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    谢晴

    • 高级工程师    
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    • 性别:女
    • 毕业院校:大连理工大学
    • 学位:博士
    • 在职信息:在职
    • 所在单位:环境学院
    • 学科:环境工程
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    Photochemical transformation of five novel brominated flame retardants: Kinetics and photoproducts

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    论文类型:期刊论文

    第一作者:Zhang, Ya-nan

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

    合写作者:Chen, Jingwen,Xie, Qing,Li, Yingjie,Zhou, Chengzhi

    发表时间:2016-05-01

    发表刊物:CHEMOSPHERE

    收录刊物:SCIE、EI、PubMed

    卷号:150

    页面范围:453-460

    ISSN号:0045-6535

    关键字:Novel brominated flame retardants; Photolytic kinetics; Direct photolysis half-lives; Phototransformation products

    摘要:Many novel brominated flame retardants (NBFRs) are used as substitutes of polybrominated diphenyl ethers (PBDEs) in recent years. However, little is known about their phototransformation behavior, which may influence the environmental fate of these chemicals. In this study, photochemical behavior of five NBFRs, allyl-2,4,6-tribromophenyl ether (ATE), 2-bromoallyl-2,4,6-tribromophenyl ether (BATE), 2,3-dibromopropyl-2,4,6-tribromophenyl ether (DPTE), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), and 246-tris(2,4,6-tribromophenoxy)-1,3,5-triazine (TTBP-TAZ) was investigated. Results show all the five NBFRs can undergo photochemical transformation under simulated sunlight irradiation. Quantum yields (Phi) of the five NBFRs varied from 0.012 of TTBP-TAZ in hexane to 0.091 of BTBPE in methanol. Half-lives (t(1/2)) relevant with solar irradiation of these NBFRs were estimated using the determined Phi, and the values are 1.5-12.0 d in summer and 17.1-165.0 d in winter. Debrominated and ether bond cleavage products were identified in the phototransformation of DPTE and BTBPE. Debromination on the phenyl is a main phototransformation pathway for DPTE, and both debromination and ether bond cleavage are main phototransformation pathways for BTBPE. This study is helpful to better understand the photo transformation behavior of the NBFRs. (C) 2015 Elsevier Ltd. All rights reserved.