United States
Environmental Protection
Agency
                        Office of
                        Emergency and
                        Remedial Response
EPA/ROD/R02-90/123
September 1990
oEPA
Superfund
Record of Decision:
          Claremont Polychemical, NY

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50272-101
 REPORT DOCUMENTATION
        PAGE
                        1. REPORT Na
                             EPA/ROD/R02-90/123
                                                                    3. Recipient. Accaulon No.
 4. TMeendSubMe
   SUPERFUND RECORD OF  DECISION
   Claremont Polychemical,  NY
   Second Remedial Action - Final
                                                                   i. Report Dste
                                                                          09/28/90
 7. AiMiorte)
                                                                    a Performing Organization Rspt No.
 9. Performing OrgdrriaUon Nun* end Address
                                                                    10. Pfo|ect/Tssk/Work Unit No.
                                                                    11. ContrsctfC) or Grsnt
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EPA/ROD/R02-90/123
Claremont Polychemical, NY
Second Remedial Action - Final

Abstract (continued)

water and soil/wastes contained onsite in drums and holding basins. The primary
contaminants of concern affecting the soil, debris, and ground water are VOCs including
PCE, TCE, toluene, and xylenes; other organics; metals including arsenic, chromium, and
lead; and inorganics including asbestos.

The selected remedial action for this site includes excavation and onsite treatment of
1,600 cubic yards of contaminated soil using low temperature enhanced volatilization,
followed by redeposition of the treated soil in the excavated areas; decontaminating
the building,  which includes removal, offsite disposal, and treatment of the asbestos
insulation; excavating, treating, and disposing of the underground tanks, tank
contents, associated equipment, liquid wastes,  and contaminated soil offsite;
backfilling the excavated area with clean soil; and pumping and treatment of ground
water using air stripping, with carbon adsorption to control offgasses, followed by
onsite reinjection of the treated ground water.  The estimated present worth cost for
this remedial action is $16,800,00, which includes an annual O&M cost of $1,100,400 for
years 0-10 and $701,900 for years 11-17.

PERFORMANCE STANDARDS OR GOALS:  No chemical-specific cleanup levels were provided.

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                          ROD FACT SHEET
SITE

Name:
Location/State:
EPA Region:
HRS Score  (date)
NPL Rank (date):

ROD

Date Signed:

Selected Remedy

Soils:


Groundwater:
Building:


Underground Tanks:



Capital Cost:
O & M:

Present Worth:

LEAD
Claremont Polychemical
Old Bethpage, Nassau County, New York
II
31.62 (June 86)
915 (August 90)
September 28, 1990
Excavation and treatment via on-site low
temperature enhance volatilization

Extraction and treatment via air stripping
and carbon adsorption and reinjection of
treated groundwater into the ground

Decontamination via vacuuming, dusting and
asbestos removal

Excavation, removal and off-site
treatment/disposal of tanks and associated
equipment

$  6,200,000
$  1,100,400 (first ten years)
$    701,900 (next six years)
$ 16,800,000
Remedial, EPA
Primary Contact  (phone):  Carlos R. Ramos  (212-264-5636)
Secondary Contact  (phone):  Douglas Garbarini  (212-264-0109)
WASTE

Type:
Soil - tetrachloroethene
Groundwater - trans-l,2-dichloroethene,
     trichlbroethene,  1,1,1-trichloeoethane
Building - copper, zinc
Underground tanks - toluene, xylenes,
     2-butanone

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Medium:             Soil, groundwater,  building, underground
                    tanks
Origin:             Pollution originated during the operation of
                    the Claremont Polychemical Corporation.  The
                    processes used resulted in the generation,
                    storage and disposal of hazardous waste
                    products.

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                 DECLARATION FOR THE RECORD OF DECISION



Site Name and Location

Claremont Polychemical, Old Bethpage,'Nassau County, New York

Statement of Basis and Purpose

This decision document presents the selected remedial action for
the Claremont Polychemical site, in Old Bethpage, Nassau County,
New York, developed in accordance with the Comprehensive
Environmental Response, Compensation and Liability Act of 1980,
as amended by the Superfund Amendments and Reauthorization Act of
1986, and, to the extent practicable, the National Contingency
Plan.  The attached index (Appendix C)  identifies the items that
comprise the administrative record upon which the selection of
the remedial action is based.

The State of New York has concurred with the selected remedy.

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, may present an imminent and
substantial endangerment of public health, welfare, or the
environment.

Description of the Selected Remedy

The remedy addresses the principal threat posed by the Site
through a combination of source control alternatives including
treatment of contaminated soils (SC-4), tank removal and
treatment (T-2), active restoration of the groundwater (GW-3B),
and building decontamination (BD-2).

This action complements the previous work conducted as part of
the second operable unit developed to address wastes contained in
several holding units  (i.e., drums, aboveground tanks, basins,
and a sump).

The major components of the selected remedy include:

  •  Excavation and on-site treatment of approximately 1,600
     cubic yards of contaminated soils via low temperature
     enhanced volatilization and redeposition of treated soils
     into the excavated areas.

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     •  Extraction and treatment of the contaminated groundwater at
       the Site via air stripping and carbon adsorption and
       reinjection of the treated water into the ground.

       Decontamination of the building via vacuuming and dusting of
       the contaminated surfaces and.removing the asbestos  .
       insulation for off-site treatment and disposal.

       Excavation, removal and off-site treatment/disposal of the
       underground tanks, associated equipment, tank contents, and
       highly contaminated soil.

  Declaration

  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 (or resource
  recovery) technologies to the maximum extent practicable and
  satisfies the statutory preference for remedies that employ
  treatment that reduces toxicity, mobility, or volume as a
  principal element.
  53
/ *
Hnstantine Sidamon-Eristoff
egional Administrator
                        ~~

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            DECISION  SUMMARY
      CLAREMONT POLYCHEMICAL SITE
             OLD  BETHPA6E
        NASSAU  COUNTY, NEW YORK
United States Environmental Protection Agency
             Region II, New York

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                          TABLE OF CONTENTS
SECTION                                                    PAGE

SITE NAME, LOCATION AND DESCRIPTION	  1
SITE HISTORY AND ENFORCEMENT ACTIVITIES	  1
HIGHLIGHTS OF COMMUNITY PARTICIPATION	  2
SCOPE AND ROLE OF OPERABLE UNIT	  3
SUMMARY OF SITE CHARACTERISTICS	  4
SUMMARY OF SITE RISKS	  8
DESCRIPTION OF ALTERNATIVES	  11
SUMMARY OF COMPARATIVE ANALYSIS OF ALTERNATIVES	  19
SELECTED REMEDY	  30
STATUTORY DETERMINATIONS	  31
DOCUMENTATION OF SIGNIFICANT CHANGES	  33
APPENDICES

APPENDIX A. FIGURES
APPENDIX B. TABLES
APPENDIX C. ADMINISTRATIVE RECORD INDEX
APPENDIX D. NYSDEC LETTER OF CONCURRENCE
APPENDIX E. RESPONSIVENESS SUMMARY
                                ii

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                         LIST OF FIGURES

Number      Name
1           Claremont Polychemical Site Location Map
2           Claremont Polychemical Site Plan
3           Surface Soil Sampling Locations
4           Soil Boring Sampling Locations
5           Estimated Area of Soil Contamination
6           Monitoring Well Location
7           Approximate Extent of Groundwater
            Contamination
                               iii

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                          LIST OF TABLES


Number      Name

1           Site History Summary

2           Summary of Chemicals Detected in Surface
            Soil

3           Summary of Chemicals Detected in Soil
            Borings

4           Summary of Chemicals Detected in
            Groundwater Samples

5           Summary of Chemicals Detected in Air
            samples

6           Summary of Chemicals Detected in Building
            Samples

7           Indicator Chemicals

8           Summary of Exposure Pathways

9           Toxicity Data for Non-Carcinogenic Effects

10          Summary of Human Non-Cancer Risk Estimates

11          Toxicity Data for Carcinogenic Effects

12          Summary of Cancer Risk Estimates

13          List of ARARs Associated with the Selected
            Remedy
                                IV

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SITE NAME/ LOCATION AND DESCRIPTION

The Claremont Polychemical site is an abandoned production
facility located in central Long Island,  in the community of Old
Bethpage, Town of Oyster Bay, Nassau County, New York (see Figure
1).  The facility is located in an area comprised of light
industrial, commercial and institutional properties (Old Bethpage
Landfill, SUNY Agricultural and Technical College at Farmingdale,
and Bethpage State Park). The Suffolk County line is approxim-
ately 800 feet east of the Site.

In 1985, Old Bethpage had a population of 5,881 persons and
Oyster Bay had a population of 305,750 persons, according to the
Current Population Report (U.S. Bureau of Census, 1987).  The
closest residences are approximately half a mile away on the west
side of the Old Bethpage Landfill ("Landfill").  The closest
public supply well is located 3,500 feet northwest of the Site.

SITE HISTORY AND ENFORCEMENT ACTIVITIES

A chronological summary of activities associated with the
Claremont Polychemical site is presented in Table 1.  The Site
occupies approximately 9.5 acres on which a 35,000 square foot,
one story, concrete building is located  (see Figure 2).  Other
features include: treatment basins, aboveground tanks,
underground tanks, leaching basins, dry wells, and water supply
wells.

From 1968 until its closure in 1980, Claremont Polychemical
manufactured inks and pigments for plastics, coated metallic
flakes, and vinyl stabilizers. The principal wastes generated
were organic solvents, resins, and wash wastes (mineral spirits).

Concern for contamination  was linked to a discovery in 1979 by
the Nassau County Department of Health (NCDOH) of 2,000 to 3,000
drums scattered throughout the Site, some uncovered and others
leaking. By September 1980 most of the drums were
sorted and either removed from the Site or reused in the plant.
Some of the material was burned in the plant's boiler. NCDOH
inspectors noted at the time that an area east of the building
(spill area) was contaminated with organic solvents as a result
of accidental and/or incidental spills and discharges. A
subsequent removal action by the property owners, in 1980,
excavated the upper ten feet of a seventy-five foot by seventy-
five foot area. The excavated material was placed on a plastic
liner. Over the years, this liner has degraded and no longer is
an impermeable layer.  Groundwater samples from a monitoring well
installed at the time (1980) indicated the presence of
groundwater contamination directly under the Site.

Claremont Polychemical and its affiliated companies  (Winding Road
Estates and Winding Road Properties) entered into receivership  in

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1980.  In 1983, Woodward-Clyde Consultants,  under the direction
of the New York State Department of Environmental Conservation,
conducted a preliminary investigation of the Site. In 1984,  Velzy
Associates conducted a limited study of the Site for the property
owners.  Additional sampling was performed and a report was
written by C.A. Rich Consultants in response to questions by the
U.S. Bankruptcy Court.  For the last four to five years two
tenant businesses have been operating at the Site.

The Claremont Polychemical site was first proposed for inclusion
on the National Priorities List (NPL) in October 1984 and was
listed in June 1986.  On December 4, 1987, EPA issued a special
notice letter to Mr. Walter Neitlich (Claremont Polychemical
Officer) requesting a good faith offer to undertake or finance
the remedial investigation and feasibility study.  No response
was received from Mr. Neitlich or a company representative,  so in
March 1988 EPA obligated funds and started a comprehensive
Remedial Investigation and Feasibility Study ("RI/FS") for the
first operable unit.

A preliminary evaluation by EPA in July 1988 revealed the
presence of hazardous waste held in containers (e.g. drums)  and
other holding units  (treatment basins, aboveground tanks, and a
sump). In September 1988, EPA performed work consisting of the
overpacking and/or stabilization of deteriorated containers and
holding units.  A second operable unit RI/FS (OU-II) dealing with
the ultimate disposal of the above mentioned hazardous wastes was
completed by EPA in July 1989.  The Record of Decision for OU-II
was issued in September 1989.  The selected remedy is currently
being implemented and consists of compatibility testing,
bulking/consolidation, and treatment/disposal of the wastes at
off-site, EPA-approved, treatment facilities.

HIGHLIGHTS OF COMMUNITY PARTICIPATION

The RI/FS Reports, and the Proposed Plan for remedial action were
released for public comment on August 24, 1990.  These documents
were available to the public in both the administrative record
file and the information repository maintained at the EPA docket
room in Region 2 and at the Plainview-Old Bethpage Public
Library.  A press release announcing the availability of these
documents was issued on August 4, 1990.  The public comment
period set by EPA concluded on September 25, 1990.

During the public comment period EPA held a public meeting to
present the RI/FS Report and the Proposed Plan, answer questions,
and accept both oral and written comments.  The public meeting
was held in the auditorium of the Old Bethpage Village Restora-
tion, Old Bethpage, New York on September 5, 1990.  Comments
received be EPA are addressed in the Responsiveness Summary
(Appendix E) appended to the Record of Decision.  This decision
document presents the selected remedial action tor the Claremont

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Polychemical site, in Old Bethpage, New York,  chosen in
accordance with CERCLA, as amended by SARA and to the extent
practicable, the National Contingency Plan ("NCP").   The decision
for this site is based in the administrative record.

SCOPE AND ROLE OF OPERABLE UNIT

EPA divided the remedial work being conducted at the Claremont
Polychemical site into two operable units.  The first operable
unit addresses the overall site remediation (groundwater and
soil) and is the focus of this document.  The RI/FS for the first
operable unit contains the detailed information and data used in
determining the nature and extent of the problem and the
development of remedial alternatives to address the problem.

The second operable unit deals only with the wastes held in
containers and holding units.  In September 1989, EPA decided to
remove these wastes and treat/dispose of the materials off-site.
This action, which includes the containers found inside the
building (e.g. drums) and the wastes contained inside the holding
units (e.g. treatment basins, aboveground tanks), is currently
ongoing.

The overall objective of the remediation is to reduce the
concentrations of contaminants in various media and structures at
the Site to levels which are protective of human health and the
environment.  The remedy selected should eliminate long-term
sources of contamination of groundwater and other media, and will
achieve this objective through:

  o  Soil Treatment.  On-site treatment of the soil to remove the
     mobile organic contamination will result in the elimination
     of a long-term source of contamination of the groundwater.

  o  Groundwater Treatment.  Extraction and treatment of the
     contaminated groundwater will contain the migration of the
     plume and, in time, will achieve federal and state standards
     for the volatile organic contaminants.

  o  Building Decontamination.  Removal of all hazardous
     materials from the building will eliminate any potential
     risk to human health and the environment.

  o  Removal and Treatment of Underground Tanks, Liquid Wastes.
     and Associated Soils.  Removal and off-site treatment of
     these wastes will result in the elimination of the threat to
     human health and the environment from possible contact with
     the wastes.  It also will result in the eradication of a
     potential long-term source of groundwater contamination.

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SUMMARY OF SITE CHARACTERISTICS

SOILS

Soil samples for chemical characterization collected at the
Claremont Polychemical site consisted of two types:  surface
soils and subsurface soils.  Surface soil samples were obtained
from the upper six inches of soil whereas subsurface soil samples
were obtained from two foot intervals at various depths below
grade up to a depth of 82 feet beneath the Site.

Surface Soil

Surface soil samples collected on-site were analyzed for metals.
Soil sample results were compared with typical background levels
and are summarized in Table 2.  Of the metals detected, only
cadmium (33.1 ppm), copper (230 ppm), lead (327 ppm), magnesium
(29,200 ppm), and zinc (3,200 ppm) exceeded typical eastern U.S.
soil background levels at a few of the surface soil sampling
locations, primarily in the soils adjacent to the treatment
basins (see Figure 3).  These metals are most probably found in
surface soil due to overflow from the treatment basins and
current site use  (i.e., vehicular traffic, storage of
construction debris).

Subsurface Soil

Volatile organic compounds detected in the subsurface soil
samples included tetrachloroethene  (26,000 ppb), 1,2-
dichloroethene (71 ppb), trichloroethene  (17 ppb), acetone
(14,000 ppb), toluene  (82 ppb), 2-butanone (3,300 ppb), xylenes
(150 ppb)  and 4-methyl-2-pentanone  (360 ppb).  In general, total
volatile organic concentrations were greatest to the east of the
process building in proximity to the former spill area at boring
locations SB-19 and SB-21 which are shown in Figure 4.  Overall,
the volatile organic concentrations decrease rapidly with depth.
A summary of the results is presented in Table 3.

Several base/neutral acid extractable organic compounds  (BNA)
were detected within soil boring samples, a majority of which
were polynuclear aromatic hydrocarbons  (PAH's) that are
constituents of fuel, oil and grease.  In addition, phthalates
(270,000 ppb), benzoic acid (120 ppb), 2-chloronaphthalene
(33,000 ppb) and pentachlorophenol  (360 ppb) also were found in
some samples.  The greatest concentrations of the three most
prevalent phthalates; bis(2-ethylhexyl)phthalate  (BEHP) at 70,000
ug/kg, di-n-butylphthalate at 3,900 ug/kg and butylbenzyphthalate
at 8,200 ug/kg were found at 0-2 ft at SB-19 in the spill area.

Relatively low levels of five pesticides, i.e., dieldrin  {26
ppb), heptachlor  (18 ppb), DDT  (88 ppb), ODD  (180 ppb), and DDE

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(110 ppb) were detected, predominantly in the western and
northern portions of the Site.  PCBs were detected only at soil
boring locations S6-02, 08, and 25 with a maximum concentration
of 1,100 ppb.  Surficial oil spillage in these areas appears to
be the most likely source of these PCBs since elevated PNAs,
typically associated with oil, were also present at these
locations.

Metals detected in soil boring samples which exceeded typical
eastern U.S. soil background levels included arsenic (35 ppm),
cadmium  (14.1 ppm), copper (152 ppm), lead (90.8 ppm),  magnesium
(29,100), and selenium  (2.0 ppm).  Selenium, lead and magnesium
exceeded background at several locations, generally at the 0-4
feet depth, but with no apparent spatial distribution.   The
elevated levels of these metals could be associated with the
presence of fill material, vehicular emissions and surficial
spills of fuel-related products.

Volume of Contaminated Soil

Tetrachloroethene  (PCE) is identified as the only chemical of
concern in soil due to the leaching of PCE from the soil to the
underlying groundwater.  The estimated volume of contaminated
soil that requires remediation is based on the extent of PCE
contamination in the soil.  Soil-to-groundwater models have
indicated the potential for PCE to contaminate the aquifer above
potable water standards.  In order to minimize the impact of the
PCE on the groundwater and enhance the groundwater treatment
remedy, the first two feet of soil in the spill area will be
treated.  Treatment to a depth of two feet will remove the
significant contamination from the soil, including the location
where the highest level of contamination, 26 ppm of PCE, was
found.  Based on soil boring information collected from the Site,
this will reduce the average PCE contamination in the soil to
much less than 200 ppb.  A 21,000 ft2 area  of soil,  generally
located in the spill area, as shown in Figure 5, is identified as
requiring remediation.  The preliminary volume of contaminated
soil from this area which requires remediation is estimated to be
1,600 cubic yards.

GROUNDWATER

Two rounds of groundwater sampling were conducted, the first was
conducted in April 1989 and the second in June 1989.  The wells
were distributed upgradient, in the immediate vicinity, and
downgradient of the Site in order to define the nature and extent
of contamination originating at the Site.  In addition, three
wells were located to the west of the Site to define the
contaminant plume emanating from the Old Bethpage Landfill.
Figure 6 shows the location of these wells and the approximate
extent of the contaminated groundwater plume.  The groundwater
flow in the region was generally from the north-northwest -to the

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south-southeast.

Groundwater samples were analyzed for volatile organics, semi-
volatile organics, pesticides and PCBs, inorganics and several
standard water quality parameters.  A summary of the results is
presented in Table 4.           .

Results

Tetrachloroethene had the greatest spatial extent and highest
groundwater concentrations of any contaminant found in site
groundwater.  Figure 7 shows the maximum groundwater
concentrations for tetrachloroethene in all wells analyzed for
during this investigation.  The maximum detected concentration
occurs near the property's boundary and the concentration
gradually attenuates to the southeast.  Maximum detected levels
of tetrachloroethene (1,300 ppb), trans-l,2-dichloroethene (830
ppb), trichloroethene (260 ppb), 1,1,1-trichloroethane (100 ppb),
ethylbenzene (160 ppb), acetone (540 ppb), benzene (60 ppb), 1,1-
dichloroethane (17 ppb), methylene chloride (14 ppb), total
xylenes (40 ppb) and vinyl chloride (7 ppb) were found which
exceeded federal and/or New York State Maximum Contaminant Levels
("MCLs").  Maximum detected values were generally found in the
shallow portion of the aquifer  (0-45 ft).

The frequency and levels of semivolatiles and pesticides detected
were much lower than those generally found for volatile organics.
The highest concentration found was 92 ug/1 for bis(2-
ethylhexyl)phthalate (BEHP) however, this level was comparable to
that found  (88 ug/1) in an upgradient well.   No PCBs were found.

Several metals were detected in concentrations exceeding federal
and state standards including arsenic  (56.5 ppm), chromium (159
ppm), lead  (464 ppm) and manganese (3,130 ppm).  However, of
these metals chromium and lead also occurred above MCLs in
upgradient wells.

AIR

The ambient air samples collected show low concentrations of
volatile contaminants namely chloroform (0.07 ppb), 1,1,1-
trichloroethane (0.7 ppb), carbon tetrachloride (0.12 ppb),
trichloroethene (1.14 ppb), tetrachloroethene  (3.42 ppb), toluene
(2.1 ppb), and styrene (0.37 ppb).  However, these concentrations
were generally comparable, and in several cases lower, than
upwind concentrations (i.e., chloroform, carbon tetrachloride,
1,1,1 trichloroethane, toluene and styrene).  Table 5 presents a
summary of the analytical results.

UNDERGROUND STORAGE TANKS

An underground tank farm consisting of fourteen tanks was

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uncovered and sampled.  Of the fourteen tanks, ten were made of
steel and four were made of fiberglass.  Eleven contained
sufficient materials to obtain liquid and/or sludge samples.  The
amount of material contained in the tanks (approximately 16,000
gallons) varied from a few inches to several feet deep.  Samples
were analyzed for one or more of the following parameters: TCL
volatiles, semivolatiles, inorganics and pesticide/PCB compounds,
total recoverable petroleum hydrocarbons (TRPH), corrosivity,
flash point, reactive cyanide and reactive sulfide.

In general, results show that the number of organic compounds
detected in any given sample was usually less than three
compounds with a maximum of eight compounds.  The maximum number
of water immiscible organic compounds was found in the eastern
steel tank EST-04.  The contents in three of the tanks were
dominated by: 2-butanone (92%) in western steel tank WST-03;
toluene (2.6%) and xylenes (3.6%) in the water immiscible phase
in eastern steel tank EST-04; and bis(2-ethylhexyl)phthalate
(BEHP)  (23%) in eastern steel tank EST-06.  No pesticides or PCBs
were detected in any tank investigation samples analyzed for
these compounds.

For most of the tanks, the TRPH was less than 40 mg/1.  However,
for western steel tank WST-03 and eastern steel tank EST-06, the
levels were 1.4% (14,000 mg/1) and 14.5% (145,000 mg/1),
respectively.  These tanks contain high levels of 2-butanone and
BEHP, respectively.  Most of the corrosivity results fell in the
range of 3 to 5.8 mm/yr.  The flash points of most of the tank
fluids fell above 100°C.  Western steel tank WST-03  and eastern
steel tank EST-04 contained fluids having flash points below
15°C.   Fiberglass tank FG-04  contains  fluid  with a  flash point of
30°C.

Four organic compounds were found in the soil directly next to
the tanks, however, three of them, tetrachloroethene, chloroform
and di-n-butylphthalate, occurred at trace levels (less than 26
ppb).  The fourth compound, bis(2-ethylhexyl) phthalate  (BEHP),
occurred at substantially higher levels, in the range of 50 to
3,000,000 ppb (i.e. up to^O.3%), in all samples.

BUILDING

Within the Claremont process building, samples were collected to
characterize any contamination associated with accumulated dust,
standing water (in floor drains and previously operating
condensers), and insulation materials.  Results are summarized in
Table 6.

Building Dust Wipes

Analysis of wipe samples taken from floors and walls show the
widespread presence of metals within the building.  Inorganics

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                                8

were detected at consistently high concentrations - aluminum at
1,696 ug/ft2  to  45,013 ug/ft2 and copper from 142 ug/ft2 to 2,091
ug/ft2.   BNA  and pesticide analysis showed bis(2-
ethyhexyl)phthalate as the principal contaminant at
concentrations of 107 to 3,200 ug/ft2.

Condensers and Floor Drains

Water samples were collected from two condensers and two floor
drains within the building.   A wipe sample was also taken from
one condenser.  All samples showed elevated levels of inorganics.
Principal contaminants include copper (17.9 - 43,900 ug/1)  and
zinc (up to 12,200 ug/1 in water samples, and 77,653 ug/ft2  in
the condenser).

Pipes

Analyses of 17 samples of insulating material collected from the
pipes within the building showed that 14 out of 17 samples had
greater than 5% asbestos.  Asbestos concentrations in the
building materials analyzed ranged from non detect to 25%
asbestos.

