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在微生物还原溶解和磁铁矿转化过程中铁氧化物还原性的降低。

Decreases in Iron Oxide Reducibility during Microbial Reductive Dissolution and Transformation of Ferrihydrite.

机构信息

Institute of Biogeochemistry and Pollutant Dynamics , ETH Zürich , 8092 Zürich , Switzerland.

Swiss Federal Institute of Aquatic Science and Technology ( Eawag ), 8600 Dübendorf , Switzerland.

出版信息

Environ Sci Technol. 2019 Aug 6;53(15):8736-8746. doi: 10.1021/acs.est.9b01299. Epub 2019 Jul 24.

Abstract

Ferrous iron formed during microbial ferric iron reduction induces phase transformations of poorly crystalline into more crystalline and thermodynamically more stable iron (oxyhydr)oxides. Yet, characterizing the resulting decreases in the reactivity of the remaining oxide ferric iron toward reduction (i.e., its reducibility) has been challenging. Here, we used the reduction of six-line ferrihydrite by MR-1 as a model system to demonstrate that mediated electrochemical reduction (MER) allows directly following decreases in oxide ferric iron reducibility during the transformation of ferrihydrite into goethite and magnetite which we characterized by X-ray diffraction analysis and transmission electron microscopy imaging. Ferrihydrite was fully reducible in MER at both pH of 5.0 and 7.5. Decreases in iron oxide reducibility associated with ferrihydrite transformation into magnetite were accessible at both pH because the formed magnetite was not reducible under either of these conditions. Conversely, decreases in iron oxide reducibility associated with goethite formation were apparent only at the highest tested pH of 7.5 and thus the thermodynamically least favorable conditions for iron oxide reductive dissolution. The unique capability to adjust the thermodynamic boundary conditions in MER to the specific reducibilities of individual iron (oxyhydr)oxides makes this electrochemical approach broadly applicable for studying changes in iron oxide reducibility in heterogeneous environmental samples such as soils and sediments.

摘要

亚铁在微生物铁还原过程中形成,会诱导非晶态向更具结晶度和热力学更稳定的铁(氧)氢氧化物的相变。然而,表征剩余氧化物铁在还原(即可还原性)方面的反应性降低一直具有挑战性。在这里,我们使用 MR-1 还原六线水铁矿作为模型系统,证明介导的电化学还原(MER)允许直接跟踪在水铁矿向针铁矿和磁铁矿转化过程中氧化物铁可还原性的降低,我们通过 X 射线衍射分析和透射电子显微镜成像对其进行了表征。在 pH 值为 5.0 和 7.5 的 MER 中,水铁矿完全可还原。与水铁矿向磁铁矿转化相关的氧化铁可还原性降低在两种条件下都可获得,因为形成的磁铁矿在这两种条件下都不可还原。相反,与针铁矿形成相关的氧化铁可还原性降低仅在测试的最高 pH 值 7.5 时明显,因此是氧化铁还原溶解的热力学最不利条件。MER 中调整热力学边界条件以适应单个铁(氧)氢氧化物特定可还原性的独特能力,使这种电化学方法广泛适用于研究土壤和沉积物等非均相环境样品中氧化铁可还原性的变化。

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