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Partial condenser analogy

Figure 7.1. Continuous single-stage equilibrium separation, (a) Flash vaporization. (Adiabatic flash with valve isothermal flash without valve when Tv is specified. (6) Partial condensation. (Analogous to isothermal flash when Ty is specified. Figure 7.1. Continuous single-stage equilibrium separation, (a) Flash vaporization. (Adiabatic flash with valve isothermal flash without valve when Tv is specified. (6) Partial condensation. (Analogous to isothermal flash when Ty is specified.
In some services (e.g., refinery fractionators), vapor approaching the chimney tray is hotter than the chimney tray liquid. Heat will be transferred from the vapor to the liquid. If the vapor is condensable, some will condense on the bottom face of the chimney tray. The net result is analogous to leakage. The author is familiar with situations where refractory was installed on the bottom face of the chimney tray. In all these cases, steps were also taken to minimize leakage, making it difficult to independently assess the effectiveness of the refractory. For multicomponent, partially condensable vapor condensing on an uninsulated bottom face of a chimney tray (e.g., in a refinery fractionator), a typical heat transfer coefficient is 15 Btu/(h ft °F) (237). [Pg.110]

For the systematic synthesis of naturally occurring bile pigments, the most versatile method is still the stepwise coupling of pyrrole—or partially reduced analogs— to form dipyrrolic units, cf. which can be coupled together. C-labeled bilirubin IXa (40), for example, has now been synthesized by condensation of an a-unsubstituted oxopyrromethene (38) with an oxopyrromethene Mannich base (39) the label was incorporated in the dimethylaminomethyl res-... [Pg.254]

A process analogous to distillation is partial condensation. Here, a vapor feed is fractionated in a condenser. In principle, the operation modes shown in Fig. 5.1-1 can also be applied to partial condensation by replacing the evaporator with a condenser. [Pg.233]

According to the discussion in Chapter 2.2, liquid mixtures containing different boiling components are partially separated by supplying heat to the system. Analogous to this, vapor mixtures with different condensing components are partially separated by partial condensation which is achieved by removing heat from the system. [Pg.230]

The map in Figure 4.20 shows how the operating temperature affects the partial pressure of benzene in the effluent. This map is a design tool for our condenser analogous to the equations we developed as design tools in the previous chapter. More on graphical design tools will be presented later. [Pg.149]

This process of countercurrent contact of a vapor with a liquid which has been produced by partial condensation of the vapor is termed rectification. Its result is equivalent to a series of redistillations with the consumption of no additional heat and is analogous in this respect to multieffect evaporation. However, it is only the result that is similar and not the mechanism of obtaining it. [Pg.106]

Equilibrium partial condensation is handled mathematically in a manner completely analogous to that for equilibrium distillation. It is a type of condition that is frequently encountered in the partial condenser of a rectification unit in which the uncondensed vapor and the condensate flow along together and reach a close approach to equilibrium. [Pg.116]

When a gas comes in contact with a solid surface, under suitable conditions of temperature and pressure, the concentration of the gas (the adsorbate) is always found to be greater near the surface (the adsorbent) than in the bulk of the gas phase. This process is known as adsorption. In all solids, the surface atoms are influenced by unbalanced attractive forces normal to the surface plane adsorption of gas molecules at the interface partially restores the balance of forces. Adsorption is spontaneous and is accompanied by a decrease in the free energy of the system. In the gas phase the adsorbate has three degrees of freedom in the adsorbed phase it has only two. This decrease in entropy means that the adsorption process is always exothermic. Adsorption may be either physical or chemical in nature. In the former, the process is dominated by molecular interaction forces, e.g., van der Waals and dispersion forces. The formation of the physically adsorbed layer is analogous to the condensation of a vapor into a liquid in fret, the heat of adsorption for this process is similar to that of liquefoction. [Pg.736]

Three different types of condensed diazaquinones, as exemplified by benzo analogs 81-83 can be formally anticipated. All reported attempts to prepare 81 have failed to date (76MI1, 760PP45) and the author is not aware of any reported synthesis of compounds similar to 82. On the other hand, 83 and other diazaquinones derived from 68 are important both from a theoretical point of view and as intermediates in organic synthesis, and this subject has been partially reviewed (78H1771). In keeping with the consistency of this review, the author has decided to cover the most important achievements in the field as well as all relevant publications that have appeared after the aforementioned review was published. However, additional pertinent information and literature references are cited in the previously mentioned review. [Pg.157]

The rate of hydrolysis is slower than the corresponding silicon analog, with hydrolysis occurring only partially. When heated with hydrogen at 1,000°C in a quartz reactor, it is converted into germanium(I) chloride, condensing onto the wall of the reactor ... [Pg.317]

Table II presents some consequences of these analogies for a vapor phase and a condensed phase together with the thermal analogs. Here rti is the concentration of the vapor in molecules per unit volume, Nt is the mole fraction in the condensed phase, Vc is the molar volume of the substrate, p< is the partial pressure, and y< is the rational activity coefficient. Table II presents some consequences of these analogies for a vapor phase and a condensed phase together with the thermal analogs. Here rti is the concentration of the vapor in molecules per unit volume, Nt is the mole fraction in the condensed phase, Vc is the molar volume of the substrate, p< is the partial pressure, and y< is the rational activity coefficient.
If the lid is removed, and the external surroundings have partial pressure Ph2o less than 23.8 Torr ( relative humidity < 100% ), then water will evaporate from the beaker into the surroundings until the beaker is empty, because only vapor is stable under these conditions. However, if the external surroundings have partial pressure Ph2o >23.8 Torr, water will condense from the surroundings to fill the beaker, because only liquid is stable under these conditions. Thus, the saturation vapor pressure ( 100% relative humidity ) corresponds to the unique concentration (partial pressure) of water vapor that can coexist at equilibrium in the atmosphere above liquid water at 25°C. Other (T, P) points on the vapor-pressure curve can be interpreted analogously. [Pg.218]

A new route, from 1-thio-D-aldohexofuranosides, was developed by Wolfrom and coworkers ethyl 1-thio-a-D-glucofuranoside was converted by chlorine into the chloride,101 arid this was condensed with the chloro-mercuri derivative of a 2,6-diacetamidopurine to give, on partial deacetylation, a 2-acetamido-9- f-D-glucofuranosyladenine.70 D-Galactofuranosyl analogs were also prepared. [Pg.123]

Gas-liquid analysis of the product obtained by polycondensation of 1,5-dichlorohexaphenylcyclo-tetrasiloxane with 1,3-dihydroxytetramethyldisiloxane has shown that initial compounds are absent in it and octamethylcyclotetrasiloxane, which would be formed by homocondensation of disiloxane-diol in acidic medium is also absent, but products with higher boiling points, i.e. the products of partial intramolecular condensation are present. In the presence of pyridine, HFC reaction of 1,5-dichlorohexaphenylcyclotetrasiloxane with a,co-dihydroxydimethylsiloxanes proceeds by analogy (at low values of n). [Pg.219]


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See also in sourсe #XX -- [ Pg.117 ]




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