A model for the CaO—SiO2—H2O system at 25°C is proposed, and based upon this, more complex systems including the effect of SO42-, Cl-, CO32-, Na+ and K+ on phase relations and solubilities in the title system have been calculated by thermodynamic modelling. At sea-water concentrations of NaCl, mixed sea-water-pore fluid compositions enhance the solubility of calcium from Ca(OH)2 and C-S-H but do not otherwise affect the stabilities of these phases. Carbonate and sulfate, on the other hand, react strongly with cement substances both with and without sodium being present; the complex solubility and reaction paths are quantified. Comparison of calculated reactions with literature data are made where possible; generally good agreement is obtained.
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October 1997
Research Article|
October 01 1997
Modelling the impact of abundant geochemical components on phase stability and solubility of the CaO—SiO2—H2O system at 25°C: Na+, K+, SO42-, Cl- and CO32 - Available to Purchase
F. P. Glasser
University of Aberdeen
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Department of Chemistry, Meston Building, University of Aberdeen, Aberdeen AB24 3UE, UK.
Publisher: Emerald Publishing
Online ISSN: 1751-7605
Print ISSN: 0951-7197
© 1997 Thomas Telford Ltd
1997
Advances in Cement Research (1997) 9 (36): 167–181.
Citation
Stronach SA, Glasser FP (1997), "Modelling the impact of abundant geochemical components on phase stability and solubility of the CaO—SiO2—H2O system at 25°C: Na+, K+, SO42-, Cl- and CO32 -". Advances in Cement Research, Vol. 9 No. 36 pp. 167–181, doi: https://doi.org/10.1680/adcr.1997.9.36.167
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