Influence of Organoclay Structure on Nanostructured Materials Based on Eva

This article reports the preparation of a series of EVA nanocomposites employing solution casting methods using different types of organo-modified montmorillonite clay. The effect of the organoclay type on the structural organization and thermal behavior of EVA nanostructured materials were systematically investigated. Regarding thermal behavior, the thermogravimetric analysis showed that the nanocomposites presented a slight decrease in thermal degradation temperature compared to EVA, while differential scanning calorimetry, in general, did not show a significant change in the thermal transition temperatures such as glass transition, melting temperature and crystallization temperature of the nanocomposites, regardless of the type and proportion of organoclay in the systems. With respect to structural aspect, the X-ray diffractograms showed that all systems presented a heterogeneous distribution of the nanoparticles, containing part intercalated. Nuclear magnetic resonance relaxometry data provided complementary information for the X-ray results, showing that the EVA systems containing 5 wt% of both studied organoclays presented a mixture of intercalated and exfoliated structures, evidencing that there was a surface interaction between polymer chains and clay lamellae.

The Evaluation of Polyethylene/Clay Composite from Solid State NMR

Polymeric nanocomposites based on polyethylene (PE) and Brazilian natural montmorillonite clay (MN) were obtained by melt processing, using a twin-screw extruder. The main objective of this work is focusing on the characterization of composites materials by solid-state nuclear magnetic resonance (NMR). The solid-state NMR measurements were used to observe both polymer matrix (through carbon-13 and hydrogen nuclei) and the clay (silicon-29 and aluminum-27). The polymer matrix analyses were carried out applying solid state techniques, such as: cross-polarization magic angle spinning (CPMAS), variable contact time (VCT) and by the proton spin-lattice relaxation time in the rotating frame parameter (T1ρH), detected from the resolved carbon-13 decay of the VCT experiment and through the determination of spin-lattice relaxation time, T1H (using low field NMR). The clay was analyzed by 29Si and 27Al, employing MAS NMR technique. From those techniques we can have principally response on clay dispersion in the polyethylene matrix, as well as the interactions between both components in the nanostructured material. The T1H response was an important result which showed, that the materials formed, presented different molecular domains (according to the domain size that varied from 25 to 50 nm, measured by relaxation), considering the clay dispersion mode in terms of intercalation and/or exfoliation in the polymer matrix.

Effect of Carbon Fillers in Ultrahigh Molecular Weight Polyethylene Matrix Prepared by Twin-Screw Extrusion

Oxidized (GO) and expanded (G-Exp) graphite were employed to prepare composites with ultrahigh molecular weight polyethylene (UHMWPE) matrix using masterbatches of polyethylene with different compositions. The materials and a blend of UHMWPE/HDPE were prepared by extrusion and their properties were evaluated. The effect of carbon fillers on the crystalline structure, thermo dynamic-mechanical (DMTA) and thermal properties (melting and crystallization temperatures) of the composites were discussed. The thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and wide-angle X-ray diffraction (WAXD) measurements showed that the addition of masterbatch with GO and G-Exp significantly increased the crystallite size of composites, increasing the temperatures of melting, degradation, glass transition and the degree of crystallinity of polyethylene. DMTA analysis indicated the storage and loss moduli of composites in relation to neat UHMWPE, the blend and UHMWPE/composites. SEM micrographs showed a flatter, continuous and uniform surface meaning a compact lamellar structure. The present work resulted in interesting findings on the effects of GO on the crystalline structures, mechanical and thermal properties of UHMWPE, which can lead to generalizations useful for future work.