In this article, the effectiveness of the co-mixing processing technique and surface modification of zinc oxide (ZnO) filler on the characteristics of the developed high-density polyethylene (HDPE)/ZnO was investigated. ZnO was treated and co-mixed with stearic acid (SA) at a ratio of 50/50 wt% using kitchen coffee grinder and the mixture was then added to the HDPE matrix in a Brabender plastograph with various ZnO contents of 0.5, 1 and 2 wt%. The morphology of the nanocomposites was characterized using scanning electron microscopy (SEM). The micrographs showed well and uniform dispersion of both treated and untreated ZnO nanofiller; however, the treated ZnO particles showed better dispersion. The nanocomposite containing 1 wt% ZnO nanoparticles was found to have the optimal properties. The results of the SEM were supported by the atomic force microscopic technique. The uniform dispersion of ZnO was further investigated through X-ray diffraction spectra. The minor peaks of ZnO in the HDPE/treated and untreated ZnO nanocomposites are considered as an evidence for the presence of uniform and well-dispersed ZnO. The electrical conductivity of the nanocomposite samples is higher than that of neat HDPE due to the semiconducting nature of ZnO and increases with ZnO content. The results of this work proved that dispersibility can be achieved through the addition of SA and conductivity of the nanocomposite depends on the ZnO content. Moreover, co-mixing technique and the surface modification of the nanofillers are very effective in producing the HDPE/ZnO nanocomposites that have many potential industrial applications such as food packaging, drug and pharmaceutical bottles.

Reversibly crosslinked isotactic polypropylene (iPP) was prepared in the presence of dicumyl peroxide. The effects of the peroxide oxy-radicals in the melt were investigated in relation to the modification of the polymer. The dynamic rheology analysis of the crosslinking process was carried out by using a plastograph. The crosslinking reaction was evaluated by the Monsanto method. The resulting structure of the modified samples was studied by means of differential scanning calorimetry (DSC), wide-angle X-ray scattering (WAXS), microhardness, and mechanical properties. The degree of crystallinity of the modified iPP, derived from DSC and WAXS, remains almost unchanged, i.e., the crystalline structure is unaffected, though the lamellar thickness slightly decreases. The impact strength of the crosslinked iPP is greatly improved with reference to that of the unmodified material. A transition from brittle to ductile behavior appears in the modified iPP for all the crosslinking agents studied.

ABSTRACT:The effects of two compatibilizing agents, polystyrene-poly(ethylene butylene)-polystyrene copolymer (SEBS) and SEBS-grafted maleic anhydride (SEBS-g-MAH), on the morphology of binary and ternary blends of polyethylene, polypropylene, and polyamide 6,6 were investigated with scanning electron microscopy and melt rheology measurements. The addition of the compatibilizers led to finer dispersions of the particles of the minor component and a decrease in their size; this induced a significant change in the blend morphology. The rheological measurements confirmed the increased interaction between the blend components, especially with SEBS-g-MAH as the compatibilizer. New covalent bonds could be expected to form through an amine-anhydride reaction.

Recent developments concerning the methodology used to prepare composites of iPP and nanoclays are reported. Conventional (reactive melt mixing) and in situ preparations were performed, and the structural properties exhibited by the composites are discussed. Results suggest that the nanoclay could exhibit partial and, maybe, total exfoliation within the composites. Adhesion between the polymeric matrix and the nanoclay layers is similar to that obtained after grafting. The experimental procedure used and the analysis performed by means of the wide-angle X-ray scattering and differential scanning calorimetry techniques permit to describe, at nanoscale level, the contribution of the nanoclay to the polymer composite system. The microhardness values of the iPP-clay composites depend on the clay content and on the preparation method, and linearly correlate, according to the additivity law, with the degree of crystallinity.

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Mechanical property changes, thermal stability, and water absorption capacity of poly(vinyl chloride) (PVC)/sisal fiber composites were assessed with respect to the effect of maleic anhydride chemical treatments of the sisal fiber, for five different sisal fiber contents, varying from 0 to 30% by weight in the composite. The composites prepared with the untreated sisal exhibited higher tensile modulus and hardness than the unloaded resin, while elongation and tensile strength were reduced. The deterioration in the mechanical properties of PVC blended with sisal fiber is attributed to the presence of moisture, interfacial defects at the fiber and polymer interface, and fiber dispersion in the PVC matrix. The amount of absorbed water is a function of the amount of fiber in the composite (F0 ¼ 0 phr, F5 ¼ 0.77 phr, and F20 ¼ 4.83 phr). The comparison of the results of characterization of F5, F20, and F30 formulations prepared with the untreated fibers and the treated ones showed a reduction in absorbed water after the chemical treatment of fiber with maleic anhydride (F0 ¼ 0 phr, F5 ¼ 0.28 phr, and F20 ¼ 2.99 phr), thus improving the mechanical properties of composites prepared with the treated sisal.

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