Bio-based poly(decylene terephthalate-co-decylene furandicarboxylate)s derived from 2,5-furandicarboxylic acid (FDCA): Synthesis and properties

Currently, a growing focus is devoted to the creation and utilization of renewable resources for bio-based polyesters due to the shortage of oil resources. Since 2,5-furandicarboxylic acid (FDCA) has been described as one of the most promising platform compounds, FDCA-based polyesters have been rapidly developed. Poly(decylene terephthalate-co-decylene furandicarboxylate) (PDTFs) in this study were prepared from dimethyl terephthalate (DMT), 1,10-decanediol (DDO) and dimethyl 2,5-furandicarboxylate (DMFD). By using 1H NMR and 13C NMR, the polyesters' chemical structure was verified. The thermal properties and the thermal stability of the polyesters were analyzed by Differential Scanning Calorimetry (DSC) and Thermogravimetric analysis (TGA). All polyesters underwent mechanical testing to ascertain their Young's modulus, tensile strength, and elongation at break. All polymers are semi-crystalline materials. The crystal texture of PDTF24 is equivalent to that of poly(decylene terephthalate) (PDT). However, the crystal structures of PDTF48 and PDTF76 are similar to that of poly(decylene furandicarboxylate) (PDF). All polymers exhibit high thermal stability. PDF has the highest tensile strength, probably because the oxygen atom on the furan ring results in stronger intermolecular interactions. When the content of the decylene furandicarboxylate unit reaches 48%, Young's modulus reaches its lowest value (96.6 MPa), but its elongation at break reaches its highest value (1098%) due to the lowest crystallinity. © 2022 Elsevier B.V.