The cure reaction of a commercial phenolic resin (FRD-5002, Borden Chimie S.A.) has been studied by IR spectroscopy (Fourier transform IR). A phenomenological approach was used to characterize the kinetic of reaction. Various kinetic models, including homogeneous reactions, diffusion-controlled reactions, phase boundary movement, and nucleation and growth-type kinetic, have been tested. Kinetic analyses using integral procedures on isothermal data indicate that the cure reaction data can be described above 140°C using the homogeneous first-order reaction model. The activation energy has been found to be about 49.6 kJ mol-1. At lower temperature, a diffusive mechanism was active, and the kinetic of reaction was well described by the Jander kinetic model. Because of the simple kinetic control active above 140°C, a mechanistic model for the resol cure at these temperatures has been also proposed.

Kinetic study of phenolic resin cure by IR spectroscopy

Nicolais L
1999

Abstract

The cure reaction of a commercial phenolic resin (FRD-5002, Borden Chimie S.A.) has been studied by IR spectroscopy (Fourier transform IR). A phenomenological approach was used to characterize the kinetic of reaction. Various kinetic models, including homogeneous reactions, diffusion-controlled reactions, phase boundary movement, and nucleation and growth-type kinetic, have been tested. Kinetic analyses using integral procedures on isothermal data indicate that the cure reaction data can be described above 140°C using the homogeneous first-order reaction model. The activation energy has been found to be about 49.6 kJ mol-1. At lower temperature, a diffusive mechanism was active, and the kinetic of reaction was well described by the Jander kinetic model. Because of the simple kinetic control active above 140°C, a mechanistic model for the resol cure at these temperatures has been also proposed.
1999
Activation energy
Crystal growth
Curing
Diffusion
Fourier transform infrared spectroscopy
High temperature operations
Integral equations
Mathematical models
Nucleation
Phase transitions
Reaction kinetics
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/303438
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