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Graphene oxide (GO) derived from oxidation of natural graphite contains many active groups that can interact with a great variety of polar moieties. In this work, polypropylene (PP)/graphene oxide nanocomposites using polypropylene (PP) grafted with amine‐alcohol (PPgDMAE) as compatibilizer were prepared by two different methods. Maleic anhydride grafted PP (PPgMA) was reacted with 2‐[2‐(dimethylamine)‐ethoxy] ethanol (DMAE) in the melt for forming amine‐alcohol functionalized polypropylene (PPgDMAE). Nanocomposites were prepared by two methods. In one method, PP/GO nanocomposite was prepared by direct melt mixing in an internal batch mixer using PPgDMAE as compatibilizer. In another method, a previous mixing of PPgDMAE with GO in hot Xilene was done and then, once the solvent was evaporated, it was incorporated into PP by melt‐mixing. The microstructure and interface enhancement of the prepared composites were analyzed by Fourier transform infrared spectroscopy (FTIR), Raman, X‐ray difraction (DRX) contact angle, scanning and transmission electron microscopy (STEM), mechanical, thermal, and electrical properties measurements. Fourier transform infrared spectroscopy (FTIR) revealed the interaction between GO and PPgDMAE. The loading of GO conducted to enhance the composite mechanical properties attributed to the strong interfacial interactions between GO and PPgDMAE. A significant improvement in mechanical thermal stability and electrical properties was observed when nanocomposites were prepared by the solution blending method compared with melt mixing method. This work suggests a potential application of GO in preparation of high performance PP composites. POLYM. COMPOS., 39:1361–1369, 2018. © 2016 Society of Plastics Engineers

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Nucleation mechanisms of poly(ethylene terephthalate) (PET), poly(butylene terephthalate) (PBT), and poly(ethylene naphthalate) (PEN) on single-wall carbon nanotubes (SWNTs) are proposed, based on experimental evidence, theoretical epitaxy analysis, and semiempirical quantum chemical calculations. In order to elucidate early nucleation stages polyester-coated nanotubes were obtained from highly diluted solutions. High-resolution transmission electron microscopy (HRTEM) revealed helical morphologies for PET/SWNTs and PEN/SWNTs and the formation of lobules with different orientations for PBT/SWNTs. To explain the morphological behavior one model was proposed based on crystallographic interactions, that is, epitaxy. Theoretical epitaxy calculations indicated that epitaxy is not possible from the strict epitaxy point of view. Instead, aromatic self-assembly mechanism was proposed based onπ-πinteractions and the chirality of the nanotube. It was proposed that the mechanism implies two steps to produce helical or lobular morphologies with different orientations. In the first step polymer chains were approached, aligned parallel to the nanotube axis and adsorbed due to electrostatic interactions and the flexibility of the molecule. However, due toπ-πinteractions between the aromatic rings of the polymer and the nanotube, in the second step chains reoriented on the nanotube surface depending on the chirality of the nanotube. The mechanism was supported by semi-empirical calculations.