Cementitious material based on synergistic industrial wastes can be used as a new product for low-carbon transformation. It can aid in resource recycling and suitable consumption and utilisation of various industrial wastes. The proposed material can reduce a large amount of CO₂ emitted during calcination in cement production and the decomposition of raw limestone. In addition, the material exhibits high durability and high resistance to corrosion in the marine environment that can further reduce CO₂ emissions over the lifecycle of the carbon footprint of the building. Currently, many similar chemical kinetic processes and mineralogical reaction processes of particle migration and rebinding exist in the hydration and hardening reactions, service processes and durability evolution of different industrial waste cementitious systems for low-carbon production. The theoretical basis of preparing various low-carbon cementitious materials (LCCMs) with industrial waste systems is discussed herein, including the two theories of ‘complex salt effect’ and ‘isomorphic effect from tetrahedral coordination of silicon-oxygen’. Further research on LCCM is based on the theoretical foundation of ‘passive hydration kinetics’. Furthermore, this study presents the CO₂ reduction potential of LCCM prepared using industrial wastes and provides future research directions in this regard.

Steel slag, desulphurised ash, desulphurised gypsum and ultra-fine iron tailing sand are common industrial solid wastes with low utilisation rates. Herein, industrial solid wastes (steel slag, desulphurised gypsum and desulphurised ash) were used as the main raw materials to prepare a gelling material and ultra-fine tailing was used as an aggregate to prepare a new type of cementing filler for mine filling. The optimal composition of the cementing filler was 75% steel slag, 16.5% desulphurised gypsum, 8.75% desulphurised ash, 1:4 binders and tailing mass ration and 70% concentration. The compressive strength of the 28-day sample reached 1.24 MPa, meeting the mine-filling requirements, while that of the 90-day sample was 3.16 MPa. The microscopic analysis results showed that a small amount of C₃A reacted with the sulphate in the desulphurised gypsum to form ettringite at the early stage of hydration after the steel slag was activated by the desulphurisation by-products. In addition, C₂S produced hydrated calcium silicate gel in an alkaline environment. As hydration proceeded, the sulphite in the desulphurised ash was converted to provide sulphate for the later sustained reaction. Under the long-term joint action of alkali and sulphate, the reactive silica–oxygen tetrahedra and alumina–oxygen tetrahedra depolymerised and then polymerised, further promoting the hydration reaction to generate hydrated calcium silicate gel and ettringite. The low-carbon and low-cost filler studied in this paper represents a new methodology for the synergistic utilisation of multiple forms of solid waste.