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Exponential function limiting

The solution of the simultaneous differential equations implied by the mechanism can be expressed to give the time-varying concentrations of reactants, products, and intermediates in terms of increasing and decreasing exponential functions (8). Expressions for each component become comphcated very rapidly and thus approximations are built in at the level of the differential equations so that these may be treated at various limiting cases. In equations 2222 and 2323, the first reaction may reach equiUbrium for [i] much more rapidly than I is converted to P. This is described as a case of pre-equihbrium. At equihbrium, / y[A][S] = k [I]. Hence,... [Pg.514]

No general rule for breaking an integrand can be given. Experience alone limits the use of this technique. It is particularly useful for trigonometric and exponential functions. [Pg.446]

This is an indication of the collective nature of the effect. Although collisions between hard spheres are instantaneous the model itself is not binary. Very careful analysis of the free-path distribution has been undertaken in an excellent old work [74], It showed quite definite although small deviations from Poissonian statistics not only in solids, but also in a liquid hard-sphere system. The mean free-path X is used as a scaling length to make a dimensionless free-path distribution, Xp, as a function of a free-path length r/X. In the zero-density limit this is an ideal exponential function (Ap)o- In a one-dimensional system this is an exact result, i.e., Xp/(Xp)0 = 1 at any density. In two dimensions the dense-fluid scaled free-path distributions agree quite well with each other, but not so well with the zero-density scaled distribution, which is represented by a horizontal line (Fig. 1.21(a)). The maximum deviation is about... [Pg.52]

The hard-core limiting forms of U(r) do not lead to physically acceptable results. We conclude that this is caused by a complete neglect of the effect of the attractive forces on the slope of the repulsive part in U(r). If the interaction energy is assumed as the sum of a Morse exponential function and the polarization energy evaluated at r = r°, the resulting transition probabilities appear useful for analyzing ion-molecule collisions. [Pg.67]

The inner integral is done by parts, to increase the exponent of the (u-1) term. Then, since the exponential function in the inner integral is small at the upper limit one may take the limit to infinity, and the lower limit will be adequately replaced by unity. [Pg.255]

The exponential and limiting regions of cell growth can be described by a single relation, in which /x is a function of substrate concentration, i.e., the Monod equation... [Pg.42]

Noncompartmental analysis is limited in that it is not descriptive or predictive concentrations must be interpolated from data. The appeal of noncompartmental analysis is that the shape of the blood concentration-versus-time curve is not assumed to be represented by an exponential function and, therefore, estimates of metabolic and pharmacokinetic parameters are not biased by this assumption. In order to minimize errors in parameter estimates that are introduced by interpolation, a large number of data points that adequately define the concentration-versus-tie curve are needed. [Pg.727]

Nonexponential luminescence decays are not well understood. However, regardless of the lack of understanding, it is a tradition to fit complex decays to sums of exponential functions either discrete or continuous (lifetime distributions). An important limitation of this approach is introduced by the nonorthogonal nature of the exponential function. The practice of fitting nonexponential luminescence decays to... [Pg.267]

This relationship for Newtonian viscosity is valid normally for temperatures higher than 50 °C or more above the Tg. The utility of the Arrhenius correlation can be limited to a relatively small temperature range for accurate predictions. The viscosity is usually described in this exponential function form in terms of an activation energy, Af, absolute temperature T in Kelvin, the reference temperature in Kelvin, the viscosity at the reference T, and the gas law constant Rg. As the temperature approaches Tg for PS (Tg = 100°C), which could be as high as 150°C, the viscosity becomes more temperature sensitive and is often described by the WLF equation [10] ... [Pg.102]

In the limit of zero gradient, the sequence reduces to the Hahn echo, and it is conventional to expand the echo amplitude as a multiple exponential function of T, and define, the usual transverse relaxation times, T,... [Pg.107]

Using a simple kinetic model, Solomon demonstrated that the spin-lattice relaxation of the I and S spins was described by a system of coupled differential equations, with bi-exponential functions as general solutions. A single exponential relaxation for the I spin, corresponding to a well-defined Tu, could only be obtained in certain limiting situations, e.g., if the other spin, S, was different from I and had an independent and highly efficient relaxation pathway. This limit is normally fulfilled if S represents an electron spin. The spin-lattice relaxation rate, for the nuclear spin, I, is in such a situation given by ... [Pg.45]

In the standard overdamped version of the Kramers problem, the escape of a particle subject to a Gaussian white noise over a potential barrier is considered in the limit of low diffusivity—that is, where the barrier height AV is large in comparison to the diffusion constant K [14] (compare Fig.6). Then, the probability current over the potential barrier top near xmax is small, and the time change of the pdf is equally small. In this quasi-stationary situation, the probability current is approximately position independent. The temporal decay of the probability to find the particle within the potential well is then given by the exponential function [14, 22]... [Pg.246]

The above reasoning shows that the stretched exponential function (4.14), or Weibull function as it is known, may be considered as an approximate solution of the diffusion equation with a variable diffusion coefficient due to the presence of particle interactions. Of course, it can be used to model release results even when no interaction is present (since this is just a limiting case of particles that are weakly interacting). [Pg.72]


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Function limit

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