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Quantum Theory of Chemical Reactions: Vol. III: Chemisorption, Catalysis, Biochemical Reactions Book

Quantum Theory of Chemical Reactions: Vol. III: Chemisorption, Catalysis, Biochemical Reactions
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Quantum Theory of Chemical Reactions: Vol. III: Chemisorption, Catalysis, Biochemical Reactions, , Quantum Theory of Chemical Reactions: Vol. III: Chemisorption, Catalysis, Biochemical Reactions
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  • Quantum Theory of Chemical Reactions: Vol. III: Chemisorption, Catalysis, Biochemical Reactions
  • Written by author R. Daudel
  • Published by Springer-Verlag New York, LLC, August 1982
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The third and last volume of this treatise IS concerned with important applications of the quantum theory of chemical reactions to chemisorption, catalysis and biochemical reactions. The book begins with an important paper devoted to the theoretical background of heterogeneous catalysis. It is followed by two papers showing typical applications of wave mechanics to the analysis of chemisorption. Catalysed gas-solid reactions are chosen to illustrate gas, organic solid state reaction and some aspects of the mechanism of the FISCHER-TROPSCH synthesis are presented. The second part of the book is devoted to biochemical applications of quantum chemistry. Two papers are concerned with the quantum theory of enzyme activity. Two others present recent progress of quantum pharmacology. Finally an important contribution to the theory of intermolecular forces is made in the view of possible applications to biochemical problems. vii R. Daudel, A. Pullman, L. Salem, and A. Viellard reds.), Quantum Theory o/Chemical Reactions, Volume III, vii. Copyright (c) 1982 by D. Reidel Publishing Company. THEORETICAL BACKGROUND OF HETEROGENEOUS CATALYSIS J.E.Germain Laboratoire de Catalyse Appliquee et Cinetique Heterogene L.A. 231 du Centre National de la Recherche Scientifique Universite Claude Bernard Lyon I, E.S.C.I.L. 43 Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex. Heterogeneous Catalysis is a surface Kinetic phenomenon by which a chemical reaction between molecules of a fluid phase is accelerated (activity) and oriented (selectivity) by contact with a solid phase (catalysts, without change of the soli


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