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Jie Dang, Guo-hua Zhang, Xiao-jun Hu, and Kuo-chih Chou, Non-isothermal reduction kinetics of titanomagnetite by hydrogen, Int. J. Miner. Metall. Mater., 20(2013), No. 12, pp.1134-1140. https://dx.doi.org/10.1007/s12613-013-0846-9
Jie Dang, Guo-hua Zhang, Xiao-jun Hu, and Kuo-chih Chou, Non-isothermal reduction kinetics of titanomagnetite by hydrogen, Int. J. Miner. Metall. Mater., 20(2013), No. 12, pp.1134-1140. https://dx.doi.org/10.1007/s12613-013-0846-9
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Non-isothermal reduction kinetics of titanomagnetite by hydrogen

摘要: Reduction of titanomagnetite (TTM) powders by H2-Ar gas mixtures was investigated under a non-isothermal condition by using a thermogravimetric analysis system. It was found that non-isothermal reduction of TTM proceeded via a dual-reaction mechanism. The first reaction was reduction of TTM to wüstite and ilmenite, whereas the second one was reduction of wüstite and ilmenite to iron and titanium dioxide. By using a new model for the dual reactions, which was in an analytical form and incorporated different variables, such as time, temperature, particle size, and hydrogen partial pressure, rate-controlling steps for the dual reactions were obtained with the apparent activation energies calculated to be 90–98 and 115–132 kJ/mol for the first and second reactions, respectively.

 

Non-isothermal reduction kinetics of titanomagnetite by hydrogen

Abstract: Reduction of titanomagnetite (TTM) powders by H2-Ar gas mixtures was investigated under a non-isothermal condition by using a thermogravimetric analysis system. It was found that non-isothermal reduction of TTM proceeded via a dual-reaction mechanism. The first reaction was reduction of TTM to wüstite and ilmenite, whereas the second one was reduction of wüstite and ilmenite to iron and titanium dioxide. By using a new model for the dual reactions, which was in an analytical form and incorporated different variables, such as time, temperature, particle size, and hydrogen partial pressure, rate-controlling steps for the dual reactions were obtained with the apparent activation energies calculated to be 90–98 and 115–132 kJ/mol for the first and second reactions, respectively.

 

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