A series of Ce1-xFexO2 （x=0, 0.2, 0.4, 0.6, 0.8, 1） complex oxide catalysts were prepared using the coprecipitation method. The catalysts were characterized by means of XRD and H2-TPR. The reactions between methane ...A series of Ce1-xFexO2 （x=0, 0.2, 0.4, 0.6, 0.8, 1） complex oxide catalysts were prepared using the coprecipitation method. The catalysts were characterized by means of XRD and H2-TPR. The reactions between methane and lattice oxygen from the complex oxides were investigated. The characteristic results revealed that the combination of Ce and Fe oxide in the catalysts could lower the temperature necessary to reduce the cerium oxide. The catalytic activity for selective CH4 oxidation was strongly influenced by dropped Fe species. Adding the appropriate amount of Fe2O3 to CeO2 could promote the action between CH4 and CeO2. Dispersed Fe2O3 first returned to the original state and would then virtually form the Fe species on the catalyst, which could be considered as the active site for selective CH4 oxidation. The appearance of carbon formation was significant and the oxidation of carbon appeared to be the rate-determining step; the amounts of surface reducible oxygen species in CeO2 were also relevant to the activity. Among all the catalysts, Ce0.6Fe0.402 exhibited the best activity, which converted 94.52% of CH4 at 900 ℃.展开更多
Three series of CeO2/CuO samples were prepared by impregnation method and characterized by XRD, N2 adsorption-desorption, temperatureprogrammed reduction （TPR）, XPS and TEM techniques. In comparison with the samples...Three series of CeO2/CuO samples were prepared by impregnation method and characterized by XRD, N2 adsorption-desorption, temperatureprogrammed reduction （TPR）, XPS and TEM techniques. In comparison with the samples prepared with CuO as initial support, the samples with Cu（OH）2 as initial support have higher reducibilities and smaller relative TPR peak areas, and also larger specific surface areas at calcina- tion temperatures of 400 ℃--600 ℃. As a result, Cu（OH）2 is better than CuO as initial support for preferential oxidation of CO in excess H2 （CO-PROX）. The best catalytic performance was achieved on the sample calcined at 600 ℃ and with an atomic ratio of Ce/Cu at 40%. XPS analyses indicate that more interface linkages Ce-O-Cu could be formed when it was calcined at 600 ℃. And the atomic ratio of Ce/Cu at 40% led to a proper reducibility for the sample as illustrated by the TPR measurements.展开更多
A series of Co (10.7 wt. %)-CeO2/SiO2 catalysts with various cerium contents was prepared and evaluated. The optimized ceria-promoted catalyst exhibits good activity, high selectivity towards long chain hydrocarbons, ...A series of Co (10.7 wt. %)-CeO2/SiO2 catalysts with various cerium contents was prepared and evaluated. The optimized ceria-promoted catalyst exhibits good activity, high selectivity towards long chain hydrocarbons, and excellent stability. The promotion mechanism of ceria was investigated using X-ray diffraction (XRD), temperature programmed reduction (TPR), H2 temperature programmed surface reaction (H2-TPSR) and transient response technique. It is suggested that the improved catalytic performance of the catalyst modified by ceria be attributed to (1) the improvement in the dispersion of metallic cobalt and the amount of active sites for Fischer-Tropsch Synthesis (FTS), leading to an increased concentration of surface active carbon species and high selectivity towards long chain hydrocarbons; (2) the inhibition of disproportionation of CO and the removal of inactive surface carbon species.展开更多
The effect of BaO doping to the Pt-Rh catalysts on its three-way catalytic activity and water-gas transfer was investigated. The results show that the light-off temperatures of hydrocarbon and carbon monoxide and nitr...The effect of BaO doping to the Pt-Rh catalysts on its three-way catalytic activity and water-gas transfer was investigated. The results show that the light-off temperatures of hydrocarbon and carbon monoxide and nitrogen oxides have little difference in the fresh catalysts. But after the hydrothermal-aged 5 h at 1000 ℃, the catalysts containing CeO2-ZrO2-BaO has lower light-off temperature and better catalytic activity than the catalysts containing BaO and CeO2-ZrO2,展开更多
