The reactivity between liquid uranium and polycrystalline yttria subst
rates of various grain-sizes is studied at 1673 K under high vacuum-lo
w p(O2) conditions (p(O2) approximate to 10(-7) Pa). At short contact
times, uranium oxidation occurs at the metal/oxide interface from oxyg
en transferred from the yttria substrate which is transformed to an un
der-stoichiometric state. At long contact times, deoxidation occurring
at the uranium free surface predominates and leads to complete elimin
ation of oxidized uranium by a dissolution-evaporation mechanism. (C)
1998 Elsevier Science B.V.