This work analyzes the morphology and behavior of hybrid composites reinforced with carbon nanotubes (CNTs) and graphene nanoplatelets (GNPs). In order to avoid the weak interface of laminar nanofillers, GNPs were functionalized with amine groups. Different tendencies were observed as a function of the measured property. Storage modulus showed a synergic trend, being the stiffness of hybrid CNT/GNP/epoxy composites higher than the corresponding ones measured in neat epoxy composites reinforced with CNTs or GNPs. In contrast, the thermal and electrical conductivity increased with the nanofiller addition, the final value of the mentioned properties in the hybrid composites was strongly influenced by specific graphitic nanofiller. Neat GNP/epoxy composites showed the highest thermal conductivity, while neat CNT/epoxy composites presented the highest electrical conductivity. This behavior is explained by the observed morphology. All composites exhibited a suitable nanofiller dispersion. However, on hybrid GNP/CNT/epoxy composites, CNTs tend to be placed between nanoplatelets, forming bridges between nanoplatelets. This morphology implies a less effective electrical network, limiting the synergic effect in the properties, which requires percolation. In spite of this, the hybrid GNP/CNT/epoxy composites showed a better combination of properties than the neat composites. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46475.

a b s t r a c tThe glass transition temperature and the crystallization behaviour of poly(ethylene terephthalate) PET ultra-thin layers (a few tens of nm) within multilayered PET/polycarbonate (PC) coextruded films are investigated as a function of layer thickness by means of calorimetric measurements. Results are discussed in terms of reduced thickness and interface effects. The appearance and evolution of lamellar orientation upon isothermal crystallization of ultra-thin PET layers from the glassy state are explored based on real time small-angle X-ray scattering (SAXS) studies. Analysis of the SAXS measurements reveals that finite size effects hamper the crystallization process. However, the final lamellar structure is similar in both, the nanolayered PET and the bulk material. Results suggest that not only lamellar insertion but also some lamellar thickening contribute to the development of the final lamellar structure. Room temperature SAXS and wide-angle X-ray diffraction (WAXS) measurements indicate that two lamellar populations develop: edge-on lamellae are proposed to appear close to the interphases while flat-on lamellae, arising as a consequence of confinement, should be preferentially located in the layers core.

The influence of graphene nanoplatelets (GNPs) on the curing of an epoxy resin based on diglycidyl ether of bisphenol A (DGEBA) and cross-linked with 4,4'-diaminodiphenylmethane (DDM) was studied. Dynamic mechanical properties and tensile properties of the corresponding graphene/epoxy nanocomposites were obtained. Two compositions 1 and 5 mass% of GNPs were studied. The cross-linking reaction of the epoxy resin is accelerated in dispersions with 5 mass% GNPs. In the presence of GNPs, the curing reaction becomes less exothermic, obtaining less perfect epoxy networks compared to neat epoxy (DGEBA-DDM) thermoset. Accordingly, the glass transition temperatures (T g ) of the nanocomposites are lower than that of the neat epoxy thermoset. This effect is not detected for low content of graphene (1 mass%). Protocol of curing having two isothermal steps leads to more perfect networks than the dynamic curing in the DSC. The Tg reduction is minimized in the samples cured through two isothermal steps. The storage moduli of the nanocomposite containing 5 mass% graphene, both in the glassy (T < T g ) and the rubbery (T > T g ) states, are higher than the ones of neat epoxy thermoset, being most pronounced this effect at T > T g . Tensile tests confirmed the higher elastic moduli of the nanocomposites; however, a decrease in strain at break and tensile strength was observed for the nanocomposite containing 5 mass% of GNPs. This brittle behavior is consistent with the morphology of the samples studied by scanning electron microscopy.

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a b s t r a c tThe development of crystalline lamellae in ultra-thin layers of poly(ethylene terephthalate) PET confined between polycarbonate (PC) layers in an alternating assembly is investigated as a function of layer thickness by means of X-ray diffraction methods. Isothermal crystallization from the glassy state is insitu followed by means of small-angle X-ray diffraction. It is found that the reduced size of the PET layers influences the lamellar nanostructure and induces a preferential lamellar orientation. Two lamellar populations, flat-on and edge-on, are found to coexist in a wide range of crystallization temperatures (T c ¼ 117e150 C) and within layer thicknesses down to 35 nm. Flat-on lamellae appear at a reduced crystallization rate with respect to bulk PET giving rise to crystals of similar dimensions separated by larger amorphous regions. In addition, a narrower distribution of lamellar orientations develops when the layer thickness is reduced or the crystallization temperature is raised. In case of edgeon lamellae, crystallization conditions also influence the development of lamellar orientation; however, the latter is little affected by the reduced size of the layers. Results suggest that flat-on lamellae arise as a consequence of spatial confinement and edge-on lamellae could be generated due to the interactions with the PC interface.