Thermal Decomposition of Cyanate Ester Resins

Abstract

Polycyanurate networks were prepared by thermal polymerization of cyanate ester monomers containing two or more cyanate ester (-O-C<triple bond>N) functional groups. The thermal decomposition chemistry of nine different polycyanurates was studied by thermogravimetry and infrared analysis of solid films and analysis of the gases evolved during pyrolysis using infrared spectroscopy and gas chromatography-mass spectrometry. It was found that the thermal stability of the polycyanurates was essentially independent of monomer chemical structure with the major mass loss occurring at about 450 deg C for all materials. Analysis of the solid-state and gas phase thermal degradation chemistry indicates a thermal decomposition mechanism for polycyanurates which begins with hydrocarbon chain scission and cross-linking at temperatures between 400 deg - 450 deg C with negligible mass loss, followed by decyclization of the triazine ring at 450 deg C that liberates volatile cyanate-ester decomposition products. The solid residue after pyrolysis increases with the aromatic content of the polymer and incorporates about two thirds of the nitrogen and oxygen present in the original material.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2001
Accession Number
ADA397376

Entities

Organizations

  • United States Department of Transportation

Tags

Communities of Interest

  • Advanced Electronics

DTIC Thesaurus Topics

  • Chemical Synthesis
  • Chemistry
  • Combustion
  • Fire Resistance
  • Fires
  • Gas Chromatography
  • Glass Transition Temperature
  • Infrared Spectra
  • Infrared Spectroscopy
  • Mass Spectra
  • Mass Spectrometers
  • Mass Spectrometry
  • Materials Science
  • Spectra
  • Spectrometry
  • Spectroscopy
  • Transition Temperature

Fields of Study

  • Materials science

Readers

  • Electrochemical Engineering/ Fuel Cell Technologies
  • Organic Chemistry
  • Polymer Science and Engineering.