Big Chemical Encyclopedia

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

Articles Figures Tables About

Function F itting

The concluding step in the argument is to note that many can be approximated, as closely as desired, by means of a staircase function. This means that, given such a function , it is possible to find a sequence of staircase functions fa with the property... [Pg.113]

The function f(it) can be given in a concrete expression as "S"-shape nonlinear function, schematically shown on the left in Figure 8A. For the convenience of analysis we take the approximation to express the "S"-shape characteristics with the combination of two straight lines as shown on the right in Figure 8A. The third term of Equation 2-2 means the increment of [D] with compression at the air/water interface. To simplify the analysis, we further assume kj k i. This assumption is consistent with the observed stability of the bilayers formed at the zero surface pressure point. The kinetics of [D] can be then expressed as... [Pg.234]

Due to the simple structure of the function f, its first and second partial derivatives are easy to compute... [Pg.132]

These two expressions are found to coincide one with the other. This encouraging result can also be used to move in the same direction to find an analytical expression for the fa-old correlation function (f). It is plausible that the memory kernel ,u(t), of a generic age, intermediate between lM=o = and / (/) =oo = oo(0>is given by... [Pg.430]

The following development of chemical relaxation theory is taken from Bernasconi (1976), Schwarz (1986) and Sparks (1989). Let us consider a physicochemical system where a single independent variable z can be observed. The equilibrium of the system can be determined by a parameter Q (e.g., temperature or pressure). Due to changes in 0, the instantaneous equilibrium may vary with time, t. If it were actually established, the variable z would assume a respective value z t). Should, however, z be different from z t) the inherent tendency for equilibrium must give rise to a rate, dz/dt = z(r), which is described as a pertinent function f It can be linearized if the system slays close enough to an appropriately chosen reference state z , as expressed by... [Pg.63]

The latter distribution function, F it), is a complement function to Fit) and is defined according to the following expression. [Pg.100]

Finding the equilibrium distribution function f(it) by minimizing the form of (1.1) is the next step in the Onsager method. Direct minimization results in an integral equation which can only be solved numaically (cf. [11]). For this reason, an approximate variation method with the following trial function was used in [7]... [Pg.4]

Equations (2) and (3) are physically meaningful only in the temperature range bounded by the triple-point temperature and the critical temperature. Nevertheless, it is often useful to extrapolate these equations either to lower or, more often, to higher temperatures. In this monograph we have extrapolated the function F [Equation (3)] to a reduced temperature of nearly 2. We do not recommend further extrapolation. For highly supercritical components it is better to use the unsymmetric normalization for activity coefficients as indicated in Chapter 2 and as discussed further in a later section of this chapter. [Pg.40]

In practice, however, it is recommended to adjust the coefficient m, in order to obtain either the experimental vapor pressure curve or the normal boiling point. The function f T ) proposed by Soave can be improved if accurate experimental values for vapor pressure are available or if it is desired that the Soave equation produce values estimated by another correlation. [Pg.156]

Each country adopts such and such a class as a function of its climatic conditions. France has chosen classes B, E, and F, respectively for the summer, winter, and cold wave periods. The first is from 1 May to 31 October, the second is from 1 November to 30 April, while the third has... [Pg.215]

The problem of synthesis in Fresnel s approximation is that it is not always solvable. Let s suppose that ,F=Lj It is possible to show that there are functions f, so... [Pg.266]

In the graphical representation of the integral shown above, a line represents the Mayer function f r.p between two particles and j. The coordinates are represented by open circles that are labelled, unless it is integrated over the volume of the system, when the circle representing it is blackened and the label erased. The black circle in the above graph represents an integration over the coordinates of particle 3, and is not labelled. The coefficient of is the sum of tln-ee tenns represented graphically as... [Pg.469]

The integral of the Gaussian distribution function does not exist in closed form over an arbitrary interval, but it is a simple matter to calculate the value of p(z) for any value of z, hence numerical integration is appropriate. Like the test function, f x) = 100 — x, the accepted value (Young, 1962) of the definite integral (1-23) is approached rapidly by Simpson s rule. We have obtained four-place accuracy or better at millisecond run time. For many applications in applied probability and statistics, four significant figures are more than can be supported by the data. [Pg.16]

When this overall sign is positive, the function F is gerade and its term symbol is appended with a "g" subscript (e.g., the level of the O2 molecule, which has 7iu" 7ig 2 occupancy is labeled 2ig) if the sign is negative, F is ungerade and the term symbol is so amended (e.g., the If level of the ItIu configuration of the... [Pg.262]

