Abstract
Containerless melting was employed to evaluate the influence of increasing ZrO2 additions on the glass-forming ability of peraluminous melts in the magnesium aluminosilicate system. The saturation limit of this oxide in glasses along the silica-cordierite join (SiO2–Mg2Al4Si5O18) is inversely proportional to the SiO2 content; however, a limited solubility of ZrO2 in melt-quenched silica exists (∼2 mol%). Peraluminous samples (particularly MgO-free samples) exhibited a substantially higher capability of incorporating ZrO2 without undergoing devitrification during cooling. TEM investigations revealed phase separation in all amorphous samples off the MgO = Al2O3 line, with ZrO2 preferentially segregating into a SiO2-depleted phase. These results identify the key role of Al2O3 for the structural incorporation of ZrO2 in silicate melts, opening up alternative pathways for the development of glasses and glass-ceramics respectively based on the homogeneous distribution of ZrO2 or, in turn, on its exploitation to induce phase separation and crystal nucleation.
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