United States
Environmental Protection
Agency
Office of
Emergency and
Remedial Response
EPA/ROD/R04-91/101
June 1991
&EPA Superfund
Record of Decision:
Velsicol Chemical, TN
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REPORT DOCUMENTATION 1" REPORT NO. I 2. 3. Reciplent'a Acceaaion No.
PAGE EPA/ROD/R04-91/101
4. nUe and SubtiUe S. Report Date
SUPERFUND RECORD OF DECISION 06/27/91
Velsicol Chemical, TN 6.
First Remedial Action
7. Author(a) 8. Perfonning OrganlZ8l1on Repl No.
9. Perfonnlng Orgalnlzation Name and Addreaa 10. Project/Ta8k/Work Unit No.
11. Contrscl(C) or Grant(G) No.
(C)
(G)
12. Sponsoring Organization Name and Addreaa 13. Type 01 Report & Period Covered
U.S. Environmental Protection Agency 800/000
401 M Street, S.W.
Washington, D.C. 20460 14.
1 S. Supplementary Notea
16. Abstract (limit: 200 won!s)
The 242-acre Velsicol Chemical site is a former plant waste landfill located near the
city of Toone, Hardeman County, Tennessee. Land use in the area is predominantly
agricultural with a wetlands area, 26 residences, and numerous creeks located within
1 mile of the site. In addition, part of the site overlies a surficial aquifer that
was used as a potable water supply in the area. From 1964 to 1973, Velsicol Chemical
Corporation used the site to dispose of industrial and chemical plant wastes. Waste
was disposed of in trenches excavated on 27 acres of the property. The site was
closed in 1973 because of the possibility of contaminated ground water migrating
offsite. By late 1978, State and Federal investigations had confirmed ground water
contamination in private wells, and a public water supply was provided in early 1979.
In 1980, a 35-acre low permeability clay cap was placed over the disposal area to
control and minimize additional impacts from the site. This Record of Decision (ROD)
addresses offsite ground water contamination, as Operable Unit 1 and will prevent
additional onsite ground water contamination from migrating from the disposal areas.
Future RODs will address other site contamination and principal threats. The primary
(See Attached Page)
17. Document Analysia L Descriptors
Record of Decision - Velsicol Chemical, TN
First Remedial Action
Contaminated Medium: gw
Key Contaminants: VOCs (carbon tetrachloride, chloroform, toluene, xylenes),
other organics (pesticides)
b. Identifiers/Open-Ended Terma
c. COSA n Reid/Group
18. Availsbility Sistement 19. Security Class (Thia Report) 21. No. 01 Pagea
None 72
20. Security Claaa (Thia Page) 22. Prtce
None
See A 9.18 Iructi I 272 (4-77)
50272.101
NSI Z3
See Ins
ons on Reverse
(Formetly NTlS-35)
Department 01 Conwnerce
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EPA/ROD/R04-91/101
Velsicol Chemical, TN
First Remedial Action
Abstract (Continued)
contaminants of concern affecting the ground water are VOCs including carbon
tetrachloride, chloroform, toluene, and xylenes; and other organics including
pesticides.
The selected remedial action for this site includes installing extraction wells onsite
and offsite to restore the contaminated ground water to acceptable drinking water
standards; constructing an onsite ground water treatment plant and treating
contaminated ground water using solids removal, air stripping, and final ground water
polishing prior to discharge; discharging the treated water onsite to nearby surface
water bodies; treating off-gases with carbon adsorption; monitoring ground water;
maintaining the ground water treatment system and the disposal area cover; and
implementing institutional controls including deed and ground water use restrictions.
The selected remedial action is contingent upon the performance data collected during
operation. If the selected remedy cannot meet the specified remediation goals,
contingency measures may include alternating pumping at wells to eliminate stagnation
points; pulse pumping at wells to allow aquifer equilibration and encourage adsorbed
contaminants to partition into ground water; and installing additional extraction wells
to facilitate or accelerate cleanup of the contaminant plume. The estimated present
worth cost for this remedial action is $11,644,000, which includes an annual O&M cost
of $696,000.
PERFORMANCE STANDARDS OR GOALS: Chemical-specific ground water clean-up goals are
based on SDWA MCLs and health-based criteria, and include carbon tetrachloride
0.005 mg/l (MCL), chloroform, 0.006 mg/l, toluene 1 mg/l (MCL), and xylenes
10 mg/l (MCL). .
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0001
SUMMARY OF REMEDIAL ALTERNATIVE SELECTION
RECORD OF DECISION
REMEDIAL ALTERNATIVE SELECTION
VELSICOL/BARDEHAN COUNTY LANDFILL
GROUNDWATER, OPERABLE UNIT I
TOONE, TENNESSEE
PREPARED BY:
U.S. ENVIRONMENTAL PROTECTION
REGION IV
ATLANTA, GEORGIA
AGENCY
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UUuL
RECORD OF DECISION
Remedial Alternative selection
First operable Un~t
S:TE NAME AND LOCATION
Velslcol/Hardeman County Landfill
rlrst operable Unit (Groundwater)
Toone, Tennessee
STATEMENT OF BASIS AND PURPOSE
ThlS decision document presents the selected remedial action for the
Groundwater Operable Unit of the velsicol/Hardeman county Landfill site in
Toone, Tennessee developed in accordance with CERCLA, as amended by SARA, and
to the extent practicable, the National Contingency Plan.
ThlS decision is based upon the contents of the Administrative Record for the
velslcol/Hardeman County Landfill site.
The United States Environmental Protection Agency and the State of Tennessee
agree on 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 ("ROD"), may present an imminent and substantial endangerment to
public health, welfare, or the environment.
DESCRIPTION OF THE SELECTED REMEDY
Th~s operable Unit is the first of at least two that are planned for the site.
This operable unit remedy addre.ses remediation of the on-site and off-site
groundwater contamination by eliminating or reducing the risk. posed by the
slte through treatment, engineering and institutional controls.
The major component. of the selected remedy include:
Install and maintain approximately five extraction wells along the
northern boundary of the disposal areas located within the site
developing a hydraulic gradient to prevent groundwater contamination
above MCLs from leaving the disposal area.
Install and maintain approximately ten extraction wells into the
off-site groundwater contamination pl~ to control the groundwater
contaminant migration and remediate the groundwater off-site to MCLs.
Build and operate a groundwater treatment system for the removal of
contaminants from the extracted groundwater to NPDES requirements prior
to the water being discharged to a nearby surface water body. The
groundwater treatment is expected to be performed using, at a minimum,
settling tanks for precipitation of dissolved solids, an air stripper
and a carbon adsorption system.
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Monitor groundwater contaminant levels to verify that remediation goals
are reached.
Impose groundwater use restrictions for the affected area and post
appropriate hazardous waste disposal signs on and around the site.
Maintain the disposal area including fences and soil cover.
Identify and evaluate possible ~dditional remedial actions (Operable
units) required for addressing the contamination of the entire site
including the contaminant source (the disposal areas) and possible
environmental/ecological concerns.
STATUTORY DETERMINATIONS
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.
As this remedy will initially result in hazardous substances remaining on sit,
above health-based levels, a review will be conducted within five years after
the commencement of remedial action to ensure that the remedy continues to
provide adequate protection of human health and the environment.
~fY}JM;~
~Greer C. Tidwell
1- Regional Administrator
Date
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SUMMARY OF REMEDIAL ALTERNATIVE SELECTION
RECORD OF DECISION
REMEDIAL ALTERNATIVE SELECTION
VELSICOL/BARDEMAN COUNTY LANDFILL
GROUNDWATER, OPERABLE UNIT I
TOONE, TENNESSEE
PREPARED BY:
U.S. ENVIRONMENTAL PROTECTION
REGION IV
ATLANTA, GEORGIA
AGENCY
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SECTION
III.
IV.
VI.
VII.
VIII.
9
0005
TABLE OF CONTENTS
PAGE
I.
INTRODUCTION. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
II.
SITE NAME,
LOCATION AND DESCRIPTION........................ 1
SITE HISTORY AND ENFORCEMENT ACTIVITIES....................2
HISTORICAL LANDFILLING PRACTICES...........................2
INVESTIGATIONS AND STUDIES COMPLETED TO DATE.......
. . . . . . . .5
HIGHLIGHTS OF COKHUNITY PARTICIPATION......................5
V.
SCOPE AND ROLE OF RESPONSE ACTION..................
. . . . . . . .6
SUMMARY OF SITE CHARACTERISTICS.............................7
GEOLOGY AND
S'1'RA.TIGRA.PBY. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
HYDROGEOLOGY....
......................................... .11
NATURE AND EXTENT OF CONTAMINATION........................l7
SUMMARY OF SITE
RISKS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .'. . . . . 25
IDENTIFICATION OF CHEMICALS OF CONCERN....................25
EXPOSURE
ASSESSICEN'l'. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .25
TOXICITY ASSESSMENT......
.................................31
RISK CHARACTERIZATION..................................... 33
UNCERTAINTIES. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . J 9
ENVIRONMENTAL
RI Sits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
DESCRIPTIOH OF ALTERNATIVES...............................42
ALTERNATIVE
1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43
ALTERNATIVE
2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43
ALTERNATIVE
3......... ....... . . . . . .... ........ ....... . ... .44
ALTERNATIVE
4.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
ALTERNATIVE
5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
ALTERNATIVE
6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .46
.
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SECTION
XI.
XII.
9
OOC6
~ ~
TABLE OF CONTENTS (Cant'd)
PAGE
ARARs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
X.
SUMMARY OF COMPARATIVE ANALYSIS OF ALTERNATIVES...........49
SELECTED REMEDY........................................... 51
CONTINGENCY MEASURES...................................... 57
STATUARY DETERMINATIONS................................... 60
PROTECTION OF HUMAN HEALTH AND THE ENVIRONMENT............60
COMPLIANCE WITH ARARa..................................... 6 1
COST EFFECTIVENESS........................................ 62
UTILIZATION OF PERMANENT SOLUTIONS AND ALTERNATIVE
TREATMENT TECHNOLOGIES OR RESOURCE RECOVERY TECHNOLOGIES
TO THE MAXIMUM EXTENT PRACTICABLE.........................62
PREFERENCE FOR TREATMENT AS A PRINCIPLE ELEMENT...........62
...
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0007
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LIST OF FIGURES
FI GURE
PAGE
1
SITE LOCATION[[[2
2
DISPOSAL SITE[[[ 8
3
MISSISSIPPI EMBAYMENT........................................... 9
4
AREA CROSS SECTION............................................. 10
5
GROUNDWATER CONTOURS.......................................... .12
6
GEOLOGIC CROSS SECTION A-A'.................................... 13
7
GEOLOGIC CROSS SECTION 8-8'................................... .14
8
A-A'....."......................... .15
HYDROGEOLOGIC CROSS SECTION
9
HYDROGEOLOGIC CROSS SECTION 8-8'...............................16
10
FINITE ELEMENT MESH........................................... .19
11 CALCULATED CARBON
12 CALCULATED CARBON
13 CALCULATED CARBON
14 PREDICTED CARBON
TETRACHLORIDE DISTRI8UTION FOR YEAR 1990.....20
TETRACHLORIDE DISTRI8UTION FOR YEAR 2000.....21
TETRACHLORIDE DISTRI8UTION FOR YEAR 2010.....22
TETRACHLORIDE PROFILE.........................23
15
PREDICTED CHLOROFORM PROFILE................................... 24
16
COLLECTION DRAIN............................................... 45
17
COMPLI.ANCE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
POINT OF
18
CO~ONENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . .53
ALTERNATIVE 2 - REMEDIAL
19
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LIST OF TABLES
':'ABLE
PAGE
SUMMARY OF WASTE DISPOSAL.................... .... ........ .... ...4
2
EXPOSURE POINT CONCENTRATIONS................................. .18
3
FUTURE EXPOSURE POINT CONCENTRATIONS...........................28
4
CLOVER CREEK WATER CHEMISTRY................................... 29
5
PUGH CREEK WATER CHEMISTRY...... ...... ..... ..... ... ........... .30
6
FUTURE CLOVER CREEK CHEMISTRY..................................32
7
SUMMARY OF TOXICOLOGY AND CHEMICAL CONSTANTS...................34
8
SUMMARY OF GROUNDWATER CANCER RISK AND RA2ARD INDEX............37
9
SUMMARY OF SURFACE WATER CANCER RISK AND HAZARD INDEX..........38
10
SUKHARY OF FUTURE GROUNDWATER CANCER RIS~ AND HAZARD INDEX.....40
11
SUKHARY OF FUTURE SURFACE WATER CANCER RIS~ AND HAZARD INDEX...41
12
GROUNDWATER REMEDIATION LEVELS................................. 47
13
IN-STREAM DISCHARGE LEVELS..................................... 48
14
EVALUATION OF GROUNDWATER REMEDIAL ALTERNATIVES................52
15
REMEDIAL COST ESTIMATE - ALTERNATIVE 2.........................58
16
REMEDIAL COST ESTIMATE - ALTERNATIVE 6.........................59
APPENDIX A - RESPONSIVENESS SUMMARY
APPENDIX B - LETTERS FROM SUPPORT AGENCIES
APPENDIX C - RIS~ ASSESSMENT CERTIFICATION
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(JOC9
RECORD OF DECISION
SUMMARY OF REMEDIAL ALTERNATIVE SELECTION
VELSICOL/HARDEKAN COUNTY LANDFILL
GROUNDWATER, OPERABLE UNIT I
TOONE, TENNESSEE
INTRODUCTION
The Velsicol/Hardeman County Landfill was proposed for inclusion on the
National Priorities List ("NPL") in December of 1982 and was finalized onto the
NPL in September of 1983. On 242 acres in Hardeman County, Tennessee, Velsicol
Chemical Corporation operated the 27 acre landfill for the disposal of plant
waste generated at their Memphis, Tennessee plant. The Remedial Investigation
("RI") report which examines air, sediment, soil, surface water, and
groundwater ~ontamination was completed in April 1991. The Operable Unit I
Feasibility study ("FS") which develops and examines alternatives for
remediation of the groundwater was submitted to the public information
repository with the RI Report in April of 1991.
