U.S. Environmental Protection Agency

Cost and Performance Report:
Slurry Phase Bioremediation Application at the Southeastern Wood Preserving Superfund Site
Canton, Mississippi




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 slurry phase bioremediation application at the Southeastern Wood Preserving Superfund site, in Canton, Mississippi. Slurry phase bioremediation was used at the Southeastern Wood site to treat soil and sludge contaminated with polynuclear aromatic hydrocarbons (PAHs), including acenaphthene, acenaphthylene, anthracene, benzo(a)anthracene, benzo(b and k)fluoranthenes, benzo(ghi)perylene, benzo(a)pyrene, chrysene, dibenzo(a,h)anthracene, fluoranthene, fluorene, indeno(1,2,3-cd)pyrene, naphthalene, phenanthrene, and pyrene.

The Southeastern Wood site was the location of a creosote wood preserving facility that operated from 1928 to 1979, and included three unlined wastewater treatment surface impoundments. Bottom sediment sludge from the impoundments was found to contain PAHs at levels of approximately 4,000 mg/kg, and was identified as a RCRA K001-listed hazardous waste. PAH concentrations measured included acenaphthene at 705 mg/kg, naphthalene at 673 mg/kg, and benzo(a)pyrene (B(a)P) at 224 mg/kg.

The application at Southeastern Wood was completed as a removal action, under an action memorandum signed in September 1990. A slurry phase bioremediation system was operated from July 1991 until 1994, and consisted of a power screen, a slurry mix tank, four slurry phase bioremediation reactors (bioreactors), and a slurry dewatering unit. The bioreactors were 38 feet in diameter and 24 feet in height, and were equipped with a blower for aeration and an impeller for mixing and keeping the slurry in suspension. Cleanup goals for this application were developed based on the results of laboratory and field pilot tests and a site-specific health-based risk analysis, and consisted of the following: total PAHs - 950 mg/kg, and B(a)P-equivalent PAHs - 180 mg/kg. These goals were provided in an LDR treatability variance for this application.

The bioreactors were operated on a batch basis, and each batch was monitored during treatment to evaluate performance with respect to the cleanup goals. Treatment performance data are available for 13 of the 61 bioreactor batches, and show that the average total PAH concentration was reduced from 8,545 to 634 mg/kg, which corresponds to a treatment efficiency of 93 percent. The average B(a)P-equivalent concentration was reduced from 467 to 152 mg/kg, or 67 percent. The analytical data indicate that the majority of biodegradation occurred during the first 5 to 10 days of treatment, and the cleanup goal for total PAHs was met for 12 of the 13 batches within approximately 19 days of treatment.

Approximately $2,900,000 were expended in this application, consisting of $2,400,000 for activities directly attributed to treatment (mobilization/setup, startup/testing/permits, and operation), and $500,000 for after-treatment activities (site restoration). The cost for activities directly attributed to treatment corresponds to $170 per ton ($230 per cubic yard) of soil and sludge treated (14,140 tons, or 10,500 cubic yards).

Table of Contents | Forward to Site Information


Site Information

Identifying Information

Southeastern Wood Preserving Superfund Site
Canton, Mississippi
CERCLIS # MSD0008258558
Action Memorandum Date: 9/30/90


Treatment Application

Type of Action: Removal
Treatability Study Associated with Application? Yes (see additional information under Background and Operation below)
EPA SITE Program Test Associated with Application? No
Operating Period: 1991-1994
Quantity of Soil Treated During Application: 14,140 tons (10,500 cubic yards) of soil and sludge


Background

Historical Activity That Generated Contamination at the Site: Creosote wood preserving
Corresponding SIC Code: 2491B (Wood Preserving Using Creosote)
Waste Management Practices That Contributed to Contamination: Manufacturing Process, Surface Impoundment/Lagoon


Site History: The Southeastern Wood Preserving Superfund Site is an abandoned wood preserving facility located in Canton, Mississippi, as shown in Figure 1. The facility was used for creosote wood preserving activities between 1928 and 1979. In 1986, EPA initiated an emergency response action at the site to stabilize three unlined surface impoundments which were overflowing.

The impoundments were dewatered and bottom sediment sludge was excavated and stabilized using approximately 70 cubic yards of cement kiln dust.

Excavation was based on a visual assessment of contamination. EPA sampled this material in April 1989, and found it to be contaminated with polynuclear aromatic hydrocarbons (PAHs), at levels of approximately 4,000 mg/kg, as shown in Table 1. The contaminated material from the lagoon was classified as a RCRA K001-listed hazardous waste (bottom sediment sludge from the treatment of wastewaters from wood preserving processes which used creosote). The excavated material was stockpiled on site for further treatment. [1, 2, 12]

Regulatory Context: This application was conducted as part of a removal action at the site. Cleanup goals were developed based on the results of bench-scale and field pilot studies using bioremediation and a site-specific health-based risk analysis.

