GB719911A - Purifying acrylonitrile by extractive distillation - Google Patents
Purifying acrylonitrile by extractive distillationInfo
- Publication number
- GB719911A GB719911A GB28514/52A GB2851452A GB719911A GB 719911 A GB719911 A GB 719911A GB 28514/52 A GB28514/52 A GB 28514/52A GB 2851452 A GB2851452 A GB 2851452A GB 719911 A GB719911 A GB 719911A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acrylonitrile
- water
- per cent
- column
- acetonitrile
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/32—Separation; Purification; Stabilisation; Use of additives
- C07C253/34—Separation; Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Acrylonitrile is purified from acetonitrile by submitting the crude acrylonitrile to extractive distillation employing water as extractant and maintaining a very high concentration of water in the liquid phase in the distillation column, whereby purified acrylonitrile vapours leave the head of the column together with water vapours. The overhead vapours are condensed, and the condensate is allowed to separate into two liquid layers; the aqueous layer is returned to the column as reflux, and the acrylonitrile layer is submitted to further distillation to remove water. In an example, 404 parts per minute of a vapour mixture containing acrylonitrile (94 per cent.), acetonitrile (3 per cent.) and water (3 per cent.), are fed to the second tray from the base of a 30-tray perforated plate column, while 1,600 parts per minute of water at 70 DEG -80 DEG C. are fed to the second tray from the top of the column. The temperature of the column-reboiler is maintained at about 85 DEG C.; and the liquid-temperature in the column below the water feed point is maintained at about 71 DEG C. The upper layer of the distillate contains acrylonitrile (95.5 per cent.), water (3.5 per cent.), and less than 1 per cent. of acetonitrile. The base product, withdrawn from the reboiler at the rate of 1,659 parts per minute contains water (96.6 per cent.), acetonitrile (0.4 per cent.), and acrylonitrile (2.3 per cent.) This product is distilled in a conventional column to recover a distillate containing the acrylonitrile, which is recycled to the extractive distillation.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US719911XA | 1951-11-14 | 1951-11-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB719911A true GB719911A (en) | 1954-12-08 |
Family
ID=22104876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28514/52A Expired GB719911A (en) | 1951-11-14 | 1952-11-12 | Purifying acrylonitrile by extractive distillation |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB719911A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1189989B (en) * | 1958-10-31 | 1965-04-01 | Knapsack Ag | Process for the separation of acrylonitrile from its gas mixtures |
DE1203758B (en) * | 1955-06-02 | 1965-10-28 | Lonza Ag | Continuous process for the production of acrylic acid nitrile from acetylene and hydrocyanic acid |
DE1230015B (en) * | 1960-04-07 | 1966-12-08 | Distillers Co Yeast Ltd | Process for the production of acrylonitrile from its mixture with acetonitrile |
DE1239294B (en) * | 1961-05-17 | 1967-04-27 | Bayer Ag | Process for the production of acrylonitrile from its mixture with acetonitrile by extraction in countercurrent |
US3328268A (en) * | 1962-07-21 | 1967-06-27 | Electro Chimie Metal | Continuous recovery of acrylonitrile and acetonitrile from mixtures by plural extractive distillation with water |
DE1255103B (en) * | 1961-05-27 | 1967-11-30 | Lentia Gmbh | Process for the continuous recovery of acrylic acid nitrile and acetonitrile from their aqueous solutions |
-
1952
- 1952-11-12 GB GB28514/52A patent/GB719911A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1203758B (en) * | 1955-06-02 | 1965-10-28 | Lonza Ag | Continuous process for the production of acrylic acid nitrile from acetylene and hydrocyanic acid |
DE1189989B (en) * | 1958-10-31 | 1965-04-01 | Knapsack Ag | Process for the separation of acrylonitrile from its gas mixtures |
DE1230015B (en) * | 1960-04-07 | 1966-12-08 | Distillers Co Yeast Ltd | Process for the production of acrylonitrile from its mixture with acetonitrile |
DE1239294B (en) * | 1961-05-17 | 1967-04-27 | Bayer Ag | Process for the production of acrylonitrile from its mixture with acetonitrile by extraction in countercurrent |
DE1255103B (en) * | 1961-05-27 | 1967-11-30 | Lentia Gmbh | Process for the continuous recovery of acrylic acid nitrile and acetonitrile from their aqueous solutions |
US3328268A (en) * | 1962-07-21 | 1967-06-27 | Electro Chimie Metal | Continuous recovery of acrylonitrile and acetonitrile from mixtures by plural extractive distillation with water |
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