Coating composition, process for producing antireflective coatings, and coated articles

Claim 2

A process for preparing an antireflective coating on a solid substrate comprising: (a) applying to a surface of said substrate a coating composition comprising the composition obtaines by mixing (1) the acid catalyzed hydrolysis and condensation products of a water-silane monomer mixture, and (2) a film-forming amount of an organic polymer having functional groups selected from the group consisting of amino, hydroxy and carboxy, hydroxy and amino, amino and carboxy, and amino, hydroxy and carboxy, said polymer being compatible with said silane monomer and the acid catalyzed hydrolysis and condensation products of said silane monomer, said coating composition being substantially free of preformed metal oxide sol and water-soluble metal salt; (b) curing the applied coating composition; and (c) treating said cured coating with an aqueous inorganic electrolyte solution for a time sufficient to produce a coating having a graded porosity.

Claim 3

The process of claim 1 wherein said aqueous electrolyte solution is an aqueous solution of hydrogen chloride, tetra(C 1 -C 12 )alkyl ammonium salt, tetra (C 1 -C 12 )alkyl ammonium hydroxide, metal salts, metal hydroxide, hydrates of said salts, hydrates of said hydroxides, or mixtures thereof, said solution having a pH from about 4 to about 11.

Claim 4

The process of claim 2 wherein said salt of the aqueous electrolyte solution of tetra(C 1 -C 12 )alkyl ammonium salt or metal salts is selected from the group consisting of carbonate, carboxylate, sulfonate, sulfate, nitrate, perchlorate, phosphate, halide, and mixtures of such salts, and wherein said aqueous electrolyte solution has a pH from about 7 to about 9.

Claim 5

The process of claim 3 wherein said metal of the metal salts is an alkaline earth or alkali metal.

Claim 6

The process of claim 1 further comprising the steps of contacting said treated cured coating with an aqueous rinsing solution for a time sufficient to remove from the surface of the coating residual products resulting from step (c), and drying the coating.

Claim 7

The process of claim 1 wherein the coating composition is cured by heating it at temperatures of between about 80° C. and temperatures above which the substrate is damaged due to such heating.

Claim 8

The process of claim 6 wherein the curing temperature is between about 80° C. and about 130° C.

Claim 9

The process of claim 1 wherein the aqueous electrolyte solution is at a temperature from about 20° C. to about its boiling temperature.

Claim 10

The process of claim 8 wherein the temperature is from about 20° C. to about 103° C.

Claim 11

The process of claim 4 wherein the metal salt is magnesium carbonate.

Claim 12

The process of claim 2 wherein the concentration of the electrolyte varies from about 0.0001 to 1.0 weight percent.

Claim 13

The process of claim 1 wherein said organic polymer is prepared from functional group-containing monomers selected from the group consisting of hydroxy (C 2 -C 4 ) alkyl acrylates, hydroxy (C 2 -C 4 )alkyl methacrylates, acrylic acid, methacrylic acid, carboxy (C 1 -C 4 ) alkyl acrylates, carboxy (C 1 -C 4 ) alkyl methacrylates, amino substituted phenyl acrylates, amino substituted phenyl methacrylates, amino substituted phenyl(C 1 -C 9 )alkyl acrylates, amino substituted phenyl(C 1 -C 9 )alkyl methacrylates, amino substituted phenoxy acrylates, amino substituted phenoxy methacrylates, amino substituted phenoxy(C 1 -C 9 )alkyl acrylates, amino substituted phenoxy(C 1 -C 9 )alkyl methacrylates, amino(C 1 -C 9 )alkyl acrylates, amino(C 1 -C 9 )alkyl methacrylates, vinylamines, mixtures of said monomers, and mixtures of said monomers with other monomers substantially free of hydroxy, carboxy or amino functional groups.

Claim 14

The process of claim 12 wherein said monomer is selected from the group consisting of hydroxy (C 2 -C 4 )alkyl methacrylates, acrylic acid, methacrylic acid, carboxy (C 1 -C 4 )alkyl acrylate, amino(C 1 -C 9 )alkyl acrylates, amino (C 1 -C 9 )alkyl methacrylates and mixtures of said monomers.

