Characterization of δ-PuGa (1 at%. Ga) Oxidation Under Dry Oxygen Atmosphere Exposure

Abstract The oxidation of δ-stabilized plutonium alloy was studied under dry oxygen exposures for temperatures varying from 100 up to 300 °C and oxygen partial pressures varying from 10 –4 up to 500 mbar. The coupling of X-ray diffraction, Raman spectroscopy and FIB-SEM has allowed to show that the oxide scale is composed of an outer layer of PuO 2 and an inner mixed layer of α + β-Pu 2 O 3 platelets propagating into a metallic zone corresponding to the stable phase of unalloyed Pu. Furthermore, the analysis of Pu oxidation kinetics has displayed first a parabolic growth governed by the diffusion of interstitial oxygen. This step consists of the thickening of the Pu 2 O 3 layer with a decrease in α-Pu 2 O 3 ratio in favor of β-Pu 2 O 3 . Then, a second step occurs consisting of a linear growth of the PuO 2 -layer with the formation of thick nodules which tend to cover the whole oxide surface. Based on the results of this work, a general oxidation mechanism for δ-Pu alloy is provided.

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Publication Details

Journal
High Temperature Corrosion of Materials
Published
2024-08-20
DOI
https://doi.org/10.1007/s11085-024-10267-6
Citations
3
Primary Topic
Nuclear Materials and Properties
Type
article
Field-Weighted Citation Impact
0.35

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article

Characterization of δ-PuGa (1 at%. Ga) Oxidation Under Dry Oxygen Atmosphere Exposure

Denis Menut, L. Jolly, I. Zacharie-Aubrun, P. Martín et al.
3 citations
High Temperature Corrosion of Materials
Nuclear Materials and Properties
0.35
article

Characterization of δ-PuGa (1 at%. Ga) Oxidation Under Dry Oxygen Atmosphere Exposure

Denis Menut, L. Jolly, I. Zacharie-Aubrun, P. Martín, N. Favart, B. Ravat, B. Oudot, Iolanda Valentina Popa
article en
3 citations

Abstract

Abstract The oxidation of δ-stabilized plutonium alloy was studied under dry oxygen exposures for temperatures varying from 100 up to 300 °C and oxygen partial pressures varying from 10 –4 up to 500 mbar. The coupling of X-ray diffraction, Raman spectroscopy and FIB-SEM has allowed to show that the oxide scale is composed of an outer layer of PuO 2 and an inner mixed layer of α + β-Pu 2 O 3 platelets propagating into a metallic zone corresponding to the stable phase of unalloyed Pu. Furthermore, the analysis of Pu oxidation kinetics has displayed first a parabolic growth governed by the diffusion of interstitial oxygen. This step consists of the thickening of the Pu 2 O 3 layer with a decrease in α-Pu 2 O 3 ratio in favor of β-Pu 2 O 3 . Then, a second step occurs consisting of a linear growth of the PuO 2 -layer with the formation of thick nodules which tend to cover the whole oxide surface. Based on the results of this work, a general oxidation mechanism for δ-Pu alloy is provided.

High Temperature Corrosion of MaterialsVol. 101(5)
Centre National de la Recherche Scientifique (FR), Université de Bourgogne (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), CEA Valduc (FR), Synchrotron soleil (FR), CEA Grenoble (FR), CEA Cadarache (FR), Laboratoire Interdisciplinaire Carnot de Bourgogne (FR), CEA Marcoule (FR), Institut des Sciences et technologies pour une Economie Circulaire des énergies bas carbone (FR)
Commissariat à l'Énergie Atomique et aux Énergies Alternatives
Clean water and sanitation
Openalex Percentile: Top 45%
Nuclear Materials and Properties
0.35
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