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The action of diffusion

The system described forms the basis of the two-film theory. Because of the mutual solubility of acetone in water, the rate at which molecules of acetone move through the liquid film is large. Consequently, acetone molecules in the air that approach the liquid film are removed at such a fast rate that the concentration of acetone in the air film becomes less than it is in the main body of gas. This concentration gradient between the air film and main air body supplies the main driving force for the transfer of mass. [Pg.47]

We can think of the air and liquid films as being resistances in series. In this respect, they are similar to thermal resistances. If we designate the acetone by subscript A (i.e., the diffusing species) and the air by subscript B (i.e., the inert or insoluble species), we can write an expression for the concentration of each species in terms of their individual molar densities  [Pg.47]

For the insoluble gas species the net diffusion is zero, vg = 0, and if we define Na as the number of moles per unit time transferred through the film surface area A, [Pg.48]

Looking back at Equation (3.15), the continuity equation, we can write a material balance for the steady-state condition where there is no accumulation of species A in the gas film  [Pg.48]

Looking back to our molar flux expression (Equation 3.43), [Pg.49]


The action of diffusion is illustrated in Figure 3.5 for a system consisting of air, acetone and water. Let us assume we have a column in which fresh water continuously flows down the walls in the form of a film or thin layer. If we introduce a gaseous mixture of acetone and air to the column, the acetone will diffuse into the water phase. For the purposes of this example, assume the air to be insoluble in water. In our idealized system a stagnant... [Pg.46]

Fig. 5. Case 3. Sherwood numbers far the transpart of finite size particles through a stagnant fluid to n spherical cellectnr under the action of diffusion and London forces... Fig. 5. Case 3. Sherwood numbers far the transpart of finite size particles through a stagnant fluid to n spherical cellectnr under the action of diffusion and London forces...
Scale of segregation is a measure of the large scale breakup process (bulk and eddy diffusivity) without the action of diffusion, shown in Figure 2- a. It is the size of the packets of B that can be distinguished from the surrounding fluid A. [Pg.24]

Electrical trees consist of visible permanent hoUow channels, resulting from decomposition of the material, and show up clearly in polyethylene and other translucent soHd dielectrics when examined with an optical microscope. Eresh, unstained water trees appear diffuse and temporary. Water trees consist of very fine paths along which moisture has penetrated under the action of a voltage gradient. Considerable force is required to effect this... [Pg.326]

MicrobiologicaHy influenced corrosion, which results from the interaction of microorganisms and a metal, is receiving increased emphasis (1,3,9). The action of microorganisms is at least one of the reasons why natural seawater is more corrosive than either artificial seawater or sodium chloride solutions. Microorganisms attach to the surfaces of metals and can, for example, act as diffusion barriers produce metaboHtes that enhance or initiate... [Pg.274]

The ESR spectrum of the pyridazine radical anion, generated by the action of sodium or potassium, has been reported, and oxidation of 6-hydroxypyridazin-3(2//)-one with cerium(IV) sulfate in sulfuric acid results in an intense ESR spectrum (79TL2821). The self-diffusion coefficient and activation energy, the half-wave potential (-2.16 eV) magnetic susceptibility and room temperature fluorescence in-solution (Amax = 23 800cm life time 2.6 X 10 s) are reported. [Pg.8]

Equations (22-86) and (22-89) are the turbulent- and laminar-flow flux equations for the pressure-independent portion of the ultrafiltra-tion operating curve. They assume complete retention of solute. Appropriate values of diffusivity and kinematic viscosity are rarely known, so an a priori solution of the equations isn t usually possible. Interpolation, extrapolation, even precuction of an operating cui ve may be done from limited data. For turbulent flow over an unfouled membrane of a solution containing no particulates, the exponent on Q is usually 0.8. Fouhng reduces the exponent and particulates can increase the exponent to a value as high as 2. These equations also apply to some cases of reverse osmosis and microfiltration. In the former, the constancy of may not be assumed, and in the latter, D is usually enhanced very significantly by the action of materials not in true solution. [Pg.2040]

It is a consequence of the action of different pH values in the aeration cell that these cells do not arise in well-buffered media [4] and in fast-flowing waters [5-7]. The enforced uniform corrosion leads to the formation of homogeneous surface films in solutions containing Oj [7-9]. This process is encouraged by film-forming inhibitors (HCOj, phosphate, silicate, Ca and AP ) and disrupted by peptizing anions (CP, SO ") [10]. In pure salt water, no protective films are formed. In this case the corrosion rate is determined by oxygen diffusion [6,7,10]... [Pg.142]

Hypochlorous acid and hypochlorite ion are known as free available chlorine. The chloramines are known as combined available chlorine and are slower than free chlorine in killing microorganisms. For identical conditions of contact time, temperature, and pH in the range of 6 to 8, it takes at least 25 times more combined available chlorine to produce the same germicidal efficiency. The difference in potency between chloramines and HOCl can be explained by the difference in their oxidation potentials, assuming the action of chloramine is of an electrochemical nature rather than one of diffusion, as seems to be the case for HOCl. [Pg.468]

FIGURE9.il Phospholipids can be flipped across a bilayer membrane by the action of flippase proteins. Wlien, by normal diffusion through the bilayer, the lipid encounters a flippase, it can be moved quickly to the other face of the bilayer. [Pg.268]

Pollard s Test for Stability of Propellants. This test, proposed in 1924—25, is based upon the action of nitric peroxide on colloidal Ag oxide Procedure. A current of air is passed over a sample of proplnt in storage into a colloidal soln of Ag oxide. If free nitrogen peroxide is present, it reacts with the colloid and decreases the amt of light diffused by it. The larger the decrease, the higher the amt of N02 present, and the more decompd is the proplnt Ref Reilly (1938), 80... [Pg.793]

Another form of interaction between the transfer processes is responsible for the phenomenon of thermal diffusion in which a component in a mixture moves under the action of a temperature gradient. Although there are important applications of thermal diffusion, the magnitude of the effect is usually small relative to that arising from concentration gradients. [Pg.694]

Irrespective of the physical form of the carotenoid in the plant tissue it needs to be dissolved directly into the bulk lipid phase (emulsion) and then into the mixed micelles formed from the emulsion droplets by the action of lipases and bile. Alternatively it can dissolve directly into the mixed micelles. The micelles then diffuse through the unstirred water layer covering the brush border of the enterocytes and dissociate, and the components are then absorbed. Although lipid absorption at this point is essentially complete, bile salts and sterols (cholesterol) may not be fully absorbed and are not wholly recovered more distally, some being lost into the large intestine. It is not known whether carotenoids incorporated into mixed micelles are fully or only partially absorbed. [Pg.118]

A pemB mutant showed a reduced growth on methylated oligogalacturonides as the sole carbon source, indicating the possible role of PemB in pectin catabolism. The action of extracellular pectinases on pectin may liberate small methylated oligogalacturonides that can enter by diffusion into the periplasm. PemB could demethylate these molecules in the periplasm or during their passage to periplasm. [Pg.844]

The mechanism of adhesion to various substrates has not been fully explained. Brauer Stansbury (1984b) consider that bonding to composite resins occurs by the diffusion of methacrylate polymer chains into the resin. Bonding to base metals is, perhaps, by salt or chelate bridges. Here it is significant that ZOE cements do not bond, so perhaps bonding is due to the action of free EBA on the substrate. The adhesion to porcelain is surprising. Porcelain is inert so that the attachment can hardly be chemical. Also, it would be expected that if a cement adheres to porcelain then it should adhere to untreated enamel and dentine, but this is not so. [Pg.346]


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The Diffusion

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