For the more general case of a homogeneous fluid in which the vary for whatever reason, it is assumed that n J is a function, F, of the as well as of nS and nV ... [Pg.486]

Because the Multiflow had multiple functional units, it would simultaneously perform both A = B + C and D = E + F storing both results in registers. If the result of the comparison turned out to be false, then it would not store the result D back into memory, and the calculation would be discarded. Because the two operations were done in parallel, this method took no extra time. The integer operation, 7 = 7 -H 1, as well as four other operations, could also be performed simultaneously. [Pg.94]

The goal of all minimization algorithms is to find a local minimum of a given function. They differ in how closely they try to mimic the way a drop of water or a small ball would roll down the slope, following the surface curvature, until it ends up at the bottom. Consider a Taylor expansion around a minimum point Xq of the general one-dimensional function F(X), which can be written as... [Pg.78]

From the time function F t) and the calculation of [IT], the values of G may be found. One way to calculate the G matrix is by a fast Fourier technique called the Cooley-Tukey method. It is based on an expression of the matrix as a product of q square matrices, where q is again related to N by = 2 . For large N, the number of matrix operations is greatly reduced by this procedure. In recent years, more advanced high-speed processors have been developed to carry out the fast Fourier transform. The calculation method is basically the same for both the discrete Fourier transform and the fast Fourier transform. The difference in the two methods lies in the use of certain relationships to minimize calculation time prior to performing a discrete Fourier transform. [Pg.564]

The function f(k ) is shown plotted against the thermodynamic capacity ratio in Figure 1. It is seen that for peaks having capacity ratios greater than about 2, the magnitude of (k ) has only a small effect on the optimum particle diameter because the efficiency required to effect the separation tends to a constant value for strongly retained peaks. From equation (1) it is seen that the optimum particle diameter varies as the square root of the solute diffusivity and the solvent viscosity. As, in... [Pg.396]

Outside the jet and away from the boundaries of the workbench the flow will behave as if it is inviscid and hence potential flow is appropriate. Further, in the central region of the workbench we expect the airflow to be approximately two-dimensional, which has been confirmed by the above experimental investigations. In practice it is expected that the worker will be releasing contaminant in this region and hence the assumption of two-dimensional flow" appears to be sound. Under these assumptions the nondimensional stream function F satisfies Laplace s equation, i.e.. [Pg.962]

The symmetry of the structure we are looking for is imposed on the field 0(r) by building up the field inside a unit cubic cell of a smaller polyhedron, replicating it by reflections, translations, and rotations. Such a procedure not only guarantees that the field has the required symmetry but also enables substantial reduction of independent variables 0/ the function F (f)ij k )- For example, structures having the symmetry of the simple cubic phase are built of quadrirectangular tetrahedron replicated by reflection. The faces of the tetrahedron lie in the planes of mirror symmetry. The volume of the tetrahedron is 1 /48 of the unit cell volume. [Pg.695]

The distribution of the vectors normal to the surface is particularly interesting since it can be obtained experimentally. The nuclear magnetic resonance (NMR) bandshape problem, for polymerized surfaces, can be transformed into the mathematical problem of finding the distribution function f x) of... [Pg.701]

Each of these sine functions represents a discrete component of the vibration signature discussed previously. The amplitudes of each discrete component and their phase angles can be determined by integral calculus when the function /(f) is known. Because the subject of integral calculus is beyond the scope of this chapter, the math required to determine these integrals are not presented. A vibration analyzer and its associated software perform this determination using FFT. [Pg.686]


See other pages where Function F itting is mentioned: [Pg.173]    [Pg.86]    [Pg.849]    [Pg.31]    [Pg.70]    [Pg.5]    [Pg.13]    [Pg.256]    [Pg.173]    [Pg.86]    [Pg.849]    [Pg.31]    [Pg.70]    [Pg.5]    [Pg.13]    [Pg.256]    [Pg.655]    [Pg.610]    [Pg.552]    [Pg.252]    [Pg.320]    [Pg.614]    [Pg.9]    [Pg.151]    [Pg.314]    [Pg.179]    [Pg.447]    [Pg.113]    [Pg.18]    [Pg.161]    [Pg.491]    [Pg.222]    [Pg.153]    [Pg.163]    [Pg.177]    [Pg.375]   
See also in sourсe #XX -- [ Pg.519 ]




SEARCH



F-function

© 2024 chempedia.info