Calcium silicate hydrates: Solid and liquid phase composition

• Published in: Cement and concrete research Vol. 78; no. Part A; pp. 57 - 70
• Main Authors: Lothenbach, Barbara, Nonat, André
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01.12.2015
• Subjects: Alkalis (D); ALUMINIUM; Aluminum; CALCIUM; CALCIUM SILICATES; Chains; CHEMICAL COMPOSITION; Concentration (composition); CONCENTRATION RATIO; C–S–H (B); HYDRATES; LIQUIDS; MATERIALS SCIENCE; Mathematical models; Pore solution (B); POTASSIUM; SILICA; SILICON; Silicon dioxide; SODIUM; SOLUBILITY; UPTAKE; C–S–H (B); Alkalis (D); Aluminium; Pore solution (B)
• ISSN: 0008-8846; 1873-3948
• DOI: 10.1016/j.cemconres.2015.03.019

This paper presents a review on the relationship between the composition, the structure and the solution in which calcium silicate hydrate (C–S–H) is equilibrated. The silica chain length in C–S–H increases with the silicon concentration and the calcium content in the interlayer space with the calcium concentrations. Sodium and potassium are taken up in the interlayer space, preferentially at low calcium concentrations and thus by low Ca/Si C–S–H. Aluminium uptake in C–S–H increases strongly at higher aluminium concentrations in the solution. At low Ca/Si, aluminium substitutes silica in the bridging position, at Ca/Si>1 aluminium is bound in TAH. Recently developed thermodynamic models are closely related to the structure of C–S–H and tobermorite, and able to model not only the solubility and the chemical composition of the C–S–H, but also to predict the mean silica chain length and the uptake of aluminium.