On growth and morphology of tio2 nanotubes on ti6al4v by anodic oxidation in ethylene glycol electrolyte: Influence of microstructure and anodization parameters

Different studies demonstrated the possibility to produce TiO2 nanotubes (TNTs) on Ti6Al4V alloy by electrochemical anodization. However, the anodizing behavior of \u3b1 and \u3b2-phases in organic electrolytes is not yet clarified. This study reports on the anodizing behavior of the two phases in an ethylene glycol electrolyte using different applied potentials and anodizing times. Atomic force and scanning electron microscopies were used to highlight the anodic oxides differences in morphology. It was demonstrated that the initial compact oxide grew faster over the \u3b2-phase as the higher Al content of the \u3b1-phase caused its re-passivation, and the higher solubility of the V-rich oxide led to earlier pores formation over the \u3b2-phase. The trend was inverted once the pores formed over the compact oxide of the \u3b1-phase. The growth rate of the \u3b1-phase TNTs was higher than that of the \u3b2-phase ones, leading to the formation of long and well defined nanotubes with thin walls and a honeycomb tubular structure, while the ones grown over the \u3b2-phase were individual, shorter, and with thicker walls

Monolayered versus multilayered electroless NiP coatings: Impact of the plating approach on the microstructure, mechanical and corrosion properties of the coatings

Electroless nickel-phosphorous (NiP) coatings were produced on low carbon steel substrates for a total plating time of 3\u202fh. Different preparation modalities were pursued. Multilayered coatings were produced by stacking three layers of the same composition by successive electroless plating with rinsing steps in between. On the other hand, coatings termed \u2018monolayered\u2019 for the sake of comparison were deposited by one step electroless process, with and without undergoing bath replenishment of the electrolyte during plating. All the samples were subjected to thermal annealing at 400\u202f\ub0C for 1\u202fh under argon atmosphere. The results show that the multilayer approach prevents crack propagation in the as-deposited coatings because the interfaces between layers block the advance of defects. Bath replenishment during monolayered coatings production creates pseudo-interfaces similar to those of the multilayered case but they are ineffective in terms of corrosion protection. Un-replenishment of the electrolyte promotes a change in the coating's microstructure from lamellar to columnar which severely worsens their performance. Upon annealing, the presence of interfaces, along with the recrystallization of the metallic matrix, promotes an upgrading of the corrosion performance of the multi-layered coatings. The corrosion products spread laterally at the interface where they stockpile. At a certain point, the accumulation of these by-products provokes the exfoliation of the outermost layer exposing the layer underneath to the corrosive media, thereby delaying the advancement of the corrosion attack. The results of this study highlight the importance of the plating approach selection, as well as the need for proper electrolyte maintenance during the production of high-performance electroless coatings

Effect of hydrogen peroxide on bovine serum albumin adsorption on Ti6Al4V alloy: A scanning Kelvin probe force microscopy study

Abstract Protein adsorption on the surface of implant materials greatly affects the performance of the implants, such as their stability as well as the release of metal ions from and the adhesion of cells to their surface. In addition, the production of extracellular H2O2 from the activation of inflammatory cells could interfere with protein–metal interactions and/or modify the conformation of adsorbed proteins. In this study, we utilised scanning Kelvin probe force microscopy (SKPFM) to visualise the impact of H2O2 on bovine serum albumin (BSA) adsorption on the positively polarised Ti6Al4V alloy in a phosphate-buffered saline (PBS) solution. We show that the negatively charged BSA adsorbs onto the surface of polished and anodically polarised Ti6Al4V in a dense layer with a continuous network-like morphology or cluster shape and reduces the variation in the total surface potential compared to that of blank Ti6Al4V. However, addition of H2O2 to the PBS solution interferes with the formation of the dense protein network, and only a thin and discontinuous protein layer adsorbs onto the surface of the Ti6Al4V alloy, lowering the total surface potential difference. The information presented in this work provides new insights into the adsorption distribution of proteins on metallic substrates in biomaterials field

Electronic properties and surface potential evaluations at the protein nano-biofilm/oxide interface: Impact on corrosion and biodegradation

The formation of a protein nano-biofilm, which exhibits a special electronic behavior, on the surface of metals or oxide biomaterials considerably influences the crucial subsequent interactions, particularly the corrosion and biodegradation processes. This study discusses the impact of electrical surface potential (ESP) of a single or nano-biofilm of albumin protein on the electrochemical interactions and electronic property evolutions (e.g., charge carriers, space charge capacitance (SCC), and band bending) occurring on the surface oxide of CoCrMo implants. Scanning Kelvin probe force microscopy (SKPFM) results indicated that ESP or surface charge distribution on a single or nano-biofilm of the albumin protein is lower than that of a CoCrMo complex oxide layer, which hinders the charge transfer at the protein/electrolyte interface. Using a complementary approach, which involved performing Mott-Schottky analysis at the electrolyte/protein/oxide interface, it was revealed that the albumin protein significantly increases the SCC magnitude and number of n-type charge carrier owing to increased band bending at the SCC/protein interface; this facilitated the acceleration of metal ion release and metal-protein complex formation. The nanoscale SKPFM and electrochemical analyses performed in this study provide a better understanding of the role of protein molecules in corrosion/biodegradation of metallic biomaterials at the protein nano-biofilm/oxide interface

Albumin Protein Adsorption on CoCrMo Implant Alloy: Impact on the Corrosion Behaviour at Localized Scale

The protein adsorption and both its conformational arrangements and electrochemical interactions on the surface of metallic biomaterials has an immense impact on corrosion/biodegradation and biocompatibility of implantable metals. In this study, we used scanning Kelvin probe force microscopy (SKPFM) to reveal the synergistic effect of various bovine serum albumin (BSA) concentrations and overpotential conditions on BSA protein adsorption mechanisms and its influence on the corrosion behaviour of the CoCrMo alloy in phosphate-buffered saline solution. Electrochemical measurements showed that CoCrMo alloy was more resistant to corrosion in the 2 g l-1 BSA protein medium than in the 0.5 g l-1 one. The SKPFM analysis revealed a lower surface potential on the regions where BSA was adsorbed forming clusters, than on the un-covered CoCrMo substrate. When the surface overpotential and the protein concentration were increased from the OCP to +300 mV vs Ag/AgCl and from 0.5 to 2 g l-1, respectively, on both protein covering and surface potential were increased. Field emission scanning electron microscopy indicated that localized corrosion eventually occurred at the BSA protein/substrate interface owing to the adsorption of counterions and the difference between the surface potential values

Heat treatments hardening effect on Ni\u2013Al composite electrodeposits

Pure Ni galvanic coatings show good mechanical properties at room temperature but exhibit a progressive decrease by increasing the temperature due to the recrystallisation. A possible solution to hinder the recrystallisation is the co-electrodeposition of metal particles which could lead to the formation at high temperature of Ni alloy coatings with higher mechanical properties. Ni matrix composite deposits containing either micro (4\u2005\u3bcm) or nano (130\u2005nm) particles of Al were produced in a parallel plate geometry. The deposits were characterised regarding their microstructure both prior and after heat treatments for 3\u2005h at 400, 600 and 800\ub0C in order to evaluate the formation of Ni/Al phases. This work focused on the evaluation of the hardness on coatings cross-section by means of Vickers microhardness and Berkovich nano-indentation mapping. The results obtained with the two methods have been compared and correlated to the microstructural modifications in order to understand the hardening mechanisms. \ua9 2018 Institute of Materials, Minerals and Mining Published by Taylor & Francis on behalf of the Institut