Non-hazardous water-based polyurethane dispersion
US-12110373-B2 · Oct 8, 2024 · US
US11059992B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11059992-B2 |
| Application number | US-201816478177-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 17, 2018 |
| Priority date | Jan 19, 2017 |
| Publication date | Jul 13, 2021 |
| Grant date | Jul 13, 2021 |
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The present invention provides waterborne polyurethane coating compositions. When applied to a substrate, the coating compositions of the present invention have good adhesion, transparency, scratch resistance, mar resistance, hardness, solvent resistance, water resistance, and dishwashing resistance. The coating compositions are suitable for application to any suitable substrate, including glass.
Opening claim text (preview).
What is claimed is: 1. A coating composition comprising: a) a water dilutable carboxyl, or hydroxyl, or carboxyl and hydroxyl, functional polyurethane dispersion, in an amount of 1 wt % to 99 wt %, based on the total weight of the coating composition; and b) one or more cross-linking agents, in an amount of 1 wt % to 99 wt %, based on the total weight of the coating composition; wherein the one or more cross-linking agents are selected from the group consisting of carbodiimides, carbodiimide derivatives, aminoplasts, blocked isocyanates, and combinations thereof; wherein the polyurethane has a glass transition temperature of −40° C. to 50° C.; wherein the polyurethane has an elongation at break of 10% to 250%; wherein the acid number of the polyurethane is greater than 20 mg KOH/g; wherein at least one crosslinker is a carbodiimide or carbodiimide derivative; wherein the moles of carbodiimide (—NCN—) groups in the carbodiimide crosslinker to the moles of carboxylic (—COOH) groups in the polyurethane is 0.2:1 to 1.2:1; and wherein when the coating composition is applied to a substrate and dried and/or cured, the dried and cured coating has a pencil hardness of equal to or greater than 6H. 2. The coating composition of claim 1 , wherein the polyurethane dispersion is present in an amount of 25 wt % to 95 wt %, based on the total weight of the coating composition. 3. The coating composition of claim 1 , wherein the one or more cross-linking agents are present in an amount of 5 wt % to 75 wt %, based on the total weight of the coating composition. 4. The coating composition of claim 1 , wherein the polyurethane dispersion has a solids content of 5 wt % to 60 wt %, based on the total weight of the polyurethane dispersion. 5. The coating composition of claim 1 , wherein the viscosity of the polyurethane dispersion is 5 cP to 5000 cP. 6. The coating of claim 1 , wherein the glass transition temperature of the polyurethane is −40° C. to 50° C. 7. The coating composition of claim 1 , wherein the minimum film forming temperature of the polyurethane is −40° C. to 40° C. 8. The coating composition of claim 1 , wherein the acid number of the polyurethane is greater than 25 mg KOH/g. 9. The coating composition of claim 1 , wherein the sum of the acid number and hydroxyl number of the polyurethane is greater than 20 mg KOH/g. 10. The coating composition of claim 1 , wherein the polyurethane comprises an aliphatic or cycloaliphatic diisocyanate repeat unit. 11. The coating composition of claim 1 , further comprising one or more silane, oxysilane, or combinations thereof, adhesion promoters. 12. The coating composition of claim 1 , having a volatile organic compound content of less than 10 wt %, based on the total weight of the coating composition. 13. The coating composition of claim 1 , wherein the tensile strength of the polyurethane is 5 MPa to 150 MPa. 14. The coating composition of claim 1 , wherein the elongation of the polyurethane is 20% to 200%. 15. A method of applying a coating composition on a substrate, comprising: a) providing the coating composition of claim 1 ; b) applying the coating composition to the substrate; and c) drying and/or curing the composition on the substrate. 16. The method of claim 15 , wherein step b) is carried out using a method selected from the group consisting of spray coating, dip coating, flow coating, spin coating, curtain coating, and roll coating. 17. The method of claim 15 , wherein the substrate is selected from the group consisting of glass, wood, metal, paper, leather, textiles, felt, concrete, masonry, ceramic, stone, plastics, combinations of the and materials. 18. A substrate or an article comprising the coating composition of claim 1 . 19. A method of formulating a coating composition, comprising mixing: a) a water dilutable carboxyl, or hydroxyl, or carboxyl and hydroxyl, functional polyurethane dispersion, in an amount of 1 wt % to 99 wt %, based on the total weight of the coating composition; and b) one or more cross-linking agents, in an amount of 1 wt % to 99 wt %, based on the total weight of the coating composition; wherein the one or more cross-linking agents are selected from the group consisting of carbodiimides, carbodiimide derivatives, aminoplasts, blocked isocyanates, and combinations thereof; wherein the polyurethane has a glass transition temperature of −40° C. to 50° C.; and wherein the polyurethane has an elongation at break of 10% to 250%; and wherein the acid number of the polyurethane is greater than 20 mg KOH/g; wherein at least one crosslinker is a carbodiimide or carbodiimide derivative; and wherein the moles of carbodiimide (—NCN—) groups in the carbodiimide crosslinker to the moles of carboxylic (—COOH) groups in the polyurethane is 0.2:1 to 1.2:1, and wherein when the coating composition is applied to a substrate and dried and/or cured, the dried and cured coating has a pencil hardness of equal or greater than 6H. 20. The method of claim 15 , wherein the dried and cured coating has a pencil hardness of equal or greater than 6H; and/or a dishwashing resistance of equal to or greater than 50 dishwashing cycles. 21. The coating composition of claim 1 , wherein the polyurethane has an elongation at break of 10% to 75%.
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