SUMMARY OF SITE RISKS

EPA conducted an Endangerment Assessment (EA) of the "no action"
alternative to evaluate the potential risks to human health and
the environment associated with the Claremont Polychemical site
in its current state.  The EA focused on the contaminants in the
air, building dust, soil, and ground water which are likely to
pose the most significant risks to human health and the
environment  (indicator chemicals).  The summary of "indicator
chemicals" in sampled matrices is listed in Table 7.

EPA's EA identified several potential exposure pathways by which
the public may be exposed to contaminant releases at the Site.
Potential pathways were developed based on current (residential,
industrial) and future land use  (residential, industrial)
scenarios at the Site.  Several pathways (Direct contact,
inhalation and ingestion) were evaluated for each scenario.
Under the present land use,  ingestion of ground water, inhalation
of fugitive dust, and contaminated air were considered complete
exposure pathways.  Ground water downgradient of the Site was
used for present and future off-site land use exposure scenarios,
whereas site ground water was used, for on-site future land use
scenario.  Site air and soil concentrations, were used for both
scenarios, as applicable.  These pathways and the populations
potentially affected are shown in Table 8.  Potentially exposed
populations include on-site and off-site residents, farm workers,
and construction workers.  Two risks were calculated,
corresponding to the average and maximum plausible case.

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Under current EPA guidelines, the likelihood of carcinogenic
(cancer causing) and non-carcinogenic effects due to exposure to
site chemicals are considered separately.  It was assumed that
the toxic effects of the site related chemicals would be
additive.  Thus, carcinogenic and non-carcinogenic risks
associated with exposures to individual indicator compounds were
summed to indicate the potential risks associated with mixtures
of potential carcinogens and non-carcinogens, respectively.

Non-carcinogenic risks were assessed using a hazard index (HI)
approach, based on a comparison of expected contaminant intakes
and safe levels of intake (Reference Doses).  Reference doses
(RfDs) have been developed by EPA for indicating the potential
for adverse health effects.  RfDs, which are expressed in units
of mg/kg-day, are estimates of daily exposure levels for humans
which are thought to be safe over a lifetime (including sensitive
individuals).  Estimated intakes of chemicals from environmental
media (e.g., the amount of a chemical ingested from contaminated
drinking water) are compared with the RfD to derive the hazard
quotient for the contaminant in the particular media.  The hazard
index is obtained by adding the hazard quotients for all
compounds across all media.  A hazard index greater than 1
indicates that potential exists for non-carcinogenic health
effects to occur as a result of site-related exposures.  The HI
provides a useful reference point for gauging the potential
significance of multiple contaminant exposures within a single
medium or across media.  The reference doses for the indicator
chemicals at the Claremont Polychemical site are presented in
Table 9.

The hazard indices for non-carcinogenic effects from the Site are
listed in Table 10.  All total His listed under current and
future off-site and on-site land uses are greater than 1,
suggesting that non-cancer effects may occur.

Potential carcinogenic risks were evaluated using the cancer
potency factors developed by the EPA for the indicator compounds.
Cancer potency factors (CPFs) have been developed by EPA's
Carcinogenic Risk Assessment Verification Endeavor for estimating
excess lifetime cancer risks associated with exposure to
potentially carcinogenic chemicals.  CPFs, which are expressed in
units of (mg/kg-day) ',  are multiplied by the estimated intake of
a potential carcinogen, in mg/kg-day, to generate an upper-bound
estimate of the excess lifetime cancer risk associated with
exposure to the compound at that intake level.  The term "upper
bound" reflects the conservative estimate of the risks calculated
from the CPF.  Use of this approach makes the underestimation of
the risk highly unlikely.  The CPFs for the indicator chemicals
are presented in Table 11.

For known or suspected carcinogens, the USEPA considers excess
upper bound individual lifetime cancer risks of between lO'4 to

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                                10

10"6 to be acceptable.  This level indicates that an individual
has not greater than a one in ten thousand to one in a million
chance of developing cancer as a result of exposure to site
conditions.

The potential risks due to carcinogens at the Site are listed in
Table 12.  The estimated risk for the current use of the
recreational areas located downgradient of the Site ranged
between 1.88 x 10"6 and 1.4 x 10 .  Under  future  off-site  land use
conditions, inhalation of the site air and ingestion of
unfiltered downgradient ground water posed a total risk varying
between 1.2 x 10s and 5.0 x 10s.  Higher  risks were estimated for
future on-site land use.  The risks from all pathways range from
1.84 x lO'4 to 6.61 x 10~*.   The primary risk to workers was  due  to
inhalation of resuspended dust inside the building  (2.37 x 10* to
5.09 x 103).   The risk for inhalation of  building resuspended
dust is above the risk range for carcinogens at the Site and the
remaining risks fall within EPA's acceptable risk range.

Uncertainties

The procedures and inputs used to assess risks in this
evaluation, as in all such assessments, are subject to a wide
variety of uncertainties.  In general, the main sources of
uncertainty include:

- environmental chemistry sampling and analysis
- environmental parameter measurement
- fate and transport modeling
- exposure parameter estimation
- toxicological data

Uncertainty in environmental sampling arises in part from the
potentially uneven distribution of chemicals in the media
sampled.  Consequently, there is significant uncertainty as to
the actual levels present.  Dermal adsorption and ingestion of
soil were not included in the exposure pathways for future off-
site land use because of the lack of off-site soil data.
Environmental chemistry analysis error can stem from several
sources including the errors inherent in the analytical methods
and characteristics of the matrix being sampled.

Uncertainties in the exposure assessment are related to estimates
of how often an individual would actually come in contact with
the chemicals of concern, the period of time over which such
exposure would occur, and in the models used to estimate the
concentrations of the chemicals of concern at the point of
exposure.

Uncertainties in toxicological data occur in extrapolating both
from animals to humans and from high to low doses of exposure, as

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                                11


well as from the difficulties in assessing the toxicity of a
mixture of chemicals.  These uncertainties are addressed by
making conservative assumptions concerning risk and exposure
parameters throughout the assessment.  As a result, the EA
provides upper bound estimates of the risks to populations near
the Landfill, and is highly unlikely to underestimate actual
risks related to the Site.f,

More specific information concerning public health risks,
including quantitative evaluation of the degree of risk
associated with various exposure pathways is presented in the Rl
Report.

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 health, welfare, or the environment.

DESCRIPTION OF ALTERNATIVES

Following a screening of remedial technologies in accordance with
the NCP, ten remedial alternatives were developed for
contaminated groundwater; five remedial alternatives were
developed for treatment of soil; and two alternatives were
developed to remediate the building and underground tank areas,
respectively.

These alternatives were screened based on implementability,
effectiveness, and cost. The screening resulted in remedial
alternatives upon which a detailed analysis was performed.  The
remedial alternatives not retained for a detailed evaluation
were: capping (SC-2); and, groundwater alternatives which relayed
solely on carbon adsorption  (GW-4A and 4B) and carbon
adsorption/enhanced activated sludge treatment (GW-6A and 6B).

Those alternatives considered in detail are discussed below.  The
time to implement as used herein means the time required for site
preparation and for actual on-site construction, start-up
activities and cleanup except for groundwater alternatives which
do not include actual remediation time.  It includes the remedial
design phase which typically takes 2-3 years to complete and
starts from the signing of the ROD.  The remedial alternatives
are organized according to the media or specific structures which
they address: soil  (SC), groundwater (GW), building  (BD) and
underground tanks (T).

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                               12
SOILS

Alternative SC-1:  No Further Action

Capital Cost: none
O & M Cost: $34,900 per year
Present Worth Cost: $564,300
Time to Implement: 1 month

The No Action alternative provides the baseline case for
comparison with other soil alternatives.   Under this alternative,
the contaminated soil is left in place without treatment.  A
long-term groundwater monitoring program would be implemented to
track the migration of contaminants from the soil into the
groundwater.  Existing monitoring wells would be used for
monitoring.  Five year reviews would be performed to assess the
need for further actions.

Roll-off containers and drums containing soils and drilling mud
generated during the remedial investigation would have to be
transported off-site for treatment and disposal in accordance
with state and federal regulations.

Alternative SC-3:  Excavation/Off-Site Incineration/Backfill with
Clean Soil

Capital Cost: $5,000,000
0 & M Cost: none
Present Worth Cost: $5,000,000
Time to Implement: 3.5 years

Site preparation for the remedial implementation would include a
parking area, equipment staging area and stockpile area.  Support
facilities (e.g. offices) also would also be installed on the
Site.  An estimated total of 1,600 cubic yards (cy) of soil would
be excavated.  Excavation would be conducted under moistened
conditions by spraying water over the surface to minimize
fugitive dust and volatile contaminant emissions.  The soil would
be stockpiled prior to transportation to an off-site facility.
The excavated soil would be transported to an off-site, EPA-
permitted incineration facility for treatment and disposal.  The
roll-off containers and drums containing soil from the remedial
investigation also would be re-packed into the same type of
containers and transported for off-site incineration along with
the excavated soil.  Clean soil would be used to backfill the
excavated area.  Site restoration would include the application
of topsoil and seeding.

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                               13


Alternative SC-4:  Excavation/On-8ite Low Temperature Enhanced
Volatilization/on-Site Redeposition

Capital Cost: $700,000
0 & H Cost: none
Present Worth Cost: $700,000
Time to Implement: 3.5 years

Site preparation and soil excavation would be performed as in
Alternative SC-3.  An estimated 1,600 cy of contaminated soil
would be treated in a mobile enhanced volatilization (low
temperature thermal extraction) unit brought on site.  Low
temperature thermal extraction consists of a feed system, thermal
processor, afterburner, and scrubber.  The excavated contaminated
soil is placed in the feed hopper with a backhoe.  The soil is
then conveyed from the hopper to the thermal processor.  Hot air
from an air heater is injected into the thermal processors at a
normal operating temperature of 260°C (500°F)  which is well above
the boiling points of most volatile organic compounds  (VOCs).
The volatilized compounds and moisture in the contaminated soil
is then burned at 1,090°C  (2,000°F)  in an afterburner operated to
ensure complete destruction.  A portion of the off-gas is
recirculated as combustion air to minimize fuel usage.  The
off-gas is then treated at the scrubber for particulate removal
and acid gas adsorption.  The off-gas leaves the system at a
temperature of less than 93°C  (200°F) .

The volatilized contaminant-laden gas also can be treated by an
activated carbon adsorption unit instead of an afterburner for
PCE removal.  A bag filter would be used to remove particulates
from the gas before it enters the carbon adsorption unit.  The
treated soil would be free of volatile organics and would be
stored for sampling and then used as backfill in the excavated
areas.  Site restoration would be performed as in Alternative
SC-3.  The roll-off containers and drums containing RI soil also
would be treated with the excavated soil.

Alternative 8C-5:  In-Situ Vacuum Extraction

Capital Cost: $385,600
O & M Cost: none
Present Worth Cost: $385,600
Time to Implement: 4 years

Site preparation would be performed as in Alternative  SC-3.
However, the soil is left in place undisturbed, therefore no
excavation would be required.  This alternative involves the
installation of vacuum extraction wells over the contaminated
soils.  Each well would have a maximum depth of 10 feet.  The
vacuum wells would be connected via a pipe system to a
skid-mounted high volume vacuum pump.  The vacuum would pull air

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                               14

through 'the contaminated soils,  within a radius of approximately
20 feet from the wells, depending on soil composition and
volatility of the contaminant.   The air containing the stripped
VOCs from the soil would be fed through a condenser to recover
the free product and moisture,  and then through an emissions
control system, i.e., a vapor phase carbon adsorption system.  The
condensed product would be drummed and transported to an off-site
treatment and disposal facility (most likely an incinerator).
The roll-offs and drums containing soil would also be treated
on-site via this technology by using a one-pipe system within the
drum connected to a vacuum pump.   The treated soils would be used
on-site for backfilling and regrading.

GROUNDWATER

Alternative GW-l:  No Further Action

Capital Cost: none
0 & M Cost: $28,400
Present Worth Cost: $464,400
Time to Implement: 1 year

This alternative includes the use of existing wells to conduct a
long-term groundwater sampling program which would monitor the
migration of contaminants of concern in the aquifer.  A total of
ten wells, including existing upgradient, on-site and
downgradient wells, would be utilized in order to sample the
groundwater from the shallow to deeper portions of the aquifer
and to track contaminant migration off-site.  Regular five-year
reviews would be performed to assess the need for additional
remedial actions.  Under this alternative, it would take 100
years to achieve groundwater remediation.

Alternative GW-2:  Pumping/Pretreatment/Air Stripping/Carbon
Adsorption/Reinjection; Pumping at the Site Boundary  (0.2 mgd)

Capital Cost: $214,800
O & M Cost: $378,700
Present Worth Cost: $3,350,500
Time to Implement: 3 years

This alternative includes the installation of three extraction
wells downgradient of the Site in order to extract 0.2 million
gallons per day (mgd) of groundwater from the site contaminant
plume.  This groundwater would be.piped to the Old Bethpage
Landfill groundwater treatment system for treatment and disposal.
The Landfill groundwater treatment system is currently under
construction and scheduled to be completed in 1991.  The 0.2 mgd
is the maximum allowable input from the Claremont site to fhe
Landfill pump and treatment system due to design limitations of
the Landfill system.  The treated effluent would be reinjected
into the aquifer through a recharge basin being constructed as

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                               15

basin being constructed as part of the Landfill system.   This
flow rate is below the modeled maximum pumping rate of 1.9 mgd
estimated for removal and treatment of the Claremont contaminant
plume.  (The original estimate of the volume of contaminated
groundwater to be treated was much less than the current
estimate.)  In addition, the landfill treatment system is only
planned to operate for 10 years based upon the time estimated for
remediation to be completed for the Old Bethpage plume.
Long-term monitoring using the new extraction wells and existing
wells would be performed for 30 years in order to monitor any
continued migration of remaining contamination in the
groundwater, both during and* after the operation of the landfill
treatment system.

Alternative 6W-3A:  Pumping/Pretreatment/Air Stripping/Carbon
Adsorption/Reinjaction; Pumping at the Leading Edge of the Plume
(1.9 mgd)

Capital Cost: $4,044,700
O & M Cost: $1,622,900
Present Worth Cost: $28,978,000
Time to Implement: 3 years

In this alternative, three extraction wells would be installed
downgradient of the site on the Bethpage State Park property in
order to capture the entire site contaminant plume.
Approximately 1.9 mgd would be pumped to an on-site treatment
facility.  The treated groundwater would be pumped to a discharge
system for reinjection to the aquifer via three reinjection
wells.  The siting of the extraction wells would be completed
during the design phase based* on technical criteria.

The groundwater treatment facility would consist of two major
processes: pretreatment to remove metals (iron, manganese,
arsenic, and thallium) and air strippers followed by a carbon
adsorption system to remove volatile and semivolatile organics.
The pretreatment system would be designed to effectively reduce
the metal concentrations in the groundwater below the federal and
New York State Groundwater Standards.  This pretreatment system
would consist of a metals precipitation system and dual media
pressure filter.  The resulting sludge would require off-site
treatment and disposal.

Two air strippers in series followed by liquid phase carbon
adsorption would be used to lower the levels of organic
contamination below the state groundwater standards.
Approximately 95 to 99 percent of the volatile organics would be
removed by air stripping.  The stripped groundwater would be
pumped to a two-stage liquid phase carbon adsorber for removal of
the remaining volatiles and BEHP, and phenol.  The volatile
organic emissions from the air stripping would be adsorbed on a
vapor phase activated carbon system in order to meet air quality

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                               16

standards.  Spent carbon would be removed for off-site
regeneration or incineration,  thus destroying all organic
contaminants.  Two treatment trains (parallel systems for
treating the groundwater) rated at 660 gallons per minute (gpm)
each would be required.

Environmental monitoring would be required during the life of the
treatment plant operation (i.e.,  30 years).  Air emissions would
be monitored to confirm compliance with the air discharge limit.
Groundwater samples would be taken every six months to monitor
groundwater contamination migration and the effectiveness of
remediation.  Under this alternative it is estimated to take 62
years to achieve remediation^of the groundwater plume.

Alternative GW-3B:  Pumping/Pretreatment/Air Stripping/Carbon
Adsorption/Reinjaction; Pumping at the site Boundary and
Downgradient (1.0 mgd)

Capital Cost: $4,936,000
O & M Cost: $1,100,400 (first;-t^n years)
            $701,900  (next six years)
Present Worth Cost: $15,620,400
Time to Implement: 3 years

In this Alternative, two extraction wells would be installed at
the boundary of the Site to capture the most contaminated
groundwater.  Additional extraction wells would be located
downgradient from the Site to capture the off-site migrating
plume.  Sufficient information exists at this time to locate the
on-site wells which would pump the concentrated contaminant plume
for treatment, however additional information would be required
before the downgradient extraction wells could be sited.  These
information needs include information regarding the actual extent
of the downgradient plume, as well as potential impacts the Old
Bethpage Landfill may have on this plume once it begins
operation.  Additional sampling would be conducted to obtain this
information.  For these reasons it is likely that the on-site
extraction wells would be installed (0-2 years) prior to the off-
site and downgradient wells.

During the first phase extraction wells would be installed at the
site boundary, requiring two treatment trains each rated at 250
gpd to treat the concentrated groundwater plume.  During the
second phase the downgradient groundwater plume would be
extracted, requiring the installation of two additional treatment
trains also rated at 250 gpd.'  The treatment trains would be
located on-site and operated in parallel.  The extracted
groundwater would be treated as in Alternative 3A.  The on-site
and off-site extraction wells would treat 1 mgd for approximately
10 years.  After 10 years it is anticipated that the downgradient

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                                17


plume would be significantly treated.  Thereafter, on-site
extraction and treatment of 0.5 mgd would continue for
aproximately six additional years.

Implementing this remedy in two phases would provide increased
overall efficiency and flexibility.  This optimized extraction
and treatment system design would be better able to address the
remediation of the Claremont site plume.

Alternative GW-5A:  Pumping/Pretreatment/UV-Chemical
Oxidation/Reinjection; Pumping at the Leading Edge of the Plume
(1.9 mgd)

Capital Cost: $4,088,900
O & M Cost: $1,108,000
Present Worth Cost: $21,121,100
Time to Implement: 3 years

This remedial alternative is%similar to Alternative GW-3A except
that a chemical oxidation process rather than air
stripping/adsorption process would be used to remove the volatile
and semivolatile organics in the groundwater.  An ultraviolet
light-hydrogen peroxide oxidation system is selected as the
representative process to treat the contaminated groundwater.
This oxidation system would employ a combination of hydrogen
peroxide (H202) and ultraviolet  (UV) light to chemically oxidize
the organic contaminants in the groundwater to carbon dioxide,
water and chlorides.  Multiple units would be required.  The
treated groundwater would have organic concentrations below state
and federal standards.  The time necessary to achieve remediation
would be 62 years.           *

Alternative GW-5B:  Pumping/Pretreatment/UV-chemical
Oxidation/Reinjection; Pumping at the Site Boundary and
Oowngradient  (1.0 mgd)

Capital Cost: $4,069,800
0 & M Cost: $1,008,600 (first ten years)
            $656,000 (next six years)
Present Worth Cost: $13,902,300
Time to Implement: 3 years

Groundwater extraction, pretreatment, and reinjection would be
accomplished as in Alternative GW-3B.  The UV-H202 system would
operate as in Alternative GW-5A except that smaller treatment
units would be used.  The time necessary to achieve groundwater
remediation would be 16 years-.

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                               18


BUILDING

Alternative BD-1:  No Further Action

Capital Cost: $8,800
O & M Cost: $2,100 per year
Present Worth Cost: $41,100
Time to Implement: 1 month

The No Action alternative provides the baseline against which
other alternatives can be compared.  It would result in leaving
the contaminated dust, asbestos insulation, and contaminated
water in floor drains and condensers intact in the building.  The
only additional security measure implemented to completely seal
the building would be waterproofing of the building ceiling.
A long-term maintenance program,  including site inspections,
would be implemented in order to ensure that the building is
completely sealed and is not accessible to the public in the
future.

Alternative BD-2:  Building Decontamination

Capital Cost: $186,200
O & M Cost: none
Present Worth Cost: $186,200
Time to Implement: 6 months

The inside contaminated surfaces of the building (i.e., walls,
floors, and hoods) would be decontaminated using dusting,
vacuuming and wiping procedures.   In addition three dust
collectors on the roof would be emptied.  The collected dust
would be transported to an off-site EPA-permitted treatment and
disposal facility.  The contaminated water in the floor drains
and condensers also would be removed and disposed of off-site.

UNDERGROUND STORAGE TANKS
                             »
Alternative T-l:  Mo Further Action

Capital Cost: $2,600
O & M Cost: $2,200 per year
Present Worth Cost: $64,300
Time to Implement: 1 month

Under this alternative the underground tanks and contents would
be left in place.  The large amounts of hazardous materials
contained in the tanks would continue to constitute a potential
source of soil and groundwater contamination.  A monitoring
program using the existing monitoring wells would be established
to detect the movement of these compounds  into the groundwater.

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                                19

Alternative T-2:  Removal and Off-Site Treatment/Disposal

Capital Cost: $336,300
O & M Cost: none
Present Worth Cost: $336,300
Time to Implement: 6 months

This alternative entails excavation of overburden soils, pumping
of tank contents, tank cleaning, removal of tanks and associated
equipment, off-site disposal/treatment of tanks, equipment and
liquid waste, and backfilling with clean soil.  A portion of the
wastes (tank content) could be reused if practical.

The underground tanks and associated piping would be drained and
cleaned of any residual sludge.  Tanks would be hoisted and
subsequently loaded on trucks and hauled off-site for disposal.
Other components of the tank farm, such as pumps, concrete pads,
and the pumphouse, would be demolished and transported off-site
for disposal.  At the disposal facility, the steel tanks would be
retested for hazardous waste contents.  Nonhazardous tanks would
either be sold for scrap or landfilled, depending on the extent
to which they could be decontaminated.  Hazardous tanks and tank
contents would be disposed of at an off-site EPA-approved
hazardous waste treatment and disposal facility.

Contaminated soils discovered during tank excavation would be
stockpiled in roll-off containers and subsequently transported to
an off-site EPA-permitted treatment and disposal facility.
Alternately, the contaminated soils could be treated on-site
using the low temperature thermal treatment unit.  After
treatment, the soils would no longer be deemed to contain listed
RCRA hazardous constituents because the soils would be treated to
below health-based levels and would be treated in accordance with
the treatment standards required by RCRA Land Disposal
Restrictions (LDRs).  Because the soils would no longer contain
any listed RCRA hazardous constituents above health-based levels,
they would not be subject to regulation under Subtitle C of RCRA
and may be used to backfill the excavated areas on-site.

Sampling of the soils underlying the tank farm would be conducted
as part of this alternative to further delineate the nature and
extent of soil contamination within this area and to assess
effectiveness of the remedy.

A description of the remedial alternatives retained and evaluated
in detail is provided below.

SUMMARY OF COMPARATIVE ANALYSIS OF ALTERNATIVES
                             *
EPA has developed nine criteria in "The Feasibility Study:
Detailed Analysis of Remedial Action Alternatives" (OSWER.
Directive 9355.3-01) to evaluate potential alternatives to ensure

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                               20

all important considerations are  factored into remedy selection
decisions.  The major objective of this section is to .evaluate
the relative performance of the alternatives with respect to the
criteria so that the advantages and disadvantages associated with
each cleanup option are clearly understood.

The evaluation criteria are noted and explained below.

  o  Overall protection of human  health and  the environment
     addresses whether or not a remedy provides adequate
     protection and describes how risks posed through each
     exposure pathway (based on a reasonable maximum exposure
     scenario) are eliminated, reduced, or controlled through
     treatment, engineering controls, or institutional controls.

  o  Compliance with applicable or relevant  and appropriate
     requirements (ARAR's) addresses whether or not a remedy
     would meet all of the applicable or relevant and appropriate
     requirements of other federal and state environmental
     statutes and requirements or provide grounds for invoking a
     waiver.

  o  Long-term effectiveness and  permanence  refers to the ability
     of a remedy to maintain reliable protection of human health
     and the environment over time, once cleanup goals have been
     met.  It also addresses the  magnitude and effectiveness of
     the measures that may be required to manage the risk posed
     by treatment residuals and/or untreated wastes.

  o  Reduction of toxicity. mobility, or volume through treatment
     is the anticipated performance of the treatment
     technologies, with respect to these parameters, a remedy may
     employ.

  o  Short-term effectiveness addresses the  period of time needed
     to achieve protection and any adverse impacts on human
     health and the environment that may be  posed during the
     construction and implementation periods until cleanup goals
     are achieved.

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

  o  Cost includes estimated capital and operation and
     maintenance costs, and net present worth costs.

  o  State acceptance indicates whether, based on its review of
     the RI/FS and Proposed Plan, the State  concurs with,
     opposes, or has no comment on the selected remedy at; the
     present time.

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                                21


  o  Community acceptance refers to the public's general response
     to the alternatives described in the Proposed Plan and the
     RI/FS reports.

