首页 | 本学科首页   官方微博 | 高级检索  
     

形稳阳极Ti/IrO_2-Ta_2O_5电Fenton法催化降解含酚废水
引用本文:高璟,闫俊娟,刘有智,郭志远,管张斌.形稳阳极Ti/IrO_2-Ta_2O_5电Fenton法催化降解含酚废水[J].含能材料,2017,25(10):866-872.
作者姓名:高璟  闫俊娟  刘有智  郭志远  管张斌
作者单位:1. 中北大学超重力化工过程山西省重点实验室,山西太原030051;中北大学化工与环境学院,山西太原030051;2. 中北大学化工与环境学院,山西太原,030051
基金项目:国家自然科学基金(21376229); 山西省青年科技研究基金(2015021033)
摘    要:针对电芬顿(Fenton)降解含酚废水时,铁阳极Fe易溶解从而影响降解效率的问题,采用形稳阳极Ti/IrO_2-Ta_2O_5进行电Fenton降解含酚废水的研究。采用高效液相去谱法推测了Ti/IrO_2-Ta_2O_5阳极和Fe阳极电Fenton降解苯酚的中间产物和降解过程。结果表明,FeSO_4·7H_2O投加量0.1 g·L~(-1),H_2O_2投加量2.94 mmol·L~(-1),初始pH值3.5,电压5.0 V,降解时间2 min,苯酚和化学需氧量(COD)去除率分别达94.14%和40.74%。在相同初始pH值、电压和降解时间下,使用铁阳极,苯酚和COD的去除率分别为40.74%和26.41%。相比Fe阳极电Fenton过程,Ti/IrO_2-Ta_2O_5阳极电Fenton过程降解废水时具有H_2O_2投加量少、降解时间短、电解电压低,并且耗酸量少、处理效果好、电极不易溶解的优点。Ti/IrO_2-Ta_2O_5阳极和Fe阳极电Fenton降解苯酚的过程是相同的,但在相同降解时间内,Ti/IrO_2-Ta_2O_5阳极电Fenton法降解含酚废水效率较高,这是由于Ti/IrO_2-Ta_2O_5阳极电催化反应与Fenton反应形成协同效应,协同降解废水的效率大于单独Fe阳极Fenton反应降解废水的效率。

关 键 词:Ti/IrO2-Ta2O5  电芬顿(Fenton)  电解  催化  含酚废水
收稿时间:2017/4/13 0:00:00
修稿时间:2017/6/26 0:00:00

Degradation of Phenol Wastewater by Electro-Fenton Method with Dimensionally Stable Anode of Ti/IrO2-Ta2O5
GAO Jing,YAN Jun-juan,LIU You-zhi,GUO Zhi-yuan and GUAN Zhang-bin.Degradation of Phenol Wastewater by Electro-Fenton Method with Dimensionally Stable Anode of Ti/IrO2-Ta2O5[J].Chinese Journal of Energetic Materials,2017,25(10):866-872.
Authors:GAO Jing  YAN Jun-juan  LIU You-zhi  GUO Zhi-yuan and GUAN Zhang-bin
Affiliation:Shanxi Province Key Laboratory of Higee-Oriented Chemical Engineering, North University of China, Taiyuan 030051, China ;School of Chemical and Environmental Engineering, Taiyuan 030051, China,Shanxi Province Key Laboratory of Higee-Oriented Chemical Engineering, North University of China, Taiyuan 030051, China ;School of Chemical and Environmental Engineering, Taiyuan 030051, China,Shanxi Province Key Laboratory of Higee-Oriented Chemical Engineering, North University of China, Taiyuan 030051, China ;School of Chemical and Environmental Engineering, Taiyuan 030051, China,School of Chemical and Environmental Engineering, Taiyuan 030051, China and School of Chemical and Environmental Engineering, Taiyuan 030051, China
Abstract:Aiming at the problem that in the degradation of phenol wastewater by Electro-Fenton, Fe of Fe anode is easily dissolved, which affects the degradation efficiency, the study on the degradation of phenol wastewater by Electro-Fenton was carried out using ghe dimensionally stable anode of Ti/IrO2-Ta2O5. The degradation intermediate products and degradation process of phenol wastewater of Ti/IrO2-Ta2O5 anode and Fe anode for Fenton degradation of phenol were detected by high performance liquid chromatography(HPLC). Results show that when FeSO4·7H2O dosage is 0.1 g·L-1, H2O2 dosage is 2.94 mmoL·L-1, initial pH is 3.5, voltage is 5 V and degradation time is 2 min, by using Ti/IrO2-Ta2O5 anode, the removal efficiency of phenol and COD can reach 94.14% and 40.74%, respectively. When Fe anode is used, at the same initial pH, voltage and degradation time, the removal efficiencies of phenol and COD are 40.74% and 26.41%, respectively. Compared with the Electro-Fenton process of Fe anode, the Electro-Fenton method of Ti/IrO2-Ta2O5 anode has the advantages of less acid consumption, less H2O2 dosage, shorter reaction time, lower electrolysis votage, lower consumption of electrode and better treatment effect for degradating phenol wastewater. The degradation process of phenol wastewater of Ti/IrO2-Ta2O5 anode and Fe anode for Fenton degradation of phenol are the same, but the degradation efficiency of phenol wastewater by Electro-Fenton method with Ti/IrO2-Ta2O5 anode is higher in the same degradation time. This is because the electrocatalysis reaction using Ti/IrO2-Ta2O5 anod and Electro-Fenton reaction can form a synergisic effect, the synergistic degradation of wastewater is more than that of alone Electro-Fenton reaction using Fe anode.
Keywords:Ti/IrO2-Ta2O5  electro-Fenton  electrolysis  catalysis  phenol wastewater
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《含能材料》浏览原始摘要信息
点击此处可从《含能材料》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号