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Laboratory Study on Evolution Mechanisms of Non-metallic Inclusions in High Strength Alloyed Steel Refined by High Basicity Slag

机译:高碱度渣精炼高强度合金钢中非金属夹杂物演变机理的室内研究

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Laboratory study was carried out to discuss evolution mechanisms of non-metallic inclusions in high strength alloyed steel refined by high basicity slag, aiming at formation of lower melting temperature inclusions to improve anti-fatigue properties of steel.It is found that steel/slag reaction time had great effect on inclusion types, compositions and shapes. With reaction time extended from 30 to 180 min, solid MgO–Al_(2)O_(3) and MgO-based inclusions were finally changed into CaO–MgO–Al_(2)O_(3) system inclusions lower melting temperature (<1773 K). While shapes of inclusions varied in the route blocky/angular→near spherical→spherical.Al_(2)O_(3)/MgO·Al_(2)O_(3)/MgO and MgO/MgO·Al_(2)O_(3)/CaO·2Al_(2)O_(3) stability diagram were obtained by thermodynamic calculation. The results indicated that MgO and MgO·Al_(2)O_(3) inclusion would be formed at early stage of steel-slag reaction because activity of Mg is much larger than that of Ca in steel. However, with increase of Ca activity, solid MgO·Al_(2)O_(3) and MgO inclusions would be inevitably and gradually transferred into complex liquid inclusions even dissolved [Ca] is as low as 0.0002%. Thus, SEM-EDS mappings of CaO–MgO–Al_(2)O_(3) system inclusions are characterized by high melting temperature solid MgO·Al_(2)O_(3) or MgO-based inclusion cores surrounded by lower melting temperature CaO–Al_(2)O_(3) outer surface layers, which would be softer during hot rolling and therefore be helpful to improve anti-fatigue properties of steel.Model was established to elucidate change mechanisms of inclusions. Transferring kinetics of inclusions was discussed qualitatively to analyze velocity controlled steps. It is found that diffusion of Mg and Ca in solid inclusion core and the formed CaO–Al_(2)O_(3) outer surface layer would be probably the limited step during evolution of inclusions. However, further work should be done to discuss evolution kinetics of inclusions quantitatively.
机译:通过实验室研究探讨了高碱度渣精制的高强度合金钢中非金属夹杂物的演化机理,旨在形成较低熔点的夹杂物以提高钢的抗疲劳性能。时间对夹杂物的类型,成分和形状影响很大。随着反应时间从30分钟延长到180分钟,固态MgO–Al_(2)O_(3)和基于MgO的夹杂物最终变为CaO–MgO–Al_(2)O_(3)系统夹杂物,降低了熔融温度(<1773 K)。夹杂物的形状在块状/角→近球形→球形时变化.Al_(2)O_(3)/ MgO·Al_(2)O_(3)/ MgO和MgO / MgO·Al_(2)O_(3通过热力学计算得到)/ CaO·2Al_(2)O_(3)稳定性图。结果表明,钢中Mg的活度比Ca大得多,MgO和MgO·Al_(2)O_(3)夹杂物会在钢渣反应的早期形成。然而,随着Ca活性的提高,即使溶解[Ca]的比例低至0.0002%,固体MgO·Al_(2)O_(3)和MgO夹杂物也将不可避免地逐渐转移成复杂的液体夹杂物。因此,CaO–MgO–Al_(2)O_(3)夹杂物的SEM-EDS映射的特征是高熔点固体MgO·Al_(2)O_(3)或被较低熔点CaO包围的基于MgO的夹杂物核–Al_(2)O_(3)的外表面层,在热轧过程中会较软,因此有助于改善钢的抗疲劳性能。建立了模型以阐明夹杂物的变化机理。定性地讨论了夹杂物的传输动力学,以分析速度控制步骤。结果发现,Mg和Ca在固态夹杂物核中以及形成的CaO–Al_(2)O_(3)外表面层中的扩散可能是夹杂物演化过程中的受限步骤。但是,应该做进一步的工作来定量讨论夹杂物的演化动力学。

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