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    Effect of pH and ammonia concentration on the shape and size of fluorapatite nanoparticles obtained by chemical reaction
    (Elsevier, 2021-11-15)
    Nanoparticles of fluorapatite (FAp Nps) were prepared by one step chemical reaction in aqueous solutions. The pH of the system was kept constant at 6 and 8. The FAp Nps were characterized with Scanning Electron Microscopy-Energy Dispersive X-Ray Spectroscopy (SEM-EDAX), X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR). The Ca/P calculated from EDAX analysis was 1.69. The results of XRD analysis and FTIR showed the presence of FAp phases. The DRX results confirm the formation of FAp with a hexagonal structure. TEM images show semispherical and elongated nanoparticles with mean diameter of 3.78 nm, 8.63 nm and 10.46 nm, when the pH and ammonia concentrations is varied. Ammonia concentration and pH influence the morphology and size of the FAp Nps.
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    Effects of preparation method on catalytic behavior of Ni-Me (Me = Co, Nb)/?-Al2O3 for oxidative dehydrogenation of ethane
    (Sociedade Brasileira de Quimica, 2025-01-01)
    Catalysts based on Ni-Me (Me = Co, Nb) supported on γ-Al2O3 were prepared by the coprecipitation-chemical deposition method via reflux, and hydrothermal method for oxidative dehydrogenation of ethane. For coprecipitation method, ammonia and urea were used as precipitating agents. In both methods, the Ni content was 30 wt.%, whereas that of Me (Co, Ni) was 5 wt.%. The activity and selectivity towards ethylene appeared to depend strongly on the composition of the catalysts and, interestingly, on the preparation conditions. In the present article, it is shown that mixed hydrothermal samples using urea showed the best performance. Specifically, the hydrothermally prepared NiNb/γ-Al2O3 sample was the one that showed the highest values. The of Nb to Ni framework allowed to enrich with nucleophilic oxygen sites displayed via X-ray photoelectronic spectra (XPS) which lead to the formation of low reducible and selective sites.
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