Composition for painting/coating applications containing a particular acrylate copolymer dispersant
US-2024254338-A1 · Aug 1, 2024 · US
US9309438B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9309438-B2 |
| Application number | US-201214004756-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 30, 2012 |
| Priority date | Apr 5, 2011 |
| Publication date | Apr 12, 2016 |
| Grant date | Apr 12, 2016 |
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The present invention relates to a radiation curable composition comprising at least one (meth)acrylated compound compound (A); and at least one inert polyester (B) that is prepared from a (i) polyol component comprising at least one cyclic ether polyol and (ii) from a polyacid component. The present invention further relates to their preparation and uses.
Opening claim text (preview).
The invention claimed is: 1. A radiation curable composition comprising at least one (meth)acrylated compound (A); and at least one inert OH-terminated polyester (B) that is prepared from a polyol component comprising at least one cyclic ether polyol and from a polyacid component, wherein said inert OH-terminated polyester (B) has a hydroxyl value of between 30 and 150 mg KOH/g. 2. The composition of claim 1 , wherein said polyol component comprises from 5 to 100 wt % of cyclic ether polyols. 3. The composition of claim 1 , wherein said polyol component comprises isosorbide as well as one or more of: as ethylene glycol, diethylene glycol and/or hydrogenated bisphenol A, and optionally neopentylgycol; and wherein the polyacid component comprises phthalic acid and/or phthalic anhydride. 4. The composition of claim 1 , wherein the inert OH-terminated polyester (B) is further prepared from one or more mono-carboxylic compounds. 5. The composition of claim 4 , wherein said mono-carboxylic compounds are selected from one or more of 2-(4-chlorobenzoyl) benzoic acid, o-benzoylbenzoic acid, 2-(4-phenylbenzoyl)benzoic acid, benzoic acid and substituted benzoic acid. 6. The composition of claim 4 , wherein the hydroxyl value of the inert OH-terminated polyester (B) is between 30 and 120 mg KOH/g. 7. The composition of claim 1 , comprising at least one inert OH-terminated polyester (B) that is prepared from a polyol component comprising at least one cyclic ether polyol and from a polyacid component, and at least one inert OH-terminated polyester (B) that is prepared from one or more mono-carboxylic compounds. 8. The composition of claim 1 , wherein the inert OH-terminated polyester (B) has a number average molecular weight of between 500 and 5000 Daltons. 9. The composition of claim 1 , wherein the (meth)acrylated compound (A) is a reactive diluent selected from di(meth)acrylates and/or tri(meth)acrylates. 10. The composition of claim 1 comprising at least 15% by weight of inert resins based upon the total weight of the composition, wherein the inert resins comprise the at least one inert OH-terminated polyester (B) and, optionally, other inert resins (C) that are different from the at least one inert OH-terminated polyester (B). 11. A coating composition, ink or varnish prepared from a composition according to claim 1 . 12. An article coated, partially or entirely, with a composition according to claim 11 . 13. A method comprising applying the composition according to claim 1 as a primer on metal or plastic and/or as an adhesion promoter for inks on a plastic. 14. A method comprising applying the inert OH-terminated polyester (B) of claim 1 as a primer on metal or plastic and/or as an adhesion promoter for inks on a plastic.
Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing · CPC title
Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain (based on polyester-amides C09D177/12; based on polyester-imides C09D179/08); Coating compositions based on derivatives of such polymers · CPC title
Photosensitive materials (G03F7/12, G03F7/14 take precedence) · CPC title
Processes for applying liquids or other fluent materials (B05D5/00, B05D7/00 take precedence) · CPC title
Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds (G03F7/075 takes precedence) · CPC title
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