The effects of potassium addition on the rate of quartz dissolution in the CMAS and CAS systems

Abstract

Quartz dissolution in melts in the KCAS and KCMAS systems results in the formation of a silica- and potassium-enriched boundary layer next to the dissolving crystals. The presence of potassium in CAS melts has no discernible effect on dissolution rate compared with that in K-free melts with otherwise similar composition despite a small decrease in the diffusivity of silica in the potassium-bearing melts. The decrease in silica diffusivity is offset by an increase in the solubility of silica in the K-bearing melts. Addition of potassium to CMAS melts results in a large decrease in the dissolution rate of quartz. Even though the solubility of silica is enhanced, the addition of potassium leads to large changes in the structure of the melt in the boundary layer (as measured by NBO/T), which results in a large decrease in the diffusivity of silica and thus slower dissolution. There is significant diffusive coupling of Al2O3, CaO and MgO during dissolution, which leads to local uphill diffusion of these components. K2O is decoupled from the other components, as shown by its much thicker diffusion zone. Potassium moves through the boundary layer as a result of two homogeneous reactions: uphill diffusion in which potassium diffuses into the silica-enriched melt adjacent to the dissolving quartz crystal and downhill diffusion in the region furthest from the crystal–melt interface where SiO2 and K2O diffuse away from the interface together.