm & Haas
 product  to Rohm & Haas'  customers and then cleaned product
 residue  from CLTL's tanker trucks and hauled it to the William
 Dick Lagoons Site.

      On  June 28,  1991,  EPA issued a Record of Decision for
 Operable Units One and  Two at the Site.  The major components of
 the  remedies selected included (1) with respect to an alternative
 water supply,  providing an extension of the City of Coatesville
 Authority water line to at least 50 homes impacted or potentially
 impacted by  the Site and, (2) with respect to the interim action
 for  groundwater clean-up, performing a hydrogeological study
 aimed at determining the proper design of a groundwater
 remediation  system,  and pumping and treating the contaminated
 ground water to remove  site-related contaminants for a limited
 time frame.

      EPA deferred the decision regarding soil remediation (OU 3)
 until a  Soil Vapor Extraction/Bioremediation (SVE/BIO)
 treatability study and  Focused Feasibility Study was performed at
 the  Site by  CLTL.

      After EPA issued the June 1991 ROD, CLTL entered into
 negotiations with EPA to implement the clean-up activities
 described in the ROD.   These negotiations continued, without
 resolution,  until March 1992.  On June 30, 1992,, EPA issued an
 Administrative Order requiring the PRPs to undertake the remedies
 respecting alternate water supplies and interim groundwater
 studies  and  remediation defined in the ROD.  The PRPs did not
 agree to comply with all of  the terms of the order.
 Consequently,  EPA hired a contractor to perform the design work
 for  the  water  line,  ground water investigation and interim
 groundwater  remediation.  Currently, EPA is reviewing the
 contractor's work plan  for the pre-design groundwater
 investigation.   The pre-design groundwater investigation needs to
 be performed prior to the completion of the design of the water
 line and groundwater pump and treat system.

      In  June 1991,  EPA  verbally approved CLTL's performance of a
 SVE/BIO  treatability at the  Site.  In August 1991, EPA confirmed
 this  approval  in writing.  The SVE/BIO treatability study was
performed pursuant to Section 6.2.2 of the Final Remedial Site
Operations Plan (RISOP)  prepared by CLTL in November 1988.  This
RISOP was incorporated  into  the September 1988 RI/FS Consent
Order between  EPA and CLTL,  as described in Section VIII (C) of
 this Order.  CLTL submitted  its workplan for the treatability
 study  in February 1992.  This workplan was disapproved by EPA in
April  1992.  CLTL submitted  a revised workplan in June 1992.
This workplan  was subsequently disapproved by EPA.  A second
revision was submitted  to EPA in August 1992.  EPA verbally
approved of  this workplan in August 1992.  Written approval was

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 provided in September 1992.

      CLTL (through its contractor)  performed a SVE/BIO
 treatability study in former Lagoon #1 at the Site from August
 1992 to November l"992 and submitted a Focused Feasibility Study
 which evaluated alternatives for remediating the  soils at the
 Site.  The purpose of this study was to determine the  feasibility
 of using this technology to remove  contamination  from  the soils
 on the Site.

      In addition to this work,  CLTL (through its  contractor) also
 used several mathematical models to calculate the level of
 contamination that can remain in the soil without releasing
 contaminants to groundwater above levels acceptable to EPA.
 These soil clean-up levels were developed using a combination of
 the fate and transport mathematical models,  HELP  and PRZM, as
 well as a groundwater mixing zone model.   Compounds which have
 been identified in the groundwater  were used in the model.  The
 groundwater concentration input data into this model was based on
 Maximum Contaminant Levels ("MCLs")  and health-based drinking
 water concentrations.   Health-based drinking water concentrations
 were established based on a  carcinogenic risk of  10E-05 or 10E-
 04.   A cancer risk of 10E-05 means  that one  additional person per
 100,000 has a chance of contracting cancer given  the relevant
 exposure scenario.   The NCP directs hazardous substance responses
 for Sites presenting risks outside  the established acceptable
 carcinogenic  risk range for  Superfund Sites  of between 10E-06 (l
 additional chance in one million) and 10E-04 (one additional
 chance in 10,000).   EPA used a  carcinogenic  risk  of either 10E-04
 or  10E-05 as  the basis for the  health-based  drinking water
 concentrations for chemicals without an MCL  at this Site rather
 than use the  more conservative  10E-06 carcinogenic risk values
 since the 10E-06 carcinogenic value for some compounds are below
 the  contract  required quantitation  limit for the  drinking water
 analytical technique,  EPA Method 524.2.   The contract  required
 quantitation  limit is the detection level required for a
 particular analytical method under  EPA's Contract Laboratory
 Program (CLP).   Use of either 10E-04 or 10E-05 carcinogenic risk
 is protective of human health since it falls within the EPA's
 acceptable risk range of 10E-06 to  10E-04.

      For those chemicals without an MCL or with a health-based
drinking water concentration greater that 10 ppb, a groundwater
concentration of 10 ppb was  used.   The use of 10  ppb was based on
the  contract  required quantitation  limits as established under
the  Contract  Laboratory Program (CLP)  Statement of Work for
Organics Analysis (CLP Document Number OLM01.1).   The  10 ppb
level was established in the focused feasibility  study by CLTL in
an attempt to conform to PADER's groundwater protection strategy,
which,  although not an applicable or relevant and appropriate
regulation for this ROD,  is  a "To Be Considered"  policy.  Soil
clean-up levels calculated on the assumption that a vegetative

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 soil cover would be placed over  the  site after soil treatment are
 listed in Table 1.

      A vegetative soil cover  is  defined in this ROD as a layer of
 soil which will support the germination and propagation of
 vegetation and will provide dermal protection from the treated
 soils.   The vegetated soil cover will not restrict the
 infiltration of rainwater or  surface water through the soils.

      According to the model,  some of the compounds listed in
 Table 1 will degrade prior to reaching the groundwater and,
 therefore,  no soil clean-up level was provided.  However, if the
 contaminated soils are treated and placed back on-site, certain
 contaminants (i.e.,  those compounds related to F001-F005 wastes)
 will have to meet the treatment  standards established by the Land
 Disposal Restrictions (LOR) listed at 40 CFR $268.43.  The LOR
 levels  for the relevant compounds are listed in Table l.  For the
 remaining compounds which are not F001-F005 wastes but do,
 according to the model,  degrade  before reaching the groundwater,
 EPA  believes that it is appropriate to establish soil clean-up
 levels  based on direct contact risks.  These levels are also
 noted in Table 1.   The groundwater concentrations used in the
 fate and transport  models- to  calculate the soil clean-up levels
 are  listed in Table 1 and are based on either MCLs, health-based
 concentrations under a drinking  water exposure scenario or 10 ppb
 as described above.

      Some of the soil clean-up levels that were calculated by the
 model exceeded the  concentrations for a direct contact risk.  The
 soil  concentrations that need to be met so that the direct
 contact  risk is acceptable to EPA are provided in Table 2.
 Attainment  of  the direct contact risk levels listed in this table
 are not  required for this ROD, because placement of a cover or
 cap over the soils  and implementation of institutional controls
will  prevent exposure to the  soils through direct contact.
However,  if  the values listed in Table 2 can be met during remedy
 implementation,  deed restrictions on the property may be
eliminated.

      CLTL also  calculated contamination levels that can remain  in
the soil with various types of caps proposed to be placed over
the site to reduce  infiltration  of rain water.  These soil clean-
up values are described and summarized in the Appendix C of the
Focused  Feasibility Study,  dated November 16, 1992.  This
document is located in the Administrative Record  (AR300569-
AR300597).   The soil clean-up levels in this Appendix do not take
MCLs  or  health-based drinking water concentrations into account,
therefore,  these values are considered preliminary by EPA.

     The results of  the SVE/BIO  treatability study indicate that
significant  quantities of VOCs can be removed from the soils
through  SVE/BIO.  Approximately  610 pounds of VOCs were removed

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 during six weeks of  continuous  operation.  Good subsurface air
 flow conditions  were observed during  the treatability study.
 After the  six week treatability study,  it  could not be
 conclusively demonstrated  that  bioremediation  ("BIO") could be
 effective  in reducing the  levels of VOCs and Semi-volatile
 organic compounds (SVOCs)  in the soils  at  the William Dick
 Lagoons Site.  During the  RI and the  treatability study, soil
 samples were taken in the  former lagoon area.  Thin layers of a
 black,  sticky, fibrous  (i.e., tar-like) substance were found at
 depths ranging from  2 to 6 feet in former  Lagoon #l.  Analysis of
 this layer showed that  it  contained the VOCs and SVOCs found in
 the  soil.  The impact of this layer on  the operation of the
 SVE/BIO system was not  analyzed during  the treatability study.
 According  to CLTL, an additional 6-12 month pilot study would be
 necessary  during the remedial design  to determine how this layer
 would  affect SVE/BIO remediation.  If this layer can not be
 remediated with  SVE/BIO, CLTL proposed  to  excavate this material
 and  treat  it by  either  thermal  desorption  or incineration.

     In addition to  the thin layers of  a black, sticky, fibrous
 substance, other materials were identified in the three former
 lagoons.   These  materials  were  classified  as "spongy", "rubber-
 like",  "dry,  matted  and latex-like" and were observed at depths
 ranging from 2 to 14  feet  in all three  lagoons.  These materials
 could also impact a  full-scale  SVE/BIO  remediation.

 III. Highlights  of Community Participation

     .In accordance with CERCLA  Sections 113(k)(2)(B)(i-v) and
 117, EPA instituted  several measures  to contact and correspond
with residents in the community surrounding the William Dick
Lagoons Site concerning Operable Unit 3.   Following is a listing
of the community  relations efforts conducted by EPA:

     June 1991- issued  the Record of  Decision for OU l and OU 2
     to persons on the  site nailing list site and government
     officials.  This ROD  discussed why the decision on
     remediating the soils at the site  would be deferred.

     July 1991- held a public meeting with interested individuals
     to describe the components of the  Record of Decision for OU
     l and OU 2.

     August 1992- issued a fact sheet to persons on the site
     mailing list and government officials describing the Soil
     Vapor Extraction/ Bioremediation treatability study.

     January 1993 - issued the Proposed Plan for the site
     respecting OU 3  via  press release, newspaper publication,
     and direct mailing to all individuals on the site mailing
     list;  announced public meeting in  February.

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      February 1993  - held  public meeting with approximately 50
      interested individuals  to explain EPA's rationale  for the
      proposed remedial  alternatives presented in the January 25,
      1993  Proposed  Plan and  to solicit comments on this Proposed
      Plan  during the 30 day  public comment period which was held
      from  January 25, 1993 to February 24, 1993.

      In addition, EPA has  updated the information repository and
 administrative record,  available for public review at the West
 Cain  Township Building,  with the reports relating to the Soil
 Vapor Extraction/ Bioremediation Treatability Study and the
 Focused Feasibility Study  for OU 3.  The index to the
 administrative record for  OU 3 is attached to this Record of
 Decision in Appendix B.

      A response to  the  comments received during the public
 comment period,  including  the public meeting, is included in the
 Responsiveness Summary,  which is part of this Record of Decision
 and is attached in  Appendix  A.

 IV. SCOPE  AHD ROLE  Of OPERABLE UNIT 3

   Based'on the results of the Preliminary Final RI/FS, EPA has
 decided that  remediation of  the entire site can best be
 approached by considering  the site as consisting of three
 separate "units'*.   These units are:

 (l)   Residential Water  Use fi.e.. Alternate Water Supply)- which
      involves a remedy  to  protect residents from contaminated
      private  well water

 (2)   Groundwater- which involves a remedy to remediate  all or
      portions of the contaminated groundwater aquifer

 (3)   Source Control- which involves a remedy to clean up
      contaminated soils at the Site (contaminated soil  is the
      media considered to be  the "principal threat" at the Site
      per the  definition of principal threat in the NCP  40 CFR
      Section  300.430(a)(1)(iii)).

      A ROD was issued for  Operable Unit 1 and for an interim
action on  Operable  Unit 2  in June 1991.

      Operable Unit  3 (Source Control) is being addressed by this
ROD.  The  goal of this  remedy is to clean soils to contaminant
levels which,  along with the installation of a vegetative soil
cover or multi-layer cap (as defined in Section VII. of this
ROD),  are  sufficient to ensure that any residual contaminants
migrating  or  leaching to the groundwater will not exceed risk-
based levels  or  Federal standards for drinking water.   In
addition,  the vegetative soil cover or multi-layer cap  will
ensure against erosion  and direct contact by the surrounding

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 community and trespassers with site soils.

      Reducing the  source of  contamination impacting the
 groundwater  at the site will allow an effective final remedy for
 groundwater  clean-up  to be designed.  The final remedy for the
 groundwater  remediation (OU  2) will be outlined in a future ROD.

 V. SUMMARY OF SITE CHARACTERISTICS

      The  purpose of the remedy under OU 3 is to address the soil
 contamination on-site so that it does not continue to impact
 groundwater  above  acceptable levels and so that any risks
 associated with direct contact with the soil are minimized.
 Therefore, this section of the ROD summarizes the site
 characteristics related to soils and groundwater as determined
 during the RI and  the Soil Vapor Extraction/Bioremediation
 Treatability Study performed in Fall 1992.  A detailed discussion
 of all site  conditions can be found in the Preliminary Final RI
 (September 1990) and  the Focused Feasibility Study (November
 1992).  The  groundwater and  soil findings are summarized below:

 Geology and  Qroundvater:

 •    The  site is located in  the Honeybrook Uplift in an outcrop
     belt of a geological structure known as the Chickies
     Formation. It is situated on the crest of the Baron Hills
     Anticline in  a fault block bounded by two normal faults to
     the  north and south.  (The Chickies is a white to light grey
     quartzite with interbedded phyllitic beds.)  The site is
     located on a  groundwater divide.  The bedrock beneath the
     lagoons is highly weathered and forms a thick saprolite up
     to 100  feet thick.  Although laboratory analysis indicates
     that  the  saprolite material is of low permeability,
     contaminants  have migrated to the groundwater table
     (approximately 50 feet  below the surface) through joints and
     fractures  in  the saprolite.

•    Groundwater at the site, as determined by monitoring well
     sampling,  is  contaminated primarily by VOCs and, to a lesser
     extent  in  frequency and concentration, semi-volatile organic
     compounds  (SVOCs).  TCE is the predominant VOC (average
     concentration •  1200 ppb, maximum concentration * 16,000
     ppb)  and phenol  is the  predominant semi-VOC (average * 800
     ppb,  maximum  * 14,000 ppb).  Other compounds found less
     frequently and/or in lover concentrations include
     chloroform, benzene, acetone, 2-methylphenol, 4-
   .  methylphenol,  isophorone and other organic compounds.  Vinyl
     chloride was detected on only one occasion in one monitoring
     well  during post-RI/FS  sampling.  Table 3 lists the maximum
     and average groundwater concentrations in onsite monitoring
     wells.

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                           10

 The highest groundwater concentrations of organic chemicals
 are found in two of the thirteen monitoring wells installed
 at the site, wells MW-5D and MW-7D.   The seven  deeper
 monitoring wells (MW-1D,  MW-3D,  MW-5D,  MW-7D, MW-9D,  MW-llD
 and MW-20D) (110 to 397 feet deep)  are generally  more
 contaminated than the six shallow wells (MW-2S, MW-4S, MW-
 6S, MW-8S, MW-lOS,  MW-12S)  (70 to 80  feet deep).   All wells
 were installed in bedrock (See Figure 4).   At well MW-20,
 the southwest corner of the  site, groundwater was found to
 be contaminated down to a depth  of  397  feet.

 The groundwater surrounding  the  Site,  which is  utilized by
 residents, is also characterized by low-level TCE
 concentrations.  Of the approximately 130 residential wells
 sampled (See Figure 5),  roughly  30  to 40 appear to have some
 site-related contamination.   Of  these 30 to 40, eleven have
 concentrations of TCE in the 5 to 15  ppb range  (the MCL is  5
 ppb)  and one well contains TCE at levels from 20  to 280 ppb,
 dependent on the sampling season.   Residential  wells  within
 a radius of the site are sampled at least once  a  year; those
 homes found to have a detectable level of TCE are sampled
 twice a year.   The radius was established by CLTL and EPA
 under the Removal Order.   Due to the  number of  homes  within
 the radius of the site (1 mile south,  1/2 mile  north) the
 sampling schedule is set up  so that samples are collected
 from 20 to 25 home wells every quarter of the year.

The results of the RI and four years  of residential well
 sampling data indicate that  TCE  levels have not changed
 significantly at the edge of the contaminant plume where
 residential wells are generally  located.  Based on this
 information, the boundary of the groundwater area affected
 by site-related contaminants has been relatively  well-
 defined (See Figure 6),  although additional characterization
 work is needed.

 The regional groundwater flow at the  Site appears to  be •
 toward the southeast.  Three significant bedrock  fracture
 features (two of which are faults)  are believed to exist  in
 the vicinity of the site. Each  appears to provide pathways
 for contaminant migration to vary froa the overall
 southeasterly flow direction and two  may serve  to partially
 block the) flow of groundwater beyond  the fractures.
 However,  it seems that intersecting smaller fractures act as
 conduits for groundwater contamination to migrate beyond  the
 three larger fractures,  resulting in  a rather complex flow
 pattern.

 Additional groundwater monitoring wells are needed and
 further studies are necessary to confirm the theory  that
 groundwater flow is controlled by site geologic fractures,
 to determine the extent of groundwater flow to  the north,

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                               11

     and to determine the severity of contamination in the area
     generally south of the site.
soil:
     Soils in the former lagoon area are contaminated by volatile
     organic compounds (VOCs),  principally trichloroethene (TCE),
     which was used at one time to clean out chemical, tank
     trailers disposing material at the site,  and semi-VOCs,
     which appear to be primarily associated with fuel oil
     residues.  Other than TCE, compounds found at significant
     levels in site soils are 2-butanone, toluene, styrene,
     xylenes, ethylbenzene, chlorobenzene, and tetrachloroethene
     (all VOCs); and several semi-VOCs, especially phenol, 1,2,4-
     trichlorobenzene, naphthalene and bis(2-ethylhexyl)
     phthalate.   The pesticide ODE was also found in
     concentrations suggesting that it was disposed of at the
     site. Table 4 presents a listing of average and maximum
     concentrations of soil contaminants.