ANALYSIS

Comparison Among Soil (SC) Alternatives

  o  Overall Protection of Human Health and the Environment

Alternative SC-1 does not meet the remedial objectives, thus it
is not protective of human health and the environment.  As a
result of this alternative, the groundwater would continue to be
contaminated directly or indirectly by the soil (groundwater
percolating through soil into the groundwater) for some unknown
period.  Alternatives SC-3, SC-4 and to some extent SC-5 would
meet the remedial objective of protecting the groundwater from
the soil source by achieving the cleanup levels in soils.
Therefore, alternatives SC-3, SC-4 and SC-5 (to a lesser extent)
are protective of human health and the environment.

  o  Compliance with ARARs

All technologies proposed for use in Alternative SC-3 through
SC-5 would be designed and implemented to satisfy all ARARs.
federal and state regulations dealing with the handling and
transportation of hazardous wastes to a fully EPA-approved off-
site treatment facility would be followed.  Under Alternative SC-
4, treated soils would not longer constitute a potential source
of groundwater contamination and could therefore, be redeposited
on-site in compliance with all RCRA standards.

  o  Long—Term Effectiveness and Permanence

Alternative SC-1 would only monitor the migration of the
contaminants and would not provide treatment or containment.
Therefore, it would not provide effective or permanent long-term
protection of groundwater at the Site.

Alternatives SC-3, SC-4 and SC-5 have similar abilities to
mitigate the risks through the removal and treatment of site
contaminants to meet the required cleanup levels.  Alternatives
SC-3 and SC-4 are highly effective, since they effectively can
remove the contaminants from the soil.  Alternative SC-5 is
intended to have a similar ability to mitigate soil
contamination, however due to the technical limitations of the
in-situ process, SC-5 may not leisure complete remediation of
soils.  The technical limitations inherent in this technology
include decreased efficiency for very shallow contamination, and
because of the possible need for supplementation with other
treatment methods.

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                               22
  o  Reduction in Toxicity. Mobility,  or Volume

Alternative SOI would provide a very  slow and gradual reduction
in toxicity through rainfall percolation,  but there would be no
treatment to reduce the mobility, toxicity or volume of
contamination in a reasonable timeframe.  It would provide no
reduction in contaminant mobility or volume.

Alternatives SC-3, SC-4, and'SC-5 are  similar in that each would
result in significant reductions in the toxicity, mobility, and
volume of the treated material through treatment.  Material
toxicity would be reduced by thermal destruction of contaminants
in Alternatives SC-3 and SC-4 and by off-site treatment of the
condensed organic product in SC-5.  Alternative SC-3 would
provide the greatest degree ofttreduction in toxicity of the
contaminants followed by SC-4 and SC-5.

  o  Short-Term Effectiveness

The implementation of Alternative SC-1 would not result in
additional risk to the community during implementation, since no
action would be taken. Alternatives SC-3,  SC-4, and SC-5 include
activities such as contaminated soil excavation and off-site
transport or on-site treatment that could potentially expose
residents to volatilized contaminants  and contaminated dust.
Engineering controls and other measures (e.g. restricting access
to the Site to authorized personnel only)  would effectively
eliminate any significant impact these activities would have on
nearby residents.  Alternative SC-5 includes in-situ treatment of
contaminated soils, so exposure risks  to residents from
excavation is much less of a concern for this alternative than
SC-3 and SC-4.  Under alternatives SC-4 and SC-5, proper air
emission control units would .be installed to minimize the
potential for public health exposures  because of low-level
emissions from the on-site treatment units.

Alternative SC-1 would result in a lower overall risks to workers
than other alternatives, since^subsurface soil is not disturbed.
Alternatives SC-4 and SC-5 provide treatment on-site, thereby
reducing potential risks to residents  along transportation
routes.  Alternatives SC-3, SC-4, and  SC-5 would present a
potential for worker exposure to volatilized contaminants during
waste excavation and/or handling.  To  minimize and/or prevent
such exposures, use of personal protection equipment would be
necessary.

SC-1 would be implemented in approximately one month.
Alternatives SC-3, SC-4 and SC-5 would be implemented in about
3.5, 3.5 and 4 years, respectively.

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                                23


  o  Implementability

Components of Alternatives SC-1, SC-3, SC-4 and SC-5 would
utilize relatively common construction equipment and materials.
Little construction difficulty would be encountered with any of
the alternatives.  However, Alternative SC-1 would be the easiest
to implement.

The technologies proposed for use in the alternatives are proven
and reliable in achieving the specified process efficiencies and
performance goals.  Low temperature thermal enhanced
volatilization and in-situ vacuum extraction have been
successfully tested at other Superfund sites.  However, there is
a greater degree of uncertainty regarding the achieving of
cleanup levels using in-situ vacuum extraction, since this
technology only has been utilized on a limited full-scale basis
at similar contaminant concentration levels.

  o  Cost

The total present worth costs *for the alternatives evaluated
range from $385,600 (in-situ vacuum extraction) to $5,000,000
(off-site treatment and disposal).  The present worth calculation
uses a 5% discount rate, and a 30-year operational period in the
case of SC-1.  All other source control alternatives would not
require any operation and maintenance cost.  Therefore, present
worth for these alternatives  (SC-3, SC-4 and SC-5) would be the
same as the capital cost.  SC-4 provides the same protection as
Alternative SC-3 at a fraction of the cost  ($700,000 versus
$5,000,000).  Although Alternative SC-5 is significantly less
expensive than SC-3 and SC-4, it may not provide the same level
of protection.

  o  State Acceptance

NYSDEC concurred with the selection of Alternative SC-4.

  o  Community Acceptance

The community have expressed support for the alternative selected
for the remediation of the soils.

Comparison of the Groundwater (GW) Alternatives

  o  Overall Protection of Human Health and the Environment

The no-action alternative would not protect human health and the
environment.  Existing contamination would continue to degrade
the aquifer and migrate off-site.

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                               24


Alternative GW-2 would not ensure protection of the health of
future users of the aquifer nor would it improve the overall
quality of the aquifer or prevent the continued migration of
contamination.

Each of the alternatives GW-3A, GW-3B,  GW-5A and GW-5B would be
significantly more protective than GW-1 or GW-2, since they would
reduce the toxicity, mobility, and volume of contaminants in the
aquifers.  Each treatment alternative considered would equally
protect human health and the environment; however,  the amount of
time required to achieve the ARARs varies greatly among
alternatives.

  o  Compliance with ARARs

Alternatives GW-1 and GW-2 would result in contaminant
concentrations remaining above ARARs (for drinking water or
protection of the groundwater resources) for a long period of
time (estimated at 100 years).

Alternatives GW-3A, GW-3B, GW-5A and GW-5B would be designed to
achieve all drinking water standards as well as those required
for groundwater protection in the treated water stream which is
to be reinjected.  Each of the^e alternatives would be capable of
providing the required contaminant removal levels.   Because
experience with UV-chemical systems is limited, its effectiveness
is slightly less certain but considered achievable.  Each of the
alternatives would comply with federal and state air emission
standards as well as regulations for the handling and disposal of
the generated wastes (e.g. spent carbon).

  o  Lona-Term Effectiveness and Permanence

Alternative GW-1 does not provide treatment but would attempt to
restrict usage of contaminated groundwater.  Alternative GW-2
provides short-term treatment, but would not restore the
contaminated aquifer for its best beneficial future use.

Alternatives GW-3A, GW-3B, GW-5A, and GW-5B all reduce the
potential risks associated with groundwater ingestion by
extracting, treating, and recharging the treated groundwater to
remove contaminants from the aquifer.  The time required to
achieve these risk reductions depends on the effective extraction
rates from the aquifer and limitations on extraction system
placement due to the large area of the contaminant plume.
Long-term effectiveness of each system is dependent on monitoring
and maintenance of the treatment system.

Alternatives GW-l and GW-2 would take approximately 100 years to
achieve the remedial action objectives.  Alternatives GW-3A and
5A would theoretically achieve the remedial action objectives in

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                                25

62 years, whereas GW-3B and 5B would achieve the remedial action
objectives in approximately 16 years.

Proper air pollution control measures would be established under
alternatives GW-3A and GW-3B to offset potential risks from the
air stripper(s), while no air pollution control measures are
deemed necessary for alternatives GW-5B and 5A.  Alternatives
GW-3A and GW-3B require the disposal of more spent carbon than
GW-5A and GW-5B, since carbon- adsorption is used.

  o  Reduction in Toxicity, Mobility, or Volume

Alternative GW-1 would very slowly and gradually reduce the
toxicity of contaminants through dilution but there would be no
treatment to reduce toxicity, mobility or volume.  Alternative
GW-2 would reduce the toxicity and volume of contaminants more
rapidly than GW-l.  Neither Alternative GW-l nor GW-2 would
permanently reduce the mobility of the contaminants.  For
alternative GW-2, the off-site portion of the contaminated
groundwater plume would continue to migrate downgradient, and
reduction of toxicity, mobility and volume would be achieved only
by natural attenuation.

Alternatives GW-3A, GW-3B, GW-5A and GW-5B would reduce the
toxicity, mobility, and volume of contaminants in the aquifers to
a greater extent than GW-l and GW-2.  Alternatives GW-3B and 5B
would reduce the toxicity, mobility, and volume to a greater
extent and at a much faster rate than the other alternatives.
Alternatives GW-3A and GW-3B would use air stripping and carbon
adsorption to remove the contaminants, while GW-5A and GW-5B
would oxidize most of the organic compounds.

  o  Short-Term Effectiveness^

Implementation of Alternative GW-l would result in no additional
risk to the community during remedial activities, since no
treatment would occur.  Alternative GW-2 could present additional
risks to the community resulting from the installation of the
extraction wells and pipelines for transportation of contaminated
groundwater. Alternatives GW-3A, GW-3B, GW-5A and GW-5B include
excavation activities, installation of the collection and
reinjection system, and construction of the treatment plant which
could result in potentially exposing residents to volatilized
contaminants and contaminated dust.  The treatment plant would be
constructed on-site.  Proper ei»girieering controls would ensure
that the impact of such activities would be insignificant.  All
alternatives except Alternatives GW-l and GW-2 would provide a
process residual requiring proper handling and disposal.

Alternative GW-l would result in no additional risk to workers,
and GW-2 would result in a lower overall worker risk than other
alternatives because of the limited soil disturbance activities.

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                               26

Personal protection equipment would be used under alternatives
GW-3A, GW-3B, GW-5A and GW-5B to minimize the worker's potential
exposure to volatilized contaminants during installation of the
collection, treatment, and recharge systems.

GW-1 would be implemented in approximately one year.  Each of the
remaining alternatives would be implemented in about 3 years.

  o  Implementability
                              *'
Alternative GW-l would be easily implemented. Alternative GW-2
would require institutional management to maintain and operate
the pumping system and to coordinate with the Old Bethpage
Landfill treatment system.  Alternatives GW-3A, GW-3B, GW-5A and
GW-5B would utilize relatively common construction equipment and
materials.  Little construction difficulty would occur with any
of the alternatives.

The air stripping and carbon adsorption technologies proposed for
use in Alternatives GW-3A and GW-3B are proven and reliable in
achieving specified process efficiencies and performance goals.
While there has been limited experience with UV-chemical
oxidation,  it has been successful in several groundwater
treatment facilities.

All proposed technologies are readily available from a number of
sources, with the exception of UV-chemical oxidation.

Alternatives GW-3A, GW-3B, GW-5A, and GW-5B would require
institutional management of the operation and maintenance of the
treated groundwater reinjection systems.  Siting the treatment
facility would not present any problems as there is enough space
available on-site.  Location of associated off-site facilities
(e.g. piping, pumps, extraction wells and reinjection wells)
would be more complex as both technical and land use factors
would be considered.

Off-site disposal facilities are available for the disposal of
the pretreatment sludge and spent carbon generated from
Alternatives GW-3A, GW-3B, GW-5A and GW-5B.

  o  Cost

The present worth costs of all GW.alternatives ranged from
$464,400 (GW-1) to $28,987,000 (GW-3A).  Alternative GW-1 would
be least expensive followed by GW-2, GW-5B, GW-3B, GW-5A and
GW-3A.  Of the alternatives providing complete remediation of the
groundwater contamination, Alternative GW-3B provides the lowest
present worth cost, $15,620,400.

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                                27
  o  State Acceptance

NYSDEC concurs with the selection of Alternative GW-3A for
groundwater treatment.

  o  Community Acceptance

The community have expressed support for the alternative selected
for the remediation of the groundvater.

Comparison of Building Alternatives (BD)

  o  Overall Protection of Human Health and the Environment

In Alternative BD-1, hazardous material would be left in the
building.  Human health and the environment remain protected only
as long as building security could be effectively enforced and
building integrity maintained.  Alternative BD-2 would remove all
hazardous material from the building, so it would be fully
protective of human health and the environment.  In addition,
Alternative BD-2 allows for future reuse of the building.

  o  Compliance with ARARs

Alternative BD-1 would not contravene any ARARs, since no action
would be taken.  Alternative BD-2 would comply with the ARARs
including RCRA land disposal restrictions as well as those
regulations related to the transport of the wastes to an off-
site facility.  The off-site treatment facility would be fully
EPA-permitted and therefore meet applicable regulations.

  o  Long-Term Effectiveness and Permanence

Alternative BD-1 would not alter conditions within the building;
hazardous materials would remain in the building.  Public
protection would rely on maintaining building security which
might be difficult to enforce.  The building could not be used
for any purpose.  Alternative BD-2 would remove all hazardous
materials from the building for off-site treatment and disposal
so that long-term exposure risks from the building would be
eliminated.  Painting and sealing the building  (Alternative BD-2)
would provide additional protection and would allow for
unrestricted use of the building in the future.

  o  Reduction in Toxicity. Mobility or Volume

Alternative BD-1 would provide no reduction in toxicity or volume
of contaminants; mobility is not an issue since the building is
self-contained.  Alternative BD-2 would provide for complete
reduction in toxicity and volume, since all contaminated material
would be removed from the building.

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                               28
  o  Short-Term Effectiveness

Implementation of BD-1 would result in no additional risks to the
community or the environment as long as building security and
integrity could be maintained.  Alternative BD-2 involves removal
and transport of the contaminants from the building, so there
would be some minimal public exposure risks as well as
environmental impacts from potential waste spills resulting from
possible transport accidents during remedial activities.  Worker
exposure risks would be minimized through the use of personal
protection equipment.  Long-term maintenance would continue
indefinitely for Alternative BD-1.  Building decontamination,
Alternative BD-2, could be accomplished in approximately 3
months.

  o  Implementability

Both alternatives are readily ^Lmplementable; neither involves any
major construction activities.  Methods and services for building
decontamination are technically feasible and readily available.
Alternative BD-1 would require institutional management i.e., a
long-term building maintenance program, whereas Alternative BD-2
would not require any long-term management.

  o  Cost

The present worth costs for Alternatives BD-1 and BD-2 are
$41,100 and $186,200, respectively.

  o  State Acceptance

NYSDEC concurs with the preferred building alternative selected.

  o  Community Acceptance

The community have expressed support for the alternative selected
for the remediation of the building.

Comparison of the Underground Tank  (T) Alternatives

  o  Overall Protection of Human Health and the Environment

Alternative T-l would not protect human health and the
environment as the threat of soil and groundwater contamination
would not be reduced.  The excavation and removal of contaminated
tanks and their contents from the Site (T-2) would significantly
reduce the potential human health and environmental risks
associated with potential leaking of contaminants from tanks into
the .soil and groundwater.

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                               29
  o  Compliance With ARARs

Alternative T-l would not facilitate compliance with groundwater
ARARs,.as a continual source*of contamination would not be
removed.  The disposal of the underground tanks (T-2) would
eliminate the source of contamination and would satisfy state and
federal ARARs.  The tanks wastes would be removed, transported,
and disposed of in accordance with all regulations.  Contaminated
soils would be disposed off in accordance with all applicable
state and federal ARARs.  Soils would be transported to an off-
site EPA-permitted treatment and disposal facility; or in the
alternative, the soils could be treated on-site using the low
temperature thermal treatment unit.  After treatment, the soils
would not longer be deemed to contain listed RCRA hazardous
constituents because it would be treated to below health-based
levels and would be treated in accordance with the treatment
standards required by RCRA Land Disposal Restrictions.

  o  Lona-Term Effectiveness and Permanence

Under Alternative T-l, the tanks and their associated hazardous
wastes would remain as a potential source of soil and groundwater
contamination.  Alternative T-2, excavation and removal of the
underground storage tanks, tank debris, and highly contaminated
soil from the Site, would reduce the potential human health and
environmental risks associated with the tanks' potential for
leaking contaminants into the soil and groundwater in the future.

  o  Reduction of Toxicitv. Mobility or Volume

No significant reduction of toxicity, mobility or volume would
result from the implementation of the no-action alternative.
Alternative T-2, excavation and off-site treatment, would result
in a permanent reduction of toxicity, mobility and volume.  The
wastes would be completely removed and either destroyed at the
treatment facility or reused if practical.

  o  Short-Term Effectiveness

Alternative T-l would result in no additional risk to the
community during implementation.

The potential public health threats to workers and area residents
associated with the implementation of Alternative T-2 include:
direct contact of workers with tank contents and potentially
contaminated soils; inhalation of fugitive dust, organic vapors,
and emissions generated during construction and excavation
activities; and improper handling of soil and hazardous liquids.
Several steps would be taken to minimize these threats including:
Site access would be restricted to authorized personnel only;
and, dust control measures such as wind screens and water sprays

-------
                               30

would be used to minimize fugitive dust emissions.

The risk to workers during excavation would be minimized by the
use of adequate personal protection equipment to prevent direct
contact with potentially contaminated soil, liquids,  and
inhalation of fugitive dust and volatile organic compounds.

Other potential short-term impacts contemplated as part of T-2
would be an increase in traffic and noise pollution resulting
from hauling soils (as necessary), hazardous liquids, and tanks
to an off-site treatment facility, as well as the traffic
associated with transporting new soil for backfill to the Site.
Transportation of excavated hazardous liquids might introduce
short-term risks with the possibility of spillage along the
transport route and potential exposure of the public to hazardous
material.  A spill contingency plan would be developed to address
and minimize the likelihood and potential impact of this
occurrence.  The actual remediation period for this alternative
is estimated to be 8 weeks.

  o  Implementab i1ity

Alternative T-l is easily implementable, since no action would be
taken.  All the components of Alternative T-2 are well developed
and commercially available.  The contained tanks and related
wastes would have to undergo a series of analyses prior
to acceptance for treatment at the EPA-permitted off-site
facility.  Sufficient land is available at the Site for
mobilization and temporary storage of the excavated soil and
materials awaiting pre-transport decontamination.  Excavation,
treatment tank decommissioning, transportation to an off-site
treatment facility, solid and liquid waste disposal, and
restoration of the Site can be performed without any major
difficulties.

  6  Cost                     M

The total present worth cost of Alternative T-l is $64,300.  The
total present worth cost of Alternative T-2, which represents the
estimated construction cost for the eight week remediation
program, is estimated at $336,300.  Operation and maintenance
costs have not been included in the cost estimate since the
duration of the remediation program is less than one year.

  o  State Acceptance

NYSDEC concurs with the selection of underground tank alternative
T-2.

  o  Community Acceptance

The community has expressed support for the alternative selected

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                               31

for the remediation of the underground tanks.

SELECTED REMEDY

The preferred alternative will achieve substantial risk reduction
through a combination of source control alternatives SC-4 (low
temperature enhanced volatilization of soil contaminants) and T-
2 (tank removal and off-site treatment),  with active restoration
of the groundwater (GW-3B), and building decontamination (BD-2).

The preferred alternative achieves this risk reduction more
quickly and at substantially less cost than the other options.
Therefore, the preferred alternative will provide the best
balance of trade-offs among alternatives with respect to the
evaluating criteria.  Based on the information available at this
time, EPA and the NYSDEC believe that the preferred alternative
will be protective of human health and the environment, will
comply with ARARs, will be cost effective, and will utilize
permanent solutions and alternative treatment technologies or
resource recovery technologies to the maximum extent practicable.
The remedy also will meet the statutory preference for the use of
treatment as a principal element.

STATUTORY DETERMINATIONS

1. Protection of Human Health and the Environment

The selected remedy is considered fully protective of human
health and the environment.  The treatment of the contaminated
soils through the low temperature enhanced volatilization process
will remove the organic contaminants from the soil.  When
combined with the removal of the underground tanks, it will
result in the elimination of both long-term sources of
groundwater contamination.  The extraction and treatment of the
contaminated groundwater using^air stripping and carbon
adsorption will provide excellent protection of both human health
and the environment.  Decontamination of the building will ensure
that public health is protected.

2. Compliance with ARARs

The soil portion of the remedy (SC-4: excavation and on-site
treatment of the contaminated soils) will comply with all action-
specific ARAR's.  Contaminated soils will be treated to health-
based levels.  Since the treated soils no longer will constitute
a source of groundwater contamination, they will be redeposited
on-site in compliance with all RCRA standards.  The groundwater
portion of the selected remedy (GW-3B: extraction and treatment
of the contaminant plume) will comply with all related ARARs
including NY Groundwater Quality Standards and Federal Maximum
Contaminant Levels.

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                               32

The building decontamination (BD-2)  and underground tank removal
(T-2) will comply with all ARAR's.   The off -site treatment
facility will be fully RCRA permitted and,  therefore,  will meet
all applicable regulations.  Wastes  will be treated using
specific technologies or specific treatment levels. The remedy
will comply with regulations including RCRA Standards Applicable
to Owners and Operators of TSD Facilities,  RCRA Standards
Applicable to Transport of Hazardous Wastes, NY Air Quality
Standards, NY Hazardous Waste Manifest System Rules, and NY
Hazardous Waste Treatment Storage and Disposal Facility
Permitting Requirements.

A summary of ARARs associated with the selected remedy is
presented in Table 13.

3. Cost Effectiveness

The selected remedy is cost effective in that it provides overall
effectiveness proportional to its cost.  The total capital and
present worth costs of the remedy are $6,200,000 and $16,800,000,
respectively.  In proportion to the  total capital cost, 11 per
cent is attributed to the soil portion;  80 per cent to the
groundwater portion; and the remaining 9 per cent to the building
and underground tank portion.  The cost of the soil component is
higher than the in-situ vacuum, extraction option; however, low
temperature treatment provides complete certainty with regard to
efficiency, at a fraction of the cost associated with the off-
site treatment option.  Likewise, although the cost of the air
stripping/carbon adsorption is higher than the UV/oxidation, air
stripping/ carbon adsorption provides a higher degree of certainty
that all groundwater contaminants will be removed.

4. Utilization of Permanent Solutions and Alternative Treatment
Technoloies to the Maximum Extent Practicable
The selected remedy utilizes permanent solutions and treatment
technologies to the maximum extent practicable.  Of those
alternatives which are protective of human health and the
environment, and comply with ARARs, the selected remedy best
balances the goals of long-term effectiveness and permanence,
reduction of toxicity, mobility or volume achieved through
treatment, short-term effectiveness, implementability, cost, and
also achieves the statutory preference for treatment as a
principal element and has state and community acceptance.
                              •   •
After the soil is treated and the underground tanks are removed,
the potential for future releases of waste to the environment
will be eliminated.  The indirect and direct risks posed by the
soil and tanks as a continued source of groundwater contamination
will be eliminated.  This action, in conjunction with the
groundwater extraction and treatment component, will restore the
aquifer to its most beneficial use and will meet all federal and

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                                33

state standards.

No short-term adverse impacts and threats to human health and the
environment are foreseen as the result of implementing the
selected remedy.  However, to minimize and/or prevent worker
exposure to contaminants, personal protection equipment will be
used.

The selected remedy will require construction of on-site soil and
groundwater treatment facilities.  No technological problems
should arise as all the treatment technologies are well
established, readily available and possess a proven track record.
                              <
5. Preference for Treatment as the Principal Element

The selected remedy fully satisfies this criterion for the source
of contamination (soil and underground tanks), groundwater, and
building contamination which are considered the principal threats
at the Site.  Therefore, the statutory preference for remedies
that employ treatment as a principal element is satisfied.

DOCUMENTATION OF SIGNIFICANT CHANGES

The Proposed Plan for the Claremont Polychemical site was
released to the public on August 24, 1990.  The Proposed Plan
identified Alternative SC-4 combined with Alternatives GW-3B,
BD-2 and T-2 as the preferred alternative.  EPA reviewed all
written and verbal comments submitted during the public comment
period.  Upon review of these comments, EPA determined that no
significant changes to the selected remedy, as it was originally
identified in the Proposed Plan, are necessary.

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APPENDIX A.  FIGURES

-------
                 V-  y^'-x\';V/.'**J
    .o^
NASSAU COUNTY
FIREMEN'S TRAINING
CENTER	\/   j • /: '••;.
-3	T	=——J\ 7...-, .il/. ."
                      • ^
                      s.

