When concrete is used for construction in cold-temperature regions, cold-resistant accelerators based on calcium nitrite (Ca(NO₂)₂) and calcium nitrate (Ca(NO₃)₂) are added to prevent early freezing damage. Although cold-resistant accelerators increase the early compressive strength and prevent early freezing damage by promoting cement hydration, the strength enhancement effect owing to the formation of such hydrates has not been evaluated quantitatively thus far. This study covers various types of analysis to understand the relationship between cement hydrate formation behavior and strength development upon the addition of varying amounts of nitrite-based accelerator. We find that the early compressive strength is enhanced by the addition of nitrite-based accelerator via the promotion of the relative production of monosulfate and C-S-H in the early age. However, the development of compressive strength decreases with an increase in the curing age. Furthermore, we find that the promotion of hydration reactions at an early age with the addition of nitrite-based accelerator can affect the formation ratio of each hydrate at a late age. We believe our findings can significantly contribute to developments in concrete application and allied fields.

Alkali-activated cements prepared from aluminosilicate powders, such as blast furnace slag and fly ash, are rapidly attracting attention as alternatives to cement because they can significantly reduce CO₂ emissions compared to conventional cement concrete. In this study, we investigated the relationship between the physical and chemical changes by accelerated carbonation conditions of alkali-activated cements. Alkali-activated cements were prepared from binders composed of blast furnace slag and fly ash as well as alkali activators sodium silicate and sodium hydroxide. Physical changes were analyzed from compressive strength, pH, and neutralization depth, and chemical changes were analyzed from XRD, TG-DTG, and ²⁹Si MAS NMR. The C–(N)–A–S–H structure is noted to change via carbonation, and the compressive strength is observed to decrease. However, in the case of Na-rich specimens, the compressive strength does not decrease by accelerated carbonation. This work is expected to contribute to the field of alkali-activated cements in the future.

The purpose of this study is to evaluate the temperature distribution, strength development, porosity, scanning electron microscopy observation, shrinkage, and surface properties of concrete in order to apply microwave heat curing to the precast method and to analyze the CO₂ emissions and economic feasibility of microwave heat curing. The heating of a steel form by microwave heating enabled concrete to be efficiently cured at a temperature within a range of ±5 °C. After the curing, demolding strength could be cleared through the densification of the concrete by decreasing the porosity of the concrete. Microwave heat curing exhibited excellent performance compared to conventional steam curing in terms of efficient temperature control, occurrence of cracks due to shrinkage, surface condition of concrete after curing, economic efficiency, and CO₂ emissions. However, verification and supplementation based on actual data are necessary so that environments applicable to the various sizes and shapes of forms can be prepared.

The frost damage resistance of blast-furnace slag (BFS) cement is affected by carbonation. Hence, this study investigates the carbonation properties of pastes incorporating BFS with different replacement ratios, such as 15%, 45%, and 65% by weight, and different curing conditions, including air and carbonation. The BFS replacement ratio properties, determined by the Ca/Si ratio of calcium silicate hydrate in the cement paste sample, were experimentally investigated using mercury intrusion porosimetry, X-ray diffraction, and thermal analysis. The experimental investigation of the pore structure revealed that total porosity decreased after carbonation. In addition, the porosity decreased at a higher rate as the BFS replacement rate increased. Results obtained from this study show that the chemical change led to the higher replacement rate of BFS, which produced a higher amount of vaterite. In addition, the lower the Ca/Si ratio, the higher the amount of calcium carbonate originating from calcium silicate hydrate rather than from calcium hydroxide. As a result of the pore structure change, the number of ink-bottle pores was remarkably reduced by carbonation. Comparing the pore structure change in air-cured and carbonation test specimens, it was found that as the replacement rate of BFS increased, the number of pores with a diameter of 100 nm or more also increased. The higher the replacement rate of BFS, the higher the amount of calcium carbonate produced compared with the amount of calcium hydroxide produced during water curing. Due to the generation of calcium carbonate and the change in pores, the overall number of pores decreased as the amount of calcium carbonate increased.