Abrasion resistant coatings by siloxane oligomers
View Patent ↗A process including forming a siloxane oligomer from a mixture including at least one alkoxysilane, at least one phase transfer catalyst, and water, and adding at least one latent curing catalyst to the siloxane oligomer to form a coating composition is described. Also described is a process for producing a rapidly cured abrasion resistant coating, including providing a coating composition including a siloxane oligomer and a thermal latent curing catalyst, applying the coating composition to an article, and curing the coating composition for less than about 10 minutes to form a coating that has a Bayer ratio of abrasion resistance of at least about 2.0. A coating composition including at least one siloxane oligomer, at least one phase transfer catalyst, and at least one latent curing catalyst is also described.
1. A process, comprising:
forming a siloxane oligomer from a mixture comprising at least one alkoxysilane, at least one phase transfer catalyst, and water; and
adding at least one latent curing catalyst comprising ammonium antimonite to the siloxane oligomer to form a coaling composition.
2. The process of claim 1 , wherein the alkoxysilane has a general structure represented by formula (I):
wherein x equals 0, 1,2 or 3;
OR is a hydrolyzable alkoxy group;
R is an alkyl group; and
OFG is an organofunctional group.
3. The process of claim 2 , wherein each R independently has from 1 to 20 carbon atoms.
4. The process of claim 2 , wherein each R independently has from 1 to 4 carbon atoms.
5. The process of claim 2 , wherein each OFG independently has from 1 to 100 carbon atoms.
6. The process of claim 2 , wherein each OFG independently has from 1 to 20 carbon atoms.
7. The process of claim 2 , wherein each OFO independently includes at least one functional group selected from the group consisting of epoxy, acrylate, methacrylate, amino, aectyl, cyano, halogen, mercapto, vinyl, alkoxyalkyl, carbamate, carboxyl, ester, aromatic, or alkyl (straight, branched, or cyclic) functional groups.
8. The process of claim 7 , wherein each GPO has at least one carbon atom in addition to the at least one functional group.
9. The process of claim 1 , wherein the at least one alkoxysilane is selected from the group consisting of (3-glyeidoxypropyl)trimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 2-(3,4-epoxycyelohexyl)ethyltriethoxysilane, 5,6-epoxyhexyltriethoxysilane, (3-methacryloxypropyl)trimethoxysilane, (3-methaeryloxypropyl)triethoxysilane, (3-acryloxypropyl) trimethoxysilane, tetraethoxysilane, tetramethoxysilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, acetoxypropyltrimethoxysilane, 3-cyanopropyltrimethoxysilane, (3,3,3-trifluoropropyl)trimethoxysilane, (tridecafluoro-1,1,2,2-tetrahydrooetyl)triethoxysilane, 3-mercaptopropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, and mixtures thereof.
10. The process of claim 1 , wherein the at least one alkoxysilane is selected from the group consisting of (3-glyeidoxypropyl)trimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 2-(3,4-epoxycyclohexyl)cthyltriethoxysilane, 5,6-epoxyhexyltriethoxysilane, (3-methacryloxypropyl)trimethoxysilane, (3-methacryloxypropyl)triethoxysilane, (3-acryloxypropyl) trimethoxysilane and mixtures thereof.
11. The process of claim 1 , wherein the at least one alkoxysilane is selected from the group consisting of (3-glycidoxypropyl)trimethoxysilane, (3-methacryloxypropyl)trimethoxysilane, (3-methacryloxypropyl)tri ethoxysilane, and mixtures thereof.
12. The process of claim 1 , wherein the at least one phase transfer catalyst is present in the mixture in an amount from about 0.0005 grams per gram of the alkoxysilane to 0.2 grams per gram of the alkoxysilane.
13. The process of claim 1 , wherein the at least one phase transfer catalyst is present in the mixture in an amount from about 0.00 1 grams per mole of the alkoxysilane to 0.2 grams per gram of the alkoxysilane.
14. The process of claim 1 , wherein water is present in the mixture in an amount from about 0.5 moles per mole of the alkoxysilane to 20 moles per mole of the alkoxysilane.
15. The process of claim 1 , wherein water is present in the mixture in an amount from about 0.5 moles per mole of the alkoxysilane to 5 moles per mole of the alkoxysilane.
