GB814238A - Process for the preparation of acrylonitrile - Google Patents
Process for the preparation of acrylonitrileInfo
- Publication number
- GB814238A GB814238A GB22049/57A GB2204957A GB814238A GB 814238 A GB814238 A GB 814238A GB 22049/57 A GB22049/57 A GB 22049/57A GB 2204957 A GB2204957 A GB 2204957A GB 814238 A GB814238 A GB 814238A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetylene
- hcn
- acrylonitrile
- chloride
- grams
- 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
- C07C253/08—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds
- C07C253/12—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds to compounds containing carbon-to-carbon triple bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
A process for the simultaneous production of acrylonitrile, monovinyl acetylene and acetaldehyde comprises introducing acetylene and HCN under a pressure of substantially 1-4 atmospheres absolute and at substantially 70-110 DEG C. into an aqueous solution of cuprous chloride containing hydrochloric acid, and ammonium chloride, sodium chloride, and/or potassium chloride, the quantity of HCN used being substantially 50-103 per cent of that quantity which would be converted into acrylonitrile when employing a large excess (more than 103 per cent) of HCN under corresponding reaction conditions. By operating in this manner, the acetaldehyde formed is not significantly converted into lactic acid nitrile by excess HCN, and may be recovered as such. The acetylene partial pressure is preferably 1-3.5 atmospheres, and the preferred temperature 80-90 DEG C. In a preferred embodiment, acetylene at 1.5 atmospheres pressure and 80 DEG C. is passed into an aqueous solution containing hydrochloric acid and 680 grams of CuCl per litre and 515 grams of KCl per litre, simultaneously introducing 3.8-7.8 grams of HCN per hour per litre of solution. The ratio of acrylonitrile to monovinyl acetylene produced may be increased by: (i) increasing the quantity of HCN (within the above limits); (ii) by decreasing the acetylene partial pressure; and/or (iii) by increasing, within the limits of 1 : 1 to 1 : 0.8, the mol. proportion of CuCl to the additional chloride. By-products obtained include lactic acid nitrile, cyanbutadiene, divinyl acetylene, higher acetylene polymers, and chloroprene.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE814238X | 1956-07-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB814238A true GB814238A (en) | 1959-06-03 |
Family
ID=6734492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22049/57A Expired GB814238A (en) | 1956-07-11 | 1957-07-11 | Process for the preparation of acrylonitrile |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB814238A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1212516B (en) * | 1960-08-02 | 1966-03-17 | Knapsack Ag | Process for the production of acrylic acid nitrile from acetylene and hydrocyanic acid |
-
1957
- 1957-07-11 GB GB22049/57A patent/GB814238A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1212516B (en) * | 1960-08-02 | 1966-03-17 | Knapsack Ag | Process for the production of acrylic acid nitrile from acetylene and hydrocyanic acid |
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