                      >
   SCALE IN FEET

R • RECHARGE BASIN
                           ENVIRONMENTAL PROTECTION
                                AGENCY
                          CLAREMONT POLYCHE^CAL FACILITY
            FIGURE 1

          SITE LOCATION
                          E3A5CO SERV^CJI

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                                                                         U.S. ENVIRONMENTAL rflOUCTION
                                                                                     AGENCY
                                                                          ClAflEUONT PtXTCHfMICA! SITE
KALI
          •4   104
             Mir
FIGURE  2

BITE  RAP

-------
»         U
                              »         U        »~

                                                II         IT
                                                                                  H-
                                                                                 OQ
                                                                                  C
                                                                                  >-t
                                                                                  n

                                                                                  u>

-------
(X)
 c
 n>

 *-

-------
                                                                PROCESS
                                                                BUILDING
EXTENT OF PCC CONTAMINATION
                                  MS OftAMMC OUSTS ON A CAM) fH£.  DO HOI RTMSf If UANUAU.Y
                                                                                        EBASCO SERVICES INCORPORATED
                                                                                                                               us DcvnrainitNTAL PROTFCTION
P1LFS OF RECOITIY
otpoarn) DEBRIS OR son.
nun* orrsin:
MTt . 9<0    W

D.K . OSW    „
CURE MOW f POLYUICUICAL SITE
                                                                                                                                                           ClARfTSJDWR  "»"

-------
Figure  6
 _12_
                              &MOMKT ML1MMCM. ft
                                 miautf^e auTaa

-------
                                 Figure  7
                                                                             STATl UMVWSTT
                                                                             AGDlCULTUKE AND
                                                                         i   Tt.CH COUXSt
  U • NON-OETECT

    ii ESTIMATED CONCENTRATION CONTOURS


NOTE: COK.TOUH INTERVALS INCHEAS»«T A »*CTO* OF 1« •— •
    ' HIGHEST CONTOUR LEVEL REPRESENTS 1000 ug/1

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APPENDIX B.  TABLES

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                        Table 1
                  Site History Summary


CONSTRUCTION OF THE CLAREMONT POLYCHEMICAL FACILITY BEGAN IN
1966

PLANT OPERATION BEGAN IN 1968

MORE THAN A THOUSAND DRUMS WERE DISCOVERED IN 1979 BY THE
NASSAU COUNTY DEPARTMENT OF HEALTH  (NCDOH)

MUST OF THE DRUMS WERE GONE AND AREA  OF CONTAMINATED SOIL
(SPILL AREA) WAS DISCOVERED IN 1980 BY NCDOH

SOILS WERE EXCAVATED AND PLACED ON PLASTIC LINERS IN 1980 BY
THE COMPANY

COMPANY ENTERED INTO CHAPTER  11 PROCEEDINGS IN  1980

NEW YORK DEPARTMENT OF LAW ASSUMES THE LEAD ON  THE SITE AND
ATTEMPTS TO NEGOTIATE AN AGREEMENT WITH RESPONSIBLE PARTY

SITE RECOMMENDED FOR PLACEMENT IN NATIONAL PRIORITY LIST IN
OCTOBER 1984

SITE WAS FINALLY INCLUDED IN  NATIONAL PRIORITY  LIST IN JUNE
1986 (RANKED 614)

EPA ASSUMES THE LEAD IN 1986  AND SENDS OUT NOTIFICATION
LETTER TO POTENTIALLY RESPONSIBLE PARTY  (PRP) IN NOVEMBER
1987

NO RESPONSE WAS RECEIVED AND  FUNDS FOR REMEDIAL
INVESTIGATION/FEASIBILITY STUDY  (RI/FS) ARE ALLOCATED IN
MARCH 1988

EBASCO SERVICES IS CONTRACTED BY EPA  TO CONDUCT RI/FS  (l"
OPERABLE UNIT) IN MARCH 1988

EPA CONDUCTS REMOVAL ACTION IN OCTOBER 1988 TO  STABILIZE
fc'ASTES

SECOWD RI/FS (2nd OPERABLE UNIT) IS OPEN IN APRIL 1989 TO
ADDRESS THE DISPOSAL OF WASTES CONTAIN IN HOLDING UNITS
(DRUMS, BASINS, ETC)

IMPLEMENTATION OF REMEDY FOR  2- OPERABLE UNIT STARTS IN
SEPTEMBER 1989

RI/FS FOR 1" OPERABLE  UNIT IS FINALIZED AND REPORTS ARE
RELEASED FOR PUBLIC CCMKENT IN AUGUST 1990

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                     TABLE   2

 COMPARISON OF CONCENTRATION RANGKS  Ol:> METALS IN
SURFACE SOIL TO TYPICAL  REGIONAL IIACKOKOUW)  I.KVIiL
      Concentration  Rnngc in
      Typical Eastern U.S.
Conccn t rn I i on
     Su i T m.'c So i I
n
Al
Sb
As
Ba
Be
Cd
Ca
Cr
Co
Cu
Fe
Pb
Mg
Mn
Wg
Ni
K
Se
Na
V
Zn
<")
c.>
(ND)
10000-300000
<1-500(1)
5-15(1)
100-3500
<1-7(1)
0.01-7
100-400000
10-00(1)
<3-70(1)
2-100
7000-550000
3-30U)
GOO-GOOO
100-4000
0.2-O.G(1)
4-30(1)
400-30000
0.1-2.0
750-7500
20-500
10-300
- Dragun, 1900.
- Conner, J.J. and II. T. Shacklcttc,
- Not detected
J72u-5n:i<)
NU-(iO
2.2-9.3
G.H--?.:.U
HD-J .2
ND-33. J
7Q.7-4'J700
3.0-75.'}
NO-3. 1
(..4-230
2'1GO-J3'.»00
7.2-377
31.4-29;! 00
](). (.-203
ND-0.22
NH- 14 . 1
ND-331>
ND-1 .3
ND-2G3
'J.2-2G. 0
6.7-32UO
1'JTj .


-------
Vp 1 a I i 1 e 0 rg an ?cs

Methylen? Chloride
Tetrachloroe1. r.ene
'. -1,2-Oichloroethene
Trichloroelher.e
1,1.2-Trichloroe th
Acetone
Toluene
2-Bu'.anone
Xy>nes

9en2e!a)anthracene
Chrysone
?enzo(b)f1uoranlhene
3enzo( k ) '1 uoranlhene
Senio!a)pyr?ne
indenol 1 ,2.3-C,d)pyrene
0 i benzol a. b) anthracene
Benzulg.h. . )perylene
Oimeti-.ylphthalal*
?i -o-hut ylphthalat J
3ut yi ipniylr'hthala'.S
?i -n-oc t ylphthalat*
3ii(2«elhyl»>exyl Jphthalate
5enj» c Ac i d
HO- 130
NO- jbO
NO-63
HO- 130
HO- 3 3
ND-33000
NO-390
NO- 90
NO- 130
MO- 170
NO- 7 5
HO-150
NO- 1100
HO-590
MD-2000
MO- 1900
NO- 7 80
"0-960
MO-8BO
•10-880
NO-820
HD-330
ND-200
HD-420
_
NO-3900
HO-8200
NO-87
NO-270000
NO-120
-
ND-11
_
-
-
ND-3 10
NO- 140
ND-67
-
ND-200
NO- 110
HO- 180
NO- 1500
ND-340
NO- 1500
NO-950
ND-700
ND-700
NO- 700
NO-580
NO- 7 40
NO-260
ND-KO
NO- 2 80
NO-48
NO-2100
NO- 1500
-
ND-4QOOI
-
              Table  3

  CLARF.MONT I'OLYCHF.MICAL SITE
Subsurface  Soil  Borings   (ug/kg)
                                                                                                                             Unsaturated Saturated
                                                                                                                                 Soi1        Soi1
                                                                                                                                         >55 rtgt
HD-8
HD-26000
ND-1
HO- 1 1
NO- 11
NO-82
_
NO- 150
ND-7
NO- 100
HO- 36
-
ND-270
NP-55
NO- 10
-
'
HD-210
HO -3
ND-1 7
ND-6
ND-7
NO-26
NO- 2 7
   ND-3
             W-19
NO-
NO-5
ND-170

HD-1




ND-70
                                      no-s
                                      NO- 3 A
                                      ND-7
                                                HO-15
NO-20
110-15
_
NO-: 3
HO- 18
ND-3
-
_
ND-200
NO- 2 5
NO- 13
ND-4
ND-5
ND-110
ND-71
ND-9
_
NO-32
ND-H
NO-110
NO II
NO-J300

NO-360
                                                                                              NO--J1
                                                 NO-/10
                                                 ND-270
                                                 NO-7 4
                                                                     NO-62
                                                           NO-100    NO-1SOO
                         ND-53


                         ND-1600
                        NO-1300
                        ND-50

                        NO-190
ND-65


NO-150
                                                                                                                    NO-170
                                                                                                                                ND-17
                                                                                                                                NO-520
                                                                                                                                         NO-390

-------
                                                                     TABLE   J tlont-oi
   Etsiic ii«i

   HeptacMor
   Oieldrin
   DOE
   ODD
   00 T

   KB'3

   PCB 1218
   PCB 1254
   PCB 1260
                                                       CONCENTRATION RANGES  OF  ORGANIC COMPOUNDS  IN
                                                              SUBSURFACE  SOIL DOR INGS  (ug/kg)

                                                                                                                                    Unsaturaled Saturated
                                                                                                                                        Soil       Soil
                                                    5-10  Feet  10-15 Teet 15=2P_fj.ei  2JblO_r«A  30-dQ Feet  4Jb5.0_F{ei  50-65 Feet  >65 Feet  >6S Feet
NO-18
NO-26
ND-70
ND-35
NO-61
ND-660
NO-120
HO-650
NO-110
NO-IBO
ND-88
NO-1)00
   (NO) or (-) - Not delected.
)_i All concentration*  
-------
                                                                      TABU   3

                                                         CONCENTRATION RANGES Of METAIS IM
                                 SUBSUHrACE SOIL BORINGS AND IHEIR COMPARISON 10 TYPICAL REGIONAL BACKGROUND LEVELS
Oncent rat • DO
Ranoe
LL?!>?'
Sb
As
Ba
Ee
Cd
Ca
Cr
Co
Cu
fe
rb
Mg
Mn
Ho
Mi
K
Se
Ag
Na
V
2n
Typical
;.. T Iqroun;)
:'. S ;i 1 ' Ippir.j*
t; 00-300000
,: 500">
t.15M)
100-3500
 65_£isA
201-1330
MO-5.3
1.0-13.2
NO-15.2 *•
-
ND-2.0 '
25.1-1070
ND- 1 . 9
NO- ' . 7
2. £-1:2
1200-7070
1.2-5.S
NO- 103
3.1-13.6
-
HO-2.5
NO-233
NC-0 . 51
ND-0: 65
-
2.7-10.9
ND-31.1
(•)  - Oragun,  J..  1963.
(1)  - Conner,  J.  J.  and  H.  T.  Shacklett*.  1975.

-------
                                                                      TABLE 4

                                                 CONCENTRATION RANGES OF VOLATILE ORGANIC COMPOUNDS
                                                    IN GROUNOUATER BY AREA AT THE CLAREMONT SITE
                                                                Rounds  I  & 2  Combined
Safe Drinking
Water Act
C'.MinO'jnd . HCl (ua/l)
A-:eAfl.ne.
0' nzene.
('.. rbon 0:sulf ide
O lorobpniene
Ci loroeH-ane
(. 'orofr .a
j. L-0'ff uroethanj
• ('-Oic!'. oroethane
• '. '-Oich'-oroethene
! J-nicl. ropropane
E'.'iy ibe*"' ene
£ Methyl 2-Pentanone
ML thirl Chloride
L. irachl . roethene
Tc luene
LI tal Xylenes
L ans-l .'• -Oichloroethent
.1 . 1 , l-Trl chloroethane
Lc ichloroethene
Vinyl Chipride
.
5
_
-
-
-
-
5
7
-
-
-
-
_
_
«
_
200
5
2
HYS OOH
MCL (ua/l)
50
5
SO
9
5
100' '
5
5
5
S
5
SO
5
S
5
5
S
S
5
2
NYS Ambient Water
Quality Criteria - Upgradient
Class GA Groundwater (uq/1) Wells (ua/1)

NO
_
20('»
_
100.,
5°r 1
0.8< »,
0.07' '
50;
50< '
-
so*;!.
07''
50 ')
50
SO
50< )
10
2
NO-2
NO
NO
NO
NO
NO
NO
NO
NO
NO
NO
NO-2.0
NO
NO-0. 8
NO
NO
NO
NO-0.2
NO-0 . 3
NO
Site Vicinity
•nd Downgradient
Wells (ua/l)
NO-540
NO-60
NO-0.2
NO-0 . 4
ND-0.8
ND-I
NO- 17
NO-6
NO-4
NO
NO- 160
NO-6
NO- 14
NO- 1300
NO-2
NO-40
ND-830
NO- 100
NO-260
ND-7
landfill/
Off-Site
Plume We,Us (uq/11
ND-7 10
NO-24
ND-4
NO- 19
NO- 7
NO-0 . 2
NO- 12
NO-2
NO
NO-0. 3
NO-0. 6
NO
NO
NO-3.0
NO-0 . 4
NO-0. 6
NO-8
ND-0.6
NO-0. 6
NO-4
(NO)  Not detected.

(*)   Guidance value.

(I)   Applies to sum of trihalomethanes.

(-)   Standard currently not available.

	  ''Underlined compounds w«r» found In  concentrations exceeding the Federal or New York State Maiimum Concentration Levels (."CLs)  or  Ambient Water
      Quality Criteria (AWQC).

-------
                                                                      TABLE 4

                                                   CONCENTRATION RANGES OF SEMI VOLATILE ORGANIC!
                                                        AND  PESTICIDES IN  GROUNOWATER BY AREA
                                                                Rounds I ft 2 Combined
Safe Drinking
Water Act
Comooui J MCL (ug/1)
Semi voi.it i les
Benzoir. Acid
Bis(2-» chylhe, yMphthalate -
"Chrysene -
"1 .4-Q-; chlorpl;en*ene 75
1,2-Oi nlorot niene
Diethyl,ihthal, te
Oi-n-butylphthalate
Fluorai Ihene —
Isopho. jne —
2-Meth; inaphtlialene
Naphih; Lsofi
2-Nitr HvioV.
4-Nlt;-. -henol
Pentacr . oroph nol
Phenri.. ire:'. -
Phenoi .
Pyrene
Pestic ies
XA1 h "HC
A "d" nf T —
'Heptaciilor

NYS DOH
MCL Jug/1)

50
4200
SO
s
5
50
770
SO
SO
SO
50
SO
50
21
50
1
SO

NO
NO
NO
NYS Ambient Water
Qual i ty Criteria -
Class GA Grojtndwater (ug/1)

^
4200
0.002J >
1 ft t
50« >
770
50' '
ioc.
-
50<'>
50«'>

NO
NO
NO

Upgradient
Wells (ug/H

NO
NO-88
NO
NO
NO
NO
NO
NO
NO
NO
NO
NO
NO
NO
NO
NO- 13
NO

NO
NO
NO
Site Vicinity
and Oowngradient
Wells fuo/11

NO-5
NO-92
NO
NO
NO
NO-2
NO-3
NO
NO-4
NO-4
NO-SI
NO- 13
NO-6
NO-2
NO
NO- 30
NO

NO
NO-0 . 1 1
NO
Landfill/
Off-Site
Plume Wells (ug/1)

NO
NO-27
NO-3
NO- 15
NO-3
ND-2
NO
NO-6
NO
NO
NO- 7
NO
NO
NO
NO-4
NO
NO-5

NO-0. 16
NO
NO-0. 047
(NO)  Not detected.

(•)   Guidance value.

(I)   Applies to sum of para (1.4) and ortho (1,2) isowers only.

(-)   Standard currently not available.

	   Underlined compounds *er* found in concentrations exceeding the Federal or New York State Maximum Concentration Levels  (*Cls)  or Ambient Water
      Qualit/ Criteria (AWQC).

<•      compounds found above MCLs/AWQC in Landfill Plume wells only.


2-l-HK

-------
                                                                          TABLE 4

                                                            CONCENTRATION RANGES OF TOTAL METALS
                                                                   IN GROUNOWATER 8V ARF.A
                                                                    Rounds I  & 2 Combined
Element
Aluminum (A1 )
Antimony (Sb)
Arsenic (As)
Barium (Ba)
Beryllium (Be)
Cadnrum (Cd)
Calcium (Ca)
Chroiiiiun (Cr)
Coba't (Co)
Copper (Cu)
Iron (Fe)
Lead (Pb)
Magnesium (Mg)
Manganese (Mn)
Mercury (Hg)
Nick 1 (Ni)
Pota- sium (K)
Sel; um (Se)
Sodio.n (Na)
Thai mm (T1)
Van* um (V)
Zinc (In)
Safe Drinking
Water Act
MCL luo/n
—
-
50
1000
-
10
.
so
-
-
-
so
-
-
2
-
-
10
-
-
-
™
NYS Ambient Water
Qual i ty Criteria -
Clais GA Groundwater (ua/1)
—
3*"*
25
1000
3'*)
10
-
SO
-
1000
300
25
35000* *>
300
2
.
-
20
-
,)(•)
-
5000
Upgradient
Wells lud/l)
NO-43.700
NO
NO-2 1.3
46.2-305
NO-6.6
NO-4.9
37.600-72.100
NO- II 2
NO-45.8
NO- 165
204-90.700
NO-55.1
6,910-15,800
218-549
NO
NO-86.7
10,500-28.200
NO-3.2
9.900-148.000
NO-8.5
NO-465
30.2-650
Site Vicinity and
Oowngradient
Wells (uo/1)
NO-50.800
NO-82.2
NO-29 . 7
NO-310
NO-10.1
NO-IO.I
NO-95.300
NO- 159
NO-76.4
NO-2 14
NO-374.000
NO-464
838-16.100
12.6-2.900
NO-2 . 4
NO-92.7
604-21.300.
NO- 7
NO-93.400
NO-17.3
NO-595
NO-838
Landrill/Off-Site
Plume Wells
(uo/1)
NO-8.400
NO-36.4
N6-S4.7
27.2-15.2
NO-2 . 4
NO-4.2
2.110-66,600
NO-28.6
NO-IS. 3
NO-43.5
79.1-83.200
NO-346
8.580-32.000
80.2-3.130
NO-I
NO-29
924-13.5000
NO
3.900-274.000
NO
NO-2 3. 7
NO- 1 40
(*)  - Guidance value.
(MOJ - Note detected.
(-T  - None currently available.
2449K .

-------
                                                        TABLE
                                                CLAREHEONT  POLYCHEHICAL  SITE
                            AIR QUALITY SAMPLING (CHARCOAL)  RESULTS  FOR  VOLATILE  ORGANIC* (PPB)1
 SAMPLE  1.0.
 LOCATION

 vinyl chloride
 1.1-dichlorotthene
 •ethylene chloride
 acrylonltrile
 chloroform
 1,1,1-trlcMorotthane
 carbon  tetrachlorlde
 benzene
 toluene*
 1,2-dtchloroethane
 trlchlorofluoromethane
 I.l,2-trlch1oro-1.2.2-
   trifluoroethane
 trlchloroethene
 tetrachloroethene
 ethylbenzene
 m- ft p-xylene
 o-xylene
 cyclohexanone
 propylbenzene
J - estimated
N - tentative Identification
R - rejected
U - non-detect due to presence In blank
222SK
CHS 154
Spill Area
'',',
1.2u
(Q ( |
<0. 1
0.7
<0.1
0.6u
1.8
3. OR
0.3NJ
2.1NJ
4.6NJ
0.5NJ
1.4NJ
0.7NJ
0.7NJ
0.1NJ
CMS 193
Treatment
Basins
<0. 1
<0. 1
3.7U
0.6
<0.l
0.8u
2.4
2.4R
0.3NJ
2.INJ
3.INJ
O.BNJ
2.3NJ
I.ONJ
0.5NJ
<0.1
CMS 158
Downwind
!!'.!
2.6u
0.6
<0.1
O.Su
1.7
2.4R
0.3NJ
2.1NJ
2.6NJ
0.4NJ
I.3NJ
0.6NJ
O.BNJ
<0.1
CHS 190
Upwind
<0 . 1
<0. 1
9.3u
0.7
0.1
0.7u
2.1
7.2R
0.3NJ
I.ONJ
2.7NJ
0.6NJ
1.8NJ
0.9NJ
0.9NJ
0.2NJ
CHS070
Malnten-
enance Room

-------
                                                        TABLE  5

                                                CLAREMONT  POLYCHEM1CAL  SITE
                               ANALYTICAL RESULTS OF  AIR SAMPLES  -  (TENAX) VOLATILE ORGAMICS
                                                                     Concentration  (ppb)">
SAMPLE ID.
LOCATION
l.l-dlcMarotthene
l.l-dtcfcloroetfcant
1.2- than*
1 ,2-dichlorop'oMne
cis-1,3 dlch1on>propene
trlchloroethfn*
dlbroMochloronethane
1.1.2-tricMoroethane
trans-1,3-dlch)oropropene
bronofom
2-Jiexanone
tetrachloroethent
1 , 1 ,2.2-telracM rooethene
chlorobenzene
styrene
U
Spill Area
BOL
BOL
BOL
0.0668J
BOL
0.1 16J
BOL
BDL
BOL
R
BOL
BOL
BDL
BOL
BOL
3.42J
BOL
BDL
0.374J
12
Treatnent
Basin*
BOL
BOL
BOL
BDL
BOL
0.112J
BDL
BDL
BOL
l.12Jb
BOL
BDL
BDL
BDL
BDL
1.76J
BOL
BOL
0.243J
D
Downwind
BOL
BDL
BOL
0.0338J
BOL
0.0941J
BDL
BDL
BDL
I.HJb
BDL
BDL
BDL
BDL
BDL
1.56J
BDL
BDL
O.I74J
14
Upwind
BDL
BOL
BOL
O.OS82J
BDL
0.117J
BDL
BDL
BDL
0.448Jb
BOL
BDL
BDL
BOL
BOL
1.54J
BDL
BOL
0.261J
16
Maintenance
ROOM
BOL
BDL
BOL
BOL
BDL
BDL
BDL
BDL
BOL
U
BOL
BOL
BDL
BOL
BOL
0.184J
BOL
BDL
0.117J
u
Maintenance
ROOM
BOl
BOL
BDL
0.0258J
BDL
BDL
BOL
BOL
BDL
0.16Ub
BDL
BDL
BOL
BDL
BDL
0.405J
BDL
BOL
0.295J
BDL - below detection 1t*it
  J - estimated
  u - non-detect due to presence in blank
  R - rejected due to presence in blank
  1 - values (including BOL) qualified as estimates
because sample holding time exceeded
2225K

-------
                                                                        TABLE 6

                                                                CLAREMONT  POLYCHEMICAL SITE
                                     ANALYTICAL RESULTS FROH WIPE SAMPLES  IN THE  PROCESS BUILDING - ORGANIC  (og/wlpe)'
  Sample

Location


SNA

Behzoic Acid
Phenanthreie
Dt-n-Buty1phtha1«t«
Fluaranthene
          IhexyDPhthalatt
Di-i-Octy. PhthaUl*

EEST.CIPE/PCJ
CONCENTRATION
CPS
WP09-1
Wall
NO
CPS
WP09-Z
Floor
2J
2J
2J
IJ
230
CPS
WPflfl-J
Wall
5J
22
CPS
WPOB-4
Floor
2400
CPS CPS
WP07-5 WP07r6
Wall Floor
NO
1400
1SOO
CPS CPS CPS
WP06-7 WP06-8 WPQ6-9
Hood Hood Floor
NO NO
270
CPS CCS CPS
WPQ6-10 WPQ5-11 WP05-12
Hood Wall Floor
V
420 100 3000
1  *,pproxi"Wtely 63 \fi  wiped per sample
NO   lot detected
J - tstirred concentration

-------
                                                                    TABLE  6
                                 (Cont'd.)
                                                                 CLARCMONT POLYCHEMICAL  SITE
                                      ANALYTICAL RESULTS FROM WIPE SAMPLES IN THE  PROCESS  BUILDING -  ORGANIC (ug/wipe)1

                                                                                           CONCENTRATION
  Samp «

Locati.-n
CPS
wppi-ia
Wall
CPS
WP04-14
Floor
CPS
WPQ2rJ$
Wall
CPS
WP02-16
Wall
CPS
WP02-17
Floor
CPS
WP01-19
Wall
NO
CPS
WP01-20
Floor
CPS
WP03-21
Floor
CPS
Floor
CPS
WP02-23
Wall
B.NA,

Phenol
Benzoic Acid
Di-n-bijtylpht'nalat*
bii(2-lthy1hn«y1)Phtha1al«
Oi-n-Octyl Phthalat*

PESTIC^DE/PTB
17J
59J

110
5200J
90J
I10J
1300
6100
1300
                                                             43J
                                                   340
                                                   24J

                                                   4200
75J
6600
1300
                                                                                 72J
Undetected
                 63 in* wiped per sa«ple
NO  Nut detected
J - Estimated concentration

-------
                                                                          TABLE  6

                                                                 CLAREHONT POLYCHEMICAL  SITE
                                     ANALYTICAL RESULTS FROM WIPE SAMPLES  IN  THE  PROCESS BUILDING -  INORGANIC (ug/wipe)

Sample
Locr.tlon
Aluminum
Antimony
Arsenic
Barium
Beryllium
Cadmium
Calcium
Chromium
Cobalt
Copper
Iron
Lead
Magnesium
Manganese
Mercury
Nickel
Potassium
SeKnium
SlUer
Sodium
Thaclium
Vanuatu*
Zinc "
CPS
WPQ9-1
Wall
114.0

