http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011173954-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_430d1c909e9d461a5b0f23e0a94f41c4
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F290-06
filingDate 2010-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c9ff1fdfb8af5bf64d8e4707e0b3b14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9f66fb2bc8a3fca33fcf5260c4866255
publicationDate 2011-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2011173954-A
titleOfInvention Method for producing aqueous urethane-modified (meth) acrylic resin dispersion
abstract [PROBLEMS] To produce a water-based urethane-modified (meth) acrylic resin dispersion capable of forming a coating film having good solvent resistance and water resistance, and having excellent alcohol shock resistance, durability against freeze-thaw cycles, and thermal stability. Offer. In a (meth) acrylic monomer (A) having no active hydrogen, it has two or more functional groups selected from polyisocyanate (a), hydroxyl group and amino group, and one or more acidic functional groups. Isocyanate-terminated urethane prepolymer having a polymerizable unsaturated group and an acidic functional group by reacting compound (b), polyol (c) having no acidic functional group, compound (d) having a glycidyl group and a polymerizable unsaturated group (B) is produced, neutralized acidic functional groups in the prepolymer (B), diluted with water and emulsified, and then the chain extension reaction of the prepolymer (B), the monomer (A) and the prepolymer (B ) Radical polymerization reaction of water-based urethane-modified (meth) acrylic resin dispersion. [Selection figure] None
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