IP Library Granted Patent US 8,455,177
Granted Patent B2
US 8,455,177 · App. 12/742,466 · Granted Jun 4, 2013

Method for making a lithographic printing plate

Inventors: Stefaan Lingier (Wondelgem, BE); Karen Demmers (Antwerp, BE)
Assignee: Agfa Graphics NV
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Quick Facts
Patent No.
US 8,455,177
App. No.
12/742,466
Granted
Jun 4, 2013
Kind
B2
Abstract

A method for making a positive-working lithographic printing plate includes the steps of: (1) providing a heat-sensitive printing plate precursor including on a support, having a hydrophilic surface or which is provided with a hydrophilic layer, a heat-sensitive coating; (2) image-wise exposing the precursor with heat and/or light; and (3) developing the exposed precursor with an aqueous alkaline developing solution including lithium ions at a concentration of at least 0.05% wt and a salt of an aliphatic carboxylic acid; wherein the molar ratio of the aliphatic carboxylic acid to the lithium ions is ≧1.

Claims (76)

1. A method for making a positive-working lithographic printing plate, the method comprising the steps of:

providing a heat-sensitive printing plate precursor including on a support, having a hydrophilic surface or which is provided with a hydrophilic layer, a heat-sensitive coating;

image-wise exposing the precursor with heat and/or light; and

developing the exposed precursor with an aqueous alkaline, silicate based developing solution including lithium ions at a concentration of at least 0.05% wt and a salt of an aliphatic carboxylic acid; wherein

a molar ratio of the salt of the aliphatic carboxylic acid to the lithium ions is >1; and

the salt of the aliphatic carboxylic acid comprises 8 to 12 carbon atoms.

2. A method according to claim 1 , wherein the concentration of the lithium ions is at least 0.1% wt.

3. A method according to claim 1 , wherein the molar ratio of the salt of the aliphatic carboxylic acid to the lithium ions is greater than 1.

4. A method according to claim 2 , wherein the molar ratio of the salt of the aliphatic carboxylic acid to the lithium ions is greater than 1.

5. A method according to claim 1 , wherein the developing solution includes an image dissolution inhibiting agent.

6. A method according to claim 5 , wherein the image dissolution inhibiting agent is selected from:

(a) polyglycols with the following structure:

R a O—(CH 2 —CHR b —O) n —R c

wherein

R a represents hydrogen, an optionally substituted alkyl group including 1 to 30 carbon atoms, —COR t , or an optionally substituted aryl or aralkyl group;

R b represents hydrogen, methyl, ethyl, and/or mixtures thereof;

R c represents hydrogen, an alkyl group, —COR d , —NR d R e , —CH 2 COOH, or —CH 2 COO − M + ; and

M + represents NH 4 + , Na + , or K + and R d , R e , and R t independently represent hydrogen, an optionally substituted alkyl group including 1 to 30 carbon atoms, an optionally substituted aryl group or aralkyl group;

(b) polycondensation products of one or more alkylene groups and/or one or more polyoxyalkylene groups with an alkylene diamine, an alkylene triamine, an alkylene polyamine, or an alkylene imine group;

(c) cationic surfactants including primary, secondary, tertiary, or quaternary ammonium salts, phosphonium salts, or sulfonium salts.

7. A method according to claim 1 , wherein the heat-sensitive coating comprises at least two layers including:

a first layer including a water-insoluble and alkali soluble resin which exhibits an increased solubility upon exposure to heat and/or light; and

a second layer, which is located between the support and the first layer, including a water-insoluble and alkali soluble resin.

8. A method according to claim 7 , wherein the second layer includes a sulphonamide binder.

9. A method according to claim 8 , wherein the sulfonamide binder is represented by:

wherein

R 9 represents hydrogen or a hydrocarbon group including up to 12 carbon atoms;

X 1 represents a single bond or a divalent linking group;

Y 4 is a bivalent sulphonamide group; and

Z 1 represents a terminal group.

10. A method according to claim 2 , wherein the heat-sensitive coating comprises at least two layers including:

a first layer including a water-insoluble and alkali soluble resin which exhibits an increased solubility upon exposure to heat and/or light; and

a second layer, which is located between the support and the first layer, including a water-insoluble and alkali soluble resin.

11. A method according to claim 10 , wherein the developing solution includes an image dissolution inhibiting agent.

12. A method according to claim 4 , wherein the heat-sensitive coating comprises at least two layers including:

a first layer including a water-insoluble and alkali soluble resin which exhibits an increased solubility upon exposure to heat and/or light; and

a second layer, which is located between the support and the first layer, including a water-insoluble and alkali soluble resin.

