In this study, melt-crystallization behaviors of poly(butylene terephthalate) (PBT) composites including different types of inorganic fillers were investigated. Composite samples having 5 wt % of fillers were prepared by melt processing in a twin screw extruder using commercial grades of calcite (CA), halloysite (HL), and organomontmorillonite (OM) as filler. Depending on the filler type and geometry, crystallization kinetics of the samples was studied by differential scanning calorimetry (DSC) methods. Effect of filler type on the nonisothermal meltcrystallization kinetics of the PBT was analyzed with various kinetic models, namely, the Ozawa, Avrami modified by Jeziorny and Liu-Mo. Crystallization activation energies of the samples were also determined by the Kissinger, Takhor, and Augis-Bennett models. From the kinetics study, it was found that the melt-crystallization rates of the samples including CA and HL-nanotube were higher than PBT at a given cooling rate. On the other hand, it was also found that organo-montmorillonite reduced the melt-crystallization rate of PBT. It can be concluded that organic ammonium groups in the OM decelerate the crystallization rate of PBT chains possibly due to affecting the chain diffusion through growing crystal face and folding. This study shows that introducing organically modified alumina-silicate layers into the PBT-based composites could significantly reduce the production rate of the injection molded parts during the processing operations. V C 2011Wiley Periodicals, Inc. J Appl Polym Sci 123: [77][78][79][80][81][82][83][84][85][86][87][88][89][90][91] 2012
In this study, nonisothermal crystallization kinetics of glass fiber (GF) and clay-type mineral (MN)-reinforced polyamide-6 (PA6) composites prepared in a twin screw extruder were investigated by differential scanning calorimetry method in the presence and absence of an organic nucleating agent (NA). Kinetic parameters for the nonisothermal melt-crystallization process of samples were determined with several models namely Ozawa, Avrami, Jeziorny, and Liu-Mo. Crystallization rate parameters of the samples and nucleation activity of the fillers and additives were also calculated by the models suggested by Zhang and Dobreva and Gutzow, respectively. Crystallization activation energies of the samples were determined by the Kissinger model. It was found that the MN filler accelerates dramatically the crystallization rate of PA6 even without a NA. Small amount of NA also has a significant acceleration effect on the crystallization rate of PA6 composites. The rate acceleration effect of NA was found to be more pronounced in the composite sample reinforced with GF. Based on the kinetic study using of GF as major filler and small amount of clay-like MN in the PA6 composites could improve the mechanical properties and crystallization rate of injection-molded parts. V C 2012 Wiley Periodicals, Inc. J Appl Polym Sci 125: E268-E281, 2012
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