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Layering oscillation

In many materials, the relaxations between the layers oscillate. For example, if the first-to-second layer spacing is reduced by a few percent, the second-to-third layer spacing would be increased, but by a smaller amount, as illustrated in figure Al,7,31b). These oscillatory relaxations have been measured with FEED [4, 5] and ion scattering [6, 7] to extend to at least the fifth atomic layer into the material. The oscillatory nature of the relaxations results from oscillations in the electron density perpendicular to the surface, which are called Eriedel oscillations [8]. The Eriedel oscillations arise from Eenni-Dirac statistics and impart oscillatory forces to the ion cores. [Pg.289]

Holman, J. P.. H. E. Gartrell, and E. E. Soehngen An Interferometric Method of Studying Boundary Layer Oscillations, J. Heat Transfer, ser. C, vol. 80. August I960. [Pg.368]

Pfenninger, W. and Bacon, J.W. (1969). Amplified laminar boundary-layer oscillation and transition at the front attachment-line of a 45° swept flat-nosed wing with and without suction. In Viscous Drag Reduction (Ed. C.S. Wells), 85-105, Plenum Press. [Pg.312]

In addition, a layer by layer oscillating composition is expected in depth for alloys whose mixing enthalpy is negative. In these predictions, surface reconstruction has not been considered. Actually, this is not always justified, mainly in the case of open surfaces, as will be shown below. [Pg.414]

Figure 4-74. Distribution of ion density and potential as well as boundary-layer oscillation in RF-CCP discharge. Figure 4-74. Distribution of ion density and potential as well as boundary-layer oscillation in RF-CCP discharge.
Fig. 3.21. Forces (a) and refractive indices (b) for a 5CB droplet between aligned bare mica sheets (T=27°C). (a) Force runs approaching the surfaces (filled circles and triangles) a residual repulsion is observed in retraction (open circles) a jump-out from the minimum of a layering oscillations is shown. The continuous lines represent the elastic twist force F D)/R = ttK220 /D (see [50] for details), calculated assuming an infinite anchoring strength with K22 = 6.5 x N. The twist... Fig. 3.21. Forces (a) and refractive indices (b) for a 5CB droplet between aligned bare mica sheets (T=27°C). (a) Force runs approaching the surfaces (filled circles and triangles) a residual repulsion is observed in retraction (open circles) a jump-out from the minimum of a layering oscillations is shown. The continuous lines represent the elastic twist force F D)/R = ttK220 /D (see [50] for details), calculated assuming an infinite anchoring strength with K22 = 6.5 x N. The twist...
Fig. 3.20. Layering oscillations in a discotic nematic (T=29°). Filled/open circles compression/decompression. A layer of micelles is adsorbed on each mica surface, resulting in a contact separation of about 9nm. The fit is done using the (3.13) with 11 nm. Fig. 3.20. Layering oscillations in a discotic nematic (T=29°). Filled/open circles compression/decompression. A layer of micelles is adsorbed on each mica surface, resulting in a contact separation of about 9nm. The fit is done using the (3.13) with 11 nm.
Anonymous (1938). Schubauer, G.B. Proc. 5 Inti. lUTAMCongress Cambridge MA. P Anonymous (1948). Galen B. Schubauer. Aeronautical Engineering Review 7(2) 7. P Anonymous (1956). Schubauer wins GoldMedaX. Aeronautical Engineering Review 15(7) 22. P Schubauer, G.B., Skramstad, H.K. (1947). Laminar boundary-layer oscillations and stability of laminar flow. Journal of the Aeronautical Sciences 14(2) 69-78. [Pg.788]

Schubauer, G.B., Skramstad, H.K. (1947). Laminar boundary-layer oscillations and stability of laminar flow. Journal of the Aeronautical Sciences 14(2) 69-78. [Pg.814]

The damped oscillations with a period of about 1 nm corresponded well to the size of the OMCST molecules and extended to about 5 nm, or about five solvent layers. An example of these forces for the same system from Christenson and Blom [68] is shown in Fig. VI-7. [Pg.244]

For a fluid, with no underlying regular structure, the mecin squared displacement gradually increases with time (Figure 6.9). For a solid, however, the mean squared displacement typically oscillates about a mean value. Flowever, if there is diffusion within a solid then tliis can be detected from the mean squared displacement and may be restricted to fewer than three dimensions. For example. Figure 6.10 shows the mean squared displacement calculated for Li+ ions in Li3N at 400 K [Wolf et al. 1984]. This material contains layers of LiiN mobility of the Li" " ions is much greater within these planes than perpendicular to them. [Pg.337]

For water, organic and water-organic metal salts mixtures the dependence of integral and spectral intensities of coherent and non-coherent scattered radiation on the atomic number (Z), density, oscillator layer thickness, chemical composition, and the conditions of the registering of analytical signals (voltage and tube current, tube anode material, crystal-analyzer) was investigated. The dependence obtained was compared to that for the solid probes (metals, alloys, pressed powder probes). [Pg.444]

In films that grow 2D for many layers, intensity oscillations have been observed for certain growth conditions using RHEED and LEED. Observation is made by monitoring the intensity of a diffracted beam as a function of time during growth. The period of an oscillation corresponds to the time it takes to deposit a monolayer. In practice, oscillations are ffequendy used to calibrate deposition rates. [Pg.274]

When two layers of the substance are displaced relative to one another, the nuclei of phase A, located between them, can be regarded as kind of a roller about which oscillations are executed. - - - when the two layers of phase AB are displaced relative to one another, they transport past the nucleus, in its immediate vicinity, a multiplicity of atoms of both kinds. - - - it follows that all the atoms A passing in the immediate vicinity of the nucieus have sufficient time to combine with the latter and this in fact may be the mechanism of the growth of the nuclei of the new phase. ... [Pg.40]

Fig. 5(a) contains the oxygen and hydrogen density profiles it demonstrates clearly the major differences between the water structure next to a metal surface and near a free or nonpolar surface (compare to Fig. 3). Due to the significant adsorption energy of water on transition metal surfaces (typically of the order of 20-50kJmoP see, e.g., [136]), strong density oscillations are observed next to the metal. Between three and four water layers have also been identified in most simulations near uncharged metal surfaces, depending on the model and on statistical accuracy. Beyond about... Fig. 5(a) contains the oxygen and hydrogen density profiles it demonstrates clearly the major differences between the water structure next to a metal surface and near a free or nonpolar surface (compare to Fig. 3). Due to the significant adsorption energy of water on transition metal surfaces (typically of the order of 20-50kJmoP see, e.g., [136]), strong density oscillations are observed next to the metal. Between three and four water layers have also been identified in most simulations near uncharged metal surfaces, depending on the model and on statistical accuracy. Beyond about...
In the process of MBE, the surface structure can be investigated by reflected high energy electron diffraction (RHEED). During MBE growth, one often observes an oscillation in the intensity of the specular reflected beam as a function of time. This is interpreted to be due to the layer-by-layer growth of a two-dimensional island. [Pg.886]


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