13. A method according to claim 12 , wherein the developing solution includes an image dissolution inhibiting agent.

14. A method according to claim 1 , wherein the heat-sensitive coating comprises at least two layers including:

a first layer including a water-insoluble and alkali soluble resin which exhibits an increased solubility upon exposure to heat and/or light; and

a second layer, which is located between the support and the first layer, including a water-insoluble and alkali soluble resin.

15. A method according to claim 14 , wherein the second layer includes a sulphonamide binder.

16. A method according to claim 15 , wherein the sulfonamide binder is represented by:

wherein

R 9 represents hydrogen or a hydrocarbon group including up to 2 carbon atoms;

X 1 represents a single bond or a divalent linking group;

Y 4 is a bivalent sulphonamide group; and

Z 1 represents a terminal group.

17. A method according to claim 14 , wherein the developing solution includes an image dissolution inhibiting agent.

18. A method according to claim 17 , wherein the image dissolution inhibiting agent is selected from:

(a) polyglycols with the following structure:

R a O—(CH 2 —CHR b —O) n —R c

wherein

R a represents hydrogen, an optionally substituted alkyl group including 1 to 30 carbon atoms, —COR t , or an optionally substituted aryl or aralkyl group;

R b represents hydrogen, methyl, ethyl, and/or mixtures thereof;

R c represents hydrogen, an alkyl group, —COR d , —NR d R e , —CH 2 COOH, or —CH 2 COO − M + ; and

wherein M+ represents NH 4 +, Na+, or K+ and R d , R e , and R t independently represent hydrogen, an optionally substituted alkyl group including 1 to 30 carbon atoms, or an optionally substituted aryl group or aralkyl group;

(b) polycondensation products of one or more alkylene groups and/or one or more polyoxyalkylene groups with an alkylene diamine, an alkylene triamine, an alkylene polyamine, or an alkylene imine group;

(c) cationic surfactants including primary, secondary, tertiary, or quaternary ammonium salts, phosphonium salts, or sulfonium salts.

19. A method for making a positive-working lithographic printing plate, the method comprising the steps of:

providing a heat-sensitive printing plate precursor including on a support, having a hydrophilic surface or which is provided with a hydrophilic layer, a heat-sensitive coating;

image-wise exposing the precursor with heat and/or light; and

developing the exposed precursor with an aqueous alkaline, silicate based developing solution including lithium ions at a concentration of at least 0.05% wt and a salt of an aliphatic carboxylic acid; wherein

a molar ratio of the salt of the aliphatic carboxylic acid to the lithium ions is ≧1;

the developing solution includes an image dissolution inhibiting agent;

the image dissolution inhibiting agent is selected from:

(a) polyglycols with the following structure:

R a O—(CH 2 —CHR b —O) n —R c

wherein

R a represents hydrogen, an optionally substituted alkyl group including 1 to 30 carbon atoms, —COR t , or an optionally substituted aryl or aralkyl group;

R b represents hydrogen, methyl, ethyl, and/or mixtures thereof;

R c represents hydrogen, an alkyl group, —COR d , —NR d R e , —CH 2 COOH, or —CH 2 COO − M + ; and

M + represents NH 4 + , Na + ,or K + and R d , R e and R t independently represent hydrogen, an optionally substituted alkyl group including 1 to 30 carbon atoms, an optionally substituted aryl group or aralkyl group;

(b) polycondensation products of one or more alkylene groups and/or one or more polyoxyalkylene groups with an alkylene diamine, an alkylene triamine, an alkylene polyamine, or an alkylene imine group;

(c) cationic surfactants including primary, secondary, tertiary, or quaternary ammonium salts, phosphonium salts, or sulfonium salts; and

the image dissolution inhibiting agent is the polycondensation product of the one or more alkylene groups and/or the one or more polyoxyalkylene groups with an alkylene diamine, an alkylene triamine, an alkylene polyamine, or an alkylene imine group.

Assignments (2)
CHANGE OF NAME Recorded Jan 3, 2018
From: AGFA GRAPHICS NV
To: AGFA NV
Reel/Frame 045742/0598 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2010
From: LINGIER, STEFAAN; DEMMERS, KAREN
To: AGFA GRAPHICS NV
Reel/Frame 024372/0380 →
Priority Claims (1)
EP 07120542 · Nov 13, 2007 · regional
Continuity (2)
Provisional Application 60987795 · Nov 14, 2007
Related Publication 20110111347A1 · May 12, 2011