Healable, recyclable and mechanically robust elastomers with multiple dynamic cross-linking bonds

The cross-linked network structure bestows rubber with excellent mechanical properties, but it greatly limits the self-healing and reprocessing ability of rubber. Herein, to address the above problem, we propose a simple cross-linking strategy with the cross-linker consisting of triple dynamic coval...

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Veröffentlicht in:Polymer (Guilford) 2022-06, Vol.252, p.124900, Article 124900
Hauptverfasser: Liu, Wei, Huang, Jiarong, Gong, Zhou, Fan, Jianfeng, Chen, Yukun
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Sprache:eng
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Zusammenfassung:The cross-linked network structure bestows rubber with excellent mechanical properties, but it greatly limits the self-healing and reprocessing ability of rubber. Herein, to address the above problem, we propose a simple cross-linking strategy with the cross-linker consisting of triple dynamic covalent bonds to vulcanize epoxidized natural rubber (ENR). A dynamic covalent network remarkably enhanced the mechanical properties of ENR through the combination of dynamic covalent bonds in the cross-linked network. At the same time, abundant dynamic covalent bonds rearranged the network topology through reversible exchange. As a result, a novel self-healing ENR with high tensile strength (2.06 ± 0.12 MPa) has been successfully developed. The ENR exhibits a high (97 ± 3%) self-healing efficiency (after 30 h at 70 °C) without applying any external force. Furthermore, it can be recycled more than three times. This work could enlighten researchers in academia and industry to develop self-healing elastomers with mechanical strength and reprocessing ability. [Display omitted] •A novel cross-linker containing triple dynamic covalent bonds was synthesized.•Triple dynamic covalent bonds is simultaneously introduced into the cross-linked network.•The covalent cross-linking driven by dynamic covalent bonds reinforce the mechanical properties of rubber.•Reversible interactions enable the self-healing ability and recyclability of rubber.
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2022.124900