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生物成因的磁黄铁矿对 U(VI)的非生物还原性固定。

Abiotic reductive immobilization of U(VI) by biogenic mackinawite.

机构信息

Department of Geosciences, Virginia Tech , Blacksburg, Virginia, United States.

出版信息

Environ Sci Technol. 2013 Mar 5;47(5):2361-9. doi: 10.1021/es304025x. Epub 2013 Feb 20.

Abstract

During subsurface bioremediation of uranium-contaminated sites, indigenous metal and sulfate-reducing bacteria may utilize a variety of electron acceptors, including ferric iron and sulfate that could lead to the formation of various biogenic minerals in situ. Sulfides, as well as structural and adsorbed Fe(II) associated with biogenic Fe(II)-sulfide phases, can potentially catalyze abiotic U(VI) reduction via direct electron transfer processes. In the present work, the propensity of biogenic mackinawite (Fe 1+x S, x = 0 to 0.11) to reduce U(VI) abiotically was investigated. The biogenic mackinawite produced by Shewanella putrefaciens strain CN32 was characterized by employing a suite of analytical techniques including TEM, SEM, XAS, and Mössbauer analyses. Nanoscale and bulk analyses (microscopic and spectroscopic techniques, respectively) of biogenic mackinawite after exposure to U(VI) indicate the formation of nanoparticulate UO2. This study suggests the relevance of sulfide-bearing biogenic minerals in mediating abiotic U(VI) reduction, an alternative pathway in addition to direct enzymatic U(VI) reduction.

摘要

在铀污染场地的地下生物修复过程中,土著金属和硫酸盐还原菌可能会利用多种电子受体,包括三价铁和硫酸盐,这可能导致各种生物成因矿物在原地形成。硫化物以及与生物成因 Fe(II)-硫化物相相关的结构和吸附态 Fe(II),可以通过直接电子转移过程潜在地催化非生物 U(VI)还原。在本工作中,研究了生物成因的磁黄铁矿(Fe 1+x S,x = 0 至 0.11)非生物还原 U(VI)的倾向。使用一系列分析技术,包括 TEM、SEM、XAS 和 Mössbauer 分析,对 Shewanella putrefaciens 菌株 CN32 产生的生物成因磁黄铁矿进行了表征。暴露于 U(VI)后的生物成因磁黄铁矿的纳米级和体相分析(分别为微观和光谱技术)表明形成了纳米颗粒 UO2。这项研究表明,含硫的生物成因矿物在介导非生物 U(VI)还原方面具有重要意义,这是除直接酶促 U(VI)还原之外的另一种途径。

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