Nelson Marcos Larocca

Preparation and Chracterization of Nanocomposites of Polyamide 6/Brazilian Clay with Different Organic Modifiers

Nanocomposites of PA6 / organoclay at different concentration were prepared via melt intercalation method using a corotating twin screw extruder. The composites were prepared with Brazilian clay that was treated with different modifiers based on quaternary ammonium salts to obtain three types of organoclays. After extrusion the mixtures were injection molded into specimens that were tested to obtain the properties of tensile strength, notched izod impact and heat deflection temperature. The structure and morphology of the nanocomposites were characterized by x-rays diffraction (XRD) and transmission electron microscopy (TEM). The results showed that the modifier “dodigen” which promoted the intermediate expansion of the bentonite clay within the three salts used for the modification of the clay affects more significantly the mechanical properties, HDT and morphology of the polyamide 6 due to the higher level of exfoliation observed in these systems compared to the others modifiers. The improvement of the properties was correlated to the level of exfoliation/intercalation obtained which depends on the process technique used, surface treatment of the Brazilian clays with organic salts and interaction between polymer and clay.

Polyethylene cellulose nanofibrils nanocomposites

This paper investigates the use of an aqueous dispersion of polyethylene copolymer with a relatively high content of acrylic acid as a compatibilizer and as an alternative medium to obtain polyethylene CNF nanocomposites. The CNF content was varied from 1 to 90wt% and the appearance, optical, thermal, mechanical and rheological properties, as well the morphology of the films were evaluated. The PE/CNF films are transparent up to 20wt% of NFC indicating a good dispersion of CNF, but a poor distribution, with PE-rich and CNF-rich regions observed by SEM. Improved mechanical properties were achieved, with a 100% and 15,900% increase in the Youngs modulus with 1wt% and 90wt% NFC, respectively. The rheological behavior indicated good melt processability. According to these results, aqueous polyolefin dispersions seem to be a promising, easy and relatively fast route for obtaining cellulose/polyolefins nanocomposites with low to high contents of cellulose nanofibrils.

Efeito da sequência de mistura nas propriedades de blendas PA6/ABS compatibilizadas com o copolímero SMA

Blends of polyamide 6 (PA6) with acrylonitrile-butadiene-estyrene (ABS) were prepared in a twin-screw extruder, using the styrene-maleic anhydride (SMA) copolymer containing 7% of maleic anhydride as compatibilizer. The effects from three blending sequences on the microstructure and properties of the blends were investigated. The morphology and mechanical properties of the materials were characterized by transmission electron microscopy and tensile and impact tests. The results showed that the morphology and mechanical properties of ternary blends depend on the sequence of blend preparation. The blend prepared using the mixture of all components in a single-pass extrusion showed the more significant improvement in the material toughness. However, when the ABS and SMA were melt mixed together in a first extrusion step prior to incorporating PA6 in a second extrusion, the impact strength is lower than that of the blend without compatibilizer PA6/ABS and PA6 matrix. Evidence of chemical reactions between the compatibilizer SMA and PA6 was also obtained using a torque rheometer.

Influência das condições de processamento na obtenção de blendas PBT/ABS

In order to correlate processing conditions in intermeshing co-rotational twin-screw extrusion (ICTSE) and properties of PBT/ABS blends, devices have been developed to obtain extruded strips from PBT/ABS blends. The PBT/ABS blend compatibilized with reactive copolymer methyl methacrylate- glycidyl methacrylate (MGE) has shown higher viscosity, lower heat of fusion and lower ductile-brittle transition temperature (DBTT) when compared to the non compatibilized PBT/ABS blend, possibly due to chemical reactions between MGE epoxy groups and the molecule end groups from PBT. Concerning the screw rotation, the compatibilized blend processed with 120 rpm has shown higher viscosity, lower heat of fusion and better impact strength properties than the one processed with 240 rpm. This could be a consequence of degradation of the blend components, caused by higher screw rotation. The feeding rate has presented itself as the processing parameter with the greater influence on blend properties. A feeding rate of 3.5 kg/h has severely compromised impact strength properties, reduced the viscosity and increased the heat of fusion, in contrast to a feeding rate of 7.0 kg/h. These observations can be attributed to a higher residence time, with the blend being submitted to higher temperature and shear for a long time, leading to the degradation of blend constituents.

Study of the Crystalline Morphology Evolution of PET and PET/PC Blends by Time‐resolved Synchrotron Small Angle X‐ray Scattering (SAXS) and DSC

Isothermal melt crystallization of poly(ethylene terephthalate) (PET) and PET/PC (polycarbonate) blend, with and without a transesterification catalyst, was studied by time‐resolved small‐angle X‐ray scattering (SAXS) and differential scanning calorimetry (DSC) in order to achieve the variation of the morphological parameters throughout the whole crystallization time. For neat PET, the catalyst promotes a decrease of the crystal lamellar thickness but for the blend no variations were observed. The effect of incorporation of catalyst in crystallization kinetics was very distinct in PET pure and the blend: in the former the catalyst leads to an increase of this kinetics while for the latter it was observed a decreasing.