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双酚A在河口水中的光解动力学
引用本文:房岐,徐子豪,刘宁彧,赵群,田森林,李英杰.双酚A在河口水中的光解动力学[J].中国环境科学,2020,40(4):1659-1666.
作者姓名:房岐  徐子豪  刘宁彧  赵群  田森林  李英杰
作者单位:昆明理工大学环境科学与工程学院, 云南 昆明 650500
基金项目:国家自然科学基金资助项目(21707058);云南省优秀青年基金资助项目(2019FI004);昆明理工大学引进高层次人才学科建设经费资助项目(1411909411)
摘    要:为研究双酚A(BPA)在河口水中的光解动力学及水中重要溶解性组分对其光解的影响,在广西钦州大榄江连接茅尾海的河口水域采取水样,通过模拟日光实验研究了河口水中BPA的光解动力学,及河口水中的重要溶解性组分Cl-,Br-,溶解性有机质(DOM),NO3-和HCO3-对BPA光解的影响.结果表明,河口水中BPA的光解速率常数k值比纯水中大,且上游水样中BPA的k值是下游水样的2.5倍.稳态光解实验表明DOM及其与卤素离子作用显著影响BPA的光解,虽然NO3-也影响BPA光解,但与DOM共存时,NO3-的影响不明显.自由基淬灭和竞争反应动力学实验发现激发三重态DOM(3DOM*)和卤素自由基(HRS)是决定河口水样中BPA光降解的主要活性物种,且3DOM*与BPA的反应活性(二级反应速率常数k3DOM*,BPA=4.42×108L/(mol·s)要高于HRS与BPA的反应活性(kBPA,Cl·=2.11×108L/(mol·s),kBPA,Cl2·-=8.5×106L/(mol·s).下游水样中高含量的卤素离子(292mmol/L)易淬灭3DOM*产生反应活性较低的HRS,致使下游水体中BPA的光解速率低于上游水体.

关 键 词:双酚A  河口水  光解动力学  激发三重态溶解性有机质  卤素自由基  二级反应速率常数  
收稿时间:2019-09-19

Photodegradation kinetics of bisphenol A in estuarine water
FANG Qi,XU Zi-hao,LIU Ning-yu,ZHAO Qun,TIAN Sen-lin,LI Ying-jie.Photodegradation kinetics of bisphenol A in estuarine water[J].China Environmental Science,2020,40(4):1659-1666.
Authors:FANG Qi  XU Zi-hao  LIU Ning-yu  ZHAO Qun  TIAN Sen-lin  LI Ying-jie
Institution:Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming 650500, China
Abstract:To study the photodegradation kinetics of bisphenol A (BPA) and the photolysis effect of the main water components in estuarine water, the real water sample was collected in the estuarine waters connecting the Maowei Sea and the Dalan River in Qinzhou city, China. The photodegradation kinetics of BPA in estuarine water sample and the effects of Cl-, Br-, dissolved organic matter (DOM), NO3-, HCO3-, and ionic strength on the photolysis of BPA were studied by simulated sunlight experiment. The results showed that the photolysis rate constant (k) value of BPA in estuarine water was higher than that in pure water, and the k value of BPA in the upstream water sample was 2.5 times as compared to the downstream water sample. Steady-state photolysis experiments showed that DOM and its interaction with halogen ions significantly affect the photolysis of BPA. Although NO3- also affected the photodegradation kinetics of BPA, the effect of NO3- was not obvious when it was concomitant with DOM. Radical quenching and competitive reaction kinetics experiments found that the triplet-excited state DOM (3DOM*) and halogen radicals (HRS) are the main reactive species that dominate the photodegradation of BPA in estuarine water samples. Moreover, the reactivity of 3DOM* with BPA (second-order reaction rate constant, k3DOM*,BPA=4.42×108L/(mol·s) was higher than that of HRS with BPA (kBPA,Cl·=2.11×108L/(mol·s),kBPA,Cl2·-=8.5×106L/(mol·s). The relatively high concentrations of halide ions (292mmol/L) in downstream water samples can easily quench 3DOM* to generate HRS with relatively low reactivity towards BPA,which can explain the phenomenon that the photolysis rate constant of BPA in the downstream water sample was lower than that of the upstream water sample.
Keywords:bisphenol A  estuarine water  photodegradation kinetics  triplet-excited state dissolved organic matter  halogen radicals  second-order reaction rate constant  
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