Abstract.Microwave devulcanization is known to be a promising and an efficient rubber recycling method which makes possible for the rubber to regain its fluidity, and makes it capable of being remolded and revulcanized. The focus of this work is to understand the physical and chemical changes that occur in the ground tire rubber after different microwave exposure periods. For this purpose chemical, thermal, rheological and morphological analyses were performed on the tire rubber, which contains natural rubber (NR) and styrene-butadiene rubber (SBR) as polymeric material. The results showed that the microwave treatment promoted the breaking of sulfur cross-links and consequently increased the rubber fluidity. However, long periods of exposure led to degradation and modification of some properties. At nanoscale, the deformation of the devulcanized NR domain under stress was observed, and the morphology obtained appears to be a droplet dispersion morphology. The most exposed samples presented only one glass transition temperature, and from this it was concluded that the treatment may have played an important role in the compatibilization of the elastomeric blend. Based on the results, it is required to control the microwave exposure time and polymeric degradation in order to achieve a regenerated rubber with satisfactory properties.

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Nanocomposites of cellulose acetate and an organically modified montmorillonite (CA/MMTO) were prepared by melt intercalation in a twin‐screw extruder, using two different plasticizers: di‐octyl phthalate (DOP) and triethyl citrate (TEC). The influence of plasticizer type and the organoclay added to the structure, the morphology, and the thermal properties of the nanocomposites was investigated. XRD and SAXS results indicated a significant CA or/and plasticizer intercalation in the clay gallery for the CA/MMTO nanocomposites. In addition, the images obtained by TEM show that the morphology of CA/MMTO nanocomposites is made up of intercalated and exfoliated silicate layers. The glass transition temperature (Tg) of CA with DOP or TEC decreased in at almost same value, which shows the characteristics of both additives as plasticizers for cellulose acetate chains. Tensile tests indicate that the nanocomposites with either of the two plasticizers presented the same performance with respect to material properties. The results demonstrated that, for some applications, TEC is an useful alternative to plasticize CA in order to substitute DOP, a non eco‐friendly plasticizer. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011

The aim of this work is to investigate the degradation of low molar mass poly(ethylene terephthalate) (PET)/organically modified montmorillonite (OMMT) clay nanocomposites prepared by melt processing. The rheological behavior in combination with transmission electron microscopic images suggests an intercalation and therefore a percolating network. Furthermore, the results indicate that the increase of organoclay content caused a degradation of PET during processing of PET/OMMT nanocomposites, once it was observed the PET molar mass decreases. The effect mentioned could be attributed to an increase of Brønsted acidic sites on the platelet surface, which is produced by the Hofmann elimination reaction of ammonium, and also the presence of residual metal compounds on clay surface might possibly favored the polymer matrix degradation process.