ISIJ International
Online ISSN : 1347-5460
Print ISSN : 0915-1559
ISSN-L : 0915-1559
Regular Article
Reduction Reactions in Al2O3–C–Fe and Al2O3–Fe2O3–C Systems at 1823 K
Rita KhannaMuhammad Ikram-Ul-HaqSeyed Fahandej SadiVeena SahajwallaPartho Sarathy MukherjeeSeshadri Seetharaman
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2014 Volume 54 Issue 7 Pages 1485-1490

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Abstract

With a view to produce Fe–Al alloys for deoxidation during steel refining, chemical reactions were investigated in Al2O3–C–Fe and Al2O3–Fe2O3–C systems at 1823 K. Using a horizontal tube furnace and argon atmosphere, interactions were investigated for time periods up to 2 hours. Two sets of blends were prepared from initial constituents, which were later used to prepare two types of substrates. Alumina and synthetic graphite powders were blended in a 70: 30 proportion (blend I), and in the second set, Fe2O3 was blended with C in a proportion of 75:25 (blend II). In one case, blend I was mixed thoroughly with iron powder (Fe (2.7 pct C)) in a ratio of 80:20; in the second case, blend I was mixed with blend II in the ratio of 70:30. We report significant reduction reactions in both cases. SEM/EDS studies on the Al2O3–C–Fe system showed unambiguous evidence for the pick-up of aluminium by molten iron after 1 hour. Levels of aluminium in molten iron were found to increase significantly with time. Due to in-situ reduction of Fe2O3, the generation of CO gas and associated turbulence, the reactions were quite fast in the Al2O3–Fe2O3–C system. X-ray diffraction studies showed the presence of additional diffraction peaks belonging to Fe3AlC and Fe3Al systems. Molten iron was found to act as a reducing agent and a metallic solvent in both cases. This study provides evidence for the carbothermic reduction of alumina at 1823 K and for the formation of ferroalloys directly from mixed oxides of aluminium and iron.

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© 2014 by The Iron and Steel Institute of Japan
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