U.S. Environmental Protection Agency

Cost and Performance Report:
Thermal Desorption at the
Pristine, Inc. Superfund Site
Reading, Ohio




Table of Contents




Prepared By:

U.S. Environmental Protection Agency
Office of Solid Waste and Emergency Response
Technology Innovation Office
March 1995

Preparation of this report has been funded wholly or in part by the U.S. Environmental Protection Agency under Contract Number 68-W3-0001. It has been subject to administrative review by EPA headquarters and Regional staff and by the technology vendor. Mention of trade names for commercial products does not constitute endorsement or recommendation for use.


Executive Summary

This report presents cost and performance data for a thermal desorption treatment application at the Pristine, Inc. Superfund Site, located in Reading, Ohio. Pristine, Inc. performed liquid waste disposal operations at the site from 1974 to 1981 and operated as a sulfuric acid manufacturing facility prior to 1974. As a result of spills and on-site disposal of wastes, soils at the Pristine site became contaminated with volatile and semivolatile organics, polynuclear aromatic hydrocarbons (PAHs), pesticides, and inorganic metals. The soils also contained high levels of elemental sulfur (greater than 2%).

SoilTech’s 10 ton/hr mobile Anaerobic Thermal Processor (ATP) system was used for treating contaminated soil at the Pristine site. The ATP system included a feed system, the ATP unit (rotary kiln thermal desorber), a vapor recovery system, a flue gas treatment system, and a tailings handling system. Wastewater from the vapor recovery system was treated in an on-site wastewater treatment system.

The ATP system was operated at the site from November 1, 1993 until March 4, 1994 and was used to treat approximately 12,800 tons of contaminated soil. The ATP System treated contaminants in soil to levels below the cleanup goals. Levels of six of the 11 target constituents were reduced to concentrations at or below the reported detection limits. All stack gas air emission performance standards were met in this application. Average throughput was approximately 6.5 tons/hr, and average on-line availability was approximately 62 percent, in this application. This application was notable for treating soil with a wide range of pH and moisture conditions. Treated soil was backfilled on site.

No information on treatment system cost was available at the time of this report.

Table of Contents | Forward to Site Identifying Information





Site Identifying Information

Identifying Information

Pristine, Inc. Superfund Site
Reading, Ohio
CERCLIS #: OHD076773712

ROD Date: 30 March 1990


Treatment Application

Type of Action: Remedial

Treatability Study Associated with Application?
No

EPA SITE Program Test Associated with Application?
No

Operating Period:
November 1993 to March 1994

Quantity of Soil Treated During Application:
Approximately 12,800 tons of soil


Background

Historical Activity That Generated Contamination at the Site: Liquid waste storage, disposal, and treatmentoperations

Corresponding SIC Code: 4953 W - Waste Management; Refuse Systems (Waste Processing Facility, miscellaneous)

Waste Management Practices That Contributed to Contamination:
Storage - Drums/Containers; Waste Treatment Plant

Site History: Pristine, Inc., a former liquid waste disposal facility that operated from 1974 to 1981, is located on a 3-acre site in Reading, Ohio, as shown in Figure 1. Prior to 1974, the Pristine site was the location of a sulfuric acid manufacturing facility. Between 1974 and 1981, the Pristine facility accepted a variety of bulk and drummed liquid waste products, including acids, solvents, pesticides, and PCBs. The types of wastes stored at Pristine are shown in Table 1. These wastes were treated by acid neutralization or incineration, and disposed on site. In December 1977, the Ohio Environmental Protection Agency modified Pristine’s operating permit to require that Pristine reduce the amount of waste maintained at the site to the equivalent of no more than 2,000 drums. [1, 2, and 3]

Figure 1. Site Location

Figure 1. Site Location [
1]



Table 1. Types of Wastes Stored at Pristine [
3]

Mixed paint sludges Sodium
Acid-contaminated soil Adipoyl chloride
Neutralized acid sludge Kepone
DDT and other pesticides Acetomethoxane (originally listed as dioxin)
Contaminated soap, cosmetics, corn syrup, and fatty acids Inorganic peroxides
Dimethyl sulfate Tetrahydrofuran
Hydrazine Amines
Flammable solvents Biological waste
Cyanide wastes Pharmaceutical waste
Chlorinated solvent sludge Freons
Sulfuric and nitric acid Adhesives
PCB-contaminated solvents Mercaptans
Ink solvent Alcohols
Neutralized acid Cadmium and plating waste
PCB-contaminated soybean oil Phenolic plastics and resins
Sulfuric acid sludge Phosphorus
Chrome wastes Picric acid
Scrubber process wastes Laboratory packs

In 1979, an on-site inspection of Pristine’s facilities by the Ohio EPA found 13 bulk storage tanks that each contained from 500 to 10,000 gallons of liquid waste material and as many as 10,000 drums on site. As a result of state enforcement actions, which cited Pristine’s failure to comply with the terms of its waste incinerator operating permit and violations of water pollution control regulations, Pristine, Inc. ceased disposal activities at the site in 1981. Samples taken on and near the Pristine site during Remedial Investigation/Feasibility Study (RI/FS) indicated that soils and sediment at the site were contaminated with volatile organic compounds (VOCs), semivolatile organic compounds, including polynuclear aromatic hydrocarbons (PAHs), pesticides, compounds, and inorganic metals. [1,2]

