http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2008146738-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S165-051 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F2400-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F2410-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S165-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/F28D2021-0022 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F2-01 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F2-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F2-38 |
| filingDate | 2007-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2010-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2008146738-A |
| titleOfInvention | METHOD FOR FREE RADICAL POLYMERIZATION OR SEWING IN THE PRESENCE OF A CHOSEN ORGANIC PEROXIDE OBTAINED BY EX SITU METHOD |
| abstract | 1. The method of free radical polymerization or crosslinking, in which at least one polymerizable monomer or at least one crosslinkable compound is reacted in the presence of at least one organic peroxide selected from the group consisting of di (n-propyl ) peroxydicarbonate, di (sec-butyl) peroxydicarbonate, di (2-ethylhexyl) peroxydicarbonate, 1,1-dimethyl-3-hydroxybutyl peroxyneodecanoate, α-cumyl peroxyneodecanoate, α-cumyl peroxyneoheptanoate, tert-amyl peroxine butane decanoate, ta-amyl peroxypivalate, tert-butyl peroxypivalate, 2,5-dimethyl-2,5-di (2-ethylhexanoylperoxy) hexane, tert-amylperoxy-2-ethylhexanoate, tert-butylperoxy-2-ethylhexanoate, tert-amylperoxyacetate, tert- butyl peroxyacetate, tert-amyl perbenzoate, tert-butyl perbenzoate, OO-tert-amyl-O- (2-ethylhexyl) monoperoxycarbonate, OO-tert-butyl-O-isopropyl monoperoxycarbonate, OO-tert-butyl-1- (2-ethylophexyl) poly (tert-butyl peroxycarbonate) polyester, decanoyl peroxide, lauroyl peroxide, succinic acid peroxide, benzo peroxide la, 1,1-di (tert-butylperoxy) -3,3,5-trimethylcyclohexane, 1,1-di (tert-butylperoxy) cyclohexane, 1,1-di (tert-amylperoxy) cyclohexane, n-butyl-4 , 4-di (tert-butyl peroxy) valerate, ethyl 3,3-di (tert-amyl peroxy) butyrate, tert-butyl peroctoate, ethyl 3,3-di (tert-butyl peroxy) butyrate, cumene hydroperoxide and tert-butyl hydroperoxide , as well as mixtures thereof, characterized in that the organic peroxide is produced continuously by the ex situ method using a closed plate heat exchanger. ! 2. The method according to claim 1, characterized in that the organic peroxide is obtained at |
| priorityDate | 2006-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 89.