     Soils are heavily contaminated from a depth of about one
     foot below the surface down to approximately 20 feet,
     depending on site location.  Former lagoon #1 is most
     heavily contaminated,  with concentrations decreasing as  one
     moves across the site to former lagoon #2 and lagoon £3.
     (See Figures 2 and 7)   Because groundwater is contaminated,
     and  the water table lies at approximately 50 feet below  the
     site, low-level subsurface soil contamination exists as  deep
     as 50 feet  although a significant drop-off in levels occurs
     after approximately 20 feet (See Figure 8 and 9).
     Contamination of soils at and below the surface appears  to
     be confined to the area of the three former lagoons.

     As a result of the reported occasional burning of floating
     oils on the surface of the lagoons, the RI included an
     analyses for dioxins in the soil (dioxins can be created
     from the burning of chlorinated phenols and hydrocarbons).
     Although dioxins were detected in the parts per trillion
     (ppt)  range (See Table 5), the levels do not present an
     unacceptable risk and will not require remediation.   EPA
     generally considers the potential need for remediation of
     dioxins when levels are found to exist in the ppb range  or
     higher.

     Based on the results of RCRA Subtitle C 40 CFR §261.24
     Toxicity Characteristic Leaching Procedure (TCLP) analyses
     of three of six soil boring samples, the soil/waste mixture
     at the site would be classified as characteristic hazardous
     waste under RCRA.  In addition, based on EPA's understanding
     of the nature of the operations leading to the generation of
     waste materials disposed of at the site,  EPA Region III  has
     determined  that the soil/waste mixture also would be

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                                12

      classified as  a land  disposal restricted hazardous waste
      under the RCRA program  (See  CFR Part 268).  The waste
      disposed at the site  contains F001-F005 waata.
 •     The former spray irrigation  and berm borrow areas (See
      Figure 7)  only have minor  levels of organic contamination
      which is not expected to present a direct contact risk. (See
      Table 6 for spray irrigation area sampling results.)

 •     Activities at  the site  does  not appear to have caused
      inorganic contamination of site soils, although levels were
      occasionally above background concentrations.  This finding
      is  in agreement with  EPA's understanding that only organic
      chemical rinsewaters  and wastes were disposed of at the
      site.

 •     During the RI  and the Soil Vapor Extraction/ Bioremediation
      treatability study, soil samples were taken in the former
      lagoon area.   Thin layers  of a black, sticky, fibrous
      substance were found  at depths ranging from 2 to 6 feet in
      former Lagoon  /I.  Analysis  of this layer showed that it
      contained the  vocs and  SVOCs found in the soil.  In addition
      to  the thin layers of a black, sticky, fibrous substance,
      other materials were  identified in the three former lagoons.
      These materials were  classified as "spongy1*, "rubber-like",
      "dry,  matted and latex-like* and were observed  at depths
      ranging from 2 to 14  feet  in all three lagoons.

VI. SUMMARY Or 8ITB RISKS

      The baseline risk assessment (RA) provides the basis for
taking remedial action and indicates the exposure pathways that
need  to  be addressed by the  remedial action  The RA was performed
for the  Site in accordance with EPA guidelines.    It involves
assessing  the toxicity or  degree  of hazard posed by substances
found at the site by considering  the levels at which these
substances  are  present.  The RA also entails describing the
exposure routes by  which humans and the environment could come
into  contact with these substances.

     When estimating an individual's exposure to sit* substances,
conservative assumptions regarding such factors as length of the
exposure period,  frequency of exposure, amount of skin exposed
and/or quantity of  substance ingested, are purposely used to
ensure that the risk is not  underestimated.  After evaluation of
the site data,  an assessment of toxicological information and
potential exposure  is performed,  followed by calculations of the
risks posed.  Separate calculations are made for those substances
that  can cause  cancer and  for those that can cause other, non-
carcinogenic health effects.  Risks to both childen and adults
are presented.

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                                13

A) Contaminant  Identification

     The  initial phase of the RA  involves reviewing all RI data
and  identifying the contaminants  of potential concern found in
all  exposure media at the site for further risk evaluation.  The
exposure  media  include onsite soil, groundwater, surface water,
springwater, fugitive dust and air emissions, and deer which
might graze at  the site.  Identified contaminants are primarily
chosen based on their relatively  high toxicity, mobility,
persistence and prevalence when compared to all contaminants
present at the  site.  The chosen  contaminants also provide a
representative  analysis of the potential risks at the site.
Arithmetic average and maximum concentration levels of the chosen
contaminants are utilized to develop most probable and maximum
exposure  scenarios in a later phase of the RA.  A listing of the
identified contaminants of concern or "indicator" contaminants
appears in Table 7.  Based on RI  data, the selected contaminants
represent 99% of the risk associated with each exposure scenario
for each medium.  Sources of uncertainty in selecting the
indicator contaminants are discussed in the RA and in Section F,
below.

B)
     The objectives of the exposure assessment are to identify
potential exposures associated with the contaminants of concern
at the site and to estimate the magnitude of these exposures.

     Based on the site's environmental setting, the RA identified
five potential populations which could be exposed to site
contaminants.  Actual exposure of these groups is currently
severely limited however, due to controls implemented at the site
to date.  The "potential exposure pathways" for this site are:

          Use of groundwater (via private well) as a residential
          water supply by residents living in the area of.
          estimated site-related impact.  Exposure includes .
          dermal contact with and ingestion of groundwater as
          well as inhalation of volatile organic chemicals
          released during showering and other activities.

          Dermal contact with and incidental ingestion of
          contaminated onsite soils by a casual trespasser.

          Ingestion of venison from deer that may graze onsite.

          Inhalation of volatile organic chemicals and fugitive
          dust released from on-site soils, and

          Recreational use of the ponds fed by spring #48 (a.k.a.
          the Baldwin Campground spring) (Figure 5).  Exposure
          includes dermal contact with and incidental ingestion

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                                14

           of  water,  as well as inhalation of volatiles released
           from the water.

           Hypothetical residential use of groundwater from the
           onsite monitoring wells installed during RI field work.

      The rationale for the selection of these potential exposure
 pathways appears in  Table 8.  When calculating the risks
 associated with each of these pathways, the RA considers three
 age  groups as potentially exposed: adults, children ages 6 to 12,
 and  children  ages 2  to 6.  Table 9 provides additional
 information on exposure duration.

      Actual quantification of potential exposure involves
 estimating exposure  point concentrations and calculating
 potential intakes for each exposure pathway identified above.
 Exposure point concentrations (the contaminant concentration at
 the  point at  which the resident is exposed) were based on the
 arithmetic average and maximum values for each indicator chemical
 found in each medium at the site.  To determine the concentration
 of VOCs  released from onsite soils and the pond fed by Spring
 #48,  and to determine the concentrations in fugitive dust
 released from onsite soils, air screening models were utilized.
 When estimating VOC  concentrations released during showering with
 private  residential  well water, an inhalation dose equivalent to
 that experienced via ingestion of such water was assumed.
 Summaries of  the average and maximum exposure point
 concentrations appear in Appendix 0 of this ROD.

      In  the calculation of potential intakes (how much and for
 how  long one  is exposed to the exposure point concentrations),
 the  characteristics  of the various exposure pathways must be
 defined.   Important  parameters include the frequency, duration,
 and  degree of exposure as well as physiologic characteristics of
 the  exposed population, such as body weight and skin surface
 area. Estimates of these parameters are based on EPA guidelines,
 recommendations found in the current literature, and professional
 judgment.  The exposure assumptions used in calculating the
 potential intakes appear in Table 9.

     Several  assumptions wars made regarding both the nature and
 extent of contamination present at the site as well as the
 behavior and  characteristics of the populations potentially
 exposed  to the contamination.  These assumptions include use of
 the  following:  monitoring data to represent exposure
 concentrations across a medium; screening level models to
 represent exposure concentrations across a medium; single values
 for exposure  parameters to characterize the behavior of an entire
population over an extended period of time, and the intake
calculations  for the deer ingestion scenario, which should be
considered semi-quantitative in light of the numerous assumptions
required.

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                                 15

 C) Toglcitv Assessment gmgq*^v

      This task requires the assessment of the intrinsic
 toxicological properties of the contaminants of potential
 concern.  Both carcinogenic and non-carcinogenic effects from the
 indicator contaminants must be presented.  A summary of
 toxicological information on all indicator compounds assessed for
 the site appears in Table 10.  This table identifies those
 compounds which are considered potential carcinogens and those
 identified for non-carcinogenic effects.  In some cases,
 compounds are evaluated for both types of effect. The acronyms
 used in Table 10 are defined as:

 Cancer Potency Factors fCPFsl have been developed by EPA for
 estimating excess lifetime cancer risks associated with exposure
 to potentially carcinogenic chemicals.  CPFs are multiplied by
 the estimated intake of a potential carcinogen to provide a
 conservative estimate of the excess lifetime cancer risk
 associated with exposure at that intake level.  CPFs are generally
 derived from human epidemiological studies or chronic animal
 bioassays.

 Reference doses fRfDs)  have been developed by EPA for indicating
 the potential for adverse health effects from exposure to
 chemicals exhibiting noncarcinogenic effects.  RfDs are estimates
 of daily exposure levels for humans, including sensitive
 individuals that are likely to be without an appreciable risk of
 adverse health effects.   RfDs are derived from human
 epidemiological studies or animal studies to which uncertainty
 factors have been applied (e.g.  to account for the use of animal
 data to predict effects on humans).

 Carcinogenic class refers to EPA's weight-of-evidence system for
 classifying chemicals suspected of being human carcinogens.  The
 classes appearing on Table 10 are defined as Group A - human
 carcinogen;  Group Bl - Probable human carcinogen based on limited
 human data;  Group B2 - Probable human carcinogen based on
 sufficient  evidence in animals but little or no evidence in
 humans;  Group C - Possible human carcinogen; Group D - Not
 classified  as to human carcinogenicity;  Group E - Evidence of
 noncarcinogenicity for humans.

 0) Risk Characterisation

The  final task of the RA is to integrate the results of the
Exposure Assessment and Toxicity Assessment to quantitatively
estimate the potential  risk associated with the six exposure
pathways previously identified.   Both carcinogenic and
noncarcinogenic effects are considered.

Carcinogenic risk - Carcinogenic risk is calculated by
multiplying  the daily intake of  each chemical,  averaged over the

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                                16

 years  of  exposure,  by the appropriate CPF.  Results are presented
 in  probabilities  expressed  in scientific notation.  A result of
 1E-04  (ixlO"4) indicates that an individual has a one in ten
 thousand  chance of  developing cancer as a result of site-related
 exposure  to  that  chemical under the specific exposure conditions
 at  the site.   Based on EPA  policy, a risk exceeding the range of
 1E-04  to  1E-06 is generally considered as exceeding the
 acceptable risk level.

 The risk  associated with exposure to a set of chemicals is
 estimated by adding the risks associated with exposure to each
 chemical.  Several  of the exposure scenarios at the site may
 involve more than one route of exposure.  A summary of the
 results of the calculations for each age group under each
 exposure  scenario,  as well  as a lifetime exposure scenario
 (calculated  by adding the risk for each age group), is presented
 in  Table  11.   This  table also provides a summation of risk
 associated with simultaneous exposure under multiple scenarios.

 Noncarcinoaenic Risk  - Noncarcinogenic risk is determined by
 calculating  the Hazard Index (HI).  This number is found by
 dividing  the daily  intake by the appropriate RfD.  The HI
 provides  an  estimate  of the potential for toxic effects to
 develop as a result of exposure to a chemical or set of chemicals
 under  the assumed conditions of exposure.

 A HI less than one  indicates that no toxic effects are expected
 to  occur  as  a result  of a given exposure, while a HI of greater
 than one  indicates  that there is a potential for an individual to
 experience adverse  health effects as a result of a given
 exposure.  Noncarcinogenic  risk associated with exposure to a set
 of  chemicals  is conservatively estimated by adding the risks
 associated with exposure to each chemical.  A summary of the
 results of the HZ calculations for each age group under each
 exposure  scenario,  including a lifetime exposure scenario,
appears in Table  12.  A multiple exposure summation appears in
this table.
E)
During the RX, an ecological investigation of the surrounding
site area was conducted to assess site-related impacts to the
local flora and fauna.  The objectives of this work were to:

     l) characterize the terrestrial and wetland communities of
     the site and surrounding area,

     2) identify the macroinvertebrate communities of the
     downgradient tributaries,

     3) assess any site-related impacts on these various
     ecological communities.

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                                17

 Utilizing the data obtained from  the  above tasks,  an ecological
 assessment of the site  was  conducted  in  a methodology similar to
 that described above for public health impact.  After completion
 of  the Exposure Assessment  and  Toxicity  Assessment phases of the
 total ecological  assessment,  it was determined that RI analytical
 results of surrounding  stream samples did not indicate an
 exposure of aquatic ecological  receptors to site-related
 contaminants.   In fact,  the macro invert br ate community in the
 streams surrounding the site were found  to be diverse and
 healthy.

 The only terrestrial receptors  experiencing site-related impact
 would be those trespassing  or residing directly on the 2.2 acre
 former lagoon area.   The chain  link fence around the site and the
 lack of an adequate food supply onsite acts to prevent
 surrounding wildlife from coming  into direct contact with site
 soils.   The vegetation  surrounding the site appears quite
 healthy,  and is not measurably  affected  by the site.  Wildlife
 residing around the site is not expected to be impacted by the
 site contamination based on evaluation of the RI data, lack of
 access to the  site,  and the RA  analysis  of potential exposure to
 grazing deer.  Due to past onsite  dumping activities, onsite
 vegetation is  quite sparse,  resulting in the one measurable
 effect of the  site to the local ecology.

 Finally,  although fringe, forested wetlands exist  along the
 streams  surrounding the site, they have  been determined not to be
 impacted  based on both  visual inspection and the analytical
 results of  stream surface water and sediment samples.  Based on
 consultation with the appropriate state  and Federal agencies, no
 threatened  or  endangered species  are  known to exist in the site
 area,  save  the occasional transient species.
P) Significant Sources of Uncert

The RA for the sit* is based on conservative assumptions
regarding exposure and toxicity. In making estimates of potential
exposure and resultant intake, an effort was made to select
parameters that overestimate actual exposures, so that the
resulting estimate of potential risk also overestimates the
actual risk associated with site-related exposures.  The
assumptions made for this risk assessment are:

     - an individual may be exposed to any of these exposure
     conditions over the course of a lifetime,

     - an individual may be chronically exposed to concentrations
     of contaminants approaching the values used in the RA,

     - an individual may be simultaneously exposed to multiple
     pathways of exposure over the period of a lifetime,

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                                18

      - deliberate overestimation  of  toxicity indices  where
      questions exist about the actual  toxicity or  carcinogenicity
      of a substance or group of substances.  (One exception to
      this conservative methodology is  the RA's assumption that
      the risk associated with exposure to more than one toxicant
      is additive.  In some cases,  depending  on the chemicals,
      risk may be greater than additive.)

 Several limitations of the RA should also be noted:

      - analytical results from only  five surface soil samples
      were available to evaluate the  exposure pathways associated
      with dermal contact, contaminant  air releases/fugitive dust
      emissions,  and ingestion of  venison associated with deer
      grazing onsite;

      - the method utilized during the  RI to  identify  the depth
      interval of soil borings for sample analyses  may or may not
      have excluded samples with higher concentrations of
      semivolatile organic compounds;

      - the sampling data utilized in the RA  for exposure via use
      of residential well water is solely comprised of volatile
      organic analytical results collected under the Consent Order
      between EPA and CLTL.   For this reason,  exposure of
      residents to other chemicals associated with  site soils,
      such as semivolatile compounds  and tentatively identified
      compounds (TICs),  was not determined.   Results from the one
      round of sampling of residential  wells  for semivolatile
      organic analyses were not used  based on the limited data set
      for these compounds;

      • the use of monitoring data, single concentration values,
      and screening level models (especially  in the air and
      grazing deer exposure scenarios)  all present  a measure of
      uncertainty when estimating  one's exposure to site
      contaminants;

      - the RA is based on conditions of no action  at  the site.
      Protective  measures instituted  at the site, including the
      installation of a fence around  the site and provision of
      point-of-entry carbon treatment units to homes with veil
      water exceeding MCLs,  results in  risks  considerably lower
      than that predicted in this  RA.

O) Conclusions of the Risk Assessment

The results of the calculations performed in the RA using the
aforementioned exposure routes indicate that the estimate of most
probable  risk associated with all routes of  exposure, except the
Hypothetical Residential Use of Monitoring Hell (or "Onsite")
Groundwater,  is  within EPA's range of  acceptable risk.  The

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                                19

 estimate of maximum or worst case risk exceeds EPA's range for
 two exposure routes; (1)  the Hypothetical Residential Use of
 Onsite Groundwater and (2)  the more realistic and actual
 Residential Use of -Offsite Groundwater.

 Following is a condensed  table of the lifetime carcinogenic risks
 calculated for each exposure scenario:

                             Table 13


    Exposure Route              Most Probable       Worst  Case

    Residential Use of
    Offsite Groundwater ,        1 x 10"5             3 x 10"**

    Contact and Ingestion
    of  Onsite Surface           9 x 10"6             2 x 10~5
    Soils

    Deer Meat Ingestion         5 x 10"6             i x 10"5

    Recreational Use of
    Spring Water at Campground  3 x 10~8             3 x 10"8

    Inhalation of Dust and
    Vapor from Onsite Soils      5 x 10'6             i x 1
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                                20

 directly below and adjacent to the site.   It has not  been
 determined when and if this contaminated  groundwater,  at or near
 to the concentration levels found below the  site, could reach
 residential wells. - Using a conservative  approach to  public
 health protection, EPA assumed that groundwater contaminant
 concentrations approaching the levels below  the site  would
 ultimately reach residential wells if either the pollutant source
 or contaminated groundwater is not contained or remediated.

