Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Transition-state theory equilibrium

Flere, we shall concentrate on basic approaches which lie at the foundations of the most widely used models. Simplified collision theories for bimolecular reactions are frequently used for the interpretation of experimental gas-phase kinetic data. The general transition state theory of elementary reactions fomis the starting point of many more elaborate versions of quasi-equilibrium theories of chemical reaction kinetics [27, M, 37 and 38]. [Pg.774]

The quasi-equilibrium assumption in the above canonical fonn of the transition state theory usually gives an upper bound to the real rate constant. This is sometimes corrected for by multiplying (A3.4.98) and (A3.4.99) with a transmission coefifiwient 0 < k < 1. [Pg.780]

There is still some debate regarding the form of a dynamical equation for the time evolution of the density distribution in the 9 / 1 regime. Fortunately, to evaluate the rate constant in the transition state theory approximation, we need only know the form of the equilibrium distribution. It is only when we wish to obtain a more accurate estimate of the rate constant, including an estimate of the transmission coefficient, that we need to define the system s dynamics. [Pg.203]

Do we expect this model to be accurate for a dynamics dictated by Tsallis statistics A jump diffusion process that randomly samples the equilibrium canonical Tsallis distribution has been shown to lead to anomalous diffusion and Levy flights in the 5/3 < q < 3 regime. [3] Due to the delocalized nature of the equilibrium distributions, we might find that the microstates of our master equation are not well defined. Even at low temperatures, it may be difficult to identify distinct microstates of the system. The same delocalization can lead to large transition probabilities for states that are not adjacent ill configuration space. This would be a violation of the assumptions of the transition state theory - that once the system crosses the transition state from the reactant microstate it will be deactivated and equilibrated in the product state. Concerted transitions between spatially far-separated states may be common. This would lead to a highly connected master equation where each state is connected to a significant fraction of all other microstates of the system. [9, 10]... [Pg.211]

A more general, and for the moment, less detailed description of the progress of chemical reactions, was developed in the transition state theory of kinetics. This approach considers tire reacting molecules at the point of collision to form a complex intermediate molecule before the final products are formed. This molecular species is assumed to be in thermodynamic equilibrium with the reactant species. An equilibrium constant can therefore be described for the activation process, and this, in turn, can be related to a Gibbs energy of activation ... [Pg.47]

Given the foregoing assumptions, it is a simple matter to construct an expression for the transition state theory rate constant as the probability of (1) reaching the transition state dividing surface and (2) having a momenrnm along the reaction coordinate directed from reactant to product. Stated another way, is the equilibrium flux of reactant states across... [Pg.201]

The transition state theory rate constant can be constructed as follows. The total flux of trajectories across the transition state dividing surface will be equal to the rate of transition times the population of reactants at equilibrium N, or... [Pg.202]

It is a remarkable fact that the microscopic rate constant of transition state theory depends only on the equilibrium properties of the system. No knowledge of the system dynamics is required to compute the transition state theory estimate of the reaction rate constant... [Pg.203]

The assumptions of transition state theory allow for the derivation of a kinetic rate constant from equilibrium properties of the system. That seems almost too good to be true. In fact, it sometimes is [8,18-21]. Violations of the assumptions of TST do occur. In those cases, a more detailed description of the system dynamics is necessary for the accurate estimate of the kinetic rate constant. Keck [22] first demonstrated how molecular dynamics could be combined with transition state theory to evaluate the reaction rate constant (see also Ref. 17). In this section, an attempt is made to explain the essence of these dynamic corrections to TST. [Pg.204]

The collision theory considers the rate to be governed by the number of energetic collisions between the reactants. The transition state theory considers the reaction rate to be governed by the rate of the decomposition of intermediate. Tlie formation rate of tlie intermediate is assumed to be rapid because it is present in equilibrium concentrations. [Pg.16]

Let us examine the equilibrium assumption of transition state theory. Consider a reversible elementary reaction at equilibrium. Because the initial and final states are at equilibrium, assuredly the transition state is in equilibrium with each of these. (It follows that for a reaction at equilibrium, transition state theory is exact insofar as the equilibrium assumption is concerned.)... [Pg.201]

If the transition state theory is applied to the reaction of two hard spheres, the result is identical with that of simple collision theory. - pp Because transition state theory is an equilibrium theory, it can be inferred that collision theory is also an equilibrium theory. [Pg.207]

The numerical values of AG and A5 depend upon the choice of standard states in solution kinetics the molar concentration scale is usually used. Notice (Eq. 5-43) that in transition state theory the temperature dependence of the rate constant is accounted for principally by the temperature dependence of an equilibrium constant. [Pg.208]

