Radiation curable acrylated polyurethane oligomer compositions

• US 4,607,084 A
• Filed: 12/16/1985
• Issued: 08/19/1986
• Est. Priority Date: 06/11/1984
• Status: Expired due to Fees

• Current Assignee: Rhodia Incorporated
• Original Assignee: Celanese Specialty Resins Incorporated
• Inventors: Morris, deceased, William J.
• Primary Examiner(s): WELSH JR, MAURICE
• Application Number:
  US06/809,450
• Time in Patent Office: 246 Days
• Field of Search: 525/454
• US Class Current: 525/454
• CPC Class Codes: C08G 18/48 Polyethers
• CPC Class Codes: C08G 18/4812 Mixtures of polyetherdiols with polyetherpolyols having at least three hydroxy groups
• CPC Class Codes: C08G 18/672 Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
• CPC Class Codes: C08G 18/73 acyclic
• CPC Class Codes: C08G 18/75 cycloaliphatic
• CPC Class Codes: C08G 18/758 containing two or more cycloaliphatic rings
• CPC Class Codes: C08G 18/8141 masked
• CPC Class Codes: C08G 18/8175 with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
• CPC Class Codes: C08L 75/04 Polyurethanes
• CPC Class Codes: C09D 175/16 having terminal carbon-to-carbon unsaturated bonds

Abstract

Radiation cured compositions having improved abrasion resistance and cure response are made from blends of the reaction product of a diisocyanate, a hydroxyalkyl acrylate and a polyether diol with the reaction product of a diisocyanate, a hydroxyalkyl acrylate and a polyether triol wherein the average acrylate functionality of the blends is from about 2.4 to about 2.6. Such cured compositions are useful as coatings for various substrates.

Claims

1. A radiation curable composition which comprises acrylated polyurethane oligomers which are the reaction product of

(a) an organic diisocyanate,

(b) a polyether diol, and

(c) a hydroxyalkyl acrylate or methacrylate blended with the reaction product of

(d) an organic diisocyanate,

(e) a polyether triol, and

(f) a hydroxyalkyl acrylate or methacrylate

wherein the organic diisocyanate, (a) and (d), is an aliphatic or cycloaliphatic diisocyanate;

wherein the polyether diol, (b), is a dihydroxy terminated polyalkylene oxide which contains 2 to 4 carbon atoms in each alkylene group and which has a molecular weight of about 800 to about 2000;

wherein the polyether triol, (e), is a trihydroxy terminated polyalkylene oxide which contains 2 to 3 carbon atoms in each alkylene group and which has a molecular weight of about 300 to about 750;

wherein the alkyl group of the hydroxyalkyl acrylate or methacrylate contains 2 or 3 carbon atoms;

wherein (b) and (e) are in such molar ratios that the resultant composition has an average acrylate or methacrylate functionality of about 2.4 to about 2.6;

wherein 1 mole of diisocyanate is reacted per hydroxyl group of the polyether diol and triol; and

wherein 1 mole of hydroxyalkyl acrylate or methacrylate is reacted per mole of diisocyanate.

2. The composition of claim 1 wherein the polyether diol and the polyether triol are preblended in a molar ratio of 0.9:

1 to 1.1;

1 and the reactions of the diisocyanate and the hydroxyalkyl acrylate or methacrylate are conducted with the blend.

3. The composition of claim 1 wherein the average acrylate or methacrylate functionality is 2.5.

4. The composition of claim 2 wherein the polyether diol and the polyether triol are preblended in a molar ratio of 1:

1.

5. The composition of claim 1 wherein the diisocyanate is 4,4'"'"'-methylene-bis(cyclohexylisocyanate).

6. The composition of claim 1 wherein the diisocyanate is isophorone diisocyanate.

7. The composition of claim 1 wherein the polyether diol is a dihydroxy terminated polyalkylene oxide which contains 4 carbon atoms in each alkylene group.

8. The composition of claim 7 wherein the polyether diol is derived from tetrahydrofuran.

9. The composition of claim 1 wherein the polyether triol has a molecular weight of about 400 and the polyether diol has a molecular weight of about 1000.

10. The composition of claim 1 wherein the hydroxyalkyl acrylate is hydroxyethyl acrylate.

11. The composition of claim 1 wherein the hydroxyalkyl acrylate is hydroxypropyl acrylate.

12. A method for providing improved abrasion resistance and cure response to radiation cured compositions which comprises using as the radiation curable composition the reaction product of

(a) an organic diisocyanate,

(b) a polyether diol, and

(c) a hydroxyalkyl acrylate or methacrylate blended with the reaction product of

(d) an organic diisocyanate,

(e) a polyether triol, and

(f) a hydroxyalkyl acrylate or methacrylate

wherein the organic diisocyanate, (a) and (d), is an aliphatic or cycloaliphatic diisocyanate;

wherein the polyether diol, (b), is a dihydroxy terminated polyalkylene oxide which contains 2 to 4 carbon atoms in each alkylene group and which has a molecular weight of about 800 to about 2000;

wherein the polyether triol, (e), is a trihydroxy terminated polyalkylene oxide which contains 2 to 3 carbon atoms in each alkylene group and which has a molecular weight of about 300 to about 750;

wherein the alkyl group of the hydroxyalkyl acrylate or methacrylate contains 2 or 3 carbon atoms;

wherein (b) and (e) are in such molar ratios that the resultant composition has an average acrylate or methacrylate functionality of about 2.4 to about 2.6;

wherein 1 mole of diisocyanate is reacted per hydroxyl group of the polyether diol and triol; and

wherein 1 mole of hydroxyalkyl acrylate or methacrylate is reacted per mole of diisocyanate.

13. The method of claim 12 wherein the polyether diol and the polyether triol are preblended in a molar ratio of 0.9:

1 to 1.1;

1 and the reactions of the diisocyanate and the hydroxyalkyl acrylate or methacrylate are conducted with the blend.

14. The method of claim 12 wherein the average acrylate or methacrylate functionality is 2.5.

15. The method of claim 13 wherein the polyether diol and the polyether triol are preblended in a molar ratio of 1:

1.

16. The method of claim 12 wherein the diisocyanate is 4,4'"'"'-methylene-bis(cyclohexylisocyanate).

17. The method of claim 12 wherein the diisocyanate is isophorone diisocyanate.

18. The method claim 12 wherein the polyether diol is a dihydroxy terminated polyalkylene oxide which contains 4 carbon atoms in each alkylene group.

19. The method of claim 18 wherein the polyether diol is derived from tetrahydrofuran.

20. The method of claim 12 wherein the polyether triol has a molecular weight of about 400 and the polyether diol has a molecular weight of about 1000.

21. The method of claim 12 wherein the hydroxyalkyl acrylate is hydroxyethyl acrylate.

22. The method of claim 12 wherein the hydroxyalkyl acrylate is hydroxypropyl acrylate.