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Structure and Properties of Aromatic Poly(benzimidazole-imide) Copolymer Fibers

机译:芳族聚苯并咪唑共聚物纤维的结构与性能

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摘要

A series of co-polyimide fibers were prepared by thermal imidization of copolyamic acids derived from 3,3',4,4'-biphenyltertracarboxylic dianhydride (BPDA) and pyromellitic dianhydride (PMDA) in various molar ratios with 2-(4-aminophenyl) 25-aminobenzimidazole (BIA). The dynamic mechanical behaviors of these polyimide (PI) fibers revealed that the glass transition temperature (T-g) was significantly improved upon increasing PMDA content. Heat-drawing process led to dramatic change on the glass transition behavior of BPDA/BIA system, but had a small impact on BPDA/PMDA/BIA co-polyimide fibers. This difference for PI fibers is attributed to the different degree of ordered structure of the fibers affected by heat-drawing. The incorporation of PMDA obviously improved the dimensional stability against high temperature, due to the restricted movement of polymer chains. In addition, the obtained fibers show excellent mechanical and thermal properties because of the strong hydrogen bonding due to the incorporation of benzimidazole moieties. (C) 2014 Wiley Periodicals, Inc.
机译:通过将3,3',4,4'-联苯四羧酸二酐(BPDA)和均苯四甲酸二酐(PMDA)衍生的共聚酰胺酸与2-(4-氨基苯基)进行各种摩尔比的热酰亚胺化制备了一系列共聚酰亚胺纤维25-氨基苯并咪唑(BIA)。这些聚酰亚胺(PI)纤维的动态力学行为表明,随着PMDA含量的增加,玻璃化转变温度(T-g)显着提高。吸热过程导致BPDA / BIA系统的玻璃化转变行为发生了巨大变化,但对BPDA / PMDA / BIA共聚酰亚胺纤维的影响很小。 PI纤维的这种差异归因于受热影响的纤维的有序结构的不同程度。由于聚合物链的运动受限,PMDA的加入明显改善了高温下的尺寸稳定性。另外,由于并入了苯并咪唑基团,氢键很强,因此获得的纤维具有优异的机械性能和热性能。 (C)2014威利期刊公司

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