Improved thermal oxidation stability of polypropylene films in the presence of β-nucleating agent

Abstract

Thermal oxidation behavior of isotactic polypropylene (PP) films with and without nucleating agent was investigated at 100 °C in air. The crystal form of PP was modified with a specific aryl amide derivative as β-nucleating agent (β-NA). Fourier transform infrared spectroscopy (FTIR), polarized optical microscopy (POM), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA) and tensile tests were performed to determine the extent of chemical degradation and the variations of microstructure of the two kinds of PP films during thermal oxidation. It was found that the mechanism of thermal oxidation of PP films was not changed in the presence of β-NA, but the time to initiation and the rate of oxidation both declined. Moreover, during the thermal oxidation aging, the melting temperature of neat PP significantly decreased while only a slight decrease of the melting temperature occurred for β-PP. Overall, the investigation indicated that the thermal oxidative stability of β-PP was higher than that of neat PP. The underlying mechanism was further analyzed by considering the change in the physical structure, especially the crystalline and the amorphous structure, of PP in the presence of β-NA.