http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004503619-A
Outgoing Links
Predicate | Object |
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classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10T428-2891 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10T428-2852 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F8-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09J7-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09J4-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09J133-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F8-00 |
filingDate | 2001-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2004-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2004503619-A |
titleOfInvention | Method for producing crosslinkable contact adhesive acrylate material |
abstract | The present invention relates to a method for producing a cross-linked acrylic contact adhesive material, the method comprising firstly the following monomer: (d) the following structure: Embedded image Acrylic and methacrylic acid monomers with [where R 1 = H or CH 3 , and R 2 = alkyl chain having 2-20 C atoms] are used in an amount of 45-99.5 weight of the monomer mixture. % (E) 0.5 to 25% by weight of the monomer mixture of one or several carboxylic anhydrides containing olefinic double bonds, (f) further unsaturation containing functional groups A It is characterized in that polyacrylate is produced by free radical (co) polymerization using an olefinic monomer in a ratio of 0 to 30% by weight of the monomer mixture. By concentrating the polymer thus formed, a polyacrylate material having a solvent content of ≦ 2% by weight is obtained, wherein the polyacrylate material has at least two functional groups B and C (group B). Is a group capable of undergoing a polymerization-type reaction with a carboxylic anhydride, and the group C is a crosslinkable group). By causing a reaction between the functional group B and the carboxylic anhydride, the monomer containing the functional group B is bonded to the polymer in a side chain form. After the reaction between the functional group B and the carboxylic anhydride has occurred, the polymer is crosslinked using radiation having energy. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9802294-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013147569-A1 |
priorityDate | 2000-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 73.