IFIBA   22255
INSTITUTO DE FISICA DE BUENOS AIRES
Unidad Ejecutora - UE
artículos
Título:
Correlation between nanohole volume and mechanical properties of amine-cured epoxy resin blended with poly(ethylene oxide)
Autor/es:
RAMOS, J.A; LARRAÑAGA, M; MONDRAGON IÑAKI,; SALGUEIRO, WALTER; SOMOZA ALBERTO,; GOYANES, SILVIA; RUBIOLO, G.H.
Revista:
POLYMERS FOR ADVANCED TECHNOLOGIES
Editorial:
Wiley
Referencias:
Año: 2009 vol. 20 p. 35 - 38
ISSN:
1042-7147
Resumen:
A set of diglycidylether of bisphenol-A (DGEBA)/4,4(-diaminodiphenylmethane (DDM) epoxy matrix modified with poly(ethylene oxide) (PEO), pre-cured at two different temperatures, was examined by positron annihilation lifetime spectroscopy (PALS). The aim was to investigate the correlation between local free volume and mechanical properties. A negative deviation from the linear additivity rule of the local free volume is observed at both cure schedules. Using together the local free volume and mechanical results allows to conclude that the cure temperature makes small contribution to the flexural strength and modulus of blends but is responsible for the composition-dependent rise of the fracture toughness. It is proposed that this behavior is a consequence of the nearest-neighbor intrachain contacts or self-association of the epoxy-OH groups during cure leading to a non-uniform space distribution of the DGEBA–PEO contacts, which causes the deflection of the crack path. (-diaminodiphenylmethane (DDM) epoxy matrix modified with poly(ethylene oxide) (PEO), pre-cured at two different temperatures, was examined by positron annihilation lifetime spectroscopy (PALS). The aim was to investigate the correlation between local free volume and mechanical properties. A negative deviation from the linear additivity rule of the local free volume is observed at both cure schedules. Using together the local free volume and mechanical results allows to conclude that the cure temperature makes small contribution to the flexural strength and modulus of blends but is responsible for the composition-dependent rise of the fracture toughness. It is proposed that this behavior is a consequence of the nearest-neighbor intrachain contacts or self-association of the epoxy-OH groups during cure leading to a non-uniform space distribution of the DGEBA–PEO contacts, which causes the deflection of the crack path.