Thermal degradation mechanism and kinetics of polycarbonate/silica nanocomposites

Polycarbonate nanocomposites filled with pristine and modified silica were prepared by simple melt compounding. The thermal degradation behavior of composites was investigated by thermogravimetric analysis coupled with differential scanning calorimetry (TGA/DSC). To understand the thermal degradation mechanism, the chemical structures of gaseous and solid degradation products were detected by thermogravimetric analysis coupled with Fourier transform infrared spectrometry (TGA/FTIR) and X-ray photoelectron spectroscopy (XPS), respectively. Kissinger Akahira Sunose (KAS) and Flynn Wall Ozawa (FWO) methods were employed to analyze the thermal degradation kinetics. High thermal degradation temperature was obtained by incorporating both types of nanoparticles into matrix, but the maximum mass loss rate increased. According to the DSC curves for degradation process, the change of the number and position of absorption peaks meant that the degradation mechanism of composites was different from that of neat PC. The analysis for TGA chars confirmed the presence of alcoholysis reaction between PC and silica nanoparticles during the thermal decomposition. TGA/FTIR results proved that no new degradation volatiles were produced during the thermal degradation of composites, but the total amounts of all gaseous products decreased by adding silica nanoparticles. The degradation activation energies of both composites increased significantly relative to neat PC, especially for the composite with modified silica. (C) 2014 Elsevier Ltd. All rights reserved.