http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-985497-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_70ec63d39d6704bacc5c7068c93ded43 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-78 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-78 |
| filingDate | 1962-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1965-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-985497-A |
| titleOfInvention | Process for stabilising ketonic compounds |
| abstract | Normally liquid aliphatic ketones are stabilized against changes in colour and/or odour by treatment with gaseous hydrogen at 70 DEG to 200 DEG F. and 40 to 250 p.s.i.g. in the presence of a hydrogenation catalyst, the duration of hydrogenation being such that no substantial conversion of the ketones occurs, and are stored either as the resulting mixture of ketone and catalyst or after separation of the catalyst. Any known hydrogenation catalyst may be used but preferred catalysts are the nickel catalysts, e.g. nickel-chromium and nickel-molybdenum alloys and, especially, Raney nickel. The preferred reaction time is 5 to 120 minutes. The hydrogenation may be performed batchwise, intermittently or continuously, in which case it is advantageous to employ a stationary catalyst bed and 50 to 100 p.s.i.g. for 5 to 40 minutes. Inert solvents may be used but it is generally preferred to effect the hydrogenation with the liquid ketone alone. In the examples, methylethyl ketone, diacetone alcohol and mesityl oxide are stabilized by hydrogenation in the presence of a Raney nickel catalyst. |
| priorityDate | 1961-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 22.