Discontinuous precipitation (DP) and discontinuous coarsening (DC) reactions have been observed in numerous alloy systems [1]. DP has been observed in the U-Nb system [2, 3, 4, 5]. The U-Nb phase diagram (Fig. 1) exhibits a continuous γ-BCC solid solution at high temperatures and a two-phase mixture of a-orthorhombic and γ-BCC below the 647°C monotectoid isotherm. The DP reaction occurs during continuous cooling and isothermal aging over 300-647°C. No metallographic evidence of a DC reaction in U-Nb has been published, although this is suggested from x-ray observations of distinct changes in the Nb content of the γ phase upon prolonged holding after the DP reaction [2, 3, 6]. This study will provide direct evidence for a DC reaction. Discontinuous and other aging reactions [7] are undesirable in U-Nb alloys, since they degrade corrosion resistance [5], ductility [8], and the shape-memory effect [9]. Hence, an improved understanding of the kinetics of these discontinuous phase transformations in U-Nb alloys is of practical interest.
Low-enriched uranium-10 wt.% molybdenum (LEU-10wt.%Mo) is of interest for the fabrication of monolithic fuels to replace highly-enriched uranium (HEU) dispersion fuels in high performance research and test reactors around the world. In this work, depleted uranium-10wt.%Mo (DU-10wt.%Mo) is used to simulate the solidification and microstructural evolution of LEU-10wt.%Mo. Electron backscatter diffraction (EBSD) and complementary electron probe microanalysis (EPMA) reveal significant microsegregation present in the metastable γ-phase after solidification. Homogenization is performed at 800 and 1000 °C for times ranging from 1 to 32 h to explore the time-temperature combinations that will reduce the extent of microsegregation, as regions of higher and lower Mo content may influence local mechanical properties and provide preferred regions for γ-phase decomposition. We show for the first time that EBSD can be used to qualitatively assess microstructural evolution in DU-10wt.%Mo after homogenization treatments. Complementary EPMA is used to quantitatively confirm this finding. Homogenization at 1000 °C for 2 to 4 h reduces the regions that contain 8 wt.% Mo or lower, whereas homogenization at 1000 °C for longer than 8 h effectively saturates Mo chemical homogeneity, but results in substantial grain growth. The appropriate homogenization time will depend upon additional microstructural considerations, such as grain growth and intended subsequent processing. Higher carbon LEU-10wt.%Mo generally contains more inclusions within the grains and at grain boundaries after solidification. The effect of these inclusions on microstructural evolution (e.g. grain growth) during homogenization and as potential γ-phase decomposition nucleation sites is unclear, but likely requires additional study.
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