Silica/polypyrrole nanocomposites without dopant (SiO2/PPy) and with oxalate dopant (SiO2/PPyOx) were synthesized using polymerization of pyrrole in the presence of nano SiO2. Synthesized SiO2/PPy and SiO2/PPyOx were characterized by FTIR, SEM, TEM and EDX and their electrical conductivities were determined by CV method through the two-point-electrode without electrolyte. The corrosion protection performance of polyvinylbutyral (PVB) coatings containing SiO2/PPyOx was evaluated and compared with that of pure PVB coatings and of PVB coatings containing SiO2/PPy by electrochemical impedance spectroscopy and adhesion measurement. The results show that electrical conductivities of SiO2/PPy and SiO2/PPyOx were 0.181 and 0.109 S/cm, respectively. The ratio of PPy on SiO2 in SiO2/PPy and SiO2/PPyOx composites was 0.77/1 and the ratio of oxalate on PPy in SiO2/PPyOx composite was 1.24/1. SiO2/PPy and SiO2/PPyOx improved corrosion resistance and adhesion of PVB coatings. The presence of oxalate in SiO2/PPyOx significantly enhanced the effect of SiO2/PPy on the protection performance of PVB coatings.
The deposition of TiN on stainless steel substrates may improve the stability and compatibility of this material with bone, which may be advantageously exploited for the elaboration of advanced pros- thetic devices. In this work, TiN-coated 316LSS (by way of DC magnetron sputtering) was used as a starting material for investigating the electrochemical post-deposition of hydroxyapatite (HAp) which has a composition close to that of bone. Electrodeposition was carried out starting from an aqueous medium containing solubilized Ca(NO3)2 and NH4H2PO4 in the presence of H2O2. We report the influence of experimental conditions on the morphology of the obtained HAp coating on TiN/316LSS. The effect of applied potential, temperature, H2O2 concentration, pH and duration of reaction were thoroughly discussed on the basis of X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier Transform Infrared (FTIR) spectroscopy and Energy Dispersive X-ray Spectroscopy (EDX) results. This method appears advantageous for producing HAp-coated implant materials.
Reduced graphene oxide (rGO) were prepared by thermal reduction technique from graphene oxide (GO) in N 2 gas atmosphere at 600 o C for 1 h. The results shown that rGO possessed a multiple layer structure and a specific surface area BET of 389.9 m 2 /g. The electrochemical properties of the rGO materials have been investigated for supercapacitors. Electrochemical measurements show that rGO exhibit a specific capacitance of 85.3 F/g at 1 A/g, and still kept 85 % capacitance after 1000 cycles at 1 A/g, indicating rGO could be a promising candidate for highperformance supercapacitor applications.
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