This paper presents the results of an experimental study performed to investigate the effect of activator modulus (SiO₂/Na₂O) and slag addition on the fresh and hardened properties of alkali-activated fly ash/slag (AAFS) pastes. Four activator moduli (SiO₂/Na₂O), i.e., 0.0, 1.0, 1.5, and 2.0, and five slag-to-binder ratios, i.e., 0, 0.3, 0.5, 0.7, 1.0, were used to prepare AAFS mixtures. The setting time, flowability, heat evolution, compressive strength, microstructure, and reaction products of AAFS pastes were studied. The results showed that the activator modulus and slag content had a combined effect on the setting behavior and workability of AAFS mixtures. Both the activator modulus and slag content affected the types of reaction products formed in AAFS. The coexistence of N–A–S–H gel and C–A–S–H gel was identified in AAFS activated with high pH but low SiO₂ content (low modulus). C–A–S–H gel had a higher space-filling ability than N–A–S–H gel. Thus, AAFS with higher slag content had a finer pore structure and higher heat release (degree of reaction), corresponding to a higher compressive strength. The dissolution of slag was more pronounced when NaOH (modulus of 0.0) was applied as the activator. The use of Na₂SiO₃ as activator significantly refined the pores in AAFS by incorporating soluble Si in the activator, while further increasing the modulus from 1.5 to 2.0 prohibited the reaction process of AAFS, resulting in a lower heat release, coarser pore structure, and reduced compressive strength. Therefore, in view of the strength and microstructure, the optimum modulus is 1.5.

Graphene (G) and graphene oxide (GO) have been shown to significantly improve the mechanical properties of cement-based materials. In this study, the effect of the G/GO on cement hydration was investigated. First, the zeta potential of G/GO in simulated solutions was tested, and the interaction between G/GO’s surface and Ca ²⁺ was explored. Subsequently, scanning electron microscopy was used to observe the morphology of C–S–H nucleation and growth on the cement surface in the cement paste containing G/GO. Furthermore, XRD and TGA analyses were carried out on the hydration products of the sample. At last, isothermal calorimetry was applied to investigate the influence of G/GO on the early hydration of cement. The results showed that the addition of G/GO significantly accelerates C–S–H nucleation and growth on the cement surface. It is indicated that the high mobility ions derived by G/GO in the cement paste dominate the reason for the accelerated hydration of cement. The presence of G, especially GO, facilitates the mobility of ions, especially Ca ²⁺ , thus enhances the interaction between the cement surface and the ions. This strong interaction promotes the C–S–H nucleation and growth, and therefore, the hydration of the cement.

Using eggshell powder (EP) to replace partial cement in cement-based materials can abate pollution caused by eggshell discard and cement production. In this paper, the surface property of EP and its influence on cement hydration were studied. Quartz powder (QP) and limestone powder (LP) were used as references. First, the chemical composition of EP was characterized. Then, the surface charge properties of these materials were analyzed using zeta potential measurement. The interactions between EP surface and Ca²⁺ were discussed based on the zeta potential test. Afterward, a scanning electron microscope (SEM) was applied to observe the morphology of hydrates on the surfaces of these materials. The results indicated that, although the compositions of EP and LP are similar, the surface charge properties are significantly different. This is likely due to the existence of organic matter on the surface of EP and the difference in the atomic structure. As shown from the zeta potential test, EP exhibits similar interaction with Ca²⁺ as QP. The interactions between EP surface and Ca²⁺ are much weaker than that between LP and Ca²⁺. These weak interactions lead to the growth of C–S–H on the surface of EP particles less than that of LP particles. The chemical reactivity of EP can be improved by using heat treatment, electrical oven, etc. This study will provide theoretical support for the better use of EP in cement-based materials.