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Morphology and mechanical properties of fibers from blends of a liquid crystalline polymer and poly(ethylene terephthalate)

机译:液晶聚合物和聚对苯二甲酸乙二醇酯共混物纤维的形态和机械性能

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AbstractThe domain morphology and mechanical properties of fibers spun from blends of a thermotropic liquid crystalline polymer, Vectra A‐900, and poly(ethylene terephthalate) (PET) have been studied across the entire composition range. The PET phase was removed by etching to reveal fibrillar LCP domains in the blends of all compositions. The 0.5μm fibril appeared to be the basic structural entity of the LCP domains. A primary effect of composition was the change from discontinuous fibrils when the composition was 35 and 60 by weight LCP to continuous fibrils when the composition was 85 and 96 LCP. This transition had major ramifications on the mechanical properties: the modulus increased abruptly between 60 and 85 LCP, and a change in the fracture mode from brittle fracture to a splitting mode was accompanied by an increase in fracture strength. Different models were required to describe the mechanical properties of the discontinuous and continuous fibril morphologies. Analytic models for short aligned fibers of Nielsen, and Kelly and Tyson were applicable when the LCP fibrils were discontinuous, while modulus and strength of blend fibers with continuous LCP fibrils were discribed by the rule of mixtur
机译:摘要研究了由热致液晶聚合物Vectra A-900和聚对苯二甲酸乙二醇酯(PET)共混纺制纤维的畴形貌和力学性能。通过蚀刻去除PET相,以显示所有组合物混合物中的纤维状LCP结构域。0.5μm原纤维似乎是LCP结构域的基本结构实体。组合物的主要作用是从组合物为35%和60%重量LCP时的不连续原纤维变为组合物为85%和96%LCP时的连续原纤维。这种转变对力学性能产生了重大影响:在60%至85%LCP之间模量突然增加,断裂模式从脆性断裂模式转变为分裂模式,同时断裂强度增加。需要不同的模型来描述不连续和连续原纤维形态的力学特性。当LCP原纤维不连续时,Nielsen、Kelly和Tyson的短取向纤维的分析模型适用,而具有连续LCP原纤维的混合纤维的模量和强度则由混合法则描述

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