Scratch-resistant aqueous 2K PU coatings

US10544327B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10544327-B2
Application numberUS-201615758450-A
CountryUS
Kind codeB2
Filing dateSep 7, 2016
Priority dateSep 9, 2015
Publication dateJan 28, 2020
Grant dateJan 28, 2020

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The invention relates to aqueous two-component coating compositions based on preferably hydroxy-functional and/or amino-functional aqueous polymer dispersions and thioallophanates containing silane groups as crosslinking agents, to a method for producing them and to the use of these coating compositions for producing coatings.

First claim

Opening claim text (preview).

The invention claimed is: 1. An aqueous coating composition comprising A) at least one polyisocyanate component, B) at least one aqueous polymer dispersion, C) optionally at least one catalyst for the crosslinking of silane groups and D) optionally further auxiliaries and additives, where the polyisocyanate component A) comprises at least one thioallophanate containing silane groups, of the general formula (I), in which R 1 , R 2 and R 3 are identical or different radicals and are each a saturated or unsaturated, linear or branched, aliphatic or cycloaliphatic or an optionally substituted aromatic or araliphatic radical having up to 18 carbon atoms, which may optionally contain up to 3 heteroatoms from the series of oxygen, sulphur and nitrogen, X is a linear or branched organic radical having at least 2 carbon atoms, Y is a linear or branched, aliphatic or cycloaliphatic, an ariphatic or aromatic radical having up to 18 carbon atoms and n is an integer from 1 to 20. 2. The coating composition according to claim 1 , characterized in that the polyisocyanate component A) comprises at least one thioallophanate containing silane groups, of the formula (I), in which R 1 , R 2 and R 3 are identical or different radicals and are each a saturated, linear or branched, aliphatic or cycloaliphatic radical having up to 6 carbon atoms, and optionally contain up to 3 oxygen atoms, and X is a linear or branched alkylene radical having 2 to 10 carbon atoms, and Y and n are as defined in claim 1 . 3. The coating composition according to claim 1 , characterized in that the polyisocyanate component A) comprises at least one thioallophanate containing silane groups, of the formula (I), in which R 1 , R 2 and R 3 are each alkyl radicals having up to 6 carbon atoms and/or alkoxy radicals which contain up to 3 oxygen atoms, with the proviso that at least one of the radicals R 1 , R 2 and R 3 is such an alkoxy radical, and X is a propylene radical (—CH 2 —CH 2 —CH 2 —), Y and n are as defined in claim 1 . 4. The coating composition according to claim 1 , characterized in that the polyisocyanate component A) comprises at least one thioallophanate containing silane groups, of the formula (I), in which R 1 , R 2 and R 3 are identical or different radicals and are each methyl, methoxy or ethoxy, with the proviso that at least one of the radicals R 1 , R 2 and R 3 is a methoxy or ethoxy radical, X is a propylene radical (—CH 2 —CH 2 —CH 2 —), and Y and n are as defined in claim 1 . 5. The coating composition according to claim 1 , characterized in that the polyisocyanate component A) comprises at least one thioallophanate containing silane groups, of the formula (I), in which Y is a linear or branched, aliphatic or cycloaliphatic radical having 5 to 13 carbon atoms. 6. The coating composition according to claim 1 , characterized in that the polyisocyanate component A) comprises at least one thioallophanate containing silane groups, of the formula (I), in which Y is an aliphatic and/or cycloaliphatic radical as obtained by removing the isocyanate groups from a diisocyanate selected from the series of 1,5-diisocyanatopentane, 1,6-diisocyanatohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane, 2,4′- and/or 4,4′-diisocyanatodicyclohexylmethane. 7. The coating composition according to claim 1 , characterized in that the aqueous polymer dispersion B) comprises at least one aqueous or water-dispersible polyacrylate resin, polyester resin, polyurethane resin, polyurea resin, polycarbonate resin and/or polyether resin. 8. The coating composition according to claim 7 , characterized in that the aqueous polymer dispersion B) comprises at least one aqueous secondary polyacrylate dispersion B 1 ), a polyester-polyacrylate-dispersion B 3 ) and/or a polyurethane dispersion B 4 ) based on polyester polyols, polycarbonate polyols and/or C3 and C4 polyether polyols. 9. The coating composition according to claim 7 , characterized in that the aqueous polymer dispersion B) contains hydroxyl groups and/or amino groups. 10. The coating composition according to claim 9 , characterized in that the catalyst C) comprises at least one amine-blocked acidic phosphoric ester, an amine-blocked sulphonic acid and/or at least one tetraalkylammonium carboxylate. 11. The coating composition according to claim 9 , characterized in that the catalyst component C) comprises at least one amine-blocked phosphoric acid phenyl ester, an amine-blocked phosphoric acid bis(2-ethylhexyl) ester, tetraethylammonium benzoate and/or tetrabutylammonium benzoate. 12. A method for producing the coating composition according to claim 1 , comprising mixing components A), B), optionally C) and optionally D) in any order in succession or together in proportions such that for each hydroxyl and/or amino group of the polymer dispersion B) there are from 0.5 to 2.0 isocyanate groups of the polyisocyanate component A). 13. A method for producing polyurethane paints and coatings comprising curing the coating composition according to claim 1 . 14. The method according to claim 13 , characterized in that the coating compositions are cured in a temperature range from 20 to 200° C. during a time of 1 min to 24 h. 15. A substrates coated with the coating composition according to claim 1 . 16. A method for producing the coating composition according to claim 1 , comprising mixing components A), B), optionally C) and optionally D) in any order in succession or together in proportions such that for each hydroxyl and/or amino group of the polymer dispersion B) there are from 0.6 to 1.8 isocyanate groups of the polyisocyanate component A). 17. A method for producing the coating composition according to claim 1 , comprising mixing components A), B), optionally C) and optionally D) in any order in succession or together in proportions such that for each hydroxyl and/or amino group of the polymer dispersion B) there are from 0.7 to 1.5 isocyanate groups of the polyisocyanate component A). 18. The method according to claim 13 , characterized in that the coating compositions are cured in a temperature range from 30 to 190° C. during a time of 2 min to 12 h. 19. The method according to claim 13 , characterized in that the coating compositions are cured in a temperature range from 50 to 180° C. during a time of 3 min to 8 h.

Assignees

Inventors

Classifications

  • Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced {(electrically insulating plastics, resins or waxes H01B3/30)}; Filling pastes · CPC title

  • formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates · CPC title

  • containing silicon · CPC title

  • acyclic · CPC title

  • containing allophanate groups · CPC title

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What does patent US10544327B2 cover?
The invention relates to aqueous two-component coating compositions based on preferably hydroxy-functional and/or amino-functional aqueous polymer dispersions and thioallophanates containing silane groups as crosslinking agents, to a method for producing them and to the use of these coating compositions for producing coatings.
Who is the assignee on this patent?
Covestro Deutschland Ag
What technology area does this patent fall under?
Primary CPC classification C09D175/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 28 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).