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基于AC/SnO2-Sb粒子电极的苯酚电催化氧化

杨胜翔 王立章 伍波 张波 李哲楠

化工进展2016,Vol.35Issue(4):1230-1236,7.
化工进展2016,Vol.35Issue(4):1230-1236,7.DOI:10.16085/j.issn.1000-6613.2016.04.042

基于AC/SnO2-Sb粒子电极的苯酚电催化氧化

Electrochemical oxidation of phenol on AC/SnO2-Sb particle electrodes

杨胜翔 1王立章 1伍波 1张波 1李哲楠1

作者信息

  • 1. 中国矿业大学 徐州 环境与测绘学院,江苏徐州 221116
  • 折叠

摘要

Abstract

As SnO2-Sb solid solution have excellent catalytic activity,a kind of AC/SnO2-Sb particle electrodes was manufactured with thermal decomposition method. Nitrogen adsorption,scanning electron microscopy(SEM),X-ray diffraction(XRD) and electrochemical test were used to analyze the surface area,porosity,phase composition,the crystal structure and electrocatalytic activity of modified activated carbon(AC). The results showed that SnO2-Sb as continuous solid solution reduced quantity of mesoporous structures but not damaged high porosity of AC that is beneficial to the electrocatalysis. In addition,these metal oxide coatings widely distributed in the channel of AC,which could improve not only electrical catalytic activity to ·OH but also the direct oxidation activity on the surface of the electrode. Meanwhile cyclic voltammetry curve of AC/SnO2-Sb showed an obvious oxidation peak at 1.10V,which indicated direct oxidation of phenol can occur at the surface of AC/SnO2-Sb. Bulk electrolysis experiments with AC and AC/SnO2-Sb were conducted with simulated phenol wastewater. The results indicated the removal of COD and phenol with AC/SnO2-Sb(78.43% and 79.52%) were better than that of AC under 12.0mA/cm2 current density during 3h electrolysis.Moreover excellent electrochemical stability of AC/SnO2 - Sb can be shown in 30 days continuous water treatment.

关键词

电化学/催化剂/活性碳/水处理/苯酚

Key words

electrochemistry/catalyst/activated carbon/wastewater treatment/phenol

分类

资源环境

引用本文复制引用

杨胜翔,王立章,伍波,张波,李哲楠..基于AC/SnO2-Sb粒子电极的苯酚电催化氧化[J].化工进展,2016,35(4):1230-1236,7.

基金项目

江苏省基础研究计划(自然科学基金)(BK2011224)、中央高校基本科研业务费专项资金(2013QNA20)及中国矿业大学大学生创新创业基金立项大学生创新项目(201563)。 ()

化工进展

OA北大核心CSCDCSTPCD

1000-6613

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