Phase Separation-Driven Concurrent High Elasticity and Reextrudability for Biobased Elastomers

The recycling challenges of thermosetting polymers and the environmental burden from petroleum-based polymers drive the rapid development of recyclable biobased elastomers. However, cross-linked biobased elastomers face an inherent trade-off between high elasticity and high-throughput recycling: robust elastic recovery requires sufficiently cross-linked topologies, whereas efficient reprocessing favors low cross-linking densities. Herein, we address this dilemma by integrating phase separation modulation with dynamic covalent cross-linking to synthesize biobased thermoplastic elastomers via one-step in situ cross-linking. Using maleic anhydride-grafted ethylene-vinyl acetate copolymer (M-<i>g</i>-EVA) as the compatibilizer, biobased monomers, epoxidized soybean oil (ESO), and dimer acid (DFA) were in situ polymerized within the ethylene-propylene-diene rubber (EPDM) matrix to form a vitrimer dispersed phase. During thermal mechanical mixing, M-<i>g</i>-EVA was first selectively predispersed in the EPDM matrix. Subsequent in situ polymerization drives the cross-linked ESO/DFA aggregates to localize within the M-<i>g</i>-EVA phase, creating a distinct third phase. Meanwhile, M-<i>g</i>-EVA forms interfacial cross-linking with ESO and physically entangles with EPDM chains, thus constructing a stable multiphase network composed of a "continuous - interfacial - dispersed phase". The resulting material demonstrates enhanced elastic performance, featuring excellent room-temperature creep resistance (0.00184%/min), improved low-temperature compression set resistance (14% reduction at -25 °C relative to a traditional commercial TPV with similar hardness), and outstanding cyclic fatigue stability (stress retention rate >97% following 300 loading-unloading cycles). Owing to β-hydroxyester bond exchange and lubricating effect of EPDM, the multiphase polymer can be continuously extruded and reprocessed with high flux, retaining >85% of its mechanical property after 5 reprocessing cycles. In short, this study provides a scalable route to high-performance and recyclable biobased elastomers and offers design insights for sustainable elastomers.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2026-02-06
DOI
https://doi.org/10.1021/acsami.5c25884
Primary Topic
Polymer composites and self-healing
Type
article
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article

Phase Separation-Driven Concurrent High Elasticity and Reextrudability for Biobased Elastomers

Binjie Jin, Guangzhi Jin, Shuangjian Yu, Liang Zhang et al.
ACS Applied Materials & Interfaces
Polymer composites and self-healing
article

Phase Separation-Driven Concurrent High Elasticity and Reextrudability for Biobased Elastomers

Binjie Jin, Guangzhi Jin, Shuangjian Yu, Liang Zhang, Yanfang Li, Siwu Wu, Baochun Guo, Zhenghai Tang, Huawei Qiao
article en

Abstract

The recycling challenges of thermosetting polymers and the environmental burden from petroleum-based polymers drive the rapid development of recyclable biobased elastomers. However, cross-linked biobased elastomers face an inherent trade-off between high elasticity and high-throughput recycling: robust elastic recovery requires sufficiently cross-linked topologies, whereas efficient reprocessing favors low cross-linking densities. Herein, we address this dilemma by integrating phase separation modulation with dynamic covalent cross-linking to synthesize biobased thermoplastic elastomers via one-step in situ cross-linking. Using maleic anhydride-grafted ethylene-vinyl acetate copolymer (M-<i>g</i>-EVA) as the compatibilizer, biobased monomers, epoxidized soybean oil (ESO), and dimer acid (DFA) were in situ polymerized within the ethylene-propylene-diene rubber (EPDM) matrix to form a vitrimer dispersed phase. During thermal mechanical mixing, M-<i>g</i>-EVA was first selectively predispersed in the EPDM matrix. Subsequent in situ polymerization drives the cross-linked ESO/DFA aggregates to localize within the M-<i>g</i>-EVA phase, creating a distinct third phase. Meanwhile, M-<i>g</i>-EVA forms interfacial cross-linking with ESO and physically entangles with EPDM chains, thus constructing a stable multiphase network composed of a "continuous - interfacial - dispersed phase". The resulting material demonstrates enhanced elastic performance, featuring excellent room-temperature creep resistance (0.00184%/min), improved low-temperature compression set resistance (14% reduction at -25 °C relative to a traditional commercial TPV with similar hardness), and outstanding cyclic fatigue stability (stress retention rate >97% following 300 loading-unloading cycles). Owing to β-hydroxyester bond exchange and lubricating effect of EPDM, the multiphase polymer can be continuously extruded and reprocessed with high flux, retaining >85% of its mechanical property after 5 reprocessing cycles. In short, this study provides a scalable route to high-performance and recyclable biobased elastomers and offers design insights for sustainable elastomers.

ACS Applied Materials & InterfacesVol. 18(6)
Division of Materials Science and Engineering (AU), Xi'an Jiaotong University (CN), South China University of Technology (CN)
Responsible consumption and production
Openalex Percentile: Top 66%
Polymer composites and self-healing
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