A simple method of synthesis of TiO₂ nanotubes (TiNT) loaded with hydroxyapatite (HAP) is described. Such nanotubes find wide applications in various fields, including biomedicine, solar cells, and drug delivery, due to their bioactivity and potential for osseointegration. The Cp-Ti substrate was anodized at a constant voltage of 40 V, with the subsequent heat treatment at 450 °C. The resulting TiNT had a diameter of 100.3 ± 2.8 nm and a length of 3.5 ± 0.04 μm. The best result of the growth rate of HAP in Hanks’ balanced salt solution (Hanks’ BSS) was obtained in calcium glycerophosphate (CG = 0.1 g/L) when precipitates formed on the bottom and walls of the nanotubes. Structural properties, surface wettability, corrosion resistance, and growth rate of HAP as an indicator of the bioactivity of the coating have been studied. X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), potentiodynamic polarization test (PPC), electrochemical impedance spectroscopy (EIS), and contact angle (CA) measurements were used to characterize HAP-loaded nanotubes (HAP-TiNT). The CA, also serving as an indirect indicator of bioactivity, was 30.4 ± 1.1° for the TiNT not containing HAP. The contact angle value for HAP-TiNT produced in 0.1 g/L CG was 18.2 ± 1.2°, and for HAP-TiNT exposed to Hanks’ BSS for 7 days, the CA was 7.2 ± 0.5°. The corrosion studies and measurement of HAP growth rates after a 7-day exposure to Hanks’ BSS confirmed the result that TiNT processed in 0.1 g/L of CG exhibited the most significant capacity for HAP formation compared to the other tested samples.

Titanium-zirconium dioxide nanostructures loaded by hydroxyapatite were produced on the surface of Ti65Zr alloy. The alloy was treated by anodization with the subsequent immersion in calcium glycerophosphate (CG) solutions. The resulting surfaces present TiO₂-ZrO₂ nanotubular (TiZr-NT) structures enriched with hydroxyapatite (HAP). The nanotube texture is expected to enhance the surface’s corrosion resistance and promote integration with bone tissue in dental implants. The TiZr-NT structure had a diameter of 73 ± 2.2 nm and a length of 10.1 ± 0.5 μm. The most favorable result for the growth of HAP in Hanks’ balanced salt solution (Hanks’ BSS) was obtained at a CG concentration of 0.5 g/L. Samples soaked in CG at a concentration of 0.5 g/L demonstrated in a decrease of the contact angles to 25.2°; after 3 days of exposure to Hanks’ BSS, the contact angles further reduced to 18.5°. The corrosion studies also showed that the TiZr-NT structure soaked in the CG = 0.5 g/L solution exhibited the best corrosion stability.

Electro-conductive carbon felt (CF) material is composed by bonding together different lengths of carbon filaments resulting in a porous structure with a significant internal surface that facilitates enhanced electrochemical reactions. Owing to its excellent electrical properties, CF is found in numerous electrochemical applications, such as electrodes in redox flow batteries, fuel cells, and electrochemical desalination apparatus. CF electro-conductivity mostly arises from the close contact between the surface of two electrodes and the long carbon fibers located between them. Electrical conductivity can be improved by a moderate pressing of the CF between conducting electrodes. There exist large amounts of experimental data regarding CF electro-conductivity. However, there is a lack of analytical theoretical models explaining the CF electrical characteristics and the effects of compression. Moreover, CF electrodes in electrochemical cells are immersed in different electrolytes that affect the interconnections of fibers and their contacts with electrodes, which in turn influence conductivity. In this paper, we investigated both the role of CF compression, as well as the impact of electrolyte characteristics on electro-conductivity. The article presents results of measurements, mathematical analysis of CF electrical properties, and a theoretical analytical explanation of the CF electrical conductivity which was done by a stochastic description of carbon filaments disposition inside a CF frame.

Electroconductive carbon felt (CF) material, having a permeable structure and significant electroconductive surface, is widely used for electrodes in numerous electrochemical applications such as redox flow batteries, fuel cells, electrochemical desalination apparatus, etc. The internal structure of CF is composed of different lengths of carbon filaments bonded together. This structure creates a large number of stochastically oriented and stochastically linked channels that have different lengths and cross sections. Therefore, the CF hydraulic permeability is similar to that of porous media and is determined by the internal empty volume and arrangement of carbon fibers. Its electroconductivity is ensured by the conductivity of the carbon filaments and by the electrical interconnections between fibers. Both of these properties (permeability and electrical conductivity) are extremely important for the efficient functioning of electrochemical devices. However, their influences counter each other during CF compressing. Increasing the stress on a felt element provides supplementary electrical contacts of carbon filaments, which lead to improved electrical conductivity. Thus, the active surface of the felt electrode is increased, which also boosts redox chemical reactions. On the other hand, compressed felt possesses reduced hydrodynamic permeability as a result of a diminished free volume of porous media and intrinsic channels. This causes increasing hydrodynamic expenditures of electrolyte pumping through electrodes and lessened cell (battery) efficiency. The designer of specific electrochemical systems has to take into account both of these properties when selecting the optimal construction for a cell. This article presents the results of measurements and novel approximating expressions of electrical and hydraulic characteristics of a CF during its compression. Since electrical conductivity plays a determining role in providing electrochemical reactions, it was measured in dry conditions and when the CF was immersed in several non-conductive liquids. The choice of such liquids prevented side effects of electrolyte ionic conductivity impact on electrical resistivity of the CF. This gave an opportunity to determine the influences of dielectric parameters of electrolytes to increase or decrease the density of interconnectivity of carbon fibers either between themselves or between them and electrodes. The experiments showed the influence of liquid permittivity on the conductivity of CF, probably by changing the density of fiber interconnections inside the felt.

Different surfaces were obtained by Plasma Electrolytic Oxidation (PEO) of the Ti–6Al–4V alloy; followed by hydrothermal treatment (HT). The surfaces were studied by scanning electron microscopy (SEM); Energy Dispersive Spectroscopy (EDS); X-ray Diffraction (XRD); Brunauer–Emmett–Teller (BET) absorption and abrasion wear tests. The resulting surface contains hydroxyapatite (HA); which contributes to superior implant osseointegration. Treated implants were introduced into rabbits and their osseointegration was studied after two and six months. It was established that implant surface area increases due to pore formation. Pore formation and hydroxyapatite on the surface of the implant qualitatively change contact osseogenesis processes with reduced duration of osseointegration of implants. The treatment of the surface of the implants by the combination of PEO and HT provided better results in the medico-biological investigations than PEO alone. Abrasion tests demonstrated that the HA will be preserved after the procedure of implantation; ensuring effective osseointegration.