Reports: ND756168-ND7: Elucidation of Chemical Reaction Pathway and Structure of Polyacrylonitrile Stabilized under Air and Inert Atmosphere by Solid-State NMR
Toshikazu Miyoshi, PhD, The University of Akron
Inter- and intra-molecular chemical reactions and their kinetics for 13C labeled atactic-polyacrylonitrile (aPAN) powder heat treated at 220 – 290 ºC under air and vacuum were investigated by various solid-state nuclear magnetic resonance (ssNMR) techniques. By applying 13C direct polarization magic angle spinning (DPMAS) as well as through-bond and through-space double quantum / single quantum ssNMR techniques, it was concluded that aPAN heat treated under air at 290 ºC for 300 min adopted ladder formation, namely, conjugated six-membered aromatic rings with partially crosslinked and oxidized rings, and polyene components. In contrast, aPAN heat treated under vacuum at the same condition thermally decomposed into oligomeric chains that were mainly composed of isolated aromatic rings connected by alkyl segments. Furthermore, early stages of the chemical reactions were investigated by 13C cross polarization (CP) and DPMAS spectra. The latter provided quantitative information regarding the kinetics of the chemical reactions. As a result, it was shown that chemical reactions under oxygen occurred homogeneously with a higher activation energy (Ea) of 122 ± 3 kJ / mol compared to that of vacuum at 47 ± 2 kJ / mol. By comparing both chemical structures and kinetics under two different conditions, the chemical reaction mechanisms of aPAN will be discussed in detail.