过冷
差示扫描量热法
材料科学
结晶
成核
共聚物
共晶体系
共单体
化学工程
等温过程
偏振光显微镜
动力学
共聚酯
相(物质)
高分子化学
结晶学
复合材料
热力学
聚合物
微观结构
化学
聚酯纤维
有机化学
光学
物理
量子力学
工程类
作者
Maryam Safari,Agurtzane Múgica,Manuela Zubitur,Antxon Martı́nez de Ilarduya,Sebastián Muñoz‐Guerra,Alejandro J. Müller
出处
期刊:Polymers
[Multidisciplinary Digital Publishing Institute]
日期:2019-12-20
卷期号:12 (1): 17-17
被引量:35
标识
DOI:10.3390/polym12010017
摘要
In this work, we study for the first time, the isothermal crystallization behavior of isodimorphic random poly(butylene succinate)-ran-poly(ε-caprolactone) copolyesters, PBS-ran-PCL, previously synthesized by us. We perform nucleation and spherulitic growth kinetics by polarized light optical microscopy (PLOM) and overall isothermal crystallization kinetics by differential scanning calorimetry (DSC). Selected samples were also studied by real-time wide angle X-ray diffraction (WAXS). Under isothermal conditions, only the PBS-rich phase or the PCL-rich phase could crystallize as long as the composition was away from the pseudo-eutectic point. In comparison with the parent homopolymers, as comonomer content increased, both PBS-rich and PCL-rich phases nucleated much faster, but their spherulitic growth rates were much slower. Therefore, the overall crystallization kinetics was a strong function of composition and supercooling. The only copolymer with the eutectic composition exhibited a remarkable behavior. By tuning the crystallization temperature, this copolyester could form either a single crystalline phase or both phases, with remarkably different thermal properties.
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