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含乐果废水的循环电-Fenton氧化过程及其影响因素
引用本文:吴进华,李小明,曾光明,杨麒,黄昱,易婷.含乐果废水的循环电-Fenton氧化过程及其影响因素[J].环境科学学报,2008,28(8):1534-1541.
作者姓名:吴进华  李小明  曾光明  杨麒  黄昱  易婷
作者单位:湖南大学环境科学与工程学院,长沙,410082
基金项目:国际科技合作重点项目 , 新世纪优秀人才支持计划资助
摘    要:为克服传统Fenton(Conventional Fenton,简称CF)法中存在着Fe2 在反应初始时即被氧化且反应过程中产生大量铁泥(Fe的复杂络合物)的不足,研究了循环电-Fenton(Circulating Electro Fenton,简称CEF-FeRe)法氧化降解自配乐果废水的过程及其各影响因子的作用机制.CEF-FeRe反应所需的H2O2通过蠕动泵缓慢加入到电解池中,而被氧化了的Fe2 又在阴极被还原,使得Fenton反应能持续进行.在乐果浓度为200mg·L-1时,通过多个单因素试验确定最佳CEF-FeRe反应条件为:常温、pH值为3.0、H2O2/Fe2 的摩尔比为10、H2O2的加入量为理论剂量、恒流0.5A.结果表明,在此条件下反应120min后COD去除率为81.67%,乐果在25min内去除率为99.4%.通过测定CEF-FeRe以及CF反应过程中Fe2 和H2O2的变化情况验证了CEF-FeRe反应的机理.动力学研究结果表明.乐果废水的CEF-FeRe反应符合一级动力学反应规律.CEF-FeRe法处理实际乐果废水也可以得到91.16%的乐果去除及68.53%的COD去除,这表明CEF-FeRe法处理乐果废水效率高且运行费用较低的特点.

关 键 词:CEF-FeRe法  乐果  一级反应动力学  反应机理
收稿时间:7/5/2007 7:07:39 PM
修稿时间:2007/12/14 0:00:00

Oxidation treatment of dimethoate-containing wastewater by a circulating electro fenton method
WU Jinhu,LI Xiaoming,ZENG Guangming,YANG Qi,HUANG Yu and YI Ting.Oxidation treatment of dimethoate-containing wastewater by a circulating electro fenton method[J].Acta Scientiae Circumstantiae,2008,28(8):1534-1541.
Authors:WU Jinhu  LI Xiaoming  ZENG Guangming  YANG Qi  HUANG Yu and YI Ting
Institution:College of Environmental Science and Engineering, Hunan University, Changsha 410082,College of Environmental Science and Engineering, Hunan University, Changsha 410082,College of Environmental Science and Engineering, Hunan University, Changsha 410082,College of Environmental Science and Engineering, Hunan University, Changsha 410082,College of Environmental Science and Engineering, Hunan University, Changsha 410082 and College of Environmental Science and Engineering, Hunan University, Changsha 410082
Abstract:The main disadvantage of Conventional Fenton (CF) treatment is the lack of Fe2+ due to the rapid oxidation of Fe2+ to Fe3+.To solve this problem, a Circulating Electro-Fenton reactor (CEF-FeRe) was employed to degrade dimethoate, during which H2O2 was added to the electrolytic cell continuously by a peristaltic pump and Fe2+ could be regenerated to Fe3+ on the cathode. The operating conditions for this CEF-FeRe, such as pH value, electric current, Fenton reagent dosage, and the molar ratio of Fe2+ to H2O2, were optimized by individual factor experiments. The research results showed that the optimal conditions for dimethoate (200 mg·L-1) degradation are: pH=3.0, n(Fe2+)/n(H2O2)=0.1, electric current=0.5 A and Fenton's reagent dosage at its theoretical dosage. Under these conditions, COD removal rates reached 81.67% within 120 min, while 99.4% of dimethoate was degraded within 25 min. The mechanism of the CEF-FeRe reaction was investigated by monitoring the changes of H2O2 and Fe2+concentration during the process. Kinetics results revealed that dimethoate oxidation follows the pseudo-first-order kinetic model at different pH values. Treatment of actual dimethoate wastewater by the CEF-FeRe showed that the removal rates of dimethoate and COD were about 91.16% and 68.53%, respectively, which indicated that the CEF-FeRe could be a cost-efficient method for dimethoate degradation.
Keywords:CEF-FeRe  dimethoate  pseudo-first-order kinetic model  reaction mechanism
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