Elaboration of the hydroxyapatite with different precursors and application for the retention of the lead

Carbonate hydroxyapatite (CHAP) was synthesized from different precursors; synthetic (CaCO3 and Ca(OH)2) and natural (egg shell before and after calcinations at 900 degrees C) under different conditions and characterized by using TG/DTG analysis, X-ray powder diffraction (XRD) method and Fourier transform infrared (FT-IR) spectroscopy techniques. The results of these analyses indicate that the four powders present the same structure of hydroxyapatite. Furthermore the four powders obtained were used for the retention of lead. The results obtained indicated that all powders present high adsorption capacity for lead, but from environmental and economic views, the hydroxyapatite synthesized from eggshell no calcined (HA2) is most advantageous. The influence of different sorption parameters, such as: initial metal concentration, equilibration time, solution pH and sorbent dosage was studied and discussed.     

New synthesis method of HA/P(D,L)LA composites: study of fibronectin adsorption and their effects in osteoblastic behavior for bone tissue engineering

A novel synthetic method to synthesize hydroxyapatite/poly (D,L) lactic acid biocomposite is presented in this study by mixing only the precursors hydroxyapatite and (D,L) LA monomer without adding neither solvent nor catalyst. Three compositions were successfully synthesized with the weight ratios of 1/1, 1/3, and 3/5 (hydroxyapatite/(D,L) lactic acid), and the grafting efficiency of poly (D,L) lactic acid on hydroxyapatite surface reaches up to 84?%. Scanning electron microscopy and Fourier transform infrared spectroscopy showed that the hydroxyapatite particles were successfully incorporated into the poly (D,L) lactic acid polymer and X ray diffraction analysis showed that hydroxyapatite preserved its crystallinity after poly (D,L) lactic acid grafting. Differential scanning calorimetry shows that Tg of hydroxyapatite/poly (D,L) lactic acid composite is less than Tg of pure poly (D,L) lactic acid, which facilitates the shaping of the composite obtained. The addition of poly (D,L) lactic acid improves the adsorption properties of hydroxyapatite for fibronectin extracellular matrix protein. Furthermore, the presence of poly (D,L) lactic acid on hydroxyapatite surface coated with fibronectin enhanced pre-osteoblast STRO-1 adhesion and cell spreading. These results show the promising potential of hydroxyapatite/poly (D,L) lactic acid composite as a bone substitute material for orthopedic applications and bone tissue engineering.     

Factorial design analysis for sorption of zinc on hydroxyapatite

A factorial design was employed to evaluate the quantitative removal of zinc from aqueous solutions on synthesized hydroxyapatite. The experimental factors and their respective levels studied were the initial zinc concentration in solution (35≤C(Zn)≤85 mg/L), adsorbent dosage (4.5≤C(susp)≤9.5 g/L), Ca/P molar ratio (1.667≤Ca/P≤2) and calcination temperature of hydroxyapatite (600≤T(Cal)≤800 °C). The adsorption parameters were analysed statistically by means of variance analysis by using the STATISTICA software. The experimental results and statistical analysis show that increasing in the calcination temperature from 600 to 800 °C decrease the zinc adsorption whereas the increase of adsorbent dosage increases it. Based on the analysis of variance and the factorial design of experiments, adsorbent dosage has a positive effect on the removal of zinc, whereas zinc concentration, Ca/P molar ratio and calcination temperature have a negative effect on this process. The factorial results also demonstrate the existence of statistically significant binary interactions of the experimental factors. The experimental results were fitted to the Langmuir and Freundlich equations to find out adsorption capacities. In most cases, the results indicate that the sorption data fits well in the Freundlich isotherm model. The results of XRD analysis, pH(PZC) and pH(Final) values indicated that ion exchange and dissolution/precipitation mechanisms predominate for the sorption of zinc on our hydroxyapatite.     

Hydroxyapatite-TiO2-SiO2-Coated 316L Stainless Steel for Biomedical Application

Metallurgical and Materials Transactions A - This study investigated the effectiveness of titania (TiO2) as a reinforcing phase in the hydroxyapatite (HAP) coating and silica (SiO2) single layer as...     

