Experimental Test of a Transition State Theory for Diffusion Coefficients in Multicomponent Liquids

1975 ◽  
Vol 14 (2) ◽  
pp. 114-119 ◽  
Author(s):  
Robert G. Mortimer ◽  
William R. Marlow ◽  
Jerry L. Shenep
Keyword(s):  
Transition State ◽  
Experimental Test ◽  
Diffusion Coefficients ◽  
Transition State Theory ◽  
State Theory

Transition-State Theory Model for the Diffusion Coefficients of Small Penetrants in Glassy Polymers

1997 ◽  
Vol 30 (23) ◽  
pp. 7296-7306 ◽  
Author(s):  
Angus A. Gray-Weale ◽  
Richard H. Henchman ◽  
Robert G. Gilbert ◽  
Michael L. Greenfield ◽  
Doros N. Theodorou
Keyword(s):  
Transition State ◽  
Diffusion Coefficients ◽  
Transition State Theory ◽  
Theory Model ◽  
State Theory ◽  
Glassy Polymers

Dimensionality reduction of free energy profiles of benzene in silicalite-1: calculation of diffusion coefficients using transition state theory

2013 ◽  
Vol 40 (1-3) ◽  
pp. 80-100 ◽  
Author(s):  
Panagiotis D. Kolokathis ◽  
Evangelia Pantatosaki ◽  
Christina-Anna Gatsiou ◽  
Hervé Jobic ◽  
George K. Papadopoulos ◽  
...  
Keyword(s):  
Free Energy ◽  
Transition State ◽  
Dimensionality Reduction ◽  
Diffusion Coefficients ◽  
Transition State Theory ◽  
State Theory ◽  
Energy Profiles ◽  
Free Energy Profiles

Microscopic Interpretation of Arrhenius Parameters

2018 ◽  
Author(s):  
Niels Engholm Henriksen ◽  
Flemming Yssing Hansen
Keyword(s):  
Activation Energy ◽  
Transition State ◽  
Transition State Theory ◽  
Average Energy ◽  
Zero Point ◽  
State Theory ◽  
Exponential Factor ◽  
Quantum Tunnelling ◽  
Microscopic Interpretation ◽  
The Difference

This chapter reviews the microscopic interpretation of the pre-exponential factor and the activation energy in rate constant expressions of the Arrhenius form. The pre-exponential factor of apparent unimolecular reactions is, roughly, expected to be of the order of a vibrational frequency, whereas the pre-exponential factor of bimolecular reactions, roughly, is related to the number of collisions per unit time and per unit volume. The activation energy of an elementary reaction can be interpreted as the average energy of the molecules that react minus the average energy of the reactants. Specializing to conventional transition-state theory, the activation energy is related to the classical barrier height of the potential energy surface plus the difference in zero-point energies and average internal energies between the activated complex and the reactants. When quantum tunnelling is included in transition-state theory, the activation energy is reduced, compared to the interpretation given in conventional transition-state theory.

Bimolecular Reactions, Transition-State Theory

2018 ◽  
Author(s):  
Niels Engholm Henriksen ◽  
Flemming Yssing Hansen
Keyword(s):  
Transition State ◽  
Saddle Point ◽  
Transition State Theory ◽  
Classical Mechanics ◽  
Small Degree ◽  
State Theory ◽  
Reaction Coordinate ◽  
Partition Functions ◽  
Bimolecular Reactions ◽  
Activated Complex

This chapter discusses an approximate approach—transition-state theory—to the calculation of rate constants for bimolecular reactions. A reaction coordinate is identified from a normal-mode coordinate analysis of the activated complex, that is, the supermolecule on the saddle-point of the potential energy surface. Motion along this coordinate is treated by classical mechanics and recrossings of the saddle point from the product to the reactant side are neglected, leading to the result of conventional transition-state theory expressed in terms of relevant partition functions. Various alternative derivations are presented. Corrections that incorporate quantum mechanical tunnelling along the reaction coordinate are described. Tunnelling through an Eckart barrier is discussed and the approximate Wigner tunnelling correction factor is derived in the limit of a small degree of tunnelling. It concludes with applications of transition-state theory to, for example, the F + H2 reaction, and comparisons with results based on quasi-classical mechanics as well as exact quantum mechanics.

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