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Kinetics and mechanism of carbothermic reduction of magnesia
Authors:Li Rongti  Pan Wei  Masamichi Sano
Affiliation:(1) the Department of Materials Science and Engineering, Tsinghua University, 100084 Beijing, People’s Republic of China;(2) the Department of Materials Process Engineering, Graduate School of Engineering, Nagoya University, 464-8603 Aichi-ken, Japan
Abstract:The reaction between MgO and graphite powders under flowing argon atmosphere was studied using a dynamic thermogravimetric method. In the temperature range 293 to 1973 K, the effects of compacting pressure, magnesia/carbon ratio, heating rate, Ar carrier-gas flow rate, and CO-partial pressure were investigated. An experimentally determined reaction mechanism was proposed and discussed. The reduction process could be divided into two stages. The first stage includes the direct reaction between MgO and graphite particles and partial gas-solid reaction at relatively low temperature (below 1750 K). The overall reaction rate depends on the solid phase-boundary reaction between magnesia and carbon particles. The second stage is the gas-solid reaction between CO and MgO, which determines the overall reaction rate. The apparent activation energies of the two stages were estimated to be 208.29 and 374.13 kJ/mol, respectively.
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