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Liquid overall

Panel Coils Immersed in Liquid Overall Average Heat-Transfer Coefficients ... [Pg.1056]

The notation used here and in Section 7.7 is standard in the literature on this subject and originates in the pioneering work of Martinelli and co-workers. There are two aspects of the notation that may lead to confusion and error. First, note that LO and GO do not denote liquid only and gas only reference flows, as might be expected. On the contrary, they denote flows in which the whole of the flow rate is liquid or gas. It may help to remember them as liquid overall and gas overall . The second point to note is that 2 denotes the two-phase multiplier. Correlations may present values of but it must be remembered that this is the square root of the two-phase multiplier. [Pg.250]

Much has been reported in recent years about phosphate ester for use as a deflocculant/dispersant for tape casting slips. Phosphate ester is a very powerful dispersant for many oxide powders, including BaTiOg, AI2O3, and TiOg. Phosphate ester is soluble in either water or a number of organic solvents and is described as an anionic surfactant in polar liquids.Overall conclusions about this additive are that it functions both as an ionic repulsion and steric hindrance deflocculant. [Pg.35]

The linear rate suggests the rate-controlling step is simply the reaction of metal with oxygen. Any corrosion product or scale formed is generally assumed to be non-protective, due to its porous, non-adherent, powdery, or volatile structure. In some cases, the corrosion product may even be a liquid. Overall reaction rates may be veiy fast up to and including ignition. Magnesium, cerium, and lanthanum are typical examples of pure metals that exhibit linear oxidation rates over a wide variety of conditions. [Pg.436]

At constant electrode geometry, the solution consists of an adequate selection of Urd resulting from a compromise between mixing and floe stability. This can be obtained first by optimizing the axial position of the electrodes using both the conductivity tracer technique for ULd estimation and turbidity measurements to estimate the amount of dispersed A1 particles in the downcomer. Experimental results show that no liquid overall circulation can be detected when the electrodes were placed in the upper part of riser, for Hi approximately higher than 60 cm. For 7 cm axial positions are reported in figure 14 at various current densities. [Pg.63]

Z(I) Vector (length 20) of overall feed composition resulting from combined liquid and vapor feeds (I = 1,N). [Pg.321]

MISCIBLE N COMPONENT LIQUID SYSTEMS IN.LF.ZOI OF OVERALL COMPOSITION... [Pg.336]

Overall formula Structural formula Molecular weight Bolling, point, °C (1 atm) Specific gravity < (liquid)... [Pg.4]

An example of an application of CAO is its use in optimising the distribution of gas in a gas lift system (Fig. 11.3). Each well will have a particular optimum gas-liquid ratio (GLR), which would maximise the oil production from that well. A CAO system may be used to determine the optimum distribution of a fixed amount of compressed gas between the gas lifted wells, with the objective of maximising the overall oil production from the field. Measurement of the production rate of each well and its producing GOR (using the test separator) provides a CAO system with the information to calculate the optimum gas lift gas required by each well, and then distributes the available gas lift gas (a limited resource) between the producing wells. [Pg.282]

In order to describe any electrochemical cell a convention is required for writing down the cells, such as the concentration cell described above. This convention should establish clearly where the boundaries between the different phases exist and, also, what the overall cell reaction is. It is now standard to use vertical lines to delineate phase boundaries, such as those between a solid and a liquid or between two innniscible liquids. The junction between two miscible liquids, which might be maintained by the use of a porous glass frit, is represented by a single vertical dashed line, j, and two dashed lines, jj, are used to indicate two liquid phases... [Pg.602]

As the temperature of the liquid phase is increased, the system ultimately reaches a phase boundary, the bubble point at which the gas phase (vapour) begins to appear, with the composition shown at the left end of the horizontal two-phase tie-line . As the temperature rises more gas appears and the relative amounts of the two phases are detemiined by applying a lever-ami principle to the tie-line the ratio of the fractionof molecules in the gas phase to that hn the liquid phase is given by the inverse of the ratio of the distances from the phase boundary to the position of the overall mole fraction Xq of the system. [Pg.613]

