TY - JOUR
T1 - Si-contamination driven phase evolution in Nd-doped UO2 porous microspheres
AU - Çolak, Gamze
AU - Leinders, Gregory
AU - Delville, Rémi
AU - Van Renterghem, Wouter
AU - Mai, Tommy
AU - Verwerft, Marc
AU - Vleugels, Jef
N1 - Score=10
Funding Information:
The authors gratefully acknowledge Koen Vanaken and Peter Dries for their technical support and the Energy Transition Fund of the Belgian FPS Economy (project: ASOF – Advanced Separation for Optimal management of Spent Fuel) for the financial support of this research. Gamze Colak thanks Simon Billiet and Dr. Christian Schreinemachers for helpful discussions and Jelle Van Eyken and Nico Vanhove for their support during microscopy investigations at SCK CEN.
Publisher Copyright:
© 2024 Elsevier Ltd and Techna Group S.r.l.
PY - 2024/5/1
Y1 - 2024/5/1
N2 - The distribution of neodymium dopant (as surrogate for americium) within the porous network of sintered (U,Nd)O2 microspheres prepared via a sol-gel infiltration technique was comprehensively assessed. Powder X-ray diffraction (XRD) results indicated the formation of a neodymium oxyapatite secondary phase with Nd4.69(SiO4)3O composition, alongside the principal U1-yNdyO2 face-centered cubic phase for y = 20 and 30 mol%. The hexagonal oxyapatite phase was likely formed during sintering under reducing conditions, when volatile SiO from an external contamination reacted with the Nd3+ in the microspheres. Transmission electron microscopy (TEM) analyses on lamellae prepared via focused ion beam (FIB) further confirmed a distinct phase separation between the main (fluorite U1-yNdyO2) phase and the oxyapatite phase, without mutual solubility of Si and U. To gain a deeper insight into the microstructure, energy dispersive X-ray spectroscopy (EDS) and electron probe microanalysis (EPMA) were performed at different locations in cross-sectioned U1-yNdyO2 microspheres. The elemental mappings showed a higher intensity of combined Nd and Si content in the periphery region, where a higher filling of the porosity network is to be expected. XRD lattice parameter analysis was found to be the most reliable method to elucidate the Nd metal fraction y in U1-yNdyO2, as compared to local quantification methods using electron beam induced X-ray fluorescence. The sintered microspheres with a targeted 20 and 30 mol% Nd dopant concentration contain around 3 ± 2 wt% and 5 ± 2 wt% Nd-oxyapatite phase. The formation mechanism of the oxyapatite phase appears to involve capillary infiltration in the liquid state, during high temperature sintering, and it may be of interest for other applications. Despite the phase heterogeneity, the method was successful in infiltrating Nd throughout the porous microspheres at high loading levels, as intended for the fabrication of transmutation targets. The distribution of the Nd-dopant throughout the microsphere was achieved as desired, and this study presents a successful fabrication and detailed characterization of porous uranium oxide microspheres doped with Nd3+, contributing to the development of transmutation target research.
AB - The distribution of neodymium dopant (as surrogate for americium) within the porous network of sintered (U,Nd)O2 microspheres prepared via a sol-gel infiltration technique was comprehensively assessed. Powder X-ray diffraction (XRD) results indicated the formation of a neodymium oxyapatite secondary phase with Nd4.69(SiO4)3O composition, alongside the principal U1-yNdyO2 face-centered cubic phase for y = 20 and 30 mol%. The hexagonal oxyapatite phase was likely formed during sintering under reducing conditions, when volatile SiO from an external contamination reacted with the Nd3+ in the microspheres. Transmission electron microscopy (TEM) analyses on lamellae prepared via focused ion beam (FIB) further confirmed a distinct phase separation between the main (fluorite U1-yNdyO2) phase and the oxyapatite phase, without mutual solubility of Si and U. To gain a deeper insight into the microstructure, energy dispersive X-ray spectroscopy (EDS) and electron probe microanalysis (EPMA) were performed at different locations in cross-sectioned U1-yNdyO2 microspheres. The elemental mappings showed a higher intensity of combined Nd and Si content in the periphery region, where a higher filling of the porosity network is to be expected. XRD lattice parameter analysis was found to be the most reliable method to elucidate the Nd metal fraction y in U1-yNdyO2, as compared to local quantification methods using electron beam induced X-ray fluorescence. The sintered microspheres with a targeted 20 and 30 mol% Nd dopant concentration contain around 3 ± 2 wt% and 5 ± 2 wt% Nd-oxyapatite phase. The formation mechanism of the oxyapatite phase appears to involve capillary infiltration in the liquid state, during high temperature sintering, and it may be of interest for other applications. Despite the phase heterogeneity, the method was successful in infiltrating Nd throughout the porous microspheres at high loading levels, as intended for the fabrication of transmutation targets. The distribution of the Nd-dopant throughout the microsphere was achieved as desired, and this study presents a successful fabrication and detailed characterization of porous uranium oxide microspheres doped with Nd3+, contributing to the development of transmutation target research.
KW - Uranium dioxide
KW - Neodymium
KW - Infiltration
KW - Rare-earth silicate
KW - Oxyapatite
UR - http://www.scopus.com/inward/record.url?scp=85184054569&partnerID=8YFLogxK
U2 - 10.1016/j.ceramint.2024.01.338
DO - 10.1016/j.ceramint.2024.01.338
M3 - Article
SN - 0272-8842
VL - 50
SP - 14307
EP - 14317
JO - Ceramics International
JF - Ceramics International
IS - 9
ER -