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Propagation constant integral expressions

The corrections SPi to the scalar propagation constant are given in Table 14-1 in terms of /j and I2. In the numerator of each expression, the derivative d//d J is the Dirac delta function 3(R — 1), as explained in Section 14-6, and the integral in the denominator is given in Table 14-6. This leads to the expressions for SPi and the corresponding SUt in the same table. There is no correction for the TEo modes, whose fields satisfy the scalar wave equation exactly. [Pg.320]

Integral expressions for the propagation constant 31-S Stored electric and magnetic energies 31-6 Phase and group velocities... [Pg.601]

In Section 11-13 we showed that the exact propagation constant is given explicitly in terms of integrals over the vector modal fields. Here we derive the analogous expression for the scalar propagation constant in terms of scalar solutions of the scalar wave equation. Starting with Eq. (33-1), we multiply by P and integrate over the infinite cross-section to obtain... [Pg.643]

It is useful to think of the total field (Eq, Hq) as being composed of three partial fields an incident and a scattered field outside the particle, as well as a field within the particle. Solutions for these fields can be expressed as expansions in u and V with undetermined coefficients, each term representing a particular integral. The coefficients can then be determined from the boundary conditions, which are that the four tangential components of the total field Eqs, Eq, Hoe, and Ho,p remain continuous across the spherical surface r = a even though the propagation constant k and magnetic permeability /x are discontinuous. The conditions that the radial components Eor and Hor are also continuous across the surface then follow automatically from Maxwell s equations. [Pg.117]

Fig. 6. All paths leading from the initial to the final points in time t contribute an interfering amplitude to the path sum describing the resultant probability amplitude for the quantum propagation. In this double slit free particle case, two paths of constant speed are local functional stationary points of the action, and these two dominant paths provide the basis for a (semiclassical) classification of subsets of paths which contribute to the path integral. In the statistical thermodynamic path expression, the path sum is equal to the off-diagonal electronic thermal density matrix... Fig. 6. All paths leading from the initial to the final points in time t contribute an interfering amplitude to the path sum describing the resultant probability amplitude for the quantum propagation. In this double slit free particle case, two paths of constant speed are local functional stationary points of the action, and these two dominant paths provide the basis for a (semiclassical) classification of subsets of paths which contribute to the path integral. In the statistical thermodynamic path expression, the path sum is equal to the off-diagonal electronic thermal density matrix...
Constant Pattern Behavior. In a real system the finite resistance to mass transfer and axial mixing in the column lead to departures from the idealized response predicted by equilibrium theory. In the case of a favorable isotherm the shock wave solution is replaced by a constant pattern solution. The concentration profile spreads in the initial region until a stable situation is reached in which the mass transfer rate is the same at all points along the wave front and exactly matches the shock velocity. In this situation the fluid-phase and adsorbed-pliase profiles become coincident, as illustrated in Figure 13. This represents a stable situation and the profile propagates without further change in shape—lienee the term constant pattern. The form of the concentration profile under constant pattern conditions may be easily deduced by integrating the mass transfer rate expression subject to the condition c/c0 = q/qQy where qfj is the adsorbed phase concentration in equilibrium with c(y... [Pg.262]

When the ROMP of a monomer M is initiated by a metal carbene complex I it is frequently found that when all the monomer has been consumed there is still some residual initiator present. This is either because the propagation rate constant kp is larger than the initiation rate constant ki and/or because the initial monomer to initiator concentration ratio [M]q/[I]q is not very large. From the observed ratio of the initial initiator to final initiator concentrations [I]oo/[I]o is possible to determine the value of kp l from eqn. (5), obtained by integrating the appropriate rate expressions for the consumption of M and I. [43]. This relationship may be expressed in graphical form, plotting kp i against [I]oo/[I]o different values of [M]q/[I]q [44]. [Pg.7]


See other pages where Propagation constant integral expressions is mentioned: [Pg.216]    [Pg.312]    [Pg.385]    [Pg.519]    [Pg.602]    [Pg.606]    [Pg.612]    [Pg.643]    [Pg.643]    [Pg.661]    [Pg.262]    [Pg.192]    [Pg.192]    [Pg.18]    [Pg.545]    [Pg.736]    [Pg.53]    [Pg.525]   
See also in sourсe #XX -- [ Pg.222 , Pg.292 , Pg.606 , Pg.643 ]




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