Aqueous coating agent and article using same
US-2016369106-A1 · Dec 22, 2016 · US
US2016145444A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016145444-A1 |
| Application number | US-201615012905-A |
| Country | US |
| Kind code | A1 |
| Filing date | Feb 2, 2016 |
| Priority date | Aug 6, 2013 |
| Publication date | May 26, 2016 |
| Grant date | — |
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This invention provided an aqueous coating composition for metal surface pre-treatment comprising: (i) at least one organosilane with at least one hydrolyzable substituent; (ii) at least one water soluble and/or water dispersible silane-functional oligomer; (iii) at least one water-soluble compound of the elements Zr and/or Ti; The resultant sol-gel coating composition reveals an extended shelf life and after surface pre-treatment using the invented coating compositions the metal substrates have higher resistance to corrosion, humidity and solvent and at the same time have better surface conductivity and paintability.
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1 . An aqueous coating composition for metal surface pre-treatment having a pH in a range of from 3 to 6, comprising: (i) at least one organosilane with at least one hydrolyzable substituent; (ii) at least one water soluble and/or water dispersible silane-functional oligomer; (iii) at least one water-soluble compound of elements Zr and/or Ti. 2 . The coating composition according to claim 1 , wherein the organosilane is selected from a compound according to Formula (I): wherein n is an integer from 1 to 3; residue R is selected from C1 to C6 alkyl groups; residue Y is selected from alkyl groups having not more than 10 carbon atoms carrying at least one epoxy, amino, hydroxyl, vinyl and/or thiol group wherein the residues Y are selected mutually independently from each other. 3 . The coating composition according to claim 1 , wherein the organosilane has a weight-average molecular weight of less than 400 g/mol. 4 . The coating composition according to claim 1 , wherein the organosilane is selected from vinyltriacetoxysilane, vinyltrialkoxysilanes, aminoethyltrialkoxysilanes, aminopropylalkoxysilanes, bis-trialkoxysilypropylamines, aminoethylaminopropyltrialkoxysilanes, aminoethylaminopropyltrialkoxysilanes, mercaptopropyltrialkoxysilanes, bis-trialkoxysilylpropyl-tetrasulfides, 3-glycidoxypropyltrialkoxysilanes, and mixtures thereof, wherein any alkoxy groups present have not more than 3 carbon atoms. 5 . The coating composition according to claim 1 , wherein the coating composition further comprises a silane according to Formula (II): wherein R′ is selected from C1 to C6 alkyl groups. 6 . The coating composition according claim 1 , wherein the silane-functional oligomer (ii) has a weight-average molecular weight from 400 g/mol to 10,000 g/mol. 7 . The coating composition according to claim 1 , wherein the silane-functional oligomer (ii) includes at least one of a polyurethane, polyacrylate, polyester and/or polyether backbone. 8 . The coating composition according to claim 7 , wherein the silane-functional oligomer (ii) includes a polyurethane backbone and is a reaction product of at least one diisocyanate, at least one hydroxyl-functional tertiary amine, at least one amino-functional organosilane and at least one polyol. 9 . The coating composition according to claim 7 , wherein the silane-functional oligomer (ii) includes a polyacrylate backbone and is a reaction product of at least one (meth)acrylate, at least one vinyl-functional silane, and at least one tertiary amine acrylate. 10 . The coating composition according to claim 7 , wherein the silane-functional oligomer (ii) includes a polyether backbone and is a reaction product of at least one epoxy resin, at least one amino-functional organosilane, and at least one multifunctional organic compound having at least two functional groups selected from hydroxyl and/or amino groups. 11 . The coating composition according to claim 1 , wherein the said water-soluble compound (iii) is one or more selected from hexafluorotitanic acid, hexafluorozirconic acid, zirconium aceto acetate, zirconium acetate and ammonium zirconium carbonate. 12 . The coating composition according to claim 1 , wherein a molar ratio of element Si to a sum of the elements Zr and/or Ti is from 10 to 500. 13 . The coating composition according to claim 1 , wherein the amount of the water-soluble compound (iii) of the elements Zr and/or Ti in the overall composition is from 0.1 wt.-% to 5 wt.-%, with respect to the elements Zr and Ti. 14 . The coating composition according to claim 8 , wherein the silane-functional polyurethane oligomer (ii) is obtained through a process wherein i) hydroxyl-functional tertiary amines, amino-functional organosilanes and polyols are pre-mixed under water-free conditions thereby forming a pre-mixture, and ii) the diisocyanates are added dropwise to the pre-mixture while the temperature is kept in a range of from 60° C.-90° C. 15 . The coating composition according to claim 14 , wherein the amino-functional organosilanes in step i) are selected from aminopropyltrialkoxysilanes, aminophenyltrialkoxysilanes, aminopropylmethyldialkoxysilanes, wherein the alkoxy groups have not more than 3 carbon atoms. 16 . A process for electroless coating of metal substrates wherein the metal substrate is contacted with the coating composition according to claim 1 . 17 . The process according to claim 16 , wherein the metal substrates are selected from hot dip galvanized steel, electrolytically galvanized steel, steel, iron, zinc, aluminum and aluminum alloys. 18 . A metal substrate coated with a coating composition according to claim 1 .
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