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Toughening of a Carbon-Fibre Composite Using Electrospun Poly(Hydroxyether of Bisphenol A) Nanofibrous Membranes Through Inverse Phase Separation and Inter-Domain Etherification

机译:通过反相分离和域间醚化使用静电纺丝双酚A纳米纤维膜的碳纤维复合材料的增韧

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摘要

The interlaminar toughening of a carbon fibre reinforced composite by interleaving a thin layer (~20 microns) of poly(hydroxyether of bisphenol A) (phenoxy) nanofibres was explored in this work. Nanofibres, free of defect and averaging several hundred nanometres, were produced by electrospinning directly onto a pre-impregnated carbon fibre material (Toray G83C) at various concentrations between 0.5 wt % and 2 wt %. During curing at 150 °C, phenoxy diffuses through the epoxy resin to form a semi interpenetrating network with an inverse phase type of morphology where the epoxy became the co-continuous phase with a nodular morphology. This type of morphology improved the fracture toughness in mode I (opening failure) and mode II (in-plane shear failure) by up to 150% and 30%, respectively. Interlaminar shear stress test results showed that the interleaving did not negatively affect the effective in-plane strength of the composites. Furthermore, there was some evidence from DMTA and FT-IR analysis to suggest that inter-domain etherification between the residual epoxide groups with the pendant hydroxyl groups of the phenoxy occurred, also leading to an increase in glass transition temperature (~7.5 °C).
机译:在这项工作中,研究了通过交织双酚A(苯氧基)纳米纤维的聚(羟基醚)薄层(〜20微米)实现碳纤维增强复合材料的层间增韧。通过直接电纺到预浸渍的碳纤维材料(东丽G83C)上以0.5 wt%至2 wt%的不同浓度生产无缺陷且平均数百纳米的纳米纤维。在150°C的固化过程中,苯氧基会扩散穿过环氧树脂,以形成具有反相形态的半互穿网络,其中环氧树脂变成具有结节形态的共连续相。这种类型的形态分别将模式I(打开破坏)和模式II(面内剪切破坏)的断裂韧性分别提高了150%和30%。层间剪切应力测试结果表明,交织不会对复合材料的有效面内强度产生负面影响。此外,从DMTA和FT-IR分析中获得的一些证据表明,残留的环氧基与苯氧基的侧链羟基之间发生了域间醚化,还导致玻璃化转变温度(约7.5°C)升高。

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