期刊
SCIENCE OF THE TOTAL ENVIRONMENT
卷 842, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.scitotenv.2022.156837
关键词
Kaolinite; Muscovite; Uranium; Calcium bridge; C -S -H; TRLFS
This study comprehensively evaluates the effect of Ca2+ on the retention of U(VI) and Np(VI) on alumosilicate minerals using batch sorption experiments and time-resolved laser-induced luminescence spectroscopy (TRLFS). The results confirm that alkaline earth elements enable strong retention of hexavalent actinides on clay minerals under hyperalkaline repository conditions.
complex geochemical conditions involving complex solution compositions and high pH resulting from degradation of cementitious geo-engineered barriers. Ca2+ cations have been hypothesized to play an important role as mediators for the retention of U(VI) on Ca-bentonite at (hyper)alkaline conditions, despite the anionic character of both the mineral surface and the aqueous uranyl species. To gain deeper insight into this sorption process, the effect of Ca2+ on U(VI) and Np(VI) retention on alumosilicate minerals has been comprehensively evaluated, using batch sorption experiments and time-resolved laser-induced luminescence spectroscopy (TRLFS). Sorption experiments with Ca2+ or Sr2+ and zeta potential measurements showed that the alkaline earth metals sorb strongly onto Ca-bentonite at pH 8-13, leading to a partial compensation of the negative surface charge, thereby generating potential sorption sites for anionic actinyl species. U(VI) and Np(VI) sorption experiments in the absence and presence of Ca2+ or Sr2+ confirmed that these cations strongly enhance radionuclide retention on kaolinite and muscovite at pH >_ 10. Concerning the underlying retention mechanisms, site-selective TRLFS provided spectroscopic proof for two dominating U(VI) species at the alumosilicate surfaces: (i) A ternary U(VI) complex, where U(VI) is bound to the surface via bridging Ca cations with the configuration surface equivalent to Ca - OH - U(VI) and, (ii) U(VI) sorption into the interlayer space of calcium (aluminum) silicate hydrates (C-(A-)S-H), which form as secondary phases in the presence of Ca due to partial dissolution of alumosilicates under hyperalkaline conditions. Consequently, the present study confirms that alkaline earth elements, which are ubiquitous in geologic systems, enable strong retention of hexavalent actinides on clay minerals under hyperalkaline repository conditions.
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