The formulation of transition state theory has been in terms of reactant and transition state concentrations let us now define an equilibrium constant in terms of activities. [Pg.209]

A more interesting possibility, one that has attracted much attention, is that the activation parameters may be temperature dependent. In Chapter 5 we saw that theoiy predicts that the preexponential factor contains the quantity T", where n = 5 according to collision theory, and n = 1 according to the transition state theory. In view of the uncertainty associated with estimation of the preexponential factor, it is not possible to distinguish between these theories on the basis of the observed temperature dependence, yet we have the possibility of a source of curvature. Nevertheless, the exponential term in the Arrhenius equation dominates the temperature behavior. From Eq. (6-4), we may examine this in terms either of or A//. By analogy with equilibrium thermodynamics, we write... [Pg.251]

A first-order rate constant has the dimension time, but all other rate constants include a concentration unit. It follows that a change of concentration scale results in a change in the magnitude of such a rate constant. From the equilibrium assumption of transition state theory we developed these equations in Chapter 5 ... [Pg.253]

The transition state theory allows us to apply results of equilibrium thermodynamics, and we, therefore, write, for a reactant or transition state species i. [Pg.254]

The extension to rates draws on the equilibrium assumption of transition state theory to yield the analogous result, with rate constants replacing the equilibrium constants of Eq. (6-96). Kresge has generalized this argument, the result being... [Pg.302]

Transition state theory assumes an equilibrium energy distribution among all possible quantum states at all points along the reaction coordinate. The probability of finding a molecule in a given quantum state is proportional to which is a Boltzmann... [Pg.297]

Various statistical treatments of reaction kinetics provide a physical picture for the underlying molecular basis for Arrhenius temperature dependence. One of the most common approaches is Eyring transition state theory, which postulates a thermal equilibrium between reactants and the transition state. Applying statistical mechanical methods to this equilibrium and to the inherent rate of activated molecules transiting the barrier leads to the Eyring equation (Eq. 10.3), where k is the Boltzmann constant, h is the Planck s constant, and AG is the relative free energy of the transition state [note Eq. (10.3) ignores a transmission factor, which is normally 1, in the preexponential term]. [Pg.417]

The classical approach for discussing adsorption states was through Lennard-Jones potential energy diagrams and for their desorption through the application of transition state theory. The essential assumption of this is that the reactants follow a potential energy surface where the products are separated from the reactants by a transition state. The concentration of the activated complex associated with the transition state is assumed to be in equilibrium... [Pg.13]

As in classical transition state theory, the PMF, w(z), can be computed from the equilibrium average ... [Pg.82]

The classical derivation of transition-state theory starts by assuming that the transition state, Xj, is in equilibrium with the reactants A and B as represented in (1). The rate of reaction, v, is given by (2) where vt is some... [Pg.140]

From transition state theory, we know that the equilibrium constant for formation of the transition state (FC ) is related to the free energy by the relationship... [Pg.268]

The effect of pressure on chemical equilibria and rates of reactions can be described by the well-known equations resulting from the pressure dependence of the Gibbs enthalpy of reaction and activation, respectively, shown in Scheme 1. The volume of reaction (AV) corresponds to the difference between the partial molar volumes of reactants and products. Within the scope of transition state theory the volume of activation can be, accordingly, considered to be a measure of the partial molar volume of the transition state (TS) with respect to the partial molar volumes of the reactants. Volumes of reaction can be determined in three ways (a) from the pressure dependence of the equilibrium constant (from the plot of In K vs p) (b) from the measurement of partial molar volumes of all reactants and products derived from the densities, d, of the solution of each individual component measured at various concentrations, c, and extrapolation of the apparent molar volume 4>... [Pg.548]


See other pages where Transition-state theory equilibrium is mentioned: [Pg.128]    [Pg.128]    [Pg.778]    [Pg.830]    [Pg.1069]    [Pg.197]    [Pg.166]    [Pg.390]    [Pg.438]    [Pg.207]    [Pg.211]    [Pg.396]    [Pg.111]    [Pg.279]    [Pg.3]    [Pg.424]    [Pg.112]    [Pg.233]    [Pg.118]    [Pg.139]    [Pg.150]    [Pg.26]    [Pg.28]    [Pg.42]   
See also in sourсe #XX -- [ Pg.36 ]




SEARCH



Equilibrium Theory of Reaction Rates The Transition-state Method

Equilibrium state

Equilibrium theory

Transition equilibrium

Transition state theory , development equilibrium

Transition state theory equilibrium hypothesis

Transition state theory relative equilibrium

© 2024 chempedia.info