材料科学
聚氨酯
聚丁二烯
弹性体
韧性
相容性(地球化学)
极限抗拉强度
热稳定性
复合材料
聚合物
侧链
热的
扩展器
玻璃化转变
极地的
灵活性(工程)
端羟基聚丁二烯
异氰酸酯
高分子化学
化学工程
弹性(物理)
溶剂
混溶性
分层(地质)
对称(几何)
作者
Yushu Tian,M. F. Wang,J L Wang,Yi Wei,Yixuan Chang,Xuan Qin,Liqun Zhang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2026-01-05
卷期号:59 (2): 763-774
被引量:1
标识
DOI:10.1021/acs.macromol.5c02654
摘要
Polyurethane elastomers (PUs) with nonpolar soft segments exhibit excellent flexibility and hydrophobicity, but the poor compatibility between nonpolar soft segments and polar hard segments limits their overall performance. In this work, hydroxyl-terminated polybutadiene (HTPB) and p-phenylene diisocyanate (PPDI) were combined with chain extenders differing in symmetry and side methyl substitution to tune hard-segment regularity. Symmetric extenders promoted excessive aggregation and heterogeneous microstructures, whereas asymmetric or methyl-substituted extenders suppressed ordered microphase separation, yielding more uniform morphologies and superior properties. The optimized sample, C3-1, achieved high tensile strength (16.9 MPa), toughness (34.3 MJ·m–3), and thermal stability (320.8 °C), representing the most flexible heat-resistant HTPB-based PU reported to date. These results demonstrate that hard-segment regularity governs both microphase morphology and macroscopic properties. Furthermore, two effective design strategies, reducing extender symmetry and introducing side methyl groups, are established for developing advanced nonpolar PUs with balanced strength, flexibility, and stability.
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