Abstract

Electrochemical studies on plutonium have been supporting the development of pyrochemical processes involving plutonium at CEA. The electrochemical properties of plutonium have been studied in molten salts – ternary eutectic mixture NaCl–KCl–BaCl 2, equimolar mixture NaCl–KCl and pure CaCl 2 – and in liquid gallium at 1073 K. The formal, or apparent, standard potential of Pu(III)/Pu redox couple in eutectic mixture of NaCl–KCl–BaCl 2 at 1073 K determined by potentiometry is equal to −2.56 V (versus Cl 2, 1 atm/Cl − reference electrode). In NaCl–KCl eutectic mixture and in pure CaCl 2 the formal standard potentials deduced from cyclic voltammetry are respectively −2.54 V and −2.51 V. These potentials led to the calculation of the activity coefficients of Pu(III) in the molten salts. Chronoamperometry on plutonium in liquid gallium using molten chlorides – CaCl 2 and equimolar NaCl/KCl – led to the determination of the activity coefficient of Pu in liquid Ga, log γ = −7.3. This new data is a key parameter to assess the thermodynamic feasibility of a process using gallium as solvent metal. By comparing gallium with other solvent metals – cadmium, bismuth, aluminum – gallium appears to be, with aluminum, more favorable for the selectivity of the separation at 1073 K of plutonium from cerium. In fact, compared with a solid tungsten electrode, none of these solvent liquid metals is a real asset for the selectivity of the separation. The role of a solvent liquid metal is mainly to trap the elements.

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