Aref Sardari, Eskandar Keshavarz Alamdari, Mohammad Noaparast, and Sied Ziaedin Shafaei, Kinetics of magnetite oxidation under non-isothermal conditions, Int. J. Miner. Metall. Mater., 24(2017), No. 5, pp. 486-492. https://doi.org/10.1007/s12613-017-1429-y
Cite this article as:
Aref Sardari, Eskandar Keshavarz Alamdari, Mohammad Noaparast, and Sied Ziaedin Shafaei, Kinetics of magnetite oxidation under non-isothermal conditions, Int. J. Miner. Metall. Mater., 24(2017), No. 5, pp. 486-492. https://doi.org/10.1007/s12613-017-1429-y
Research Article

Kinetics of magnetite oxidation under non-isothermal conditions

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  • Corresponding author:

    Eskandar Keshavarz Alamdari    E-mail: alamdari@aut.ac.ir

  • Received: 10 May 2016Revised: 6 November 2016Accepted: 10 November 2016
  • Oxidation of magnetite concentrates, which occurs during the pellet induration process, must be deeply understood to enable the appropriate design of induration machines. In the present paper, the kinetics of the magnetite oxidation reaction was studied. Primary samples were obtained from the Gol-e-Gohar iron ore deposit. Magnetic separation and flotation decreased the sulfur content in the samples to be approximately 0.1wt%. Thermogravimetric analysis was used to measure mass changes during the oxidation of magnetite and, consequently, the conversion values. The aim of this study was to use isoconversional methods to calculate the kinetic parameters. The Coats-Redfern method was also used to obtain the activation energy. Thermogravimetric analyses were run at three different heating rates. The Coats-Redfern results were too ambiguous for a meaningful interpretation. In the case of the isoconversional method, however, the mean activation energy and pre-exponential factor of the oxidation reaction were obtained as 67.55 kJ and 15.32×108 min-1, respectively. Such a large activation energy implies that temperature strongly affects the reaction rate. The oxidation reaction exhibits a true multi-step nature that is predominantly controlled by chemical reaction and diffusion mechanisms.
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