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   <subfield code="a">Electrochemistry of uranium in sodium chloroaluminate melts</subfield>
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   <subfield code="c">[W. D'olieslager, F. Meuris, L. Heerman]</subfield>
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   <subfield code="a">The electrochemical behaviour of uranium has been studied in basic, NaCl-saturated NaAlCl4 melts at 175°C. Solutions of UO3 exhibit two oxidation/reduction waves (cyclic voltammetry). The first wave corresponds to the U(VI)/U(IV) redox couple and is irreversible (slow electron transfer). The second wave corresponds to the deposition and stripping of an insoluble U(III) compound (U(IV)/U(III)). Solutions of UO2 or UCl4 and U(IV) solutions prepared by exhaustive electrolysis of UO3 behave identically. The cyclic voltammograms of U(IV) solutions are the same as those of UO3, but they show additional anodic peaks. Analysis of the peak currents (cyclic voltammetry), the limiting currents (pulse polarography) and the non-linear log i-t curves (anodic controlled potential coulometry) leads to the conclusion that uranium (IV) in the basic chloroaluminate melt exists as two different species in slow equilibrium with one another, of which only one species can be oxidized to U(VI). E.m.f. measurements of U(VI)-U(IV) mixtures indicate that the electron transfer process involves the formation of an intermediate U(V) species in a disproportionation equilibrium.</subfield>
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