Bismaleimide resin co‐modified by allyl ether of resveratrol and allyl ether of eugenol‐grafted polysiloxane with enhanced toughness, heat resistance, and flame retardancy

Abstract

AbstractModifying bismaleimide (BMI) resin to improve its toughness and flame retardancy without sacrificing the glass transition temperature (Tg) and thermal decomposition stability is still a challenge. In this study, we employed the allyl ether of resveratrol (AER) and eugenol allyl ether grafted polysiloxane (PMES‐Allyl) to co‐modify BMI resin. For the BMI/AER/PMES‐Allyl (BAPA) resin, the content of PMES‐Allyl was 15 wt%, and the molar ratio of maleimide and allyl groups was controlled as 1:0.8. Compared to commercial 2,2′‐diallyl bisphenol A modified BMI (BD) resin, the BAPA resin exhibited superior thermal properties after curing, due to the role of AER in improving the crosslinking density and chain rigidity of the network. The cured BAPA resin had a Tg more than 380°C, and its initial thermal decomposition temperature (Td5%) and char yield (Y800°C) reached 424.8°C and 46.4%, respectively. Meanwhile, PMES‐Allyl as a rubber phase could effectively improve the toughness of the cured resin. The impact strength of the cured BAPA resin was 15.2 kJ/m2. Moreover, the two modifiers both helped to improve the flame retardancy of the material. Compared with the cured BD resin, the cured BAPA resin showed a decrease of peak heat release rate (PHRR), total heat release (THR), and maximum average rate of heat emission (MARHE) by 25.5%, 35.5%, and 31.5%, respectively. Its total smoke production (TSP) was only 35.6% of that of the cured BD resin. In addition, the cured BAPA resin also displayed a lowered water absorption and improved thermal aging resistance. Therefore, it is suggested to be a promising and high‐performance thermosetting resin for cutting‐edge applications.