Granted Patent B2

US 7,553,906 · App. 10/738,879 · Granted Jun 30, 2009

Abstract

Claims (44)

1. Blocked organic polyisocyanates comprising at least one unsaturated functional group that is capable of copolymerizing with ethylene-unsaturated compounds when exposed to actinic radiation, the polyisocyanates further comprising structural units having the formula (1)

in which

X is an electron-attracting group,

R 1 , and R 2 are independently selected from the group consisting of a hydrogen atom, a saturated or unsaturated aliphatic or cycloaliphatic radical, an optionally substituted aromatic or araliphatic radical and each radical contains up to 12 carbon atoms and optionally up to 3 heteroatoms of the elements oxygen, sulfur, or nitrogen and are optionally substituted by halogen atoms; and

n is an integer of from 0 to 5.

2. The polyisocyanates according to claim 1 , wherein the electron-attracting group X is an ester, sulfoxide, sulfo, nitro, phosphonate, nitrile, isonitrile or carbonyl group.

3. A process for producing the polyisocyanates according to claim 1 , comprising reacting

A1) one or more organic polyisocyanates together with

A2) one or more compounds comprising at least one isocyanate-reactive group and at least one group that is capable of copolymerizing with ethylene-unsaturated compounds when exposed to actinic radiation,

A3) optionally other isocyanate-reactive compounds and

A4) blocking agents containing at least one CH-acid cyclic ketone having the general formula (2),

in which

X is an electron-attracting group,

R 1 , and R 2 are independently selected from the group consisting of a hydrogen atom, a saturated or unsaturated aliphatic or cycloaliphatic radical, an optionally substituted aromatic or araliphatic radical and each radical contains up to 12 carbon atoms and optionally up to 3 heteroatoms of the elements oxygen, sulfur, nitrogen and are optionally substituted by halogen atoms and

n is an integer of from 0 to 5,

A5) in the presence of one or more catalysts and

A6) optionally auxiliary substances and additives and

A7) optionally solvents.

4. A method of making paints, coatings, sizes, adhesives and moulded articles comprising combining the polyisocyanate according to claim 1 with one or more compounds containing isocyanate-reactive groups.

5. Coating compositions comprising

B1) one or more polyisocyanates according to claim 1 and/or

B2) one or more blocked organic polyisocyanates displaying structural units having formula (1)

in which

X is an electron-attracting group,

R 1 , and R 2 are independently selected from the group consisting of a hydrogen atom, a saturated or unsaturated aliphatic or cycloaliphatic radical, an optionally substituted aromatic or araliphatic radical and each contain up to 12 carbon atoms and optionally up to 3 heteroatoms of the elements oxygen, sulfur, nitrogen and are optionally substituted by halogen atoms and

n is an integer of from 0 to 5,

B3) one or more compounds comprising at least one isocyanate-reactive group and optionally containing one or more functional groups that are capable of copolymerizing with ethylene-unsaturated compounds when exposed to actinic radiation,

B4) optionally compounds comprising functional groups that are capable of copolymerizing with ethylene-unsaturated compounds when exposed to actinic radiation and that do not contain NCO groups or NCO-reactive groups,

B5) optionally catalysts and

B6) optionally auxiliary substances and additives

B7) optionally products from reactions of components B1) to B6) with one another

with the proviso that when compounds of B2 are combined with compounds of B3, in the absence of compounds of B1, at least one of the compounds of B3 will contain a functional group that is capable of copolymerizing with ethylene-unsaturated compounds when exposed to actinic radiation.

