IP Library Granted Patent US 8,653,213
Granted Patent B2
US 8,653,213 · App. 13/210,674 · Granted Feb 18, 2014

Hydrophobic coating compositions and articles coated with said compositions

Inventor: James F Brown (Clifton, VA)
Assignee: Cytonix, LLC
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Quick Facts
Patent No.
US 8,653,213
App. No.
13/210,674
Granted
Feb 18, 2014
Kind
B2
Abstract

Hydrophobic coating compositions are provided as are processes to coat articles with the compositions. Extremely hydrophobic coatings are provided by the compositions. Compositions that include perfluorohexyl(meth)acrylate and a branched or high Tg monomer are provided as are articles coated with the polymerization product of the composition. Methods are also provided for forming hydrophobic coatings on articles.

Claims (18)

1. A coating composition consisting of a perfluorohexyl(meth)acrylate and a monomer, the monomer consisting of (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C.

2. A coating composition comprising a perfluorohexyl(meth)acrylate and a monomer, the monomer comprising (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer comprises isobornyl(meth)acrylate.

3. A coating composition comprising a perfluorohexyl(meth)acrylate and a monomer, the monomer comprising (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer comprises allyl(meth)acrylate.

4. A coating composition comprising a perfluorohexyl(meth)acrylate and a monomer, the monomer comprising (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer comprises phenoxyethyl(meth)acrylate.

5. A coating composition comprising a perfluorohexyl(meth)acrylate and a monomer, the monomer comprising (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer comprises cyclohexyl(meth)acrylate.

6. A coating composition comprising a perfluorohexyl(meth)acrylate and a monomer, the monomer comprising (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer comprises isodecyl(meth)acrylate.

7. A coating composition comprising a perfluorohexyl(meth)acrylate and a monomer, the monomer comprising (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer comprises ethylhexyl(meth)acrylate.

8. A coating composition comprising a perfluorohexyl(meth)acrylate and a monomer, the monomer comprising (a) a branched monomer, (b) a monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, or (c) a branched monomer that forms a homopolymer exhibiting a glass transition temperature of 50° C. or higher, the coating composition being formulated to be polymerizable to form a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer comprises isooctyl(meth)acrylate.

9. A polymerization product of the coating composition of claim 1 .

10. A method comprising:

applying the coating composition of claim 1 to a surface; and

polymerizing the coating composition.

11. The method of claim 10 , wherein the surface is a surface of a laboratory vessel, and the laboratory vessel is a member selected from the group consisting of pipette tips, microcentrifuge tubes, vials, syringes, microtiter plates, microscope slides, microscope slide assemblies, sample chambers for analytical devices, and tubing.

12. A laboratory vessel produced by the method of claim 11 .

13. The method of claim 10 , wherein the surface is a surface of an article, and the article is a member selected from the group consisting of windshields, rainshields, satellite dishes, radar dishes, signal receivers, signal transmitters, radomes, antennas, vehicular surfaces, architectural surfaces, outdoor furniture, household goods, kitchen articles, and bath articles.

14. A laboratory vessel, said vessel comprising a vessel material having a surface intended to contact a liquid and a coating applied to at least a portion of the surface, wherein said coating comprises the polymerization product of a perfluorohexyl(meth)acrylate and a monomer, the coating comprising a coating surface having a surface area populated with 30% by area or more trifluoromethyl groups and a surface energy of about 22 dynes/cm or lower at 20° C., wherein the monomer is selected from isobornyl(meth)acrylate, allyl(meth)acrylate, tetrahydrofurfuryl(meth)acrylate, phenoxyethyl(meth)acrylate, cyclohexyl(meth)acrylate, isodecyl(meth)acrylate, ethylhexyl(meth)acrylate, isooctyl(meth)acrylate, and combinations thereof.

15. The laboratory vessel of claim 14 , wherein the coating consists essentially of the perfluorohexyl(meth)acrylate and the monomer.

16. The laboratory vessel as defined in claim 14 , wherein said vessel is a member selected from the group consisting of pipette tips, microcentrifuge tubes, vials, syringes, microtiter plates, microscope slides, microscope slide assemblies, sample chambers for analytical devices, and tubing.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2011
From: BROWN, JAMES F.
To: CYTONIX, LLC
Reel/Frame 027304/0505 →
Continuity (8)
Continuation In Part 12816703 · Jun 16, 2010
Continuation 10898773 · Jul 26, 2004
Continuation 10272982 · Oct 17, 2002
Division 09823853 · Mar 30, 2001
Continuation In Part 09593847 · Jun 14, 2000
Division 09220884 · Dec 28, 1998
Continuation In Part 08795316 · Feb 3, 1997
Related Publication 20120067908A1 · Mar 22, 2012