IP Library Granted Patent US 6,962,763
Granted Patent B2
US 6,962,763 · App. 10/786,851 · Granted Nov 8, 2005

Silver-free black-and-white thermographic materials

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Quick Facts
Patent No.
US 6,962,763
App. No.
10/786,851
Granted
Nov 8, 2005
Kind
B2
Abstract

Silver-free, aqueous-based direct thermographic materials are designed to have image tone with near neutral density. Without the use of organic silver salts containing reducible silver ions, the image is formed using a color developing agent precursor that releases a color developing agent when heated to a temperature of at least 80° C., a combination of cyan, yellow and magenta dye-forming color couplers that provide cyan, yellow, and magenta dyes, and a hindered-amine N-oxyl as an oxidizing agent. No silver metal or silver ions are purposely added to these materials. This combination of components provides a means for controlling image tone without reliance upon conventional toning agents.

Claims (41)

1. A silver-free black-and-white thermographic material comprising a support having thereon at least one imaging layer comprising predominantly a hydrophilic or water-dispersible polymeric latex binder, and further comprising:

a) a color developing agent precursor that releases a color developing agent when heated to a temperature of at least 80° C., and

b) a cyan dye-forming color coupler that is capable of reacting with said released color developing agent to produce a cyan dye,

c) a magenta dye-forming color coupler that is capable of reacting with said released color developing agent to produce a magenta dye,

d) a yellow dye-forming color coupler that is capable of reacting with said released color developing agent to produce a yellow dye, and

e) an oxidizing agent that is a hindered-amine N-oxyl that is capable of oxidizing the released color developing agent,

said material being substantially free of silver metal or reducible silver ions.

2. The material of claim 1 wherein said oxidizing agent is represented by the following Structure I:

wherein R 1 , R 2 , R 3 , and R 4 are independently substituted or unsubstituted alkyl groups, substituted or unsubstituted aryl groups, or substituted or unsubstituted cycloalkyl groups, or R 1 and R 2 or R 3 and R 4 are combined to form a substituted or unsubstituted carbocyclic or heterocyclic ring, and Z represents the carbon or nitrogen atoms necessary to complete a 5- to 14-membered heterocyclic ring.

3. The material of claim 2 wherein R 1 , R 2 , R 3 , and R 4 are independently substituted or unsubstituted alkyl groups having 1 to 4 carbon atoms, substituted or unsubstituted cyclohexyl groups, or substituted or unsubstituted phenyl groups, and Z represents the carbon or nitrogen atoms necessary to complete a 5- or 6-membered heterocyclic ring.

4. The material of claim 2 wherein R 1 , R 2 , R 3 , and R 4 are independently unsubstituted methyl, ethyl, cyclohexyl, or phenyl groups.

5. The material of claim 1 wherein said oxidizing agent is represented by the following Structure II:

wherein R 1 , R 2 , R 3 , and R 4 are independently substituted or unsubstituted alkyl groups, substituted or unsubstituted aryl groups, or substituted or unsubstituted cycloalkyl groups, or R 1 and R 2 or R 3 and R 4 are combined to form a substituted or unsubstituted carbocyclic or heterocyclic ring, R 5 and R 6 are independently hydrogen, substituted or substituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted cycloalkyl groups, hydroxy, alkyl esters, aryl esters, or sulfonyl esters, or R 5 and R 6 are combined to form an oxo group or a substituted or unsubstituted carbocyclic or heterocyclic ring.

6. The material of claim 5 wherein at least one of R 5 and R 6 is hydrogen.

7. The material of claim 6 wherein at least one or R 5 and R 6 is hydrogen and the other is hydroxy, an alkyl group, or an alkyl or aryl ester.

8. The material of claim 5 wherein R 5 and R 6 are combined to form an oxo group.

9. The material of claim 1 wherein said oxidizing agent is 2,2,6,6-tetramethylpiperidinyloxy, free radical, 4-hydroxy-2,2,6,6-tetramethylpiperidinyloxy, free radical, 4-hydroxy-2,2,6,6-tetramethylpiperidinyloxy benzoate, free radical, or 2,2,6,6,-tetramethyl-4-(methylsulfonyloxy)-1-piperidinooxy, free radical.

10. The thermographic material of claim 1 wherein said oxidizing agent is present in an amount of from about 0.5 to about 20 mol/mol of color developing agent precursor.

11. The material of claim 1 wherein said color developing agent precursor releases p-phenylenediamine color developing agent upon heating to a temperature of at least 80° C.

12. The material of claim 1 wherein said color developing agent precursor is present in an amount of from about 0.0001 to about 0.1 mol/m 2 .

13. The material of claim 1 wherein said cyan dye-forming color coupler, said magenta dye-forming color coupler, and said yellow dye-forming color coupler are independently present in an amount of from about 0.01 to about 1 mol/mol of color developing agent precursor.

14. The material of claim 1 wherein said binder is a hydrophilic binder is gelatin, a gelatin derivative, a cellulosic material, or a poly(vinyl alcohol).

15. The material of claim 1 that is duplitized, having one or more of the same or different imaging layers on both sides of said support.

