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Continuous disperse phases

Ct, Ctp heat capacity at constant pressure of continuous, dispersed phase... [Pg.360]

Sherwood number factor defined by Eq. (9-22) velocity ratio defined by Eq. (9-25) mass transfer factor defined by Eq. (9-21) thermal conductivity of continuous, dispersed phase velocity ratio defined by Eq. (9-7) viscosity ratio defined by Eq. (9-8)... [Pg.362]

The onset of high electrical conductivity with increasing volume fraction of metallic particles has also been of interest in relation to theoretical treatments which consider the factors which control formation of a continuous disperse phase of randomly distributed particles. In pursuance of such work, the distribution of metallic particles was studied experimentally by quantitative microscopy of polished plane sections. A marked increase in conductivity was observed when the fractional volume loading of silver particles in Bakelite reached 0.36-0.38 ( 3). [Pg.582]

Slope of equilibrium line in mole fractions Slope of equilibrium line continuous/dispersed phase Slope of equilibrium distribution curve, dcE/dcp Slope of equilibrium line in concentration, c, units Slope of equilibrium curve, dc Q /dcE)... [Pg.1450]

The experimental results confirmed the expectations based on the calculations. Figure 4 shows the dq>endence of the sucked-in dispersed phase on the flow rate of the continuous phase for the old and new geometries, respectively. It can be seen that the suction of the dispersed phase is much hi er with the new geometry, so no extra pump is needed to achieve the desired phase ratio of about 3 1 (continuous dispersed phase). The drop size distribution was about the same for both devices. Using the following conditions a mean diameter of around 1.5 pm and a Sauter mean diameter of around 2.5 pm could be obtained continuous phase dispersed phase ... [Pg.105]

Fig. 8. Emulsion morphology diagram, illustrating where the microemulsion in various macroemulsion morphologies is a continuous phase or dispersed phase. Morphology boundaries (—), aqueous, continuous (--------------), oleic, continuous (--), microemulsion, continuous. Fig. 8. Emulsion morphology diagram, illustrating where the microemulsion in various macroemulsion morphologies is a continuous phase or dispersed phase. Morphology boundaries (—), aqueous, continuous (--------------), oleic, continuous (--), microemulsion, continuous.
The values of k and hence Sb depend on whether the phase under consideration is the continuous phase, c, surrounding the drop, or the dispersed phase, d, comprising the drop. The notations and Sh are used for the respective mass-transfer coefficients and Sherwood numbers. [Pg.63]

Type of drop Dispersed phase, Sh Continuous phase, Sh... [Pg.63]

Holdup and Flooding. The volume fraction of the dispersed phase, commonly known as the holdup can be adjusted in a batch extractor by means of the relative volumes of each Hquid phase added. In a continuously operated weU-mixed tank, the holdup is also in proportion to the volume flow rates because the phases become intimately dispersed as soon as they enter the tank. [Pg.69]

However, in a countercurrent column contactor as sketched in Figure 8, the holdup of the dispersed phase is considerably less than this, because the dispersed drops travel quite fast through the continuous phase and therefore have a relatively short residence time in the equipment. The holdup is related to the superficial velocities U of each phase, defined as the flow rate per unit cross section of the contactor, and to a sHp velocity U (71,72) ... [Pg.69]

The role of coalescence within a contactor is not always obvious. Sometimes the effect of coalescence can be inferred when the holdup is a factor in determining the Sauter mean diameter (67). If mass transfer occurs from the dispersed (d) to the continuous (e) phase, the approach of two drops can lead to the formation of a local surface tension gradient which promotes the drainage of the intervening film of the continuous phase (75) and thereby enhances coalescence. It has been observed that d-X.o-c mass transfer can lead to the formation of much larger drops than for the reverse mass-transfer direction, c to... [Pg.69]

L tex Foa.m Rubber. Latex foam mbber was the first ceUular polymer to be produced by frothing. (/) A gas is dispersed in a suitable latex 2) the mbber latex particles are caused to coalesce and form a continuous mbber phase in the water phase (7) the aqueous soap film breaks owing to... [Pg.407]

