K-A-S-H (K2O-Al2O3-SiO2-H2O) gel is a key phase that forms in most alkali-activated binders (eco-friendly binders which utilize a substantial amount of industrial by-product). An in-depth understanding of the microstructure and performance of this nano-sized key phase facilitates better application to alkali-activated binders. However, such studies remain little and undetailed. Therefore, our research aims to provide insights into the microstructure of K-A-S-H particles synthesized with accurate stoichiometric control by the hydrothermal method through thermogravimetric analysis (TG), Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and BET surface area. The results show that for materials prepared at the curing temperature lower than 80 °C, the K-A-S-H products were completely amorphous. With increased curing temperature and time, the K-A-S-H products were transformed from the amorphous phase to the crystalline zeolite phase structure, with a reduction in the specific surface area. The TG results indicate that the crystalline phase contains more non-evaporated water or zeolite water for structural rearrangement. The degree of tetrahedral polymerization slightly decreased with an increase of the K2O/SiO2 ratio as the amount of non-bridged oxygen atoms increased, whereas it gradually increased with an increase of curing temperature and time, as suggested by the FTIR and NMR results. Various K2O/SiO2 ratios resulted in the formation of zeolite K-H and K-G zeolite, both of which exhibited highly polymerized three-dimensional network structures. However, there was no significant effect of the SiO2/Al2O3 ratio on the structure of K-A-S-H products. Overall, these results provide insight into understanding the chemical stability of K-A-S-H.
This study investigated the influence of alkali content on the early-age hydration process of slag-based geopolymer and the feasibility of non-destructive resistivity. Results showed that there existed a threshold of alkali content in adjusting the early-age hydration. Initially, increasing the alkali content tended to accelerate the dissolution period (detected by resistivity and heat release rate) and resulted in a denser microstructure (detected by TEM). When the alkali content surpassed 6 wt%, the increasing alkali content mitigated the structural development of a slag-based geopolymer, as it lowered the liquid water content and caused local precipitation, which trapped the early-age ions transmission and, therefore, the later-age mechanical development was inhibited. It was proven that the resistivity acted as a linkage among the reaction degree, workability, and strength development.
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