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The Integral Equation

Let us denote by P the class of boundary value problems for which a unique solution to (2.5.1) exists. We shall not seek to determine the size of this class. However, in Chap. 3, it will emerge that simple contact problems involving transverse motion are members of P, so that at least it is non-empty. It is likely in fact that P is quite extensive, in which case (2.5.1) provides a general method for solving non-inertial boundary value problems. For certain problem categories, the question of whether or not they belong to P is irrelevant because easier methods exist for solving them, as we shall see in Sect. 2.6. [Pg.67]

For contact problems involving transverse motion, it would seem that no simpler method than solving (2.5.1) is available, without special assumptions on the form of the viscoelastic functions. [Pg.67]

Equation (2.5.1) involves both space and time variables occurring in an interdependent manner, which renders it unlikely that exact solutions will be available, even for simple problems. The two methods of solution, with any wide degree of applicability, are (a) numerical and (b) iterative. In the former case. [Pg.67]

General Theorems and Methods of Solution of Boundary Value Problems [Pg.68]

Considerable simplification is achieved if only steady-state solutions, involving uniform linear motion, are sought. We shall see, in Chap. 3, that the time variable is essentially eliminated, leaving an integral equation in the space variable. At least for simple problems, it is possible to make considerable analytical progress before resorting to numerical methods. [Pg.68]


These equations are the coupled system of discrete equations that define the rigorous forward problem. Note that we can take advantage of the convolution form for indices (i — I) and (j — J). Then, by exciting the conductive media with a number N/ oi frequencies, one can obtain the multifrequency model. The kernels of the integral equations are described in [13] and [3j. [Pg.328]

If the impulse response function g(x) of a system is known, the output signal y(x) of the system is given for any input signal u(x). The integral equation, which is called superposition integral. [Pg.366]

The step response function h(x) is also determined by the integral equation (1). The relationship between step response h(x) and the impulse response g(x) is represented by... [Pg.366]

One may choose 6(Q,P,T) such that the integral equation can be inverted to give f Q) from the observed isotherm. Hobson [150] chose a local isotherm function that was essentially a stylized van der Waals form with a linear low-pressure region followed by a vertical step tod = 1. Sips [151] showed that Eq. XVII-127 could be converted to a standard transform if the Langmuir adsorption model was used. One writes... [Pg.656]

The integral equation approach has also been explored in detail for electrolyte solutions, with the PY equation proving less usefiil than the HNC equation. This is partly because the latter model reduces cleanly to the MSA model for small h 2) since... [Pg.583]

Assuming explicit time dependence in L (A3.2.38) is equivalent to the integral equation... [Pg.708]

Eirst decide what the integral equation corresponding to Eq. (6-29) is for the approximate wave function (6-30), then integrate it for various values of y. Report both Y at the minimum energy and Cmin for the Gaussian approximation function. This is a least upper bound to the energy of the system. Your report should include a... [Pg.182]

Fig. 21. Control volumes for appHcation of the integral equations of motion where 1, 2, and 3 are the location of control surfaces and Sy (a) general,... Fig. 21. Control volumes for appHcation of the integral equations of motion where 1, 2, and 3 are the location of control surfaces and Sy (a) general,...
The integral equation method is free of the disadvantages of the continuum model and simulation techniques mentioned in the foregoing, and it gives a microscopic picture of the solvent effect within a reasonable computational time. Since details of the RISM-SCF/ MCSCF method are discussed in the following section we here briefly sketch the reference interaction site model (RISM) theory. [Pg.419]

We recently proposed a new method referred to as RISM-SCF/MCSCF based on the ab initio electronic structure theory and the integral equation theory of molecular liquids (RISM). Ten-no et al. [12,13] proposed the original RISM-SCF method in 1993. The basic idea of the method is to replace the reaction field in the continuum models with a microscopic expression in terms of the site-site radial distribution functions between solute and solvent, which can be calculated from the RISM theory. Exploiting the microscopic reaction field, the Fock operator of a molecule in solution can be expressed by... [Pg.420]

Discretizating by substituting the various finite-difference type approximations for the terms in the integrated equation representing flow processes, which converts the integral equations into a system of algebraic equations. [Pg.785]

If the cavity function does not change fast in the region of interest, then the derivative Viy(ri3) is small and thus the integral involved may be neglected. In this approximation on integrating Eq. (27), we obtain the integral equation... [Pg.142]

The above-quoted integral equation has been widely used over the last 50 years and to give a detailed aeeount of all its divergent appheations would require a whole book. The interested reader is advised to eonsult several already available review artieles [8-10] as well as a number of exeellent monographs [4-6,11,12]. Here we only mention some direetions of researeh that use the integral equation approaeh and will shortly point some of its advantages as well as limitations and drawbaeks it suffers from. [Pg.246]

We proceed with cluster series which yield the integral equations. Evidently the correlation functions presented above can be defined by their diagrammatic expansions. In particular, the blocking correlation function is the subset of graphs of h rx2), such that all paths between... [Pg.302]

Wilkinson" has generalized the fractional time method in the following way. For rate equation dcldt = —kc", the integrated equation, for n 1, is... [Pg.30]

The constant is determined by the initial conditions. Suppose Cb = 0 at t = 0 then we obtain constant = —dkiKk2 — k,), and the integrated equation becomes... [Pg.67]

Figure 7 shows schematically the main components of the water balance in soils, the integral equation for which in terms used in the figure can be written as follows ... [Pg.121]

Exercise Derive the integral equation for the stationary density function/(x) by differentiating the expression in F(x) with respect to x. [Pg.283]

This peculiar form applies when a dimeric molecule dissociates to a reactive monomer that then undergoes a first-order or pseudo-first-order reaction. This scheme is considered in Section 4.3. Unless one can work at either of the limits, the form is such that a numerical solution or the method of initial rates will be needed, since the integrated equation has no solution for [A]r. [Pg.35]

It is necessary to get insight into the kernel of the integral equation (3.26). Since frequency exchange is initiated by non-adiabatic collisions, it is reasonable to use the Keilson-Storer model. However, before employing kernel (1.16) it should be integrated over the angle... [Pg.98]

In the case of weak collisions the change in J is so slight that one may proceed from an integral description of the process to a differential one, just as in Eq. (1.23). However, the kernel of the integral equation (3.26) specified in Eq. (3.28) is different from that in the Feller equation. Thus, the standard procedure described in [20] is more complicated and gives different results (see Appendix 3). The final form of the equation obtained in the limit y — 1, to —> 0 with... [Pg.100]

For an unbalanced polymer with [-C00H] - C-NH ] = D and the assumption that D has a constant value results in the integrated equation... [Pg.138]

We have given the integrated equations for simple first- and second-order kinetics. For integrated equations for a large number of kinetic types, see Margerison, D. Ref. 52, p. 361. See Hammett, L.P. Ref 42, p. 62. [Pg.303]

Very recently Husain et al.(12) obtained an analytical solution to the integral equation describing peak broadening for a turbidity detector in the Mie scattering regime. [Pg.48]


See other pages where The Integral Equation is mentioned: [Pg.656]    [Pg.656]    [Pg.474]    [Pg.564]    [Pg.577]    [Pg.637]    [Pg.127]    [Pg.461]    [Pg.461]    [Pg.461]    [Pg.461]    [Pg.461]    [Pg.556]    [Pg.681]    [Pg.688]    [Pg.331]    [Pg.181]    [Pg.24]    [Pg.52]    [Pg.154]    [Pg.31]    [Pg.655]    [Pg.99]    [Pg.270]    [Pg.376]    [Pg.101]    [Pg.633]   


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Integral equations

The Integral

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