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Synergistic enhancement of fracture toughness in multiphase epoxy matrices modified by thermoplastic and carbon nanotubes

机译:热塑性和碳纳米管改性多相环氧基质中断裂韧性的协同性

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Herein, we report the development of multiphase epoxy-based nanocomposite blends with enhanced fracture toughness and controlled microstructure. The blends are based on bifunctional and tetrafunctional epoxy resins, suitable for a wide range of applications particularly as matrices for advanced high temperature fibre reinforced composites with glass transition temperatures exceeding 200 degrees Celsius. The multiphase blends comprise nanoscale (carbon nanotubes) and microscale (phase separating thermoplastic) inclusions which together form unique multiscale morphologies capable of dissipating crack energy through different energy absorption mechanisms. This work provides, for the first time, an in-depth investigation of the interactions between the nano- and microscale toughness modifiers which under appropriate conditions lead to a synergistic enhancement in the fracture toughness of the resin. A secondary agglomeration of carbon nanotubes during curing was shown to be suppressed by the phase separating thermoplastic particles, leading to a well dispersed state, justifying the synergistic increase in fracture toughness of the resulting blends. The molecular architecture of the epoxy matrix, in particular, the number of epoxide functional groups, was shown to be of significant importance in determining the final microstructure of the modified blends following curing reaction.
机译:在此,我们报告了具有增强的断裂韧性和控制微观结构的多相环氧基纳米复合材料的开发。共混物基于双功能和四官能环氧树脂,适用于各种应用,特别是作为先进的高温纤维增强复合材料的基质,玻璃化转变温度超过200摄氏度。多相共混物包括纳米级(碳纳米管)和微尺寸(相分离热塑性塑料)夹杂物,其共同形成通过不同的能量吸收机制来散发裂纹能量的独特的多尺度形态。这项工作首次提供了对纳米和微观韧性改性剂之间的相互作用的深入研究,其在适当的条件下导致树脂的断裂韧性的协同增强。显示在固化过程中的碳纳米管的二次凝聚,被相位分离热塑性颗粒抑制,导致井分散状态,证明了所得共混物的断裂韧性的协同增加。特别是环氧基质的分子结构,特别是环氧化物官能团的数量在确定固化反应后修饰的共混物的最终微观结构方面具有重要意义。

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