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Kinetics of the crosslinking reaction of a bisnadimide model compound in thermal and microwave cure processes

✍ Scribed by Yumin Liu; X. D. Sun; X.-Q. Xie; D. A. Scola


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
330 KB
Volume
36
Category
Article
ISSN
0887-624X

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✦ Synopsis


The kinetic studies of the crosslinking reaction of a nadic end-capped imide model compound, N,NЈ-(oxydi-3,4Ј-phenylene) bis(5-norbornene-2,3-dicarboximide), a bisnadimide, in thermal and microwave processes were investigated. The conversion of the endo isomer to exo isomer proceeds at a much lower temperature than the crosslinking reaction. The crosslinking reaction was monitored by the combined decrease in the infrared absorptions of the endo and exo isomers at 840 and 780 cm Οͺ1 , respectively. The decrease in the concentration of starting materials follows first-order kinetics in the thermal and microwave processes. At the same temperatures (230 or 280Β°C), the crosslinking reaction proceeds at about 10 times faster in the microwave process than in the thermal process. Solid-state 13 C-NMR showed no significant loss in CAC double bond resonance in the cured products by comparison with the starting material. This study provides direct evidence that the microwave process may be an efficient method to cure nadic end-capped polyimides.


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