This Record of Decision ("ROD") has been prepared to summarize the remedial
alternative selection process and to present the selected remedial alternative,
in accordance with Section 113(K)(2)(B)(V) and Section 117(b) of the
Comprehensive Environmental Response, Compensation, and Liability Act of 1980
("CERCLA"), as amended by the Superfund Amendments and Reauthorization Act
«"SARA") P.L. 99-499). The Administrative Record for the velsicol/Bardeman .
county Landfill Site forms the basis for the Record of Decision contained
herein.
SITE NAME. LOCATION. AND DESCRIPTION
The Velsicol/Bardeman County Landfill is located on an approximately 242-acre
parcel approximately one mile north of Tennessee State Bwy 100 on the east side
of Toone-Teague Road (see Figure 1). The Velsicol/Bardeman County Landfill and
the contaminated areas associated with the landfill will hereinafter be
referred to as the "Site".
The 242-acre parcel was purchased by Velsicol Chemical corporation ("velsicol")
for use as a landfill and is presently owned by a hOlding company for
Velsicol. From 1964 to 1973, the landfill was operated by Velsicol for the
disposal of their Memphi., Tennessee pesticide manufacturing plant's production
waste.
Waste from the plant was di8posed of in trenches excavated on 27 acres of the
property (the "di8posal areas"). The top 'of the disposal areas i8 generally
flat; however, the 8ide8 of the dispo.al areas slope down toward the drainage
areas and creek.. The di8posal areas are located on the we8t side of Pugh
Creek and are approximately one mile south of clover Creek which contains a
large wetlands area. The creeks are used recreationally but are not used as a
drinking water source.
The Sit. is locat.d in a rural part of Bar4eman County, Tenn..... and most of
the land use in the ar.a i8 agricultural. Groundwater beneath the Site
property is encountered at approximately 30 feet below land surface down to a
depth between 110 to 170 feet. An artesian aquifer i. locate4 at approximately
220 feet below land .urface. The surficial aquifer beneath the Site property,
comprised of the Wilcox and Claiborne Formation., was u..~ a. a potable water
-8upply in the area. Approximately 26 re.idence. are locat.d within 1 mile of
"
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SITE lOCATION - VElSICOUHARDEMAN COUNTY LANDFilL
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the disposal areas with the nearest residence within one-quarter of a mile from
the disposal areas.
Due to the disposal of the industrial and chemical wastes in the disposal
areas, government agencies and the nearby community have raised concerns
regarding potential impact from the Site.
SITE HISTORY AND ENFORCEMENT ACTIVITIES
Historical LandfillinQ Practices
In July 1964~ velsicol purchased the
Tennessee, specifically for use as a
Velsicol's Memphis, Tennessee plant.
by the Toone-Teague Road to the west
242 acres of land in Hardeman County,
landfill to dispose of plant waste from
The property, shown on Figure 1, is bound
and pugh creek to the east.
Immediately 'upon purchasing this property, velsicol began erecting a fence
around a portion of the property where the landfilling was to commence. The
purpose of the fence was to prevent local livestock from wandering onto the
area during active landfilling. The fence ~as comprised of three strand barbed
wire. A gate was provided at the access point off of the Toone-Teague Road.
The landfilling operation commenced in October 1964 and continued until June'
1973. At the time of closure, waste had been disposed of in three specific
disposal areas which covered a total area of approximately 27 acres. It was
initially estimated that an equivalent of. approximately 300,000 drums of plant
waste from Velsicol's Memphis plant were dispo8ed of in these three disposal
areas. During the development of the RI work Plan, velsicol completed a more
detailed estimate of waste volumes based on extensive evaluations of detailed
plant production rates. A more accurate estimate of waste quantity and type,
based on this second review by velsicol, is summarized in Table 1.
Development of the landfill began in October 1964 with the northern disposal
area since it was the only area on the property which was cleared of trees.
Waste disposal commenced along the east side of the north disposal area and was
carried out. longitudinally in the direction of the property ridges. The middle
and south disposal areas were developed sometime in the late 1960s or early
1970s. Subsequent to a public meeting held in Jackson, Tennessee in March
1971, the Tennessee Department of Health and Environment (-TDBE-) evaluated the
landfilling operation at the site. On the basis of this evaluation, a
Commissioner's Order was issued to Velsicol by TDBE which required Velsicol to
cease disposal operations in the south disposal area in August 1972, but
allowed limited waste disposal in the middle and north disposal areas until
June 1973. Therefore, after closure of the south disposal area, selected
wastes continued to be disposed of in the north and middle disposal areas until
the landfill was permanently closed in June 1973.
Plant waste was disposed of in trenches which were excavated longitudinally
along the top of the property ridges. Velsicol's records indicate that each
trench was excavated to a depth of 12 to 15 feet~ to a width of 10 to 12 feet~
and to a length of 200 to 500 feet. Trenches were placed approximately four to
eight feet apart.
As each transport vehicle arrived at the disposal areas, the containerized
waste was dumped off the truck into one of the excavated disposal trench.s.
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IAIIIII
SUMMAUY 01 WASil. IHSI'OSAI. AI IIAIU)J:MAN ( (II IN I) I ANIIIIII Ul
IIAIWI:MAN COUNT\' I.ANDHI.I. Hili S
\,.Q
Weight T(lt~1 Tot~1 1 'I '", ,,1"111 .
Utllsity Wtigh' Vol","t [qllil)ala-,,' M..,""" ..f I'""",. C)
IV/lslt' (lbslgal) (/bs' (Gal) , of "rulllS of III "/'" ,,1 , ,",,11111,'/ 0
-~
I h'pl,H:hlor Catalyst 111.1 2,539,000 251,386 4,571 II 1 ',/I 1'0
Ilcplanc Hl'sidul' 6.3 14 .5)1), 1100 2.)07,778 4 I ,IJ(,() 1/11
hl)l'r Drums 45,417 II 4',..11/
\I' A Still D- 30 Bolloms 12.0 16,128,000 I,J44,OOO 24,43h °1/1\ I\KH I
, AN2K 994,605 18,004 1/ II
Acclic Acid 80110015 19.9 19,351.1I()O 972,412 17,68() °1/11 11..1'11
H.' 2 Bol\oms 7.1 D,854,94() 1,951,400 35,480 °l/ll/~) 2 1.f)It.>
(hlon-ndic Anhydride
SIIiI Uotloms 10.8 10,1 25,O()0 937,500 17,045 01/11 11.11/'1
I'CL Bollums )-11 14.1 n,988,(X)() 9'J2,057 18,037 01/11 II,!! I
Carbon 8t.-ds 9.4 1,515,1X)() 161,170 2,930 If 1." Itl
HanJanc Filter Cakc 15.6 3,122,000 200,128 3,639 If 1.1t 19
-
95,161,940 10,112,436 229,279 129.;"//
NotC$:
II .'
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II
Disposal by landfillint; al I larJeman Counly Landfill
Disposal by mum'r.IIIOII ..1 Ml'ml'his 1'1.1111 S,ll'
I )ISPUSl'J as Iud ill pl.1I11 hoilt'r
I ),sposal by Jisch.nglllg to Iht' Itlt.al s.lIIilJry sl'wer
W.lsll' d,SI)(,<,t'd 01 hy IIWllIl'rJllon II0wt'vI'r, WIU'IIIIICIfH'r.,'or WdS nol oper.llm!; (It', I','n ,'nl 011..111'/. w.I',I,' dl"I~,'.,,1 11/1'1'
..1 'IMd"III.ln (.o""ly 1.11,.11111
1.111.11 II III "'.
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0013
On occasion; drums were set upright in the trenches upon disposal. In most
cases, however, the containerized waste was left in the trench in the random
order and orientation of which it had been dumped. Disposed waste. was covered
daily with soil excavated from the trenches. Upon filling with waste, each
trench was covered with a minimum of three feet of soil which had previously
been excavated from the area. The cover material was placed and compacted with.
a bulldozer and was mounded over the backfilled trenches to allow for future
settlement. periodically, as the backfilled areas settled, repairs were made
by backfilling with additional soil.
Investiqations and Studies comcleted to Date
Investigative studies at the site were started as early as 1967 when the United
States Geological Survey ("USGS") reported on the potential of the disposed
wastes to contaminate the groundwater beneath the disposal areas. Findings of
these studies lead to the above-referenced commissioner's order limiting
additional disposal in the trenches and finally closing the disposal areas in
1973. By late 1978, state and Federal investigations had confirmed groundwater
contamination in private wells. The use of wells by residences in the vicinity
of the disposal areas for domestic water supply was halted, and in early 1979,
a public water supply replaced the private drinking water wells. In 1980,
based on studies prepared by the united states Environmental Protection Agency
("USEPA"), TDRE, USGS and contractors working for velsicol, a low permeability
clay cap covering approximately 35 acres was placed over the disposal areas to
control and minimize additional impacts from the site.
After the completion of the cap, a monitoring program was implemented by
Velsicol and overseen by USEPA and TDRE to assess the effectiveness of the
cap. The monitoring program included the regular monitoring of groundwater
quality, surface water and sediment quality in pugh and clover creeks, a
regional groundwater elevation survey surrounding the Site and the installation
of lysimeters beneath the clay cap.
In December 1982, the site was proposed for inclusion on the NPL. The results
of the monitoring program were presented in February of 1985, and on November
5, 1985, TDRE issued a notice to Velsicol stating that a Remedial
Investigation/Feasibility study ("RI/FS") would have to be performed for the
site. USEPA and TDRE entered into a site Enforcement Agreement in July of 1986
making TDRE the lead agency responsible for enforcing the remedial activities
performed at the site. On January 7, 1987, TDRE issued a commissioner's order
requiring velsicol to perform the RI/FS for the site. In late 1988, EPA Region
IV became the lead agency, and in February of 1989 entered into an
Administrative order on Con.ent with Velsicol to complete the RI/FS. The RI
and FS reports were completed in early April of 1991 and were placed in the
information repository along with the Administrative Record ("AR") prior to
April 15, 1991.
HIGHLIGHTS OF COMMUNITY PARTICIPATION
I
During the early 1980s, numerous community relations meetings were held to
address community concerns. After contaminated well usage was replaced with
public water, and the landfill was covered with the low-permeability cap, the
community was informed through fact aheets, information placed in the Site
repository, and contact with State and Federal officials.
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In February of 1988, as part of the RI, a Community Relations plan ("CRP") was
prepared by the TDHE with assistance from the university of Tennessee. This
document lists contacts and ~nterested parties throughout government and the
local community. It also establishes communication pathways to ensure timely
dlssemination of pertinent information. Based on the CRP, a public meet~ng was
held to discuss the RIfFS process with the community.
In April of 1991, the RIfFS and the Proposed Plan for the groundwater operable
Un~t ("Proposed Plan") were released to the public.
All of these documents were made available in the Administrative
at USEPA, Region IV and the information repository maintained at
aol~var-Hardeman County public Library.
Record located
the
A public comment period was held from April 25, 1991 to May 24, 1991. In
add~tlon, a public meeting was held on April 25, 1991 to present the results of
the RIfFS and the preferred alternative as presented in the Proposed Plan. All
comments which were received by USEPA prior to the end of the public comment
per~od, including those expressed verbally at the public meeting, are addressed
in the Responsiveness summary which is attached, as Appendix A, to this Record
of Decision.
SCOPE AND ROLE OF RESPONSE ACTION
The scope of this response action is to address the off-site groundwater
contamination and prevent additional contamination from leaving the disposal
areas via migration through the groundwater. This response action is the first
of two or more operable units ("OP unit") or remediation phas.s that will be
used to address the contamination of the entire sit. including the landfill
wastes and any long term environmental effects caused by the migration of waste
from the disposal areas. The preferred alternatives for the groundwater OP
Unit ("OP unit t1") will address the remediation of contamination in the
groundwater beyond the disposal areas boundaries prior to its discharge into
the nearby surface water bodies of Clover and Pugh creeks.
A remedy for the groundwater is proposed to protect public health and the
environment by controlling exposure to the contaminated groundwAter and
controlling migration of the contamination through the groundwater to soils,
sediments and surface water bodies. The groundwater is being addressed first
for a number of reasons I
1.
Contaminants in the groundwater are above Maximum Contaminant Levels
(-MCLS-) for drinking water and pose a health risk for anyone using
the groundwater. presently, homes in the area are being supplied
water due to the groundwater contamination.
2.
