Influence of compatibilizer on the properties of low-density polyethylene/polyamide 6 blends obtained by mechanical recycling of multilayer film waste.

Polymeric wastes have caused increasing environmental problems, mainly in oceans that accumulate large amounts of non-degradable plastic waste. Particularly, waste of polymeric multilayer films for packaging presents low interest for mechanical recycling due to the poor properties and low commercial value of the recycled material generated as polymeric blends. Multilayer films of low-density polyethylene (LDPE) and polyamide 6 (PA6) is a typical material used for packaging applications. The aim of this study was to evaluate the action of the concentration of maleic anhydride grafted polyethylene (PE- g-MA) on the compatibilization of LDPE/PA6 blends generated from mechanical recycling of multilayer films containing both polymers. The action of the PE- g-MA on the properties of the LDPE/PA6 blends was evaluated by tensile tests, optical microscopy, melt flow rate, and scanning electron microscopy. The use of PE- g-MA at 2.5 wt% as a compatibilizer during reactive extrusion of the multilayer films waste has showed the best result for production of the respective recycled LDPE/PA6 blends.

Organoclay nanocomposites of post-industrial waste poly(butylene terephthalate) from automotive parts.

Polymeric nanocomposites are novel materials of huge interest owing to their favourable cost/performance ratio with low amount of nanofillers, improved thermal resistance, flame retardancy and mechanical properties in relation to their matrices. In this work, composites based on post-industrial waste or primary recycled poly(butylene terephthalate) and 5 wt.% of organic modified montmorillonite clays were melt compounded using a twin-screw extruder. A 2(2) factorial experimental design was used to study the compounding and processing variables: Organic modified montmorillonite with one or two hydrogenated tallow (initial basal spacing) and screw speed of the extruder. X-ray diffraction and transmission electron microscopy suggest that a partial exfoliation of the organoclay in the recycled poly(butylene terephthalate) matrix was achieved for organic modified montmorillonite with lower initial basal spacing. On the other hand, formulations containing organic modified montmorillonite with higher initial basal spacing showed only intercalated structure. The recycled poly(butylene terephthalate)-organic modified montmorillonite nanocomposites did not drip flaming material during burning tests. Storage of dynamic-mechanical, tensile and flexural moduli of the recycled poly(butylene terephthalate)-organic modified montmorillonite were improved when compared with both virgin and recycled poly(butylene terephthalate)s, mainly for nanocomposites formulated at a lower initial basal spacing organoclay. This could be related to a better diffusion of polymer into organic modified montmorillonite layers compared with the higher initial basal spacing organoclay. The improvements on the physical properties of recycled poly(butylene terephthalate) showed the feasibility to add value to primary recycled engineering thermoplastics with a very small amount of organic modified montmorillonite.