16. The process of claim 1 , wherein the mixture further comprises a solvent.
17. The process of claim 16 , wherein the solvent is selected from the group consisting of ethanol, isopropanol, 1-methoxy-2-propanol, ethyl acetate, n-butylacetate, t-butylacetate, 2-propoxyethanol, propylene glycol monomethyl ether acetate, and mixtures thereof.
18. The process of claim 16 , wherein the solvent comprises isopropanol.
19. The process of claim 16 , wherein the solvent is present in the mixture in an amount at least about 0.01 moles per mole of the alkoxysilane.
20. The process of claim 16 , wherein the solvent is present in the mixture in an amount at least about 0.1 moles per mole of the alkoxysilane.
21. The process of claim 16 , wherein the solvent is present in the mixture in an amount at least about 1 mole per mole of the alkoxysilane.
22. The process of claim 1 , wherein forming a siloxane oligomer continues for a period sufficient to hydrolyze at least 40 percent of all OR groups.
23. The process of claim 1 , wherein forming a siloxane oligomer continues for a period sufficient to hydrolyze at least 70 percent of all OR groups.
24. The process of claim 1 , wherein forming a siloxane oligomer continues for a period sufficient to hydrolyze at least 80 percent of all OR groups.
25. The process of claim 1 , wherein forming a siloxane oligomer continues for a period sufficient to form a siloxane oligomer with a weight average molecular weight from about 500 to about 100,000.
26. The process of claim 1 , wherein forming a siloxane oligomer continues for a period sufficient to form a siloxane oligomer with a weight average molecular weight from about 1,000 to about 50,000.
27. The process of claim 1 , wherein forming a siloxane oligomer continues for a period sufficient to form a siloxane oligomer with a weight average molecular weight from about 2,000 to about 20,000.
28. The process of claim 1 , wherein the coating composition has a latent curing catalyst ratio from about 0.1 to about 5.0.
29. The process of claim 1 , wherein the coating composition has a latent curing catalyst ratio from about 1.0 to about 3.0.
30. The process of claim 1 , further comprising adding at least one solvent to the coating composition.
31. The process of claim 30 , wherein the at least one solvent is selected from the group consisting of ethanol, isopropanol, 1-methoxy-2-propanol, ethyl acetate, n-butylaeetate, t-butylacetate, 2-propoxyethanol, propylene glycol monomethyl ether acetate, and mixtures thereof.
32. The process of claim 1 , further comprising adding metal oxide particles to the coating composition.
33. The process of claim 32 , wherein the metal oxide particles are selected from the group consisting of particles of silica, zirconium oxide, zinc oxide, titanium oxide, aluminum oxide, cerium oxide, tin oxide, Atrium oxide, antimony pentoxide, silica-titania, indium tin oxide, antimony tin oxide, and mixtures thereof.
34. The process of claim 32 , wherein the metal oxide particles have functional groups on their surfaces.
35. The process of claim 32 , wherein the coating composition has a particle ratio from about 0.1 to about 200.
36. The process of claim 32 , wherein the coating composition has a particle ratio from about 20 to about 100.
37. The process of claim 32 , wherein the coating composition has a particle ratio from about 30 to about 70.
38. The process of claim 1 , wherein the coating composition has a solid content from about 20% to about 60%.
39. The process of claim 1 , wherein the coating composition has a solid content from about 30% to about 50%.
40. The process of claim 1 , wherein the coating composition has a viscosity from about 1 centipoise to about 150 centipoises.
41. The process of claim 1 , wherein the coating composition has a viscosity from about 2 centipoises to about 30 centipoises.
42. The process of claim 1 , wherein the coating composition has a viscosity from about 3 centipoises to about 10 centipoises.
43. The process of claim 1 , further comprising:
applying the coating composition to an article to form a coated article.
44. The process of claim 43 , further comprising preparing the surface of the article prior to applying the coating composition.
45. The process of claim 44 , wherein preparing the surface comprises applying a primer layer to the surface of the article.
46. The process of claim 1 , further comprising purifying the formed siloxane oligomer before forming the coating composition.
47. The process of claim 46 , wherein purifying the formed siloxane oligomer comprises separating a first liquid phase from a second liquid phase.
48. The process of claim 1 , wherein adding at least one latent curing catalyst comprises adding the at least one latent curing catalyst without separating the phase transfer catalyst from the siloxane oligomer.
49. The process of claim 1 , wherein adding at least one latent curing catalyst comprises adding the at least one latent curing catalyst afier separating the phase transfer catalyst from the siloxane oligomer.