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Jan Tits, Kazuki Iijima, Erich Wieland, Gento Kamei
The uptake of radium by calcium silicate hydrates and hardened cement paste
Keywords: Radium, C-S-H, Cement, Adsorption, Ion-exchange
In the present study the interaction of Ra(II) with calcium silicate hydrates (C-S-H) as well as with fresh and degraded hardened cement pastes (HCP) has been investigated using batch-type sorption tests. Synthetic C-S-H phases with varying CaO:SiO2 (C:S)mol ratios, relevant to non-degraded HCP and degraded HCP, were prepared in the absence of alkalis (Na(I), K(I)) and in an alkali-rich artificial cement pore water (ACW). The Ra(II) sorption kinetics, the effect of the solid to liquid ratio and the C:S mol ratio on the Ra(II) uptake were investigated. In addition, the reversibility of Ra(II) sorption was tested using dilution tests. Comparison with data on the uptake of Sr(II) by C-S-H phases obtained from previous in-house studies showed that the same model concept could be applied to interpret the immobilization of Sr(II) and Ra(II) in these systems. Ra(II) sorption on C-S-H in the absence of alkalis could be interpreted in terms of a Ra2+-Ca2+ cation exchange model. The Ra2+-Ca2+ exchange selectivity coefficient, RaCaKC, was determined to be (6±4). There are indications that, in the presence of alkalis, the Ra(II) sorption by C-S-H phases can only be described with the help of an ion-exchange model involving Ra2+, Ca2+ and the monovalent alkalis.
The cation exchange model developed for C-S-H phases in the absence of alkalis was successfully applied to predict the sorption of Ra(II) on degraded HCP, assuming that the Ra(II) sorbs solely on the C-S-H fraction of the HCP. Model predictions and experimental data were found to agree well in view of the simplified sorption model used.
Radiochimica Acta, Oldenbourg Wissenschaftsverlag
Print ISSN: 0033-8230
Volume: 94, 09/2006
Pages: 637 - 643