      In addition to carcinogenic  risks, the  RA calculated risks
 to humans of contracting non-carcinogenic health effects from
 substances associated with the site using the same identified
 exposure routes.  The results of  these calculations for non-
 carcinogenic health effects were  below the EPA guideline of i.o
 for children and adults for all exposure  scenarios except both
 the most probable and maximum Hypothetical Use of Onsite
 Groundwater scenarios.  These results suggest that exposure to
 non-carcinogenic chemicals at the site is not anticipated to
 result in adverse health effects  under the current conditions of
 exposure.   As stated above,  however, it implies that  groundwater
 contaminants found at levels directly below  and adjacent to the
 site could pose non-carcinogenic  health effects to users.
 Therefore,  if groundwater contaminant concentrations  at or
 approaching these levels were to  migrate  to  residences, non-
 carcinogenic health effects would be expected.

      For the two groundwater exposure scenarios exceeding EPA's
 carcinogenic and noncarcinogenic  guidelines  (Residential Use of
 Of fsite and Onsite Groundwater),  TCE is the  contaminant which
 poses the greatest carcinogenic risk and  chloroform and
 tetrachloroethene pose the greatest noncarcinogenic risk.

      Under the scenario Hypothetical Residential Use  of
 Monitoring Well Groundwater,  it should be emphasized  that no one
 is  currently using this water.  This scenario presents the risk
 which could be posed if the site  were left unaddreseed and the
 contaminant plume continued to spread.

      From  an environmental risk perspective, analyses of surface
 water and  sediment samples near the William  Dick Lagoons Site do
 not indicate that these media are currently  measurably affected
 by  site-related contamination.  Further,  except for that of the
 immediate  area of the former lagoons, the assessment  made of the
 local  environment did not identify any potentially adverse
 effects of site~related contamination to  the wellbeing of plants
 and animals.   Thus,  it appears that the Sit* has had  no
 persistent  adverse effect upon the surrounding ecosystem.

     EPA has determined that actual or threatened releases of
hazardous substances from this site, if not  addressed by
 implementing the response action  selected in this ROD, may
present an  imminent and substantial endangerment to public

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                                21

 health,  welfare,  or the environment.

 vzi.  Description  of Alternatives

      The draft Focused Feasibility Study (FFS) discusses the
 alternatives evaluated for the  soil and  provides supporting
 information leading to alternative selection by EPA.  EPA's
 comments to this  draft document did not  affect EPA's selection
 process  but may effect the design and  implementation of the
 remedy.   Both the draft FFS and EPA's  comments to the draft are
 included in the Administrative  Record.   The index for this
 administrative record is attached to this ROD in Appendix B.

      CERCLA Section 121 requires  that  the alternative chosen in
 the ROD  meet several criteria.  The alternative must protect
 human health and  the environment,  be cost effective, and meet the
 requirements of environmental regulations.  Permanent solutions
 to contamination  problems should  be developed wherever possible.
 These solutions should reduce the volume, toxicity, or mobility
 of the contaminants.   Emphasis  is also placed on treating the
 wastes at the Site,  whenever possible, and on applying innovative
 technologies to clean up the contaminants.

      The soil clean-up levels listed in  Table 1 were used as a
 basis for the comparison of alternatives for this ROD.  These
 levels were calculated based on the assumption that a vegetative
 soil  cover would  be placed over the site after treatment.  A
 vegetative soil cover is defined  in this ROD as a layer of soil
 which will support the germination and propagation of vegetation
 and will provide  dermal protection from  the treated soils.  The
 vegetated soil cover will not restrict the infiltration of
 rainwater or surface water through the soils.

      EPA's goal is to restore the site to a condition as close as
 possible to the pre-disposal conditions  within a reasonable cost.
 Restoration of the site to a state similar to pre-disposal
 conditions may be achievable if the soil clean-up levels in Table
 l are met.  These  soil clean-up  levels  do not take into account
 the risk of direct contact with the soils for all of the
 compounds listed  because the installation of a the vegetative
 soil  cover and implementation of  institutional controls, which
 are included as part of all of  the alternatives listed below,
 will  provide acceptable protection against direct contact with
 the subsurface soils.   Although reducing contaminants in the soil
 to levels that do not pose an unacceptable direct contact risk is
 not a requirement of  this ROD,  if the  treatment technology used
 in this  remedy can remediate the  soils to the direct contact risk
 levels provided in Table 2,  the site could be used with
 unrestricted access.   If the direct contact risk levels are not
met by the remedy,  than deed restrictions will need to b«
 implemented so that the the treated soil at the site is not
 excavated or uncovered.

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                                22

      If the levels listed  in Table  1 cannot be obtained by any of
 the treatment technologies listed below, than a multi-layer cap
 that will restrict- infiltration of  water so that contaminants
 will not leach into  groundwater above an acceptable level will be
 installed at the site.   Therefore,  for the remedy described in
 this ROD,  the soil clean-up levels  described in Table l may be
 refined during the Remedial Design  by incorporating any
 information generated by any future treatability studies
 conducted at the Site.   In addition, data generated during the
 hydrogeological study,  which is expected to be completed during
 1993,  may, be incorporated  into the  model to refine the soil
 clean-up levels to ensure  compliance with the MCLs and health-
 based drinking water concentrations, as described in Section II.

      The alternatives evaluated in  this ROD for OU 3 are
 described below.   The method and detail of the alternative
 evaluation differs from that presented in the FFS.  Specifically,
 EPA arranged the separate  SVE/BIO alternatives into one
 alternative and the  separate thermal desorption alternatives into
 one alternative.   The SVE/BIO alternative and the thermal
 desorption alternative  described in this ROD outline all of the
 variations of alternatives in the FFS.  In addition, although
 incineration was screened  out of the detailed analysis of
 alternatives in the  FFS, EPA has included it in its evaluation.

     All of the costs and  implementation times listed in this
 Proposed Plan are estimates.

 The alternatives evaluated for Source Control - Oerable Unit 3
Alternative 1: No Action
Alternative 2: Capping
Alternative 3: SVE/BIO with Multi-layer Cap
Alternative 4: Thermal Desorption with Vegetative Soil Cover or
               Multi-layer Cap
Alternative 5: On-«ite Incineration with Vegetative Soil
               Cover

COKMOM BLEKENTSs  All of the alternatives which were considered,
except for the No Action alternative, contain common elements.
Prior to remedy implementation, alternatives 2 through 5 will
require a minor amount of surface soil sampling in the former
lagoon berm borrow area (Figure 2) to determine if a vegetative
soil cover is appropriate in this area to limit direct contact
with soils.  Because only a limited number of surface soil
samples were obtained during the RI from the former lagoon berm
borrow area for evaluation of the direct contact exposure
scenario, additional sampling is required.  The remediation
design work for Alternatives 2 through 5 will delineate those
areas of the site requiring source control activities,
specifically, the former lagoon area and those areas requiring

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                                23

 only a vegetative soil cover.   Based on the sampling performed,
 the subsurface soil in this area may require treatment as
 described in Alternatives 2 through 5.   This treatment will be
 performed as part of this ROD.

      Because a cap or cover would be installed in Alternatives 2
 through 5, long term monitoring and maintenence will be required.
 The cap or cover shall (l)  provide dermal protection from the
 treated soils; (2)  support the  germination and propagation of
 vegetative cover; and (3)  compact veil  and be stable when dry.
 The cap or cover shall be maintained for 30 years.

    .. Alternatives 4 and 5 require excavation of contaminated
 soils.   Because of the high levels of VOCs in the soils,
 excavation will need to be performed under controlled conditions
 to reduce the risks to workers  and nearby residents.  The risks
 associated with the excavation  will be  determined during the
 remedial design phase.   A preliminary risk assessment for the air
 emissions from excavation was performed by EPA's toxicologist.
 Air emission rates were calculated by personnel in EPA's Region
 III Air,  Radiation, and Toxics  Division.  The air emission model
 report  and the preliminary risk assessment are attached to this
 ROD in  Appendix C.   Results from this preliminary risk assessment
 indicate that the potential carcinogenic risk to a young child
 exposed to air emissions of TCE for 90  days,  which is the
 predicted duration of soil remediation, is 2.77E-06.  This is
 within  the EPA's generally acceptable carcinogenic risk range of
 l.OE-06 to l.OE-04.  These values are preliminary and may be
 refined during the  remedial design.   If calculations performed
 during  the remedial design indicate an  unacceptable risk,  than
 the risk will be mitigated.  Possible options for mitigating the
 risks include continued operation of the SVE system until VOC
 levels  are reduced  to an acceptable level, staging the excavation
 so  that only a small amount of  soil is  excavated at a time,
 excavating during the winter months or  containing the excavation
 process under a tent-type enclosure.  In addition, appropriate
 monitoring will occur to ensure that any excavation emissions do
 not present a health threat.

 Alternative 1:  No Action                                •

     •  Capital Cost:  $0
     •  Annual Operation and Maintenance (O&M): $0
     •  Present Worth:  $0
     •  Time to Implement: None

     The.NCP requires that  the  "no action* alternative be
 evaluated for each  site unit in order to establish a baseline for
 comparison..   Under  this alternative,  EPA would take no action
with respect to the contaminated  soils  at the former lagoons.
This approach would allow contaminants  to continue to leach into
the groundwater thereby preventing an effective groundwater

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                                24

 remediation program.   It would also permit access to the site
 which would increase  the risk of  direct contact with subsurface
 contaminated soils.   Any future use of the site property which
 disturbs site soils would present an inhalation and direct
 contact threat.

      The no action alternative is .not protective of human health
 and the environment and, therefore,  will not be considered
 further in this  ROD.

 Alternative 2: Capping

      • Capital Cost:  $500,000 to  $850,000
      • Annual O&M: $19,600 to $32,600
      • Present Worth:  $800,000 to $1,350,000
      • Time to Implement:  14  months

      This alternative involves multi-layer capping of the lagoon
 area soils.   A multi-layer cap is defined in this ROD as an upper
 vegetative layer (topsoil) underlain by a drainage layer (sand)
 over a low permeability layer fi.e..  natural soils, admixed
 soils,  a synthetic liner or membrane, or any combination of these
 materials).   The area to- be capped is expected to be
 approximately 2.2 acres, although the actual extent of the cap
 will be determined during design.   The total area of the cap will
 be  somewhat larger than the area  of contaminated soil to prevent
 any lateral infiltration of precipitation.  The cap may need to
 extend over portions  of the former lagoon borrow area as
 determined by the sampling described in the Common Elements
 section,  above.   The  cap would be designed to conform to the
 substantive performance standards outlined in the Pennsylvania
 closure regulations set forth in  25 Pa. Code 265.110-.119 and the
 landfill closure regulations  at 265.310 which are relevant and
 appropriate regulations..

     Because the contaminated soil would not be removed or
 treated under this alternative, the soil clean-up levels listed
 in Table 1 would net  be net.   However, the cap would be designed
 to eliminate direct contact with  the soils.  The cap would also
 limit the amount of rainwater infiltration through the
 contaminated soils so that the leaching of contaminants from the
 soil to the groundwater is reduced to levels which would not
 result  in groundwater contamination above MCLs or health-based
 levels.

     The range in O&M costs reflects the use of either an
 "alternative" cap or  a "RCRA" cap.   CLTL defined a so-called
 "RCRA"  cap  in the focused feasibility study as an upper
 vegetative layer (topsoil) underlain by a drainage layer  (sand)
over a  low permeability layer (i.e..  natural soils, admixed
 soils,  a  synthetic liner,  or  any  combination of these materials).
The "alternative" cap,  as defined by CLTL in the focused

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                                25

 feasibility study/  substitutes a  synthetic membrane for the low .
 permeability layer used in the "RCRA"  cap definition,  above.
 Using the mathematical models that were developed  during the
 focused feasibility study,  the specific cap  structure  will be
 determined during the remedial design.

      Institutional controls (i.e..  deed restrictions)  would need
 to be implemented under this alternative so  that access to the
 property is limited.   The integrity of the cap would be
 maintained to ensure adequate protection against direct contact
 with the soils and infiltration of surface and rain water.

 Alternative 3:  SVE/BIO with a Multi-layer Cap

      •  Capital Cost:  $1,700,000 to $4,100,000
      •  Annual O&M:  $280,000
      •  Present Worth:  $2,700,000  to $5,100,000
      •  Time to Implement:  33-35 months (+3-5 years of  operation)

      This alternative  involves the in-situ treatment of
 approximately 24,000 cubic  yards  of site soil via  Soil Vapor
 Extraction (SVE)  and Bioremedition (BIO).  This estimated volume
 was  determined during  the Focused Feasibility Study by assuming
 that the contaminated  soil  extends out: to a  distance halfway
 between each contaminated sample  location and the  closest "clean"
 boring.   "Clean"  borings are defined as those with chemical
 constituent levels  below clean-up levels defined in Table 1.  SVE
 consists of a network  of air withdrawal (or  vacuum)  wells
 installed throughout the contaminated  soils.  The  walls are
 connected to a  vacuum  pump  systea to provide continuous air flow
 through the soil, resulting in the removal or stripping
 (volatilization)  of contaminants  from  the soil.  SVE would be
 used in conjunction with bioremediation.  BXO is the use of
 indigenous microorganisms to degrade the chemicals in  the soils.
 The  addition of air through the soil with the SVE  would stimulate
 bacterial growth.   The bioremediation  could  be enhanced with the
 addition of nutrients,  such as nitrogen and  phosphorous.  This
 would be accomplished  by spraying a water solution containing the
 nutrients over  the  area to  be treated.   The  types  of chemicals
 degraded depends  on the types of  organisms which are naturally
 occurring in the  soil.

     During the operation of this remedy, air emissions controls
 would be required to meet appropriate  State  and Federal hazardous
waste and air standards.  Any contaminants generated by these
 emissions controls  would be disposed of off-site in accordance
with Resource Conservation  and Recovery.Act  (RCRA)  requirements.

     The  SVE/BIO  remedy would be  concluded at the  point in time
when no  significant reduction in  voc and SVOC soil concentrations
result after continuous operation.  A statistically valid
confirmatory soil sampling  program would be  established during

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                                26

 the remedial  design to determine  the endpoint of remediation.

      Based on the results  of  the  SVE/BIO treatability study
 conducted in  August 1992 and  SVE  studies performed at similar
 sites,  it is  not anticipated  that this technology can meet the
 soil clean-up levels listed in Table 1, which were based on
 installation  of  a vegetative  soil cover over the area containing
 the treated soils once the soil has been remediated.  Therefore,
 after completion of the SVE/BIO process, it is anticipated that a
 multi-layer cap  (similar to the "alternative" or "RCRA" cap, as
 described in  alternative 2),  would have to be placed on the site.
 The cap would be designed  to  eliminate direct contact with the
 contaminants  remaining in  the soils   The cap would also limit
 the amount of rainwater infiltration through the remaining
 contaminated  soils so that the leach .ig of contaminants from the
 soil  to the groundwater is reduced to levels which do not exceed
 MCLs  or health based levels.  A final decision on the type of
 multi-layer cap  would depend  on the success in achieving the soil
 remediation goals.   For costing purposes, an "alternative" cap,
 as  described  under alternative 2, is proposed.  The cap would be
 designed  to conform to substantive Pennsylvania closure
 regulations set  forth in 25 Pa. Code 265.110-.119 and the
 landfill  closure regulations  at 265.310 which are relevant and
 appropriate regulations.

      The  results of the SVE/BIO treatability study indicate that
 significant quantities of  VOCs can be removed from the soils.
 Approximately 610 pounds of VOCs  were removed during the six week
 continuous operation of the treatability study.  Good subsurface
 air flow  conditions were observed during the treatability study.
 Because the treatability study was only operated for six weeks,
 it  did  not conclusively demonstrate that bioremediation could be
 effective in  degrading the VOCs and SVOCs in the soils.

      Even though the SVE/BIO  treatability study showed that this
 technology removed large amounts  of VOCs, it did not confirm that
 the soil  cleanup criteria  could be net, especially with respect
 to  SVOCs.  Because the lagoon  soils are not uniform, it is
 possible  that the air flow during SVE/BIO remediation would
 short-circuit throughout the  subsurface.  This short-circuiting
may result in minimal treatment of subsurface areas which have a
 low permeability.

     As described in the Site Characteristics section, thin
 layers.of a black,  sticky, fibrous substance and materials
 classified as "spongy", "rubber-like", "dry, matted and latex-
 like" were identified in the  three former lagoons during the RI
and treatability study.  The  impact of these layers on the
operation of  the SVE/BIO system was not analyzed during the
treatability  study.   According to CLTL, an additional 6-12 month
pilot study would be necessary during the remedial design to
determine how this layer would affect SVE/BIO remediation.  CLTL

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                                27

 proposed that if this layer could not be remediated with SVE/BIO,
 this material should be excavated and treated by either thermal
 desorption or incineration.  EPA agrees that additional studies
 would be necessary during the remedial design to determine the
 impact of these materials on the SVE/BIO remediation.   These
 materials could adversely impact a full-scale SVE/BIO
 remediation.   The type of cap installed under this  alternative if
 thermal desorption or incineration of the tar-like  material is
 necessary would be determined during  the remedial design.

      The range in costs listed above  reflect the possible need
 for thermal treatment (either off-site incineration or  on-site
 thermal desorption)  of the tar-like layer identified in former
 lagoon area after operation of the SVE/BIO system.   The need for
 thermal treatment of the tar-like layer and  the  type of thermal
 treatment required would be assessed  during  a pilot study
 conducted during the remedial design.

