IP Library Granted Patent US 10,599,035
Granted Patent B2
US 10,599,035 · App. 15/485,504 · Granted Mar 24, 2020

Method of improving light stability of flexographic printing plates featuring flat top dots

Inventors: Chouaib Boukaftane (Decatur, GA); Eric Lee (Woodstock, GA)
Assignee: MacDermid Graphics Solutions, LLC
G03F7/031G03F7/2055G03F7/24B29C2035/0827B29C2035/0833B41N1/12
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Quick Facts
Patent No.
US 10,599,035
App. No.
15/485,504
Granted
Mar 24, 2020
Kind
B2
Abstract

A photocurable relief image printing blank comprising: (a) a support layer; (b) one or more photocurable layers disposed on the support layer, wherein the one or more photocurable layers comprise: i) a binder; ii) one or more monomers; iii) an alpha-aminoketone photoinitiator; and optionally, iv) an additive selected from the group consisting of phosphites, phosphines, thioether amine compounds, and combinations of one or more of the foregoing; (c) a laser ablatable masking layer disposed on the one or more photocurable layers, the laser ablatable masking layer comprising a radiation opaque material; and (d) optionally, a removable coversheet. Upon exposure and development, the resulting relief image printing element does not degrade if left under ambient lights for an extended period of time.

Claims (38)

1. A photocurable flexographic printing blank comprising:

a) a support layer;

b) one or more photocurable layers disposed on the support layer, wherein the one or more photocurable layers comprise:

i) a binder;

ii) one or more monomers;

iii) an alpha-aminoketone photoinitiator, wherein the alpha-aminoketone photoinitiator comprises 2-methyl-1-(4-methylthiophenyl)-2-morpholinpropan-1-one; and

iv) an additive selected from the group consisting of phosphites, phosphines, thioether amine compounds, and combinations of one or more of the foregoing;

c) a laser ablatable masking layer disposed on the one or more photocurable layers, the laser ablatable masking layer comprising a radiation opaque material; and

d) optionally, a removable coversheet.

2. The photocurable flexographic printing blank according to claim 1 , wherein the one or more photocurable layers comprises an additive which comprises tris(nonylphenyl)phosphite.

3. The photocurable flexographic printing blank according to claim 1 , wherein the one or more photocurable layers comprises an additive which comprises a thioether amine compound selected from the group consisting of 2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino)phenol, 4-[[4,6-bis(nonylsulfanyl)-1,3,5-triazin-2-yl ] amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(octadecylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-octylsulfanyl) -1,3,5-triazin-2-yl]amino]-2,6-bis(2-methylnonan-2-yl)phenol, 4-[[4,6-bis(hexylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(heptylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2-tert-butyl-6-m -ethylphenol, 4-[[4,6-bis(ethylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(2,4,4-trimethylpentan-2-ylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(2-octylsulfanylethylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-dibutylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-dimethylphenol, 2,6-ditert-butyl-4-[[4-(3,5-ditert-butyl-4-hydroxyanilino)-6-octylsulfany-1-1,3,5-triazin-2-yl]amino]phenol, 4-[[4,6-bis(pentylsulfanyl) -1,3,5-triazin-2-yl]amino-2,6-dimethylphenol, 4-[[4,6-bis(hexylsulfanyl)-1,3,5-triazin-2-yl]amino]-2-tert-butylphenol, 2,6-ditert-butyl-4-[(4-octylsulfanyl-1,3,5-triazin-2-yl)amino]phenol, 4[[4,6-bis(ethylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-dimethylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]-butylamino]-2,6-ditert-butylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]-cyclohexylamino]-2,6-ditert-butylphenol, 2-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-6-tert-butylphenol, 2-tert-butyl-6-methyl-4-[[4-octylsulfanyl-6-[(2,2,6,6,-tetramethylpiperidin-4-yl)amino]-1,3,5-triazin-2-yl]amino]phenol, 4-[[4,6-bis(octylsulfanylmethyl)-1,3,5-triazin-2-yl)amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl)methylamino]-2,6-ditert-butylphenol, 4-[(4-amino-6-chloro-1,3,5-triazin-2-yl)amino]-2,6-ditert-butylphenol, and 4-[(4-cyclohexyl-6-cyclohexylsulfanyl-1,3,5-triazin-2-yl)amino]-2,6-di(propan-2-yl)phenol.

4. The photocurable flexographic printing blank according to claim 3 , wherein the additive comprises 2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino)phenol.

