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Synthesis and properties of polyimides derived from diamine monomer containing bi-benzimidazole unit

机译:含联苯并咪唑单元的二胺单体衍生的聚酰亚胺的合成及性能

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摘要

A new aromatic heterocyclic diamine monomer containing bi-benzimidazole unit, 2,2-bis(4′-aminophenyl)- 5,5-bi-1H-benzimidazole, was synthesized from 2,2-bis(4′-nitrophenyl)- 5,5-bi-1H-benzimidazole (BNPBBI) prepared via the reaction of 3,3′,4,4′-biphenyltetramine and pnitrobenzaldehyde with a high yield. Their compositions and chemical structures containing polybenzimidazole backbone were characterized by FTIR, 1H NMR and elemental analysis. A series of aromatic polyimides containing the heterocyclic moiety in the main chain were prepared by the reaction of BAPBBI with various aromatic dianhydrides of 3,3′,4,4′- biphenyltetracarboxylic dianhydride, 4,4′-oxydiphthalic anhydride or pyromellitic dianhydride. The polymers possess a high glass transition temperature of >415 °C and a good thermal stability up to 566 °C with a 5 % weight loss. The combination of polybenzimidazole and polyimide via introducing BAPBBI into the main chains provides the rigid structure, and macromolecular interactions are thus enhanced, resulting in the outstanding mechanical properties. These polyimides exhibit the strong tensile strength of 201 to 327 MPa, and the ultrahigh tensile moduli of 10.7 to 15.5 GPa without post stretching.
机译:由2,2-双(4'-硝基苯基)-5合成了一种新型的含双苯并咪唑单元的芳香族杂环二胺单体2,2-双(4'-氨基苯基)-5,5-双-1H-苯并咪唑通过3,3',4,4'-联苯四胺与对硝基苯甲醛的反应制备高产率的1,5-双-1H-苯并咪唑(BNPBBI)。通过FTIR,1H NMR和元素分析对它们的组成和含有聚苯并咪唑骨架的化学结构进行了表征。通过BAPBBI与3,3',4,4'-联苯四甲酸二酐,4,4'-氧二邻苯二甲酸酐或均苯四甲酸二酐的各种芳族二酐反应,制备了一系列在主链中包含杂环部分的芳族聚酰亚胺。该聚合物具有> 415°C的高玻璃化转变温度和高达566°C的良好热稳定性,重量损失为5%。通过将BAPBBI引入主链中的聚苯并咪唑和聚酰亚胺的结合提供了刚性结构,从而增强了大分子的相互作用,从而获得了出色的机械性能。这些聚酰亚胺在没有后拉伸的情况下表现出201至327 MPa的强拉伸强度,以及10.7至15.5 GPa的超高拉伸模量。

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