Hostname: page-component-77c89778f8-sh8wx Total loading time: 0 Render date: 2024-07-17T01:49:38.875Z Has data issue: false hasContentIssue false

Reducing the uncertainty of nuclear fuel dissolution: an investigation of UO2 analogue CeO2

Published online by Cambridge University Press:  25 January 2013

Claire L. Corkhill
Affiliation:
The Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK, S1 3JD.
Daniel J. Bailey
Affiliation:
The Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK, S1 3JD.
Stephanie M. Thornber
Affiliation:
The Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK, S1 3JD.
Martin C. Stennett
Affiliation:
The Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK, S1 3JD.
Neil C. Hyatt
Affiliation:
The Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, UK, S1 3JD.
Get access

Abstract

In this investigation, CeO2 analogues, which approximate as closely as possible the characteristics of fuel-grade UO2, were characterised after dissolution under a wide range of conditions. Powdered samples were subject to a range of aggressive and environmentally relevant alteration media with different solubility controls, and reacted at 70 °C and 90 °C. Dissolution kinetics were monitored through analysis of the coexisting aqueous solution. Monolith samples were monitored for development of surface defects such as pores and dissolution pits, in addition to morphological changes at grain boundaries and surface pores upon dissolution under aggressive conditions. The surfaces were analysed using confocal profilometry, vertical scanning interferometry and scanning electron microscopy. Dissolution rates were found to be greatest in low pH solutions and at higher temperatures. Preferential dissolution appears to occur at grain boundaries and on particular grains, suggesting a crystallographic control on dissolution.

Type
Articles
Copyright
Copyright © Materials Research Society 2013 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Shoesmith, D. W., Journal of Nuclear Materials 282, 1 (2000).CrossRefGoogle Scholar
Ollila, K. and Oversby, V, SKB Technical Report TR-05-07 (2005).Google Scholar
Ollila, K., Posiva Work Report 2008-75 (2008).Google Scholar
Stennett, M. C., Corkhill, C. L., Marshall, L. A. and Hyatt, N. C. Journal of Nuclear Materials 432, 182 (2013).CrossRefGoogle Scholar
Claparede, L., Clavier, N., Dacheux, N., Moisy, P., Podor, R. and Ravaux, J., Inorganic Chemistry 50, 9059 (2011).CrossRefGoogle Scholar
Icenhower, J. P., Strachan, D. M., Lindberg, M. M., Rodriguez, E. A. and Steele, J. L. PNNL Report 14252 (2003).Google Scholar
Godinho, J. R. A., Piazolo, S., Stennett, M. C. and Hyatt, N. C. Journal of Nuclear Materials 419, 46 (2011).CrossRefGoogle Scholar
Godinho, J. R. A., Piazolo, S. and Evins, L. Z.. Geochimica et Cosmochimica Acta 86, 392 (2012).CrossRefGoogle Scholar