IP Library Granted Patent US 7,396,638
Granted Patent B2
US 7,396,638 · App. 10/766,939 · Granted Jul 8, 2008

Photothermographic material and image forming method

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Quick Facts
Patent No.
US 7,396,638
App. No.
10/766,939
Granted
Jul 8, 2008
Kind
B2
Abstract

The present invention relates to a photothermographic material including, on a same surface of a support, a photosensitive silver halide, a non-photosensitive organic silver salt, a reducing agent and a binder, wherein the photosensitive silver halide has a silver iodide content within a range from 40 to 100 mol %, and the material is thermally developed within a developing time of 12 seconds or less. The invention also relates to an image forming method using the photothermographic material.

Claims (26)

1. An image forming method comprising:

image-wise exposing to a blue semiconductor laser which has a light emission peak intensity within a wavelength range of 350 to 450 nm a photothermographic material comprising, on a same surface of a support, a photosensitive silver halide having a silver iodide content of 40 to 100 mol %, a non-photosensitive organic silver salt of an aliphatic carboxylic acid including a silver behenate, a reducing agent, a binder, and an adsorbable redox compound represented by Formula (I), wherein, in Formula (I), A represents a group that can be adsorbed by silver halide; W represents a divalent connecting group; n represents 0 or 1; B represents a reducing group that is capable of reducing silver ions and is a residue derived from a compound represented Formula B 13 ; and

thermally developing the image-wise exposed photothermographic material with a developing time of 1 to 12 seconds and with a developing temperature of 110° C. to 140° C.;

wherein in Formula B 13 , R b13 , represents a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group; R H13 represents a hydrogen atom, an alkyl group, an aryl group, an acyl group, an alkylsulfonyl group or an arylsulfonyl group; R b130 to R b133 each independently represent a hydrogen atom or a substituent;

A-(W) n —B  Formula (1)

wherein the photothermographic material further includes a compound represented by the following formula (H):

Q-(Y) n —C(Z 1 )(Z 2 )X  Formula (H)

wherein in formula (H), Q represents an alkyl group, an aryl group or a heterocyclic group; Y represents a divalent connecting group; n represents 0 or 1; Z 1 and Z 2 each independently represent a halogen atom; and X represents a hydrogen atom or an electron attracting group

and wherein the reducing agent is a compound represented by the following formula (R-1):

wherein in formula (R-1), R 11 and R 11 ′ each independently represent an alkyl group having 1 to 20 carbon atoms; R 12 and R 12 ′ each independently represent an alkyl group having 2 to 20 carbon atoms; L represents a —S—group or a —CHR 13 — group; R 13 represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; X 1 and X 1 ′ each independently represent a hydrogen atom or a group that can substitute a benzene ring.

2. The image forming method according to claim 1 , wherein the developing time is 2 to 10 seconds.

3. The image forming method according to claim 1 , wherein the thermal development is conducted at a temperature of 110° C. to 130° C.

4. The image forming method according to claim 1 , wherein the photothermographic material further includes an antifogging agent.

5. The image forming method according to claim 1 , wherein the photosensitive silver halide has an average grain size of 5 to 50 nm.

6. The image forming method according to claim 1 , wherein the photothermographic material further includes a development accelerator.

7. The image forming method according to claim 1 , wherein the photothermographic material further includes a toning agent.

8. The image forming method according to claim 1 , wherein the photothermographic material further includes an ultra-high contrast agent.

9. The image forming method according to claim 1 , wherein the photothermographic material further includes a matting agent.

10. The method of claim 1 wherein the silver halide has a silver iodide content of 80 to 100 mol %.

11. The method of claim 1 wherein the silver halide has a silver iodide content of 90 to 100 mol %.

12. The method of claim 1 , wherein an adsorbable group represented by A is a mercapto group, a salt thereof, a thion group (—C(═S)—), a heterocyclic group containing at least an atom selected from a nitrogen atom, a sulfur atom, a selenium atom and a tellurium atom, a sulfide group, a disulfide group, a cationic group, or an ethynyl group.

13. The method of claim 1 , wherein the adsorbable redox compound is represented by any of the following formulas (71) to (79):

14. The method of claim 1 , wherein the photothermographic material further comprises a compound represented by the following formula (H):

Q-(Y) n —C(Z 1 )(Z 2 )X  Formula (H)

wherein in formula (H), X is a bromine atom; Y is SO 2 ; N is 1; and Q is an aryl group or a heterocyclic group.

15. The method of claim 1 , wherein the photothermographic material is thermally developed by a plate heater.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2007
From: FUJIFILM HOLDINGS CORPORATION (FORMERLY FUJI PHOTO FILM CO. LTD.)
To: FUJIFILM CORPORATION
Reel/Frame 019331/0493 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 15, 2004
From: CRARY, LYNWOOD F.; FORGE, JOHN R.; JOHANSEN, MARK R.
To: TI GROUP AUTOMOTIVE SYSTEMS, L.L.C.
Reel/Frame 015565/0690 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2004
From: NARIYUKI, FUMITO
To: FUJI PHOTO FILM CO, LTD
Reel/Frame 014944/0609 →