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Development of Fe-doped g-C_3N_4/graphite mediated peroxymonosulfate activation for degradation of aromatic pollutants via nonradical pathway

机译:Fe掺杂的g-C_3N_4 /石墨介导的过氧单硫酸盐活化通过非自由基途径降解芳香族污染物的研究进展

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摘要

A new composite catalyst, i.e., Fe doped g-C3N4/graphite (Fe-CN/G), was successfully constructed to activate peroxymonosulfate (PMS) for efficient phenolic compounds (i.e., p-chlorophenol, 4-CP) degradation in the pH range of 3-10. The optimized Fe-CN/G, i.e., Fe-3.75-CN/G(5.0), was fabricated at the dosage of 3.75 mmol FeCl3 center dot 6H(2)O, 5.0 g dicyandiamide, and 5.0 mmol glucose. Fe complexed in the nitrogen pots of Fe-3.75-CN/G(5.0) was demonstrated to be the primary active site for PMS activation, and the introduction of graphite favored the exposure of more accessible active sites in Fe-3.75-CN/G(5.0), suggesting a synergistic effect between the Fe and graphite of Fe-3.75-CN/G(5.0) on 4-CP degradation. Multiple experiments confirmed that sulfate radical (SO4 center dot(-)), hydroxyl radical (HO center dot), singlet oxygen (O-1(2)) and superoxide radical (O-2 center dot(-)) exerted negligible contribution on 4-CP degradation. The in-situ Fe K-edge X-ray absorption near-edge structure (XANEX) analysis revealed a redox cycle of Fe in PMS/Fe-3.75-CN/G(5.0), suggesting the formation of high-valent iron-oxo species ( Fe-IV=O) was responsible for 4-CP degradation. In addition, PMS/Fe-3.75-CN/G(5.0) exhibited acceptable degradation of 4-CP in the presence of coexisting anions and natural organic matters (NOM). We believe this study provides new insights into the design and development of Fe-based heterogeneous catalysts for PMS-based wastewater treatment. (C) 2019 Elsevier B.V. All rights reserved.
机译:成功构建了一种新型的复合催化剂,即铁掺杂的g-C3N4 /石墨(Fe-CN / G),以活化过氧单硫酸盐(PMS),以在pH值下有效降解酚类化合物(即对氯苯酚,4-CP)。范围3-10。以3.75 mmol FeCl3中心点6H(2)O,5.0 g双氰胺和5.0 mmol葡萄糖的剂量制备了优化的Fe-CN / G,即Fe-3.75-CN / G(5.0)。事实证明,在氮罐Fe-3.75-CN / G(5.0)中络合的铁是PMS活化的主要活性部位,而石墨的引入有利于在Fe-3.75-CN / G(G)中暴露更多易接近的活性部位。 (5.0),表明Fe-3.75-CN / G(5.0)的Fe和石墨之间对4-CP降解具有协同作用。多次实验证实,硫酸根(SO4中心点(-)),羟基(HO中心点),单线态氧(O-1(2))和超氧自由基(O-2中心点(-))的贡献可忽略不计4-CP降解。原位Fe K边缘X射线吸收近边缘结构(XANEX)分析揭示了PMS / Fe-3.75-CN / G(5.0)中Fe的氧化还原循环,表明形成了高价铁-氧物种(Fe-IV = O)导致4-CP降解。此外,PMS / Fe-3.75-CN / G(5.0)在共存阴离子和天然有机物(NOM)的存在下表现出可接受的4-CP降解。我们相信这项研究为基于PMS的废水处理的铁基非均相催化剂的设计和开发提供了新的见识。 (C)2019 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《The Science of the Total Environment》 |2019年第20期|62-72|共11页
  • 作者单位

    Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China|Nanjing Univ, Res Ctr Environm Nanotechnol ReCENT, Nanjing 210023, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China|Nanjing Univ, Res Ctr Environm Nanotechnol ReCENT, Nanjing 210023, Jiangsu, Peoples R China;

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

    Fe-doped graphic carbon nitrate; Graphite; Peroxymonosulfate activation; High-valent iron-oxo species; In-situ XANES;

    机译:掺铁图形硝酸碳;石墨;过氧单硫酸盐活化;高价铁-氧代物质;原位XANES;

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