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Phase Morphology and Fracture Behaviour of CNT and Thermoplastic Modified Epoxy Ternary Nanocomposite by Different Processing Methods

机译:不同加工方法CNT和热塑性改性环氧三元纳米复合材料的相形态及断裂行为

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CNT modified thermoplastic toughened epoxy nanocomposites used as potential matrix materials for fibre reinforced composites were prepared and compared. During the preparation step, CNTs were added, in two different ways to investigate the consequences of changing the order of addition in the final properties of the nanocomposites. It was shown that the presence of CNTs has a great impact on different aspects of the phase separation process of the thermoplastic particles and the resulting phase morphologies. Nanotubes in ternary blends with CNTs initially added to the epoxy phase showed a better dispersion in comparison with the other type where CNTs were initially added to the thermoplastic phase. The difference in morphology and micro structure of the blends including nanotubes with those without CNTs were attributed to the increase in the local viscosity, limiting the mobility and hence the growth of the thermoplastic phase following phase separation. This resulted in the formation of smaller particles with a wider distribution in particle size. Mode-I fracture toughness of the ternary blends with CNTs initially added to the epoxy phase, showed a synergistic increase where the gain in fracture toughness was higher than the combined increases resulted from addition of the thermoplastic and nanotubes individually. A more uniform distribution of carbon nanotubes in this system made it possible for the thermoplastic microparticles to exhibit a plastic deformation during crack propagation, as evident from the micrographs of the fracture surfaces. This together with the formation of shear bands in the epoxy matrix and the pull-out of the nanotubes were identified as the most important energy dissipation mechanisms, largely contributing into the observed synergistic increase in the fracture toughness.
机译:制备了CNT改性的热塑性韧性增韧作为纤维增强复合材料潜在基质材料的环氧纳米复合材料。在制备步骤中,以两种不同的方式加入CNT以研究改变纳米复合材料的最终性质的添加顺序的后果。结果表明,CNT的存在对热塑性颗粒的相分离过程的不同方面产生了很大的影响和所得相形态的不同方面。与最初添加到环氧相的CNT中的三元共混物的纳米管显示出与最初加入到热塑性相中的其他类型的其他类型相比更好的分散体。将包含纳米管的混合物的形态和微结构的差异归因于局部粘度的增加,限制了迁移率,因此分离后热塑性相的生长。这导致形成较小的颗粒,其颗粒尺寸较宽。 Mode-I最初加入环氧相的CNT的三元共混物的裂缝韧性显示出协同增加,其中断裂韧性的增益高于添加热塑性和纳米管的增加。该系统中的碳纳米管的更均匀分布使得热塑性微粒可以在裂纹繁殖期间表现出塑性变形,从断裂表面的显微照片中显而易见。这与环氧基质中的剪切带的形成和纳米管中的剪切带一起被鉴定为最重要的能量耗散机制,很大程度上有助于观察到的裂缝韧性的协同增加。

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