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六价铬在自然结构土壤和沉积物中的生成。

Hexavalent Chromium Generation within Naturally Structured Soils and Sediments.

机构信息

Earth System Science Department, Stanford University , Stanford, California 94305, United States.

出版信息

Environ Sci Technol. 2017 Feb 21;51(4):2058-2067. doi: 10.1021/acs.est.6b04039. Epub 2017 Feb 7.

DOI:10.1021/acs.est.6b04039
PMID:28084730
Abstract

Chromium(VI) produced from the oxidation of indigenous Cr(III) minerals is increasingly being recognized as a threat to groundwater quality. A critical determinant of Cr(VI) generation within soils and sediments is the necessary interaction of two low-solubility phases-Cr(III) silicates or (hydr)oxides and Mn(III/IV) oxides-that lead to its production. Here we investigate the potential for Cr(III) oxidation by Mn oxides within fixed solid matrices common to soils and sediments. Artificial aggregates were constructed from Cr(OH)- and CrFe(OH)-coated quartz grains and either mixed with synthetic birnessite or inoculated with the Mn(II)-oxidizing bacterium Leptothrix cholodnii. In aggregates simulating low organic carbon environments, we observe Cr(VI) concentrations within advecting solutes at levels more than twenty-times the California drinking water standard. Chromium(VI) production is highly dependent on Cr-mineral solubility; increasing Fe-substitution (x = 0 to x = 0.75) decreases the solubility of the solid and concomitantly decreases total Cr(VI) generation by 37%. In environments with high organic carbon, reducing conditions within aggregate cores (microbially) generate sufficient Fe(II) to suppress Cr(VI) efflux. Our results illustrate Cr(VI) generation from reaction with Mn oxides within structured media simulating soils and sediments and provide insight into how fluctuating hydrologic and redox conditions impact coupled processes controlling Cr and Mn cycling.

摘要

六价铬(Cr(VI))是由原生 Cr(III) 矿物氧化产生的,它对地下水质量的威胁日益受到关注。在土壤和沉积物中生成 Cr(VI) 的关键决定因素是两种低溶解度相——Cr(III)硅酸盐或(水合)氧化物和 Mn(III/IV)氧化物——之间必要的相互作用,这导致了 Cr(VI)的生成。在这里,我们研究了 Mn 氧化物在土壤和沉积物中常见的固定固体基质中氧化 Cr(III)的潜力。人工聚集体由 Cr(OH)-和 CrFe(OH)-涂层的石英颗粒构建而成,要么与合成的水钠锰矿混合,要么接种 Mn(II)氧化细菌 Leptothrix cholodnii。在模拟低有机碳环境的聚集体中,我们观察到在运移溶质中 Cr(VI)的浓度达到了加利福尼亚饮用水标准的二十多倍。Cr(VI)的生成高度依赖于 Cr 矿物的溶解度;增加 Fe 取代(x = 0 至 x = 0.75)会降低固体的溶解度,同时将总 Cr(VI)生成量降低 37%。在高有机碳环境中,聚集体核心(微生物)内的还原条件会产生足够的 Fe(II)来抑制 Cr(VI)的流出。我们的结果说明了在模拟土壤和沉积物的结构化介质中与 Mn 氧化物反应生成 Cr(VI)的情况,并深入了解了水文学和氧化还原条件的波动如何影响控制 Cr 和 Mn 循环的耦合过程。

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