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Microbial mobilization of plutonium and other actinides from contaminated soil

机译:微生物从污染土壤中迁移ton和其他act系元素

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We examined the dissolution of Pu, U, and Am in contaminated soil from the Nevada Test Site (NTS) due to indigenous microbial activity. Scanning transmission x-ray microscopy (STXM) analysis of the soil showed that Pu was present in its polymeric form and associated with Fe- and Mn- oxides and aluminosilicates. Uranium analysis by x-ray diffraction (mu-XRD) revealed discrete U-containing mineral phases, viz., schoepite, sharpite, and liebigite; synchrotron x-ray fluorescence (mu-XRF) mapping showed its association with Fe- and Ca-phases; and mu-x-ray absorption near edge structure (mu-XANES) confirmed U(IV) and U(VI) oxidation states. Addition of citric acid or glucose to the soil and incubated under aerobic or anaerobic conditions enhanced indigenous microbial activity and the dissolution of Pu. Detectable amount of Am and no U was observed in solution. In the citric acid-amended sample, Pu concentration increased with time and decreased to below detection levels when the citric acid was completely consumed. In contrast, with glucose amendment, Pu remained in solution. Pu speciation studies suggest that it exists in mixed oxidation states (III/IV) in a polymeric form as colloids. Although Pu(IV) is the most prevalent and generally considered to be more stable chemical form in the environment, our findings suggest that under the appropriate conditions, microbial activity could affect its solubility and long-term stability in contaminated environments. (C) 2015 Elsevier Ltd. All rights reserved.
机译:我们检查了由于内在微生物活动导致内华达州测试点(NTS)污染的土壤中Pu,U和Am的溶解情况。对土壤的扫描透射X射线显微镜(STXM)分析表明,Pu以其聚合物形式存在,并与Fe和Mn-氧化物和铝硅酸盐有关。通过X射线衍射(mu-XRD)进行的铀分析显示出离散的含U矿物相,即闪锌矿,尖晶石和褐铁矿。同步加速器的X射线荧光(mu-XRF)作图表明其与Fe和Ca相有关。和在边缘结构附近的mu-x射线吸收(mu-XANES)证实了U(IV)和U(VI)的氧化态。向土壤中添加柠檬酸或葡萄糖,并在需氧或厌氧条件下孵育可增强原生微生物活性和Pu的溶出度。在溶液中可检测到的Am量没有U。在柠檬酸修饰的样品中,当柠檬酸被完全消耗时,Pu浓度会随时间增加而降低到检测水平以下。相反,通过葡萄糖修正,Pu保留在溶液中。 Pu形态研究表明,它以胶体形式以聚合物形式存在于混合氧化态(III / IV)中。尽管Pu(IV)是环境中最普遍的化合物,并且通常被认为是更稳定的化学形式,但我们的发现表明,在适当的条件下,微生物活性可能会影响其在污染环境中的溶解度和长期稳定性。 (C)2015 Elsevier Ltd.保留所有权利。

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