Regulatory Context: A Record of Decision (ROD) was signed in December 1987 and amended in 1990. An Explanation of Significant Differences (ESD) amended the 1990 ROD and specified thermal desorption to remediate site soils. Thermal desorption was selected based on its ability to remove PAHs and pesticides from the site soil. [4, 5, 6]


Site Logistics/Contacts

Site Management: PRP Lead

Oversight: EPA

Remedial Project Manager:

Mr. Tom Alcamo
USEPA Region 5
230 South Dearborn Street
Chicago, Illinois 60604
(312) 886-7278


Vendor:

Mr. Thomas J. Froman
Project Engineer
Canonie Environmental Services Corp. (prime contractor)
800 Canonie Drive
Porter, IN 46304
(219) 926-8651

Mr. Joseph H. Hutton
SoilTech ATP Systems, Inc. (subcontractor)
800 Canonie Drive
Porter, IN 46304
(219) 926-8651

Back to Executive Summary | Table of Contents | Forward to Matrix Description


Matrix Description

Matrix Identification

Type of Matrix Processed Through the Treatment System: Soil (ex situ), sediment (ex situ)


Contaminant Characterization

Primary Contaminant Groups: Volatiles, semivolatiles (primarily polynuclear aromatic hydrocarbons), pesticides, metals, and sulfur.

To characterize soils for thermal desorption, composite samples were collected from twelve separate areas across the Pristine site. Concentrations of volatile organics ranged from non-detect to 140 parts per billion (ppb), semivolatile organics ranged from non-detect to 130 ppm, lead ranged from 26 parts per million (ppm) to 1,100 ppm, and 4,4'-DDT ranged from 110 ppb to 8,200 ppb. Samples analyzed for PCBs were all non-detect. One composite sample was collected from the area near the former waste incinerator and analyzed for dioxins and furans. Laboratory analytical results for this sample indicated that concentrations of furans ranged from 26.7 parts per trillion to 722 parts per trillion, and concentrations dioxins ranged from 3.0 parts per trillion to 792 parts per trillion. [9]

The soil was also determined to contain sulfur in excess of 2% by weight. [20]

Table 2 presents the concentrations of 17 contaminants in the untreated soil that was fed to the desorber during the three-day proof-of-process test. [16, 20]

Table 2. Feed Soil Concentrations [16, 20]

Constituent Number of Samples Minimum Concentration (µg/kg) Maximum Concentration
(µg/kg)
Benzo(a)anthracene 3 530 J 1,100
Benzo(a)pyrene 3 420 J 750
Benzo(b)fluoranthene 3 980 1,900
Benzo(k)fluoranthene 3 290 J 440
Chrysene 3 790 890
Dibenzo(a,h)anthracene 3 ND (380) ND (770)
Indeno(1,2,3-cd)pyrene 3 290 J 370 J
Aldrin 3 ND (460) ND (2,300)
4,4'-DDT 3 3,200 4,800
Dieldrin 3 160 J ND (2,300)
2,3,7,8-TCDD (equivalent) 4 9.93 E-04 1.06 E-02
Benzene 3 ND (6) ND (6)
Chloroform 3 3 J ND (6)
1,2-Dichloroethane 3 5 J 8
1,1-Dichloroethene 3 ND (6) ND (6)
Tetrachloroethene 3 11 70
Trichloroethene 3 ND (6) 6

J-Result is an estimated value below the reporting limit.
ND - Not detected (detection limit shown in parentheses).


Matrix Characteristics Affecting Treatment Cost or Performance

Table 3 presents the major matrix characteristics affecting cost or performance for this application.

Table 3. Matrix Characteristics [9, 20]

Parameter Value Measurement Procedure
Soil Classification Silty clays with some sand Not available
Clay Content and/or Particle Size Distribution Not available --
Bulk Density 53-104 lbs/ft³ Not available
Lower Explosive Limit Not available --
Moisture Content 15-20% Not available
pH 1-2 for some feed soils Not available
Oil and Grease or Total Petroleum Hydrocarbons Not available --


Back to Site Identifying Information | Table of Contents | Forward to Treatment System Description


Treatment System Description

Primary Treatment Technology Type

Thermal desorption


Supplemental Treatment Technology

Post-treatment (air) - cyclone, quench, baghouse, carbon adsorption, condenser, and gas-oil-water separators.

Post-treatment (water) - oil/water separation (using a gravity separator, a coalescing plate system, an oleophilic membrane packing, and a dissolved air flotation system), hydrogen peroxide oxidation, sand filtration, and activated carbon filtration.