Claim 15

The process of claim 12 wherein said monomer is selected from the group consisting of hydroxy(C 2 -C 4 )alkyl methacrylates, acrylic acid, amino(C 1 -C 9 )alkyl methacrylates, mixtures of said monomers, and mixtures of said monomers with methyl methacrylate.

Claim 16

The process of claim 1 wherein at least one silane monomer is used to form the water-silane monomer mixture, said silane being representable by the following general formula: R.sup.1.sub.m (R.sup.2).sub.n SiX.sub.4-(m+n) wherein R 1 is C 1 -C 20 alkyl, C 1 -C 20 haloalkyl, C 2 -C 20 alkenyl, C 2 -C 20 haloalkenyl, phenyl, phenyl(C 1 -C 20 )alkyl, C 1 -C 20 alkylphenyl, phenyl(C 2 -C 20 )alkenyl, C 2 -C 20 alkenylphenyl, glycidoxy(C 1 -C 20 )alkyl, epoxycyclohexyl(C 1 -C 20 )alkyl, morpholino, amino(C 1 -C 20 )alkyl, amino(C 2 -C 20 )alkenyl, mercapto(C 1 -C 20 )alkyl, mercapto(C 2 -C 20 )alkenyl, cyano(C 1 -C 20 )alkyl, cyano(C 2 -C 20 )alkenyl, acryloxy, methacryloxy or halogen, R 2 is C 1 -C 20 alkylene, C 2 -C 20 alkenylene, phenylene, C 1 -C 20 alkylenephenylene, amino(C 1 -C 20 )alkylene or amino(C 2 -C 20 ) alkenylene, X is hydrogen, halogen, hydroxy, C 1 -C 5 alkoxy, C 1 -C 5 alkoxy(C 1 -C 5 )alkoxy, C 1 -C 4 acyloxy, phenoxy, C 1 -C 3 alkylphenoxy or C 1 -C 3 alkoxyphenoxy, the halo or halogen of R 1 or X being bromo, chloro or fluoro, m and n are each an integer of from 0 to 2, and the sum of m and n is an integer of from 0 to 3.

Claim 17

The process of claim 15 wherein: (a) R 1 is a C 1 -C 10 alkyl, C 1 -C 10 haloalkyl, C 2 -C 10 alkenyl, phenyl, phenyl(C 1 -C 10 )alkyl, C 1 -C 10 alkylphenyl, glycidoxy(C 1 -C 10 ) alkyl, epoxycyclohexyl(C 1 -C 10 )alkyl, morpholino, amino(C 1 -C 10 )aklyl, amino(C 2 -C 10 )alkenyl, mercapto(C 1 -C 10 )alkyl, mercapto(C 2 -C 10 )alkenyl, cyano(C 1 -C 10 )alkyl, cyano(C 2 -C 10 )alkenyl or halogen, R 2 is a C 1 -C 10 alkylene or C 2 -C 10 alkenylene group, phenylene, C 1 -C 10 alkylenephenylene, amino(C 1 -C 10 )alkylene, amino(C 2 -C 10 )alkenylene, X is hydrogen, halogen, hydroxy, C 1 -C 3 alkoxy, C 1 -C 3 alkoxy(C 1 -C 3 )alkoxy, 1 -C 2 acyloxy, phenoxy, C 1 -C 2 alkylphenoxy or C 1 -C 2 alkoxyphenoxy, the halo or halogen of R 1 or X being chloro or fluoro; and (b) a catalytic amount of a water-soluble acid selected from the group consisting of acetic, formic, glutaric, maleic, nitric, sulfuric and hydrochloric acids is present in the water-silane monomer mixture.