Remedy Selection: Slurry-phase bioremediation was selected for this application on the basis of cost. In addition, slurry-phase bioremediation was identified as preferable to land treatment because it was believed to treat the soil in a shorter period of time and to achieve lower concentrations in the residual soil. [4, 9]

Table 1. Concentrations of PAHs in Excavated Material* [12]

Constituent

Concentration (mg/kg)

Acenaphthene

705

Acenaphthylene

78.8

Anthracene

2.44

Benzo(a)anthracene

496

Benzo(b)fluoranthene/ Benzo(k)fluoranthene

513

Benzo(ghi)perylene

9.8

Benzo(a)pyrene

224

Chrysene

305

Dibenzo(ah)anthracene

27.05

Fluoranthene

419

Fluorene

32.2

Indeno(1,2,3-cd)pyrene

64.1

Naphthalene

673

Phenanthrene

266

Pyrene

ND (0.36)

Total PAHs

3,815

ND - Not detected. Value in parentheses is the reported detection limit.
*Sample collected April 4, 1989.

Figure 1. Site Location
Figure 1. Site Location[1]


Site Logistics/Contacts

Site Management: Fund-Lead

Oversight: EPA

On-Scene Coordinator: R. Donald Rigger
USEPA Region 4
345 Courtland Street, N.E.
Atlanta, GA 30365
(404) 347-3931

Treatment System Vendor: Douglas E. Jerger/Pat Woodhull
OHM Remediation Services Corp.
16406 U.S. Route 224 East
P.O. Box 551
Findlay, OH 45840
(419) 425-6175

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) and sludge (ex situ)


Contaminant Characterization

Primary Contaminant Group: Polynuclear Aromatic Hydrocarbons (PAHs)

The excavated material at the site contained PAH concentrations of approximately 4,000 mg/kg dry weight for total PAHs and from 1,000 to 2,500 mg/kg dry weight carcinogenic PAHs. Total PAHs are defined as the sum of the 16 constituents listed below. Carcinogenic PAHs are defined as the total concentration of the seven PAHs marked with an asterisk: [3]

  • Acenaphthene;
  • Acenaphthylene;
  • Anthracene;
  • Benzo(a)anthracene*;
  • Benzo(b)fluoranthene*/
  • Benzo(k)fluoranthene*;
  • Benzo(ghi)perylene;
  • Benzo(a)pyrene*;
  • Chrysene*;
  • Dibenzo(a,h)anthracene*;
  • Fluoranthene;
  • Fluorene;
  • Indeno(1,2,3-cd)pyrene*;
  • Naphthalene;
  • Phenanthrene; and
  • Pyrene.


Matrix Characteristics Affecting Treatment Cost or Performance

The major matrix characteristics affecting cost or performance for this technology and the values measured for each are shown in Table 2.

Table 2. Matrix Characteristics [2, 9, 12]

Parameter

Value

Measurement Method

Soil Classification

Information not provided

Information not provided

Clay Content and/or Particle Size Distribution*

>10 mesh (gravel) 5%
<10->200 mesh (sand) 40%
<200 mesh (clay) 55%

Information not provided

Bulk density (of stockpiled material)

1.83 gm/cm3

ASTM-D1298

Ash

66.8%

ASTM-D482

Sulfur

0.08%

ASTM-D129

Free liquids

None

SW-846-9095

Total Solids

71.5%

SM-209F

*Information was not provided in the available references on whether this distribution was for soil excavated from the site and/or treated in the bioreactors.

Various types of debris were present in the contaminated soil and sludge excavated at the site. The debris included large stones, plastic sheeting, concrete, and railroad ties. [2]

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


Treatment System Description

Primary Treatment Technology Type

Slurry phase bioremediation


Supplemental Treatment Technology Types

Pretreatment (Solids): screening, mixing
Post-Treatment (Solids): dewatering


Slurry Phase Bioremediation System Description and Operation

The slurry phase bioremediation system used at Southeastern Wood Preserving included a power screen, a slurry mix tank, four slurry phase bioremediation reactors (bioreactors), and a slurry dewatering unit. This system, shown in Figure 2, was used to separate out the larger particles (greater than 200 mesh, or 0.0029 inches) from the stockpiled soil and sludge, and to biologically treat the remaining soil and sludge particles (less than 200 mesh).

As shown on Figure 2, soil and sludge from the stockpile were power-screened to remove debris greater than 0.5 inches such as large stones, plastic sheeting, and railroad ties. The power-screening step removed approximately 450 cubic yards of material.

Figure 2. Slurry Phase Bioremediation System Used at Southeastern Wood Preserving

Figure 2. Slurry Phase Bioremediation System Used at Southeastern Wood Preserving [6]

Soil and sludge that passed the power screening step were loaded into a slurry mix tank for soil washing. The mix tank contained three compartments:

In addition, nutrients and slurry conditioning chemicals (including a dispersant and defoaming agent) were added and mixed with the slurry in this compartment.

Materials removed by the shaker screen and hydrocyclone were stockpiled on site.

The slurry mixing/soil washing process was performed on a batch basis, with 20-30 minutes of processing time per batch.

Bioreactors [1, 2, 16, 26]

Four closed-top bioreactors were used in this application. Each bioreactor was 38 feet in diameter and 24 feet in height, and was equipped with diffusers and a blower for aeration and an impeller for mixing and keeping the slurry in suspension. Each bioreactor had an operating capacity of 180,000 gallons. The system was operated on a batch process, with each batch consisting of 160 to 180 cubic yards of material. Sixty-one batches were treated in this application, consisting of 17 batches in reactor 1, 23 batches in reactor 2, 14 batches in reactor 3, and 7 batches in reactor 4. During treatment, the slurry in the reactors was monitored daily for pH, temperature, dissolved oxygen, and other biological monitoring parameters, such as nutrient and biomass concentrations. Operating parameters and values for this application are shown in Table 3.

