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The Influence of Ligands and Precipitates on the Release of Nuclides from the Near Field under Natural Repository Conditions

Published online by Cambridge University Press:  21 March 2011

L. Liu
Affiliation:
Department of Chemical Engineering and Technology, Royal Institute of Technology, SE-100 44 Stockholm, Sweden
I. Neretnieks
Affiliation:
Department of Chemical Engineering and Technology, Royal Institute of Technology, SE-100 44 Stockholm, Sweden
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Abstract

Once groundwater intrudes into a damaged canister and wets the spent fuel pellets, radiation emitted from the spent nuclear fuel splits nearby water into oxidizing and reducing species. This may lead to an oxidizing condition near the fuel pellets. As a result, uranium oxide that makes up the fuel matrix will become more soluble, and the incorporated radionuclides will be released more rapidly. The dissolution process is, however, a dynamic one that can be influenced by many factors. Of great importance are the radiation power of the fuel matrix, the concentration of ligands near the fuel surface, and the transport resistance of the near field. Consequently, the escape of nuclides from the damaged canister is dominated mainly by the intrusion of ligands, and the precipitation/dissolution of secondary phases within the fuel rods. To investigate the possible effects of ligands and precipitates, a coupled dissolution and transport model, which includes the barrier effect of the Zircaloy claddings, is developed. The application of the model to a SKB-specified reference scenario indicates that by far the largest fraction of the oxidized uranium will reprecipitate within the canister. This may significantly decrease the fuel surface available for oxidation and the water available for radiolysis. Subsequently, much less fuel matrix will be dissolved and much less of the other nuclides will be released. Simulations further identify that carbonate and silicate have the greatest influences on the formation of secondary phases, and on the release of nuclides, under natural repository conditions.

Type
Research Article
Copyright
Copyright © Materials Research Society 2001

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References

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