成核
战术性
层状结构
材料科学
结晶
结晶学
光学显微镜
外延
聚结(物理)
化学工程
化学物理
聚合
复合材料
化学
图层(电子)
扫描电子显微镜
聚合物
有机化学
工程类
物理
天体生物学
作者
Binghua Wang,Gang Wang,Shanshan He,Taicheng Sun,Jingbo Chen,Changyu Shen,Bin Zhang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2021-12-08
卷期号:54 (24): 11404-11411
被引量:24
标识
DOI:10.1021/acs.macromol.1c02057
摘要
The self-nucleation behavior of β-form isotactic polypropylene (β-iPP) crystals in ultrathin films has been probed by atomic force microscopy (AFM) and optical microscopy (OM). The hexagonal β-iPP single crystals can be obtained via a self-seeding method at much higher crystallization temperatures (e.g., 156 °C). We found that the average number nucleation density (N) of β-iPP lamellar crystals deceases with increasing self-nucleation temperature (Ts) and heating rate (Vh). Upon heating the polymorphic structures induced by shear flow to a temperature between 143 and 156 °C, since α-iPP grows about 20–2400% faster than β-iPP, the former overtakes and engulfs the growth front of the later when crystallized for a sufficiently long time. However, the morphological observations show that both α-iPP and β-iPP were grown by homoepitaxy on their own crystals, and no trace of the epitaxial overgrowth of α-iPP lamellae on the entire growth front of β-iPP was observed, that is, a high-temperature βα growth transition appears to be absent, which probably indicates that the free energy barrier for secondary αα nucleation and ββ nucleation is much lower than that of βα nucleation in ultrathin films.
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