首页> 外文期刊>Glass Physics and Chemistry: A Journal on the Structural, Physical, and Chemical Properties and Nature of Inorganic Glasses and Glass-Forming Melts >Calculation of temperature dependences of the viscosity and volume relaxation time for oxide glass-forming melts from chemical composition and dilatometric glass transition temperature
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Calculation of temperature dependences of the viscosity and volume relaxation time for oxide glass-forming melts from chemical composition and dilatometric glass transition temperature

机译:从化学成分和膨胀玻璃化转变温度计算出氧化物玻璃形成熔体的粘度和体积弛豫时间的温度依赖性

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The relaxation parameter K_s that is equal to the ratio of the viscosity #eta# to the Kohlrausch volume relaxation time #tau#_s is analyzed. It is shown that htis parameter can be evaluated from the temperature T_(13) (corresponding to a viscosity of 10~(13) P) and the glass transition temperature T_g~+ determined from the dilatometric heting curve. The maximum error of the estimate with due regard for experimental errors is equal to +-(0.4-0.5)logK_s for "strong"glasses and +-(0.6-0.8)logK_s for "fragile" glasses, which, in both cases, corresponds to a change in the relaxation times with a change in the temperature by +-(8-10)K. It is revealed that the viscosity, the Kohlrausch volume relaxation time #tau#_s, and the shear modulus G of glass-forming materials in silicate, borate, and germanate systems satisfy the relationship log(#tau#_sG/#eta#)approx=1. The procedure for calculating the temperatur edependences of the viscosity and the relaxation times in the glass transition range from the chemical composition and the T_g~+ temperature for glass-forming melts in the above systems is proposed. The root-meansquare deviations between the calculated and experimental temperatures T_(11) and T_(13) are equal to +-(6-8) K for all the studied (silicate, borate, germanate, and mixed) oxide glass-forming systems. The proposed relationships can be useful for evaluating the boundaries of the annealing range and changes in the properties and their temperature coefficients upon cooling of glass-forming melts.
机译:分析等于粘度#eta#与Kohlrausch体积弛豫时间#tau#_s之比的弛豫参数K_s。结果表明,htis参数可以从温度T_(13)(对应于10〜(13)P的粘度)和由热膨胀曲线确定的玻璃化转变温度T_g〜+进行评估。在适当考虑实验误差的情况下,估算值的最大误差等于“强”眼镜的+-(0.4-0.5)logK_s和“易碎”眼镜的+-(0.6-0.8)logK_s,在这两种情况下,都对应随温度变化+-(8-10)K来改变弛豫时间。结果表明,在硅酸盐,硼酸盐和锗酸盐体系中,形成玻璃的材料的粘度,Kohlrausch体积弛豫时间#tau#_s和剪切模量G满足log(#tau#_sG /#eta#)的关系= 1。提出了在上述系统中,由化学成分和玻璃形成熔体的T_g〜+温度计算粘度和玻璃化转变范围内的弛豫时间的温度依赖性的程序。对于所有研究的(硅酸盐,硼酸盐,锗酸盐和混合氧化物)氧化物玻璃形成系统,计算温度T_(11)和实验温度T_(13)之间的均方根偏差等于+-(6-8)K 。所建议的关系对于评估退火范围的边界以及冷却玻璃成形熔体时特性及其温度系数的变化可能有用。

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