Excess water generated in the bioreactors was occasionally removed from the reactors. This excess water was first sampled, and, as appropriate, discharged to a POTW.

Operation [2, 9, 10]

Construction of the treatment facilities began in January 1991 and was completed in mid-April 1991. Demonstration testing began at that time and consisted of batch treatment of 700 cubic yards of soil. By late June 1991, the treatment vendor had demonstrated that the soil could be treated in the reactors to the cleanup standards set in the contract. During the demonstration tests, the vendor also evaluated the performance of a land treatment unit (LTU) for this application. However, soil applied directly to the LTU did not meet the cleanup standards within this timeframe. In order to complete the demonstration test and receive EPA authorization to proceed with the project, the vendor decided to forego applying soil directly to the LTU and treated all soil in the reactors.

Operation of the full-scale soil treatment system began in July 1991. During full-scale operation, the vendor refined the operation by adding a slurry mix tank/soil washing (desanding) operation. The vendor found that keeping sand-sized particles in suspension in the reactors was extremely difficult, and they removed the sand prior to pumping the slurry to the reactors. The sand was analyzed separately and subject to the same clean up criteria as the fine grained particles.

Soon after full-scale operation began, the vendor began to have problems meeting the clean up standards within the anticipated 30 to 35 day reactor residence time. Specifically, problems were encountered with two compounds, pyrene and phenanthrene, which both have a K001 treatment standard of 1.5 mg/kg. The vendor identified non-homogeneity in the contaminated soil stockpile as the cause. During this early period of system operation, reactor residence time was running in the 60 to 80 day range. This problem was resolved by modifying the cleanup standards to be based on total PAH concentrations (i.e., the sum of 16 specific PAHs). This was accomplished by removing the K001 treatment standards - see additional discussion under Cleanup Goals.

Progress of the bioremediation process was measured using oxygen uptake rate (OUR). When the OUR showed a significant decline, the vendor would collect samples for chemical analysis.

The vendor noted that there was a problem with foam production during bioreactor operation. Foam would overflow the bioreactors, and the vendor had trouble containing the overflow. To correct this problem, the combination of dispersant and defoamer was revised, including addition of a lignin.

The bioreactors were located outdoors, and operated year round, but were not heated. The vendor specified that during the colder winter months, much slower degradation was observed. The bioreactor temperature ranged from 15°C to 21°C during the winter months. During the spring, summer, and fall, bioreactor temperatures ranged from 25°C to 40°C.

Air Dispersion Modelling [11]

To assess emissions of volatile organic compounds (VOCs) and PAHs from the bioremediation process, the treatment vendor performed air dispersion modeling. The vendor modeled off-property ground-level VOC and PAH concentrations using the EPA Industrial Source Complex (ISC) dispersion simulation model. The results of the modeling showed that proposed activities would not result in any exceedence of accepted long-term exposure screening levels for this application.

Slurry Dewatering [9]

After treatment in the bioreactors, the slurry was transferred to a slurry dewatering unit, which was a 425-foot long, 160-foot wide, and 6-foot deep high density polyethylene (HDPE)-lined cell. The water recovery system, consisting of drain tiles in coarse sand, was sloped to a sump to collect excess water. Excess water was pumped to a 350,000-gallon water management tank and was reused for slurry preparation. Soil remaining in the slurry dewatering unit was tilled to further dry the treated material.

Treated soil and sludge were placed in a lined, capped disposal cell on site. Debris and sand were also placed in the cell.


Operating Parameters Affecting Treatment Cost or Performance

The major operating parameters affecting cost or performance for this technology and the values measured for each are shown in Table 3.

Table 3. Bioreactor Operating Parameters [1, 2, 16]

Parameter

Value

Measurement Method

Air Flow Rate (SCFM)

350 ± 100

N/A

pH

7.2  ± 1.0

N/A

Residence Time (days)

8 to 29

N/A

System Throughput (yd3 per batch)

160 to 180

N/A

No. of Batches Treated

61

N/A

Temperature (°C)

15 - 40

N/A

Biomass Concentration (cfu/ml)

107 - 108

Information not provided

Hydrocarbon Degradation

Not measured

---

Operating Volume (gallons)

180,000

N/A

Impeller Speed (RPM)

900

N/A

Solids Loading %

20

N/A

Initial Defoamer (mg/L)

200

N/A

Initial Dispersant (mg/L)

1,000

N/A

Dissolved Oxygen (mg/L)

>2.0

N/A

NH4-N (mg/L)

60 ± 20

Information not provided

PO4-P (mg/L)

10

Information not provided

N/A - Measurement method not reported for this parameter because resulting value not expected to vary among measurement methods.


Timeline

A timeline for this application is shown in Table 4.

Table 4. Timeline [1, 2]

Start Date

End Date Activity

1928

1979

Southeastern Wood Preserving operated as creosote wood treatment facility

April 1989

---

Initial samples collected from excavated materials

September 1990

---

Action memorandum signed

January 1991

April 1991

Treatment facility construction

April 1991

June 1991

Demonstration tests performed

July 1991

1994

Slurry phase bioremediation of soil and sludge performed

No additional details on the timeline for this application (e.g., for bioremediation activities) are provided in the available references.

