Anaerobic Dissolution Rates of U(IV)-Oxide by Abiotic and Nitrate-Dependent Bacterial Pathways

The long-term stability of U­(IV) solid phases in anaerobic aquifers depends upon their reactivity in the presence of oxidizing chemical species and microbial catalysts. We performed flow-through column experiments under anaerobic conditions to investigate the mechanisms and dissolution rates of biogenic, noncrystalline UO2(s) by chemical oxidants (nitrate and/or nitrite) or by Thiobacillus denitrificans, a widespread, denitrifying, chemolithoautotrophic model bacterium. Dissolution rates of UO2(s) with dissolved nitrite were approximately 5 to 10 times greater than with nitrate alone. In the presence of wild-type T. denitrificans and nitrate, UO2(s) dissolution rates were similar to those of abiotic experiments with nitrite (from 1.15 × 10–14 to 4.94 × 10–13 mol m–2 s–1). Experiments with a T. dentrificans mutant strain defective in U­(IV) oxidation supported microbially mediated U­(IV) oxidation. X-ray absorption spectroscopy (XAS) analysis of post-reaction solids showed the presence of mononuclear U­(VI) species rather than a solid U­(VI) phase. At steady-state U release, kinetic and spectroscopic results suggest detachment of oxidized U­(VI) from the UO2(s) surface as the rate-determining step rather than electron transfer or ion diffusion. Under anaerobic conditions, production of nitrite by nitrate-reducing microorganisms and enzymatically catalyzed, nitrate-dependent U­(IV) oxidation are likely dual processes by which reduced U solids may be oxidized and mobilized in the aqueous phase.