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Phase contacting

Fig. X-16. (a) Microscopic appearance of the three-phase contact region, (b) Wetting meniscus against a vertical plate showing the meniscus only, adsorbed film only, and joined profile. (From Ref. 226 with permission. Copyright 1980 American Chemical Society.)... Fig. X-16. (a) Microscopic appearance of the three-phase contact region, (b) Wetting meniscus against a vertical plate showing the meniscus only, adsorbed film only, and joined profile. (From Ref. 226 with permission. Copyright 1980 American Chemical Society.)...
D. Platikanov and M. Nedyalkov, Contact Angles and Line Tension at Microscopic Three Phase Contacts, in Microscopic Aspects of Adhesion and Lubrication, J. M. Georges, ed., Elsevier, Amsterdam, 1982. [Pg.386]

In practice, it may be possible with care to float somewhat larger particles than those corresponding to the theoretical maximum. As illustrated in Fig. XIII-7, if the particle has an irregular shape, it will tend to float such that the three-phase contact occurs at an asperity since the particle would have to be depressed considerably for the line of contact to advance further. The resistance to rounding a sharp edge has been investigated by Mason and co-workers [62]. [Pg.474]

Interfacial Mass-Transfer Coefficients. Whereas equiHbrium relationships are important in determining the ultimate degree of extraction attainable, in practice the rate of extraction is of equal importance. EquiHbrium is approached asymptotically with increasing contact time in a batch extraction. In continuous extractors the approach to equiHbrium is determined primarily by the residence time, defined as the volume of the phase contact region divided by the volume flow rate of the phases. [Pg.62]

Fig. 7. The concept of contact angle with a captive bubble in an aqueous medium, adhering to a hydrophobic sofld P is the three-phase contact point. Here, the vector passes through P and forms a tangent to the curved surface of the air bubble. The contact angle 0 is drawn into the Hquid. Fig. 7. The concept of contact angle with a captive bubble in an aqueous medium, adhering to a hydrophobic sofld P is the three-phase contact point. Here, the vector passes through P and forms a tangent to the curved surface of the air bubble. The contact angle 0 is drawn into the Hquid.
Parallel flow. The direction of gas flow is parallel to the surface of the sohds phase. Contacting is primarily at the interface between phases, with possibly some penetration of gas into the voids among the solids near the surface. The solids bed is usually in a static-condition (Fig. 12-30). [Pg.1173]

Operating holdup contributes effectively to mass-transfer rate, since it provides residence time for phase contact and surface regeneration via agglomeration and dispersion. Static holdup is hmited in its contribution to mass-transfer rates, as indicated by Thoenes and Kramers [Chem. Eng. ScL, 8, 271 (1958)]. In laminar regions holdup in general has a negative effecl on the efficiency of separation. [Pg.1394]

The effective friction loss, or gas-phase contacting power, is easily determined by direct measurements. However, the liquid-phase contacting power, supplied from the stream of scrubbing liquid, and the mechanical contacting power, supplied by a mechanically driven rotor, are not direc tly measurable the theoretical power inputs can be estimated, but the portions of these quantities effectively converted to contac ting power can only be inferred from comparison with gas-phase contacting power. Such data as are available indicate that the contributions or contacting power from different sources are directly additive in their relation to scrubber performance. [Pg.1592]

The gas-phase contacting power Pc may be calculated from the effective fric tion loss by the following relationships ... [Pg.1592]

The power input from a liquid stream injected with a hydraulic spray nozzle may usually be taken as approximately equal to the product of the nozzle feed pressure pf and the volumetric hquid rate. The liquid-phase contacting power Pe may then be calculated from the following formulas ... [Pg.1592]

PHASE CONTACTING AND LIQUID-SOLID PROCESSING AGITATION OF LOW-VISCOSITY PARTICLE SUSPENSIONS... [Pg.1620]

BBT solution on unmodified sorbents of different nature was studied. Silica gel Merck 60 (SG) was chosen for further investigations. BBT immobilization on SG was realized by adsoi ption from chloroform-hexane solution (1 10) in batch mode. The isotherm of BBT adsoi ption can be referred to H3-type. Interaction of Co(II), Cu(II), Cd(II), Ni(II), Zn(II) ions with immobilized BBT has been studied in batch mode as a function of pH of solution, time of phase contact and concentration of metals in solution. In the presence of sodium citrate absorbance (at X = 620 nm) of immobilized BBT grows with the increase of Cd(II) concentration in solution. No interference was observed from Zn(II), Pb(II), Cu(II), Ni(II), Co(II) and macrocomponents of natural waters. This was assumed as a basis of soi ption-spectroscopic and visual test determination of Cd(II). Heavy metals eluted from BBT-SG easily and quantitatively with a small volume of HNO -ethanol mixture. This became a basis of soi ption-atomic-absoi ption determination of the total concentration of heavy metals in natural objects. [Pg.292]

In a processing facility, the primary aim is to impart effective phase-contacting in the constituents within the safety and temporal constraints prescribed by the particular application. The basic design features of the equipment described in this section help to discern the performance capabilities of candidate geometries in this context. [Pg.717]

The static mixer is also useful for direct contact heat transfer between fluids, nvo phase contacting, and other useful applications such as mass transfer. [Pg.339]

