Poly(lactic acid) (PLA)-rich poly(lactic acid)/poly(e-caprolactone) (PLA/PCL) blends were melt-blended at different compositions. The compositions such as 90/10 and 80/20 were obtained using three different blending methods and processed by injection molding and hot pressing. All blends were immiscible. The crystallinity of PLA increased slightly in the presence of poly(ecaprolactone) (PCL), and the PCL exhibited fractionated crystallization in the presence of PLA. Injection molded specimens, compared with hot pressed specimens, presented much smaller PCL particles regardless of the blending method used. Some interfacial adhesion was observed in all cases. The stiffness of PLA/PCL blends decreased as the PCL content was increased and was independent of processing. Injection molded specimens showed ductile behavior and broke at elongation values close to 140%, while the elongation at break of the hot pressed specimens was clearly lower, most likely due to the larger size of the PCL particles. Although the impact strength of the blends remained low, it improved by approximately 200% with 30% PCL and by 350% with 40% PCL. V C 2015Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 42641.

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There is need for developing novel conductive polymers for Digital Light Processing (DLP) 3D printing. In this work, photorheology, in combination with Jacobs working curves, efficaciously predict the printability of polyaniline (PANI)/acrylate formulations with different contents of PANI and photoinitiator. The adjustment of the layer thickness according to cure depth values (Cd) allows printing of most formulations, except those with the highest gel point times determined by photorheology. In the working conditions, the maximum amount of PANI embedded within the resin was ≃3 wt% with a conductivity of 10−5 S cm−1, three orders of magnitude higher than the pure resin. Higher PANI loadings hinder printing quality without improving electrical conductivity. The optimal photoinitiator concentration was found between 6 and 7 wt%. The mechanical properties of the acrylic matrix are maintained in the composites, confirming the viability of these simple, low-cost, conductive composites for applications in flexible electronic devices.

Bio-based polymeric nanocomposites (NCs) with enhanced electrical conductivity and rigidity were obtained by adding multi-walled carbon nanotubes (CNTs) to a commercial bio-based polyamide 4,10 (PA410). Two different types of commercial CNTs (Cheap Tubes and Nanocyl NC7000 TM ) and two different preparation methods (using CNTs in powder form and a PA6-based masterbatch, respectively) were used to obtain melt-mixed PA410/CNT NCs. The effect of the preparation method as well as the degree of dispersion and aspect ratio of the CNTs on the electrical and mechanical properties of the processed NCs was studied. Superior electrical and mechanical behavior was observed in the Nanocyl CNTs-based NCs due to the enhanced dispersion and higher aspect ratio of the nanotubes. A much more significant reduction in aspect ratio was observed in the Cheap Tubes CNTs than in the Nanocyl CNTs. This was attributed to the fact that the shear stress applied during melt processing reduced the length of the CNTs to similar lengths in all cases, which pointed to the diameter of the CNTs as the key factor determing the properties of the NCs. The PA6 in the ternary PA410/PA6/CNT system led to improved Young's modulus values because the reinforcing effect of CNTs was greater in PA6 than in PA410.