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Wai Li Ling

Publications and source records attributed to Wai Li Ling.

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Mechanisms and kinetics of C-S-H nucleation approaching the spinodal line: Insights into the role of organics additives

Wet chemistry C-S-H precipitation experiments were performed under controlled conditions of solution supersaturation in the presence and absence of gluconate and three hexitol molecules. Characterization of the precipitates with SAXS and cryo-TEM experiments confirmed the presence of a multi-step nucleation pathway. Induction times for the formation of the amorphous C-S-H spheroids were determined from light transmittance. Analysis of those data with the classical nucleation theory revealed a significant increase of the kinetic prefactor in the same order as the complexation constants of calcium and silicate with each of the organics. Finally, two distinct precipitation regimes of the C-S-H amorphous precursor were identified: i) a nucleation regime at low saturation indexes (SI) and ii) a spinodal nucleation regime at high SI where the free energy barrier to the phase transition is found to be of the order of the kinetic energy or less.

cond-mat.mtrl-sci

Impact of gluconate and hexitol additives on the precipitation mechanism and kinetics of C-S-H

The present paper investigates the influence of gluconate and hexitol additives on the precipitation mechanism and kinetics of C-S-H. To this end, wet chemistry C-S-H precipitation experiments were performed under controlled conditions of solution supersaturation, under varying silicate concentration, while the transmittance of the solution was followed. This allowed determining induction times for the formation of C-S-H precursors in the presence and absence of gluconate and three hexitol molecules. Characterization of the precipitates was performed via small angle X-ray scattering and cryo-transmission electron microscopy experiments, which allowed the identification of a multi-step nucleation pathway also in the presence of the organics. Analysis of the induction time data in the framework of the classical nucleation theory revealed a significant increase of the kinetic pre-factor, which is associated to physical rates of cluster collision and aggregation during the nucleation process. Values of the kinetic pre-factor increase in the same order as the complexation constants of calcium and silicate with the each of the organics. This points to a retarding mechanism of crystallization related to steric hindrance of the aggregation of the early formed clusters via adsorption of the organics at their surfaces.

cond-mat.mtrl-sci