Coating composition comprising autoxidisable component

Patent metadata

Field	Value
Publication number	US-8945681-B2
Application number	US-201313864062-A
Country	US
Kind code	B2
Filing date	Apr 16, 2013
Priority date	Mar 31, 2008
Publication date	Feb 3, 2015
Grant date	Feb 3, 2015

Abstract

There is described (pref. non-adhesive) coating compositions (which may be either water or solvent borne) that comprise an autoxidisable vinyl polymer, the autoxidisable polymer having a vinyl polymer backbone 25% to 75% by wt of the autoxidisable polymer; fatty acid residue 25% to 75% by wt of the autoxidisable polymer; T g from −60° C. to +20° C., M w from 3500 to 50000 g/mol; and polydispersity from 2 to 10; the autoxidisable polymer obtained by a process of: (A) polymerising ethylenically unsaturated vinyl monomers comprising: at least one epoxy functional vinyl monomer 15% to 100% by wt total monomers in (A); 0 to 85% of at least one other ethylenically unsaturated vinyl monomer, (preferably other than styrenic monomers) by wt total monomers in (A); (B) reacting the epoxy functional polymer from (A) with fatty acids having an average iodine value from 30 to 250 g I 2 /100 g fatty acid; where composition has: a) a opt. co-solvent content ≦40% by wt of the composition; b) a solids content either ≧30% (aqueous) ≧60% (solvent based) by wt of the composition, the composition as a coating film having a telegraphing value of less than 10 gloss units (difference between an initial smooth gloss minus an initial rough gloss of the film).

First claim

The invention claimed is:

1. A coating composition that comprises an autoxidisable vinyl polymer, said composition being selected from the group consisting of aqueous coating compositions and solvent-based coating compositions, wherein
I) said autoxidisable vinyl polymer has:
i) vinyl polymer backbone in an amount from 25% to 75% by weight of said autoxidisable vinyl polymer;
ii) fatty acid residue in an amount from 25% to 75% by weight of said autoxidisable vinyl polymer;
iii) a T g from −60° C. to +20° C.,
iv) a weight average molecular weight (M w ) from 3,500 to 50,000 g/mol; and
v) a PDi from 2 to 10; wherein

II) said autoxidisable vinyl polymer is obtained by a process comprising the steps of:
(A) polymerising ethylenically unsaturated vinyl monomers comprising:
i) at least one epoxy functional vinyl monomer in an amount from 15% to 100% by weight of the total monomers in step (A); and
ii) at least one other ethylenically unsaturated vinyl monomer in an amount from 0% to 85% by weight of the total monomers in step (A);
to obtain an epoxy functional vinyl polymer, and

(B) reacting said epoxy functional vinyl polymer obtained in step (A) with fatty acids having an average iodine value from 30 to 250 g I 2 /100 g fatty acid; wherein

III) said composition has:
a) optionally a co-solvent content less than or equal to 40% by total weight of said composition;
1) a solids content when aqueous of greater than or equal to 30% by total weight of said aqueous composition; and
2) a solids content when solvent-based of greater than or equal to 60% by total weight of said solvent-based composition; and wherein

IV) said composition when in the form of a film has a telegraphing value of less than 10 gloss units, where the telegraphing value is a difference between an initial smooth gloss value minus an initial rough gloss value of the film, where
the initial smooth gloss value is the gloss when the film is cast on smooth PVC (R z =1 μm [±0.25 μm]);
the initial rough gloss value is the gloss when the film is cast on rough PVC (R z =25 microns [μm] [±5 μm]); and where
the film has a dry film thickness of 52 μm [±6 μm]; and
the initial gloss value is measured at a 20° angle, one day (24 hours) after the film has been cast.

2. A coating composition according to claim 1 , wherein the coating composition is a non-adhesive composition.

3. A coating composition according to claim 1 , wherein the epoxy functional vinyl polymer prepared in step (II)(A) has a M n from 1,500 to 10,000 g/mol.

4. A coating composition according to claim 1 , wherein the epoxy functional vinyl polymer prepared in step (II)(A) comprises 0 to 1% of acid functional vinyl monomers by weight of the epoxy vinyl functional polymer.

