IP Library Granted Patent US 6,906,136
Granted Patent B2
US 6,906,136 · App. 10/420,680 · Granted Jun 14, 2005

UV-curable compositions

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Quick Facts
Patent No.
US 6,906,136
App. No.
10/420,680
Granted
Jun 14, 2005
Kind
B2
Abstract

A UV-curable composition is disclosed. The composition comprises a crosslinking agent, a hydroxyalkyl acrylate or methacrylate, and an acrylic polyol. The crosslinking agent is selected from the group consisting of multifunctional isocyanates, melamines, and silanes. The acrylic polyol comprises recurring units of an allylic alcohol. The composition can be irradiated to be solidified and then fully cured by the urethane, melamine, or silane reactions. Alternatively, the composition can be cured by the urethane, melamine, or silane reactions, and then fully cured by radiation. The invention provides low VOC but high performance coatings. More importantly, the invention provides a UV-curable system without the need for acrylated oligomers.

Claims (27)

1. A UV-curable composition comprising

(a) a crosslinking agent selected from the group consisting of multifunctional isocyanates, melamines, and silanes;

(b) a hydroxyalkyl acrylate or hydroxyalkyl methacrylate; and

(c) an acrylic polyol comprising recurring units of an allylic alcohol.

2. The composition of claim 1 wherein the crosslinking agent is a multifunctional isocyanate.

3. The composition of claim 2 wherein the multifunctional isocyanate is selected from the group consisting of toluene diisocyanate (TDI), polymeric TDI, diphenylmethane diisocyanate (MDI), polymeric MDI, 1,6-hexamethylene diisocyanate (HDI), polymeric HDI, isophorone diisocyanate (IPDI), polymeric IPDI, dicyclohexylmethane diisocyanate (H 12 MDI), and polymeric H 12 MDI, and mixtures thereof.

4. The composition of claim 2 wherein the crosslinking agent is a multifunctional isocyanate selected from the group consisting of HDI, polymeric HDI, IPDI, polymeric IPDI, H 12 MDI, and polymeric H 12 MDI.

5. The composition of claim 1 wherein the crosslinking agent is a melamine.

6. The composition of claim 1 wherein the crosslinking agent is a silane.

7. The composition of claim 1 wherein the hydroxyalkyl acrylate or hydroxyalkyl methacrylate is selected from the group consisting of hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, hydroxypropyl methacrylate, hydroxybutyl acrylate, hydroxybutyl methacrylate, caprolactone acrylate, caprolactone methacrylate, and mixtures thereof.

8. The composition of claim 1 wherein the acrylic polyol is a polyol blend comprising a liquid acrylic polyol and a resinous polyol in a ratio within the range of 10/90 to 90/10 by weight; wherein the liquid acrylic polyol has Mn within the range of about 500 to about 10,000, hydroxyl number within the range of about 20 mg KOH/g to about 500 mg KOH/g, and a glass transition temperature (T g ) within the range of about −70° C. to about 0° C.; and the resinous polyol has Mn within the range of about 500 to about 10,000, hydroxyl number within the range of about 20 mg KOH/g to about 500 mg KOH/g, and T g greater than about 25° C.

9. The composition of claim 8 wherein the liquid acrylic polyol comprises:

(a) from about 2% to about 60% by weight of recurring units of a hydroxy-functional monomer selected from the group consisting of allyl and methallyl alcohols, alkoxylated allyl and methallyl alcohols;

(b) from about 40% to about 98% by weight of recurring units of a C 1 to C 20 alkyl acrylate or methacrylate whose homopolymer has a T g below about 25° C.; and

(c) optionally, up to about 25% by weight of recurring units of a third monomer that is selected from the group consisting of vinyl aromatics, vinyl halides, vinyl ethers, vinyl esters, acrylic and methacrylic acids, unsaturated nitriles, conjugated dienes, and mixtures thereof.

10. The composition of claim 8 wherein the resinous polyol comprises:

(a) from about 2% to about 60% by weight of recurring units of a hydroxyl functional monomer selected from the group consisting of allyl and methallyl alcohols, alkoxylated allyl and methallyl alcohols;

(b) from about 40% to about 98% by weight of recurring units of a monomer selected from the group consisting of vinyl aromatics, and C 1 to C 20 alkyl, aryl, and cyclic acrylates and methacrylates whose homopolymers have a T g greater than or equal to 25° C.; and

(c) optionally, up to about 25% by weight of recurring units of a third monomer selected from the group consisting of vinyl halides, vinyl ethers, vinyl esters, acrylic and methacrylic acids, conjugated dienes, and mixtures thereof.

11. The composition of claim 8 wherein the liquid acrylic polyol is a copolymer of n-butyl acrylate and an allylic alcohol selected from the group consisting of allyl and methallyl alcohols, ethoxylated allyl and methallyl alcohols of 1 to 5 oxyethylene units, propoxylated allyl and methallyl alcohols of 1 to 5 oxypropylene units, and mixtures thereof.

12. The composition of claim 8 wherein the liquid acrylic polyol is a copolymer of n-butyl acrylate and allyl propoxylate of 1 to 5 oxypropylene units.

13. The composition of claim 8 wherein the resinous polyol is a copolymer of styrene and an allylic alcohol selected from the group consisting of allyl alcohol, ethoxylated allyl alcohols of 1 to 5 oxyethylene units, propoxylated allyl alcohols of 1 to 5 oxypropylene units, and mixtures thereof.

14. The composition of claim 8 wherein the resinous polyol is a copolymer of styrene and allyl alcohol.

15. The composition of 8 wherein the resinous polyol is a copolymer of styrene, isobornyl methacrylate, and allyl propoxylate.

16. The composition of claim 1 further comprising a reactive diluent selected from the group consisting of acrylates, methacrylates, and vinyl ethers.

17. The composition of claim 1 wherein the composition is packaged into AB two separate parts, wherein part A comprises the crosslinking agent and part B comprises the hydroxyalkyl acrylate or hydroxyalkyl methacrylate and the acrylic polyol.

18. The composition of claim 1 containing no VOC.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0705 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0856 →
SECURITY AGREEMENT Recorded Aug 4, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; BASELL POLYOLEFIN GMBH; LYONDELL CHEMICAL COMPANY; EQUISTAR CHEMICALS, L.P.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 021354/0708 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AND PATENT APPLICATIONS Recorded Mar 26, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; EQUISTAR CHEMICALS. LP.; LYONDELL CHEMICAL COMPANY; LYONDELL CHEMICAL TECHNOLOGY, L.P.; LYONDELL PETROCHEMICAL COMPANY; NATIONAL DISTILLERS AND CHEMICAL CORPORATION; OCCIDENTAL CHEMICAL CORPORATION; OLIN CORPORATION; QUANTUM CHEMICAL CORPORATION; BASELL POLYOLEFIN GMBH
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 020704/0562 →
RELEASE OF LYONDELL CHEMICAL TECHNOLOGY, L.P. PATENT SECURITY AGREEMENT Recorded Mar 20, 2008
From: JPMORGAN CHASE BANK, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 020679/0063 →
SECURITY AGREEMENT Recorded Sep 15, 2006
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: JPMORGAN CHASE BANK N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 018260/0306 →