IP Library Granted Patent US 9,266,987
Granted Patent B2
US 9,266,987 · App. 11/919,945 · Granted Feb 23, 2016

Method of making low extractable coatings using radiation curable compositions containing aminoacrylates

Inventors: Vincent Stone (Brussels, BE); Francis Bergiers (La Hulpe, BE); Thierry Randoux (Braine l'Alleud, BE); Christian Lucot (Limas, FR)
Assignee: ALLNEX BELGIUM S.A.
C08F220/34C09D133/14
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Quick Facts
Patent No.
US 9,266,987
App. No.
11/919,945
Granted
Feb 23, 2016
Kind
B2
Abstract

A method of making low extractable coatings, varnishes, adhesives or inks comprising the steps of: (a) providing a radiation curable composition, (b) applying said composition onto a surface, and (c) irradiating the surface with actinic radiation or electron beam, wherein the radiation curable composition comprises at least one amino(meth)acrylate obtained by reacting at least one primary and/or secondary amine (A) with at least one (meth)acrylated ethoxylated polyol (B) having a degree of alkoxylation of at least 4.

Claims (36)

1. A method of making a low extractable coating, which comprises:

(a) providing a radiation curable composition comprising:

at least one amino(meth)acrylate,

wherein the amino(meth)acrylate is produced by a method consisting essentially of

reacting at least one primary or secondary amine (A) with at least one (meth)acrylated ethoxylated and propoxylated polyol (B) having a degree of alkoxylation of at least 4 and at least 3 (meth)acrylic groups,

wherein the polyol (B) is a (meth)acrylated ethoxylated and propoxylated polyol having a molar ratio of propoxyl to ethoxyl units of 1:4,

(b) applying said composition onto a surface,

(c) irradiating the surface with actinic radiation or electron beam radiation, and

(d) obtaining the low extractable coating.

2. The method according to claim 1 , wherein the polyol (B) is selected from ethoxylated and propoxylated glycerol tri(meth)acrylates, ethoxylated and propoxylated trimethylolpropane tri(meth)acrylates or ethoxylated and propoxylated pentaerythritol tetra(meth)acrylates.

3. The method according to claim 1 , wherein the polyol (B) is selected from the tetra(meth)acrylates of ethoxylated and propoxylated pentaerythritol having a degree of alkoxylation of 5 to 15.

4. The method according to claim 1 , wherein the amine (A) corresponds to formula (I)

wherein R 1 is an alkyl, optionally substituted by hydroxy, alkoxy, tertiary amine and/or aryl, and, R 2 is hydrogen or an alkyl, optionally substituted by hydroxy, alkoxy, tertiary amine and/or aryl, with the proviso that R 1 and R 2 may be linked together in order to form a ring.

5. The method according to claim 1 , wherein the amine (A) is selected from alkylamines and dialkylamines, wherein the alkyl groups, each independently, comprise from 1 to 12 carbon atoms, optionally substituted by a hydroxy.

6. The method according to claim 1 , wherein the radiation curable composition comprises from 5 to 99% by weight of the amino(meth)acrylate.

7. The method according to claim 1 , wherein the composition further comprises from 1 to 95% by weight of a (meth)acrylated ethoxylated and/or propoxylated polyol (B) having a degree of alkoxylation of at least 4.

8. The method according to claim 1 , wherein the low extractable coating is a low extractable varnish, adhesive or ink.

9. The method according to claim 1 , wherein the amount of the at least one primary or secondary amine (A) is less than 500 ppm after the reaction of the at least one primary or secondary amine (A) with at least one (meth)acrylated ethoxylated and propoxylated polyol (B) having a degree of alkoxylation of at least 4 and at least 3 (meth)acrylic groups is complete.

10. The method according to claim 1 , wherein the amount of the at least one primary or secondary amine (A) is less than 200 ppm after the reaction of the at least one primary or secondary amine (A) with at least one (meth)acrylated ethoxylated and propoxylated polyol (B) having a degree of alkoxylation of at least 4 and at least 3 (meth)acrylic groups is complete.

