IP Library Granted Patent US 10,167,359
Granted Patent B2
US 10,167,359 · App. 15/532,637 · Granted Jan 1, 2019

Radiation curing coating composition

Inventors: Vanessa Maurin (Perstorp, SE); Paul Kelly (Sale, GB)
Assignee: PERSTORP AB
C08G18/4277C08F220/18C08G18/0842C08G18/10C08G18/4825C08G18/4833C08G18/4887C08G18/6755C08G18/755C08G18/8175C09D4/00C09D133/14C09D175/16
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Quick Facts
Patent No.
US 10,167,359
App. No.
15/532,637
Granted
Jan 1, 2019
Kind
B2
Abstract

Disclosed is a UV-curing coating composition comprising (a) 40-70% by weight of at least one urethane (meth)acrylate being a product of a reaction between at least one polycaprolactone polyol (a1) and at least one adduct (a2), said adduct (a2) being a product of a reaction between at least one polyisocyanate (a3) and at least one hydroxyalkyl (meth)acrylate (a4), said polycaprolactone polyol (a1) being a product of a reaction between at least one polyalkoxylated polyol (a5) and at least one caprolactone monomer (a6), (b) 20-50% by weight of at least one reactive diluent having at least one olefinic carbon-carbon double bond, and (c) 0.5-10% by weight of at least one photoinitiator, and optionally (d) 1-15% by weight of at least one matting agent.

Claims (24)

1. A coating composition characterised in, that said coating composition is a UV-curing coating composition comprising:

(a) 40-70% by weight of at least one urethane (meth)acrylate being a product of a reaction between at least one polycaprolactone polyol (a1) and at least one adduct (a2), said adduct (a2) being a product of a reaction between at least one polyisocyanate (a3) and at least one hydroxyalkyl (meth)acrylate (a4), and said polycaprolactone polyol (a1) being a product of a reaction between at least one polyalkoxylated polyol (a5) and at least one caprolactone monomer (a6),

(b) 20-50% by weight of at least one reactive diluent having at least one olefinic carbon-carbon double bond, and

(c) 0.5-10% by weight of at least one photoinitiator.

2. The coating composition according to claim 1 characterised in, that it additionally comprises:

(d) 1-15% by weight, calculated on subtotal of said components (a) to (c), of at least one matting agent.

3. The coating composition according to claim 2 characterised in, that said matting agent (d) is a haptic matting agent.

4. The coating composition according to claim 2 characterised in, that said matting agent (d) is a polyamide, a micronised biopolymer, a synthetic amorphous and optionally surface treated silica, a corpuscular crypto-cristalline amorphous silica, lamellar kaolin and/or an inorganically modified polyethylene wax dispersion.

5. The coating composition according to claim 1 characterised in, that said polycaprolactone polyol (a1) has 2-10 caprolactone units/molecule.

6. The coating composition according to claim 1 characterised in, that said polycaprolactone polyol (a1) has a glass transition temperature (Tg) of less than −40° C.

7. The coating composition according claim 1 characterised in, that said polycaprolactone polyol (a1) has a molecular weight (Mw) of 1000-6000 g/mol.

8. The coating composition according to claim 1 characterised in, that said adduct (a2) is obtained at a molar ratio polyisocyanate (a3) to hydroxyalkyl (meth)acrylate (a4) of between 1 to 0.8 and 1 to 1.

9. The coating composition according to claim 1 characterised in, that said polyisocyanate (a3) is an aliphatic or cycloaliphatic di or triisocyanate and/or a a NCO-functional dimer, trimer or polymer thereof or therewith.

10. The coating composition according to claim 1 characterised in, that said polyisocyanate (a3) is hexamethylene diisocyanate, isophorone diisocyanate, dicyclohexyl methane diisocyanate, tetrahydrofuran diisocyanate, cyclohexylene diisocyanate and/or nonane triisocyanate, and/or a NCO-functional dimer, trimer or polymer thereof or therewith.

11. The coating composition according to claim 1 characterised in, that said hydroxyalkyl (meth)acrylate (a4) is hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, trimethylolethane di(meth)acrylate, trimethylolpropane di(meth)acrylate, trimethylolbutane di(meth)acrylate and/or pentaerythritol tri(meth)acrylate.

12. The coating composition according to claim 1 characterised in, that said polyalkoxylated polyol (a5) is a polyethoxylated, polypropoxylated and/or polybutoxylated diol or triol having 1-30 ethoxy, propoxy and/or butoxy units/molecule.

13. The coating composition according to claim 1 characterised in, that said polyalkoxylated polyol (a5) is a polyethoxylated and/or polypropoxylated neopentyl glycol, glycerol, trimethylolethane, trimethylolpropane or trimethylolbutane.

14. The coating composition according to claim 1 characterised in, that said caprolactone monomer (a6) is ε-caprolactone.

15. The coating composition according to claim 1 characterised in, that said reactive diluent (b) is at least one alkyl (meth)acrylate, vinyl (meth)acrylate, (meth)allyl (meth)acrylate, polyester (meth)acrylate, epoxy (meth)acrylate, urethane (meth)acrylate and/or melamine (meth)acrylate.

16. The coating composition according to claim 1 characterised in, that said reactive diluent (b) is isobornyl (meth)acrylate, dipropylene glycol di(meth)acrylate, tripropyleneglycol di(meth)acrylate, hexanediol di(meth)acrylate and/or trimethylolpropane tri(meth)acrylate.

17. The coating composition according to claim 1 characterised in, that said photoinitiator (c) is a benzoin ether, an acylphosphine, an acetophenone, an aminoalkyl phenone, a benzophenone and/or an antraquinone.

18. The coating composition according to claim 1 characterised in, that it additionally comprises at least one pigment, filler and/or dye.

19. The coating composition according to claim 1 characterised in, that it additionally comprises at least one UV-stabiliser, flow/levelling agent, rheological agent, inhibitor and/or UV-absorber.

20. A method for obtaining a decorative and/or protective topcoat comprising applying a coating composition of claim 1 to a substrate.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2019
From: PERSTORP AB
To: PERSTORP UK LTD
Reel/Frame 049601/0396 →
CHANGE OF NAME Recorded Jun 26, 2019
From: PERSTORP UK LTD
To: INGEVITY UK LTD
Reel/Frame 049601/0464 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 29, 2018
From: MAURIN, VANESSA; KELLY, PAUL
To: PERSTORP AB
Reel/Frame 044755/0216 →
Priority Claims (1)
SE 1400571 · Dec 4, 2014 · national
Continuity (1)
Related Publication 20170355807A1 · Dec 14, 2017