Dissolution of Oxide Particles in Multi-component Slags Governed by Diffusive and Convective Fluxes

Daniel Marian Ogris, Susanne Michelic, Ernst Gamsjäger
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Abstract

The kinetics of the dissolution of oxide particles in metallurgical slags is simulated by means of a sharp-interface finite difference model where multi-component diffusion is considered. The effect of convective fluxes on the dissolution kinetics is being considered by a constrained boundary layer thickness. The thickness of this boundary layer can be estimated from theory and is used together with the interdiffusivity matrix to predict the dissolution kinetics of spherical alumina particles in various CaO–SiO2–Al2O3 slags. The numerical results are compared to experimental observations using High-Temperature Confocal Scanning Laser Microscopy (HT-CSLM). The results imply that the processes controlling the dissolution kinetics are multi-component diffusion with density-driven convective fluxes in the liquid slag gaining more influence in the later stages of the dissolution process

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多组分炉渣中氧化物颗粒的溶解受扩散和对流通量控制
通过锐面有限差分模型模拟了冶金渣中氧化物颗粒的溶解动力学,其中考虑了多组分扩散。对流通量对溶解动力学的影响是通过限制边界层厚度来考虑的。该边界层的厚度可以从理论上估算出来,并与相互扩散矩阵一起用于预测球形氧化铝颗粒在各种 CaO-SiO2-Al2O3 矿渣中的溶解动力学。数值结果与使用高温共焦激光扫描显微镜(HT-CSLM)进行的实验观察结果进行了比较。结果表明,控制溶解动力学的过程是多组分扩散过程,在溶解过程的后期阶段,液渣中的密度驱动对流通量的影响更大。
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