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亚铁诱导针铁矿有机矿物转化过程中铬和碳的行为和归宿。

Behavior and Fate of Chromium and Carbon during Fe(II)-Induced Transformation of Ferrihydrite Organominerals.

机构信息

State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012, China.

School of Earth & Environment, University of Leeds, Leeds LS2 9JT, U.K.

出版信息

Environ Sci Technol. 2023 Nov 14;57(45):17501-17510. doi: 10.1021/acs.est.3c05487. Epub 2023 Nov 3.

Abstract

The mobility of chromium (Cr) is controlled by minerals, especially iron (oxyhydr)oxides. The influence of organic carbon (OC) on the mobility and fate of Cr(VI) during Fe(II)-induced transformation of iron (oxyhydr)oxide, however, is still unclear. We investigate how low-weight carboxyl-rich OC influences the transformation of ferrihydrite (Fh) and controls the mobility of Cr(VI/III) in reducing environments and how Cr influences the formation of secondary Fe minerals and the stabilization of OC. With respect to the transformation of Fe minerals, the presence of low-weight carboxyl-rich OC retards the growth of goethite crystals and stabilizes lepidocrocite for a longer time. With respect to the mobility of Cr, low-weight carboxyl-rich OC suppresses the Cr(III) associated with Fe minerals, and this suppression is enhanced with increasing carboxyl-richness of OC and decreasing pH. The presence of Cr(III) mitigates the decrease in total C associated with Fe minerals and increases the C especially for Fh organominerals made with carboxyl-rich OC. Our study sheds new light on the mobility and fate of Cr in reducing environments and suggests that there is a potential synergy between Cr(VI) remediation and OC stabilization.

摘要

铬(Cr)的迁移性受矿物的控制,特别是铁(氧)氢氧化物。然而,有机碳(OC)对 Fe(II)诱导的铁(氧)氢氧化物转化过程中 Cr(VI)的迁移性和归宿的影响尚不清楚。我们研究了低分子量富含羧基的 OC 如何影响 Fh 的转化并控制还原环境中 Cr(VI/III)的迁移性,以及 Cr 如何影响次生铁矿物的形成和 OC 的稳定。就 Fe 矿物的转化而言,低分子量富含羧基的 OC 会延迟针铁矿晶体的生长,并使纤铁矿更长时间保持稳定。就 Cr 的迁移性而言,低分子量富含羧基的 OC 会抑制与 Fe 矿物结合的 Cr(III),并且这种抑制作用随着 OC 中羧基含量的增加和 pH 值的降低而增强。Cr(III)的存在减轻了与 Fe 矿物结合的总 C 的减少,并增加了 C 的含量,特别是对于使用富含羧基的 OC 形成的 Fh 有机矿物。我们的研究为还原环境中 Cr 的迁移性和归宿提供了新的认识,并表明 Cr(VI)修复和 OC 稳定之间存在潜在的协同作用。

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