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Phase quadratic

EARLY PERSPECTIVES ON GEOMETRIC PHASE Quadratic case lower surface... [Pg.23]

Since there is a definite phase relation between the fiindamental pump radiation and the nonlinear source tenn, coherent SH radiation is emitted in well-defined directions. From the quadratic variation of P(2cii) with (m), we expect that the SH intensity 12 will also vary quadratically with the pump intensity 1 ... [Pg.1270]

EO effects can be linear or quadratic, depending on whether the degree of phase retardation varies with either the first or second power of apphed voltage. The variation of birefringence with potential takes the form... [Pg.340]

Rule i 4, on the other hand, has both a linear and quadratic term, so that / (p = 0) > 0 in general, and is therefore predicted to have a second order (or continuous) phase transition. Although the mean-field predictions are, of course, dimension-independent, they are expected to become exact as the dimension d —7 oo. In practice, it is often found that there exists a critical dimension dc above which the mean-field critical exponents are recovered exactly. [Pg.356]

Chapter 3 is devoted to pressure transformation of the unresolved isotropic Raman scattering spectrum which consists of a single Q-branch much narrower than other branches (shaded in Fig. 0.2(a)). Therefore rotational collapse of the Q-branch is accomplished much earlier than that of the IR spectrum as a whole (e.g. in the gas phase). Attention is concentrated on the isotropic Q-branch of N2, which is significantly narrowed before the broadening produced by weak vibrational dephasing becomes dominant. It is remarkable that isotropic Q-branch collapse is indifferent to orientational relaxation. It is affected solely by rotational energy relaxation. This is an exceptional case of pure frequency modulation similar to the Dicke effect in atomic spectroscopy [13]. The only difference is that the frequency in the Q-branch is quadratic in J whereas in the Doppler contour it is linear in translational velocity v. Consequently the rotational frequency modulation is not Gaussian but is still Markovian and therefore subject to the impact theory. The Keilson-... [Pg.6]

In the high-temperature limit microscopic calculation [186] led to a formula quadratic in scattering phases ... [Pg.166]

Using acetonitrile, the correlahon between isocratic logk and organic modifier percentages in the mobile phase (< )) can be described by the general quadratic equahon ... [Pg.334]

Baczek, T., Markuszewski, M., Kaliszan, R. Linear and quadratic relationships between retention and organic modifier content in eluent in reversed phase high-performance liquid chromatography a systematic comparative statistical study. [Pg.352]

This expansion is exact there are no terms of higher order than quadratic. From equation (1.40) we see that the phase velocity Uph of the wave packet is given by... [Pg.20]

The heptane water and toluene water interfaces were simulated by the use of the DREIDING force field on the software of Cerius2 Dynamics and Minimizer modules (MSI, San Diego) [6]. The two-phase systems were constructed from 62 heptane molecules and 500 water molecules or 100 toluene molecules and 500 water molecules in a quadratic prism cell. Each bulk phase was optimized for 500 ps at 300 K under NET ensemble in advance. The periodic boundary conditions were applied along all three directions. The calculations of the two-phase system were run under NVT ensemble. The dimensions of the cells in the final calculations were 23.5 A x 22.6 Ax 52.4 A for the heptane-water system and 24.5 A x 24.3 A x 55.2 A for the toluene-water system. The timestep was 1 fs in all cases and the simulation almost reached equilibrium after 50 ps. The density vs. distance profile showed a clear interface with a thickness of ca. 10 A in both systems. The result in the heptane-water system is shown in Fig. 3. Interfacial adsorption of an extractant can be simulated by a similar procedure after the introduction of the extractant molecule at the position from where the dynamics will be started. [Pg.364]

Figure 10.11 A well-ordered 2D AuS phase develops during annealing to 450 K. (A) The structure exhibits a very complex LEED pattern, which can be explained by an incommensurate structure with a nearly quadratic unit cell. (B) STM reveals the formation of large vacancy islands by Oswald ripening which cover about 50% of the surface, thus indicating the incorporation of 0.5 ML of Au atoms into the 2D AuS phase. The 2D AuS phase exhibits a quasi-rectangular structure (inset) and uniformly covers both vacancy islands and terrace areas. (Reproduced from Ref. 37). Figure 10.11 A well-ordered 2D AuS phase develops during annealing to 450 K. (A) The structure exhibits a very complex LEED pattern, which can be explained by an incommensurate structure with a nearly quadratic unit cell. (B) STM reveals the formation of large vacancy islands by Oswald ripening which cover about 50% of the surface, thus indicating the incorporation of 0.5 ML of Au atoms into the 2D AuS phase. The 2D AuS phase exhibits a quasi-rectangular structure (inset) and uniformly covers both vacancy islands and terrace areas. (Reproduced from Ref. 37).

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See also in sourсe #XX -- [ Pg.12 ]




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