The effects of BaO doping on the three-way catalytic activity of Pt-Rh catalyst and on water-gas shift were investigated. The results show that the light-off temperatures of hydrocarbon and carbon monoxide and nitroge...The effects of BaO doping on the three-way catalytic activity of Pt-Rh catalyst and on water-gas shift were investigated. The results show that the light-off temperatures of hydrocarbon and carbon monoxide and nitrogen oxides of the fresh catalysts slightly differ from those of the aged catalysts, and the catalysts containing CeO2-ZrO2-BaO have lower lightoff temperature and better catalytic activity than these containing BaO and CeO2-ZrO2 after hydrothermal aging for 5 h at 1000 ℃. The catalysts were characterized by means of the temperature-programmed reduction （TPR） in hydrogen and the temperature-programmed desorption （TPD） in oxygen. It is confirmed that the suggested route of CeO2-ZrO2-BaO by coprecipitation can improve the catalytic activity of catalysts.展开更多
The Pd-only catalysts for motorcycle were prepared by impregnating CeO2-ZrO2-Al2O3 and CeO2-ZrO2+Al2O3 with PdCl2 aqueous solution and characterized by X-ray diffraction (XRD), oxygen storage capacity (OSC) and H2-tem...The Pd-only catalysts for motorcycle were prepared by impregnating CeO2-ZrO2-Al2O3 and CeO2-ZrO2+Al2O3 with PdCl2 aqueous solution and characterized by X-ray diffraction (XRD), oxygen storage capacity (OSC) and H2-temperature-programmed reduction (H2-TPR) methods. The XRD result indicated that the CeO2-ZrO2-Al2O3 compound prepared by co-precipitation formed a single solid solution and had good thermal stability, and Pd phase was not observed in all catalysts. The TPR results showed that the reduction temperature of Pd/CeO2-ZrO2-Al2O3 catalyst was lower than that of Pd/CeO2-ZrO2+Al2O3 catalyst whether they were fresh or aged catalysts. The Pd/CeO2-ZrO2-Al2O3 exhibited high three-way catalytic activity at low temperature, high thermal stability, and wide working window, suggesting a great potential for applications.展开更多
CeVO4, CeMo0.01V0.99O4 and CeMo0.03V0.97O4 were prepared by co-precipitation method. The addition of molybdenum as promoter shows a positive effect on the catalytic behavior of CeVO4 in oxidative dehydrogenation of pr...CeVO4, CeMo0.01V0.99O4 and CeMo0.03V0.97O4 were prepared by co-precipitation method. The addition of molybdenum as promoter shows a positive effect on the catalytic behavior of CeVO4 in oxidative dehydrogenation of propane to propylene. The reduction behaviors of the catalysts were characterized by temperature-programmed reduction. The activation energies of reduction process for the catalysts were obtained at different reduction rates by Kissinger method. The addition of Mo to CeVO4 enhances the selectivity to propylene.展开更多
Various manganese oxide nanorods with similar one-dimensional morphology were prepared by calcination of MnOOH nanorods under different gas atmosphere and at different temper- atures, which were synthesized by a hydro...Various manganese oxide nanorods with similar one-dimensional morphology were prepared by calcination of MnOOH nanorods under different gas atmosphere and at different temper- atures, which were synthesized by a hydrothermal route. The morphology and structure of MnOx catalysts were characterized by a series of techniques including X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, and tempera- ture programmed reduction （TPR）. The catalytic activities of the prepared MnO~ nanorods were tested in the liquid phase aerobic oxidation of benzyl alcohol, which follow a sequence as MnO2〉Mn203~Mn304〉MnOOH with benzaldehyde being the main product. On the basis of H2-TPR results, the superior activity of MnO2 is ascribed to its lower reduction temperature and therefore high oxygen mobility and excellent redox ability. Moreover, a good recycling ability was observed over MnO2 catalysts by simply thermal treatment in air.展开更多
