| Summary: | The processes of iron oxides’ reduction have a complex physicochemical mechanism, with the participation of solid, liquid, and gaseous substances. The article discusses the existing models for the reduction of iron oxides and provides data on the thermodynamic possibility of carrying out the reactions of their reduction through the solid and gas phases. Experimental data on the reduction of iron from industrial scale, obtained by the DSC (differential scanning calorimetry) method, show the kinetic dependence of the rate and completeness of recovery on external factors: pressing pressure during sample preparation and the reagents’ composition. The pressing pressure, under conditions of iron ions’ solid-phase diffusion, has the significant effect by increasing the reagents’ contact area. Under conditions of iron ions’ comprehensive diffusion, the pressing pressure does not affect the reduction processes rate. The introduction of 10 mass.% flux into the raw mixture composition leads to a partially liquid-phase diffusion of iron ions and weakens the effect of the pressing pressure in this process. An ion diffusion-catalytic mechanism is proposed to describe the observed effects during the reduction of iron oxide of technogenic origin.
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