- Acetic acid/toluene
- Acetonitrile/ethanol
- Acetonitrile/water
- Acetone/methanol
- Benzene/cyclohexane
- Benzene/ethanol
- Benzene
/isopropyl alcohol (IPA)
- Benzene/1-propanol
- Benzene/methanol
- Benzene/methyl-ethyl ketone (MEK)
- 1-Butanol/n-butyl acetate
- 1-Butanol/n-octane
- Diisopropyl ether (DIPE)
/isopropyl alcohol (IPA)
- 1,4-Dioxane/water
- Ethanol/ethyl acetate
- Ethanol/heptane
- Ethanol/methyl-ethyl ketone (MEK)
- Ethanol/water
- Ethyl acetate/methanol
- Methanol/methyl acetate
- Methanol/methyl-ethyl ketone (MEK)
- Methyl-ethyl ketone (MEK)
/isopropyl alcohol (IPA)
- 1-Propanol/cyclohexane
- Tetrahydrofuran/water
(The list could have been very long. These are just a few examples)
Example:
[Ethanol-Water]
The ethanol-water azeotrope has been reported to disappear at 306K (source: DDBST Gmbh) (i e 33 Celsius or 91 Farenheit) or 80 mmHg dew pressure (International Journal of BioChemiPhysics, Vol. 13, No.2, December 2004, page 46). Hence, sub-azeotropic ethanol-water,e.g. 94 mass%, distilled in a column with a sufficient number of actual plates, with a reboiler temperature of +10C (i e 50 Farenheit), a condenser temperature of +4C (39 Farenheit) and in the presence of inert gas (e.g. nitrogen) circulating through the column and thereafter from the condenser back into the reboiler and so forth can produce 100% pure ethanol as distillate.
Hence with a chemical laboratory having a distillation setup with a nitrogen circulation means inside a large refrigerator, a nitrogen gas tube and a means for heating the reboiler, 100% pure ethanol as distillate should be possible to obtain.
- Acetophenone/phenol
- Acetone/chloroform
- Ethylene diamine/water
- Formic acid/water
- Hydrochloric acid/water
- N,N-Dimethylacetamide (DMAC)/water
(The list could have been very long. These are just a few examples)