Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Stable boundary layer

Sengupta, T.K., Kameswara Rao, A. and Venkatasubbaiah, K. (2006). Spatiotemporal growing wave fronts in spatially stable boundary layer. Phys. Rev. Letters, 96, 224504. [Pg.315]

The shape of the flow passage that guides the air to the sensor element plays an important role in the function of an air-flow sensor (the bypass, Fig. 7.6.8). Cross section and length are the important factors. As an accelerated flow has the most stable boundary layers and therefore is less vulnerable to flow separation, it would be favorable to have a decreasing cross section (in the flow direction). To avoid a restriction of air flow in the bypass the cross section at the outlet should not be too small in relation to the inlet. Therefore a reduction of cross section for stable accelerated flow is only done in the vicinity of the sensor element and in curved parts of the bypass (Fig. 7.6.8). [Pg.365]

Methods based on temporal gradients This approach is used at all scales, including small chambers operated in fully enclosed mode for short periods, boundary-layer budget methods in both the daytime convective boundary layer (CBL) and the nocturnal stable boundary layer (SBL), and global atmospheric budget methods. The dominant terms are I and IV. [Pg.42]

In desalination, localized concentrations of solute build up at the point where the solvent leaves the solution and enters the membrane. The solute accumulates in a relatively stable boundary layer (Fig. 13.9-3) next to the membrane. Concentration polarization, is defined as the ratio of the salt concentration at the membrane surface... [Pg.789]

The unstable boundary layer is a commonly occurring regime in environmental flows, and reverts to the stable boundary layer if the stability terms are zero. Assume a logarithmic velocity profile in the air boundary layer, altered by a stability function (Brutsaert, 1982), and assign = pw to be the flux of momentum at height z. Then, the momentum/unit volume difference between heights z and z = 0 is... [Pg.236]

Sweating, the other powerful heat loss mechanism actively regulated by the thermoregulatory center, is most developed in humans. With about 2,6 million sweat glands distributed over the skin and neurally controlled, sweat secretion can vary from 0 to 1 I7(h m ). The other, lesser, passive evaporative process of the skin is from the diffusion of water. The primary resistance to this flow is the stratum corneum or outermost 15 pm of the skin. The diffusion resistance of the skin is high in comparison to that of clothing and the boundary layer resistance and as a result makes water loss by diffusion fairly stable at about 500 grams/day. [Pg.179]

Normally the vortex finder should extend down into the conical portion of the cyclone. It is thought that the vortex finder plays an important role in the maintenance of a stable spiraling fluid flow in the cyclone, and this makes it more difficult for the particles to leak through the boundary layer on the roof of the lid of the cyclone to the overflow tube.- Without a vortex finder, the efficiency may be reduced by 4-5%. However, an excessive long vortex finder may hinder the high spin velocity in the fluid flow and thus reduce the efficiency of the cyclone. [Pg.1210]

Contamination of the biosphere by stable OCPs (DDT, HCH, aldrin, dieldrin, heptachlor, and toxafene) has become a global phenomenon. With global transfer, pesticides may reach countries that never produced or used them. In the northern hemisphere, where winds tend to blow from west to east, the rate of the wind in the boundary layer between the troposphere and the atmosphere is approximately 35 m/sec. Pesticide particles may completely orbit the Earth in approximately 12 days. Over this time, the probability of the particles falling to Earth may vary, and depends on the height of their orbit at a height of 3 km above sea level, particles will remain in the atmosphere for about seven days at a height of 6 km, for 30 days at a height of 30 km, for two years [31]. [Pg.39]

Wyngaard, J. C. (1975). Modeling the planetary boundary layer-extension to the stable case. Boundary Layer Meteorol. 9, 441-460. [Pg.298]

