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论文类型：期刊论文

第一作者：Xie, Qing

通讯作者：Chen, JW (reprint author), Dalian Univ Technol, Key Lab Ind Ecol & Environm Engn, Minist Educ, Sch Environm Sci & Technol, Dalian 116024, Peoples R China.

合写作者：Chen, Jingwen,Zhao, Hongxia,Wang, Xingbao,Xie, Hong-Bin

发表时间：2015-02-01

发表刊物：ENVIRONMENTAL SCIENCE-PROCESSES & IMPACTS

收录刊物：SCIE、PubMed、Scopus

卷号：17

期号：2

页面范围：351-357

ISSN号：2050-7887

摘要：Hydroxylated polyhalodiphenyl ethers (HO-PXDEs) are emerging aquatic pollutants. Previous studies have shown that HO-PXDEs can photogenerate dioxins and phenolic compounds. However, it is unclear which photochemical pathways are responsible for the various photoproducts. This study investigates the direct photolysis and photooxidation initiated by O-1(2) and (OH)-O-center dot that can be formed by photosensitization, taking 2'-HO-2,3',4,5'-tetrabromodiphenyl ether (2'-HO-BDE-68) as a case study. The results show that 1,3,8-tribromodibenzo-p-dioxin can only be produced during direct photolysis. By mass spectrum analysis, four dihydroxylated polybromodiphenyl ethers, generated from both direct and indirect photodegradation were confirmed. Among them, di-HO-tribromodiphenyl ether (di-HO-TBDE) was the main product generated from direct photohydrolysis. Most probably, the di-HO-TBDE is 2',5'-HO-2,3',4-tribromodiphenyl ether, as was suggested by density functional theory calculations. Ether bond cleavage is a dominant pathway for the direct photolysis and photooxidation reactions leading to 2,4-dibromophenol as the dominant product. The yields of the products, which are irrespective of reaction time and can be employed to compare the ability of different HO-PXDEs to photogenerate a given product, were reported. This study indicates that for accurate ecological risk assessment of HO-PXDEs, their different photodegradation pathways that may lead to different photoproducts should be considered.