The epoxy resin containing a typical mesogenic group such as biphenol was cured with catechol novolak and aromatic diamines which have neighboring active hydrogens. In the biphenol-type epoxy resin cured with catechol novolak, 4,4-diaminodiphenylmethane, and p-phenylenediamine (PPD), the glass-rubbe
Effect of network structure on thermal and mechanical properties of biphenol-type epoxy resins cured with phenols
โ Scribed by M. Ochi; N. Tsuyuno; K. Sakaga; Y. Nakanishi; Y. Murata
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 491 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
In the biphenol-type epoxy resin cured with catechol novolac (CN), a very weak glass transition and, thus, a very high rubbery modulus were observed. On the other hand, the glass transition was clearly observed in the system cured with phenol novolac (PN). This means that the micro-Brownian motion of network chains is highly suppressed in the system cured with CN. The reason for this suppression of the chain motion in the CNcured system has been pursued from the viewpoint of the conformation of network chains. The disappearance of the glass transition in the biphenol-type resin depends on the formation of the active hydrogens in the curing agents. Thus, it was suggested that the suppression of the micro-Brownian motion is due to the orientation of the biphenyl groups in the network. Moreover, it has been shown that the mechanical and bonding strength a t high temperature is considerably improved by the suppression of the network chain motion in the CN-cured biphenol resin system.
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