K. Sasaki et al., HIGHLY REACTIVE BETA-DICALCIUM SILICATE .5. INFLUENCE OF SPECIFIC SURFACE-AREA ON HYDRATION, Journal of the American Ceramic Society, 76(4), 1993, pp. 870-874
The hydration of beta-C2S prepared from hillebrandite [Ca2(SiO3)(OH)2]
and having specific surface areas of 6.8, 5.5, and 3.1 m2/g was inves
tigated. Different specific areas were obtained by varying the dissoci
ation temperature of hillebrandite. In addition, the hydration of beta
-C2S synthesized from high-temperature solid-state reaction was also s
tudied as a comparison. The specific surface area exerts a strong infl
uence on the hydration rate, which increases as the surface area incre
ases. The degree of influence changes with the reaction, becoming grea
ter as hydration progresses. There is initially a linear relationship
between specific area and the time required to complete a specific rea
ction. The specific surface area also affects the reaction mechanism.
In the case of specific areas of 5.5 m2/g or less, the reaction change
s from a chemical reaction to a diffusion-controlled one, and the degr
ee of reaction comes almost to a halt at 80% to 85%. The Ca/Si ratios
of hydrate and the silicate anion structures were also investigated in
this study.