5. The photocurable flexographic printing blank according to claim 1 , wherein the one or more photocurable layers comprises an additive which comprises a phosphine selected from the group consisting of triphenyl phosphine, tri-p-tolylphosphine, diphenylmethylphosphine, diphenylethylphosphine, diphenylpropylphosphine, dimethylphenylphosphine, diethylphenylphosphine, dipropylphenylphosphine, divinylphenylphosphine, divinyl-p-methoxyphenylphosphine, divinyl-p-bromophenylphosphine, divinyl-p-tolylphosphine, diallylphenylphosphine, divinyl-p-bromophenylphosphine, and diallyl-p-tolylphosphine and combinations of one or more of the foregoing.

6. The photocurable flexographic printing blank according to claim 1 , further comprising a material selected from the group consisting of amine acrylates, amine reaction accelerators, and combinations of one or more of the foregoing.

7. The photocurable flexographic printing blank according to claim 1 , wherein the one or more photocurable layers further comprises one or more compounds selected from the group consisting of plasticizers, antiozonants, fillers, reinforcing agents, UV absorbers and combinations of one or more of the foregoing.

8. The photocurable flexographic printing blank according to claim 1 , wherein the one or more photocurable layers does not contain butylated hydroxytoluene, 2,4-Bis(octylthio)-6-(4-hydroxy-3,5-di-tert-butylanilino)-1,3,5-triazine, or 1,3,5-Trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxybenzyl)benzene.

9. The photocurable flexographic printing blank according to claim 7 , wherein the one or more compounds comprise a plasticizer.

10. A method of producing a flexographic relief image printing element from a photocurable flexographic printing blank, the method comprising the steps of:

a) providing a photocurable flexographic printing blank, the photocurable flexographic printing blank comprising:

i) a backing or support layer;

ii) one or more photocurable layers disposed on the backing or support layer, wherein the one or more photocurable layers comprise:

1) a binder;

2) one or more monomers;

3) an alpha-aminoketone photoinitiator, wherein the alpha-aminoketone photoinitiator comprises 2-methyl-1-(4-methylthiophenyl) -2-morpholinpropan-1-one; and

4) an additive selected from the group consisting of phosphites, phosphines, thioether amine compounds, and combinations of one or more of the foregoing; and

iii) a laser ablatable masking layer disposed on the one or more photocurable layers, the laser ablatable masking layer comprising a radiation opaque material;

b) selectively ablating the laser ablatable masking layer to create an in situ negative of a desired image in the laser ablatable masking layer;

c) exposing the one or more photocurable layers to actinic radiation through the in situ negative to selectively crosslink and cure portions of the one or more photocurable layers; and

d) developing the exposed one or more photocurable layers of the photocurable printing blank to reveal the relief image therein, said relief image comprising a plurality of relief printing dots.

11. The method according to claim 10 , wherein the one or more photocurable layers comprises an additive which comprises tris(nonylphenyl)phosphite.

12. The method according to claim 10 , wherein the one or more photocurable layers comprises an additive which comprises a thioether amine compound selected from the group consisting of 2,6-di-tert -butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino)phenol, 4-[[4,6-bis(nonylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(octadecylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-bis(2-methylnonan-2-yl)phenol, 4[[4,6-bis(hexylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(heptylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2-tert-butyl-6-m-ethylphenol, 4-[[4,6-bis(ethylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(2,4,4-trimethylpentan-2-ylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(2-octylsulfanylethylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-ditert-butylphenol 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-dibutylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-dimethylphenol, 2,6-ditert-butyl-4[[4-(3,5-ditert-butyl-4-hydroxyanilino)-6-octylsulfany-1-1,3,5-triazin-2-yl]amino]phenol, 4-[[4,6-bis(pentylsulfanyl) -1,3,5-triazin-2-yl]amino-2,6-dimethylphenol, 4-[[4,6-bis(hexylsulfanyl)-1,3,5-triazin-2-yl]amino]-2-tert-butylphenol, 2,6-ditert-butyl-4-[(4-octylsulfanyl-1,3,5-triazin-2-yl)amino]phenol, 4-[[4,6-bis(ethylsulfanyl)-1,3,5-triazin-2-yl]amino]-2,6-dimethylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]butylamino]-2,6-ditert-butylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]-cyclohexylamino]-2,6-ditert-butylphenol, 2-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl]amino]-6-tert-butylphenol, 2-tert-butyl-6-methyl-4-[[4-octylsulfanyl-6-[(2,2,6,6,-tetramethylpiperidin-4-yl]amino]-1,3,5-triazin-2-yl]amino]phenol, 4-[[4,6-bis(octylsulfanylmethyl)-1,3,5-triazin-2-yl)amino]-2,6-ditert-butylphenol, 4-[[4,6-bis(octylsulfanyl)-1,3,5-triazin-2-yl)methylamino]-2,6-ditert-butylphenol, 4-[(4-amino-6-chloro-1,3,5-triazin-2-yl)amino]-2,6-ditert-butylphenol, and 4-[(4-cyclohexyl-6-cyclohexylsulfanyl-1,3,5-triazin-2-yl)amino]-2,6-di(propan-2-yl)phenol.

