The effects of CeO2 contents and silica carrier porosity with their pore diameters ranging from 5.2 nm to 12.5 nm of CuO-CeO2/SiO2 cata-lysts in CO oxidation were investigated.The catalysts were characterized by N2 ad...The effects of CeO2 contents and silica carrier porosity with their pore diameters ranging from 5.2 nm to 12.5 nm of CuO-CeO2/SiO2 cata-lysts in CO oxidation were investigated.The catalysts were characterized by N2 adsorption/desorption at low temperature,X-ray diffraction （XRD）,temperature-programmed reduction by H2 （H2-TPR）,oxygen temperature programmed desorption （O2-TPD） and X-ray photoelectron spectroscopy （XPS）.The results suggested that,the ceria content and the porosity of SiO2 carrier possessed great impacts on the structures and catalytic performances of CuO-CeO2/SiO2 catalysts.When appropriate content of CeO2 （Ce content 8 wt%） was added,the catalytic activity was greatly enhanced.In the catalyst supported on silica carrier with larger pore diameter,higher dispersion of CuO was observed,better agglomeration-resistant capacity was displayed and more lattice oxygen could be found,thus the CuO-CeO2 supported on Si-1 showed higher catalytic activity for low-temperature CO oxidation.展开更多
Mesoporous silica-zirconia supported phosphotungstic acid was synthesized by evaporation induced self-assembly method and used as oxidative desulfurization catalysts. The structural properties of as-prepared catalysts...Mesoporous silica-zirconia supported phosphotungstic acid was synthesized by evaporation induced self-assembly method and used as oxidative desulfurization catalysts. The structural properties of as-prepared catalysts were characterized using various analytical techniques including X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and nitrogen adsorption desorption. The experimental results showed that HPW was highly dispersed on mesoporous framework. The surface acidity of catalysts was analyzed by FTIR measurement of adsorbed pyridine.The surface Lewis acidity was improved with increasing the content of zirconium in the samples. The mesoporous composites were used as catalysts with H2O2 as oxidant for oxidative desulfurization of model fuel. The catalytic activity results showed that the surface Lewis acid sites acted as selective adsorption active sites for dibenzothiophene, which facilitated the sulfur removal from model fuel in the presence of arene. A slight decrease in activity of the recovered catalyst used in the proceeding rounds indicated the reusability of the catalyst.展开更多
Co,K-Supported hexagonal mesoporous silicas（HMS） have been prepared by incipient wetness impregnation with cobalt acetate tetrahydrate and potassium acetate as metal precursors, and ethylene glycol as impregnation s...Co,K-Supported hexagonal mesoporous silicas（HMS） have been prepared by incipient wetness impregnation with cobalt acetate tetrahydrate and potassium acetate as metal precursors, and ethylene glycol as impregnation solvent. The products have been characterized via powder X-ray diffraction, N2 adsorption-desorption isotherms and diffuse reflectance UV-Vis spectroscopy. The divalent cobalt with a tetrahedral oxygen coordination exists mainly in the calcined samples. The catalytic properties have been tested for the oxidation of 4-t-butyltoluene with dioxygen in liquid phase at mild conditions. The products offered good catalytic activities in the oxidation reactions. Co-K-HMS catalyst with loading 4% Co and 2% K（mass fraction） affords a higher yield（22.4%） of 4-t-butylbenzaldehyde at a conversion of 28.3% under the reaction conditions. Adding a proper amount of potassium in Co-HMS results in an improvement catalytic activity and stability.展开更多
The gas phase methane oxidative carbonylation was studied in the presence of molecular oxygen over silica materials including their mechanical mixtures with rhodium chalcogen chlorides obtained in non-aqueous inorgani...The gas phase methane oxidative carbonylation was studied in the presence of molecular oxygen over silica materials including their mechanical mixtures with rhodium chalcogen chlorides obtained in non-aqueous inorganic media. The formation of Rh4SCl7, Rh4S9Cl2, Rh4SesCl3 and Rh3Se3Cl solids was confirmed by elemental analysis, IR absorption spectroscopy, XPS and X-ray diffraction. Silica, vanadium-, and molybdenum-containing mesoporous molecular sieves have been used as supports. It was found that productivity of oxygenates （methanol, methyl acetate and acetic acid） depends mainly on the method of the catalyst preparation and the type of the support.展开更多