Claim 18

The process of claim 12 wherein at least one silane monomer is used to form the water-silane monomer mixture, said silane being representable by the following general formula: R.sup.1.sub.m (R.sup.2).sub.n SiX.sub.4-(m+n) wherein R 1 is C 1 -C 20 alkyl, C 1 -C 20 haloalkyl, C 2 -C 20 alkenyl, C 2 -C 20 haloalkenyl, phenyl, phenyl(C 1 -C 20 )alkyl, C 1 -C 20 alkylphenyl, phenyl(C 2 -C 20 )alkenyl, C 2 -C 20 alkenylphenyl, glycidoxy (C 1 -C 20 )alkyl, epoxycyclohexyl(C 1 -C 20 )alkyl, morpholino, amino(C 1 -C 20 )alkyl, amino(C 2 -C 20 )alkenyl, mercapto(C 1 -C 20 )alkyl, mercapto(C 2 -C 20 )alkenyl, cyano(C 1 -C 20 )alkyl, cyano(C 2 -C 20 )alkenyl, acryloxy, methacryloxy or halogen, R 2 is C 1 -C 20 alkylene, C 2 -C 20 alkenylene, phenylene, C 1 -C 20 alkylenephenylene, amino(C 1 -C 20 )alkylene or amino(C 2 -C 20 ) alkenylene, X is hydrogen, halogen, hydroxy, C 1 -C 5 alkoxy, C 1 -C 5 alkoxy(C 1 -C 5 )alkoxy, C 1 -C 4 acyloxy, phenoxy, C 1 -C 3 alkylphenoxy or C 1 -C 3 alkoxyphenoxy, the halo or halogen of R 1 or X being bromo, chloro or fluoro, m and n are each an integer of from 0 to 2, and the sum of m and n is an integer of from 0 to 3.

Claim 19

The process of claim 17 wherein the aqueous electrolyte solution is at a temperature from about 20° C. to about its boiling temperature and the aqueous electrolyte solution is an aqueous solution of hydrogen chloride, tetra(C 1 -C 12 )alkyl ammonium salt, tetra (C 1 -C 12 )alkyl ammonium hydroxide, metal salts, metal hydroxide, hydrates of said salts, hydrates of said hydroxides, or mixtures thereof, said solution having a pH from about 4 to about 11.

Claim 20

The process of claim 13 wherein: (a) R 1 is a C 1 -C 10 alkyl; C 1 -C 10 haloalkyl, C 2 -C 10 alkenyl, phenyl, phenyl(C 1 -C 10 )alkyl, C 1 -C 10 alkylphenyl, glycidoxy(C 1 -C 10 ) alkyl, epoxycyclohexyl(C 1 -C 10 )alkyl, morpholino, amino(C 1 -C 10 )alkyl, amino(C 2 -C 10 )alkenyl, mercapto(C 1 -C 10 )alkyl, mercapto(C 2 -C 10 )alkenyl, cyano(C 1 -C 10 )alkyl, cyano(C 2 -C 10 )alkenyl or halogen, R 2 is a C 1 -C 10 alkylene or C 2 -C 10 alkenylene group, phenylene, C 1 -C 10 alkylenephenylene, amino(C 1 -C 10 )alkylene, amino(C 2 -C 10 )alkenylene, X is hydrogen, halogen, hydroxy, C 1 -C 3 alkoxy, C 1 -C 3 alkoxy(C 1 -C 3 )alkoxy, C 1 -C 2 acyloxy, phenoxy, C 1 -C 2 alkylphenoxy, or C 1 -C 2 alkoxyphenoxy, the halo or halogen of R 1 or X being chloro or fluoro; and (b) a catalytic amount of a water-soluble acid selected from the group consisting of acetic, formic, glutaric, maleic, nitric, sulfuric and hydrochloric acids is present in the water-silane monomer mixture.

Claim 21

The process of claim 19 wherein said salt of the aqueous electrolyte solution of tetra(C 1 -C 12 )alkyl ammonium salt or metal salts is selected from the group consisting of carbonated carboxylate, sulfonate, sulfate, nitrate, perchlorate, phosphate, halide and mixtures of such salts, and wherein said aqueous electrolyte solution has a pH from about 7 to about 9.

Claim 22

The process of claim 20 wherein said metal of the metal salts is an alkaline earth or alkali metal.

