Big Chemical Encyclopedia

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

Articles Figures Tables About

Approximation linear

A linear stability analysis of (A3.3.57) can provide some insight into the structure of solutions to model B. The linear approximation to (A3.3.57) can be easily solved by taking a spatial Fourier transfomi. The result for the Ml Fourier mode is... [Pg.739]

The limitations and range of validity of the linear theory have been discussed in [17, 23, 24]- The linear approximation to equation (A3.3.54) and equation (A3.3.57) assumes that the nonlinear temis are small compared to the linear temis. As t[increases with time, at some crossover time i the linear... [Pg.740]

In the linear approximation there is a direct Fourier relationship between the FID and the spectrum and, in the great majority of experunents, the spectrum is produced by Fourier transfonnation of the FID. It is a tacit assumption that everything behaves in a linear fashion with, for example, imifonn excitation (or effective RF field) across the spectrum. For many cases this situation is closely approximated but distortions may occur for some of the broad lines that may be encountered in solids. The power spectrum P(v) of a pulse applied at Vq is given by a smc fiinction 18]... [Pg.1471]

Sun X, Wang H B and Miller W H 1998 Semiclassical theory of electronically nonadiabatic dynamics Results of a linearized approximation to the initial value representation J. Chem. Phys. 109 7064... [Pg.2330]

A linear approximation for the nonpenetration condition between the rod and rigid punch can be written as follows ... [Pg.342]

In real-life problems ia the process iadustry, aeady always there is a nonlinear objective fuactioa. The gradieats deteroiiaed at any particular poiat ia the space of the variables to be optimized can be used to approximate the objective function at that poiat as a linear fuactioa similar techniques can be used to represent nonlinear constraints as linear approximations. The linear programming code can then be used to find an optimum for the linearized problem. At this optimum poiat, the objective can be reevaluated, the gradients can be recomputed, and a new linearized problem can be generated. The new problem can be solved and the optimum found. If the new optimum is the same as the previous one then the computations are terminated. [Pg.79]

Otherwise, the iterations consisting of formulation of linear approximations and the solution of the linear programming problem are continually repeated (48). [Pg.79]

If the accuracy afforded by a linear approximation is inadequate, a generally more accurate result may be based upon the assumption thedfix) may be approximated by a polynomial of degree 2 or higher over certain ranges. This assumption leads to Newtons fundamental interpolation formula with divided differences... [Pg.470]

Figure 26-65 illustrates that Eq. (26-90) provides a linear approximation to the nonlinear relationship between two-phase specific volume and reciprocal pressure (v vs. P or vs. T ). For single components, me initial slope of the curve is found using me Clapeyron equation to give ... [Pg.2349]

A first approximation is obtained by setting a to zero (linear approximation). Hence... [Pg.254]

For times less than the transit time of the wave, the current is proportional to the stress at the input electrode in a linear approximation. For times greater than the wave transit time, the current is proportional to the stress difference between the electrodes. Thus, the thin-film nature of PVDF provides a means to measure stress differences, and, given mechanical tolerances that limit loading times to a few nanoseconds, measurements are difficult to... [Pg.106]

This treatment illustrates several important aspects of relaxation kinetics. One of these is that the method is applicable to equilibrium systems. Another is that we can always generate a first-order relaxation process by adopting the linearization approximation. This condition usually requires that the perturbation be small (in the sense that higher-order terms be negligible relative to the first-order term). The relaxation time is a function of rate constants and, often, concentrations. [Pg.139]

The onset of flow instability in a heated capillary with vaporizing meniscus is considered in Chap 11. The behavior of a vapor/liquid system undergoing small perturbations is analyzed by linear approximation, in the frame work of a onedimensional model of capillary flow with a distinct interface. The effect of the physical properties of both phases, the wall heat flux and the capillary sizes on the flow stability is studied. A scenario of a possible process at small and moderate Peclet number is considered. The boundaries of stability separating the domains of stable and unstable flow are outlined and the values of the geometrical and operating parameters corresponding to the transition are estimated. [Pg.4]

In capillary flow with a distinct meniscus separating the regions of pure liquid and pure vapor flows, it is possible to neglect the change in densities of the phases and assume po and pu are constant. For flow of incompressible fluid (p = const., p = 0, duildx = 0) the substitution of (11.8) in Eqs. (11.1-11.3) leads, in a linear approximation, to the following system of equations... [Pg.441]

A first approach to the definition of the confidence regions in parameter space follows the linear approximation to the parameter joint distribution that we have already used If the estimates are approximately normally distributed around 9 with dispersion [U. U.] then an approximate 100(1 - a)%... [Pg.83]

