Uranium–35 wt.% zirconium (U–35 wt.% Zr) alloy was annealed for 1 h and 24 h at 650 °C and characterized to understand the early-stage microstructure evolution. Dendritic microstructure with fine (∼300 nm in length) α-U precipitates clustered between dendrite branches were observed in the 1-h annealed sample. After 24-h annealing at 650 °C, the α-U precipitates coarsened, and the dendritic microstructure disappeared because of microstructure homogenization. Furthermore, microchemical homogenization observed with energy-dispersive X-ray spectroscopy analysis suggests that α-U precipitates are approaching thermodynamic equilibrium in the 24-h annealed sample. The findings from this study have potential impacts on the manufacturing and computer modeling of metallic nuclear fuel.

Concentrated solid-solution alloys (CSAs) demonstrate excellent mechanical properties and promising irradiation resistance depending on their compositions. Existing experimental and simulation results indicate that their heterogeneous structures induced by the random arrangement of different elements are one of the most important reasons responsible for their outstanding properties. Nevertheless, the details of this heterogeneity remain unclear. Specifically, which properties induced by heterogeneity are most relevant to their irradiation response? In this work, we scrutinize the role of heterogeneity in CSAs played in damage evolution in different aspects through atomistic simulations, including lattice misfit, thermodynamic mixing, point defect energetics, point defect diffusion, and dislocation properties. Our results reveal that structural parameters, such as lattice misfit and enthalpy of mixing, are generally not suitable to assess their irradiation response under cascade conditions. Instead, atomic-level defect properties are the keys to understand defect evolution in CSAs. Therefore, tuning chemical disorder to tailor defect properties is a possible way to further improve the irradiation performance of CSAs.

The breakdown of the columnar grains and lamellar α + β colony microstructure in two-phase Ti alloys during conversion of ingot to billet is critical to the development of desired combination of mechanical properties. Colony breakdown occurs during a series of thermomechanical processing steps in the α + β phase field. However, fundamental knowledge of the microstructural dependence of this transformation is limited, particularly its dependence on the initial orientation of the α + β colony relative to the imposed strain-path. In this study, the viscoplastic self-consistent polycrystal plasticity model is used to examine deformation behavior as a function of crystal loading direction. Criteria were developed to predict relative globularization rates; it was found that both slip system activities in the α phase and relative crystal rotations of each phase must be considered. Predictions are demonstrated to be consistent with literature and suggest that further experimental investigation of relative globularization rates is necessary.