      Institutional controls (i.e.,  deed restrictions) would be
 implemented under this alternative so that access to the property
 is  limited.   The integrity of the cap must be maintained to
 ensure adequate protection against direct contact with  the soils
 and infiltration of surface and rain  water.

 Alternative 4:  Thermal Desorption with Vegetative Soil  Cover or
                Multi-layer Cap

      • Capital  Cost:  $7,500,000 to $9,000,000
      • Annual O&M:  $20,000
      • Present  Worth:  $7,800,000 to $9,300,000
      • Time to  Implement:  25 months

      This alternative involves the excavation and treatment of
 approximately 24,000 cubic yards of site soil via thermal
 desorption.   This estimated volume was determined during the
 Focused Feasibility Study by assuming that the contaminated soi
 extends out to  a distance halfway between each contaminated
 sample location and the closest "clean" boring.   "Clean" borings
 are defined as  those with chemical constituent levels below
 cleanup levels  defined in Table 1.  Thermal  desorption  generally
 consists  of a rotary dryer designed to accept contaminated soils
 which are then  heated to a sufficient temperature to volatilize
 the contaminants froa the soil into the air.   The rotary dryer
rotates to allow for proper mixing and the contaminated air
 stream is treated in a control system consisting of a fabric
 filter for particulate removal,  a wet scrubber for  acidic gas
 conversion, and a carbon adsorption systea for capture  of the
contaminants.   Excavation of contaminated soil and  replacement of
 treated soil  would be  performed using conventional  construction
equipment.  Soils would be stockpiled onsite before loading into
the rotary dryer for treatment.

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                                28

      Based  on  the  nature of the operations  leading to the
 generation  of  the  waste materials at the site, EPA Region III has
 determined  that the'contaminated soil, prior to treatment, either
 constitutes or must be managed as a hazardous waste bearing the
 hazardous waste identification numbers F001 through F005 under
 State and Federal  law.  EPA anticipates that following treatment,
 the  soil will  no longer "contain1* hazardous wastes and thus need
 no longer be managed as a hazardous waste for purposes of Federal
 law.   EPA also anticipates that for State law purposes, the
 levels of contaminants in the soils after treatment will be such
 that the soils may be "delisted" and no longer considered a
 hazardous waste under State law.  (Any such "delisting"
 determination  will be made by EPA in accordance with the
 substantive requirements of 25 Pa. Code Section 260.22, and the
 applicable  requirements of CERCLA and the National Contingency
 Plan,  40 C.F.R. Part 300.).  It is not expected that the treated
 soil  will constitute "contaminated soil1* for the purposes of PA's
 Residual Waste Management Regulations, 25 Pa. Code Ch. 287 et.
 3«q.

      After  completion of the thermal desorption process and
 replacement of treated soils, a vegetative  soil cover or multi-
 layer cap will be  placed on the site.  The  cap or cover will be
 designed to eliminate direct: contact with the any contaminants
 remaining in the soils.  The thermal desorption system will be
 designed to reduce the levels of contaminants in the soil so that
 infiltration of rainwater through these soils will not leach
 contaminants into  the groundwater above MCLs or health based
 levels, as  describe in Section II.  Soil levels which meet these
 criteria are listed in Table 1.  A final decision on the type of
 cap or cover will  depend on the success in  achieving the soil
 remediation goals.  If, during the thermal  desorption
 treatability study, EPA determines that the soil clean-up levels
 listed in Table 1  are not achievable, a multi-layer cap  (as
 described under Alternative 3) designed to  limit the amount of
 rainwater and  surface water infiltration through the
 contamination  remaining in the soils so that the leaching of
 contaminants froa  the soil to the groundwater is reduced to MCLs
 or health based levels, will be installed.

     The success in obtaining the soil remediation goals listed
 in Table 1 will be determined by performing a thermal desorption
 treatability study during the remedial design.  The soil clean-up
 levels may need to be modified based on the results of the
 thermal desorption treatability study. Any  such modification
 shall  be made  in accordance with the National Oil and Hazardous
 Substance Pollution Contingency Plan  ("NCP"), 40 CRF Part 300,
 and applicable agency guidance.

     For costing purposes for this ROD, an  "alternative" cap,  as
described under Alternative 2, is proposed.  It is possible,
however, that  thermal desorption could reduce the soil

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                                29

 concentrations to a level which would require only a  vegetative
 soil cover,  as described in Table 1.   if  only a  vegetative soil
 cover was required, the present worth cost  of this remedy would
 be reduced by approximately $620,000.

      As in Alternative 3, air emissions from  the treatment
 operation would be controlled to meet appropriate  State and
 Federal standards.  Any emission control  residues  generated by
 the treatment system would be disposed of off-site in accordance
 with federal and state waste disposal reguations.   Any
 wastewaters generated by any treatment component of the thermal
 desorption system, including a scrubber,  would be  disposed of
 off-site in accordance with applicable or relevent and
 appropriate state and federal waste disposal  regulations.

      Wastewaters generated during the thermal desorption process
 would be stored on-site in containers or  a  tank  and be disposed
 off-site in accordance with federal and/or  state hazardous waste
 storage and disposal requirements.    Treated  off-gases would be .
 released at the site after passage through  an emissions control
 system and would be required to meet  State  and Federal air
 standards.   Off-site disposal of treatment  residuals, if anyr
 will  comply with federal and/or state hazardous  waste disposal
 regulations.   Operation of the incinerator, if required, would be
 comply with  the standards set forth in PA Code 264.340 through
 264.353.

     As stated in the Genoa Elements section above,  the
 excavation process will need to be controlled to reduce the risks
 to workers and nearby residents posed by  the  emission of VOCs.
 Appropriate  monitoring will occur to  ensure that any  excavation
 emissions do not pose a health threat.

     Based on thermal desorption remediation  performed at. similar
 sites with similar contamination,  EPA believes that the thermal
desorption unit will b« able to process the tar-like  materials
 found in  the  former lagoons.   Because of  the  possibility that the
tar-like  layer cannot be treated by thermal desorption, EPA
considered the possibility of off-site incineration of the tar-
 like layer to meet the soil clean-up  goals.   The rang* in costs
 listed  above  reflects the possible need for off-site  incineration
of the  tar-like layer identified in the former lagoon area.  The
need for  incineration of the tar-like layer will be assessed
during  the remedial design.   It the thermal desorption
treatability  study indicates that off-site  incineration of the
tar-like  material is necessary,  the off-site  incinerator must
comply  with all Federal and State applicable  or  relevent and
appropriate requirements for the operation  of an incinerator.

     Depending on the soil clean-up level that is  achieved at the
Site, institutional control* (i.e., deed  restrictions) may need
to be implemented so that access to the property is limited.  The

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                                30

 integrity of  the  cap or vegetative soil cover must be maintained
 to  ensure adequate protection against direct contact with the
 soils  and infiltration of surface and rain water.

 Alternative 5: Onsite Incineration With Vegetative Soil Cover

     Estimated Capital Cost: $19,500,000
     Estimated Annual O&M: $0
     Estimated Present Worth: $19,500,000
     Time to  implement: 28-34 months

     This alternative achieves source control by excavating an
 estimated 24,000  cubic yards or more of contaminated soil and
 incinerating  it onsite.  This estimated volume was determined
 during the Focused Feasibility Study by assuming that the
 contaminated  soil extends out to a distance halfway between each
 contaminated  sample location and the closest "clean" boring.
 "Clean" borings are defined as those with chemical constituent
 levels below  cleanup levels defined in Table 1.  Incineration, or
 thermal destruction, uses high temperature oxidation under
 controlled conditions to degrade soils containing organics into
 by-products that  include carbon dioxide, water vapor, inert ash,
 and hydrogen  chloride gas (if chlorinated organics are present in
 the soil).  Soils would be stockpiled onsite before loading into
 the incinerator for treatment,  once all soils are incinerated,
 the remaining ash along with clean fill will be deposited onsite,
 graded and revegetated to restore the sit* to a natural
 condition.

     EPA  expects  that the characterization and management of the
 residual  ash  under the State hazardous and residual waste
 regulations will  be equivalent to that accorded the treated soil
 in Alternative 4.  It is anticipated that the ash generated as a
 result of  the incineration process will meet the soil clean-up
 levels listed in  Table 1.  After the ash and clean fill are
 deposited  on  site, a vegetative soil cover would be installed to
 eliminate direct  contact with the any contaminants remaining in
 the soils.  The incineration system will be designed to reduce
 the levels of contaminants in the soil so that infiltration of
 rainwater through these soils will not leach contaminants into
 the groundwater above MCLs or health based levels.

     wastewaters  generated during the incineration process would
 be stored on-site in containers or a tank and be disposed off-
 site in accordance with federal and/or state hazardous waste
 storage and disposal requirements.   Treated off-gases would be
 released at the site after passage through an emissions control
 system and would  be required to meet State and Federal air
 standards.  Off-site disposal of treatment residuals, if any,
will comply with  federal and/or state hazardous waste disposal
regulations.  Operation of the incinerator would be comply with
the substantive standards set forth in PA Code 264.340 through

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                                31

 264.353.

      As stated in the common Elements section above/  the
 excavation process^will need to be controlled to reduce the risks
 to workers and nearby residents posed by the emission of VOCs.
 Appropriate monitoring will occur to ensure  that any  excavation
 emissions do not pose a health threat.

 vin. summary of Comparative Analysis of Alternatives

      Each of the remedial  alternatives for this  operable unit has
 been compared and evaluated with  respect to  the  nine  evaluation
 criteria  in the NCP,  40 CFR Part  300.430(e)(9).   The  nine
 criteria  are listed in Figure 3.   The nine criteria are:

 A.  Overall Protection of Human Health and the Environment

      Overall protection of human  health and  the  environment
 addresses whether a remedy provides adequate protection and
 describes hov risks posed  through each pathway are eliminated,
 reduced,  or controlled through treatment, engineering controls,
 or institutional controls.

      The  "No Action"  alternative  is not protective of human
 health  and the environment because the site  would be  open to
 public  access and,  therefore,  the risk of exposure to VOCs via
 ingestion or dermal contact of subsurface soil,  if excavated or
 uncovered,  or inhalation of VOC vapors from  the  subsurface soil,
 if  excavated or uncovered,  would  not be addressed.  The "No
 Action" alternative would  not prevent the continued leaching of
 contaminants from the soil to the groundwater.   Therefore, the
 "No Action"  alternative will not  be considered further in this
 Proposed  Plan.

     Alternatives 2 through 5 would protect  human health by
 reducing  the leaching of contaminants from soil  to groundwater.
 Installation of a vegetative soil cover or multi-layer cap and
 implementation of institutional controls under Alternatives 2
 through 5 would provide additional protection against direct
 contact with the VOCs and  SVOCs in the subsurface soil.

     Alternatives 3,  4 and 5 would provide more  protection of
human health and the  environment  than Alternative 2 by not only
preventing direct contact  and reducing the level of contaminants
 leached to groundwater but by also reducing  and  controlling the
risk of exposure to source contaminants through  treatment of the
soils in the former lagoons.

B. Compliance with Applicable or  Relevant and Appropriate
Requirements (ARARs)

     Section 121(d) of CERCLA requires that  remedial  actions at

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                                32

 CERCLA sites at least attain  legally applicable or relevant and
 appropriate federal and State standards, requirements, criteria,
 and limitations which are collectively referred to as "ARARs",
 unless such ARARs are waived  under CERCLA Section 121(d)(4).

      Applicable requirements  are  those cleanup standards,
 standards of control,  or other substantive requirements,
 criteria,  or limitations promulgated under federal environmental
 or state environmental law or facility siting laws that
 specifically address hazardous substance, pollutant, contaminant,
 remedial- action,  location, or other circumstance at a CERCLA
 Site.   Only those state standards that are identified by a state
 in a timely manner and that are more stringent than federal
 requirements may be applicable.

      Relevant and appropriate requirements are those cleanup
 standards,  standards of control,  and other substantive
 requirements,  criteria,  or limitations promulgated under federal
 environmental or state environmental law or facility siting laws
 that,  while not applicable to a hazardous substance, pollutant,
 contaminant,  remedial  action,  location or circumstance at a
 CERCLA Site,  address problems or  situations sufficiently similar
 to those encountered at the CERCLA Sit* that their use is well
 suited to the particular Sit*.  Only those state standards that
 are identified in a timely manner and are more stringent than
 federal requirements may be relevant and appropriate.

     ARARs may relate  to the  substances addressed by the remedial
 action (chemical-specific), to the location (location-specific),
 or the manner in which the remedial action is implemented
 (action-specific).

        The Applicable  and Relevant or Appropriate Requirements
 for the alternatives developed in this ROD are listed below.

     Alternatives 2 through 5 would meet the respective ARARs for
 the Federal and State  environmental laws for this action.  The
 ARARs  for  this action  and the alternatives which are affected by
 each alternative are described below.

     EPA recognizes that under the Commonwealth of Pennsylvania's
 regulations governing  remediation of groundwater contaminated by
hazardous wastes,  the  standard for remediation is the achievement
 of  background levels for such hazardous wastes   (sjje. 25 Pa. Code
 S264.ioo(a) (9).   This  standard is a State ARAR for CERCLA
remedial actions  requiring remediation of groundwater.  Although
 the remedy  selected in this ROD for operable Unit 3 does not
require the remediation of groundwater contamination, EPA
recognizes  that the cleanup levels selected for contaminated
soils  at the site in this ROD may impact groundwater at  the Site.
At  such time as a final groundwater remedy is selected  for the
Site,  the  State's groundwater remediation standard, if  effective

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                                33

 at that tine,  will be considered  an ARAR which must  be net by the
 remedy unless  waived in accordance  with Section  121(d)(4) of
 CERCLA,  42  U.S.C.  (d)(4).

 Chemical Specific  ARARs

      a.   The  Resource Conservation and Recovery Act (RCRA)
          regulations at 40  CFR Part 264 Subpart AA- Air Emission
          Standards for Process Vents is relevant and appropriate
          for  Alternatives 3,  4,  and 5 because the SVE, thermal
        • desorption and incinertion have a stack vented to the
          atmosphere.   The total  organic emissions from all
          affected process vents  at the Site  are required to be
          below  1.4 kg/hr and  2800  kg/hr or reduce,  by use of a
          control  device total organic emissions from all
          affected process vents  at the facility by  95 weight
          percent  under this regulation.

      b.   The  emissions from the  treatment system must comply
          with the special permit requirements for sources
          located  in or siginificantly impacting nonattainment
          areas  set forth at Pa.  Code 5127.61-73.  These
          requirements are applicable to Alternatives 3, 4, and
          5.

      c.   The  emissions from the  treatment system must comply
          with the National  Ambient Air Quality  Standards  (NAAQS)
          as implemented under the  Pa.  State  Implementation Plan
          ("SIP").   This regulation,  which deals with the release
          of volatile  organic  emissions,  applies to  this action
          because  the  sit* lies in  an ozone non-attainment area.
          Alternatives 3, 4  and 5 must comply affected by this
          ARAR.

      d.   The  emission standards  set forth in 40 CFR Part 61,
          Subpart  F and Subpart J  which regulate vinyl chloride
          and  benzene  emissions under the Clean  Air  Act, Section
          112, 42  U.S.C. $7412 and  are Known  as  National Emission
          Standards for Hazardous Air Pollutants (NESHAPs) are
          relevant and appropriate  requirements  for  Alternatives
          3, 4 and 5.

a. Location specifie ABAfts:  There  are no location specific ARARs
for this Operable  Unit at the  Site.

3. Action specific ARABS<

     a.   The requirement in 25 PA  Code S127.12(a) (5) that air
          emissions be reduced to the minimum obtainable levels
          through  the  use of test available technology  (BAT), as
          defined  in 25 PA Code Section 121.1, will  apply to
          Alternatives 3, 4  and 5.

