We have studied the relative rates of oxidative corrosion of U-Nb alloys co
ntaining 2-8 wt. % Nb, using x-ray photoelectron spectroscopy and depth pro
filing by sputtered neutrals mass spectroscopy. The alloys have been charac
terized after exposure to dry and humidified air (up to 50% relative humidi
ty) at temperatures from 25 to 125 degreesC, and after exposure to electroc
hemical solutions. Oxidation of the U-Nb alloys in a tube furnace results i
n oxide layers comprised of UO2 and Nb2O5 under all experimental conditions
used. The thickness of the oxides increased with treatment time and temper
ature, but decreased with increasing Nb alloy content. For example, a 48 h
treatment at 75 degreesC and 50% relative humidity results in an oxide laye
r on U-2% Nb that is approximately 1.5 times as thick as that on U-8% Nb. E
lectrochemical oxidation of U-Nb alloys facilely generated UO3( . nH(2)O) a
nd Nb2O5 layers similar to 1000 Angstrom thick, qualitatively similar to th
ermal oxidation results. U-Nb alloys electrochemically oxidized at low pH e
xhibit oxide layers with near-surface regions (50 Angstrom) enhanced in Nb
content, as compared to the bulk material. Surface UO3 (. nH(2)O) was not r
eadily reduced upon exposure to molecular D-2; however, D atoms facilely re
duced UO3(. nH(2)O) to UO2.