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U(VI) retention in compact Callovo-Oxfordian clay stone at temperature (20-80 °C); What is the applicability of adsorption models?
被引:2
|作者:
Montavon, G.
[1
]
Ribet, S.
[1
]
Bailly, C.
[1
]
Loni, Y. Hassan
[1
]
Made, B.
[2
]
Grambow, B.
[1
]
机构:
[1] Univ Nantes, SUBATECH, IMT A, CNRS IN2P3, 4 rue Alfred Kastler, F-44307 Nantes, France
[2] ANDRA, 1-7 rue Jean Monnet,Parc Croix Blanche, F-92298 Chdtenay Malabry, France
关键词:
Uranium;
COx;
Clay materials;
Adsorption;
Temperature;
Nuclear waste;
D O I:
10.1016/j.clay.2023.107093
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
In the context of the radioactive waste management in deep geological formations, U(VI) retention by intact Callovo-Oxfordian claystone (COx) was studied by percolation-type experiments at 20 and 80 degrees C. The experimental results were confronted with modelling prediction based on a published adsorption model developed from dispersed media in the 20-80 degrees C temperature range. For the experiments at 20 degrees C, the adsorption model allowed to explain the results for the intact system; the retention was weak (R-d similar to 10 L.kg(-1)) and the analysis of the COx phases at the end of the experiment confirmed a retention of U by the clay fraction. The adsorption model in temperature also explained the observed trend of increasing retention with increasing temperature. However, it underestimated the temperature effect on the adsorption of U(VI) by the COx clay fraction, and other phases contributed to the retention. Solid-state analysis of the percolation-doped samples indicated a reactivity in the order pyrite>clay>calcite phases. The transposition of the knowledge at 20 degrees C from the dispersed system to the intact medium was therefore not possible at 80 degrees C for the studied U(VI)/COx system.
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