A novel Pt/CeO(2)-ZrO(2)-Bi(2)O(3) catalyst was prepared to realize complete CO oxidation at room temperature or below even in the presence of moisture. Using this catalyst, a high CO oxidation activity and a high stability against moisture have been realized simultaneously. 相似文献
Comparative results (specific area, metallic dispersion, and activity in the carbon monoxide oxidation) on sol-gel and impregnated Pt/TiO2 catalysts are presented. In order to explain the important differences between the two preparations, among them high resistivity of sol-gel catalyst to sintering, the formation of anchored and/or partially buried particles into the support is proposed. 相似文献
The effect of Ce doping and pretreatment of Pt/Al2O3 on its catalysis of propane oxidation was investigated after aging the catalysts. The Ce amount and pretreatment conditions were varied, and the propane oxidation activity was measured. The properties of the catalysts were investigated by means of XRD, STEM-EDX, FT-IR, and H2-TPR. The size of the Pt nanoparticles (PtNPs) decreased for water-treated catalysts doped with a small amount of Ce, suggesting that water treatment of Ce-doped catalysts inhibits Pt sintering. The minimum PtNP size was obtained with ca. 3.6 wt% of Ce. The Ce species with less than 3.6 wt% existed in a dispersed state, whereas above this value, CeO2 particulates co-existed. The propane oxidation temperature of the water-treated catalysts was lowered to an extent that depended on the Ce content. This tendency is consistent with the PtNP size in the catalysts. It is considered that highly dispersed Ce species take a primary role in promoting propane oxidation on PtNPs. The reduction temperature of Ce species on water-treated catalysts was lower than that of untreated catalysts, probably owing to a stronger interaction between Pt and Ce, demonstrated by FT-IR measurements. The increased reducibility of Ce species may be the reason for the improved oxidation activity of the catalysts.
Molecular structures and vibrational spectra of the CO species adsorbed on the Pt/TiO2, Pt/CeO2 and FeOx/Pt/CeO2 have been investigated by means of density functional theory (DFT) calculation and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). The geometrical structures and vibrational frequencies were obtained at the MPW1PW91/SDD level. Theoretical calculation shows that the calculated IR spectra were in good agreement with the experimental results. The calculated results clarify the assignment of the adsorbed CO species on the surface of Pt/TiO2, Pt/CeO2 and FeOx/Pt/CeO2. 相似文献
The laser-induced luminescence of Cr3+ impurity ions in model Fe/Al2O3 and Cr/Al2O3 catalysts with different calcination temperatures was studied. It was found that an additional luminescence band at 770 nm appeared in the luminescence spectra of low-temperature samples as a result of the interaction of octahedrally coordinated Cr3+ ions with Fe3+ impurity ions. In the θ-Al2O3 phase with a concentration of Cr3+ ions higher than 0.1 wt %, the interaction of the Cr3+-Cr3+ ion pairs in the immediate surroundings resulted in the appearance of Nθ lines due to the splitting of Rθ lines. The differences of these lines from the Nα lines of α-Al2O3 were related to the individuality of the crystal lattice of the θ phase and the coordination of Cr3+ impurity ions in the immediate surroundings, which is different from that in the α phase. Based on the laser-induced luminescence spectroscopic data, it was found that regions with a local Cr3+ concentration higher than the average Cr3+ concentration in the bulk of a catalyst by one order of magnitude were formed in the α-Al2O3-Fe2O3 system with the bulk Fe and Cr concentrations of 2.5 and 0.04 wt %, respectively, which was calcined at 1220°C, as a result of the diffusion of chromium and iron ions. 相似文献
Au/Al2O3 catalyst was prepared by a modified anion impregnation method and investigated with respect to its initial activity and stability for low-temperature CO oxidation. The activity changes of the catalyst were examined after separate treatment in CO+O2 or CO2+O2. Furthermore, in situ FT-IR studies were performed to investigate the species on the surface when CO or CO+O2 or CO2+O2 was selected separately as adsorption gas. The results showed that Au/Al2O3 catalyst exhibited very high initial activity, but the catalytic activity was found to decrease gradually during CO oxidation with time on stream. And also, the activity of the catalyst declined after treatment in CO+O2 or CO2+O2. The formation and accumulation of carbonate-like species during CO oxidation or treatment in CO+O2 or CO2+O2 might be mainly responsible for the activity decrease, which was reversible. 相似文献
The structure of Ti/Al2O3 supports (0–14 wt% Ti) and Co/Ti/Al2O3 catalysts (3 wt% Co) was examined by EXAFS. The results indicated that the Ti was present primarily as a highly dispersed surface phase. The Ti EXAFS results indicated that the Ti species were octahedrally coordinated. Evidence of Ti—Ti interactions was found for all loadings (2–14 wt% Ti) suggesting that the Ti surface species are present as small clusters of TiO2.The Co EXAFS results showed evidence for several structurally different Co surface phases as a function of Ti loading. Evidence of a Co species interacting with the Ti surface phase was observed for the 3% Co/2% Ti-3%Co/6%Ti catalysts. At the highest loadings studied, 3%Co/8%Ti and 3%Co/14%Ti, evidence was found for a CoTiO3-like phase. 相似文献
Heptene-2 aromatization on Pt/Al2O3 in a pulse microcatalytic reactor has been studied under H2 and N2 atmosphere at temperatures between 330 to 500°C and at a total pressure of 4.0 kg/cm2. Results showed that the production of only cracked products (mainly methane) from deep fragmentation of heptene-2 in H2 sharply contrasts with the reaction in N2 in which the catalyst showed aromatic selectivity with the production of methane, benzene and toluene. In H2-N2 mixtures, 75% H2 was required to reduce the aromatization activity of the catalyst to zero. A test of the kinetic data using Sica's method [15] of pulse kinetic analysis suggests a first order in heptene-2 with an activation energy of 102.61 kJ/mol in N2 and 124.71 kJ/mol in H2. The difference in activation energies has been attributed to a difference in reaction mechanisms in both gases. 相似文献
The microstructure of 2% Pt/CeO2-TiO2 catalysts has an effect on their catalytic properties in CO oxidation. The nanostructured catalysts as platinum clusters 0.3–0.5 nm in size are the most active. These clusters are stabilized at crystal boundaries formed by irregularly intergrown anatase particles. The catalyst containing platinum particles 2–5 nm in size is less active because of the decrease in the extent of dispersion of platinum and the change of its electron state. 相似文献
The oxidation of CO in excess oxygen in a reaction mixture on Ni/Al2O3 gives a nonuniform catalyst surface containing NiO. The amount of stationary states of the system increases. The critical effects involving sharp change in catalyst are smoothed out and the activity remains high.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 29, No. 4, pp. 350–355, July–August, 1993. 相似文献