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Three hydrodynamics

One fundamental question concerning the new approach seems to have passed unnoticed despite the many arguments that have been raised aginst it. In the derivation of the and 5-functions, Scheraga and Mandelkern have assumed that the three hydrodynamic properties can be represented by an identical equivalent ellipsoid. If either F, or p of this fictitious ellipsoid is arbitrarily fixed the other is automatically defined. But there is no a priori reason to assume that the particles under shearing stress and sedimentation should fit the same hydrodynamic model. If Ve is kept identical the appropriate p value for describing one property might differ from the... [Pg.342]

L is the specimen length, D is the diffusion coefficient of oxygen. Re = XV/u, and Sc= v/D. The equation correlating the corrosion rates for the three hydrodynamic geometries is given as... [Pg.138]

The use of a second downstream electrode to monitor chemical fluxes at the working electrode is proving to be an important technique for the investigation of electrode mechanisms. This is particularly true for electrodes which have a more complicated structure than a simple metallic surface. Examples are modified electrodes, oxide electrodes, or enzyme electrodes. For these more complex systems, the separate measurement of the fluxes at the electrolyte-electrode interface provides unique and valuable information. Double electrodes can be constructed for all three hydrodynamic systems. A crucial parameter for such a double electrode is the collection efficiency, N, which, in the steady state, relates the flux of material detected as a limiting current on the downstream electrode to the flux of material generated on the upstream electrode. The collection efficiency is a function of the geometry of the electrode and is given for all three systems by [4, 9]... [Pg.133]

The R variation range (of a reactive mixture V, in conditions of constant linear velocity) includes three hydrodynamic modes of liquid flow laminar (small R), transient, and turbulent, depending on the numerical values of a characteristic mixing time = RVD(., b (Figure 1.4). [Pg.15]

Table 1 Experimental values for different chromatographic systems eluted in two types of column packings at three hydrodynamic volumes (in ml/mol). Table 1 Experimental values for different chromatographic systems eluted in two types of column packings at three hydrodynamic volumes (in ml/mol).
Fig. 3 Plot of the preferential solvation coefficient. A, as a function of the volume fraction of polymer(2), (f>2, at three hydrodynamic volumes, Vij = 10 (O ) lO ( ). and 10 (AA.) ml/mol for different systems (a) Tol/PDMS/PS (b) Bz/ PDMS/PS and (c) CHX/PDMS/PS eluted in p.-Styragel (empty symbols) and TSK Gel Hhr (solid symbols) columns. Solid line has been calculated with equations and 3 values given in Ref. 28. Source From An analysis of the concentration effects on elution volumes through the preferential solvation parameter in two SEC packings, in Macromol. Chem. Phys. ... Fig. 3 Plot of the preferential solvation coefficient. A, as a function of the volume fraction of polymer(2), (f>2, at three hydrodynamic volumes, Vij = 10 (O ) lO ( ). and 10 (AA.) ml/mol for different systems (a) Tol/PDMS/PS (b) Bz/ PDMS/PS and (c) CHX/PDMS/PS eluted in p.-Styragel (empty symbols) and TSK Gel Hhr (solid symbols) columns. Solid line has been calculated with equations and 3 values given in Ref. 28. Source From An analysis of the concentration effects on elution volumes through the preferential solvation parameter in two SEC packings, in Macromol. Chem. Phys. ...
Table 6. Transport relationships for three hydrodynamic systems... Table 6. Transport relationships for three hydrodynamic systems...
The correlation for Cd (Uke the friction factor and the impeller power number, Np) covers several hydrodynamic regimes. The corresponding ranges for Rep and the correlating expression for Cd are shown in Table 10-1 for three hydrodynamic regimes. [Pg.551]

The cleaning process proceeds by one of three primary mechanisms solubilization, emulsification, and roll-up [229]. In solubilization the oily phase partitions into surfactant micelles that desorb from the solid surface and diffuse into the bulk. As mentioned above, there is a body of theoretical work on solubilization [146, 147] and numerous experimental studies by a variety of spectroscopic techniques [143-145,230]. Emulsification involves the formation and removal of an emulsion at the oil-water interface the removal step may involve hydrodynamic as well as surface chemical forces. Emulsion formation is covered in Chapter XIV. In roll-up the surfactant reduces the contact angle of the liquid soil or the surface free energy of a solid particle aiding its detachment and subsequent removal by hydrodynamic forces. Adam and Stevenson s beautiful photographs illustrate roll-up of lanoline on wood fibers [231]. In order to achieve roll-up, one requires the surface free energies for soil detachment illustrated in Fig. XIII-14 to obey... [Pg.485]

