Thermodynamic Parameters of Crosslinked Elastomers (BR, SBR and NBR) and Their Blends.

Herein, a methodology is employed based on the Flory-Rehner equation for estimating the Flory-Huggins interaction parameter (χ12*) of crosslinked elastomer blends. For this purpose, binary elastomer blends containing polybutadiene rubber (BR), styrene-butadiene rubber (SBR) and nitrile-butadiene rubber (NBR), were prepared in a mixing chamber at a temperature below the activation of the crosslinking agent. Swelling tests with benzene were employed to determine the crosslinked fraction, finding that after 20 min of thermal annealing, the BR and NBR were almost completely crosslinked, while the SBR only reached 60%. Additionally, the BR-SBR blend increased by 2-3 times its volume than its pure components; this could be explained based on the crosslink density. From the mechanical tests, a negative deviation from the rule of mixtures was observed, which suggested that the crosslinking was preferably carried out in the phases and not at the interface. Furthermore, tensile tests and swelling fraction (ϕsw) results were employed to determine the average molecular weight between two crosslinking points (Mc), and subsequently χ12*. Calculated χ12* values were slightly higher than those reported in the literature. The calculated thermodynamic parameters for the blends showed positive ΔGmix values and endothermic behavior, suggesting their immiscible nature.

Morphology and thermal properties of clay/PMMA nanocomposites obtained by miniemulsion polymerization.

Miniemulsion polymerization was used as the synthetic method to produce clay/poly(methyl methacrylate) nanocomposites. Two kinds of interfacial interactions clay-polymer particle were observed by electron microscopy, one where the polymer particles are adhered on the surface of the larger fragments of clay, and another where nanometric fragments of clay are encapsulated by polymer particles. Variations in the glass transition temperature (T(g)) and thermomechanical properties of the matrix, as function of clay content, were observed. In particular, at the highest clay loading (1.0 wt%) depression of T(g) and thermomechanical properties were observed. The increased clay-polymer matrix interfacial area appears to be the conditioning factor that determines such behavior.

Comparative study on the mechanical and fracture properties of acrylic bone cements prepared with monomers containing amine groups.

In this work, the effect of the incorporation of comonomers containing amine groups on the mechanical and fracture properties of acrylic bone cements was studied. Cements were prepared with either diethyl amino ethyl acrylate (DEAEA), dimethyl amino ethyl methacrylate (DMAEM) or diethyl amino ethyl methacrylate (DEAEM) as comonomer in the liquid phase. It was found that strength and modulus decreased with increasing comonomer content in the bending and compressive tests. It was also observed that fracture toughness (K(IC)) and the critical strain energy release rate (G(IC)) increase with increasing comonomer concentration and are significantly higher compared to the control formulation. The mechanical and fracture properties of cements were also evaluated after soaking the specimens in Simulated Body Fluid (SBF) for 3 and 6 months. It was found that the mechanical properties of cements decreased when the samples were stored in SBF, although the impact strength increased in the first 3 months and then decreased. SEM micrographs were in agreement with the results obtained during mechanical characterization as the increase in toughness was confirmed by the appearance of ductile tearing pattern which is associated with plastic deformation.

Evidence of multi-walled carbon nanotube fragmentation induced by sonication during nanotube encapsulation via bulk-suspension polymerization.

The synthesis of multi-walled carbon nanotube/polystyrene composites, with nanotube concentrations of 0.04, 0.08 and 0.16 wt%, was carried out by in situ bulk-suspension polymerization with the assistance of sonication. By using this method both encapsulation and exfoliation of the nanotubes into the polymer host were achieved. Evidence of significant nanotube fragmentation was found by scanning electron microscopy; the cause of such fragmentation was attributed to the induction of strong cavitation due to the application of ultrasound during the synthesis. Infrared spectroscopy showed no evidence of the formation of covalent bonds between the nanotubes and the polystyrene during the process of synthesis. The thermal stability was not improved by the inclusion of the nanotubes, it was attributed to the low nanotube concentrations; however, composites glass transition temperature showed improvements.