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新型溴代苯酚类消毒副产物的氯化降解机制
引用本文:李欢,李正魁,李爱民,周庆,王莹,潘旸.新型溴代苯酚类消毒副产物的氯化降解机制[J].环境科学,2017,38(8):3273-3280.
作者姓名:李欢  李正魁  李爱民  周庆  王莹  潘旸
作者单位:南京大学环境学院, 污染控制与资源化研究国家重点实验室, 南京 210023,南京大学环境学院, 污染控制与资源化研究国家重点实验室, 南京 210023,南京大学环境学院, 污染控制与资源化研究国家重点实验室, 南京 210023,南京大学环境学院, 污染控制与资源化研究国家重点实验室, 南京 210023,南京大学环境学院, 污染控制与资源化研究国家重点实验室, 南京 210023,南京大学环境学院, 污染控制与资源化研究国家重点实验室, 南京 210023
基金项目:国家自然科学基金项目(51438008,51408296);江苏省自然科学基金项目(BK20140607)
摘    要:最近,13种新型极性卤代苯酚类消毒副产物在氯化消毒后的饮用水中被发现,它们按结构被分成4组,分别是二卤-4-羟基苯甲醛、二卤-4-羟基苯甲酸、二卤水杨酸和三卤苯酚.为研究它们在氯化消毒过程中的降解机制,选取了其中的4种全溴代种类,即3,5-二溴-4-羟基苯甲醛、3,5-二溴-4-羟基苯甲酸、3,5-二溴水杨酸以及2,4,6-三溴苯酚,利用UPLC/ESI-tq MS中的前体离子扫描,多反应监测和子离子扫描,鉴定了这几种消毒副产物在氯化消毒过程中的中间产物以及终产物,并根据这些中间产物和终产物与消毒时间的关系推测了其降解路径.结果表明,除了3,5-二溴水杨酸相对较稳定外,其余3种消毒副产物在氯化消毒过程中不稳定,通过取代、水解以及氧化等过程最终降解为卤乙酸等脂肪族小分子消毒副产物.在降解过程中有许多中间产物被检测并鉴定出来,其中包含一组具有五元环结构的新型消毒副产物(三卤代-羟基环戊烯二酮).

关 键 词:消毒副产物  苯酚类消毒副产物  氯化消毒  降解机制
收稿时间:2016/12/26 0:00:00
修稿时间:2017/3/8 0:00:00

New Bromated Phenolic Disinfection Byproducts: Mechanism of Their Decomposition During Chlorination
LI Huan,LI Zheng-kui,LI Ai-min,ZHOU Qing,WANG Ying and PAN Yang.New Bromated Phenolic Disinfection Byproducts: Mechanism of Their Decomposition During Chlorination[J].Chinese Journal of Environmental Science,2017,38(8):3273-3280.
Authors:LI Huan  LI Zheng-kui  LI Ai-min  ZHOU Qing  WANG Ying and PAN Yang
Affiliation:State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China,State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China,State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China,State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China,State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China and State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China
Abstract:Recently, 13 new phenolic halogenated disinfection by-products (DBPs) have been reported in chlorinated drinking water and have been classified into four groups: dihalo-4-hydroxybenzaldehydes, dihalo-4-hydroxybenzoic acid, dihalo-salicylic acids, and trihalo-phenols. In this work, the four fully brominated species (3,5-dibromo-4-hydroxybenzoic acid, 3,5-dibromosalicylic acid, 2,4,6-tribromophenol, and 3,5-dibromo-4-hydroxybenzaldehyde) were selected as representatives, and the decomposition mechanism of these new DBPs during chlorination was studied with the aid of ultra performance liquid chromatography/electrospray ionization triple-quadrupole mass spectrometry (precursor ion scan, multiple reaction monitoring, and product ion scan). Except for 3,5-dibromosalicylic acid, the new DBPs were not stable and could be finally decomposed to haloacetic acids through multistep substitution, hydrolysis, and oxidation. Various decomposition intermediate DBPs were detected, including a new group of halogenated DBPs with cyclic structures (trihalo-hydroxyl-cyclopetene-diones).
Keywords:disinfection by-products  phenolic disinfection by-products  chlorination  decomposition mechanism
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