Thermodynamic equilibrium between the CaO–SiO
2–Al
2O
3–MgO
satd–CaF
2(–TiO
x) slags and the Fe–11mass%Cr melt was investigated at 1873 K in order to understand the thermodynamic behavior of titanium oxide in the refining slags. The equilibrium between silicon and titanium in steel melts and their oxides in the slags are theoretically expected and experimentally proved well. The activity coefficient of TiO
2 increases by increasing the basicity in logarithmic scale. By combining this with the previous results, in multi component calcium(–magnesium) silicate slags containing Al
2O
3 and TiO
2, TiO
2 could be considered as a basic oxide in silicate base melts, while it could be the relatively acidic oxide in the aluminate (very low silica) base melts. The activity coefficient of TiO
2 gradually decreases by substituting silica for alumina, indicating that the attraction between TiO
2 and SiO
2 is greater than that between TiO
2 and Al
2O
3 in the present slag system. This could be explained from the electronegativity difference between each cation involved. The activity of TiO
2 in the 10%MgO slag system shows a negative deviation from an ideality, while that in the CaO–SiO
2–Al
2O
3–MgO
satd(–CaF
2) system is relatively close to the ideal behavior up to about 10 mol% TiO
2. This is mainly due to the relatively basic characteristic of TiO
2.
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