SoilTech ATP Thermal Desorption System Description and Operation

System Description

The SoilTech Anaerobic Thermal Processor, shown in Figure 2, is a mobile treatment system consisting of six main process units, including a soil pretreatment system, a feed system, an anaerobic thermal processor unit, a vapor recovery system, a flue gas treatment system, a tailings handling system, and a wastewater treatment system. [14, 17, 20]

Figure 2. ATP Schematic

Figure 2. ATP Schematic [
19]

The feed system consists of two feed hoppers and a conveyor belt. One feed hopper contains the contaminated soil and the other contains clean sand. The sand is fed to the ATP unit during system startup and shutdown periods, and acts as a heat carrier. [14, 18]

The ATP unit is a rotary kiln which contains four separate internal zones separated using proprietary sand seals. As shown in Figure 3, these include the preheat, retort, combustion, and cooling zones. The feed enters the preheat zone where it is heated to approximately 450°F and mixed, vaporizing water, volatile organics, and some semivolatile organics. The solids then enter the retort zone where they are heated to a target temperature range of 950 to 1,200°F, causing vaporization of heavy oils and some thermal cracking of hydrocarbons, resulting in the formation of coked solids and decontaminated solids. The solids from the retort zone then enter the combustion zone where coked solids are combusted. A portion of the decontaminated solids are recycled to the retort zone via a recycle channel. The recycling of these solids helps to maintain an elevated temperature in the retort zone. The decontaminated solids remaining in the combustion zone enter the cooling zone where they are cooled to a specified exit temperature. [14, 18]

Figure 3. Simplified Sectional Diagram Showing the Four Internal Zones

Figure 3. Simplified Sectional Diagram Showing the Four Internal Zones [
14]

The vapor recovery system consists of two parallel systems. One system condenses water and vapors from the preheat zone of the ATP unit and consists of a cyclone, a condenser, and a gas-oil-water separator. The other system condenses water and vapors from the retort zone and consists of two cyclones, a scrubber, a fractionator, a condenser, and a gas-oil-water separator. Condensed water from the vapor recovery system is treated in an on-site wastewater treatment system which consists of the following processes:

The flue gas treatment system consists of a cyclone with fines conveyor, flue gas quencher chamber, baghouse with dust conveyor, acid gas scrubber, and activated carbon unit. This system removes particulates and trace hydrocarbons from the flue gas exiting the combustion zone of the ATP. Fines from the baghouse and cyclone are mixed with the treated solids exiting the ATP unit. The treated flue gas is released to the atmosphere. [14, 18]

The tailings (treated solids) handling system is used to cool and remove treated solids from the ATP. The treated solids exiting the ATP are quenched with process and scrubber water and transported to storage piles using belt and screw conveyors. [14, 18]

Treated soil was backfilled on site. The soil was placed in trenches that were used for a soil vapor extraction system. The vendor stated that this area will be capped. [21, 22]

The primary innovative features of this ATP unit are the four internal zones and the use of proprietary sand seals at each end of the retort zone which are designed to maintain an oxygen-free environment in the retort zone. The oxygen-free environment in the retort zone helps to prevent the oxidation of hydrocarbons and coke. [14, 18]

System Operation

SoilTech conducted a proof-of-process performance test prior to full-scale operation to demonstrate compliance with soil treatment cleanup goals and stack gas emission performance standards. Four test runs (sampling windows) were completed during the proof-of-process test. [20]

Sulfur dioxide (SO2) control was a particular concern in this application because of concerns with SO2 emissions and the impact of SO2 on corrosion of process equipment and on the pH of aqueous condensate streams. Several SO2 control methods were used during the proof-of-process and full-scale operations, including lime (calcium oxide) addition, caustic solution, desorption, recovery of elemental sulfur under anaerobic conditions, and wet scrubbing of ATP flue gasses. [20]

During full-scale operation of the ATP system, 12,839 tons of soil and sediment were treated. Average throughput was approximately 6.5 tons/hr, and average on-line availability was approximately 62 percent. The wastewater from this system was treated and discharged to a sanitary sewer. [17,20]

Operating Parameters Affecting Treatment Cost or Performance [14, 20]

Table 4 lists the major operating parameters affecting cost or performance for this technology. Values measured for these parameters during the proof-of-process period are included in this table. Automatic waste feed shutoff controls were used for key operating parameters, including retort and combustion zone temperatures and preheat, retort, and combustion zone pressures.

Table 4. Operating Parameters [14, 20]

Parameter Value Measurement Procedure
Preheat and Retort Zone Residence Time Approximately 5 minutes Engineering design calculations
Preheat Zone Temperature 411.9-446.1°F Thermocouples in preheat zone
Retort Zone Temperature 1,009.9-1,034.1°F Thermocouples in retort zone
Combustion Zone Temperature 1,386.0-1,412.0°F Thermocouples in combustion zone
Cooling Zone Temperature 623.8-688.8°F Thermocouples in cooling zone
System Throughput 7.84-10 tons/hr Weight of untreated solids measured using a truck scale
Preheat Zone Pressure -0.10 inches water column Pressure to electrical transducer
Retort Zone Pressure -0.12 inches water column Pressure to electrical transducer
Combustion Zone Pressure -0.08 inches water column Pressure to electrical transducer
Stack Gas Exit Temperature 135°F Thermocouples in stack
Stack Gas Flow Rate 8,200 acfm @ 450°F Orifice Plate Flowmeter

The data collected during the proof-of-process period indicated that the ATP system met all established performance criteria for flue gas stack emissions and for treated soil. Based on these results, EPA approved the continued operation of the ATP system at these target operating conditions.


