http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1130125-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_90bfbc2f04cecd74ee6cd031f847d2a6 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-20 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-20 |
filingDate | 1967-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf12d0a8b71c89b596ac597bba450d52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89e73624b90fd62131caf98cf85f7348 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e76c1cdf35f3b02c6fa2710061f73bb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b46198ca25077a4a02d0f0766af966c9 |
publicationDate | 1968-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-1130125-A |
titleOfInvention | Process for the production of organic sulphonates |
abstract | 1,130,125. Production of organic sulphonates. MARATHON OIL CO. 12 Jan., 1967 [14 Jan., 1966], No.1811/67. Heading C2C. A process for producing organic sulphonates comprises preaerating a hydrocarbon compound containing non-aromatic carbon to carbon unsaturation by intimately contacting said compound with a free-oxygen-containing gas until the reaction mixture has a titratable peroxide number of at least 10 inilliequivalents of titratable peroxide per kilogram of reaction mixture and thereafter reacting the resulting reaction mixture with a soluble, non-interfering bisulphite so as to produce an organic sulphonate. The preaeration and reaction with the bisulphite are preferably carried out at a temperature of 15-200‹ C. and a pressure of 0À1- 10,000 p.s.i.a., the reaction with the bisulphite being carried out in the presence of from 0À25- 10 volumes of inert organic solvent per volume of hydrocarbon compound. Hydrocarbon compounds preferred are acyclic olefins and bisulphites preferred are alkali metal and ammonium bisulphites. Air may be sparged into the reaction during bisulphite addition. Reaction of sodium bisulphite with pre-aerated α-olefins yields a sodium alkane sulphonate. |
priorityDate | 1966-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 27.