Multi-functional unsaturated polyester polyols

• US 6,916,547 B2
• Filed: 02/01/2002
• Issued: 07/12/2005
• Est. Priority Date: 02/01/2002
• Status: Expired due to Term

• Current Assignee: AFI Licensing LLC (Armstrong World Industries Incorporated)
• Original Assignee: AWI Licensing Company
• Inventors: Ross, Jeff S., Tian, Dong
• Primary Examiner(s): Chen, Vivian
• Application Number:
  US10/062,380
• Publication Number:
  US 20030148126A1
• Time in Patent Office: 1,257 Days
• Field of Search: 428/195, 428/480, 428/323, 428/141, 428/329, 528/298, 528/300, 528/302, 528/303, 528/306, 528/354, 528/361, 528/363
• US Class Current: 428/480
• CPC Class Codes: C08G 63/08 Lactones or lactides
• CPC Class Codes: C09D 167/06 Unsaturated polyesters having carbon-to-carbon unsaturation
• CPC Class Codes: C09D 167/07 having terminal carbon-to-carbon unsaturated bonds
• CPC Class Codes: Y10T 428/24355 Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
• CPC Class Codes: Y10T 428/25 Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
• CPC Class Codes: Y10T 428/257 Iron oxide or aluminum oxide
• CPC Class Codes: Y10T 428/31786 Of polyester [e.g., alkyd, etc.]

Abstract

Novel multifunctional unsaturated polyester polyols, UV-curable top coat formulations including these polyols, and a one-step process for preparing these polyols, are disclosed. Surface coverings and surface covering components including these top coat formulations are also disclosed. The polyols are generally formed by the ring opening polymerization of a lactone with a compound of the formula (R¹)_aR(OH)_b, where a+b>2. R¹ is a double bond-containing moiety such as allyl, vinyl, vinylidene, vinyl ether, acrylate, and the like. R is generally an alkyl, aryl, aralkyl, alkaryl, ether or ester group, including substituted versions thereof. R can be a polymer, including polymers with a plurality of functional groups. Examples of lactone groups which can be used include caprolactone, lactide and glycolide. The polyols can be used in 100% solids, solvent and water based radiation cured coatings, thermal cured coatings, dual cure (thermal with UV/e-beam, or UV/e-beam with thermal curing) coatings, and other types of coatings. These new resins enhance coating performance due to their multi-functional groups in the polymer chain.

Claims

1. A top coat formulation comprising a multifunctional unsaturated polyester polyol of the formula:

(R¹)_aR—

[O—

(C(O)—

(CR²R³)_n—

O—

)_mH]_b

wherein;

a and b are, independently, equal to or greater than 1, and a+b combined are greater than 2,

n is a number between 1 and 20, inclusive, m is a number between 1 and 50, inclusive,

R is an alkyl, aryl, aralkyl or alkaryl, or substituted versions thereof,

R¹ is an olefin-containing moiety, and

R² and R³ are, independently, H, alkyl, aryl, aralkyl, alkaryl, ether, alkoxy, acetal, ester, or substituted versions thereof, or R² and R³ combine to form a cycloalkane wherein one or more of the carbons is optionally replaced with a heteroatom,

wherein one or more of the C(R²R³) groups can be replaced with a heteroatom.

2. The top coat formulation of claim 1, wherein at least one R¹ comprises an allyl, vinyl ether, vinyl, vinylidine or (meth)acrylate group.

3. The top coat formulation of claim 1, wherein R is selected from the group consisting of alkyl and alkaryl.

4. The top coat formulation of claim 1, wherein R² and R³ are, independently, selected from the group consisting of H and C_1-6 alkyl.

5. The top coat formulation of claim 1, wherein a is between 2 and 6, inclusive.

6. The top coat formulation of claim 1, wherein b is between 2 and 6, inclusive.

7. The top coat formulation of claim 1, further comprising one or more additional components, selected from the group consisting of flatting agents, photoinitiators, reactive diluents, hard particles and adhesion promoters.

8. The top coat formulation of claim 7, wherein hard particles are aluminum oxide particles.

9. The top coat formulation of claim 1, wherein the formulation is radiation-curable.

10. The top coat formulation of claim 1, wherein the formulation is thermally curable.

11. The top coat formulation of claim 10, further comprising a cross-linking compound selected from the group consisting of melamine and isocyanate.

12. A surface covering comprising a top coat layer, the top coat layer comprising the reaction product of the top coat formulation of claim 11.

13. The surface covering of claim 12, wherein the top coat layer further comprises one or more additional components, selected from the group consisting of flatting agents, photoinitiators, reactive diluents, hard particles and adhesion, promoters.

14. The top coat formulation of claim 1, wherein the formulation is radiation-curable and thermally curable.

15. A surface covering comprising a top coat layer, the top coat layer comprising the cured top coat formulation of claim 1.

16. The surface covering of claim 15, wherein the surface covering is a floor covering.

17. The surface covering of claim 16, further comprising a wear layer.

18. The surface covering of claim 16, further comprising a design layer.

19. The surface covering of claim 16, further comprising a foam layer.

20. The surface covering of claim 16, further comprising a base layer.

21. The surface covering of claim 15, wherein the top coat layer further comprises one or more additional components, selected from the group consisting of flatting agents, photoinitiators, reactive diluents, hard particles and adhesion promoters.

22. The top coat formulation of claim 1, wherein n is a number between 3 and 14, inclusive.

23. A method of forming the top coat formulation comprising a multifunctional unsaturated polyester polyol of the formula:

(R¹)_aR—

[O—

(C(O)—

(CR²R³)_n—

O—

)_mH]_b

wherein;

a and b are, independently, equal to or greater than 1, and a+b combined are greater than 2,

n is a number between 1 and 20, inclusive,

m is a number between 1 and 50, inclusive,

R is an alkyl, aryl, aralkyl, alkaryl, ether or ester group, or substituted versions thereof,

R¹ is an olefin-containing moiety, and

R² and R³ are, independently, H, alkyl, aryl, aralkyl, alkaryl, ether, alkoxy, acetal, ester, or substituted versions thereof, or R² and R³ combine to form a cycloalkane wherein one or more of the carbons is optionally replaced with a heteroatom,

wherein one or more of the C(R²R³) groups can be replaced with a heteroatom, the method comprising reacting a compound of the formula (R¹)_aR(OH)_b, where a+b>

2, and a and b are, independently, equal to or greater than one, with a lactone in the presence of a suitable acid catalyst, wherein R is an alkyl, aryl, aralkyl, alkaryl, ether or ester group, or substituted versions thereof, and R¹ is an olefin-containing moiety.

24. The method of claim 23, further comprising adding a cross-linking compound selected from the group consisting of melamine and isocyanate.

25. The method of claim 24, wherein the cross-linking compound is added after the reaction of the compound of the formula (R¹)_aR(OH)_b with the lactone.

26. The method of claim 23, further comprising adding one or more additional components, selected from the group consisting of flatting agents, photoinitiators, reactive diluents, hard particles and adhesion promoters to the top coat formulation.

27. The method of claim 26, further comprising adding a cross-linking compound selected from the group consisting of melamine and isocyanate.

28. The method of claim 27, wherein the cross-linking compound is added after the reaction of the compound of the formula (R¹)_aR(OH)_b with the lactone.