Examining structure property relationships in coatings based on substituted linear aromatic polycyanurates

I. Hamerton*, B. J. Howlin, D. A. Tilbrook

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

3 Citations (Scopus)


Three series of halogenated and non-halogenated polycyanurates are prepared in good yield and purity, and fully characterised. Many of the resulting polymers, formed at room temperature using phase transfer catalysis, can be cast into films with good resilience and high thermal stability (some examples suffer no mass loss when held isothermally at 190°C and only display appreciable losses when held continuously at 300°C). Char yields of 35-65% are achieved in nitrogen depending on backbone structure. Some problems were encountered with solubility, particularly with heavily halogenated dichlorotriazines, which limited molecular weights (Mn = 2000-4000 g mol-1 depending on backbone structure) although when the phase volume ratio was altered to 0.25 higher molecular weights (Mn = 10,000-30,000 g mol-1) were possible. Best solubility was achieved by using aromatic diols with at least two equivalent phenylene units per dichlorotriazine unit. DSC reveals polymerisation exotherms with maxima at 190-260°C (ΔHp = 35-57 kJ/mol) followed by embrittlement and shrinkage (when heated to 300°C). These phenomena may be due to the formation of poorly formed crystallites (activation energies span 155-380 kJ/mol) combined with thermal isomerisation.

Original languageEnglish
Pages (from-to)1046-1057
Number of pages12
JournalReactive and Functional Polymers
Issue number8
Publication statusPublished - 2013


  • Crystallisation
  • Polycyanurates
  • Thermal properties


Dive into the research topics of 'Examining structure property relationships in coatings based on substituted linear aromatic polycyanurates'. Together they form a unique fingerprint.

Cite this