Claim 23

The process of claim 21 wherein the metal salt is magnesium carbonate.

Claim 24

The process of claim 20 wherein the aqueous electrolyte solution is at a temperature of from about 20° C. to about its boiling temperature.

Claim 25

The process of claim 23 wherein the concentration of the electrolyte varies from about 0.0001 to about 1.0 weight percent.

Claim 26

An article comprising, in combination, a substrate and on at least one surface thereof an antireflective coating prepared by the process of claim 1.

Claim 27

The article of claim 25 wherein said substrate is selected from the group consisting of glass, ceramics, metals and solid organic polymeric materials.

Claim 28

The article of claim 26 wherein said solid organic polymeric material is selected from the group consisting of polyacrylates, polymethacrylates, poly(C 1 -C 12 )alkyl methacrylates, polyoxy(alkylene methacrylates), poly (alkoxylated phenol methacrylates), cellulose acetate, cellulose triacetate, cellulose acetate propionate, cellulose acetate butyrate, poly(vinyl acetate), poly(vinyl alcohol), poly(vinyl chloride), poly(vinylidene chloride), thermoplastic polycarbonates, polyesters, polyurethanes, poly(ethylene terephthalate), polystyrene, poly(alpha methylstyrene), copoly(styrene-methylmethacrylate), copoly(styrene-acrylonitrile), polyvinylbutyral and polymers of members of the group consisting of polyol(allyl carbonate) monomers, polyfunctional acrylate monomers, polyfunctional methacrylate monomers, diethylene glycol dimethacrylate monomers, diisopropenyl benzene monomers, alkoxylated polyhydric alcohol monomers and diallylidene pentaerythritol monomers.

Claim 29

The article of claim 27 wherein said solid organic polymeric material is a homopolymer or copolymer of a monomers selected from the group consisting of acrylates, methacrylates, methyl methacrylate, ethylene glycol bis methacrylate, ethoxylated bisphenol A dimethacrylate, vinyl acetate, vinylbutyral, urethane, diethylene glycol bis(allyl carbonate), diethylene glycol dimethacrylate, diisopropenyl benzene, and ethoxylated trimethylol propane triacrylate.

Claim 30

An article comprising, in combination, a substrate and on at least one surface thereof an artireflective coating prepared by the process of claim 18.

Claim 31

The article of claim 29 wherein said substrate is selected from the group consisting of glass, ceramics, metals and solid organic polymeric materials.

Claim 32

The article of claim 30 wherein said solid organic polymeric material is a homopolymer or copolymer of a monomer selected from the group consisting of acrylates, methacrylates, methyl methacrylate, ethylene glycol bis methacrylate, ethoxylated bisphenol A dimethacrylate, vinyl acetate, vinylbutyral, urethane, diethylene glycol bis(allyl carbonate), diethylene glycol dimethacrylate, diisopropenyl benzene, and ethoxylated trimethylol propane triacrylate.

Claim 33

An article comprising, in combination, a substrate and on at least one surface thereof an antireflective coating prepared by the process of claim 20.

Claim 34

The article of claim 32 wherein said substrate is selected from the group consisting of glass, ceramics, metals and solid organic polymeric materials.

Claim 35

The article of claim 33 wherein said solid organic polymeric material is a homopolymer or copolymer of a monomer selected from the group consisting of acrylates, methacrylates, methyl methacrylate, ethylene glycol bis methacrylate, ethoxylated bisphenol A dimethacrylate, vinyl acetate, vinylbutyral, urethane, diethylene glycol bis(allyl carbonate), diethylene glycol dimethacrylate, diisopropenyl benzene, and ethoxylated trimethylol propane triacrylate.

