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Heterogeneous catalysis between

There are two areas of catalysis based on whether the catalyst belongs to the same phase as the main constituents or a separate phase (usually a solid). The first case is essentially homogeneous catalysis in the liquid phase the second is heterogeneous catalysis between gas reactions catalyzed by a solid. [Pg.323]

Diffusivity and tortuosity affect resistance to diffusion caused by collision with other molecules (bulk diffusion) or by collision with the walls of the pore (Knudsen diffusion). Actual diffusivity in common porous catalysts is intermediate between the two types. Measurements and correlations of diffusivities of both types are Known. Diffusion is expressed per unit cross section and unit thickness of the pellet. Diffusion rate through the pellet then depends on the porosity d and a tortuosity faclor 1 that accounts for increased resistance of crooked and varied-diameter pores. Effective diffusion coefficient is D ff = Empirical porosities range from 0.3 to 0.7, tortuosities from 2 to 7. In the absence of other information, Satterfield Heterogeneous Catalysis in Practice, McGraw-HiU, 1991) recommends taking d = 0.5 and T = 4. In this area, clearly, precision is not a feature. [Pg.2095]

However, research into transition metal catalysis in ionic liquids should not focus only on the question of how to make some specific products more economical or ecological by use of a new solvent and, presumably, a new multiphasic process. Since it bridges the gap between homogeneous and heterogeneous catalysis, in a novel and highly attractive manner, the application of ionic liquids in transition metal catalysis gives access to some much more fundamental and conceptual questions for basic research. [Pg.253]

The Eley-Rideal mechanism for gas-solid heterogeneous catalysis envisions reaction between a molecule adsorbed on the solid surface and one that is still in the gas phase. Consider a reaction of the form... [Pg.377]

Reactivity studies of organic ligands with mixed-metal clusters have been utilized in an attempt to shed light on the fundamental steps that occur in heterogeneous catalysis (Table VIII), although the correspondence between cluster chemistry and surface-adsorbate interactions is often poor. While some of these studies have been mentioned in Section ll.D., it is useful to revisit them in the context of the catalytic process for which they are models. Shapley and co-workers have examined the solution chemistry of tungsten-iridium clusters in an effort to understand hydrogenolysis of butane. The reaction of excess diphenylacetylene with... [Pg.106]

The next level is that of small catalytically active particles, with typical dimensions of between 1 and 10 nm, and inside the pores of support particles (pm range). The questions of interest are the size, shape, structure and composition of the active particles, in particular of their surfaces, and how these properties relate to catalytic reactivity. Although we will deal with heterogeneous catalysis, the anchoring of catalytic... [Pg.17]

Adsorption of reactants on the surface of the catalyst is the first step in every reaction of heterogeneous catalysis. Flere we focus on gases reacting on solid catalysts. Although we will deal with the adsorption of gases in a separate chapter, we need to discuss the relationship between the coverage of a particular gas and its partial pressure above the surface. Such relations are called isotherms, and they form the basis of the kinetics of catalytic reactions. [Pg.53]

Explain the differences and similarities between homogeneous and heterogeneous catalysis. [Pg.401]

The examples of the model studies presented show how the meshing of modern surface techniques with reaction kinetics can provide valuable Insights Into the mechanisms of surface reactions and serve as a useful complement to the more traditional techniques. Close correlations between these two areas holds great promise for a better understanding of the many subtleties of heterogeneous catalysis. [Pg.197]

Drastic sampling and subjective judgment was required to condense 40 years of research in heterogeneous catalysis into a few thousand words. There might be rather little overlap between this paper and that with the same title written by another author. References have been omitted to avoid presenting a sampling of names with the implication that they alone were responsible for the advances. [Pg.68]

J.L Margitfalvi J and M. Hegedus, 8th International Congress on the Relation Between Homogeneous and Heterogeneous Catalysis, Balatonfured, Hungary, Sept. 1995 N°21 oral presentation accepted for publication in J. Mol Cat... [Pg.250]

In 1982, Laine reviewed simple chemical tests and application of some techniques to distinguish between homogeneous and heterogeneous catalysis. He proposed five criteria for detecting homogeneous cluster catalysts ... [Pg.427]

These systematic studies suggest that an intrinsic connection between the adsorbate structure, mobility, and the formation of product can be established with the aid of structural information obtained from high-pressure STM. It further demonstrated the importance of STM in studies of heterogeneous catalysis at high pressure. [Pg.213]


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See also in sourсe #XX -- [ Pg.138 ]




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