A general flow map of different hydrodynamic conditions (Fig. 23) consists of regions of flooding, dispersion, and recirculation on a plot of N vs for a Rushton turbine. For a low viscosity aqueous/air system, the gas flow numbers for the three conditions are given hy FI = 30Fr[D/TY for flooding, = 0.2Fr° (F/r)° for complete dispersion, and =13FF D/TY for recirculation. [Pg.432]

The traditional view of emulsion stability (1,2) was concerned with systems of two isotropic, Newtonian Hquids of which one is dispersed in the other in the form of spherical droplets. The stabilization of such a system was achieved by adsorbed amphiphiles, which modify interfacial properties and to some extent the colloidal forces across a thin Hquid film, after the hydrodynamic conditions of the latter had been taken into consideration. However, a large number of emulsions, in fact, contain more than two phases. The importance of the third phase was recognized early (3) and the lUPAC definition of an emulsion included a third phase (4). With this relation in mind, this article deals with two-phase emulsions as an introduction. These systems are useful in discussing the details of formation and destabilization, because of their relative simplicity. The subsequent treatment focuses on three-phase emulsions, outlining three special cases. The presence of the third phase is shown in order to monitor the properties of the emulsion in a significant manner. [Pg.196]

Cavitation has three negative side effects in valves—noise and vibration, material removal, and reduced flow. The bubble-collapse process is a violent asymmetrical implosion that forms a high-speed microjet and induces pressure waves in the fluid. This hydrodynamic noise and the mechanical vibration that it can produce are far stronger than other noise-generation sources in liquid flows. If implosions occur adjacent to a solid component, minute pieces of material can be removed, which, over time, will leave a rough, cinderlike surface. [Pg.789]

Particle-Bubble Attachment. In the above, principles leading to creation of desired hydrophobicity/hydrophihcity of the particles has been discussed. The next step is to create conditions for particle-bubble contact, attachment, and their removal, which is simply described as a combination of three stochastic events with which are associated the probability of particle-bubble colhsion, probabihty of attachment, and probability of retention of attachment. The first term is controlled by the hydrodynamic conditions prevaihng in the flotation unit. The second is determined by the surface forces. The third is dependent on the s irvival of the laden bubble by liq ud t irbulence and impacts by the other suspended particles. A detailed description of the hydrodynamic and other physical aspects of flotation is found in the monograph by Schulze (19 ). [Pg.1810]

H.E. Trease, Three-Dimensional Free Lagrangian Hydrodynamics, in The Free-Lagrange Method (edited by M.J. Fritts, W.P. Crowley and H.E. Trease), Lecture Notes in Physics, Number 238, Springer-Verlag, New York, 1985. [Pg.350]

Calibration curves for PS and PMMA are shown in Figs. 15.3-15.5. The slight differences in courses of calibration curves for PS in THF, chloroform, and toluene, as well as the curve for PMMA in THF (Fig. 15.3), can be explained by the flow rate variations for different pumping systems and by the hydrodynamic volume effects, respectively. The calibration curves for PMMA in mixed eluents THF/toluene are shown in Fig. 15.4. Three percent of THF in toluene assured a reasonable SEC elution of PMMA. However, more chloroform was needed to obtain a good SEC elution of PMMA in mixed eluent chloroform/toluene... [Pg.451]

A more rigorous treatment takes into account the hydrodynamic characteristics of the flowing solution. Expressions for the limiting currents (under steady-state conditions) have been derived for various electrodes geometries by solving the three-dimensional convective diffusion equation ... [Pg.91]

Models of atmospheric phenomena are similar to those of combustion and involve the coupling of exceedingly complex chemistry and physics with three-dimensional hydrodynamics. The distribution and transport of chemicals introduced into groundwater also involve a coupling of chemical reactions and transports through porous solid media. The development of groundwater models is critical to understanding the effects of land disposal of toxic waste (see Chapter 7). [Pg.155]

Dudukovic, M. P., Trends in catalytic reaction engineering, Catal. Today, 48, 5-15 (1999). A comprehensive review of the complex hydrodynamic issues associated with three-phase reactors is given in... [Pg.432]


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See also in sourсe #XX -- [ Pg.331 ]




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