GB645754A - Production of nitriles - Google Patents
Production of nitrilesInfo
- Publication number
- GB645754A GB645754A GB20153/47A GB2015347A GB645754A GB 645754 A GB645754 A GB 645754A GB 20153/47 A GB20153/47 A GB 20153/47A GB 2015347 A GB2015347 A GB 2015347A GB 645754 A GB645754 A GB 645754A
- Authority
- GB
- United Kingdom
- Prior art keywords
- catalyst
- hydrocarbon
- ammonia
- dioxide
- treatment
- 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
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aromatic nitriles are manufactured by contacting an alkyl-substituted aromatic hydrocarbon with ammonia, in gaseous phase, at temperatures between about 900 DEG F. and the decomposition temperature of ammonia (preferably at 980-1030 DEG F.), in the presence of a catalyst comprising a molybdenum oxide (e.g. the sesquioxide, dioxide, pentoxide or especially the trioxide), preferably supported on alumina. The molecular proportion of hydrocarbon in the reaction mixture may vary widely (e.g. from about 20 to about 90 per cent), but it is preferable to use a molar excess of ammonia. If the catalyst becomes fouled it may be regenerated by careful oxidation, e.g. by passing a stream of air over it. The pressure at which the reaction is effected may be subatmospheric, atmospheric or superatmospheric. Examples describe the preparation of benzonitrile from toluene, tolunitriles from xylenes and xylylnitriles from trimethylbenzenes. Other starting materials specified are methylnaphthalenes, and hydrocarbon fractions containing mixed alkylbenzenes or alkylnaphthalenes. The Specification as open to inspection under Sect. 91 comprises also the use of catalysts containing a tungsten oxide (e.g. the dioxide or trioxide) and of catalyst supports other than alumina (e.g. silica gel, the material sold under the Registered Trade Mark "Carborundum," pumice or clays), the use of temperatures down to about 850 DEG F. (the preferred range being about 925-1075 DEG F.), and the use as starting materials of other hydrocarbons having at least two carbon atoms to at least one of which at least two hydrogen atoms are attached (including alkenyl substituted aromatic hydrocarbons, especially styrene). Reference is made to the use of air diluted with flue gases for the oxidation treatment for the regeneration of the catalyst, and it is stated that this treatment is preferably followed by a purging treatment, e.g. by passing over the catalyst a stream of nitrogen, carbon dioxide or hydrocarbon gases. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US645754XA | 1943-11-10 | 1943-11-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB645754A true GB645754A (en) | 1950-11-08 |
Family
ID=22056895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB20153/47A Expired GB645754A (en) | 1943-11-10 | 1947-07-25 | Production of nitriles |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB645754A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3497545A (en) * | 1966-03-10 | 1970-02-24 | Halcon International Inc | Preparation of polynitriles by ammoxidation of polyalkyl substituted aromatic hydrocarbons utilizing recycle of unreacted hydrocarbons and intermediate nitriles |
US4883897A (en) * | 1986-12-19 | 1989-11-28 | Nitto Chemical Industry Co., Ltd. | Process for producing 2,6-dichlorobenzonitrile |
-
1947
- 1947-07-25 GB GB20153/47A patent/GB645754A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3497545A (en) * | 1966-03-10 | 1970-02-24 | Halcon International Inc | Preparation of polynitriles by ammoxidation of polyalkyl substituted aromatic hydrocarbons utilizing recycle of unreacted hydrocarbons and intermediate nitriles |
US4883897A (en) * | 1986-12-19 | 1989-11-28 | Nitto Chemical Industry Co., Ltd. | Process for producing 2,6-dichlorobenzonitrile |
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