Low temperature cure coating formed via resin-facilitated catalyst migration between layers in a double layer curing mechanism

Patent metadata

Field	Value
Publication number	US-11034857-B2
Application number	US-201715660454-A
Country	US
Kind code	B2
Filing date	Jul 26, 2017
Priority date	Jul 26, 2017
Publication date	Jun 15, 2021
Grant date	Jun 15, 2021

Abstract

A double coating, curing method, cured coating, and kit are provided. A first layer of the double coating can be a first cure coating composition, which has a first hydroxy-functional resin, a first crosslinking agent, and a first catalyst. A second layer of a second cure coating composition can have a low hydrophilicity acrylic resin as a second hydroxy-functional resin, a second crosslinking agent, and a second catalyst. The first catalyst catalyzes crosslinking between the second hydroxy-functional resin and crosslinking agent, and not between the first hydroxy-functional resin and crosslinking agent. The second catalyst catalyzes crosslinking between the first hydroxy-functional resin and crosslinking agent, and not between the second hydroxy-functional resin and crosslinking agent. The first and/or second hydroxy functional resins can facilitate catalyst migration from one layer to the other. The separate compositions can be shelf-stable and/or the curing can occur at low temperature.

First claim

What is claimed is:

1. A double coating, comprising:
a substrate;
a first layer comprising a first low-temperature cure coating composition, which comprises
a first hydroxy-functional resin,
an aminoplast resin low-temperature crosslinking agent, and
a first catalyst;

and
a second layer comprising a second low-temperature cure coating composition, which is a solventborne composition comprising
a second hydroxy-functional resin, which is a low hydrophilicity acrylic resin,
a second low-temperature crosslinking agent, which is an isocyanate resin,
a second catalyst, and
an organic solvent,

wherein the first layer and the second layer are adjacent to each other,
wherein the first catalyst catalyzes a crosslinking reaction between the second hydroxy-functional resin and the second low-temperature crosslinking agent, and does not catalyze a crosslinking reaction between the first hydroxy-functional resin and the aminoplast resin low-temperature crosslinking agent,
wherein the second catalyst catalyzes a crosslinking reaction between the first hydroxy-functional resin and the aminoplast resin low-temperature crosslinking agent, and does not catalyze a crosslinking reaction between the second hydroxy-functional resin and the second low-temperature crosslinking agent.

2. The coating of claim 1 , wherein the first and second low-temperature cure coating compositions cure within 20 minutes at a temperature of 100° C.

3. The coating of claim 1 , wherein the low hydrophilicity acrylic resin as the second hydroxy-functional resin comprises, in polymerized form, at least one alkyl (meth)acrylate monomer.

4. The coating of claim 1 , wherein the low hydrophilicity acrylic resin as the second hydroxy-functional resin comprises, in polymerized form, at least one unsubstituted alkyl (meth)acrylate monomer in a content of at least 25 mol % with respect to total monomers in the low hydrophilicity acrylic resin.

5. The coating of claim 1 wherein the low hydrophilicity acrylic resin as the second hydroxy-functional resin comprises, in polymerized form, at least one cycloalkyl (meth)acrylate monomer in a content of at most 75 mol % with respect to total monomers in the low hydrophilicity acrylic resin.

6. The coating of claim 1 , wherein the low hydrophilicity acrylic resin as the second hydroxy-functional resin comprises, in polymerized form, at least one hydroxy-substituted alkyl (meth)acrylate monomer in a content of at most 75 mol % with respect to total monomers in the low hydrophilicity acrylic resin.

7. The coating of claim 1 , wherein the low hydrophilicity acrylic resin as the second hydroxy-functional resin comprises, in polymerized form with respect to total monomers in the low hydrophilicity acrylic resin:
at least one unsubstituted alkyl (meth)acrylate monomer in a content of from 25 mol % to 100 mol %,
optionally, a hydroxy-substituted alkyl (meth)acrylate monomer, if present, in a content of from 0 to 75 mol %,
optionally, a (meth)acrylic acid monomer, if present, in a content of from 0 to 25 mol %, and
optionally, a cycloalkyl (meth)acrylate monomer, if present, in a content of from 0 to 75 mol %.

8. The coating of claim 7 , wherein the low hydrophilicity acrylic resin as the second hydroxy-functional resin further comprises, in polymerized form, a substituted alkyl (meth)acrylate monomer comprising a substituent that is not a hydroxyl group.

9. The coating of claim 1 , wherein each of the first and second layers has a stable pot life of at least 30 days.

10. The coating of claim 1 , wherein the second layer is a non-polar clearcoat and the first layer comprises water.

11. The coating of claim 1 , wherein the substrate comprises, as at least one thermoplastic material, a polyolefin, a polyamide, a polyurethane, a polyester, a polycarbonate, an acrylonitrile-butadiene-styrene (ABS) copolymer, an EPDM rubber, an acrylic polymer, or a vinyl polymer.

12. The coating of claim 1 , wherein the first low-temperature cure coating composition comprises, based on a total weight of resin solids in the composition:
from 35 to 65 percent by weight of the first hydroxy-functional resin:
from 15 to 65 percent by weight of the aminoplast resin low-temperature crosslinking agent; and
from 0.05 to 7.5 percent by weight of the first catalyst, and
wherein the second low-temperature cure coating composition comprises, based on a total weight of resin solids in the composition:
from 35 to 65 percent by weight of the second hydroxy-functional resin:
from 35 to 65 percent by weight of the second low-temperature crosslinking agent; and
from 0.25 to 7.5 percent by weight of the second catalyst.

13. A method of curing the coating of claim 1 , the method comprising curing the coating at a temperature of from 80° C. to less than 120° C.

14. A method of coating a substrate by curing the double coating of claim 1 , the method comprising:
depositing the first layer on the substrate,
depositing the second layer directly on the first layer, thereby obtaining the double coating, and
curing the double coating at a temperature of from 80° C. to less than 120° C., thereby obtaining a cured double coating.

15. The method of claim 14 , wherein an amount of the second catalyst in the first layer after the curing is greater than 50% by mass of an initial amount of the second catalyst in the second layer immediately after the second layer is deposited, and
an amount of the first catalyst in the second layer after the curing is greater than 50% by mass of an initial amount of the first catalyst in the first layer immediately after the first layer is deposited.

Assignees

• Basf Coatings Gmbh

Inventors

• December Timothy S
• Clark Timothy
• Ozvald Adam M
• Campbell Donald H

Classifications

• C09D7/63 Primary

  organic · CPC title

• C08G18/6254

  Polymers of alpha-beta ethylenically unsaturated carboxylic acids and of esters of these acids containing hydroxy groups · CPC title

• C09D133/066

  containing -OH groups · CPC title

• B05D1/36

  Successively applying liquids or other fluent materials, e.g. without intermediate treatment · CPC title

• B05D7/544

  the first layer is let to dry at least partially before applying the second layer · CPC title