Abstract
AbstractWe have investigated the structures of U(VI) oxides precipitated from room temperature aqueous solutions at low ionic strength as a function of pH. Using the uranium LIII - edge extended x-ray absorption fine structure (EXAFS) as a probe of the local structure around the uranium, a trend is observed whereby the axial oxygen bond lengths from the uranyl groups increase from 1.80 Å at pH=7 to 1.86 Å at pH=11. A concomitant decrease in the equatorial oxygen and nearest-neighbor uranium bond lengths also occurs with increasing pH. Expansion of the linear O=U=O group is seen directly at the L111 absorption edge where multiple scattering resonances systematically shift in energy. EXAFS curve-fitting analysis on these precipitates and a sample of synthetic schoepite indicate that the structure of the species formed at pH=7 is similar to the structure of schoepite. At pH=11, the precipitate structure is similar to that of a uranate.
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