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Acid site from reaction rates

Number of Acid Sites from Reaction Rates. 112... [Pg.97]

Since the salt uptake process takes place at near neutral pH levels where the proton concentration is very low, the rate of salt adsorption by the resin system is extremely slow The rate-limiting step in thermally regenerable ion-exchange resins is the transfer of protons from the acidic to the basic sites. Rapid reaction rates in these resins have been achieved through the use of different methods. [Pg.100]

All the samples shown in Figure 16.9 contain 0.5% Ru so the dispersion on the x-axis is proportional to the number of surface metal sites. The phthalate hydrogenation reaction is well behaved with activities proportional to the number of metal sites - a phenomenon that occurs when there is no structure sensitivity nor any transport restrictions nor issues with aromatic adsorption on acid sites controlling hydrogenation rates. The most active sample is the one produced from the 400 °C reduction of the partially decomposed Ru impregnate. [Pg.363]

In contrast, there are fewer limitations from the chemical point of view. The preparation of large, well-defined, libraries that involve amino acid building blocks has been demonstrated many times. Carefully optimized reaction conditions for the preparation of other mixed libraries can also ensure that each desired compound is present in sufficient amount. However, the reaction rates of some individual selectors with the activated solid support may be lower than that of others. As a result, the more reactive selectors would occupy a majority of the sites within the beads. Since the most reactive selectors may not be the most selective, testing of a slightly larger number of specifically designed CSPs may be required to reduce the effect of falsenegative results. [Pg.90]

The activity and stability of catalysts for methane-carbon dioxide reforming depend subtly upon the support and the active metal. Methane decomposes to carbon and hydrogen, forming carbon on the oxide support and the metal. Carbon on the metal is reactive and can be oxidized to CO by oxygen from dissociatively adsorbed COj. For noble metals this reaction is fast, leading to low coke accumulation on the metal particles The rate of carbon formation on the support is proportional to the concentration of Lewis acid sites. This carbon is non reactive and may cover the Pt particles causing catalyst deactivation. Hence, the combination of Pt with a support low in acid sites, such as ZrO, is well suited for long term stable operation. For non-noble metals such as Ni, the rate of CH4 dissociation exceeds the rate of oxidation drastically and carbon forms rapidly on the metal in the form of filaments. The rate of carbon filament formation is proportional to the particle size of Ni Below a critical Ni particle size (d<2 nm), formation of carbon slowed down dramatically Well dispersed Ni supported on ZrO is thus a viable alternative to the noble metal based materials. [Pg.463]

Figure 12.17 Sites at which insulin stimulates protein synthesis in a muscle. The sites are indicated by 0. Insulin has its anabolic effect on protein synthesis in muscle by affecb ng six processes or reactions (i) it inhibits protein degradab on in the muscle (ii) it sb mulates amino acid transport from the blood into the muscle (iii) it stimulates the inib ab on-reacb on of the pathway for protein synthesis, i.e. formab on of the complex (tRNA-amino acid-mRNA-ribosomal RNA) (iv) it increases the rate of mRNA synthesis, and therefore the number of mRNA molecules (v) it stimulates ribosomal RNA synthesis (vi) it sb mulates elongabon of the pepbde (see Chapter 20). Figure 12.17 Sites at which insulin stimulates protein synthesis in a muscle. The sites are indicated by 0. Insulin has its anabolic effect on protein synthesis in muscle by affecb ng six processes or reactions (i) it inhibits protein degradab on in the muscle (ii) it sb mulates amino acid transport from the blood into the muscle (iii) it stimulates the inib ab on-reacb on of the pathway for protein synthesis, i.e. formab on of the complex (tRNA-amino acid-mRNA-ribosomal RNA) (iv) it increases the rate of mRNA synthesis, and therefore the number of mRNA molecules (v) it stimulates ribosomal RNA synthesis (vi) it sb mulates elongabon of the pepbde (see Chapter 20).

See other pages where Acid site from reaction rates is mentioned: [Pg.470]    [Pg.616]    [Pg.198]    [Pg.520]    [Pg.2789]    [Pg.419]    [Pg.206]    [Pg.114]    [Pg.162]    [Pg.455]    [Pg.63]    [Pg.246]    [Pg.77]    [Pg.533]    [Pg.601]    [Pg.182]    [Pg.452]    [Pg.104]    [Pg.127]    [Pg.283]    [Pg.46]    [Pg.390]    [Pg.95]    [Pg.470]    [Pg.368]    [Pg.200]    [Pg.82]    [Pg.105]    [Pg.282]    [Pg.259]    [Pg.105]    [Pg.666]    [Pg.123]    [Pg.262]    [Pg.259]    [Pg.368]    [Pg.287]    [Pg.324]    [Pg.423]    [Pg.459]    [Pg.508]    [Pg.525]    [Pg.552]   
See also in sourсe #XX -- [ Pg.111 , Pg.112 , Pg.113 ]




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