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Stefan flow convection

Analysis. To answer this question formally the fuel species and oxidizer species conservation equations would have to be solved. But again, we found a posteriori that the condition for group combustion corresponded to such a dilute cloud that these continuity equations could be approximated accurately enough by neglecting the terms involving Stefan flow convection. Therefore ... [Pg.70]

Figures 4.34 and 4.35 represent two extreme cases. Drying processes represent the case shown in Fig. 4.34 and distillation processes represent Fig. 4.35. Neither case represents a convective mass transfer case while the gas flow is in the boundary layer, other flows are Stefan flow and turbulence. Thus Eqs. (4.243) and (4.244) can seldom be used in practice, but their forms are used in determining the mass transfer factor for different cases. Figures 4.34 and 4.35 represent two extreme cases. Drying processes represent the case shown in Fig. 4.34 and distillation processes represent Fig. 4.35. Neither case represents a convective mass transfer case while the gas flow is in the boundary layer, other flows are Stefan flow and turbulence. Thus Eqs. (4.243) and (4.244) can seldom be used in practice, but their forms are used in determining the mass transfer factor for different cases.
Rapid evaporation introduces complications, for the heat and mass transfer processes are then coupled. The heat of vaporization must be supplied by conduction heat transfer from the gas and liquid phases, chiefly from the gas phase. Furthermore, convective flow associated with vapor transport from the surface, Stefan flow, occurs, and thermal diffusion and the thermal energy of the diffusing species must be taken into account. Wagner 1982) reviewed the theory and principles involved, and a higher-order quasisteady-state analysis leads to the following energy balance between the net heat transferred from the gas phase and the latent heat transferred by the diffusing species ... [Pg.56]

These two conditions (Eqs. (4.97) and (4.98)) are usually sufficient for assuming the medium as quiescent in dilute systems in which both cua.s and cda,oo are small. However, in nondilute or concentrated systems the mass transfer process can give rise to a convection normal to the surface, which is known as the Stefan flow [Taylor and Krishna, 1993]. Consider a chemical species A which is transferred from the solid surface to the bulk with a mass concentration cua.oo- When the surface concentration coa,s is high, and the carrier gas B does not penetrate the surface, then there must be a diffusion-induced Stefan convective outflux, which counterbalances the Fickian influx of species B. In such situations the additional condition for neglecting convection in mass transport systems is [Rosner, 1986]... [Pg.158]

The Stefan convection, however, does not alter the analogy between heat and mass transfer because the laws governing the change in the Nusselt number with the Stefan flow are identical to those governing Shs. [Pg.159]

This relation is known as Stefan s law, and the induced convective flow described that enhance.s mass diffusion is called the Stefan flow. Noting that y, — P/P and C = P/RJT for an ideal gas mixture, the evaporation rate of spccie /4 can also be expressed a.s... [Pg.818]

The flow induced by evaporating molecules is called Stefan flow. The contribution of the th evaporating species to the Stefan flow is given by the convection term, pJ/u, for i = 1,..., F, in (12.9), and the total Stefan flow is obtained as the sum... [Pg.267]

The /th species mass flux, j, and the total heat flux, q, can be expressed in terms of transfer coefficients. This is useful in situations where the liquid or gas phase is not completely resolved, or when the flow conditions are not exactly known. Often, these transfer coefficients are determined experimentally for a particular flow situation. For instance, different expressions are used, depending on whether the transfer is due to pure conduction or whether it is dominated by ccaivection. Also, the type of convection plays a role, that is, if the convection is forced or non-forced. A forced convection has a non-zero relative velocity between droplet and environment, whereas for a non-forced convection, the relative drop-gas velocity is zero and only the Stefan flow dominates. Note that the natural convection due to gravity is taken to be zero since gravity is an external force, and external forces are neglected in this article. In addition, in forced convection, the nature of the flow, that is, whether the flow is laminar or turbulent, plays an important role. These issues will be discussed in more detail in the following subsections. [Pg.269]

Note that diffusion may cause convection Stefan flow). Figure 3.2.24 shows an example to illustrate this for the case of evaporation. Further quantitative details are given in Topic 3.2.5. [Pg.86]