11. The method according to claim 1 , wherein the at least one primary or secondary amine (A) is stripped from the reaction product of the at least one primary or secondary amine (A) with at least one (meth)acrylated ethoxylated and propoxylated polyol (B) having a degree of alkoxylation of at least 4 and at least 3 (meth)acrylic groups.

12. The method according to claim 1 , wherein the low extractable coating is suitable to be used for food packaging applications.

13. A method of making a low extractable coating, which comprises:

(a) providing a radiation curable composition comprising:

at least one amino(meth)acrylate and from 1 to 95% by weight of a (meth)acrylated ethoxylated and propoxylated polyol (B) having a degree of alkoxylation of at least 4,

wherein the amino(meth)acrylate is produced by a method consisting essentially of

reacting at least one primary or secondary amine (A) with at least one (meth)acrylated ethoxylated and propoxylated polyol (B),

wherein the amine (A) is selected from the group consisting of methylamine, ethylamine, propylamine, butylamine, hexylamine, 2-ethylhexylamine, cyclohexylamine, dimethylamine, diethylamine, dipropylamine, dibutylamine, ethanolamine and mixtures thereof,

wherein the polyols (B) are tetra(meth)acrylates of ethoxylated and propoxylated pentaerythritol having a degree of alkoxylation of 5 to 15, wherein a molar ratio of propoxyl toethoxyl units of 1:4, and wherein the molar ratio of amino groups of (A) to (meth)acrylic double bonds of (B) is 0.01:1 to 0.5:1

(b) applying said composition onto a surface,

(c) irradiating the surface with actinic radiation or electron beam radiation, and

(d) obtaining the low extractable coating.

14. The method according to claim 13 , wherein the amine (A) is selected from the group consisting of diethylamine, dipropylamine, butylamine, and ethanolamine.

15. The method according to claim 1 , wherein the amine (A) is selected from the group consisting of methylamine, ethylamine, propylamine, butylamine, hexylamine, 2-ethylhexylamine, cyclohexylamine, dimethylamine, diethylamine, dipropylamine, dibutylamine, ethanolamine and mixtures thereof.

16. The method according to claim 15 , wherein the amine (A) is selected from the group consisting of diethylamine, dipropylamine, butylamine, and ethanolamine.

17. The method according to claim 1 , wherein the molar ratio of amino groups of (A) to (meth)acrylic double bonds of (B) is 0.01:1 to 0.5:1.

18. The method according to claim 1 , wherein the amount of the at least one primary or secondary amine (A) is less than 1000 ppm after the reaction of the at least one primary or secondary amine (A) with at least one (meth)acrylated ethoxylated and propoxylated polyol (B) having a degree of alkoxylation of at least 4 and at least 3 (meth)acrylic groups is complete.

Assignments (4)
CHANGE OF ADDRESS OF ASSIGNEE Recorded Sep 21, 2017
From: ALLNEX BELGIUM S.A.
To: ALLNEX BELGIUM S.A.
Reel/Frame 044168/0952 →
CORRECTIVE ASSIGNMENT TO CORRECT THE OWNER NAME PREVIOUSLY RECORDED ON REEL 031970 FRAME 0134. ASSIGNOR(S) HEREBY CONFIRMS THE OWNER NAME SHOULD BE ALLNEX BELGIUM S.A. AND NOT ALLNEX BELGIUM SA. WITHOUT THE PERIOD BETWEEN SA.. Recorded May 22, 2014
From: CYTEC SURFACE SPECIALTIES S.A.
To: ALLNEX BELGIUM S.A.
Reel/Frame 032983/0488 →
CHANGE OF NAME Recorded Jan 13, 2014
From: CYTEC SURFACE SPECIALTIES S.A.
To: ALLNEX BELGIUM SA.
Reel/Frame 031970/0134 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2007
From: STONE, VINCENT; BERGIERS, FRANCIS; RANDOUX, THIERRY; LUCOT, CHRISTIAN
To: CYTEC SURFACE SPECIALTIES, S.A.
Reel/Frame 020315/0276 →
Priority Claims (1)
EP 05012507 · Jun 10, 2005 · regional
Continuity (1)
Related Publication 20090098304A1 · Apr 16, 2009