Abstract: A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethylenic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups. Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

Abstract: A film-forming thermoset coating composition includes: (a) an aqueous medium; and Option 1 and/or Option 2 as follows: Option 1: (b1) polyurethane-acrylate core-shell particles including a polymeric acrylic core at least partially encapsulated by a polymeric shell including urethane linkages, where the polymeric shell includes an acid functional group and two or more hydrazide functional groups, where the polymeric shell is covalently bonded to at least a portion of the polymeric core; and (c1) (i) formaldehyde; (ii) polyformaldehyde; and/or (iii) a compound that generates formaldehyde; Option 2: (b2) polyurethane-acrylate core-shell particles including a polymeric acrylic core at least partially encapsulated by a polymeric shell including urethane linkages, where the polymeric shell includes an acid functional group and two or more N-methylolated hydrazide functional groups, where the polymeric shell is covalently bonded to at least a portion of the polymeric core.

Abstract: The present invention provides multilayer coated substrates, prepared using primer and/or sealer compositions comprising waterborne curable film-forming compositions, in turn comprising: a) an aqueous dispersion of a pigment and i) polymeric urethane-shell particles having a care-shell morphology and having hydroxyl functional groups, wherein the core is prepared from a monomer mixture comprising hydrophobic, ethylenically unsaturated monomers and the shell comprises a polyurethane or polyurethane-urea polymer; or ii) polymeric acrylic-shell particles having a core-shell morphology and having hydroxyl functional groups, wherein the core is prepared from a monomer mixture comprising hydrophobic, ethylenically unsaturated monomers and the shell is prepared from a monomer mixture comprising hydrophilic, ethylenically unsaturated monomers; b) a polyisocyanate crosslinking agent; and optionally c) a hydroxyl functional, water dispersible acrylic polymer.

Abstract: A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethyl enic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups, Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

Abstract: A coating composition includes: (a) an acid functional polyol polymer having an acid value of greater than 9 mg KOH/g and less than 60 mg KOH/g, and a hydroxyl value of from 100 to 300 mg KOH/g; (b) a non-aminoplast derived crosslinker reactive with the acid functional polyol polymer; and (c) a non-aqueous liquid medium. Further, an equivalent ratio of functional groups on the crosslinker reactive with hydroxyl functional groups to hydroxyl functional groups on the acid functional polyol polymer is within a range of from 0.5 to 1.5. The coating composition is substantially free of an external catalyst. The coating composition cures at a temperature of less than 80° C.

Abstract: A coating composition includes: (a) a phosphorus acid functional polyol polymer having an acid value within a range of greater than 7 mg KOH/g and 33 mg KOH/g or less, and a hydroxyl value within a range of from 60 to 200 mg KOH/g; (b) an aminoplast derived crosslinker reactive with the phosphorus acid functional polyol polymer; and (c) a non-aqueous liquid medium. Further, if an external catalyst is present, the coating composition comprises less than 0.25 weight % of the external catalyst based on the total weight of the coating composition. The coating composition cures at a temperature of 100° C. or less.

Abstract: A coating composition includes (a) a melamine resin having imino and methylol functional groups that together comprise 30 mole % or greater of the total functionality of the melamine resin; and (b) at least one polymer reactive with (a) that is obtained from components including polytetrahydrofuran and a carboxylic acid or anhydride thereof. The polytetrahydrofuran includes greater than 20 weight % of the components that form the polymer (b) and the carboxylic acid or anhydride thereof includes greater than 5 weight % of the components that form the polymer (b). The polymer (b) has an acid value of at least 15 based on the total resin solids of the polymer (b).

Abstract: A polyol polymer is obtained from reactants including: a) a non-aromatic epoxy functional compound that includes at least 30 weight % of the total solids weight of the reactants; and b) an aromatic mono-carboxylic acid functional compound, or anhydride thereof, that is substantially free of non-aromatic ethylenic unsaturation. The polyol polymer has ester linkages and hydroxyl functional groups. Further, if the reactants further include an aromatic polycarboxylic acid, the aromatic polycarboxylic acid makes up less than 15 weight % of the total solids weight of the reactants. A coating composition is also prepared with the polyol polymer.

