Abstract
Desulfurization of molten iron by molten slag is an electrochemical reaction. Previous investigations confirmed that applying electricity could enhance the desulfurization of molten iron, but a quantitative relation between the electricity and the desulfurization was not fully elucidated. The present study attempted to correlate the extent of the electrochemical desulfurization with the applied electricity via a series of high-temperature desulfurization experiments and thermodynamic analyses. A molten iron containing C and S was allowed to react with CaO–\(\hbox {Al}_{{2}}\hbox {O}_{{3}}\)–\(\hbox {MgO}_{\text {sat.}}\) slag at 1673 K (1400 \(^\circ \)C), with and without the electricity of constant current. S distribution coefficients (\(L_{\text {S}}\) = (pct S)/[pct S]) were obtained after the normal and the electrochemical equilibria, respectively. The obtained results were interpreted by employing the Nernst equation in order to extract the potential difference (\(\varDelta \phi _{\text {S}}\)) for the electrochemical desulfurization. It was found that applying electric current (I) increased the \(L_{\text {S}}\) after the electrochemical desulfurization, which resulted in the increase of \(\varDelta \phi _{\text {S}}\). A resistance, \(R_{\text {DeS}} = \varDelta \phi _{\text {S}}\)/I, or a specific resistivity, \(\rho _{\text {DeS}} = \varDelta \phi _{\text {S}}\)/(I/A), where A is the cathodic area, for the electrochemical desulfurization was defined, which can be used to characterize the susceptibility to the electrochemical desulfurization. It was found that \(R_{\text {DeS}}\) was independent of the I within the range of this investigation, decreased as (pct CaO)/(pct \(\hbox {Al}_{{2}}\hbox {O}_{{3}}\)) increased and was proportional to the resistance of the slag (\(R_{\text {slag}}\)). A favorable condition for the electrochemical desulfurization is not the same as that for the normal desulfurization condition. The \(\varDelta \phi _{\text {S}}\), which is an indicator of the extent of electrochemical desulfurization, was independently predicted by employing a thermodynamic model for the oxysulfide slag. The model prediction was in a good agreement with the experimental data. The model was used to predict necessary current level for a desired electrochemical desulfurization.
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One of the authors (YBK) thanks Prof. M.A. Rhamdhani, Swinburne University of Technology, Australia, for his kind discussion on the electrochemical reaction.
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Manuscript submitted March 29, 2021; accepted July 15, 2021.
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Kim, DH., Kang, YB. An Attempt to Correlate Electrochemical Desulfurization of Molten Iron Using CaO–Al2O3–MgOsat. Molten Slag and Applied Electricity at 1673 K (1400 °C). Metall Mater Trans B 52, 2960–2970 (2021). https://doi.org/10.1007/s11663-021-02289-1
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DOI: https://doi.org/10.1007/s11663-021-02289-1