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Integration changes

The two volume integrals change the dependence on x and introduce the number density of atoms n (number/cm ) such that the energy now varies as... [Pg.232]

Different values of will result if the integral limits (i.e., band width) or modulation transfer function in the integral change. All surface characterization instruments have a band width and modulation transfer function. If rms roughness values for the same surface obtained using different instruments are to be compared, optimally the band widths and modulation transfer functions would be the same they should at least be known. In the case of isotropic surface structure, the spatial frequencies p and q are identical, and a single spatial frequency (/>) or spatial wavelength d= /p) is used to describe the lateral dimension of structure of the sample. [Pg.714]

Figure 6-15. Nephelauxetic expansions of the d orbitals are expected to be less than those resulting from integral changes in oxidation state. Figure 6-15. Nephelauxetic expansions of the d orbitals are expected to be less than those resulting from integral changes in oxidation state.
Fig. 3.4.7 The linear relationship between the integrated change in SPI image intensity and the gravimetric mass loss due to drying of concrete specimens [9]. Fig. 3.4.7 The linear relationship between the integrated change in SPI image intensity and the gravimetric mass loss due to drying of concrete specimens [9].
Figure 5.19 Diagram to illustrate order of integration change. Figure 5.19 Diagram to illustrate order of integration change.
To simplify the integration we can switch the order of integration. The order of integration change, schematically depicted Fig. 5.19. [Pg.236]

AadsX is an integral change and involves contributions as the fractional coverage varies from 0 9. Usually, we are interested in how thermodynamic properties vary with coverage and want the differential change... [Pg.349]

Some Relations between Macroscopic and Microscopic Adsorption Parameters The molar integral change of free energy at a temperature T during adsorption is [2,13]... [Pg.288]

The integral change in entropy, AS, is determined from the temperature coefficient of AG. The change in differential entropy of the adsorbent, AS, can be determined either from the difference between the changes in entropy of the integral... [Pg.363]

The integral change in free energy, AGt, and the contribution to AG by barium sulfate, n1AG1t, and by water, n2AG2, are plotted in Figure 5. The dashed lines are extrapolations to zero coverage based upon the empirical equations fitted to the data at low pressures. [Pg.368]

Integral change in free energy, AGt, is for system containing 1 mole of barium... [Pg.369]

These arguments lead us to the conclusions that the integrated change in the solvation free energy is... [Pg.122]

Fig. 38. Integrated changes ol charge associated with potential dependence of coverage by the CP intermediate at the reduced Pt electrodes, derived for various initial potentials from the curves of Fig. 37A (340). Fig. 38. Integrated changes ol charge associated with potential dependence of coverage by the CP intermediate at the reduced Pt electrodes, derived for various initial potentials from the curves of Fig. 37A (340).
Finally, if the upper and lower limits of integration are reversed, the sign of the integral changes as well. This is easily seen from the antiderivative form ... [Pg.986]

In practice, it is more precise to evaluate the viscosity from a step strain experiment by transforming the integration of Eq. (7.117) to a logarithmic time scale using the identity td nt = dt, and the lower limit of integration changes because when = 0, In f = - 00 ... [Pg.287]


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See also in sourсe #XX -- [ Pg.78 , Pg.79 ]




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