Molecular dynamics of the α-relaxation during crystallization of a low-molecular-weight compound:: A real-time dielectric spectroscopy study

被引:32
|
作者
Dobbertin, J
Hannemann, J
Schick, C
Pötter, M
Dehne, H
机构
[1] Univ Rostock, Dept Phys, D-18051 Rostock, Germany
[2] Univ Rostock, Dept Chem, D-18051 Rostock, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 1998年 / 108卷 / 21期
关键词
D O I
10.1063/1.476352
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Low-molecular-weight compounds often crystallizes to systems with 100% crystallinity. There are only a few examples where a small amorphous fraction, characterized by a glass transition, remains after long time crystallization from the melt. The crystallization of such a glass-forming low-molecular-weight compound was investigated in order to monitor the change of the molecular dynamics with increasing crystallinity by dielectric spectroscopy and differential scanning calorimetry (DSC). The measurement of the dielectric alpha-relaxation was performed in real time during isothermal crystallization above the glass transition. At high crystallinities (above 90%) a shift of the peak position and a broadening of the dielectric spectrum was observed. The calorimetric glass transition temperature shifts in the same region for about 15 K to higher temperatures. No direct information about the morphology of the samples is available at the moment but indirect measurements indicate a layerlike crystalline structure. Then the remaining amorphous fraction can be considered between the crystal layers and the observed changes in the relaxation behavior may be caused by spatial confinement in the order of nanometer. (C) 1998 American Institute of Physics. [S0021-9606(98)50321-2].
引用
收藏
页码:9062 / 9068
页数:7
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