http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1090041-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d2bb724dd58cbb2a73b244e79b0c9e42
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08L63-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G59-16
filingDate 1978-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07cbcbca5abcc744d2148ef88ef45011
publicationDate 1980-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1090041-A
titleOfInvention Radiation curable coating composition and method for preparation of the same
abstract ABSTRACT OF THE DISCLOSURE 3-Halo-2-hydroxypropyl acrylates nod methacrylates and 2-halo-1 (hydroxymethyl)ethyl acrylates and methacrylates are used as reactive solvent for an acrylic or (meth)acrylic terminated polyether resin in radiation curable coating compositions. Mixtures of the (meth)acrylic terminated polyether resin and 3-halo-2-hydroxypropyl (meth)acrylate and/or 2-halo-1-(hydroxymethyl)ethyl (meth)acrylate are usually prepared by adding diglycidyl either of bisphenol A to (meth)acrylic acid while the weight of 3-halo-2-hydroxypropyl (meth)acrylate and 2-halo-1-(hydroxymethyl)ethyl (meth)acrylate in the reaction mixture is at least about 5 percent by weight of the sum of the weights of the (meth)acrylic terminated polyether resin, the 3-halo-2hydroxypropyl (meth)acrylate and the 2-halo-1-(hydroxymethyl)ethyl (meth)acrylate present in the reaction mixture. In a preferred embodiment, both epihalohydrin and diglycidyl ether of bisphenol A are added to the (meth)acrylic acid. This application is directed to the preparation of the mixtures of the resin and reactive solvent.
priorityDate 1976-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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