Another type of polyol often used in the manufacture of flexible polyurethane foams contains a dispersed soHd phase of organic chemical particles (234—236). The continuous phase is one of the polyols described above for either slab or molded foam as required. The dispersed phase reacts in the polyol using an addition reaction with styrene and acrylonitrile monomers in one type or a coupling reaction with an amine such as hydrazine and isocyanate in another. The soHds content ranges from about 21% with either system to nearly 40% in the styrene—acrylonitrile system. The dispersed soHds confer increased load bearing and in the case of flexible molded foams also act as a ceU opener. [Pg.417]

Water-in-OilEmulsions. A water-in-od or invert emulsion consists of a continuous od phase which surrounds finely divided water droplets that are uniformly dispersed throughout the mixture. The invert emulsion ensures that the od is in constant contact with the hydrauHc system s moving parts, so as to minimise wear. [Pg.263]

Figure 4b represents the case where a reactant dissolved in the dispersed phase reacts with the continuous phase to produce a co-reactant. The co-reactant and any remaining unreacted original reactant left in the dispersed phase then proceed to react with each other at the dispersed phase side of the interface and produce a capsule shell. Capsule shell formation occurs entirely because of reaction of reactants present in the droplets of dispersed phase. No reactant is added to the aqueous phase. As in the case of the process described by Figure 4a, a reactive species must be dissolved in the core material in order to produce a capsule shell. [Pg.320]

Figure 4c illustrates interfacial polymerisation encapsulation processes in which the reactant(s) that polymerise to form the capsule shell is transported exclusively from the continuous phase of the system to the dispersed phase—continuous phase interface where polymerisation occurs and a capsule shell is produced. This type of encapsulation process has been carried out at Hquid—Hquid and soHd—Hquid interfaces. An example of the Hquid—Hquid case is the spontaneous polymerisation reaction of cyanoacrylate monomers at the water—solvent interface formed by dispersing water in a continuous solvent phase (14). The poly(alkyl cyanoacrylate) produced by this spontaneous reaction encapsulates the dispersed water droplets. An example of the soHd—Hquid process is where a core material is dispersed in aqueous media that contains a water-immiscible surfactant along with a controUed amount of surfactant. A water-immiscible monomer that polymerises by free-radical polymerisation is added to the system and free-radical polymerisation localised at the core material—aqueous phase interface is initiated thereby generating a capsule sheU (15). [Pg.320]

Static mixing of immiscible Hquids can provide exceUent enhancement of the interphase area for increasing mass-transfer rate. The drop size distribution is relatively narrow compared to agitated tanks. Three forces are known to influence the formation of drops in a static mixer shear stress, surface tension, and viscous stress in the dispersed phase. Dimensional analysis shows that the drop size of the dispersed phase is controUed by the Weber number. The average drop size, in a Kenics mixer is a function of Weber number We = df /a, and the ratio of dispersed to continuous-phase viscosities (Eig. 32). [Pg.436]

Drilling fluids are classified as to the nature of the continuous phase gas, water, oil, or synthetic. Within each classification are divisions based on composition or chemistry of the fluid or the dispersed phase. [Pg.174]


See other pages where Continuous disperse phases is mentioned: [Pg.360]    [Pg.364]    [Pg.365]    [Pg.365]    [Pg.367]    [Pg.367]    [Pg.201]    [Pg.53]    [Pg.76]    [Pg.1269]    [Pg.1031]    [Pg.266]    [Pg.587]    [Pg.110]    [Pg.3909]    [Pg.436]    [Pg.920]    [Pg.420]    [Pg.95]    [Pg.612]    [Pg.360]    [Pg.364]    [Pg.365]    [Pg.365]    [Pg.367]    [Pg.367]    [Pg.201]    [Pg.53]    [Pg.76]    [Pg.1269]    [Pg.1031]    [Pg.266]    [Pg.587]    [Pg.110]    [Pg.3909]    [Pg.436]    [Pg.920]    [Pg.420]    [Pg.95]    [Pg.612]    [Pg.2585]    [Pg.154]    [Pg.63]    [Pg.69]    [Pg.74]    [Pg.279]    [Pg.284]    [Pg.112]    [Pg.112]    [Pg.476]    [Pg.99]    [Pg.318]    [Pg.321]   
See also in sourсe #XX -- [ Pg.231 , Pg.232 ]




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Disperse phase

Dispersion polymerization continuous phase

Dispersive phase

Phase dispersion

Water-continuous emulsions, determining dispersed phase

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