Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1568877 | Journal of Nuclear Materials | 2008 | 4 Pages |
Abstract
Using the recently developed steady-state model for simulation of radiation induced dissolution of spent nuclear fuel in water we have estimated the rate of dissolution for relatively fresh fuel to 1.64 Ã 10â9 mol mâ2 sâ1. A series of experiments have been performed on fuel fragments in deoxygenated water containing 10 mM HCO3â. The dissolution rates obtained from these experiments range from 2.6 Ã 10â10 to 1.6 Ã 10â9 mol mâ2 sâ1. The leaching time in the experiments is 40 days or less and during this time the amount of released uranium increases linearly with time which indicates that the system has reached steady-state. The excellent agreement between the estimated dissolution rate and the dissolution rates obtained from the spent nuclear fuel leaching experiments indicates that the steady-state approach can indeed be used to predict the rate of spent nuclear fuel dissolution.
Related Topics
Physical Sciences and Engineering
Energy
Nuclear Energy and Engineering
Authors
Fredrik Nielsen, Ella Ekeroth, Trygve E. Eriksen, Mats Jonsson,