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Uranyl acetate speciation in aqueous solutions—an XAS study between 25°C and 250°C
Authors:EH Bailey  JFW Mosselmans
Institution:1 School of Life and Environmental Sciences, University of Nottingham, Nottingham, NG7 2RD, UK
2 CCLRC Daresbury Laboratory, Daresbury, Warrington, WA4 4AD, UK
3 Department of Mineralogy, Natural History Museum, Cromwell Road, London, SW7 5BD, UK
Abstract:Speciation of uranium (VI) in acetate solutions between 25 and 250°C, at pH values between 1.8 and 3.8 and acetate/uranium (Ac/U) ratios of 0.5 to 100 has been investigated using uranium LIII-edge X-ray absorption spectroscopy. With increasing pH the UO2(Ac)20 species becomes more important than UO2(Ac)+ species, which is predominant below pH 2. It remains the dominant species as pH is further increased to 3.8 at an Ac/U ratio of 20. Decrease in U-Oeq bond distance and coordination number with increasing solution age indicates that steric/kinetic factors are important and that equilibrium is attained slowly in this system with initial acetate coordination to the uranyl ion being monodentate or pseudo-bridging before slow conversion to bidentate chelation. Acetate coordination to the uranyl ion appears to decrease as temperature is increased from room temperature to ∼100°C before increasing in solutions of Ac/U > 2. For solutions where Ac/U ≤ 2 at pH 2.1, there is no evidence for uranyl acetate speciation at low temperatures, but at elevated temperature bidentate uranyl-acetate ion-pairing is evident. The existence of the uranyl acetate species in the temperature range 200 to 240°C demonstrates the importance of including acetate and other organic ligands in models of uranium transport at elevated temperatures.
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