Claim 36

A process for preparing an antireflective coating on a solid organic polymeric substrate comprising: (a) applying to a surface of said substrate a coating composition comprising the composition obtained by mixing (1) the acid catalyzed hydrolysis and condensation products of a water-silane monomer mixture, said silane monomer being selected from the group consisting of glycidoxy(C 1 -C 10 )alkyl tri(C 1 -C 5 )alkoxy silane, C 1 -C 10 alkyl tri(C 1 -C 5 )alkoxy silane, tetramethylorthosilicate, tetraethylorthosilicate and mixtures of said silane monomers, and (2) a film forming amount of an organic polymer having functional groups selected from the group consisting of amino, hydroxy and carboxy, hydroxy and amino, amino and carboxy, and amino, hydroxy and carboxy, said organic polymer being prepared from functional group-containing monomers selected from the group consisting of hydroxy (C 2 -C 4 )alkyl methacrylates, acrylic acid, methacrylic acid, carboxy(C 1 -C 4 )alkyl acrylate, amino (C 1 -C 9 )alkyl acrylates, amino(C 1 -C 9 )alkyl methacrylates and mixtures of said monomers, said polymers being compatible with said silane monomer and the acid catalyzed hydrolysis and condensation products of said silane monomer, said coating composition being substantially free of preformed metal oxide sol and water-soluble metal salt; (b) curing the applied coating composition; and (c) treating said cured coating with an aqueous inorganic electrolyte solution for a time sufficient to produce a coating having a graded porosity, said inorganic electrolyte being selected from hydrogen chloride, tetra(C 1 -C 12 )alkyl ammonium salt, tetra (C 1 -C 12 )alkyl ammonium hydroxide, metal salts, metal hydroxide, hydrates of said salts, hydrates of said hydroxides, or mixtures thereof, said solution having a pH from about 4 to about 11 and a temperature of from about 20° C. to about 103° C.

Claim 37

A process for preparing an antireflective coating on a solid organic polymeric substrate comprising: (a) applying to a surface of said substrate a coating composition comprising the composition obtained by mixing (1) the acid catalyzed hydrolysis and condensation products of a water-silane monomer mixture, said silane monomer being selected from the group consisting of glycidoxy(C 1 -C 10 )alkyl tri(C 1 -C 5 )alkoxy silane, C 1 -C 10 alkyl tri(C 1 -C 5 )alkoxy silane, tetramethylorthosilicate, tetraethylorthosilicate and mixtures of said silane monomers, and (2) a film forming amount of an organic polymer having functional groups selected from the group consisting of amino, hydroxy and carboxy, hydroxy and amino, amino and carboxy, and amino, hydroxy and carboxy, said organic polymer being prepared from functional group-containing monomers selected from the group consisting of hydroxy (C 2 -C 4 )alkyl methacrylates, acrylic acid, methacrylic acid, carboxy(C 1 -C 4 )alkyl acrylate, amino (C 1 -C 9 )alkyl acrylates, amino(C 1 -C 9 )alkyl methacrylates and mixtures of said monomers, said polymers being compatible with said silane monomer and the acid catalyzed hydrolysis and condensation products of said silane monomer, said coating composition being substantially free of preformed metal oxide sol and water-soluble metal salt; (b) curing the applied coating composition; and (c) treating said cured coating with an aqueous inorganic electrolyte solution for a time sufficient to produce a coating having a graded porosity, said inorganic electrolyte being selected from hydrogen chloride, tetra(C 1 -C 12 )alkyl ammonium salt, tetra (C 1 -C 12 )alkyl ammonium hydroxide, metal salts, metal hydroxide, hydrates of said salts, hydrates of said hydroxides, or mixtures thereof, said solution having a pH from about 4 to about 11 and a temperature of from about 20° C. to about 103° C.

Claim 38

An article comprising, in combination, an organic polymeric substrate and on at least one surface thereof an antireflective coating prepared by the process of claim 35.

Claim 39

The article of claim 36 wherein the organic polymeric substrate is a homopolymer or copolymer of a monomer selected from the group consisting of acrylates, methacrylates, methyl methacrylate, ethylene glycol bis methacrylate, ethoxylated bisphenol A dimethacrylate, vinyl acetate, vinylbutyral, urethane, diethylene glycol bis(allyl carbonate), diethylene glycol dimethacrylate, diisopropenyl benzene, and ethoxylated trimethylol propane triacrylate.