Patent classifications
C08F20/54
(Meth)acrylamide polymers for contact lens and intraocular lens
An contact lens or intraocular lens (IOL) with very high water content polymers that have increased hydrolytic stability to withstand high temperatures such as autoclave temperatures, 123 C or even higher temperatures while in an aqueous environment comprising at least one polymer comprising one or more monomeric subunits comprising a polymerized acrylamide or methacrylamide group, at least one side group comprising an aliphatic carbon moiety substituted by at least one hydroxyl moiety, wherein the one or more monomeric subunits comprising a polymerized acrylamide or methacrylamide group, at least one side group comprising an aliphatic carbon moiety substituted by at least one hydroxyl moiety, comprise at least 50 wt. % of the polymer.
(Meth)acrylamide polymers for contact lens and intraocular lens
An contact lens or intraocular lens (IOL) with very high water content polymers that have increased hydrolytic stability to withstand high temperatures such as autoclave temperatures, 123 C or even higher temperatures while in an aqueous environment comprising at least one polymer comprising one or more monomeric subunits comprising a polymerized acrylamide or methacrylamide group, at least one side group comprising an aliphatic carbon moiety substituted by at least one hydroxyl moiety, wherein the one or more monomeric subunits comprising a polymerized acrylamide or methacrylamide group, at least one side group comprising an aliphatic carbon moiety substituted by at least one hydroxyl moiety, comprise at least 50 wt. % of the polymer.
Free-radical polymerization methods and articles thereby
A method of curing a curable composition includes contacting the free-radically curable composition with the solid primer layer thereby causing at least partial curing of the curable composition. The solid primer layer includes a binder material, optional beta-dicarbonyl compound, and an organic peroxide. The curable composition includes at least one free-radically polymerizable compound, a polyvalent metal compound, and a quaternary ammonium halide. The method can be used for adhesive bonding of substrates and preparation of various articles.
Free-radical polymerization methods and articles thereby
A method of curing a curable composition includes contacting the free-radically curable composition with the solid primer layer thereby causing at least partial curing of the curable composition. The solid primer layer includes a binder material, optional beta-dicarbonyl compound, and an organic peroxide. The curable composition includes at least one free-radically polymerizable compound, a polyvalent metal compound, and a quaternary ammonium halide. The method can be used for adhesive bonding of substrates and preparation of various articles.
Free-radical polymerization methods and articles thereby
A method of curing a curable composition includes contacting the free-radically curable composition with the solid primer layer thereby causing at least partial curing of the curable composition. The solid primer layer includes a binder material, optional beta-dicarbonyl compound, and an organic peroxide. The curable composition includes at least one free-radically polymerizable compound, a polyvalent metal compound, and a quaternary ammonium halide. The method can be used for adhesive bonding of substrates and preparation of various articles.
End-functionalized polymers
