Kinetics of the cyclization and isomerization reactions in polyacrylonitrile based carbon fiber precursors during thermal‐oxidative stabilization

Abstract

ABSTRACTThe kinetics of reactions in polyacrylonitrile (PAN) based carbon fiber (CF) production should be of significance to the guidance of process control, fiber structure formation. PAN precursor fibers were isothermally stabilized at 210, 225, 240, 255, and 270 °C, respectively, for 10 to 100 min in an air oven to study the kinetics of the cyclization and isomerization reactions. The structural evolution of PAN precursor fibers during thermal‐oxidative stabilization was characterized by Fourier transform infrared (FTIR) spectroscopy and solid state 13C nuclear magnetic resonance (13C NMR). The results indicate that the FTIR absorbance of CN (the resultant of the cyclization) in PAN shows a trend of first increasing and then decreasing. And then the NMR peak assigned to the carbon atoms linking imino groups (NH) proves the isomerization of CN into NH in pyridone structure. Based upon the FTIR absorbance method, the entire process of the cyclization and isomerization reactions is considered as a consecutive first‐order reaction. A kinetic model for the consecutive reaction has been established via the evaluation of the reaction rate constants of two single reactions. According to the model, the simulated kinetic curves of the characteristic groups (CN, CN, and NH) conform to the FTIR absorbance trends of these groups based on experimental data. This study is expected to furnish in‐depth information on the crucial reaction kinetics during stabilization of PAN precursors, which is of advantage to the process optimization of the CF production. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020, 137, 48819.