Degradation characteristic of 4-bromdiphenyl ether in mixed solutions by electron beam irradiation

The degradation characteristic of 4-bromdiphenyl ether (BDE-4) was investigated in different solutions.The study indicates that the process of direct degradation of this compound is dependent upon the bromine and the ether bond connected to diphenyl by electron beam.laser flash photolysis was employ...

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Published inJournal of Shanghai University Vol. 14; no. 2; pp. 89 - 93
Main Author 施文彦 焦正 顾建忠 郭瑞云 吴文静 徐刚 胡谷雨 雷建求 吴明红
Format Journal Article
LanguageEnglish
Published Heidelberg Shanghai University Press 01.04.2010
School of Environmental and Chemical Engineering,Shanghai University,Shanghai 200444,P.R.China%Shanghai Institute of Optics and Fine Mechanics,Chinese Academy of Sciences,Shanghai 201800,P.R.China
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ISSN1007-6417
1863-236X
DOI10.1007/s11741-010-0203-3

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Summary:The degradation characteristic of 4-bromdiphenyl ether (BDE-4) was investigated in different solutions.The study indicates that the process of direct degradation of this compound is dependent upon the bromine and the ether bond connected to diphenyl by electron beam.laser flash photolysis was employed to determine the degradation of each species (cationic,neutral,and anionic).From these data,intermediate products of BDE-4 degradation were shown for direct irradiationdegradation.The neutral radical was formed during the photolysis of these compounds.For all the compounds,diphenyl ether and hydroxybiphenyl were observed as common products.Reaction of the BDE-4 under electron beam was debromide.The debromide rate of BDE-4 at pH=5.5 is somewhat lower than that of BDE-4 at pH=10.0.The decomposition rate for BDE-4 is 99.8% at pH=10.0 on the dose of 14 kGy.BDE-4 from its radical could provide bromine ion into water and the cation radical of BDE-4 formed quickly recombine with hydrogen radical and formed phenyl ether.
Bibliography:TQ325.12
31-1735/N
TQ243.24
4-bromdiphenyl ether (BDE-4), laser flash photolysis, electron beam (EB), transient absorption
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ISSN:1007-6417
1863-236X
DOI:10.1007/s11741-010-0203-3