16. The material of claim 1 further comprising a protective layer over said one or more imaging layers.

17. A silver-free, black-and-white, non-photosensitive thermographic material that comprises a transparent polymer support having on only one side thereof one or more thermally sensitive imaging layers and an outermost non-thermally sensitive protective layer over said one or more thermally sensitive imaging layers,

said one or more thermally sensitive imaging layers comprising predominantly one or more hydrophilic binders, and in reactive association, imaging chemistry consisting essentially of:

a) a color developing agent precursor that releases a p-phenylenediamine color developing agent when heated to a temperature of at least 80° C., said color developing agent precursor being present in an amount of from about 0.001 to about 0.05 mol/m 2 ,

b) a cyan dye-forming color coupler that is capable of reacting with said released color developing agent to produce a cyan dye,

c) a magenta dye-forming color coupler that is capable of reacting with said released color developing agent to produce a magenta dye,

d) a yellow dye-forming color coupler that is capable of reacting with said released color developing agent to produce a yellow dye,

e) an oxidizing agent that is 2,2,6,6-tetramethylpiperidinyloxy, free radical, 4-hydroxy-2,2,6,6-tetramethylpiperidinyloxy, free radical, or 4-hydroxy-2,2,6,6-tetramethylpiperidinyloxy benzoate, free radical, and is present in an amount of from about 1 to about 10 mol/mol of said color developing agent precursor, and

f) a development enhancing toning agent,

said material being substantially free of silver metal or reducible silver ions, and said cyan dye-forming color coupler, magenta dye-forming color coupler, and yellow dye-forming color coupler being independently present in an amount from about 0.05 to about 0.5 mol/mol of said color developing agent precursor.

18. The material of claim 12 wherein said hydrophilic binder is gelatin or a derivative thereof, a cellulosic material, or a poly(vinyl alcohol).

19. A method comprising imaging the thermographic material of claim 1 with a thermal imaging source to provide a visible image.

20. The method of claim 19 wherein said thermographic material comprises a transparent support and said image-forming method further comprises:

positioning said imaged thermographic material with the visible image thereon between a source of imaging radiation and an imageable material that is sensitive to said imaging radiation, and

thereafter exposing said imageable material to said imaging radiation through the visible image in said imaged thermographic material to provide an image in said imageable material.

21. A method comprising imaging the thermographic material of claim 17 with a thermal imaging source to provide a visible image.

22. The method of claim 21 wherein said imaging is carried out using a thermal print head or a laser.

23. The method of claim 19 further comprising using said imaged thermographic material for medical diagnostic purposes.

Assignments (17)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (061579/0341) Recorded Mar 16, 2026
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: CARESTREAM HEALTH, INC.
Reel/Frame 075100/0653 →
SECURITY INTEREST Recorded Mar 13, 2026
From: CARESTREAM HEALTH, INC.
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS ADMINISTRATIVE AGENT
Reel/Frame 075081/0379 →
RELEASE OF SECURITY INTEREST Recorded Oct 14, 2022
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: CARESTREAM HEALTH, INC.; CARESTREAM DENTAL, LLC; QUANTUM MEDICAL IMAGING, L.L.C.; QUANTUM MEDICAL HOLDINGS, LLC; TROPHY DENTAL INC.
Reel/Frame 061681/0380 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY (FIRST LIEN) Recorded Oct 14, 2022
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: CARESTREAM HEALTH, INC.; CARESTREAM DENTAL LLC; QUANTUM MEDICAL IMAGING, L.L.C.; TROPHY DENTAL INC.
Reel/Frame 061683/0441 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY (SECOND LIEN) Recorded Oct 14, 2022
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: CARESTREAM HEALTH, INC.; CARESTREAM DENTAL LLC; QUANTUM MEDICAL IMAGING, L.L.C.; TROPHY DENTAL INC.
Reel/Frame 061683/0601 →
GRANT OF SECURITY INTEREST IN PATENT RIGHTS - TL Recorded Sep 30, 2022
From: CARESTREAM HEALTH, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 061579/0341 →
GRANT OF SECURITY INTEREST IN PATENT RIGHTS - ABL Recorded Sep 30, 2022
From: CARESTREAM HEALTH, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 061579/0301 →
SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jul 1, 2013
From: CARESTREAM HEALTH, INC.; CARESTREAM DENTAL LLC; QUANTUM MEDICAL IMAGING, L.L.C.; TROPHY DENTAL INC.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
Reel/Frame 030724/0154 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT (FIRST LIEN) Recorded Jun 28, 2013
From: CARESTREAM HEALTH, INC.; CARESTREAM DENTAL LLC; QUANTUM MEDICAL IMAGING, L.L.C.; TROPHY DENTAL INC.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
Reel/Frame 030711/0648 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY (SECOND LIEN) Recorded Mar 13, 2012
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: CARESTREAM HEALTH, INC.
Reel/Frame 027851/0812 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 12, 2011
From: CARESTREAM HEALTH, INC.; CARESTREAM DENTAL, LLC; QUANTUM MEDICAL IMAGING, L.L.C.; QUANTUM MEDICAL HOLDINGS, LLC; TROPHY DENTAL INC.
To: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
Reel/Frame 026269/0411 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY (FIRST LIEN) Recorded Apr 4, 2011
From: CREDIT SUISSE AG, CAYMAN ISLANDS BRANCH
To: CARESTREAM HEALTH, INC.
Reel/Frame 026069/0012 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2008
From: EASTMAN KODAK COMPANY
To: CARESTREAM HEALTH, INC.
Reel/Frame 020756/0500 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2008
From: EASTMAN KODAK COMPANY
To: CARESTREAM HEALTH, INC.
Reel/Frame 020741/0126 →
FIRST LIEN OF INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jul 27, 2007
From: CARESTREAM HEALTH, INC.
To: CREDIT SUISSE, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT
Reel/Frame 019649/0454 →
SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEME Recorded Jul 27, 2007
From: CARESTREAM HEALTH, INC.
To: CREDIT SUISSE, CAYMAN ISLANDS BRANCH, AS ADMINISTRATIVE AGENT
Reel/Frame 019773/0319 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2004
From: MASKASKY, JOE E.; SCACCIA, VICTOR P.
To: EASTMAN KODAK COMPANY
Reel/Frame 014997/0302 →