Setting time and mechanical properties are key metrics needed to assess the properties of municipal solid waste incineration (MSWI) bottom ash alkali-activated samples. This study investigated the solidification law, polymerization, and strength development mechanism in response to NaOH and liquid sodium silicate addition. Scanning electron microscopy and X-ray diffraction were used to identify the formation rules of polymerization products and the mechanism of the underlying polymerization reaction under different excitation conditions. The results identify a strongly alkaline environment as the key factor for the dissolution of active substances as well as for the formation of polymerization products. The self-condensation reaction of liquid sodium silicate in the supersaturated state (caused by the loss of free water) is the major reason for the rapid coagulation of alkali-activated samples. The combination of both NaOH and liquid sodium silicate achieves the optimal effect, because they play a compatible coupling role.

In deep coal mining, grouting reinforcement and water blockage are the most effective means for reinforcing the rock mass of extremely broken coal. However, traditional cement grouting materials are not suitable for use in complex strata because of their insufficient early mechanical strength and slow setting time. This study innovatively proposes using alkali-activated grouting material to compensate for the shortcomings of traditional grouting materials and strengthen the reinforcement of extremely unstable broken coal and rock mass. The alkali-activated grouting material was prepared using slag as raw material combined with sodium hydroxide and liquid sodium silicate activation. The compressive strength of specimens cured for 1 d, 3 d, and 28 d was regularly measured and the condensation behavior was analyzed. Using X-ray diffraction and scanning electron microscopy, formation behavior of mineral crystals and microstructure characteristics were further analyzed. The results showed that alkali-activated slag grouting material features prompt and high strength and offers the advantages of rapid setting and adjustable setting time. With an increase in sodium hydroxide content, the compressive strength first increased (maximum increase was 21.1%) and then decreased, while the setting time continued to shorten. With an increase in liquid sodium silicate level, the compressive strength increased significantly (and remained unchanged, maximum increase was 35.9%), while the setting time decreased significantly (and remained unchanged). X-ray diffraction analysis identified the formation of aluminosilicate minerals as the main reason for the excellent mechanical properties and accelerated coagulation rate.

To study the key factors that affect the mechanical properties of polymer materials and explore the relationship between mineral crystal formation and strength development, fly ash (FA) polymer samples were prepared using sodium hydroxide, slag, liquid sodium silicate, and hydrated lime as activators. A change in the compressive strength was observed, and X-ray diffraction measurements were carried out to confirm the change. The effects of different types and amounts of activators on the formation and transformation of mineral crystals in FA polymer samples as well as on the development of compressive strength were studied. Moreover, the relationship between the formation and transformation of mineral crystals and the development of compressive strength was established. The results show that the strongly alkaline excitation environment established by sodium hydroxide is the prerequisite for crystal formation and development of compressive strength. Under this strongly alkaline excitation environment, slag, hydrated lime, and liquid sodium silicate can increase the amounts of calcium and silicon, which promote the formation and development of hydrated calcium silicate and hydrated calcium silicoaluminate in polymers and significantly improve the compressive strength.

In this study, coralline-activated materials were prepared using ball-milled coral powder as cementitious material and coral sand as fine aggregate. XRF (X-ray fluorescence) and chemical dissolution tests were carried out to determine the content and reactivity of various elements in coral powder. The compressive strength of the developed composites was evaluated at different ages, and the formation and transformation of mineral crystals in coralline-activated samples were further analyzed by XRD (X-ray diffractometer). The results show that the calcium content in coral powder was as high as 89.5% (loss on ignition). However, only 56% of the active calcium could participate in the polymerization reaction. The silicon and aluminum content was too low, and the slag addition could improve the deficiency of silicon and aluminum in coral powder. With the increase in slag content (from 0% to 50%), the compressive strength of the composites increases significantly. Nevertheless, the enhancement is not pronounced when the slag content exceeds 50%. The increase in slag amount can stimulate the transformation of calcium minerals, e.g., aragonite and calcite, into hydrated calcium silicate and calcium aluminosilicate gels, which significantly enhances the resulting compressive strength.

To further enhance the compressive strength of alkali-activated materials and reveal their condensation behavior, the reactivity of alkali-activated slag materials was enhanced through the addition of different kinds and proportions of sodium silicate. The mechanical properties of the specimens were observed regularly and the condensation behavior was further analyzed. The results showed that both solid and liquid sodium silicate could significantly improve the compressive strength. The maximum increase in compressive strength was 123.7%, while the initial and final setting times were significantly shortened to 9 min. When solid sodium silicate content increased from 5% to 15%, the compressive strength first increased to 34.6 MPa and then decreased to 28.6 MPa, indicating that 10% was the optimum solid sodium silicate content. The large amount of crystallized solid sodium silicate in the specimen led to the decrease in mechanical properties. When liquid sodium silicate content increased from 5% to 15%, the compressive strength first increased to 52.8 MPa and then tended to be stable, implying that 10% was the optimum content. This shows that its reinforcement effect has a maximum limit. The activation effect of liquid sodium silicate was better than that of solid.

This paper presents the preparation of alkali-activated red mud (RM) light material by an ultra-high liquid–solid ratio (1.98) based on the super water absorption characteristic of RM particles. Compressive strength, dry density, and water absorption are analyzed over time. Besides, the characteristic distributions of porosity and pore size are measured by mercury injection tests, and the microstructure is further analyzed by scanning electron microscopy. The results show that the ultra-high liquid–solid ratio can be used to prepare light samples with superior mechanical properties, low water absorption, reasonable pore distribution, and fine microstructures compared with light samples prepared with a foaming agent. The reason is that the significant increase in the free water does not change the dense microstructure of samples and effectively limits the increase in the detrimental pores. This effectively alleviates the sudden decrease in compressive strength and limits the increase in water absorption.