Carbothermal solid state reduction of stable metal oxides

Authors

Oleg Ostrovski, University of New South Wales
Guangqing Zhang, University of WollongongFollow
R Kononov, University of New South Wales, Sydney, Australia
Mohammad A. R Dewan
J Li, University of New South Wales

RIS ID

62813

Publication Details

Ostrovski, O., Zhang, G., Kononov, R., Dewan, M. A. R. Li, J. (2010). Carbothermal solid state reduction of stable metal oxides. Steel Research International, 81 (10), 841-846.

Abstract

The paper considers carbothermal solid state reduction of manganese, titanium and aluminium oxides in argon, helium and hydrogen. The difference in reduction in helium and argon was reflected by different diffusion coefficients of gaseous reactants and products, which are much higher in helium than in argon. When carbothermal reduction took place in hydrogen, it was involved in the reduction process by reducing oxides to suboxides and forming methane.

Manganese and titanium oxides were reduced to carbide Mn₇C₃ and oxycarbide Ti(O_xC_1-x) correspondingly, while products of alumina reduction included carbide Al₄C₃ and vapours of Al and Al₂O, which were re-oxidised to Al₄O₄C outside the reactor and deposited in the lower temperature zone. Gas atmosphere had a profound effect on the extent and rate of reduction. This effect was different in reduction of different oxides. Reduction of manganese oxides was the fastest in hydrogen, and faster in helium than in argon. Reduction of titania in argon and helium proceeded with about the same rate and was much faster in hydrogen than in the inert atmospheres. The rate and extent of alumina reduction in hydrogen and helium were higher than in argon, although no significant difference was observed in alumina reduction in hydrogen and helium. This reflects differences in reduction mechanisms, which are discussed in the paper.