Uranium oxide weathering: spectroscopy and kinetics

Abstract Particles of UO 2+ x ( x ≅0.16 ± 0.06) exposed to the atmosphere react by oxidation and formation of complexes (hydrates, hydroxides and carbonates). Surface reactions alter and erode the UO 2 particles. This paper outlines results for measurements of oxidation rates on uranium oxide particles using in situ photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and secondary ion mass spectrometry (SIMS). Phosphorescence spectra observed during oxidation of UO 2+ x were attributed to U(VI) in uranyl-type coordination and in octahedral coordination. Uranyl-type spectra formed during wet oxidation of UO 2+ x , and U(VI) octahedral spectra formed during dry oxidation of UO 2+ x . The uranyl-type species, although more stable, is more kinetically labile for vacuum reduction than is the octahedral U(VI). Oxidation of U(IV) species are diffusion controlled. Vacuum reduction of uranyl U(VI) in UO 3 follows a field-enhanced cationic diffusion rate law, while re-oxidation follows a diffusion rate law. Post-oxidation core and valence band XPS and SIMS measurements provided qualitative and quantitative measures of uranium oxidation states near uranium oxide surfaces.