Hydrothermal conversion of mixed uranium(iv)–cerium(iii) oxalates into U1−xCexO2+δ·nH2O solid solutions

Uranium–cerium oxide solid solutions, U1−xCexO2+δ·nH2O, were prepared through hydrothermal conversion of mixed U(iv)–Ce(iii) oxalate precursors, cerium being used as a surrogate for plutonium. Whatever the starting pH, the fluorite-type structure of AnO2 was obtained after heating at 250 °C for 24 h...

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Published inDalton transactions : an international journal of inorganic chemistry Vol. 52; no. 31; pp. 10951 - 10968
Main Authors Benarib, S, Dacheux, N, Le Goff, X F, Lautru, J, L Di Mascio, Clavier, N
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 08.08.2023
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Abstract Uranium–cerium oxide solid solutions, U1−xCexO2+δ·nH2O, were prepared through hydrothermal conversion of mixed U(iv)–Ce(iii) oxalate precursors, cerium being used as a surrogate for plutonium. Whatever the starting pH, the fluorite-type structure of AnO2 was obtained after heating at 250 °C for 24 h. The initial pH of the reaction media appeared to affect significantly the oxide morphology: for pH ≤ 2, the powder was found to be composed of microspheres, whereas for more alkaline pH values, agglomerates of nanocrystallites were found. Furthermore, a study of the hydrothermal treatment duration (T = 250 °C, pH = 8, t = 1–48 h) showed that fluorite-type mixed dioxides started to form after only 1 h, and then became single phase after 3 h. SEM and TEM/EDS analyses revealed that the cationic distribution narrowed with time to finally form highly homogeneous mixed oxides. Such a preparation route was then applied to various cerium incorporation rates and it was found that the formation of U1−xCexO2+δ·nH2O mixed oxides was possible for 0.1 ≤ x ≤ 0.75. In all the systems investigated, the speciation of uranium and cerium was questioned in both the solid and liquid phases. Thermodynamic calculations and evaluation of the O/M ratio in the final oxides led us to understand the complex redox behaviour of uranium and cerium in solution during hydrothermal processes and to propose a conversion mechanism.
AbstractList Uranium–cerium oxide solid solutions, U1−xCexO2+δ·nH2O, were prepared through hydrothermal conversion of mixed U(iv)–Ce(iii) oxalate precursors, cerium being used as a surrogate for plutonium. Whatever the starting pH, the fluorite-type structure of AnO2 was obtained after heating at 250 °C for 24 h. The initial pH of the reaction media appeared to affect significantly the oxide morphology: for pH ≤ 2, the powder was found to be composed of microspheres, whereas for more alkaline pH values, agglomerates of nanocrystallites were found. Furthermore, a study of the hydrothermal treatment duration (T = 250 °C, pH = 8, t = 1–48 h) showed that fluorite-type mixed dioxides started to form after only 1 h, and then became single phase after 3 h. SEM and TEM/EDS analyses revealed that the cationic distribution narrowed with time to finally form highly homogeneous mixed oxides. Such a preparation route was then applied to various cerium incorporation rates and it was found that the formation of U1−xCexO2+δ·nH2O mixed oxides was possible for 0.1 ≤ x ≤ 0.75. In all the systems investigated, the speciation of uranium and cerium was questioned in both the solid and liquid phases. Thermodynamic calculations and evaluation of the O/M ratio in the final oxides led us to understand the complex redox behaviour of uranium and cerium in solution during hydrothermal processes and to propose a conversion mechanism.
Author Benarib, S
Dacheux, N
Le Goff, X F
Clavier, N
L Di Mascio
Lautru, J
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SubjectTerms Cerium oxides
Conversion
Fluorite
Hydrothermal treatment
Liquid phases
Microspheres
Mixed oxides
Oxalates
Plutonium
Solid phases
Solid solutions
Speciation
Uranium
Title Hydrothermal conversion of mixed uranium(iv)–cerium(iii) oxalates into U1−xCexO2+δ·nH2O solid solutions
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