Abstract: The present invention provides multilayer coated substrates, prepared using primer and/or sealer compositions comprising waterborne curable film-forming compositions, in turn comprising: a) an aqueous dispersion of a pigment and i) polymeric urethane-shell particles having a care-shell morphology and having hydroxyl functional groups, wherein the core is prepared from a monomer mixture comprising hydrophobic, ethylenically unsaturated monomers and the shell comprises a polyurethane or polyurethane-urea polymer; or ii) polymeric acrylic-shell particles having a core-shell morphology and having hydroxyl functional groups, wherein the core is prepared from a monomer mixture comprising hydrophobic, ethylenically unsaturated monomers and the shell is prepared from a monomer mixture comprising hydrophilic, ethylenically unsaturated monomers; b) a polyisocyanate crosslinking agent; and optionally c) a hydroxyl functional, water dispersible acrylic polymer.

Abstract: The present invention is directed to a method for forming a composite coating on a bare, untreated metal substrate comprising: (A) applying a first, waterborne coating composition directly to a surface of the bare substrate to form a first coating; and (B) applying a second, transparent coating composition to the first coating formed in step (A) to form a secondary coating thereon and yielding a composite coating; wherein the first coating composition comprises an aqueous dispersion of polymeric microparticles having a core-shell morphology and having reactive functional groups, wherein the core of the polymeric microparticles is prepared from a monomer mixture comprising substantially hydrophobic ethylenically unsaturated monomers and wherein the shell of the polymeric microparticles comprises a polyurethane polymer containing acid functional groups and/or a polyurethane-urea polymer containing acid functional groups. Coated metal substrates prepared by this method are also provided.

Abstract: The present invention is directed to a method for forming a composite coating on a substrate. The method comprises: (A) applying a first, waterborne coating composition to a surface of the substrate, the composition comprising: (a) a polymeric component containing acid functional groups and an additional, different functional group; (b) a curing agent having functional groups reactive with the additional functional groups on the polymeric component; and (c) microgel particles different from the curing agent, prepared from a diamine and an acid functional polyisocyanate, wherein the polyisocyanate contains an average of 0.75 acid functional groups per molecule and the wherein the polyisocyanate has at least three isocyanate functional groups, to form a substantially uncured first coating thereon; and (B) applying a second coating composition to the uncured first coating, to form a substantially uncured secondary coating thereon. Also provided are coated substrates prepared using the above method.

Abstract: The present invention provides a curable, organic polymeric photochromic composition comprising: a photochromic amount of at least one photochromic material; a polymeric polyol having carbonate groups along its backbone and having a number average molecular weight greater than 5000 g/mole; and a curing agent having reactive functional groups capable of reacting with hydroxyl groups on the polymeric polyol. After curing and after the Photochromic Performance Test the composition demonstrates a T1/2 fade rate of less than 200 seconds. Also provided is a photochromic article comprising a rigid substrate and a photochromic organic polymeric coating applied to a surface of the substrate. The photochromic organic polymeric coating comprises the composition described above.

Abstract: Described are non-aqueous dispersions of photosensitive polymeric microparticles, comprising: a) an organic continuous phase comprising an organic solvent; and b) photosensitive polymeric microparticles dispersed in the organic continuous phase. The microparticles comprise an at least partially polymerized component having integral surface and interior domains, wherein the surface domain comprises a polymeric material that is solubilized by the organic solvent, the interior domain comprises a polymeric material that is insoluble in the organic solvent, and the surface domain and/or interior domain is photosensitive. Also described are methods of producing such non-aqueous dispersions, curable film-forming compositions containing them, and photosensitive coated substrates.