6. A process for producing the coating compositions according to claim 5 comprising mixing components B1) to B6).

7. Coatings obtained from coating compositions according to claim 5 .

8. Substrates coated with coatings according to claim 7 .

9. The process of claim 3 , wherein the organic polyisocyanates of A1) are one or more selected from the group consisting of 1,4-diisocyanatobutane, 1,5-diisocyanatopentane, 1,6-diisocyanatohexane, 2-methyl-1,5-diisocyanato-pentane, 1,5-diisocyanato-2,2-dimethyl pentane, 2,2,4-trimethyl-1,6-diisocyanato-hexane, 2,4,4-trimethyl-1,6-diisocyanatohexane, 1,10-diisocyanatodecane, 1,3-diisocyanatocyclohexane, 1,4-diisocyanatocyclohexane, 1,3-bis-(isocyanato-methyl) cyclohexane, 1,4-bis-(isocyanatomethyl) cyclohexane, isophorone diisocyanate, 4,4′-diisocyanato-dicyclohexyl methane, 4-isocyanatomethyl-1,8-octane diisocyanate, ω,ω′-diisocyanato-1,3-dimethyl cyclohexane, 1-isocyanato-1-methyl-3-isocyanato-methyl cyclohexane, 1-isocyanato-1-methyl-4-isocyanato-methyl cyclohexane, bis-(isocyanatomethyl) norbornane, 1,5-naphthalene diisocyanate, 1,3-bis-(2-isocyanatoprop-2-yl) benzene, 1,4-bis-(2-isocyanatoprop-2-yl) benzene, 2,4-diisocyanatotoluene, 2,6-diisocyanatotoluene, 2,4-diisocyanatotoluene, 2,4′-diisocyanatodiphenyl methane, 4,4′-diisocyanato-diphenyl methane, 1,5-diisocyanatonaphthaline, and 1,3-bis(isocyanatomethyl) benzene.

10. The process of claim 3 , wherein the compounds of A2) are one or more selected from the group consisting of acrylates, methacrytates, maleinates, fumarates, maleimides, and acrylamides.

11. The process of claim 3 , wherein the compounds of A2) are one or more selected from the group consisting of 2-hydroxyethyl methacrylate; 2-hydroxyethyl acrylate; polyethylene oxide monomethacrylates; polyethylene oxide monoacrylates; polypropylene oxide monomethacrylates; polypropylene oxide monoacrylates; polyalkylene oxide monomethacrylates; polyalkylene oxide monoacrylates; poly(ε-caprolactone) monomethacrylates; poly (ε-caprolactone) monoacrylates; 2-hydroxypropyl methacrylate; 2-hydroxypropyl acrylate; 4-hydroxybutyl methacrylate; 4-hydroxybutyl acrylate; 3-hydroxy-2,2-dimethyl propyl methacrylate; 3-hydroxy-2,2-dimethyl propyl acrylate; the hydroxy-functional monoacrylates, diacrylates or tetraacrylates of polyhydric alcohols selected from trimethylol propane, glycerol, pentaerythritol, dipentaerythritol, ethoxylated, propoxylated, alkoxylated trimethylol propane, alkoxylated glycerol, alkoxylated pentaerythritol, and alkoxylated dipentaerythritol; the reaction products of acrylic acid or methacrylic acid with glycidyl (meth)acrylate; and the reaction products of acrylic acid or methacrylic acid with the glycidyl ester of versatic acid.

12. The process of claim 3 , wherein the CH-acid cyclic ketone of A4) is one or more selected from the group consisting of cyclopentanone-2-carboxymethyl ester, cyclopentanone-2-carboxyethyl ester, cyclopentanone-2-carboxylic acid nitrile, cyclohexanone-2-carboxylmethyl ester, cyclohexanone-2-carboxyethyl ester, and cyclopentanone-2-carbonyl methane.

13. The process of claim 3 , wherein the catalyst A5) is one or more selected from the group consisting of sodium carbonate, trisodium phosphate, 1,4-diazabicyclo[2.2.2]octane, potassium carbonate, and zinc-2-ethyl hexanoate.

14. A method of thermoforming comprising

forming a film comprising the coating compositions of claim 5 ;

curing the film by exposure to actinic radiation to form an elastic layer; and

drawing the elastic layer over a moulded part at a temperature at which crosslinking occurs in the elastic layer.

Assignments (9)