Abstract

The effect of B2O3 content on the rheological behavior and molten structure of the MgO–SiO2-based ferronickel slag were studied at a fixed (SiO2+Al2O3)/(MgO + CaO) mass ratio of 1.4. Results show that the viscosity of the slag melt decreased with the addition of B2O3, and B2O3 had a relatively little effect when its content was over 7 mass%. The break temperature of ferronickel slag reduced from 1711 to 1596 K and its apparent activation energy deceased from 95.34 ± 2.61 to 23.08 ± 1.65 kJ/mol with the addition of B2O3 from 3 to 9 mass%. Structural analyses indicate that B2O3 stripped the oxygen from the silicate structure. The formation of B–O–B structures connected by non-ring [BO3]-trihedral and [BO4]-tetrahedral structural units led to boroxol rings. These resulted in higher degree of polymerization (DOP) of both silicate and borate structures. However, the O− in [BO2O−], the dominant 2D [BO3]-trihedral structure and the formation of asymmetric Si–O–B structural units could depolymerize the network structures of ferronickel slag.

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