Groundwater treatment can be started while additional studies are
performed and evaluated. These additional studies are required for
determining remediation technologies for controlling the source are
performed And evaluated.
3.
Groundwater
bodies, and
creeks over
is presently discharging into
higher levels of contaminants
the next four years.
the nearby surface water
will be discharging to the
-
-------
-7 -
5
9
0015
Future response actions will address other Site contamination and principal
threats completing remediation of the entire site.
SUMMARY OF SITE CHARACTERISTICS
The source of the Site contamination including the groundwater is the 27-acre
waste disposal areas (see Figure 2) located within the site.
sampling of the disposal areas, nearby soils, surface water, sediments and
groundwater was performed during the Remedial Investigation ("RI"), and the
results of the sampling are contained in the April 1991 RI report. This Record
of Decision for OP unit t1 will address only the results of the groundwater
portion of the RI since additional studies are required to evaluate final
disposal area remedies.
Geoloqy and stratigraphv
The site is located on the eastern flank of the Mississippi Embayment (see
Figure 3). The embayment is a thick suite of sediments deposited in a large
syncline or geologic trough, covering approximately 100,000 square miles in the
Gulf Coastal plain. The axis of the syncline plunges to the south, Le. the
sediments thicken to the south, with its axis roughly following the Mississippi
River. A cross section of -the area is shown in Figure 4.
The Porter's Creek clay is a thick sequence, averaging approximately 120 feet
of largely gray to black Paleocene clay, with noncontinuou8 subordinate lenses
of sand. This sequence of clays effectively seal. off the lower formations
from any contamination in the overlying Wilcox and claiborne (Eocene)
Formations.
The wilcox Formation unconformably overlies the Porter's creek clay, i.e. there
is an erosional break between the two :ormations. The Wilcox, estimated to be
75 to 125 feet thick in the .tudy area, ia a heterogeneou. unit of sand with
some silt and clay, with occasional beds of lignite, kaolin, and siderite
(FeC03). Theae sediments are interbedded and interlensed, and are not
laterally persistent. They are typical of nonmarine fluvial or deltaic
depoaita. This lack of lateral continuity is one of the key factors in
questioning the ability of the formations to receive continuous reinjection of
treated groundwater at tbe site.
The claiborne Pormation ia similar to the wilcox witb many vertical and
horizontal di.continuitie.. The Claiborne is comprised predominantly of
interbedded .and. with len.e. and thin bed. of clay and sandy clay, and 80me
thin len... of kaolin. It. maximum thickne.. in we.tern Tenne..ee is up to
1100 feet, but in the .tudy area it range. from 0 to 125 feet.
The Wilcox-Claiborne contact uaually is not discernible in Tennessee because
(1) the lithologies are similar, (2) th. stratigraphies of th. two formations
are so variable, and (3) the boundary between the two is erosional and,
therefore, not at all uniform.
Quaternary alluvial sediment. overlie mo.t of the Claiborne Formation in this
area. Thi. alluvium ia similar to the Claiborne .ediments and could not be
differentiated from them in the study ar.a. The alluvium i. usually capped by
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5 9
0016
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0019
loess, which is glacially derived, wind blown, very anqular silt. silt was
present at the surface at 9 of 12 well locations drilled near the Site. The
thickness of the loess deposits ranges from 0 to about 12 feet.
HVdroaeoloQV
The Porter's Creek Clay is'an aquitard that forms the lower boundary of the
water table aquifer in northern Hardeman County. The sands of the Wilcox and
Claiborne Formations are hydrologically connected and form one
hydrostratigraphic unit as the water table aquifer. This aquifer ranges from
approximately 6S to 12S feet thick in the study area and is considered a Class
IIa aquifer,'
Precipitation is the principal source of groundwater recharge. On a broad,
regional scale, movement of groundwater generally follows the dip of the
sediments, which is to the west toward the Mississippi River. Flow directions
within the water table aquifer in the outcrop area, such as at the Site, are
primarily controlled, however, by the local topography and nearby stream
systems. Clover Creek and the Hatchie River are the primary discharge areas
for the water table aquifer in northern Hardeman county, with Clover Creek
establishing the direction of groundwater flow to the north and northwest in
the area of ,the site (see Fiqure S).
The water table aquifer is the primary source of groundwater in northern
Hardeman County. Cross sections from south to north are shown in Fiqures 6 and
7. Sand thicknesses are circled to indicate the many potential pathways for
contaminant movement through these heterogeneous strata. Although there are
many low permeability lenses, studies near the edge of the Site showed that
perched water on top of these lenses is seldom found.
Corresponding well placements and the elevations of the groundwater and ground
surface are shown in Fiqures 8 and 9. At the disposal areas, contaminants have
to diffuse and percolate through 7S to 9S feet of sediments in the unsaturated
zone before they reach the groundwater. A two-foot thick clay cap installed on
the disposal areas in 1980 has sUbstantially reduced percolation through the
trenches and waste.
Although private wells in the vicinity of the disposal areas were monitored
extensively during the early phases of groundwater contamination, these wells
have been largely abandoned or plugged after Velsicol provided for an
alternative water supply to the residences affected by the downgradient
contamination. All groundwater monitoring is now done from carefully installed
and logged monitoring wells.
Vertical hydraulic gradients were calculated for each monitoring well nest.
Well nests are indicated schematically on Fiqures 8 and 9 by multiple screens
at the same location. Downward gradients ranging from 0.0004 to 0.02 feet/foot
were found at five of the eleven locations: while upward gradients ranging from
0.002 to 0.18 feet/foot were determined at the remaining six wells. The
relatively low magnitudes of the downward gradients adjacent to Pugh and Clover
creeks, however, suggests that horizontal flow parallel to and beneath the
creeks is occurring in Scme reaches. The complete groundwater and surface
water elevation data support the conclusion that these creeks form the
hydrologic boundaries of the groundwater flow from the Site. '
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5
9
-17-
0025
Nature and Extent of Contamination
In monitoring the downgradient movement of contaminants beyond the disposal
areas, only carbon tetrachloride (CCI4) and chloroform (CBCI3) were detected in
1989 in all six samples from two rounds of sampling (in samples from each of
three selected downgradient wells as shown in Table 2).
Contaminants detected in five of the six samples were acetone (which may. have
been a result of laboratory contamination), methylene chloride, and
tetrachloroethylene.
Two contaminants were detected in four of the six samples:
chlorobenzene and toluene.
These mobile contaminants are all volatile organic compounds ("VOCS")
characterized by:
high vapor pressures,
moderate to high solubilities,
relatively high Benry's Law constants (partitioning between air and
water), and
relatively weak sorption to soil organic matter.
Pesticides and related compounds were either not found at all in the
groundwater or were mainly found in the groundwater on-site.
Groundwater flow and contaminant transport were modeled with a two-dimensional
integrated depth model, GWPGK3, developed by J. F. Sykes at the university of
Waterloo, Waterloo, Ontario, in 1987. This is a finite element, numerical
model used for two-dimensional analyses of steady state flow and mass transport
in variably saturated cross-sections and integrated depth confined or phreatic
(water table) aquifers. .
The finite element mesh used for the model is shown in Figure 10. Simulations
of predicted carbon tetrachloride concentrations are shown in Figures 11 to 13,
with a predicted concentration profile shown in Figure 14. similar
distributions of chloroform were developed; its concentration profile is shown
in Figure 15.
While the model was calibrated against measured contaminant concentrations in
the field, these modeling results can only be interpreted qualitatively. The
heterogeneous nature of the geology of the area precludes an accurate
prediction of future conditions, which must be modeled from the assumptions of
hydraulic conductivity, longitudinal and transverse dispersivity, etc. Using
these assumptions, the calibrated hydraulic conductivity used in the model was
O.OOS cm/sec. This value is significantly lower than the maximum value of
0.0111 em/see as determined by slug tests. Yet even the value of 0.0111 em/see
resulted in a calculation of a travel time of approximately 26 years for
groundwater beneath the disposal areas to reach Clover Creek; whereas the
actual travel time was l.s. than 23 years. The actual tran.port time must
necessarily be the result of groundwater flow through the many interconnected,
highly permeable sand lenses highlighted in Figure. 6 and 7.
~
-------
'"' 9 0026 TABLE
'-' -
EXPOSL"RE POI~-r CO~CE~'TRATION (mg/lJ
GROL;..L>WATER. OOW~GRADrr::-..-r PtL~
HARDE.'.{A."i COL':-..n LA~1JmL RIfFS
.
Round 1 Round:
CkLmlcal CM.5 IJ C,\fJ'.5 GM.5 13 C,',fP-j
.o...:erone 3.38 758 0.021 1.68 ~ ~~ :x
' j
-:JrtxJn 7' etrac....londe :.76 '" -... :.19 1:.0 505 :: ':8
..:: I
C hiorobenzene 0.009 0.038 0.00 0.006 0.051 ,J)J
C;uorororm O. 707 0.914 0.807 .., ~- :.09 : :-~9
_.~,
\lethvlene C:-Uonde 0.503 0..91 0.00 a.:~ 054: -. ,""" ("\,
... """ j, v
-:- errac!-joroethvlene 0.014 0.0:1 0.00 0.010 0036 = J06
7oiue1"e 0.11.5 0.302 0.00 0.095 0...01 000
Xvle1"e 0.00 0.007 0.00 0.00 0.00 0.00
3is(: ethvlhexyDphth..1.l.1te 0.00 0.00 0.200 0.087 0.00 0 . ()()
:JI-n-butvlphttaare 0.00 0.00 0.00 0.00 0.00 J:xJ
:Jt-n-octy! ph thalate 0.00 0.00 0.010 0.00 0.00 'JJO
: 4- :>1 c.....lorop henol 0.00 0.00 0.00 0.00 000 ' ':-\
. ,\.:
Endnn 0.00 0.00 0.00 0.00 000 :X
Endnn ketone 0.00 0.00 0.00 0.00 0.00 J),;
Endr:n Aldehyde 0.00 0.00 0.00 0.00 0.00 JX)
Heptachlor 0.00 0.00 O. (XX}2 0.00 0.00 Joo
.
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CALCULA TED CARBON TETRACHLORIDE
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CALCULA TED CARBON TETRACHLORIDE
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5
-25-
9
0033
SUMMARY OF SITE RISKS
A baseline risk assessment was conducted for the Site and is presented in the
RI report. The risk assessment consisted of a chemicals of concern
identification, an exposure assessment, a toxicity assessment and a risk
characterization for human health effects.
Environment risks were briefly discussed based on available data; however,
additional information is required, and an environmental evaluation will be
conducted as a part of OP Unit 42.
Identification of Chemicals of Concern
The identification section involves the selection of the contaminants of
concern ("COCS") used in evaluating the risks associated with the Site. The
COCs are detected cont~inants which have inherent toxic/carcinogenic
properties that are likely to pose the greatest concern with respect to the
protection of public health and the environment. Selected contaminants of
concern at the Site include:
Carbon tetrachloride
Chlorobenzene
Chloroform
Tetrachloroethene
Toluene
Xylene
Acetone
Methylene Chloride
Bis (2-ethylhexyl)phthalate
Di-n-butyl phthalate
Di-n-octyl phthalate
2,4-Dichlorophenol
Enarin
Enarin Ketone
Enarin Aldehyde
Heptachlor
All of the contaminants above except Methylene Chloride and 2,4 -
Dichlorophenol (which were detected only in groundwater) were detected in both
soil and groundwater beneath the disposal areas.
EXDosure Assessment
The exposure assessment identified potential pathways and routes for
contaminants of concern to reach the receptors and the e8timated contaminant
concentration at the points of exposure. Contaminant release mechanisms from
environmental media, based on relevant hyarologic and hyarogeologic information
(fate and transport, and other pertinent Site-8pecific information, such as
local land and water us. or demographic information), were also presented.
At the Site, the current receptor population Was identified as limited to the
residential community surrounding the disposal areas.
Groundwater 'is the current release medium which can transport chemicals from
the Site. Prior to capping the disposal areas in October 1980, direct contact
with the waste and surface water transport Was a potential release medium.
Bowever, the graded and grassed cap presently precludes any direct contact with
wastes or erosion of wastes into surface water. The cap also limits air
dispersion of volatile organic chemicals from the waste. The aquifer under the
Site was the aquifer from which local residents' wel18 previously arew water
for household use. Although the present residents now receive their household
water from a public water supply, the potential to use the aquifer for
residential water exists and thus has been evaluated as a potential exposure
pathway. This pathway includes the consumption of contaminated groundwater and
the inhalation of volatiles through bathing-
,.
-------
5
-26-
9
0034
The contaminated groundwater discharges to the surface either at seeps or
d~rectly to Pugh and clover creeks. All of the identified continuous seeps
presently flow into Pugh or clover Creek. Because of the remote locations of
the seeps, direct human contact is considered unlikely. However, if contact
d~d occur, it would most likely be single or occasional exposure resulting in
an ~ns~gnificant total dose. Therefore, potential human exposure to the seep
cor.tam~nation ~s considered to be via the surface water in Pugh and Clover
Creeks.
Because the volatile organics which are migrating from the site biodegrade and
volatilize in open waters, they are not persistent in the above-ground
env~ronment. This lack of persistence significantly limits their potential
r~sk and hazard to human health when evaluating the surface water exposure
pathway.
