JOURNAL OF NUCLEAR MATERIALS | 卷:484 |
The high-temperature heat capacity of the (Th,U)O2 and (U,Pu)O2 solid solutions | |
Article | |
Valu, S. O.1,2 Benes, O.1 Manara, D.1 Konings, R. J. M.1,2 Cooper, M. W. D.3,4 Grimes, R. W.3 Gueneau, C.5 | |
[1] European Commiss, Joint Res Ctr, POB 2340, D-76125 Karlsruhe, Germany | |
[2] Delft Univ Technol, Fac Appl Phys, Mekelweg 15, NL-2629 JB Delft, Netherlands | |
[3] Imperial Coll, Dept Mat, London SW7 2AZ, England | |
[4] Los Alamos Lab, Div Mat Sci & Technol, POB 1663, Los Alamos, NM 87545 USA | |
[5] Ctr Saclay, LM2T, SCCME, CEA,DANS,DPC, Gif Sur Yvette, France | |
关键词: Actinide mixed oxides; Calorimetry; Heat capacity; | |
DOI : 10.1016/j.jnucmat.2016.11.010 | |
来源: Elsevier | |
![]() |
【 摘 要 】
The enthalpy increment data for the (Th,U)O-2 and (U,Pu)O-2 solid solutions are reviewed and complemented with new experimental data (400-1773 K) and many-body potential model simulations. The results of the review show that from room temperature up to about 2000 K the enthalpy data are in agreement with the additivity rule (Neumann-Kopp) in the whole composition range. Above 2000 K the effect of Oxygen Frenkel Pair (OFP) formation leads to an excess enthalpy (heat capacity) that is modeled using the enthalpy and entropy of OFP formation from the end-members. A good agreement with existing experimental work is observed, and a reasonable agreement with the results of the many-body potential model, which indicate the presence of the diffuse Bredig (superionic) transition that is not found in the experimental enthalpy increment data. (C) 2016 Published by Elsevier B.V.
【 授权许可】
Free
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
10_1016_j_jnucmat_2016_11_010.pdf | 673KB | ![]() |