In this study, polymeric nanocomposites based on poly(methyl methacrylate) (PMMA) and silicon carbide (SiC) nanoparticles were prepared by radical mass polymerization in the presence of filler. Nanoparticles of SiC with and without surface treatment with organosilane were obtained .The nanocomposites were characterized by X-ray fluorescence (XRF), infrared spectroscopy (FTIR), thermogravimetry (TGA) and Field Emission Gun Scanning Electron Microscopy (FEG SEM) with an energy dispersive x-ray spectroscopy (EDS) detector. The produced nanocomposites showed well-dispersed SiC incorporation in the PMMA matrix. The results pointed that the surface treatment on SiC fillers was successful on enhancing the interaction between the organic matrix and the inorganic filler.

In the present work, the synthetic route to obtain crosslinked polyethylene (PEX) was studied using vinyltrimethoxy silane (VTMS) as crosslink agent and commercial polyethylene (HDPE and LLDPE). Materials were processed with increasing amounts of VTMS (2.5, 5.0 and 7.5 wt.%). After insertion of silane onto polymer chain in solid state, samples were molded by compression. Gel content was used to measure the extension of crosslinking. Melting temperature and degree of crystallinity were evaluated using differential scanning calorimetry (DSC). The microstructure of the starting polyethylene was correlated with the effectiveness of crosslinking and the resultant thermal and mechanical properties of the PEX. Hydroxylated liquid polybutadiene (HLPB) was employed to improve crosslink efficiency, as well as mechanical properties of the material.

Nanocomposites of high-impact polypropylene resin and organosilane-functionalized nanotubes in halloysite clay were prepared with the introduction of peroxide to promote selective incorporation of the filler into the polypropylene phase of the matrix, with minor insertion into the EPR elastomeric phase, thus improving the stiffness while preserving the high toughness of the material. Silica composites were also prepared as standard filler. The effect of increasing load content on the morphological and mechanical properties of this material was evaluated by SEM and DMA. The content of the hexane-extracted fraction of these composites after processing was evaluated. Halloysite was well-dispersed in the matrix. Composites with 10% of filler and 0.5% w/w of dicumyl peroxide had increased stiffness and higher loss factor. An increase of the E’ was generated by halloysite addition, but there was a higher decrease in Tan delta. Studies using experimental planning as a tool enabled choosing appropriate amounts of DCP to obtain a high performance composite.

Aiming to improve the dispersion of carbon nanotubes (CNT) in a polymer matrix, a fourth-generation Ziegler-Natta, ZN, catalyst was prepared in the presence of CNT to synthesize nanocomposites of polypropylene (PP/CNT) by in situ polymerization. The performance of the ZN catalyst was evaluated along with the thermal (TGA and DSC) and dynamic-mechanical properties of the nanocomposites and they were compared with those of neat PP synthesized with the standard catalyst prepared without carbon nanoparticles. The thermal degradation temperature of the PP/CNT nanocomposite increased in comparison with that of neat PP. Moreover, the crystallization temperature and the degree of crystallinity sharply increased in PP/CNT materials. Finally, the storage modulus of the nanocomposite prepared by 30 min of polymerization increased, as well as the Tg.