Si-Mn脱氧钢中夹杂物连铸过程中的演变

Evolution behaviors of inclusions in Si-Mn deoxidized steel during continuous casting

  • 摘要: 本文以SWRH82B为例探究了Si-Mn脱氧钢在连铸过程中夹杂物的特征演变规律。通过在国内某厂生产82B时对炼钢-连铸过程进行取样,利用自动扫描电镜分析了钢中夹杂物类型、尺寸、成分等特征变化。结果表明:从RH出站到中间包浇铸过程,钢液发生二次氧化,钢中的TO和N增加。热力学计算表明,中间包内发生二次氧化时,CaO-Al2O3-SiO2系夹杂物不会自发生成,该类夹杂物为外来夹杂物;当TO含量在0.0020%~0.0023%时,Ca与O反应的吉布斯自由能变ΔG小于Si、Mn与O反应的ΔG,导致MnO-Al2O3-SiO2系夹杂物中含有少量的CaO成分;当TO达到0.0027%时,Al、Si、Ca与O反应的ΔG分别为-68.36 kJ·mol-1、-20.59 kJ·mol-1、-15.30 kJ·mol-1,远小于Ca和Mg与O反应的ΔG(分别为-2.00 kJ·mol-1和111.21 kJ·mol-1),因而生成大量MnO-Al2O3-SiO2系夹杂物,其数量占比达84.92%。结晶器内保护渣颗粒与已有的夹杂物碰撞聚合,导致夹杂物中的(CaO)/(SiO2)增加并接近保护渣二元碱度(R=0.75),因而结晶器内所取钢样中CaO-Al2O3-SiO2系夹杂物的数量占比明显上升。热力学计算还表明,在中间包浇铸过程中,当钢液温度T从1758 K降至1597 K时,Al可还原夹杂物中的SiO2和MnO,其反应的ΔG范围分别为-131.25 kJ·mol-1~-115.33 kJ·mol-1和-35.57 kJ·mol-1~-28.95 kJ·mol-1,因而导致结晶器内夹杂物中Al2O3含量增加。热力学计算结果与工业试验取样分析结果一致。

     

    Abstract: To investigate the evolution of inclusions in Si-Mn deoxidized steel during continuous casting, samplings of liquid steel in refining and casting of the commercial steel SWRH82B were conducted in a domestic steel work. Varied features of inclusions in steel, such as type, size and composition etc., were analyzed by an automatic SEM machine. The results showed that re-oxidation of molten steel occurred during RH departure and tundish casting, resulting in pick-ups of total oxygen TO and nitrogen N contents in steel. During secondary oxidation in the tundish, the CaO-SiO2-Al2O3 inclusions can’t form spontaneously and were classified as exogenous inclusions. When re-oxidation occurred in the tundish with TO content increased from 0.0020% to 0.0023%, the changes of Gibbs free energy viz. ΔG of the reaction between Ca and O was lower than that of reactions between Si, Mn and O, resulting in a small amount of CaO constituent in the MnO-SiO2-Al2O3 system inclusions. When TO approached about 0.0027%, the ΔG for reactions of Al, Si, Ca with O were -68.36 kJ·mol-1, -20.59 kJ·mol-1 and -15.30 kJ·mol-1 respectively, which were much lower than those of reactions between Ca, Mg and O (-2.00 kJ·mol-1 and 111.21 kJ·mol-1, respectively). Accordingly, a large number of MnO-Al2O3-SiO2 inclusions were formed at this stage, accounting for a number fraction about 84.92% of inclusions. In the mold, collisions and aggregations between entrapped mold flux particles and existing inclusions caused an increase in the (CaO)/(SiO2) ratio in inclusions, which is close to the binary basicity of mold flux (R=0.75). The proportions of CaO-SiO2-Al2O3 inclusions in steel samples taken from casting mold increased significantly. Thermodynamic calculations indicated that during tundish casting, as the temperature T decreased from 1758 K to 1597 K, the ΔG ranges for the reduction of SiO2 and MnO by Al were -131.25 kJ·mol-1~-115.33 kJ·mol-1 and -35.57 kJ·mol-1~-28.95 kJ·mol-1, respectively. This demonstrated that Al reduced SiO2 and MnO in inclusions, resulting in increased Al2O3 contents in inclusions in the mold. The thermodynamic calculation results were consistent with the analysis results of industrial samples.

     

/

返回文章
返回