http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-2345291-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c72d118f5664072de841f9c5c34b9d99 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G77-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G77-08 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G77-24 |
filingDate | 1999-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a9b9af6562d2d4a384a4f5d44c7c3fe5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_141635fde8efee7f4d2a5a596a82aac6 |
publicationDate | 2000-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-2345291-A |
titleOfInvention | Polymerization process for fluorosilicone polymers |
abstract | A process for making organosilyl end-stopped diorganopolysiloxane fluid is provided comprising the steps of reacting an organic end-stopping compound with a fluorosilicone trimer in the presence of a catalytic amount of linear phosphonitrillic acid, and inactivating the linear phosphonitrilic acid, thereby forming organosilyl end-stopped diorganopolysiloxane fluid. The fluoro-substituted cyclosiloxane is preferably 1,3,5-tris(3,3,3-trifluoropropyl)-1,3,5-trimethylcyclotrisiloxane. This is preferably reacted with hexamethyldisiloxane or trimethylchlorosilane with LPNC as a catalyst. |
priorityDate | 1998-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 85.