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


Treatment System Performance

Cleanup Goals/Standards

The results of laboratory and field pilot tests and a site-specific health-based risk analysis were used to develop the following cleanup goals for this application:

Total PAHs were defined in this application as the sum of the concentrations for the 16 constituents shown in Table 7. EPA used published toxicity-equivalent factors to calculate the B(a)P-equivalent of the carcinogenic PAHs (the carcinogenic PAHs are identified in Table 7). In calculating B(a)P-equivalent concentrations, the concentration of each PAH is multiplied by a factor which is equal to its carcinogenicity relative to benzo(a)pyrene. The resulting weighted concentrations are summed to calculate the B(a)P-equivalent carcinogenic PAH value. [6, 7]

In addition, the cleanup goals allowed 15% of the treated soil to have a total PAH concentration less than 1,100 mg/kg, and 25% of the treated soil to have a B(a)P-equivalent concentration less than 230 mg/kg. [2, 6]


Additional Information on Goals

At the beginning of this application, soil was classified as RCRA hazardous waste K001. However, in February 1992, soon after full-scale operation began, an LDR treatability variance was obtained so that the soil would not need to be treated to meet the LDR treatment standards for K001. The treatability variance was obtained under 40 CFR Section 268.44, and resulted in the cleanup goals for total and carcinogenic PAHs shown above. Additional information is provided in reference 10 on the process used to obtain the variance. [10, 26]


Treatment Performance Data

Treatment performance data are available from 13 of the 61 bioreactor batches. Slurry samples were collected at the start of biotreatment and on a periodic basis during treatment. The sampling point for slurry samples is marked on Figure 2 with an “X.” No additional information on how samples were collected is provided in the available references.

Table 5 presents the initial concentrations of PAHs in the slurry, and Table 6 presents the concentrations of PAHs in the slurry after treatment had occurred. [NOTE: No information is provided in the available references to explain how specific days were selected for use in calculating treatment efficiency - e.g., how Day 10 was selected for calculating treatment efficiency for bioreactor batch R1 B5; what data were used to select this day; or why treatment continued beyond this date.] Tables 5 and 6 show the concentrations of 16 individual PAH constituents measured in each of the bioreactor batches, as well as the sum of the concentrations for all 16 PAHs and for the 7 carcinogenic PAHs, and the B(a)P-equivalent for the sum of the 16 PAHs. The average concentration of each PAH is also shown on these tables. Figures 3 through 8 show the total PAH concentrations as a function of time for the first six batches shown in Tables 5 and 6, based on data in References 2 and 24.

Table 7 presents a summary of the PAH treatment performance data for the first six batches according to the number of rings in the PAH constituent (two, three, four, or five and six ring PAHs). This table shows the cleanup goals for this application, and the average results for PAHs at the start of treatment (from Table 5) and after treatment (from Table 6). The treatment efficiency included in the table was calculated based on the reduction in concentration for these average results.

No data are provided in the available references to characterize the performance of the soil washing step.


Performance Data Assessment

For the 13 batches with available data, the average total PAH concentration was reduced from 8,545 mg/kg to 634 mg/kg, which corresponds to a treatment efficiency of 93 percent. The average B(a)P-equivalent concentration was reduced from 467 mg/kg to 152 mg/kg, or 67 percent. Carcinogenic PAHs showed a similar reduction, from 1,160 mg/kg to 374 mg/kg, or 67 percent.

Table 6 shows that 12 of the 13 bioreactor batches met the cleanup goal of 950 mg/kg for total PAHs; for the 12 batches, total PAH concentrations ranged from 421 mg/kg to 898 mg/kg. For batch R1 B7, the total PAH concentration on Day 20 was 1,126 mg/kg, exceeding the maximum cleanup goal. According to the OSC, further treatment was performed on this batch, however, additional data on treatment performance for this batch are not provided in the available references. [26]

Table 5. Concentrations of PAHs in Slurry at Start of Treatment [2, 24]

 

Bioreactor/Batch ID#

 

R1 B5

R1 B8

R1 B9**


R1 B10


R2 B9


R2 B10


R1 B4


R1 B6

R1 B7


R2 B5


R2 B6


R2 B7


R2 B8

Constituent

Concentration (mg/kg Dry Weight)

Acenaphthene

642

968

692

892

1,280

981

465

574

723

508

1,440

846

949

Acenaphthylene

34

ND
(163)

28

ND(59)

ND(223)

ND(51)

ND(155)

37.2

31.9

ND(50.5)

ND(373)

ND
(67.1)

ND(120)

Anthracene

1,050

1,560

2,140

2,280

2,340

2,330

1,540

1,720

1,620

1,580

2,870

2,020

1,490

Benzo(a)anthracenec

224

287

283

237

370

277

327

279

230

245

597

241

279

Benzo(b)fluoranthenec/ Benzo(k)fluoranthene*c

367

337

278

296

345

304

233

323

344

290

710

287

349

Benzo(ghi)perylene

21

ND
(163)

33

ND(59)

ND(223)

ND(51)

ND(155)

ND(32.7)

20.8

ND(50.5)

ND(373)

ND
(67.1)

ND(120)

Benzo(a)pyrenec

92

ND
(163)

105

100

ND(223)

98

ND(155)

98.2

87.4

81.5

ND(373)

94.7

ND(120)

