کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1477115 | 991173 | 2006 | 8 صفحه PDF | دانلود رایگان |

The elasticity and structure of lithium silicate glasses Li2O·3SiO2, Li2O·2SiO2, and Li2O·2SiO2·0.135ZrO2 were studied at ambient conditions, using both Raman and Brillouin spectroscopies. The conventional nucleating agent, i.e., Zr4+ caused a more polymerized silicate network, amorphous phase separation before crystallization, and a significant drop in shear, Young's and bulk moduli, though Raman spectra have revealed that the partial substitution of Zr for Si occurred chiefly in the less polymerized Q2 species. The compiled data of alkali silicate glasses M2O–SiO2 (M = Li, Na, K) showed that each glass displays different M2O concentrations for getting minimum bulk modulus due to difference in field strength of cations, depolymerization of silicate network, and coordination number of cations. The specific M2O concentrations for such minima increase with increasing cation size. Different composition dependences of elastic moduli for the glasses having same constituents can be ascribed to different mechanisms for compression and shear deformation.
Journal: Journal of the European Ceramic Society - Volume 26, Issue 16, 2006, Pages 3613–3620