Radionuclide release from research reactor spent fuel

• Published in: Journal of nuclear materials Vol. 416; no. 1; pp. 211 - 215
• Main Authors: Curtius, H., Kaiser, G., Müller, E., Bosbach, D.
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Amsterdam Elsevier B.V 01.09.2011; Elsevier
• Subjects: Applied sciences; Controled nuclear fusion plants; Corrosion; Dispersion; Energy; Energy. Thermal use of fuels; Exact sciences and technology; Fission nuclear power plants; Fuels; Installations for energy generation and conversion: thermal and electrical energy; Nuclear fuels; Nuclear research reactors; Preparation and processing of nuclear fuels; Salt water; Solid phases; Solubility; Spent fuels; Lanthanide; Solubility; Aluminium; Clad; Leaching; Light water reactor; Nuclear reactor; Sorption; Actinide; Corrosion; Zircaloy; Nuclear power plant; Concentration effect; Lixiviation; Solid phase; Uranium dioxide; Isotopes; Research reactor; Irradiated nuclear fuel
• ISSN: 0022-3115; 1873-4820
• DOI: 10.1016/j.jnucmat.2010.12.221

Numerous investigations with respect to LWR fuel under non oxidizing repository relevant conditions were performed. The results obtained indicate slow corrosion rates for the UO 2 fuel matrix. Special fuel-types (mostly dispersed fuels, high enriched in 235U, cladded with aluminium) are used in German research reactors, whereas in German nuclear power plants, UO 2-fuel (LWR fuel, enrichment in 235U up to 5%, zircaloy as cladding) is used. Irradiated research reactor fuels contribute less than 1% to the total waste volume. In Germany, the state is responsible for fuel operation and for fuel back-end options. The institute for energy research (IEF-6) at the Research Center Jülich performs investigation with irradiated research reactor spent fuels under repository relevant conditions. In the study, the corrosion of research reactor spent fuel has been investigated in MgCl 2-rich salt brine and the radionuclide release fractions have been determined. Leaching experiments in brine with two different research reactor fuel-types were performed in a hot cell facility in order to determine the corrosion behaviour and the radionuclide release fractions. The corrosion of two dispersed research reactor fuel-types (UAl x -Al and U 3Si 2-Al) was studied in 400 mL MgCl 2-rich salt brine in the presence of Fe 2+ under static and initially anoxic conditions. Within these experimental parameters, both fuel types corroded in the experimental time period of 3.5 years completely, and secondary alteration phases were formed. After complete corrosion of the used research reactor fuel samples, the inventories of Cs and Sr were quantitatively detected in solution. Solution concentrations of Am and Eu were lower than the solubility of Am(OH) 3(s) and Eu(OH) 3(s) solid phases respectively, and may be controlled by sorption processes. Pu concentrations may be controlled by Pu(IV) polymer species, but the presence of Pu(V) and Pu(IV) oxyhydroxides species due to radiolytic effects cannot completely be ruled out. Solution concentrations of U were within the range of the solubility limits of the solid phase U(OH) 4(am). The determined concentrations of U and Am in solution were about one order of magnitude higher for the U 3Si 2-Al fuel sample. Here, the formation of U/Si containing secondary phase components and their influence on radionuclide solubility cannot be ruled out. Results of this work show that the U 3Si 2-Al and UAl x -Al dispersed research reactor spent fuel samples dissolved completely within the test period of 3.5 years in MgCl 2-rich brine in the presence of Fe 2+. In view of final disposal this means that these fuel matrices represent no barrier. The radionuclides will be released instantaneously. Cs (the long-lived isotope 135Cs is of special concern with respect to final disposal) and Sr were classified as mobile radionuclide species. For U, Am, Pu and Eu, a reimmobilization was observed. Sorption is the process which is assumed to be responsible for the reimmobilization of the long-lived actinide Am and the lanthanide Eu. Solution concentrations of U and Pu seem to be controlled by their solubility controlling solid phases.