New hyperbranched polyester modified DGEBA thermosets with improved chemical reworkability

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • David Foix - , Universidad Rovira i Virgili (Author)
  • Michael Erber - , Leibniz Institute of Polymer Research Dresden (Author)
  • Brigitte Voit - , Leibniz Institute of Polymer Research Dresden (Author)
  • Albena Lederer - , Leibniz Institute of Polymer Research Dresden (Author)
  • Xavier Ramis - , UPC Polytechnic University of Catalonia (Barcelona Tech) (Author)
  • Ana Mantecon - , Universidad Rovira i Virgili (Author)
  • Angels Serra - , Universidad Rovira i Virgili (Author)

Abstract

The chemical reworkability of epoxy thermosets in alkaline solutions has been increased by adding a hyperbranched polyester (HBPE) as a reactive modifier to the diglycidyl ether of bisphenol A (DGEBA) cured by lanthanide triflates as cationic initiators. The presence of hydroxyl chain-ends in the HBPE allows the modifier to be linked covalently to the epoxy matrix through the monomer activated propagation mechanism, which occurs in cationic polymerizations. Yb(OTf)(3) leads to quicker curing than the lanthanum salt and to materials with the highest glass transition temperature (T-g). The addition of HBPE does not affect adversely the thermal stability and leads to a slight reduction of the global shrinkage. The T-g of the materials, the relaxed modulus and the linear thermal expansion coefficients are practically maintained by the addition of HBPE. (C) 2010 Elsevier Ltd. All rights reserved.

Details

Original languageEnglish
Pages (from-to)445-452
Number of pages8
JournalPolymer degradation and stability
Volume95
Issue number4
Publication statusPublished - Apr 2010
Peer-reviewedYes
Externally publishedYes

External IDs

Scopus 77349100141
ORCID /0000-0002-4531-691X/work/148607810

Keywords

Keywords

  • Cationic polymerization, Epoxy resins, Hyperbranched polymers, Reworkability, Shrinkage