.98
79.0J


2500.0


28.6

4.2J
218.08
4.4J


271. OB






CPS
WP09-2
Floor
2850.0
24. 1J
4.5
549.0J

117.0
7340.0
172.0

1840.0
9200.0
1600.0
1600.0
95.2

1S.4J
1290.0




13.0
929.0
CPS

Wall
341.0


2380. OJ

406.0
4900.0
15.3

519.0
1010.0
99.6
293.08
15.8


474.08
0.6BB




816.0
CPS
WP8-4
Floor
8980. OJ
59.6
8.1
1180.0
0.688
590.0
18.300.0
566.0
11.1
1040.0
65,600.0
3030. OJ
4130. OJ
443. OJ

72.4
3080.0


38,400.0

28.4
38,400.0
CPS CPS
WP07-5 VP07-6
Wall Floor
1180.0J
35. BJ
7.0
7.38

5.0

4.6

1290
395.0
186. OJ
216.08
5.9J

6.78
656.08





17,700.0
CPS
WP06-7
Hood
224.0
19. 3J

11. OB

4.0

9.7

438.0
182.0
77.3
133.08
3. OB
0.62

248.08





3610.0
CPS
WP06-8
Hood
1080.0


39.6BJ

2.1J
3290.0
25.2

1760.0
980.0
121.0
764.08
11.3


384.08





719.0
CPS
WP06-9
Floor
42.200.0
59.4
8.5
747. OJ
0.74J
186.0
16.200.0
486.01
11.6
1960.0
135.000
1810.0
2970.0
709.0
0.68
91.3
2630.0




21.6
23,000.0
CPS
WP06-10
Hood
75.9


5.5B

1.5J

20.4

201.0

99.1
191.08
2.4B


203.08





1230.0
CPS
WPQ5-11
Wall
327.0
41.0

104. OJ

21.9
5130.0
534.0

253.0
611.0
2410.0
246. OB
8.2J


294.08





217.0
CPS
WPOS-12
Floor
3280.0
183.0
7.3
807. OJ

585.0
9380.0
5940.0
10.9
3710.0
67.400.0
29.900.0
1200.0
432.0

49.0
1340.0





1430.0
CPS
WP04-13
Wall
117.0
12. OJ

28.5BJ '

4.6

22.5

iar.0
194.0
112.0
188.0
4.5J


338. OB






CPS
WP04-14
Floor
5210.0
182.0
1.6B
4020. OJ

1070.0
4990.0
1570.0
6.68
1570.0
20.900.0
6100.0
1860.0
140.0

22. OJ
3690.0




8.08
937.0
??69K

-------
                                                                     TABLE   6   (Cont'd)
                                                                 CLAREMONT  TOLYCHEM1CAL  SITE
Sample

Location
Aluminum
Antimony
Arsenic
BariuM
Beryllium
Cadmium
Calcium
Chromium
Cobalt
Copper
Iron
Lead
Magnesium
Manganese
Mercury
Nickel
Potassium
Selenium
Silver
Sodium
Thallium
Vanadium
Zinc

CPS
WP02-15.
Wall
77.6
15. OJ

87.1

13.0

30.8

54.2
270.0
368. OJ
427.08
2.38


225.08



1
CPS
iJM/D ic
•^**y t ^ i o
Wall
51.8
10.2

45. 7 J

S.4

18.6

33.6
167.0
203.0
307. OB
2.08
0.55
4.6
202.08



ANALYTICAL RESULTS FROM WIPE SAMPLES

CPS
WP02-17
Floor
6380.0
114.0
4.3
1120. OJ
0.83B
397.0
13,000.0
1650.0
7.5B
6030.0
32.100.0
12.400.0
4030.0
242.0
1.11
23. 9 J
27,300.0

19.0
4420.0
IN I HE PROCESS BUILDING •
- INORGANIC
CONCENTRAJJON
CPS
WPQ1-19
Wall
294.0


71. U

3.1
3290.0
29.4

133.0
440.0
162.0
300.08
8.4J


294.08
149.000

107.0
CPS
WP01-20
Floor
1840.0

2.8J
86. 4 J

9.4
8970.0
123.0

154.0
4190.0
523.0
947.08
28.0


2560.0

3.28
138.0
CPS
WP03-21
Floor
1740.0
25. 7 J
13. 2J
339. OJ

82.2
4670.0
264.0

1100.0
17.900.0
1220.0
740. OB
92.7

8.08
905.08

5.98
1270.0
CPS
WP03-22
Floor
1590.0
28. U
4.0
275. OJ

87.3
4120.0
250.0

1140.0
15,200.0
1200.0
644.08
86.3

8.08
564.08

7.2B
1280.0
CPS
WP03-23
Wall
911.0
23. 7 J
2.3
147. OJ

5.6
5650.0
73.6

1500.0
1370.0
357.0
903.08
17.3


520. OB

3.4B
454.0
'  Approximately 135 in2 wiped per sample.
8 - The concentration listed It below the analysis required detection limit but above the instrument detection  limit.
J - Estimated concentration.

-------
                                 Table 7
                    Summary of Indicator Chemicals in
             Sar.pled Matrices at Claremont Polychemical Site
  Antimony
  Arsenic
  Barium
  Benzene
  Benzoic  Acid
  Beryllium
  Bi s (2-e thy IhexyDph thai ate
  Butyl benzyl phthalate
  Cadmium
  Chlorobenzene
  Chloroethane3
 Chloroform
 Chromium
 Cobalt
 Copper
 1,2-Dichlorobcnzene(a/
   4-Dichlorobenzene(a)
   1-Dichloroethane
   1-Dichloroethene
 1,2-Dichloroethane
 Diethylphthalate
 Di-n-butylphthalate
 Di-n-octyl-phthalate(a)
 Ethylbenzene
 Iron
 Isophcrone
 Lead
 Manganese
 Mercury
 Nickel
 PAHs - Naphthalene
     - Benzo(a)pyrene
Pentachlorophenol
Pesticides -  4,4'-DDT
             4,4'-DDD
1
1
   c
   o
   c
   0
   0
   0
   c
   o
   0
   0
   0
  o
  o
  0
  o
  0
  0
  0
  o
  o
  c
  0
  o
 o
 o
 o
 o
 0
 c

 0
 0
                Alpha-BKC
 o  Phenol
 c  Seier.ium
 c  Tetrachioroethene
 o  Thalium
 o  Toluene
b  7rans-l,2-Dichic roethene*
c  Trichloroethcne
o  Vanadium
o  Zinc
                                X
                               X
                                   BuiIding
                                   	Ryit	  5.0_i.l

                                      X        X
                                      X
                                      X
                                      V
                                     X
                                     X
                                     X
                                     X

                                     X

                                     X
                                     X
                                     X
                                     X
                                         •f
                                         *«

                                         X
X

X
X
X
                                              X
                                              X
                                              X
                                              X
                                              X
                                              X
                                              X
                                             X
                                             X

                                             X
                                             X
                                             X
                                                             A
                                                             X
                                                             X
                                                             X
                                                             X


                                                             X
                                                             X


                                                             X
                                                             X
                                                             X
                                                             V

                                                             X
                                                             X
         X
         X
         X
         X
         X
         X
         X
         X
         X
         X
        X
        X
        X
        X
        X

        V
X  Selected chemical of potential concern
— Net selected az a chemical of potential cToncern
(a)   No Toxicity data

-------
Exposure Hediuit/
_ Sciriarjg _

I •  PMjenLJ,*niLJhe

    Air

    Soli

    Groundwater

2.
A.  On-Slle

    Air

    Building

    Soli



    Groundwater




 B.  QfJbSitt

    Air

     Soil

    Groundwater
                                                       Table  8
                                               CLAREMONT POLYCHEMICAL SITE
                              SlimARY OF EXPOSURE PATHWAYS UNDER CURRENT AND FUTURE  LAND USE
                                       Potentially Exposed
                                       _Pj)P.o. J.3 LUM	
Residents, workers, students

Residents, workers, students

Residents, workers, students
Residents, construct Ion-workers

Workers  InsIHe building

Residents, construction workers
Residents, construction workers
Residents, construction workers

Residents
Inhalation of Volatile*

Inhalation of Fugitive Oust

Incidental Ingestlon
Inhalation of Volatile!

Inhalation of dust

Inhalation of Fugitive Dust
Dernal  contact
Ingestlon

Inhalation of Volatlles  while
showering
Dermal  contact  while showering
Ingest ion
 Inhalation of Volatlles

 Inhalation of Fugitive Dust

 Inhalation of Volatiles while
 showering
 Dermal contact while showering
 Ingestlon
 Residents, workers

 Residents, workers

 Residents

 Residents

-------
                                                     Table  9
                            Toxicity  Data for  Non-Carcinogenic Effects
                                     Dose  Response  Evaluation  (a)
Chemical Name
Volatile*:
Benzene
Ch I orobenzene
Chloroform
1,1-Dichtoroethane
1,2-0ichtoro« thane
1,1'Dichloroethene
Ethytbenzene
Toluene
Tetrachloroethene
1,1.1-Trfchloroethane
Trichloroethene
Vinyl Chloride
Xylene*
Seni volatile*:
•enioic Acid
1 sophorone
Pent ach I orophenol
Phenol
8enzo(a)pyrene >
Naphthalene
HONCARC IMOGENS
Oral RfO
(ing/kg-day)

-
3.00E-02
1.00E-02
1.00E-01
-
9.00E-03
1.00E-01
3.00E-01
1.00E-02
9.00E-02
-
-
2.00E»00

*.00€»00
2.00E-01
3. 006-02
6.00E-01
-
4.00E-01
Bis(2-ethytheiyl)phtha(ate 2.006-02
Butyl benzyl phthalate
Oi -n-butylpftthalate
OiethytpMhalat*
Pesticides:
Alpha «HC
4.4'-DDT
Inorganics:
Ant iMony
Arsenic
•ariuM
•cry Him
Cadmiui

Chromiin (VI)
Copper (a)«
lead***
Xaogane**
Mercury
MiekcV
Seleniun
Th«Uitn
Vanadim
Zinc
2.00E-01
1.00E-01
8.00C-01

8.00E-W
5.00E-04

4.00E-04
1.00E-03
S. 006-02
S. 006-03
1E-03 (food)
SE-Ot (Mater)
S. 006 -03
3. 706-02
1.436 -04
2.00E-01
3.00E-04
2.00E-02
3.006-03
7.006-05
7.006-03
2.001-01
: Reference Doses
Inhalation RfO
(mg/kg-day)

.
5. 006-03
NO
1.006-01
-
NO
NO
1.006*00
HO
3.006-01
-
•
A. 006-01

NO
NO
NO
NO
.
NO
NO
NO
NO
NO

NO
NO

NO
- •
1.006-04
NO
NO
NO
NO
1.006-02
NO
3.006-04
NO
NO
1.006-03
NO
NO
NO
(•) Health effects Assessment Surmary Tables - Second and Third  Quarters. USEPA. 1989.
/i (USEP*-

-------
                                Table  10
                  Claremont  Polychemical Site   _
       Summary  of  Human Non-cancer  Risk  Estimates
                                            Hazard Index for
                                          Noncareinedenie Effects
Eioosur* Pathway
                                   Average
                                    Cai*
                                               Kaximum
                                              Plausible
                                                Cast
Inhalation of air
Ingestion of soil
Dermal adsorption of soil
Inhalation of Fugitive Oust
Ingestion of ground*ater
0.8
0.15
0.01
15.2
3.2'/•>

                      Total        10         II*

Futuri Qn-Site Land Use Conditions
                                                           PCE

                                                           Pb
                                                            PC-
                                                            Sb. TL. ?CE
Dermal adsorption of  ground»atfr     —        0.01
Inhalation or uround«ater Volatile*   2.83       N/A
                                                            PC-
                       Total
Inhalation of resuspendsd building
dust
rutun  6ui IJinT Use
                                              2:*
                                                           Barium,  iron.
                         H[ Jbo./e  \  |.id''«Jf •l».al  risk  or HI is

                                     —15 'Jltd

-------
                                                          Table 11
                                 Toxicity  Data  For  Carcinogenic  Effects
                                         Dose Response  Evaluation  (a)

volatile*:
Benierw
Chlorobenzene
Chloroform
1,1-Oichlorotthifw
1,2-Dichloro«th«nt
1,1-Dichloroethene
Ethylbetutnt
Toluene
Tetrachloro»th«nt
1, 1.1 -Inch loroethane
Trichtorocthent
Vinyl Chloride
Seanvol •til**:
Benzoic Acid
Isophorone
Pemach 1 orophenol
Phenol
8enzo(a)pyrene (b)
Naphthalene
Cere i nog ens:
Or* I CPF
(mg/kg-day)'

2.90E-02
6.10E-03
9.10E-02
9.106-02
6.00E-01
™
5.10E-02
-
1.10E-02
2.30E«00

-
4.10E-03
-
•
1.15E-01
•
8is<2-ethylhexyl)phthalat* 1.40E-02
Butyl benzyl pri thai ate
Di-ri-butytphthalate
Oiethylphthal««
Pesticides :
Alpha BHC
4,4'-ODT
Inorganics:
Ant iseny
Arsenic
••ritM
Beryl I ium
Cadmium
Chromium (VI)
Copper
lead
Manganese
Mercury
nickel (c)
Sri mum
thai 1 iuai
VanadiuB
Zinc
HO
HO
HO

1 . 70E*00
3.40E-01

-
1.50E*00 (b)
•
«>
HO
MO
-
HO
-
-
HO
•

•
-
Cancer Potency
Weight of
•1 Evidence

A
12
•2
•2
C

•2
"
•2
A

-
C
0
•
•2
•
•2
C
D
0

•2
•2

•
A
•
•2
•
.
-
•2
•
•
•
•
•
-
•
Factors
Inhalation CPF
(i»9/k9-dayr-1

2.90E-02
8.10E-02
HO
9.10E-02
1.20E»00

3.30E-03
"
1.30E-02
2.9SE-01
^B..
.
HO
-
.
6.10E*00
•
MO
MO
NO
NO

1.70E-00
3.406-01

-
S.OOE*01
-
a.*OE*oo
6. 10E*00
«.10E*01
•
HO
•
-
1.70E*00
•
•
•
•
Weight of
Evidence

A
82
MO
82
C

82

82
A
.
.
C
0
.
82
.
82
.
0
0

82
82

.
A
.
82
81
A
-
82
•
-
A
•
-
-
-
C?A Weight of Evidence Claitifieations are  as follows:
   Croup A • Muwn Carcinogen.  Sufficient  evidence fro* epideaiologic studies  to sipport a causal  association between exposure
   and cancer.
   Croup II - Probable Hunan Carcinogen.  United evidence of carcinogenic!ty in himans  fron epidenioiogtcal studies.
   Croup 12 - Probable Hunan Carcinogen.  Sufficient evidence of carcinogenicity in animals.  Inadequate evidence of
   careirvogsrii-i- • in hir?r...
   Croup C - Posiible Human Carcinogen.  Limited evider:e of circinogenicity in animals. """
   Group 0 - Hot Classified.  Inadequate evidence of carcinogenicity in animals.
!. '  :'.c.--' .  ~f-;-  . . Astis-r-nt '- •—-r;- r-*ilc.-    ' -••     ' "  '    :. .   ...  .j;PA, "589.
(a:* Calculated  froi the current drinking water standard of  1.3 nj/l assuming an ingest ion of 2.0 I/day for a 70 kg person.
(b)  Integrated llsk Information System. 1987.
(c)  The CPF represents the nickel subsulfide font of the  chemical.

-------
                                  Table 12

                       Claremont Polychemical  Site
                   Summary  of Cancer  Risk Estimates
                                          Excess Lifetime Cancgr Bisk
Exoosur" Pathway
                                   Averagt
                                    Case
   flaxinuo)
Plausible Case
Predominant
 Chemical s
Current Land Use Conditions

Inhalation of air
Inhalation of soil
Ingestion of Groundwatcr
                                   1.81E-06
                                   I.05E-09
                                   4.23E-OS
  1.38E-06
  9.48E-08
                       Total        1.88E-06

Future  Off-Sit? Land Use Conditions
                                                1.40E-05
                       Total

fulur» On-$ite Land Us* Conditions
                                   1.20E-05
  5.0E-05
Inhalation of a
-------
Table 13.  List of Applicable or Relevant and Appropriate Requirements (ARARs) for the Selected
Remedy.
SOILS
Regulatory Level

Federal
State
GROUNDWATER

Federal

State



OTHERS
Description

National Ambient Air Quality Standards for Hazardous Air
Pollutants (NAAQS)
40 CFR 52

RCRA - Land Disposal Restrictions (40 CFR 268)

RCRA - Standards Applicable to Transport of Hazardous
Waste (CFR 263.11, 263.20-21
and 263.30-31)

RCRA - Standards for Owners/Operators of Permitted
Hazardous Waste Facilities (40 CFR 264.10-264.18)

RCRA - Preparedness and Prevention (40 CFR 264.10-
264.18)

RCRA - Contingency Plan and  Emergency Procedures (40
CFR 264.50-264.56)

DOT - Rules for Transportation of Hazardous Materials (49
CFR Parts 107, 171.1-172.558)

New York Hazardous Waste Manifest System Rules  (6
NYCRR 372)

New York Hazardous Waste Treatment Storage and Disposal
Facility Permitting Requirements
(6 NYCRR 370 and 373)
SDWA Maximum Contaminant Levels (MCLs)

Groundwater Quality Regulations (6 NYCRR Part 703.5)

Drinking Water Standards (10 NYCRR Part 5)



OSHA - Safety and Health Standards (29 CFR 1926)

OSHA - Record Keeping, Reporting and Related Regulations
(29 CFR 1904)

-------
APPENDIX C.  ADMINISTRATIVE RECORD INDEX

-------
89/27/9B                             Index Docuient Nuiber Order                                              Page: 1
                                     CLAREHONT POLYCHEHICAL Oocuients



Docuient Nuaber: CLR-001-8801 To 0151                                                Date: 07/01/90

Title: Draft Final Reaedial Investigation Report:  Clareiont Polycheiical Site, Volute 1 of 6:  Sections
       1, 2 and 3

     Type: PLAN
Condition: DRAFT
   Author: Nivargikar, Rao:  Ebasco Services
Recipient: none:  US EPA


Docuient Nuiber: CLR-001-0152 To 0356                                                Date: 07/01/90

Title: Draft Final Reiedial Investigation Report Clareiont Polycheiical Site, Volute 2 of 6:  Sections
       4 and 5

     Tyoe: PLAN
Condition: DRAFT
   Author: none:  Ebasco Services
Recipient: none:  US EPA


DocLeer.t Nuabe-: CLR-aZi-Z357 To 0557                                                Date: 07/81/90

Title: Craft Final RBsedia! Investigation Report, Clarenont Polycheiical Site, Voluie 3 of 6:  Sections
       i, 7 and References

     Type: PLAN
Condition: DRArT
   fijthor: none:  Ebasco Services
Recipient: none:  US EPA


Docuaent Nuiber: CLR-001-055S To 0845                                                Date: 07/01/90

Title: Draft Final Reiedial Investigation Report, Clareiont Polycheiical Site, Voluie 4 of 6:  Appendices
       A-H

     Type: PLAN
Condition: DRAFT
   Author: none:  Ebasco Services
Recipient: none:  US EPA

-------
B9/27/9B                             Index Docuient Nueber Order                                              Page:  2
                                     CLAREHONT POLYCKEHICAL Docuients
Docuient Nuaber: CLR-8B1-8846 To 1889                                                Date: B7/B1/9B

Title: Draft final Reiedial Investigation Report, Clareiont Polycheiical Site, Volute 5 of 6:  Appendices
       I-L

     Type: PLAN
Condition: DRAFT
   Author: none:  Ebasco Services
Recipient: none:  US EPA


Docuient Nuiber: CLR-B81-1B98 To 1460                                                Date: B7/B1/9B

Title: Draft Final Reaediai Investigation Report, Claresont Polycheiical Site, Voluie 6 of 6:  Chesical
       Results Appendices

     Type: PLAN
Condition: DRAFT
   Author: none:  Ebasco Services
Recipient: none:  US EPA


Docuaer.t NaiDer: CLR-B81-146i To 1914                                                Date: 87/81/98

Titls: Draft rinal Feasibility Study Report - Clareiont Polyche»i:al Site

     Type: PLAN
Condition: DF>."
   Author: Nivarcitar, Rao:  Ebasco Services
Recipient: none:  US EPA


Docuient Nuiaber: CLR-881-1915 To 1929                                                Date: 88/81/98

Title: Superfund Proposed Plan - Clareiont Polycheiical Site

     Type: PLAN
   Author: none:  US EPA
Recipient: none:  none

-------
89/27/90                             Index Document Nuaber Order                                              Page: 3
                                     CLARENONT POLYCHEHICAL Docuients
Docutent Nusber: CLR-BB1-193B To 1931                                                Date: 88/29/98

Title: (Letter advising of concurrence with proposed reaedial action alternatives for Clareiont Polycheaical
       site)

     Type: CORRESPONDENCE
   Author: O'Toole, Michael J Jr:  NY Dept of Environmental Conservation
Recipient: Casoe, Richard L:  US EPA
Docuaent Nuaber: CLR-081-1932 To 1985                                                Date: 89/22/89

Title: Declaration for the Record of Decision and Decision Suaaary - Clareiont Polycheiical Site
       Operable Unit II

     Type: LE6AL DOCUMENT
   Author: Hiisiynsfci, Hiliiaa J:  US EPA
Re::oient: none:  none

-------
APPENDIX D.  NYSDEC LETTER OF CONCURRENCE

-------
  SEP-25-1990  08=04  FROM   NYS.ENUIR.CONSERUfiTI ON     TO     6-55265?2i2ib466«
New York State Department of Environmental Conservation
SO Wolf Road, Albany, New York 12233*7010
                                                                         Thomas C. Jortlno.
                                                                         Conunte»ion«r
   Mr. Richard L. Caspe, P.E.
   Di rector
   Emergency & Remedial Response  Division
   U.S.  Environmental Protection  Agency              .oEP  2 4 1990
   Region  II
   26 Federal Plaza
   New York, NY   10278

   Dear  Mr. Caspe:

               Re:  Claremont  Polychemical Site - ID. No.  130015
                    Old Bethpage, Nassau County, New York

   The New York State Department  of  Environmental Conservation (NYSDEC) has
   reviewed the draft Operable Unit  One Declaration for the Record of Decision
   (ROD) for the  above-referenced site.  The NYSDEC concurs with the selected
   remedies which include:

   1.    Alternative SC-4,  Contaminated Soils - Excavation of approximately
         1600 cubic yards of contaminated soil, on-site Low Temperature Enhanced
         Volatilization and on-site  redeposition.

   2.    Alternative GW-3B, Groundwater - Extraction of 1.0 mgd of contaminated
         groundwater, followed by treatment (metal precipitation, air stripping
         and carbon adsorption) and  reinjection of the treated water into the
         aquifer.

   3.    Alternative BD-2 - Building decontamination and off-site treatment/
         disposal of collected dust, asbestos insulation,  and contaminated water
         from the floor drains and condensers.

   4.    Alternative T-2, Underground Storage Tanks: Removal and Off-Site
         Treatment/Disposal -  This alternative includes excavation of overburden
         soil, pumping of the  tank contents, tank cleaning,  removal of tanks  and
         appurtenant equipment, off-site disposal/treatment  of tanks, equipment
         and liquid waste,  and backfilling with clean soil.

   If you  have any questions,  please call Mr. Kama! Gupta,  of my staff, at
   (518) 457-3976.
                                        Sincerely,
                                        Edwirjn OTstrtTTvan
                                        Deputy Commissioner
    cc:    C.  Ramos,  USEPA,  Region II
          R.  Tramontane,  NYSDOH

-------
APPENDIX E.  RESPONSIVENESS SUMMARY

-------
                      RESPONSIVENESS SUMMARY

                   Claremont Polychemical sit*
                   Old Bethpage, Nassau County
                            New York


The U..S. Environmental Protection Agency (EPA) held a public
comment period from August 25, 1990 through September 25, 1990 to
receive comments from interested parties on the final Remedial
Investigation and Feasibility Study (RI/FS) reports and Proposed
Plan for the Claremont Polychemical Superfund Site (Site).

A public participation meeting was conducted by EPA on
September 5, 1990 at the Old Bethpage Village Restoration, Old
Bethpage, New York to discuss the remedial alternatives, to
present EPA's preferred alternative for the remediation of the
site, and to provide an opportunity for the interested parties to
present oral comments and questions to EPA.

This responsiveness summary provides a synopsis of citizen's
comments and concerns about the Site as raised during the public
comment period, and EPA's responses to those comments.  All
comments summarized in this document were factored into EPA's
final decision for selection of the remedial activities for
cleanup of the Claremont Polychemical Site.

This responsiveness summary is divided into the following
sections:

     I.   Responsiveness Summary Overview.  This section briefly
          describes the background of the Claremont Polychemical
          Site and outlines the proposed alternatives.

    II.   Background on Community Involvement and Concerns.  This
          section provides a brief history of community interests
          and concerns regarding the Claremont Polychemical Site.