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                           34

b.   25  PA Code  §123.1, which prohibits the emission of
     fugitive  air contaminants and regulates emissions
     during construction activities, is applicable to
     Alternatives 3, 4 and 5.

c.   25  PA Code  §123.2, which prohibits the emission of
     fugitive  air contaminants from crossing the facility's
     property  line, is applicable to Alternatives 3, 4 and
     5.

d. •  25  PA Code  §123.31, which prohibits the emission of
    ; malodorous  air contaminants from crossing the property
     line, is  applicable to Alternatives 3, 4 and 5.

e.   25  PA Code  §123.41, which prohibits the emission of
     visible emissions of greater that 20% opacity, is
     applicable  to Alternatives 3, 4 and 5.

t.   RCRA regulations 25 Pa. Code S262.ll  (a) and (b)  (this
     section establishes standards for generators of
     hazardous waste and relates to hazardous waste
     determination), §262.20 (relating to manifesting
     requirements for off-site shipments of spent carbon or
     other hazardous wastes), and $262.30-33 (relating to
     pretransport requirements) are applicable to
     Alternatives 3, 4 and 5.

g.   With respect to Alternative 2 and Alternative 3
     (assuming the cleanup levels cannot be attained as part
     of  that remedial alternative), the substantive closure
     requirements set forth at 25 PA. Code §§265.110-119 and
     the landfill closure requirements set forth at 25 Pa.
     Code §265.310 are relevant and appropriate; the
     groundwater monitoring requirements at 25 Pa. Code
     §§264.90-110 are relevant and appropriate.  To the
     extent that the treated soils in Alternative 4 or
     residual  ash in Alternative 5 constitute hazardous
     wastes, the requirements of 25 Pa. Code Sections
     264.13-15 (General Facility standards); 264.31, 37 (PPC
     Plan and  Emergency Procedures); 264.90, .91, .97, and
     .98-.100  (Groundwater Monitoring); 264.111, .114, and
     .117-.119   (Closure and Postclosure); and 264.301,
     .302, .303, .305, .309, and .310 (Landfills) would be
     applicable  to the design, construction and maintenance
     of the area into which the treated soils or residual
     ash are deposited.  To the extent that the treated
     soils or  residual ash are not hazardous wastes due to
     application of the "centained-in" rule under federal
     lav and delisting under State lav, they may
     nevertheless constitute "contaminanted soil" for the
     purposes  of PA'S Residual Waste Management Regulations.
     In that event, management of those wastes may be

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                           35

     subject to the substantive requirements of
     Pennsylvania's residual waste regulations to the extent
     required under 25 Pa. Code Section 287.101(d).

h.   With respect to Alternative 3, the container storage
     standards set forth at 25 Pa. Code SS264.171-180 and
     the substantive closure requirements set forth at 25
     Pa. Code SS264.110-119 are applicable to the container
     storage of contaminants collected by the air emissions
     controls unless they are stored on-site in accordance
   -  with 25 Pa. Code $262.34; the regulations set forth at
     25 Pa. Code §263.10-263.32 are applicable when the air
     emission control residues are transported off-site; if
     thermal desorption and/or incineration are utilized as
     part of this remedy, the ARARs set forth in paragraphs
     i. and j., infra, respectively, are applicable or
     relevant and appropriate, as indicated; the groundwater
     monitoring requirements at 25 Pa. Code 264.90-100 are
     relevant and appropriate.

i.   With respect to Alternative 4, the container storage
     standards set forth at 25 Pa. Code SS264.171-180 and
     the closure requirements set forth at 25 Pa. Code
     §§264.110-119 are applicable to the container storage
     of contaminants collected by the air emissions controls
     unless they are stored on-site in accordance with 25
     Pa. Code §262.34; the regulation set forth at 25 Pa.
     Code 5263.10-263.32 are applicable when the air
     emission control residues are transported off-site; 40
     CFR §264, Subpart X, is applicable to the operation,
     closure and post-closure care of the thermal desorption
     unit; the waste pile design, operation and closure
     requirements set forth at 25 Pa. Code §§264.250-.258
     are applicable to the stockpile of excavated soil; the
     substantive closure and post-closure requirements set
     forth at 25 Pa. Code §§264.110-119 are applicable to
     the stockpile of excavated soil; the container
     management requirements at 25 Pa. Code §§264.171-180 or
     the tank standards at 25 Pa. Code §§264.190-199 are
     applicable to the on-site storage of wastewater
     dependent upon how the wastewaters are stored; the
     substantive closure and post-closure requirements set
     forth at 25 Pa. Code §264.110-119 are applicable to the
     closure of the units used to store wastewater unless
     the wastewater is stored on-site in accordance with 25
     Pa. Code §262.34; the regulations set forth at 25 Pa.
     Code 263.10-263.32 are applicable when the wastewater
     is transported off-site;  if off-site incineration of
     the tar-like material is necessary, the substantive
     standards of 25 Pa. Code §262 relating to generators of
     hazardous waste apply ot the tar-like material and the
     container or tank storage standards set forth at 25 Pa.

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                           36

     Code  §264.171-180 and/or §264.190-.199 for storage of
     the tar-like material prior to transport for off-site
     incineration are applicable; the substantive
     requirements of 25 Pa. Code 265.373, .375, .377, and
     .381  are relevant and appropriate to the operation and
     closure of the thermal desorption unit (to the extent
     that  such requirements are more stringent than those
     imposed by 40 CFR Part 264, Subpart X).

j.   With  respect to Alterative 5, the container storage
     standards set forth at 25 Pa. Code §§264.171-180 and
     the substantive closure requirements set forth at 25
     Pa. Code §§264.110-119 are applicable to the container
     storage of contaminants collected by the air emissions
     controls unless they are stored on-site in accordance
     with  25 Pa. Code 262.34; the operation and closure
     standards for incinerators set forth at 25 Pa. Code
     264.340-353 are applicable; the substantive general
     closure standards set forth at 25 Pa. Code 264.110-119
     are applicable to the closure of the incinerator unit;
     the waste pile design, operation and closure
     requirements set forth at 25 Pa. Code §§264.250-258 are
     applicable to the stockpile of excavated soil; the
     container management requirements at 25 Pa. Code
     §§264.171-180 and/or the tank standards at 25 Pa. Code
     §§264.190-199 are applicable to the on-site storage of
     wastewater dependent upon how the wastewaters are
     stored; the substantive closure and post-closure
     requirements set forth at 25 Pa. Code §264.110-119 are
     applicable to the closure of the units used to store
     wastewater unless the wastewater is stored on-site in
     accordance with 25 Pa. Code §262.34; the regulations
     set forth at 25 Pa. Code 263.10-263.32 are applicable
     when the wastewater is transported off-site; the
     provisions of RCRA 3004(o)(1)(B), 42 U.S.C.
     §6244(0)(1)(B), and the regulations thereunder, minimum
     technology requirements, apply to operation of the
     incinerator.

k.   DOT regulations 49 CFR Parts 107 (Hazardous Material
     Program Procedures) and 171.1-172.604 apply to
     Alternatives 3, 4, and 5 for the transport of hazardous
     materials.

1.   The land disposal restrictions as described in RCRA 40
     CFR Part 268 are applicable since the remedy involves
     the excavation and treatment of the soils and the re-
     placement of treated soils which were "hazardous
     wastes1* at the point of generation into a land disposal
     unit at the Site.  The untreated soils contain FOOi-
     F005 hazardous wastes and, therefore, the treated soils
     or residual ash must meet, at a minimum, the

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                                37

           concentration  levels  listed  in  40 CFR part  268.43.
           Because the  soil  clean-up  levels for some of  the
           chemicals  listed  in Table  l  are more stringent than the
           LDR levels,  the levels  listed in Table  1 shall be met
           prior  to placement.   For chemicals which do not have a
           calculated clean-up level  as described  in Table 1, the
           levels listed  in 40  CFR Part 268.43 shall  be met.
           Alternatives 4 and 5  are affected by this ARAR.

      m.    The provision  of  Section 121(a)(3) of CERCLA, 42 U.S.C.
           S962l(d)(3), apply to the  off-site disposal of any
           hazardous  substance under  Alternatives  3, 4,  and 5.

4.    To  Be Considered

      a.    The policies set  forth  in  PADER's "Groundwater
           Protection Strategy", February  1992, and the  MCLs, and
           risk-based drinking water  concentrations are  "to be
           considered"  (TBC)  in  developing soil clean-up levels.
           Soil clean-up  levels  were  developed using a combination
           of  the fate  and transport  mathematical  models, HELP and
           PRZH as well as a groundwater mixing zone model.  The
           groundwater  concentration  input data into this model
           was based  on MCLs and risk-based drinking water
           concentrations.   For  those chemicals without  an MCL or
           with a risk-based drinking water concentration greater
           that 10 pppb, a groundwater  concentration of  10 ppb was
           used.   Soil  clean-up  TBCs  are listed in Table 1.  These
           levels may be refined during the Remedial Design by
           incorporating  data generated during the
           hydrogeological study which  is  currently ongoing to
           ensure compliance with  MCLs  and risk-based  drinking
           water  concentrations.   Alternatives 2,  3, 4,  and 5 are
           affected by  this  TBC.

     b.    The policies set  forth  in  EPA's "Revised Procedures for
           Planning and Implementing  Off-Site Response Actions11,
           (November  13, 1987) is  a TBC for Alternatives 3, 4, and
           5.

C. Lona-Term  Effectiveness  and  Permanence

     Long-term effectiveness and  permamence refers to expected
residual risk and the  ability of  a remedy to maintain reliable
protection of human  health  and  the environment over time once
clean-up goals have  been met.

     Alternatives 2  through 5   require long-term  maintenance of a
vegetative soil  cover  or multi-layer cap.  Because Alternative 5
would require only a vegetative soil cover, only  routine mowing
would be required.   The cap installed  under Alternative 2 would
probably require the most maintenance  because it  would  be the

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                                38

 most  complex cap.   Not only would it require routine mowing but
 inspections  and, possibly repairs, to the cap would be necessary.
 In  addition,  monitoring of surrounding wells may be necessary to
 confirm that the cap  is operating effectively.  Although it is
 not known what  type of cap would be required for Alternatives 3
 and 4, it is anticipated that the cap installed under Alternative
 4 would be less complex than the cap for Alternative 3 and,
 therefore, may  require less maintenance.  Alternative 4 is
 expected to  require a less complex cap than alternative 3 because
 more  contaminants will be removed from the soil under Alternative
 4.  It is .possible  that only a vegetative soil cover would be
 required for Alternative 4.

      The direct contact risk will be eliminated under
 Alternatives 2  through 5 because a vegetative soil cover or
 multi-layer  cap will  be installed.  The risk associated with
 contaminant  migration to groundwater would be virtually
 eliminated under Alternative 5 because the contaminants would be
 destroyed.   If  the  cap was not installed or maintained properly,
 Alternative  2 would exhibit the highest risk of contaminant
 migration to groundwater because the contaminants would remain in
 the soil.  If operation and maintenance was not implemented
 properly, the risk  of contaminant migration to groundwater for
 Alternatives 3  would  be greater than that for Alternative 4
 because more contaminants are expected to remain in the
 subsurface under Alternative 3.

 D.  Reduction of toxicitv. mobility, or volume of the contaminants
 through treatment

     Reduction  of toxicity, mobility, or volume through treatment
 refers to the anticipated performance of the treatment
 technologies  a  remedy may employ.

     Alternatives 3,  4 and 5 are the only alternatives which
would result  in a reduction of the toxicity, mobility and volume
of  contaminants in  the soil through treatment.  Alternatives 3,
4,  and 5 would  reduce the level of VOCs in the soils.
Alternatives  4  and  5  would also reduce the levels of SVOCs in the
soil.  Alternative  3  may reduce the levels of SVOCs in the soil,
although the treatability study did not determine the
effectiveness of this reduction.  Alternative 5 destroys the
contaminants  in the immediate environment.   Because previous
studies have  confirmed that thermal desorption can remove site-
related VOCs  and SVOCs,  Alternative 4 is expected to be more
effective than  Alternative 3 in reducing the contaminants at the
Site.  Alternatives 3 and 4 would remove contaminants from the
immediate environment,  although disposal of the residual waste
 (i.e. spent carbon, pure product, wastewater, etc.) or
destruction of  the  extracted contaminants in a safe and effective
manner would  be required.  Alternative 2 would not reduce the
toxicity, mobility  or volume of the contaminants through

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                                39

 treatment.   Under Alternative  2,  the contaminants will remain in
 the  soil  and a  cap will  be  installed over the contamination.

 E. Short  Term Effectiveness

      Short term effectiveness  refers to the period of time needed
 to complete  the remedy and  any adverse impacts on human health
 and  the environment that may be posed during the construction and
 implementation  of the remedy until clean-up levels are achieved.

      Alternative 4 could be implemented within 25 months of the
 ROD.  This time frame includes a  6-month treatability study.
 Alternative  2 would take the shortest amount of time to implement
 (19  months).  Alternative 3 would take the longest time to
 implement because a 6 to 12 month treatability study would be
 required  prior  to remedy implementation and an SVE/BIO operation
 and  maintenance period of 3 years, or possibly more, is expected.
 Alternative  5 is expected to take 21 months to implement.

      Alternative 2 would be the alternative least likely to
 impact the community, workers  and the environment during
 construction and implementation because removal of hazardous
 substances would not occur.  The  short term risks associated with
 Alternatives 4  and 5 would  be  greater than Alternative 3 because
 these alternatives would involve  the excavation of soils.  If the
 excavation is implemented under controlled conditions and if
 worker safety procedures are properly adhered to, these risks
 would be  minimal.

 F. Implementability

      Implementability is the technical and adminstrative
 feasibility  of  a remedy, including the availability of materials
 and  services needed to implement  a particular option.

     Alternatives 3, 4 and  5 would require initial testing of the
 treatment system operation  and periodic sampling to ensure
 efficient operation of the  treatment system.

     Alternative 2 is the most easily implemented alternative
 because no treatment is  required.  The treatment technologies
used in Alternatives 4 and  5 are  well established and have.been
proven reliable at similar  sites.

     Although the soil vapor extraction portion of Alternative 3
has been proven at this  Site and  other Sites to remove
significant  quantities of VOCs, the heterogeneity of the soils at
this Site could limit its effectiveness.  "Tar-like", "spongy",
and  "latex"  layers have  been identified at various depths in the
former lagoons.  These layers  could limit air flow through the
soil.  If additional studies show that these layers do reduce the
effectiveness of the technology,  these layers may need to be

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                                40

 excavated and treated using a different technology,  such as
 thermal  desorption or incineration.   Due to time constraints on
 the treatability study,  bioremediation was not proven effective
 in the removal of SVOCs.   These  factors could delay  and increase
 the difficulty in implementation of the remedy.

      Services and materials are  readily available for all
 alternatives.
      Cost  includes  estimated  capital and operation and
 maintenance  costs as  well as  present worth costs.

      This  criteria  examines the capital, annual O&M, and present
 worth costs  for  each  alternative.  These costs are presented in
 the Description  of  Alternatives section, above.  The present
 worth cost for Alternative 4  is $7,300,000 to $9,000,000.  The
 range provided takes  into account the possibility of incineration
 of the tar-like  layer.   The lowest cost alternative is
 Alternative  2 at $800,000 to  $1,350,000. The range takes into
 account the  possibility of several types of caps.  The present
 worth cost estimate for Alternative 3 is $2,700,000 to
 $5,100,000.  The range  provided takes into account the
 possibility  of thermal  desorption or incineration of the tar-like
 layer.  The  costs for Alternative 3 are based on a 3-year pilot
 operation.   If an additional  two years is necessary for
 operation, the present  worth  costs would be increased to
 $3,100,000 to $5,500,000.   The highest cost is for Alternative 5
 at $19,500,000.

      Because the costs  generated are only estimates. (-30% to
 +50%) and  are dependent on the type of cap required and the
 effectiveness of the  technology used (which will be determined
 during the design phase),  the difference in costs between
 Alternative  4 and Alternative 3 may not be significant.

 F. State Acceptance

     The Commonwealth of Pennsylvania has evaluated and commented
 on the alternatives presented in this ROD and has initially
 agreed with  the  technical remedy selected.  The official position
 of the Commonwealth of  Pennsylvania will be documented in the
Adminstrative Record  for this Site upon receipt.

G. Community Acceptance

     Comments received  from the public are specifically addressed
 in the Responsiveness Summary which is attached to this ROD  in
Appendix A.

     Comments received  from some community members, including 15

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                                41

 homeowners near the William Dick  Lagoons Site and a local
 remediation contractor,  indicate  a preference for incineration.
 The 15 homeowners believe that only incineration can restore the
 the site to a condition  close to  its pre-disposal condition.  EPA
 believes that thermal desorption  provides acceptable protection
 of human health and the  environment without  the  additional cost
 required by incineration.

      One potentially responsible  party  (PRP)  indicated a
 preference for use of soil vapor  extraction/bioremediation in
 conjuction with thermal  desorption.   The PRP proposed excavating
 the soils to remove the  tar-like  materials.   The tar-like
 materials would be treated by thermal desorption and the
 excavated soils would be treated  above  ground by SVE/BIO.  The
 remaining contaminated soils in the subsurface would be treated
 in-situ by SVE/BIO.   Given the random locations  of the tar-like
 layers in the former lagoons,  EPA believes that  the technique
 used in this proposal may not indentify all  of the
 heterogeneities in the subsurface.   Therefore, this proposal may
 not adequately treat the soils so that  only  a vegetative  soil
 cover is required over the treated material.   In addition, this
 proposal may not treat the SVOCs  to levels which will not impact
 groundwater above MCLs or health  based  levels.   It is anticipated
 that this proposal will  require a more  complex cap (i.e., a
 multi-layer cap)  than a  vegatative soil cover.   Therefore, the
 site will not be returned to a condition close to its pre-
 disposal condition.

 IX.   Selected Remedy and Performance standards

      A.  General Description of the Selected  Remedy

      Based upon consideration of  the requirements of CERCLA, the
 detailed analysis of the alternatives using  the  nine criteria and
 public comments,  EPA has determined that Alternative 4 (Thermal
 Desorption with a Vegetative Soil Cover or Multi-layer Cap)  is
 the most appropriate remedy for the William  Dick Lagoons  Site.

      This remedy was selected to  reduce the  chemical
 concentrations in the soils so that leaching of  contaminants into
 the groundwater will be  minimized.   Reduction of the source of
 contamination in the soils is necessary so that  it does not
 continue to impact groundwater above MCLs or health based levels.
 The   soil  clean-up goals are listed in  Table 1 and were
 calculated based on  mathematical  models developed during  the
 Focused  Feasibility  Study.   This  alternative will also prevent
exposure to the site-related chemicals  through inhalation,
 ingestion,  and dermal contact through the installation of a
vegetative  soil cover or multi-layer cap over the treated soils.
Based on current  information,  Alternative 4  provides the  best
balance  among the alternatives with respect  to the nine criteria
EPA uses to evaluate each  alternative.

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                                42

      Under this  alternative, prior to remedy implementation, a
 minor amount  of  surface  soil sampling will be performed in the
 former lagoon berm borrow area  (Figure 2) to determine if a
 vegetative soil  cover  is appropriate in this area to limit direct
 contact with  soils.  Because only a limited number of surface
 soil samples  were  obtained during the RI from the former lagoon
 borrow area for  evaluation of the direct contact exposure
 scenario,  additional sampling is  required.  The remediation
 design work for  this alternative  will delineate those areas of
 the site requiring source control activities, specifically the
 former lagoon area, and  those areas requiring a vegetative soil
 cover.

      This  alternative  involves the excavation and treatment of
 approximately 24,000 cubic yards  of site soil via thermal
 desorption.   This  estimated volume was determined during the
 Focused Feasibility Study by assuming that the contaminated soi
 extends out to a distance halfway between each contaminated
 sample  location  and the  closest "clean" boring.  "Clean" borings
 are defined as those with chemical constituent levels below
 cleanup levels defined in Table 1.