The theory on the level of the electrode and on the electrochemical cell is sufficiently advanced [4-7]. In this connection, it is necessary to mention the works of J.Newman and R.White s group [8-12], In the majority of publications, the macroscopical approach is used. The authors take into account the transport process and material balance within the system in a proper way. The analysis of the flows in the porous matrix or in the cell takes generally into consideration the diffusion, migration and convection processes. While computing transport processes in the concentrated electrolytes the Stefan-Maxwell equations are used. To calculate electron transfer in a solid phase the Ohm s law in its differential form is used. The electrochemical transformations within the electrodes are described by the Batler-Volmer equation. The internal surface of the electrode, where electrochemical process runs, is frequently presented as a certain function of the porosity or as a certain state of the reagents transformation. To describe this function, various modeling or empirical equations are offered, and they... [Pg.462]

In order to assess transport mechanisms due to convection various correlation for heat and mass transfer coefficients in a packed bed have been derived. For the present application the transfer coefficient in the bed is related to the transfer coefficient of a single particle in a gas flow according to [15]. Due to the outflow of the gases during pyrolysis and char conversion the calculated transfer coefficient is decreased, thus Stefan correction is included to calculate the transfer coefficient at a finite flow over the boundary. [Pg.592]

However, if convective transport of heat and species mass in porous catalyst pellets have to be taken into account simulating catal3dic reactor processes, either the Maxwell-Stefan mass flux equations (2.394) or dusty gas model for the mass fluxes (2.427) have to be used with a variable pressure driving force expressed in terms of mass fractions (2.426). The reason for this demand is that any viscous flow in the catalyst pores is driven by a pressure gradient induced by the potential non-uniform spatial species composition and temperature evolution created by the chemical reactions. The pressure gradient in porous media is usually related to the consistent viscous gas velocity through a correlation inspired by the Darcy s law [21] (see e.g., [5] [49] [89], p 197) ... [Pg.308]

For porous membranes the mass transport mechanisms that prevail depend mainly on the membrane s mean pore size [1.1, 1.3], and the size and type of the diffusing molecules. For mesoporous and macroporous membranes molecular and Knudsen diffusion, and convective flow are the prevailing means of transport [1.15, 1.16]. The description of transport in such membranes has either utilized a Fickian description of diffusion [1.16] or more elaborate Dusty Gas Model (DGM) approaches [1.17]. For microporous membranes the interaction between the diffusing molecules and the membrane pore surface is of great importance to determine the transport characteristics. The description of transport through such membranes has either utilized the Stefan-Maxwell formulation [1.18, 1.19, 1.20] or more involved molecular dynamics simulation techniques [1.21]. [Pg.4]

A classical method for measuring the diffusion coefficient or the vapor of a volatile liquid in air or other gas (e.g,. toluene in N2) employs the Stefan tube shown in Fig. 2.3-8. a long tube of narrow diameter (to suppress convection) partially filled with a pure volatile liquid A and maintained in a constanl-tempeiaUire bath. A gcotle flow of air is sometimes established acmes the top of the tube to sweep away the vapor reaching the top of the lube. The fall of the liquid level with lime is observed. [Pg.1094]

Transport in OSN membranes occurs by mechanisms similar to those in membranes used for aqueous separations. Most theoretical analyses rely on either irreversible thermodynamics, the pore-flow model and the extended Nemst-Planck equation, or the solution-diffusion model [135]. To account for coupling between solute and solvent transport (i.e., convective mass transfer effects), the Stefan-Maxwell equations commonly are used. The solution-diffusion model appears to provide a better description of mixed-solvent transport and allow prediction of mixture transport rates from pure component measurements [136]. Experimental transport measurements may depend significantly on membrane preconditioning due to strong solvent-membrane interactions that lead to swelling or solvent phase separation in the membrane pore structure [137]. [Pg.320]

We shall try to cover all the membrane processes within one model at the end of fliis chapter, in order to relate the various membrane processes with each other in terms of driving forces, fluxes and basic separation principles. To do so, the starting point must be a simple model, such as a generalised Pick equation [41 or a generalised Stefan-MaxweU equation [42]. In order to describe transport through a porous membrane or through a nonporous membrane, two contributions must be taken into account, the diffusional flow (v) and the convective flow (u). The flux of component i through a membrane can be described as the product of velocity and concentration, i.e. [Pg.260]


See other pages where Stefan flow convection is mentioned: [Pg.316]    [Pg.316]    [Pg.127]    [Pg.127]    [Pg.236]    [Pg.86]    [Pg.599]    [Pg.710]    [Pg.658]    [Pg.473]    [Pg.853]    [Pg.491]    [Pg.540]    [Pg.512]    [Pg.45]   
See also in sourсe #XX -- [ Pg.70 ]




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