The role of reactive oxygen species and carbonate radical in oxcarbazepine degradation via UV, UV/H2O2: Kinetics, mechanisms and toxicity evaluation

被引:111
作者
Liu, Tongcai [1 ]
Yin, Kai [1 ]
Liu, Chengbin [1 ]
Luo, Jinming [2 ,3 ]
Crittenden, John [2 ,3 ]
Zhang, Weiqiu [2 ,3 ]
Luo, Shenglian [1 ,4 ]
He, Qunying [1 ]
Deng, Yongxiu [1 ]
Liu, Hui [1 ]
Zhang, Danyu [1 ]
机构
[1] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[2] Georgia Inst Technol, Brook Byers Inst Sustainable Syst, 828 West Peachtree St, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, Sch Civil & Environm Engn, 828 West Peachtree St, Atlanta, GA 30332 USA
[4] Nanchang Hongkong Univ, Dept Environm & Chem Engn, Nanchang 330063, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxcarbazepine; Carbonate radical; Reactive oxygen species; Toxicity; Ultraviolet light hydrogen peroxide; Advanced oxidation processes; ADVANCED OXIDATION PROCESSES; SYNTHETIC HUMAN URINE; WASTE-WATER TREATMENT; SINGLET OXYGEN; TRANSFORMATION PRODUCTS; PHOTOCHEMICAL DEGRADATION; MICROCYSTIN-LR; RATE CONSTANTS; UV/CHLORINE TREATMENT; EFFICIENT REMOVAL;
D O I
10.1016/j.watres.2018.10.007
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Oxcarbazepine (OXC) is ubiquitous in the aqueous environment. And due to its ecotoxicological effects and potential risks to human, an effective way to eliminate OXC from aqueous environment has aroused public concerns in recent years. Radical-based reactions have been shown to be an efficient way for OXC destruction, but the reactions of OXC with reactive oxygen species (ROS) and carbonate radical (CO3 center dot-) are still unclear. In this study, we focused the degradation of OXC and ROS, CO3 center dot- generation mechanism, and their roles in OXC degradation via UV and UV/H2O2. The triplet state of oxcarbazepine ((OXC)-O-3*) was found to play an important role in OXC degradation via UV. And hydroxyl radicals ((OH)-O-center dot) and singlet oxygen (O-1(2)) were found to be the dominant ROS in OXC degradation. Superoxide radical (Or) did not react with OXC directly, but it may react with intermediate byproducts. Generation of CO3 center dot- played a positive role on OXC degradation for both UV and UV/H2O2. In addition to (OH)-O-center dot, (OXC)-O-3* also contribute to CO3 center dot- production. The second-order rate constants of OXC with (OH)-O-center dot and CO3 center dot- were 1.7 x 10(10) M-1 s(-1) and 8.6 x 10(7) M-1 s(-1), respectively. Potential OXC degradation mechanisms by (OH)-O-center dot were proposed and included hydroxylation, a-ketol rearrangement, and benzylic acid rearrangement. Compared with nonselective (OH)-O-center dot, the reactions involving CO3 center dot- are mainly electron transfer and hydrogen abstraction. And the acute toxicity of OXC was lower after UV/H2O2 and UV/H2O2/HCO3- treatments, which was confirmed by luminescent bacterial assay (Vibrio fischeri bacterium). (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:204 / 213
页数:10
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