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Yeast biomass-induced Co_2P/biochar composite for sulfonamide antibiotics degradation through peroxymonosulfate activation

机译:酵母生物质诱导的CO_2P / BioCHAR通过过氧键硫酸盐活化来降解磺酰胺酰胺抗生素。

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摘要

Advanced oxidation processes (AOPs) based on peroxymonosulfate (PMS) activation have attracted increasing attention in recent years for organic pollutants removal. Herein, we put forward a facile method to form cobalt phosphide/carbon composite for PMS activation. Combining impregnation approach with pyrolysis treatment enabled the formation of Co2P/biochar composites using baker's yeast and Co2+ as precursors. The as-synthesized products exhibited excellent catalytic activity for sulfamethoxazole (SMX) degradation over the pH range 3.0-9.0 by activating PMS. For example, 100% of SMX (20 mg L-1) removal was achieved in 20 min with catalyst dosage of 0.4 g L-1 and PMS loading of 0.4 g L-1. Near zero Co2+ leaching was observed during catalytic reaction, which remarkably lowered the toxic risk of transition metal ion in water. Meanwhile, the reusability of catalyst could be attained by thermal treatment. SMX degradation intermediates were identified by liquid chromatography-mass spectrometry (LC-MS), which facilitated the proposal of possible SMX degradation pathways. Ecological Structure Activity Relationships (ECOSAR) analysis indicated that SMX degradation intermediates may not pose ecological toxicity to the environment. Further investigation verified that Co2P/biochar composites could set off PMS activation not only for the degradation of SMX but also for other sulfonamides. In this study, we not only developed a facile method of utilizing environmental-benign biomass for transition metal phosphide/carbon composite formation, but also achieved highly efficient antibiotic elimination by PMS-based AOP. (C) 2020 Elsevier Ltd. All rights reserved.
机译:基于过氧键磺酸盐(PMS)活化的先进氧化方法(AOP)近年来对有机污染物的去除引起了近年来的越来越长。在此,我们提出了一种容易法形成磷化钴/碳复合物的PMS活化。将浸渍方法与热解性处理相结合,使得使用面包酵母和CO2 +作为前体形成CO 2P / BioChOS复合材料。通过活化PMS,AS合成的产品表现出磺胺甲氧唑(SMX)降解的优异催化活性。例如,在20分钟内实现了100%的SMX(20mg L-1),催化剂剂量为0.4g L-1和0.4g L-1的PMS负载量。在催化反应过程中观察到邻零CO2 +浸出,这显着降低了水中过渡金属离子的毒性风险。同时,可以通过热处理获得催化剂的可重用性。通过液相色谱 - 质谱(LC-MS)鉴定SMX降解中间体,其促进了可能的SMX降解途径的提议。生态结构活动关系(Ecosar)分析表明,SMX降解中间体可能不会对环境产生生态毒性。进一步调查证实,CO 2P / BioChOS复合材料可以脱离PMS激活,而不仅可以用于SMX的降解,还可以脱离SMX,但也可以用于其他磺胺酰胺。在这项研究中,我们不仅开发了利用环境良性生物质用于过渡金属磷化物/碳复合材料形成的容易方法,而且还通过PMS的AOP实现了高效的抗生素消除。 (c)2020 elestvier有限公司保留所有权利。

著录项

  • 来源
    《Environmental Pollution》 |2021年第2期|115930.1-115930.9|共9页
  • 作者单位

    Sichuan Univ Sch Chem Engn Chengdu 610065 Peoples R China;

    Sichuan Univ Sch Chem Engn Chengdu 610065 Peoples R China;

    Sichuan Univ Sch Chem Engn Chengdu 610065 Peoples R China;

    Sichuan Univ Sch Chem Engn Chengdu 610065 Peoples R China;

    Sichuan Univ Sch Chem Engn Chengdu 610065 Peoples R China;

    Sichuan Univ Sch Chem Engn Chengdu 610065 Peoples R China;

    Sichuan Univ Sch Chem Engn Chengdu 610065 Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Impregnation; Biomass; Cobalt phosphide; Advanced oxidation process; Sulfonamide;

    机译:浸渍;生物量;钴磷化物;晚期氧化过程;磺酰胺;

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