Application of polycolloid-releasing substrate to remediate trichloroethylene-contaminated groundwater: A pilot-scale study

Journal of Hazardous Materials

Volumn 268, Issue , 2014, Pages 92-101

  Tsai, T T ^a   Liu, J K ^a   Chang, Y M ^b   Chen, K F ^c   Kao, C M ^a  

^a NATIONAL SUN YAT SEN UNIVERSITY   (Taiwan)

^b NATIONAL TAIPEI UNIVERSITY OF TECHNOLOGY   (Taiwan)

^c NATIONAL CHI NAN UNIVERSITY   (Taiwan)

Author keywords

Anaerobic bioremediation; Groundwater contamination; Real time polymerase chain reaction (PCR); Reductive dechlorination; Slow polycolloid releasing substrate

Indexed keywords

ANAEROBIC BIOREMEDIATION; CONTAMINATED GROUNDWATER; DEHALOCOCCOIDES SPP; GROUNDWATER CONTAMINATION; MICROBIAL ANALYSIS; REAL-TIME POLYMERASE CHAIN REACTION; REDUCTIVE DECHLORINATION; TOTAL ORGANIC CARBON;

ANESTHETICS; BIODEGRADATION; BIOREMEDIATION; BIOTECHNOLOGY; BYPRODUCTS; DECHLORINATION; DNA SEQUENCES; GENES; GROUNDWATER; INJECTION (OIL WELLS); TRICHLOROETHYLENE; VEGETABLE OILS;

POLYMERASE CHAIN REACTION;

GROUND WATER; TRICHLOROETHYLENE;

BIODEGRADATION; BIOREMEDIATION; COLLOID; CONCENTRATION (COMPOSITION); DECHLORINATION; DNA; GROUNDWATER POLLUTION; MICROBIAL ACTIVITY; POLYMERASE CHAIN REACTION; SAMPLING; SUBSTRATE; WATER MANAGEMENT; WATER POLLUTION; WATER QUALITY;

ARTICLE; BIODEGRADATION; BIOREMEDIATION; CONTROLLED STUDY; DECHLORINATION; DEHALOCOCCOIDES; DNA EXTRACTION; DNA SEQUENCE; GENETIC ANALYSIS; MICROBIAL DIVERSITY; NONHUMAN; NUCLEOTIDE SEQUENCE; PILOT STUDY; REAL TIME POLYMERASE CHAIN REACTION; TOTAL ORGANIC CARBON; WATER CONTAMINATION;

ANAEROBIC BIOREMEDIATION; GROUNDWATER CONTAMINATION; REAL-TIME POLYMERASE CHAIN REACTION (PCR); REDUCTIVE DECHLORINATION; SLOW POLYCOLLOID-RELEASING SUBSTRATE;

BIODEGRADATION, ENVIRONMENTAL; CHLOROFLEXI; COLLOIDS; DNA, BACTERIAL; GROUNDWATER; PILOT PROJECTS; RNA, RIBOSOMAL, 16S; TAIWAN; TRICHLOROETHYLENE; WATER MICROBIOLOGY; WATER POLLUTANTS, CHEMICAL; WATER PURIFICATION;

EID: 84892900114     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2014.01.004     Document Type: Article

References (65)