Schemes for classifying surfactants are based upon physical properties or upon functionality. Charge is tire most prevalent physical property used in classifying surfactants. Surfactants are charged or uncharged, ionic or nonionic. Charged surfactants are furtlier classified as to whetlier tire amphipatliic portion is anionic, cationic or zwitterionic. Anotlier physical classification scheme is based upon overall size and molecular weight. Copolymeric nonionic surfactants may reach sizes corresponding to 10 000-20 000 Daltons. Physical state is anotlier important physical property, as surfactants may be obtained as crystalline solids, amoriDhous pastes or liquids under standard conditions. The number of tailgroups in a surfactant has recently become an important parameter. Many surfactants have eitlier one or two hydrocarbon tailgroups, and recent advances in surfactant science include even more complex assemblies [7, 8 and 9]. Schemes for classifying surfactants are based upon physical properties or upon functionality. Charge is tire most prevalent physical property used in classifying surfactants. Surfactants are charged or uncharged, ionic or nonionic. Charged surfactants are furtlier classified as to whetlier tire amphipatliic portion is anionic, cationic or zwitterionic. Anotlier physical classification scheme is based upon overall size and molecular weight. Copolymeric nonionic surfactants may reach sizes corresponding to 10 000-20 000 Daltons. Physical state is anotlier important physical property, as surfactants may be obtained as crystalline solids, amoriDhous pastes or liquids under standard conditions. The number of tailgroups in a surfactant has recently become an important parameter. Many surfactants have eitlier one or two hydrocarbon tailgroups, and recent advances in surfactant science include even more complex assemblies [7, 8 and 9].
Condensed phase vibrational or vibronic lineshapes (vibronic transitions create vibrational excitations of electronic excited states) rarely provide infonnation about VER (see example C3.5.6.4). Experimental measurements of VER need much more than just the vibrational spectmm. The earliest VER measurements in condensed phases were ultrasonic attenuation studies of liquids [15], which provided an overall relaxation time for slowly (>10 ns) relaxing small molecule liquids. [Pg.3034]

Thermospray nebulizers are somewhat expensive but can be used on-line to a liquid chromatographic column. About 10% of sample solution is transferred to the plasma flame. The overall performance of the thermospray device compares well with pneumatic and ultrasonic sprays. When used with microbore liquid chromatographic columns, which produce only about 100 pl/min of eluant, the need for spray and desolvation chambers is reduced, and detection sensitivities similar to those of the ultrasonic devices can be attained both are some 20 times better than the sensitivities routinely found in pneumatic nebulizers. [Pg.150]

In the liquid state molecules are in intimate contact, so the energetics of molecular interactions generally make a contribution to the overall picture of the mixing process. There are several aspects of the situation that we should be aware of before attempting to formulate a theory for ... [Pg.521]

Equation 28 and its liquid-phase equivalent are very general and valid in all situations. Similarly, the overall mass transfer coefficients may be made independent of the effect of bulk fiux through the films and thus nearly concentration independent for straight equilibrium lines ... [Pg.23]

Combustion. The primary reaction carried out in the gas turbine combustion chamber is oxidation of a fuel to release its heat content at constant pressure. Atomized fuel mixed with enough air to form a close-to-stoichiometric mixture is continuously fed into a primary zone. There its heat of formation is released at flame temperatures deterruined by the pressure. The heat content of the fuel is therefore a primary measure of the attainable efficiency of the overall system in terms of fuel consumed per unit of work output. Table 6 fists the net heat content of a number of typical gas turbine fuels. Net rather than gross heat content is a more significant measure because heat of vaporization of the water formed in combustion cannot be recovered in aircraft exhaust. The most desirable gas turbine fuels for use in aircraft, after hydrogen, are hydrocarbons. Fuels that are liquid at normal atmospheric pressure and temperature are the most practical and widely used aircraft fuels kerosene, with a distillation range from 150 to 300 °C, is the best compromise to combine maximum mass —heat content with other desirable properties. For ground turbines, a wide variety of gaseous and heavy fuels are acceptable. [Pg.412]


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See also in sourсe #XX -- [ Pg.357 , Pg.359 ]




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Overall gas—liquid mass transfer

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