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Synergetic Transformations of Multiple Pollutants Driven by Cr(Ⅵ)-Sulfite Reactions

机译:Cr(Ⅵ)-亚硫酸盐反应驱动的多种污染物的协同转化

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摘要

Reduction of Cr(Ⅵ) is often deemed necessary to detoxify chromium contaminants; however, few investigations utilized this reaction for the purpose of treating other industrial wastewaters. Here a widely used Cr(Ⅵ)-sulfite reaction system was upgraded to simultaneously transform multiple pollutants, namely, the reduction of Cr(Ⅵ) and oxidation of sulfite and other organic/inorganic pollutants in an acidic solution. As(Ⅲ) was selected as a probe pollutant to examine the oxidation capacity of a Cr(Ⅲ)-sulfite system. Both ~·OH and SO_4~(·-) were considered as the primary oxidants for As(Ⅲ) oxidation, based on the results of electron spin resonance, fluorescence spectroscopy, and specific radicals quenching. As (Ⅲ)-scavenging, oxidative radicals greatly accelerated Cr(Ⅵ) reduction and simultaneously consumed less sulfite. In comparison with a Cr(Ⅵ)-H_2O_2 system with 50 μM Cr(Ⅵ), Cr(Ⅵ), the sulfite system had excellent performance for both As(Ⅲ) oxidation and Cr(Ⅵ) reduction at pH 3.5. Moreover, in this escalated process, less sulfite was required to reduce Cr(Ⅵ) than the traditional Cr(Ⅵ) reduction by sulfite process. This effectively improves the environmental compatibility of this Cr(Ⅵ) detoxification process, alleviating the potential for SO_2 release and sulfate ion production in water. Generally, this study provides an excellent example of a "waste control by waste" strategy for the detoxification of multiple industrial pollutants.
机译:通常认为还原Cr(Ⅵ)可以使铬污染物解毒。但是,很少有研究将这种反应用于处理其他工业废水。在此升级了广泛使用的Cr(Ⅵ)-亚硫酸盐反应系统,以同时转化多种污染物,即在酸性溶液中还原Cr(Ⅵ)以及亚硫酸盐和其他有机/无机污染物的氧化。选择砷(Ⅲ)作为探针污染物,考察了Cr(Ⅲ)-亚硫酸盐体系的氧化能力。根据电子自旋共振,荧光光谱和特定自由基猝灭的结果,〜·OH和SO_4〜(·-)均被认为是As(Ⅲ)氧化的主要氧化剂。由于清除了(Ⅲ),氧化自由基极大地促进了Cr(Ⅵ)的还原,同时消耗了较少的亚硫酸盐。与具有50μMCr(Ⅵ),Cr(Ⅵ)的Cr(Ⅵ)-H_2O_2体系相比,亚硫酸盐体系在pH 3.5时具有良好的As(Ⅲ)氧化和Cr(Ⅵ)还原性能。此外,在该逐步升级的方法中,与传统的亚硫酸盐法还原Cr(Ⅵ)相比,还原Cr(Ⅵ)所需的亚硫酸盐更少。这有效地改善了这种Cr(Ⅵ)脱毒工艺的环境相容性,减轻了水中SO_2释放和产生硫酸根离子的可能性。通常,该研究为多种工业污染物的排毒提供了“废物控制废物”策略的极好例子。

著录项

  • 来源
    《Environmental Science & Technology》 |2015年第20期|12363-12371|共9页
  • 作者单位

    State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong, P.R. China,School of Environmental and Municipal Engineering, Qingdao University of Technology, Qingdao 266033, China;

    State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong, P.R. China;

    State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong, P.R. China;

    State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong, P.R. China;

    College of Environmental Science and Engineering, Donghua University, Shanghai, 201620, China,Southern Cross GeoScience, Southern Cross University, Lismore, NSW 2480, Australia;

    State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong, P.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);
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  • 正文语种 eng
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