Congratulations to Ke Yuan who successfully defended his dissertation on April 9, 2015.
Advisor: Udo Becker


Uranium has a unique chemical behavior because of the presence of the localized 5f electrons. The redox chemistry of uranium influences its mobility in the aqueous environment. Thus, this thesis investigates the redox processes of aqueous uranium (uranyl, [O=U=O]2+), in order to understand and predict its behavior in the environment. In addition, the UO2-HfO2solid-solution behavior (Hf being a neutron absorber) is modeled to study under which conditions the mixture forms solid solution or exsolves, which is essential for the thermal conductivity and melting point of the fuel.

Soluble uranyl(VI) can be reduced on surfaces of Fe(II) bearing minerals to solid U(IV)O2, resulting in the decrease of its mobility in the environment. However, the previously considered one-step two-electron reduction pathway from U(VI) to U(IV) has been challenged by the presence of stable pentavalent U(V). The experiments here investigate the pathways of uranium reduction by reducing uranyl(VI) electrochemically on powdered and bulk magnetite electrodes. The number of electrons transferred per redox change is found to be one, which confirms the one-electron reduction from U(VI) to U(V). Nano-size uranium precipitates were found on the surface of magnetite by in situ electrochemical AFM. Further spectroscopic evidence (XPS, AES, XANES, and EXAFS) suggests these precipitates are poorly crystallized mixed-valence state U(V)/U(VI) solids,which stabilize U(V) by preventing its disproportionation (2U(V)→U(VI)+U(IV)). In contrast, the catalytic properties of the surface of powdered magnetite facilitates the disproportionation of U(V), which is attributed to the adsorption/desorption kinetics of protons on the particulate magnetite.

In order to better control the power distribution in a nuclear reactor, UO2, a nuclear fuel material, gets mechanically mixed with the neutron absorber HfO2. The thermodynamic mixing properties of the UO2-HfO2 (limited in experimental data) were simulated using DFT and Monte Carlo simulations. The calculated binary forms extensive solid solution across the entire compositional range, with a variety of exsolution phenomena associated with the different HfO2 polymorphs. Close to the UO2end member, which is relevant to the nuclear fuel, the isometric uranium-rich solid solutions exsolve as the fuel cools, and there is a tendency to form the monoclinic hafnium-rich phase in the matrix of the isometric, uranium-rich solid solution phase.