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Ethanol binary azeotropes

However, there is a problem. Water and ethanol form an azeotrope, as mentioned before, but benzene also forms a binary azeotrope with ethanol. The benzene-ethanol binary azeotrope boils at 67.8°C and consists of 67.6% benzene and 32.4% ethanol. This means that as the benzene-water azeotrope is distilled, ethanol is also removed. An excess of ethanol is therefore essential. [Pg.864]

Absolute (100%) ethanol is often made by adding benzene to the ethanol -water binary azeotrope (two components), to make a ternary azeotrope (three components). This ternary alcohol-water-benzene (18.5 7.4 74.1) azeotrope comes over until all the water is gone, followed by a benzene-ethanol mixture. Finally, absolute ethanol gets its chance to appear, marred only slightly by traces of benzene. [Pg.307]

B. Ethyl a-(bromomethyl)acry late. In a nitrogen-flushed, 1-L, round-bottomed flask equipped with a magnetic stirrer, Dean-Stark trap, and condenser are placed 42.0 g (0.25 mol) of a-(bromomethyl)acrylic acid and 300 mL of benzene. Approximately 50 mL of a binary azeotrope of benzene and water is distilled (Note 7). The Dean-Stark trap is removed and 100 mL of absolute ethanol (Note 8) and 1 mL of concentrated sulfuric acid are added slowly. The contents of the flask are boiled in a nitrogen atmosphere for 36 hr, the condensate being passed through 100 g of molecular sieves (Linde 3A) before being returned to the flask. About 125 mL of a mixture of benzene and ethanol is removed from the reaction... [Pg.29]

Figure 43 shows these azeotropes as well as a ternary one we now wish to find. Starting at the ethanol/water binary azeotrope, the infinite-dilution f-value for toluene is 2.78. Allowing for two liquid phases, the above algorithm locates the ternary azeotrope without difficulty. If we do not allow for two liquid phases, computations indicate there is no ternary azeotrope. [Pg.137]

MgS04, CaO, K2CO3, Ca or solid NaOH, followed by refluxing with, and distn from, calcium, magnesium activated with iodine, aluminium amalgam or sodium. Can also dry with molecular sieves, or by refluxing with n-butyl phthalate or succinate. (For method, see Ethanol.) n-Butanol can also be dried by efficient fractional distn, water passing over in the first fractn as a binary azeotrope (contains about 37% water). An ultraviolet-... [Pg.143]

The quantity of hexane necessary to entrain water, methanol, ethanol, acetone, and acetaldehyde dimethyl acetal to the top was estimated as the sum of the hexane quantities required to form the binary azeotropes with the quantities of water, methanol, ethanol, acetone, and acetaldehyde dimethyl acetal in the mixture. [Pg.140]

An example of azeotropic distillation is the use of benzene to permit the complete separation of ethanol and water, which forms a minimum-boiling azeotrope with 95.6 weight percent alcohol. The alcohol-water mixture with about 95 percent alcohol is fed to the azeotropic distillation column with a benzene-rich stream added at the top. The bottom product is nearly pure alcohol, and the overhead vapor is a ternary azeotrope. The overhead vapor is condensed and separated into two phases. The organic layer is refluxed, and the water layer is sent to a benzene recovery column. All the benzene and some alcohol is taken overhead and sent back to the first column, and the bottoms stream is distilled in a third column to give pure water and some of the binary azeotrope. [Pg.610]

Liquid with pungent odor. bp7 81.4. tig 1.4086. dj 0.8636 dj5 0 8407. Easily soluble in water, methanol, ethanol, ether, acetone, glacial acetic acid. Slightly sol in hydrocarbons. Forms a binary azeotrope with water, bp 75 (12% water), uv spectrum and electric moments Rogers, J. Am. Chem. Soc. 69, 2544 (1947). Polymerizes on standing, LDm in mioe and rats 35 mg/kg, C.A. 72, 124809b 0970). [Pg.963]

The ethanol column (C-1) has practically only stripping zone. Fig. 9.31-left shows composition profile both for liquid and vapour phase. The examination of the composition profiles highlights the role of the entrainer. In the zone close to the top the benzene extracts the ethanol in the liquid phase, and as a result increases the volatility of water, so that on lower stages the water is completely removed. In the lower part practically only the binary ethanol/benzene remains. The distillation trajectory starts from the ternary azeotrope, goes along the ethanol/ benzene saddle and terminates in the ethanol vertex. Because the boiling point of the azeotrope ethanol-water is close to the pure ethanol, the profile could easily jump to the ethanol/water azeotrope. Consequently, the design and operation of the column (C-1) is very sensitive. [Pg.381]

When the water has been eliminated, there follows at 68.3°C a binary azeotrope containing 32.4% of ethanol and 67.6% of benzene, and finally at 78.4°C alcohol of about 99.8% purity distils over. On an industrial scale the preparation takes place continuously, but in the laboratory it is often more convenient to operate in batch and work up the two layers of the ternary azeotrope and the binary azeotrope in portions. [Pg.327]

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]

Thus, when a mixture of 95% ethanol and benzene Is distilled, the above ternary azeotrope distills first, followed by the binary azeotrope, and the final Action (b.p. 78.30 C) is absolute alcohol. [Pg.11]

Comparing the two plots in Figure 2.8a and b, it can be seen that the composition of the low-boding binary azeotrope that exists between acetone and methanol has a strong dependence on pressure, moving from about 80 mol% acetone at 1 atm to 40mol% at 10 atm. More importantly, however, is to notice the change in the node type at pure acetone at 1 atm, pure acetone is a saddle point, while at 10 atm, this point becomes a stable node. Further, there is now also a saddle node in the form of a binary azeotrope between acetone and ethanol at 10 atm that never existed at 1 atm. [Pg.29]

In a nonideal system such as ethyl acetate/water/ ethanol, for instance, there exists considerable complexity from a phase equilibrium point of view because of the presence of a liquid liquid-equilibrium (LLE) envelope, as well as the presence of three binary azeotropes and a single ternary azeotrope. Attempts have been made to... [Pg.103]

In a situation in which fractionating power is known to be barely adequate, the two solvents (DIPE and chloroform) with low-boiling binary azeotropes including water rather than ethanol have the advantage that it is positively helpful to have their water binaries admixed with the ternary in the decanter (Table 7.6). [Pg.102]

The boiling points of the pure components at atmospheric pressure are as follows ethyl acetate (ETAC) 77.2 C ethanol (ETOH) 78.3 C water (H20) 100.0 C acetic acid (HAG) 118.0 G. There are three binary azeotropes and one ternary azeotrope summarized in Table 10.2, with respective boiling points at atmospheric pressure. The normal boiling points for the pure components as well as the compositions of the azeotropes are obtained from ASPEN Properties Plus using UNIQUAG and show satisfactory agreement with the data available elsewhere [105]. [Pg.344]


See other pages where Ethanol binary azeotropes is mentioned: [Pg.79]    [Pg.79]    [Pg.194]    [Pg.143]    [Pg.618]    [Pg.123]    [Pg.123]    [Pg.377]    [Pg.588]    [Pg.52]    [Pg.44]    [Pg.70]    [Pg.103]    [Pg.1133]    [Pg.414]    [Pg.42]    [Pg.55]    [Pg.136]    [Pg.230]    [Pg.1504]    [Pg.94]    [Pg.106]    [Pg.186]    [Pg.1501]    [Pg.377]    [Pg.379]    [Pg.1314]    [Pg.111]    [Pg.45]    [Pg.79]    [Pg.382]   
See also in sourсe #XX -- [ Pg.4 , Pg.34 ]




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