Chrysenec

228

302

301

247

397

302

316

297

254

225

573

257

310

Dibenzo(ah)anthracenec

15

ND
(163)

ND(40)

ND(59)

ND(223)

ND(51)

ND(155)

ND(32.7)

14.6

ND(50.5)

ND(373)

ND
(67.1)

ND(120)

Fluoranthene

1,060

1,570

1,950

1,850

2,210

1,610

1,590

1,850

1,260

1,490

3,470

1,810

1,630

Fluorene

181

669

499

661

1,040

732

195

204

663

281

483

850

833

Indeno(1,2,3-cd)pyrenec

30

ND
(163)

40

ND(59)

ND(223)

ND(51)

ND(155)

35.4

28.2

ND(50.5)

ND(373)

ND
(67.1)

ND(120)

Naphthalene

19

ND
(163)

ND(40)

ND(59)

ND(223)

ND(51)

ND(155)

ND(32.7)

24.7

ND(50.5)

ND(373)

87.3

ND(120)

Phenanthrene

220

1,250

395

2,030

1,300

988

253

279

1,360

272

639

2,710

1,680

Pyrene

878

1,080

1,220

1,010

1,610

1,090

1,130

1,270

974

950

2,430

989

1,080

Total PAHs

5,061

8,512

8,004

9,751

11,561

8,840

6,694

7,016

7,636

6,023

14,331

10,326

8,960

Total Carcinogenic PAHs

956

1,171

1,027

939

1,447

1,032

1,109

1,049

958

892

2,440

947

1,118

Benzo(a)pyrene Equivalent

245

585

295

334

818

318

570

268

245

283

1,313

349

454

cCarcinogenic PAHs.
*Sum of b and k isomers reported.
**The vendor specified that some concentration values were estimated for this batch. However, which values were estimated was not specified.
ND - Not detected. Value in parentheses is the reported detection limit. For calculation of averages and totals, ½ the detection limit was used for values that were not detected.

Table 6. Concentrations of PAHs in Slurry After Treatment [2, 24]

 

Bioreactor/Batch ID#

 

R1 B5
Day 10

R1 B8
Day 13

R1 B9
Day 10

R1 B10
Day 10

R2 B9
Day 11

R2 B10
Day 27

R1 B4
Day 33

R1 B6
Day 11

R1 B7
Day 20

R2 B5
Day 20

R2 B6
Day 17

R2 B7
Day 13

R2 B8
Day 23

Constituent

Concentration (mg/kg Dry Weight)

Acenaphthene

ND(7)

ND(14)

ND(16)

9

ND(7)

ND(13)

ND(11.3)

ND
(6.06)

ND
(34.5)

ND
(10.3)

ND(27.3)

ND(12.3)

ND(22.7)

Acenaphthylene

11

13

ND(16)

19

14

23

12.1

6.63

ND
(34.5)

10.5

ND(27.3)

ND(12.3)

ND(22.7)

Anthracene

104

55

102

230

135

100

115

125

229

84.1

39.6

89.3

68.2

Benzo(a)anthracenec

10

ND(14)

ND(16)

20

10

16

16.5

ND
(6.06)

ND
(34.5)

12

ND(27.3)

ND(12.3)

ND(22.7)

Benzo(b)fluoranthenec/

Benzo(k)fluoranthene*c

155

240

131

254

259

213

138

95

476

149

282

166

226

Benzo(ghi)perylene

23

26

25

ND(7)

ND(7)

29

22

13.9

ND
(34.5)

18

ND(27.3)

14.8

ND(22.7)

Benzo(a)pyrenec

52

80

74

95

91

82

63.6

46

83.4

38.9

82.9

49.8

70.6

Chrysenec

24

55

30

41

33

31

57.1

31.1

69.6

18.2

61.6

33.8

57.4

Dibenzo(ah)anthracenec

10

ND(14)

ND(16)

ND(7)

ND(7)

20

ND(11.3)

ND
(6.06)

ND
(34.5)

ND
(10.3)

ND(27.3)

ND(12.3)

ND(22.7)

Fluoranthene

25

32

26

31

37

43

41.3

21

40.2

37

26

21.4

24.9

Fluorene

14

ND(14)

ND(16)

25

16

15

ND(11.3)

16.2

ND
(34.5)

ND
(10.3)

ND(27.3)

ND(12.3)

ND(22.7)

Indeno(1,2,3-cd)pyrenec

28

33

31

31

24

40

28.3

17.9

ND
(34.5)

23.6

33.1

19

30.7

Naphthalene

ND(7)

ND(14)

ND(16)

9

ND(7)

ND(13)

ND(11.3)

ND
(6.06)

ND
(34.5)

ND
(10.3)

ND(27.3)

ND(12.3)

ND(22.7)

Phenanthrene

27

14

23

79

30

31

22.3

24.6

53.9

19.9

11.3

20.7

15.9

Pyrene

25

18

30

48

46

33

40.4

11.7

36.2

29

14.7

28

17

Total PAHs

515

601

520

898

709

689

579

421

1,126

461

646

480

591

Total Carcinogenic PAHs

279

422

282

445

421

402

309

196

681

247

487

281

407

Benzo(a)pyrene Equivalent

123

144

133

146

140

211

112

74

224

84

185

249

156

cCarcinogenic PAHs.
*Sum of b and k isomers reported.
ND - Not detected. Value in parentheses is the reported detection limit. For calculation of averages and totals, ½ the detection limit was used for values that were not detected.