The oxygen storage material (OSM) Ce0.35Zr0.55Y0.1O1.95 was prepared by co-precipitation routine and studied by means of TEM, XRD, XPS, BET, H2-TPR and oxygen storage capacity (OSC) measurements. The results indicated...The oxygen storage material (OSM) Ce0.35Zr0.55Y0.1O1.95 was prepared by co-precipitation routine and studied by means of TEM, XRD, XPS, BET, H2-TPR and oxygen storage capacity (OSC) measurements. The results indicated that this material possessed plenty of Ce3+ and lattice oxygen vacancy (percentage of Ce3+ was 59.6%) and high cerium atom utilization ratio (80.04%). The porous material was with an average BET surface area of 97 m2·g-1 and pore volume of 0.26 mL·g-1. After aged at 1 000 ℃ in air for 5 h, the sample still possessed plenty of Ce3+ and lattice oxygen vacancy (percentage of Ce3+ was 57.1%), and showed high cerium atom utilization ratio (78.25%), and high thermal stability.展开更多
基金the National Natural Science Foundation of China (50574046)National Natural Science Foundation of Major Research Projects (90610035)+1 种基金Natural Science Foundation of Yunnan Province (2004E0058Q)High School Doctoral Subject Special Science and Re- search Foundation of Ministry of Education (20040674005)
文摘A series of Ce1-xFexO2 （x=0, 0.2, 0.4, 0.6, 0.8, 1） complex oxide catalysts were prepared using the coprecipitation method. The catalysts were characterized by means of XRD and H2-TPR. The reactions between methane and lattice oxygen from the complex oxides were investigated. The characteristic results revealed that the combination of Ce and Fe oxide in the catalysts could lower the temperature necessary to reduce the cerium oxide. The catalytic activity for selective CH4 oxidation was strongly influenced by dropped Fe species. Adding the appropriate amount of Fe2O3 to CeO2 could promote the action between CH4 and CeO2. Dispersed Fe2O3 first returned to the original state and would then virtually form the Fe species on the catalyst, which could be considered as the active site for selective CH4 oxidation. The appearance of carbon formation was significant and the oxidation of carbon appeared to be the rate-determining step; the amounts of surface reducible oxygen species in CeO2 were also relevant to the activity. Among all the catalysts, Ce0.6Fe0.402 exhibited the best activity, which converted 94.52% of CH4 at 900 ℃.
文摘Three series of CeO2/CuO samples were prepared by impregnation method and characterized by XRD, N2 adsorption-desorption, temperatureprogrammed reduction （TPR）, XPS and TEM techniques. In comparison with the samples prepared with CuO as initial support, the samples with Cu（OH）2 as initial support have higher reducibilities and smaller relative TPR peak areas, and also larger specific surface areas at calcina- tion temperatures of 400 ℃--600 ℃. As a result, Cu（OH）2 is better than CuO as initial support for preferential oxidation of CO in excess H2 （CO-PROX）. The best catalytic performance was achieved on the sample calcined at 600 ℃ and with an atomic ratio of Ce/Cu at 40%. XPS analyses indicate that more interface linkages Ce-O-Cu could be formed when it was calcined at 600 ℃. And the atomic ratio of Ce/Cu at 40% led to a proper reducibility for the sample as illustrated by the TPR measurements.
文摘A series of Co (10.7 wt. %)-CeO2/SiO2 catalysts with various cerium contents was prepared and evaluated. The optimized ceria-promoted catalyst exhibits good activity, high selectivity towards long chain hydrocarbons, and excellent stability. The promotion mechanism of ceria was investigated using X-ray diffraction (XRD), temperature programmed reduction (TPR), H2 temperature programmed surface reaction (H2-TPSR) and transient response technique. It is suggested that the improved catalytic performance of the catalyst modified by ceria be attributed to (1) the improvement in the dispersion of metallic cobalt and the amount of active sites for Fischer-Tropsch Synthesis (FTS), leading to an increased concentration of surface active carbon species and high selectivity towards long chain hydrocarbons; (2) the inhibition of disproportionation of CO and the removal of inactive surface carbon species.