Potential exposure to the water in pugh and Clover creeks is through
recreational activities, primarily fishing and hunting. Although fishing would
probably be limited to Clover Creek, since Pugh Creek is too shallow to support
a game fish population of fishing size, data from both creeks has been
evaluated. Game animals could drink from either Pugh Creek or clover creek.
Human exposure would be limited to eating fish caught in clover Creek or eating
game animals which might drink from the creeks. Although neither Pugh nor
Clover creek would be expected to be used for swimming, a sw~ing scenario has
been included in the assessment to conservatively address any occasional
wad~ng, swimming, or water contact by residents.
The following human exposure pathways were evaluated for potential exposure
po~nt concentration., e.t~ated daily intake and potential risk andlor hazard:
o
the use of contaminated groundwater for household use,
o
recreational fishing and fish consumption from clover Creeks,
o
occasional skin contact while fishing, swimming, or wading, and
o
inhalation of volatile compounds detected in clover Creek while
fishing.
Three levels of as.umption. are presented for each .cenario. -Levell-
assumptions pre.ent the average or mean value for the exposure assumption,
-Level 2- pre.ents assumptions which will include, statistically, 90 to 95
percent of the population, and -Level 3- pre.ents as.umptions that are
considered maximum wor.t ca.e a..umption. which are individually po..ible. For
example, occupancy of a re.idence at one location for 10 years i. considered
to repre.ent the average length of tim8 that individual. will pre.ide at one
location (-level 1-). The -90th- percentile value for length of occupancy for
one residence is 30 year. (-level 2-). It i. pos.ible that an individual could
spend their entire life in a single location so the Level 3 value is assumed to
be 70 years.
The mean of all .ample concentration., including non-detect. at half the
detection limit, in the media being evaluated i. u.ed for the Levell
calculations, and the statistical 95th percentile on this mean is applied for
the Level 2 calculations. For the Level 3 calculation., the mean of only the
analytically detected values is used as the applicable media concentration for
.
-------
5
9
0035
-27-
a possible maximum exposure. In those cases where a single well or sampling
location is evaluated, the single value is evaluated using all three exposure
levels of each applicable scenario.
To evaluate the exposure to groundwater under present conditions, the reported
concentrations of the chemicals of concern were evaluated in Wells GM-5, 13 and
GHP-5 for sampling rounds 'in FebruarY/March 1989, November 1989, and November
1989 (Table 2). Selection of these wells provides information on concentration
along the approximate center line of the plume between the northern boundary of
the disposal areas and the edge of Clover Creek.
The concentrations of carbon tetrachloride and chloroform were estimated in
wells GM-5, 13, 7 and GHP-5 for the years 1968-2011. Years 1995, 2000 and 2010
were evaluated for potential risk and hazard. The calculated concentrations of
carbon tetrachloride and chloroform in each of the four wells for these three
time intervals are summarized in Table 3.
The only expected human exposures to potential contamination in the surface
water is by consumption of fish which have been exposed to contaminated water,
the consumption of wild terrestrial animals ~hich may drink contaminated water,
the occasional skin contact while wading or while fishing or the potential
inhalation of volatile compounds which could potentially volatilize from the.
surface water while fishing. .
Tables 4 and 5 summarize the environmental data from Pugh and clover Creeks.
only Clover Creek appears large enough to support a game fish population. Game
animals could drink from either creek. The analytical data indicate that there
is no consistency in the reported concentrations., Acetone,
bis(2-ethylhexyl)phthalate, di-n-octyl phthalate, and endrin ketone are
reported in upstream locations which are not impacted by the contaminated
groundwater plume from the Site. Beptachlor, heptachlor epoxide and b-BBC were
reported in only a single sample in the two sampling rounds. Based on the
presence of pesticides in the upstream samples and the pattern of positive
detects it presently appears that the pesticides detected in the creek water
are not exclusively, if at all, from the discharge of contaminated groundwater
from the Site.
Carbon tetrachloride and chloroform are the only chemicals reported in the
creeks which appear to be Site related. Although the.e volatile organics are
migrating from the Site and may enter the creeks, their volatility and
susceptibility to degradation apparently prevent their accumulation in the
creeks at concentrations that are consistently detectable. Although the source
is not definite, the concentrations of the volatiles reported in the creeks
(Tables 4 and 5, Round 2) were evaluated for their potential exposure and
estimated total incremental risk and hazard to human health.
To evaluate
Pugh creek,
where water
used Clover
public health impacts of Site-related chemicals in Clover Creek and
it was assumed that game fish were caught and consumed in areas
contained Site-related chemicals and that the same individual also
creek and Pugh Creek for recreational swimming.
A scenario for potential exposure from
which may drink the contaminated water
concern which are discharging into the
consumption of game animals and birds
was not developed. The chemicals of
stream tram the Site (carbon
,.
-------
- -
5 9
0036
TABLE 3
ESTIMATED EXPOSURE POINT CONCENTRATIONS FOR GROt:~DWATER
FtJTURE MODELED CONDITIONS. DOWNGRADIENT PLt.:ME
HARDEMAN COt:~TY LA~"DmL RIIFS
Well Year Carbon Tetrachloride ChIaro form
(mgl L) (mgiL)
GM-3 1995 10.989 :.S:~
2000 6.689 1.029
2010 2.513 0.33:
13 1995 8.833 1 ~'''"'
..-""1'-
2000 3.846 0.936
2010 2.410 0.3::-
.. 1995 7.654 1--*63
I
2000 3.892 1.003 .
2010 2.7i1 0.387
GMP-3 1995 3.526 ., .-~
;. . .. .J
2000 3.025 0.9::-
2010 2.7'23 8.39:
..
-------
'-)
0037
TABLE :,
CLOVU alEEJC WA1'U CHEMISTRY (~8ft)
HARDEMAN COUNTY LANDFTLL R1IFS
CJwMic.l
RcnuuI I Rown4 2
CII. C. Ob C4 CII. C. 06 C-I
13.2 13.7 23-
.:J
.),.~erone
.:..uOon Tea-achlonde
13.67
:3
::-.iorororm
SIS\ :~th vlhexyl)?nt~te
470
:'\. n-«:~ipnthalare
:.:'\c~rl
0.224
~::C:-::'L KelCne
0.32
H et) laC !\lor
0.172
He?lachlor Epoxide-
0.118
Hexac.:.uoroc:ycloncun8 (b.;BHO-
0.163
.\,'otes:
. :: . Locanons u!"num of Ira wnere contaminatKi downpdient piume discha~es to creek.
~, - COnSQN8nCl not det8l:18d llIanglKl banngs and nOt sei8C18d IS concaaunanCl or concern.
.3) Other contamtnanCl or CDnC1!m not det8l:1l!d in Cover Creek lamples.
~
-------
r-
J
9
o CJ 38
'7" AiLE
I"..:GH am W41"EJ. or£MISTlY (~
HAAOEM AN co l:NT'r LA .'lOFTU. R1I'FS
R""... 1 Ro",",,:
Pt' P"~' P'2b' PJ. P4 PS ;>6" P"'~" P'2b" P3,0" p,
18.8 ~
44.9 ZS.9 51..3 :'
.
:::3
\00 31 \0 15 11
0.196 04 04 007 0..3.5
o..-ui
....:'~ne
~J"'tIOn -:-.r.ncniOnd.
-=~cl"'Ororm
3...,: -4lt1vI ncxvI ~rllna...
="n~lonthAu..
~ar./'I
~~cr./'I K.u:>,.,.
'-"~QcNor
-:~oac..""'or EooXJ~
,.,u...a'l\Joroevc:JOn.un. ,'t>-8Ha.
"'C3 IArodor ::U).
2.514
'.0..
.. , 9.ac~und 5A!IIot~ loc:nON ....",en ~ nOf rwc..... ~.....t.. tftIIft ~ s....
:. - ~.xaDO/'l nor &naIV28I rhI8 n:Nnd.
JI . w:>ruDNI'IU:I root aft8Cl8d '" ~18d bann~.nd nO( ~ .. contamlNna of oanam.
.. 2!t1er ::::>/'IQI!Iln&r\1I 01 amarn not Cl8l8Cted 1/'1 Pu~n Crwu. 'AII'Ipt8.
.
-------
-31-
5
9
0039
tetrachloride and chloroform) would be metabolized and/or excreted from animals
or birds. Due to the low levels of Site-related volatile compounds in the
surface water samples, bioconcentration and tissue retention are expected to be
negligible in mammals and birds who ingest the water. Concentrations of carbon
tetrachloride and chloroform in game animals and game birds as a result of
drinking water from Clover creek or Pugh Creek would be de minimis.
As noted, carbon tetrachloride and chloroform are the main contaminants
presently expected to migrate in high concentrations into the creeks. The
potential Clover Creek concentrations at the years 1995, 2000 and 2010 are
summarized in Table 6.
To evaluate potential inhalation exposure of fisherman to chemicals in the
Creek, an estimated air concentration at the air water interface was estimated
by applying the same air/water partition constant (-PR-) as was used to
evaluate the shower/bath exposure scenario for household use (see the RI,
Section 6). Applying the PR of 1.3 to the highest water concentration of
carbon tetrachloride predicted in Clover Creek of 1.164 mg/L, the estimated air
concentration would be 1.5 mg/L. Assuming an immediate air dilution factor of
10 at the creek surface and an additional 10-fold dilution due to mixing from
the water surface zone to the breathing zone, the inhaled concentration would
be 0.015 mg/~~'
This would be in the general range of odor detection and approximately 50% of
the time weighted average (-TWA-) for an acceptable level in the workplace.
considering that the water concentration is based on the 3Q20 (low flow)
estimate, that a fisherman would be exposed to the air on a contaminated area
of the Creek only a few days per year, and that any wind velocity would greatly
diminish exposure levels beyond the 100-fold aS8umption, the estimated
potential air levels and related exposure levels are conservatively high and
are not a health concern.
Toxicitv Asse8sment
The toxicity asse8sment presents" available human health and environmental
criteria based on pertinent standards, advisories and guidelines developed for
the protection of human health and the environment. An explanation of how
these values were derived and how they should be applied is presented below.
Cancer potency factor. (WCPFSW) have been developed by EPA's Carcinogenic
Assessment Group for estimating exce.s lifetime cancer risks associated with
exposure to potentially carcinogenic chemicals. CPFs, which are expressed in
units of (mg/kg/day)-l, are multiplied by the e.timated intake of a potential
carcinogen, in mg/kg/day, to provide an upper-bound estimate of the exceS8
lifetime cancer risk a..ociated with exposure at that intake level. The term
.upper-bound. reflect. the conservative estimate of the risk. calculated from
the CPF. Use of this approach makes underestimation of the actual cancer risk
highly unlikely. Cancer potency factors are derived from the re.ult8 of human
epidemiological studies or chronic animal bjoas.ays to which animal-to-human
extrapolation has been applied.
Reference dose8 (-RfDS-) have been developed by EPA for indicating the
potential for adverse health ettect. from expo.ure to chemicals exhibiting
noncarcinogenic eftect.. RfD., which are expre..ed in unit. ot mg/kg/day, are
e.timate. ot litetime daily exposure level. tor human., including .ensitive
individuals.
~
-------
- -
5 9
0040
TAB LE 6
ESTIMATED CLOVER CREEK CHEMISTR Y (mg/U
fUT1JRE MODELED CONDITIONS
HARDEMAN COUNTY LANDFILL RUFS
Year Cuban Tetrachloride Chloroform
3Q20 (l) Overall (2) Ann\U1 (3) 3Q20 (l) Overall (2) Annual (3)
Low Average Average Low Average Average
Flow Flow Flow Flow Flow Flow
:995 1.164 0.069 0.088 0.238 0.01~ 0.013
:000 1.000 0.059 O.OiS 0.182 0.011 O.Ol-y
2010 0.549 0.033 0.041 0.082 0.005 0.006
~otes:
" : )
Lowest average daily flow over a 3 day period during 20 years.
(:!)
Annual average daily flow calculated from 17 measurements from 1980
through 1987.
':3)
Average daily flow based on the average annual flow from 1980 through 198:-
..
-------
-33-
5
9
0041
Estimated intakes of chemicals from environmental media (e.g., the amount of a
chemical ingested from contaminated drinking water) can be compared to the
RfD. The ratio of dose over RfD gives the hazard index ("HI"). Values of HI
greater than l indicate an unacceptable exposure. RfDs are derived from human
epidemiological studies or animal studies to which uncertainty factors have
been applied (e.g., to account for the use of animal data to predict the
effects on humans). These uncertainty factors help ensure that the RfDs will
not underestimate the potential for adverse noncarcinogenic effects to occur.
In evaluating the hazard from the non-carcinogenic effects of chemicals, the
average daily exposure was based on potential shorter term (non-lifetime)
exposure estimates, generally the average daily exposure for a year. To
maintain a conservative approach, if the average daily exposure was
significantly greater for a young child than for an adult (shower/bath and
sWimming), the child's exposure was used to estimate the potential hazard.
The RfDs used to calculate the hazard indices are presented in Table 7. These
RfD values are taken from the Integrated Risk Assessment Information system
("IRIS") data base, if available from that source, or from the Health Effects
Assessment Summary Tables ("BEAST"). No reference values were found for endrin
ketone and endrin aldehyde, therefore the values for endrin are applied as
surrogate values. The RfD value for di-n-butyl phthalate is applied to
di-n-octyl phthalate as a surrogate value. These surrogate substitutions
should result in conservative evaluations based on structure-activity
relationships.
