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|Title:||Plutonium and americium aluminate perovskites|
|Authors:||VIGIER JEAN-FRANCOIS; POPA KARIN; MARTEL LAURA; MANARA DARIO; DIESTE BLANCO OLIVER; FREIS DANIEL; KONINGS RUDY|
|Citation:||INORGANIC CHEMISTRY vol. 58 no. 14 p. 9118-9126|
|Publisher:||AMER CHEMICAL SOC|
|Type:||Articles in periodicals and books|
|Abstract:||Both AmAlO3 and PuAlO3 perovskites have been synthesised and characterised using powder X Ray Diffraction (XRD), Raman spectroscopy, Fourier-transform infrared spectroscopy (FT IR) and 27Al Magic Angle Spinning - Nuclear Magnetic Resonance spectroscopy (MAS-NMR). AmAlO3 perovskite showed a rhombohedral configuration (Space group R-3c) in agreement with previous studies. The effect of americium alpha-decay on this material has been followed by XRD and 27Al MAS-NMR analyses. In a first step, a progressive increase of disorder in the crystalline phase was detected, associated with a significant crystallographic swelling of the material. In a second step the crystalline AmAlO3 perovskite was progressively converted into amorphous AmAlO3, with a total amorphisation occurring after 8 months and 2 x 1018 alpha-decay/g. For the first time, PuAlO3 perovskite was synthesised with an orthorhombic configuration (Space group Imma), showing an interesting parallel to CeAlO3 and PrAlO3 lanthanide analogues. High-temperature XRD was performed and showed a phase transition Imma→R-3c occurring between 473 K and 573 K. The thermal behaviour of R-3c PuAlO3 was followed from 573 K to 1273 K, and extrapolation of the data suggests that cubic plutonium perovskite should become stable at around 1850 K (R-3c→Pm-3m transition).|
|JRC Directorate:||Nuclear Safety and Security|
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