The rate of extraction depends on the mass transport coefficient (f), the phase contact area (F) and the difference between the equilibrium concentration and the initial concentration of the dissolved component, which is usually expressed as the driving force of the process (a). The rate of extraction (V) can be calculated as shown in Equation (135) ... [Pg.267]

As can be seen from Equation (135), the only effective way to increase the extraction rate is by increasing the phase contact area. This can be achieved by... [Pg.267]

Fig. 123 shows the typical construction of a mixer-settler extractor. The main parameters usually required for the design of an extractor are maximum output, total holding capacity, organic reagent capacity, mixer capacity, phase contact time, settler surface area and specific settler output. [Pg.273]

In order to prove the limitation of the process by quasi-diffusion in the grain, it is most convenient to carry out experiments with phase contact interruption [107], For the sorption of organic ions after this interruption and the restoration of the contact after a certain period of time, the dependence usually the shape of... [Pg.39]

Equations describing the transfer rate in gas-liquid dispersions have been derived and solved, based on the film-, penetration-, film-penetration-, and more advanced models for the cases of absorption with and without simultaneous chemical reaction. Some of the models reviewed in the following paragraphs were derived specifically for gas-liquid dispersion, whereas others were derived for more general cases of two-phase contact. [Pg.334]

Some of the additional mathematical models mentioned below were derived for the characterization of swarms of bubbles whereas others were derived for the specific case of a single bubble or the general case of two-phase contact. Most models for the bubble-liquid contact are limited to the case of a single bubble, and consequently their direct applicability to gas-liquid dispersions is very restricted. [Pg.386]

For the solid-liquid system changes of the state of interface on formation of surfactant adsorption layers are of special importance with respect to application aspects. When a liquid is in contact with a solid and surfactant is added, the solid-liquid interface tension will be reduced by the formation of a new solid-liquid interface created by adsorption of surfactant. This influences the wetting as demonstrated by the change of the contact angle between the liquid and the solid surface. The equilibrium at the three-phase contact solid-liquid-air or oil is described by the Young equation ... [Pg.182]

Pyruvic acid is the simplest homologue of the a-keto acid, whose established procedures for synthesis are the dehydrative decarboxylation of tartaric acid and the hydrolysis of acetyl cyanide. On the other hand, vapor-phase contact oxidation of alkyl lactates to corresponding alkyl pyruvates using V2C - and MoOa-baseds mixed oxide catalysts has also been known [1-4]. Recently we found that pyruvic acid is obtained directly from a vapor-phase oxidative-dehydrogenation of lactic acid over iron phosphate catalysts with a P/Fe atomic ratio of 1.2 at a temperature around 230°C [5]. [Pg.201]

The constraint to be implemented at the three-phase contact line between the two fluids and a solid surface requires that the contact angle 0 (compare Figure 2.58) assumes a prescribed value. As discussed in Section 2.2.3, the contact angle might also be allowed to vary with the velocity of the contact line. Especially in microfluidic... [Pg.231]

The disadvantage of the two-phase contacting principle is related to the technical expenditure of realizing phase separation throughout the complete reactor passage. Special measures have to be taken to prevent phase inter-mixing. Also, this has to be controlled during the process. Hence inspection windows are essential (for the first prototype they may be eliminated later). [Pg.577]


See other pages where Phase contacting is mentioned: [Pg.113]    [Pg.466]    [Pg.73]    [Pg.53]    [Pg.481]    [Pg.155]    [Pg.1578]    [Pg.1578]    [Pg.1625]    [Pg.1627]    [Pg.1629]    [Pg.1631]    [Pg.1633]    [Pg.1635]    [Pg.1637]    [Pg.1639]    [Pg.1641]    [Pg.1881]    [Pg.2015]    [Pg.718]    [Pg.719]    [Pg.57]    [Pg.299]    [Pg.202]    [Pg.577]   
See also in sourсe #XX -- [ Pg.427 ]




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Classification of Microreactors - Phase-contacting Principles

Contact Between Three Phases Wetting

Contact angle mobile phase velocity

Contact of phases

Contact phase

Contact phase

Contact phase proteinases

Contact-phase activation

Contacting with Continuous Phases

Contacting with Disperse Phases

Disperse phase contact

Equilibrium of a Species Between Two Phases in Contact

Liquid Phase Contact

Liquid phase sintering contact flattening

Liquid-solid phase-contacting principles

Mechanical contact vapor-phase

Phase Contacts between Particles in Disperse Structures

Phase contact line

Phase contact ratio

Phase contact structures

Phase contact structures chemical modifiers

Phase contact structures mechanical stresses

Phase contact structures particle bridging

Phase contact structures silica particles

Phase contact systems

Phase contacting conditions

Phases contact time behaviour

Potential difference between two contacting phases

Reaction phase-contacting principles

Rules of Thumb about the Context for a Chemical Process Heterogenous Phase contacting

Stationary phases contact angle

Structures with Phase Contacts

Surface force three-phase contact line

Surface state contacting phase

Three-Phase Contact Line Wetting

Three-phase contact

Three-phase contact extension

Three-phase contact line

Three-phase contact line wetting front

Three-phase contact wetting perimeter

Three-phase contacting

Three-phase line/perimeter, contact

Three-phase line/perimeter, contact angle

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