Synthesis and Characterization of Brannerite Compositions for MOX Residue Disposal. (19th December 2016)

• Record Type: Journal Article
• Authors: Bailey, D.J.; Stennett, M.C.; Hyatt, N.C.
• Is Part Of: MRS advances. Volume 2:Number 10(2017)
• Page Start: 557
• Page End: 562
• Publication Date: 2016-12-19
• Subjects: U, -- ceramic, -- microstructure; Electrical engineering -- Congresses; Physics -- Congresses; Materials -- Research -- Congresses; Materials science -- Congresses; 620.11
• DOI: 10.1557/adv.2016.631
• Languages: English
• ISSNs: 2059-8521

Abstract

ABSTRACT: Due to their high actinide content MOX residues require immobilization within a robust host matrix. Although it is possible to immobilize actinides in vitreous wasteforms; ceramic phases, such as brannerite (UTi2 O6 ), are attractive due to their high waste loading capacity and relative insolubility. Brannerites Gd0.1 U0.9 Ti2 O6, Ce0.1 U0.9 Ti2 O6 and Gd0.1 U0.81 Ce0.09 Ti2 O6 were prepared using an oxide route. Charge compensation of trivalent cations was expected to occur via the oxidation of U (IV) to higher valence states (U (V) or U (VI)). Gd was added to act as a neutron absorber in the final Pu bearing wasteform and Ce was used as a structural surrogate for Pu. X-ray absorption spectroscopy showed that Ce (IV) was reduced to Ce (III) in all cases. X-ray powder diffraction of synthesized specimens found that the final phase assemblage was strongly affected by processing atmosphere (air or argon). Prototypical brannerite was formed in all compositions, secondary phases observed were found to vary according to processing atmosphere and stoichiometry. Microstructural analysis (SEM) of the sintered samples confirmed the results of the X-ray powder diffraction.