4,4′-Bismaleimidediphenylmethane (BMI) was cured finally at 250 °C with cardanol (CD) or CD novolac (CDN) prepared by the reaction of CD and paraformaldehyde with CD/maleimide unit ratios 1/2, 1/4 and 1/6. The obtained cured resins with CD/maleimide ratio lower than 1/2 did not show glass transition until 300°C and had 5% weight loss temperature higher than 450°C. The curing mechanism was elucidated by means of the proton nuclear magnetic resonance (1H-NMR) and Fourier transform infrared spectroscopy (FTIR) analyses of the model reaction products of CD and N-phenylmaleimide (PMI) and the cured resins.
- Mitsuhiro Shibata
- Yusuke Itakura
- Hironori Watanabe