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The role of synergistic effects between ozone and coagulants (SOC) in the electro-hybrid ozonation-coagulation process

机译:在电杂交臭氧化凝固过程中臭氧和凝结剂(SOC)之间协同作用的作用

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摘要

In order to improve the dissolved organic matter removal efficiency, an electro-hybrid ozonation-coagulation (E-HOC) system was developed in this study, in which the electro-coagulation (EC) and ozonation occurred simultaneously in one integrated unit. Higher removal efficiency was observed for the E-HOC process compared with those of EC, ozonation and pre-ozonation-EC process for the treatment of wastewater treatment plant (WWTP) effluent and ibuprofen (IBP). 58.6% dissolved organic carbon (DOC) removal efficiency was achieved in the E-HOC process for the treatment of WWTP effluent at optimal operational condition (current density 15 mA/cm(2), initial pH 5 and ozone dosage 1.5 mg O-3/mg DOC). Based on the reactive oxygen species (ROS) detection and reactions on the electrodes, the synergistic effects between ozone and coagulants (SOC) were found to be involved in the E-HOC process. According to pseudo-first-order rate constant analyses, the contribution of five possible organic removal pathways was quantified. It was revealed that the peroxone and SOC effects exhibited almost equal contribution to IBP removal at initial pH 5 under different current densities, both of which played the dominant role in the E-HOC process. However, the contribution of the SOC effects decreased significantly when the initial pH increased to 7 and 9. As an important pathway for organic removal in the E-HOC process at initial pH 5, the mechanism of the SOC effects was analysed at initial pH 5. It was revealed the SOC effects can further improve hydroxyl radicals (center dot OH) generation, and the surface hydroxyl groups of the hydrolysed Al species generated from anode electrolysis were determined to be the active sites to generate ROS in the SOC effects. (C) 2020 Elsevier Ltd. All rights reserved.
机译:为了提高溶解的有机物质去除效率,在该研究中开发了电杂交臭氧凝固(E-HOC)系统,其中在一个集成单元中同时发生电凝固(EC)和臭氧。与EC,臭氧化和臭氧型-EC处理相比,对E-HOC过程观察到更高的去除效率,用于治疗废水处理厂(WWTP)流出物和布洛芬(IBP)。 58.6%溶解有机碳(DOC)在E-HOC过程中实现了去除效率,用于在最佳操作状态下处理WWTP流出物(电流密度15mA / cm(2),初始pH5和臭氧剂量1.5mg O-3 / mg doc)。基于对电极的反应性氧物质(ROS)检测和反应,发现臭氧和凝结剂(SOC)之间的协同效应参与E-HoC过程。根据伪一阶率常数分析,量化了五种可能的有机去除途径的贡献。据透露,过氧化物和SOC效应在不同电流密度下在初始pH 5下表现出对IBP除去的几乎等同贡献,这两者都在E-HoC过程中发挥了显着作用。然而,当初始pH增加到7和9时,SOC效应的贡献显着降低。作为在初始pH 5的E-Hoc过程中有机移除的重要途径,SOC效应的机制在初始pH 5中分析。揭示了SOC效应可以进一步改善羟基自由基(中央点OH)产生,并且从阳极电解产生的水解的Al物种的表面羟基被确定为在SOC效应中产生RO的活性位点。 (c)2020 elestvier有限公司保留所有权利。

著录项

  • 来源
    《Water Research 》 |2020年第15期| 115800.1-115800.12| 共12页
  • 作者单位

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Key Lab Northwest Water Resource Environm & Ecol MOE Xian 710055 Peoples R China;

    Xian Univ Architecture & Technol Shaanxi Key Lab Environm Engn Xian 710055 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

    Electro-HOC process; Reactive oxygen species; Synergistic effects; Surface hydroxyl groups;

    机译:电力氧化物;活性氧物种;协同效应;表面羟基;

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