位阻效应
结晶度
材料科学
热塑性聚氨酯
热塑性塑料
氢键
极限抗拉强度
复合材料
超分子化学
弹性体
结晶
高分子化学
化学工程
结晶学
晶体结构
分子
化学
有机化学
工程类
作者
Hang-Tian Zhang,Fang Zhang,Yixian Wu
标识
DOI:10.1021/acs.iecr.9b06107
摘要
Thermoplastic polyurethane (TPU) elastomers based on polyoxytetramethylene glycol (PTMG) with 2000 g·mol–1 as soft segments (SSs) and isocyanates as well as their reaction with butanediol as hard segments (HSs) were synthesized. The three-dimensional supramolecular networks were constructed in TPU by the formation of physical HSs-rich domains via microphase separation, hydrogen bonding, and microcrystallization, which are dominated by the chemical structure of HSs. The robust stretchable TPU with an excellent tensile strength of 32 MPa and elongation of 1378% at break could be successfully prepared, and no crystallization happened to keep the elasticity even at a low temperature (−90 °C) when the steric semisymmetric bis(4-isocyanatocyclohexyl)methane (HMDI) was introduced into HSs-rich domains. The crystallinity and ordered hydrogen bonding content decreased in HSs-rich domains with increases in steric hindrance and asymmetry of diisocyanates. A new approach was developed to construct the high-performance TPUs by introducing long PTMG SSs for the flexibility and elasticity and steric semisymmetric HMDI hard segments.
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