Claims
- 1. A method of producing a non-glare coating on a reflective surface which comprises spraying a polymerizable composition onto a reflective surface and allowing said composition to cure in the presence of water, said composition being sprayed in the form of fine droplets, and said composition comprising 5-40% by weight of solids in solution, said solids comprising:
- (1) 75-100% by weight of an epoxy prepolymer comprised of 90-50% by weight of an epoxyterminated silane and 10-50% by weight of alicyclic, aliphatic, or mixed aliphaticcyclic oxiranes, the prepolymer having a number average molecular size of 50-400 Angstroms, and
- (2) 0-25% by weight of hydrophobic silica particles of 0.0005 to 0.050 microns in average diameter,
- the composition further comprising a catalytically active amount of a silane hydrolysis catalyst.
- 2. The method of claim 1 wherein said epoxy-terminated silane is represented by the formula: ##STR10## wherein R is alkylene of 1 to 8 carbon atoms and R.sup.2 is alkyl of 1 to 6 carbon atoms.
- 3. The method of claim 2 wherein the oxiranes are represented by the formulae: ##STR11## wherein n is a positive integer of 1 to 12.
- 4. The method of claim 3 in which the silane hydrolysis catalyst is selected from the group consisting of (1) highly fluorinated aliphatic sulfonyl catalysts, (2) highly fluorinated aliphatic sulfonic acid or salt catalysts, (3) Lewis acids, (4) Bronstad acids, or (5)protonic acids which can cure tetraethoxy silane to a tack free state at 90.degree. C. and 60% relative humidity in less than 30 minutes.
- 5. The method of claim 4 in which the hydrophobic silica has less than 1% by weight surface hydroxyl groups and is present at 10-25% by weight solids in the composition.
- 6. The method of claim 4 in which the composition further comprises an effective amount of ultraviolet absorbers.
- 7. The method of claim 2 in which the silane hydrolysis catalyst is selected from the group consisting of (1) highly fluorinated aliphatic sulfonyl catalysts, (2) highly fluorinated aliphatic sulfonic acid or salt catalysts, (3) Lewis acids, (4) Bronstad acids, or (5) protonic acids which can cure tetraethoxy silane to a tack free state at 90.degree. C. and 60% relative humidity in less than 30 minutes.
- 8. A composition of 5-40% by weight solids in solution which can be sprayed to form a non-glare abrasion resistant coating, the solids of which comprise:
- (1) 75-100% by weight of an epoxy prepolymer comprised of 90-50% by weight of an epoxy-terminated silane and 10-50% by weight of alicyclic, aliphatic, or mixed aliphaticcyclic oxiranes, the prepolymer having a number average molecular size of 50-400 Angstroms, and
- (2) hydrophobic silica particles having an average diameter of 0.0005 to 0.050 microns in an amount up to 25% by weight
- and in the solution, a catalytically active amount of a silane hydrolysis catalyst capable of curing tetraethoxy silane tack free in less than 30 minutes at 90.degree. C. and 60% relative humidity.
- 9. The composition of claim 8 in which the oxirane is represented by any of the formulae: ##STR12## wherein n is a positive integer of 1 to 12.
- 10. An aerosol can containing the composition of claim 9.
- 11. The aerosol can and composition of claim 10 wherein the epoxy-terminated silane is represented by the formula: ##STR13## wherein R is alkylene of 1 to 8 carbon atoms and R.sup.2 is alkyl of 1 to 6 carbon atoms.
- 12. The aerosol can and composition of claim 11 wherein the silane hydrolysis catalyst is selected from the group consisting of (1) highly fluorinated aliphatic sulfonyl catalysts, (2) highly fluorinated aliphatic sulfonic acid or salt catalysts, (3) Lewis acids, (4) Bronstad acids, or (5) protonic acids which can cure tetraethoxy silane to a tack free state at 90.degree. C. and 60% relative humidity in less than 30 minutes.
- 13. An aerosol can containing the composition of claim 8.
Parent Case Info
This application is a continuation-in-part of copending application Ser. No. 843,875, filed Oct. 20, 1977, and now abandoned.
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
3955035 |
Ito et al. |
May 1976 |
|
4049986 |
Nozari |
Sep 1977 |
|
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
843875 |
Oct 1977 |
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