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Waves coefficient

Crowding factor Permeability of porous medium Rate constant, I th-order homogeneous reaction Thermal conductivity or thermal conduction coefficient Wave number, Eqs. (10.4.2b), (10.4.28) Wetting coefficient, Eq. (10.1.9)... [Pg.17]

The quotient of the second-order kinetic rate constant over the energy of transition is called the Einstein coefficient of emission, denoted A.j and expressed in m s f Precise, quantum-mechanical calculations give the following equation for the absorption coefficient (wave-number basis) ... [Pg.44]

For some values of 7, this expression will yield MOs that are not normalized.) Equation (15-6) tells us that MO continuous function [by replacing n — )/6 with the continuous variable 0] and then locate the places on this coefficient wave that correspond to the discrete points of interest. Sketches for this coefficient wave when 7 = 3 and 7 = 9 are shown in Fig. 15-6. The special points of interest, where actual coefficient values are given... [Pg.532]

Figure 15-6 Coefficient waves for 7 = 3 dashed curve) and 7 = 9 dotted curve). Both curves intercept the same coefficient values (ibl/VS) at the positions related to carbon atoms 1-6, so the curves produce the same MO. Figure 15-6 Coefficient waves for 7 = 3 dashed curve) and 7 = 9 dotted curve). Both curves intercept the same coefficient values (ibl/VS) at the positions related to carbon atoms 1-6, so the curves produce the same MO.
Equation (15-17) tells us how to produce wavefunctions. We simply take exp(/fa) times our basis set, with k taking on all values between —nja and n ja, and pick off values at discrete points corresponding to carbon atom positions. Since it is more convenient to work with the real forms of solutions, we in effect choose a pair of k values (e.g., —7r/4a and 7r/4a) so that we can generate a pair of trigonometric coefficient waves [cos(7Tx/4a) and sin(7rx/4a)]. Thejr MOs for regular polyacetylene produced from Bloch sums are shown in Fig. 15-8 for selected values of k. These can be used to illustrate some important points ... [Pg.538]

As k increases, the coefficient wave goes to shorter wavelength and more nodes. [Pg.538]

Figure 15-8 Coefficient waves times a periodic basis set of one 2p7r AO on each carbon. (a)A =0, so the coefficient wave is a constant and the periodic basis is unmodulated, (b)-(d) Plus and minus A -value exponentials are mixed to give trigonometric coefficient waves. In (d), one of these waves has nodes at every carbon so no Bloch sum function exists for this case. Figure 15-8 Coefficient waves times a periodic basis set of one 2p7r AO on each carbon. (a)A =0, so the coefficient wave is a constant and the periodic basis is unmodulated, (b)-(d) Plus and minus A -value exponentials are mixed to give trigonometric coefficient waves. In (d), one of these waves has nodes at every carbon so no Bloch sum function exists for this case.
Consider the reflection of a normally incident time-harmonic electromagnetic wave from an inhomogeneous layered medium of unknown refractive index n(x). The complex reflection coefficient r(k,x) satisfies the Riccati nonlinear differential equation [2] ... [Pg.128]

The transmission coefficient Cl (Qj,t), considering transient (broadband) sources, is time-dependent and therefore accounts for the possible pulse deformation in the refraction process. It also takes account of the quantity actually computed in the solid (displacement, velocity potential,...) and the possible mode-conversion into shear waves and is given by... [Pg.736]

The beam-defect interaction is modelled using Kirchhoff s diffraction theory applied to elastodynamics. This theory (see [10] for the scattering by cracks and [11] for the scattering by volumetric flaws) gives the amplitude of the scattered wave in the fonn of coefficients after interaction with defects and takes account of the possible mode-conversion that may occur. [Pg.738]

As a result, the interference of the reflectional wave is shown the change for the position both the defects and the interfaces, and the size of the defect. And, the defect detection quantitatively clarified the change for the wave lengths, the reflection coefficient of sound pressure between materials and the reverse of phase. [Pg.833]

The echo height F/B of the expression (1) is changed that the wave length X becomes shorter, the frequency becomes increaser and the reflective coefficient of sound pressure in the bonding interface becomes higher. [Pg.838]

The use of air-bome ultrasound for the excitation and reception of surface or bulk waves introduces a number of problems. The acoustic impedance mismatch which exists at the transducer/air and the air/sample interfaces is the dominant factor to be overcome in this system. Typical values for these three media are about 35 MRayls for a piezo-ceramic (PZT) element and 45 MRayls for steel, compared with just 0.0004 MRayls for air. The transmission coefficient T for energy from a medium 1 into a medium 2 is given by... [Pg.840]

