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EN
The adsorption of CO2 on a nano-calcium oxide (nano-CaO) adsorbent was investigated under different conditions of temperature and supply pressure, considering kinetic, isotherm, and thermodynamic parameters. CaO is a crystalline material with a high surface area and nanosized particles with high porosity, which showed rapid initial CO2 adsorption rates in the moderate temperature range studied. The adsorption was well described by the pseudo-second-order and the intraparticle diffusion kinetic models. The Langmuir isotherm model fitted the experimental data well, indicating a monolayer-type process. The thermodynamic parameters revealed that the CO2/nano-CaO adsorption was endothermic, not spontaneous, and proceeded via physical and chemical processes. The activation energy value confirmed that the mechanism involved is a chemical process. In addition, the nano-CaO adsorbent could be regenerated five times without any significant loss of performance or properties. All the obtained results reveal that this porous nanoadsorbent has huge potential to be applied for CO2-capture technologies on a large scale.
EN
This work addresses the synthesis of nanocrystalline barium, strontium, and calcium hydroxyapatites (Ca-HAps) via the chemical precipitation method, followed by calcination. To give a coherent picture of the most important structural, textural, and morphological properties of these materials and to investigate the influence of these characteristics over Co2+ ion adsorption capacity from aqueous solutions, the powders prepared were systematically characterized by X-ray diffraction, N2-physisorption measurements, scanning electron microscopy (SEM), energy dispersive X-ray spectrometry, and Fourier Transformed Infrared spectroscopy (FTIR). The results clearly showed that the Ca-HAp obtained exhibits better nanocrystallinity, greater structural stability, high surface area, high total pore volume, and mesoporosity, compared with the other synthesized hydroxyapatites, and that these physicochemical properties share a direct correlation with favorable Co2+ ion adsorption capacity at room temperature and pressure. The results proved that the physicochemical features of resulting alkaline-earth hydroxyapatites, prepared via the chemical precipitation method, played a fundamental role during the adsorption of heavy metal (with high toxicity) from aqueous solutions.
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