Table 7. Summary of PAH Treatment Performance Data [2]

Constituent

Cleanup Goal (mg/kg)

Average Concentration at Outset of Treatment*** (mg/kg)

Average Concentration After Treatment*** (mg/kg)

Treatment Efficiency (%)

Two Ring PAHs
Naphthalene

 
N/A


 48


6

 
88

Three Ring PAHs
Acenaphthene
Acenaphthylene
Anthracene
Fluorene
Phenanthrene

 
N/A
N/A
N/A
N/A
N/A

 
909
52
1,950
630
1,031

 
6
15
121
14
34

 
99
71
94
98
97

Four Ring PAHs
Benzo(a)anthracene*
Chrysene*
Fluoranthene
Pyrene

 
N/A
N/A
N/A
N/A

 
280
296
1,708
1,148

 
12
36
32
33

 
96
88
98
97

Five and Six Ring PAHs
Benzo(b)fluoranthene*
Benzo(k)fluoranthene*
Benzo(ghi)perylene
Benzo(a)pyrene*
Dibenzo(ah)anthracene*
Indeno(1,2,3-cd)pyrene*

 
N/A
N/A
N/A
N/A
N/A
N/A

 
321
**
50
98
47
53

 
209
**
18
79
9
31

 
35
**
64
19
81
42

Total PAHs

950

8,621

655

92

Carcinogenic PAHs

N/A

1,095

376

66

Benzo(a)pyrene Equivalent

180

433

150

65

*Carcinogenic PAHs.
**Combined with benzo(b)fluoranthene.
***Concentration values are averages from first six batches shown on Tables 5 and 6, and are reported as mg/kg dry weight.
N/A - Not applicable. No cleanup goal established for this constituent/group of constituents.

Figure 3. Total PAH Concentration vs. Time Bioreactor/Batch R1 B5

Figure 3. Total PAH Concentration vs. Time Bioreactor/Batch R1 B5 [2]

Figure 4. PAH Concentration vs. Time Bioreactor/Batch R1 B8

Figure 4. PAH Concentration vs. Time Bioreactor/Batch R1 B8 [2]

Figure 5. PAH Concentration vs. Time Bioreactor/Batch R1 B9

Figure 5. PAH Concentration vs. Time Bioreactor/Batch R1 B9 [2]

Figure 6. PAH Concentration vs. Time Bioreactor/Batch R1 B10

Figure 6. PAH Concentration vs. Time Bioreactor/Batch R1 B10 [2]

Figure 7. PAH Concentrations vs. Time Bioreactor/Batch R2 B9

Figure 7. PAH Concentrations vs. Time Bioreactor/Batch R2 B9 [2]

Figure 8. PAH Concentrations vs. Time Bioreactor/Batch R2 B10

Figure 8. PAH Concentrations vs. Time Bioreactor/Batch R2 B10 [2]

Nine of the 13 batches met the cleanup goal of 180 mg/kg for B(a)P-equivalent; the batches that met the cleanup goal ranged from 24 to 156 mg/kg. According to the OSC, further treatment was also performed on the four batches that did not appear to meet the cleanup goal for B(a)P (R2 B20 at 211 mg/kg; R1 B7 at 224 mg/kg; R2 B6 at 185 mg/kg; and R2 B7 at 249 mg/kg). However, additional data on treatment performance for these batches are not provided in the available references. [26]

As shown in Figures 3 through 8, the majority of the biodegradation occurred during the first 5 to 10 days of treatment, and the cleanup goal for total PAHs was met for 12 of the 13 batches within approximately 19 days of treatment.

The data in Table 7 show that the number of ring structures in the PAH constituent (two, three, four, or five and six rings) affected the treatment efficiency. The concentrations of constituents with two to four rings were reduced 71% to 99%, while five and six ring constituents were reduced 19% to 81%. These results are consistent with reports in the technical literature that show that higher molecular weight PAHs (e.g., five and six ring structures) are more difficult to biodegrade than two to four ring structures. [8]


Performance Data Completeness

Analytical data for 16 PAHs are available for 13 of the 61 batches processed through the treatment system during the course of remediation. Data are available for specific days during each batch treatment, as well as for the range of operating conditions over the course of the treatment application.


Performance Data Quality

Limited information is contained in the available references on performance data quality. A quality assurance program plan (QAPP) for this application was developed by a commercial analytical laboratory (Analytical Services Corp.). The QAPP addressed project organization and responsibilities, QA objectives, sampling procedures, sample custody, analytical procedures, and other items.

PAH slurry samples were centrifuged and extracted following SW846 Method 3540. PAH concentrations were quantified using gas chromatography with a mass spectrometer detector following SW846 Method 8270. As shown in Appendix A, detection limits for individual PAHs ranged from 5 mg/kg to 223 mg/kg for the first six batches shown in Table 5 for this application.

The vendor noted two problems related to performance data quality for this application. Problems were noted concerning implementation of the sampling plan, and for sample extraction and quantification. These problems were resolved by developing an approved sampling plan, and by performing audits on the extraction and analytical methodology.

