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Enzymatic synthesis of 2,5-furandicarboxylic acid-based semi-aromatic polyamides: enzymatic polymerization kinetics, effect of diamine chain length and thermal properties

机译:酶合成2,5-呋喃羧酸的半芳族聚酰胺:酶聚合动力学,二胺链长度和热性能的作用

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2,5-Furandicarboxylic acid (FDCA)-based semi-aromatic polyamides are novel biobased alternatives to petrol-based semi-aromatic polyamides (polyphthalamides), that have a broad commercial interest as engineering thermoplastics and high performance materials. In this study, a series of FDCA-based semi-aromatic polyamides is successfully produced via Novozym?435 (N435, an immobilized form of Candida antarctica lipase b (CALB))-catalyzed polycondensation of (potentially) biobased dimethyl 2,5-furandicarboxylate and aliphatic diamines differing in chain length (C4–C12), using a one-stage method at 90 °C in toluene. The obtained polyamides reach high weight-average molecular weights ranging from 15?800 to 48?300 g mol ~(?1) ; and N435 shows the highest selectivity towards 1,8-octanediame (C8). MALDI-ToF MS analysis indicates that no byproducts are formed during the enzymatic polymerization. Study of the kinetics of the enzymatic polymerization suggests that phase separation of FDCA-based oligoamides/polyamides takes place in the early stage of polymerization, and the isolated products undergo an enzyme-catalyzed solid-state polymerization. However, the isolation yields of the purified products from the enzymatic polymerizations are less than ~50% due to the production of a large amount of low molecular weight products that are washed away during the purification steps. Furthermore, the thermal properties of the enzymatic FDCA-based semi-aromatic polyamides are carefully investigated, and compared to those of the FDCA-based and petrol-based counterparts produced via conventional synthesis techniques as reported in literature.
机译:基于汽油基半芳族聚酰胺(聚邻苯二甲酰胺)的新型生物化替代品是具有广泛的商业兴趣作为工程热塑性塑料和高性能材料的新型生物化替代品。在本研究中,通过Novozymα435(N435,念珠菌抗野胶脂肪酶B(CALB)的固定化形式的基于FDCA的半芳族聚酰胺。(潜在的)生物化二甲基2,5-呋喃二甲酸酯的致氢缩聚在连锁长度(C4-C12)中不同的脂族二胺在甲苯中使用一阶段方法。得到的聚酰胺达到高重量平均分子量,范围为15〜800至48〜48〜(α1); N435显示了对1,8-Octanediame(C8)的最高选择性。 MALDI-TOF MS分析表明在酶聚合过程中没有形成副产物。研究酶聚合动力学表明,在聚合的早期阶段进行FDCA的寡酰胺/聚酰胺的相分离,并且分离的产物经历酶催化的固态聚合。然而,由于在纯化步骤期间洗去的大量低分子量产物,纯化产物的分离产率小于〜50%。此外,仔细研究了酶促FDCA的半芳族聚酰胺的热性质,并与通过在文献中报道的常规合成技术产生的FDCA基和基于汽油的对应物的热性能。

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