In this study, the effects of graphene oxide (GO) on the microstructure of cement mortars were studied using scanning electron microscopy (SEM), thermogravimetric (TG), and X-ray diffraction (XRD) techniques. Cement mortar samples with different proportions of GO (0.02, 0.04, 0.06, and 0.08 wt % based on the weight of cement) were prepared. The test results showed that GO affected the crystallization of cement hydration products, C–S–H (calcium silicate hydrate is the main hydrate product) and CH (calcium hydroxide). The morphology of hydration products changed with the increase of GO content. Furthermore, the results of XRD analyses showed that the diffraction peak intensity and the crystal grain size of CH (001), (100), (101), and (102) for GO samples increased considerably compared with the control sample. Based on the results, it can be understood that GO can modify the crystal surface of CH, leading to the formation of larger crystals.

C-A-S-H (CaO-Al₂O₃-SiO₂-H₂O) and N-A-S-H (Na₂O-Al₂O₃-SiO₂-H₂O) have a wide range of chemical compositions and structures and are difficult to separate from alkali-activated materials. Therefore, it is difficult to analyze their microscopic properties directly. This paper reports research on the synthesis of C-A-S-H and N-A-S-H particles with an average particle size smaller than 300 nm by applying the hydrothermal method. The composition and microstructure of the products with different CaO(Na₂O)/SiO₂ ratios and curing conditions were characterized using XRD, the RIR method, FTIR, SEM, TEM, and laser particle size analysis. The results showed that the C-A-S-H system products with a low CaO/SiO₂ ratio were mainly amorphous C-A-S-H gels. With an increase in the CaO/SiO₂ ratio, an excess of Ca(OH)₂ was observed at room temperature, while in a high-temperature reaction system, katoite, C₄AcH₁₁, and other crystallized products were observed. The katoite content was related to the curing temperature and the content of Ca(OH)₂ and it tended to form at a high-temperature and high-calcium environment, and an increase in the temperature renders the C-A-S-H gels more compact. The main products of the N-A-S-H system at room temperature were amorphous N-A-S-H gels and a small amount of sodalite. An increase in the curing temperature promoted the formation of the crystalline products faujasite and zeolite-P. The crystallization products consisted of only zeolite-P in the high-temperature N-A-S-H system and its content were stable above 70%. An increase in the Na₂O/SiO₂ ratio resulted in more non-bridging oxygen and the TO₄ was more isolated in the N-A-S-H structure. The composition and microstructure of the C-A-S-H and N-A-S-H system products synthesized by the hydrothermal method were closely related to the ratio of the raw materials and the curing conditions. The results of this study increase our understanding of the hydration products of alkali-activated materials.

Energy piles—A fairly new renewable energy concept—Use a ground heat exchanger (GHE) in the foundation piles to supply heating and cooling loads to the supported building. Applying phase change materials (PCMs) to piles can help in maintaining a stable temperature within the piles and can then influence the axial load acting on the piles. In this study, two kinds of carbon-based composite PCMs (expanded graphite-based PCM and graphite nanoplatelet-based PCM) were prepared by vacuum impregnation for potential application in energy piles. Thereafter, a systematic study was performed and different characterization tests were carried out on two composite PCMs. The composite PCMs retained up to 93.1% of paraffin and were chemically compatible, thermally stable and reliable. The latent heat of the composite PCM was up to 152.8 J/g while the compressive strength of cement paste containing 10 wt % GNP-PCM was found to be 37 MPa. Hence, the developed composite PCM has potential for thermal energy storage applications.

The relatively high shrinkage of the alkali-activated slag (AAS) has restricted its application as a widely-used building material. This research attempts to study the effect of a hydrothermally synthesized C-A-S-H gel, which has a similar composition to that of the main AAS product, on the shrinkage performance of the AAS. The C-A-S-H nano-particles were mixed into AAS mortars in a proportion ranging from 1 wt % to 5 wt % using two different methods, and the drying and autogenous shrinkage ratio of modified AAS mortars were measured at various ages. The effect of C-A-S-H on their microstructures was also characterized. Results obtained indicated that the addition of C-A-S-H gel to AAS mortars had reduced their drying and autogenous shrinkage, with the addition of 3 wt % reaching the maximum reduction. However, the added amount was not directly proportional to the decrease of shrinkage; the proportion of early-stage drying shrinkage of AAS mortars was greater than that of autogenous shrinkage; the dispersion method was slightly better than the dry mixing method in both shrinkage reduction. MIP results suggested that the addition of C-A-S-H gel had reduced the total porosity and the average pore size of AAS mortars, optimized their pore structure distribution, and significantly reduced the volume of mesopores (<0.05 µm) which resulted in high shrinkage, while the adding method had no significant effect on the pore size distribution of AAS mortars. SEM results showed that the addition of C-A-S-H gel can reduce the crack width of mortars, obtain a dense and uniform matrix structure, increase the density, and effectively suppress both shrinkage deformation of the system, whereas the adding method has no obvious effect on the crack width of the mortar. This research provides a novel approach of the AAS shrinkage reduction and structure refinement, shedding lights on nano-material modification of the AAS.

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.

In the present research work, the ternary effects of varying dosages of graphene oxide encapsulated silica fume (GOSF), nano-silica sol (SS), and fly ash (FA) on the rheological properties, compressive strength, the content and crystal size of calcium hydroxide (CH), porosity, water absorption, and microstructure of cement were studied. The results showed that the incorporation of SF improved the dispersion of GO in the cement matrix. GOSF was prepared through electrostatic attraction between the positively charged SF and negatively charged GO. The ternary mixture of GOSF, SS, and FA had a synergistic effect that improved the performance of cement. When the curing age of cement reached 28 days, the compressive strength reached a peak of 86.5 MPa, the minimum values of content and crystal size of CH were 11.55% and 45.69 nm, respectively, and the minimum values of water absorption and porosity were 0.0011 cm/s^0.5 and 13.56%, respectively. In terms of microstructure, the denser structure of C-S-H gel and the regular arrangement of CH were noticed.