Using seawater for concrete production is potentially
advantageous
from a sustainability perspective. However, the fundamental mechanisms
underlying seawater-mixed concrete are far from being understood,
especially from the nanoscale. Herein, molecular models are developed
to study, for the first time, the influence of seawater (NaCl solutions)
on the behavior of calcium silicate hydrate (C-S-H, the main binding
phase of concrete). Thermodynamically, Na+ showed a strong
adsorption capacity on the C-S-H surface, resulting in the partial
release of Ca2+ from the surface (termed as “Na–Ca
cation exchange”). Mechanically, the presence of NaCl in the
interlayer solutions enhanced the bond performance between the C-S-H
layers because Na+ ions provided a greater stress transfer
capacity than H2O molecules. Under shear loading, the C-S-H
layers slid over each other, with the interlayer solutions acting
as a lubricant. An increase in NaCl concentration enhanced the sliding
resistance, which was attributed to the increased viscosity of the
interlayer solutions and strengthening of the solid–solution
interfaces. The above atomic-level findings facilitate a better understanding
of the influence of seawater on concrete properties.