Adsorption carbon oxide

C2O2H] has been deduced from isotopic studies of carbon oxide adsorption... 

Lukaszewski M, Siwek H, Czerwinski A (2010) Analysis of the electrochemical quartz crystal microbai-ance response during oxidation of carbon oxides adsorption products on platinum group metals and alloys. J Solid State Electrochem 14(7) 1279-1292... 

Co-adsorption experiments show a complex role of the nature and concentration of chemisorbed ammonia species. Ammonia is not only one of the reactants for the synthesis of acrylonitrile, but also reaction with Br()>nsted sites inhibits their reactivity. In particular, IR experiments show that two pathways of reaction are possible from chemisorbed propylene (i) to acetone via isopropoxylate intermediate or (ii) to acrolein via allyl alcoholate intermediate. The first reaction occurs preferentially at lower temperatures and in the presence of hydroxyl groups. When their reactivity is blocked by the faster reaction with ammonia, the second pathway of reaction becomes preferential. The first pathway of reaction is responsible for a degradative pathway, because acetone further transform to an acetate species with carbon chain breakage. Ammonia as NH4 reacts faster with acrylate species (formed by transformation of the acrolein intermediate) to give an acrylamide intermediate. At higher temperatures the amide may be transformed to acrylonitrile, but when Brreform ammonia and free, weakly bonded, acrylic acid. The latter easily decarboxylate forming carbon oxides. 

Kunimatsu K, Golden WG, Seki H, Philpott MR. 1985a. Carbon monoxide adsorption on a platinum electrode studied by polarization modulated FT-IRRAS. 1. Co Adsorbed in the double-layer potential region and its oxidation in acids. Langmuir 1 245 -250. 

Gilman S. 1963. The mechanism of electrochemical oxidation of carbon monoxide and methanol on platinum. I. Carbon monoxide adsorption and desorption and simultaneous oxidation of the platinum surface at constant potential. J Phys Chem 67 1989-1905. 

Cuesta A, Lopez N, Gutierrez C. 2003. Electrolyte electroreflectance study of carbon monoxide adsorption on polycrystalline silver and gold electrodes. Electrochim Acta 48 2949-2956. Date M, Hamta M. 2001. Moisture effect on CO oxidation over Au/Ti02 catalyst. J Catal 201 221-224. 

Carbon corrosion, 300 Carbon monoxide adsorption, 248,250,255, 325-327, 347, 386-391,528-532 Carbon monoxide oxidation... 

The adsorption of oxygen on diamond was studied by Barrer (156). Essentially no chemisorption was observed at —78°. From 0 to 144° oxygen was chemisorbed, but no carbon oxides were liberated. Some carbon dioxide was formed as well from 244 to 370° by interaction of oxygen and diamond surface not covered with surface oxides. Surfaee oxide formation was observed at low pressures. The coefficient of friction of diamond increases considerably after heating in a high vacuum. The measurements by Bowden and Hanwell (157) showed a decrease in the friction on access of oxygen, even at very low pressures. 

In this work, we will show that the addition of TCM to the feedstream in the methane conversion process results in the enhancement of the conversion of methane and the selectivity to C2 hydrocarbons on praseodymium oxide primarily as a result of the formation of praseodymium oxychloride, in contrast with the production of carbon oxides on praseodymium oxide in the absence of TCM (8-10). The surface properties of these catalysts are characterized by application of adsorption experiments and X-ray photoelectron spectroscopy (XPS). 

Fig. 19. Illustration of carbon monoxide adsorption followed by oxygen adsorption on metal oxides [W. G. Garner, J. Chem. Soc. 1239 (1947)].

Iron molybdates, well known as selective methanol oxidation catalysts, are also active for the propene oxidation, but not particularly selective with respect to acrolein. Acetone is the chief product at low temperature (200°C), whereas carbon oxides, besides some acrolein, predominate at higher temperatures [182,257], Firsova et al. [112,113] report that adsorption of propene on iron molybdate (Fe/Me = 1/2) at 80—120°C causes cation reduction (Fe3+ -> Fe2+) as revealed by 7-resonance spectroscopy. Treatment with oxygen at 400°C could not effect reoxidation (in contrast to similarly reduced tin molybdate). The authors assume that this phenomenon is related to the low selectivity of iron molybdate. 

According to the International Union of Pure and Applied Chemistry (IUPAC O)) the turnover frequency of a catalytic reac tion is defined as the number of molecules reacting per active site in unit time. The term active sites is applied to those sites for adsorption which are effective sites for a particular heterogeneous catalytic reaction. Because it is often impossible to measure the amount of active sites, some indirect method is needed to express the rate data in terms of turnover frequencies In some cases a realistic measure of the number of active sites may be the number of molecules of some compound that can be adsorbed on the catalyst. This measure is frequently used in the literature of the Fischer-Tropsch synthesis, where the amount of adsorption sites is determined by carbon monoxide adsorption on the reduced catalyst. However, it is questionable whether the number of adsorption sites on the reduced catalyst is really an indication of the number of sites on the catalyst active during the synthesis, because the metallic phase of the Fischer-Tropsch catalysts is often carbided or oxidized during the process. 

Carbon monoxide adsorption on ZnO has been found to depend strongly on the pretreatment of the oxide. Kortiim and Knehr (94) detected a weakly bound CO with at least one rotational degree of freedom showing rotational-vibrational bands with maxima at 2188 and 2120 cm-1 and a strongly bound complex similar to bidentate carbonate. In addition, well-degassed ZnO specimens adsorbed CO with the IR frequency within the carbonyl... 

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