IP Library Patent Application 11952601
Patent Application
App. No. 11/952,601

SELF-PHOTOINITIATING WATER-DISPERSIBLE ACRYLATE IONOMERS AND SYNTHETIC METHODS

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Patent No.
US None
App. No.
11/952,601
Abstract

The invention detailed herein comprises a family of novel multifunctional acrylate ionomeric resins, which are water-dispersible, and have built-in photoinitiator. The inventive resins are made self-photoinitiating by their reaction with β-keto esters (e.g., acetoacetates), β-diketones (e.g., 2,4-pentanedione), β-keto amides (e.g., acetoacetanilide, acetoacetamide), and/or other β-dicarbonyl compounds that can participate in the Michael addition reaction as “Michael donors.” These water-dispersible resins cure under standard ultraviolet (UV) cure conditions to give tack-free coatings without the addition of traditional photoinitiators. The present invention further relates to the use of these resins in coatings.

Claims (56)

1 . An ionomer comprising:

an ionic, UV-curable Michael resin,

an amount of water; and

a counter-ion wherein the ionic,

wherein the UV-curable Michael resin comprises:

at least one hydroxy-functional Michael resin and

at least one ionic isocyanate-terminated urethane oligomer

wherein said at least one hydroxy-functional Michael resin comprises a β-dicarbonyl monomer, a hydroxy-functional acrylate monomer and a multifunctional acrylate and

wherein said at least one ionic isocyanate-terminated urethane oligomer comprises an isocyanate-reactive hydrophilic monomer, a polyol and at least one multifunctional isocyanate.

2 . The ionomer of claim 1 , further comprising at least one additive selected from the group consisting of pigments, gloss modifiers, flow and leveling agents and other additives as appropriate to formulate coatings, paints, laminates, sealants, adhesives, foundry sand binders, and inks.

3 . A polymerized product comprising the ionomer according to claim 1 , cured with a free radical generator.

4 . The polymerized product, according to claim 3 , wherein said free-radical generator is actinic light.

5 . The polymerized product, according to claim 3 , wherein said free-radical generator is electron beam radiation.

6 . The polymerized product, according to claim 3 , wherein said free-radical generator is a peroxide.

7 . The polymerized product, according to claim 6 , wherein said peroxide is selected from the group consisting of methyl ethyl ketone peroxide (MEKP), tert-butyl perbenzoate (TBPB), cumyl peroxide, and t-butyl peroxide.

8 . The polymerized product, according to claim 3 , further comprising at least one additive selected from the group consisting of pigments, gloss modifiers, flow and leveling agents and other additives as appropriate to formulate coatings, paints, laminates, sealants, adhesives, foundry sand binders, and inks.

9 . A method of utilizing an ionic Michael resin comprising:

providing a substrate;

applying the ionomer of claim 1 to said substrate; and

curing said resin.

10 . The method of using an ionic Michael resin, according to claim 9 , wherein applying comprises a coating method selected from the group consisting of roll-coating, spray-coating, brush-coating, dip-coating, and electrocoating.

11 . A method of fabricating a backbone-ionic, UV-curable ionomer comprising:

providing a resin reactor having a dry atmosphere;

providing a polyol to said reactor;

providing an isocyanate-reactive, hydrophilic monomer to said reactor;

providing a urethanation catalyst to said reactor;

providing a polyisocyanate to said reactor;

maintaining a reaction mixture at a reaction-effective temperature; and

providing a hydroxy-functional, multifunctional acrylate Michael oligomer.

12 . The method of fabricating a backbone-ionic, UV-curable ionomer, according to claim 11 , wherein a preferred isocyanate-reactive, hydrophilic monomer is dimethylolpropionic acid.

13 . The method of fabricating a backbone-ionic, UV-curable ionomer, according to claim 11 , wherein said urethanation catalyst is selected from the group consisting of dibutyltin dilaurate, tin(II) octoate, and diazabicyclo[2.2.2]octane.

14 . The method of fabricating a backbone-ionic, UV-curable ionomer, according to claim 11 , wherein providing a hydroxy-functional, multifunctional acrylate d Michael oligomer comprises:

providing a resin reactor;

providing a polyol multifunctional acrylate monomer to said reactor;

providing a hydroxyacrylate monomer to said reactor;

providing a β-dicarbonyl monomer to said reactor; and

providing a Michael addition catalyst.

15 . The method of fabricating a backbone-ionic, UV-curable ionomer, according to claim 14 , wherein said Michael addition catalyst is a strong base that is readily soluble in the monomer mixtures.

16 . The method of fabricating a backbone-ionic, UV-curable ionomer, according to claim 14 , wherein said Michael addition catalyst is selected from the group consisting of diazabicycloundecene, diazabicyclononene, 1,1,3,3-tetramethyl guanidine, Group I alkoxide bases, quaternary hydroxides and alkoxides, and organophilic alkoxide bases generated in situ from the reaction between a halide anion and an epoxide moiety.

17 . The method of fabricating a backbone-ionic, UV-curable ionomer, according to claim 11 , further comprising:

adding an amount of water; and optionally

adding a counter-ion.

18 . The method of fabricating a backbone-ionic, UV-curable ionomer, according to claim 17 , further comprising adding at least one additive selected from the group consisting of pigments, gloss modifiers, flow and leveling agents and other additives as appropriate to formulate coatings, paints, laminates, sealants, adhesives, foundry sand binders, and inks.

19 . A method of fabricating a pendant-ionic, UV-curable ionomer comprising:

providing a resin reactor having a dry atmosphere;

providing a β-dicarbonyl;

providing a multifunctional acrylate;

providing a Michael addition catalyst; and

maintaining a reaction-effective temperature.

20 . The method of fabricating a pendant-ionic, UV-curable ionomer, according to claim 19 further comprising:

adding an amount of water; and optionally

adding a counter-ion.

21 . The method of fabricating a pendant-ionic, UV-curable ionomer, according to claim 19 further comprising adding at least one additive selected from the group consisting of pigments, gloss modifiers, flow and leveling agents and other additives as appropriate to formulate coatings, paints, laminates, sealants, adhesives, foundry sand binders, and inks.

22 . An oligomerized pendant-ionic, multifunctional acrylate Michael resin comprising:

at least two equivalents of a pendant-ionic multifunctional acrylate Michael resin; and

a primary amine, wherein said amine is disubstituted with said resin.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Apr 13, 2010
From: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
To: ASHLAND LICENSING AND INTELLECTUAL PROPERTY LLC; AQUALON COMPANY; HERCULES INCORPORATED
Reel/Frame 024218/0928 →
SECURITY AGREEMENT Recorded Dec 3, 2008
From: ASHLAND LICENSING AND INTELLECTUAL PROPERTY...; AQUALON COMPANY; HERCULES INCORPORATED
To: BANK OF AMERICA, N.A. AS ADMINISTRATIVE AGENT
Reel/Frame 021924/0001 →