In evaluating the hazard from the carcinogenic effects, the average daily
exposure is based on lifetime exposure estimates. Lifetime estimated average
.exposure levels are based on exposure for 10, 30, or 70 years of a 70-year
lifetime. To maintain a conservative approach in each case, 6 years are
considered to be childhood years and the daily dose for those 6 years were
based on assumptions for a child's weight and exposure to estimate the
potential additional lifetime cancer risk.
The CPFs used to calculate the additional lifetime cancer risks are presented
in Table 7. These CPF values are taken from the IRIS database, if available
from that source, or from BEAST.
water quality standards, criteria and advisories are also presented in Table 7
for comparison with the reported concentrations in groundwater and surface
water.
Absorption efficiency of individual chemicals i8 not applied in the asse8sments
of water exposure. orally ingested and inhaled doses are assumed to have 100\
absorption. For dermal absorption, the permeability constant for water is used
to determine water absorptions and the chemicals are assumed to be absorbed
with the water in a proportional manner based on the reported concentration.
The toxicity and chemical information for the contaminants of concern which was
applied in this assessment is summarized in Table 7.
Risk Characterization
Excess lifetime cancer risks are determined by multiplying the intake level
~
-------
,f'
\D
CJ
C~I
-+-
T AilE 7 I"I\~ I 01 2 1'0
SUMMARY OF TOXICOI.OCY ANU O'EMJ '"KILKIJ
,
Acrtu.w <;818 27U )'J4'J'i41 ~ 24 221:tllU 1111',/11 NA I III; III ,It_I'
,.,beN> Telr.,hl...KW IS) 84 117 HIli 281 I 11'.112 1'11..111 I 1/ HI 7111. H4 I.VI'I '" ),1111 Y 1111.'
(hionUnLf.."W 112S6 2b 4t111 HI4 1 11'.112 1 fN; .111 NA 2 III. 112 II\in '" hllltY 11111
( hlufU'O.1n 119 J8 ]4~ 71111 191 ) I bill 2 'I': .111 h II 411 I II'. III In",-, IHIII
Mdhyk". ( 101,,,..J,- 84 9) '>11 1'J7tU I II) HilI' .,1' ,111- ,III 1 (Jt. 411 b III II! 11\0\'1 !111M
1t't'luhlUftlt'lhylcM I to'> 9) l4 41\'> 1 till ) bl'tll] 1 fI- 1111 tji\ I III. III I. VI f
,.4..."", 9114 Jl '>ltI 17 1 (N; .lIl 111.1111 Ni\ 1111. III
Jlyl"11C C '..ull lOb lto 1(1 1'11\ 11 241:.11] Ni\ !III: II_I
11,..42 ,"I.ylh...yllph'h"~IC )'J() '>7 h lI' ,III II WI .. II ,HI .lIi I ~I II' !III II' 1111. I 1111,'
'" " hu'yl,4.lhA"'c 27H)~ 1111. liS ~tU ~h I 7J. II' i ! 11 ,III N,\ 1111 III t< 1'1'11 ..I... II ~. 11'.,1
I »t n till Iylphth.lloah.' 1'J1I,7 141; H4 ) '11 I I/- ,H, 1 II. .111 N,\ 111'111
2.4/1... 111...",4"'''0' IbJ III H '11.112 ~',UI 11 1 "'" III 4 fl. ,III N,\ 1111 lit
/1/1. )'>4 4'J 711- 417 11,1" b2 141 III '> ,>,. 114
I'",'ro" 31111 9U 7 fit- 117 II 1b '> 14 H 1/: .111 NA 1111- 114 (Ivn. t-.,llwy 111..11
F...Jro" 1(,-,...". (]J JIlin 2 lit; 117 1126 ~b H 110HI NA 1111. (~I
f...Jro" AI.J~hy~ 01 31111119 2 Ilf 117 II 2b ) IS 7 21' ,112 NA 1 III. H4
, ".,>c., h".. 17.JU ' hI- U1 1112 ~44 I 21- .CI4 I hi; .114 4 >~ .UI I U:II'>
IIr.....h&... Ff'u...Jr J8'1]2 2 bl: jib U}'i '> 411 'I It ,II) I II- (/'i
-------
0"..;. .,
,
At "tunr
Co.h", 1t......I,I",""r
( hi...........,......
( hl......."m
M"lhr"'..r (.hI."..I"
",',tI.. hlu.u,.lhr'"oM
"".'K"'C
.IIr"'''''lr..~"
1"'" ,"hr'h"rlll'''''h~'''k
I" .. "ulrl....'h~Lolr
2.4 I lit hr................
Encl'III
1'".I.."k...."", '11
I:......i" Aldeh,.", 1.11
II....... hi...
Nu4.~.
en
'0
UltE 7 I'."r 1... 1
C)
WATER STANUAIIOS ANU (JlITERIA C'
IIAIIUEMAN COUNn lANUI'II.L IIiit'S +.:..
'-.Ill
'''''''I'S'' <..N
W.,,. U-.'ify ('.iI.... '''.'11 _..!~~~~..." 1/,."10 ,U..i,.,., !~!~-- ,,..,, H,,"' '"K
,.Mn w.,,. w.,.. ri.. 0.... 11.'1 ,.,.. .I., I ''''1'' J",.,.. ..f.,;.... c .."." w.",
w'U O~" b ri.. 0.''1 "', IDa, 'OAIC 1Daj( IU, Hhi ~,....J"fJ
7111 Nil Nil Nil Nil Nil NA
~ 11'00111' IIln'42 11111" IIn"'I4 4 III" 111111 Ill'> Nil 1/1. 1_. II'A
"I' U4W U41111 Nil Nil Nil Nil Nil riA MI I,
"I' II...." IIInll9 II I UII 'I 11111\1 Nfl NI' NI' Nil Nil I II- III
11.1111'1 IIlnll'l 11111'" III I; H; 10 NA ) II. II/ Wt}....
Ilfl'; IIlnlllll II IU... IIln'lI 1 1 I ~ IIII'll! rI,\
11111 I:; 14 ) 414 !II , I III '"I. .UI NA
..nl' 411 .111 .UI "" III tlA
14 I'» > -.., Nfl Nil Nil NIl Nil I III. II/
.. '4 1~4 Nil Nil Nil Nil Nil NA
111'1 )(1'1 1
)119 Nil Nfl NI' Nfl Nil N/\ GJ
1111'1 11"..11 II nil 111111 11111 II II! tlUIl 11111 u..t! NA v.
1
NA
NA
111.l1.li14 I II, II:; 1111: III 1 'It: III 11111 11111 III'" 111111> Nil 111.111
MUI. WT = .........Lo. Wr,sh'
nom III/JUC = Mill;li/no Mr......., r.nou....,:II1 1)'11"""0 (."kiuo
Soolut>iti'r: Soolul>di(r in w.lr. ., )() 11rs'ft"0 C "".uo
1"11 kow = 11.ri,hm I........ III ulllw Ot.""uIlW~'", ..."... rquiliIM,um
k... = W.1n /("........ «_""".1101\ ..1'" wlwn. .,bun ..... ..~..,. .1 '"'tuhbllum
ecl' = lIouo:onr-II..ion ."'... loom ".Ift tuli.h
(.W = e 8MWI P_, l''''kM..1w> I~.med (........ SIt'l'" F"."..I. ............ o"lio,,,.1 ......10:1 loom ........1 oJ.l.
1110 = ............doH cw d.- nul ...pe"'" lu ........ 8
-------
r
"
'-'
9
n 0 ' ~
U '-tLf
-36-
wlth the cancer potency factor. These risks are probabilities that are
generally expressed in scientific notation (e.g., 1x10-6 or 1E-6). An excess
lifetlme cancer risk of 1X10-6 indicates that, as a plausible upper bound, an
lndlvldual has a one in one mlllion chance of developing cancer as a result of
slte-related exposure to a carclnogen over a 70-year llfetime under the
speclfic exposure conditions at a site. The Agency considers indivldua1 excess
cancer rlsks ln the range of 10-4 to 10 -6 as protective.
Potentlal concern for noncarcinogenic effects of a single contaminant in a
slng1e medium is expressed as the hazard quotient ("BQ") (or the ratio of the
estlmated intake derived from the contaminant concentration in a given medium
to the contaminant's reference dose). By adding the HQs for all contaminants
withln a medium or across all media to which a given population may reasonably
be exposed, the Hazard Index ("HI") can be generated. The BI provides a useful
reference point for gauging the potential significance of multiple contaminant
exposures within a single medium or across media.
Estimated total incremental lifetime cancer risk from future household use of
groundwater using present conditions was calculated for wells GH-S, 13 and
GHP-5. These wells are located on the appro~imate center line of the
downgradient plume and are positioned between the northern boundary of the
disposal area and the edge of Pugh and clover creeks.
The risk and hazards from individual chemicals show that the calculated risks
and hazards are related primarily to the presence of carbon tetrachloride which
accounts for over 90\ of the total risk and hazard at each well.
The chemicals of concern at the site are primarily liver toxicants and as such
it is appropriate to sum the incremental risks and hazards for the several
primary chemicals reported in groundwater. since the exposures would all
relate to the local population, it is also appropriate to sum the risks from
the two household uses of groundwater, namely drinking and bathing. The total
incremental risks and hazard presented by household use of the groundwater are
summarized in Table 8 based on level 1 assumptions (see page 26). It is
apparent that the risks and hazards all exceed acceptable levels by several
orders of magnitude. This is to be expected since the reported concentrations
exceed Water Quality criteria for drinking water by several orders of magnitude
and the Health Advisories for drinking water by 2 to 3 orders of magnitude.
The additional lifetim8 risk of cancer and the non-carcinogenic hazard from
exposure to surface waters of the creeks based on the site-specific indicator
chemlcals are 8ummarized in Table 9.
In the 8ingle instance where the assessment shows unacceptable risk from
surface water (eating fish from Pugh creek, P3a), the risk is almo8t totally
from the reported level of PCBs which is probably not originating from the
site. As discussed earlier, the reported concentrations of pesticides, PCBs
and phthalates are apparently from background sources or are analytical
artifacts, and are not considered to be Site-related. The reported
concentrations of organic solvents in the ROund 2 creek samples co~ld
rea80nably be Site-related although the upstream sample from location C2a has
the highest concentration of carbon tetrachloride reported in clover Creek.
...
-------
-37-
5
9
0045
TABLE 8
St.iMMARY OF CA~CER RISK A~D HAZARD [~DEX
AVERAGE EXPOSL"RE SCE~ARIO ill
GROt:~DWATER I="i DOW~GRAQ[E~'" PlL~E
HARDE~A.\l COt:~'TY LA~DFILL RL'FS
Cancer Risk Ha:ard [ndn
Well I.D. Round I Round 2 Round I Round 2
On-Site Average 1.4E.ol 1.1E+OO UE+04 1.1E.OS
C\o1-S 4.2E.ol 1.8E+OO 4.4E+04 1.9E.OS
1~ 3.9E.ol 7.7E-ol 4.1E+04 1.:!.E+OS
CMP-S 3.3E.ol 4.7E.ol 3.SE+04 4.9E+04
(1)
Average exposure scenario is the Level 1 scenario for future
household use fran current carbon tetrachloride and chloroform
levels in grourdwater
,.
-------
-3.3-
5 9
0046
TABLE 9
SUMMARY OF CANCER RISK AND HAZARD INDEX
AVERAGE EXPOSURE SCENARIO (1)
PRESENT REPORTED CONCENTRATIONS
SURFACE WATER IN CLOVER AND PUGH CREEKS
HARDEMAN LANDFILL SITE RifFS
Welll.D.
Cancer Risk
Round 1 Round 2
Hazard Index
Round 1 Round 2
Clcn'er Creek
C2a Cpstream
C2 Upstream
C3b
C4
O.OE+OO
1.4E-06
O.OE+OO
4.0E-05
1.3E-07
4.7E-08
~A
8.1 E-08
9.5E-02
3.9E-02
3.2E-05
3.8E+00
1.4E-02
5.1 E-03
NA
8.9E-03
Pugh Creek
P2a Upstream 7.0E-08 NA 1. 9E-01 NA
P2b Upstream O.OE+OO NA 1.9E-01 ~A
P3a 3.3E-03 NA 5.6E-01 NA
P4 1.4E-07 1.6E.07 2.1E-01 1.7E-02
P5 3.3E-07 6.5E-06 3.6E-01 4.2£-01
P6 O.OE+OO \lA 9.5£-02 \!A
;..; otes:
~ A - Not Analyzed
(1) A verage Exposure Scenario is the Levell Scenario
....
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1
0047
-39-
Assuming the carbon tetrachloride is Site-related, examination of the risk and
hazard assessment results show that the reported concentrations do not present
a concern for fish consumption or for occasional skin contact. The swimming
exposure component of the assessment calculations would greatly exceed any
casual skin exposure component related to wading or fishing.
Based on the results of the risk calculations, it is evident that the potential
exposure to volatile compounds in the air due to specific chemicals
volatilizing from the surface waters while fishing does not represent a
significant risk to the general public.
