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Solvent Effect on the Glass Transition Temperature of Syndiotactic Polystyrene Viewed from Time-Resolved Measurements of Infrared Spectra at the Various Temperatures and Its Simulation by Molecular Dynamics Calculation

机译:从不同温度下红外光谱的时间分辨测量看溶剂对间规聚苯乙烯玻璃化转变温度的影响及其分子动力学模拟

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Time-resolved infrared spectral measurement was performed in the solvent-induced crystallization process of syndiotactic polystyrene (sPS) glass at the various temperatures,and the crystallization kinetics were analyzed quantitatively.Both of the crystallization rate constant and the crystallinity estimated after passage of long time were found to decrease with decrease in the crystallization temperature.The extrapolation of the rate constant and the crystallinity to the zero values allowed us to estimate the glass transition temperature (T_g) in the organic solvent atmosphere.The Tg of the original glass sample (ca.100 deg C) was found to shift to -90 +- 10 deg C for chloroform,-70 +- 10 deg C for benzene,and -30 +- 10 deg C for toluene.The solvent with higher solubility or higher interaction with sPS was found to shift the T_g at higher degree.To understand this plasticizing effect of solvent from the microscopic point of view,the molecular dynamics calculation was performed for sPS-toluene and sPS-chloroform systems,and a good correspondence was obtained about the T_g shift between the observed and calculated results.
机译:在不同温度下,间规聚苯乙烯(sPS)玻璃在溶剂诱导的结晶过程中进行时间分辨红外光谱测量,并对结晶动力学进行定量分析。结晶速率常数和经过长时间后的结晶度发现随着结晶温度的降低而降低。速率常数和结晶度外推至零值使我们能够估计有机溶剂气氛中的玻璃化转变温度(T_g)。对于氯仿,发现(.100摄氏度)转移到-90 +-10摄氏度,对于苯来说转移到-70 +-10摄氏度,对于甲苯转移到-30 +-10摄氏度。 sPS被发现会较高程度地改变T_g。为了从微观角度了解溶剂的这种增塑作用,对sPS-进行了分子动力学计算甲苯和sPS-氯仿体系,并且观察到的和计算的结果之间的T_g位移具有良好的对应关系。

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