Inorganic glasses and glass-ceramics studied by isothermal mechanical spectroscopy

被引:0
作者
Riviere, A. [1 ]
Chocinski-Arnault, L. [1 ]
机构
[1] ENSMA, CNRS, UMR 6617, Mecan & Phys Mat Lab, F-86961 Futuroscope, France
来源
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING | 2006年 / 442卷 / 1-2期
关键词
isothermal mechanical spectroscopy; mixed alkali effect; inorganic glass; glass-ceramic; point defect;
D O I
10.1016/j.msea.2006.03.123
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This paper describes isothermal mechanical spectroscopy measurements carried out in silicate glasses and LAS (Li2O-Al2O3-SiO2)-type glass-ceramics. Single alkali silicate glass Na(2)O(center dot)3SiO(2) exhibits two relaxation peaks. The first one located at a low temperature is generally assigned to the stress-induced diffusion of alkali ions. The second relaxation peak is attributed to the "non-bridging oxygen". Mixed alkali silicate glasses (1-x)Na2O center dot xLi(2)O center dot 3SiO(2) with x=0, 0.25, 0.5, 0.75 exhibit the mixed alkali peak. And also the "non-bridging oxygen" peak. Two LAS-type glass-ceramics having the same chemical composition but different microstructures: "beta-quartz" and beta-spodumene" type, respectively, and their parent glass have been studied. For the glass which does not contain "non-bridging oxygen", a single mechanical relaxation peak linked with the stress-induced movement of lithium ions is observed. On the contrary, two peaks occur in the beta p-quartz" and "beta-spodumene" glass-ceramics. The "low-temperature" peak (similar to 340 K for 1 Hz) is linked with ion mobility in the respective main crystalline phase. The origin of the "high-temperature" peak is totally different for the two glass-ceramics; in the "beta-quartz" glass-ceramic, it is due to Mg2+ and Zn2+ ion relaxation in the crystalline phase, whereas in the "beta-spodurnene" glass-ceramic, it is linked with a complex entity within the residual vitreous phase. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:243 / 249
页数:7
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