Shear viscosity of glass-forming melts in the liquid-glass transition region

被引:0
作者
D. S. Sanditov
机构
[1] Buryat State University,Department of Physical Problems, Buryat Scientific Center, Siberian Branch
[2] Russian Academy of Sciences,undefined
来源
Journal of Experimental and Theoretical Physics | 2010年 / 110卷
关键词
Viscous Flow; Silicate Glass; Valence Bond; Hole Formation; Bridge Oxygen Atom;
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学科分类号
摘要
A new approach to interpreting the hole-activation model of a viscous flow of glass-forming liquids is proposed. This model underlies the development of the concept on the exponential temperature dependence of the free energy of activation of a flow within the range of the liquid-glass transition in complete agreement with available experimental data. The “formation of a fluctuation hole” in high-heat glass-forming melts is considered as a small-scale low-activation local deformation of a structural network, i.e., the quasi-lattice necessary for the switching of the valence bond, which is the main elementary event of viscous flow of glasses and their melts. In this sense, the hole formation is a conditioned process. A drastic increase in the activation free energy of viscous flow in the liquid-glass transition region is explained by a structural transformation that is reduced to a limiting local elastic deformation of the structural network, which, in turn, originates from the excitation (critical displacement) of a bridging atom like the oxygen atom in the Si-O-Si bridge. At elevated temperatures, as a rule, a necessary amount of excited bridging atoms (locally deformed regions of the structural network) always exists, and the activation free energy of viscous flow is almost independent of temperature. The hole-activation model is closely connected with a number of well-known models describing the viscous flow of glass-forming liquids (the Avramov-Milchev, Nemilov, Ojovan, and other models).
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页码:675 / 688
页数:13
相关论文
共 64 条
[1]  
Avramov I.(2005)undefined J. Non-Cryst. Solids 351 3163-undefined
[2]  
Doremus R. H.(2002)undefined J. Appl. Phys. 92 7619-undefined
[3]  
Ojovan M. I.(2007)undefined J. Phys.: Condens. Matter 19 415 107-undefined
[4]  
Travis K. P.(1996)undefined Phys. Rev. B: Condens. Matter 53 2171-undefined
[5]  
Hand R. J.(1994)undefined Vysokomol. Soedin., Ser. A 36 1156-undefined
[6]  
Dure J. C.(1955)undefined Zh. Prikl. Khim. (Leningrad) 28 1077-undefined
[7]  
Olsen N. B.(1975)undefined Fiz. Khim. Stekla 1 256-undefined
[8]  
Christensen T.(1976)undefined Fiz. Khim. Stekla 2 515-undefined
[9]  
Maksimov V. L.(1992)undefined Fiz. Khim. Stekla 18 3-undefined
[10]  
Myuller R. L.(1978)undefined Fiz. Khim. Stekla 4 662-undefined