J. Rose et al., X-ray absorption spectroscopy study of immobilization processes for heavy metals in calcium silicate hydrates. 2. Zinc, LANGMUIR, 17(12), 2001, pp. 3658-3665
Tricalcium silicate (C3S), the major phase of cement-based materials, conta
ins naturally a few hundred parts per million of heavy metals. An X-ray abs
orption spectroscopy (XAS) study at the Zn K-edge has been carried out to e
lucidate the binding mechanisms of Zn by calcium silicate hydrates, which i
s important to predict the long-term behavior of Zn. At low concentration,
under the threshold of precipitation of the oxide, oxy hydroxide, and calci
um zinc hydroxide, no retardation of the hydration of the C3S has been obse
rved for C3S doped with Zn. A previous Si-29 NMR (Moulin, I.; Stone, W. E.
E.; Sanz, J.; Bottero, J.-Y.; Mosnier, J-Y.; Haehnel, C. Langmuir 1999, 151
2829-2835) study has demonstrated that the structure of the hydrated CBS (
called C-S-H for calcium silicate hydrates) does not change if Zn is presen
t initially or not. XAS experiments have shown that Zn tetrahedra are incor
porated within the matrix of C-S-H and linked directly at the end of the si
licate chains through Zn-O-Si bonds. The Zn-Si distance is approximate to3.
1 Angstrom. Extended X-ray absorption fine structure results have been conf
irmed by ab initio calculations including multiple scattering.