In the present study the adsorption of Reactive Blue 19 dye on the hydroxyapatite (HAp) nanopowders was investigated. The batch adsorption experiments were performed by monitoring the adsorbent dosage, contact time, dye solution concentration, pH and temperature. At pH 3 and 20°C, high dye removal rates of about 95.58% and 86.95% for the uncalcined and calcined nanohydroxyapatites, respectively, were obtained. The kinetic studies indicated the dye adsorption onto nanohydroxyapatite samples to follow a pseudo-second order model. The Langmuir isotherm was found to be the best to represent the equilibrium with experimental data. The maximum adsorption capacity of uncalcined and calcined nanohydroxyapatite samples has been found to be 90.09 mg/g and 74.97 mg/g, respectively.

Biocompatible coatings produced on the basis of the chemically extracted natural hydroxyapatite (HAp) from the animal bones were deposited using multiplex method comprising glow discharge nitriding (GDN) of the titanium alloy substrate and pulsed laser deposition (PLD) of HAp on the formerly fabricated titanium nitride layer (TiN). The TiN interlayer plays an important role improving adhesion of HAp to substrate and preserves the direct contact of the tissue with metallic substrate in the case of possible cracking of HAp coating. Surface morphology of deposited layers, crystallographic texture and residual stress were studied in relation to the type of laser applied to ablation (Nd:YAG or ArF excimer), laser repetition, temperature of substrate and atmosphere in the reactive chamber.

Generally, the metallic implants do not exhibit any bio-integration properties in contact with bone tissues. To improve the interfacial properties of metallic implants in contact with bone, the coatings with thin biocompatible films are used. Two methods to coating titanium implants with hydroxyapatite are described. The first is a two phase method, where by cathodic polarization is deposed a monetite film followed by an alkaline treatment when the monetite is converted to hydroxyapatite. The second method is a biomimetic deposition on an alkaline activate titanium surface, using a five time more concentrated simulated body fluid (5xSBF). After deposition this samples was drying at 120℃ and was sintered at 700℃ for three hours. Optical microscopy, Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM) and Energy-dispersive X-ray (EDX) were used to characterize structure, morphology and compositions of the deposed films. In this study, electrochemical deposition and biomimetic deposition of hydroxyapatite are compared.

In order to enhance bioactive properties of titanium 99.2 used in implantology and various biomedical applications, numerous methods to form tight oxide coatings are being investigated. Some of these interesting techniques for generating TiO2 coatings include: electrochemical methods with anodizing, electric discharge treatment, plasma methods (PVD) and diffusive methods (i.e. oxidation in a fluidized bed). Each method aims to create a thin homogenous oxide coating characterized with thermal stability and repassivation ability in the presence of body fluid environment. However, new methods are still sought for increasing the biocompatibility of the substrate following a change in the intensity of depositing on the oxide coating compounds with high biocompatibility with body tissues, including hydroxyapatite, which constitutes the basis for subsequent osseointegration processes. The article presents investigation of HAp formation on titanium substrate surface after hybrid oxidation process. Hybrid surface treatments combine methods of fluidized bed atmospheric diffusive treatment FADT with the PVD surface treatment realized with different parameters (FADT – 640°C / 8h and PVD – magnetron sputtering with TiO2 target). In order to investigate the effects of hybrid oxidation and the formation of HAp molecules, SEM-EDS, SEM-EBSD, STEM-EDS, RS, nanoindentation and Kokubo bioactivity tests (c-SBF2) were carried out. The hybrid method of titanium oxidation, proposed by the Author, presents a new outlook on the modification and development of the properties of oxide coatings in the area of biomedical applications. Combining the ways of Ti Grade 2 oxidation in the hybrid method highly improves the formation of hydroxyapatite compounds and shows the potential of applying such a technique in implantology, where the intensive growth of bone tissues is crucial.

Because of excellent properties, similar to natural bone minerals, and variety of possible biomedical applications, hydroxyapatite (HAp) is a valuable compound among the calcium phosphate salts. A number of synthesis routes for producing HAp powders have been reported. Despite this fact, it is important to develop new methods providing precise control over the reaction and having potential to scale-up. The main motivation for the current paper is a view of continuous synthesis methods toward medical application of produced hydroxyapatite, especially in the form of nanoparticles.

Hydroxyapatite (HAp) has been attracting widespread interest in medical applications. In a form of coating, it enables to create a durable bond between an implant and surrounding bone tissues. With addition of silver nanoparticles HAp should also provide antibacterial activity. The aim of this research was to evaluate the composition of hydroxyapatite with silver nanoparticles in a non-destructive and non-contact way. For control measurements of HAp molecular composition and solvent evaporation efficiency the Raman spectroscopy has been chosen. In order to evaluate dispersion and concentration of the silver nanoparticles inside the hydroxyapatite matrix, the optical coherence tomography (OCT) has been used. Five samples were developed and examined ‒ a reference sample of pure HAp sol and four samples of HAp colloids with different silver nanoparticle solution volume ratios. The Raman spectra for each solution have been obtained and analyzed. Furthermore, a transverse-sectional visualization of every sample has been created and examined by means of OCT.

