Chain Conformation and Crystallization Behavior of the Syndiotactic Polystyrene Nanocomposites Studied Using Fourier Transform Infrared Analysis

Abstract

Analyses of the effects of montmorillonite (clay) on the chain conformation and crystallization of syndiotactic polystyrene (s-PS) thin films are investigated using FTIR spectroscopy, X-ray diffraction, and TEM. The clay is dispersed into the s-PS matrix using a solution blending with scale in 1−2 nm or in a few tenths to 100 nm, depending on whether a surfactant is added or not. Upon adding clay, the chain conformation of s-PS tends to convert to TTTT from TTGG after drying because the highly dispersed clay overcomes the energy barrier of chain conformation transformation. This phenomenon leads to a change in a conventional mechanism of molecular packing for s-PS in the drying stage. During melt-crystallization, clay plays a vital role in facilitating the formation of the thermodynamically favored all-trans β form crystal, particularly on the s-PS thin film samples. When the s-PS is melt-crystallized at a cooling rate of 1 °C/min from 320 °C, the highest absolute crystallinity of β form up to 0.56 occurs in the clay dispersibility of few tenths to 100 nm in the s-PS matrix; then dispersibility is of 1−2 nm (0.49), and the final one is of pure s-PS (0.42). Evidently, clay significantly affects the chain conformation and crystallization of s-PS.