Abstract
The oxidative dephosphorization of carbon-saturated Fe-Mn alloys was successfully demonstrated by measuring the phosphorus partition ratio between BaO-MnO, BaO-MnO-BaF2, and BaO-CaOsatd.-MnO fluxes and liquid Fe-Mn-Csatd. alloy between 1573 and 1673 K. The phosphorus partition ratio increases with increasing BaO content of the flux. The phosphate capacity of the BaO-MnO flux is as high as that of the BaO-BaF2 flux and is far larger than those of CaO-bearing fluxes. Addition of BaF2 to the BaO-MnO flux increases BaO solubility, which increases the phosphate capacity. The manganese partition ratios between the BaO-MnO flux and Fe-Mn-Csatd. alloy were approximately constant at 0.64, 0.33, and 0.23 at 1573, 1623, and 1673 K, respectively. The carbon content of the BaO-MnO flux was measured as functions of slag composition, temperature, and partial pressure of CO. A stable species of carbon in the BaO-MnO flux was found to be BaC2 experimentally and thermodynamically. The sulfide capacity of the BaO-MnO system at 1573 K has been shown to be far larger than any known flux systems and to be a few times larger than that for the BaO-BaF2 system.
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Formerly Graduate Student, Department of Metallurgy, The University of Tokyo
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Watanabe, Y., Kitamura, K., Rachev, I.P. et al. Thermodynamics of phosphorus and sulfur in the BaO-MnO flux system between 1573 and 1673 K. Metall Trans B 24, 339–347 (1993). https://doi.org/10.1007/BF02659137
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DOI: https://doi.org/10.1007/BF02659137