Moisture acts as a debonding agent through one of or a combination of the following mechanisms 1) attack of the metallic surface to form a weak, hydrated oxide interface, 2) moisture assisted chemical bond breakdown, or 3) attack of the adhesive. (2 ) A primary drawback to good durability of metal/adhesive bonds in wet environments is the ever present substrate surface oxide. Under normal circumstances, the oxide layer can be altered, but not entirely removed. Since both metal oxides and water are relatively polar, water will preferentially adsorb onto the oxide surface, and so create a weak boundary layer at the adhesive/metal interface. For the purposes of this work, the detrimental effects of moisture upon the adhesive itself will be neglected. The nitrile rubber modified adhesive used here contains few hydrolyzable ester linkages and therefore will be considered to remain essentially stable. [Pg.181]

Boundary layer thickness used in 8-notation of stable isotope ratios also used for 8 functions Molar absorptivity temporary constant Viscosity dummy variable Angle, such as contact angle... [Pg.657]

By comparison, all bonds other than Sn - C in the tin hydroxides are quite strong. In ClsSnOH the bond energies are 125 kcalmor 95 kcal mol and 87 kcal mol for the 0 - H, Sn - 0, and Sn - Cl bonds, respectively. Thus, it appears likely that the hydroxide ligand is quite stable and could survive transit through the thermal boundary layer in a CVD reactor and form tin oxide. [Pg.27]

Figure8.15. Freeandforcedconvectionregimes (o)freeconvectiveplume,where(6)convective plume deflected by wind (c) unstable boundary layer and (d) stable or neutral boundary layer, where Ts < (Adams et al., 1990). Figure8.15. Freeandforcedconvectionregimes (o)freeconvectiveplume,where(6)convective plume deflected by wind (c) unstable boundary layer and (d) stable or neutral boundary layer, where Ts < (Adams et al., 1990).
It seems possible, therefore, that in this initial region the upper part of the film, outside the growing boundary layer, is in potential-like flow, and that once the boundary layer reaches the free surface, its vorticity is sufficient to trigger the wave disturbances, which can then propagate or not, depending on whether the flow is unstable or stable (jVFr > 1 or N < 1). [Pg.191]

The rather fast reaction rate of halomethanes with Cl atoms suggests that this process may play a primary role in the removal of halomethanes from the troposphere and results in the formation of HC1 or 1C1 molecules. These degradation pathways do not lead to bromine or iodine atoms but to relatively stable molecules, which may initiate a different bromine and iodine cycles in the marine boundary layer. The atmospheric lifetime of IC1 is probably controlled by its sunlight photodissociation to iodine and chlorine atoms. Another possible degradation pathway of IC1 may be the hydrolysis to hypoiodous acid IOH, which may further be dissolved in seawater. [Pg.291]

To explain the particles that formed in both the ethylene/oxygen and hydrogen/oxygen mixtures, it was postulated that they form in the gas phase and that the overall etching process takes place in three steps. First, free radicals are formed homogeneously in a boundary layer adjacent to the surface. Second, these radicals interact with metal atoms in the surface. This interaction results in the formation of volatile intermediates. Third, the metastable, volatile intermediates interact in the gas phase so that metal particles are formed and stable product molecules released. Individual metastable species presumably interact with each other and also with particles formed from multiple collisions. The larger particles interact with each other as well. [Pg.401]


See other pages where Stable boundary layer is mentioned: [Pg.1006]    [Pg.225]    [Pg.137]    [Pg.519]    [Pg.153]    [Pg.1941]    [Pg.1946]    [Pg.148]    [Pg.35]    [Pg.569]    [Pg.570]    [Pg.571]    [Pg.1006]    [Pg.225]    [Pg.137]    [Pg.519]    [Pg.153]    [Pg.1941]    [Pg.1946]    [Pg.148]    [Pg.35]    [Pg.569]    [Pg.570]    [Pg.571]    [Pg.1060]    [Pg.129]    [Pg.169]    [Pg.664]    [Pg.21]    [Pg.345]    [Pg.156]    [Pg.157]    [Pg.63]    [Pg.345]    [Pg.196]    [Pg.93]    [Pg.225]    [Pg.30]    [Pg.80]    [Pg.223]    [Pg.544]    [Pg.917]    [Pg.439]    [Pg.326]   
See also in sourсe #XX -- [ Pg.42 ]




SEARCH



© 2024 chempedia.info