This invention relates to end-functionalized living polymers or copolymers having a structure represented by the general formula 1 or 2, wherein R.sub.1 is a hydrogen atom, a methyl group, or a radically non-polymerizable organic group containing 1 to 20 carbon atoms. R.sub.2 is a functional end group of a vinyl hetero monomer selected from the group consisting of hydroxy, epoxy, silyl, NH.sub.2, NH(C.sub.1-C.sub.6alkyl), N(C.sub.1-C.sub.6alkyl).sub.2, CHCH.sub.2, CCH, C(CH.sub.3)CH.sub.2, OCHCH.sub.2, (OCH.sub.2CH.sub.2).sub.1-10OH, OR.sub.20, COOR.sub.20, CONHR.sub.20, OCONHR.sub.20, OCOR.sub.20 and NHCOR.sub.20, wherein R.sub.20 is linear or branched C.sub.1-C.sub.20 alkyl or linear or branched C.sub.1-C.sub.20 alkyl substituted with hydroxy, epoxy, silyl, NH.sub.2 or N(C.sub.1-C.sub.6alkyl).sub.2; or R.sub.20 is phenyl, benzyl, CHCH.sub.2, CCH or C(CH.sub.3)CH.sub.2, or R.sub.2 is a residue of an acrylic acid (CH.sub.2CHCOO*), methacrylic acid, (CH.sub.2C(CH.sub.3)COO*) or CH(CH.sub.3)CHCOO* or R.sub.2 is a residue of a dicarboxylic acid HOOCR.sub.cCOO* or C.sub.1-C.sub.6alkyl-OOCR.sub.cCOO* wherein R.sub.c is C.sub.1-C.sub.20 alkylene, C.sub.1-C.sub.20alkenylene or phenylene; or R.sub.2 is a residue derived from the reaction of an isocyanate R.sub.aNCO with the hydroxy group or with the amine group of the vinyl hetero monomer, said residue being R.sub.aNHCOO* or R.sub.aNHCONH* wherein R.sub.a is unsubstituted C.sub.1-C.sub.20alkyl, C.sub.1-C.sub.20cycloalkyl or C.sub.1-C.sub.20alkyl substituted with hydroxy, epoxy, silyl, NH.sub.2, NH(C.sub.1-C.sub.6alkyl) or N(C.sub.1-C.sub.6alkyl).sub.2; or R.sub.2 is a residue derived from the reaction of a diisocyanate residue OCNR.sub.bNCO with the hydroxy group or with the amine group of the vinyl hetero monomer, said residue being *OOCNHR.sub.bNCO or *HNOCNHR.sub.bNCO or *OOCNHR.sub.bNHCOR.sub.30 wherein R.sub.b is C.sub.1-C.sub.20 alkylene or C.sub.1-C.sub.20cycloalkylene or phenylene and R.sub.30 is a residue of hydroxyethylacrylate (CH.sub.2CHCOO(CH.sub.2).sub.2O*), hydroxyethylmethacrylate (CH.sub.2C(CH.sub.3)COO(CH.sub.2).sub.2O*), hydroxybutylacrylate (CH.sub.2CHCOO(CH.sub.2).sub.4O*) or hydroxybutylmethacrylate (CH.sub.2C(CH.sub.3)COO(CH.sub.2).sub.4O*), A is the hetero atom of the vinyl hetero monomer selected from the group consisting of oxygen, nitrogen, sulfur and silicon; and if R.sub.2 is silyl and M is a direct bond, A is a direct bond; M is a bond or a divalent group linking the heteroatom of the vinyl hetero monomer and the functional end group of the vinyl hetero monomer said M being selected from the group consisting of C.sub.1-50 alkylene, C.sub.1-50 (hetero)alkylene, arylene and heteroarylen
THERMOREVERSIBLE POLYMERS AND METHODS OF USE THEREOF
The present disclosure provides thermoreversible polymers, hydrogel compositions comprising the thermoreversible polymers, as well as methods of making and using the thermoreversible polymers.
CURABLE RESIN COMPOSITION, COMPOSITION FOR MOLDING, RESIN MOLDED ARTICLE, AND METHOD FOR PRODUCING RESIN MOLDED ARTICLE
Disclosed is a curable resin composition that includes radical polymerizable monomers including a monofunctional radical polymerizable monomer, a linear or branched polymer containing a polyoxyalkylene chain, and a radical polymerization initiator.
CURABLE RESIN COMPOSITION, COMPOSITION FOR MOLDING, RESIN MOLDED ARTICLE, AND METHOD FOR PRODUCING RESIN MOLDED ARTICLE
Disclosed is a curable resin composition that includes radical polymerizable monomers including a monofunctional radical polymerizable monomer, a linear or branched polymer containing a polyoxyalkylene chain, and a radical polymerization initiator.
MATERIALS AND DEVICES
A reversible cycle phase change liquid comprises a polar working fluid, nanoparticles of a material having a density greater than 3000 kg/m.sup.3, and a controllable gel. The gel is switchable between hydrophilic and hydrophobic phases by application of a phase change driver. The gel coats the nanoparticles to a first thickness when the gel is in the hydrophilic phase and is swollen by the polar working fluid, and coats the nanoparticles to a reduced thickness when in the hydrophobic phase. The coated nanoparticles form clusters, or comprise individual unclustered nanoparticles, when the gel is in the hydrophilic phase, and form larger clusters when the gel is in the hydrophobic phase. In embodiments aggregation of the nanoparticles into clusters is self-limiting because of electrical charges on the nanoparticles, such that when the gel is in the hydrophobic phase the clusters remain soluble within the liquid.