Aqueous thermally bleachable composition useful in a photothermographic element

Abstract

This invention relates to a photothermographic element comprising a support, at least one photothermographic imaging layer, and at least one antihalation layer or a filter layer, wherein the antihalation or filer layer comprises an aqueous heat-bleachable composition comprising a 1-aminopyridinium filter dye having a methine linkage terminated by a substituted or unsubstituted heterocyclic nucleus of the type contained in cyanine dyes, which filter dye is in the presence of an effective amount of a thermal solvent.

Description

FIELD OF THE INVENTION

This invention relates to colored, aqueous heat-bleachable compositions that can undergo a change in electromagnetic absorption characteristics upon application of heat. These compositions are useful as antihalation or filter components of photothermographic elements. In particular, 1-aminopyridinium dyes in combination with a thermal solvent has been found to provide improved bleaching characteristics in photothermographic elements.

BACKGROUND OF THE INVENTION

Photographic materials usually contain various layers and components, including antihalation or filter layers, overcoats and radiation sensitive layers. The antihalation layer of an imaging element helps to prevent light that has passed through the radiation sensitive layer(s) from reflecting back into those layers. If reflection is not prevented, the resulting image is less sharp. In wet processes, the antihalation layer is generally removed or rendered colorless during wet-chemical processing. A filter layer is used to absorb light of a color not completely absorbed by a color layer or color layer unit above the filter layer, while transmitting light of a color intended to be absorbed by a color layer or a color layer below the filter layer. In other words, a filter layer is used to selectively absorb light not used for image capture. An antihalation layer can be viewed as a type of filter layer positioned below all the color layers, wherein no light needs to be transmitted to any color layer below the antihalation layer, but reflection of light back through the antihalation unit is prevented or minimized. Both an antihalation layer and a filter layer will typically employ a filter dye which absorbs, or filters out, light not intended to be absorbed by a color layer.

Imaging elements that can be processed, after imagewise exposure, simply by heating the element are referred to as photothermographic elements. It is often desired that such elements include an antihalation or filter layer. In most cases, the antihalation layer must be rendered substantially transparent upon heat processing in order to avoid unwanted absorption of light during scanning, which would undesirably result in a higher level of minimum density (an increased “D min ”). Particularly in the case of a color film, bleaching to transparency and avoiding or minimizing any tint is desirable.

It is generally desirable to employ light-filtering dyes which can be quickly and readily rendered ineffective, i.e., decolorized or destroyed and removed prior to or during or after photographic processing. For conventional processing of conventional film, it has been found to be particularly convenient to employ dyes which are rendered ineffective by one of the photographic baths used in processing the exposed element, such as a photographic developer or fixer. The de-coloration or destruction of a light-absorbing dye will hereinafter be referred to as bleaching.

Prior-art dyes having desirable absorption characteristics have not always had good thermal bleaching characteristics. Visible images made from photographic elements containing some such dyes have been subject to undesirable stains. Other dyes have not had the desired stability that is required for normal storage of the photographic element. Many dry photographic processes, that is, those photographic processes that require no liquids for the preparation of a visible image, have employed light-absorbing dyes that could only be removed by subjecting them to some form of liquid treatment for example, an acid bath or an alkaline bath. However, many of these dry processes lose their attractiveness when liquids are required for dye removal. Typical processes employing prior art light-absorbing layers are described in U.S. Pat. No. 3,260,601 and U.S. Pat. No. 3,282,699.

Furthermore, many if not most of the bleachable antihalation compositions in the prior art were designed for solvent systems in which the dyes and the bleaching agents were soluble as individual molecules. Furthermore, most of the bleachable antihalation compositions in the prior art have been directed to health imaging or graphic arts (monochrome systems), as compared to photothermographic color film for consumer use. In the latter context, the dark keeping of a thermally bleachable dye composition would be a challenge. For such compositions to be useful, it would be crucial that they have the least amount of dark keeping loss, and at the same time undergo almost complete bleaching at higher temperatures.

