Synthesis of polyamide 6 with aramid units by combination of anionic ring-opening and condensation reactions

Camille Bakkali-Hassani, Mikaël Planes, Kevin Roos, Anne Laure Wirotius, Emmanuel Ibarboure, Stephane Carlotti

Research output: Contribution to journalArticleResearchpeer-review

5 Citations (Scopus)

Abstract

Polyamides with different percentages of aromatic/aliphatic units and molar masses were synthesized in a one-step bulk copolymerization of ε-caprolactam and ethyl 4-aminobenzoate at 140 °C keeping the same experimental conditions basically used for the synthesis of polyamides by anionic ring opening polymerization (AROP). Copolyamides were characterized by NMR spectroscopy, size exclusion chromatography and thermo-mechanical analysis (DSC, TGA and DMA). This methodology, combining simultaneous anionic ring-opening and condensation reactions, affords a new route to introduce aromatic amides into an aliphatic polyamide backbone and tune its properties. Modified polyamides 6 (PA6) obtained from ε-caprolactam by an activated monomer mechanism and containing up to 17% mol of aromatic moiety were prepared. The new materials exhibited in particular high thermal stability and high glass transition temperature up to 79 °C.

Original languageEnglish
Pages (from-to)231-237
Number of pages7
JournalEuropean Polymer Journal
Volume102
DOIs
Publication statusPublished - 1 May 2018
Externally publishedYes

Keywords

  • Activated Monomer mechanism
  • Aliphatic-aromatic polyamides
  • Anionic polymerization
  • Condensation
  • Ring-opening

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