Biodegradation of UV-irradiated polychlorinated biphenyls in surfactant micelles
Potential enhancement of biodegradability of commercial polychlorinated biphenyls (PCBs) mediated by photodechlorination was investigated. Used in tandem, photolysis and biodegradation of Aroclor 1242 (MW≈260), a commercial PCB mixture, dissolved in micellar solution of a nonionic surfactant, polyox...
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Published in | Water Science & Technology Vol. 38; no. 7; pp. 25 - 32 |
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Main Authors | , , , , , , |
Format | Journal Article Conference Proceeding |
Language | English |
Published |
New York NY
Elsevier Ltd
1998
Oxford Pergamon Press IWA Publishing |
Subjects | |
Online Access | Get full text |
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Summary: | Potential enhancement of biodegradability of commercial polychlorinated biphenyls (PCBs) mediated by photodechlorination was investigated. Used in tandem, photolysis and biodegradation of Aroclor 1242 (MW≈260), a commercial PCB mixture, dissolved in micellar solution of a nonionic surfactant, polyoxyethylene 10 lauryl ether (POL(10)), was studied. A mixed population of two genetically engineered microorganisms (GEMs), Pseudomonas putida IPL5∷TnPCB and Ralstonia eutropha B30P4∷TnPCB, was used for the aerobic biodegradation of POL (10) while cometabolizing Aroclor 1242. UV-irradiation at 254 nm for 40 minutes caused 63% degradation of Aroclor 1242 in a solution containing 210 mg/L of PCB congeners in 4 g/L POL(10). In the same period, 42% of the PCB chlorine appeared as chloride in solution. Gas chromatograms of UV-irradiated Aroclor 1242 solutions indicated that almost all biorecalcitrant PCB congeners, especially the highly chlorinated ones, were photolyzed. PCB GEMs removed an additional 30 mg/L (14.3%) of the PCBs in 96 hr from the UV-irradiated micellar PCB solution. Seemingly, the products of photolysis did not inhibit biodegradation of the remaining congeners or the surfactant. |
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Bibliography: | SourceType-Books-1 ObjectType-Book-1 content type line 25 ObjectType-Conference-2 SourceType-Conference Papers & Proceedings-2 |
ISBN: | 0080433944 9780080433943 |
ISSN: | 0273-1223 1996-9732 |
DOI: | 10.1016/S0273-1223(98)00603-9 |