Timeline

The timeline for this application is presented in Table 5.

Table 5. Timeline [4, 5, 14]

Start Date End Date Activity
12/82 -- Pristine added to National Priorites List
-- '87 RI/FS conducted
12/87 -- ROD signed
3/90 -- ROD amended
11/93 3/94 Thermal desorption completed
11/93 11/93 Three day proof-of-process test conducted

Back to Matrix Description | Table of Contents | Forward to Treatment System Performance


Treatment System Performance

Cleanup Goals/Standards

An Explanation of Significant Differences (ESD), which amended the 1990 ROD, identified the cleanup goals shown in Table 6 for treatment of on-site soils and sediments at the site.

Table 6. Cleanup Goals [6]

Constituent Cleanup Goal (µg/kg)
Total Carcinogenic PAHs* 1,000
Aldrin 15
DDT 487
Dieldrin 6
2,3,7,8-TCDD (Equivalent)** 0.990
Benzene 116
Chloroform 2,043
1,2-Dichloroethane 19
1,1-Dichloroethane 285
Tetrachloroethane 3,244
Trichloroethane 175

*Total Carcinogenic PAHs are defined as teh total of benz(a)anthracene, benz(a)pyrene, benz(b)fluoranthene, benz(k)fluoranthene, chrysene, dibenzo(a,h)anthracene, and ideno(1, 2, 3-cd)pyrene.
**Cleanup goal for 2, 3, 7, 8-TCDD (Equivalent) taken from Treated Soil Analytical Results. [
16]

While the ROD and ESD did not specify stack gas emission standards, standards for stack gas emissions were established for the proof-of-process period during project planning. Table 7 lists performance standards for stack gas emissions. In addition, a Destruction and Removal Efficiency (DRE) of 99.99% was required to be demonstrated for PAHs and pesticides in this application. [20]

Table 7. Proof-of-Process Tests Stack Gas Emissions Performance Standards [20]

Parameter Performance Standard
Particulates 0.015 grains per dry standard cubic foot
(gr/dscf) corrected to 7% oxygen
Opacity <20%
Total Dioxin and Furan Emissions <30 nanograms (ng)/dscm @ 7% O
Hydrogen Chloride <4 lbs/hr
Total Hydrocarbons (THC) <20 ppm corrected to 7% O
Sulfur Dioxide 16.6 gm/sec

Treatment Performance Data [16, 20]

Table 8 summarizes the results of the analysis of treated soil from 40 of the 44 piles. Data on the minimum and maximum constituent concentrations are presented; data on analysis by soil pile is included in Appendix A. Sampling was performed between November 1, 1993 and March 4, 1994. No data were reported for four of the piles (nos. 34-37).

Table 8. Treatment Performance Data [16]

Constituent Number Soil Piles Analyzed Cleanup Goal (µg/kg) Minimum Concentration (µg/kg) Maximum Concentration (µg/kg)
Benzo(a)anthracene 40 ND (370) ND (370) ND (400)
Benzo(a)pyrene 40 ND (370) ND (370) ND (400)
Benzo(b)fluroanthene 40 ND (370) ND (370) ND (400)
Benzo(k)fluroanthene 40 ND (370) ND (370) ND (400)
Chrysene 40 ND (370) ND (370) ND (400)
Dibenzo(a,h)anthracene 40 ND (370) ND (370) ND (400)
Indeno(1,2,3-cd)pyrene 40 ND (370) ND (370) ND (400)
Total Carcinogenic PAHs 40 1000 ND ND
Aldrin 40 15 ND (4.3) ND (4.9)
4,4'-DDT 40 487 ND (8.6) 9.6
Dieldrin 40 6 ND (4.0) 4.8
2,3,7,8-TCDD
(equivalent)
40 0.99 0.000028 0.0123
Benzene 40 116 ND (5) 9
Chloroform 40 2043 ND (5) 9
1,2-Dichloroethane 40 19 ND (5) ND (6)
1,1-Dichloroethane 40 285 ND (5) ND (6)
Tetrachloroethane 40 3244 ND (5) ND (6)
Trichloroethane 40 175 ND (5) ND (6)

ND - Not detected (detection limit shown in parentheses).

Performance standards and analytical results for selected parameters in stack gas emissions during the proof-of-process tests as presented in Table 9. Air modelling using the ICST-2 model, was conducted to assess ground level concentrations of specific metals and other compounds.

