Insight into the Cationic Charge Distribution in U1–y– z Pu y Am z O2±x Mixed Oxides

Uranium–plutonium mixed oxides, containing few mol % of Am, are currently studied as fuel for Sodium Fast Reactors. The study of the O/M ratio of these fuels is of main interest, as its variation can induce issues for reactor safety. For this purpose, four U1–y–z Pu y Am z O2±x samples (0.235 ≤ y ≤...

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Veröffentlicht in:Inorganic chemistry 2024-10, Vol.63 (43), p.20482-20491
Hauptverfasser: Fouquet-Métivier, Pauline, Medyk, Laetitia, Lebreton, Florent, Guéneau, Christine, Hunault, Myrtille O. J. Y., Solari, Pier-Lorenzo, Dardenne, Kathy, Rothe, Jörg, Martin, Philippe M.
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Sprache:eng
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Zusammenfassung:Uranium–plutonium mixed oxides, containing few mol % of Am, are currently studied as fuel for Sodium Fast Reactors. The study of the O/M ratio of these fuels is of main interest, as its variation can induce issues for reactor safety. For this purpose, four U1–y–z Pu y Am z O2±x samples (0.235 ≤ y ≤ 0.39 and 0.005 ≤ z ≤ 0.02) were studied using electron probe microanalysis (EPMA), X-ray powder diffraction (XRD), and X-ray absorption spectroscopy (XAS) experiments. EPMA analyses revealed a homogeneous matrix phase with few U- and Pu-rich agglomerates. A matrix phase of fluorite structure (face-centered cubic), as well as a small contribution of a UO2 phase of the same structure, was evidenced for all of the samples by XRD. The O/M ratios of the (U,Pu)­O2±x matrix were calculated based on the obtained lattice parameters. XANES experiments highlighted the simultaneous presence of U5+ and Pu3+/Am3+ for all of the samples, indicating a charge compensation mechanism even for stoichiometric samples. Based on the EPMA and XRD results, it was evidenced that this coexistence of U4+, U5+, Pu3+, Pu4+, and Am3+ was not originating from the U- and Pu-rich agglomerates. It was found to be rather a peculiarity of the U1–y–z Pu y Am z O2±x matrix phase, discussed with the help of thermodynamic calculations performed on the U–Pu–Am–O system.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.4c03084