Bluma G. Soares

Electrical conductivity in carbon black-loaded polystyrene-polyisoprene blends. Selective localization of carbon black at the interface

SummaryThe electrical conductivity of carbon-black loaded polystyrene-polyisoprene blends has been studied. In this ternary system, the filler is at the interface of co-continuous polyblends as confirmed by the very low value of the filler percolation threshold (0.2 vol % for blends compression molded at 250°C) and by optical microscopy. As a result of the selective localization of carbon black at the interface, the percolation threshold is very sensitive to the compression molding temperature.

Electrical conductivity of polystyrene-rubber blends loaded with carbon black

Abstract Polystyrene/rubber blends have been loaded with carbon black (CB) and the filler localization in the two-phase polyblends has been studied in relation to the chemical structure of the rubber. The CB localization and the electrical conductivity are greatly influenced by the substitution of the rubber chains. In polystyrene/polybutadiene blends, the filler is localized within the polybutadiene phase. In contrast, in polystyrene/polyisoprene and polystyrene/ethylene—propylene rubber (EPM) blends, CB is mainly localized at the interface, so that the CB percolation threshold in cocontinuous two-phase polyblends is dramatically decreased.

Cationic polymerization in iodine/liquid sulfur dioxide system: I. The polymerization of alpha-methylstyrene

Investigations concerning the initiation step in cationic polymerization of alpha-methylstyrene in liquid SO2 initiated by iodine have been made, based on the analysis of the low molecular weight components soluble in methanol by gas chromatography coupled with mass spectrometry. The results suggest that the formation of the alpha-methylstyrene diiodide is not possible, probably due to steric hindrance. HI formed from the carbocation (generated by the attack of iodine on the monomer at-60°) may initiate the polymerization.

PA6/NBR blends: improvement of processability and mechanical properties

Abstract This work deals with the study of the processability of blends based on PA6 and NBR. The aim is to achieve reduced PA 6 melting temperatures in order to avoid degradation of the NBR phase during processing. The effect of different additives in PA has been studied. For this purpose PA6 was blended with nonylphenol, EVA 18, EVA 33 and EVAMA. Among several masterbatches based on PA6; the sample containing 5% of EVAMA presented the best combination of processability and mechanical properties. The influence of additives in the processing behavior, crystallinity of the PA6 phase, mechanical and physicochemical properties are discussed in the present work.

Utilization of maleic anhydride modified ground eva waste in nbr vulcanizates

Abstract The influence of poly(ethylene-co-vinyl acetate) (EVA) waste (EVAW) on the rheological and mechanical properties of NBR vulcanizates compounds was studied. The optimum concentration of EVAW, which has presented higher ultimate tensile strength, was found to be 70 phr. In addition, the influence of EVAW modified with maleic anhydride as adhesion promoter was studied. Two distinct routes of modification with maleic anhydride were selected, originating a carboxylated EVA waste (EVAWCOOH) and an anhydride EVA waste (EVAWMA). An improvement of tensile strength and aging resistance was observed with the substitution of EVAW by EVAWCOOH or EVAWMA. A very good resistance to compression set has been achieved with the addition of EVAWCOOH. The improvement of mechanical performance was attributed to a better dispersion of EVAW along NBR matrix, promoted by the enhanced modified-waste polarity, which allowed a good interaction with polar NBR. The presence of anhydride group in functionalized EVAW resulted in...

THERMAL PROTECTION OF POLYAMIDE 6/ACRYLONITRILE–BUTADIENE RUBBER THERMOPLASTIC-VULCANIZATES: INFLUENCE OF TYPE AND CONTENT ON BLEND PROPERTIES

ABSTRACT Polyamide 6 (PA6)/NBR blends are interesting because of their supposed properties at elevated temperatures. The blend, however, has a critical problem in terms of processing stability, as a result of the thermal degradation of the NBR phase. We evaluate a system of dissimilar addition of antioxidant in each phase (a combination of Irganox®/Irgafos® for the PA phase, and Naugard 445® for the NBR phase) and study the influence of these antioxidants on the properties of the blend. The evaluation was performed through tensile strength, differential scanning calorimetry (DSC), thermogravimetric analysis, and X-ray diffraction analysis. The influence of the antioxidant system on the crystallization process of the PA phase was evaluated through isothermal DSC analysis. Results showed the best combination of antioxidant addition in master batches and during processing.

Modificação de fibra de carbono com PBLH e sua utilização em compósitos com resina epoxídica

Carbon fibers containing 1,4 e 2,1 mmol/g of carboxyl and phenolic hydroxyl groups, respectively, were modified through the reaction with TDI. The presence of isocyanate groups at the fiber surface made possible the fiber modification with hydroxyl terminated polybutadiene (HTPB). These modified and unmodified carbon fibers were employed in the preparation of epoxy resin-based composites. A substantial improvement in the impact properties was observed in the composites with HTPB-grafted carbon fibers when compared to unmodified carbon fibers. These results may be attributed to a higher interfacial adhesion promoted by reactions between the functional groups present at the modified carbon fiber surface and the epoxy matrix.