   III.   Summary of Major Questions and Comments Received Purina
          the Public Comment Period and EPA's Responses.  This
          section summarizes comments submitted to EPA at the
          public meeting and during the comment period and
          provides EPA's responses to these comments.

    IV.   Appendices.  This section includes a copy of the agenda
          for the public meeting (Appendix A), Proposed Plan
          (Appendix B), public meeting sign-in sheet  (Appendix
          C), and the overhead transparencies used at the public
          meeting (Appendix D).

-------
Z.   RESPONSIVENESS SUMMARY OVERVIEW

Site Background

The Claremont Polychemical Site is an abandoned production
facility located in central Long Island, in the community of Old
Bethpage, Town of Oyster Bay, Nassau County, New York.  The
facility is situated in an area comprised of light industrial,
commercial and institutional properties (Oyster Bay Solid Waste
Disposal Complex, SUNY Agricultural and Technical College at Far-
mingdale, and Bethpage State Park).  The Suffolk County line is
approximately 800 feet east of the Site.

In 1985, Old Bethpage had a population of 5,881 persons and
Oyster Bay had a population of 305,750 persons, according to the
Current Population Report (U.S. Bureau of Census, 1987).  The
closest residences are approximately half a mile away on the west
side of the landfill.  The closest public supply well is located
3,500 feet northwest of the Site.

The Site occupies approximately 9.5 acres on which a 35,000
square foot, one story, concrete building is located.  Other
features include: treatment basins, aboveground tanks,
underground tanks, leaching basins, dry wells, and water supply
wells.

From 1968 until its closure in 1980, Claremont Polychemical
manufactured inks and pigments for plastics, coated metallic
flakes, and vinyl stabilizers.  The principal wastes generated
were organic solvents, resins, and wash wastes (mineral spirits).

Concern for contamination was linked to a discovery in 1979 by
the Nassau County Department of Health  (NCDOH) of 2,000 to 3,000
drums scattered throughout the Site, some uncovered and others
leaking.  By September 1980 most of the drums were sorted and
either removed from the Site or reused in the plant. Some of the
material was burned in the plant's boiler.  NCDOH inspectors
noted at the time that an area east of the building (spill area)
was contaminated with organic solvents as a result of accidental
and/or incidental spills and discharges.  A subsequent removal
action by the property owners, in 1980, excavated the upper ten
feet of a seventy-five foot by seventy-five foot area.  The
excavated material was placed on a plastic liner. Over the years,
this liner degraded and no longer is an impermeable layer.
Groundwater samples from a monitoring well installed at the time
indicated the presence of groundwater contamination directly
under the Site.

Claremont Polychemical and its affiliated companies entered into
receivership in 1980. In 1983, Woodward-Clyde Consultants, under
the direction of the New York State Department of Environmental
Conservation, conducted a preliminary investigation of the Site.

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In 1984, Velzy Associates conducted a limited study of the Site
for the property owners.  Additional work was performed by C.A.
Rich Consultants.  For the last four to five years two tenant
businesses have been operating at the Site.

The Claremont Polychemical Site was first proposed for inclusion
on the National Priorities List (NPL) in October 1984 and
received a final listing status in June 1986.  On December 4,
1987, EPA issued a special notice letter to Mr. Walter Neitlich
(Claremont Polychemical Officer) requesting a good faith offer to
undertake or finance the remedial investigation and feasibility
study.  No response was received from Mr. Neitlich or from the
company.  In March 1988 EPA obligated funds and started a
comprehensive RI/FS for the first operable unit.

A preliminary evaluation by EPA in July 1988 revealed the
presence of hazardous waste held in containers (e.g. drums) and
other holding units (treatment basins, aboveground tanks, and a
sump). In September 1988, EPA performed work consisting of the
overpacking and/or stabilization of deteriorated containers and
holding units.  A second operable unit RI/FS (OU-II) dealing with
the ultimate disposal of the above mentioned hazardous wastes was
completed by EPA in July 1989.  The Record of Decision for OU-II
was issued in September 1989.  The selected remedy is currently
being implemented and consists of compatibility testing,
bulking/consolidation, and treatment/disposal of the wastes at
off-site, EPA-approved, treatment facilities.

Summary of Remedial Alternatives

The remedial alternatives considered for the Claremont
Polychemical Site are described in the RI/FS and Proposed Plan
for this operable unit  (referred to as operable unit one).  Those
alternatives considered are detailed below:

Remedial Alternatives for Contaminated Soils (SC)

  o SC-l No Further Action
  o SC-3 Excavation/Off-Site Incineration/Backfill with Clean
    Soil
  o SC-4 Excavation/Low Temperature Enhanced Volatilization/On-
    Site Redeposition
  o SC-5 In-Situ Vacuum Extraction

Remedial Alternatives for Contaminated Groundwater  (GW)

  o GW-l No Further Action
  o GW-2 Pumping/Air Stripping/Reinjection; Site Boundary  (0.2
    mgd)
  o GW-3A Pumping/Air Stripping/Reinjection; Leading Edge of
    Plume (1.9 mgd)

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  o GW-3B Pumping/Air Stripping/Reinjaction; Site Boundary and
    Downgradient (1.0 ingd)
  o GW-5A Pumping/UV-Chemical Oxidation/Reinjaction; Leading Edge
    of Plume (1.9 mgd)
  o GW-5B Pumping/UV-chemical Oxidation/Reinjaction; Site
    Boundary and Downgradient (1.0 mgd)

Remedial Alternatives for Building (BD)

  o BD-1 No Further Action
  o BD-2 Building Decontamination/Waste Treatment and Disposal

Remedial Alternatives for Underground Storage Tanks (T)

  o T-l No Further Action
  o T-2 Removal and Off-Site Disposal

EPA, with concurrence from the New York State Department of
Environmental Conservation, chose a remedy which addresses the
principal threats posed by the Site through a combination of
source control alternatives - treatment of contaminated soils
(SC-4) and tank removal and treatment  (T-2), with active
restoration of the groundwater (GW-3B), and building
decontamination (BD-2).  Based on the current information, these
alternatives provide the best protection of human health and the
environment.

II.   BACKGROUND OF COMMUNITY INVOLVEMENT

Community interest in the Claremont Polychemical Site has been
moderate throughout the RI/FS process and removal actions.
Locally, the community has been active at public meetings related
to various environmental problems associated with the Old
Bethpage Landfill Site (OBL), Liberty Industrial Finishing Site,
and the Nassau County Fire Service Academy.  Several remedial
activities are currently being conducted at the landfill,
including extraction and treatment of groundwater contamination.
The community 'has been aware of the Claremont Polychemical Site
through newspaper articles, fact sheets, press releases, public
notices, and public information meetings.  Organized groups
include the Citizens for Pure Water in South Farmingdale.

The major concern expressed by the community is migration of
contaminants through groundwater.  Local officials and the public
in general have focused their concern on the potential for
groundwater contamination and the impact on the drinking water
supply wells located in the area.

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III.   SUMMARY OF MAJOR QUESTIONS AND COMMENTS RECEIVED DURING
       THE PUBLIC COMMENT PERIOD AND EPA'8 RESPONSES

Comments raised during the public comment period for the
Claremont Polychemical Site are summarized below.

COMMENT:  Local officials inquired about whether or not EPA
foresees any problems reinjecting the volume of groundwater to be
treated as part of the groundwater remedy.

RESPONSE:  EPA does not foresee any technical problems related to
the reinjection of the treated groundwater into the aquifer.  Our
current hydrogeological model indicates that the aquifer should
be able to assimilate this volume of water (1.0 million gallons
per day).  Construction and operation of the proposed groundwater
reinjection wells is technically feasible at the Site.  Normal
potential problems such as clogging of the well screens due to
suspended matter will be taken into account in the facility
design.

COMMENT:  A resident asked whether a risk assessment has been
prepared which calculates the overall risk to the population
exposed to contaminated groundwater, not only from the Claremont
Polychemical Site, but from the combination of all Superfund
sites in the vicinity.

RESPONSE:  The risk assessment developed by EPA for the Claremont
site addresses potential risk to human health and the environment
from exposure to the Claremont Polychemical Site-related
contamination only.  Calculation of a "global or regional" risk
figure would be difficult to accomplish since relationships
between sources and exposed population would need to be
determined for a variety of sources.  However, due to the
proximity of Claremont Polychemical with the Old Bethpage
Landfill (OBL), and the potential for overlapping plumes, the
risk calculated by EPA for exposure to groundwater at Claremont
Polychemical may be influenced by contamination from the
Landfill.  Remediation of the Claremont Polychemical contaminant
plume takes into consideration the potential impact of remedial
activities taking place at OBL (i.e., groundwater extraction and
treatment) in order to restore the aquifer to its best potential
use.

COMMENT:  A resident asked whether the remedial action taken by
the company's owners in 1980  (i.e., excavation of soils and
placement on plastic liner), and the use of liners in general,
constitutes a good remedial action.

RESPONSE:  It is difficult to assess the effectiveness of the
1980 action, since air and groundwater monitoring was not
conducted concurrently with the action.  Although liners are
effective in reducing the potential for soil contaminants to

-------
leach into the groundvater, they do not control the spread of
leachate unless a collection system is in place.  They also allow
for the volatilization of contaminants into the air phase without
treatment.  Such releases are generally not acceptable to EPA or •
New York State.  Generally speaking, liners without proper
controls are not standard EPA response techniques.

COMMENT:  Concern was expressed about other sources of
groundwater contamination  (e.g., the high number of Superfund
sites in the area), and how all these affect the groundwater
remediation.

RESPONSE:  When EPA takes action at superfund sites, it takes
into account potential upgradient or off-site contributions to
the site groundwater contamination.

In other cases, EPA selected a remedy to address site
contamination which is followed by a second operable unit to
address remediation of an upgradient source, if one has been
identified.  If a source has not been identified, EPA may conduct
a second operable unit investigation to assist in the
identification of an off-site source.

When EPA takes action at Superfund sites, it takes into account
potential upgradient or off-site contributions to the site
groundwater contamination.  In the case of the Claremont
Polychemical Site, a great amount of communication and
coordination has taken place between EPA and the Town of Oyster
Bay (which is in charge of remedial activities at OBL).  The
groundwater remedy selected at Claremont Polychemical foresees a
close coordination between the remedial activities taking place
at both the OBL and Claremont Polychemical Sites.

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APPENDIX A.  PUBLIC MEETING AGENDA

-------
<° «•«»,
(SB
         UNITED STATES ENVIRONMENTAL PROTECTION AGENCY

                             REGION I I
                          26 FEDERAL PLAZA
                       NEW YORK. NEW YORK 1O278
                              AGENDA
                          Public Meeting
               Claremont Polychemical  Superfund sit*
                 Old Bethpage Village Restoration
                      Old Bethpage, Mew York

                         September 5.  1990
                             7:00  P.M.
 I. Welcome & Introduction
 II.  Overview of Superfund
 III.  Remedial Investigation/
      Feasibility Study and
      Preferred Alternative
 VI.  Questions and Answers

 V.  Closing
                                         Cecilia Echols
                                         Community Relations
                                          Coordinator
                                         U.S. EPA, Region 2

                                         Douglas Garbarini
                                         Chief, Eastern New York &
                                          Caribbean Remedial Action
                                          Section
                                         U.S. EPA, Region 2

                                         Carlos R. Ramos
                                         Remedial Project Manager
                                         Claremont Polychemical
                                          Superfund Site
                                         U.S. EPA, Region 2

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APPENDIX B.  PROPOSED PLAN

-------
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    feyjyj^'t^y^^^^^-*^*^^^'^*-*^*^^^^*^*3^

 Superfund Proposed Plan
                                         Claremont  Polychemical  Site
                                           Old  Bethpage, Nassau County, New York
 EPA
 Region  2
                                  August 1990
 ANNOUNCEMENT OF PROPOSED PLAN

 The Proposed Plan describes the remedial alternatives
 considered for the Claremont Polychemical Superfund
 site and identifies the preferred remedial alternative
 wfth the rationale for this preference.  The Proposed
 Plan was developed by the U.S. Environmental
 Protection Agency (EPA) with support from the New
 York State Department of Environmental Conservation
 (NYSDEC). EPA is issuing the Proposed Plan as part
 of its public participation responsibilities under Section
 117(a)  of the Comprehensive Environmental Response,
 Compensation,  and Liability Act (CERCLA) of 1980. as
 amended and Section 300.430(f) of the National
 Contingency Plan (NCP). The alternatives summarized
 here are described in the remedial investigation and
 feasibility study (RI/FS) for this operable unit (referred
 to as operable  unit one in the RI/FS), which should be
 consulted for a more detailed description of all the
 alternatives.

 This Proposed Plan is being distributed to solicit public
 comments pertaining to all the remedial alternatives
 evaluated, as well as the preferred alternative.

 COMMUNITY ROLE IN SELECTION PROCESS

 EPA and NYSDEC rely on public input to ensure that
 the concerns of the community are considered in
 selecting an effective remedy for each Superfund site.
 EPA has set a public comment period which concludes
 on September 25, 1990. The public comment period
 includes a public meeting at which EPA will present the
 RI/FS Report and the Proposed Plan, answer
 questions, and  accept both crci and wiiHen ccmrne; its.

 A public meeting will be held in the auditorium of the
 Old  Bethpage Village Restoration, Round Swamp Road,
 Old  Bethpage, New York on  September 5, 1990 at 7:00
 p.m. to allow EPA to present the conclusions of the
 .RI/FS. to further elaborate on the preferred remedial
||fterric..;ve, a;'.j to receive
Documentation of the final remedy selection will be
presented in the ROD after consideration of all the
public comments. Comments will be summarized in
the Responsiveness Summary Section of the Record of
Decision.
  The administrative record file, which contains the
  information  upon which  the selection of the
  response action will be based, is available at the
  following location:

  Plainview-Old Bethpage
  Public Library
  999 Country Road
  Plainview, New York
  Tel. (516) 938-0077
  Hours:  Mon-Fri., 9:00 a.m to 9:00 p.m.
         Sat., 9:30 a.m. to 5:30 p.m.
         Sun., 1:00 p.m. to 9:00 p.m.
   Dates to remember
   MARK YOUR CALENDAR

   August 25 to September 25, 1990
   Public comment period on remedies

   September 5, 1990
   Public  meeting  at   the  Old  Bethpage
   Restoration Auditorium,  Old Bethpage, New
   York at 7:00 p.m.

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SHE BACKGROUND

The Claremont Polychemical site is an abandoned
production facility located in central Long Island, in the
community of Old Bethpage, Town of Oyster Bay,
Nassau County. New York.  The facility is situated in
an area comprised of light industrial, commercial and
Institutional properties (Oyster Bay Solid Waste
Disposal Complex, SUNY Agricultural and Technical
College at Farmingdale,  and Bethpage State Park). The
Suffolk County line is approximately 800 feet east of
the site.

The Site occupies approximately 9.5 acres on which  a
35,000 square foot, one story, concrete building is
located (see Figure 1).   Other features include:
treatment basins, aboveground tanks, underground
tanks, leaching basins, dry wells, and water supply
wells.

From 1968 until its closure in 1980. Claremont Polych-
emical  manufactured inks and pigments for plastics,
coated metallic flakes, and viny' stabilizers. The
principal wastes generated wer- organic solvents,
resins,  and wash wastes (mineral spirits).

Concern for contamination  was linked to a discovery
in 1979 by the Nassau County Department of Health
(NCDH) of 2,000 to 3,000 drums were scattered
throughout the Site; some uncovered and others
leaking. By September 1980 most of the drums were
sorted and either removed from the site, or reused in
the plant.  Some of the material was burned in the
plant's boiler. NCDH  inspectors  noted at the  time mat
an area east of the building (spill area) was
contaminated with organic solvents as a result of
accidental and/or incidental spills and discharges. A
subsequent removal action, in 1980, excavated the
upper ten feet of  a seventy-five foot by seventy-five foot
area.  The excavated  material was placed on  a plastic
liner.  Over the years, this liner has  degraded and no
longer is an  impermeable layer. Groundwater samples
from a monitoring well installed at the time indicated
the presence of groundwater contamination directly
under the site.

Claremont Polychemical and its affiliated companies
entered into receivership in 1980. In 1983,  Woodward-
Clyde Consultants, under the direction of the New York
State Department of Environmental Conservation,
conducted a preliminary investigation of the site. In
1984, Velzy Associates conducted a limited study of
the site for the  property owners. Additfonal wort; was
performed by C.A. Rich Consultants in response to a

-------
request for information by the U.S., Bankruptcy Court.
For the last four to five years two tenant businesses
have been operating at the site under the supervision
of the Bankruptcy court

A preliminary evaluation by EPA on July 1988 revealed
the presence of hazardous waste held in containers
(e.g. drums) and other holding units (treatment basins,
aboveground tanks, and a sump). In September 1988,
EPA performed work consisting of the overpacking
and/or stabilization of deteriorated containers and
holding units.  A second operable unit RI/FS (OU-II)
dealing with the ultimate disposal of the above
mentioned hazardous wastes was completed by EPA in
July 1989.  The Record of Decision for  OU-II was
issued on September 1989.  The selected remedy is
currently  being implemented  and consists of
compatibility testing, bulking/consolidation, and
treatment/disposal of the wastes at off-site, EPA-
approved, treatment facilities.

SCOPE AND ROLE OF OPERABLE UNIT

EPA divided the remedial work being conducted at the
Claremont Polychemical site into two operable units.
The first operable unit addresses the overall site
remediation (groundwater and soil) and is the focus of
this document.  This RI/FS contains the detailed
information and data used in determining the nature
and extent of the problem, and the development of
remedial  alternatives to address the problem.

As discussed above, the second operable unit  deals
only with the wastes held in containers and holding
units.  In September 1989, EPA decided to  remove
these wastes and treat/dispose of the materials off-site.
This action, which includes the containers found inside
the building (e.g. drums) and the wastes contained
inside the holding units (e.g.  treatment  basins,
aboveground tanks), is currently ongoing.

The overall objective of the remediation is to reduce
the concentrations of  contaminants to levels which  are
protective of human health and the environment  The
remedy selected will achieve this objective by:

  o    Soil Treatment.  Treatment of the soil to remove
       the mobile organic contamination will result in
       the elimination of a long-term source of
       contamination of the groundwater.

  o    Groundwater Treatment.  Extraction  and
       treatment of the contaminated groundwater will
       contain the migration of the plume and in time
       will achieve Federal and State standards for the
       volatile organic contaminants.
  o     Building Decontamination.  Removal of all
        hazardous materials from the building will
        eliminate any potential risk to human hearth
        and the environment,  and will allow for
        unrestricted use of the building in the future.

  o     Removal/Treatment of Underground Tanks.
        Liquid Wastes,  and Associated  Soils.
        Removal and treatment of these wastes will
        result in the elimination of the threat  to human
        health and the  environment from possible
        contact with the wastes. Also will result in the
        eradication of a long-term source of
        groundwater contamination.

SUMMARY OF SfTE RISKS

A baseline risk assessment was developed as part of
the remedial investigation for Claremont  Polychemical.
The risk assessment evaluates the potential impacts on
human health and  the environment if the contamination
at the site is not remediated. This information is used
by EPA to make a determination as to whether
remediation of the  site may be required.

Two basic scenarios were developed based on present
(industrial) and possible future (residential) land use at
the Site.  Under both scenarios several pathways
(direct contact, inhalation and ingestion) were
evaluated  for exposure to surface and subsurface soils,
air, resuspended building  dust, and ground water used
for drinking and domestic purposes. The populations
evaluated  included on-site residents; off-site residents
(including students and  recreational users); and
workers.  Two estimates were developed,
corresponding to the maximum concentration  detected
or 'worst case scenario* and a representative  exposure
or 'most reasonable case'.  EPA considers risks in the
range of 10"4 to 10* to be acceptable.  This risk range
can be interpreted to mean than an individual may
have a one in ten  thousand to a one in a million
increased  chance of developing cancer  as result of
site-related exposure to  a carcinogen over a 70-year
lifetime under the specific exposure conditions at the
Site.

Based on  the Rl report some of the contaminants of
concern are: tetrachloroethene (PCE) and bis(2-
ethylhRxynphthalate (BEHP) in soil; 1,1.1-
trichloroethane, tetrachloroethene and bis(2-
ethylhexyOphthalate in groundwater; cadmium,
chromium and copper in the building; and 2-butanone.
toluene and bis(2-ethylhexyQphthalate in the
underground storage tanks.

rDYs bnselinc :n^=ngerment assessment indicates
  ^l the most significant--public health risk results from

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Maximum Concentration of Selected
Contaminants Delected in Soil. '
Groundwater. Building a/id Underground
Tank Content
CONCEN-
MATRIX COMPOUND TRAT1ON
SOIL
(ma/Kg)


GROUND
WATER
(ug/Kg)




BUILDING
(ug/wipe)




TANKS
(mg/Kg)


bi((2-«thylhexyl)
phthalole
tetrachloroelhen*
toad
1.1.1-
tiichloroethana
trichloroethen*
letrachloroelhene
•Ihylbenzen*
bis(2-ethylhexyl)
phthalate
chromium
bis(2-ethylhexyl)
phthalate
cadmium
chromium
copper
lead
2-bu:anon«
toluene
xylene
bis(2-ethylhexy<)
Dhthalate
270
26
98
100
260
1.300
160
50
159
70
313
1.103
24.600
7.974
92.000
2.600
3.600
23.000
the ingestion of grounbwater, inhalation of groundwater
volatiles (e.g. wh'i'.e showering), and the inhalation of
resuspended dust inside the building under the future
use scenario.  Under the representative and worst-
case scenario, the lifetime excess cancer risk of
drinking the on-site groundwater are 1.36 x 10" and
4.53 x 10", respectively. This indicates that an
individual has a one in ten thousand and, a five in ten
thousand chance a' developing cancer as a result of
drinking this water.  Similarly, the representative and
worst-case risk for people inhaling the on-site
groundwater volatiles are 4.36 x 10s and 1.45 x 10",
respectively. Under the representative-case scenario,
the potential excess cancer risk associated with
exposure to  rssuspended building dust is 2.37 x 10",
and 5.09 x 103 under the worse-case scenario. For
ingestion of off-site groundwater the representative-
case risk is 9.59 x 10*; the worst-case risk is
3.20 x 10".

The risk assessment contains the conclusion that direct
exposure to site soils does not represent a significant
risk to human health and the environment. However,
they do pose a significant indirect risk by  being a
continuous source of groundwater contamination.
Contaminants in excess of Federal and State standards
were detected in the site groundwater plume.  EPA
policies and regulations allow remedial actions to be
taken whenever cross-media impacts  result in the
exceedance of one or more Maximum Contaminant
Levels.  Consequently,  soil remediation is  warranted to
remove this continuous source of contamination into
the groundwater and expedite compliance with Federal
and State groundwater standards.

Actual or threatened releases of hazardous substances
from this site, if not  addressed by the preferred
alternative or one of the other active measures
considered, may present  a current or potential threat to
the environment through the groundwater  pathway.

SUMMARY OF REMEDIAL ALTERNATIVES

The remedial alternatives are organized according to
the media areas which they  address:  soil  (SC),
groundwater  (GW), building (BD) and underground
tanks (T).  These alternatives were screened based  on
implementability, effectiveness,  and cost. The screening
resulted in remedial alternatives upon which a detailed
analysis was  performed.  Those alternatives considered
in detail are discussed below.  Time  to implement*  is
defined as the period  of time needed for the alternative
to be started (e.g. amount of time needed for the
construction of a treatment facility). It does include the
time required for remedial design activities which is
assumed to take 2 years.

SOILS
   Remedial Alternatives for Contaminated Soils (SC)

    o    SC-1 No Further Action
    o    SC-3   Excavation/Off-sit e
         'mcineration/Sackfiu with Clean Soil
    o    SC-4   Excavation/Low   Temperature
         Enhanced  Volatilization/On-Site
         Redeposition    ;  :   :  :   ;;
    o    SC-5 In-Situ Vacuum Extraction

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 Alternative SC-1: No Further Action

 Capital Cost: none
 O & M Cost: $34,909 per year
 Present Worth Cost: $564,300
 Time to Implement: 1 month

 The  No Action alternative provides the baseline case
 for comparison -with other soil alternatives. Under this
 alternative, the contaminated soil is left in place without
 treatment. A long-term groundwater monitoring
 program would be implemented to track the  migration
 of contaminants from the soil into the groundwater.
 Existing monitoring wells would be used for monitoring.
 Five year reviews would be performed to assess the
 need for further actions.

 Remedial investigation-related roll-off containers and
 drums containing soils  and drilling mud would have to
 be transported off-site for treatment and disposal.

 Alternative SC-3: Excavation/OfT-Site
 Incineration/Backfill with Clean  Soil

 Capital Cost: $18,535,100
 O & M Cost: none
 Present Worth Cost: $18,535,100
 Time to Implement: 3.5 years

i Site  preparation for the remedial  implementation would
 include a parking area, equipment staging area and
 stockpile area. Support facilities  (e.g.  offices) would
 also be  installed on the site. An estimated total of
 6,240 cubic yards (cy) of soil would be excavated.
 Excavation would be  conducted under moistened
 conditions by spraying  water over the  surface to
 minimize fugitive dust and volatile contaminant
 emissions.  The soil would be  stockpiled  prior to
 transportation to an off-site facility. The excavated soil
 would be transported to an off-site, EPA-permitted
 incineration facility for treatment and disposal.  The
 roll-off containers and drums containing soil can also
 be re-packed into the same type of containers and
 transported for off-site incineration along with the soil.
 Clean soil would be used to backfill the excavated
 area. Sits restoration would include the application of
 topsoil and seeding.

