Degradation of an Amine‐Based Epoxy Resin–Kinetics Analysis and Chemical Behavior

ABSTRACT This study investigates the thermal decomposition of a crosslinked epoxy resin system based on diglycidyl ether of bisphenol A (DGEBA) and diamines in both inert and oxidative atmospheres. First, kinetic modeling of the degradation process was performed. Under nitrogen, the reaction was described by two successive steps with activation energies of 157 kJ/mol (first step) and 208 kJ/mol (second step). In air, a five‐step model was applied with activation energy varying between 120 and 225 kJ/mol, depending on the step. Gaseous decomposition products were analyzed using a Fourier‐transform infrared (FTIR) spectrometer and a gas chromatograph–mass spectrometer (GC‐MS), both coupled with a thermobalance. The results indicate that the surrounding atmosphere had only a minor impact on the nature of the degradation products, which predominantly included water, phenol, phenolic derivatives, and ammonia. However, in addition to the products detected in nitrogen, carbon dioxide, and carbon monoxide were additionally detected in the oxidative environment.

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Publication Details

Journal
Macromolecular Theory and Simulations
Published
2026-04-30
DOI
https://doi.org/10.1002/mats.70043
Primary Topic
Epoxy Resin Curing Processes
Type
article
Field-Weighted Citation Impact
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article

Degradation of an Amine‐Based Epoxy Resin–Kinetics Analysis and Chemical Behavior

Jürgen Hartmann, Claire Strasser, Elena Moukhina, Carolin Fischer
Macromolecular Theory and Simulations
Epoxy Resin Curing Processes
article

Degradation of an Amine‐Based Epoxy Resin–Kinetics Analysis and Chemical Behavior

Jürgen Hartmann, Claire Strasser, Elena Moukhina, Carolin Fischer
article en

Abstract

ABSTRACT This study investigates the thermal decomposition of a crosslinked epoxy resin system based on diglycidyl ether of bisphenol A (DGEBA) and diamines in both inert and oxidative atmospheres. First, kinetic modeling of the degradation process was performed. Under nitrogen, the reaction was described by two successive steps with activation energies of 157 kJ/mol (first step) and 208 kJ/mol (second step). In air, a five‐step model was applied with activation energy varying between 120 and 225 kJ/mol, depending on the step. Gaseous decomposition products were analyzed using a Fourier‐transform infrared (FTIR) spectrometer and a gas chromatograph–mass spectrometer (GC‐MS), both coupled with a thermobalance. The results indicate that the surrounding atmosphere had only a minor impact on the nature of the degradation products, which predominantly included water, phenol, phenolic derivatives, and ammonia. However, in addition to the products detected in nitrogen, carbon dioxide, and carbon monoxide were additionally detected in the oxidative environment.

Macromolecular Theory and SimulationsVol. 35(3)
Technical University of Applied Sciences Würzburg-Schweinfurt (DE), Bavarian Center for Applied Energy Research (DE)
Openalex Percentile: Top 11%
Epoxy Resin Curing Processes
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