A variety of antihalation compositions have been reported in the literature for use in photothermographic systems which avoid the use of processing solutions. Such compositions generally include heat bleachable antihalation dyes or incorporated addenda that act as bleaching agents. Furthermore, many if not most prior arts (references cited below) describing thermally bleachable dye compositions use many-fold excesses of the bleaching reagents to decolorize the dyes. For example, prior patents teaching the use of excess of bleaching reagents: include, for example, Fuji EP 911,693 A1, DuPont U.S. Pat. No. 5,312,721, 3M U.S. Pat. No. 5,258,274, and Kodak U.S. Pat. Nos. 4,201,590, 4,196,002, and 4,081,278.

Prior-art patents in which bleaching reagents are not used to decolorize bleachable dyes are very limited. Dyes containing 1-aminopyridinium nucleus represent one such class of dyes. In particular, the use of 1-aminopyridinium dyes in antihalation or filter compositions for photographic imaging systems are known, being described in U.S. Pat. No. 3,619,194 (Mitchell). But these dyes, as disclosed in this patent, are not useful as they do not bleach efficiently enough at acceptable processing temperatures.

Thermal solvents for use in photothermographic and thermographic systems are generally known. Heat processable photosensitive elements can be constructed so that after exposure, they can be processed in a substantially dry state by applying heat. Because of the much greater challenges involved in developing a dry or substantially dry color photothermographic system, however, most of the activity to date has been limited to black and white photothermographic systems, especially in the areas of health imaging and microfiche.

It is known how to develop latent image in a photographic element not containing silver halide wherein organic silver salts are used as a source of silver for image formation and amplification. Such processes are described in U.S. Pat. Nos. 3,429,706 (Shepard et al.) and 3,442,682 (Fukawa et al.). Dry processing thermographic systems are described in U.S. Pat. Nos. 3,152,904 (Sorenson et al.) and 3,457,075 (Morgan and Shely). A variety of compounds have been proposed as “carriers” or “thermal solvents” or “heat solvents” for such systems, whereby these additives serve as solvents for incorporated developing agents, or otherwise facilitate the resulting development or silver diffusion processes. Acid amides and carbamates have been proposed as such thermal solvents by Henn and Miller (U.S. Pat. No. 3,347,675) and by Yudelson (U.S. Pat. No. 3,438,776). Bojara and de Mauriac (U.S. Pat. No. 3,667,959) disclose the use of non-aqueous polar solvents containing thione, —SO 2 — and —CO— groups as thermal solvents and carriers in such photographic elements. Similarly, La Rossa (U.S. Pat. No. 4,168,980) discloses the use of imidazoline-2-thiones as processing addenda in heat developable photographic materials. Takahashi (U.S. Pat. No. 4,927,731) discloses a microencapsulated base activated heat developable photographic polymerization element containing silver halide, a reducing agent, a polymerizable compound, contained in a microcapsule and separate from a base or base precursor. In addition, a sulfonamide compound is included as a development accelerator.

Thermal solvents for use in substantially dry color photothermographic systems have been disclosed by Komamura et al. (U.S. Pat. No. 4,770,981), Komamura (U.S. Pat. No. 4,948,698), Aomo and Nakamaura (U.S. Pat. No. 4,952,479), and Ohbayashi et al. (U.S. Pat. No. 4,983,502). The terms “heat solvent” and “thermal solvent” in these disclosures refer to a substantially non-hydrolyzable organic material which is a liquid at ambient temperature or a solid at an ambient temperature but mixes (dissolves or melts or both) with other components at a temperature of heat treatment or below but higher than 40° C., preferably above 50° C. Such solvents may also be solids at temperatures above the thermal processing temperature. Their preferred examples include compounds which can act as a solvent for the developing agent and compounds having a high dielectric constant which accelerate physical development of silver salts. Alkyl and aryl amides are disclosed as “heat solvents” by Komamura et al. (U.S. Pat. No. 4,770,981), and a variety of benzamides have been disclosed as “heat solvents” by Ohbayashi et al. (U.S. Pat. No. 4,983,502). Polyglycols, derivatives of polyethylene oxides, beeswax, monostearin, high dielectric constant compounds having an —SO 2 — or —CO— group such as acetamide, ethylcarbamate, urea, methylsulfonamide, polar substances described in U.S. Pat. No. 3,667,959, lactone of 4-hydroxybutanoic acid, methyl anisate, and related compounds are disclosed as thermal solvents in such systems. The role of thermal solvents in these systems is not clear, but it is believed that such thermal solvents promote the diffusion of reactants at the time of thermal development. Masukawa and Koshizuka disclose (in U.S. Pat. No. 4,584,267) the use of similar components (such as methyl anisate) as “heat fusers” in thermally developable light-sensitive materials. Baxendale and Wood in the Defensive Publication corresponding to U.S. application Ser. No. 825,478 filed Mar. 17, 1969 disclose water soluble lower-alkyl hydroxybenzoates as preprocessing stabilizers in silver salt heat-developable photographic elements.

