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Carbothermal synthesis of titanium oxycarbide

The aim of the project was to establish the rate and mechanisms of solid stage reduction of titania and ilmenite ores. The project examined carbothermal reduction of titania and various types of ilmenite ores in argon, helium, hydrogen, and their mixtures. Effect of CO in the gas atmosphere on reduction behavior of titania and primary ilmenite ore was also studied. Isothermal and non-isothermal reduction experiments were conducted in a fixed bed reactor in the high temperature furnace in the temperature range up to 1500oC. The off-gas composition in the reduction process was monitored by a CO/CO2/CH4 infrared analyser. The extent of reduction was calculated using data on gas composition and LECO oxygen analysis. Phase composition and morphology of reduced samples were studied using XRD, SEM and optical microscopy. The major findings of this project are as follows: • The reduction of titania to titanium oxycarbide occurred in the following sequence: TiO2 → Ti5O9 → Ti4O7 → Ti3O5 → Ti2O3 → (TiO-TiC) solid solution. • Carbothermal reduction of ilmenite concentrates proceeded in two main stages. In the first stage pseudorutile and ilmenite were reduced to metallic iron and titania. Second stage involved the reduction of titania to titanium oxycarbide. • Rate and degree of reduction of titania and ilmenite concentrates increased with increasing temperature. • Reduction rate of titania and ilmenite concentrates was faster in hydrogen than in helium and argon. The difference in the reduction behavior in helium and argon was insignificant; reduction rate of ilmenite was slightly faster in helium than in argon. • High rate of reduction of titania and ilmenite in hydrogen was attributed to formation of methane which facilitated mass transfer of carbon from graphite to oxide. Hydrogen was also directly involved in reduction of titania and ilmenite concentrates; hydrogen reduced pseudorutile to iron and titania. Titania was further reduced to titanium oxycarbide by carbon through methane. • Increased gas flow rate slightly improved the reduction rate in hydrogen and suppressed the reduction in inert gases. • Addition of CO to hydrogen and inert gases above 3 vol% suppressed the reduction process.

Identiferoai:union.ndltd.org:ADTP/258608
Date January 2009
CreatorsDewan, Mohammad Ashikur Rahman, Materials Science & Engineering, Faculty of Science, UNSW
PublisherAwarded By:University of New South Wales. Materials Science & Engineering
Source SetsAustraliasian Digital Theses Program
LanguageEnglish
Detected LanguageEnglish
Rightshttp://unsworks.unsw.edu.au/copyright, http://unsworks.unsw.edu.au/copyright

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