      Because  of  the high levels of VOCs in the soils, excavation
 shall be performed under controlled conditions to reduce the
 risks to workers and nearby residents.  The risks associated with
 the excavation shall be  determined during the remedial design
 phase.   A  preliminary  risk assessment for the air emissions from
 excavation was performed by EPA's toxicologist.  Air emission
 rates were calculated  by personnel in EPA's Region III Air,
 Radiation,  and Toxics  Division.   The air emission model report
 and the  preliminary risk assessment are attached to this ROD in
 Appendix C.   Results from this preliminary risk assessment
 indicate that the  potential carcinogenic risk to a young child
 exposed  to air emissions of TCE for 90 days, which is the
 predicted  duration of  soil remediation, is 2.77E-06.  This is
 within the EPA's generally acceptable carcinogenic risk range of
 l.OE-06  to l.OE-04.  These values are preliminary and may be
 refined  during the remedial design,  if calculations performed
 during the remedial design indicate an unacceptable risk, than
 the risk will  b« mitigated. Possible options for mitigating the
 risks include  continued  operation of the SVE system until VOC
 levels arc reduced to  an levels which do not: pose a risk through
 inhalationfor  excavation, staging the excavation so that only a
 small amount of coil is  excavated at a time, excavating during
 the winter months  or containing the excavation process under a
 tent-type  enclosure.   In addition, appropriate air monitoring
will be performed  on-site to ensure that any excavation emissions
do not present a health  threat.

     Thermal desorption  generally consists of a rotary dryer
designed to accept contaminated soils which are then heated to a
sufficient temperature to volatilize the contaminants from the

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                                43

 soil into the air.   The rotary dryer rotates to allow for proper
 mixing and the contaminated air stream is  treated in a control
 system consisting of a fabric filter for particulate removal, a
 wet scrubber for acidic gas conversion,  and a carbon adsorption
 system for capture of the contaminants.  Excavation  of
 contaminated soil and replacement  of treated soil would be
 performed using conventional construction  equipment.   Soils would
 be stockpiled onsite before loading  into the rotary  dryer for
 treatment.

      Based on the nature of the operations leading to the
 generation of the waste materials  at the site,  EPA Region III has
 determined that the contaminated soil, prior to treatment,
 constitutes a hazardous waste bearing the  hazardous  waste
 identification numbers F001 through  F005 under State and Federal
 law.   EPA anticipates that following treatment,  the  soil will no
 longer "contain" hazardous wastes  and thus will cease to be a
 hazardous waste for purposes of Federal  law.   EPA also
 anticipates that for State law purposes, the levels  of
 contaminants in the soils will be  such that the soils may be
 "delisted"  and no longer considered  a State hazardous waste.
 (Any such "delisting" determination  will be made by  EPA in
 accordance  with the substantive requirements of 25 Pa.  Code
 Section 260.22,  and the applicable requirements of CERCLA and the
 National  Contingency Plan,  40 C.F.R.  Part  300.)   Nonetheless, the
 treated soils may still constitute "residual waste"  under
 Pennsylvania law,  and be subject to  the  substantive  requirements
 of  Pennsylvania's residual waste regulations to the  extent
 required  under 25 Pa.  Code Section 287.101(d).

     After  completion of the thermal desorption process, a
 vegetative  soil  cover or multi-layer cap will be placed on the
 site.   The  cap or cover will be designed to eliminate direct
 contact with the any contaminants  remaining in the soils.  The
 thermal desorption  system will be  designed to reduce the levels
 of  contaminants  in  the soil so that  infiltration of  rainwater
 through these soils will not leach contaminants into the
 groundwater above MCLs or health based levels,  as describe in
 Section II.   Soil levels which meet  these  criteria are listed in
 Table  1.  A final decision on the  type of  cover or cap will
 depend  on the success in achieving the soil remediation goals.
 The success in obtaining the soil  remediation goals  listed in
 Table  1 will  be  determined by performing a thermal desorption
 treatability study  during the remedial design.   The  soil clean-up
 levels may  need  to  be modified based on  the results  of the
 thermal desorption  treatability study.

     The soil  clean-up levels,  listed .in Table 1,  were developed
using a combination of the fate and  transport mathematical
models, HELP  and PRZM,  as well as  a  groundwater mixing zone
model.  Compounds which have been  identified in the  groundwater
were used in the model.   The groundwater concentration input data

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                                44

 into  this model was based on Maximum Contaminant Levels  ("MCLs")
 and health-based drinking water concentrations.  Health-based
 drinking water concentrations were established based on a
 carcinogenic risk of 10E-05 or 10E-04.  A cancer risk of 10E-05
 means that one additional person per 100,000 has a chance of
 contracting cancer given the relevant exposure scenario.  The NCP
 directs hazardous substance responses for Sites presenting risks
 outside the established acceptable carcinogenic risk range for
 Superfund Sites of between 10E-06 (l additional chance in one
 million) and 10E-04 (one additional chance in 10,000).  EPA used
 a carcinogenic risk of either 10E-04 or 10E-05 as the basis for
 the health-based drinking water concentrations for chemicals
 without an MCL at this Site rather than use the more conservative
 10E-06 carcinogenic risk values since the 10E-06 carcinogenic
 value for some compounds are below the contract required
 quantitation limit for the drinking water analytical technique,
 EPA Method 524.2.  The contract required quantitation limit is
 the detection level required for a particular analytical method
 under EPA's Contract Laboratory Program (CLP).  Use of either
 10E-04 or 10E-05 carcinogenic risk is protective of human health
 since it falls within the EPA's acceptable risk range of 10E-06
 to 10E-04.

      For those chemicals without an MCL or with a health-based
 drinking water concentration greater that 10 ppb, a groundwater
 concentration of 10 ppb was used.  The use of 10 ppb was based on
 the contract required quantitation limits as established under
 the Contract Laboratory Program (CLP) Statement of Work for
 Organics Analysis (CLP Document Number OLM01.1).  The 10 ppb
 level was established in the focused feasibility study by CLTL in
 an attempt to conform to PADER's groundwater protection strategy,
 which, although not an applicable or relevant and appropriate
 regulation for this ROD, is a "To Be Considered1* policy.  Soil
 clean-up levels calculated assuming that a vegetative soil cover
 would be placed over the Site after soil treatment are listed in
 Table 1.

     According to the model, some of the compounds listed in
 Table l will degrade prior to reaching the groundwater and,
 therefore, no soil clean-up level was provided.  However, if the
 contaminated soils are treated and placed back on-site, certain
 contaminants fi.e.. those compounds related to F001-F005 wastes)
which degrade before reaching the groundwater (as calculated by
 the model) nonetheless will have to meet the treatment standards
 established by the Land Disposal Restrictions (LDR) listed at 40
 CFR S268.43.  The LDR levels for the relevant compounds are
 listed in Table 1.  Finally, for the remaining compounds which
 are not F001-F005 wastes but do, according to the model, degrade
before reaching the groundwater, EPA believes that it is
appropriate to establish soil clean-up levels based on direct
contact risks.  These levels are also noted in Table  1.  The
groundwater concentrations used in the fate and transport models

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                                45

 to  calculate  the  soil  clean-up  levels are  listed  in Table  1 and
 are based  on  either MCLs,  health-based concentrations under a
 drinking water  exposure  scenario  or  10 ppb as described above.

      Some  of  the  soil  clean-up  levels that were calculated by the
 model exceeded  the concentrations for a direct contact risk.  The
 soil concentrations that need to  be  met so that the direct
 contact risk  is acceptable to EPA are provided in Table 2.
 Attainment of the direct contact  risk levels listed in this table
 are not required  for this  ROD,  because placement  of a vegetative
 soil cover or multi-layer  cap over the soils and  implementation
 of  institutional  controls  will  prevent exposure to the soils
 through direct  contact.  However, if the values listed in  Table 2
 can be met during remedy implementation, deed restrictions on the
 property may  be eliminated.

      If, during the thermal desorption treatability study, EPA
 determines that the soil clean-up levels listed in Table 1 are
 not achievable, a multi-layer cap will be  designed to limit the
 amount of  rainwater and  surface water infiltration through the
 contamination remaining  in the  soils so that the  leaching  of
 contaminants  from the  soil to the groundwater is  reduced to MCLs
 or  health  based levels.  A multi-layer cap is defined in this ROD
 as  an upper vegetative layer (topsoil) underlain  by a drainage
 layer (sand)  over a low  permeability layer (i.e.  natural soils,
 admixed soils,  a  synthetic liner, or any combination of these
 materials). The final  cap  design  will be determined during the
 remedial design.  Because  a cover or cap will be  installed under
 the  Selected  Remedy, long  term  monitoring  and maintenence  for the
 operation  and maintenence  of the  cover or  cap will be required.

      In addition, the  treatability study to be performed during
 the  remedial  design will determine if the  heterogeneities  in the
 soil  (i.e.. the tar-like,  fibrous, sticky, latex  materials, etc.)
 requires additional treatment to  meet the  soil clean-up goals.

      Depending  on the  soil clean-up  level  that is achieved at the
 Site,  institutional controls, in  the form  of deed restrictions,
may need to be  implemented under  so  that access to the property
 is limited.   The  integrity of the cap or vegetative soil cover
must  be maintained to  ensure adequate protection  against direct
contact with  the  soils and infiltration of surface and rain
water.

B. Performance  Standards

Determination of  Extent  of Soil Contamination:  Prior to the
design of the thermal  desorption  unit, additional soil sampling
shall be performed in  the  former  lagoon berm area, as well as the
former lagoon area, to define the extent of soil  contamination.
Soil contamination shall be defined  as levels of  contamination
which exceed  the  levels  listed  in Table 1.   The  number,

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                                46

 location,   and depth of these sampling points shall be subject to
 approval by EPA.

 Excavation  and Operation of the Thermal Oesorption Unit:  All
 soils containing chemicals above the concentrations listed in
 Table l shall be excavated, stockpiled, and remediated on-site by
 a  thermal desorption treatment system.  The soils shall be
 remediated  to the concentration levels listed in Table 1.  These
 levels may  be refined during the Remedial Design by incorporating
 data generated during the hydrogeological study which is
 currently ongoing to ensure compliance with MCLs and health-based
 drinking water concentrations.

 The thermal desorption unit shall comply with the regulations
 outlined in 40 CFR $264, Subpart X- Miscellaneous Units and the
 provisions  of RCRA 3004(o) (42 U.S.C. S6244(o).  The design,
 operation and closure and post-closure of the waste piles
 generated during the stockpiling of excavated soil shall comply
 with the substantive regulations set forth in 25 Pa. Code
 §§264.250-258, 25 Pa. Code §§264.110-119 and 25 Pa. Code
 §264.310.   If off-site incineration of the tar-like material is
 necessary,  such material shall be transported to and managed at
 an incinerator which satisfies applicable federal and state
 requirements for incinerators.  The operation and closure of the
 thermal desorption unit shall comply with the substantive
 requirements of 25 Pa. Code 265.373, .375, .377, and .381 (to the
 extent that such requirements are more stringent than those
 imposed by  40 CRF Part 264, Supart X).

     Prior  to excavation, a risk assessment shall be performed to
 determine the risk associated with air emissions from the
 excavation  process.  Emissions from the excavation process shall
 not exceed  a carcinogenic risk of 1 x 10~4.   If this level is
 exceeded, emission control measures shall be implemented to
 reduce emissions below this level.  The emission control measures
 shall be subject to approval by EPA.  In addition, an EPA-
 approved air monitoring program for the excavation of soils shall
be established prior to remedial action.

Treatment of Air Emissions from the Thermal Desorption Unit:
contaminants in the effluent air from the thermal desorption unit
shall be removed with a treatment unit, the specifications of
which shall be determined during the remedial design and subject
to EPA and FADER approval.  The treatment unit(s) shall comply
with the following ARARs which are performance standards: the
Resource Conservation and Recovery Act (RCRA) regulations 40 CFR
Part 264 Subpart AA- Air Emission Standards for Process Vents;
the special permit requirements for sources locating in or
siginificantly impacting nonattainment areas set forth at Pa.
Code §127.61-73; the National Ambient Air Quality Standards
 (NAAQS)  under the Clean Air Act (40 CFR SS 50.1-3, 50.9, Appendix
D,  and Appendix H); 40 CFR Part 61, Subpart F and Subpart J which

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                                47

 are requirements which regulate vinyl  chloride  and  benzene
 emissions under the Clean Air Act,  Section  112,  42  U.S.C. §7412
 and are known as National Emission  Standards  for Hazardous Air
 Pollutants (NESHAPs);  the requirement  in  25 PA  Code S127.12(a)(5)
 that air emission be reduced to the minimum obtainable levels
 through the use of best available technology  (BAT),  as defined in
 25  PA Code Section 121.1; 25 PA Code 5123.1,  which  prohibits the
 emission of fugitive air contaminants  and regulates emissions
 during construction activities; 25  PA  Code  $123.2,  which
 prohibits the emission of fugitive  air contaminants from crossing
 the facility's property line;  25 PA Code  5123.31, which prohibits
 the emission of malodorous air contaminants from crossing the
 property line; 25 PA Code 5123.41,  which  prohibits  the emission
 of  visible emissions of greater that 20%  opacity.

 Management and Disposal of Treatment Residuals:  The management
 and ultimate disposal  of the treatment residuals shall be
 determined,  subject to EPA approval, during the  remedial design.
 Such management may entail treatment and/or disposal of carbon
 filters or contaminated water.   In  the event  the treatment
 residuals are a hazardous waste, as determined by EPA, the
 following ARARS will apply as  the Performance Standards.  The on-
 site storage of wastewater shall comply with  the container
 management regulations set forth in 25 Pa.  Code  55264.171-180 or
 the tank standards at  25 Pa.  Code 55264.190-199, dependent on how
 the wastewater is stored.   The closure and  post-closure of the
 waste water  storage units shall comply with the  requirements set
 forth at 25  Pa.  Code 5264.110-119 unless  the  wastewater is stored
 on-site in accordance  with 25  Pa. Code 5262.34.  The
 transportation of wastewater off-site  shall comply  with the
 requirements of 25 Pa.  Code 5263.10-32.   The  container storage of
 contaminants collected by the  air emissions control system shall
 comply with  25 Pa.  Code SS264.171.180  and 25  Pa. Code SS264.110-
 119  unless the containers are  stored on-site  in  accordance with
 25  Pa.  Code  S262.34.   The off-site  transporation of the air
 emission control devices shall comply  with  25 Pa. Code 5263.10-
 32.    The transport of hazardous materials  shall comply with DOT
 regulations  49 CFR Parts 107  (Hazardous Program  Procedures) and
 171.1-172.604.   The generation of hazardous waste on-site and the
 transporation of hazardous waste shall comply with  25 Pa. Code
 §262.11  (a)  and (b), §262.20,  and 5262.30-33.

 Backfilling  of Treated Soils and Placement  of a  Vegetative Soil
 cover  or  Multi-layer caps   The treated soils  shall  be backfilled
 into excavated areas.   The backfilling of treated soils shall
 comply with  the Land Disposal  Restriction regulations as
 described in 40 CFR Part 268.   The  untreated  soils  contain
 "hazardous wastes"  in  the F001-F005 category  at  the point of
 generation and,  therefore,  the treated soils  must meet, at a
minimum,  the concentration levels listed  in 40 CFR  Part 268.43.
 Because the  soil clean-up levels for some of  the chemicals listed
 in Table  1 are more stringent  than  the LDR  levels,  the levels

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                                48

 listed  in Table  1  shall be met prior to placement.  For chemicals
 which do not have  a calculated clean-up level as described in
 Table l, the levels listed in under the F001-F005 category in 40
 CFR Part 268.43  shall be met.

     Once the treated soils are placed on-site, a protective,
 vegetative  soil  cover will be placed over the backfilled area if
 the treatment levels in Table 1 are attained by the thermal
 desorption  treatment.  The vegetative soil cover shall: (1)
 provide dermal protection from the treated soils; (2)  support the
 germination and  propagation of vegetation; and (3) compact well
 and not crack excessively when dry.  EPA anticipates that
 following treatment, the soil will no longer "contain" hazardous
 wastes  and  thus  will cease to be a hazardous waste for purposes
 of  Federal  law.  EPA also anticipates that for State law
 purposes, the levels of contaminants in the soils will be such
 that the soils may be "delisted" and no longer considered a State
 hazardous waste.   (Any such "delisting" determination will be
 made by EPA in accordance with the substantive requirements of 25
 Pa.  Code Section 260.22, and the applicable requirements of
 CERCLA  and  the National Contingency Plan, 40 C.F.R. Part 300.)
 Nonetheless, the treated soils may still constitute "residual
 waste"  under Pennsylvania law, and be subject to the substantive
 requirements of  Pennsylvania's residual waste regulations to the
 extent  required  under 25 Pa. Code Section 287.101(d).

     If, during  the design of the thermal desorption unit, it is
 determined  that  the technology can not meet the soil clean-up
 levels  outlined  in Table 1, technology-based criteria shall be
 determined  by EPA.  Using the technology-based criteria as the
 treatment standards for the thermal desorption unit and the
 mathematical models developed in the Focused Feasibility Study, a
 suitable cap will  be designed to reduce the leaching of
 contaminants into  the groundwater to MCLs or health-based levels.
 The permeability of the cap will be determined with the model
 used to determine  soil clean-up levels in the Focused Feasibility
 Study (and  subsequent revisions) prepared for this Site.

