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Strength, defined

In fig. 26 the Arrhenius plot ln[k(r)/coo] versus TojT = Pl2n is shown for V /(Oo = 3, co = 0.1, C = 0.0357. The disconnected points are the data from Hontscha et al. [1990]. The solid line was obtained with the two-dimensional instanton method. One sees that the agreement between the instanton result and the exact quantal calculations is perfect. The low-temperature limit found with the use of the periodic-orbit theory expression for kio (dashed line) also excellently agrees with the exact result. Figure 27 presents the dependence ln(/Cc/( o) on the coupling strength defined as C fQ. The dashed line corresponds to the exact result from Hontscha et al. [1990], and the disconnected points are obtained with the instanton method. For most practical purposes the instanton results may be considered exact. [Pg.66]

It should be noted that no such difficulty appears with the integral of an absorption spectrum because the absorption coefficient is proportional to the logarithm of a ratio of intensities, so that e(A) = e(v). For instance, in the calculation of an oscillator strength (defined in Chapter 2), integration can be done either in the wavelength scale or in the wavenumber scale. [Pg.53]

Another important quantity in the context of El transitions is the electric dipole line strength, defined as [7]... [Pg.275]

For octahedral dl, d > d3, d , and d cases, the ground state is derived from the lowest term of the free ion for all values of the crystal field strength (defined by AJ. Hence the multiplicity, the number of unpaired spins and, if the spin-only formula applies, the effective magnetic moment must all be the same as that of the free ion, no matter how strong the interaction between the ion and the ligands. For octahedral d4, d , d , and d7 cases the ground state is derived from... [Pg.274]

The generalized oscillator strength defined by (II.4) has a number of important properties that have been listed by Inokuti.5 Of great importance practically are the sum rules... [Pg.15]

Figure 23. Dependence of MacMillan-Mayer osmotic coefficient on concentration for lithium chloride aqueous solutions at 298 K dotted line indicates calculated and full line indicates experimental dependence on IM, the ionic strength defined in terms of MacMillan-Mayer variables (Friedman and Krishnan, 1973a). Figure 23. Dependence of MacMillan-Mayer osmotic coefficient on concentration for lithium chloride aqueous solutions at 298 K dotted line indicates calculated and full line indicates experimental dependence on IM, the ionic strength defined in terms of MacMillan-Mayer variables (Friedman and Krishnan, 1973a).
The extremes of these coupling strengths define two distinct functional roles for protons ... [Pg.95]

Both definitions are natural since wq turns out to be the ratio of the microwave frequency w and the Kepler firequency H of the Rydberg electron, and Sq is the ratio of the microwave field strength and the field strength experienced by an electron in the noth Bohr orbit of the hydrogen atom. Motivated by the above discussion we have redrawn the results obtained by Bayfield and Koch (1974) and present them in Fig. 7.2 as an ionization signal (in arbitrary units) versus the scaled field strength defined in (7.1.3). For no in (7.1.3) we chose no = 66, the centroid of the band of Rydberg states present in the atomic beam. [Pg.184]

Strength of PS specimens rose about 25% and the strength tended to approach a constant value in the high M range. In contrast, the fatigue strength, defined as the stress level below which no failure occurred in 10 cycles, doubled in value over the M ran studied and it continued to rise with increasing M... [Pg.97]

The procedure now consists in adding other strong electrolytes to the solution. Since remains unaffected by this step while of the electrolyte of interest necessarily changes, m will change in the opposite direction. One thus measures m from the observed solubilities of the salt My Ay in the presence of other salts added in varying amounts. The results may then be extrapolated to infinite dilution on a plot of m versus where S is the ionic strength defined in Eq. (4.2.1). This permits an extrapolation to zero molarity where y — 1. The mean molarity obtained from this extrapolation thus yields. Measuring m for any other value of S then provides the desired y ... [Pg.261]

Thus the phase space structure of the classical dynamics depends not on field strength e and frequency co independently, but only on the scaled field strength defined by Eq. (7). Scaled energies E and scaled actions T derived from the equations of motion in the scaled variables are related to the energies E and actions / in atomic units by... [Pg.104]


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See also in sourсe #XX -- [ Pg.136 ]




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Bond strength, defined

Frictional shear strength, defined

Impact strength defined

Ionic strength defined

Tensile strength defined

Ultimate tensile strength defined

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