Table 9. Stack Gas Emissions Results from Proof-of-Process Tests [20]

Parameter Performance Analytical Results
Particulates 0.015 grains per dry standard cubic foot
(gr/dscf) corrected to 7% oxygen
<0.00078 gr/dscf @ 7% O2
Opacity <20% <20%
Total Dioxin and Furan
Emission
<30 nanograms (ng)/dscm @ 7% O2 0.26 ng/dscm @7% O (window no.1);
2,3,7,8-TCDD equivalent=0.013
ng/dscm @ 7% O2
Hydrogen Chloride <4 lbs/hr 0.00851 - 0.0144 lbs/hr
Total Hydrocarbons (THC) <20 ppm corrected to 7% O2 5.6 - 8.8 ppm (occasional spikes over 20 ppm*)
Sulfer Dioxide 16.6 gm/sec <1 gm/sec

*Waste feed to the ATP was disconected when THC concentrations exceeded 20 ppm. THC spikes (above 20 ppm) were attributed by the vendor to burner malfunction causing uncombusted propane fuel to be emitted from the stack.

To assess compliance with the 99.99% DRE for PAHs and pesticides during the proof-of-process period, surrogate organic compounds were added to the feed soil in window numbers 2, 3, and 4 of the proof-of-process test. 1,2,3-Trichlorobenzene was used as a surrogate to represent PAHs, and chloromethyl-benzene (benzyl chloride) was used as a surrogate for pesticides. The results of the testing showed a 99.99% (four-nines) DRE for 1,2,3-trichlorobenzene in windows 2 and 3 (six-nines in window 4) and 99.999% (five-nines) DRE for benzyl chloride in windows 2, 3, and 4.


Performance Data Assessment

A review of the treatment performance data in Table 8 indicates that the cleanup goals for all constituents were met for the 40 piles of treated soil that were analyzed. The performance data show that the technology removed six of the 11 targeted constituents to levels at or below the detection limit. Only 4,4'-DDT, dieldrin, 2,3,7,8-TCDD (equivalent), benzene, and chloroform remained in the treated soil above the detection limit, at maximum concentration levels of 4.8 to 9.6 µg/kg.

For the seven PAH constituents analyzed, this technology was effective in removing these constituents to the reported detection limit (400 µg/kg).

A review of the stack gas emissions sampling results, presented in Table 9, show that during the proof-of-process tests, all stack gas emissions performance standards were met. Occasional THC spikes were measured at levels greater than the performance standard of 20 ppm. The vendor attributed these THC spikes to burner malfunction which caused uncombusted propane fuel to be emitted from the stack.


Performance Data Completeness

Treatment performance data are available for assessing the concentrations of individual constituents in 40 of 44 soil piles treated, and for assessing the concentrations in feed soil and stack gas air emissions from the proof-of-process test.


Performance Data Quality

Project specifications were prepared for this application by Conestoga-Rovers Associates (CRA). The remedial action was monitored by CRA for the PRPs.

Soil samples were analyzed using SW-846 Methods 8270, 8080, 8290, and 8240. No exceptions to the QA/QC objectives were noted by the vendor for this application.

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Treatment System Cost

Procurement Process

The PRPs contracted with Canonie Environmental Services Corp. to thermally treat soil and sediment at this site. Canonie contracted with SoilTech to perform the thermal treatment portion of the project. Conestoga-Rovers Associates was selected by the PRPs to monitor the remedial action. [20] No additional information is available on the competitive nature of the procurement process.


Treatment System Cost

No information was available on treatment system cost at the time of this report's preparation.


Vendor Input

According to the treatment vendor, in general, the costs for treatment using the SoilTech ATP system vary depending on the character of the waste material, with treatment costs ranging from $150 to $250 per ton for a 10 ton/hr ATP system. The factors identified by the vendor that affect costs include:

Vendor estimates for mobilization and demobilization costs for a 10-ton per hour system range from $700,000 to $1.5 million. [17]

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Observations And Lessons Learned

