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Thermodynamics of Simultaneous Desulfurization and Dephosphorization of Silicomanganese Alloy

机译:硅锰合金同时脱硫和脱磷的热力学

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Because sulfur and phosphorus are very harmful in steel products, there are increasing requirements for refining these elements from ferroalloys industries. Hence, in the present study, simultaneous desulfurization (de-S) and reducing dephosphorization (Rde-P) from silicomanganese (SiMn) alloy were investigated using metal-slag equilibration method under highly reducing condition at 1773 K. Experiments were carried out by equilibration between SiMn alloy and MnO-based slag in graphite crucible under p(O_2) = 10~(-18) atm. Slag composition was designed by changing basicity (CaO/SiO_2) and MnO content at fixed Al_2O_3 (=20%) and MgO (=5%) contents. De-S ratio increased with increasing basicity until C/S = 1.5 whereas Rde-P ratio was not significantly affected by slag basicity. This was because thermodynamic driving force of de-S reaction was greater than that of Rde-P reaction under present experimental conditions. The de-S and Rde-P ratios commonly increased with decreasing oxygen partial pressure.
机译:由于硫和磷在钢铁产品中非常有害,因此对从铁合金行业提炼这些元素的要求不断提高。因此,在本研究中,采用金属渣平衡法在1773 K的高还原条件下研究了硅锰(SiMn)合金的同时脱硫(de-S)和还原性脱磷(Rde-P)。通过平衡进行实验p(O_2)= 10〜(-18)atm下石墨坩埚中SiMn合金与MnO基炉渣的比值通过改变碱度(CaO / SiO_2)和固定Al_2O_3(= 20%)和MgO(= 5%)含量下MnO含量来设计炉渣成分。 De-S比随碱度的提高而增加,直至C / S = 1.5,而Rde-P比不受渣碱度的影响。这是因为在目前的实验条件下,de-S反应的热力学驱动力大于Rde-P反应的热力学驱动力。 de-S和Rde-P之比通常随氧气分压的降低而增加。

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