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Q function

It would seem better to transform chemisorption isotherms into corresponding site energy distributions in the manner reviewed in Section XVII-14 than to make choices of analytical convenience regarding the f(Q) function. The second procedure tends to give equations whose fit to data is empirical and deductions from which can be spurious. [Pg.700]

Here, 8(5) is the Dirac 6 function and /(0) is an arbitrary function to be determined [it can be shown that any function of the type/(g,0) leads to the same result because of the h q) function]. By considering Eq. 046) for the z component, we obtain (employing polar coordinates) ... [Pg.690]

A(Q) function defined by equations 3.3.17 inlet, or at mouth of catalyst pore... [Pg.578]

Equation 4.139 has been written for the case where the isotopic substitution is on reactant molecule A only. Therefore the qs ratio in the numerator cancels. The partition function ratio qA2/qAi in the numerator can be replaced by isotopic ratios of translational, rotational, and vibrational partition functions as in Equation 4.76. However, in the denominator one has to be careful to remember that the isotopic partition ratio involves the q functions which contain only 3N -7 (for a linear... [Pg.123]

Figure 5.11 The shape of the lxo(2)l and x2o(Q) functions for a quantum harmonic oscillator. Figure 5.11 The shape of the lxo(2)l and x2o(Q) functions for a quantum harmonic oscillator.
The ( )j(q)Qm (Q) is a set of linearly independent functions the Qm(Q) functions are not orthogonal in Q-space for arbitrary electronic states the overlap integrals Jd Q Qm(Q) Q m (Q) are the well known Franck-Condon factors. The hypothesis is that an arbitrary quantum molecular state is given by the linear superposition jus as in the general case ... [Pg.184]

If a liquid with constant viscosity r flows through a tube, the P(Q) function is described by the well known Poiseuille equation, which can be written as... [Pg.145]

A solid-phase-supported version of the Pictet-Spengler reaction has been demonstrated for the synthesis of mono- and disubstituted tetrahydro-P-carbolines [40,41], Disubstituted quinolines have been prepared via solid-phase synthesis utilizing three classes of building blocks aiyl methyl ketones, (Q-functionalized acids, and primary amines [42],... [Pg.35]

It is useful to calibrate the EQCM, i.e., to determine Cf, e.g., by electrodeposition and electrodissolution of silver. The rigidity layer behavior can be tested by depositing films of different thicknesses. Usually relatively thin films (10 nm-some hundreds nm) show rigid layer behavior. The deviation from linearity regarding the Am vs. Q function is related to the appearance of the viscoelastic effect. By the help of impedance measurements... [Pg.193]

Crane FL and Navas P (1997) The diversity of coenzyme Q function. Moiecuiar Aspects of Medicine 18(Suppl), S1-S6. [Pg.420]

By successively eliminating the Q functions, this gives a general equation in recursive fonu as before ... [Pg.416]

Figure 10. Neutron total scattering S(Q) functions from powdered samples of the high and low temperature phases of cristobalite and quartz, shown over two ranges of Q. The scattering functions show well-defined Bragg peaks at lower values of Q superimposed above structured diffuse scattering, and at high Q the scattering shows well-defined oscillations. Figure 10. Neutron total scattering S(Q) functions from powdered samples of the high and low temperature phases of cristobalite and quartz, shown over two ranges of Q. The scattering functions show well-defined Bragg peaks at lower values of Q superimposed above structured diffuse scattering, and at high Q the scattering shows well-defined oscillations.
Therefore, it is tempting to formulate the properties of molecules in terms of the q function rather than to refer to a highly abstract many-electron wave function. Unfortunately, just because q is a quasi-classical quantity, it is impossible to base on it a whole exact or approximate treatment of atoms or molecules its role remains that of a description of the results obtained through the calculation of the wave function W itself a>. [Pg.13]

Demonstrate that the weight fraction h vb.a l of randomly branched polymers of N-q/-functional and A l bifunctional monomers N = N-q + is... [Pg.248]

Total scattering data can be analyzed by fitting models directly in reciprocal-space [i.e., the S Q) function is fit]. However, an alternative and intuitive approaeh is to Fourier transform the data to real-spaee to obtain the atomic pair distribution function (PDF), which is then fit in real-space. The reduced pair distribution function, G r), is related to S Q) through a sine Fourier transform aeeording to ... [Pg.468]

In a similar way, integrating (139) over d2a we obtain the Q function for the second-harmonic mode, which has the form... [Pg.46]

Figure 11. Contour plots for the Q function (a) fundamental mode and (b) second-harmonic mode, for the mean number of photons Na = 10. Contours are taken at 0.1 of the maximum. Figure 11. Contour plots for the Q function (a) fundamental mode and (b) second-harmonic mode, for the mean number of photons Na = 10. Contours are taken at 0.1 of the maximum.

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See also in sourсe #XX -- [ Pg.265 , Pg.266 , Pg.291 , Pg.295 , Pg.302 ]




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Separating q Nuclear and Electronic Partition Functions

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