A. Nonat et al., PHYSICOCHEMICAL PARAMETERS DETERMINING HYDRATION AND PARTICLE INTERACTIONS DURING THE SETTING OF SILICATE CEMENTS, Solid state ionics, 101, 1997, pp. 923-930
Hydration of tricalcium silicate (Ca3SiO5), the pure phase used as a m
odel of the portland cements, is the chemical process leading to the f
ormation of hydrates, while setting is a definite time event correspon
ding to the change of the paste from the soft to the hard state. Setti
ng results from interactions between anhydrous or very partially hydra
ted particles. The analysis of these interactions leads to the identif
ication of two fundamental steps: the coagulation of cement grains dur
ing the first minutes following the mixing and the rigidification of t
he coagulated structure which arises simultaneously with the accelerat
ion of the calcium silicate hydrates (C-S-H) formation. The chemical e
volution of the system, which controls the lime concentration in solut
ion, determines the nature of particle interactions and the physical e
volution of the suspension or paste: there exists a critical range of
lime concentration required to initiate the coagulation of cement part
icles and the ability of C-S-H to make rigid the coagulated structure
depends on the solubility of these particles.