Blocked polyisocyanates curing free from elimination products for dualcure systems

• US 8,957,176 B2
• Filed: 09/02/2005
• Issued: 02/17/2015
• Est. Priority Date: 09/08/2004
• Status: Active Grant

• Current Assignee: Allnex Netherlands B.V. (Allnex (Luxembourg) & Cy SCA)
• Original Assignee: Allnex IP SARL
• Inventors: Weikard, Jan, Fischer, Wolfgang, Fcke, Thomas
• Primary Examiner(s): SERGENT, RABON A
• Application Number:
  US11/219,395
• Publication Number:
  US 20060052573A1
• Time in Patent Office: 3,455 Days
• Field of Search: 525/126, 525/440.02, 522/90, 428/424.2, 528/45, 528/75, 528/73, 540/202, 544/67, 544/222, 548/951, 548/952, 560/115, 560/157, 560/158, 564/38, 564/44
• US Class Current: 528/45
• CPC Class Codes: C08G 18/8175 with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
• CPC Class Codes: C09D 175/16 having terminal carbon-to-carbon unsaturated bonds

Abstract

The invention provides innovative blocked polyisocyanates whose crosslinking is initiated thermally and photochemically. The polyisocyanates comprise at least one thermally reversibly blocked NCO group whose blocking agent contains at least one group which on exposure to actinic radiation reacts, with polymerization, with ethylenically unsaturated compounds. A process for preparing the polyisocyanates, and their use in binders, is also provided.

Claims

1. A polyisocyanate which:

A) comprises at least one thermally reversibly blocked NCO group whose blocking agent is selected from the group consisting of (meth)acryloyloxyethyl acetoacetate, (meth)acryloyloxypropyl acetoacetate, (meth)acryloyloxybutyl acetoacetate and combinations thereof,

B) has exclusively aliphatically and/or cycloaliphatically attached isocyanate groups, and

C) is prepared from an organic polyisocyanate having an NCO functionality >

2.

2. The polyisocyanate of claim 1 which further comprises one or more groups which on exposure to actinic radiation reacts, with polymerization, with ethylenically unsaturated compounds, wherein the one or more groups is different from the (meth)acryolyl group of the at least one thermally reversibly blocked NCO group.

3. A process for preparing the polyisocyanate according to claim 1, which comprises reacting with one another:

A1) one or more organic polyisocyanates having exclusively aliphatically and/or cycloaliphatically attached isocyanate groups and an NCO functionality >

2 with

A2) optionally one or more compounds which are different from A4 and comprise at least one isocyanate-reactive group and at least one group which on exposure to actinic radiation reacts, with polymerization, with ethylenically unsaturated compounds,

A3) optionally further isocyanate-reactive compounds other than the compounds of component A2) and A4), and

A4) a blocking agent selected from the group consisting of (meth)acryloyloxyethyl acetoacetate, (meth)acryloyloxypropyl acetoacetate, (meth)acryloyloxybutyl acetoacetate and combinations thereof,

A5) optionally in the presence of one or more catalysts and solvents, reactive diluents and/or auxiliaries and additives.

4. A process for preparing the polyisocyanate according to claim 3, wherein in A2) acrylates, methacrylates, maleates, fumarates, maleimdies, acrylamides, vinyl ethers, propenyl ethers, allyl ethers and/or compounds containing dicyclopentadienyl units are used which contain at least one isocyanate-reactive group.

5. A process for preparing polyisocyanate according to claim 3, wherein (i) for each equivalent of NCO in A1) 0.2 to 0.8 equivalent of A4) is used, (ii) for each equivalent of NCO in A1) 0.2 to 0.8 equivalent of A2) is used, and (iii) the sum of the equivalents of components A2) and A4) that are used is not greater than 1 per NCO group from A1).

6. The process for preparing the polyisocyanate according to claim 3, wherein A1 comprises a uretdione, carbodiimide, isocyanurate, iminooxadiazinedione, biuret, urethane, allophanate, oxadiazinetrione or acylurea structure.

7. A coating material comprising

B1) one or more polyisocyanates according to claim 1,

B2) one or more compounds comprising at least one isocyanate-reactive group and containing optionally one or more functional groups which on exposure to actinic radiation react, with polymerization, with ethylenically unsaturated compounds,

B3) optionally compounds which carry functional groups which on exposure to actinic radiation react, with polymerization, with ethylenically unsaturated compounds and which contain neither NCO groups nor NCO-reactive groups,

B4) optionally catalysts and

B5) optionally auxiliaries and additives.