In this study, Hydroxyapatite (HAp) is extracted from the Rihu fish scales which are generally dumped as garbage. The aluminium composite was fabricated through the powder metallurgy technique by reinforcing HAp (0, 5, 10 and 15 wt%) as a reinforcement. The fabricated samples were sintered through microwave sintering at 530℃ for 15 min under an argon gas environment. The fabricated composites were subjected to X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS) analysis to confirm the constituting elements and to describe the reinforcement dispersion in the matrix. Uniform reinforcement dispersion was observed for the composite reinforces with 5%HAp, 10%HAp particles. The mechanical characterization results reveal that the Al-10% HAp composite exhibits a microhardness value of 123 ± 3 Hv and maximum ultimate tensile strength of 263 ± 10 MPa and 299 ± 9 MPa compression strength was obtained due to the presence of a strong bond among the aluminium and HAp particles.

In the present work, Hydroxyapatite synthesis was carried out using hydrothermal method with calcium nitrate tetrahydrate (Ca(NO ₃) ₂.4H ₂O) and fosfor pentaoksit (P ₂O ₅) as precursors. For the hydrothermal method, constant reaction temperature (180°C) and different reaction times (6 hours, 12 hours, 18 hours and 24 hours) were determined. The samples produced were divided into two groups. Four samples were not heat treatment; four samples were heat treatment at 700°C for 1 hour. The obtained products were characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) techniques, X-ray diffraction (XRD) and UV-Vis spectrometer. SEM photos showed that the Hydroxyapatite powders produced are in the form of the agglomerate. According to EDS results, Hydroxyapatite samples are of high purity. XRD’s findings confirm that the diffraction peaks correspond to the pure phase of Hydroxyapatite. A general decrease was observed in the energy band gap of the samples with increasing hydrothermal reaction time.

The HAp (hydroxyapatite) excellent ion exchange resin and has adsorption properties of heavy metals and organic materials. It is used as an adsorption material and as an organic drug-delivery material due to these characteristics, that are essentially controlled the specific surface area. In this paper, the specific surface area was controlled by adding polymers of polyvinylpyrrolidone (PVP), polystyrene beads (PSB), and polyethylene glycol (PEG). Through the USP process, the HAp powder is able to synthesize into the spherical shape, specific surface area, and pore were controlled by the properties of the polymers.

Phosphorus removal and recovery from domestic wastewater is urgent nowadays. A novel process of nutrients removal coupled with phosphorus recovery from domestic sewage was proposed and optimization of induced crystallization reaction was performed in this study. The results showed that 92.3% of phosphorus recovery via induced Hydroxyapatite crystallization was achieved at the optimum process parameters: reaction time of 80 min, seed crystal loads of 60 g/L, pH of 8.5, Ca/P mole ratio of 2.0 and 4.0 L/min aeration rate when the PO43--P concentration was 10 mg/L in the influent, displaying an excellent phosphorus recovery performance. Importantly, it was found that the effect of reaction temperature on induced Hydroxyapatite crystallization was slight, thus favoring practical application of phosphorus recovery method described in this study. From these results, the proposed method of induced HAP crystallization to recover phosphorus combined with nutrients removal can be an economical and effective technology, probably favoring the water pollution control and phosphate rock recycle.

The purpose of the study was to assess the effect of autologous activated platelet-rich plasma on healing of a bone substitute - tricalcium phosphate hydroxyapatite in experimental long bone defects using an animal model.

The experiment involved an animal model of femoral defect. 24 Termond white rabbits were used in the study. We evaluated the effect of autologous platelet-rich plasma on tricalcium phos- phate using classical radiology, micro-CT studies, strength tests and histological evaluation.

Radiological and histological assessment did not show a beneficial effect of PRP together with a bone substitute in comparison to filling the defects only with bone replacement material. The only benefit of adding platelet-rich plasma to a bone substitute was shown in microCT imaging.

Autologous, activated platelet-rich plasma combined with hydroxyapatite tricalcium phos- phate has a positive effect on the remodeling of the newly formed bone tissue, increasing its density.

Polymer coatings are increasingly used in varied fields and applications from simple coatings of barrier to intricated nanotechnology based composite. In the present study, polyvinylidene fluoride(PVDF)/Hydroxyapatite (HA )coatings were produced by spin coating technique over 316L SS. Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) were used to observe the coated 316L SS substrates surface morphology. The corrosion protection efficiency of pure polyvinylidene fluoride and polyvinylidene fluoride/HA nanocomposite coatings on 316L SS was inspected using potentiodynamic polarization along with the ions release techniques in Hank’s solution. A superior biocompatibility and an improved protection performance against corrosion were obtained for the 316L SS samples with nanocomposite coatings compared with the pure polyvinylidene fluoride coatings and pristine 316L SS counterparts. The 316L SS samples coated by PVDF/HA nanocomposite showed enhanced corrosion protection within Hank’s solution. The corrosion of 316L SS samples within Hank’s solution increased from 92.99% to 99.99% when using 3wt% HA due to increasing the PVDF inhibition efficiency. Good agreements in the electrochemical corrosion parameters were obtained from using ions release and potentiodynamic polarization tests.

In this work, gel-casting of foams method was used to produce ZrO2 porous ceramics. The obtained foams with total porosity of 89.5 vol% were composed of approximately spherical cells having the mean diameter of 537 ± 153 μm interconnected by circular cell windows having the mean diameter of 152 ± 82 μm. Next, the ZrO2 foams were coated with fluorapatite (FA) and hydroxyapatite (HA) layers by slurry infiltration. The intermediate fluorapatite (FA) layer was introduced to prevent the chemical reactions between ZrO2 and HA at high temperatures during sintering process. The ZrO2 samples containing only HA coatings, were also tested, for comparison. The obtained ceramic biomaterials were subjected to in vitro tests in the simulated body fluid (SBF) solution. The results show that the ZrO2 foams with FA/HA layers possessed better bioactivity than the foams with the HA/HA coating.