Thermodynamical and Structural Study of Protactinium(V) Oxalate Complexes in Solution


Thermodynamical and Structural Study of Protactinium(V) Oxalate Complexes in Solution

Mendes, M.; Hamadi, S.; Le Naour, C.; Roques, J.; Jeanson, A.; Den Auwer, C.; Moisy, P.; Topin, S.; Aupiais, J.; Hennig, C.; Di Giandomenico, M. V.

The complexation of protactinium(V) by oxalate is studied by X-ray absorption spectroscopy (XAS), capillary electrophoresis coupled with ICP-MS (CE-ICP-MS ) and solvent extraction. XAS measurements show unambiguously the presence of a short single oxo-bond. CE-ICP-MS results indicate the formation of a highly charged anionic complex. The formation constant of PaO(C2O4)+, PaO(C2O4)2– and PaO(C2O4)33– are determined from solvent extraction data by using protactinium at tracer scale (CPa < 10–10M) and different temperatures. Complexation reactions of Pa(V) with oxalate are found to be exothermic with relatively high positive entropic variation.

Keywords: Pa(V) oxalate; Thermodynamics; EXAFS

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