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The beneficial effect of cathodic hydrogen peroxide generation on mitigating chlorinated by-product formation during water treatment by an electro-peroxone process

机译:通过电过氧工艺在水处理过程中减轻氯化氯化氯化含氯化氯化副产物形成的有益效果

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摘要

The formation of chlorinated by-products is a major concern associated with electrochemical water treatment processes. This study investigated the formation of chlorinated by-products during surface water treatment by a newly developed electrochemical advanced oxidation process (EAOP), the electroperoxone (E-peroxone) process, which couples ozonation with in situ electro-generation of hydrogen peroxide (H2O2) from cathodic oxygen reduction. Due to the enhanced ozone (03) conversion to hydroxyl radicals (center dot OH) by electro-generated H2O2, the E-peroxone process considerably accelerated the abatement of ozone-refractory micropollutants such as clofibric acid and chloramphenicol in the selected surface water compared to conventional ozonation. In addition, the cathodically generated H2O2 effectively quenched hypochlorous acid (HOCl) derived from the anodic oxidation of chloride in the surface water. Therefore, the formation of trichloromethane (TCM) and chloroacetic acids (CAAs) from the reactions of HOCl with dissolved organic matter (DOM) was insignificant during the E-peroxone process, and similar levels of TCM and CAAs were generally observed in the conventional ozonation and E-peroxone treated water. In contrast, considerable amounts of HOCl could be generated from the anodic oxidation of chloride and then accumulated in the surface water during conventional electrolysis process, which resulted in significantly higher concentrations of TCM and CAAs in the electrolysis treated water. The results of this study suggest that the E-peroxone process can overcome the major limitation of conventional electrochemical processes and provide an effective and safe EAOP alternative for micro pollutant abatement during water treatment. (C) 2019 Elsevier Ltd. All rights reserved.
机译:氯化副产物的形成是与电化学水处理过程相关的主要关注点。本研究通过新开发的电化学先进的氧化过程(EAOP),通过新开发的电化学先进的氧化过程(EAOP),将臭氧(E-Peroxone)方法进行研究,将氯化酮(E-氧化锆)加工在原位电解中的过氧化氢(H2O2)中的氟化物(H2O2)中的氯化酮(EAOP)进行了氯化副产物的形成来自阴极氧还原。由于增强的臭氧(03)转化为羟基自由基(中心点OH),通过电生H 2 O 2,E-氧化锆过程相比,E-氧化氢气过程显着加速了臭氧耐火微拷贝的臭氧和氯霉素的剥离,与常规臭氧化。另外,阴极产生的H 2 O 2有效地淬灭衍生自氯化物在地表水中阳极氧化的次氯酸(HOCl)。因此,在E-过氧化物过程中,将三氯甲烷(TCM)和氯乙酸(CAA)从HOCl的反应中形成,在E-过氧酮过程中,通常在常规臭氧化中观察到类似水平的TCM和CAAs和E-过氧酮处理的水。相反,可以从氯化物的阳极氧化产生相当大量的HoCl,然后在常规电解过程中积聚在地表水中,这导致电解处理水中显着较高的TCM和CAAs。本研究的结果表明E-氧化锆工艺可以克服传统电化学过程的主要限制,并在水处理过程中提供微污染物减排的有效和安全的助剂。 (c)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Water Research》 |2019年第15期|209-217|共9页
  • 作者单位

    Tsinghua Univ Beijing Key Lab Emerging Organ Contaminants Contr State Key Joint Lab Environm Simulat & Pollut Con Sch Environm Key Lab Solid Waste Management & Env Beijing 100084 Peoples R China;

    Tsinghua Univ Beijing Key Lab Emerging Organ Contaminants Contr State Key Joint Lab Environm Simulat & Pollut Con Sch Environm Key Lab Solid Waste Management & Env Beijing 100084 Peoples R China;

    Tsinghua Univ Beijing Key Lab Emerging Organ Contaminants Contr State Key Joint Lab Environm Simulat & Pollut Con Sch Environm Key Lab Solid Waste Management & Env Beijing 100084 Peoples R China;

    Tsinghua Univ Beijing Key Lab Emerging Organ Contaminants Contr State Key Joint Lab Environm Simulat & Pollut Con Sch Environm Key Lab Solid Waste Management & Env Beijing 100084 Peoples R China;

    Tsinghua Univ Beijing Key Lab Emerging Organ Contaminants Contr State Key Joint Lab Environm Simulat & Pollut Con Sch Environm Key Lab Solid Waste Management & Env Beijing 100084 Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Bromate; Chlorinated by-products; Electrochemical advanced oxidation process; Electro-peroxone; Micropollutant; Ozonation;

    机译:溴酸盐;氯化副产品;电化学先进的氧化过程;电氧化锆;微润肤剂;臭氧化;
  • 入库时间 2022-08-18 22:34:30

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