JOURNAL ARTICLE

Diels–Alder‐based crosslinked self‐healing polyurethane/urea from polymeric methylene diphenyl diisocyanate

Abstract

ABSTRACT Crosslinked self‐healing polyurethane/urea based on a Diels–Alder reaction (C‐PMPU–DA) was synthesized from a multiple‐furan monomer and a commercial bismaleimide. The multiple‐furan monomer (PMPU–furan) was obtained from a functionalized prepolymer (polymeric MDI: PBA‐2000 = 2:1) by furfuryl amine. The structures of both the PMPU–furan and C‐PMPU–DA were characterized by attenuated total reflectance (ATR)–Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and 1 H‐NMR. The Diels–Alder bonds enabled C‐PMPU–DA thermal reversibility, which was investigated by ATR–FTIR spectroscopy, 1 H‐NMR, gel–solution–gel experiments, and viscosity tests. Meanwhile, the self‐healing properties of C‐PMPU–DA were also investigated by the recovery of the mechanical properties. The results showed that C‐PMPU–DA exhibited good thermal reversibility and self‐healing properties. C‐PMPU–DA exhibited thermosetting properties at room temperature, although it exhibited thermoplastic properties at higher temperatures and may find applications in self‐healing materials, recyclable materials, or removable materials. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40234.

Keywords:
Polyurethane Thermogravimetric analysis Materials science Polymer chemistry Monomer Fourier transform infrared spectroscopy Differential scanning calorimetry Furan Melamine Prepolymer Condensation polymer Organic chemistry Chemical engineering Chemistry Composite material Polymer

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Citation History

Topics

Polymer composites and self-healing
Physical Sciences →  Materials Science →  Polymers and Plastics
Carbon dioxide utilization in catalysis
Physical Sciences →  Chemical Engineering →  Process Chemistry and Technology
Synthesis and properties of polymers
Physical Sciences →  Materials Science →  Polymers and Plastics
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