8. A substrate coated with coatings obtained from one or more polyisocyanates according to claim 1.

9. A polyisocyanate which:

A) comprises at least one thermally reversibly blocked NCO group whose blocking agent is selected from the group consisting of (meth)acryloyloxyethyl acetoacetate, (meth)acryloyloxypropyl acetoacetate, (meth)acryloyloxybutyl acetoacetate and combinations thereof and

B) has exclusively aliphatically and/or cycloaliphatically attached isocyanate groups,

C) comprises a uretdione, carbodiimide, isocyanurate, iminooxadiazinedione, biuret, urethane, allophanate, oxadiazinetrione or acylurea structure, and

D) is prepared from an organic polyisocyanate having an NCO functionality of >

2.

10. The polyisocyanate of claim 9 which further comprises one or more groups which on exposure to actinic radiation reacts, with polymerization, with ethylenically unsaturated compounds, wherein the one or more groups is different from the (meth)acryolyl group of the at least one thermally reversibly blocked NCO group.

11. A process for preparing the polyisocyanate according to claim 9, which comprises reacting with one another:

A1) one or more organic polyisocyanates having exclusively aliphatically and/or cycloaliphatically attached isocyanate groups and comprising a uretdione, carbodimide, isocyanurate, iminooxadiazinedione, biuret, urethane, allophonate, oxadiazinetrione or acylurea structure with

A2) optionally one or more compounds which are different from A4 and comprise at least one isocyanate-reactive group and at least one group which on exposure to actinic radiation reacts, with polymierzation, with ethylenically unsaturated compounds,

A3) optionally further isocyanate-reactive compounds other than the compounds of component A2) and A4), and

A4) a blocking agent selected from the group consisting of (meth)acryloyloxyethyl acetoacetate, (meth)acryloyloxypropyl acetoacetate, (meth)acryloyloxybutyl acetoacetate and combinations thereof,

A5) optionally in the presence of one or more catalysts, solvents, reactive diluents, auxiliaries and/or additives,

wherein A1) has an NCO functionality of >

2.

12. A process for preparing the polyisocyanate according to claim 11, wherein A2) acrylates, methacrylates, maleates, fumarates, maleimides, acrylamides, vinyl ethers, propenyl ethers, allyl ethers and/or compounds containing dicyclopentadienyl units are used which contain at least one isocyanate-reactive group.

13. A process for preparing the polyisocyanate according to claim 11, wherein (i) for each equivalent of NCO in A1) 0.2 to 0.8 equivalent of A4) is used, (ii) for each equivalent of NCO in A1) 0.2 to 0.8 equivalent of A2) is used, and (iii) the sum of the equivalents of compounds A2) and A4) that are used is not greater than 1 per NCO group from A 1).

14. A coating material comprising

B1) one or more polyisocyanates according to claim 9,

B2) one or more compounds comprising at least one isocyanate-reactive group and containing optionally one or more functional groups which on exposure to actinic radiation react, with polymerization, with ethylenically unsaturated compounds,

B3) optionally compounds which carry functional groups which on exposure to actinic radiation react, with polymerization, with ethylenically unsaturated compounds and which contain neither NCO groups nor NCO-reactive groups,

B4) optionally catalysts and

B5) optionally auxiliaries and additives.

15. A substrate coated with coatings obtained from one or more polyisocyanates according to claim 14.

16. A coating material comprising:

B1) one or more polyisocyanates comprises a reaction product of;

A1) one or more organic polyisocyantes having exclusively aliphatically and/or cycloaliphatically attached isocyanate groups, wherein the organic polyisocyanates have an NCO functionality of >

2;

A2) optionally one or more compounds, different from A4), which comprise at least one isocyanate-reactive group and contain at least one group which on exposure to actinic radiation reacts, with polymerization, with ethylenically unsaturated compounds,

A3) optionally further isocyanate-reactive compounds other than the compounds of component A2) and A4), and

A4) a blocking agent selected from the group consisting of (meth)acryloyloxyethyl acetoacetate, (meth)acryloyloxypropyl acetoacetate, (meth)acryloyloxybutyl acetoacetate and combinations thereof,

A5) optionally in the presence of one or more catalysts and/or solvents, reactive diluents and/or auxiliaries and additives,

B2) one or more compounds comprising at least one isocyanate-reactive group and containing optionally one or more functional groups which on exposure to actinic radiation react, with polymerization, with ethylenically unsaturated compounds,

B3) one or more compounds which carry functional groups which on exposure to actinic radiation react, with polymerization, with ethylenically unsaturated compounds and which contain neither NCO groups nor NCO-reactive groups,

B4) optionally catalysts and

B5) optionally auxiliaries and additives.

17. The coating material of claim 16, wherein A1) comprises a uretdione, carbodiimide, isocyanurate, iminooxadiazinedione, biuret, urethane, allophonate, oxadiazinetrione or acylurea structure.

18. The coating material of claim 16, wherein (i) for each equivalent of NCO in A1) 0.2 to 0.8 equivalent of A4) is used, (ii) for each equivalent of NCO in A1) 0.2 to 0.8 equivalent of A2) is used, and (iii) the sum of the equivalents of components A2) and A4) that are used is not greater than 1 per NCO group from A1).