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Synthesis of Nanocrystalline PuO 2 by Hydrothermal and Thermal Decomposition of Pu(IV) Oxalate: A Comparative Study

Affiliation
Univ. Lille, CNRS, Centrale Lille, Univ. Artois, UMR 8181—UCCS—Unité de Catalyse et Chimie du Solide, F-59000 Lille, France
Baumann, Viktoria;
ORCID
0000-0003-2759-6492
Affiliation
European Commission, Joint Research Centre, 76344 Karlsruhe, Germany
Popa, Karin;
ORCID
0000-0002-2679-1715
Affiliation
European Commission, Joint Research Centre, 76344 Karlsruhe, Germany
Walter, Olaf;
Affiliation
Univ. Lille, CNRS, Centrale Lille, Univ. Artois, UMR 8181—UCCS—Unité de Catalyse et Chimie du Solide, F-59000 Lille, France
Rivenet, Murielle;
Affiliation
ORANO, 92320 Chatillon, France
Senentz, Gérald;
Affiliation
ORANO, 92320 Chatillon, France
Morel, Bertrand;
ORCID
0000-0001-6113-2128
Affiliation
European Commission, Joint Research Centre, 76344 Karlsruhe, Germany
Konings, Rudy J.M.

In recent years, the hydrothermal conversion of actinide (IV) oxalates into nanometric actinide dioxides ( An O 2 ) has begun to be investigated as an alternative to the widely implemented thermal decomposition method. We present here a comparison between the hydrothermal and the conventional thermal decomposition of Pu(IV) oxalate in terms of particle size, morphology and residual carbon content. A parametric study was carried out in order to define the temperature and time applied in the hydrothermal conversion of tetravalent Pu-oxalate into PuO 2 and to optimize the reaction conditions.

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