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The kinetics of the glass transition and physical aging in germanium selenide glasses

机译:硒化锗玻璃的玻璃态转变动力学和物理时效

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摘要

The kinetics associated with the glass transition is investigated using differential scanning calorimetry (DSC) for germanium selenide glasses with Ge content ranging from 0 to 30 at.% and average coordination numbers ranging from 2.0 to 2.6. As Ge content increases, the glass transition region broadens and the step change in heat capacity at Tg decreases. As a result of physical aging, enthalpy overshoots are observed in DSC heating scans and the corresponding change in enthalpy can be calculated as a function of aging time. The change in enthalpy linearly increases with the logarithm of aging time and then levels off at an equilibrium value that increases with decreasing aging temperature. The time required to reach equilibrium increases with decreasing aging temperature and, at a given distance from T_g, the time increases with decreasing germanium content. The results indicate that all samples show expected physical aging behavior, and no evidence is found for a Boolchand intermediate phase characterized by high stability and absence of physical aging.
机译:使用差示扫描量热法(DSC)研究了锗含量为0到30 at。%,平均配位数为2.0到2.6的硒化锗玻璃的与玻璃化转变有关的动力学。随着Ge含量的增加,玻璃化转变区域变宽,并且在Tg处的热容量的阶跃变化减小。由于物理老化,在DSC加热扫描中会观察到焓过冲,并且可以根据老化时间计算出相应的焓变化。焓的变化随老化时间的对数线性增加,然后稳定在一个随老化温度降低而增加的平衡值上。达到平衡所需的时间随着老化温度的降低而增加,并且在距T_g的给定距离下,该时间随着锗含量的降低而增加。结果表明,所有样品均显示出预期的物理老化行为,并且没有发现以高稳定性和无物理老化为特征的Boolchand中间相的证据。

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