Isothermal Crystallization Kinetics of Polypropylene Latex-Based Nanocomposites with Organo-Modified Clay

The effect of organo-modified clay (Cloisite 93A) on the crystal structure and isothermal crystallization behavior of isotactic polypropylene (iPP) in iPP/clay nanocomposites prepared by latex technology was investigated by wide angle Xray diffraction, differential scanning calorimetry and polarized optical microscopy. The X-ray diffraction results indicated that the higher clay loading promotes the formation of the beta-phase crystallites, as evidenced by the appearance of a new peak corresponding to the (300) reflection of beta-iPP. Analysis of the isothermal crystallization showed that the PP nanocomposite (1% C93A) exhibited higher crystallization rates than the neat PP. The unfilled iPP matrix and nanocomposites clearly shows double melting behavior; the shape of the melting transition progressively changes toward single melting with increasing crystallization temperature. The fold surface free energy (sigma(e)) of polymer chains in the nanocomposites was lower than that in the PP latex (PPL). It should be reasonable to treat C93A as a good nucleating agent for the crystallization of PPL, which plays a determinant effect on the reduction in sigma(e) during the isothermal crystallization of the nanocomposites. The activation energy, Delta E-a, decreased with the incorporation of clay nanoparticles into the matrix, which in turn indicates that the nucleation process is facilitated by the presence of clay. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 1927-1938, 2010