Mechanisms of Plutonium Redox Reactions in Nitric Acid Solutions.

Abstract

Plutonium (Pu) exhibits a complex redox behavior in aqueous solutions. This is due to the ability of the element to adapt a wide range of oxidation states typically from +3 to +6 and the tendency for dynamic interconversion between the oxidation states that primarily depend upon acid concentration and presence of coordinating ligands. This work interrogates the Pu redox behavior in aqueous nitric acid via a combination of voltammetry and in situ vis-NIR spectroelectrochemistry under controlled potentials to map the interconversion between the various Pu oxidation states. The NIR-spectroelectrochemistry studies used to complement the visible spectroscopy bring a new and more complete perspective into the plutonium redox transformations. This allows elucidation of the mechanisms of the involved redox reactions facilitating an in-depth understanding of the relative stability of the Pu oxidation states as a function of redox potentials and nitric acid concentrations. It is observed that oxidation of Pu(III) results in generation of Pu(IV) and Pu(VI) (the latter as PuO22+), bypassing the Pu(V) oxidation state. Further, with increasing acid concentrations, the formation of the Pu(VI) species progressively decreases so that the dynamic equilibrium between the Pu(III) and Pu(IV) oxidation states dominates. These findings have significant implications for developing separation processes for used nuclear fuel reprocessing and treatment.