NMR and vibrational spectroscopic study of the order and mobility in polycarbonate and polycarbonate — poly(ethylene oxide) blends

Abstract

AbstractTime dependence of the gel formation in toluene solutions of polycarbonate (PC) was investigated by two‐dimensional Fourier‐transform infrared (2D FT‐IR) correlation spectroscopy. The 2D correlation approach reveals that there are at least three bands in the C=O stretching region. The intensity increase of the band at 1771 cm−1 occurs later compared with the onset of the intensity changes of the bands at 1778 and 1765 cm−1 corresponding to amorphous and crystalline‐like domains, respectively. The band at 1771 cm−1 is assigned to the chain conformations occurring in the partial‐order regions accompanying crystalline‐like domains. Splitting of the signals of aromatic carbons in the solid‐state 13C CP/MAS NMR spectra of semicrystalline PC and PC‐PEO blends indicates restricted mobility resulting from the fixed ordering due to partial crystallinity of PC itself and from blending of PC with PEO. The decreasing mobility of PC with the increasing content of highly mobile PEO in the blends was proved by the dipolar dephasing rates obtained in the 1H‐1H CRAMPS (combined rotation and multi‐pulse spectroscopy) NMR experiments.