IP Library Granted Patent US 10,328,455
Granted Patent B2
US 10,328,455 · App. 14/858,187 · Granted Jun 25, 2019

One component heat-curable powder coating composition

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Quick Facts
Patent No.
US 10,328,455
App. No.
14/858,187
Granted
Jun 25, 2019
Kind
B2
Abstract

The invention relates to a one component heat-curable powder coating composition comprising a resin containing reactive unsaturations and wherein all said reactive unsaturations are carbon carbon double bonds connected directly to an electron withdrawing group, a thermal initiation system comprising a transition metal catalyst and a peroxide, wherein the peroxide is chosen from the group of peroxyesters, mono-peroxycarbonates and mixtures thereof and a co-crosslinker chosen from the group of vinylethers, vinylesters, vinylamides, itaconates, enamines and mixtures thereof.

Claims (84)

1. A one component heat curable powder coating composition comprising:

(i) a polyester resin containing reactive unsaturations, the polyester resin having a weight per the reactive unsaturations (WPU) as determined using 1H-NMR which is higher than 250 and lower than 1500 g/mole,

(ii) a thermal initiation system comprising (a) a transition metal catalyst and (b) a peroxide, wherein

(a) the transition metal catalyst is selected from the group consisting of transition metal salts, transition metal complexes and mixtures thereof, wherein the transition metal is Mn, Fe, Co or Cu, and wherein

(b) the peroxide is selected from the group consisting of peroxyesters, monoperoxycarbonates and mixtures thereof, and wherein the peroxide is represented by formula (1):

wherein

R 1 , R 2 and R 3 each independently stand for an alkyl, and wherein X stands for R 4 or for OR 4 , wherein R 4 stands for an alkyl, an aryl or for an oligomer or polymer, and wherein

the amount of peroxide is at least 10 mmol peroxide/Kg resin containing reactive unsaturations and co-crosslinker, and

(iii) a co-crosslinker having a weight per unsaturation (WPU) as determined using 1H-NMR higher than 150 and lower than 870 g/mole, said crosslinker being chosen from the group consisting of vinylethers, vinyletherurethanes, vinylesters, vinylamides, itaconates, enamines and mixtures thereof, wherein

all of the reactive unsaturations of the polyester resin are carbon-carbon double bonds connected directly to an electron withdrawing group and are reactive towards radicals generated by the peroxide, and wherein

the thermal initiation system is present in an amount such that when the powder coating composition is applied to a substrate and cured at a temperature of 130° C. for 20 minutes, the resulting coating resists at least 70 acetone double rubs (ADR), wherein each ADR is a back and forward movement over a surface of the coating having a thickness of approximately 60 μm using a cotton cloth drenched in acetone covering a hammer head having a weight of 980 grams and a contact surface area with the coating of 2 cm 2 .

2. The composition according to claim 1 , wherein the resin has a WPU higher than 250 and less than 1150 g/mole.

3. The composition according to claim 1 , wherein the resin has a WPU higher than 500 and less than 1500 g/mole.

4. The composition according to claim 1 , wherein the resin has a WPU higher than 500 and less than 1150 g/mole.

5. The composition according to claim 1 , wherein the co-crosslinker has a WPU higher than 150 and lower than 650 g/mole.

6. The composition according to claim 1 , wherein the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole.

7. The composition according to claim 1 , wherein the resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin.

8. The composition according to claim 1 , wherein the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid.

9. The composition according to claim 1 , wherein the reactive unsaturations of the resin are based on maleic acid, fumaric acid, citraconic acid, itaconic acid, and/or mesaconic acid.

10. The composition according to claim 1 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

11. The composition according to claim 1 , wherein the reactive unsaturations of the resin are based on fumaric acid.

12. The composition according to claim 1 , wherein the peroxide is t-butyl peroxybenzoate, t-butyl peroxy-2-ethyl hexanoate, t-amyl peroxy (2-ethyl) hexanoate or t-butyl peroxy-2-ethylhexyl carbonate.

13. The composition according to claim 1 , wherein the transition metal is a Mn, Fe, or Cu salt or complex.

14. The composition according to claim 1 , wherein the co-crosslinker is chosen from the group of vinylethers, vinylesters and mixtures thereof.

