Comparative Developmental Toxicity of New Aromatic Halogenated DBPs in a Chlorinated Saline Sewage Effluent to the Marine Polychaete Platynereis dumerilii

被引:510
作者
Yang, Mengting [1 ]
Zhang, Xiangru [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Civil & Environm Engn, Environm Engn Program, Hong Kong, Hong Kong, Peoples R China
关键词
DISINFECTION BY-PRODUCTS; MAMMALIAN-CELL CYTOTOXICITY; DRINKING-WATER; TETRAHYMENA-PYRIFORMIS; NITROBENZENE TOXICITY; AQUATIC TOXICITY; WASTE-WATER; CHEMICALS; GENOTOXICITY; PHENOLS;
D O I
10.1021/es401841t
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Using seawater for toilet flushing may introduce high levels of bromide and iodide into a city's sewage treatment works, and result in the formation of brominated and iodinated disinfection byproducts (DBPs) during chlorination to disinfect sewage effluents. In a previous study, the authors' group has detected the presence of many brominated DBPs and identified five new aromatic brominated DBPs in chlorinated saline sewage effluents. The presence of brominated DBPs in chlorinated saline effluents may pose adverse implications for marine ecology. In this study, besides the detection and identification of another seven new aromatic halogenated DBPs in a chlorinated saline sewage effluent, their developmental toxicity was evaluated using the marine polychaete Platynereis dumerilii. For comparison, the developmental toxicity of some commonly known halogenated DBPs was also examined. The rank order of the developmental toxicity of 20 halogenated DBPs was 2,5-dibromohydroquinone > 2,6-diiodo-4-nitrophenol >= 2,4,6-triiodophenol > 4-bromo-2-chlorophenol >= 4-bromophenol > 2,4-dibromophenol >= 2,6-dibromo-4-nitrophenol > 2-bromo-4-chlorophenol > 2,6-dichloro-4-nitrophenol > 2,4-dichlorophenol > 2,4,6-tribromophenol > 3,3-dibromo-4-hydroxybenzaldehyde > bromoform >= 2,4,6-trichlorophenol > 2,6-dibromophenol > 2,6-dichlorophenol > iodoacetic acid >= tribromoacetic acid > bromoacetic acid > chloroacetic acid. On the basis of developmental toxicity data, a quantitative structure-activity relationship (QSAR) was established. The QSAR involved two physical-chemical property descriptors (log P and pK(a)) and two electronic descriptors (the lowest unoccupied molecular orbital energy and the highest occupied molecular orbital energy) to indicate the transport, biouptake, and biointeraction of these DBPs. It can well predict the developmental toxicity of most of the DBPs tested.
引用
收藏
页码:10868 / 10876
页数:9
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