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Experimentally determined uranium isotope Fractionation during reduction of hexavalent U by bacteria and zero valent iron

机译:实验确定的细菌和零价铁还原六价铀过程中的铀同位素分馏

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摘要

Variations in stable isotope ratios of redox sensitive elements are often used to understand redox processes occurring near the Earth's surface. Presented here are measurements of mass-dependent U isotope fractionation induced by U(VI) reduction by zerovalent iron (Fe-0) and bacteria under controlled pH and HCO3- conditions. In abiotic experiments, Fe-0 reduced U(VI), but the reaction failed to induce an analytically significant isotopic fractionation. Bacterial reduction experiments using Geobacter sulfurreducens and Anaeromyxobacter dehalogenans reduced dissolved U(VI) and caused enrichment of U-238 relative to U-235 in the remaining U(VI). Enrichment factors (epsilon) calculated using a Rayleigh distillation model are -0.31 parts per thousand and -0.34 parts per thousand for G. sulfurreducens and A. dehalogenans, respectively, under identical experimental conditions. Further studies are required to determine the range of possible values for U-238/U-235 fractionation factors under a variety of experimental conditions before broad application of these results is possible. However, the measurable variations in delta U-238 show promise as indicators of reduction for future studies of groundwater contamination, geochronology, U ore deposit formation, and U biogeochemical cycling.
机译:氧化还原敏感元素的稳定同位素比率的变化通常用于了解地球表面附近发生的氧化还原过程。此处介绍的是在受控pH和HCO3-条件下,零价铁(Fe-0)和细菌对U(VI)还原引起的质量依赖性U同位素分级的测量。在非生物实验中,Fe-0还原了U(VI),但该反应未能诱导出具有分析意义的同位素分馏。细菌还原实验使用地球还原菌硫还原菌和脱氧厌氧杆菌减少了溶解的U(VI)并导致U-238在剩余的U(VI)中相对于U-235富集。在相同的实验条件下,使用瑞利(Rayleigh)蒸馏模型计算的富集因子(ε)分别为-0.31份和-0.34份。在可能广泛应用这些结果之前,需要进一步的研究来确定各种实验条件下U-238 / U-235分馏因子的可能值范围。但是,三角洲U-238的可测量变化显示出有望作为减少地下水污染,地质年代,铀矿床形成和铀生物地球化学循环研究的指标。

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