Water's behaviour on Ca-rich tricalcium silicate surfaces for various degrees of hydration: A molecular dynamics investigation

被引：22

作者：

Claverie, Jerome ^{[1
,2
]}

Bernard, Fabrice ^{[1
]}

Marques Cordeiro, Joao Manuel ^{[2
]}

Kamali-Bernard, Siham ^{[1
]}

机构：

[1] INSA Rennes, Lab Civil Engn & Mech Engn LGCGM, Rennes, France

[2] Sao Paulo State Univ UNESP, Sch Nat Sci & Engn, Dept Chem & Phys, BR-15385000 Sao Paulo, Brazil

来源：

JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS | 2019年 / 132卷

关键词：

Hydration; Tricalcium silicateC(3)S; Molecular dynamics (MD) simulations; Hydrogen bonding; REACTIVE FORCE-FIELD; ATOMISTIC SIMULATIONS; MECHANICAL-PROPERTIES; SCREW DISLOCATIONS; S-H; CALCIUM; ENERGETICS; IMPACT; STABILITY; ADSORPTION;

D O I：

10.1016/j.jpcs.2019.03.020

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Tricalcium silicate (C3S) hydration is a highly relevant topic toward a better understanding of ordinary Portland cement. Molecular Dynamics (MD) simulations can provide relevant information about water behaviour at interface with mineral surfaces. For the first time, the influence of C3S protonation on water structure and dynamics is assessed by simulating the Ca-rich (040) surface in contact with water. The recently extended INTERFACE force field for C3S, including parameters for hydroxyl and silanol groups, was used to perform classical MD calculations. The water layered structure arising from strong hydrogen bonding with the mineral surface decays with increasing hydration of the first atomic layer. We found that the presence of hydroxyl and silanol groups, as well as desorption of calcium cations strongly influence the structural and dynamical properties of water.

引用

页码：48 / 55

页数：8