1. Interstate Technology Regulatory Council (ITRC) Technical and Regulatory Guidance for In Situ Chemical Oxidation of Contaminated Soil and Groundwater 2005, Interstate Technology and Regulatory Council, Washington, DC.
2. Scheutz C., Durant N.D., Hansen M.H., Bjerg P.L. Natural and enhanced anaerobic degradation of 1,1,1-trichloroethane and its degradation products in the subsurface - a critical review. Water Res. 2011, 45:2701-2723.
3. Adamson D.A., Lyon D.Y., Hughes J.B. Flux and product distribution during biological treatment of tetrachloroethene dense non-aqueous-phase liquid. Environ. Sci. Technol. 2004, 38:2021-2028.
4. U.S.Environmental Protection Agency CERCLIS Database 2005, United States Environmental Protection Agency, Washington, DC. http://cfpub.epa.gov/supercpad/cursites/srchsites.cfmS.
5. Tsai T.T., Kao C.M., Hong A., Liang S.H., Chien H.Y. Remediation of TCE-contaminated aquifer by an in situ three-stage treatment train system. Colloids Surf. A 2008, 322(1-3):130-137.
6. Long C.M., Borden R.C. Enhanced reductive dechlorination in columns treated with edible oil emulsion. J. Contam. Hydrol. 2006, 87:54-72.
7. Yu S., Semprini L. Enhanced reductive dechlorination of PCE DNAPL with TBOS as a slow-release electron donor. J. Hazard. Mater. 2009, 167:97-104.
8. Pant P., Pant S. A review: advances in microbial remediation of trichloroethylene (TCE). J. Environ. Sci. 2010, 22:116-126.
9. Duhamel M., Mo K., Edwards E.A. Characterization of a highly enriched Dehalococcoides-containing culture that grows on vinyl chloride and trichloroethene. Appl. Environ. Microbiol. 2004, 70:5538-5545.
10. Da Silva M.L.B., Daprato R.C., Gomez D.E., Hughes J.B., Ward C.H., Alvarez P.J.J. Comparison of bioaugmentation and biostimulation for the enhancement of dense nonaqueous phase liquid source zone bioremediation. Water Environ. Res. 2006, 78:2456-2465.
11. Cupples A.M., Spormann A.M., McCarty P.L. Vinyl chloride and cis-dichloroethene dechlorination kinetics and microorganism growth under substrate limiting conditions. Environ. Sci. Technol. 2004, 38(4):1102-1107.
12. Fletcher G.C., Youssef J.F., Gupta S. Research issues in inactivation of Listeria monocytogenes associated with New Zealand greenshell mussel meat (Perna canaliculus) using high pressure processing. J. Aquat. Food Prod. Technol. 2008, 17:173-194.
13. Futamata H., Harayama S., Hiraishi A., Watanabe K. Functional and structural analyses of trichloroethylene-degrading bacterial communities under different phenol-feeding conditions: laboratory experiments. Appl. Microbiol. Biotechnol. 2003, 60:594-600.
14. Friis A.K., Heimann A.C., Jakobsen R., Albrechtsen H.J., Cox E., Bjerg P.L. Temperature dependence of anaerobic TCE-dechlorination in a highly enriched Dehalococcoides-containing culture. Water Res. 2007, 41:355-364.
15. He J., Ritalahti K.M., Aiello M.R., Loffler F.E. Complete detoxification of vinyl chloride (VC) by an anaerobic enrichment culture and identification of the reductively dechlorinating population as a Dehalococcoides population. Appl. Environ. Microbiol. 2003, 69:996-1003.
16. Harkness M.R., Farnum R. How slow is slow in slow release? Remediation of chlorinated and recalcitrant compounds. The Fourth International Conference 2004, 24-27.
17. Jin H.H., Nakajima-Kambe T., Akutsu-Shigeno Y., Nakashima M., Shigeno T., Nomura N., Uchiyama H. Isolation and characterization of bacteria that degrade poly(lactic acid-glycerol ester)-type time-release electron donors for accelerated biological reductive dechlorination. Macromol. Symp. 2005, 224:155-165.
18. He J.Z., Holmes V.F., Lee P.K.H., Alvarez-Cohen L. Influence of vitamin B-12 and cocultures on the growth of Dehalococcoides isolates in defined medium. Appl. Environ. Microbiol. 2007, 73:2847-2853.
19. Hendrickson E.R., Payne J.A., Young R.M., Starr M.G., Perry M.P., Fahnestock S., Ellis D.E., Ebersole R.C. Molecular analysis of Dehalococcoides 16S ribosomal DNA from chloroethene-contaminated sites throughout North America and Europe. Appl. Environ. Microbiol. 2002, 68:485-495.
20. Pfeiffer P., Bielefeldt A.R., Illangasekare T., Henry B. Physical properties of vegetable oil and chlorinated ethene mixtures. J. Environ. Eng. 2005, 131:1447-1452.
21. Bedard D.L., Ritalahti K.A., Löffler F.E. The Dehalococcoides population in sediment-free mixed cultures metabolically dechlorinates the commercial polychlorinated biphenyl mixture Aroclor 1260. Appl. Environ. Microbiol. 2007, 73:2513-2521.
