Research examines reactivity of C3A in electric clinkers compared to commercial types, indicating key roles of morphology and hydration.
Scalable electrical production of clinker is possible under reducing conditions, and the reactivity of C 3 A produced in such conditions has only been superficially described. We examined electric clinkers made over molten steel with a range of fineness and compared them against commercial clinkers. Using x‐ray diffraction, calorimetry, and backscattered electron microscopy/image analysis, we investigated the roles of morphology, crystal structure, and phase interaction. Shortage of Fe 3+ ions in the interstitial in electric clinkers makes its C 3 A more reactive like white cements and synthetic systems. In the presence of ferric oxides, ferrite is formed and the concentration of dissolved Fe 3+ ions in C 3 A increases. The kinetics of C 3 A hydration are hindered both by the ferrite phases intermixing with the C 3 A phase, hence acting as a physical barrier for dissolution, and by Fe 3+ ions dissolving in C 3 A, thereby reducing its intrinsic reactivity. Although this higher reactivity of C 3 A requires more gypsum to ensure proper sulfation, this can be managed by controlling fineness and blending with supplementary cementitious materials.
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Joseph et al. (2025) studied this question.
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