     The vegetative soil cover or multi-layer cap shall be
maintained  for 30  years.  The vegetative soil cover or multi-
 layer cap design shall include a cost/benefit analysis for
maximizing  the biodiversity of the cover or cap.  This analysis
shall compare the  capital and operation and maintenance costs of
a conventional cap or cover (i.e. grass or similar vegetation) to
the costs associated with a cap or cover which promotes
biodiversiy on the site.  This evaluation shall be used to allow
 EPA to determine the vegetation on the soil cover or cap.

operation and Maintenance ("OUT*):  The vegetative soil cover or
multi-layer cap  shall be given routine maintenance for at  least
30 years to maintain the integrity and effectiveness of the  final
cover or cap, including making repairs to the cover or cap as

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                                49

 necessary  to  correct  cracks  and the effects  of  settling,
 subsidence, erosion,  etc.  Natural  vegetation (grasses and weeds)
 shall  be maintained on  the cover or cap.   An O&M plan shall be
 developed, based  on the type of cover or cap selected by EPA, and
 implemented.   Because the  selected alternative  shall result in
 contaminants  remaining  on-site, 5-year Site  reviews under Section
 121(c)  of  CERCLA  will be required.

 Institutional Controls:  If  the soil clean-up levels listed in
 Table  2 are not achieved,  deed restrictions  shall be placed on
 the  deed to the portion of the property that comprises the
 excavated  and capped  area.   This is required to limit the use of
 this land  and prevent excavation or construction on the capped
 and  closed former lagoon area and  any other  area on-site which
 requires soil treatment or a cap so that threats to human health
 and  the environment are minimized.

 Worker Safety:  During  all Site work, Occupational Safety and
 Health Administration ("OSHA") standards set forth at 29 C.F.R.
 Parts  1910, 1926  and  1904  governing worker safety during
 hazardous  waste operations,  shall  be complied with.

 X.   Statutory Determinations

     EPA's primary responsibility  at Superfund  sites is to select
 remedial actions  that are  protective of human health and the
 environment.   Section 121  of CERCLA also requires that the
 selected remedial action comply with ARARs,  be  cost-effective,
 and  utilize permanent treatment technologies to the maximum
 extent  practicable.   The following section discuss how the
 selected remedyfor the  William Dick Lagoons  Site meets these
 statutory  requirements.

 A.   Protection of Human Health and the Environment

     The Selected Remedy protects  human health  and the
 environment by reducing the  level  of contaminants in the soils at
 the  Site which, in turn, reduces the leaching of contaminants
 into the groundwater  beneath the Site.  By reducing the source of
 contamination to  the  groundwater,  a groundwater remediation
 system  can be designed  and installed to reduce  the level of
 contaminants  in groundwater  to background levels or, if
 background levels are unattainable, to the maximum contaminant
 levels  (MCLs)  established  under the Safe Drinking Water Act
 (SWDA).

     Installation of  a vegetative  soil cover or multi-layer cap
over the treated  soil will prevent exposure  to  the site-related
 chemicals through inhalation, ingestion, and dermal contact.

     Implementation of the selected remedy will not pose
unacceptable  short-term risks or cross-media impacts.  The

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                                50

 remedial  technologies employed  in  the  selected  remedy are proved
 to  reduce the concentrations  of the organic  compounds identified
 on-site to acceptable levels.

 B.    Compliance with Applicable or Relevant  and Appropriate
      Requirements  (ARARS)

 Chemical  Specific  ARARs

      a.    The Resource Conservation and Recovery Act (RCRA)
        •   regulations 40 CFR  Part  264  Subpart AA- Air Emission
           Standards  for Process Vents  is relevant and appropriate
           for the  selected alternative because  the SVE, thermal
           desorption and incinertion have a  stack vented to
           atmosphere.  The total organic emissions from all
           affected process vents at the Site are required to be
           below 1.4  kg/hr and 2800 kg/hr or  reduce, by use of a
           control  device total  organic emissions from all
           affected process vents at the facility by 95 weight
           percent  under this  regulation.

      b.    The emissions from  the treatment system must comply
           with the special permit  requirements  for sources
           locating in or siginificantly impacting nonattainment
           areas set  forth at  Pa. Code  $127.61-73.

      b.    The emissions from  the treatment system must comply
           with the National Ambient Air Quality Standards (NAAQS)
           under the  Clean Air Act  (40  CFR SS 50.1-3, 50.9,
           Appendix D,  and Appendix H).  This regulation, which
           deals with the release of volatile organic emissions,
           applies  to this action because the site lies in an
           ozone non-attainment  area.

     c.    40  CFR Part 61, Subpart  F and Subpart J are relavant
           and appropriate requirements which regulate vinyl
           chloride and benzene  emissions under  the Clean Air. Act,
           Section  112, 42 U.S.C. S7412 and are  known as National
           Emission Standards  for Hazardous Air  Pollutants
           (NESHAPs).

2. Location Specific AJUtR*:  There are no location specific ARARs
for this Operable  Unit at the Site.

3. Action  Specifie ARARs:

     a.    The requirement in  25 PA Code S127.12(a)(5) that air
           emission be reduced to the minimum obtainable levels
           through  the use of  best  available  technology  (BAT), as
           defined  in 25 PA Code Section 121.1,  will apply to  the
           seltected  alternative.

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                           51

 b.    25  PA Code §123.1,  which prohibits  the emission of
      fugitive air  contaminants and  regulates emissions
      during construction activities,  is  applicable to  the
      selected alternative.

 c.    25  PA Code §123.2,  which prohibits  the emission of
      fugitive air  contaminants from crossing the facility's
      property line,  is applicable to  the selected
      alternative.

 d. .   25  PA Code §123.31,  which prohibits the emission of
      malodorous air  contaminants from crossing the property
      line,  is applicable to the selected alternative.

 e.    25  PA Code §123.41,  which prohibits the emission of
      visible emissions of greater that 20% opacity, is
      applicable to the selected alternative.

 f.    RCRA  regulations 25 Pa.  Code §262.11  (a) and (b)  (this
      section establishes standards  for generators of
      hazardous waste and relates to hazardous waste
      determination), §262.20  (relating to manifesting
      requirements  for off-site shipments of spent carbon or
      other hazardous wastes),  and §262.30-.34 (relating to
      pretransport  requirements) are applicable to the
      selected alternative.

 g.    To  the extent that  the treated soils constitute
      hazardous wastes, the requirements  of 25 Pa. Code
      Sections 264.13-15  (General Facility Standards);
      264.31,  37 (PPC Plan and Emergency  Procedures); 264.90,
      .91,  .97,  and .98-.100 (Groundwater Monitoring);
      264.111,  .114,  and  .117-.119   (Closure and
      Postclosure); and 264.301, .302, .303, .305, .309, and
      .310  (Landfills) and regulations at 40 CFR Part 264,
      Subpart N which implement the  minimum technological
      requirements  for replacement of  an  existing landfill or
      surface impoundment unit set forth  at 42 U.S.C.
      §6924(o)  would  be applicable to  the design,
      construction  and maintenance of  the area into which the
      treated soils or residual ash  are deposited.  To the
      extent that the treated  soils  or residual ash are not
      hazardous wastes due to  delisting,  the management of
      those  .wastes  may be subject to the  substantive
      requirements  of Pennsylvania's residual waste
      regulations to  the  extent required  under 25 Pa. Code
      Section 287.101(d).

h.    The container storage standards  set forth at 25 Pa.
      Code §§264.171-180  and the substantive closure
      requirements  set forth at 25 Pa. Code §§264.110-119 are
      applicable to the container storage of contaminants

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                           52

     collected  by  the air emissions controls unless they are
     stored on-site  in accordance with 25 Pa. Code §262.34;
     the regulation  set forth at 25 Pa. Code §263.10-263.32
     are applicable  when the air emission controls are
     transported off-site; 40 CFR §264, Subpart X, is
     applicable to the operation, closure and post-closure
     care of the thermal desorption unit; the waste pile
     design, operation and closure requirements set forth at
     25 Pa. Code §$264.250-258 are applicable to the
     stockpile  of  excavated soil; the substantive closure
   •  and post-closure requirements set forth at 25 Pa. Code
     §§264.110-119 and 25 Pa. Code §264.310 are applicable
     to the stockpile of excavated soil; the container
     management requirements at 25 Pa. Code §§264.171-180 or
     the tank standards at 25 Pa. Code §§264.190-199 are
     applicable to the on-site storage of wastewater
     dependent  upon  how the wastewaters are stored; the
     substantive closure and post-closure requirements set
     forth at 25 Pa. Code §264.110-119 are applicable to the
     closure of the  units used to store wastewater unless
     the wastewater  is stored on-site in accordance with 25
     Pa. Code §262.34; the regulations set forth at 25 Pa.
     Code 263.10-263.32 are applicable when the wastewater
     is transported  off-site; the substantive standards of
     25 Pa. Code §262 relating to generators of hazardous
     waste apply ot  the tar-like material and the container
     or tank storage standards set forth at 25 Pa. Code
     §264.171-180  and/or §264.190-.199 for storage of the
     tar-like material prior to transport for off-site
     incineration  are applicable; the substantive
     requirements  of 25 Pa. Code 265.373, 375, .377, and
     .381 are relevant and appropriate to the operation and
     closure of the  thermal desorption unit (to the extent
     that such  requirements are more stringent than those
     imposed by 40 CFR Part 264, Subpart X).

i.   DOT regulations 49 CFR Parts 107 (Hazardous Material
     Program Procedures) and 171.1-172.604 apply to the
     selected alternative for the transport of hazardous
     materials.

j.   The land disposal restrictions as described in 40 CFR
     Part 268 are  applicable since the remedy involves the
     excavation and  treatment of the soils and the placement
     of the treated  soils back onto the Site.  The untreated
     soils contain F001-F005 RCRA wastes and, therefore,
     must meet, at a minimum, the concentration levels
     listed in  40  CFR Part 268.43.  Because the soil clean-
     up levels  for some of the chemicals listed in Table 1
     are more stringent than the LOR levels, the levels
     listed in Table l shall be met prior to placement.  For
     chemicals which do not have a calculated clean-up level

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                                53

           as described in Table 1,  the levels listed  in 40 CFR
           Part 268.43 shall be met.

      k.    The provisions of Section 121(a)(3)  of CERCLA (42
           U.S.C.  §9621 (d)(3))  apply to the off-site disposal of
           any hazardous substance under the selected alternative.

 4.    To  Be Considered

      a.    The policies set forth  in FADER's "Groundwater
        .  Protection Strategy", February 1992,  and the  MCLs, and
    •'      risk-based drinking water concentrations are  "to  be
           considered" (TBC)  in developing soil clean-up levels.
           Soil clean-up levels were developed using  a combination
           of the  fate and transport mathematical models,  HELP and
           PRZM as well as a groundwater mixing zone  model.   The
           groundwater concentration input data into  this model
           was based  on MCLs and risk-based  drinking  water
           concentrations.   For those chemicals without  an MCL or
           with a  risk-based drinking water  concentration greater
           that 10 pppb,  a groundwater concentration  of  10 ppb was
           used.   Soil clean-up TBCs  are listed in Table l.   These
           levels  may be refined during the  Remedial  Design  by
           incorporating  data generated during the
           hydrogeological study which is currently ongoing  to
           ensure  compliance with  MCLs and risk-based drinking
           water concentrations.


      b.    The policies set forth  in EPA's "Revised Procedures for
           Planning and Implementing Off-Site Response Actions",
           (November  13,  1987)  is  a TBC for  the selected
           alternative.

c. cost-effectiveness

     The selected remedy is  cost-effective  in providing overall
protection in proportion to  cost, and meets all other
requirements  of CERCLA.  The NCP, 40 CFR Section
300.340(f)(ii)(D), requires  EPA to  evaluate cost-effectiveness by
comparing  all the alternatives  which meet the threshold
criteria - protection of human  health and the environment and
compliance with ARARs -  against three additional balancing
criteria:  long-term  effectiveness and permanence; reduction of
toxicity,  mobility,  or volume through treatment; and short-term
effectiveness.  The  selected remedy  meets these criteria and
provides for  overall effectiveness  in proportion to  its cost.
The estimated present worth  cost  for the selected remedy is
$7,800,000-$9,000,000.   The  range of costs  accounts  for possible
added treatment for  the  tar-like  material and possible  need for a
more complex  cap  (i.e. a multi-layer cap) once treatment is
complete.  The type  of cap and  need  for additional treatment will

-------
                                54

 be  determined during remedial design.

 D.  Utilization  of  Permanent Solutions and Alternative Treatment
 Technologies or Resource Recovery Technologies to the Maximum
 Extent Practicable

      EPA has determined that the selected remedy represents the
 maximum extent  to  which permanent solutions and treatment
 technologies can be utilized while providing the best balance
 among the other evaluation criteria.  Of those alternatives
 evaluated that  are protective of human health and the environment
 and meet ARARs, the selected remedy provides the best balance of
 tradeoffs in terms of  long-term and short-term effectiveness and
 permanence, cost,  implementability, reduction in toxicity,
 mobility and volume through treatment, State and community
 acceptance, and preference for treatment as a principal element.

      Under the  selected remedy, thermal desorption of the soils
 will  provide a  greater degree of reduction of toxicity, mobility,
 and volume than soley  capping the contaminanted soils or using
 soil  vapor extraction  and bioremediation.  Thermal desorption
 will  provide similar long-term effectiveness and implementability
 to  incineration, while reducing the toxicity, mobility and volume
 through treatment  to acceptable levels, at a significant cost
 reduction.  The State  is supportive of the selected remedy.

      Some members  of the community requested that incineration be
 used  at the site to restore the site to conditions as close to
 the pre-disposal conditions as possible.  EPA believes that
 thermal desorption will reduce the risk associated with the soils
 on  Site at an acceptable cost and that the added cost of
 incineration does  not  provide any additional protection benefits.
 In  designing the thermal desorption system, EPA will attempt to
 reduce the levels  in the soils to levels which would require only
 a vegetative soil  cover, therefore, returning the site to
 conditions as close to the pre-disposal conditions as possible.

 E.  Preference for  Treatment as a Principle Element

     The selected  remedy employs a treatment process which has
 been demonstrated  to effectively reduce VOC and SVOC
 contamination at other Superfund sites.  Therefore/ the statutory
 preference for  remedies that employ treatment as a principal
 element is satisfied.

 XX.  Documentation of  Significant Changes

     The Proposed  Plan for OU 3 for the William Dick Lagoons Sie
was released for public comment in January 1993.  The Proposed
Plan identified Alternative 4 as the preferred alternative.  EPA
reviewed all written and oral comments submitted during the
comment period.  Upon  review of these comments, it determined

-------
                                55

 that the soil cleanup levels,  as  described in the Focused
 Feasibility Study,  needed to be modified to conform with the
 health-based drinking water concentrations,  Land Disposal
 Restrictions, and direct contact  risks.

      As described in Section II.  of  this ROD,  preliminary soil
 cleanup goals were  based on a  mathematical model which calculated
 soil levels using specified groundwater  concentrations.  Although
 the  PRP performing  the focused feasibility study (FFS) did modify
 the  soil cleanup levels to conform with  existing MCLs, as
 required by EPA,  the PRPs did  not modify the soil cleanup levels
 to conform with health-based drinking water concentrations for
 compounds without MCLs or for  compounds  with health-based
 drinking water concentrations  less than  10 ppb,  as required by
 EPA.

      EPA believes the model should incorporate health-based
 drinking water standards for compounds with health-based drinking
 water levels greater tha 10 ppb.  Therefore,  the soil clean-up
 levels were modified by EPA using health-based drinking water
 concentrations.   Health-based  drinking water concentrations were
 established based on a carcinogenic  risk of 10E-05 or 10E-04.  A
 cancer risk of 10E-05 means that  one additional  person per
 100,000 has a chance of contracting  cancer given the relevant
 exposure scenario.   The NCP directs  hazardous substance responses
 for  Sites presenting risks outside the established acceptable
 carcinogenic risk range for Superfund Sites of between 10E-06 (1
 additional chance in one million) and 10E-04 (one additional
 chance in 10,000).   EPA used a carcinogenic risk of either 10E-04
 or 10E-05 as the  basis for the health-based drinking water
 concentrations for  chemicals without an  MCL at this Site rather
 than  use the more conservative 10E-06 carcinogenic risk values
 since the 10E-06  carcinogenic  value  for  some compounds are below
 the contract required quantitation limit for the drinking water
 analytical technique,  EPA Method  524.2.   The contract required
 quantitation limit  is the detection  level required for a
 particular analytical method under EPA's Contract Laboratory
 Program (CLP).  Use of either  10E-04 or  10E-05 carcinogenic risk
 is protective of  human health  since  it falls within the EPA's
 acceptable risk range of 10E-06 to 10E-04.   (The 10 ppb level was
 established during  the FFS by  the PRP in an attempt to conform to
 PADER's groundwater protection strategy,  which,  although not an
 applicable or relevant and appropriate regulation for this ROD,
 is a  "To Be Considered"  policy.)

      In addition, EPA modified the cleanup criteria for some
 compounds  because of requirements under  the Land Disposal
Restrictions (LDRs).   According to the model,  some of the
compounds  listed  in Table 1 will  degrade prior to reaching the
groundwater and,  therefore,  no soil  clean-up level was provided.
However,  if the contaminated soils are treated and placed back
on-site,  certain  contaminants  (i.e.  those compounds related to

-------
                                56

F001-F005 wastes) which degrade before reaching the groundwater
(as calculated by the model) will have to meet the treatment
standards established by the LOR listed at 40 CFR §268.43.  The
LOR levels for the relevant compounds are listed in Table 1.
Finally, for the remaining compounds which are not F001-F005
wastes but do, according to the model, degrade before reaching
the groundwater, EPA believes that it is appropriate to establish
soil clean-up levels based on direct contact risks.  These levels
are also noted in Table 1.  The groundwater concentrations used
in the fate and transport models to calculate the soil clean-up
levels are.listed in Table 1 and are based on either MCLs,
health-based concentrations under a drinking water exposure
scenario or 10 ppb as described above.

