聚丁烯
结晶
差示扫描量热法
战术性
熔点
活化能
热力学
材料科学
结晶学
聚合物
分析化学(期刊)
化学
高分子化学
物理化学
聚合
有机化学
复合材料
物理
作者
Kaushal Kishore,R. Vasanthakumari,TG Ramesh
标识
DOI:10.1002/pola.1986.080240821
摘要
Abstract An equation has been developed for the study of the kinetics of polymer crystallization at high pressures using differential scanning calorimetry (DSC) in the dynamic mode of operation. The activation energy for the crystallization of isotactic polybutene‐1 (PB‐1) has been determined to be ca. 20 kcals/mol; this has been attributed to the transport of chain segments to the site of crystallization. The melting behavior of form‐I PB‐1 crystals has been studied by using a high‐pressure differential thermal analyzer (DTA) setup and high‐pressure DSC. The melting temperature Tm does not show any significant change with pressure in the low‐pressure region up to 1.2 kbar; beyond this point a large increase in Tm with pressure was observed. This unusual low‐pressure behavior of PB‐1 has been attributed to formation of intermediate form I′, which has a lower melting point than form I.
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