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Effect of Mn(ll) on the Structure and Reactivity of Biogenic Uraninite

机译:Mn(ll)对生物铀铀矿结构和反应活性的影响

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摘要

The efficacy of a site remediation strategy involving the stimulation of microbial U(VI) reduction hinges in part upon the long-term stability of the product biogenic uraninite, toward environmental oxidants. Geological sedimentary uraninites (nominal formula UO_2) reportedly contain abundant cation impurities that enhance their resistance to oxidation. By analogy, incorporation of common groundwater solutes into biogenic uraninite could also impart stability-enhancing properties. Mn(II) is a common groundwater cation, which has a favorable ionic radius for substitution reactions. The structure and reactivity of Mn(II)-reacted biogenic uraninite are investigated in this study. Up to4.4 weight percent Mn(II) was found to be structurally bound in biogenic uraninite. This Mn(II) incorporation was associated with decreasing uraninite particle size and structural order. Importantly, the equilibrium solubility of Mn-reacted uraninite was halved relative to unreacted uraninite, demonstrating changes in thermodynamic properties, while the dissolution rate was up to 38-fold lower than that of unreacted biogenic uraninite. We conclude that structural incorporation of Mn(II)into uraninite has an important stabilizing effect, leading to the prediction that other groundwater solutes may similarly stabilize biogenic uraninite.
机译:涉及刺激微生物U(VI)还原的现场修复策略的功效部分取决于产品生物成尿素对环境氧化剂的长期稳定性。据报道,地质沉积的尿素矿(标称式为UO_2)含有丰富的阳离子杂质,可增强其抗氧化性。以此类推,将常见的地下水溶质掺入生物尿素中也可以提高稳定性。 Mn(II)是一种常见的地下水阳离子,对于取代反应而言,它具有良好的离子半径。在这项研究中,研究了锰(Ⅱ)反应的生物型铀矿的结构和反应性。发现高达4.4重量百分比的Mn(II)在生物尿素中被结构结合。 Mn(II)的掺入与减少的尿素矿粒度和结构顺序有关。重要的是,相对于未反应的尿素,Mn反应的尿素的平衡溶解度降低了一半,这说明了热力学性质的变化,而溶出速率却比未反应的生物尿素低了38倍。我们得出的结论是,Mn(II)掺入尿素石中具有重要的稳定作用,从而导致预测其他地下水溶质可能同样稳定了生物尿素。

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  • 来源
    《Environmental Science & Technology》 |2009年第17期|6541-6547|共7页
  • 作者单位

    Environmental Microbiology Laboratory, Ecole Polytechnique Federate de Lausanne, Lausanne, CH 1015, Switzerland;

    Stanford Synchrotron Radiation Lightsource, 2575 Sand Hill Rd., Menlo Park, California 94025;

    Environmental Science and Engineering Division, Colorado School of Mines, 1500 Illinois St., Golden, Colorado 80401 Environmental Microbiology Laboratory, Ecole Polytechnique Federate de Lausanne, Lausanne, CH 1015, Switzerland;

    Environmental Microbiology Laboratory, Ecole Polytechnique Federate de Lausanne, Lausanne, CH 1015, Switzerland;

    Department of Energy, Environmental and Chemical Engineering Washington University, One Brookings Drive, St. Louis, Missouri 63130;

    Stanford Synchrotron Radiation Lightsource, 2575 Sand Hill Rd., Menlo Park, California 94025;

    Department of Energy, Environmental and Chemical Engineering Washington University, One Brookings Drive, St. Louis, Missouri 63130;

    Stanford Synchrotron Radiation Lightsource, 2575 Sand Hill Rd., Menlo Park, California 94025;

    Environmental Microbiology Laboratory, Ecole Polytechnique Federate de Lausanne, Lausanne, CH 1015, Switzerland;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-17 14:04:48

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