Metal oxide-adsorbate interactions dissociative adsorption

It has been reported that methanol is formed from C0-H2 reaction over silica-supported Pd, Pt, Ir catalysts (5). The behaviour of the metal was found to be influenced by the carrier (6,7,8, 9). The selectivity in methanol was discussed in terms of acid-base properties of the support which influenced the non dissociative adsorption of CO on the metal required for oxygenated hydrocarbon formation, in terms of electronic interaction between the metal and the support or in terms of stabilization by the carrier of oxidized metal cations which would adsorb CO non dissociatively. We have studied the C0-H2 reaction at 553 K, 30 atmospheres over Pt supported on a variety of oxides. The characteristics of the catalysts are given in table 2... 

In this chapter, recent results are discussed In which the adsorption of nitric oxide and its Interaction with co-adsorbed carbon monoxide, hydrogen, and Its own dissociation products on the hexagonally close-packed (001) surface of Ru have been characterized using EELS (13,14, 15). The data are interpreted In terms of a site-dependent model for adsorption of molecular NO at 150 K. Competition between co-adsorbed species can be observed directly, and this supports and clarifies the models of adsorption site geometries proposed for the individual adsorbates. Dissociation of one of the molecular states of NO occurs preferentially at temperatures above 150 K, with a coverage-dependent activation barrier. The data are discussed in terms of their relevance to heterogeneous catalytic reduction of NO, and in terms of their relationship to the metal-nitrosyl chemistry of metallic complexes. 

Chemisorption [114] on an oxide surface differs significantly from that on metals. One of the main reasons for this difference is the ionic character of the solid, which favors acid-base or donor-acceptor reactions. Lewis sites are localized on the cations and basic sites on the anions. An example of this type of interaction is given by CO2, which reacts with basic to give a surface carbonate COj . Similarly, a donor molecule such as H2O or NH3 can be molecularly adsorbed via its lone-pair electrons, which react with an acidic (cation) site. An alternative to the molecular adsorption is that resulting from the heterolytic dissociation of the molecule. It may occur by abstraction of H atom transferred to a basic site, producing a hydroxyl group. 

Adsorption of reactants on the surface of a catalyst represents the first elementary step in a catalytic reaction cycle. Chemisorption and physisorption are two kinds of adsorption, and differ according to the type and strength of bond. In physisorption, the adsorption bond is due to the rather weak van der Waals interactions between permanent or induced dipoles. Chemisorption occurs if a real chemical bond is formed between the substrate and the adsorbate. Molecules may adsorb intact or dissociate on the surface. Catalytic reactions almost always involve the dissociation of at least one of the reacting molecules. In certain highly stable molecules, such as methane or ethane, chemisorption is not possible without the rupture of a C-H bond. Dissociation of molecules on metals leads to predominantly neutral fragments (homolytic bond splitting), whereas on oxides, the dissociation... 

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