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Single reactant system reaction

The technique of confining the catalyst in a capsule permits various treatment or activation procedures as well as examination of multi-component adsorption effects. For a single reactant system reaction products can be preadsorbed at a known quantity to ascertain the effect these might have on reactant adsorption and... [Pg.57]

Figure B3.4.3. A schematic figure showing, for the DH2 collinear system, a reaction-path coordmate Q coimecting continuously the reactants and the single products asymptote. Also shown are the cuts denoting the coordinate perpendicular to Q. Figure B3.4.3. A schematic figure showing, for the DH2 collinear system, a reaction-path coordmate Q coimecting continuously the reactants and the single products asymptote. Also shown are the cuts denoting the coordinate perpendicular to Q.
The simplest solid—solid reactions are those involving two solid reactants and a single barrier product phase. The principles used in interpreting the results of kinetic studies on such systems, and which have been described above, can be modified for application to more complex systems. Many of these complex systems have been resolved into a series of interconnected binary reactions and some of the more fully characterized examples have already been mentioned. While certain of these rate processes are of considerable technological importance, e.g. to the cement industry [1], the difficulties of investigation are such that few quantitative kinetic studies have been attempted. Attention has more frequently been restricted to the qualitative identifications of intermediate and product phases, or, at best, empirical rate measurements for technological purposes. [Pg.282]

Lewis Bases. A variety of other ligands have been studied, but with only a few of the transition metals. There is still a lot of room for scoping work in this direction. Other reactant systems reported are ammoni a(2e), methanol (3h), and hydrogen sulfide(3b) with iron, and benzene with tungsten (Tf) and plati num(3a). In a qualitative sense all of these reactions appear to occur at, or near gas kinetic rates without distinct size selectivity. The ammonia chemisorbs on each collision with no size selective behavior. These complexes have lower ionization potential indicative of the donor type ligands. Saturation studies have indicated a variety of absorption sites on a single size cluster(51). [Pg.60]

This choice may present itself for reactions between a liquid reactant and a readily soluble gas phase reactant. Such reactions may be carried out in a two-phase system at a relatively low pressure (or a high temperature), or in a single phase system at an elevated pressure (or a low temperature). In many chemical processes the actual reaction takes place in the liquid phase only. The... [Pg.239]

Different in silico approaches have been tackled for the description of the complex system of reactions encompassing the PS. Despite the large number of biochemical species, the interactions between the single molecules are well-known. Moreover, higher-order interactions between different molecular classes seem to have a modest impact on the overall protein production [29]. Therefore, it is reasonable to approach a comprehensive description of the PS by modeling every reactant as a single entity. [Pg.154]

Properties such as large interfacial area and an ability to solubilize both oil-soluble and water-soluble reactants in a single phase system makes microemulsions ideal as reaction media (Flanagan and Singh, 2006 Gaonkar and Bagwe, 2002). For example, Morgado and co-workers (1996) nsed a continnons reversed micellar system to synthesize lysophospholipids and free fatty acids from lecithin hydrolysis, with applications to the food, pharmaceutical and chemical industries. Hydrolysis was catalyzed by porcine pancreatic phospholipase A. Carvalho and Cabral (2000) reviewed the use of reversed micellar systems as reactors to carry out lipase-catalyzed esterification, biocatalysis, transesterificadon, and hydrolysis reactions. [Pg.160]

In a single reaction (where selectivity is not a problem), the usual choice of excess reactant is to eliminate the component which is more difficult to separate in the downstream separation system. Alternatively, if one of the components is more hazardous (as is chlorine in this example), again we try to ensure complete conversion. [Pg.35]

In this chapter, we resfiict the discussion to elementary chemical reactions, which we define as reactions having a single energy bamer in both dhections. As discussed in Section I, the wave function R) of any system undergoing an elementary reaction from a reactant A to a product B on the ground-state surface, is written as a linear combination of the wave functions of the reactant, A), and the product, B) [47,54] ... [Pg.344]

In this reaction, there are twelve single bonds and one (C-O) double bond in both the reactants and products. Because of this conservation of the total number and types of bonds, very good results can be obtained relatively inexpensively for isodesmic reactions due to the cancellation of errors on the two sides of the reaction. In other words, comparing very similar systems enables us to take maximum advantage of cancellation of error. [Pg.181]

From the study of the influencing of single reactions by products and by other added substances and from the analysis of mutual influencing of reactions in coupled systems, the following conclusions can be drawn concerning adsorption of the reaction components. (1) With the exception of crotyl alcohol on the platinum-iron-silica gel catalyst, all the substances present in the coupled system, i.e. reactants, intermediate products, and final products, always adsorbed on the same sites of the catalytic surface (competitive adsorption). This nonspecificity was established also in our other studies (see Section IV.F.2) and was stated also by, for example, Smith and Prater (32), (2) The adsorption of starting reactants and the desorption of the intermediate and final products appeared in our studies always as faster, relative to the rate of chemical transformations of adsorbed substances on the surface of the catalyst. [Pg.49]


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