According to the OSC, the vendor evaluated two potential methods for PAH sample extraction (soxhlet and sonic extraction) and found “significant differences” in analytical results based on method used. Based on these results, the analytical method was standardized and written into the contract. [26]

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Treatment System Cost

Procurement Process

The contract for remediation services at Southeastern Wood was competitively procured by EPA. For this procurement, EPA's Contracting Officer (CO) obtained a deviation from the EPA Acquisition Regulations which allowed a negotiated procurement without submission of technical proposals. Performance specifications were used instead of specifying a technology. Twelve bidders submitted proposals for different technologies and price was the determining factor for award. The contract was awarded to OHM Remediation Services Corporation. EPA required the vendor to perform a technology demonstration at the site to ensure that the technology would be feasible. The contract with OHM was a firm fixed price (lump sum) service contract. Additional information on the procurement process for this application is provided in Reference 4. [4]


Treatment System Cost [1, 2, 12]

Tables 8 and 9 present the costs for the slurry phase bioremediation treatment application at Southeastern Wood. In order to standardize reporting of costs across projects, costs are shown in Tables 8 and 9 according to the format for an interagency Work Breakdown Structure (WBS). The WBS specifies 9 before-treatment cost elements, 5 after-treatment cost elements, and 12 cost elements that provide a detailed breakdown of costs directly associated with treatment. Tables 8 and 9 present the cost elements exactly as they appear in the WBS, along with the specific activities as provided by the treatment vendor.

As shown in Table 8, the vendor provided actual cost data that shows a total of $2,400,000 for activities directly associated with treatment of 14,140 tons (10,500 cubic yards) of soil and sludge (i.e., excluding after-treatment cost elements). This total consists of costs for mobilization/setup, startup/testing/permits, and operation. Included in this total are costs for treatment of 61 batches at $18,700 per batch. The total costs for activities directly attributed to treatment corresponds to $170 per ton ($230 per cubic yard) of soil and sludge treated. In addition, the vendor provided cost data that show a total of $500,000 for after-treatment activities (site preparation and closure). The vendor provided no information on before-treatment activities, such as for monitoring, sampling, testing, and analysis in this application. [3, 19]

Table 10 shows actual costs provided by the vendor for slurry preparation, slurry phase biological treatment, and dewatering on a per ton of material basis. This table shows that the relatively largest costs associated with this system are for the slurry preparation process. [1]

Table 8. Treatment Activity Cost Elements According to the WBS* [3]

Cost Elements(Directly Associated With Treatment)

Cost ($)

Actual or Estimated
(A) or (E)

Mobilization/Set Up (Design Engineering)

100,000

A

Startup/Testing/Permits (Treatability and Pilot-Scale Testing)

200,000

A

Operation (short-term - up to 3 years) (soil screening and slurry preparation, slurry treatment, slurry dewatering, and project administration and support)

2,100,000

A

TOTAL TREATMENT ACTIVITY COST

2,400,000

A

Table 9. After-Treatment Cost Elements According to the WBS* [3]

Cost Elements

Cost ($) Actual or Estimated
(A) or (E)
Site Restoration (site preparation and closure)

500,000

A

TOTAL AFTER-TREATMENT COST

500,000

A

Table 10. Unit Costs for Treatment of Soil and Sludge at Southeastern Wood Preserving Superfund Site [1]

Process

Cost per Dry Ton of Material Treated ($) Actual or Estimated
(A) or (E)
Slurry Preparation

50 - 60

A

Slurry Phase Biological Treatment

40 - 55

A

Dewatering Process

20 - 30

A

Total for Slurry Phase Biological Treatment System

110 - 145

A

*Cost figures rounded up to the nearest $100,000.


Cost Data Quality

The cost data presented above are actual costs for this application as reported by the treatment vendor, and are believed to accurately represent the costs associated with this application.


Vendor Input

The vendor specified three variables that have a significant impact on the cost of remediation using this technology: the slurry phase reactor solids concentration, residence time in the reactors, and the percentage of material removed in the slurry preparation/soil washing process. According to the vendor, increasing the solids concentration in the reactors increases the amount of soil treated per batch. This results in a decrease both in the total number of batches treated and the cost per ton of treatment. In addition, longer batch residence times reduce the system throughput and, therefore, increase the cost of treatment. The higher the percentage of material that is removed by the slurry preparation/soil washing process, the lower the cost for the bioreactors, since less material will remain to be biologically treated. [3]

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Observations And Lessons Learned

