IP Library Granted Patent US 10,519,337
Granted Patent B2
US 10,519,337 · App. 14/902,546 · Granted Dec 31, 2019

Coating compositions for packaging articles such as food and beverage containers

Inventors: Sebastien Gibanel (Givry, FR); Benoit Prouvost (L'Abergement de Cuisery, FR)
Assignee: The Sherwin-Williams Company
C09D151/003B05D7/14C09D5/022B05D1/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,519,337
App. No.
14/902,546
Granted
Dec 31, 2019
Kind
B2
Abstract

An article, comprising a food or beverage container ( 20 ), or a portion thereof, that includes a metal substrate ( 30, 32 ) and a coating ( 34 ) disposed on at least a portion of the metal substrate ( 30, 32 ). The coating ( 34 ) is preferably formed from a coating composition that comprises an emulsion polymerized latex having a first-stage emulsion polymerized copolymer and a second-stage emulsion polymerized copolymer.

Claims (24)

1. A method of making an inside spray coating composition for food or beverage containers, the method comprising:

emulsion polymerizing first-stage monomers in an aqueous carrier to produce a first-stage copolymer comprising water-dispersing groups;

emulsion polymerizing second-stage monomers, wherein at least 5% by weight of the second-stage monomers are chemically different from the first-stage monomers, in the presence of the first-stage copolymer to form a second-stage copolymer, wherein the second-stage copolymer is chemically different from the first-stage copolymer, and wherein the second-stage copolymer comprises a curing group configured to react with the first-stage copolymer during a curing step; and

formulating the coating composition for a spray coating application, wherein the coating composition is substantially free of one or more, or all, of structural units derived from each of (meth)acrylamide-type monomers and bisphenol A, and wherein the coating composition spray-applied onto an interior of a 12 ounce two-piece drawn and ironed aluminum beverage can and cured at 188° C. to 210° C. (measured at the can dome) for 60 seconds provides an inside spray beverage can coating with an average film thickness of about 0.7 mg/in 2 to about 4.0 mg/in 2 , and the can coating exhibits a global extraction result of less than 50 ppm as measured according to the extraction procedure in 21 C.F.R. § 175.300, paragraphs (d)-(e).

2. The method of claim 1 , wherein the coating has an average film thickness of about 0.9 mg/in 2 to about 2.1 mg/in 2 .

3. The method of claim 2 , wherein the first-stage copolymer has an acid number greater than about 80 milligrams potassium hydroxide per gram of first-stage copolymer.

4. The method of claim 1 , wherein the first-stage copolymer has an acid number greater than about 40 milligrams potassium hydroxide per gram of first-stage copolymer.

5. The method of claim 4 , wherein the curing group comprises an oxirane group.

6. The method of claim 5 , wherein second-stage monomers comprise greater than 5% to less than 40% by weight of monomer having an oxirane group.

7. The method of claim 1 , wherein the first-stage copolymer has an acid number greater than about 100 milligrams potassium hydroxide per gram of first-stage copolymer.

8. The method of claim 1 , wherein the curing group comprises an oxirane group, an isocyanate group, an azlactone group, an oxazoline group, a cyclocarbonate group, or a combination thereof.

9. The method of claim 1 , wherein the curing group comprises an oxirane group, and wherein the second-stage monomers comprise glycidyl methacrylate.

10. The method of claim 9 , wherein second-stage monomers comprise greater than 5% to less than 30% by weight of glycidyl methacrylate.

11. The method of claim 1 , wherein the first-stage copolymer has a glass transition temperature of greater than 30° C. and wherein the second-stage copolymer has a glass transition temperature of greater than 30° C.

12. The method of claim 1 , wherein each of the first- and second-stage copolymers are substantially free of styrene.

13. The method of claim 1 , wherein the coating has an initial metal exposure of less than 3 mA.

14. The method of claim 1 , wherein the first-stage monomers are present in an amount of greater than 30% by weight and less than 100% by weight relative to the total weight of first-stage monomers and second-stage monomers.

15. The method of claim 14 , wherein the first-stage monomers are present in an amount greater than 0% by weight of less than 75% by weight relative to the total weight of first-stage monomers and second-stage monomers.

16. The method of claim 1 , wherein the coating composition has a total solids content of greater than about 15% to less than about 25%, based on the total weight of the coating composition.

17. The method of claim 16 , wherein the coating composition includes greater than about 50% by weight of latex emulsion copolymers, based on the entire weight of the total solids in the coating composition.

18. The method of claim 17 , wherein the first-stage copolymer has an acid number greater than 40 milligrams potassium hydroxide per gram of first-stage copolymer, and wherein the first-stage monomers are present in an amount of greater than 30% by weight and less than 100% by weight relative to the total weight of first-stage monomers and second-stage monomers.

19. The method of claim 17 , wherein the first-stage copolymer has a glass transition temperature of greater than 30° C. and wherein the second-stage copolymer has a glass transition temperature of greater than 30° C.

20. The method of claim 1 , wherein the coating composition includes greater than about 50% by weight of latex emulsion copolymers, based on the entire weight of the total solids in the coating composition.

21. The method of claim 1 , wherein the coating composition includes a phenoplast resin.

Assignments (9)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2023
From: THE SHERWIN-WILLIAMS HEADQUARTERS COMPANY
To: SWIMC LLC
Reel/Frame 063275/0494 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 11, 2022
From: THE SHERWIN-WILLIAMS COMPANY
To: THE SHERWIN-WILLIAMS HEADQUARTERS COMPANY
Reel/Frame 060366/0979 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2021
From: THE VALSPAR CORPORATION
To: THE SHERWIN-WILLIAMS COMPANY
Reel/Frame 057204/0946 →
MERGER Recorded Oct 29, 2020
From: ENGINEERED POLYMER SOLUTIONS, INC.
To: THE VALSPAR CORPORATION
Reel/Frame 054443/0772 →
MERGER Recorded Sep 2, 2020
From: VALSPAR SOURCING, INC.
To: ENGINEERED POLYMER SOLUTIONS, INC.
Reel/Frame 053826/0606 →
NUNC PRO TUNC ASSIGNMENT Recorded Mar 24, 2020
From: THE SHERWIN-WILLIAMS COMPANY
To: VALSPAR SOURCING, INC.
Reel/Frame 052217/0640 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT PATENT NO. 8465946 PREVIOUSLY RECORDED AT REEL: 045281 FRAME: 0529. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER. Recorded May 4, 2018
From: VALSPAR SOURCING, INC.
To: THE SHERWIN-WILLIAMS COMPANY
Reel/Frame 046087/0150 →
MERGER Recorded Feb 8, 2018
From: VALSPAR SOURCING. INC
To: THE SHERWIN-WILLIAMS COMPANY
Reel/Frame 045281/0529 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2016
From: GIBANEL, SEBASTIEN; PROUVOST, BENOIT
To: VALSPAR SOURCING, INC.
Reel/Frame 038865/0252 →
Continuity (2)
Provisional Application 61842044 · Jul 2, 2013
Related Publication 20170002227A1 · Jan 5, 2017