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Generation of hydroxyl radicals by metal-free bifunctional electrocatalysts for enhanced organics removal

机译:通过无金属双官能电催化剂产生羟基自由基,以增强有机物去除

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摘要

Low yields of H_2O_2 and a narrow range of appropriate pH values have been two major drawbacks for electro-Fenton (EF) process. Herein, metal-free electrochemical advanced oxidation processes (EAOPs) were developed with nitrogen and sulfur co-doped electrochemically exfoliated graphene (N, S-EEGr) electrocatalysts, which was confirmed as an outstanding bifunctional catalyst for synchronous generation and activation of H_2O_2 via (2 + 1) e~- consecutive reduction reactions. Specifically, two elements (N, S) in metal-free N, S-EEGr-CF cathode synergize to promote the formation of H_2O_2 followed by its activation. With N, S-EEGr-CF cathode, phenol of initial 50 mg L"1 could be effectively removed within pH 3-11 and 6.25 mA cm~(-2), and 100% removal efficiency could be achieved within 15-min even at neutral pH. The pseudo-first-order rate constant for phenol removal in metal-free EAOPs with N,S-EEGr-CF at neutral pH was 10 times higher than that with EF process. Detection of active species, coupled with decay kinetics with specific trapping agents, confirmed that ·OH was the dominant oxidizing species promoting removal efficiencies of organics (phenol, antibiotics and dyes) at pH 3 and pH 7. In the actual wastewater treatment, the synergistic effect of bifunctional catalyst would also be used for improving the degradation efficiency of organics. Thus, the metal-free EAOPs with N,S-EEGr-CF cathode may serve as an alternative in wastewater treatment with a broadened range of solution pH values and avoiding Fe~(2+) (catalyst) addition.
机译:双氧水的低的产率和适当的pH值的窄范围已经用于电芬顿(EF)处理两个主要的缺点。在本文中,无金属的电化学高级氧化处理(EAOPs)与氮和硫共掺杂的电化学剥离的石墨烯(N,S-EEGR)电催化剂,它被确认为用于经由H_2O_2的同步产生和活化的杰出的双功能催化剂的开发( 2 + 1)E〜 - 连续还原反应。具体地,两个元件(N,S)的无金属-N,S-EEGR-CF阴极增效促进H_2O_2的形成,随后其激活。与N,S-EEGR-CF阴极,初始50毫克的L的苯酚“1可有效pH值3-11和6.25毫安厘米〜(-2),和100%的去除效率可能被15分钟内达到,甚至除去内在中性pH。伪一级速率常数为脱酚在用N-无金属EAOPs,S-EEGR-CF在中性pH下为高10倍以上,与EF处理。活性物质的检测,加上衰减动力学与特定的捕获剂,确认·OH为优势氧化物质在pH 3和pH 7.在实际废水处理促进有机物(苯酚,抗生素和染料)的去除效率,也将用于双功能催化剂的协同效应提高有机物的降解效率,因此,与N,S-EEGR-CF阴极不含金属的EAOPs可以作为废水处理的替代与溶液的pH值的范围扩大,并避免的Fe〜(2+)(催化剂)添加。

著录项

  • 来源
    《Science of the total environment》 |2021年第15期|148107.1-148107.11|共11页
  • 作者单位

    Guangdong Key Laboratory of Environmental Pollution and Health School of Environment Jinan University Guangzhou 511443 China;

    Key Laboratory of Pollution Process and Environmental Criteria (MOE) College of Environmental Science and Engineering Nankai University Tianjin 300350 China;

    Guangdong Key Laboratory of Environmental Pollution and Health School of Environment Jinan University Guangzhou 511443 China;

    Guangdong Key Laboratory of Environmental Pollution and Health School of Environment Jinan University Guangzhou 511443 China;

    Universite Gustave Eiffel Laboratoire Geomateriaux et Environnement EA 4508 77454 Marne-la-Vallee Cedex 2 France;

    Universite Gustave Eiffel Laboratoire Geomateriaux et Environnement EA 4508 77454 Marne-la-Vallee Cedex 2 France;

    Guangdong Key Laboratory of Environmental Pollution and Health School of Environment Jinan University Guangzhou 511443 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Metal-free electrochemical advanced oxidation; process; H_2O_2 activation; Bifunctional electrocatalyst; Organics degradation; Reusability;

    机译:无金属电化学先进氧化;过程;h_2O_2激活;双功能电催化剂;有机物退化;可重用性;

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