Abstract: Described are various methods of producing non-aqueous dispersions of photosensitive polymeric microparticles, comprising: (a) preparing one or more aqueous dispersions of a polymerizable component, at least one of which contains a photosensitive material and, wherein the polymerizable components comprise at least one hydrophilic functional group and/or at least one hydrophobic functional group; (b) subjecting the dispersion of (a) to conditions sufficient to form microparticles; (c) at least partially polymerizing the polymerizable component; (d) combining the dispersion with an organic continuous phase comprising an organic solvent; (e) removing water from the dispersion such that the final water content of the non-aqueous dispersion is less than 30 percent by weight; wherein e) is performed before or after d); and (f) reacting any acid functional groups on the surface of the microparticles with a reactive material having at least one epoxy functional group, at least one thiocarbonylthio functional group, a

Abstract: The present invention is directed to curable film-forming compositions comprising: a) a curing agent; and b) a film-forming material comprising a fluoropolymer, a polymer having functional groups, and a plurality of particles comprising fillers and/or nanoscale particles having an average particle size ranging from 1 to less than 1000 nanometers prior to incorporation into the composition; wherein 20 to 30 percent by weight of the film-forming material of b) comprises the fluoropolymer. In certain embodiments, after application to a substrate as a coating and after curing, the cured composition demonstrates burnish resistance and an 85° gloss of less than 50. Multi-component composite coating compositions are also provided.

Abstract: The present invention is directed to a method for forming a composite coating on a substrate. The method comprises: (A) applying a first, waterborne coating composition to a surface of the substrate, the composition comprising: (a) a polymeric component containing acid functional groups and an additional, different functional group; (b) a curing agent having functional groups reactive with the additional functional groups on the polymeric component; and (c) microgel particles different from the curing agent, prepared from a diamine and an acid functional polyisocyanate, wherein the polyisocyanate contains an average of 0.75 acid functional groups per molecule and the wherein the polyisocyanate has at least three isocyanate functional groups, to form a substantially uncured first coating thereon; and (B) applying a second coating composition to the uncured first coating, to form a substantially uncured secondary coating thereon. Also provided are coated substrates prepared using the above method.

Abstract: The present invention provides a curable, organic polymeric photochromic composition comprising: a photochromic amount of at least one photochromic material; a polymeric polyol having carbonate groups along its backbone and having a number average molecular weight greater than 5000 g/mole; and a curing agent having reactive functional groups capable of reacting with hydroxyl groups on the polymeric polyol. After curing and after the Photochromic Performance Test the composition demonstrates a T1/2 fade rate of less than 200 seconds. Also provided is a photochromic article comprising a rigid substrate and a photochromic organic polymeric coating applied to a surface of the substrate. The photochromic organic polymeric coating comprises the composition described above.

Abstract: An aqueous dispersion comprising a reaction product of trimellitic anhydride and a polyol, wherein the molar ratio of trimellitic anhydride to polyol in the reaction product ranges from 1:2 to 1:4, and wherein the reaction product is further reacted with an anhydride to form another reaction product. A method of making a resin comprising the reaction product described above is also disclosed.

Abstract: Described are various methods of producing non-aqueous dispersions of photosensitive polymeric microparticles, comprising: (a) preparing one or more aqueous dispersions of a polymerizable component, at least one of which contains a photosensitive material and, wherein the polymerizable components comprise at least one hydrophilic functional group and/or at least one hydrophobic functional group; (b) subjecting the dispersion of (a) to conditions sufficient to form microparticles; (c) at least partially polymerizing the polymerizable component; (d) combining the dispersion with an organic continuous phase comprising an organic solvent; (e) removing water from the dispersion such that the final water content of the non-aqueous dispersion is less than 30 percent by weight; wherein e) is performed before or after d); and (f) reacting any acid functional groups on the surface of the microparticles with a reactive material having at least one epoxy functional group, at least one thiocarbonylthio functional group, a

Abstract: Described are non-aqueous dispersions of photosensitive polymeric microparticles, comprising: a) an organic continuous phase comprising an organic solvent; and b) photosensitive polymeric microparticles dispersed in the organic continuous phase. The microparticles comprise an at least partially polymerized component having integral surface and interior domains, wherein the surface domain comprises a polymeric material that is solubilized by the organic solvent, the interior domain comprises a polymeric material that is insoluble in the organic solvent, and the surface domain and/or interior domain is photosensitive. Also described are methods of producing such non-aqueous dispersions, curable film-forming compositions containing them, and photosensitive coated substrates.