Abstract
In this study, experimental characterization and reactive molecular dynamics simulations were integrated to reveal the effects of NaCl on the early hydration of tricalcium silicate (C3S). The results demonstrate that NaCl significantly accelerates the early hydration of C3S by promoting Ca dissolution and silicate tetrahedra polymerization. Specifically, Cl–ions coordinate with surface Ca, weakening the Ca–O bonds in C3S and reducing the energy barrier for Ca dissolution. Meanwhile, Na+ions compete with Ca2+for the O atoms, creating localized charge imbalance and attracting protons, which destabilize Si–O bonds and facilitate the polymerization of silicate tetrahedra. These effects are further amplified at elevated temperatures, which accelerate Ca dissolution and silicate chain formation. For the first time, an atomistic dual-pathway mechanism is proposed in this study, where Cl–facilitates Ca dissolution while Na+drives silicate polymerization during early C3S hydration, advancing the molecular-level understanding of ionic effects in cement hydration.
Recommended Citation
W. Zhang et al., "Atomistic Insights into Dual Mechanisms for NaCl-Driven Dissolution and Polymerization of Tricalcium Silicate," ACS Sustainable Chemistry and Engineering, vol. 13, no. 41, pp. 17520 - 17536, American Chemical Society, Oct 2025.
The definitive version is available at https://doi.org/10.1021/acssuschemeng.5c07547
Department(s)
Civil, Architectural and Environmental Engineering
Keywords and Phrases
hydration; NaCl; reactive molecular dynamics; temperature; tricalcium silicate
International Standard Serial Number (ISSN)
2168-0485
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2025 American Chemical Society, All rights reserved.
Publication Date
20 Oct 2025
Comments
National Key Research and Development Program of China, Grant 2022YFE0133800