Curing of epoxy-urethane copolymers in a heated mold: Effect of the curing conditions on the phase-separation process

The curing process of an epoxy-urethane copolymer in a heated mold was studied. The epoxy resin (DGEBA, Araldyt GY9527; Ciba Geigy), was coreacted with a urethane prepolymer (PU, Desmocap 12; Bayer) through an amine that acted as crosslinking agent (mixture of cycloaliphatic amines; Distraltec). The...

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Bibliographic Details
Authors: Stefani, Pablo Marcelo, Moschiar, Stella Maris, Aranguren, Mirta Ines, Marieta, C., Mondragon, I.
Format: article
Status:Published version
Publication Date:2001
Country:Argentina
Institution:Consejo Nacional de Investigaciones Científicas y Técnicas
Repository:CONICET Digital (CONICET)
Language:English
OAI Identifier:oai:ri.conicet.gov.ar:11336/36799
Online Access:http://hdl.handle.net/11336/36799
Access Level:Open access
Keyword:Curing in Mold
Epoxy-Urethane Copolymers
Modified Epoxy
Phase Separation
https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
Description
Summary:The curing process of an epoxy-urethane copolymer in a heated mold was studied. The epoxy resin (DGEBA, Araldyt GY9527; Ciba Geigy), was coreacted with a urethane prepolymer (PU, Desmocap 12; Bayer) through an amine that acted as crosslinking agent (mixture of cycloaliphatic amines; Distraltec). The study focused on the effect of the curing condition and PU concentration on time-temperature profiles measured in the mold and the consequent final morphologies obtained. As the PU concentration increases, the maximum temperature reached in the mold decreases as a result of the dilution effect of the elastomer on reaction heat, whereas the Tg of the piece also decreases. Phase separation is a function of conversion and temperature reached in the curing part and was analyzed using experimental data and a mathematical model that predicts temperature and conversion throughout the thickness of the mold. Scanning electron microscopy and atomic force microscopy were used to determine the characteristics of the dispersed phase for the different formulations and conditions of curing. It was shown that the size of the dispersed phase increased with the initial PU concentration, whereas there were practically no differences in the separated phase as a function of position or temperature of curing (in the range of 70 to 100°C studied). The superposition of the phase diagrams with the conversion-temperature trajectories during cure provided an explanation of the morphologies generated.