Without loss of generality y = y can be assumed. If the dipole moment can be assumed to be a linear function of coordinate within the spread of the frozen Gaussian wave packet, the matrix element (gy,q,p, Pjt(r) Y,q, p ) can be evaluated analytically. Since the integrand in Eq. (201) has distinct maxima usually, we can introduce the linearization approximation around these maxima. Namely, the Taylor expansion with respect to bqp = Qq — Qo and 8po = Po — Po is made, where qj, and pj, represent the maximum positions. The classical action >5qj, p , ( is expanded up to the second order, the final phase-space point (q, p,) to the first order, and the Herman-Kluk preexponential factor Cy pj to the zeroth order. This approximation is the same as the ceUularization procedure used in Ref. [18]. Under the above assumptions, various integrations in U/i(y, q, p ) can be carried out analytically and we have... [Pg.174]

Here I — ma is moment of inertia, a angular acceleration, and z the resultant moment. Note that we have neglected attenuation but in reality, of course, it is always present. This equation characterizes a motion for any angle a, but we consider only the vicinity of points of equilibrium. For this reason, the resultant moment in the linear approximation can be represented as... [Pg.203]

A linear approximation for the velocity term, used to treat the DME problem [74], does not work for MEMED, because the concentration boundary layers tend to be much larger for MEMED due to the longer drop times employed. [Pg.349]

Next let us turn our attention to models described by a set of ordinary differential equations. We are interested in establishing confidence intervals for each of the response variables y, j=l,...,/w at any time t=to. The linear approximation of the output vector at time to,... [Pg.181]

Because the degrees of freedom decouple in the linear approximation, it is easy to describe the dynamics in detail. There is the motion across a harmonic barrier in one degree of freedom and N — 1 harmonic oscillators. Phase-space plots of the dynamics are shown in Fig. 1. The transition from the reactant region at q <0 to the product region at q >0 is determined solely by the dynamics in (pi,qi), which in the traditional language of reaction dynamics is called the reactive mode. [Pg.198]

So far, the discussion of the dynamics and the associated phase-space geometry has been restricted to the linearized Hamiltonian in eq. (5). However, in practice the linearization will rarely be sufficiently accurate to describe the reaction dynamics. We must then generalize the discussion to arbitrary nonlinear Hamiltonians in the vicinity of the saddle point. Fortunately, general theorems of invariant manifold theory [88] ensure that the qualitative features of the dynamics are the same as in the linear approximation for every energy not too high above the energy of the saddle point, there will be a NHIM with its associated stable and unstable manifolds that act as separatrices between reactive and nonreactive trajectories in precisely the manner that was described for the harmonic approximation. [Pg.200]


See other pages where Approximation linear is mentioned: [Pg.721]    [Pg.740]    [Pg.741]    [Pg.1263]    [Pg.10]    [Pg.129]    [Pg.80]    [Pg.469]    [Pg.224]    [Pg.110]    [Pg.612]    [Pg.76]    [Pg.39]    [Pg.770]    [Pg.941]    [Pg.97]    [Pg.438]    [Pg.442]    [Pg.86]    [Pg.8]    [Pg.168]    [Pg.102]    [Pg.102]    [Pg.179]    [Pg.180]    [Pg.28]    [Pg.52]    [Pg.200]   
See also in sourсe #XX -- [ Pg.5 , Pg.45 ]

See also in sourсe #XX -- [ Pg.115 , Pg.121 ]

See also in sourсe #XX -- [ Pg.120 ]

See also in sourсe #XX -- [ Pg.72 ]

See also in sourсe #XX -- [ Pg.237 ]

See also in sourсe #XX -- [ Pg.12 , Pg.116 ]

See also in sourсe #XX -- [ Pg.66 , Pg.67 ]

See also in sourсe #XX -- [ Pg.2 ]




SEARCH



A Non-Linear Approximation - Local Anisotropy

Approximate Methods and Linear Algebra

Approximate confidence levels and regions for non-linear models

Approximate linear dependence

Approximate linear relationship

Approximate non-linear lumping in systems with time-scale separation

Approximation linear harmonic

Approximation techniques linearization

Computing Kinetic Parameters Using Non-Linear Approximation Tools

Coupled Cluster Doubles theory, linear approximation

Domain Partition and Linear Approximation of the Yield Function

Electron transfer reactions linear response approximation

Hypernetted-chain approximation linearized

Limits Linear approximation

Linear Combination of Atomic Orbitals Approximation

Linear Interaction Approximation

Linear Interaction Approximation continuum solvent

Linear approximation excited state Hanle effect

Linear approximation of the

Linear approximations, role

Linear combination of atomic orbitals LCAO) approximation

Linear coupled-cluster approximation

Linear driving force approximation

Linear eikonal approximation

Linear noise approximation

Linear response approximation

Linear response approximation models

Linear response approximation solvation

Linear superposition approximation

Linearization approximation

Linearization approximation Debye-Hiickel

Linearized approximation

Linearized approximation

Linearized mapping approximation

Matrix form of quasi-linear approximation

Molecular orbital linear combination atomic orbitals approximation

Multi-configuration linear response approach and random phase approximation

Quasi-linear approximation

Quasi-linear approximation localized

Quasi-linear approximation of the modified Greens operator

Simplification linear approximation

The linear approximation

Theories linear driving force approximation

Three-Phase System and Linear Approximation

© 2024 chempedia.info