CO self-poisoning and slow surface kinetics pose major challenges to a CO oxidation catalyst that should work at ambient temperature.Furthermore,the presence of moisture would cause passivation of the catalyst A highl...CO self-poisoning and slow surface kinetics pose major challenges to a CO oxidation catalyst that should work at ambient temperature.Furthermore,the presence of moisture would cause passivation of the catalyst A highly active ceria promoted Pt catalyst（4%Pt-12%CeO_2/SiO_2;conversion≥99%at low（ 500 ppm） and high（ 2500 ppm） CO concentrations was developed for CO oxidation at ambient temperature in humid air.Catalyst preparation variables such as Pt and CeO_2 loading,ceria deposition method,drying and calcination conditions for the ceria and Pt precursors were optimized experimentally.The activity was correlated with surface properties using CO/H_2 chemisorption,O_2-H_2 titration,X-ray diffraction and BET surface area analysis.The method of CeO_2 deposition had a significant impact on the catalytic activity.CeO_2 deposition by impregnation resulted in a catalyst that was three times more active than that prepared by deposition precipitation or CeO_2grafting.O_2-H_2 titration results revealed that the close association of ceria and Pt in the case of CeO_2deposition by impregnation resulted in higher activity.The catalyst support used was also crucial as a silica supported catalyst was five times more active than an alumina supported catalyst.The particle size and pore structure of the catalyst support were also crucial as the reaction was diffusion controlled.The drying and calcination conditions of the ceria and Pt precursors also played a crucial role in determining the catalytic activity.The Pt-CeO_2/SiO_2 catalysts with Pt 2.5 wt%and CeO_2 15 wt%were highly active（TOF 0.02 s^（-1）） and stable（conversion 99%after 15 h） at ambient conditions.展开更多
基金supported by the National Natural Science Foundation of China(20590360)New Century Excellent Talent Project of China(NCET-05-0783)
文摘The effects of CeO2 contents and silica carrier porosity with their pore diameters ranging from 5.2 nm to 12.5 nm of CuO-CeO2/SiO2 cata-lysts in CO oxidation were investigated.The catalysts were characterized by N2 adsorption/desorption at low temperature,X-ray diffraction （XRD）,temperature-programmed reduction by H2 （H2-TPR）,oxygen temperature programmed desorption （O2-TPD） and X-ray photoelectron spectroscopy （XPS）.The results suggested that,the ceria content and the porosity of SiO2 carrier possessed great impacts on the structures and catalytic performances of CuO-CeO2/SiO2 catalysts.When appropriate content of CeO2 （Ce content 8 wt%） was added,the catalytic activity was greatly enhanced.In the catalyst supported on silica carrier with larger pore diameter,higher dispersion of CuO was observed,better agglomeration-resistant capacity was displayed and more lattice oxygen could be found,thus the CuO-CeO2 supported on Si-1 showed higher catalytic activity for low-temperature CO oxidation.
基金Funded by the National Natural Science Foundation of China(No.21106008)the Petro China Innovation Foundation(No.2013D-5006-0405)
文摘Mesoporous silica-zirconia supported phosphotungstic acid was synthesized by evaporation induced self-assembly method and used as oxidative desulfurization catalysts. The structural properties of as-prepared catalysts were characterized using various analytical techniques including X-ray diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and nitrogen adsorption desorption. The experimental results showed that HPW was highly dispersed on mesoporous framework. The surface acidity of catalysts was analyzed by FTIR measurement of adsorbed pyridine.The surface Lewis acidity was improved with increasing the content of zirconium in the samples. The mesoporous composites were used as catalysts with H2O2 as oxidant for oxidative desulfurization of model fuel. The catalytic activity results showed that the surface Lewis acid sites acted as selective adsorption active sites for dibenzothiophene, which facilitated the sulfur removal from model fuel in the presence of arene. A slight decrease in activity of the recovered catalyst used in the proceeding rounds indicated the reusability of the catalyst.
