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Volume 20 Issue 12
Dec.  2013
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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://doi.org/10.1007/s12613-013-0846-9
Cite this article as:
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://doi.org/10.1007/s12613-013-0846-9
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Non-isothermal reduction kinetics of titanomagnetite by hydrogen

  • 通讯作者:

    Guo-hua Zhang    E-mail: ghzhang_ustb@163.com

  • 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

    + Author Affiliations
    • 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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