The expression exp(-cxx) describes the reduction of the wave amplitude in absorbing materials. The damping coefficient a can be split into an absorption coefficient Oa and the scattering coefficient Oj. [Pg.866]

The damping coefficient a can be determined by measuring the exponential reduced wave amplitude p, at various points during propagation. [Pg.866]

By plotting InCp po) against x the damping coefficient a is the gradient of the resulting straight line. To separate the elements oq and Ota in a it is possible to measure the backscattering acoustic wave pressure Ps. [Pg.866]

Surface waves at an interface between two innniscible fluids involve effects due to gravity (g) and surface tension (a) forces. (In this section, o denotes surface tension and a denotes the stress tensor. The two should not be coiifiised with one another.) In a hydrodynamic approach, the interface is treated as a sharp boundary and the two bulk phases as incompressible. The Navier-Stokes equations for the two bulk phases (balance of macroscopic forces is the mgredient) along with the boundary condition at the interface (surface tension o enters here) are solved for possible hamionic oscillations of the interface of the fomi, exp [-(iu + s)t + i V-.r], where m is the frequency, is the damping coefficient, s tlie 2-d wavevector of the periodic oscillation and. ra 2-d vector parallel to the surface. For a liquid-vapour interface which we consider, away from the critical point, the vapour density is negligible compared to the liquid density and one obtains the hydrodynamic dispersion relation for surface waves + s>tf. The temi gq in the dispersion relation arises from... [Pg.725]

We call this a partial M/ave expansion. To detennine tire coefficients one matches asymptotic solutions to the radial Scln-ddinger equation with the corresponding partial wave expansion of equation (A3.11.106). It is customary to write the asymptotic radial Scln-ddinger equation solution as... [Pg.979]

Here, = q ([) ) are the wave fiinctions of the spectroscopic states and the coefficients are detennined from the initial conditions... [Pg.1060]

This is not the case for stimulated anti-Stokes radiation. There are two sources of polarization for anti-Stokes radiation [17]. The first is analogous to that in figure B1.3.3(b) where the action of the blackbody (- 2) is replaced by the action of a previously produced anti-Stokes wave, with frequency 03. This radiation actually experiences an attenuation since the value of Im x o3 ) is positive (leading to a negative gam coefficient). This is known as the stimulated Raman loss (SRL) spectroscopy [76]. Flowever the second source of anti-Stokes polarization relies on the presence of Stokes radiation [F7]. This anti-Stokes radiation will emerge from the sample in a direction given by the wavevector algebra = 2k - kg. Since the Stokes radiation is... [Pg.1205]

Another class of instabilities that are driven by differences in the diffusion coefficients of the chemical species detennines the shapes of propagating chemical wave and flame fronts [65, 66]. [Pg.3069]

In hyperspherical coordinates, the wave function changes sign when <]) is increased by 2k. Thus, the cotTect phase beatment of the (]) coordinate can be obtained using a special technique [44 8] when the kinetic energy operators are evaluated The wave function/((])) is multiplied with exp(—i(j)/2), and after the forward EFT [69] the coefficients are multiplied with slightly different frequencies. Finally, after the backward FFT, the wave function is multiplied with exp(r[Pg.60]

A term that is nearly synonymous with complex numbers or functions is their phase. The rising preoccupation with the wave function phase in the last few decades is beyond doubt, to the extent that the importance of phases has of late become comparable to that of the moduli. (We use Dirac s terminology [7], which writes a wave function by a set of coefficients, the amplitudes, each expressible in terms of its absolute value, its modulus, and its phase. ) There is a related growth of literatm e on interference effects, associated with Aharonov-Bohm and Berry phases [8-14], In parallel, one has witnessed in recent years a trend to construct selectively and to manipulate wave functions. The necessary techifiques to achieve these are also anchored in the phases of the wave function components. This bend is manifest in such diverse areas as coherent or squeezed states [15,16], elecbon bansport in mesoscopic systems [17], sculpting of Rydberg-atom wavepackets [18,19], repeated and nondemolition quantum measurements [20], wavepacket collapse [21], and quantum computations [22,23], Experimentally, the determination of phases frequently utilizes measurement of Ramsey fringes [24] or similar" methods [25]. [Pg.96]


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See also in sourсe #XX -- [ Pg.532 ]




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