Performance Observations and Lessons Learned


Other Observations and Lessons Learned

Back to Treatment System Cost | Table of Contents | Forward to References


References

  1. Feasibility Study Completed for the Pristine, Inc. Site. U.S. Environmental Protection Agency, Office of Public Affairs, Region 5, November 1987.
  2. Pristine, Inc. Source unknown.
  3. Remedial Investigation Followup Work Plan for Pristine, Inc., Reading, Ohio. Ecology and Environment, Inc., TDD R05-8607-01, September 1986.
  4. Superfund Record of Decision, Pristine, OH, First Remedial Action - Final. U.S. Environmental Protection Agency, EPA/ROD/R05-88/060, December 1987.
  5. Superfund Record of Decision, Pristine, OH, First Remedial Action (Amendment) - Final. U.S. Environmental Protection Agency, EPA/ROD/R05-90/132, March 1990.
  6. Explanation of Significant Differences for the Pristine, Inc. Superfund Site. undated.
  7. Pristine, Inc., Ohio. NPL Publications Assistance Database, U.S. Environmental Protection Agency, Region 5, EPA ID #OHD076773712, March 1992.
  8. Draft Proposed Plan, Pristine, Inc. Superfund Site, Reading, Ohio. U.S. Environmental Protection, February 1989.
  9. Final Design Report, Thermal Treatment of Soil and Sediment (One Hundred Percent Design) Pristine, Inc. Site, Pristine, Ohio. Conestoga-Rovers & Associates, Ref. No. 3250 (25), July 1993.
  10. Performance of Remedial Response Activities at Uncontrolled Hazardous Waste Sites (REM II), U.S. EPA Contract No. 68-01-6939, Final Remedial Investigation Report, Pristine, Inc. Site, Reading, Ohio. Camp Dresser & McKee, Inc., et. al., REM II Document No. 115-RIL-RT-CMKQ-1. July 1986.
  11. Soil Excavation and Handling Plan, Pristine, Inc., Reading, Ohio. Canonie Environmental Services Corp., 92-171-03, August 1993.
  12. Health and Safety Plan, Pristine, Inc., Reading, Ohio. Canonie Environmental Services Corp., 92-171-03, August 1993.
  13. Treated Soil Handling, Sampling, and Analysis Plan, Pristine, Inc., Reading, Ohio. Canonie Environmental Services Corp., 92-171-03, September 1993.
  14. SoilTech ATP System Proof of Process, Pristine, Inc. Site, Reading, Ohio. Canonie Environmental Services Corp., 92-171-03, February 1994.
  15. Letter from U.S. Environmental Protection Agency, Region 5, to Pristine Trustees. May 4, 1993.
  16. Treated Soil Analytical Results. Letters from Canonie Environmental Services Corp. to Conestoga-Rovers & Associates Limited, December 1993 through March 1994.
  17. Hutton, J. and Shanks, R. "Thermal Desorption of PCB-Contaminated Waste at the Waukegan Harbor Superfund Site." Remediation. Spring 1994.
  18. U.S. EPA. Risk Reduction Engineering Laboratory. Draft Applications Analysis Report for the SoilTech Anaerobic Thermal Processor at the Wide Beach Development and Waukegan Harbor Superfund Sites. Cincinnati, OH. May 1993.
  19. PRC Environmental Management, Inc. Results from the SITE Demonstration of the SoilTech ATP Process at the OMC Site in Waukegan, Illinois; Volume I - Draft Report. Chicago, Illinois. September 16, 1994.
  20. Hutton, J.H., and A.J. Trentini, "Thermal Desorption of Polynuclear Aromatic Hydrocarbons and Pesticides Contaminated Soils at an Ohio Superfund Site: A Case Study," 94-FA155.05, undated.
  21. Comments on Draft Report from SoilTech, Received February 16, 1995.
  22. Personal communication, Tom Alcamo, RPM, to Jim Cummings, EPA/TIO, February 14, 1995.

Analysis Preparation

This case study was prepared for the U.S. Environmental Protection Agency’s Office of Solid Waste and Emergency Response, Technology Innovation Office. Assistance was provided by Radian Corporation under EPA Contract No. 68-W3-0001.

Back to Observations and Lessons Learned | Table of Contents | Forward to Appendix A - Summary of Analytical Results for the Treated Soil Piles at the Pristine Superfund Site


Appendix A - Summary of Analytical Results for the Treated Soil Piles at the Pristine Superfund Site


Data reported in ug/kg for all constituents

Pile Number   1   2   3   4   5   6   7   8   9   10   11  
Sample Date Cleanup 1 Nov 93 8 Nov 93 9 Nov 93 11 Nov 93 12 Nov 93 15 Nov 93 17 Nov 93 18 Nov 93 20 Nov 93 25 Nov 93 29 Nov 93
EPA Method Goals 8270   8270   8270   8270   8270   8270   8270   8270   8270   8270   8270  
Benzo(a)anthracene   370 U 370 U 380 U 380 U 380 U 380 U 370 U 380 U 380 U 370 U 370 U
Benzo(a)pyrene   370 U 370 U 380 U 380 U 380 U 380 U 370 U 380 U 380 U 370 U 370 U
Benzo(b)fluoranthene   370 U 370 U 380 U 380 U 380 U 380 U 370 U 380 U 380 U 370 U 370 U
Benzo(k)fluoranthene   370 U 370 U 380 U 380 U 380 U 380 U 370 U 380 U 380 U 370 U 370 U
Chrysene   370 U 370 U 380 U 380 U 380 U 380 U 370 U 380 U 380 U 370 U 370 U
Dibenzo(a,h)anthracene   370 U 370 U 380 U 380 U 380 U 380 U 370 U 380 U 380 U 370 U 370 U
Indeno(1,2,3-cd)pyrene   370 U 370 U 380 U 380 U 380 U 380 U 370 U 380 U 380 U 370 U 370 U
Total PAHs 1000 BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL  
EPA Method   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080  
Aldrin 15 4.5 U 4.5 U 4.6 U 4.6 U 4.5 U 4.6 U 4.4 U 4.5 U 4.5 U 4.5 U 4.5 U
4,4'-DDT 487 8.9 U 9.1 U 9.2 U 9.1 U 9 U 9.3 U 8.9 U 9.1 U 9 U 9 U 9 U
Dieldrin 6 4.5 U 4.5 U 4.6 U 4.6 U 4.5 U 4 U 4.4 U 4.5 U 4.5 U 4.5 U 4.5 U
EPA Method   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290  
2,3,7,8-TCDD (Equivalent) 0.99 0.01   0   0   0 U 0 U 0.000575 0.000635 0.000027 0.000275 0   0.000 U
EPA Method   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240  
Benzene 116 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 96 U 5 U 5 U
Chloroform 2043 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 5 U 6 U 5 U
1,2-Dichloroethane 19 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 5 U 6 U 5 U
1,1-Dichloroethene 285 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 5 U 6 U 5 U
Tetrachloroethene 3244 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 5 U 6 U 5 U
Trichloroethene 175 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 5 U 6 U 5 U

BDL - Below detection limit
N/A - Not available
Data Qualifiers:
U - Constituent was not detected above the detection limit specified. The detection limit is influenced by several factors, including initial sample size, dilution factor, matrix interferences, and instrument response; therefore the detection limit may vary from sample to sample.





