Abstract Nitrile rubber (NBR) nanocomposites with different contents of synthetic Somasif ME-100 mica (sodium-fluorohectorite) were obtained by melt compounding using a Semi Efficient curing system. The effect of curing on the nanocomposties was evaluated through rheometric properties, crosslink density (CLD) and mechanical properties. The ME-100 mica dispersion in NBR was assessed by transmission electron microscopy (TEM), the Payne effect and thermodynamic properties (ΔS and ΔG). Both the curing parameters and CLD pointd out that the addition of ME-100 directly affects crosslinks formation. It could also be observed that the nanofiller dispersion state is complex, exhibiting exfoliated and agglomerated structures (TEM); besides, agglomerations rose linearly as the nanofiller was added (the Payne effect). Notwithstanding these findings, and on the basis of unfilled formulations, NBR20 nanocomposite showed improvement in mechanical properties (tensile and tear strengths) which suggests that ME-100 might be considered a semi-reinforcing filler.

This study evaluated the effect of adding poly (ethylene methyl acrylate) (EMA) and cotton linter (CL) on the properties of recycled poly (ethylene terephthalate) (PETrec). For this, PETrec/EMA blend and PETrec/EMA/CL composite were developed. In order to improve the interfacial adhesion and the properties of these materials, ethylene/methyl acrylate/glycidyl methacrylate terpolymer (EMA-GMA) and polyethylene-grafted maleic anhydride (PE-g-MAH) were added. The rheological results showed that the addition of EMA increased and the addition of 1 wt% of CL reduced the viscosity. The morphological analysis of the non-compatibilized blend and composite showed poor interfacial adhesion. Polymer blends with 2 and 6 wt% of EMA had better mechanical properties, since these formulations have the smallest average particle diameter of 0.58 and 1.00 µm, respectively. The mechanical testing of composites showed a material with higher maximum strength and elasticity modulus than polymer blend when analyzed at the same EMA phase concentration. The use of EMA-GMA was effective in reducing the size of particles of the EMA in the blend.

This study involved an evaluation of the influence of phase inversion in poly(methyl methacrylate) elastomer/poly(ethylene terephthalate) binary blends (PMMAelast/PET) and the effect of the addition of poly(methyl methacrylate-glycidyl methacrylate-ethyl acrylate) (MGE) interfacial compatibilizer on the microrheological properties of this polymer blend. Thermal, dynamic mechanical thermal, rheological and morphological analyses were performed using sensitive techniques such as differential scanning calorimetry (DSC), dynamic mechanical thermal analysis (DMTA), parallel plates rheometry in the linear viscoelastic region, and atomic force microscopy (AFM), respectively. In this study, it was found that variations in the percentage of the PET phase influenced the correlation between the rheological properties at low shear rates and the morphology of the PMMAelast/PET binary blend and of the PMMAelast/PET/MGE compatibilized blend.

Abstract In this work, the rheological, mechanical and morphological behavior of immiscible blend poly (methyl methacrylate) with elastomeric particles (PMMAelast) and post-consumer poly (ethylene terephthalate) (PET) with and without the use of the interfacial compatibilizer poly (methyl methacrylate-co-glycidyl methacrylate-co-ethyl acrylate) (MGE) was studied. The significant increase in torque presented in rheological analyses has shown a indication of chemical reactions between the epoxy group of MGE with end groups of PET chains and also with the elastomeric phase of PMMAelast. The increased concentration of PET yielded an increase in maximum strength and elasticity modulus and a decrease in elongation at break. The PMMAelast/PET binary blend (50/50 wt%) and PMMAelast/PET/MGE compatibilized blend (65/30/5 wt%) showed pronounced results in elongation at break compared to PMMAelast, whereas, in the first results were due to the evidence of a co-continuous morphological structure and in the second, due to the efficiency of the dual reactive interfacial compatibilization of PMMAelast/PET blends. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses showed that PMMAelast/PET/MGE blends exhibit complex phase morphology due to the presence of elastomeric particles in the PMMAelast copolymer and in the use of MGE terpolymer.

The search for new materials with properties suitable for specific applications has increased the number of research studies to fill the market demands. The development of polymer composites by the addition of inorganic fillers to the poly(methyl methacrylate) (PMMA) increases the potential use of this polymer in various application fields. The main objective of this work was to study the rheological and mechanical behavior of composites obtained from the addition of silica in two different types of PMMA matrix: a common (PMMAc) and an elastomeric copolymer (PMMAel). The results showed that the addition of silica particles to the PMMA matrix promoted an increase in torque, a decrease in the melt flow index of composites and an increase in hardness compared to pure polymers. The composites also showed a reduction of the maximum tensile strength for composites with PMMAc matrix and maintenance of tensile strength for composites with PMMAel matrix. The average width of scratch decreased due to a change in wear mechanism, attributed to the increase of hardness in the composites obtained.

Recent interest in polymer/organoclays nanocomposites systems is motivated by the possibility of achieving enhanced properties and added functionality at lower clay loading as compared to conventional micron size fillers. By adding montmorillonite clay to polyamide 6 increases the Young modulus, yield strength and also improves barrier properties. In this work, nanocomposites of polyamide 6 with montmorillonite clay were obtained. The clay was chemically modified with three different quaternary ammonium salts such as: Dodigen, Genamin and Cetremide. In this case, a dispersion of Na-MMT was stirred and a salt equivalent to 1:1 of cation exchange capacity (CEC) of Na-MMT was added to the dispersion. The montmorillonite clay (untreated and treated by ammonium salts) and nanocomposites were characterized by X ray diffractions. Also the nanocomposites were characterized by transmission electron microscopy and mechanical properties. The results indicated that all the quaternary ammonium salts were intercalated between the layers of clay, leading to an expansion of the interlayer spacing. The obtained nanocomposites showed better mechanical properties when compared to polyamide 6. The clay acted as reinforcing filler, increasing the rigidity of nanocomposites and decreasing its ductility.

The aim of this work was to evaluate the interfacial tension from the poly(butylene terephtalate) and poly(styrene-co-acrylonitrile) (PBT/SAN) interface region using the drop retraction method. SAN filaments were sandwiched between two PBT films; the whole system was heated up to 240 °C, in a hot stage coupled to an optical microscope. The rheological parameters of the PBT/SAN system were obtained by parallel plates rheometry. An increase of the interfacial tension with the PBT molecular weight was observed with values between 0.57 and 1.06 mN/m, depending on the molecular weight. Theoretical values were calculated using the geometric-mean and harmonic-mean equations and were found to be similar to the experimental results. Viscosity measurements showed that the higher the SAN/PBT viscosity ratio, the lower the interfacial tension of these blends.