Cost and Performance
Report:
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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.
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%).
SoilTechs 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
Pristine, Inc. Superfund Site
Reading, Ohio
CERCLIS #: OHD076773712
ROD Date: 30 March 1990
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
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 Pristines 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 [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 Pristines 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 Pristines 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 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
Type of Matrix Processed Through the Treatment System: Soil (ex situ), sediment (ex situ)
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).
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
Thermal desorption
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.
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 [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
[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.
The timeline for this application is presented in Table 5.
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
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 |
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.
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.
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.
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.
Back to Treatment System Description | Table of Contents | Forward to Treatment System Cost
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.
No information was available on treatment system cost at the time of this report's preparation.
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]
Back to Treatment System Performance | Table of Contents | Forward to Observations and Lessons Learned
Back to Treatment System Cost | Table of Contents | Forward to References
This case study was prepared for the U.S. Environmental Protection Agencys 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
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.