Actinide coordination sphere in various U, Np and Pu nitrato coordination complexes
Christophe Den Auwer, R. Revel, Marie‐Christine Charbonnel, M.T. Presson, Steven D. Conradson, E. Simoni, Jiangfeng Du, C. Madic
Abstract
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Christophe Den Auwer, R. Revel, Marie‐Christine Charbonnel, M.T. Presson, Steven D. Conradson, E. Simoni, Jiangfeng Du, C. Madic
Abstract
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Waste management of nuclear fuel represents one of the major environmental concerns of the decade. To recycle fissile valuable materials, intimate knowledge of complexation mechanisms involved in the solvent extraction processes is indispensable. Evolution of the actinide coordination sphere of AnO2(NO3)2TBP-type complexes (An = U, Np, Pu; TBP = tributylphosphate) with the actinide valence state have been probed by XAS at the metal L III edge. Dramatic changes in the actinide coordination sphere appeared when the An(VI) metal is reduced to An(IV). However, no significant evolution in the actinide environment has been noticed across the series UO2 2+, NpO2 2+ and PuO2 2+.
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Waste management of nuclear fuel represents one of the major environmental concerns of the decade. To recycle fissile valuable materials, intimate knowledge of complexation mechanisms involved in the solvent extraction processes is indispensable. Evolution of the actinide coordination sphere of AnO2(NO3)2TBP-type complexes (An = U, Np, Pu; TBP = tributylphosphate) with the actinide valence state have been probed by XAS at the metal L III edge. Dramatic changes in the actinide coordination sphere appeared when the An(VI) metal is reduced to An(IV). However, no significant evolution in the actinide environment has been noticed across the series UO2 2+, NpO2 2+ and PuO2 2+.
Key concepts: Actinide, Coordination sphere, Chemistry, Plutonium, Coordination number, Coordination complex, Lanthanide, Fissile material