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首页> 外文期刊>Chemical engineering journal >Enhancement of photoelectrocatalytic degradation of diclofenac with persulfate activated by Cu cathode
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Enhancement of photoelectrocatalytic degradation of diclofenac with persulfate activated by Cu cathode

机译:Cu阴极激活双氯芬酸的光电催化降解光电催化降解

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摘要

In this work, persulfate (S2O82-, PS) was introduced to the photoelectrocatalytic (PEC) system, which consisted of a gamma-Bi2MoO6 photoanode and a copper foil cathode (Bi2MoO6/Cu/PEC/PS system). Significant enhancement of diclofenac sodium (DCF) degradation efficiency was observed in this system under visible light irradiation. At an applied bias of 1.5 V and initial solution pH of 5.62, the removal efficiency of DCF with an initial concentration of 10 mg/L was increased from 19.4% in the PEC process to 86.3% in the PEC process with 10 mM PS addition. The pseudo-first-order kinetic rate constant of DCF degradation was increased from 0.1112 h(-1) to 1.0498 h(-1). Active free radicals involving SO center dot(-)(4) and HO center dot were produced in this process, which were confirmed by electron spin resonance analysis. Furthermore, the surface variation of copper foil cathode was characterized by FE-SEM, GI-XRD, XPS and in situ Raman spectroscopy. It was demonstrated that Cu2O formed on the surface in the reaction process with the S2O82- addition, which was further confirmed by the photoelectrochemical analysis of the cathode. The surface Cu(0)-Cu(l)-Cu(II)-Cu(0) redox cycle of cathode was proposed, which was responsible for the persulfate activation, leading to the generation of free radicals. This work may provide a new perspective on the combined utilization of different technologies for catalytic contaminant removal. (C) 2017 Published by Elsevier B.V.
机译:在这项工作中,将过硫酸盐(S2O82-,PS)引入光电催化剂(PEC)系统,其由伽马-Bi2Moo6光电码和铜箔阴极(Bi2Moo6 / Cu / PEC / PS系统)组成。在该系统下,在可见光照射下,在该系统中观察到双氯芬酸钠(DCF)降解效率显着提高。在1.5V和初始溶液pH的施用偏压下,5.62的pH值,初始浓度为10mg / L的DCF的去除效率从PEC工艺中的19.4%增加到PEC工艺中的86.3%,加入10mM PS加入。 DCF降解的伪第一阶动力率常数从0.112小时(-1)增加到1.0498小时(-1)。在该方法中生产涉及所需点( - )(4)和HO中心点的有源自由基,通过电子自旋共振分析证实。此外,通过Fe-SEM,Gi-XRD,XPS和原位拉曼光谱表征铜箔阴极的表面变化。证明Cu 2O在反应过程中形成的Cu 2 O,通过S2O82添加,通过阴极的光电化学分析进一步证实。提出了表面Cu(0)-Cu(1)-Cu(II)-Cu(II)-Cu(0)阴极的氧化还原循环,其负责过硫酸盐活化,导致自由基的产生。这项工作可以提供关于催化污染物去除的不同技术的合并利用的新视角。 (c)2017年由Elsevier B.V发布。

著录项

  • 来源
    《Chemical engineering journal》 |2017年第2017期|共10页
  • 作者单位

    Chinese Acad Sci Key Lab Drinking Water Sci &

    Technol Res Ctr Ecoenvironm Sci Beijing 100085 Peoples R China;

    Chinese Acad Sci Key Lab Drinking Water Sci &

    Technol Res Ctr Ecoenvironm Sci Beijing 100085 Peoples R China;

    Chinese Acad Sci Key Lab Drinking Water Sci &

    Technol Res Ctr Ecoenvironm Sci Beijing 100085 Peoples R China;

    Chinese Acad Sci Key Lab Drinking Water Sci &

    Technol Res Ctr Ecoenvironm Sci Beijing 100085 Peoples R China;

    Chinese Acad Sci Key Lab Drinking Water Sci &

    Technol Res Ctr Ecoenvironm Sci Beijing 100085 Peoples R China;

    Chinese Acad Sci Key Lab Drinking Water Sci &

    Technol Res Ctr Ecoenvironm Sci Beijing 100085 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;
  • 关键词

    Photoelectrocatalysis; Persulfate; Cu cathode; Cu2O; Diclofenac;

    机译:光电催化剂;过硫酸盐;Cu阴极;CU2O;双氯芬酸;

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