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Different Pathways of Secondary Phase Formation Induced by Colloidal and Dissolved Silica During the Dissolution of UO2 Nuclear Fuel in Leaching Tests

[+] Author Affiliations
M. Amme

Institute for Transuranium Elements

H. Lang, M. Stöckl

GSF National Research Centre for Environment and Health

Paper No. ICEM2003-4504, pp. 1975-1981; 7 pages
  • ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation
  • 9th ASME International Conference on Radioactive Waste Management and Environmental Remediation: Volumes 1, 2, and 3
  • Oxford, England, September 21–25, 2003
  • Conference Sponsors: Nuclear Engineering Division and Environmental Engineering Division
  • ISBN: 0-7918-3732-7 | eISBN: 0-7918-3731-9
  • Copyright © 2003 by ASME


We investigated the different dissolution behaviour of UO2 nuclear fuel material in waters containing silica in two different physical and chemical forms (dissolved ions and as SiO2 colloids, respectively) at elevated temperatures (95 °C in autoclaves). It was investigated if SiO2 colloids can act as carrier material for U ions during a interface geochemical dissolution process, a process that might possibly enhance the mobilization of uranium. Herefore, leaching / dissolution tests were conducted in batch reactors, using both dissolved Si (sodium metasilicate solution), as well as synthetic SiO2 colloids (100 nm diameter). Solid materials were examined with scanning electron microscopy (SEM-EDX) after the tests and ICP-OES was used for analysis of concentrations of U and Si in solutions. Thermodynamic calculations were applied for modelling the surface charges of the solid materials. Results show that a treatment with colloidal SiO2 has different effects on the surfaces than a leaching in dissolved silicate solutions. In the presence of colloids, well-crystallized secondary phases containing U and Si (most obviously uranyl silicates) were found on the surfaces, which were attacked by the treatment. This was not the case when dissolved Si was used. SiO2 colloids were partly found to remain on the surfaces after 1000 h at 95 °C. Dissolved U concentrations decreased with increasing Si content in the systems, especially so when colloidal Si was used. Ultrafiltration showed that the greatest part of the dissolved U was associated with Si colloids. A surface charge model suggests that the different effects are due to the development of electrostatic interactions between the UO2 and SiO2 surfaces.

Copyright © 2003 by ASME
Topics: Nuclear fuels



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