Sag control compositions, methods of forming the same, and methods of forming coating systems using the same

Patent metadata

Field	Value
Publication number	US-9856384-B2
Application number	US-201414336222-A
Country	US
Kind code	B2
Filing date	Jul 21, 2014
Priority date	Jul 21, 2014
Publication date	Jan 2, 2018
Grant date	Jan 2, 2018

Abstract

Sag control compositions, methods of forming sag control compositions, and methods of forming coating systems that include at least one coating layer including urea crystals of such sag control compositions are provided herein. In an embodiment, a sag control composition includes urea crystals and a non-polymeric organic solvent. The urea crystals include the reaction product of a polyisocyanate and a mono-amine. The sag control composition is a stable mixture with a single phase at a temperature of about 21° C. based upon visual observation for a period of at least 10 minutes after forming the mixture.

First claim

What is claimed is:

1. A sag control composition comprising:
urea crystals comprising the reaction product of a polyisocyanate and a mono-amine; and
a non-polymeric organic solvent present in an amont of from about 85 to about 95 weight % based on the total weight of the sag control composition;
wherein the sag control composition comprises the urea crystals in an amount of at least about 8 weight %, based on the total weight of the sag control composition and is a stable mixture with a single phase at a temperature of about 21° C. based upon visual observation for a period of at least 10 minutes after forming the mixture.

2. The sag control composition of claim 1 , wherein the urea crystals are present in an amount of from about 8 to about 15 weight %, based on the total weight of the sag control composition.

3. The sag control composition of claim 1 , wherein the polyisocyanate is chosen from blocked or un-blocked aliphatic, cycloaliphatic, heterocyclic, aromatic di-, tri-, polyisocyanates or a combination thereof.

4. The sag control composition of claim 1 , wherein the mono-amine is chosen from primary amines having in the range of from 1 to 20 carbon atoms.

5. The sag control composition of claim 1 , free of hydroxyl-functional resin.

6. The sag control composition of claim 5 , free of a coating resin.

7. The sag control composition of claim 1 , having a D50 particle size distribution of from about 1 to about 5 microns.

8. The sag control composition of claim 7 , wherein a content of particles having a size of greater than about 15 microns is less than about 3 weight %, based on the total weight of the sag control composition.

9. The sag control composition of claim 1 , wherein the non-polymeric organic solvent is polar and is capable of participating in hydrogen bonding.

10. The sag control composition of claim 9 , wherein the urea crystals have a solubility in the non-polymeric organic solvent of from about 0 to about 5 g/l at about 21° C.

11. The sag control composition of claim 9 , wherein the non-polymeric organic solvent has a hydrogen bonding parameter of 1.7≦X≦7.7, where X is the hydrogen bonding parameter of the solvent.

12. The sag control composition of claim 1 , wherein the sag control composition is a non-Newtonian fluid with an inverse relationship between viscosity of the sag control composition and applied shear force.

13. A method of forming a sag control composition, wherein the method comprises the steps of:
combining a mono-amine and a non-polymeric organic solvent to form a sag control pre-mix;
applying shear force to the sag control pre-mix in a mixing device chosen from an emulsifier device or a disperser;
while applying the shear force to the sag control pre-mix in the mixing device, combining a polyisocyanate with the sag control pre-mix to form a reactive composition;
continuing to apply the shear force to the reactive composition in the mixing device for a period sufficient to form the sag control composition having urea crystals with a D50 particle size distribution of from about 1 to about 5 microns;
wherein the sag control composition comprises the urea crystals in an amount of at least about 8 weight %, based on the total weight of the sag control composition, wherein the non-polymeric organic solvent is present in an amount of from about 85 to 92 weight % based on the total weight of sag control composition, based on the total weight of the sag control compositiin, and wherein the sag control composition is a stable mixture with a single phase at a temperature of about 21° C. based upon visual observation for a period of at least 10 minutes after forming the mixture.

14. A method of forming a coating system comprising at least one coating layer including urea crystals, wherein the method comprises the steps of:
providing a binder composition comprising a coating resin;
mixing the binder composition and a sag control composition to form a coating composition, wherein the sag control composition comprises:
urea crystals comprising the reaction product of a polyisocyanate and a mono-amine, wherein the urea crystals are present in an amount of at least about 8 weight %, based on the total weight of the sag control composition; and
a non-polymeric organic solvent present in an amount of from about 85 to 92 weight % based on the total weight of the sag control composition; and
wherein the coating composition comprises from about 1 to about 5 weight % of the urea crystals based on the total weight of the coating resin in the coating composition; and

wherein the sag control composition is a stable mixture with a single phase at a temperature of about 21° C. based upon visual observation for a period of at least 10 minutes after forming the mixture;
applying the coating composition onto a substrate to form a coating layer having a dry thickness;
wherein a content of urea crystals having a size of greater than the dry thickness of the coating layer is less than about 3 weight %, based on the total weight of the sag control composition.

15. The method of claim 14 , wherein mixing the binder composition and the sag control composition comprises mixing binder composition and the sag control composition free of the coating resin.

16. The method of claim 14 , further comprising storing the sag control composition for a period of at least 60 days prior to mixing the binder composition and the sag control composition.

17. The sag control composition of claim 1 , wherein the sag control composition is a stable mixture with a single phase at a temperature of about 21° C. based upon visual observation for a period of at least 24 hours after forming the mixture.

18. The sag control composition of claim 17 , wherein the sag control composition is free of hydroxyl-functional resin.

19. A sag control composition comprising:
urea crystals comprising the reaction product of a polyisocyanate and a mono-amine; and
a non-polymeric organic solvent;
wherein the sag control composition comprises the urea crystals in an amount of at least about 8 weight %, based on the total weight of the sag control composition and is a stable mixture with a single phase at a temperature of about 21 ° C. based upon visual observation for a period of at least 10 minutes after forming the mixture; and
wherein the sag control composition is free of hydroxyl-functional resin.

Assignees

• Axalta Coating Systems Ip Co
• Axalta Coatings Systems Ip Co Llc

Inventors

• Uhlianuk Peter W
• Trindade Delson J
• Ladd Brian J

Classifications

• C08G18/73

  acyclic · CPC title

• C08K5/21

  Urea; Derivatives thereof, e.g. biuret · CPC title

• C09D5/00

  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

• C09D7/69

  Particle size larger than 1000 nm · CPC title

• C08G18/2865

  Compounds having only one primary or secondary amino group; Ammonia · CPC title