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Investigation of uranium oxide hydrates with barium(ıı) ions: structural diversity, uranium valences and implications

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    SYSNO ASEP0574228
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleInvestigation of uranium oxide hydrates with barium(ıı) ions: structural diversity, uranium valences and implications
    Author(s) Lu, K.T. (AU)
    Zhang, Y. (AU)
    Wei, T. (AU)
    Ablott, T.A. (AU)
    Plášil, Jakub (FZU-D) RID, ORCID
    Karatchevtseva, I. (AU)
    Zheng, R. (AU)
    Number of authors7
    Source TitleNew Journal of Chemistry. - : Royal Society of Chemistry - ISSN 1144-0546
    Roč. 47, č. 28 (2023), s. 13286-13296
    Number of pages11 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsBarium(II) ions ; Uranium oxides ; natural weathering ; x-ray diffraction ; crystal structure
    Subject RIVDB - Geology ; Mineralogy
    OECD categoryMineralogy
    Method of publishingOpen access
    Institutional supportFZU-D - RVO:68378271
    UT WOS001021060400001
    EID SCOPUS85166291985
    DOI10.1039/d3nj01334k
    AnnotationAlthough barium(II) ions play an important role in the natural weathering of the mineral uraninite (UO2+x) and are expected to therefore do the same for spent nuclear fuel in geological disposal, the detailed structural understanding of this role is rather limited. In this work, we report the synthesis and characterisation of two new uranium oxide hydrate (UOH) phases with barium(II) ions, a layer-structured UOH-Ba1 constructed with undulating uranyl oxide hydroxide layers incorporating hydrated interlayer barium(II) ions, and UOH-Ba2 forming a complex three-dimensional structure by linking six different types of uranium polyhedrons with barium(II) ions located in the narrow channels. Both crystal structures were revealed using synchrotron single crystal X-ray diffraction and confirmed with powder X-ray or electron diffractions.
    WorkplaceInstitute of Physics
    ContactKristina Potocká, potocka@fzu.cz, Tel.: 220 318 579
    Year of Publishing2024
    Electronic addresshttps://hdl.handle.net/11104/0344570
Number of the records: 1  

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