Advances in Catalysis, Vol. 31 by D.D. Eley, Herman Pines, Paul B. Weisz (Eds.) PDF

By D.D. Eley, Herman Pines, Paul B. Weisz (Eds.)

ISBN-10: 0120078317

ISBN-13: 9780120078318

Particular medical benefit and a wealth of knowledge make the e-book tremendous precious, like different volumes within the series.(from preface)A major a part of the hassle in catalysis examine relies on an realizing extra whole wisdom of the character and behaviour of reactive intermediates or chemisorbed complexes will let us to supply greater catalysts for business approaches. The aiding funds circulate is unquestionably in accordance with this assumption. This quantity of Advances in Catalysis provides completely written bills of 4 various sectors of this attempt.

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Extra resources for Advances in Catalysis, Vol. 31

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Contrary to suggestions by the previous workers (140), it was therefore proposed that Rh(1) was the active oxidation state for the ethylene dimerization reaction. 2 - . 1 K I 0 100 200 300 400 0 500 Activation Temperature ("C) FIG. 15. Ethylene dimerization activity for RhNaY catalyst as a function of activation temperature. (Reproduced from Ref. - 40 3 20 0 100 200 300 400 500 600 Activation Temperature ("C) FIG. 16. 5 eV). perature: 0. 2 eV); 0, (Reproduced from Ref. ) 28 I . E. MAXWELL Clearly, with good evidence for Rh(1) as the active species in RhY, there is now a consistency between the homogeneous (141) and heterogeneous catalyst systems.

METHANOL Since the discovery of highly active homogeneous rhodium catalysts for methanol carbonylation by Monsanto workers (f 96), there has been considerable industrial and academic research effort in this area. The catalyst system consists not only of a rhodium complex, but also includes a halogen promoter, preferably containing iodine, typically methyl iodide, which is regenerated at the end of the catalytic cycle. , acetic acid or methyl acetate, depending on reaction conditions). The trace by-products are usually dimethyl ether and acetaldehyde.

Dependence of the catalytic activity (turnover number) of ruthenium A, X, Y, L, and mordenite zeolites for the hydrogenation of benzene on the surface area S of the ruthenium mordenite-4; 0, A-2; A, X - I ; A, X-2; m, Y-l ; W, Y-4; 0, L-2; @, L-4. (Rezeolite: 0, produced from Ref. ) 22 I. E. MAXWELL the amount of hydrogen adsorbed and the catalytic activity of PtY zeolites for cyclohexane dehydrogenation. In addition, the catalyst precalcination temperature prior to reduction had a marked influence on activity.

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Advances in Catalysis, Vol. 31 by D.D. Eley, Herman Pines, Paul B. Weisz (Eds.)

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