Effect of LaCoO3 perovskite deposition on ceria-based supports on total oxidation of VOC

Supported LaCoO3 perovskites with 10 wt.% loading were prepared by impregnation of different supports containing ceria with a solution of La and Co nitrates and citric acid. All precursors were calcined at 700 degrees C for 5 h. XRD investigations indicated the perovskite formation via "citrate" precursor only on ceria support. All catalysts were tested for toluene total oxidation in the temperature range 100-600 degrees C. In spite of a large surface area, alumina-supported perovskites showed a lower global activity. It appears then the necessity of the presence of a perovskite phase for good oxidative activity. In terms of reaction rates higher reaction rates per perovskite weight were observed for all supported catalysts when compared to bulk LaCoO3. (c) 2005 Elsevier B.V. All rights reserved

Low-temperature CO oxidation on Ag/ZSM-5 catalysts: Influence of Si/Al ratio and redox pretreatments on formation of silver active sites

Silver catalysts supported on ZSM-5 (Si/Al = 30, 50 and 80) were investigated for low-temperature CO oxidation to study the nature of the silver active sites and their formation under the influence of the support chemical composition and redox pretreatments. The catalysts were characterized by HRTEM, FTIR, XPS, diffuse reflectance UV–Vis spectroscopy, NH3 thermodesorption (NH3 TPD) and temperature-programmed reduction (H2 TPR). The chemical composition (Si/Al ratio) of the ZSM-5 zeolite support significantly affects catalytic properties of Ag/ZSM-5 samples: the lower the Broensted acidity of the zeolite support, the higher the activity of the catalysts. Interestingly, while oxidizing pretreatment of catalysts led to a significantly better performance than reducing pretreatments, the consecutive reducing treatment of the preoxidized samples significantly promoted the catalytic activity for low-temperature CO oxidation. Thus, Ag/ZMS-5 catalyst with Si/Al = 80, pretreated consecutively in oxidizing and reducing conditions, showed the highest activity, reaching 90% CO conversion at just 40 °C. Comparison of activity and characterization results showed that silver particles with size below 2 nm are the most active; larger particles are just “spectators”. The most probable silver active centers in the low-temperature CO oxidation are ionic species, mostly charged clusters Agnδ+, strongly interacting with the support. The obtained results in low-temperature CO oxidation might be of particular interest for neutralization of exhaust gases of car engines during “cold start”

Low-temperature CO oxidation on Ag/ZSM-5 catalysts: Influence of Si/Al ratio and redox pretreatments on formation of silver active sites

Silver catalysts supported on ZSM-5 (Si/Al = 30, 50 and 80) were investigated for low-temperature CO oxidation to study the nature of the silver active sites and their formation under the influence of the support chemical composition and redox pretreatments. The catalysts were characterized by HRTEM, FTIR, XPS, diffuse reflectance UV–Vis spectroscopy, NH3 thermodesorption (NH3 TPD) and temperature-programmed reduction (H2 TPR). The chemical composition (Si/Al ratio) of the ZSM-5 zeolite support significantly affects catalytic properties of Ag/ZSM-5 samples: the lower the Broensted acidity of the zeolite support, the higher the activity of the catalysts. Interestingly, while oxidizing pretreatment of catalysts led to a significantly better performance than reducing pretreatments, the consecutive reducing treatment of the preoxidized samples significantly promoted the catalytic activity for low-temperature CO oxidation. Thus, Ag/ZMS-5 catalyst with Si/Al = 80, pretreated consecutively in oxidizing and reducing conditions, showed the highest activity, reaching 90% CO conversion at just 40 °C. Comparison of activity and characterization results showed that silver particles with size below 2 nm are the most active; larger particles are just “spectators”. The most probable silver active centers in the low-temperature CO oxidation are ionic species, mostly charged clusters Agnδ+, strongly interacting with the support. The obtained results in low-temperature CO oxidation might be of particular interest for neutralization of exhaust gases of car engines during “cold start”