By the application of appropriate modeling techniques, water concentrations of
carbon tetrachloride and chloroform were predicted in the wells downgradient of
the landfill and in the creeks. Values predicted for the years 1995, 2000 and
2020 in Wells GM-5, 13, 7, and GMP-5 were evaluated for potential total
incremental lifetime cancer risk and non-carcinogenic hazard using the same
household exposure or recreation scenarios as were used for evaluation of
present conditions. The summary data are presented in Tables 10 (groundwater)
and 11 (surface water).
.
Upon examination of. Table 10, it is apparent that the estimated risks and
hazards are still far in excess of acceptable levels, even in the year 2010
after an additional 20 years of migration of the plume without further
remediation.
The predicted concentrations of carbon tetrachloride and chloroform in clover
Creek are estimated to peak in the year 1994. Table 11 shows a gradual
decrease of estimated potential risk and hazard after the year 1995. At the
estimated period of peak flux to the creek between the years of 1993 and 1995,
estimated potential risks are below the target range of 1E-04 to 1E-06
estimated total incremental lifetime risk of cancer. The estimated total
hazard level is also below a level of concern even applying the more
conservative conditions of 3Q20 creek flow where the estimated groundwater flux
from the plume area makes up approximately one-half of the total creek flow.
Uncertainties
Regardless of the type of risk estimate developed, it should be emphasized that
all estimates of risk are based upon numerous assumptions and uncertainties.
In addition to limitation. associated with Site-specific chemical data, other
assumption. and uncertainties that affect the accuracy of the Site-specific
risk characterizations result from the extrapolation of potential adverse human
health eff.ct. from animal studies, the extrapolation of effects observed at
high-dose to low-dose effects, the modeling of dose response effects, and
route-to-route extrapolation.
The use of acceptable levels (established standards, criteria and guidelines)
and unit cancer risk values which are derived from animal studies introduces
uncertainty ,into the risk estimate.. In addition, the exposure assumptions
used in estimating individual dose levels are often surrounded by
uncertainties. As such, the.e estimates should not stand alone from the
various assumptions and uncertainties upon which they are ba.ed. In developing
numerical indices of risk, an attempt i. made to evaluate the .ffect of the
a.sumptions ,and limitation. on the numerical ..timat...
~
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We/ll.D.
C\-1-5
CMP-5
(1 )
-_.1-
5
9
0048
TABLE 10
SL'MMARY OF CASCER RISK A:-';D HAZARD ISDEX
F1.rn.:RE ESTI~A TED CO:-';CE:\'TRA TIO:-.;S
GROL"NDWATER IN DOWNGRADIE:-';T PLL~E
HARDE~AN U.:-';DFILL SITE RI/FS
13
Cancer Risk (1) Ha:ard Index
2995 2000 1020 1995 1000 2.010.
1. :""E.OO 1.0E.00 -4.:2£-01 1.8E.05 1.1:: ...05 .UE...V4
l.4E.OO 8.9E-01 3.7E-01 UE.05 9.3E.04 3.8E.04
1.1E...00 9.0E-01 4.:£-01 1.1E...05 9.4E.04 4.4E...04
8.4E-01 7.7E-01 3.9E-01 8.9E.04 8.0E.04 4.1E.04
Risk estimates presented for the average (level 1) scenario for
groundwater exposure fran dri.nk~ and bathing exposure to
carbon tetrachloride and chloroform
,.
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-"'..-
5
9
0049
TABLE 11
StiM.'-fARY OF CA='iCER RISK A~D HAZARD {;...1)EX
Ft.JTt"RE EST1~ATED CO~CE~TRAT10~S
St"RFACE WATER I~ CLOVER CREEK
HARDE~A~ LA~DFlLL SITE RI/FS
Cancer Risk!I) Ha:ard Index(2)
Welll.D. 2995 2000 2020 1995 2000 2020
Carbon Tetrachlonde 3.iE.Q7 3.~E.Q7 1.8E-07 6.9E.Q1 5.9E.Q1 3.2E.Ql
Chloroform 1.5E.Q9 1.2E.Q9 5.5E-10 5.9E.Q3 ~.5E.Q3 2.0E.Q3
T 01315 3.7E.Q7 3.2E.Q7 1.3E.07 6.9E-01 5.9E.Ql 3.3E.{)1
(1 )
~dative cancer risk. based on level 1 exposure assumptions
for all relevent pathways
(2)
Hazard i.n:iex based on "3Q20" estimates
. .
. '.
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9
("'\ ,', c 0
uu"
-42-
7he uncertainty factors which are incorporated into the risK estimates are
bel~eved to be conservative. As such, when they are considered collectively,
exposure and subsequently risK may be overestimated. On the other hand, these
es~~mated risk calculations were based on present conditions at the Site,
~ncluding the cap, and no maJor ~ncreases of contaminants already in the
aqu~fer. Additional risK could occur should the concentrations increase or the
cap erode.
In conclusion, based on the results of the risk assessment, actual or
threatened releases of hazardous substances from Site, if not addressed by
~mplementing the response action selected in this ROD, may present an imminent
and substantial endangerment to public health, welfare, or the environment.
Environmental RisKS
As previously stated in this ROD, the final potential environmental risks
associated with the site will be addressed as part of the second operable unit.
Previous studies have generally indicated that the contaminants migrating from
the Site are not presenting an environmental risk since the contaminants are
highly volatile and do not concentrate or bioaccumulate in the environment.
However, additional studies concerning these waste. and the more persistent
compounds located in the di~posal areas are required for a final analysis.
Also, although previous investigations have not identified any endangered
species in the area of the site, it has recently been determined, and will have
to be verified, that an endangered species of bat may exist in the vicinity of
the site.
DESCRIPTION OF ALTERNATIVES
The surficial aquifer is under consideration for remediation due to the
.unacceptable risk associated with the con8umption of the contaminated
groundwater.
Based on the contamination detected in the aquifer at different locations, the
groundwater has been divided into two areas: on-site and off-site. The on-site
groundwater i8 that portion of the aquifer located directly beneath the
disposal areas. The off-.ite groundwater is that portion of the aquifer
located beneath all properties surrounding the dispo.al areas. The off-site
groundwater contains mainly the highly mobile contaminant. like carbon
tetrachloride and chloroform. The following is a list of the remedial
alternative. under con.ideration for the contaminated groundwater. The FS
Report contain. a more detailed evaluation of each alternative.
1 )
No action (A1 and B1 in the FS).
2 )
On-site Groundwater Extraction through well., Treatment, and surface
Water Discharge (A4 in the FS).
3 )
In.titutional Control. (B2 in the FS).
4 )
Off-site Groundwater Extraction through well. and a collection
trench along pugh and Clover creek., Treatment and Surface Water
Di.charge (B4in FS).
..
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5
9
,..,-.r-1
UU;)
-43-
5 )
Off-site Groundwater Extraction through a' collection trench along
Pugh and Clover creeks, Treatment anet surface Water Discharge (86 in
FS) .
6 )
Off-site Groundwater Extraction through wells, Treatment, and
Surface Water Discharge (88 in FS).
It should be noted that groundwater reinjection was considered in the FS for
each of the groundwater ,treatment remedies. However, groundwater reinjection
is' not considered feasible due to concerns over the ability of the aquifer to
accept all of the reinjected water, the affects of the reintroduced water on
contaminant flow, and the long-term maintenance of the injection wells, which
may plug up over time due to mineral precipitation.
All of these alternatives except -No Action- involve restrictions on land:and
well use in the vicinity of the site, upkeep of the fence arid property, and
monitoring to assess the effectiveness of the' remedy. Each alternative also
includes identifying and evaluating possible additional remedial actions
required for addr~ssing the contamination of the entire Site including the
contaminant source (the disposal areas) and posslble environmental/ecological
concerns.
ALTERNATIVE 1: NO ACTION
pre.ent Worth (PW) cost $0.00
Years to Implement: 0
CERCLA requires that the -No Action- alternative be considered at every site.
Under this alternative, no groundwater containment or treatment would take
place. The only reduction of contaminant levels would occur via natural
processes such as dispersion and attenuation. since moni1;oring' is already part
of the disposal areas maintenance, additional cost would not be incurred.
ALTERNATIVE 2: ON-SITE GROUNDWATER EXTRACTION. TREATMENT AND SURl"ACE
WATER DISCHARGE
Present Worth Cost: $7,266,000
PW capital cost: 3,146,500
PW O'H Cost: 4,120,000/30 yr.
Years to Impl8JD8nta 2
Alternative 2 provides for tbe hydraulic containment of the contaminated
on-site groundwater along tbe nortbern boundary of tbe disposal areas. ,
Approximately 5 extraction vells would be installed to,develop a bydraulic
gradient along tbis northern boundary line preventing on-site groundwater
contamination above HCLs fraa leaving tbe dis~sal areas. Extracted on-site
groundwater would be pumped to a treatment system located on the site property
for treatment of groundwater to National pollutant Discbarge Elimination Syst..
C-NPDES8) concentrations establisbed as part of the clean Water Act for surface
water discharges. The contamination, particularly carbon tetrachloride,
chloroform, and naturally occuring matals, would be treated using settling
tanka for solids removal, air stripping and carbon adsorption. Treated
,.
-------
-44-
on-site groundwater would be di~charged to one of the nearby surface water
bodies (Pugh or clover Creek) and would comply w~th NPDES discharge
requirements.
ALTERNATIVE 3: INSTITUTIONAL CONTROLS
Present worth Cost: $1,088.00
PW capital Cost: 60,000
PW O&M Cost: 1,028,000/30 yrs.
Years to Implement: 50
Alternative 3 provides only for the restrictions of land and groundwater use In
the contaminated areas. It includes the monitoring of the contaminat~on and
its migration off-site. Reduction of contaminants to acceptable levels would
occur only through natural processes and will require an estimated 50 years
before cleanup goals would be met.
ALTERNATIVE 4: OFF-SITE GROUNDWATER EXTRACT:ON THROUGH WELLS AND A COLLECTION
TRENCH ALONG PUGH AND CLOVER CREEKS. TREATMENT AND SURFACE WATER DISCHARGE
Present worth Cost: $11,791,500
PW capital Cost: 6,568.500
PW O&M Cost: 5,223,000/30 yrs.
Years to Implement: 2
Alternative 4 addresses the containment and recovery along Clover creek and the
extraction of off-site groundwater in the areas of highest contaminat~on. A
slurry wall and collection tile system would be placed along clover creek
station at the confluence of clover creek and pugh creek for approximately
8,000 feet (see Figure 16) to the western limit of the plume to collect
contamination already entering the creeks.
Approximately 10 extraction wells would be installed into the high
concentration areas of the off-site groundwater to control further migratlc~ cf
the plume toward the creeks and to treat the groundwater to MCL concentra~lon
levels. The extracted water would be pumped to an off-site system for
treatment. The system would consist of settling tanks, air stripping and
carbon absorption. Treated groundwater would be discharged to one of the
nearby surface water bodies and would comply with NPDES discharge requ~rements.
ALTERNATIVE 51 OrF-SITE GROUNDWATER EXTRACTION THROUGH A COLLECTION TRENCH
ALONG PUGH ~ CLOVER CREEKS, TREATMENT AND SURFACE WATER DISCHARGE
Present worth cost: $9,384,000
PW capital Cost: 4,727,000
PW O&M Costs: 4,657,000/30 yrs.
Years to Implement: 2
Alternative 5, like Alternative 4, addresses the containment and recovery ~~
off-site contaminated groundwater along clover Creek. A slurry wall and
collection tile system would be placed along Clover creek; however, no
-------
LEGEND
----
APPROXIWA TE: UW'TS OF PLUWE
COI.J.£CT1ON DRAIN AUGNWENT
~: . :..;. .:
CJ:..:.::.:-:-:'. :.~:'.
"
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5
9
f"\u~rl.
u. :) {~
-46 -
extraction wells would be installed in the high concentration areas of the
groundwater plume, The contaminated groundwater would be treated and.
discharged in the same manner described in Alternative 4,
ALTERNATIVE 6: OFF-SITE GROUNDWATER EXTRACTION THROUGH WELLS. TREATMENT AND
SURFACE WATER DISCHARGE
Present worth Cost: $4,378,000
PW capital Cost: 1,936,000
PW O&M Cost: 2,442,000/30 yrs,
Years to Implement: 2
Alternative 6 provides for the removal of contaminated off-site groundwater
from the plume in the areas of highest concentration. Approximately 10 wells
would be installed into the high concentration areas of the off-site plume to
control the groundwater contaminant migration and remediate the off-site
groundwater to MCL concentration levels. The off-site groundwater treatment
and discharge would be the same as Alternative 4 and would comply with NPDES
requirements.
~
Any remedy implemented for OP unit t1 shall meet the performance standards set
forth below which are the Applicable or Relevant and Appropriate Requirements
("ARARS") identified for these remedial alternatives.
