材料科学
位阻效应
聚氨酯
弹性体
韧性
相容性(地球化学)
极限抗拉强度
聚合物
复合材料
热稳定性
分子动力学
预聚物
化学工程
热的
动态力学分析
共聚物
玻璃化转变
高分子化学
支化(高分子化学)
机械强度
艾氏冲击强度试验
作者
Yushu Tian,Yi Wei,Min Wang,Jiadong Wang,Shuang Li,Xuan Qin,Liqun Zhang
标识
DOI:10.1002/marc.202500727
摘要
The segmental compatibility between soft and hard segments, along with the resulting microphase separation behavior, critically influences the mechanical and thermal properties of polyurethane elastomers (PU). In this work, we propose a steric hindrance-based molecular design strategy to regulate the microphase structure of nonpolar polybutadiene-based PU. Multiscale characterization and molecular simulations reveal that introducing chain extenders with moderate steric hindrance effectively disrupts the ordered packing of hard segments. This leads to the formation of an interfacial transition-type microphase separation (ITMS) structure. The unique interfacial state enhances interfacial compatibility and morphological uniformity, thereby improving tensile strength, toughness, and energy dissipation. The optimized sample, PU-2, achieved a tensile strength of 14.3 MPa, a toughness of 23.5 MJ·m-3, and tan δmax above 1.0. It also exhibited stable performance under dynamic loading, together with water resistance, electrical insulation, and biocompatibility. These results highlight ITMS as a design strategy for optimizing PU with nonpolar soft and rigid hard segments.
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