Molecular dynamics simulation of coupled water and ion adsorption in the nano-pores of a realistic calcium-silicate-hydrate gel. (13th September 2021)

• Record Type: Journal Article
• Authors: Tu, Yongming; Yu, Qian; Wen, Rongjia; Shi, Pan; Yuan, Lei; Ji, Yuanhui; Sas, Gabriel; Elfgren, Lennart
• Is Part Of: Construction & building materials. Volume 299(2021)
• Publication Date: 2021-09-13
• Subjects: Molecular dynamics -- Realistic C-S-H -- Water molecules -- Ion-coupled -- Interface -- Adsorption; Building materials -- Periodicals; 624.18
• DOI: 10.1016/j.conbuildmat.2021.123961
• Languages: English
• ISSNs: 0950-0618

Abstract

Highlights: A more accurate real model of C-S-H is reconstructed in our work. The structure and dynamic properties of water in different regions are compared. Effects of mixed solutions on the adsorption of sodium ions are discussed. The coupling adsorption characteristics and mechanisms of different anions on the surface are studied. Abstract: The adsorption behavior of water and ions at the surfaces of porous calcium-silicate-hydrate (C-S-H) gels affects the durability of concrete. This paper presents the results of molecular dynamics simulations performed using the Clay Force Field that were conducted to investigate the local structure, adsorption behavior, and dynamic properties of water and ions in the pores of C-S-H gels. A realistic C-S-H gel channel model was constructed and simulated with three mixed salt solutions (NaCl + Na2 SO4, NaCl + Na2 CO3, and Na2 SO4 + Na2 CO3 ) in the pores. The realistic C-S-H gel surface was found to be hydrophilic, causing water molecules to adopt an orderly arrangement near the substrate surface. This hydrophilicity is due to defective silicon chains in the substrate that provide large numbers of hydrogen bonding sites for surface water molecules. Additionally, calcium atoms near the surface attract water molecules to form hydration layers. The adsorption of cations near the substrate correlated negatively with the strengths of the ionic clusters formed by the dissolved anions and cations. As a result, the adsorption of sodium ion was strongest for the NaCl + Na2 SO4 solution and weakest for the Na2 SO4 + Na2 CO3 solution. There were also clear differences in the adsorption behaviors of the anions. Chloride adsorption was mainly driven by ion pairing with calcium atoms near the surface, while sulfate adsorption was mainly due to ion pairing with surface-adsorbed sodium ions. Conversely, carbonate ions exhibited weaker surface adsorption because of their tendency to form ionic clusters in solution. These insights into the adsorption behaviors of common ions near a realistic C-S-H gel surface will be useful in future efforts to develop modified cement-based materials with improved properties.