Abstract

Abstract In order to improve the stabilization and spinnability of polyacrylonitrile, a bifunctional comonomer containing both ester and amide groups was synthesized to prepare poly(acrylonitrile- co -3-aminocarbonyl-3-butenoic acid methyl ester) [P(AN- co -ABM)] copolymers used as the carbon fiber precursor instead of poly(acrylonitrile-acrylamide-methyl acrylate) [P(AN-AM-MA)] terpolymer. The differential scanning calorimetry and thermogravimetry results show that the stabilization of P(AN- co -ABM) have been remarkably improved by ABM compared with P(AN-AM-MA) terpolymer, such as lower initiation temperature, broadened exothermic peak and smaller activation energy. Moreover, the spinnability of P(AN- co -ABM) is also improved by ABM due to the lubrication of ester groups in ABM. This study clearly shows that P(AN- co -ABM) copolymer is a better material for use as a carbon fiber precursor than P(AN-AM-MA) terpolymer.

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