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六价铬的单独还原和与还原粘土矿物的联合还原。

Cr(VI) Reduction by Siderophore Alone and in Combination with Reduced Clay Minerals.

机构信息

State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Beijing 100083, China.

School of Water Resources and Environment, China University of Geosciences, Beijing 100083, China.

出版信息

Environ Sci Technol. 2022 Sep 6;56(17):12315-12324. doi: 10.1021/acs.est.2c04104. Epub 2022 Aug 15.

Abstract

Siderophores and iron-containing clays are known to influence the transformation of chromium in the environment. The role of clays in hexavalent chromium [Cr(VI)] reduction has been reported extensively. However, the mechanisms of Cr(VI) reduction by siderophores and their combination with iron-bearing clays are poorly known. Herein, we report the kinetics and products of Cr(VI) reduction by a siderophore alone or in combination with reduced clays. Results showed that Cr(VI) reduction by a tri-hydroxamate siderophore─desferrioxamine B (DFOB)─at a pH of 6 was achieved by one-electron transfer via the formation of Cr(V) intermediate. The formed Cr(V) was further reduced to organically complexed Cr(III). The Cr(VI) reduction rate and extent in the presence of both DFOB and reduced clays unexpectedly decreased relative to that with reduced clays alone, despite both serving as Cr(VI) reductants. The interaction between DFOB and clays (e.g., adsorption/intercalation, dissolution, and/or oxidation) was primarily responsible for Cr(VI) reduction inhibition. The extent of inhibition increased at higher DFOB concentrations in the presence of iron-rich nontronite but decreased in the presence of iron-poor montmorillonite, which may be related to their different Cr(VI) reduction mechanisms. This study highlights the importance of siderophores in chromium transformation and its impact on the reactivity of iron-bearing clays toward heavy metal reduction in the environment.

摘要

铁载体和含铁矿黏土已知会影响环境中铬的转化。黏土在六价铬[Cr(VI)]还原中的作用已被广泛报道。然而,铁载体对 Cr(VI)的还原机制及其与含铁黏土的结合仍知之甚少。在此,我们报告了单独或与还原黏土结合的铁载体还原 Cr(VI)的动力学和产物。结果表明,在 pH 值为 6 时,三羟肟酸盐铁载体—去铁胺 B(DFOB)通过形成 Cr(V)中间产物实现了 Cr(VI)的单电子转移还原。形成的 Cr(V)进一步被还原为有机络合的 Cr(III)。尽管 DFOB 和还原黏土都可以作为 Cr(VI)还原剂,但与单独使用还原黏土相比,在 DFOB 和还原黏土共存的情况下,Cr(VI)还原的速率和程度出人意料地降低了。DFOB 和黏土之间的相互作用(例如,吸附/插层、溶解和/或氧化)主要导致 Cr(VI)还原抑制。在富铁蒙脱石存在的情况下,随着 DFOB 浓度的增加,抑制程度增加,但在贫铁蒙脱石存在的情况下,抑制程度降低,这可能与其不同的 Cr(VI)还原机制有关。本研究强调了铁载体在铬转化中的重要性及其对含铁黏土在环境中重金属还原反应性的影响。

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