Compounds with the formulae CaZr1−xCexTi2O7 with x = 0.1–0.5 were synthesized by solid state reaction. Cerium was used as a surrogate for actinide elements. A transition from the 2M polymorph to the 4M polymorph (expanded unit cell due to cation ordering) in zirconolite was observed with increasing cerium content. The presence of both tri- and tetravalent Ce, contrary to formulation, was confirmed using X-ray absorption near edge spectroscopy, suggesting substitution on both Ca and Zr sites. Sintering was carried out via spark plasma sintering, during which the perovskite phase (Ca0.4Ce0.4TiO3) was stabilized due to the reducing conditions of this technique. Scanning electron microscopy and energy dispersive spectrometry revealed that the 2M polymorph was dilute in Ce content in comparison to the 4M-zirconolite. High temperature X-ray diffraction was used to detail the kinetics of perovskite to zirconolite transition. It was found that CaCeTi2O7 (cubic pyrochlore) formed as an intermediate phase during the transition. Our results show that a transition from 2M- to 4M-zirconolite occurs with increasing Ce content and can be controlled by adjusting the PO2 and the heat treatment temperature.
Hollandite-rich ceramic waste forms have been demonstrated to exhibit high durability while simultaneously accommodating a wide range of radionuclides in their matrices. This paper presents preliminary results on the preparation and characterization of ceramic waste forms prepared by two different methods-melt processing and spark plasma sintering (SPS). Both processes resulted in similar phase assemblages but exhibited different microstructures depending on processing method. The SPS samples exhibited fine-grained (<1 lm) and dispersed phases, whereas the melt-processed sample contained larger grains (10-20 lm) of specific phases. Additional data will need to be collected on the aqueous leaching durability and radiation resistance to evaluate each processing method for waste form performance.
Hollandite-rich multiphase waste form compositions processed by melt-solidification and spark plasma sintering (SPS) were characterized, compared, and validated for nuclear waste incorporation. Phase identification by x-ray diffraction (XRD) and electron back-scattered diffraction (EBSD) confirmed hollandite as the major phase present in these samples along with perovskite, pyrochlore and zirconolite. Distribution of selected elements observed by wavelength dispersive spectroscopy (WDS) maps indicated that Cs formed a secondary phase during SPS processing, which was considered undesirable. On the other hand, Cs partitioned into the hollandite phase in melt-processed samples. Further analysis of hollandite structure in melt-processed composition by selected area electron diffraction (SAED) revealed ordered arrangement of tunnel ions (Ba/Cs) and vacancies, suggesting efficient Cs incorporation into the lattice.
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