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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c72d118f5664072de841f9c5c34b9d99
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1804
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-18
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
filingDate 2000-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0621bf6383920d189390d1721bf36e0f
publicationDate 2007-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1439183-B1
titleOfInvention Use of a composition comprising a salt of a mercaptosilane
abstract An improvement on existing methods to desulfurize oligosulfide silanes generates no added raw materials or waste streams in addition to the sodium chloride which is generated as a byproduct in the current manufacturing process for polysulfide silanes. this is accomplished by using mercaptosilane salts as desulfurizing agents, which yield more product in addition to that already obtained from the desulfurized silane of higher sulphur rank. The process simply entails reacting an oligosulfide silane with a mercaptosilane salt to thereby obtain an oligosulfide silane whose average sulphur rank is less than the starting oligosulfide silane. Coproduct sulphide salts can be recycled back to the oligosulfide manufacturing process. The mercaptosilane salts are novel materials as well.
priorityDate 2000-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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