Stanley Johan, Xanthopoulou Eleftheria, Kostoglou Margaritis, Fras Zemljič Lidija, Lambropoulou Dimitra A, Bikiaris Dimitrios N
Laboratory of Chemistry and Technology of Polymers and Colors, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki, Greece.
Laboratory of Chemical and Environmental Technology, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki, Greece.
Polymers (Basel). 2024 Nov 26;16(23):3305. doi: 10.3390/polym16233305.
In recent years, bio-based poly(ethylene furanoate) has gained the attention of packaging industries owing to its remarkable properties as a promising alternative to fossil-based polymers. It is necessary to synthesize high-molecular-weight polymers using effective and straightforward techniques for their commercialization. In this present work, poly(ethylene 2,5-furan dicarboxylate) (PEF) was produced with a high molecular weight of 0.43 dL/g using 2,5-furan dicarboxylic acid (FDCA) or its derivative Dimethyl-2,5-Furan dicarboxylate (DMFD), followed by solid-state polymerization (SSP) conducted at different temperatures and reaction times. The intrinsic viscosity ([]), carboxyl end-group concentration (-COOH), and thermal properties of the produced polyesters were evaluated using differential scanning calorimetry (DSC). The results indicated that the SSP process improved the melting temperature and crystallinity of both the PEF samples as the reaction times and temperatures increased, as corroborated by DSC and X-ray diffraction (XRD) analyses. Additionally, both intrinsic viscosity and number-average molecular weight saw an increase with longer SSP durations and higher temperatures, while the concentration of carboxyl end groups decreased, aligning with expectations. The overall results indicate that PEF (DMFD) samples exhibited a significant increase in crystallization and molecular weight, attributed to their lower degree of crystallinity and their monomer's high purity.
近年来,生物基聚(2,5-呋喃二甲酸乙二酯)因其作为化石基聚合物的一种有前途的替代品所具有的卓越性能而受到包装行业的关注。有必要采用有效且直接的技术合成高分子量聚合物以实现其商业化。在本工作中,使用2,5-呋喃二甲酸(FDCA)或其衍生物2,5-呋喃二甲酸二甲酯(DMFD)制备了特性粘度为0.43 dL/g的高分子量聚(2,5-呋喃二甲酸乙二酯)(PEF),随后在不同温度和反应时间下进行固态聚合(SSP)。使用差示扫描量热法(DSC)对所制备聚酯的特性粘度([η])、羧基端基浓度(-COOH)和热性能进行了评估。结果表明,如DSC和X射线衍射(XRD)分析所证实的,随着反应时间和温度的增加,SSP过程提高了两个PEF样品的熔点和结晶度。此外,随着SSP持续时间延长和温度升高,特性粘度和数均分子量均增加,而羧基端基浓度降低,符合预期。总体结果表明,PEF(DMFD)样品的结晶度和分子量显著增加,这归因于其较低的结晶度和单体的高纯度。