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Degradation of organic pollutants by a Co_3O_4 -graphite composite electrode in an electro-Fenton-like system

ISSN号：1001-3555
期刊名称：《分子催化》
时间：0
分类：X503.23[环境科学与工程—环境工程] O646.54[理学—物理化学;理学—化学]
作者机构：[1]Engineering Research Center of Eco-environment in Three Gorges Reservoir Region,Ministry of Education,China Three Gorges University, [2]Institute of Oceanology,Chinese Academy of Sciences, [3]School of Natural Science & Mathematics,Ferrum College
相关基金：supported by the National Natural Science Foundation of China （21177072, 21207079）; the Educational Commission for Distinguished Group of Hubei Province, China （T200703）; the Natural Science Foundation for Innovation Group of Hubei Province, China（2009CDA020）

作者： LIU Shuan[1,2], GU Yan[1], WANG ShuLian[1], ZHANG Yu[1], FANG YanFen[1], JOHNSON David M[3], HUANG YingPing[1]

关键词：污染物降解, 复合电极, L系统, 石墨, 傅里叶变换红外光谱, FENTON反应, 持久性有机污染物, 硫酸盐还原菌, Co3O4-graphite electrode, electro-Fenton-like system, electro-generation of hydroxyl radicals, electro-catalytic degradation of POPs

中文摘要：

一个新奇合成电极被一起压 Co3O4 和石墨构造，它在 electro-Fenton-like (EFL ) 被用作阴极系统。Co3O4 的差的电子运输特征被合并石墨克服。在 situ 氢氧根激进分子的电镀物品催化的产生(浥

英文摘要：

A novel composite electrode was constructed by pressing together Co3O4 and graphite and it was used as the cathode in an electro-Fenton-like （EFL） system. The poor electron transport characteristic of Co3O4 was overcome by incorporating graphite. In situ electro-catalytic generation of hydroxyl radicals （·OH） occurred at high current efficiencies from pH 2-10, extending the traditional Fenton reaction pH range. Cyclic voltammetry and AC impedance spectrometry were used to characterize the composite electrode. The ability of the EFL system to degrade organic compounds was investigated using sulforhodamine B （SRB） and 2,4-dichlorophenol （2,4-DCP） as probes. Decoloration of SRB （1.0×10-5 mol/L） was complete （100%） in 150 min and SRB was effectively degraded from pH 2-10. The decomposition of SRB was studied using Fourier transform infrared spectroscopy （FT-IR） and total organic carbon （TOC） analysis and results indicated that the final degradation products were carbon dioxide, carboxylic acids and amines. The EFL system also decomposed 2,4-DCP and the degradation was 98.6% in 240 min. Electro-catalytic degradation of SRB occurs by a ·OH mechanism. After 5 times reused, the degradation rate of SRB did not significantly slow down. The electrode shows excellent potential for use in advanced oxidation processes （AOPs） used to treat persistent organic pollutants （POPs） in wastewater.

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