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A Novel kinetic model for dissolution and precipitation of oxide on stainless-steel surface in stagnant liquid sodium

河口 宗道*; 池田 明日香; 斉藤 淳一  

Kawaguchi, Munemichi*; Ikeda, Asuka; Saito, Junichi

This study performed sodium experiments and developed a new kinetic model to investigate the oxide dissolution and precipitation behavior on the stainless-steel (SS) surface in stagnant liquid sodium. The experiment revealed that the oxygen of Na$$_{4}$$FeO$$_{3}$$ on the SS surface was dissolved into the liquid sodium with v$$_{dis}$$ $$approx$$ 9.3 $$times$$10 $$^{-5}$$ wt.ratio/h in less than 20 h, and the oxide precipitation occurred on the SS surface with v$$_{pre}$$ $$approx$$ 1.4 $$times$$10$$^{-5}$$ wt.ratio/h after the dissolution. Furthermore, the phase-field (PF) calculation code was developed to investigate the dependence of six parameters (T, c$$_{0}$$, $$Upsilon$$, D $$_{L}$$, k, and $$Delta$$t) of the oxide precipitation velocity in the liquid sodium. As a result, the precipitation velocity increased linearly as the oxygen concentration (c$$_{0}$$) and the oxygen diffusion coefficient (D$$_{L}$$) in liquid sodium increased. In contrast, its velocity decreased exponentially as the sodium temperature (T) and the interfacial energy of oxide ($$Upsilon$$) increased. The quasi-partial coefficient (k) and the time step ($$Delta$$t) did not affect the calculation results at all. In these sensitivity analyses, the oxide precipitation velocity obtained by the PF calculation shows consistency with the laboratory-scale experimental findings of Latge et al.

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