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首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Preparation of poly(ether ketone)s derived from 2,5-furandicarboxylic acid via nucleophilic aromatic substitution polymerization
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Preparation of poly(ether ketone)s derived from 2,5-furandicarboxylic acid via nucleophilic aromatic substitution polymerization

机译:亲核芳族取代聚合制备2,5-呋喃二甲酸衍生的聚醚酮

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摘要

From the viewpoint of the suppression of the petroleum consumption, aromatic poly(ether ketone)s (PEKs) were prepared by the nucleophilic aromatic substitution polymerization of 2,5-bis(4-fluorobenzoyl)furan (BFBF) synthesized from biomass and aromatic bisphenols. The model reaction of BFBF and p-methoxyphenol revealed that BFBF possessed enough reactivity for the nucleophilic aromatic substitution reactions. The polymerizations of BFBF and aromatic bisphenols afforded high molecular weight polymers with good yields in N-methylpyrrolidone and diphenyl sulfone for several hours. The longer polymerization time brought about the formation of insoluble parts in any solvents and reduction of molecular weight. The obtained PEKs were thermoplastics and exhibited good thermal stability, mechanical properties, and chemical resistance comparable to common high-performance polymers. The thermal properties were tunable with the structure of bisphenols. (c) 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016, 54, 3094-3101
机译:从抑制石油消耗的观点出发,通过生物质和芳香族双酚合成的2,5-双(4-氟苯甲酰基)呋喃(BFBF)的亲核芳香取代聚合反应制得芳香族聚醚酮(PEK)。 。 BFBF与对甲氧基苯酚的模型反应表明,BFBF对亲核芳族取代反应具有足够的反应性。 BFBF和芳族双酚的聚合反应可在数小时内在N-甲基吡咯烷酮和二苯砜中提供高收率的高分子量聚合物。较长的聚合时间导致在任何溶剂中形成不溶部分并降低分子量。所获得的PEK是热塑性塑料,与常规的高性能聚合物相比,具有良好的热稳定性,机械性能和耐化学性。热性能可通过双酚的结构调节。 (c)2016 Wiley Periodicals,Inc. J. Polym。科学,A部分:Polym。化学2016,54,3094-3101

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