Abstract
Understanding of the behaviour of nuclear material in extreme conditions is essential for the analyses of the operation limits of nuclear fuels, and prediction of possible nuclear reaction accidents. In this context, the high temperature behaviour of uranium nitride and mixed uranium–plutonium nitrides has been studied in the present work by laser heating under controlled atmosphere coupled with fast multi-wavelength pyrometry. Such an approach has allowed performing a thermal arrest analysis and establishing the solid–liquid phase boundaries in the investigated compositions, whereby non-congruent vaporisation was avoided by setting a suitable nitrogen overpressure. In addition, the normal spectral emissivities of the current samples were determined by radiance spectroscopy. Besides revealing a slightly more metallic optical behaviour in plutonium-containing compositions, this latter characterisation led to the determination of the real melting/solidification temperatures of the investigated nitrides. It is confirmed that UN melts congruently at (3120±30) K in a nitrogen pressure of 0.25MPa (2.5bar). The melting/solidification temperatures decrease in plutonium containing samples, reaching (3045±25) K for x(PuN)=0.2, a composition of interest for potential applications of this material as a nuclear fuel. Besides their fundamental importance, the current results are useful for a deeper understanding of the nitride fuel behaviour under accidental conditions, whereby uncontrolled thermal excursions might occur in the nuclear reactor core.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.