Phototransformations of polychlorobiphenyls in Brij 58 micellar solutions

被引:58
作者
Chu, W
Jafvert, CT
Diehl, CA
Marley, K
Larson, RA
机构
[1] Purdue Univ, Sch Civil Engn, W Lafayette, IN 47907 USA
[2] Univ Illinois, Dept Nat Resources & Environm Sci, Urbana, IL 61801 USA
关键词
D O I
10.1021/es970960u
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Our purpose in conducting these studies was to examine photolysis as a destructive process for polychlorobiphenyls (PCBs) extracted from soils with surfactant solutions. Surfactants have shown promise as agents for removing free phase and sorbed contaminants from soils, yet information on ultimate disposal options and recycle/recovery strategies for the surfactants is generally lacking. For arylhalides, photodechlorination may result in decontamination, eliminating the need to physically separate these contaminants from the washing solution. Photochemical reactions of the PCB congener mixture, Aroclor 1254, and the specific congener, 2,3,4,5-tetrachlorobiphenyl (2,3,4,5-TeCB), were investigated in aqueous solutions containing surfactant micelles with UV light at 253.7 nm. Photoreduction through photodechlorination was shown to be the main decay pathway in which lesser chlorinated congeners were formed as intermediates. In experiments with 2,3,4,5-TeCB, final noncarbon-containing products included Cl- and H+, both produced nearly stoichiometrically from the starting materials. The quantum yield for decay of 0.1 mu M 2,3,4,5-TeCB in 0.5 mM Brij 58 micellar solutions was over six times greater than in water alone. Sequential extraction from a soil and photoreduction of 2,3,4,5-tetrachlorobiphenyl by Brij 58 solutions proved to be limited by surfactant loss to the soil.
引用
收藏
页码:1989 / 1993
页数:5
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