22. Cupples A.M. Real-time PCR quantification of Dehalococcoides populations: methods and applications. J. Microbiol. Methods 2008, 72:1-11.
23. Lindow N.L., Borden R.C. Anaerobic bioremediation of acid mine drainage using emulsified soybean oil. Mine Water Environ. 2005, 24:199-208.
24. Pfeiffer P., Bielefeldt A.R., Illangasekare T., Henry B. Partitioning of dissolved chlorinated ethenes into vegetable oil. Water Res. 2005, 39:4521-4527.
25. Borden R.C. Concurrent bioremediation of perchlorate and 1,1,1-trichloroethane in an emulsified oil barrier. J. Contam. Hydrol. 2007, 94(1-2):13-33.
26. Coulibaly K.M., Borden R.C. Impact of edible oil injection on the permeability of aquifer sands. J. Contam. Hydrol. 2004, 71(1-4):219-237.
27. Bennett P., Gandhi D., Warner S., Bussey J. In situ reductive dechlorination of chlorinated ethenes in high nitrate groundwater. J. Hazard. Mater. 2007, 149:568-573.
28. Liang S.H., Kuo Y.C., Chen S.H., Chen C.Y., Kao C.M. Development of a slow polycolloid-releasing substrate (SPRS) biobarrier to remediate TCE-contaminated aquifers. J. Hazard. Mater. 2013, 254-255:107-115.
29. Jiang H., Chen Y., Jiang P., Zhang C., Smith T.J., Murrell C.J., Xing X.H. Methanotrophs: multifunctional bacteria with promising applications in environmental bioengineering. Biochem. Eng. J. 2010, 49:277-288.
30. Kao C.M., Chen C.Y., Chen S.C., Chen Y.L. Application of in situ biosparging to remediate a petroleum-hydrocarbon spill site: field and microbial evaluation. Chemosphere 2008, 70(8):1492-1499.
31. Kao C.M., Chen C.S., Tsai F.Y., Yang K.H., Chien C.C., Liang S.H., Yang C.A., Chen S.C. Application of real-time PCR, DGGE fingerprinting, and culture-based method to evaluate the effectiveness of intrinsic bioremediation on the control of petroleum-hydrocarbon plume. J. Hazard. Mater. 2010, 178(1-3):409-416.
32. Wong M.L., Medrano J.F. Real-time PCR for mRNA quantitation. Biotechniques 2005, 39:75-85.
33. Von Felten A., Défago G., Maurhofer M. Quantification of Pseudomonas fluorescens strains F113, CHA0 and Pf153 in the rhizosphere of maize by strain-specific real-time PCR unaffected by the variability of DNA extraction efficiency. J. Microbiol. Methods 2010, 81:108-115.
34. Pascual J., Macian M.C., Arahal D.R., Garay E., Pujalte M.J. Multilocus sequence analysis of the central clade of the genus Vibrio by using the 16S rRNA, recA, pyrH, rpoD, gyrB, rctB and toxR genes. Int. J. Syst. Evol. Microbiol. 2009, 60:154-165.
35. Thompson C.C., Thompson F.L., Vicente A.C.P. Identification of Vibrio cholerae and Vibrio mimicus by multilocus sequence analysis (MLSA). Int. J. Syst. Evol. Microbiol. 2008, 58:617-621.
36. Savazzini F., Longa C.M.O., Pertot I., Gessler C. Real-time PCR for detection and quantification of the biocontrol agent Trichoderma atroviride strain SC1 in soil. J. Microbiol. Methods 2008, 73:185-194.
37. Holmberg A.-I.J., Melin P., Levenfors J.P., Sundh I. Development and evaluation of SCAR markers for a Pseudomonas brassicacearum strain used in biological control of snow mould. Biol. Control 2009, 48:181-187.
38. Aulenta F., Fuoco M., Canosa A., Papini M.P., Majone M. Use of poly-beta-hydroxy-butyrate as a slow-release electron donor for the microbial reductive dechlorination of TCE. Water Sci. Technol. 2008, 57(6):921-925.
39. Révész S., Sipos R., Kende A., Rikker T., Romsics C., Mészáros É., Mohr A., Táncsics A., Márialigeti K. Bacterial community changes in TCE biodegradation detected in microcosm experiments. Int. Biodeterior. Biodegrad. 2006, 58:239-247.
40. Jang W., Aral M.M. Effect of biotransformation on multispecies plume evolution and natural attenuation. Transp. Porous Med. 2008, 72:207-226.
41. Lee I.S., Bae J.H., McCarty P.L. Comparison between acetate and hydrogen as electron donors and implications for the reductive dehalogenation of PCE and TCE. J. Contam. Hydrol. 2007, 94:76-85.
42. Ritalahti K.M., Amos B.K., Sung Y., Wu Q.Z., Koenigsberg S.S., Löffler F.E. Quantitative PCR targeting 16S rRNA and reductive dehalogenase genes simultaneously monitors multiple Dehalococcoides strains. Appl. Environ. Microbiol. 2006, 72:2765-2774.
43. Holmes V.F., He J., He J., Lee P.K.H., Alvarez-Cohen L. Discrimination of multiple Dehalococcoides strains in a trichloroethene enrichment by quantification of their reductive dehalogenase genes. Appl. Environ. Microbiol. 2006, 72:5877-5883.
