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Oxygen chemisorption metals

It is important to notice that the work function, , of a given solid surface changes significantly with chemisorption. Thus oxygen chemisorption on transition metal surfaces causes up to 1 eV increase in while alkali chemisorption on transition metal surfaces causes up to 3 eV decrease in . In general electronegative, i.e. electron acceptor adsorbates cause an increase in 0 while electropositive, i.e. electron donor adsorbates cause a decrease in 0. Note that in the former case the dipole vector P formed by the adsorbate and the surface points to the vacuum while in the latter case P points to the surface (Fig. 4.20). [Pg.138]

The first STM evidence for the facile transport of metal atoms during chemisorption was for oxygen chemisorption at a Cu(110) surface at room temperature 10 the conventional Langmuir model is that the surface substrate atoms are immobile. The reconstruction involved the removal of copper atoms from steps [eqn (1)], resulting in an added row structure and the development of a (2 x 1)0 overlayer [eqn (2)]. The steps present at the Cu(llO) surface are... [Pg.52]

Oxygen chemisorption at cryogenic temperatures provided the clue for the presence of metastable reactive oxygen states at metal surfaces, with XPS... [Pg.55]

Influences of Oxygen Chemisorption and of Metal Ions in Ignition and Combustion... [Pg.361]

RICHARDS HSHIEH Oxygen Chemisorption and Metal Ions... [Pg.363]

Influence of Metal Ions on Oxygen Chemisorption and Ignition of Chars. We have carried out extensive studies of the influence of metal ions in wood on pyrolysis mechanisms (5.6) and this approach has now been extended to oxygen chemisorption of the chars. The metal ions occur in wood predominantly as the counterions of the uronic acid components of the hemicelluloses (12). We have shown that they can be almost completely removed by very mild acid treatment without any other major change in the chemistry of the wood. Table II shows that the major metal ions in cottonwood are Ca, K and Mg. The acid-washing process removed 98X of the metal ions in... [Pg.366]

Another way of investigating structure is through the classical method on metals of varying catalyst particle size. The key to this method is to measure active catalyst surface areas in order to determine changes in turnover rates with ensemble size. In recent years several chemisorption techniques have been developed to titrate surface metal centers on oxides (25). In this volume Rao and Narashimha and Reddy report on the use of oxygen chemisorption to characterize supported vanadium oxide. [Pg.8]

A major problem in noble metal catalyzed liquid phase alcohol oxidations -which is principally an oxidative dehydrogenation- is poisoning of the catalyst by oxygen. The catalytic oxidation requires a proper mutual tuning of oxidation of the substrate, oxygen chemisorption and water formation and desorption. When the overall rate of dehydrogenation of the substrate is lower than the rate of oxidation of adsorbed hydrogen, noble metal surface oxidation and catalyst deactivation occurs. [Pg.385]


See other pages where Oxygen chemisorption metals is mentioned: [Pg.140]    [Pg.140]    [Pg.172]    [Pg.464]    [Pg.17]    [Pg.25]    [Pg.23]    [Pg.8]    [Pg.8]    [Pg.16]    [Pg.26]    [Pg.27]    [Pg.51]    [Pg.52]    [Pg.54]    [Pg.56]    [Pg.73]    [Pg.73]    [Pg.77]    [Pg.70]    [Pg.161]    [Pg.168]    [Pg.168]    [Pg.361]    [Pg.362]    [Pg.369]    [Pg.373]    [Pg.408]    [Pg.75]    [Pg.336]    [Pg.410]    [Pg.269]    [Pg.60]    [Pg.79]    [Pg.418]    [Pg.447]   
See also in sourсe #XX -- [ Pg.2 ]




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