-------
WILLIAM DICK LAGOONS
 RECORD OP DECISION

TABLES  1 through  12

-------
                  TABLE l:   SOIL CLBAH-tTP LEVELS
                (Based on a vegetative Soil Cover)
Chemical
Soil Cleanup
Groundvater
concentration

Volatile Organic*
benzene*
butanone (MEK)
chlorobenzene
chloroform
1-2 , dichloroethane
1-2, dichloroethene (total)
1-2 , dichloropropane
ethylbenzene
4-methyl-2-pentanone (MIBK)
styrene
tetrachloroethane (PCE)
toluene
1,1, 1-trichloroethane
trichlorethene
xylene (total)
methylene chloride
Smivolatile Oronnlos
acenaphthenne
anthracene
benzo (a) anthracene
Levels
(mo/kg)

3.7*
362(NC)1
5.72(NC)1
2803(NC)1
0.047
0.36
0.17
1.7
0.064
3.7
1.2
282(NC)1
1
0.42
28* (NC)1
33*
31
94
920
used in
Model (ppbl

5
-
-
-
5
10
5
10
10
10
5
-
10
5
-
10
10
1.0

-------
 benzo(b)floranthene
 benzo(k)floranthene
 benzo(a)pyrene (BaP)
 benzo(g,h,i)perylene
 benzole acid
 bis(2-chloroethyl)ether(BCEE)
 bis(2-ethylhexyl(phthalate(DEHP)
 4-chloro-3-methylphenol
 chrysene
 disbenz(a,h)anthracene
 1,2-dichlorobenzene
 1,4-dichlorobenzene
 4,4-DDE
 2,4-dichlorophenol
 diethyl phthalate
 2,4-dimethyIphenol
 fluoranthene
 fluorene
 indeno(1,2,3-c,d)pyren*
 isophoron*
 2-methylnaphthalene
 2-methylphenol(o-cresol)
 4-methylphenol(p-cresol)
napnthalene
nitrobenzene
740
740
7300
6050
3 10, 000s (NC)1
0.01
266
5.2
390
6600
6.2*
11
7250
230s (KC)1
0.95
0.82
250
49
4400
0.68
57s (NC)1
5.62(NC)1
3.22(HC)1
3100S(MC)1
14*
2.0*
2.0*
2.04
5.54
-
1.2s
4
10
3
3
10
10
2.5*
-
10
10
10
10
4
10
-
-
-
-
-

-------
phenanthrene

phenol

pyrene

1,2-4-trichlorobenzene
94


470003(HC)1

250

 61
10




10

10
1  (NC)  Soil Clean up value not calculated by model; according to
   model compound degrades before reaching groundvater.

2  Soil  Clean up value based on Land Disposal Restrictions for
   F001-F005 wastes in mg/L  (40 CFR 268.43).

3  Soil  clean up value based on either 1 x 10"* cancer risk or a
   hazard quotient » 1 under a residential direct contact
   exposure scenario.

*  Groundvater concentration based on a 1 x 10"5 cancer risk for a
   drinking water exposure scenario.

5  Ground water concentration based on a 1 x 10*4 cancer risk for
   a drinking water exposure scenario.

-------
                             Table 2
                       CONTACT RISK CONCENTRATIONS
Volatile oraaniea

benzene
2-butanone  (MEK)
chlorobenzene
chloroform
1-2, dichloroethane
1-2, dichloroethene  (total)
1-2 , dichloropropane
ethylbenzene
4-methyl-2-pentanone  (KIBK)
styrene
t et r achl or oe thane  ( PCE )
toluene
1,1, 1-trichloroethane
trichloroethene  (TCE)
xylene (total)
Direct contact
acenaphthene
anthracene
benzo (a) anthracene
benzo (b) f loranthene
benzo (k) f loranthene
    Residential

      59
      3900
      1600
      280
      19
      700
      25
      7800
      3900
      57
      33
      16000
      7000
      150
      160,000
      4700
      23000
      1.6
      1.9
      4.4

-------
 benzo(a)pyrene(BaP)
 benzo(g,h,i)perylene
 benzole acid
 bis(2-chloroethyl)ether  (BCEE)
 bis(2-ethylhexyl)phthalate(DEHP)
 4- chloro-3-nethylphenol
 chrysene
 dibenz(a,h)anthracene
 1,2-dichlorobenzene
 1,4-dichlorobenzene
 4,4-DDE
 2,4-dichlorophenol
 diethyl phthalate
 2,4-dimethylphenol
 fluoranthene
 fluorene
 indeno(1,2,3-c,d)pyrene
 isophorone
 2-methyInaphthalene
 2-methylphenol(o-creaol)
 4-methylphenol(p-creaol)
naphthalene
phenanthrene
phenol
pyrene
1,2-4-trichlorobenzene
0.23
11
310,000
1.5
120
0.21
7000
71
5
230
63000
1600
3100
3100
0.84
1800

3900
390
3100
2300
47000
2300
780

-------
                                           TAIL!   3
                                     GflOUNO WATl» QUALITY
                                   WILLIAM DICK LAGOONS StTI
                              Maximum      Avtrag*        Av«rag«        Frequency
                                           Ma«tmum*     Caneantfitlan   of
 VOLAT1LU

 m«tftyi«n« cftlene*                36            36             3             i of ••
 •eaten*                          960          *80             39            A of -3
 careen duulfid*                   32J          17j             4             s of • 3
 i.2-dicnioro*tn«ne. (total)          210          ' 53J            20            3 of -3
 entereform                       560          «87             39            3 of -3
 1 2-dien»ero«man«                120          102J            M            3 of "3
 2-outanona                       350  '        207             '«   .         3 ot "3
 '.2-4ieniorooropan«                *7j  .         9J             «!            1 of'3
 tnemoreatnan*                 16.000        '4.300          '200           9 of'3
 o*nz*n«                          '80          170J            14            3 of 13
 4.m«inyi.2-0«manone             220          1QSJ            13            3 of 13
 tatraemorootnon*            '     320          2SOJ            19            2 of 13
 toiuana                          510          430             35            3 of 13
 enioroe«ftzon«                     32J          19J             2            2 of 13

 total iyi«*i»a                      160          127J            12            3 of ?3

 SIMIVOLATILIS

 0n*nol                         14.000        10.300          818           3 of '3
 oia  (2-cntoreamyi) •tnar           24            17             2            2 of 13
 2-cmoropnanoi                    41            14             1             i of 13
 Danzyf  aieonoi                     19            17             i             1 of 13
 2-matnyipnanoi                   300          217J            il            2 of i3
 4.m«tfiylpfi«nel           21            7             
-------
                            UGOON AMD BEflM AAEASOH. OUAUTY
                                        OICX LAGOONS SITE
                                   Avaraga      Maiimum    Fraquancy  of
    i . i -dicnioroatnana
    l.2-tficnioroatnan«. (total)
    cmoroform
    i.2-dicfiieroatr»ana
    2-outanotrieliloropli«nol
2-cftioronapfltftalana
137
3.120
« «A
1 79
741
12.040
_ «
»:
93.000.000
5.300J
2.800J
73.SOOJ
2.400.000
64,000
200.000
217.500
5.500.000
350.000J
2.200J
7.200J
36.000J
44.000J
3.400J
31.000J
20.000J
900J
31.0004
1.300.000J
1.SOO.OOOJ
130. 000 J
1.800J
3.300J
220.000J
21 OJ
1.700J
i1 wwracriai
1 Of 27
5 af 27
4 of 27
« Of 27
1 Of 27
1 Of 27
11V» 1 «' 27
12 Of 27
2 of 24
2 of 27
8 of 27
12 of 27
12 of 27
14 of 27
4 of 27
12 of 26
10 of 27
4 of 27
10 of 27
5 of 27
6 of 27
1 Of 27
2 Of 27
3 Of 27
2 of 27
Oof 27
19 of 27
19 of 27
2 of 27
1 Of 27
3 Of 27
19 of 27
1 Of 27
1 Of 27
                                    1 of 3

-------
                                        GROUND WATER QUALITY
                                      WILLIAM DICK LAGOONS SITE
Compound
METALS (dissolved) (»g/l)
aluminum
oanum •;
beryllium
calcium
cooait
copper
iron
lead
magnesium
manganese
potassium
selenium
sodium
zmc
Maximum
Caneantrf'lgn,
•
1.430
83.7
1.6
5.280
20.8
14.4
20.200
i
4.260 •
863
8.520
2.«
32.500
61.2
Average
Maximum*

1.430
83.7
1.6
S.280
20.8
144
19.800
1
4.260
863
4.260
2.4
32.500
61.2
Average
Concentration

'54
25.7
0.1
1.875
3.3
3.9
4.870
0.27
1.705
193
426
0.2
8.182
61.2
Frequency
of 0«t«etie

3 of -2
^2 v -Z
: at :Z
9 of 9
* or "2
2 3f 5
11 or :•
4 af ".
3 of *
n of .12
1 Oflfl
1 of 12
7 of 12
1 Of 1
CONVENTIONAL PARAMETERS (mg/l)
otocnomicai oxygen
demand (BOO) .
total dissolved solids (TOS)
nitrate
alkalinity (as CaCO3)
cnionae
naraness (as CaCO3)
total organic canon (TOO
91

560
3.1
20
20
64
52
PH"'
•
CQftCM!fslIIM>isl fVpOIIBd fflf • iMll flTOfll Wtl
M^MSk mar mn tt> Is* ttsA •M^BMS&AA mA •••*»> r^nnrrei
91

560
3.1
20
20
64
52
<1S

<8S
<1.3
8.2
<5
22
<&4
12 3f '2

12 of '2
12 3f -2
12 of -2
12 3f '2
12 of '2
12 3f '.2
5.6
when me) maximum
icft two or more samples
• * Out of a msflrimum of 13 wait tar erganics and 12 wotts for motats:
                   s^ek •••ASBJ A^^^B^B^^ ^^&« >^be) eeBi^hAA «^t^^^ekl^ ^B ^Mei^dkiai
                   IO IBM sample count tnose sampio n MII*UI
                 kdlt ffloA
• • • From pump tost on MW-20. October/November 1919.

Noto:   Pesoades/PCSa not eotoctsd in any weUa.

J<- Estimated concontration
                                             2 or 2

-------
                        LAGOON AND BERM AREA SOB. QUAL rrv
                                   O.CK LAGOONS
  Compound	e^A™?*	M«*»mum

  METALS (confd) (mg/kg)
  cobalt
  copper
  iron
  lead
  magnesium
 mercury
 nickel
 potassium
 silver
 sodium
 vanadium
 zinc
1.4
tA
9
7.960
24
916
64
0.01
5.4
628
04
. 1
38
1A
3
52
4.1
40J
18.000
269J
5.080
160
2.3
1 4
3.070
1.7
644
28J
253J
5 of 6
7 of 8
27 of 27
27 of 27
18 of 18
23 Of 23
3 Of 27
t7 of 27
4 of 17
2 of 27
1 Of 17
27 of 27
23 of 23
J •  estimated concentration
                           Page 3 of 3

-------
                           LAGOON AND BEAM AREA SOIL QUALITY
                               WILLIAM DICK LAGOONS SITE


                                  Avaraga      Maximum    Frequency  of
    Compcund	 ConcantrationConeanffatlon  Oafaetfon*

    SEMIVOLATILCS  (confd) (tig/kg)

    dimatnyl pfttftafata                1i          S90J         i of 27
    acanapfttfiylana                  740        7.000J        8 of 27
    acanaptnana                     3.970        47.000J       13 of 27
    oibafttofuran                     3.570        36.000J       13 of 27
    diatftyl pmftalatf                 83         1.*OOJ        2 cf 27
    fluorana                        4.240        41.000J       13 of 27
   N-nitrosodipftanylamina           734       '  5.300J        5 of 27
   ptntacnioropnanol                  2           S4j          i of 27
   pn«nantnr«n«                   16.500       280.000J      16 of 27
   antftrac«n«                      1.830        13.000J       16 of 27
   di-n-outylphtnalata             5.910       32.000J       u of 27
   fluorantnanr                   8.360      200.000J       16 of 27
   pyr«n«                         6.020      120.000J       16 of 27
   butyibanzyipmhaiata            11.300       78.000J       15 of 27
   banzo (a) amtiracana             1.860 .     30.000J      13 of 27
  cnrysana                       2.130       29.000J      16 of 27
  bis(2-ttnyihaxyi)phtfiaiata       169.000     1.200.000J     22 of 27
  di-n-octyipfttnaiatt              4.720       29.000J       15 of 27
  banzo(b and/or k)fluor«ntMana     3.940       54,000J       15 of 27
  banzo(a)pyrtnt                  1.250       2S.OOOJ       11 of 27
  indtno(1.2.3.e.d)pyrana           300         7.600J       5 of 27
  dibanzo(a.A)antftracan«             81          2.700J       3 of 27
  ban20(g.ft,i)p«ryitn«              300         8.000J       5 of 27

  PEST1CIOES/PC8S big/kg)

                                                             •
 haptaefilor tpoxida                 6            150         1 of  27
 4.4'.QOE                       34.300       220.000       17 of 27

 METALS (mgAg)


 aluminum                       8.040        15.100       27 of 27
 arsanic                          9.2           14J        27 of 27
 barium                           81           672J        27 of 27
 baryllium                       0.09          O.S1         1 of  6
 cadmium                        0.04           1.U         1  of 26
 calcium   ..-                     2.190        11.100        6 of  6
cftromium                        39           349J   '    26 of  27


                               Paga 2 of 3

-------
       TAIL! 5
      Oiom Oat* Summary
    William Oicx Lftgoofl* Sit*
W«R C*J« Townsftp. C***t*r County
EMM T.ft. Ma
3*mo<* location
3*mp<* 0*t*
unit*

2.3.78-TCOO
atn*f TCOO
2.3.7.B-TCOF
am*r rco*
2.3.7J-PCOO
otn«r PCOO
2.3.7 8.PCOF
otrw PCO«
2.3.7 8-MxCDD
om«f MiCOO
2.3.7.1-HiCDF
omcfMiCO'
2.3.7 i-WoCDO
otMfMeCOO
2.3.7 8-HBCOf
om«f MoCOF
OCO3
OCO *
2.3.7.11 TCOO •dumMmi

23297
0-8«e*qrogno
10/11/89
u«/K«










o.oot



O.OS


S.9

ud/K«
0.007
23291
0-9 (2-4)
10/11/89
ufl/Kfl




o.gt












3.t

uo/K*
0.0044
23301
0>« fO-21
10/1 1'89
u«/K«


O.Tt
0.01
O.t9

0.01
0.00«
0.024
O.Of
0.27
0.03
0.09
0.37
0.42
o.oa
0.01
4.1
0.1 •
(M/Kfl
0.0241
23299
0-4 (2-*>
t 0/1 1/89
ua/Kq




0.03S






0.09S



02i


Z4
uO/Ko
0.01 45
         tfw fMtfMd tf«t»ctten iMt IWM Mt MM f»port*d.

-------
                             wB

                               O.CK
  aluminum
  arsenic
  barium
  5«ryllium
  eitremJum
  eebtlt
  iron
 itatf
 mercury
 potassium
 sodium
vanadium
zinc
    VOUTILCS

   SI yiVOLATILf 3
      ".
   btnzoic aetd
   «.«,,.„.,.„.„,„,„„„,,

   S'«(2..enyii.,,y,,Blu(ul           ?'          <«oj       !*•
                                 *U     •     t «/• .       ' 0" «
                                             • OUJ        t af |
  PfSTICI06S/PCS«


  MfTALS (mg/kgj
tO. 843
2.2
39
0.32
10
2.7
7.899
8.8
730
121
0.1
m + A
749
294
15.5
31
14 inn
1 *.auo
^ •
•J.*
48
O.S8
20
^ •
11.700
15
1.260
291
0.69
2.170
1.070
21
39

8 of •
8 of |
8ofS
8 of 8
8ofS
7 of 8
8 Of 8
8 of 8
8of8
8of6
1 of 8
4 Of 8
2 of 8
8of9
8of8

-------
            TA8LI  7
                          or CB
                          Of EA
                   CAU or cofraunr
                      IDIf
l^-4lehIoreetjitM (tocaO
   1.2mehlenbcn>en«
.41
   l.lttIqrlheyl)pluhaUte
                                        phenol
                                 lwt«diehtorMtiitnc ItouO
                                     ehtonbenzcnc
                                 4-mtthjriph«nol (p^meO
                                   2.4-dicWorophenol

-------
                                        TABLE •
         Com
water aquifer
                                               MiriaMm «*
                                                   OMHUI


                                                                   HP • n*
Air
                  •I fcfM* AIM
VM
                                   OM
                                            Vw

-------
                             <«
                                    I.1M cma       '0.470 out
•OfcTw
it 70 iwr Ufwiv
            WATW
  WIM» SflOMnnylMMf
 •* tHH A/M Cra^M (f


MMI MOVtf I


•t ft
 r 1m*n rr'

  «»
                             (•I
                       a nun
                        71%
                        1C
                             (0

                             let

                             (0

                            (Ml
                             (0
                        0.0*
                       t«
               (0      24 IM<
               (0     3M Mr
               m
               m
               m
               (0
                                   UMIO
» liar*

 71%

 1C
                                       O.It
                                       11* •
24 IMO
                0.1*

               14 0*

                »f
               14 Mr
                                                                •Jt
                                                                  1
                                                                 24
                                                                1.4*
                                                               OJ

-------
10

-------
                                                                                    TABLE  1t
                          3C-OS • IC-03
 DMT Mm UcMttea
                                                                   flt-07 .
                                                                                       5£-Oi • IE-OS
                                  IC4S
                                                                                              IE-OS
                          3K4S  - 3C-OC
                                                                     N* . NA
 T«Ml
                                             arM  .  JfrO*        3*O«  • 3»CB        lf-OB
WOTCi
Vl

-------
                                                 12
                                          3C41
                                  8C-C8
7C-M
                                    NA • NA

                                    •t 1.0 fcr teutpnud

-------