Cost Observations and Lessons Learned


Performance Observations and Lessons Learned


Other Observations and Lessons Learned

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References

  1.  Jerger, D.E. and P.M. Woodhull. "Slurry-Phase Biological Treatment of Polycyclic Aromatic Hydrocarbons in Wood Preserving Wastes," For Presentation at the 87th Annual Meeting and Exhibition of the Air and Waste Management Association, Cincinnati, Ohio, June 19-24, 1994.
  2. Letter from Douglas E. Jerger, OHM Corporation, to EPA RCRA Docket, regarding Docket Number F-92-CS2-FFFFF, March 7, 1994.
  3. Woodhull, P.M. and D.E. Jerger. "Bioremediation Using a Commercial Slurry-Phase Biological Treatment System: Site-Specific Applications and Costs." Remediation. Summer 1994.
  4. USEPA OSWER/TIO. Procuring Innovative Treatment Technologies at Removal Sites: Regional Experiences and Process Improvements. 542/R-92/003. August 1992.
  5. Telephone conversation of Tim McLaughlin, Radian Corp., with Douglas Jerger, OHM Remediation Services Corp. May 24, 1995.
  6. Jerger, D.E., Erickson, S.A., and Rigger, R.D. "Full-Scale Slurry Phase Biological Treatment of Wood Preserving Wastes at a Superfund Site." Not dated.
  7. Nisbet, I.C., and P.K. Laboy, "Toxic Equivalency Factors (TEFs) for Polycyclic Aromatic Hydrocarbons (PAHs)." Regulatory Toxicology and Pharmacology, 16, 290-300. 1992.
  8. DOD Environmental Technology Transfer Committee. Remediation Technologies Screening Matrix and Reference Guide. Second Edition. Federal Remediation Technologies Roundtable. October 1994.
  9. Meeting Notes. Meeting between Tim McLaughlin, Radian, and Don Rigger, OSC, Atlanta Georgia, September 26, 1995.
  10. Memorandum from Greer C. Tidwell, Regional Administrator, to Donald J. Guinyard, Director, Waste Management Division, regarding Approval of Treatability Variance for the Southeastern Wood Treating Site. February 18, 1992.
  11. Michael Sullivan & Assoc., Inc., "Southeastern Wood Preserving Superfund Site Remediation, Canton, Mississippi, Air Dispersion Modeling." July 1991.
  12. OHM Remediation Services Corp. Amendment of Solicitation/ Modification of Contract. September 26, 1990.
  13. Correspondence from William E. Beck, Senior Project Manager, OHM Remediation Services Corp., to Don Rigger, Project Officer, EPA Region IV, regarding Confirmation of telecon regarding Invoice No. 9782-007, Southeast Wood Preserving Site, Canton, MS, OHM Project No. 9782. January 17, 1994.
  14. Memorandum from Pat Stamp, Laboratory Quality Assurance Specialist, Laboratory Evaluation & Quality Assurance Section, to Francis J. Garcia, On-Scene Coordinator, Emergency Response & Removal Branch, Waste Management Division, regarding Southeastern Wood Site, Quality Assurance Program Plan for Analytical Services Corporation Laboratory. August 6, 1993.
  15. Correspondence from David J. Cady, Senior Project Manager, OHM Remediation Services Corp., to Sharyn Erickson, Contracting Officer, USEPA, Region IV, regarding USEPA Contract No. 68-S0-4001, Requisition/Project No. WO-86007-F4, Southeastern Wood Preserving Site in Canton, Mississippi, OHM Remediation Services Corp. Project No. 9782, Request for Contract Reformation - Funding Availability. August 19, 1993.
  16. Summary of Bioremediation Batches Invoiced to Date, U.S. EPA Contract No. 68-SO-4001, Southeastern Wood Preserving Site, Canton, Mississippi, OHM Project No. 9782; Compilation Date: June 16, 1994.
  17. Correspondence from Sharyn A. Erickson, Contracting Officer, USEPA, Region IV, to Michael A. Szomjassy, V.P., S.E., Region, OHM Remediation Services Corp., regarding EPA Contract 68-SO-4001, for Southeastern Wood Preserving. April 14, 1993.
  18. Correspondence from Sharyn A. Erickson, Contracting Officer, USEPA, Region IV, to David J. Cady, OHM Remediation Services Corp., regarding Revised Price Breakdown for Southeastern Wood Preserving Contract 68-SO-4001. July 27, 1993.
  19. Correspondence from William E. Beck, Senior Project Manager, OHM Remediation Services Corp., to Sharyn Erickson, Contracting Officer, USEPA, Region IV, regarding USEPA Contract 68-SO-4001, Requisition/ Project No. WO-86007-F4, Southeastern Wood Preserving Site in Canton, Mississippi, OHM Remediation Services Corp. Project No. 9782, Revised Breakdown of Contract Price Incorporating Contract Modification No. 2. December 30, 1993.
  20. Breakdown of Contract Price. July 7, 1991.
  21. Memorandum from Patrick M. Tobin, Acting Regional Administrator, Region IV, to Richard J. Guimond, Acting Assistant Administrator, Office of Solid Waste and Emergency Response, regarding Request for a Removal Action Ceiling Increase for the Southeastern Wood Preserving Site in Canton, Madison County, Mississippi, Site ID# 1L. September 15, 1993.
  22. Information on OHM Remediation Services Corp. regarding Southeastern Wood Preserving. Not dated.
  23. Memorandum from V. Kansal, S&A Section Chief, to R. Singhvi, EPA/ERT, regarding Document Transmittal Under Work Assignment #4-699. January 6, 1993.
  24. Analytical Data. Southeastern Wood Preserving, Project 9782. Not dated.
  25. Correspondence from Sam Mabry, Director, Hazardous Waste Division, Mississippi Department of Natural Resources, to Pat Tobin, Waste Management Division, Environmental Protection Agency, Region IV, regarding analytical results from Southeastern Wood in Canton, Mississippi. October 8, 1987.
  26. Comments provided by Don Rigger, OSC, received March 8, 1996, on Draft Cost and Performance Report, Slurry Phase Bioremediation at the Southeastern Wood Preserving Superfund site, Canton, Mississippi, November 30, 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 International under EPA Contract No. 68-W3-0001 and U.S. Army Corps of Engineers Contract No. DACA45-96-D-0016.

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