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An aqueous solution route was employed to prepare cerium titanate oxide brannerite. Thermal analysis, X-ray diffraction, Raman spectroscopy, transmission and scanning electron spectroscopy, were used to investigate the brannerite structure formation and bulk properties. Mixed metal oxides (TiO 2 , CeO 2 and brannerite CeTi 2 O 6 ) were formed upon calcination at 800 °C for 12 h. The amount of brannerite phase decreased to form the constituent oxides with increasing calcination temperature and only pure TiO 2 and CeO 2 were present after 1200 °C calcination. The brannerite CeTi 2 O 6 phase reformed at 1300 °C, and its relative amount was increased with dwell time. After 48 h calcination at 1300 °C, brannerite with only minor metal oxide impurities (<1%) was observed. The sample melted at 1400 °C which led to the collapse of brannerite back to its constituent oxides. Further, the phase formation was influenced by pelletization of the powders, which may be explained by a molar volume increase during brannerite formation. Attempts to confirm this hypothesis using Pu brannerite were inconclusive. [ABSTRACT FROM AUTHOR]

A novel soft chemistry route was developed to synthesize Y 2 Hf x Ti 2− x O 7 (0≤ x ≤2.0) oxide solid solution. An aqueous solution containing reactants was produced to ensure the combustion reaction taking place at the molecular level. A suite of characterization techniques, including X-ray diffraction, Raman, transmission electron spectroscopy, as well as X-ray absorption near edge structure (XANES), is employed to investigate the structural and phase changes of the series. Both X-ray and electron diffraction patterns show that the Y 2 Hf x Ti 2− x O 7 system undergoes a clear composition-induced phase transition from ordered pyrochlore to disordered defect-fluorite at x ~1.5. On the other hand, Raman and XANES spectra reveal a gradual evolution of the local structure with the substitution of Hf for Ti. [ABSTRACT FROM AUTHOR]