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
Curing behavior and properties of epoxy resins cured with the diamine having the quinoxaline or triazine structure
β Scribed by Fumihiko Akutsu; Mari Inoki; Nobuyoshi Daicho; Yoshio Kasashima; Norifumi Shiraishi; Kenji Marushima
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 108 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
2,3-Bis(4-aminophenyl)quinoxaline (1a), 2,3-bis(4-aminophenyl)-6-methylquinoxaline (1b), and 5,6-bis(4-aminophenyl)-3-(2-pyridyl)-1,2,4-triazine (2) were studied as curing agents of epoxy resins. The exotherms on differential scanning calorimetry thermograms of the mixtures of diglycidyl ether of bisphenol A (DGEBA) with 1a, 1b, and 2 were observed at higher temperatures than that of the mixture of DGEBA with a commercially used diamine, for example, 4,4Π-diaminodiphenylsulfone (DDS). However, the epoxy resin cured with 1a (EP-1a) showed higher tensile strength to stainless steel at 20Β°C than that cured with DDS, and the high tensile strength of EP-1a was maintained even at 180Β°C. The epoxy resin cured with 1b or 2 also possessed higher tensile strength at 20Β°C than that cured with DDS, but the high tensile strength lowered somewhat at 120Β°C. Using diamines 1a, 1b, and 2 as a curing agent improved heat distortion temperatures of the cured epoxy resins.
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