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New Lanthanide Oxalato-nitrates Crystallized From Acidic Solutions

Published online by Cambridge University Press:  01 February 2011

Christelle Tamain
Affiliation:
[email protected], CEA MARCOULE, DEN/DRCP/SCPS, Laboratoire de Conversion et Chimie des Actinides, Bagnols sur cèze, France
Murielle Rivenet
Affiliation:
[email protected], CNRS/ENSCL/USTL, Unité de Catalyse et de Chimie du Solide - Groupe Chimie du Solide, Villeneuve d'Ascq, France
Bénédicte Arab-Chapelet
Affiliation:
[email protected], CEA MARCOULE, DEN/DRCP/SCPS, Laboratoire de Conversion et Chimie des Actinides, Bagnols sur cèze, France
Stéphane Grandjean
Affiliation:
[email protected], CEA MARCOULE, DEN/DRCP/SCPS, Laboratoire de Conversion et Chimie des Actinides, Bagnols sur cèze, France
Francis Abraham
Affiliation:
[email protected], CNRS/ENSCL/USTL, UCCS, Villeneuve d'Ascq, France
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Abstract

To identify the various oxalates and oxalato-nitrates likely to form during the nuclear fuel reprocessing we study crystallization of such compounds by various methods (slow diffusion, hydrothermal syntheses, in situ oxalate syntheses …), in different conditions and in presence of monovalent ions. In a first stage, lanthanides are used as surrogates of the actinides (III) radioactive elements. This communication reviews various lanthanides (III) compounds obtained by crystallization from nitric acid solution containing hydrazinium ions. Diethyl oxalate was used as a precursor for oxalate ions. A careful adjustment of the experimental conditions allowed us to synthesize single crystals of nitrates, oxalato-nitrates and oxalates with various ligand/Ln(III) ratio and containing nitrates as ligands or as counter ions. In all the compounds hydrazinium ions are present as counter ions. The crystal growth method is described and the crystal structures, determined by X-ray diffraction from single crystals, are discussed in terms of metal-oxalate frameworks.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

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