This work focuses on a simple approach for designing polyurethane elastomers with ultra-robust properties. Initially, polyurethane/lignin elastomers were synthesized using polytetramethylene ether glycol (PTMG) as a soft segment, hexamethylene diisocyanate (HDI) with 4,4′-dihydroxydiphenyl ether (DO) as hard segments, and lignin nanoparticles (LNP) as a biomacromolecular crosslinker. Subsequently, the resulting elastomers were pre-stretched at certain ratios (λ), and surprisingly, the pre-stretched polyurethane/lignin elastomer (at the ratio of λ = 14) displayed significant improvement in mechanical properties, while the tensile strength and toughness values were sharply enhanced from 32.4 MPa and 298.7 MJ m−3 to 116.2 MPa and 501.3 MJ m−3, respectively. This improvement can be attributed to the obtainment of dense cross-linked networks due to the combined effect of pre-stretching on both multiscale structural orientation and stress-induced crystallization (SIC). The interphase distance (dp) decreased from 15.708 to 14.612 nm, the interplanar crystal distance (dc) increased from 4.387 Å to 4.398 Å, and the Herman orientation factor (f) increased from −0.0066 to 0.0518. This work presents a novel strategy for preparing polyurethane elastomers with exceptional mechanical performance.

Ultra-robust polyurethane/lignin elastomers based on multiscale structural orientation induced by pre-stretching

Zhang, Yu;Puglia, Debora;
2025

Abstract

This work focuses on a simple approach for designing polyurethane elastomers with ultra-robust properties. Initially, polyurethane/lignin elastomers were synthesized using polytetramethylene ether glycol (PTMG) as a soft segment, hexamethylene diisocyanate (HDI) with 4,4′-dihydroxydiphenyl ether (DO) as hard segments, and lignin nanoparticles (LNP) as a biomacromolecular crosslinker. Subsequently, the resulting elastomers were pre-stretched at certain ratios (λ), and surprisingly, the pre-stretched polyurethane/lignin elastomer (at the ratio of λ = 14) displayed significant improvement in mechanical properties, while the tensile strength and toughness values were sharply enhanced from 32.4 MPa and 298.7 MJ m−3 to 116.2 MPa and 501.3 MJ m−3, respectively. This improvement can be attributed to the obtainment of dense cross-linked networks due to the combined effect of pre-stretching on both multiscale structural orientation and stress-induced crystallization (SIC). The interphase distance (dp) decreased from 15.708 to 14.612 nm, the interplanar crystal distance (dc) increased from 4.387 Å to 4.398 Å, and the Herman orientation factor (f) increased from −0.0066 to 0.0518. This work presents a novel strategy for preparing polyurethane elastomers with exceptional mechanical performance.
2025
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1609820
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