The development of alternative binders to ordinary Portland cement is motivatedby the high thermal energy demand, calcination emissions, and environmentalimpact associated with clinker production. Magnesium-based cementitious systems,particularly reactive magnesium oxide cement, magnesium oxychloride cement,magnesium oxysulfate cement, magnesium phosphate cement, and magnesium silicatehydrate cement, have attracted considerable scientific attention because of theirrelatively low-temperature processing, rapid hardening potential, chemical versatility,and ability to participate in mineral carbonation.This paper presents an advanced analysis of the physicochemical behavior ofmagnesium-based compounds as partial or complete alternatives to Portland cement. The analysis integrates hydration thermodynamics, carbonation chemistry,dissolution–precipitation kinetics, pore-structure evolution, reaction–diffusion theory,fracture mechanics, and thermodynamic phase-equilibrium concepts.The principal reactions include the formation of brucite, hydrated magnesiumcarbonates, magnesium oxychloride phases, magnesium oxysulfate phases, struvite,and magnesium silicate hydrate gel. The principal limitation of magnesium-basedcement is that its performance depends strongly on the calcination route, particle size,water-to-binder ratio, curing humidity, carbon dioxide concentration, and additivechemistry.The most technically promising approach is a tailored hybrid system based onreactive magnesium oxide, silica-rich supplementary materials, controlled carbonation,and chemical or polymeric modification.
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Khaled Aldhufri (2026) studied this question.
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