Study of Eu3+ and Tm3+ substitution effects in sol–gel fabricated calcium hydroxyapatite

In this study, an aqueous sol–gel chemistry route based on phosphoric acid as the phosphorus precursor, calcium acetate monohydrate and lanthanide (III) oxides as source of calcium and lanthanide ions, respectively, have been used to prepare europium- and thulium-substituted calcium hydroxyapatite (CHAp:Ln3+) powders. The ethylenediaminetetraacetic acid was used as complexing agent in the sol–gel processing. The final products were obtained by calcination of the dry precursor gels for 5 h at 1000 °C. The phase transformations, composition, and structural changes in the polycrystalline samples were studied by infrared spectroscopy, X-ray powder diffraction analysis, scanning electron microscopy and photoluminescence measurements. It was demonstrated, however, that the substitution of calcium by Eu or Tm proceeds in the CHAp at low concentration of lanthanide ion. Graphical abstract: Excitation and emission of Tm3+ in CHAp:Tm3+ spectra

Wet Polymeric Precipitation Synthesis for Monophasic Tricalcium Phosphate

Tricalcium phosphate (β-Ca3(PO4)2, β-TCP) powders were synthesized using wet polymeric precipitation method for the first time to our best knowledge. The results of X-ray diffraction analysis showed the formation of almost single a Ca-deficient hydroxyapatite (CDHA) phase of a poor crystallinity already at room temperature. With continuously increasing the calcination temperature up to 800 °C, the crystalline β-TCP was obtained as the main phase. It was demonstrated that infrared spectroscopy is very effective method to characterize the formation of β-TCP. The SEM results showed that β-TCP solids were homogeneous having a small particle size distribution. The β-TCP powders consisted of spherical particles varying in size from 100 to 300 nm. Fabricated β-TCP specimens were placed to the bones of the rats and maintained for 1-2 months

Effect of Mn doping on the low-temperature synthesis of tricalcium phosphate (TCP) polymorphs

Effect of Mn doping on the low-temperature synthesis of tricalcium phosphate (TCP) polymorphs was demonstrated in alpha- and beta-TCP polymorphs prepared by wet precipitation'inethod under identical conditions and annealed at 700 degrees C. Calcium phosphates with Mn doping level in the range from 1 to 5 mol% were studied and the formation of desired polymorph was controlled by varying Mn content in as-prepared precipitates. It was found that increasing Mn content resulted in the formation of beta-TCP, while alpha-TCP was obtained with low Mn doping level, whereas a mixture of two polymorphs was obtained for intermediate Mn concentrations. Moreover, doping with Mn ions allowed the synthesis of beta-TCP at relatively low temperature (700 degrees C). Synthesized compounds were characterized by X-ray diffraction (XRD) analysis, electron paramagnetic resonance (EPR), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), inductively coupled plasma optical emission spectrometry (ICP-OES) and colorimetric MTT assay

Heterogeneous Fenton Oxidation Using Magnesium Ferrite Nanoparticles for Ibuprofen Removal from Wastewater : Optimization and Kinetics Studies

In this study, the catalytic properties of Fenton-like catalyst based on magnesium ferrite nanoparticles for IBP degradation were examined. Structural and morphological studies showed the low crystallinity and mesoporous structure for the catalyst obtained via a glycine-nitrate method. The influences of catalyst dosage, oxidant concentration, and solution pH on the pollutant degradation were investigated. The pseudo-first-order model describes kinetic data, and under optimal condition (catalyst dose of 0.5 g L-1, H2O2 concentration of 20.0 mM, and pH of 8.0), apparent rate constant reached 0.091 min-1. It was shown that Fenton reaction was mainly induced by iron atoms on the catalyst surface, which is supported by very low iron leaching (up to 0.05 mg L-1) and high catalytic activity at neutral solution pH (6.0-8.0). It was found that the IBP mineralization onto magnesium ferrite catalyst was rapid and reached up to 98-100% within 40 min. Thus, prepared magnesium ferrite nanoparticles can be used as an effective Fenton-like catalyst for the IBP degradation from wastewater.peerReviewe

Effect of magnesium ferrite doping with lanthanide ions on dark-, visible- and UV-driven methylene blue degradation on heterogeneous Fenton-like catalysts

Abstract The catalytic behavior of magnesium ferrites doped with lanthanide ions (La³⁺, Ce³⁺, Sm³⁺, Gd³⁺, and Dy³⁺) on Methylene Blue (MB) degradation using Fenton process was studied. A slow increase in cubic Fd3m crystalline structure parameters and increase in crystallite size of doped samples magnesium ferrites were observed. A dramatic decrease in catalytic activity of catalysts obtained at 600 °C as compared to catalysts obtained at 300 °C was explicitly observed and this was grossly attributed to the elimination of surface hydroxyl groups as ascertained by FT-IR analysis. The initial magnesium ferrite demonstrated the highest catalytic activity under dark- (kˈ 0.0555 min⁻¹) and visible-light (kˈ 0.1029 min⁻¹) conditions. Catalytic efficiency of the lanthanides doped catalysts under UV-irradiation in accordance with the maximum appearance rate constant kˈ decreased in the following order Ce³⁺ > Dy³⁺ > La³⁺ ≈ MgFe₂O₄ > Sm³⁺ > Gd³⁺. The most active ferrites provided up to 99% of MB degradation in 60 and 20 min for visible- and UV-driven Fenton processes. Findings obtained from this study were observed to be competitive with other heterogeneous Fenton catalysts