Corrosion of uranium and its low content Zr, Nb, and Ru alloys in aqueous solutions

Corrosion of uranium and its alloys with low content (0.5-5.0 at %) of Zr, Nb, and Ru in water and bicarbonate aqueous solutions is studied; the effect of hydrogen peroxide, the main product of radiation processes, on the corrosion rate is elucidated. The rate of the primary Corrosion process U + (2 + n)H2O = UO2 center dot nH(2)O + 2H(2)up arrow is measured by electrochemical methods in anaerobic and aerobic conditions for uranium metal and its alloys containing 0.5 to 5.0 at % of Zr, Nb, and Ru. It is shown that the corrosion rates for the alloys are lower than that of reactor-grade uranium; however, the difference is rather close to the measurement error. The corrosion mechanism is studied; U(III) is shown to be rather unstable in neutral solutions when uranium(III) hydroxide is precipitated and no significant amount of U(III) and UH3 is present among the products of the metallic uranium corrosion in water. The kinetics of the second corrosion stage U(IV) + O-2 --> U(VI) is studied by spectrophotometric method. It is shown that the reaction of U(IV) oxidation by atmospheric oxygen is similar in weakly acid solutions (pH 1.5-4.0) and in bicarbonate media: in particular, it has an induction period for uranium (IV) accumulation, after which the reaction accelerates; it is formally a first-order reaction with respect to uranium. The reaction mechanisms differ in the two media: in weakly acid solutions, after the appearance of U(VI), the reproportionation reaction proceeds; thus formed U(V) interacts with O-2 faster than U(IV). In the bicarbonate medium, the acceleration of the reaction is due to the formation of a [U(IV)Sigma U(VI)] complex whose reactivity is higher than that of uranium (IV). In the absence of bicarbonate, of great importance is the formation of a copolymer of U(IV) and U(VI), which at pH >= 4 prevents formation of U(V). It is shown that on the introduction of hydrogen peroxide to aqueous solutions, the metallic uranium surface becomes transpassive, which increases the rate of corrosion process by at least an order of magnitude,. The introducing of oxidants and platinum mesh lowers the hydrogen accumulation at 120-150 degrees C and, hence, the hydrogen-explosion danger of the uranium-water-corrosion-products system. Methods of deposition of metal oxide (Tc, Ru, Mo, W) films onto uranium surfaces by immersing uranium metal into Tc(VII), Ru(VI), or Mo and W heteropoly compound solutions are studied.