Influence of material properties on the damage-reporting and self-healing performance of a mechanically active dynamic network polymer in coating applications

  • Da Hae Son
  • , Gi Young Kim
  • , Ji Eun Jeong
  • , Sang Ho Lee
  • , Young Il Park
  • , Hoyoul Kong
  • , In Woo Cheong
  • , Jin Chul Kim

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

We conducted a detailed investigation of the influence of the material properties of dynamic polymer network coatings on their self-healing and damage-reporting performance. A series of reversible polyacrylate urethane networks containing the damage-reporting diarylbibenzofuranone unit were synthesized, and their material properties (e.g., indentation modulus, hardness modulus, and glass-transition temperature) were measured conducting nanoindentation and differential scanning calorimetry experiments. The damage-reporting and self-healing performances of the dynamic polymer network coatings exhibited opposite tendencies with respect to the material properties of the polymer network coatings. Soft polymer network coatings with low glass-transition temperature (~10C) and indentation hardness (20 MPa) exhibited better self-healing performance (almost 100%) but two times worse damage-reporting properties than hard polymer network coatings with high glass-transition temperature (35~50C) and indentation hardness (150~200 MPa). These features of the dynamic polymer network coatings are unique; they are not observed in elastomers, films, and hydrogels, whereby the polymer networks are bound to the substrate surface. Evidence indicates that controlling the polymer’s physical properties is a key factor in designing high-performance self-healing and damage-reporting polymer coatings based on mechanophores.

Original languageEnglish
Article number2468
JournalMolecules
Volume26
Issue number9
DOIs
StatePublished - 2021

Keywords

  • Dynamic polymer network
  • Mechanophore
  • Polymer coating
  • Self-healing coating
  • Self-reporting polymer

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