Process for producing matt coatings on sheetlike substrates

Patent metadata

Field	Value
Publication number	US-11969753-B2
Application number	US-201816637071-A
Country	US
Kind code	B2
Filing date	Aug 15, 2018
Priority date	Aug 16, 2017
Publication date	Apr 30, 2024
Grant date	Apr 30, 2024

Abstract

The present disclosure relates to a process for producing matt coatings on sheetlike substrates. The method includes providing an uncured lacquer layer of a UV radiation-curable liquid lacquer formulation F on a surface of the substrate to be coated. The method also includes irradiating the lacquer layer with UV radiation substantially in the wavelength range of 250 to 420 nm with a radiation dose which results in partial curing of the lacquer layer. The method further includes irradiating the partially cured lacquer layer with UV radiation in the wavelength range of 150 to <250 nm under inert gas. The method further includes irradiating the partially cured lacquer layer with UV radiation substantially in the wavelength range of 250 to 420 nm or with electron radiation with a radiation dose which results in end-curing of the lacquer layer.

First claim

The invention claimed is:

1. A method for producing matt coatings on sheetlike substrates, comprising the consecutive steps i.-iv.,
i. providing an uncured coating film of a liquid coating formulation F, curable by UV radiation, on the surface of the substrate to be coated;
ii. irradiating the coating film with UV radiation which lies substantially in the wavelength range from 250 to 420 nm, with a radiation dose which leads to partial curing of the coating film;
iii. irradiating the partially cured coating film with UV radiation in the wavelength range from 150 to <250 nm under inert gas;
iv. irradiating the partially cured coating film with UV radiation which lies substantially in the wavelength range from 250 to 420 nm, or with electron beams, with a radiation dose which leads to full curing of the coating film;
wherein the coating formulation F comprises at least 80 wt %, based on the total weight of the coating-forming constituents of the coating formulation F, of one or more curable constituents which have ethylenically unsaturated double bonds,
the coating formulation F further comprising at least one photoinitiator, wherein the coating formulation F comprises at least one oligomer or polymer which carries on average at least 1.5 ethylenic double bonds per molecule and has a number-average molecular weight M n of at least 450 daltons, and
the coating formulation F fulfills at least the following features (A) and (B) or (A) and (C) and optionally (D):
(A) the number of ethylenically unsaturated double bonds, based on the coating-forming constituents present in the coating formulation F, is in the range from 3.0 to 8.0 mol/kg;
(B) the coating formulation F comprises at least 30 wt %, based on the curable constituents present therein, of an oligomer or polymer or of a mixture of oligomers and/or polymers wherein the ratio α/T o of calculated network arc length α in g/mol to the onset temperature T o in kelvins of the glass transition, determined by means of differential scanning calorimetry according to DIN EN ISO 11357-2:2014, is at least 1.2;
(C) the mass-average ratio α/T o , averaged over the weight fractions of all curable constituents of the coating formulation F, is at least 1.0;
(D) the coating formulation F comprises at least one aromatic epoxy acrylate in an amount of at least 20 wt %, based on the total weight of the curable constituents present in the coating formulation F.

2. The method according to claim 1 , wherein the irradiation in step ii. takes place with UV radiation with a radiation dose in the range from 20 to 200 mJ/cm 2 , the UV radiation lying substantially in the wavelength range from 350 to 420 nm.

3. The method according to claim 1 , wherein the irradiation in step ii. takes place under an oxygen-containing atmosphere.

4. The method according to claim 1 , wherein the irradiation in step iii. takes place in the wavelength range from 150 to 230 nm.

5. The method according to claim 1 , wherein the irradiation in step iv. takes place with UV radiation which lies substantially in the wavelength range from 350 to 420 nm.

6. The method according to claim 1 , wherein the coating formulation F is a nonaqueous coating formulation which comprises at least 80 wt %, based on the total weight of the coating formulation F, of one or more constituents which have ethylenically unsaturated double bonds.

7. The method according to claim 1 , wherein the coating formulation F is applied to the surface of the substrate to be coated, in an amount such that, after curing, the resulting film thickness is from 3 to <20 μm, more particularly from 3 to 15 μm.

8. The method according to claim 1 , wherein, in the coating formulation F, the ethylenically unsaturated double bonds of the constituents present therein are present to an extent of at least 90 mol %, based on the total amount of the ethylenically unsaturated double bonds present in the composition, in the form of acrylate groups.

9. The method according to claim 1 , wherein the coating formulation F comprises as principal constituent at least one oligomer selected from aliphatic urethane (meth)acrylates, aliphatic polyether (meth)acrylates, aliphatic polyester (meth)acrylates, aliphatic polycarbonate (meth)acrylates, and mixtures thereof.

10. The method according to claim 1 , wherein the coating formulation F further comprises at least one monomer which carries on average 1 to 3 ethylenic double bonds per molecule and has a number-average molecular weight M n <450 daltons.

11. The method according to claim 1 , wherein the irradiation in step iv. takes place with a radiation dose in the range from 150 to 600 mJ/cm 2 .

12. The method according to claim 1 , wherein the coating formulation F fulfills feature (D).

13. The method according to claim 12 , wherein the aromatic epoxy acrylate is selected from the reaction products of aromatic glycidyl ethers with hydroxyalkyl acrylates and/or acrylic acid.

14. The method according to claim 12 , wherein the coating formulation F comprises at least one additive selected from matting agents, waxes, and inert resins.

15. The method according to claim 1 , wherein the coating formulation F comprises at least one photoinitiator which has at least one absorption band having a maximum λ max in the range from 340 to 420 nm.

16. The method according to claim 15 , wherein the coating formulation F further comprises at least one photoinitiator which has at least one absorption band having a maximum λ max in the range from 220 to 340 nm.

17. The method according to claim 15 , wherein the photoinitiator has at least one absorption band having a maximum λ max in the range from 350 to 410 nm.

18. The method according to claim 16 , wherein the photoinitiator has at least one absorption band having a maximum λ max in the range from 230 to 320 nm.

19. The method according to claim 1 , wherein the substrate to be coated is a sheetlike, nonporous substrate.

Assignees

• Basf Se

Inventors

• Becker Axel
• Berger Sebastian
• Stein Stefanie

Classifications

• B05D3/067 Primary

  Curing or cross-linking the coating · CPC title

• C09D163/10

  Epoxy resins modified by unsaturated compounds · CPC title

• C09D167/07

  having terminal carbon-to-carbon unsaturated bonds · CPC title

• C09D171/00

  Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain (based on polyacetals C09D159/00; based on epoxy resins C09D163/00; based on polythioether-ethers C09D181/02; based on polyethersulfones C09D181/06); Coating compositions based on derivatives of such polymers · CPC title

• B05D5/02 Primary

  to obtain a matt or rough surface · CPC title