Remediation of contaminated groundwater for a Class IIa aquifer is required to
meet MCLs as established under the Safe Drinking Water Act (40 CFR 141, 143)
and, if possible, to attain Maximum contaminant Level Goals ("HCLGs"). HCLGs
can not be enforced as cleanup levels since they are sometimes technically
impossible to meet; however, groundwater sampling will monitor for HCLGs as a
possible result of the groundwater extraction and treatment. The groundwater
remediation levels for the contaminants of concern in the aquifer are
identified in Table 12. Reduction of the contaminants to the8e levels will
reduce the risk posed from the consumption of contaminated water from an
absolute risk over a ten year period to a risk of 8.2 X 10-sfor a 70 kg adult
over a iifetime (70 year.). Thi. ri8k falls within EPA's acceptable risk range
of 10-4to 10-6.
Any discharge to a nearby .urface water body is required to meet NPDES
standards e.tablished by the clean Water Act and regulated by the State of
Tennessee. Pugh and Clover creeks are classified for fish and aquatic life,
recreation, irrigation, live.tock watering and wildlife. The allowable
in-stream contaminant levels based on State and Federal regulations are
identified in Table 13. Final discharge levels will be determined by surface
water flow information, contaminant levels, and biological testing that will be
established by the state of Tennessee. The surface water discharge will be
required to meet the NPDES limit8 that are e.tabli.hed.
since contaminants are presently still leaching from the disposal areas, a
Point of compliance, as defined under regulation. promulgated pur.uant to the
Re.ource con.ervation. and Recovery Act ("RCRA") (40 CrR section 264.95) i8
relevant and appropriate for determining the point or line on the site beyond
which contaminant level8 in the groundwater must be remediated to HCL8. The
..
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5
9
0055
'!'ABLE :2
GROUNDWATER REME~:A'!':ON LE'JELS ~OR
CONTAMINANTS OF CONCERN AT THE
VELSICOL/HARDEMAN COUNTY NPL SITE
CONTAMINANTS GROUNDWATER
OF CONCERN REMEDIATION LEVEL ( 1) MCLG(2) RISK(3)
(mg/1) (mg/1)
VOLATILE ORGANICS
Acetone 0.7 (4)
Carbon Tetrachoride 0.005 0.0 1. 9x10-S
Ch1orobenzene 0.1 0.1
Chloroform 0.006 (5) 1. OxlO-6
Methylene Chloride 0.005 0.0 1. lx10-6
Tetrachloroethene 0.005 0.0 7.SxlO-6
Toluene 1.0 1.0
Xylenes 10.0 10.0
~
Bis (2-ethylhexyl) phthalate 0.004 0.0 1. 6x10-6
Di-n-butyl phthalate 0.7 (4)
Di-n-octyl phthalate 0.14 (4)
2,4 - Dichlorophenol 0.1 "( 4)
PESTICIDES
Endrin 0.0002 (6) 0.0002
Endrin Aldehyde 0.0002 (6) 0.0002
Endrin Ketone 0.0002 (6) 0.0002 -
Heptachlor 0.0004 0.0 5.2xlO-S
--------
TOTAL CARCINOGENIC RISK a.2xlO-S
(1) Maximum Contaminant Levels (MCLS) as promulgated under the Safe
Drinking Water Act (40CFR 141,143) were used as the remediation
level for all contaminants that have an MCL. Contaminants without
MCLs are identified numbers, and the source of the remediation
level is identified in the footnotes.
(2) MCLG - Maximum COntaminant Level Goal. A non-enforceable
concentration of a drinking water contaminant that is protective of
adverse human health effects and allows an adequate margin of
safety.
(3) Ri8k is calculated for the carcinogenic compounds
(4) Lifetim8 aealth Advisory (LHA). A lifetime exposure concentration
protective of adverse, non-cancer health effects, that assumes a
relative source contribution (RSC) of 20' of the contaminant in a
drinking water source. (January 31, 1991, Federal Register, page
3535.)
(5) Level set for a lifetime risk (70 years) of 10-6 (one in one
million exces. cancer risk level for drinking water).
(6) On July 25, 1990, a MCL and MCLG of 0.002 mq/l was proposed but is
not final for endrin. Should the MCL be made final, 0.002 mg/1
will be the endrin remediation level. The other endrin compounds
are based on the level set for endrin.
.
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5
9
"0 r"" 6
U :J
-:- .i.5~= J.:3
PLAMNING LIM!TS-:~S7R~A~
VELISCOL CHE~!CAL au~~, ~AR:E~A~ CCUNTY
The following instream limits are orov~ded for planning
pu~~oses and are valid for one year. Ary limits to be
included in a discharge per~i~ ar~ sJcje~~ to t~e ~~b:i~
~o~ice ~rocess, t~e exact locatio~ of t~e disc~arge and t~e
relative size of the discharge.
Compounds
VO~ATIL.~S
Acetone
Benzene
Carbon disulfide
Car~on tetrach: o~ ~ :~.
Chlorobenzene
Chloroform
Methylene chlorice
Tetracnloroet~er.e
Toluene
Tr-ichloroethene
Xylenes
Bis(2-ethylexyl)ph~~a1ate
Di-n-butyl phtha~ate
Di-n-octyl phthala~e
2/4-Dichlor-opheno~
Naphthalene
Dieldrin
Endr-in
Endr-in Aldehyde
Endr-in Ketone
Heptachlor
Aluminum
Arsenic
Barium
Cadmium
Calcium
Chromium VI
Total
B~As
P~ST!CIDES
"'E~AL.S
Copper
Iron
Lead
Magnesium
Manglnese
Mercury
Nickel
Potassium
Selenium
Silver
Sodium
Zinc
... Technology based limit ap~lies
~ ':J ~ ~e
,
:~st;ea~ limi~, ~g/L.
(chr"onic/a~u~e)
0.CC5*
0.005/C.044
47.0
16.0
0.088
0.010*
0.005/0.807
0.010.
0.059
~ 2 . 0
- 6 .
1.9x10 /0.0025
2.3)('0-6/0.000~8
-
2.0x~O-6
0.087/0.75
0.19/C.36
0.0007/0.002
0.0"/0.O~6
0.01 chr-onic
0.007/0.009
1.0/2.0
0.001/0.034
-
1.2x10-5/0.0024
0.088/0.79
0.005/0.020
0.001 acute
0.059/0.065
discharge.
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5
9
-49-
OuS7
Point of compliance ("PCC") for this ROD is established by identifying the
disposal areas and setting the POC at the edge of these areas as shown ~n
Figure 17. Due to the steep relief along the edge of the disposal areas at
th~s site especially along the northern and eastern sides, the POC is set at
the base of the grade of the disposal areas.
Land Disposal Restr~ctions ("LDRs") as set forth in regulations promulgated
pursuant to RCRA (40 CFR Part 268) may be applicable to the residuals of the
groundwater treatment facility, spec~fically the sludge from the settling tanks
wh~ch may requ~re RCRA disposal. spent carbon from the treatment process
should be able to be regenerated for additional use.
The Clean Air Act is an ARAR for the releases to air from the air stripper.
Releases from the stripper will comply with Federal and State Clean A~r
Standards.
Any work performed in the area of Clover Creek could affect the wetlands along
Clover creek, and 40 CFR Part 6, Appendix A concerning responses in a wetlands
would apply.
SUMMARY OF COMPARATIVE ANALYSIS OF ALTERNATIVES
The remedial alternatives developed during the site FS were evaluated by USEPA
u8ing the followi~g nine criteria. The advantage. and di.advantages of each
alternative were' then compared to identify the alternative providing the best
balance Among the.e nine criteria.
1.
overall protection of Human Health and the Environment addresses
whether or not an alternative provide. adequate protection and
describes how risks are eliminated, reduced or controlled through
treatment and engineering or institutional controls.
2.
Compliance with Applicable or Relevant and Appropriate Requirements
(ARAR.) addre8ses whether or not an alternative will meet all of the
applicable or relevant and appropriate requirement. or provide
ground. for invoking a waiver.
3.
Long-term Effectivene..
alternative to maintain
environment, over time,
ability of an
health and the
been met.
and Permanence refer. to the
reliable protection of human
once cleanup objective. have
4.
Reduction of Toxicity, Mobility or volume i. the anticipated
performance of the treatment technologies an alternative may employ.
5.
Short-term Effectivene.. involve. the period of time needed to
achieve protection and any adver.e impact. on human health and the
environment that may be po.ed during the con.truction and
implementation period until cleanup objective. are achieved.
6.
Implementability i. the technical and admini.trative fea.ibility of
an alternative, including the availability of good. and service.
needed to implement the .olution.
.
-------
.. DISPOSAL. AREAS
. APPROXIW. T! L.OC. TlON
OF I/ELSICOL DEE? 't\t:LL
--- STUDY AREA
-.- DISPOSAL. SITE
a
?E~5:~NEL. SUPPORT z:~~
_. _. - - .-
~. ..;~~ -
....... -
Point of Compliance
=':'i\-: '7" ~Y.?:":.:"'.
..
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5
9
- .
(""'\ -, r ()
LJU-J
7.
Cost lncludes capital costs, as well as operation and malntenance
costs.
8.
Agency Acceptance lndicates whether, based on its review of the
RIfFS and Proposed Plan, TORE agrees wlth USEPA on the preferred
alternative.
9.
community Acceptance lndicates the publlc support of a given
alternatlve. ThlS criterla is dlscussed in the Responslveness
swnmary.
Table 14 contains an evaluation and comparison of
the groundwater using seven of the nine crlteria.
Acceptance are discussed below.
the six (6) alternatlves for
State and communlty
State Acceptance
TOB!: has assisted USEPA in the review of reports and Site evaluations. TOBE
has reviewed and concurs with the selected remedy for the groundwater (see
Appendix B).
Community Acceptance
Community response to the alternatives is presented in the aesponsiveness
summary (Appendix A) which addresses comments received during the public
meeting and public comment period. Although the public had general questions
concernlng the remedy, no comments were received that indicated the need for a
major change in the remedy selected.
SELECTED R1!:MEDY
The selected remedy for the contaminated groundwater is a combination of
Alternatives 2 and 6. This remedy involves the hydraulic containment of the
on-site groundwater using extraction wells to prevent the on-site groundwater
above HCLs from leaving the disposal areas and the extraction of cont&mlnated
off-site groundwater to remediate the contaminated aquifer beyond the POC down
to HCLs. After groundwater is extracted, it will be treated and then
discharged to a nearby surface water body (Pugh or Clover creek).
The selected remedy will include the following:
i)
Extraction wells (approxim£tely five (5») and pumping systems wlll
be inltalled to achieve an effective hydraulic capture of
contaminantl in on-lite groundwater at the POC (see Page 46).
Approxim£te locationl of these extraction well. are .hown in Figure
18; however, locations of these well. will change to comply with the
POCo It i. e.tim£ted that the.e well. mu.t collectively recover
approxim£tely 200 qpm to achieve hydraulic containment. Piezometers
may be in.talled within the projected containment area to
demonstrate capture.
ii)
Extraction well. (approxim£tely ten (10» and pumping IYlte~ will
be in.talled to restore the contaminated off-.ite groundwater beyond
the POC to within acceptable drinking water standards by removlng
groundwater from the areas of peak contaminant concentratlon. :t
...
-------
TABLE 14:Evaluation o' Groundwater Remedial Alternatives
(J1
'-0
Ev8lual1on C.U..1a
AUe.f\8U..e 6
AI18.nall". .
AU..nal.... 2
Alte.natlv. J
AU..nal.... 4
AU..naU... S
0.... PmllIC1lUO of
PutIIIc He8lh and Ih8
Enwonmenl
No ~.prov1d8d
W. provide overa.
protection of IU*:
heaIh W. noI
inunedI8IeIv fII'*a lhe
-~ lrom .
011. SoW CIft)Uf1dIIIt....
oont8lllln8l1on
W. pruvwte overal
prot...,,,,,, of IU*:
healh. .. noI prua1
.he -1IOf1fn8f1I 'rom
.,..........
oonI_llOI1
CGmpNnm ...h
. ARAR'. 1St... and
f...eI Reyu&aIIonaI
0... noI CIDIItfJIr willi
.... ........
CompIi8a with ..
8IIIJIic88II8 .... ....
...... ........ lor
..... JIIQUfII»""
an"""'"
W. pnNlI1B ""&laY
prot""',on of puUoo;
healh ....11he
-- sp8I:''''''
by lhe 0 P lJrwfs
obfBd'ves
. Same 85 Alemalove 4
Sa,,,.. as AI"m8lhle 4
o
o
0'\
o
----__'__0______---..--- -..---- .
s ."... as AI_- 4
Doea noI ~ w8h
.... .... .....11
regulations 0IIn08fTW1U
gmundIIo- ...,...
lion.
#
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vii)
viii)
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is estimated that these extraction wells will have a pumpinq rate of
approximately 30 qpm each. Approximate locations of these
extraction wells are shown in Figure 19; however, locations of these
wells could chanqe based on movement of the contaminant plume.
iii)
Groundwater from all extraction wells will be pumped via a forcemain
system to the treatment plant on the Site property as shown in
Fiqure 19. It is estimated that approximately 8000 to 9000 lineal
feet of forcemain will be required to connect all of the extraction
wells and the treatment plant.
iv)
Contaminated qroundwater will be treated in the treatment plant
usinq a system conceptually desiqned to consist of settlinq tanks
for solids removal, air strippinq and final carbon adsorption
treatment for off qas treatment and final qroundwater polishinq
prior to discharqe. A conceptual desiqn of the system is shown
schematically in Figure 20. It is estimated that the plant will be
treatinq approximately 550 qpm of water contaminated with an
approximate total Voc concentration of 15 mqlL. The treatment
system will be required to comply with air emissions standards and
NPDES requirements (see paqe 49) prior to surface water discharqe
and may be modified to meet these requirements.