Summary of Analytical Results for the Treated Soil Piles at the Pristine Superfund Site (Cont.); Data reported in ug/kg for all constituents

Pile Number   12   13   14   15   16   17   18   19   20   21   22  
Sample Date Cleanup 30 Nov 93 2 Dec 93 3 Dec 93 6 Dec 93 7 Dec 93 12 Dec 93 14 Dec 93 17 Dec 93 20 Dec 93 20 Dec 93 22 Dec 93
EPA Method Goals 8270   8270   8270   8270   8270   8270   8270   8270   8270   8270   8270  
Benzo(a)anthracene   360 U 390 U 380 U 380 U 370 U 380 U 400 U 380 U 370 U 380 U 380 U
Benzo(a)pyrene   360 U 390 U 380 U 380 U 370 U 380 U 400 U 380 U 370 U 380 U 380 U
Benzo(b)fluoranthene   360 U 390 U 380 U 380 U 370 U 380 U 400 U 380 U 370 U 380 U 380 U
Benzo(k)fluoranthene   360 U 390 U 380 U 380 U 370 U 380 U 400 U 380 U 370 U 380 U 380 U
Chrysene   360 U 390 U 380 U 380 U 370 U 380 U 400 U 380 U 370 U 380 U 380 U
Dibenzo(a,h)anthracene   360 U 390 U 380 U 380 U 370 U 380 U 400 U 380 U 370 U 380 U 380 U
Indeno(1,2,3-cd)pyrene   360 U 390 U 380 U 380 U 370 U 380 U 400 U 380 U 370 U 380 U 380 U
Total PAHs 1000 BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL  
EPA Method   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080  
Aldrin 15 4.3 U 4.7 U 4.5 U 4.6   4.5 U 4.6 U 4.8 U 4.7 U 4.5 U 4.4 U 4.5 U
4,4'-DDT 487 8.6 U 9.4 U 9.1 U 9.2   9.1 U 9.2 U 9.6   9.3 U 8.9 U 8.9 U 9 U
Dieldrin 6 4.3 U 4.7 U 4.5 U 4.6   4.5 U 4.6 U 4.8   4.7 U 4.5 U 4.4 U 4.5 U
EPA Method   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290  
2,3,7,8-TCDD (Equivalent) 0.99 0.000405 0.000562 0.000296 0.000225 0.0000715 0.000208 0.0000859 0.000204 0.000434 0.00016 0.000514
EPA Method   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240  
Benzene 116 7   6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
Chloroform 2043 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 9  
1,2-Dichloroethane 19 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
1,1-Dichloroethene 285 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
Tetrachloroethene 3244 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
Trichloroethene 175 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U

BDL - Below detection limit
N/A - Not available
Data Qualifiers:
U - Constituent was not detected above the detection limit specified. The detection limit is influenced by several factors, including initial sample size, dilution factor, matrix interferences, and instrument response; therefore, the detection limit may vary from sample to sample.







Summary of Analytical Results for the Treated Soil Piles at the Pristine Superfund Site (Cont.); Data reported in ug/kg for all constituents