 Alternative SC-4:  Excavatton/On-Siie Low Temperature
 Enhanced Volatilization/OrhStte Redfeposftion

 Capital Cost:  $2,262,500
 0 &  M  Cost:  none
 Present  Worth Cost: $2,262,500
 Time to  Implement 3.5 years

ftSite preparation &nd sou excavation would be
 performed as in Alternative SC-3.  An estimated 6,240
 cy of contaminated soil would be treated in a mobile
 enhanced volatilization (low temperature thermal
 extraction) unit brought on site.  Low temperature
 thermal extraction consists of a feed system,  thermal
 processor, afterburner, and scrubber. The excavated
 contaminated soil is placed in the feed hopper with a
 backhoe. The  soil is then conveyed from the hopper
 to the thermal processor. Hot air from an  air heater is
 injected  into the thermal processors at a normal
 operating temperature of 260°C  (500°F) which is well
 above the boiling points of most volatile organic
 compounds (VOCs).  The volatilized compounds and
 moisture in the contaminated soil  is then burned at
 1090°C (2000°F) in an afterburner operated to ensure
 complete destruction.  A portion of the off-gas is
 recirculated as combustion air to minimize fuel usage.
 The off-gas is then treated at the scrubber for
 paniculate removal and acid gas adsorption.  The
 off-gas leaves the system at a temperature of less than
 93°C (200°F).

 The volatilized contaminant-laden gas also can be
 treated by an activated carbon adsorption unit instead
 of an afterburner for PCE removal. A bag filter would
 be used to remove particulates  from the gas before it
 enters the carbon adsorption unit. The treated soil
 would be free of volatile organics  and would  be stored
 for sampling and then used as  backfill in the excavated
 areas.  Site restoration would  be performed as in
 Alternative SC-3.  The roll-off containers and  drums
 containing Rl soil can also be treated with the soil.

 Alternative SC-5:  In-Situ Vacuum  Extraction

 Capital Cost: $385,600
 O & M Cost: none
 Present  Worth  Cost: $385,600
 Time to  Implement: 4 years

 Site preparation would be performed as in Alternative
 SC-3.  However, the soil  is left in place undisturbed,
 therefore no excavation would be required. This
 alternative involves the installation of vacuum extraction
 wells over the contaminated soils.  Each well would
 have a maximum  depth  of 10 feet. The vacuum wells
 would be connected v\t> a pipe  system to  a
 skid-mounted high volume vacuum pump.  The vacuum
 would pull air through the contaminated soils, within a
'rad/us of approximately 20 feet from the wells,
 depending on soil composition and volatility  of the
 contaminant. The air  containing the  stripped VOCs
 would be fed through a condenser to recover the free
 product  and moisture, and then through an emissions
 control system, i.e., a  vapor phase carbon adsorption
 system.  The condense, prcc'uc.'. wouj;J be drummed
 and transported to an off-site treatment and  disposal

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facility (most likely to be an incinerator). The roll-offs
and drums containing soil can also be treated on-site
via this technology by Using a one-pipe system within
the drum connected to  a vacuum pump.  The treated
soils would be used on-site for backfilling and
regrading.

GROUNOWATER
  Remedial   Alternatives   for   Contaminated
  Groundwater (GW)

    o  GW-1  No Further Action
    o  GW-2  Pumping/Air  Stripping/Reinjection;
  ::  Southern Site Boundary (0.2 mgd)
    o  GW-3A Pumping/Air  Stripping/Reinjection;
  ::    Leading Edge of Plume (1.9 mgd)
  ••'•  o  GW-3B Pumping/Air  Stripping/Reinjection;
       Southern Site Boundary and Downgradient
       (1.0 mgd)
    o  GW-5A   Pumping/UV-Chemical
       Oxidation/Reinjection;   Leading   Edge  of
       Plume (1.9 mgd)
    o  GW-5B    Pumping/UV-Chemical
       Oxidation/Reinjection;   Southern   Site
       Boundary and Oowngradient (1.0 mgd)
Alternative GW-1:  No Further Action

Capital Cost: none
0 & M Cost: $28,400
Present Worth Cost: $464,400
Time to Implement: 1 year

This alternative includes the use of existing wells to
conduct a long-term groundwater sampling program
which would monitor the migration of contaminants of
concern in the aquifer.  A total of ten wells, including
existing upgradient,  on-site and downgradient welts,
would be utilized in  order to sample  the groundwater
from the shallow xo deeper portions of the aquifer and
to track contaminant migration off-site.  Regular
five-year review's wo-jld be performed to assess the
need for additional remedial actions.

Anemaflve GW-2:  Purapng/Prefrealment/Air
Stripping/Carbon AdsorpforVReinjeciion; Pumping at
the Southern Site Boundary (0.2 rogd)

Capital Cost: $214,800
0 & M Cost: $378,700
Present Worth Cost: $3,350,500
Time to Irrplsmp?': i -5 years
This alternative includes the installation of three
extraction wells downgradient of the site in order to
extract 0.2 million gallons per day (mgd)  of
groundwater from the site contaminant plume. This
groundwater would be piped to the Old Bethpage
Landfill groundwater treatment system for treatment
and disposal. The Landfill groundwater treatment
system is currently under construction and scheduled
to be completed in 1991. The 0.2 mgd is the
maximum allowable input from the Claremont Site to
the Landfill pump and treatment system due to design
limitations of that system. The treated effluent would
be reinjected into the aquifer through a recharge basin
being constructed as part of the  Landfill system. This
flow rate is below the modeled .maximum pumping rate
of 1.9 mgd estimated for removal and treatment of the
site contaminant plume.  (The original estimate of the
volume of contaminated groundwater to be treated was
much less than the current estimate).  In addition, the
landfill treatment system is only planned  to operate for
10 years based upon the time estimated for
remediation to the completed for the Old Bethpage
plume.  Long-term monitoring using the new extraction
and existing wells would be  performed for 30 years in
order to  monitor any continued migration of remaining
contamination in the groundwater, both during and
after the operation of the landfill treatment system.

AJtematfve GW-3A:  Pumping/Pretreatment/Air
Stripping/Carbon Adsorption/Reinjection;  Pumping at
the Leading Edge of the Plume (1.9 mgd)

Capital Cost: $4,044,700
O & M Cost: $1,622,900
Present Worth Cost: $28,978,000
Time to Implement: 3 years

In this alternative, three extraction wells would be
installed downgradient of the site on the Bethpage
State Park  property in order to capture the entire site
contaminant plume. Approximately 1.9 mgd  would  be
pumped to an on-site treatment facility. The treated
groundwater would be pumped to a discharge system
for reinjection to the aquifer  via three reinjection wells.
The siting of the extraction wells would be completed
during the design.phase based on technical criteria

The groundwater treatment facility would consist of two
major processes: pretreatment to remove metals (iron,
manganese, arsenic, and thallium) and air strippers
followed by a carbon adsorption system to remove
volatile and semivolatile organics. The pretreatment
system  is designed to  effectively reduce the  metal
concentrations in the groundwater below the Federal
and New York State Groundwater Standards. This
pretreatment system would consist ci - .nelais
precipitation system and'dual media pressure filter.

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 The resulting sludge would require off-site treatment
 and disposal.

 Two air strippers in series followed by liquid phase
 carbon adsorption would be used to lower the levels of
 organic contamination below the state requirement for
 groundwater standards.  Approximately 95 to 99
 percent of the volatile organics would be removed by
 air stripping. The stripped groundwater would be
 pumped to a two-stage liquid  phase carbon adsorber
 for removal of the remaining volatiles and BEHP, and
 phenol. The volatile organic emissions from the air
 stripping would be adsorbed on a vapor phase
 activated carbon system in order to meet air quality
 standards.  Once the vapor phase and liquid phase
 carbon is exhausted, it would  be removed for off-site
 regeneration or incineration, thus destroying all organic
 contaminants. Two treatment  trains (parallel systems
 for treating the groundwater} rated at 660 gallons per
 minute (gpm) each would be required.

 Environmental monitoring would be required during the
 life of the treatment plant operation (i.e.,  30 years).  Air
 emissions would be  monitored to confirm compliance
 of the air discharge limit.  Groundwater samples would
 be taken every six months to monitor groundwater
 contamination migration and effectiveness of
 remediation. Under this  alternative it is estimated to
 take 62 years to  achieve remediation of the
 groundwater plume

 Alternative GW-3B: Pumping/Pretreatment/Air
 Stripping/Carbon Adsorption/Reinjection;  Pumping at
 the Southern Site Boundary and Downgradient (1.0
 mgd)

 Capital Cost: $4,936,000
 0 & M Cost: $1,100,400 (first ten years)
             $701,900 (next six years)
 Present Worth Cost. $15,620,400
 Time to Implement 3 years

 in this Alternative, two extraction wells would be
 installed slightly downgracltent of the southern
 boundary ol me ste to capture the most contaminated
 grounctwater. Two additional extraction wells would be
 located downgradient from the site to capture the off-
 site (diluted) migrating plume.  Groundwater would be
 pumped at a rate of 1 mgd and_traat»d on-site as in
 Alternative GW-3A.  In ihfs alternative four treatment
 trains  rated at 175 gpm would  be used.  Treated
 groundwater would be reinjected  into the aquifer.

 This alternative would be implemented m two phases.
 During the first phase extraction wells wca/d be
.installed at the southern  bound-: •/ requiring two
Itreatmetit trains to treat the concentrated groundwater
plume.  During the second phase the diluted
groundwater plume would be extracted, requiring the
installation of two additional treatment trains.  In
between these phases  (approximately 1-2 years),
critical information would  be  developed concerning the
impact of neighboring pump and treatment systems
(e.g. Old Bethpage Landfill) on the Claremont
Polychemical plume.  Additional sampling would be
conducted to further  delineate the extent of the
Claremont plume.  Implementing this remedy in two
phases would provide increased overall efficiency and
flexibility. This optimized extraction and treatment
system design would be  better able to address the
remediation  of the Claremont site plume.  It is
estimated that 16 years of pumping and treatment
would be required to complete the groundwater
remediation.

Alternative GW-5A:  Pumping/Pretreatment/UV-Chemical
OxJdation/Reinjection; Pumping at the Leading  Edge of
the Plume (1.9 mgd)

Capital Cost: $4,088,900
0 & M Cost: $108,000
Present Worth Cost:  $21,121,100
Time to Implement: 3 years

This remedial alternative  is similar to Alternative GW-3A
except that a chemical oxidation process rather than air
stripping/adsorption process would be used  to remove
the volatile and semivolatile organics in the
groundwater. An ultraviolet  light-hydrogen peroxide
oxidation system is selected as the representative
process to treat the  contaminated groundwater. This
oxidation system would employ a combination  of
hydrogen peroxide (H,Oj) and ultraviolet (UV) light to
chemically oxidize the organic contaminants  in the
groundwater to carbon dioxide, water and chlorides.
Multiple units would  be required.  The treated
groundwater would have organic concentrations below
State and Federal standards.

Alternative GW-5B:  Pumping/Pretreatment/UV-ChemicaJ
Oxidaijon/Retnjection; Pumping  at the Southern Site
Boundary and Downgradient (1.0 mgd)

Capital Cost: $4,069,800
O & M Cost: $1,008,600  (first ten years)
             656,000 (next six years)
Present Worth Cost  $13,902,300
Time to Implement: 3 years

Groundwater extraction, pretreatment, and reinjection
would be accomplished as in Alternative GW-3B. The
UV-H202 system would, operate as in Alternative GW-5A
except that smaller tr?.-tment units ryculd be used.

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BUILDING
 Alternative T-1:  No Further Action
   Remedial Alternatives for Building (BD)

  .  o  BD-1 No Further Action
    o  BD-2   Building    Decontamination/Waste
       Treatment and Disposal
Alternative BD-1: No Further Action

Capital Cost: $8,800
O & M Cost: $2,100 per year
Present Worth Cost: $41,100
Time to Implement: 1 month

The No Action alternative  provides the baseline against
which other alternatives can be compared.  It would
result in leaving the contaminated dust, asbestos
insulation, and contaminated water in floor drains and
condensers intact in the building.  The only additional
security measure implemented to completely seal the
building would be waterproofing of the building ceiling.

A long-term maintenance  program, including site
inspections, would  be implemented in order to ensure
that the building is completely sealed and is not
accessible to the public in the future.

Alternative BD-2: Building Decontamination

Capital Cost: $186,200
0 & M Cost: none
Present Worth Cost: $186,200
Time to Implement: 1 month

The inside contaminated surfaces of the building (i.e.,
walls, floors, and hoods) would be decontaminated
using dusting, vacuuming and wiping procedures.  In
addition three dust collectors on the roof would be
emptied.  The collected tfjsl wou/d be transported to
an off-site treatment aid tfsposaf facility. The
contaminated water in the floor drains and condensers
also would be removed and disposed of off-site.

UNDERGROUND STORAGE TANKS
  Remedial AftemaiNes for Underground
  Tanks (T)

    o  T-1 No Further Action
    o  T-2 Removal and Off-Site Disposal
 Capital Cost: $2,600
 O & M Cost: $2,200 per year
 Present Worth Cost: $64,300
 Time to Implement: 4 months

 Under this alternative the underground tanks and
 contents would be left in place.  The large amounts of
 hazardous materials contained in the tanks would
 continue to constitute a potential source of soil and
 groundwater contamination. A monitoring program
 using the existing monitoring wells would be
 established to detect the movement of these
 compounds into the groundwater.

 Alternative T-2  Removal and Off-Site
 Treatment/Disposal

 Capital Cost: $336,300
 O & M Cost: none
 Present Worth Cost: $336,300
 Time to Implement: 4 months

 This alternative entails excavation of overburden soils,
 pumping of tank contents,  tank cleaning, removal of
 tanks and appurtenant equipment, off-site
 disposal/treatment of tanks, equipment and liquid
 waste, and backfilling with  clean soil.

 The underground tanks and appurtenant piping would
 be drained and cleaned of any residual sludge.  Tanks
 would be hoisted and subsequently loaded on trucks
 and hauled for off-site disposal.  Other components of
 the tank farm, such  as pumps,  concrete pads, and the
 pumphouse, would be demolished and transported off-
 site for disposal. At the disposal facility, the steel
 tanks would be retested for hazardous waste contents.
 Nonhazardous tanks would either be sold for scrap or
 landfilied, depending on the extent to which they can
 be decontaminated.  Hazardous tanks and tank
 contents would be disposed of at an off-site EPA-
 approved hazardous waste treatment and disposal
 facility.

 Highly contaminated soils discovered during tank
 excavation would be stockpiled in roll-off containers
 and subsequently transported to an off-site EPA-
. licensed treatment and disposal facility.  Sampling  of
 the soils underlying  the tank farm would be conducted
 as part of this  alternative to further delineate the nature
 and extent of soil contamination within this area and to
 assess effectiveness of the remedy.

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   ALUAT1ON OF THE REMEDIAL ALTERNATIVES
 The preferred alternative* for the remediation of the site
 combines source control alternatives with active
 restoration of the groundwater.  Alternative SC-4,
 excavation of the contaminated soils, on-srte low
 temperature thermal treatment, and  on-site redeposition
 is the preferred alternative to clean up the soils.  The
 preferred alternative for  remediation  of the groundwater
 contamination is alternative GW-3B,  extraction of the
 groundwater at the site  perimeter and downgradient,
 followed by treatment (metal precipitation, air stripping
 and carbon adsorption)  and reinjection of the treated
 water into the aquifer.  Alternative BD-2 and T-2 are the
 preferred alternatives for the building and underground
 tank  areas. Alternative BD-2 entails removal of
 contaminated dust from the building by vacuuming and
 wiping, and removal of the liquid wastes from drains
 and condensers.  Under alternative  T-2, the
 underground storage tanks, tank contents, and the soil
 around it would be excavated and disposed of at an
 off-site treatment facility.

 Based on current information, this combination of
 alternatives provides the best balance among the nine
 criteria that EPA uses to evaluate alternatives and to
Censure that all important considerations are factored
into remedy selection decisions. The Analysis section
 profiles the performance of the  preferred alternative
 against the nine criteria, noting how it compares to
 other options under consideration.

 The evaluation criteria is noted  below and explained
 below.

  o    Overall protection of human health and the
        environment addresses  whether or not a
        remedy provides adequate protection and
        describes how risks posed through each
        exposure pathway (based on a reasonable
        maximum exposure scenario) are eliminated,
        reduced, or connoted through treatment,
        engineering controls, or institutional controls.

  o   . Compliance with applicable  or relevant and
        appropriate requirements (ARAR's) addresses
        whether or  not a remedy would meet all of the
        applicable or relevant and appropriate
        requirements ol  other Federal and State
        environmental statutes and requirements or
        provide grounds for invoking a waiver.

  o    Long-term effectiveness and permanence  refers
        to the ability of  a remedy to maintain reliable
        protection of human health and the
        environment over time, once cleanup goals
        have been met  It  also addresses the
        magnitude and effectiveness of the measures
        that may be required to manage the risk
        posed by treatment residuals and/or untreated
        wastes.

 o      Reduction of toxicitv, mobility, or volume
        through treatment is the anticipated
        performance of the treatment technologies,
        with respect to these parameters, a remedy
        may employ.

 o      Short-term effectiveness addresses the period
        of time needed to achieve protection and any
        adverse impacts on human health and the
        environment that may be posed  during the
        construction and implementation period until
        cleanup goals are achieved.

 o      Implementabilitv is the technical  and
        administrative  feasibility of a remedy, including
        the availability of materials and services
        needed to implement a particular option.

 o      Cost  includes  estimated capital and operation
        and maintenance costs, and net present
        worth costs.

 o      State acceptance indicates whether, based on
        its review of the RI/FS and Proposed  Plan, the
        State concurs with, opposes, or has  no
        comment on the selected remedy at the
        present time.

 o      Community  acceptance will  be assessed  in
        the Record  of Decision (ROD) and refers to
        the public's general response to the  alterna-
        tives  described in the Proposed Plan  and the
        RI/FS reports.

ANALYSIS

Comparison Among Sofl (SC) Alternatives

The following discussion compares the relative
performance of each soil alternative using the specific
evaluation criteria listed previously.

 o      Overall Protection of Human Health and the
       . Environment

Alternative SC-1 does not meet the remedial objectives,
thus it is not protective  of human health and the
environment.   As  a result of this alternative, the
groundwater would continue to be contaminated by the
soil source for some unknown period.  Alternatives
SC-3, SC-4 and to some extent SG-5 would meet  the
remedial objective of .protecting the groundwater from

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                                                     10
 the soil source by achieving the cleanup level in soils.
 Therefore, alternatives SC-3, SC-4 and SC-5 (to a
 lesser extent) are protective of hunan hearth and the
 environment

  o     Compliance with ARARs

 All technologies proposed for use in Alternative SC-3
 through SC-5 would be designed and implemented to
. satisfy all ARARs.  Federal and State regulations
 dealing with the handling and transportation of
 hazardous wastes to an off-site treatment facility would
 be followed.  The off-site treatment facility would be
 fully EPA-approved.  RCRA wastes would be treated
 using specific technologies or specific treatment levels,
 as appropriate, to comply with land disposal
 restrictions.

  o     Long-Term Effectiveness and Permanence

 Afternatfve SC-1 would only monitor the migration of
 the contaminants and does not provide treatment or
 containment.  Therefore, it does not  provide effective or
 permanent long-term protection of groundwater at the
 site.

 Alternatives SC-3, SC-4  and SC-5 are similar in their
 ability to mitigate the risks through the removal and
 treatment of site contaminants to meet the required
 cleanup levels. Alternatives SC-3 and SC-4 provide  a
 high degree of effectiveness since they can effectively
 remove the contaminants from the soil. Although
 Alternative SC-5 is intended to have  a similar ability to
 mitigate soil contamination, due to the technical
 limitations of  in-situ process, SC-5 may not ensure
 removal of contaminants to the cleanup level.

  O    Reduction in Toxicity, Mobility,  or Volume

Alternative SC-1 would provide a very slow and gradual
 reduction in toxicity through rainfall percolation,  ft
would provide no reduction in contaminant mobility.

Alternatives SC-3, SC-4, and SC-5 again are similar,  in
that each would result in significant reductions in the
toxicity, mobility, and volume of the treated material.  .
Material toxicity would be reduced by thermal
destruction of contaminants in Alternatives SC-3 and
SC-4 and by  off-site treatment of the condensed
organic product in SC-5. Alternative SC-3 would
provide the greatest degree of reduction in toxicity of
the contaminants followed by SC-4 and SC-5.

  o    Short-Term Effectiveness

The implementation of Alternative SC-1 would not result
in additional risk to the community during
implementation. Alternatives SC-3, SC-4, and SC-5
include activities such as contaminated soil excavation
and off-site transport or on-site treatment that could
potentially expose residents to volatilized contaminants
and contaminated dust  Engineering controls and
other measures (e.g. restricting access to the site to
authorized personnel only) would effectively  eliminate
any impact these activities would have on nearby
residents. Alternative SC-5 includes in-situ treatment of
contaminated soils, so exposure risks to residents from
excavation is much less of a concern for this alternative
than SC-3 and SC-4.  Under alternatives SC-4 and
SC-5, proper air emission control units would be
installed to minimize the potential for public  health
exposures because of low-level emissions from the
on-site treatment  units.

Alternative SC-1 would result in a lower overall  risk to
workers than other alternatives since subsurface soil is
not disturbed. Alternatives SC-4 and SC-5 provide
treatment on-site, thereby reducing potential risk to
residents along transportation routes.  Alternatives SC-
3, SC-4, and SC-5 would present a potential for worker
exposure to volatilized contaminants during waste
excavation and/or handling.  To minimize and/or
prevent such exposures, use of personal protection
equipment would be necessary.

SC-1  would be implemented in approximately one
month.  Alternatives SC-3,  SC-4 and SC-5 would be
implemented in about 3.5,  3.5 and 4 years,
respectively.

  o      Implementabilitv

Components of Alternatives SC-1, SC-3, SC-4 and SC-5
would utilize relatively common construction equipment
and materials. Little construction difficulty would be
encountered with any of the alternatives.  However,
Alternative SC-1 would be the easiest to implement.

The technologies proposed for use in the alternatives
are proven and reliable in achieving the specified
process efficiencies and performance goals.  Low
temperature thermal enhanced volatilization and in-situ
vacuum extraction have been successfully tested at
other Superfund sites.  However,  there is a greater
degree of uncertainty regarding the achieving of
cleanup levels using in-situ vacuum extraction since
this technology has only been performed on a  limited
full-scale basis at similar contaminant concentration
levels.
The tntqi nretjqnt worth costs for the alternatives
evaluated ranged from $385,600 (in-situ vacuum

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                                                    11
   faction) to $18,535.100 (off-site treatment and
'disposal).  Present worth considers a 5% discount rate.
and a 30-year operational period in the case of OC-1.
All other source control alternatives would not require
any operation and maintenance cost. Therefore,
present worth for these alternatives (SC-3, SC-4 and
SC-5) would be the same as the capital cost SC-4
provides the same protection as alternative SC-3 at a
fraction of the cost (52,262,500 versus $18,535,100).
Although alternative SC-5 is significantly less expensive
than SC-3 and SC-4,  it may not provide the same level
of protection.

  o    State Acceptance

MYSDEC concurs with the preferred alternative
selected.

Comparison of the Groundwater (GW) Alternatives

The following section compares the relative
performance of each  groundwater  alternative.

  o    Overall Protection of Human Health and the
       Environment

The no-action alternative would not protect human
health and the environment.  Existing contamination
would continue to degrade the aquifer and migrate
off-site.

Alternative GW-2 would not ensure protection of the
health of future  users of the aquifer nor would it
improve the overall quality of the aquifer or  prevent the
continued migration of contamination.

Each of the alternatives GW-3A. GW-3B, GW-5A and
GW-5B would be  significantly more protective than GW-
1 or GW-2 since they would reduce the toxicity,
mobility, and volume  of contaminants in the aquifers.
Each treatment  alternative considered would equally
protect human health and the environment however,
the amount of time required to achieve the ARARs
varies greatly among alternatives.

  o    Compliance with ARARs

Alternatives GVV-1 and GW-2 would result in
contaminant concentrations remaining above ARARs
(tor drinking water or protection of the groundwater
resources) for a long period of time (100 years).

Alternatives GW-3A, GW-3B. GW-5A and GW-5B would
be designed to  achieve all drinking water standards as
well as those required for groundwater protection  in the
r^ated water stream  which is to be reinjected. Each  of
these alternatives would be capable of providing the
required contaminant removal levels.  Because
experience with UV-chemical systems is limited, its
effectiveness is slightly less certain but considered
achievable. Each of the alternatives would comply with
air emission standards as well as regulations for the
handling and  disposal of the generated wastes (e.g.
spent carbon).

  o     Long-Term Effectiveness  and Permanence

Alternative GW-1 does not provide treatment but would
attempt to restrict usage of contaminated groundwater.
Alternative GW-2 provides short-term treatment, but
would not restore the contaminated aquifer for its best
beneficial  future use.

