화학공학소재연구정보센터
Korea Polymer Journal, Vol.2, No.2, 131-139, October, 1994
Cure Behavior of Diglycidyl Ether of Bisphenol A/ Diaminodiphenylmethane in the Presence of α,ω-Methyl Carboxylate-Butadiene-Acrylonitrile Copolymer
The isothermal cure behavior of diglycidyl ether of bisphenol A (DGEBA)/diaminodiphenyl methane (DDM) in the presence of α,ω-methyl carboxylate-butadiene-acrylonitrile copolymer (est-CTBN) has been analyzed by differential scanning calorimetry and rheometry. the result shows that the cure mechanism changes from the autocatalytic cure mechanism to the nth order reaction as the concentration of est-CTBN increases. This change of mechanism seems to be caused by the decrease in the degree of participation of the hydroxyl group in situ formed as a result of the reaction between an epoxide group and a primary amine of DDM during the subsequent ring opening. the lower participation of the hydroxyl group in the ring opening may arise from the fact that the probability to form hydrogen bonds between the hydroxyl groups and carbonyl groups of est-CTBN becomes greater as the concentration of est-CTBN increases.
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