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首页> 外文期刊>Composites Science and Technology >Functionalized aramid nanofibers prepared by polymerization induced self-assembly for simultaneously reinforcing and toughening of epoxy and carbon fiber/epoxy multiscale composite
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Functionalized aramid nanofibers prepared by polymerization induced self-assembly for simultaneously reinforcing and toughening of epoxy and carbon fiber/epoxy multiscale composite

机译:通过聚合诱导自组装制备的功能化芳族聚酰胺纳米纤维,可同时增强和增韧环氧和碳纤维/环氧多尺度复合材料

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摘要

Aramid nanofibers (ANFs) are polymeric nanofibers that have been drawing tremendous attention as new nanoscale building blocks of advanced composites. Herein, we report a new strategy to rapidly synthesize functionalized ANFs (fANFs) through polymerization-induced self-assembly of poly(phenylene terephthalamide) (PPTA) using soluble sulfonated PPTA to tailor the size of fANTs, and the extraordinary reinforcing and toughening effect of fANFs on epoxy (EP) resin and multiscale carbon fiber (CF)/EP composites. With a diameter of similar to 30 nm, and reactive sulfonic acid groups on the surfaces, the branched fANFs can be easily dispersed in EP and are reactive with the matrix, therefore, remarkably improve the interfacial interaction and mechanical properties (including both strength and toughness) of EP at low fANF contents. The tensile strength, Young's modulus, toughness and elongation at break of fANFs/EP nanocomposites are increased by similar to 59%, similar to 19%, similar to 112% and similar to 36%, respectively. The flexural strength, interlaminar shear strength, total energy dissipation and flexural strain at break of fANFs/CF/EP multi-scale composite are increased by similar to 57%, similar to 38%, similar to 65% and similar to 71%, respectively. To the best of our knowledge, the enhancement in the strengths is comparative with those provided by graphene oxide, and the total fracture energy and flexural strain at break are more significantly increased by fANFs than almost all of the nanofillers ever reported.
机译:芳族聚酰胺纳米纤维(ANFs)是聚合物纳米纤维,作为先进复合材料的新型纳米级结构单元,已经引起了极大的关注。在本文中,我们报告了一种新的策略,可通过使用可溶性磺化PPTA来调节fANTs的尺寸,通过聚合诱导的聚对苯二甲酰对苯二胺(PPTA)的聚合诱导的自组装来快速合成官能化的ANFs(fANFs),以及非凡的增强和增韧效果。环氧树脂(EP)和多尺度碳纤维(CF)/ EP复合材料上的fANF。支链的fANFs的直径接近30 nm,并且在表面具有反应性磺酸基团,可以轻松地分散在EP中并与基体发生反应,因此显着改善了界面相互作用和机械性能(包括强度和韧性) fANF含量低的EP)。 fANFs / EP纳米复合材料的拉伸强度,杨氏模量,韧性和断裂伸长率分别增加了约59%,约19%,约112%和约36%。 fANFs / CF / EP多尺度复合材料的抗折强度,层间剪切强度,总能量耗散和断裂时的挠曲应变分别增加了约57%,约38%,约65%和71% 。据我们所知,强度的增强可与氧化石墨烯相提并论,并且fANFs的总断裂能和断裂时的挠曲应变比几乎所有报道的纳米填料都显着提高。

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