Comparison of calculated and measured radionuclide inventory of a Zircaloy-4 cladding tube plenum section

ABSTRACTCladding tubes of water-cooled nuclear reactors are usually made of Zircaloy and are an important retaining element for radionuclides present in the fuel both during predisposal activities such as reloading of fuel assemblies from interim storage casks to final disposal casks and during final disposal in the case of canister breaching. However, cladding integrity is affected by various processes during reactor operation and beyond, e.g. fuel cladding chemical interaction and fission product precipitation onto the inner cladding surface. Using experimental and modelling methods, the radionuclide inventory of an irradiated Zircaloy-4 plenum section is analyzed. Quantities of 235/238U, 237Np, 238/239/240/241/242Pu, 241/243Am, 243/244Cm besides 14C, 55Fe, 125Sb, 154Eu, and 134/137Cs were (radio-)chemically determined in digested Zircaloy-4 subsamples. Measured inventories of activation products in the Zr-alloy are in good agreement with calculated values. However, amounts of actinides and fission products exceed the calculated inventory by factor ∼57 (minor actinides and non-volatile fission products) and ∼114 (137Cs). Excess of minor actinides and part of enhanced Cs inventory originate from fuel residues deposited on the inner cladding surface during fuel rod fabrication, whereas vast amount of cesium is volatilized from subjacent fuel pellets and transported to the plenum.

Aqueous leaching of high burnup UO2 fuel under hydrogen conditions

ABSTRACTLeaching results on fragments of high burnup (65 MWd/kgU) UO2 fuel from a commercial pressurized water reactor are presented. The experiment was performed in simplified granitic groundwater under a hydrogen pressure of up to 5 MPa, representing conditions in a water intrusion scenario for a Swedish KBS-3 design spent nuclear fuel repository. The freshly crushed fragments were pre-washed for 6 days to remove pre-oxidized matrix and part of the instant release fraction of the radionuclide inventory, and then transferred to an autoclave for leaching under hydrogen conditions. Following an initial release of U attributed to dissolution of a pre-oxidized fuel layer caused by the aerated handling mainly during the transfer from pre-washing to autoclave, the U concentration decreased with time to levels of 2-5x10-9 M, which corresponds, approximately, to the solubility of amorphous UO2. The release of radionuclides such as Cs and Sr gradually declined indicating a transition to inhibition of the fuel matrix dissolution.