聚丁烯
结晶
成核
战术性
聚合物
相变
材料科学
量子纠缠
聚合物结晶
结晶度
多态性(计算机科学)
相(物质)
化学物理
高分子化学
结晶学
热力学
聚合
化学
有机化学
量子
物理
基因型
复合材料
基因
量子力学
生物化学
作者
Lingling Ni,Shanshan Xu,Chenxuan Sun,Yanan Qin,Ying Zheng,Jian Zhou,Chengtao Yu,Pengju Pan
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2022-01-24
卷期号:11 (2): 257-263
被引量:17
标识
DOI:10.1021/acsmacrolett.1c00794
摘要
Polymorphism and crystal transition are common phenomena of semicrystalline polymers. These two behaviors are known to be controlled by the nucleation and chain mobility of polymers, both of which are constrained by the chain entanglement at the molecular level. However, the role of chain entanglement in polymorphic crystallization and crystal phase transition of polymers has not been well understood. Herein, we use isotactic polybutene-1 (PB-1) as a model polymorphic polymer and present the crucial role of chain entanglement in the polymorphic crystallization kinetics and solid-solid phase transition. A series of less-entangled PB-1 with different entanglement degrees were successfully prepared by freeze-drying the polymer dilute solution. Compared to the bulk sample and re-entangled one, chain disentangling of PB-1 suppressed the crystallization kinetics of form II but significantly increased the phase transition rate and final transition degree from form II to form I. The disentangling-promoted II-I phase transition originated from the reduced nucleation barrier and enhanced chain mobility. This work would advance the in-depth understanding on the formation and transition mechanisms of polymorphic polymer crystals at the molecular level.
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