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协同转化受六价铬-亚硫酸盐反应驱动的多种污染物。

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

机构信息

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.

出版信息

Environ Sci Technol. 2015 Oct 20;49(20):12363-71. doi: 10.1021/acs.est.5b03275. Epub 2015 Sep 29.

Abstract

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(VI)-sulfite system. Both (•)OH and SO4(•-) 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)-H2O2 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 SO2 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.

摘要

将六价铬(Cr(VI))还原通常被认为是解毒铬污染物所必需的;然而,很少有研究利用该反应来处理其他工业废水。在这里,我们将广泛使用的 Cr(VI)-亚硫酸盐反应系统进行升级,以同时转化多种污染物,即在酸性溶液中还原 Cr(VI)、氧化亚硫酸盐和其他有机/无机污染物。选择 As(III)作为探针污染物来考察 Cr(VI)-亚硫酸盐系统的氧化能力。基于电子顺磁共振、荧光光谱和特定自由基猝灭的结果,认为(•)OH 和 SO4(•-)是 As(III)氧化的主要氧化剂。As(III)-清除剂和氧化自由基大大加速了 Cr(VI)的还原,同时消耗了较少的亚硫酸盐。与 50 μM Cr(VI)的 Cr(VI)-H2O2 体系相比,在 pH 3.5 时,亚硫酸盐体系在 As(III)氧化和 Cr(VI)还原方面具有出色的性能。此外,在这个升级过程中,与传统的亚硫酸盐还原 Cr(VI)过程相比,还原 Cr(VI)所需的亚硫酸盐更少。这有效地提高了这种 Cr(VI)解毒过程的环境相容性,减轻了水中 SO2 释放和硫酸盐离子生成的潜在风险。总的来说,本研究为多种工业污染物解毒的“以废治废”策略提供了一个极好的范例。

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