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Thermal oxidation of aromatic epoxy-diamine networks

Article dans une revue avec comité de lecture
Author
DELOZANNE, Justine
300457 SAFRAN Group
86289 Laboratoire Procédés et Ingénierie en Mécanique et Matériaux [PIMM]
DESGARDIN, Nancy
302872 HERAKLES - SAFRAN
492366 Airbus Safran Launchers
CUVILLIER, Nicolas
300457 SAFRAN Group
RICHAUD, Emmanuel
86289 Laboratoire Procédés et Ingénierie en Mécanique et Matériaux [PIMM]

URI
http://hdl.handle.net/10985/15441
DOI
10.1016/j.polymdegradstab.2019.05.030
Date
2019
Journal
Polymer Degradation and Stability

Abstract

The thermal oxidation of DGEBA-DDS (bisphenol A diglycidyl ether + 4,4′-diaminodiphenyl sulfone) and TGMDA-DDS (4,4′-methylenebis(N,N-diglycidylaniline) + 4,4′-diaminodiphenyl sulfone) was performed at 80, 120, and 200 °C and was monitored by FTIR. Oxidation was shown to generate amides and carbonyls. Comparisons were done with model systems displaying some common reactive groups, which highlighted the predominating role of methylene in α position of ether in DGEBA-DDS and methylene in α position of nitrogen hold by TGMDA in TGMDA-DDS. The participation of CH2 in α position of DDS hardener group seems to depend on the temperature and decrease when lowering it. The oxidation of such complex systems must hence be described by a co-oxidation model where each kind of reactive sites is described by its own set of kinetic constants.

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