4.7 Article

Thermally Reversible Cross-Linking of Recyclable Polyamide Materials Based on Schiff Base and Diels-Alder Reactions

Journal

MACROMOLECULAR RAPID COMMUNICATIONS
Volume -, Issue -, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202300252

Keywords

Diels-Alder reaction; polyamide materials; recyclability; reprocessability; Schiff base

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A facile method for producing recyclable polyamide materials is developed by constructing linear polymer chains through a Schiff base reaction and crosslinking them with bismaleimide. The resulting polyamide material, GF-BMs, exhibits high tensile strength and good solvent resistance. The presence of thermally reversible Diels-Alder covalent bonds and dynamic imine bonds in the polymer network enables fast reprocessing, self-healing, and recyclability, offering a new idea for recyclable materials.
Recyclability of cross-link polymer materials is essential to alleviate environmental pollution caused by discarded or damaged polymers. Herein, a facile method for producing recyclable polyamide materials is developed. Linear polymer chains are constructed by Schiff base reaction between glutaraldehyde (GD) and furandiamine (FD). The linear polymer chains are crosslinked by bismaleimide (BM) to give rise to polyamide material, named GF-BMs. The resulting GF-BMs polyamide material possesses strong tensile strength (78 MPa) and good solvent resistance from room temperature to 135 & DEG;C. Especially, the thermally reversible Diels-Alder covalent bonds and dynamic imine bonds in the polymer network have a synergistic effect on fast-reprocessing, self-healing, and recyclability, which provides a new idea for recyclable materials.

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