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三种植晶度差的二氧化锰(IV)对三价铬的氧化作用。2. 固相分析。

Chromium(III) oxidation by three poorly crystalline manganese(IV) oxides. 2. Solid phase analyses.

机构信息

Plant and Soil Sciences Department, Delaware Environmental Institute, University of Delaware, 152 Townsend Hall, Newark, Delaware 19716, USA.

出版信息

Environ Sci Technol. 2012 Nov 6;46(21):11601-9. doi: 10.1021/es302384q. Epub 2012 Oct 19.

DOI:10.1021/es302384q
PMID:23050862
Abstract

Layered, poorly crystalline Mn(IV)O(2) phases are abundant in the environment. These mineral phases may rapidly oxidize Cr(III) to more mobile and toxic Cr(VI) in soils. There is still, however, little knowledge of how Cr(III) oxidation by Mn(IV)O(2) proceeds at the microscopic and molecular levels. Therefore, the sorption mechanisms of Cr(III) and Cr(VI) on Random Stacked Birnessite (RSB), δ-MnO(2), and Acid Birnessite (AB) were determined by Extended X-ray Absorption Fine Structure Spectroscopy (EXAFS). These three synthetic Mn(IV)O(2), which are poorly crystalline phases and have layered structures, were reacted with 50 mM Cr(III) at pH 2.5, 3, and 3.5 before being analyzed by EXAFS. The results indicated that Cr(VI) was loosely sorbed as an outer-sphere complex on Mn(IV)O(2), while Cr(III) was tightly sorbed as an inner-sphere complex. Further research is needed to understand why Cr(III) stopped being significantly oxidized by Mn(IV)O(2) after 30 min. This study, however, demonstrated that the formation of a Cr surface precipitate is not necessarily responsible for the cessation in Cr(III) oxidation. Indeed, no Cr surface precipitate was detected at the microscopic and molecular levels on Mn(IV)O(2) surfaces reacted with Cr(III) for 1 h, although the Cr(III) oxidation ceased before 1 h of reaction at most employed experimental conditions.

摘要

层状、结晶度差的 Mn(IV)O(2) 相在环境中大量存在。这些矿物相可能会在土壤中迅速将 Cr(III)氧化为更具移动性和毒性的 Cr(VI)。然而,对于 Mn(IV)O(2 在微观和分子水平上氧化 Cr(III)的过程,我们仍然知之甚少。因此,通过扩展 X 射线吸收精细结构光谱 (EXAFS) 确定了 Cr(III)和 Cr(VI)在随机堆积的锰矿 (RSB)、δ-MnO(2) 和酸性锰矿 (AB)上的吸附机制。这三种合成的 Mn(IV)O(2) 是结晶度差的层状结构,在 pH 2.5、3 和 3.5 下与 50 mM Cr(III)反应,然后通过 EXAFS 进行分析。结果表明,Cr(VI)以外部配位络合物的形式松散地吸附在 Mn(IV)O(2)上,而 Cr(III)则以内部配位络合物的形式紧密地吸附在 Mn(IV)O(2)上。需要进一步研究为什么 Cr(III)在 30 分钟后不再被 Mn(IV)O(2)显著氧化。然而,本研究表明,Cr 表面沉淀的形成不一定是 Cr(III)氧化停止的原因。事实上,在 Mn(IV)O(2)表面与 Cr(III)反应 1 小时后,在微观和分子水平上都没有检测到 Cr 表面沉淀,尽管在大多数实验条件下,反应不到 1 小时就停止了 Cr(III)的氧化。

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