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Dissolution Studies of Soddyite as a Long-Term Analogue of the Oxidative Alteration of the Spent Nuclear Fuel Matrix
Published online by Cambridge University Press: 03 September 2012
Abstract
The thermodynamic and kinetic dissolution properties of a synthetically obtained soddyite have been determined at different bicarbonate concentrations. This uranium-silicate is expected to be a secondary solid phase of the oxidative alteration pathway of uranium dioxide in waters with low phosphate content and, consequently, it is likely to constitute one of the long-term uranium solubility limiting solid phases.
The experimental data obtained at the end of the experiments correspond fairly well to the theoretical model calculated with a log K0S0 of 3.9±0.7.
On the other hand, the general trend of the total uranium in solution measured in the experiments as a function of time has been fitted by using a kinetic equation obtained from the principle of detailed balancing of the dissolution reaction. In addition, the EQ3/6 code has also been used to model the uranium concentrations as a function of time. In both modeling exercises comparable results were obtained. The dissolution rate, normalized to the total surface area used in the experiments as measured with the BET method, gave an average value of 6.8 (±4.4) 10−14 mol cm−2 s−1.
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- Copyright © Materials Research Society 1997
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