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Binary mixtures boiling points

Normal Binary mixture Boiling point 20 A A For test of... [Pg.148]

C), forms a ternary azeotrope (boiling point 64.9 "C), which is a minimum-boiling mixture. Benzene and Ethanol form a binary azeotrope (boiling point... [Pg.11]

The phase diagrams shown in Figures 9.4—9.7 all have T and P monotonic in the compositions of both phases. Consequently, at any fixed pressure the mixture boiling points are bounded by the pure-component boiling points, and at any fixed temperature the mixture pressures are bounded by the pure-component vapor pressures. But binary mixtures can have T and P pass through extrema with composition. Consider the slope of an isothermal Px curve for a binary mixture in VLE,... [Pg.383]

The breaking up of azeotropic mixtures. The behaviour of constant boiling point mixtures simulates that of a pure compound, because the composition of the liquid phase is identical with that of the vapour phase. The composition, however, depends upon the pressure at which the distillation is conducted and also rarely corresponds to stoichiometric proportions. The methods adopted in practice will of necessity depend upon the nature of the components of the binary azeotropic mixture, and include —... [Pg.12]

Carbon disulfide is completely miscible with many hydrocarbons, alcohols, and chlorinated hydrocarbons (9,13). Phosphoms (14) and sulfur are very soluble in carbon disulfide. Sulfur reaches a maximum solubiUty of 63% S at the 60°C atmospheric boiling point of the solution (15). SolubiUty data for carbon disulfide in Hquid sulfur at a CS2 partial pressure of 101 kPa (1 atm) and a phase diagram for the sulfur—carbon disulfide system have been published (16). Vapor—Hquid equiHbrium and freezing point data ate available for several binary mixtures containing carbon disulfide (9). [Pg.27]

Since the boiling point properties of the components in the mixture being separated are so critical to the distillation process, the vapor-liquid equilibrium (VLE) relationship is of importance. Specifically, it is the VLE data for a mixture which establishes the required height of a column for a desired degree of separation. Constant pressure VLE data is derived from boiling point diagrams, from which a VLE curve can be constructed like the one illustrated in Figure 9 for a binary mixture. The VLE plot shown expresses the bubble-point and the dew-point of a binary mixture at constant pressure. The curve is called the equilibrium line, and it describes the compositions of the liquid and vapor in equilibrium at a constant pressure condition. [Pg.172]

Figure 8. Boiling point diagram for binary mixture. Figure 8. Boiling point diagram for binary mixture.
The normal boiling point of a binary liquid mixture is the temperature at which the total vapor pressure is equal to 1 atm. If we were to heat a sample of pure benzene at a constant pressure of 1 atm, it would boil at 80.1°C. Similarly, pure toluene boils at 110.6°C. Because, at a given temperature, the vapor pressure of a mixture of benzene and toluene is intermediate between that of toluene and benzene, the boiling point of the mixture will be intermediate between that of the two pure liquids. In Fig. 8.37, which is called a temperature-composition diagram, the lower curve shows how the normal boiling point of the mixture varies with the composition. [Pg.461]

Based on the above information, the CAMD problem definition is revised as follows - The solvent can be acyclic hydrocarbons and ketones (aromatic compounds, chlorides, dioxanes are not considered for EH S concerns). The normal boiling point should be higher than that of chloroform (334 K), the molecular weight could be between 70-120, the solvent must not form azeotrope with either acetone or chloroform, and, must be totally miscible with the binary mixture of acetone and chloroform. [Pg.438]

Solvents used here for a general liquid-liquid extraction method were selected from Snyders solvent selectivity triangle. As extraction liquids have to be composed of mixtures of three solvents which may enter into maximum interaction with the analyte, three solvents had to be selected that represent a wide variety of selective interactions. In addition, the solvents should be sufficiently polar to ensure quantitative extraction. Besides selectivity and polarity requirements, the solvents should also meet a few other criteria, mainly for practical reasons they should not be miscible with water, have low boiling points (for relatively fast evaporation procedures) and have densities sufficiently different from the density of water, for pure solvents as well as for selected binary or ternary mixtures of solvents. [Pg.285]

Vapor-liquid equilibrium data at atmospheric pressure (690-700 mmHg) for the systems consisting of ethyl alcohol-water saturated with copper(II) chloride, strontium chloride, and nickel(II) chloride are presented. Also provided are the solubilities of each of these salts in the liquid binary mixture at the boiling point. Copper(II) chloride and nickel(II) chloride completely break the azeotrope, while strontium chloride moves the azeotrope up to richer compositions in ethyl alcohol. The equilibrium data are correlated by two separate methods, one based on modified mole fractions, and the other on deviations from Raoult s Law. [Pg.91]

In contrast, certain mixtures of two (binary) or three (ternary) components form constant boiling mixtures that cannot be separated by distillation. In such cases, each component contributes a fixed amount and the boiling point of the mixture is characteristic of the components. Such a system is called an azeotrope. The boihng point of an azeotrope may be higher or lower than that of the individual components. Common binary azeotropes are listed in Table 4.7 and ternary azeotropes are listed in Table 4.8. [Pg.483]

Binary mixtures of lower-boiling alcohols 181 Close-boiling-point problem... [Pg.288]

In distillation, the boiling point of, say, a binary mixture is related to its composition. The composition of the vapour can be related to that of the liquid by means of Raoult s law. [Pg.179]

The operation sequence for a single batch, shown in Figure 6.10, produces 2 main-cuts (PI and P2), 5 off-cuts and a final bottom product (P5). Specifications for products P3 and P4 could not be achieved directly because of the high purity requirement, low amount of component 3 and 4 in the feed mixture and the proximity of their boiling points with other components. Therefore, low purity off-cuts 2-5 (essentially binary or a ternary mixtures) are produced, collected in separate storage vessels and reprocessed when the amount of in each vessel reaches the full... [Pg.182]


See other pages where Binary mixtures boiling points is mentioned: [Pg.376]    [Pg.376]    [Pg.72]    [Pg.376]    [Pg.511]    [Pg.143]    [Pg.110]    [Pg.155]    [Pg.181]    [Pg.1132]    [Pg.142]    [Pg.171]    [Pg.497]    [Pg.184]    [Pg.143]    [Pg.577]    [Pg.578]    [Pg.581]    [Pg.110]    [Pg.257]    [Pg.143]    [Pg.254]    [Pg.507]    [Pg.531]    [Pg.168]    [Pg.131]    [Pg.133]    [Pg.342]    [Pg.185]   
See also in sourсe #XX -- [ Pg.547 ]

See also in sourсe #XX -- [ Pg.547 ]




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