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Updated: Jan 3, 2026

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
Published on: November 30, 2020
Bio-based thermoplastic poly(butylene succinate-co-propylene succinate) copolyesters: effect of glycerol on thermal
Kai-Hung Hsu1, Chin-Wen Chen, Li-Yuan Wang
1Institute of Organic and Polymeric Materials, Research and Development Center of Smart Textile Technology, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao East Road, Taipei, 10608, Taiwan, Republic of China. kuocc@mail.ntut.edu.tw cwchen@ntut.edu.tw.
Abstract:
Poly(butylene succinate-co-propylene succinate) (PBSPS) was polymerized using succinic acid, 1,4-butanediol, 1,3-propanediol, and glycerol (GC). The PBSPS copolyester with a BS/PS ratio of 7/3 has a low melting point (Tm, 80 °C) and crystallization temperature (Tc, 20 °C) in addition to excellent thermal stability with a thermal degradation temperature (Td) above 300 °C. Isodimorphism was observed for 30-50 mol% PS, lowering Tm and Tc. The featured crystalline lattices (021) and (110) of PBS at 2θ = 21.5° and 22.5° gradually disappeared with PS content greater than 50 mol% and transformed into a PPS crystalline lattice at 2θ = 22.3°. Young's modulus decreased with increasing PS content due to crystallinity loss. Wide-angle X-ray diffraction demonstrated that the chain movement regularity was affected by the GC content, reducing the crystallinity. The PBSPS copolyesters were elastic with 0.001 mol% GC but became rigid with GC content greater than 0.01 mol%. The chain conformation was flexible for 0.001-0.01 mol% GC and exhibited an irregular steric architecture for 0.02-0.03 mol% GC due to more GC acting as nodes. Thus, the thermal and mechanical properties of the synthesized bio-based PBSPS copolyesters can be controlled by adjusting the GC content; therefore, such copolyesters are suitable for medical support, coating, and phase-change material applications.
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