Abstract
The observed retarding effect of sulfur on the decarburization of Fe-C melts has been interpreted by means of a mixed-control mechanism involving gas-phase mass transfer and dissociative adsorption of CO2. A mathematical model formulated on the basis of the proposed mechanism gave an excellent fit to the experimental data. The application of the model to the data provided a value of 4.42 x 10−3 mole · cm−2 · s−1 · atm−1 for the dissociative adsorption rate constant for CO2 on liquid iron at 1973 K; the fraction of surface sites that cannot be occupied by sulfur, even at apparent surface-saturation, was found to be 0.085. The model predicts a residual rate of decarburization at high sulfur concentrations; this prediction is borne out by the experiment. The effect of convective motion within the levitated melt on the rate of decarburization below a characteristic carbon concentration was quantified. The liquid-phase mass transfer was greatly enhanced by the stirring effect of the electromagnetic field. The effective diffusivity of carbon in Fe-C melts under levitation conditions has been found to be 3.24 x 10−3 cm2 · s−1, a value ten times as large as that under stationary conditions.
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Lee, H.G., Rao, Y.K. Rate of decarburization of iron-carbon melts: Part II. a mixed-control model. Metall Trans B 13, 411–421 (1982). https://doi.org/10.1007/BF02667757
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DOI: https://doi.org/10.1007/BF02667757