文摘The effect of BaO doping to the Pt-Rh catalysts on its three-way catalytic activity and water-gas transfer was investigated. The results show that the light-off temperatures of hydrocarbon and carbon monoxide and nitrogen oxides have little difference in the fresh catalysts. But after the hydrothermal-aged 5 h at 1000 ℃, the catalysts containing CeO2-ZrO2-BaO has lower light-off temperature and better catalytic activity than the catalysts containing BaO and CeO2-ZrO2,
基金Project supported by the National Natural Science Foundation of China (20273043) the National Nature Science KeyFoundation of China (20333030)
文摘The effects of BaO doping on the three-way catalytic activity of Pt-Rh catalyst and on water-gas shift were investigated. The results show that the light-off temperatures of hydrocarbon and carbon monoxide and nitrogen oxides of the fresh catalysts slightly differ from those of the aged catalysts, and the catalysts containing CeO2-ZrO2-BaO have lower lightoff temperature and better catalytic activity than these containing BaO and CeO2-ZrO2 after hydrothermal aging for 5 h at 1000 ℃. The catalysts were characterized by means of the temperature-programmed reduction （TPR） in hydrogen and the temperature-programmed desorption （TPD） in oxygen. It is confirmed that the suggested route of CeO2-ZrO2-BaO by coprecipitation can improve the catalytic activity of catalysts.
基金Project supported by the National High Technology Research and Development Program of China (863 Program,2006AA06Z347)the Specialized Research Fund for the Doctoral Program of Higher Education (20070610026)
文摘The Pd-only catalysts for motorcycle were prepared by impregnating CeO2-ZrO2-Al2O3 and CeO2-ZrO2+Al2O3 with PdCl2 aqueous solution and characterized by X-ray diffraction (XRD), oxygen storage capacity (OSC) and H2-temperature-programmed reduction (H2-TPR) methods. The XRD result indicated that the CeO2-ZrO2-Al2O3 compound prepared by co-precipitation formed a single solid solution and had good thermal stability, and Pd phase was not observed in all catalysts. The TPR results showed that the reduction temperature of Pd/CeO2-ZrO2-Al2O3 catalyst was lower than that of Pd/CeO2-ZrO2+Al2O3 catalyst whether they were fresh or aged catalysts. The Pd/CeO2-ZrO2-Al2O3 exhibited high three-way catalytic activity at low temperature, high thermal stability, and wide working window, suggesting a great potential for applications.
基金supported by the National Natural Science Foundation of China (No. 21076056 and 20973096)the National Basic Research Program of China (No. 2009CB623502)the Program for Changjiang Scholars and Innovative Research Team in University (IRT0927)
文摘CeVO4, CeMo0.01V0.99O4 and CeMo0.03V0.97O4 were prepared by co-precipitation method. The addition of molybdenum as promoter shows a positive effect on the catalytic behavior of CeVO4 in oxidative dehydrogenation of propane to propylene. The reduction behaviors of the catalysts were characterized by temperature-programmed reduction. The activation energies of reduction process for the catalysts were obtained at different reduction rates by Kissinger method. The addition of Mo to CeVO4 enhances the selectivity to propylene.
文摘Various manganese oxide nanorods with similar one-dimensional morphology were prepared by calcination of MnOOH nanorods under different gas atmosphere and at different temper- atures, which were synthesized by a hydrothermal route. The morphology and structure of MnOx catalysts were characterized by a series of techniques including X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, and tempera- ture programmed reduction （TPR）. The catalytic activities of the prepared MnO~ nanorods were tested in the liquid phase aerobic oxidation of benzyl alcohol, which follow a sequence as MnO2〉Mn203~Mn304〉MnOOH with benzaldehyde being the main product. On the basis of H2-TPR results, the superior activity of MnO2 is ascribed to its lower reduction temperature and therefore high oxygen mobility and excellent redox ability. Moreover, a good recycling ability was observed over MnO2 catalysts by simply thermal treatment in air.
文摘The oxygen storage material (OSM) Ce0.35Zr0.55Y0.1O1.95 was prepared by co-precipitation routine and studied by means of TEM, XRD, XPS, BET, H2-TPR and oxygen storage capacity (OSC) measurements. The results indicated that this material possessed plenty of Ce3+ and lattice oxygen vacancy (percentage of Ce3+ was 59.6%) and high cerium atom utilization ratio (80.04%). The porous material was with an average BET surface area of 97 m2·g-1 and pore volume of 0.26 mL·g-1. After aged at 1 000 ℃ in air for 5 h, the sample still possessed plenty of Ce3+ and lattice oxygen vacancy (percentage of Ce3+ was 57.1%), and showed high cerium atom utilization ratio (78.25%), and high thermal stability.
