Mechanism and kinetics of electrochemical degradation of isothiazolin-ones using Ti/SnO2-Sb/PbO2 anode

被引:43
作者
Han, Weiqing [1 ]
Chen, Yong [1 ]
Wang, Lianjun [1 ]
Sun, Xiuyun [1 ]
Li, Jiansheng [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Environm & Biol Engn, Nanjing 210094, Jiangsu Prov, Peoples R China
关键词
Isothiazolin-ones; Electrochemical degradation; Mechanism; Kinetics; WASTE-WATER TREATMENT; DOPED DIAMOND ELECTRODES; OXIDATION; REMOVAL; FENTON; 2-CHLOROPHENOL; POLLUTANTS; CATHODE; OXIDES;
D O I
10.1016/j.desal.2011.03.027
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This study investigated the electrochemical degradation of isothiazolin-ones in aqueous solution on a Ti/SnO2-Sb/PbO2 electrode. 1-Nitro-2-crylic-acetone, acetic acid and formic acid were the main degradation intermediates identified by tandem mass spectrometry (MS/MS) and the pathway for electrochemical degradation of isothiazolin-ones was proposed. Kinetic analyses indicated that electrochemical degradation of isothiazolin-ones was a pseudo-first-order reaction. The influences of operating parameters, such as electrolysis time, initial concentration of isothiazolin-ones, current density, initial pH and electrolyte flow rate on electrochemical degradation of isothiazolin-ones were investigated. Electrochemical degradation of isothiazolin-ones as well as CODcr (chemical oxygen demand determined by potassium dichromate) was controlled by mass transport. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:82 / 88
页数:7
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