Abstract
A series of zirconolite ceramics with stoichiometry Ca1-xCexZrTi2-2xAl2xO7 (x = 0–0.35), considered as a host phase for the immobilisation of separated plutonium, were prepared from a mixture of oxide precursors by sintering in air at 1450 °C. Ce was utilised as a structural surrogate for Pu, with Al added to provide charge compensation. XRD and electron diffraction analyses indicated crystallisation of the zirconolite-2M polytype for all compositions, accompanied by various secondary phases contingent on the doping level, consistent with microstructure observation. The relative yield of zirconolite phases remained above 94 wt.% for 0.05 < x < 0.20. It was determined that Ce was partially reduced to the Ce3+ oxidation state and Al occupied mainly octahedral Ti sites. The incorporation rate of CeO2 was calculated to be 9.27 wt.% in Ca0.80Ce0.20ZrTi1.60Al0.40O7 with a comparatively high yield of 94.7 wt.%, which is representative of a PuO2 incorporation rate of 14.86 wt.%.
Original language | English |
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Article number | 153198 |
Number of pages | 8 |
Journal | Journal of Nuclear Materials |
Volume | 556 |
Early online date | 19 Jul 2021 |
DOIs | |
Publication status | Published - 1 Dec 2021 |
Bibliographical note
Publisher Copyright:© 2021 Elsevier B.V.
Keywords
- Ceramic wasteforms
- Local environment
- Plutonium immobilisation
- Waste loading
- Zirconolite