A laboratory study was carried out to better understand the factors that contribute to the formation of complex inclusions, as inclusions play an important role during steel production; if not properly managed, inclusions can cause nozzle clogging during continuous casting and also damage the steel’s mechanical properties and machineability. To determine the chemical composition of inclusions that are less detrimental to the machineability of Al-deoxidized and Ca-treated gear steels, thermodynamic calculations and automated scanning electron microscopy (SEM) coupled with energy dispersive spectroscopy (EDS), as well as electron probe micro-X-ray analysis (EPMA) with the wavelength dispersive spectroscopy (WDS) technique, were utilized. The findings demonstrated that the morphology of inclusions changed from irregular to a more spherical type and the composition also changed to dual oxy-sulfides from pure oxides and sulfides as the Ca concentration in the steel was increased up to 36 ppm. The amount of Pure MnS sulfides also reduced significantly after Ca treatment. The ternary phase diagram and stability diagram for the inclusions revealed that 15–25 ppm Ca is the optimal range for the modification of both oxides and sulfides into the desired morphology and composition under the stipulation that the concentration of O in the steel is maintained at or below 50 ppm.
To understand and clarify the formation mechanisms and evolution of complex inclusions in Ti-Ca deoxidized offshore structural steel, inclusions in industrial steel were systematically investigated. The number density of total inclusions generally decreased from Ladle Furnace (LF), Vacuum Degassing (VD), Tundish to the final product except for Ti and Ca addition. The major inclusions during the refining process were CaO-Al2O3-SiO2-(MgO)-TiOx and CaO-Al2O3-SiO2. CaO-Al2O3-SiO2-(MgO)-TiOx inclusion initially originated from the combination of CaO-SiO2-(MgO) in refining slag or refractory and deoxidization product Al2O3 and TiO2. With the refining process proceeding and Ca addition, the Al2O3 concentration in the CaO-Al2O3-SiO2-(MgO)-TiOx inclusions gradually dropped while the CaO and TiO2 concentrations gradually increased. The CaO-Al2O3-SiO2 inclusions originally came from refining slag, existing as 2CaO∙ Al2O3∙ SiO2, and maintained a liquid state during the early stage of LF. After Ca treatment, it was gradually transferred to 2CaO∙ SiO2 due to Al2O3 continuously being reduced by Ca. The liquidus of 2CaO∙ SiO2 inclusion was higher than that of molten steel, so they presented as a solid-state during the refining process. After welding thermal simulation, CaO-Al2O3-SiO2-(MgO)-TiOx inclusions were proven effective for inducing intragranular acicular ferrite (IAF) while CaO-Al2O3-SiO2 was inert for IAF promotion. Additionally, Al2O3-MgO spinel in multiphase CaO-Al2O3-SiO2-(MgO)-TiOx inclusion has different formation mechanisms: (1) initial formation as individual Al2O3-MgO spinel as a solid-state in molten steel; (2) and it presented as a part of liquid inclusion CaO-Al2O3-SiO2-(MgO)-TiOx and firstly precipitated due to its low solubility.
Modern blast furnaces with extensive operational volume demand better-quality iron agglomerates as feed for stable operation. Sinter is the principal feed used in blast furnaces across Asia. Liquid generated during the sintering process plays an essential role in the coalescence of the sinter blend and in sinter quality. Therefore, an estimation of liquid properties at peak bed conditions during sintering helps manage sintering liquid behaviour, leading to better control of final sinter properties. In this study, three different iron sinters were reheated to sinter bed conditions, followed by quenching. Electron probe X-ray microanalysis (EPMA) was used to identify the resultant phases and quantify their chemical compositions. The impact of sinter bulk compositions was analysed, especially on sintering liquid properties. Furthermore, experiments were conducted to study the softening and melting behaviour of the sinters, and the cohesive range of the sinters was identified. Finally, the effect of the sinter bulk compositions on sintering liquid properties and softening behaviour is detailed.