AbstractBecause of their high chemical durability and waste loading capacity, iron phosphate glasses are a natural candidate for a nuclear waste disposal medium. We have studied the effects of uranium on the structure of iron phosphate glasses with both neutron and high-energy x-raydiffraction. The results of neutron scattering, which is mostly sensitive to pair correlations involving light atoms i.e. O-O, Fe-O and P-O, indicate the main structural features of the base glass are largely unaffected by the addition of UO2. The nearest-neighborbour P-O, Fe-O and O- O peaks remain at the same position in real space and their intensities scale approximately with concentration. These findings are consistent with earlier results using Raman scattering and EXAFS on the Fe-K edge, where in both cases the spectra remain similar to the base glass. The results of high-energy x-ray scattering, which is sensitive to correlations involving the heavier atoms and thus complements the neutron measurements, are also consistent with the overall picture of uranium occupying interstitial sites in the relatively undisturbed base glass structure. Combining the neutron and x-ray data for a 10 mol% UO2 glass suggests the intriguing possibility of a U6+ uranyl ion configuration although further work is needed to establish the precise local structure and valence state of uranium in these glasses.
Formation of Reaction Layer and Dissolution Behavior of Alkali and Alkaline-Earth Iron Phosphate Glasses in Water
