Surface alteration evidence for a mechanism of anoxic dissolution of UO2
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Authors
Popel, AJ
Beng Thye, Tan
Thomas, Gouder
Giulio, Lampronti
Jason, Day
Rachel, Eloirdi
Alice, Seibert
Ian, Farnan
Publication Date
2019-01-15Journal Title
Applied Surface Science
ISSN
0169-4332
Publisher
Elsevier
Volume
464
Pages
376-379
Type
Article
Metadata
Show full item recordCitation
Popel, A., Beng Thye, T., Thomas, G., Giulio, L., Jason, D., Rachel, E., Alice, S., & et al. (2019). Surface alteration evidence for a mechanism of anoxic dissolution of UO2. Applied Surface Science, 464 376-379. https://doi.org/10.1016/j.apsusc.2018.09.094
Abstract
A secondary phase has been observed to nucleate on the surface of UO2 in a solution with uranium concentration values of ~10-9 mol/l. The UO2 was in the form of a 100 nm single crystalline film of UO2 epitaxially deposited on the (001) surface of a single crystalline silicon substrate. An extended (140 days) dissolution experiment with UO2 in contact with a solution in deoxygenated, deionised water, under an Ar atmosphere (~0.1 O2 ppm) at ambient temperature (~25 °C) suggests that uranium dioxide should dissolve and precipitate while remaining in the U4+ oxidation state to enable nucleation of a low solubility secondary phase. A mechanism for the anoxic dissolution of UO2 in deionised water is proposed that involves U4+ dissolution at defect sites that subsequently nucleate and precipitate in a less defective form.
Keywords
UO2, Anoxic dissolution, Secondary phases, Nucleation, Thin film, Geological disposal
Sponsorship
B.T. Tan acknowledges funding from the Singapore Nuclear and Research Safety Initiative (SNRSI).
Funder references
Engineering and Physical Sciences Research Council (EP/I036400/1)
EPSRC (via University of Leeds) (EP/S011935/1)
Identifiers
External DOI: https://doi.org/10.1016/j.apsusc.2018.09.094
This record's URL: https://www.repository.cam.ac.uk/handle/1810/285353
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