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Poly(ϵ-caprolactone) (PCL) of ca. 20,000 molecular weight is shown to be partially miscible with three aromatic-amine-cured epoxy resins. This conclusion is based on the depression of the epoxy Tg, the effect on physical and mechanical properties, and the observation that a large proportion (40-55%) of the PCL ester groups are involved in hydrogen bonding. This miscibility behavior is compared to PCL blends with anhydride-cured epoxy resins, which appear to have a two-phase morphology. The different miscibilities are rationalized on the basis of the existence of functional groups (e. g., hydroxyl) in amine-cured epoxies which are capable of hydrogen bonding to the PCL ester groups. Anhydride-cured epoxy resins contain fewer potential hydrogen bonding sites.
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Clark et al. (1984) studied this question.
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