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.
In this study, a poly (lactic acid)/hydroxyapatite (PLA/HAp) porous nanocomposite was fabricated by melt mixing method. Polyethylene oxide (PEO) was added into the nanocomposite to improve compatibility of HAp in the PLA matrix. A porous structure of the nanocomposite was created by using a salt (NaCl) which leaches in water. The influence of HAp's weight, compatibiliser content of porous agent on morphology and mechanical properties of PLA/HAp nanocomposite was investigated by SEM and tensile testing method. The obtained results indicated that the nanocomposite
Here we report a facile approach to enhance the dispersibility of ethylene vinyl acetate copolymer (EVA)/silica nanocomposites (for the EVA/silica nanocomposites and interaction between silica nanoparticles (nanosilica) and EVA by adding EVA-g-acrylic acid (EVAgAA) as a compatibilizer, which was formed by grafting acrylic acid onto EVA chains with the aid of dicumyl peroxide). The above nanocomposites with and without EVAgAA were prepared by melt mixing in a Haake intermixer with different contents of silica and EVAgAA. Their structure and morphology were characterized by Fourier transform infra-red (FT-IR) spectroscopy, field emission scanning electron microscopy (FE-SEM), and the mechanical, rheological, dielectrical, and flammability properties of the nanocomposites were also investigated. The FT-IR spectra of the nanocomposites confirmed the formation of hydrogen bonds between the surface silanol groups of nanosilica and C=O groups of EVA and/or EVAgAA. The presence of EVAgAA remarkably increased the intensity of hydrogen bonding between nanosilica and EVA which not only enhanced the dispersion of nanosilica in EVA matrix but also increased the mechanical, viscosity and storage modulus of EVA/silica nanocomposites. In addition, the flammability of EVA/silica nanocomposites is also significantly reduced after the functionalization with EVAgAA. However, the mechanical properties of EVA/silica nanocomposites tended to level off when its content was above 1.5 wt.%. It has also been found that the dielectric constant value of the EVA/EVAgAA/silica nanocomposites is much lower than that of the EVA/silica nanocomposites, which is another evidence of the hydrogen bonding formation between EVAgAA and nanosilica.
We report on the fabrication and the electrochemical behavior of TiN film on the 316L stainless steel (316LSS) material in simulated body fluid (SBF) solution for implant application. The characterization results indicate that the coated TiN is completely crystalline with (111) crystal orientation. Electrochemical results of 316LSS and TiN/316LSS material after 21 days of immersion in SBF show that the durability of the TiN/316LSS is much higher than that of 316LSS, which registers a very low corrosion current density (about tens of nA cm(-2)). The formation of hydroxyapatite on the surface of the TiN/316LSS is also confirmed by SEM, EDX, X-ray and IR spectroscopy.
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