5. A coating composition according to claim 1 , wherein the epoxy functional vinyl polymer prepared in step (II)(A) comprises less than 5% of hydroxy functional monomer(s) by weight of the epoxy vinyl functional polymer.

6. A coating composition according to claim 1 , wherein the epoxy functional vinyl polymer prepared in step (II)(A) comprises less than 40% of styrenic monomer(s) by weight of the epoxy vinyl functional polymer.

7. A coating composition according to claim 1 , wherein the fatty acid residue is free of fatty acid glycidyl esters.

8. A coating composition according to claim 1 , wherein the coating composition is an aqueous coating composition.

9. An aqueous coating composition according to claim 8 , comprising no more than 13% N-methylpyrrolidone by weight of the total composition.

10. An aqueous coating composition according to claim 8 , comprising no more than 13% by weight of polymer solids of nitrogen containing molecules with an evaporation rate <0.1, wherein the nitrogen containing molecules are aromatic, heterocyclic or aliphatic primary and secondary di-amines, and wherein the weight % of nitrogen in the nitrogen containing molecules is >5% by weight of the nitrogen containing molecules.

11. A coating composition according to claim 1 , wherein the coating composition is a solvent based coating composition.

12. A process for obtaining a polymer composition that comprises at least one autoxidisable vinyl polymer, wherein:
said autoxidisable vinyl polymer when in the form of a film has a telegraphing value of less than 10 gloss units, where
the telegraphing value is a difference between an initial smooth gloss value minus an initial rough gloss value of the film, where
the initial smooth gloss value is the gloss when the film is cast on smooth PVC (R z =1μm [±0.25 μm]);
the initial rough gloss value is the gloss when the film is cast on rough PVC (R z =25 microns [μm][±5 μm]);and where
the film has a dry film thickness of 52 μm [±6 μm]; and
the initial gloss value is measured at a 20° angle, one day (24 hours) after the film has been cast, wherein

the process comprises the steps of:
I) polymerising ethylenically unsaturated vinyl monomers comprising:
i) at least one epoxy functional vinyl monomer in an amount from 15% to 100% by weight of the total monomers in step I); and
ii) at least one other ethylenically unsaturated vinyl monomer in an amount from 0% to 85% by weight of the total monomers in step I);

to obtain an epoxy functional vinyl polymer; and
II) reacting said epoxy functional vinyl polymer obtained in step I) with fatty acids having an average iodine value from 30 to 250 g I 2 /100 g fatty acid;
where the resultant autoxidisable vinyl polymer has
i) vinyl polymer backbone in an amount from 25% to 75% by weight of said autoxidisable vinyl group containing polymer;
ii) fatty acid residue in an amount from 28% to 75% by weight of said autoxidisable vinyl polymer;
iii) a T g from −60° C. to +20° C.,
iv) a weight average molecular weight (M w ) from 3,500 to 50,000 g/mol; and
v) a PDi from 2 to 10.

13. A polymer obtained by a process as claimed in claim 12 .

14. A coating composition comprising a polymer as claimed in claim 13 .

15. A coated substrate, comprising a substrate, and a coating on the substrate, wherein the coating comprises a coating composition as claimed in claim 1 having a telegraphing value of less than 10 gloss units.

16. A method of coating a substrate comprising the steps of
i) applying a coating composition as claimed in claim 1 to a substrate;
ii) drying the substrate to form a coating thereon; wherein
the coating has a telegraphing value of less than 10 gloss units.

Assignees

• Overbeek Gerardus Cornelis
• Van Casteren Ilse
• Tennebroek Ronald
• Van Der Werf Jelle Bernardus Otto
• Dsm Ip Assets Bv

Inventors

• Overbeek Gerardus Cornelis
• Van Casteren Ilse
• Tennebroek Ronald
• Van Der Werf Jelle Bernardus Otto

Classifications

• C08F2810/30

  leading to the formation or introduction of aliphatic or alicyclic unsaturated groups · CPC title

• C09D133/068

  containing glycidyl groups · CPC title

• C08F8/14

  Esterification · CPC title

• C08F8/44

  Preparation of metal salts or ammonium salts · CPC title

• Y10T428/31855

  Of addition polymer from unsaturated monomers · CPC title