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The reduction of 4-chloronitrobenzene by Fe(II)-Fe(III) oxide systems - correlations with reduction potential and inhibition by silicate

机译:Fe(II)-Fe(III)氧化物体系还原4-氯硝基苯-与还原电位和硅酸盐抑制作用的关系

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摘要

Recent studies have demonstrated that the rate at which Fe(II)-Fe(III) oxyhydroxide systems catalyze the reduction of reducible contaminants, such as 4-chloronitrobenzene, is well correlated to their thermodynamic reduction potential. Here we confirm this effect in the presence of Fe(III) oxyhydroxide phases not previously assessed, namely ferrihydrite and nano-goethite, as well as Fe(III) oxyhydroxide phases previously examined. In addition, silicate is found to decrease the extent of Fe(II) sorption to the Fe(III) oxyhydroxide surface, increasing the reduction potential of the Fe(II)-Fe(III) oxyhydroxide suspension and, accordingly, decreasing the rate of 4-chloronitrobenzene reduction. A linear relationship between the reduction potential of the Fe(II)-Fe(III) oxyhydroxide suspensions and the reduction rate of 4-chloronitrobenzene (normalized to surface area and concentration of sorbed Fe(II)) was obtained in the presence and absence of silicate. However, when ferrihydrite was doped with Si (through co-precipitation) the reduction of 4-chloronitrobenzene was much slower than predicted from its reduction potential. The results obtained have significant implications to the likely effectiveness of naturally occurring contaminant degradation processes involving Fe(II) and Fe(III) oxyhydroxides in groundwater environments containing high concentrations of silicate, or other species which compete with Fe(II) for sorption sites. (C) 2016 Elsevier B.V. All rights reserved.
机译:最近的研究表明,Fe(II)-Fe(III)羟基氧化体系催化还原可还原污染物(例如4-氯硝基苯)的速率与它们的热力学还原潜力密切相关。在这里,我们在存在先前未评估的Fe(III)羟基氧化物相(即亚铁酸盐和纳米针铁矿)以及先前已检查的Fe(III)羟基氧化物相的存在下证实了这种效果。此外,发现硅酸盐减少了Fe(II)吸附到羟基氢氧化Fe(III)的程度,增加了Fe(II)-Fe(III)羟基氢氧化物悬浮液的还原电位,因此降低了还原4-氯硝基苯。在存在和不存在以下条件下,获得了Fe(II)-Fe(III)羟基氧化物悬浮液的还原电位与4-氯硝基苯的还原速率(相对于表面积和吸附的Fe(II)的浓度标准化)之间的线性关系。硅酸盐。但是,当水铁矿中掺有Si(通过共沉淀)时,4-氯硝基苯的还原要慢于其还原电位所预测的速度。获得的结果对于在含有高浓度硅酸盐的地下水环境中或与Fe(II)竞争吸附位点的其他地下水环境中涉及Fe(II)和Fe(III)羟基氧化物的天然污染物降解过程的可能有效性具有重大意义。 (C)2016 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Journal of Hazardous Materials》 |2016年第15期|143-149|共7页
  • 作者单位

    UNSW Australia, Sch Civil & Environm Engn, UNSW Water Res Ctr, Sydney, NSW 2052, Australia;

    UNSW Australia, Sch Civil & Environm Engn, UNSW Water Res Ctr, Sydney, NSW 2052, Australia;

    UNSW Australia, Sch Civil & Environm Engn, UNSW Water Res Ctr, Sydney, NSW 2052, Australia;

    UNSW Australia, Sch Civil & Environm Engn, UNSW Water Res Ctr, Sydney, NSW 2052, Australia;

  • 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

    Reduction kinetics; Mediated electrochemistry; Redox potential; Contaminant degradation;

    机译:还原动力学;介电电化学;氧化还原电势;污染物降解;
  • 入库时间 2022-08-17 13:22:15

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