13. The method according to claim 12 , wherein the additive comprises 2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino)phenol.

14. The method according to claim 10 , wherein the one or more photocurable layers comprises an additive which comprises a phosphine selected from the group consisting of triphenyl phosphine, tri-p-tolylphosphine, diphenylmethylphosphine, diphenylethylphosphine, diphenylpropylphosphine, dimethylphenylphosphine, diethylphenylphosphine, dipropylphenylphosphine, divinylphenylphosphine, divinyl-p-methoxyphenylphosphine, divinyl-p-bromophenylphosphine, divinyl-p-tolylphosphine, diallylphenylphosphine, divinyl-p-bromophenylphosphine, and diallyl-p-tolylphosphine and combinations of one or more of the foregoing.

15. The method according to claim 10 , wherein the one or more photocurable layers further comprises a material selected from the group consisting of amine acrylates, amine reaction accelerators, and combinations of one or more of the foregoing.

16. The method according to claim 10 , wherein the one or more photocurable layers further comprises one or more compounds selected from the group consisting of plasticizers, antiozonants, fillers, reinforcing agents, UV absorbers and combinations of one or more of the foregoing.

17. The method according to claim 10 , wherein the one or more photocurable layers does not contain butylated hydroxytoluene, 2,4-Bis(octylthio)-6-(4-hydroxy-3,5-di-tert-butylanilino) -1,3,5-triazine, or 1,3,5-Trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene.

18. The photocurable flexographic printing plate according to claim 1 , wherein the one or more photocurable layers comprises one or more additional photoinitiators, the one or more additional photoinitiators being selected from the group consisting of benzoin alkyl ethers, dialkoxyacetophenones, aldehyde and ketone carbonyl compounds having at least one aromatic nucleus attached directly to the carboxyl, and combinations of the foregoing.

19. The method according to claim 10 , wherein the one or more photocurable layers comprises one or more additional photoinitiators, the one or more additional photoinitiators being selected from the group consisting of benzoin alkyl ethers, dialkoxyacetophenones, aldehyde and ketone carbonyl compounds having at least one aromatic nucleus attached directly to the carboxyl, and combinations of the foregoing.

Assignments (6)
CHANGE OF NAME Recorded Apr 3, 2026
From: MACDERMID GRAPHICS SOLUTIONS, LLC
To: XSYS FLEXO US LLC
Reel/Frame 075338/0889 →
PARTIAL RELEASE OF SECURITY INTEREST IN PATENT COLLATERAL AT R/F 049855/0001 Recorded Feb 28, 2025
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: MACDERMID GRAPHICS SOLUTIONS, LLC
Reel/Frame 070365/0089 →
ASSIGNMENT OF SECURITY INTEREST IN PATENT COLLATERAL Recorded Nov 17, 2022
From: BARCLAYS BANK PLC
To: CITIBANK, N.A.
Reel/Frame 061956/0643 →
SECURITY INTEREST Recorded Feb 5, 2019
From: MACDERMID GRAPHICS SOLUTIONS, LLC (F/K/A MACDERMID PRINTING SOLUTIONS, LLC)
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 049855/0001 →
CHANGE OF NAME Recorded Dec 26, 2017
From: MACDERMID PRINTING SOLUTIONS, LLC
To: MACDERMID GRAPHICS SOLUTIONS, LLC
Reel/Frame 044958/0355 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2017
From: BOUKAFTANE, CHOUAIB; LEE, ERIC
To: MACDERMID PRINTING SOLUTIONS, LLC
Reel/Frame 041982/0206 →
Continuity (1)
Related Publication 20180297388A1 · Oct 18, 2018