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Interpretation of dissolution behavior at the surface of uranium-zirconium oxide solid solutions

Tonna, Ryutaro*; Sasaki, Takayuki*; Okamoto, Yoshihiro  ; Kobayashi, Taishi*

The dissolution behavior of (U,Zr)O$$_{2}$$, the primary uranium solid phase in the fuel debris from the Fukushima Daiichi nuclear power plant accidents, was investigated thermodynamically and kinetically under atmospheric conditions. Cubic (U,Zr)O$$_{2}$$ samples with a uniform solid solution of Zr were prepared using wet chemistry methods, and static batch immersion tests were conducted. In strongly acidic conditions, where the solubility of U and Zr exceeded their concentrations, congruent dissolution of both elements was observed with (U,Zr)O$$_{2}$$ dissolving at the same rate as UO$$_{2}$$. In moderately acidic conditions, where the U solubility was higher than its concentration with Zr reaching a steady state at lower solubility, the U dissolution rate from (U,Zr)O$$_{2}$$ decreased compared to UO$$_{2}$$. In the presence of oxalic acid, with increased Zr solubility due to the formation of complexes, the U dissolution rate from (U,Zr)O$$_{2}$$ did not decrease. This indicates that Zr in (U,Zr)O$$_{2}$$ formed a secondary solid phase on the solid surface under conditions of lower Zr solubility, which in turn suppressed the oxidative dissolution of U.

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