Time-Dependent Retention of a Mixture of Cs(I), Sm(III), Eu(III) and U(VI) as Waste Cocktail by Calcium Silicate Hydrate (C-S-H) Phases

In the context of the safe storage of high-level radioactive waste, the time-dependent retention of a waste cocktail (WC) consisting of Zr(IV), Mo(VI), Ru(III), Pd(II), Cs(I), Sm(III), Eu(III) and U(VI) was studied on the commercially available C-S-H phase Circosil&reg:. The herein presented results focus on Cs(I), Sm(III), Eu(III) and U(VI). Precipitation and wall adsorption studies in the absence of the solid phase show only a small amount of precipitation for Sm(III) and Eu(III) (34 &plusmn: 18%) in the high-saline diluted Gipshut solution (DGS, pH 10.6, I = 2.6 M). For Cs(I) and U(VI), no precipitation was observed. In 0.1 M NaCl (pH 10.9), the measured retention could completely be attributed to wall adsorption for all four elements. The obtained Rd values for the time-dependent retention of Sm(III), Eu(III) and U(VI) on Circosil&reg: of 105 to 106 L&middot:kg&minus:1 are in good agreement with the literature. For Cs(I) in the strongly saline background electrolytes, slightly higher Rd values of up to 8&middot:102 L&middot:kg&minus:1 were determined for the crystalline Circosil&reg: compared to the wet chemical C-S-H phases. Overall, the commercial product Circosil&reg: is suitable as an alternative to synthesised C-S-H phases to observe trends in the retention behaviour of these elements. Comparison between both background electrolytes shows an increase in the amount and velocity of retention for all four elements with decreasing salinity. This confirms adsorption processes as the fastest and initial retention mechanism. Precipitation or incorporation of Eu(III), Sm(III) and U(VI) cannot be ruled out in the long term. Comparing the kinetic of this WC study to single-element studies in the literature, a longer uptake time to reach a steady state of 7 d in 0.1 M NaCl and 28 d in DGS instead of &lt:1 d was observed for Eu(III) and Sm(III). The situation for Cs(I) is similar. This indicates competing effects between the different WC elements for adsorption sites on the C-S-H phases.