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Updated: Jun 30, 2025

Molecular Entanglement and Electrospinnability of Biopolymers
Published on: September 3, 2014
Design strategy for blends of biodegradable polyester and thermoplastic starch based on a molecular dynamics study of
Akihiro Yamaguchi1, Satoshi Arai2, Noriyoshi Arai3
1Circular Industries Research Department, Production Engineering and MONOZUKURI Innovation Center, Research and Development Group, Hitachi, Ltd., 2-9-2, Yoshida, Totsuka, Yokohama, Kanagawa 244-0817, Japan; Department of Mechanical Engineering, Keio University, 3-14-1, Hiyoshi, Kohoku, Yokohama, Kanagawa 223-8522, Japan.
Abstract:
Molecular insight into the phase-separated interface formed when biodegradable polyesters and thermoplastic starch (TPS) are melt-blended is valuable for the design of composites. In this study, eight different interfaces combining four major biodegradable polyesters (PLA, PBS, PHB and PBAT) and two TPSs [unmodified TPS (nTPS) and citrate-modified TPS (cTPS)] were investigated by using molecular dynamics (MD) simulations. According to the MD simulation results, PBS, PHB and PBAT diffuse readily into the TPS and form compatible interfaces, whereas PLA is less compatible with the TPS. The results of tensile simulations show that PBS and PBAT adhere well to TPS; in particular, PBS/cTPS and PBAT/cTPS exhibit high interfacial-fracture energy (G). Both PLA and PHB blended with TPS exhibit low G because PLA is less compatible with TPS and PHB and TPS have low electrostatic interaction. The reason for the high G of PBS/cTPS and PBAT/cTPS is thought to be a combination of three factors: (i) formation of a deep compatible interface, (ii) suppression of void growth by electrostatic interactions and (iii) absorption of strain energy by a change in the conformation of the molecular chains. These three interfacial adhesion mechanisms should be considered when designing biodegradable polyester/TPS blends with good mechanical properties.
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