基金Supported by the National Natural Science Foundation of China(No.20773110)the Science Technology Foundation of Zhejiang Province,China(No.2008C21019)
文摘Co,K-Supported hexagonal mesoporous silicas（HMS） have been prepared by incipient wetness impregnation with cobalt acetate tetrahydrate and potassium acetate as metal precursors, and ethylene glycol as impregnation solvent. The products have been characterized via powder X-ray diffraction, N2 adsorption-desorption isotherms and diffuse reflectance UV-Vis spectroscopy. The divalent cobalt with a tetrahedral oxygen coordination exists mainly in the calcined samples. The catalytic properties have been tested for the oxidation of 4-t-butyltoluene with dioxygen in liquid phase at mild conditions. The products offered good catalytic activities in the oxidation reactions. Co-K-HMS catalyst with loading 4% Co and 2% K（mass fraction） affords a higher yield（22.4%） of 4-t-butylbenzaldehyde at a conversion of 28.3% under the reaction conditions. Adding a proper amount of potassium in Co-HMS results in an improvement catalytic activity and stability.
基金supported by funds from scientific research programs of National Academy of Sciences of Ukraine and Ministry of Education and Science of Ukraine
文摘The gas phase methane oxidative carbonylation was studied in the presence of molecular oxygen over silica materials including their mechanical mixtures with rhodium chalcogen chlorides obtained in non-aqueous inorganic media. The formation of Rh4SCl7, Rh4S9Cl2, Rh4SesCl3 and Rh3Se3Cl solids was confirmed by elemental analysis, IR absorption spectroscopy, XPS and X-ray diffraction. Silica, vanadium-, and molybdenum-containing mesoporous molecular sieves have been used as supports. It was found that productivity of oxygenates （methanol, methyl acetate and acetic acid） depends mainly on the method of the catalyst preparation and the type of the support.
基金supported by US Army contract(W56HZV-05-C0686) at Auburn University administered through TARDEC
文摘CO self-poisoning and slow surface kinetics pose major challenges to a CO oxidation catalyst that should work at ambient temperature.Furthermore,the presence of moisture would cause passivation of the catalyst A highly active ceria promoted Pt catalyst（4%Pt-12%CeO_2/SiO_2;conversion≥99%at low（ 500 ppm） and high（ 2500 ppm） CO concentrations was developed for CO oxidation at ambient temperature in humid air.Catalyst preparation variables such as Pt and CeO_2 loading,ceria deposition method,drying and calcination conditions for the ceria and Pt precursors were optimized experimentally.The activity was correlated with surface properties using CO/H_2 chemisorption,O_2-H_2 titration,X-ray diffraction and BET surface area analysis.The method of CeO_2 deposition had a significant impact on the catalytic activity.CeO_2 deposition by impregnation resulted in a catalyst that was three times more active than that prepared by deposition precipitation or CeO_2grafting.O_2-H_2 titration results revealed that the close association of ceria and Pt in the case of CeO_2deposition by impregnation resulted in higher activity.The catalyst support used was also crucial as a silica supported catalyst was five times more active than an alumina supported catalyst.The particle size and pore structure of the catalyst support were also crucial as the reaction was diffusion controlled.The drying and calcination conditions of the ceria and Pt precursors also played a crucial role in determining the catalytic activity.The Pt-CeO_2/SiO_2 catalysts with Pt 2.5 wt%and CeO_2 15 wt%were highly active（TOF 0.02 s^（-1）） and stable（conversion 99%after 15 h） at ambient conditions.
