Jm. Haschke et al., Reactions of plutonium dioxide with water and hydrogen-oxygen mixtures: Mechanisms for corrosion of uranium and plutonium, J ALLOY COM, 314(1-2), 2001, pp. 78-91
Investigation shows that plutonium dioxide interacts chemically with water
and catalytically with oxygen-hydrogen mixtures to form water. Water adsorb
s strongly on the oxide below 120 degreesC and desorbs as the temperature i
s increased to 200 degreesC. Hydroxide formed by dissociative adsorption of
water promotes formation of the higher oxide (PuO2+x) plus H-2, and in the
presence of O-2, drives a water-catalyzed cycle that accelerates formation
of PuO2+x by the PuO2 + O-2 reaction. Results are consistent with kinetic
control of plutonium corrosion by the adherent oxide layer on the metal and
imply that moisture-enhanced oxidation is driven by the water-catalyzed cy
cle. Evaluation of experimental results and literature data for U and Pu le
ad to a comprehensive corrosion mechanism applicable to both metals in dry
air. water vapor, and moist air. In all cases, corrosion proceeds by diffus
ion of oxide ions through the oxide product, not by transport of hydrogen o
r hydroxide. Rates vary as changes in the concentration of adsorbed water d
etermine the rate of O2- formation and the gradient in oxygen concentration
across the oxide diffusion barrier. Results account for a sharp decrease i
n the corrosion rate of Pu by water and moist air as the temperature approa
ches 200 degreesC. (C) 2001 Elsevier Science B.V. All rights reserved.