Pile Number   23   24   25   26   26 (Dup. 27   28   29   30   31   32   33  
Sample Date Cleanup 2  Jan 94 3 Jan 94 5 Jan 94 10 Jan 94 10 Jan 94 12 Jan 94 14 Jan 94 17 Jan 94 18 Jan 94 20 Jan 94 24 Jan 94 31 Jan 94
EPA Method Goals 8270   8270   8270   8270   8270   8270   8270   8270   8270   8270   8270   8270  
Benzo(a)anthracene   380 U 390 U 400 U 380 U 380 U 400 U 370 U 410 U 400 U 370 U 380 U 380 U
Benzo(a)pyrene   380 U 390 U 400 U 380 U 380 U 400 U 370 U 410 U 400 U 370 U 380 U 380 U
Benzo(b)fluoranthene   380 U 390 U 400 U 380 U 380 U 400 U 370 U 410 U 400 U 370 U 380 U 380 U
Benzo(k)fluoranthene   380 U 390 U 400 U 380 U 380 U 400 U 370 U 410 U 400 U 370 U 380 U 380 U
Chrysene   380 U 390 U 400 U 380 U 380 U 400 U 370 U 410 U 400 U 370 U 380 U 380 U
Dibenzo(a,h)anthracene   380 U 390 U 400 U 380 U 380 U 400 U 370 U 410 U 400 U 370 U 380 U 380 U
Indeno(1,2,3-cd)pyrene   380 U 390 U 400 U 380 U 380 U 400 U 370 U 410 U 400 U 370 U 380 U 380 U
Total PAHs 1000 BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL  
EPA Method   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080  
Aldrin 15 4.5 U 4.7 U 4.7 U 4.6 U 4.6 U 4.8 U 4.6 U 4.9 U 4.8 U 4.5 U 4.6 U 4.5 U
DDT 487 9 U 9.4 U 9.3 U 9.2 U 9.2 U 9.1 U 9.1 U 9.7 U 9.8 U 9 U 9.1 U 9 U
Dieldrin 6 4.5 U 4.7 U 4.7 U 4.6 U 4.6 U 4.8 U 4.6 U 4.9 U 4.8 U 4.5 U 4.6 U 4.5 U
EPA Method   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290  
2,3,7,8-TCDD (Equivalent) 0.99 .000413 0.0000705 0.000595 0.000733 0.000415 0.000114 0.000189 0.0000542 0.0000436 0.00023 0.000138 0.000679
EPA Method   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240  
Benzene 116 6 U 5 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
Chloroform 2043 6 U 5 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
1,2-Dichloroethane 19 6 U 5 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
1,1-Dichloroethene 285 6 U 5 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
Tetrachloroethene 3244 6 U 5 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U
Trichloroethene 175 6 U 5 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U 6 U

BDL - Below detection limit
N/A - Not available
Data Qualifiers:
U - Constituent was not detected above the detection limit specified. The detection limit is influenced by several factors, including initial sample size, dilution factor, matrix interferences, and instrument response; therefore the detection limit may vary from sample to sample.

Summary of Analytical Results for the Treated Soil Piles at the Pristine Superfund Site (Cont.); Data reported in ug/kg for all constituents

Pile Number   34   35   36   37   38   39   40   41   42   42(Dup.)   43   44  
Sample Date Cleanup N/A   N/A   N/A   N/A   22 Feb 94 22 Feb 94 22 Feb 94 26 Feb 94 28 Feb 94 28 Feb 94 1 March 94 4 March 94
EPA Method Goals 8270   8270   8270   8270   8270   8270   8270   8270   8270   8270   8270   8270  
Benzo(a)anthracene   N/A   N/A   N/A   N/A   0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U
Benzo(a)pyrene   N/A   N/A   N/A   N/A   0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U
Benzo(b)fluoranthene   N/A   N/A   N/A   N/A   0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U
Benzo(k)fluoranthene   N/A   N/A   N/A   N/A   0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U
Chrysene   N/A   N/A   N/A   N/A   0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U
Dibenzo(a,h)anthracene   N/A   N/A   N/A   N/A   0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U
Indeno(1,2,3-cd)pyrene   N/A   N/A   N/A   N/A   0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U 0.4 U
Total PAHs 1000 N/A   N/A   N/A   N/A   BDL   BDL   BDL   BDL   BDL   BDL   BDL   BDL  
EPA Method   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080   8080  
Aldrin 15 N/A   N/A   N/A   N/A   4.6 U 4.5 U 4.6 U 4.3 U 4.5 U 4.5 U 4.4 U 4.4 U
DDT 487 N/A   N/A   N/A   N/A   9.1 U 9 U 9.2 U 8.6 U 9.1 U 9.1 U 8.8 U 8.9 U
Dieldrin 6 N/A   N/A   N/A   N/A   4.6 U 4.5 U 4.6 U 4.3 U 4.5 U 4.5 U 4.4 U 4.4 U
EPA Method   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290   8290  
2,3,7,8-TCDD (Equivalent) 0.99 N/A   N/A   N/A   N/A   0.00 U 0.00 U 0.00 U 0.00 U 0.000136 0.00021 0.000062 0.000144
EPA Method   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240   8240  
Benzene 116 N/A   N/A   N/A   N/A   6 U 6 U 6 U 5 U 6 U 6 U 5 U 5 U
Chloroform 2043 N/A   N/A   N/A   N/A   6 U 6 U 6 U 5 U 6 U 6 U 5 U 5 U
1,2-Dichloroethane 19 N/A   N/A   N/A   N/A   6 U 6 U 6 U 5 U 6 U 6 U 3 U 5 U
1,1-Dichloroethene 285 N/A   N/A   N/A   N/A   6 U 6 U 6 U 5 U 6 U 6 U 5 U 5 U
Tetrachloroethene 3244 N/A   N/A   N/A   N/A   6 U 6 U 6 U 5 U 6 U 6 U 5 U 5 U
Trichloroethene 175 N/A   N/A   N/A   N/A   6 U 6 U 6 U 5 U 6 U 6 U 3 U 5 U

BDL - Below detection limit
N/A - Not available
Data Qualifiers:
U - Constituent was not detected above the detection limit specified. The detection limit is influenced by several factors, including initial sample size, dilution factor, matrix interferences, and instrument response; therefore, the detection limit may vary from sample to sample.

 

 

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