Neptunium(V) partitioning to uranium(VI) oxide and peroxide solids

被引:44
作者
Douglas, M
Clark, SB [1 ]
Friese, JI
Arey, BW
Buck, EC
Hanson, BD
机构
[1] Pacific NW Natl Lab, Radiochem Sci & Engn Grp, Richland, WA 99352 USA
[2] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
关键词
D O I
10.1021/es0405169
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Metaschoepite, [(UO2)(8)O-2(OH)(12)](.)10H(2)O, and metastudtite, UO(4)(.)4H(2)O, are alteration phases anticipated in a spent nuclear fuel repository following the moist oxidation Of UO2 on a geologic time scale. Dissolved concentrations and hence potential mobility of other radionuclides in the fuel, such as the neptunyl cation (NpO2+), Will likely be determined by the extent of their partitioning into these U(VI) solids. Np-237 is of particular interest due to its potential high mobility and long half-life (2.1 x 10(6) years.) In this study, metaschoepite has been precipitated and subsequently transformed to studtite in the presence of dissolved Np. The metaschoepite and studtite solids that formed initially contained < 10 and 6500 ppm Np, respectively. Batch dissolution studies of these solids at pH 6 demonstrate release of Np that exceeds congruent dissolution of U from metastudtite; furthermore, the released Np cation remains in solution. Thus, although the Np partitions into the metastudtite solid initially, it is released to solution over time, indicating that metastudtite is not likely to serve as a host solid for Np incorporation or sorption of the neptunyl cation on long time scales.
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页码:4117 / 4124
页数:8
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