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Research on the stability of fuel debris consisting of oxides and alloys, 8; Dissolution of uranium from simulated fuel debris in the UO$$_{2}$$-Zr-SS system and formation of alteration layer

Kumagai, Yuta   ; Watanabe, Masayuki   ; Kusaka, Ryoji  ; Akiyama, Daisuke*; Kirishima, Akira*; Sato, Nobuaki*; Sasaki, Takayuki*

Fuel debris generated during the 1F accident is expected to remain in contact with water. The contact with water has possibility to cause long-term degradation of the fuel debris. One of the causes of the degradation is oxidation of the debris matrix by hydrogen peroxide (H$$_{2}$$O$$_{2}$$) due to the water radiolysis. In this study, we performed 30-day immersion tests in aqueous H$$_{2}$$O$$_{2}$$ solution using simulated fuel debris samples prepared from uranium oxide (UO$$_{2}$$), stainless steel (SUS304), and zirconium metal (Zr) or oxide (ZrO$$_{2}$$). The U dissolution by the immersion was much lower than the H$$_{2}$$O$$_{2}$$ consumed. Moreover, the H$$_{2}$$O$$_{2}$$ reaction with UO$$_{2}$$ sample once induced dissolution of U but the U concentration decreased with immersion time. Also, in the results of the simulated debris samples, increasing trend of dissolved U concentration was not clearly observed. These results indicate formation of solid uranyl peroxides as alteration layer, as it was reported in the similar immersion studies of UO$$_{2}$$.

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