15. The composition according to claim 1 , wherein the co-crosslinker is a vinylether.

16. The composition according to claim 14 , wherein the resin has an acid value of less than 10 mg KOH per g resin.

17. The composition according to claim 15 , wherein the resin has an acid value of less than 10 mg KOH per g resin.

18. The composition according to claim 14 , wherein the resin has an acid value of less than 5 mg KOH per g resin.

19. The composition according to claim 15 , wherein the resin has an acid value of less than 5 mg KOH per g resin.

20. The composition according to claim 1 , wherein the composition further comprises an inhibitor.

21. The composition according to claim 20 , wherein the inhibitor is a hydroquinone or a catechol.

22. The composition according to claim 1 , wherein the resin has a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min.

23. The composition according to claim 1 , wherein the resin has a glass transition temperature of at least 45° C. as measured via DSC at a heating rate of 5° C./min.

24. The composition according to claim 1 , wherein the resin has a glass transition temperature of at least 40 and of at most 65° C. as measured via DSC at a heating rate of 5° C./min.

25. The composition according to claim 1 , wherein the resin has a number average molecular weight in the range of from 1500 to 8000 Da.

26. The composition according to claim 1 , wherein the resin has a number average molecular weight in the range of from 2100 to 4000 Da.

27. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is chosen from the group of vinylethers, vinylesters and mixtures thereof.

28. The composition according to claim 27 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

29. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is chosen from the group of vinylethers, vinylesters and mixtures thereof; and

the composition comprises an inhibitor.

30. The composition according to claim 29 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

31. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is a vinylether.

32. The composition according to claim 31 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

33. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is a vinylether; and

the composition comprises an inhibitor.

34. The composition according to claim 33 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

35. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and an acid value of less than 10 mg KOH per g resin, and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is a vinylether.

36. The composition according to claim 35 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

37. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and an acid value of less than 5 mg KOH per g resin, and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is a vinylether.

38. The composition according to claim 37 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

39. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and an acid value of less than 10 mg KOH per g resin, and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is a vinylether; and

the composition comprises an inhibitor.

40. The composition according to claim 39 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

41. The composition according to claim 1 , wherein

the reactive unsaturations of the resin are based on maleic acid, fumaric acid, itaconic acid, acrylic acid and/or methacrylic acid, said resin has a hydroxyl value in the range of from 0 to 70 mg KOH per g resin and an acid value of less than 5 mg KOH per g resin, and a number average molecular weight in the range of from 1500 to 8000 Da and a glass transition temperature of at least 40° C. as measured via DSC at a heating rate of 5° C./min; and

the co-crosslinker has a WPU higher than 150 and lower than 630 g/mole and said co-crosslinker is a vinylether; and

the composition comprises an inhibitor.

42. The composition according to claim 41 , wherein the reactive unsaturations of the resin are based on fumaric acid and/or maleic acid.

43. A process for the preparation of a powder coating composition according to claim 1 , comprising the steps of:

(a) mixing the components of the powder coating composition to obtain a premix;

(b) heating the premix to obtain an extrudate;

(c) cooling down the extrudate to obtain a solidified extrudate; and

(d) breaking the solidified extrudate into smaller particles to obtain the powder coating composition.

44. A process for coating a substrate comprising the following steps of:

(1) applying a powder coating composition according to claim 1 to a substrate; and

(2) heating the substrate.

45. A substrate that is fully or partially coated with a powder coating composition according to claim 1 .

46. The substrate according to claim 45 , wherein the substrate is a heat-sensitive substrate.

47. The substrate according to claim 46 , wherein the heat-sensitive substrate is wood.

48. The substrate according to claim 46 , wherein the heat-sensitive substrate is plastic.

Assignments (3)
CHANGE OF CORPORATE ADDRESS Recorded Mar 30, 2022
From: COVESTRO (NETHERLANDS) B.V.
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 059546/0570 →
CHANGE OF NAME Recorded Jul 2, 2021
From: MS HOLDING B.V.
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 056756/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2021
From: DSM IP ASSETS B.V.
To: MS HOLDING B.V.
Reel/Frame 056726/0106 →