Interface interactions in UN-X-UO2 systems (X = V, Nb, Ta, Cr, Mo, W) by pressure-assisted diffusion experiments at 1773 K
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In: Journal of Nuclear Materials, Vol. 561, 153554, 01.04.2022.
Research output: Contribution to journal › Article › peer-review
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T1 - Interface interactions in UN-X-UO2 systems (X = V, Nb, Ta, Cr, Mo, W) by pressure-assisted diffusion experiments at 1773 K
AU - Costa, Diogo Ribeiro
AU - Liu, Huan
AU - Adorno-Lopez, Denise
AU - Middleburgh, Simon
AU - Wallenius, Janne
AU - Olsson, Par
PY - 2022/4/1
Y1 - 2022/4/1
N2 - UN-UO2 composite fuel is considered an advanced technology fuel (ATF) option to overcome the low oxidation resistance of the UN fuel. However, the interaction between UO2 and UN limits the performance of such composites. A possible way to avoid this interaction is to encapsulate the UN fuel with a material that has a high melting point, high thermal conductivity and reasonably low neutron cross-section. Amongst many candidates, refractory metals can be the first option. In this study, detailed investigations in UN-X-UO2 composite systems (X = V, Nb, Ta, Cr, Mo, W) were performed using SEM/FIB-EDS. The systems were heat-treated at 1773 K and 80 MPa for 10 min in vacuum using the spark plasma sintering method as a pressure-assisted diffusion apparatus. The results suggest that Mo and W are the most promising coating candidates to protect the UN fuel against interactions with UO2. Both metals are inert to N migration and preserve sharp interfaces with the nitride fuel. V, Nb, Ta and Cr strongly interact with UO2 and UN and form their respective nitrides V2N/V8N, Nb2N, and Cr2N. The formation of TaNx was not observed but Ta reacts with UO2 and forms two phases at the UO2-Ta interface (UTa2O7 and Ta2O5), while O from UO2+ x diffuses throughout the Ta foil and oxidise the UN pellet via grain boundary attack. This oxidation mechanism also occurs at the V, Nb and Cr-UN interfaces. Our recent atomic scale modelling of the X-UN interfaces also proposes Mo and W as the optimal candidates. Therefore, these results validate the coating candidates for the UN fuel and may guide further experimental/modelling development in UN-X-UO2 advanced technology fuel.
AB - UN-UO2 composite fuel is considered an advanced technology fuel (ATF) option to overcome the low oxidation resistance of the UN fuel. However, the interaction between UO2 and UN limits the performance of such composites. A possible way to avoid this interaction is to encapsulate the UN fuel with a material that has a high melting point, high thermal conductivity and reasonably low neutron cross-section. Amongst many candidates, refractory metals can be the first option. In this study, detailed investigations in UN-X-UO2 composite systems (X = V, Nb, Ta, Cr, Mo, W) were performed using SEM/FIB-EDS. The systems were heat-treated at 1773 K and 80 MPa for 10 min in vacuum using the spark plasma sintering method as a pressure-assisted diffusion apparatus. The results suggest that Mo and W are the most promising coating candidates to protect the UN fuel against interactions with UO2. Both metals are inert to N migration and preserve sharp interfaces with the nitride fuel. V, Nb, Ta and Cr strongly interact with UO2 and UN and form their respective nitrides V2N/V8N, Nb2N, and Cr2N. The formation of TaNx was not observed but Ta reacts with UO2 and forms two phases at the UO2-Ta interface (UTa2O7 and Ta2O5), while O from UO2+ x diffuses throughout the Ta foil and oxidise the UN pellet via grain boundary attack. This oxidation mechanism also occurs at the V, Nb and Cr-UN interfaces. Our recent atomic scale modelling of the X-UN interfaces also proposes Mo and W as the optimal candidates. Therefore, these results validate the coating candidates for the UN fuel and may guide further experimental/modelling development in UN-X-UO2 advanced technology fuel.
KW - Advanced technology fuel
KW - Pressure-assisted diffusion
KW - Refractory metals
KW - Spark plasma sintering
KW - UN-UO2
U2 - 10.1016/j.jnucmat.2022.153554
DO - 10.1016/j.jnucmat.2022.153554
M3 - Article
VL - 561
JO - Journal of Nuclear Materials
JF - Journal of Nuclear Materials
SN - 0022-3115
M1 - 153554
ER -