Surface modification of natural and synthetic hydroxyapatites powders by grafting polypyrrole

The modification of hydroxyapatite surface by grafting polypyrrole has been investigated with two hydroxyapatites (HA) powders. One is natural derived from bovine bone, it was prepared by calcination at 750 °C. The other is synthetic synthesized by the sol–gel method using Ca(NO₃)₂·4H₂O and P₂O₅. The presence of (C₄H₃N) _n polymeric fragment bound to HA surface was evidenced by infrared analysis. X-ray powder analysis has shown that the apatite structure remains unchanged during the surface modification. The thermogravimetric analysis has shown that the weight loss exhibited by HA increased from 8.7 to 47.8 and from 18.3 to 42.8 wt% for natural hydroxyapatite (NHA)/polypyrrole and synthetic hydroxyapatite (SHA)/polypyrrole, respectively, as the pyrrole solution concentration increased from 5 to 15 wt%. Grafting of polypyrrole on HA surface caused an increase in specific surface area up to 113 m²/g for SHA and up to 107 m²/g for NHA aged in 15 wt% pyrrole solution (HA/15Pyrrole). According to the results found for these two apatites, a mechanism of surface modification was proposed for the formation of N–H hydrogen bonds as the result of a reaction between the C₄H₅N organic reagent and OH^? ions of the HA.     

A Fast and Efficient Approach for Image Compression Using Curvelet Transform

In this paper a novel image compression technique using features of wavelet and curvelet transforms is proposed to improve efficiency and compression performance. Indeed, the curvelet transform is one of the recently developed multiscale transforms which is especially designed to represent efficiently curves and edges in an image. In the proposed method, the compression algorithm involves the Haar wavelet transform to decompose the image into four frequency sub-bands. The lowest frequency sub-band coefficients are processed using Set Partitioning In Hierarchical Trees (SPIHT) encoding. Meanwhile, Fast Discrete Curvelet Transform (FDCT) is applied to the remaining frequency sub-bands. The FDCT output coefficients are then quantized according to the sub-band they belong to. The lowest frequency FDCT output coefficients are quantized using Differential Pulse Code Modulation, the medium frequency coefficients are processed using SPIHT, whereas the high frequency coefficients are removed. Experimental results demonstrate that our method provides high performance for edge detection compared to existing techniques particularly for images with abrupt changes. In addition, this new image coding and decoding approach is powerful in terms of computation time. Moreover, the proposed method reveals significant improvement in compression ratio and decoded peak-signal-to-noise-ratio.     

Characterization of Magnesium‐Doped Hydroxyapatite Prepared by Sol‐Gel Process

Pure and doped hydroxyapatite (HA) nanocrystalline powders (Ca_10‐xMg_x(PO₄)₆OH₂) were synthesized using sol‐gel process. For this, calcium nitrate tetrahydrate, magnesium nitrate hexahydrate, and phosphorous pentoxide were used as precursors for Ca, Mg, and P, respectively. Calculated amounts of magnesium ions (Mg⁺²) especially from 0 to 10% (molar ratio) were incorporated as dopant into the calcium sol solution. The structure and morphology of the gels obtained after mixing the phosphorous and (calcium + magnesium) sol solution were different, and their condensations in time depend on the quantities of magnesium added. The several powders resulting from the gels dried and sintered at 500°C for 1 h were characterized by thermogravimetry (TG), Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), and inductively coupled plasma (ICP). Additionally, their agglomeration, morphology, and particle size were investigated using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The specific surface area of each sample was measured by the Brunauer–Emmett–Teller (BET) gas adsorption technique. The results of XRD, FTIR, and ICP values ranged between 0.45 and 2.11 mg/L indicated that the magnesium added in the calcium solution was incorporated in the lattice structure of HA so prepared, while those obtained by SEM and TEM confirmed the influence of Mg on their morphology (needle and irregular shape) and crystallite size, which is about 30–60 nm. The as‐prepared powders had a specific surface area ranged between 6.37 and 27.60 m²/g.