IP Library Granted Patent US 9,329,479
Granted Patent B2
US 9,329,479 · App. 14/390,427 · Granted May 3, 2016

Lithographic printing plate precusor

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Quick Facts
Patent No.
US 9,329,479
App. No.
14/390,427
Granted
May 3, 2016
Kind
B2
Abstract

A negative-working lithographic printing plate precursor includes a coating containing a photopolymerizable layer and optionally an intermediate layer between the photopolymerizable layer and the support, wherein the coating further includes a polysiloxane, the polysiloxane being present in the photopolymerizable layer and/or in the optional intermediate layer, and the polysiloxane is obtained by reacting at least one organosilicon compound represented by the general Formula (I) and at least one organosilicon compound represented by the general Formula (II):

Claims (29)

1. A method of preparing a negative-working lithographic printing plate precursor comprising the steps of:

providing a support having a hydrophilic surface or which is provided with a hydrophilic layer;

providing a coating on the support, the coating including a photopolymerizable layer and optionally an intermediate layer between the photopolymerizable layer and the support, the coating further including a polysiloxane present in the photopolymerizable layer and/or in the optional intermediate layer; wherein

the polysiloxane is obtained by reacting a first organosilicon compound represented by the general Formula (I) and a second organosilicon compound represented by the general Formula (II):

R 1 represents a group including at least one free radical polymerizable group;

R 2 , R 3 , R 6 , and R 7 independently represent an alkoxy, aryloxy, or an acyloxy group, or an optionally substituted alkyl, cycloalkyl, alkenyl, alkynyl, aryl, or heteroaryl group;

R 4 and R 8 independently represent an optionally substituted alkyl, cycloalkyl, alkenyl, alkynyl, aryl, heteroaryl group, or acyl group;

R 5 represents a hydrophilic group selected from a carboxylic acid or a salt thereof, a sulphonic acid or a salt thereof, a sulphuric acid or a monoester or a salt thereof, a hydrocarbon group substituted with at least one hydroxyl group, an oligoalkylene oxide group, a quaternary ammonium group, a phosphonium group, or combinations thereof; and

L 1 represents a di- or trivalent linking group; and

R 1 and L 1 are bonded to the silicon atom via a carbon atom.

2. The method according to claim 1 , wherein the polysiloxane is present in the photopolymerizable layer.

3. The method according to claim 1 , wherein R 1 includes two, three, four, or five free radical polymerizable groups.

4. The method according to claim 1 , wherein L 1 represents an alkylene, cycloalkylene, arylene, heteroarylene, —O—(CH 2 ) k —, —S—(CH 2 ) k —, —(CH 2 ) k —O—CO—(CH 2 ) l —, —CS—(CH 2 ) k —, —CO—(CH 2 ) k —, —O—CO—NH—, —(CH 2 ) k —CO—NH—, —(CH 2 ) k —NH—CO—, —NR*—CO—NH—, >N—CO—NH—, —NR*—CS—NH—, or combinations thereof;

k and l independently represent 0, 1, or an integer greater than 1; and

R* represents hydrogen or a methyl group.

5. The method according to claim 1 , wherein the polysiloxane is obtained by reacting the first organosilicon compound in an amount ranging between 10 to 50 mol % with the second organosilicon compound in an amount ranging between 20 to 90 mol %.

6. The method according to claim 1 , wherein the polysiloxane further includes a third organosilicon compound according to Formula (III):

wherein

R 9 and R 10 independently represent an alkoxy, aryloxy, or an acyloxy group, or an optionally substituted alkyl, alkenyl, alkynyl, aryl, or heteroaryl group;

L 2 represents a divalent linking group selected from an alkylene, cycloalkylene, arylene, heteroarylene, (poly)alkylene oxide group, —O—(CH 2 ) k , —S—(CH 2 ) k , —CO—(CH 2 ) k , —(CH 2 ) k —O—CO—(CH 2 ) l —, —CS—(CH 2 ) k , —CO—(CH 2 ) k —, —O—CO—NH—, —(CH 2 ) k —CO—NH—, —NR′—CO—NH—, —NH—CS—NH—, or combinations thereof;

k and l independently represent 0, 1, or an integer greater than 1;

R′ represents hydrogen or a methyl group; and

R 11 represents an optionally substituted alkyl, alkenyl, alkynyl, aryl, heteroaryl group, or acyl group.

7. The method according to claim 6 , wherein the polysiloxane is obtained by reacting the first organosilicon compound in an amount ranging between 10 to 50 mol % with the second organosilicon compound in an amount ranging between 20 to 90 mol % and the third organosilicon compound in an amount ranging between 20 to 90 mol %.

8. The method according claim 1 , wherein the photopolymerizable layer includes a polymerizable compound, a binder, and a polymerization initiator.

9. A method of preparing a lithographic printing plate comprising the steps of:

image-wise exposing the precursor obtained according to the method of claim 1 ; and

developing the precursor off-press by treating the coating of the precursor with a developing solution thus removing non-exposed areas of the coating from the support.

10. The method according to claim 9 , wherein the developing solution is a gum solution and the precursor is developed and gummed in one single step.

Assignments (4)
CHANGE OF NAME Recorded Jan 5, 2024
From: AGFA OFFSET BV
To: ECO3 BV
Reel/Frame 066206/0663 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2022
From: AGFA NV
To: AGFA OFFSET BV
Reel/Frame 060899/0240 →
CHANGE OF NAME Recorded Jan 3, 2018
From: AGFA GRAPHICS NV
To: AGFA NV
Reel/Frame 045742/0598 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2014
From: LOCCUFIER, JOHAN; STEENACKERS, MARIN; VERBRUGGHE, SAM
To: AGFA GRAPHICS NV
Reel/Frame 033889/0262 →