44. Kuo Y.C. Application of in situ emulsified biobarrier to remediate chlorinated-solvent contaminated groundwater, Ph.D. Dissertation 2012, National Sun Yat-Sen University, Kaohsiung, Taiwan.
45. American Public Health Association (APHA) Standard Methods for the Examination of Water and Wastewater 2005, APHA-AWWA-WEF, Washington, DC. 22nd ed.
46. Magnuson J.K., Romine M.F., Burris D.R., Kingsley M.T. Trichloroethene reductive dehalogenase from Dehalococcoides ethenogenes: sequence of tceA and substrate range characterization. Appl. Environ. Microbiol. 2000, 66:5141-5147.
47. Lee M.H., Clingenpeel S.C., Leiser O.P., Wymore R.A., Sorenson K.S., Watwood M.E. Activity-dependent labeling of oxygenase enzymes in a trichloroethene-contaminated groundwater site. Environ. Pollut. 2008, 153:238-246.
48. Nubel U., Engelen B., Felske A., Snaidr J., Wieshuber A., Amann R.I., Ludwig W., Backhaus H. Sequence heterogeneities of genes encoding 16S rRNAs in Paenibacillus polymyxa detected by temperature gradient gel electrophoresis. J. Bacteriol. 1996, 178:5636-5643.
49. Baldwin B.R., Nakatsu C.H., Nies L. Detection and enumeration of aromatic oxygenase genes by multiplex and real-time PCR. Appl. Environ. Microbiol. 2003, 69:3350-3358.
50. Yanru Y., Manuel P., William S., Josef Z. Identification of microorganisms involved in reductive dehalogenation of chlorinated ethenes in an anaerobic microbial community. Water Res. 2005, 39:3954-3966.
51. Sigler W.V., Zeyer J. Microbial diversity and activity along the forefields of two receding glaciers. Microb. Ecol. 2002, 43:397-407.
52. Lu X., Wilson J.T., Kampbell D.H. Comparison of an assay for Dehalococcoides DNA and a microcosm study in predicting reductive dechlorination of chlorinated ethenes in the field. Environ. Pollut. 2009, 157:809-815.
53. Takami H., Masui N., Nakasone K., Horikoshi K. Replication origin region of the chromosome of alkaliphilic Bacillus halodurans C-125. Biosci. Biotechnol. Biochem. 1999, 63:1134-1137.
54. Tsai T.T., Kao C.M., Surampalli R.Y., Weng C.H. Enhanced bioremediation of fuel-oil contaminated soils: a laboratory feasibility study. J. Environ. Eng. 2009, 135(9):845-853.
55. Mera N., Iwasaki K. Use of plate-wash samples to monitor the fates of culturable bacteria in mercury- and trichloroethylene-contaminated soils. Appl. Microbiol. Biotechnol. 2007, 77:437-445.
56. Chang Y.C., Okeke B.C., Hatsu M., Takamizawa K. In vitro dehalogenation of tetrachloroethylene (PCE) by cell-free extracts of Clostridium bifermentans DPH-1. Bioresour. Technol. 2001, 78:141-147.
57. Fries M.R., Forney L.J., Tiedje J.M. Phenol- and toluene-degrading microbial populations from an aquifer in which successful trichloroethene cometabolism occurred. Appl. Environ. Microbiol. 1997, 63:1523-1530.
58. Coleman N.V., Mattes T.E., Gossett J.M., Spain J.C. Phylogenetic and kinetic diversity of aerobic vinyl chloride-assimilating bacteria from contaminated sites. Appl. Environ. Microbiol. 2002, 68:6162-6171.
59. Watanabe K., Teramoto M., Harayama S. Stable augmentation of activated sludge with foreign catabolic genes harboured by an indigenous dominant bacterium. Environ. Microbiol. 2002, 4:577-583.
60. Lonergan D.J., Jenter H.L., Coates J.D., Phillips E.J.P., Schmidt T.M., Lovley D.R. Phylogenetic analysis of dissimilatory Fe(III)-reducing bacteria. J. Bacteriol. 1996, 178:2402-2408.
61. 2 as photocatalyst: a feasibility study in museum and nursing institutions. J. Environ. Eng. 2011, 137:163-170.
62. Shin H.Y., Singhal N., Park J.W. Regeneration of iron for trichloroethylene reduction by Shewanella alga BrY. Chemosphere 2007, 68:1129-1134.
63. Neumann A., Wohlfarth G., Diekert G. Purification and characterization of tetrachloroethene reductive dehalogenase from Dehalospirillum multivorans. J. Biol. Chem. 1996, 271:16515-16519.
64. Hörber C., Christensen N., Arvin E., Kiær Ahring B. Tetrachloroethene dechlorination kinetics by Dehalospirillum multivorans immobilized in upflow anaerobic sludge blanket reactors. Appl. Microbiol. Biotechnol. 1999, 51:694-699.
65. Ishida H., Nakamura K. Trichloroethylene degradation by Ralstonia sp. KN1-10A constitutively expressing phenol hydroxylase: transformation products, NADH limitation, and product toxicity. J. Biosci. Bioeng. 2000, 89:438-445.