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作者机构:State Key Laboratory of Pollution Control and Resource Reuse School of the Environment Nanjing University Nanjing 210093 China Jiaying University Meizhou 514015 China
出 版 物:《Journal of Environmental Sciences》 (环境科学学报(英文版))
年 卷 期:2006年第18卷第4期
页 面:771-776页
核心收录:
学科分类:083001[工学-环境科学] 0830[工学-环境科学与工程(可授工学、理学、农学学位)] 081705[工学-工业催化] 08[工学] 0817[工学-化学工程与技术]
基 金:TheNationalNaturalScienceFoundationofChina(No.20207004 50578074)andtheNationalKeyTechnologyandDevelopmentProgramofChina(No.2003BA808A17)
主 题:bisphenol A Fe(Ⅲ)-oxalate complexes photooxidation reactive oxygen species
摘 要:The aqueous photodegradation of bisphenol A (BPA) in the presence of Fe(Ⅲ)-oxalate complexes (Fe(Ⅲ)-Ox), which are common compositions of natural water, was investigated in this study. BPA underwent rapid indirect photolysis in Fe(Ⅲ)-Ox solution under simulated solar irradiation, proceeding pseudo-first-order kinetics. The photolysis rate increased with decreasing pH or initial BPA level and increasing Fe(Ⅲ)/oxalate concentration ratio. Hydroxyl radicals (·OH), which were generated from the photochemical processes of Fe(Ⅲ)-Ox complexes and contributed to the photooxidation of BPA, were determined by molecular probe and electron spin resonance (ESR) methods with the steady-state concentration of 2.56 × 10^-14 mol/L. Superoxide anion radical (O2^·-) was considered as the precursor of. OH and qualitatively determined by adding nitro blue tetrazolium as well as ESR experiments. Based on the structural analysis of the intermediate photoproducts of BPA in Fe(Ⅲ)-Ox complexes solution, the possible degradation pathways of BPA were proposed, involving ·OH addition, alkyl scission and alky oxidation. The results indicate that the photochemical reactivity of Fe(Ⅲ) may affect the environmental fate of BPA in natural water significantly.