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

• Published in: Reactive & functional polymers Vol. 73; no. 8; pp. 1046 - 1057
• Main Authors: Hamerton, I., Howlin, B.J., Tilbrook, D.A.
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier B.V 01.08.2013; Elsevier
• Subjects: Applied sciences; Backbone; Crystallisation; Exact sciences and technology; Halogenated; Manganese; Molecular structure; Molecular weight; Organic polymers; Physicochemistry of polymers; Polycondensation; Polycyanurates; Polymers; Preparation, kinetics, thermodynamics, mechanism and catalysts; Solubility; Thermal properties; Thermal properties; Crystallisation; Polycyanurates; Molecular weight distribution; Molecular structure; Bromine containing copolymer; Crystallization; Chlorine containing copolymer; Ether copolymer; Experimental study; Triazine derivative copolymer; Thermal stability; Ketone copolymer; Sulfide copolymer; Preparation; Aromatic copolymer; Interfacial polymerization; Property structure relationship; Activation energy; Film forming properties
• ISSN: 1381-5148
• DOI: 10.1016/j.reactfunctpolym.2013.04.012

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=2000–4000gmol−1 depending on backbone structure) although when the phase volume ratio was altered to 0.25 higher molecular weights (Mn=10,000–30,000gmol−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=35–57kJ/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 155–380kJ/mol) combined with thermal isomerisation.