Premium
Curing kinetics and thermomechanical behaviour of co‐anhydride cured aminoglycidyl epoxy resins
Author(s) -
Rocks Jens,
George Graeme A,
Vohwinkel Friedrich
Publication year - 2003
Publication title -
polymer international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 105
eISSN - 1097-0126
pISSN - 0959-8103
DOI - 10.1002/pi.1286
Subject(s) - curing (chemistry) , epoxy , maleic anhydride , materials science , glass transition , pyromellitic dianhydride , polymer chemistry , activation energy , catalysis , tertiary amine , kinetics , composite material , chemistry , organic chemistry , copolymer , polyimide , polymer , physics , quantum mechanics , layer (electronics)
Abstract The curing behaviour and thermomechanical properties of a technical grade of N , N , N ′, N ′‐tetraglycidyl‐4,4′‐diaminodiphenylmethane (TGDDM, Araldite ® MY721), cured in the presence of an anhydride hardener mixture consisting of maleic anhydride (MA) and pyromellitic acid dianhydride (PMDA) was studied by calorimetric and dynamic mechanical analysis. The cure kinetics and the influence of varying stoichiometric anhydride‐to‐epoxy ratios were evaluated and the apparent activation energy was calculated according to Barrett's method. High extents of conversion from DSC studies of the MY721‐resin were reached after room temperature cure, without an added catalyst, for 24 h, followed by a post‐curing step of 1 h at 90 °C. The ultimate glass transition temperatures for the molar anhydride/epoxy ratio, r = 0.8, were close to the decomposition temperature, and indications were obtained that the network structure consists of two independent sub‐networks. It is suggested that two separate mechanisms contribute to the curing reaction at room temperature. First, the tertiary amine structure, intrinsic to aminoglycidyl resins, may act as an internal catalyst for the anhydride ring opening, and secondly, the unsaturated bond of MA participates in the curing reaction by nucleophilic attack, such as from tertiary amines or carboxylate or alkoxide anions. From a study of a range of different aminoglycidyl resins, this low‐temperature curing behaviour is found to be a general phenomenon. Copyright © 2003 Society of Chemical Industry