聚酰胺
韧性
材料科学
共聚物
热稳定性
芳纶
聚合物
极限抗拉强度
增韧
刚度(电磁)
灵活性(工程)
支化(高分子化学)
高分子化学
化学工程
复合材料
高分子科学
数学
工程类
统计
纤维
作者
Xianzhu Zhong,Aniruddha Nag,Kenji Takada,Akinori Nakajima,Tatsuo Kaneko
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-02-28
卷期号:29 (5): 1058-1058
被引量:3
标识
DOI:10.3390/molecules29051058
摘要
Polybenzimidazoles (PBIs) are recognized for their remarkable thermal stability due to their unique molecular structure, which is characterized by aromaticity and rigidity. Despite their remarkable thermal attributes, their tensile properties limit their application. To improve the mechanical performance of PBIs, we made a vital modification to their molecular backbone to improve their structural flexibility. Non-π-conjugated components were introduced into PBIs by grafting meta-polyamide (MA) and para-polyamide (PA) onto PBI backbones to form the copolymers PBI-co-MA and PBI-co-PA. The results indicated that the cooperation between MA and PA significantly enhanced mechanical strain and overall toughness. Furthermore, the appropriate incorporation of aromatic polyamide components (20 mol% for MA and 15% for PA) improved thermal degradation temperatures by more than 30 °C. By investigating the copolymerization of PBIs with MA and PA, we unraveled the intricate relationships between composition, molecular structure, and material performance. These findings advance copolymer design strategies and deepen the understanding of polymer materials, offering tailored solutions that address thermal and mechanical demands across applications.
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