PROBLEM TO BE SOLVED BY THE INVENTION

There is a need for antihalation compositions that can be permanently and quickly bleached at lower temperatures in aqueous systems. Particularly in the field of color photothermographic film for consumer use, the requirements in terms of bleaching and keeping are high.

Also, the need to use excesses of bleaching reagents in a bleachable AHU or filter layer adds to the cost of thermally bleachable dye compositions. It would be desirable to obtain useful AHU dyes that do not require excessive amounts of bleaching reagents to undergo decolorization. Most preferable are the dyes that do not need any additional reagents to undergo successful bleaching and yet have good keeping characteristics.

There is a need for a photothermographic imaging element comprising an antihalation compound that promotes rapid bleaching once processing has been initiated by heating the element. The existence of such imaging chemistry would allow for very rapidly processed films that can be processed simply and efficiently in low cost photoprocessing kiosks.

These and other problems may be overcome by the practice of our invention.

SUMMARY OF THE INVENTION

The present invention relates to a photothermographic element comprising a support, at least one aqueous coatable photothermographic layer, and at least one aqueous coatable antihalation layer or a filter layer, wherein the antihalation or filer layer comprises a heat-bleachable composition comprising at least one light-absorbing filter dye that is a 1-aminopyridinium dye comprising a methine linkage terminated by a substituted or unsubstituted heterocyclic nucleus of the type contained in cyanine dyes, in assocation with a thermal solvent.

The term “filter dye” encompasses dyes used in filter layers or antihalation layers and excludes dyes resulting from developing agents or coupling agents. In one embodiment of the invention, the particles are dispersed in a matrix comprising a hydrophilic polymer or water-dispersible hydrophobic polymer.

The terms “heat solvent,” “thermal solvent,” and “melt former” in this application are used synonomously and refer to a substantially non-hydrolyzable organic material which is a solid at an ambient temperature but substantially mixes with the binder phase and dissolves or melts, or both, with the dye at a temperature of heat treatment or below but higher than 80° C., preferably higher than 90° C. The presence of the melt former increases dye bleaching by at least 10% at a time and temperature corresponding to 50% bleaching, which time is between 5 seconds and 1 minute and which temperature is between 90° C. to 180° C. More preferably, the melt former increases the dye bleaching by 15% or 20% at the same condition.

In a preferred embodiment, the thermal solvent is a phenolic compound. Such compounds are advantageous in the AHU dye provides improved decolorization compared to other thermal solvents.

Such solvents may also be solids at temperatures above the thermal processing temperature. Their preferred examples include compounds which can act as a solvent for the developing agent and compounds having a high dielectric constant which accelerate physical development of silver salts. Thermal solvents include the alkyl and aryl amides, a variety of benzamides, polyglycols, derivatives of polyethylene oxides, beeswax, monostearin, high dielectric constant compounds having an —SO 2 — or —CO— group such as acetamide, ethylcarbamate, urea, methylsulfonamide, the lactone of 4-hydroxybutanoic acid, methyl anisate, and related compounds.

