In‐Depth Microstructural Evolution Analyses of Cement‐Bonded Spinel Refractory Castables: Novel Insights Regarding Spinel and CA6 Formation

Abstract

Calcium hexaluminate (CaO·6Al2O3–CA6) is usually associated as the product reaction between alumina and CA2 (CaO·2Al2O3) in cement‐bonded refractory castables. However, some investigations related to the Al2O3–CaO–MgO ternary system have indicated that CA6 could be generated by additional routes, involving two other high‐alumina phases: CaMg2Al16O27 (CM2A8) and Ca2Mg2Al28O46 (C2M2A14). Considering the lack of conclusive studies on this subject in the refractories field, the present study addresses an in‐depth microstructural evolution analysis of high‐alumina castables containing in situ or preformed spinel (MgAl2O4) in order to check the actual CA6 development steps in the presence of an MgO‐containing phase. By scanning electron microscopy (SEM) and thermodynamic calculations, it was observed that CA6 formation took place indeed as a result of the decomposition reaction of CM2A8, which was firstly generated due to the interaction between spinel and Al2O3–CaO–Na2O–SiO2 liquid. Although, the results confirmed this complex CA6 formation route regardless of the spinel incorporation method (pre‐formed grains addition or in situ reaction), the CA6 crystals distribution after the thermal treatment was entirely affected by the previous spinel grains location. Those different microstructural profiles could be the conclusive aspects to explain the poorer slag resistance of preformed spinel‐containing castables when in contact with steel ladle slags.