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Carbon monoxide over single crystals

Ladas et al. (321) have studied the oxidation of carbon monoxide over model Pd/Al203 catalysts formed by vacuum deposition of Pd on an a-AI2O3 single-crystal support. Little structure sensitivity is found (curves 4 and 5 of Fig. 20), and the rates for low FE agree with those reported for Pd... [Pg.135]

MECHANISMS OF THE CARBON MONOXIDE OXIDATION AND NITRIC OXIDE REDUCTION REACTIONS OVER SINGLE CRYSTAL AND SUPPORTED RHODIUM CATALYSTS ... [Pg.215]

Mechanisms of the Carbon Monoxide Oxidation and Nitric Oxide Reduction Reactions over Single Crystal and Supported Rhodium Catalysts High Pressure Rates Explained using Ultrahigh Vacuum Surface Science", G.B. Fischer, Se H. Oh, J.E. Carpenter, C.L. DiMaggio, S.J. Schmieg,... [Pg.504]

G. Fisher and co-workers, "Mechanism of the Nitric Oxide—Carbon Monoxide—Oxygen Reaction Over a Single Crystal Rhodium Catalyst," in M. [Pg.496]

G. Fisher and co-workers, "Mechanism of the Nitric Oxide—Carbon Monoxide—Oxygen Reaction Over a Single Crystal Rhodium Catalyst," in M. J. Philips and M. Teman, eds., Proceedings of the 9th International Congress on Catalysis, Vol 3, Characterisation and Metal Catalysts, Chemical Institute of Canada, Ottawa, 1988. [Pg.496]

Senanayake SD, Waterhouse GIN, Idiiss H, Madey TE (2005) Coupling of carbon monoxide molecules over oxygen-defected UO fl 11) single crystal and thin film surfaces. Langmuir 21 11141... [Pg.153]

Investigations into these topics are presented in this volume. Iron, nickel, copper, cobalt, and rhodium are among the metals studied as Fischer-Tropsch catalysts results are reported over several alloys as well as single-crystal and doped metals. Ruthenium zeolites and even meteo-ritic iron have been used to catalyze carbon monoxide hydrogenation, and these findings are also included. One chapter discusses the prediction of product distribution using a computer to simulate Fischer-Tropsch chain growth. [Pg.1]

Detailed studies of the coadsorption of oxygen and carbon monoxide, hysteresis phenomena, and oscillatory reaction of CO oxidation on Pt(l 0 0) and Pd(l 1 0) single crystals, Pt- and Pd-tip surfaces have been carried out with the MB, FEM, TPR, XPS, and HREELS techniques. It has been found that the Pt(l 0 0) nanoplane under self-osciUation conditions passes reversibly from a catalytically inactive state (hex) into ahighly active state (1 x 1). The occurrence of kinetic oscillations over Pd nanosurfaces is associated with periodic formation and depletion of subsurface oxygen (Osub)- Transient kinetic experiments show that CO does not react chemically with subsurface oxygen to form CO2 below 300 K. It has been found that CO reacts with an atomic Oads/Osub state beginning at temperature 150 K. Analysis of Pd- and Pt-tip surfaces with a local resolution of 20 A shows the availability of a sharp boundary between the mobile COads and Oads fronts. The study of CO oxidation on Pt(l 0 0) and Pd(l 1 0) nanosurfaces by FEM has shown that the surface phase transition and oxygen penetration into the subsurface can lead to critical phenomena such as hysteresis, self-oscillations, and chemical waves. [Pg.175]

The current knowledge of the CO + O2 reaction mechanism makes possible to state rather justified theoretical models giving insight to the features of spatio-temporal dynamics of reaction on the platinum surface. Carbon monoxide oxidation over Pt(lOO) single crystal has been studied comprehensively. It was shown that under certain conditions (partial pressures of reactants and temperature), the adsorbate coverages and the reaction rate undergo self-oscillations attended by the spatio-temporal pattern of COads and Oads formation on the surface [1,2,94]. The observed phenomena are associated with the reversible adsorbate-induced surface phase transition hex 1 X 1. The platinum state in unreconstructed 1x1 phase is catalytically active due to the ease of oxygen molecules dissociation S (02) 0.3—0.4 S (02) 10. The CO... [Pg.176]

Chemisorption of carbon monoxide on transition metal surfaces (either single crystals or supported clusters) is a tool of general use to study the active sites present over this type of solid surfaces [42]. CO adsorption on noble metals has been the subject of a large number of papers. For instance, the adsorption behaviour of CO on surfaces of Pt single crystals, polycrystalline Pt films, and supported Pt catalysts has been discussed in terms of adsorbed species or adsorption structures formed during interaction of CO with the metal surface. [Pg.437]


See other pages where Carbon monoxide over single crystals is mentioned: [Pg.2]    [Pg.43]    [Pg.464]    [Pg.33]    [Pg.149]    [Pg.773]    [Pg.252]    [Pg.162]    [Pg.370]    [Pg.62]    [Pg.175]    [Pg.129]    [Pg.251]   
See also in sourсe #XX -- [ Pg.24 , Pg.25 , Pg.26 ]




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