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In an effort to obtain porous scaffolds with improved mechanical properties and biocompatibility, the current study discusses nanocomposite materials based on poly(propylene fumarate)/N-vinyl pyrrolidone(PPF/NVP) networks reinforced with polymer-modified graphene oxide (GO@PPF). The GO@PPF nanofiller was synthesized through a facile and convenient surface esterification reaction, and the successful functionalization was demonstrated by complementary techniques such as FT-IR, XPS, TGA and TEM. The PPF/NVP/GO@PPF porous scaffolds obtained using NaCl as a porogen were further characterized in terms of morphology, mechanical properties, sol fraction, and in vitro degradability. SEM and nanoCT examinations of NaCl-leached samples revealed networks of interconnected pores, fairly uniform in size and shape. We show that the incorporation of GO@PPF in the polymer matrix leads to a significant enhancement in the mechanical properties, which we attribute to the formation of denser and more homogenous networks, as suggested by a decreased sol fraction for the scaffolds containing a higher amount of GO@PPF. Moreover, the surface of mineralized PPF/NVP/GO@PPG scaffolds is uniformly covered in hydroxyapatite-like crystals having a morphology and Ca/P ratio similar to bone tissue. Furthermore, the preliminary biocompatibility assessment revealed a good interaction between PPF/PVP/GO@PPF scaffolds and murine pre-osteoblasts in terms of cell viability and proliferation. [ABSTRACT FROM AUTHOR]

In order to estimate electro-optical response times, measurements of the transmitted light intensity through positive uniaxial nematic thin films in planar alignment have been performed. Very fast relaxation times were experimentally found for nematic samples aligned with conductive polymers, namely, polypyrrole doped with 5 types of anions having different molecular sizes and geometries. Using undoped polypyrrole alignment layers, slower electro-optical responses were obtained. Given that the improvement in the relaxation times is induced by the presence of the anions in the polypyrrole films, the increasing of the total restoring torque of the nematic molecules to the confining surfaces-responsible for the short relaxation times-is related to the charges accumulated at the nematic-conductive polymer interface. [ABSTRACT FROM AUTHOR]

The composites based on carbon nanotubes (CNTs) and conducting polymers (CPs) are promising materials for supercapacitor devices due to their unique nanostructure that combines the large pseudocapacitance of the CPs with the fast charging/discharging double-layer capacitance and excellentmechanical properties of the CNTs. Here, we report a new electrochemical method to obtain polypyrrole (PPY)/single-walled carbon nanotube (SWCNT) composites. In the first step, the SWCNTs are covalently functionalized with monomeric units of pyrrole by esterification of acyl chloride functionalized SWCNTs and N-(6-hydroxyhexyl)pyrrole. In the second step, the PPY/SWCNTs composites are obtained by copolymerizing the pyrrole monomer with the pyrrole units grafted on SWCNTs surface using controlled potential electrolysis. The composites were further characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The results showed good electrochemical charge storage properties for the synthesized composites based on PPY and SWCNTs covalently functionalized with pyrrole units making them promising electrode materials for high power supercapacitors. [ABSTRACT FROM AUTHOR]