Curia Silvio, Biundo Antonino, Fischer Isabel, Braunschmid Verena, Gübitz Georg M, Stanzione Joseph F
Department of Chemical Engineering, Rowan University, 201 Mullica Hill Road, Glassboro, NJ, 08028, USA.
Austrian Centre of Industrial Biotechnology (ACIB), Konrad Lorenz Straße 20, 3430, Tulln an der Donau, Austria.
ChemSusChem. 2018 Aug 9;11(15):2529-2539. doi: 10.1002/cssc.201801059. Epub 2018 Jul 20.
The utilization of wood-derived building blocks (xylochemicals) to replace fossil-based precursors is an attractive research subject of modern polymer science. Here, we demonstrate that bisguaiacol (BG), a lignin-derived bisphenol analogue, can be used to prepare biobased polyesters with remarkable thermal properties. BG was treated with different activated diacids to investigate the effect of co-monomer structures on the physical properties of the products. Namely, derivatives of adipic acid, succinic acid, and 2,5-furandicarboxylic acid were used. Moreover, a terephthalic acid derivative was used for comparison purposes. The products were characterized by H NMR spectroscopy, attenuated total reflectance FTIR spectroscopy, gel-permeation chromatography, thermogravimetric analysis, and differential scanning calorimetry to assess their structural and thermal properties in detail. The polymers showed glass-transition temperatures ranging up to 160 °C and thermal stabilities in excess of 300 °C. Furthermore, the susceptibility of the polyester to enzymatic hydrolysis was investigated to assess the potential for further surface functionalization and/or recycling and biodegradation. Indeed, hydrolysis with two different enzymes from the bacteria Thermobifida cellulosilytica led to the release of monomers, as quantified by HPLC. The results of this study indicate that our new polyesters represent promising renewable and biodegradable alternatives to petroleum-based polyesters currently employed in the plastics industry, specifically for applications in which high-temperature stability is essential to ensure overall system integrity.
利用源自木材的建筑模块(木化学产品)来替代基于化石的前体是现代聚合物科学中一个具有吸引力的研究课题。在此,我们证明了双愈创木酚(BG),一种源自木质素的双酚类似物,可用于制备具有卓越热性能的生物基聚酯。用不同的活性二酸处理BG,以研究共聚单体结构对产品物理性能的影响。具体而言,使用了己二酸、琥珀酸和2,5-呋喃二甲酸的衍生物。此外,还使用了对苯二甲酸衍生物用于对比目的。通过核磁共振氢谱、衰减全反射傅里叶变换红外光谱、凝胶渗透色谱、热重分析和差示扫描量热法对产品进行表征,以详细评估其结构和热性能。这些聚合物的玻璃化转变温度高达160℃且热稳定性超过300℃。此外,研究了聚酯对酶促水解的敏感性,以评估进一步进行表面功能化和/或回收及生物降解的潜力。实际上,用来自嗜热栖热放线菌的两种不同酶进行水解导致单体释放,通过高效液相色谱法定量。本研究结果表明,我们的新型聚酯是目前塑料工业中使用的石油基聚酯有前景的可再生和可生物降解替代品,特别是对于高温稳定性对确保整个系统完整性至关重要的应用。