RESUMEN
The objective of this study is to introduce Cu into SnO2 sorbent for improving its COS adsorption capacity. Cu-doped SnO2 adsorbents were synthesized using a conventional sol-gel method with citric acid. X-ray diffraction studies revealed that up to 0.4 mol of Cu ions were well-inserted within the SnO2 framework. Scanning electron microscopy images confirmed that the addition of Cu ions reduced the particle size of the SnO2 sorbents. Additionally, it led to an increase in the Brunauer-Emmett-Teller surface area of the sorbents. The COS adsorption tests were carried out in the temperature range of 300-400 °C with a gas hourly space velocity of 8,500 h-1. It was found that Cu0.6SnO2 displayed higher COS adsorption capacity than the sorbents of other compositions, and the breakthrough time and COS adsorption capacity on it at 400 °;C were 170 min and 4.87 mg/g, respectively. X-ray photoelectron spectroscopy results indicated that the Cu2+ ions in the CuxSnO2 adsorbent converted into CuS by binding to the S2- ions in COS gas, while the remaining CO segments combined with the Sn atoms in SnO2 and then are adsorbed as SnCO. Overall, this study showed that the hard-soft acid-base rule is better followed in the Cu0.6SnO2 adsorbent than in the SnO2 adsorbent and that the adsorption is more stable.
RESUMEN
In order to enhance the photoreduction of CO2 to CH4, a new type of photocatalyst, Sb1.5Sn8.5-xTixO19.0, with high conductivity and low bandgap was developed by partially incorporating Ti into the framework of Sb1.5Sn8.5O19.0 (antimony-doped tin oxide, ATO) using a controlled hydrothermal method. XRD and TEM analyses indicated that the Sb1.5Sn8.5-xTixO19.0 particles exhibited a tetragonal crystal structure and were approximately 20 nm in size. Furthermore, the bandgap and conductivity of these materials increased with increasing Ti content. A study of the photoreduction of CO2 with H2O revealed a remarkable increase in the generation of CH4 over the Sb1.5Sn8.5-xTixO19.0 catalysts. In particular, CH4 generation was the highest when Sb1.5Sn8.5Ti1.0O19.0 was used as the photocatalyst, and was three-fold higher than that achieved by using anatase TiO2. Photoluminescence studies showed that the enhanced photocatalytic activity of the Sb1.5Sn8.5-xTixO19.0 materials could be attributed to the interfacial transfer of photogenerated charges, which led to an effective charge separation and inhibition of the recombination of photogenerated electron-hole (e-/h+) pairs.
RESUMEN
The purpose of this study was to use a spinel structure to improve the performance and stability of chemical looping combustion processes. The oxygen carrier employed was Fe2MnO4, in which Ni was substituted at the Fe sites. Fe2-xNixMnO4 spinel particles were successfully synthesized by a sol-gel method. The obtained particles were characterized by X-ray diffraction (XRD), scanning electron microscopy, and CH4-/CO-temperature programmed desorption experiments. The XRD analysis confirmed that all the synthesized particles presented spinel structure. The performance of the particles was evaluated in redox cycle experiments under H2/air and CH4/air at 850 °C using a thermogravimetric analyzer. The Ni-substituted particles exhibited a higher performance than Fe2Mn1, being Fe1Ni1Mn1 the sample with the highest oxygen transfer capacity (19.68 wt% in H2/air and 15.90 wt% in CH4/air).
RESUMEN
Layered perovskite Sr2TiO4 photocatalyst was synthesized by using sol-gel method with citric acid. In order to increase the surface area of layered perovskite Sr2TiO4, and thus to improve its photocatalytic activity for CO2 reduction, its surface was modified via hydrogen treatment or exfoliation. The physical and chemical properties of the prepared catalysts were characterized by X-ray diffraction, high-resolution transmission electron microscopy, elemental mapping analysis, energy-dispersive X-ray spectroscopy, N2 adsorption-desorption, UV-Vis spectroscopy, X-ray photoelectron spectroscopy, photoluminescence, and electrophoretic light scattering. CO2 photoreduction was performed in a closed reactor under 6 W/cm2 UV irradiation. The gaseous products were analyzed using a gas chromatograph equipped with flame ionization and thermal conductivity detectors. The exfoliated Sr2TiO4 catalyst (E-Sr2TiO4) exhibited a narrow band gap, a large surface area, and high dispersion. Owing to these advantageous properties, E-Sr2TiO4 photocatalyst showed an excellent catalytic performance for CO2 photoreduction reaction. The rate of CH4 production from the photoreduction of CO2 with H2O using E-Sr2TiO4 was about 3431.77 µmol/gcat after 8 h.
RESUMEN
Micro-/nano-structured SrSnO3/x wt.-% TiO2 composites (x = 10, 20, and 30) were designed using a mixed method, a typical hydrothermal and impregnation method, to enhance hydrogen production from MeOH/H2O photo-splitting. All the materials obtained exhibited a perovskite structure. Scanning electron microscopy revealed pure SrSnO3 to have a rod-like morphology with a square base, 0.7-1.5 µm in size, and a height of approximately 2.0-3.0 µm. Moreover, phenomena were observed in the rods similar to that of typical perovskite with a layered structure. TiO2 nanoparticles, < 100 nm in size, were observed in the SrSnO3/TiO2 materials and the number of particles increased with increasing Ti concentration. The SrSnO3 material absorbed shorter band edges of less than 300 nm compared to that of pure TiO2, and the UV-visible absorption spectra were shifted to high wavelengths with the TiO2, loading. Hydrogen evolution from MeOH/H2O (1:1) photosplitting over the micro-/nano-structured SrSnO/TiO2 composite was enhanced compared to that over pure SrSnO3. In particular, 0.033 mmol of H2 gas was collected after 10 h under an 18 W-lamp with 365 nm radiation when 0.5 g of a SrSnO3/TiO2 20 wt.-% composite was used. Based on cyclic voltammetry and ultraviolet-visible spectroscopy, it was expected that the high photo activity resulted from the decrease in electron-hole recombination on the micro-/nano-structured SrSnO3/TiO2 composite.