Catalytic properties mechanism

Metals and alloys, the principal industrial metalhc catalysts, are found in periodic group TII, which are transition elements with almost-completed 3d, 4d, and 5d electronic orbits. According to theory, electrons from adsorbed molecules can fill the vacancies in the incomplete shells and thus make a chemical bond. What happens subsequently depends on the operating conditions. Platinum, palladium, and nickel form both hydrides and oxides they are effective in hydrogenation (vegetable oils) and oxidation (ammonia or sulfur dioxide). Alloys do not always have catalytic properties intermediate between those of the component metals, since the surface condition may be different from the bulk and catalysis is a function of the surface condition. Addition of some rhenium to Pt/AlgO permits the use of lower temperatures and slows the deactivation rate. The mechanism of catalysis by alloys is still controversial in many instances. 

Additional information concerning the mechanisms of solid—solid interactions has been obtained by many diverse experimental approaches, as the following examples testify adsorptive and catalytic properties of the reactant mixture [1,111], reflectance spectroscopy [420], NMR [421], EPR [347], electromotive force determinations [421], tracer experiments [422], and doping effects [423], This list cannot be comprehensive. Electron probe microanalysis has also been used as an analytical (rather than a kinetic) tool [422,424] for the determination of distributions of elements within the reactant mixture. Infrared analyses have been used [425] for the investigation of the solid state reactions between NH3 and S02 at low temperatures in the presence and in the absence of water. 

An initial deceleratory process ( 1%) in KN3 decomposition is ascribed to reaction at superficial imperfections [712]. The subsequent constant rate of product evolution corresponds to an interface process but this is not a nucleation and growth mechanism since the product metal is volatile (as in NaN3). The catalytic properties of potassium vapour are attributed... 

Kadlec and Rosmusova [1153] believe that both Ni and Co oxalates initially yield product oxide and that the proportion of metal increases with a. Since nickel oxalate decomposes at temperatures 60 K lower than those for CoC204, even a small proportion of Ni2+ markedly increases the rate of decomposition of cobalt oxalate. The effect was attributed to the catalytic properties of the preferentially formed Ni metal. The a—time curves were generally sigmoid and showed only slight deviations in shape with changes in the Ni Co ratio. In the decomposition of a mechanical... 

V-Sb-oxide based catalysts show interesting catal)dic properties in the direct synthesis of acrylonitrile from propane [1,2], a new alternative option to the commercial process starting from propylene. However, further improvement of the selectivity to acrylonitrile would strengthen interest in the process. Optimization of the behavior of Sb-V-oxide catalysts requires a thorough analysis of the relationship between structural/surface characteristics and catalytic properties. Various studies have been reported on the analysis of this relationship [3-8] and on the reaction kinetics [9,10], but little attention has been given to the study of the surface reactivity of V-Sb-oxide in the transformation of possible intermediates and on the identification of the sxirface mechanism of reaction. 

It appears that the heme/imidazole motif can be realized in metaUoporphyrins that are available in just two steps (Fig. 18.21b). However, it is not yet known how to accomplish objectives 2 and 3. It is also important to understand the mechanism of catalyst degradation during the ORR and to identify alternative functional groups that may increase catalyst stability to be useful in fuel cells, a metaUoporphyrin catalyst would probably have to retain its catalytic properties over at least 4 x 10 turnovers (about 1000 hours of operation at a turnover frequency of 1 s ), i.e., more than a hundred times longer than the most stable metaUoporphyrin catalysts reported to date. 

After the review of literature, we report here the results of the degradation of phenol, carried out in our laboratory in the presence of ultrasound, Ti02, rare earths and transition metal ions to highlight our interpretation of the mechanism. Various transition metal salts are known for their catalytic properties due to partly filled d-orbital of the metal atom. Mesoporous transition metal oxides are used not... 

I. The Mechanism of the Influence of Illumination on the Adsorption and Catalytic Properties of a Surface. 158... 

The method of metal introduction should significantly affect the degree of proximity between the Pt and acidic sites, hence the catalytic properties. In a previous study, the behavior of Pt/MCM-22 samples in n-hexane transformation was explored by Martins et al. [11]. In this study the same reaction was used in order to evaluate the influence of the mode of Pt introduction. Three 1 wt.% Pt/MCM-22 samples were prepared, differing by the mode of platinum introduction ion exchange, incipient wetness impregnation or mechanical mixture of the zeolite with Pt/Al203. 

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