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Mechanistic insights into the catalytic ozonation process using iron oxide-impregnated activated carbon

机译:使用氧化铁浸渍的活性炭进行机械洞察催化臭氧化工艺

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摘要

In the present study, radiolabelled formate was used as a probe compound in order to gain mechanistic insight into the catalytic ozonation process using a commercially available iron oxide-impregnated activated carbon catalyst. We simultaneously analysed the adsorptive and oxidative removal of formate in order to determine the contribution of the catalyst to adsorption and oxidant generation processes respectively. Our results show that the presence of the catalyst enhanced ozone decay as well as the rate and extent of formate oxidation at pH 3.0 compared to that observed in the presence of ozone alone as a result of oxidant generation via O-3-Fe oxide interaction. A reduction in rate and extent of formate oxidation on addition of t-butanol and Cl- (known hydroxyl radical ((OH)-O-center dot) scavengers under acidic conditions) provides evidence that the oxidant generated during catalytic ozonation at pH 3.0 is (OH)-O-center dot. Moreover, the oxidation of formate during catalytic ozonation mostly occurs at the solid-liquid interface and/or in bulk solution with adsorption playing no role in the overall oxidation process with this finding supported by the exceptionally high oxidation efficiency compared to the extent of adsorption observed when no O-3 was added. While catalytic ozonation was effective in formate oxidation at pH 3.0, the presence of the catalyst did not lead to an increase in either the rate or extent of formate oxidation at pH 7.3 and 8.5 suggesting that only protonated iron oxide surface sites generate strong oxidant(s) on interaction with O-3. Based on our understanding of the processes operating during the ozonation and catalytic ozonation processes, a mathematical model has been developed that adequately describes the experimental results obtained here. Overall, this study shows that systematic measurement of ozone decay, removal of the parent compound as well as formation of the oxidized products under well controlled conditions are required for unequivocal elucidation of the mechanism of catalytic ozonation. (C) 2020 Elsevier Ltd. All rights reserved.
机译:在本研究中,将放射性标记的甲酸酯用作探针化合物,以利用市售的氧化铁浸渍的活性炭催化剂来获得催化臭氧处理的机械洞察。我们同时分析了甲酸盐的吸附和氧化去除,以便分别确定催化剂对吸附和氧化剂产生过程的贡献。我们的研究结果表明,与通过O-3-Fe氧化物相互作用的氧化剂产生的氧化剂的结果,在pH 3.0中,pH 3.0的催化剂增强臭氧衰减的存在以及在pH 3.0的氧化率和程度的速率和程度。在酸性条件下加入叔丁醇和Cl-((OH)-O-中心点)清除剂的甲酸氧化率的速率和程度的降低提供了证据表明在pH3.0处催化臭氧化生成的氧化剂是(哦)-o中心点。此外,在催化臭氧化过程中甲酸甲酸盐的氧化主要发生在固液界面和/或在本体溶液中,吸附在整个氧化过程中没有作用,与观察到的吸附程度相比,通过特殊的高氧化效率支撑当没有添加O-3时。虽然催化臭氧化在pH 3.0的甲酸氧化中,但催化剂的存在不会导致pH 7.3和8.5在pH 7.3和8.5下甲酸氧化的速率或程度增加,这表明只有质子化的氧化铁表面位点产生强氧化剂(s关于与O-3的互动。基于我们对在臭氧化和催化臭氧过程期间操作的过程的理解,已经开发了一种充分描述了这里获得的实验结果的数学模型。总体而言,本研究表明,在催化臭氧化机制的情况下,需要系统测量臭氧衰减,除去母体化合物以及在良好控制的条件下形成氧化产物。 (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|115785.1-115785.13|共13页
  • 作者单位

    Univ New South Wales UNSW Water Res Ctr Sch Civil & Environm Engn Sydney NSW 2052 Australia;

    Univ New South Wales UNSW Water Res Ctr Sch Civil & Environm Engn Sydney NSW 2052 Australia;

    Univ New South Wales UNSW Water Res Ctr Sch Civil & Environm Engn Sydney NSW 2052 Australia;

    Univ New South Wales UNSW Water Res Ctr Sch Civil & Environm Engn Sydney NSW 2052 Australia;

    Univ New South Wales UNSW Water Res Ctr Sch Civil & Environm Engn Sydney NSW 2052 Australia;

    Beijing OriginWater Technol Co Ltd Beijing Peoples R China;

    Univ New South Wales UNSW Water Res Ctr Sch Civil & Environm Engn Sydney NSW 2052 Australia;

  • 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

    Catalytic ozonation; Activated carbon; Hydroxyl radicals; Adsorption; Iron oxides;

    机译:催化臭氧化;活性炭;羟基自由基;吸附;氧化铁;

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