Accelerated photo-transformation of 2,2′,4,4′,5,5′-hexachlorobiphenyl (PCB 153) in water by dissolved organic matter

被引:11
作者
Chen, Lei [1 ]
Shen, Chaofeng [1 ,2 ]
Zhou, Minmin [1 ]
Tang, Xianjin [1 ]
Chen, Yingxu [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Environm & Resource Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Acad Water Sci & Environm Engn, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Photolysis; Polychlorinated biphenyls (PCBs); Dissolved organic matter (DOM); Reactive species; Intra-DOM; Photosensitizer; SINGLET OXYGEN; PHOTOSENSITIZED DEGRADATION; PHOTOCHEMICAL FORMATION; HYDRATED ELECTRONS; AROCLOR; 1254; PHOTODEGRADATION; LIGHT; CONSTITUENTS; IRRADIATION; CHEMISTRY;
D O I
10.1007/s11356-012-1112-9
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The ubiquitous dissolved organic matter (DOM) has an important influence on transformation of organic contaminants through the production of reactive substances, such as (OH)-O-aEuro cent, O-1(2), and (DOM)-D-3*. The photolysis of a higher chlorinated polychlorinated biphenyl (PCB) congener (2,2',4,4',5,5'-hexachlorobiphenyl, PCB 153) under simulated sunlight in presence of humic acid (HA) was investigated. Degradation of PCB 153 was accelerated significantly by the addition of HA, with a rate constant of 0.0214, 0.0413, and 0.0358 h(-1) in the initial 18 h of irradiation in presence of 1, 5, and 20 mg/L HA, respectively. The main photodegradation products analyzed by gas chromatography mass spectrometry were 4-hydroxy-2,2',4',5,5'-pentaCB and 2,4,5-trichlorobenzoic acid. Main reactive species involved were determined by the electron spin-resonance spectroscopy, including O-1(2) and (OH)-O-aEuro cent. Special scavengers were added to elucidate the photolysis mechanisms. By using the specific scavengers, it turned out that (OH)-O-aEuro cent accounted for 29.3 % of the degradation, and the intra-DOM reactive species (O-1(2), (OH)-O-aEuro cent, and (DOM)-D-3*) accounted for 59.6 % of the degradation. Photo-transformation sensitized by DOM, which involves both aqueous and intra-DOM reactions of PCBs with reactive species, may be one of the most important mechanisms for natural attenuation of PCBs.
引用
收藏
页码:1842 / 1848
页数:7
相关论文
共 38 条
[1]   Effect of light on humic substances: Production of reactive species [J].
Aguer, JP ;
Richard, C ;
Andreux, F .
ANALUSIS, 1999, 27 (05) :387-390
[2]  
Bedard DL, 2003, DEHALOGENATION: MICROBIAL PROCESSES AND ENVIRONMENTAL APPLICATIONS, P443
[3]  
Boule P., 1999, BARCELO DAMIA KOSTIA, P204
[4]   CRITICAL-REVIEW OF RATE CONSTANTS FOR REACTIONS OF HYDRATED ELECTRONS, HYDROGEN-ATOMS AND HYDROXYL RADICALS (.OH/.O-) IN AQUEOUS-SOLUTION [J].
BUXTON, GV ;
GREENSTOCK, CL ;
HELMAN, WP ;
ROSS, AB .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1988, 17 (02) :513-886
[5]   Photosensitized degradation of 2,4′,5-trichlorobiphenyl (PCB 31) by dissolved organic matter [J].
Chen, Lei ;
Tang, Xianjin ;
Shen, Chaofeng ;
Chen, Chen ;
Chen, Yingxu .
JOURNAL OF HAZARDOUS MATERIALS, 2012, 201 :1-6
[6]   Study on adverse impact of e-waste disassembly on surface sediment in East China by chemical analysis and bioassays [J].
Chen, Lei ;
Yu, Chunna ;
Shen, Chaofeng ;
Zhang, Congkai ;
Liu, Lei ;
Shen, Kaili ;
Tang, Xianjin ;
Chen, Yingxu .
JOURNAL OF SOILS AND SEDIMENTS, 2010, 10 (03) :359-367
[7]   Indirect Photodegradation of Amine Drugs in Aqueous Solution under Simulated Sunlight [J].
Chen, Yong ;
Hu, Chun ;
Hu, Xuexiang ;
Qu, Jiuhui .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (08) :2760-2765
[8]   Photosensitized degradation of bisphenol a by dissolved organic matter [J].
Chin, YP ;
Miller, PL ;
Zeng, LK ;
Cawley, K ;
Weavers, LK .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (22) :5888-5894
[9]   Quantifying Interactions between Singlet Oxygen and Aquatic Fulvic Acids [J].
Cory, Rose M. ;
Cotner, James B. ;
McNeill, Kristopher .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (03) :718-723
[10]   THE PHOTOCHEMICAL GENERATION OF HYDROGEN-PEROXIDE IN NATURAL-WATERS [J].
DRAPER, WM ;
CROSBY, DG .
ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1983, 12 (01) :121-126