The effect of epoxy excess on the kinetics of an epoxy-anhydride system

The uncatalyzed cure of a commercial tetrafunctional epoxy monomer TGDDM (N,N,N′,N′-tetraglycidyl-4,4′-diaminodiphenylmethane) with hexahydrophthalic anhydride (HHPA), using variable stoichiometric ratios is reported. The reaction was followed by differential scanning calorimetry (DSC). Two kinds of...

ver descrição completa

Detalhes bibliográficos
Autores: Mauri, Adriana Noemi, Riccardi, Carmen Cristina
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2002
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/54133
Acesso em linha:http://hdl.handle.net/11336/54133
Access Level:acceso abierto
Palavra-chave:Epoxy Excess
Anhydride
Kinetic
https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
Descrição
Resumo:The uncatalyzed cure of a commercial tetrafunctional epoxy monomer TGDDM (N,N,N′,N′-tetraglycidyl-4,4′-diaminodiphenylmethane) with hexahydrophthalic anhydride (HHPA), using variable stoichiometric ratios is reported. The reaction was followed by differential scanning calorimetry (DSC). Two kinds of experiments were performed: (1) fresh samples were run at several heating rates, and (2) samples, precured a certain time in an oil bath at constant temperature (i.e., 80 to 120°C), were run at 10°C/min. Two peaks were observed in the case of the epoxy excess but only one for the stoichiometric formulation: the peak at low temperature was attributed to the epoxy copolymerization with the anhydride while the peak at high temperature was attributed to the epoxy homopolymerization. The catalytic effect of the OH groups present in the epoxy monomer on the copolymerization reaction was demonstrated by the decrease in the activation energy of the propagation step when increasing the epoxy excess. There is a catalytic effect of the copolymerization product on the homopolymerization reaction. Our simplest model, proposed previously for a catalyzed epoxy/anhydride system [J. Polym. Sci. Part B: Polym. Phys. Ed., 37, 2799 (1999)], can be used to fit both isothermal and dynamical kinetic data.