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DSA电极电催化氧化降解四环素废水工艺优化
引用本文:张佳,王国祥,夏明芳,朱兆连,江野立,韩睿明.DSA电极电催化氧化降解四环素废水工艺优化[J].精细化工,2014,31(2).
作者姓名:张佳  王国祥  夏明芳  朱兆连  江野立  韩睿明
作者单位:南京师范大学,南京师范大学地理科学学院江苏省环境演变及生态建设重点实验室,江苏 南京,1. 南京师范大学地理科学学院江苏省环境演变及生态建设重点实验室,江苏 南京 210023;2. 南京大学环境学院污染控制与资源化研究国家重点实验室,江苏 南京 210093,南京大学环境学院污染控制与资源化研究国家重点实验室,江苏 南京 210093,南京大学环境学院污染控制与资源化研究国家重点实验室,江苏 南京 210093,南京师范大学地理科学学院江苏省环境演变及生态建设重点实验室,江苏 南京 210023
基金项目:国家自然科学基金项目(No. 41173078)
摘    要:以盐酸四环素(TC·HCl)为研究对象,钛基钌铱涂层(IrO2-RuO2/Ti)为阳极,钛板为阴极,电催化氧化降解TC·HCl模拟废水,探讨了初始质量浓度、电流密度、pH、电解质硫酸钠浓度对电催化降解TC·HCl效率的影响。结果表明,电催化氧化可有效降解水中的TC·HCl。提高电流密度,降低TC·HCl初始质量浓度、电解质硫酸钠浓度,可增大TC·HCl去除率。反应的前90 min,pH对去除率无影响,反应90 min后降解效果出现明显差别,pH为3、7和12时,反应300 min去除率分别为92%、100%和72%。降解过程遵循一级反应动力学模型。通过综合各工艺参数下的去除率、能量消耗和电流效率,得出最佳工艺参数为:TC·HCl初始质量浓度300 mg/L、电流密度10 mA/cm2、硫酸钠浓度0.05 mol/L、pH=7,在该条件下反应180 min后TC·HCl去除率达94%。该实验结果为电化学处理制药工业废水提供了基础数据和科学参考。

关 键 词:电催化  盐酸四环素  降解  反应动力学  水处理技术与环境保护
收稿时间:9/6/2013 12:00:00 AM
修稿时间:2013/10/29 0:00:00

Optimization of Electro-catalytic Oxidation of Tetracycline Hydrochloride in Aqueous Solution by DSA Electrodes
ZHANG Ji,WANG Guo-xiang,XIA Ming-fang,ZHU Zhao-lian,JIANG Ye-li and HAN Rui-ming.Optimization of Electro-catalytic Oxidation of Tetracycline Hydrochloride in Aqueous Solution by DSA Electrodes[J].Fine Chemicals,2014,31(2).
Authors:ZHANG Ji  WANG Guo-xiang  XIA Ming-fang  ZHU Zhao-lian  JIANG Ye-li and HAN Rui-ming
Affiliation:Nanjing Normal University,Jiangsu Key Laboratory of Environmental Change and Ecological Construction, College of Geographical Science, Nanjing Normal University, Nanjing 210023,1. Jiangsu Key Laboratory of Environmental Change and Ecological Construction, College of Geographical Science, Nanjing Normal University, Nanjing 210023; 2. State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210093,State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210093,State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210093,Jiangsu Key Laboratory of Environmental Change and Ecological Construction, College of Geographical Science, Nanjing Normal University, Nanjing 210023
Abstract:Tetracycline HCl (TC•HCl) in an artificial wastewater was electrochemically degraded using IrO2-RuO2/Ti as anode and Ti as cathode. The impacts of initial TC concentrations, current density, pH value, electrolyte concentrations on the degradation effect of TC were investigated. The energy consumption and current efficiency were compared according to operating conditions to reveal the optimal condition for electrochemical degradation of TC HCl. Results showed that electro-catalytic oxidation could effectively remove TC in aqueous solutions. Higher current density, lower initial concentrations of TC•HCl and/or lower concentrations of Na2SO4 as electrolyte could enhance the removal rate of TC•HCl. During 0-90 min of the reaction, pH had no effect on the removal rate. After 90 min, acidic and alkaline conditions both partly inhibited the degradation of TC HCl, for example, the removal rates at pH 3, 7 and 12 were 92 %, 100 % and 72 % after 300 min respectively. Degradation procedure was in accordance with the first-order kinetic model. With the analysis of the removal rate, energy consumption and current efficiency under various operating conditions, the optimal condition constitute the initial TC•HCl concentration of 300 mg/L, the current density of 10 mA•cm-2, the Na2SO4 concentration of 0.05 mol•L-1 and the pH value of 7 with a removal rate of TC•HCl 94 % after 180 min. The present study provides so far the primary data for wastewater management against TC HCl.
Keywords:electro-catalysis  tetracycline hydrochloride  removal rate  reaction kinetics
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