The introduction of alkaline earth oxides into Li
2O-Al
2O
3-SiO
2 glass components can improve the mechanical and optical performances of glass and glass–ceramics for various applications. In this research, microstructures, thermal properties, crystallization behavior, and mechanical performance changes
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The introduction of alkaline earth oxides into Li
2O-Al
2O
3-SiO
2 glass components can improve the mechanical and optical performances of glass and glass–ceramics for various applications. In this research, microstructures, thermal properties, crystallization behavior, and mechanical performance changes in specific Li
2O-Al
2O
3-SiO
2 glass with the introduction of different alkali earth oxides, MgO, CaO, SrO, and BaO, were investigated. From Raman and NMR spectra microstructure analysis, it was confirmed that the addition of MgO could compete with Al as a network former and charge compensator, while increasing the bridging oxygen number with Si and affecting the chemical shift in
29Si. Meanwhile, the glass structures slightly changed due to the introduction of CaO, SrO, and BaO, with larger ionic radii. Meanwhile, the glass transition and first crystallization temperatures increased due to MgO introduction and then decreased with larger-radii alkali earth oxides’ addition, due to different glass network connectivity. After heat treatment, the crystal phases in the glass–ceramics changed with the introduction of alkaline earth oxides. The main crystal phases varied from Li
2Si
2O
5, SiO
2, and LiAlSi
4O
10 in glass without alkali earth oxide introduction; to SiO
2, Li
xAl
xSi
3−xO
6, and MgAl
2Si
4O
12 in glass with MgO addition; to SiO
2 and Li
xAl
xSi
3−xO
6 with CaO addition; to SiO
2, LiAlSi
4O
10, and Li
2SiO
3 for glass with SrO addition; and further to Li
2SiO
5, SiO
2, and LiAlSi
4O
10 for glass with BaO addition. Moreover, in the mechanical performance of the glass–ceramics, the Vickers hardness and elastic modulus reached a maximum of 8.61 GPa for glass with MgO and 90.12 GPa for glass with BaO modification, respectively, probably due to different crystal phases. More importantly, the crack resistance values presented a large increase for MgO glass and MgO- or CaO-modified glass–ceramics.
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