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Chain Structure and Molecular Weight Dependent Mechanics of Poly(ethylene 2,5-furandicarboxylate) Compared to Poly(ethylene terephthalate)

机译:与聚(乙二醇酯)相比,聚(乙烯2,5-呋喃二羧酸甲酯)的链结构和分子量依赖力学

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摘要

Solution and melt viscosity relations to molecular weight were obtained for bio-based poly(ethylene 2,5-furandicarboxylate) (PEF) in comparison to poly(ethylene terephthalate) (PET). Furthermore, the rate dependent glassy state tensile properties were explored at varying molecular weights, showing ductile behavior for high molecular weight PEF at low rates. The unperturbed chain dimensions of PEF indicate similar conformational freedom to PET but lower chain packing due to the shorter bond length of 2,5-furandicarboxylic acid (FDCA), inducing a lower entanglement density as corroborated by plateau moduli measurements. The high temperature and shear rate dependence of the melt viscosity as well as the high strain rate dependence of the glassy state yield stress can be explained by this lower entanglement density, although the glassy state may furthermore be subject to chain mobility restrictions.
机译:与聚(乙二醇酯)(PET)相比,获得对生物基聚(乙烯2,5-呋喃二羧酸甲酯)(PEF)的分子量的溶液和熔体粘度关系。 此外,在不同的分子量下探讨速率依赖性玻璃状拉伸性质,显示出低速率的高分子量PEF的延性行为。 由于2,5-呋喃二羧酸(FDCA)的较短键合长度,PEF的不受干扰的PEF的链尺寸表明宠物但低链填充的较低链填充。通过高原模量测量诱导较低的缠结密度,诱导较低的缠结密度。 熔体粘度的高温和剪切速率以及玻璃状屈服应力的高应变率依赖性可以通过这种较低的缠结密度来解释,尽管玻璃状状态也可能受到链迁移率限制。

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