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Boihng point solvent

Nitrobenzene is an extremely versatile solvent, and may frequently be employed for the crystallisation of compounds which do not dissolve appreciably in the common organic solvents. The vapour is somewhat poisonous, so that recrystaUisations must be carried out in the fume cupboard. After the crystals have been collected, they should be washed with a volatile solvent, such as benzene, alcohol or ether, to remove the excess of nitrobenzene (compare Section 11,32). The only disadvantage of nitrobenzene as a solvent is that it has a pronounced oxidising action at the boihng point. [Pg.175]

Component 1 is the diffusing gas, while component 2 is the solvent. The solvent viscosity l2 in Pa sec, the solute molar volume at the normal boihng point Vi in mVkmole, and the solvent association parameter Xo multiplied by the solvent... [Pg.415]

Solvent Effects m Extractive Distillation In the distillation of ideal or nonazeotropic mixtures, the component with the lowest pure-component boihng point is always recovered primarily in the distillate, while the highest boiler is recovered primarily in the bottoms. The situation is not as straightforward for an extractive-distillation operation. With some solvents, the component with the lower pure-component boiling point wih be recovered in the distillate as in ordinaiy distillation. For another solvent, the expected order is reversed, and the component with the higher pure-component boiling point wih be... [Pg.1314]

A negative deviation reduces the activity of the solute in the solvent, which enhances the liqnid-hqnid partition ratio but also leads to maximnm-boihng-point azeotropes. Among other classes of solvents shown in Table 15-4 that suppress the escaping tendency of a ketone are classes 1 and 2, i.e., phenohcs and acids. [Pg.1452]

There are several compilations and reviews of fluorocarbon physical properties [4, 5, 6 9, 10, II 12], and only the boihng points, surface energies and activities, and solvent properties are discussed in this section to illustrate the characteristic fluonne substituent effects... [Pg.980]

Once the reagents are selected, compatible solvents are chosen. Some solvents avoided for scale-up are shown in Table 2.2. 1,2-Dichloroethane, a Class 1 solvent with toxicity similar to benzene, should be avoided. Solvents more commonly used are shown in Table 2.3. Characteristics considered include toxicity, polarity, boihng point, freezing point, miscibihty with water, and ability to remove water (and other compounds) by... [Pg.18]

Alkanes have similar chemical properties, hut their physical properties vary with molecular weight and the shape of the molecule. The low polarity of all the bonds in alkanes means that the only intermolecular forces between molecules of alkanes are the weak dipole-dipole forces (see 2.5.1), which are easily overcome. As a result, compared with other functional groups, alkanes have low melting and boihng points, and low solubility in polar solvents, e.g. water, but high solubility in nonpolar solvents, e.g. hexane and dichloromethane. Most cycloalkanes also have low polarity. [Pg.64]

Solvent mixtures that contain heat-sensitive compounds, are viscous, or have high boihng points can be separated using wiped-film evaporators (WFE) [57, 58]. A WFE operates by receiving a liquid feed into a column that contains several wiper blades. The walls of the WFE are heated at a constant temperature in order to vaporize the solvent film. As the solvent vapors migrate to the center of the WFE, they come into contact with a coohng unit that condenses the vapors, allowing them to flow down the condenser to the outlet receiver. The thin solvent film and reduced system pressure (in the case of vacuum operation) allows the solvents to be separated slowly at lower temperatures [57-59]. [Pg.78]

Crystallization is used to separate saturated fats and oleic acid from linoleic acid. If a highly concentrated product is required, the linoleic acid may be crystallized once or repeatedly as the last step in purification. Crystallization is a mild procedure but usually requires the use of a solvent (108) such as acetone or methanol. The use of low boihng point and flammable solvents raises concerns over plant safety, government regulations on manufacturing, and market acceptance of the product. Furthermore, the removal of oleic acid by crystallization in solvent is only possible by lowering the temperature of the liquor to below —40°C (108). To crystallize linoleic acid, the temperature must be reduced to —75 °C. [Pg.1376]

In order to calculate the change in boihng point it is therefore necessary to know the latent heat of the solvent, the relative lowering of the vapour pressure, and also the composition of the saturated vapour at T and Tq. The boihng point of the solution will be higher or lower than that of the pure solvent according as (Pa-Pa)j, PuT ... [Pg.245]

The change in the freezing point of substances which form solid solutions can be calculated in a similar manner. For the purposes of this calculation it is necessary to know the vapour pressures of the sohd solvent and the partial pressures of the solid solution. It is easy to show that the freezing point of a solution of this kind may even be higher than that of the pure solvent, just as (by 10) the boihng point of a solution may be, lower than that of the pure solvent. Actual cases in which the freezing point is raised have recently been observed by V. HevesyJ and Sackur. ... [Pg.245]

Pft of the solute at the boihng point of the solvent. If Pf,>Pay the boihng point will be lowered, since L/ is always negative. [Pg.259]

Table 12.2 hsts values of A), for several common solvents. Using the boihng-point elevation constant for water and Equation (12.5), you can see that if the molahty m of an aqueous solution is 1.00, the boiling point will be 100.52°C. [Pg.485]

The physical properties of alkenes, alk)mes, and aromatic compoimds are very similar to those of alkanes. They are nonpolar. As a result of the "like dissolves like" rule, they are not soluble in water but are very soluble in nonpolar solvents such as other hydrocarbons. They also have relatively low boihng points and melting points. [Pg.295]

Low toxicity solvent Easy to recycle and reuse Low reactivity in general High density to create multiphases Expensive, can require functionalized ligands Low solubility of many organic materials Low-boihng-point compounds are volatile Disposal can be problematic... [Pg.5]

The most prominent thermic basic operation is the rectification or distillation to separate individual components from a mixture. For separation, the mixture is evaporated completely and successively cooled down. The components can be effectively separated if they have different boiling points or dew points, respectively. In the case of close boihng points for the components in the feed mixture, distillation is still applicable if an auxiliary chemical (so-called solvent) is available changing the boiling or dew points of at least one component (so-called fractional distillation) P... [Pg.12]

Since all C4-sub-fractions possess similar boiling points, extractive distillation has to be applied, i.e. a solvent chemical is used to drive the boihng points apart. See Sun and Wristers (2006). [Pg.154]

Dictionary of Organic Compounds. Oxford, England Oxford University Press, 4th Ed., 1965, with annual supplements. This five-volume work, covering over 40,000 compounds, gives molecular and structural formulas, melting and boihng points, recrystallization solvents, uses, and literature references. [Pg.134]


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See also in sourсe #XX -- [ Pg.70 , Pg.74 , Pg.320 ]




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