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Synthesis and crystallinity of poly(butylene 2,5-furandicarboxylate)

机译:synthesis and crystallinity of poly(butylene 2,5-furandicarboxylate)

摘要

Poly(butylene 2,5-furandicarboxylate) (PBF) was obtained by esterification of 2,5-furandicarboxylic acid (FDCA) and 1,4-butylene glycol (BG). By using H-1 NMR at 750 MHz to recognize the trace end groups at different polymerization stages, the study provides a clear picture that the polymerization proceeds cleanly to give the desirable linear structure. On the basis of the end group analysis, the degree of polymerization of PBF was determined to be as high as 125, which is in agreement with the molecular weight from the viscosity study. Solid state C-13 NMR revealed that one of the furan carbons is sensitive to local morphology. DSC and X-ray diffraction further revealed that the polymer had high tendency to form crystalline materials (T-m = 130 degrees C & 169 degrees C; T-g = 32 degrees C). On the basis of DSC and NMR evidences, the two crystalline states are assumed to be beta-phase (less stable) and alpha-phase (more stable), respectively, by analogy with the crystalline structure of PBT. High tendency of forming crystalline structure allows the continuous fibers to be drawn from the PBF's melt. The results thus raise the hope that the biomass-derived PBF could be a promising furan counterpart of the petroleum-based poly(butylene terephthalate) (PBT). (C) 2012 Elsevier Ltd. All rights reserved.
机译:通过将2,5-呋喃二甲酸(FDCA)和1,4-丁二醇(BG)酯化获得聚(2,5-呋喃二甲酸丁二酯)(PBF)。通过在750 MHz处使用H-1 NMR识别不同聚合阶段的痕量端基,该研究提供了清晰的画面:聚合反应干净进行,得到了所需的线性结构。在端基分析的基础上,确定PBF的聚合度高达125,这与粘度研究的分子量相符。固态C-13 NMR表明,呋喃碳之一对局部形态敏感。 DSC和X射线衍射进一步显示该聚合物具有形成晶体材料的高趋势(T-m = 130℃和169℃; T-g = 32℃)。根据DSC和NMR证据,类似于PBT的晶体结构,假定两个晶态分别为β相(较不稳定)和α相(较稳定)。形成晶体结构的高度趋势允许将连续纤维从PBF的熔体中拉出。因此,结果提高了希望,即源自生物质的PBF可以成为石油基聚对苯二甲酸丁二酯(PBT)的有希望的呋喃对应物。 (C)2012 Elsevier Ltd.保留所有权利。

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