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Surface-Mediated Formation of Pu(Ⅳ) Nanoparticles at the Muscovite-Electrolyte Interface

机译:白云母-电解质界面的Pu(Ⅳ)纳米粒子的表面介导形成

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摘要

The formation of Pu(Ⅳ)-oxo-nanoparticles from Pu(Ⅲ) solutions by a surface-enhanced redox/polymerization reaction at the muscovite (001) basal plane is reported, with a continuous increase in plutonium coverage observed in situ over several hours. The sorbed Pu extends >70 A from the surface with a maximum concentration at 10.5 A and a total coverage of >9 Pu atoms per unit cell area of muscovite (0.77 μg Pu/cm~2) (determined independently by in situ resonant anomalous X-ray reflectivity and by ex-situ alpha-spectrometry). The presence of discrete nanoparticles is confirmed by high resolution atomic force microscopy. We propose that the formation of these Pu(Ⅳ) nanoparticles from an otherwise stable Pu(Ⅲ) solution can be explained by the combination of a highly concentrated interfacial Pu-ion species, the Pu(Ⅲ)- Pu(Ⅳ) redox equilibrium, and the strong proclivity of tetravalent Pu to hydrolyze and form polymeric species. These results are the first direct observation of such behavior of plutonium on a naturally occurring mineral, providing insights into understanding the environmental transport of plutonium and other contaminants capable of similar redox/polymerization reactions.
机译:据报道,在白云母(001)基面上通过表面增强的氧化还原/聚合反应从Pu(Ⅲ)溶液中形成了Pu(Ⅳ)-氧纳米颗粒,并且在数小时内就地观察到p的覆盖率不断增加。 。被吸附的Pu从表面延伸> 70 A,最大浓度为10.5 A,白云母的每晶胞面积总覆盖率> 9 Pu原子(0.77μgPu / cm〜2)(由原位共振异常X独立确定)射线反射率和非原位阿尔法光谱)。高分辨率原子力显微镜证实了离散纳米颗粒的存在。我们认为,可以通过高浓度的界面-离子物种,Pu(Ⅲ)-Pu(Ⅳ)氧化还原平衡的组合来解释从其他方式稳定的Pu(Ⅲ)溶液中形成这些Pu(Ⅳ)纳米颗粒。四价Pu具有很强的水解和形成聚合物种类的倾向。这些结果是对such在天然矿物上的这种行为的首次直接观察,为理解understanding和其他能够进行类似氧化还原/聚合反应的污染物的环境迁移提供了见识。

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  • 来源
    《Environmental Science & Technology》 |2013年第24期|14178-14184|共7页
  • 作者单位

    Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, United States,Institute of Resource Ecology, Helmholtzzentrum Dresden-Rossendorf, P.O. Box 510119, 01314 Dresden, Germany;

    Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, United States;

    Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, United States;

    Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, United States;

    Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, United States;

    Center for Advanced Radiation Sources, University of Chicago, Chicago, Illinois 60637, United States;

    Center for Advanced Radiation Sources, University of Chicago, Chicago, Illinois 60637, United States;

    Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, United States;

    Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, United States;

  • 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);
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