Alternatives GW-3A, GW-3B, GW-5A, and GW-5B all
reduce the potential risks associated with groundwater
ingestion  by extracting, treating, and recharging the
treated groundwater to remove contaminants from the
aquifer. The  time required  to achieve these risk
reductions depends on the effective extraction rates
from the aquifer and limitations on extraction system
placement due to the large area on the  contaminant
plume.  Long-term effectiveness of each system is
dependent on monitoring and maintenance of the
treatment  system.

Alternatives GW-1 and GW-2 would take approximately
100 years to  achieve the remedial action objectives.
Alternatives GW-3A and 5A would theoretically achieve
the remedial action objectives in 62 years, whereas
GW-3B and SB would achieve the remedial action
objectives in  approximately 16 years.

Proper air pollution control  measures would be
established under alternatives GW-3A and GW-3B to
offset potential risks from the air stripper(s), while no
pollution control measures  are deemed necessary for
alternatives GW-5B  and 5A. Alternatives GW-3A and
GW-3B require the  disposal of more spent carbon than
GW-5A and GW-5B since vapor phase carbon
adsorption is used.

  o      Reduction in Toxicitv. Mobility,  or Volume

Alternative GW-1 would very slowly and  gradually
reduce the toxicity of contaminants through dilution.
Alternative GW-2 would reduce the toxicity and volume
of contaminants more rapidly than GW-1.  Neither
Alternative GW-1 nor GW-2 would permanently reduce
the mobility of the contaminants.  For alternative GW-2,
the off-site portion of the contaminated groundwater
plume would continue to migrate  downgradient and
reduction of toxicity, mobility and  volume would be
achieved  only by rv:rai ?tt?nuat:c?n.

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                                                    12
Alternatives GW-3A. GW-3B, GW-5A and GW-5B would
reduce the toxicity, mobility, and volume.of
contaminants in the aquifers to a greater extent than
GW-1 and GW-2.  Alternatives GW-3B and SB would
reduce the toxicity, mobility, and volume to a greater
extent and at a much faster rate than the other
alternatives.  Alternatives GW-3A and GW-3B would use
air stripping  and carbon adsorption to  remove the
contaminants, while GW-5A and GW-5B would  oxidize
most of the organic compounds.

  o    Short-Term Effectiveness

Implementation of Alternative GW-1 would result in no
additional risk to the community during remedial
activities. Alternative GW-2 could present additional
risks to the community  resulting from the installation of
the extraction wells and pipelines for transportation of
contaminated groundwater. Alternatives GW-3A, 3B,
and  GW-5A and 5B include excavation activities,
installation of the collection and reinjection system,  and
construction of the treatment plant which could result
in potentially exposing residents to volatilized
contaminants and contaminated dust.  The treatment
plant would be constructed on-site.  Proper
engineering controls would ensure that the impact of
such activities would be insignificant.  All alternatives
except Alternative GW-1 and GW-2 would provide a
process residual requiring  proper handling and
disposal

Alternative GW-1 would result in no additional risk to
workers,  and GW-2 would  result in a lower overall
worker risk than other alternatives because of the
limited soil disturbance activities.   Personal protection
equipment would be used under alternatives GW-3A,
GW-3B, GW-5A and GW-5B to minimize  the worker's
potential exposure to volatilized contaminants during
installation of the collection, treatment, and recharge
systems.

  o    tmptementabnitv

Alternative GW-1 would be easily implemented.
Alternative GW-2 would require institutional
management to maintain and operate the pumping
system and to coordinate  with the Landfill treatment
system.  Alternatives GW-3A, GW-3B, GW-5A and
GW-5B would utilize relatively  common construction
equipment and materials.  Little construction difficulty
would occur with any of the alternatives.

The  air stripping and carbon adsorption technologies
proposed for use in Alternatives GW-3A  and GW-3B
are proven and reliable in  achieving specified process
efficiencies an* performance goals.  While there  has
been limited experience with UV-chemical oxidation, it
has been successful in several groundwater treatment
facilities.

All proposed technologies are readily available from a
number of sources, with the exception of UV-chemical
oxidation.  It is expected that additional UV-chemical
equipment manufacturers would  be available once this
technology becomes more mature.

Alternatives  GW-3A, GW-3B, GW-5A, and GW-5B would
require institutional management of the operation and
maintenance of the treated groundwater reinjection
system. Siting the treatment facility would not present
any problems  as there is enough space available on-
site. Associated off-site facilities (e.g.  piping,  pumps,
extraction wells and reinjection wells) would be
potentially more complex to locate as  both technical
and land use factors would be considered.

Off-site disposal facilities are available for the disposal
of the pretreatment sludge and spent  carbon
generated from Alternatives GW-3A, GW-3B, GW-5A
and GW-5B.
The present worth costs of all GW alternatives ranged
from $464,400 (GW-1) to $28,987,000 (GW-3A).
Alternative GW-1 would be least expensive followed by
GW-2. GW-5B, GW-3B. GW-5A and GW-3A. Of the
alternatives providing complete remediation of the
groundwater contamination, Alternative GW-3B provides
the lowest present worth cost, $15,620,400.

  o      State Acceptance

NYSDEC concurs with the preferred alternative
selected.

Comparison of Building Alternatives (BO)

Only two building alternatives:  No-Action and Building
Decontamination were evaluated.

  o      Overall Protection of Human Health and the
         Environment

In Alternative BD-1, hazardous material is left in the
building.  Human health and the environment remain
protected only as long as building security can be
effectively enforced and building integrity maintained.
Alternative BD-2 removes all hazardous material from
the building so it is fully protective of human health
and the environment.  In addition, Alternative BD-2
allows for future reuse of the  building.

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13
   o    Compliance with ARARs

FAltemative BD-1 would not contravene any ARARs
 since no action would be taken.  Alternative BD-2
 would comply with the ARARs relevant to the transport
 of the wastes to an off-site facility.  The off-site
 treatment facility would be fully EPA-permitted and
 therefore meet applicable regulations.

   o    Lono-Term Effectiveness and Permanence

 Alternative BD-1 would not alter conditions within the
 building;  hazardous materials would remain in the
 building.  Public protection would rely on maintaining
 building security which may be difficult to enforce.  The
 building could not be used for any purpose.
 Alternative BD-2 removes all  hazardous materials from
 the building for off-site treatment and disposal so that
 long-term exposure risks from the building would be
 eliminated.   Painting and sealing the building
 (alternative  BD-2)  would provide additional protection
 and would allow for unrestricted use of the building in
 the future.

   O    Reduction in Toxicitv,  Mobility or Volume

 Alternative BD-1 provides no reduction in toxicity or
 volume of contaminants; mobility is not an issue since
tthe building is self-contained. Alternative BD-2
(provides  for complete reduction in toxicity and volume
 since all contaminated material is removed from the
 building.

   o    Short-term Effectiveness

 Implementation of BD-1 should result in no additional
 risks to the community  or the environment as long  as
 building security and  integrity can be maintained.
 Alternative BD-2 involves removal and transport  of the
 contaminants from the building so there are some
 minimal public exposure risks as well as environmental
 impact from potential waste spills resulting from a
 possible transport accidents  during remedial activities.
 Worker exposure risks would be minimized through the
 use of personal protection equipment.  Long-term
 maintenance would continue indefinitely for Alternative
 BD-1. Building decontamination, Alternative BD-2,
 could be accomplished in approximately 3 months.

   o .   Implementabiliry

 Both alternatives are readily implementable; neither
 involves  any major construction activities. Methods and
 services for building decontamination are technically
 feasible and readily available. Alternative BD-1  would
require institutional manager^nt i.e., a long-term
wilding  maintenance program, whereas Alternative
   BD-2 does not require any long-term management.

     o
   The present worth costs for alternatives BD-1 and BD-2
   are $41,100 and $186,200, respectively.

     o      State Acceptance

   NYSDEC concurs with the preferred alternative
   selected.

   Comparison of the Underground Tank  CD Alternatives

     o      Overall Protection of Human Health and the
            Environment

   Alternative T-1 would not protect human health and the
   environment as the threat of soil and groundwater
   contamination would not be reduced.  The excavation
   and removal of contaminated tanks and their contents
   from the site (T-2) would significantly .reduce the
   potential human health and environmental risks
   associated with potential leaking of contaminants from
   tanks into the soil and groundwater.

     o      Compliance With ARARs

   Alternative T-1 would not comply with groundwater
   ARARs, as continual source of contamination would not
   be removed. The disposal of the underground tanks
   (T-2) would eliminate the source of contamination and
   would  satisfy applicable State and Federal ARARs, as
   the tanks and related wastes would be removed,
   transported, and disposed of in accordance with all
   regulations.

     o      Long-Term Effectiveness

   Under  alternative T-1, the tanks and their associated
   hazardous wastes would remain as a potential source
   of soil  and groundwater contamination. Alternative T-
   2, excavation and removal of the underground storage
   tanks,  tank debris, and highly contaminated soil from
   the site, would reduce the potential human health and
   environmental risks associated with the tanks' potential
   for leaking contaminants into the soil and groundwater
   in the future.

     o      Reduction of Toxicitv. Mobility or Volume

   No significant reduction of toxicity, mobility or volume
   would  result from the implementation of the no-action
   alternative.  Alternative T-2, excavation  and off-site
   treatment, would  result in a permanent reduction of
   toxicity, mobility and volume. The wastes wor'"1 ^e

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14
Summary of Alternative

REMEDY
SOIL
SC-1
SC-3
SC-4
SOS
GROUNDWATER
GW-1
GW-2
GW-3A
GW-3B
GW-5A
GW-5B
BUILDING
BD-1
BD-2
UNDERGROUND TANKS
T1
T2
Analysis.

CAPITAL COST

0
18.535.100
2.262.500
385.600

0
214,800
4,044.700
4,936.000
4,088.900
4,069.800

8,800
186,200

0
336,300

PRESENT
WORTH COST

564,300
18,535,100
2,262.500
385,600

464,400
3,350.500
28,978.100
15,620.400
21.121,100
13,902,300

41,100
186200

64,300
336,300

TIME TO ACHIEVE
REMEDY (years)

30
3.5
3.5
5

100
103
65
19
65
16

30
3.3

30
3.1

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                                                       15
  completely removed and either destroyed at the
  treatment facility or reused if practical.

    o    Short Term Effectiveness

  Alternative T-1 would result in no additional risk to the
  community during implementation.

  The potential public health threats to workers and area
  residents associated with the implementation of
  alternative T-2 include: direct contact of workers with
  tank contents and potentially contaminated soils;
  inhalation of fugitive dust, organic vapors,  and
  emissions generated during  construction and
  excavation activities; and improper handling of soil and
  hazardous liquids. Several steps would be taken to
  minimize these threats including: site access would be
  restricted to authorized personnel only, and dust
  control measures such as wind screens and water
  sprays would be used to minimize fugitive dust
  emissions.

  The risk to workers during excavation would be
  minimized by the use of adequate personal protection
  equipment to prevent direct  contact with potentially
  contaminated soil, liquids, and inhalation of fugitive
  dust and volatile organic compounds.

  Other potential short-term impacts contemplated as
  part of T-2 would be an increase in traffic  and noise
  pollution resulting from hauling soils (as necessary),
  hazardous liquids, and tanks to an off-site treatment
  facility, as well as the traffic  associated with
  transporting new soil for backfill to the Site.
  Transportation of excavated  hazardous liquids may
  introduce short-term risks with the possibility of spillage
  along the transport route and potential exposure of the
  public to hazardous material. A spill contingency plan
  would be developed to address and minimize the
  likelihood and potential impact of this occurrence.  The
  actual remediation period for this alternative is
  estimated to be 8 weeks.

    o    ImplementabiVitv

  All the components of both remedial alternatives are
  we!) developed and commercially available.  The
  contained tanks and related wastes would have to
  undergo a series of analyses prior to acceptance for
  treatment at the off-site facility.  Sufficient land is
  available at the site for mobilization and temporary
  storage of the excavated soil and materials awaiting
  pre-transport decontamination.  Excavation, treatment
  tank decommissioning, transportation to an off-she
  treatment facility, solid and liquid waste disposal,  and
Restoration of the site can be performed without any
Pmajor difficulty.
  o      Cost

The total present worth cost of alternative T-1 is
$64,300. The total present worth cost of alternative T-
2, which represents the estimated construction cost for
the eight week remediation program, is estimated at
$336,300.  Operation and maintenance costs have not
been included in the cost estimate since the duration
of the remediation program is less than one year.

  o      State Acceptance

NYSDEC concurs with the preferred alternative
selected.

SUMMARY OF THE PREFERRED ALTERNATIVE

In summary, the preferred alternative will achieve
substantial risk reduction through a combination of
source  control alternatives SC-4 (low temperature
enhanced volatilization of soil contaminants) and T-2
(tank removal and off-site treatment), with active
restoration of the groundwater (GW-3B), and building
decontamination  (BD-2).

The preferred alternative achieves this risk reduction
more quickly and at substantially less  cost than the
other options.  Therefore, the preferred alternative will
provide the best  balance of trade-offs  among
alternatives with respect to the evaluating criteria.
Based  on the information available at this time, EPA
and the NYSDEC believe that the preferred alternative
will be  protective of  human health and the environment,
will comply with ARARs, will be cost effective, and will
utilize permanent solutions and alternative treatment
technologies or resource recovery technologies to the
maximum extent  practicable.  The remedy also will
meet the statutory preference for the use of a remedy
that involves treatment as a principal element.

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APPENDIX C.  SIGN-IN SHEET

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       UNITED BT>.TBL;
                         REGIOW XI
                       PUBLIC: MEETING
                            FOR
           Claremont Polyche:*iccl Supcxfund Bite
                               .,  Kew York
                               5, 1990
                     MEETING ATTENDEEd
                       (PlWse Print)
NAME STREET
HAILING
CITY ZIP PHONE REPRESENTING LIST
fan *%}&*, lr° Ml /**"%, fan*' {MT 72/7/77 TV If
l-<&kcsrf'h/reJT' ~fo(vw. n<\\]
dvA/ &•* ;/?? / ^a?-j8oo ^^JvA^y
                          ^

/SO
                                                                        *
                                                                       \S

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APPENDIX D.  OVERHEAD TRANSPARENCIES

-------
    Public Meeting
Claremont Polychemical
    Superfund Site
     United States
     Environmental
   Protection Agency
  September 5, 1990

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            Site History
CONSTRUCTION OF THE CLAREMONT
POLYCHEMICAL FACILITY BEGAN IN 1966

PLANT OPERATION BEGAN IN 1968

MORE THAN A THOUSAND DRUMS WERE
DISCOVERED IN 1979 BY THE NASSAU COUNTY
DEPARTMENT OF HEALTH (NCDOH)

MUST OF THE  DRUMS WERE GONE AND AREA OF
CONTAMINATED SOIL (SPILL AREA) WAS
DISCOVERED IN 1980 BY NCDOH

SOILS WERE EXCAVATED AND PLACED ON
PLASTIC LINERS IN 1980 BY THE COMPANY

COMPANY ENTERED INTO CHAPTER 11
PROCEEDINGS IN 1980

NEW YORK DEPARTMENT OF LAW ASSUMES THE
LEAD ON THE SITE AND ATTEMPTS TO
NEGOTIATE AN AGREEMENT WITH RESPONSIBLE
PARTY

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            Site  History
           (Cont'n 2 of 3)
SITE RECOMMENDED FOR PLACEMENT IN
NATIONAL PRIORITY LIST IN OCTOBER 1984

SITE WAS FINALLY INCLUDED IN NATIONAL
PRIORITY LIST IN JUNE 1986 (RANKED 614)

EPA ASSUMES THE LEAD IN 1986 AND SENDS
OUT NOTIFICATION LETTER TO POTENTIALLY
RESPONSIBLE PARTY (PRP) IN NOVEMBER 1987

NO RESPONSE WAS RECEIVED AND FUNDS FOR
REMEDIAL INVESTIGATION/FEASIBILITY STUDY
(RI/FS) ARE ALLOCATED IN MARCH 1988

EBASCO SERVICES IS CONTRACTED BY EPA TO
CONDUCT RI/FS (1" OPERABLE UNIT) IN MARCH
1988

EPA CONDUCTS REMOVAL ACTION IN OCTOBER
1988 TO STABILIZE WASTES

SECOND RI/FS (2nd OPERABLE UNIT) IS OPEN IN
APRIL 1989 TO ADDRESS THE DISPOSAL OF
WASTES CONTAIN IN HOLDING UNITS (DRUMS,
BASINS, ETC)

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            Site History
          (Cont'n 3 of 3)
IMPLEMENTATION OF REMEDY FOR 2nd OPERABLE
UNIT STARTS IN SEPTEMBER 1989

RI/FS FOR 1- OPERABLE UNIT IS FINALIZED AND
REPORTS ARE RELEASED FOR PUBLIC COMMENT
IN AUGUST 1990

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REMEDIAL INVESTIGATION

-------
         Summary of Field
            Investigation
SOIL-GAS SURVEY

GEOPHYSICAL INVESTIGATION

AIR MONITORING

SURFACE SOIL SAMPLING

SUBSURFACE SOIL SAMPLING

MONITORING WELL INSTALLATION

HYDRAULIC CONDUCTIVITY TESTING

WATER LEVEL MEASUREMENTS

GROUNDWATER SAMPLING

BUILDING SAMPLING

UNDERGROUND STORAGE TANK SAMPLING

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      Summary of Samples
        Collected by EPA


SOIL GAS SURVEY - 102 samples

SOIL - 325 subsurface samples (25 locations)
      32 surface samples

GROUNDWATER - 72 samples

  - OFFSITE WELLS - 27 locations

  - SITE WELLS  - 5 locations

AIR - 10 locations

BUILDING - 57 samples

UNDERGROUND STORAGE TANKS - 23 samples

PRIOR EPA WORK

  - BASINS

  - CONTAINERS (DRUMS, ETC)

  -SUMP

  - ABOVE GROUND TANKS

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      Maximum Concentration of Selected
         Contaminants Detected in Soil,
    Groundwater, Building and Underground
                  Tank Content

                                   CONCEN-
MATRIX            COMPOUND         TRATION
SOIL              bis(2-ethylhexyl)         270
(mg/Kg)            phthalate
                 tetrachloroethene         26
                 lead                  98

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      Maximum Concentration of Selected
         Contaminants Detected  in Soil,
    Groundwater, Building and Underground
                   Tank Content
MATRIX

GROUND
WATER
(ug/Kg)
COMPOUND
1,1,1-trichloroethane
                  trichloroethene
CONCEN-
TRATION

   100
                     260
                  tetrachloroethene
                    1,300
                   ethylbenzene
                     160
                   bis(2-ethylhexyl)
                   phthalate
                      50
                   chromium
                     159

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  Maximum Concentration of Selected
    Contaminants Detected in Soil,
Groundwater, Building and Underground
             Tank Content
MATRIX
BUILDING
(ug/wipe)




TANKS
(mg/Kg)


COMPOUND
bis(2-ethylhexyl)
phthalate
cadmium
chromium
copper
lead
2-butanone
toluene
xylene
bis(2-ethylhexyl)
CONCEN
TRATION
70
313
1,103
24,600
7,974
92,000
2,600
3,600
23,000
            phthalate

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RISK ASSESSMENT

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          Exposure Routes
 SOIL

   - INGESTION

   - DIRECT CONTACT

   - INHALATION

 GROUNDWATER

   - INGESTION

   - DIRECT CONTACT

   - INHALATION OF VOLATILE EMISSIONS

 BUILDING

   - INGESTION OF RESUSPENDED DUST
• EXISTING ROUTES VS. POTENTIAL FUTURE
ROUTES

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          Public Health Evaluation
       Current Land Use Conditions
                 NON
                 CARCINOGENIC   CARCINOGENIC
EXPOSURE ROUTES   RISK           RISK
 SOIL            ACCEPTABLE    ACCEPTABLE
 SITE GROUNDWATER ACCEPTABLE    ACCEPTABLE
 AIR              ACCEPTABLE    ACCEPTABLE

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          Public Health Evaluation
    Future Off-Site Land Use Conditions
                 NON
                 CARCINOGENIC   CARCINOGENIC
EXPOSURE ROUTES   RISK           RISK
 SOIL            ACCEPTABLE    ACCEPTABLE
 GROUNDWATER    UNACCEPTABLE  ACCEPTABLE
 AIR             ACCEPTABLE    ACCEPTABLE

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          Public Health Evaluation
    Future On-Site  Land Use Conditions
                 NON
                 CARCINOGENIC   CARCINOGENIC
EXPOSURE ROUTES   RISK           RISK
 SOIL            ACCEPTABLE    ACCEPTABLE
 GROUNDWATER    UNACCEPTABLE  ACCEPTABLE
 AIR              ACCEPTABLE    ACCEPTABLE
 BUILDING         UNACCEPTABLE  UNACCEPTABLE

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FEASIBILITY STUDY

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        Remedial  Alternatives
           CONTAMINATED SOILS
o  SC-1 No Further Action
o  SC-3 Excavation/Off-site Incineration/Backfill with
   Clean Soil
o  SC-4 Excavation/Low Temperature Enhanced
   Volatilization/On-Site  Redeposition
o  SC-5 In-Situ Vacuum Extraction

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        Remedial  Alternatives
       CONTAMINATED GROUNDWATER
o  GW-1 No Further Action

o  GW-2 Pumping/Air Stripping/Reinjection;
   Southern Site Boundary (0.2 mgd)

o  GW-3A Pumping/Air Stripping/Reinjection;
   Leading Edge of Plume (1.9 mgd)

o  GW-3B Pumping/Air Stripping/Reinjection;
   Southern Site Boundary and Downgradient (1.0
   mgd)

o  GW-5A Pumping/UV-Chemical
   Oxidation/Reinjection; Leading Edge of Plume
   (1.9 mgd)

o  GW-5B Pumping/UV-Chemical
   Oxidation/Reinjection; Southern Site Boundary
   and Downgradient (1.0 mgd)

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       Remedial Alternatives
                BUILDING
o  BD-1 No Further Action

o  BD-2 Building Decontamination/Waste Treatment
   and Disposal
      UNDERGROUND STORAGE TANKS

o T-1  No Further Action

o T-2  Removal and Off-Site Disposal

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       Detailed Analysis  of
           Alternatives
1.    OVERALL PROTECTION OF HUMAN
     HEALTH AND THE ENVIRONMENT

2.    COMPLIANCE WITH ARARs

3.    LONG-TERM EFFECTIVENESS AND
     PERMANENCE

4.    REDUCTION IN TOXICITY, MOBILITY, OR
     VOLUME

5.    SHORT-TERM EFFECTIVENESS

6.    IMPLEMENTABIUTY

7.    COST

8.    STATE ACCEPTANCE

9.    COMMUNITY ACCEPTANCE
TREATMENT TECHNOLOGIES AND RESOURCE
RECOVERY

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Summary of Alternative Analysis.
             SOIL


REMEDY

SC-1
SC-3
SC-4
SC-5

CAPITAL
COST

0
18,535,100
2,262,500
385,600
PRESENT
WORTH
COST

564,300
18,535,100
2,262,500
385,600
TIME TO
ACHIEVE
REMEDY
(years)
30
3.5
3.5
5

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Summary of Alternative Analysis.
       GROUNDWATER


REMEDY

GW-1
GW-2
GW-3A
GW-3B
GW-5A
GW-5B

CAPITAL
COST

0
214,800
4,044,700
4,936,000
4,088,900
4,069,800
PRESENT
WORTH
COST

464,400
3,350,500
28,978,100
15,620,400
21,121,100
13,902,300
TIME TO
ACHIEVE
REMEDY
(years)
100
103
65
19
65
19

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    Summary of Alternative Analysis
                BUILDING


                        PRESENT     TIME TO
            CAPITAL      WORTH      ACHIEVE
REMEDY      COST        COST        REMEDY
                                    (years)

BD-1            8,800        41,100      30

BD-2           186,200       186,200       3.3

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   Summary of Alternative Analysis,
       UNDERGROUND TANKS
REMEDY
CAPITAL
COST
PRESENT
WORTH
COST
TIME TO
ACHIEVE
REMEDY
(years)
T-1              0       64,300     30




T-2          336,300      336,300     3.1

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   EPA's Preferred Alternative
SC-4     Excavation/Low
         Temperature Enhanced
         Volatilization/On-Site
         Redeposition

GW-3B   Pumping/Air
         Stripping/Reinjection;
         Southern Site Boundary
         and Downgradient (1.0
         mgd)

BD-2     Building
         Decontamination/Waste
         Treatment and Disposal

T-2      Removal and Off-Site
         Disposal

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          PREFERRED  REMEDY


REMEDY

4SC-4
4GW-3B
«BD-2
*T-2

CAPITAL
COST

2.3
4.9
0.2
0.3
PRESENT
WORTH
COST

2.3
15.6
0.2
0.3
TIME TO
ACHIEVE
REMEDY
(years)
3.5
19
3.3
3.1
TOTAL
7.7
18.3
     Costs are expressed in million dollars

-------