V)
Treated water will be discharqed to one of the nearby surface wate~
bodi.s (Puqh or Clover creek) in compliance with NPDES requirements
via a forcemain pipinq system.
vi)
Groundwater monitorinq will be conducted to determine the
effectiveness of the qroundwater extraction and verify that
qroundwater remediation qoals (Table 12) are reached for the
off-site qroundwater beyond the POCo
Deed restrictions, siqns, and institutional controls will be
established to identify the presence, quantity and nature of wastes
in the disposal area and qroundwater and limit uses of both until
remediations are complete.
Haintain the qroundwater treatment system and the disposal area.'
cover. Maintenance of the disposal areas will include:
a)
periodic inspection of the disposal areas' surface includinq
slopes;
b)
periodic inspection of the monitorinq well network and property
fence;
C)
periodic mcwinq of the veqetation over the disposal areas'
cover;
d)
the application of fertilizer at a specified frequency;
e)
re-establishment of veqetation over distressed areas;
f)
periodic repair of areas eroded by surtace water runoff,
q)
maintenance of the property fence and signs; and
h)
control of burrowinq animals.
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AL tERN A TIVt: '-REMEDIAL COMPONENTS I
I
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EXTRACTION
SYSTE"
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~
<:::=::: GROUNDWATER
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EQUALIZATION
AND S£nuNG TANK
;t
~ ~ AIR INTAKE
o~
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SLUDGE HANDLING
SYSTEM
PUMP
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000
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2 STAGE VAPOUR PIIASE
CARBOt4 ADSORPTION SYSTEM
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MIST
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9
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2 STAGE AQUEOUS
PHASE CAlmON
ADSORPTION
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PROPOSED GROUNDWATER TREATMENT SYSTLM
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ix)
Identify and evaluate possible additional remedial actions requ~red
for addressing the contam~natlon of the ent:re S~te ~nclud~ng the
contaminant source (disposal areas) and possible environmental/
ecological concerns and prepare a feasib~lity study to discuss the
alternat~ves. possible treatao::ity stud:es and/or add:t:onal
sampling may be requ~red.
In additlon to the above activit:es, varlOUS support act:vities :ncluding the
implementat~on of a worker health & safety program and env:ronmental mon:torlng
for ind~cator chemlcal em~ss:ons will be conducted.
The estimated costs of alternatives 2 and 6 are shown in Tables 15
combined cost for this selected remedy, excluding the cost for the
identified in paragraph ix above, is estimated to be approximately
dollars.
and 16. The
work
11,644,000
Continqency Measures
The goal of this remedial action is to restore the groundwater to its
beneficial use, which is that of a drinking water source. Based on information
obtained during the remedial investigation and the analysis of all remedial
alternatives, EPA believes that the selected remedy may be able to ach:eve this
goal.
It may become apparent, during implementation or operation of the groundwater
extraction system and its modifications, that contaminant levels have ceased to
decline and are remaining constant at levels higher than the remediat~on goals
in Table 12 over some portion of the contaminated plume. In such a case, the
remediation goals and/or the remedy may be r~evaluated.
If the selected remedy cannot meet the specified remediation goals, at any or
all of the monitoring points during implen. tation, the contingency measures
and goals described in this section may rep~ace the selected remedy and goals
for these portions of the plume. such contingency measures will, at a minLmum,
prevent further migration of the plume and include a combination of conta:nment
technologies and institutional controls. These measures axe considered to be
protective of human health and the environment, and axe technically pract~cable
under the corresponding circumstances.
The selected remedy will include groundwater extraction for an estimated per~od
of 30 years, during wbicb time the system's performance will be carefully
monitored on a regular basis and adjusted as warranted by the performance data
collected during operation. MOdifications may include any or all of the
followingl
a)
at individual wells where cleanup goals have been attained, pump:ng
may be discontinued;
b)
alternating pumping at wells to eliminate stagnation points;
C)
pulse pumping to allow aquifer equilibration and encourage adsorbed
contaminants to partition into groundwater; and
d)
installation of additional extraction wells to facilitate or
accelerate cleanup of the contaminant plume.
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5
9
Q 0 ,S G
TABLE ~S
REMEDIAL COST ESTThiA TE. At TER.'iA TIVE A2.
HARDEMA.'l COlJ~ lA.'iDFILL SITE
.4""1<411 Prts~t Worth T.Jt4l1 Prutflt
1 ttm Ducri p ti Oft C4Ip"t4l1 Costs O&M Costs of O&M Costs Worth Costs
1. !I1stiN[ional Conrrols S 3.5,000 S 68 ,COO S 641.000 S 67"6.C(()
~ ~1aintain Existing Clay Cap 9 ,COO as ,000 8= C(()
3. On-Site Hydraulic Containment 550,000 25 ,000 US,.500 ;- 55 ,.5.)J
4. Groundwater Treatment 1 ,J8S ,cro 325,000 3 ,064 ,cro H49,ro::J
5. Discharge 200,000 10,COO 94,000 294.ro::J
6. !I1direct Capital Costs 976.300 ° ° 9iL,,"'(J
Subtotals S 3,146,500 5 ~37,COO 5 4,120,000
Total &timated Present Worth C08t . Altemative A2. S 7,266,(0)
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-59-
5
9
,0067
TABLE 16
R£',.~ro[AL COST ESTIMATE. ALTERNATIVE ("
HARD£',.{A." COl::-.n L\:-.iDFILL SITE
"'""11,,1 Pru"t Worth Tot"l Prtsmt
ftrm Drscr;pho" CiJp"t,,[ Costs O&M Costs of O&.~ Costs Worth Costs
1. ::"cstit1Jtional Controls S 40 ,COO S l09,COO S 1.028,COO S 1.:60 ,COO
, Off-Site Hydraulic Removal 970,COO 40 ,COO 377.COO U47.XO
3. Groundwater Tn!atment 2i5,COO 100 ,COO 94J,COO 1.2:8,COO
(additiona! costs)
.{. Discharge 50,000 10,000 94 ,COO 144.COO
5. lr1direct Capita! Costs 601 ,COO 0 0 60 1. COO
Subtotals S 1.9J6,COO S 259,COO S 2,-44:,COO
Totoll utimolt~d Pres~nt Worth Cost. Alt~matin"'" S 40378,000
,
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5
9
,0068
-60-
To ensure that the remediation goals continue to be maintained, the aquifer
will be monitored at those wells where pumping has ceased on an occurrence of
every quarter for 5 years following di~continuation_of groundwater extraction.
If it is 'determined, on the basis of the preceding criteria and the system
performance data, 'that certain portions of the aquifer cannot be restored to
their benet'icial use, any or all of the following measures invclving long-term
management may occur, for an indefinite period of time, as a modification of
the existing system:
a)
engineering controls such as physical barriers, or long-term
gradient control provided by low level pumping, as containment
measures;
b)
chemical-specific ARARs will be waived for the cleanup of those
portions of the aquifer based on the technical impracticability of
achieving further contaminant reduction;
C)
institutional controls will be provided/maintained to restrict
access to those portions of the aquifer which remain above
remediation goals;
d),
continued monitoring of specified wells; and
e)
periodic reevaluation of remedial technologies for groundwater
restoration.
The decision to invoke any or all of these measures may be made during
periodic review of the remedial action, which will occur at leAst once
five (5) years. If any or all of these measures are determined to be
necessary, an Explaination of significant Differences ("ESD"), or a ROD
Ammendment will be issued to inform the public of these actions.
a
every
STATUTORY DETERMINATIONS
Under its legal authorities, EPA's primary responsibility at superfund sites is
to undertake remedial actions that achieve adequate protection of human health
and the environment. In addition, section 121 of CERCLA establishes several
other statutory requirements and preferences. These specify that when
complete, the selected remedial action for this site must comply with
applicable or relevant and appropriate environmental standards established
under Federal and State environmental laws unless a statutory waiver is
justified. The selected remedy also must be cost effective and utilize
permanent solutions and alternative treatment technologies or resource recovery
technologies to the maximum extent practicable. Finally, the statute
includes a preference for remedies that employ treatment that permanently and
significantly reduce the volume, toxicity, or mobility of hazardous wastes as
their principal element. The following sections discuss how the selected
reme~y meets these statutory requirements.
protection of Human Health and the Environment
Based on tbe site risk assessment, long term exposure to contaminants through
the consumption and use of contaminated groundwater is the identified risk
associated with the Site. Althougb no excessive risk was identified for
exposure to the wastes contained in the disposal areas, th~s risk level was
~
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5
9
0069
-~~-
based on present conditions which include a temporary cover over the disposal
areas.
The selected remedy protects human health and the environment through
extract~on and treatment of the contaminated groundwater. The contaminants
will be permanently removed from the groundwater by air str~pp~ng. The
volatile d~ssolved gases w~ll be transferred to the air stream for treatment by
carbon adsorpt~on and release to the atmosphere in compliance with Clean A~r
Act regulations.
Extraction of the contaminated groundwater also will eventually eliminate the
threat of exposure to the most mobile contaminants from direct contact or from
ingestion of contaminated groundwater. The future carcinogenic r~sks
associated with these exposure pathways are as high as a one in one for
consumption of the contaminated groundwater. By extracting the contam~nated
groundwater and treating, the cancer risk in the consumption of off-site
groundwater will be reduced to about 8.2 X 10-5 and an Hazard Indices (HI)
ratio of less than 1. These levels are within the range of acceptable exposure
levels of between 10-4 and 10-6 and an HI ratio of less than 1. There are
no short-term threats associated with the selected remedy that cannot be
readily controlled. In addition, no adverse cros.-media impacts are expected
from the remedy.
The contingency r~medy, if required, will provide overall protection of
health and the environment through a combination of ma.. reduction and
institutional and/or engineering control..
human
Compliance with ARARs
The selected remedy of hydraulic containment and treatment
groundwater at the PCC and extraction and treatment of the
beyond the PCC will comply with all Applicable or Relevant
Requirements (ARAR8) or the contingency remedy will attain
waiver of any ARARs. The ARARs are pre.ented below:
of the on-site
off-site groundwater
and Appropriate
or justify the
Action specific ARARs:
*
clean Water Act (40 CFR Part 122)
*
Tenne..ee water Quality Control Act, TN code 69-3-104
*
clean Air Act (40 CFR Parts 50-62)
Chemical Specific ARARs:
*
Safe Drinking Water Act (40 CFR Part. 141, and 143)
*
Tenne..ee Water Quality criteria (1200-4)
Location specific ARARs
*
Response in a Floodplan or wetlands (40 CFR Part 6, Append~x A)
*
RCRA (40 CFR Section 264.95)
*
clean Water Act (section 404) (40 CFR Part 230) (33 CFR Parts
320-330)
,
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-62-
5
9
0070
RCRA LDRs are not generally applicable to the groundwater extraction and
treatment process; however, should levels in the waste residuals in the sludge
from the treatment process exceed allowable standards, the sludge will be
disposed of in accordance with LDRs.
Cost Effectiveness
The selected remedies are cost-effective because they have been determined to
provide overall effectiveness proportional to their costs. Alternatives 2 and
6 have an estimated net present worth value of $11,644,000. Alternative 6 is
the least costly and the mostly easily implemented of Alternatives 4,5 and 6
which meet all off-site ARARs.
Utilization of Permanent solutions and Alternative Treatment Technoloqies (or
Resource Recoverv Technoloqies) to the Maximum Extent practicable
The State of Tennessee and EPA have determined that the selected remedy
represents the maximum extent to which permanent solutions and treatment
technologies can be utilized in a cost-effective manner for op Unit i1. of
those alternatives that are protective of human health and the environment and
comply with ARARs, the state of Tennessee and EPA have determined that this
selected remedy provides the best balance of tradeoffs in terms of long-term .
effectiveness and permanence, reduction in toxicity, mobility, or volume
achieved through treatment, short-term effectiveness, implementability, cost,
also considering the statutory preference for treatment as a principal element
and considering state and community input.
The selected remedy reduces the toxicity, mobility, and volume of the
contaminants in the groundwater: complies with ARARs; provides short-term
effectiveness; and protects human health and the environment. The selected
remedy will be easier to implement technically because it requires less
construction and is less likely to destroy the wetlands around clover creek.
Finally, the off-site portion of the remedy costs the least of the equally
protective off-site alternatives. The major tradeoffs that provide the basis
for this selection decision are long-term effectiveness, implementability, and
cost. .
The selected remedy is more reliable and can be implemented more quickly, with
less difficulty and at less cost that the other treatment alternatives and is
therefore determined to be the most appropriate solution for the contaminated
groundwater caused by the release of hazardous substances from or at the site.
Preference for Treatment as a principal Element
By treating the contaminated groundwater in an on-site treatment plant
consisting of an air stripper and carbon adsorption then discharging the
treated effluent to one of the nearby surface water bodies, the selected remedy
addresses the principal threat of future direct contact/ingestion of
contaminated groundwater posed by the site through the use of treatment
technologies. Therefore, the statutory preference for remedies that employ
treatment as a principal element is satisfied.
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