Assessing the Accuracy of Isothermal Kinetic Tests in Reproducing Light-Off Profiles for Pd/Al₂O₃ Catalyzed NO–CO Reactions

Activation energy calculation of NO–CO reaction on rhodium surface by density functional theory

Mechanism and kinetics of the NOCO reaction on Rh

The effect of O2 on the NO–CO reaction over Ag–Pd/Al2O3: An in situ infrared study

Mechanistic Studies of the NO–CO Reaction onRh/Al2O3under Net-Oxidizing Conditions

Investigation into the catalytic reduction of NOx at copper–ceria interface active sites

Copper–cobalt oxide spinel supported on high-temperature aluminosilicate carriers as catalyst for CO–O 2 and CO–NO reactions

Catalytic conversion of CO, NO and SO 2 on supported sulfide catalysts : II. Catalytic reduction of NO and SO 2 by CO

The catalytic property of a [PtMo6]/MgO catalyst prepared by using a [PtMo6O24]8− precursor for NO–CO reactions and a structural analysis by means of Pt L3- and Mo K-edge EXAFS spectroscopy was studied. The catalytic activity of the bimetallic ensemble catalyst appeared due to the incorporation of Pt ions into the MgO surface, where Pt4+ ions substituted Mg2+ ions in the first layer of the MgO surface. It seems that the NO–CO reaction proceeded on the Pt sites embedded in the MgO surface by a redox mechanism, whereas metallic Pt particles on MgO were inactive under the present reaction conditions, characterized by an in-situ EXAFS analysis.

An integrated study of Pt/WO 3/SiO 2 catalysts for the NOCO reaction : III. FTIR kinetic study and correlation of promotional effects

Isolation of Active Adsorbates for the NO–CO Reaction on Pd/Al2O3by Selective Enhancement and Selective Poisoning

Investigation of the physicochemical properties of CuO/Sm2O3/γ-Al2O3 catalysts and their activity for NO removal by CO

In the catalytic NO–CO reaction over metal oxide catalysts, the surface states of reduced metal oxides were studied with ESCA, and the correlation of the activities of the reduced metal oxide catalysts for the NO–CO reaction with their surface states was investigated. The surfaces of the catalysts were studied with ESCA after treatments in situ. It was revealed that the surface states of the metal oxides did not always agree with their bulk constituents. For example, it was found that the oxygen in the surface layer of the cobalt oxide after a proper reduction treatment by CO was richer than in its bulk. Moreover, the correlation between the surface states and the activities of those oxides was successfully explained. It was also concluded that, in the NO–CO reaction, the metal states were most active for the cobalt, iron, and nickel oxides, while the Cu+ state was more active than the Gu metal state for the copper oxide.

Characterization of rhodium oxide nanoparticles in MCM-41 and their catalytic performances for NO–CO reactions in excess O 2

A novel mechanism for spectator CO-mediated reaction with unique cis-(NO) 2 dimer on a Co 2+-dimer/γ-Al 2O 3(1 1 0) model catalyst: Density functional theory calculations

Preparation and characterization of Pd loaded Sr-deficient K2NiF4-type (La, Sr)2MnO4 catalysts for NO–CO reaction