Comparison of the effects of carbon-based and inorganic nanomaterials on early cement hydration

This study delves into the impact of nanomaterials on early cement hydration, aiming to elucidate their mechanism of action. Four nanomaterials were selected, including carbon-based nanomaterials (multi-walled carbon nanotubes (CNT) and graphene oxide (GO)) and inorganic nanomaterials (nano-SiO2 and nano-CaCO3). Initially, the zeta potential was employed to examine nanomaterial adsorption on relevant ions in simulated solutions. Subsequently, SEM NMR, XRD, and TGA were utilized to assess the influence of different nanomaterials on hydration product morphology, content, and structure. Utilizing the Krstulovic-Dabic model, the hydration kinetics based on the heat of hydration in cement paste containing nanomaterials was simulated. Results revealed nanomaterials exhibited stronger Ca2+ ion adsorption than cement particles, with CNT and GO particles displaying weaker adsorption relative to SO42- ions. Conversely, nano-SiO2 and nano-CaCO3 particles exhibited a stronger adsorption capacity for Ca2+ ions than SO4 2- ions. This robust adsorption facilitated hydration product generation, yielding fine and regular C-S-H particles in carbon-based nanomaterial-containing cement pastes, contrasting with coarse and irregular particles in inorganic nanomaterial-containing pastes. Nanomaterial introduction increased polymerization and the average chain length of hydration products. Furthermore, it heightened exothermic peak intensity and total exothermic amount, while reducing the induction period and exothermic peak length. Hydration kinetics, simulated through the Krstulovic-Dabic model, aligned with the nucleation and growth (NG)-phase boundary reaction (I)-diffusion (D) process. In the NG stage, nanomaterials accelerated hydration by reducing reaction stages (n) and increasing the rate constant (K1'). In the I stage, hindered Ca2+ ion migration led to decreased K2', slowing hydration. Stage D witnessed a rapid decline in K3'.