MULTILAYER IMAGEABLE ELEMENT CONTAINING SULFONAMIDO RESIN

Abstract

A positive-working imageable element comprises inner and outer layers and a radiation absorbing compound such as an IR absorbing dye. The inner layer includes a first polymeric material. The ink receptive outer layer includes a second polymeric binder comprising a polymer backbone and an —X—C(=T)-NR—S(═O)2— moiety that is attached to the polymer backbone, wherein —X— is an oxy or —NR′— group, T is O or S, R and R′ are independently hydrogen, halo, or an alkyl group having 1 to 6 carbon atoms. After thermal imaging, the element can be developed using an alkaline developer. Use of the particular second polymeric binder reduces sludging in the developer. Its dissolution rate in the developer is slow enough to resist developer attack in the non-imaged areas of the outer layer but rapid enough for the second polymeric binder to be quickly loosened from imaged areas and kept suspended or dissolved for a considerable time.

Description

Claims

1. A positive-working imageable element that comprises a radiation absorbing compound and a substrate having thereon, in order: an inner layer comprising a first polymeric binder, andan ink receptive outer layer comprising a second polymeric binder different than said first polymeric binder, said polymeric binder comprising a hydrophobic backbone,wherein said second polymeric binder has a pKa of from about 6 to about 9, and the pKa of said second polymeric binder is greater than the pKa of said first polymeric binder.

2. The element of claim 1 wherein said second polymeric binder has a pKa of from about 6 to about 8.

3. The element of claim 1 wherein the difference in pKa values between said first and second polymeric binders is from about 2 to about 5 units.

4. The element of claim 1 wherein said second polymeric binder comprises one or more mercapto, sulfonamido, N-substituted sulfonamido, α-cyano esters, α-cyano ketones, β-diketones, and α-nitro ester groups, or mixtures thereof, in sufficient amounts to provide said second polymeric binder pKa value.

5. The element of claim 4 wherein said mercapto, sulfonamido, N-substituted sulfonamido, α-cyano esters, α-cyano ketones, β-diketones, and α-nitro ester groups, or mixtures thereof, are present as pendant groups on said hydrophobic backbone.

6. The element of claim 1 wherein said second polymeric binder also comprises recurring units derived from a (meth)acrylate, (meth)acrylamide, vinyl ether, vinyl ester, vinyl ketone, olefin, unsaturated imide, unsaturated anhydride, N-vinyl pyrrolidone, N-vinyl carbazole, 4-vinyl pyridine, (meth)acrylonitrile, styrenic monomer, or combinations thereof.

7. The element of claim 6 wherein said second polymeric binder comprises recurring units derived from one or more (meth)acrylates, styrenic monomers, (meth)acrylonitriles, (meth)acrylamides, or combinations thereof.

8. The element of claim 1 wherein said infrared radiation absorbing compound is a carbon black or IR absorbing dye having a maximum absorption at from about 700 to about 1200 nm and is present in said inner layer in an amount of at least 5 weight %.

9. The element of claim 1 wherein said outer layer further comprises a colorant, a coating surfactant, or both.

10. The element of claim 1 wherein said first polymeric binder is a (meth)acrylic resin comprising carboxy groups, a vinyl acetate-crotonate-vinyl neodecanoate copolymer phenolic resin, a maleated wood rosin, a styrene-maleic anhydride copolymer, a (meth)acrylamide polymer, a (meth)acrylonitrile polymer, or a polymer derived from an N-substituted cyclic imide.

11. The element of claim 1 wherein said first polymeric binder is a copolymer derived from an N-substituted cyclic imide, a (meth)acrylonitrile, a (meth)acrylamide, and (meth)acrylic acid.

12. The element of claim 11 wherein said inner layer further comprises a secondary additional polymeric material.

13. The element of claim 1 wherein said inner layer has a dry coating weight of from about 0.5 to about 2.5 g/m2 and said outer layer has a dry coating weight of from about 0.2 to about 1 g/m2.

14. A method for forming an image comprising: A) thermally imaging the positive-working imageable element of claim 1, thereby forming an imaged element with imaged and non-imaged regions,B) contacting said imaged element with an alkaline developer to remove only said imaged regions, andC) optionally, baking said imaged and developed element.

15. The method of claim 14 wherein imaging in step A is carried out using infrared radiation in the range of from about 700 nm to about 1200 nm.

16. The method of claim 14 wherein said alkaline developer is a solvent-based developer containing benzyl alcohol or ethylene glycol phenyl ether (phenoxy ethanol).

17. The method of claim 14 wherein said second polymeric binder has a pKa of from about 6 to about 8, and the difference in pKa values between said first and second polymeric binders is from about 2 to about 5 units.

18. The method of claim 14 wherein said second polymeric binder comprises one or more mercapto, sulfonamido, N-substituted sulfonamido, α-cyano esters, α-cyano ketones, β-diketones, and α-nitro ester groups, or mixtures thereof, in sufficient amounts to provide said second polymeric binder pKa value, and said groups are present as pendant groups on said hydrophobic backbone.

19. The method of claim 14 wherein said second polymeric binder also comprises recurring units derived from a (meth)acrylate, (meth)acrylamide, vinyl ether, vinyl ester, vinyl ketone, olefin, unsaturated imide, unsaturated anhydride, N-vinyl pyrrolidone, N-vinyl carbazole, 4-vinyl pyridine, (meth)acrylonitrile, styrenic monomer, or combinations thereof.