The invention is also directed to a method of processing a photothermographic element and the use of the photothermographic element, wherein the antihalation or filter layer becomes at least 40%, preferably at least 50%, more preferably at least 90%, colorless within about 20 minutes, preferably within about 5 minutes, more preferably within about 0.5 minutes, upon heating to a temperature of at least about 90° C. (according to controlled tests of such a layer essentially alone on the same support used in the product). The described antihalation or filter layer is especially advantageous because of the speed with which the layer becomes at least 40% colorless upon heating and its good shelf life storage stability. Preferred embodiments provide thermal bleaching of greater than 75% in less than 20 seconds at a temperature below 170° C.

The invention is also directed to a method of forming an image in the multicolor photothermographic element, including scanning the developed image.

DETAILED DESCRIPTION OF THE INVENTION

As indicated above, a feature of the invention is the use, in a photothermographic element of a filter or antihalation layer comprising a 1-aminopyridinium filter dye having a methine linkage terminated by a substituted or unsubstituted heterocyclic nucleus of the type contained in cyanine dyes, e.g., those set forth in Mees and James, The Theory of the Photographic Process, MacMillan, 4th ed., pp. 194-290, hereby incorporated by reference. This filter dye has found to produce significantly improved results when combined with a melt former.

In general, when reference in this application is made to a particular moiety or group it is to be understood that such reference encompasses that moiety whether unsubstituted or substituted with one or more substituents (up to the maximum possible number). For example, “alkyl” or “alkyl group” refers to a substituted or unsubstituted alkyl, while “benzene group” refers to a substituted or unsubstituted benzene (with up to six substituents). Generally, unless otherwise specifically stated, substituent groups usable on molecules herein include any groups, whether substituted or unsubstituted, which do not destroy properties necessary for the photographic utility. Examples of substituents on any of the mentioned groups can include known substituents, such as: halogen, for example, chloro, fluoro, bromo, iodo; hydroxy; alkoxy, particularly those “lower alkyl” (that is, with 1 to 6 carbon atoms, for example, methoxy, ethoxy; substituted or unsubstituted alkyl, particularly lower alkyl (for example, methyl, trifluoromethyl), thioalkyl (for example, methylthio or ethylthio), particularly either of those with 1 to 6 carbon atoms; substituted or unsubstituted alkenyl, preferably of 2 to 10 carbon atoms (for example, ethenyl, propenyl, or butenyl); substituted and unsubstituted aryl, particularly those having from 6 to 20 carbon atoms (for example, phenyl); and substituted or unsubstituted heteroaryl, particularly those having a 5 or 6-membered ring containing 1 to 3 heteroatoms selected from N, O, or S (for example, pyridyl, thienyl, furyl, pyrrolyl); acid or acid salt groups such as any of those described below; hydroxylate, amino, alkylamino, cyano, nitro, carboxy, carboxylate, acyl, alkoxycarbonyl, aminocarbonyl, sulfonamido, sulfamoyl, sulfo, sulfonate, alkylammonium, and an ionizable group with a pKa value below 4 in water; and others known in the art. Alkyl substituents may specifically include “lower alkyl” (that is, having 1-6 carbon atoms), for example, methyl, ethyl, and the like. Further, with regard to any alkyl group or alkylene group, it will be understood that these can be branched or unbranched and include ring structures.

In a preferred embodiment of the present invention, the filter dye is represented by the following formulae I:

wherein:

R 1 and R 2 can be either:

(a) an alkyl group, preferably having one to eight carbon atoms such as methyl, ethyl, propyl, butyl, etc. including a substituted alkyl radical such as aralkyl, e.g., benzyl; hydroxyalkyl such as hydroxypropyl, hydroxyethyl; etc.;

(b) an acyl group, e.g.,

 including a thioacyl group, e.g.,

wherein R 5 is an alkyl group preferably having one to eight carbon atoms such as methyl, ethyl, propyl, butyl, etc., an aryl group such as phenyl, naphthyl, tolyl, etc., an alkoxy group containing one to eight carbon atoms such as methoxy, ethoxy, butoxy, isobutoxy, etc., an amino group such as arylamino, alkylamino, etc., a heterocyclic nucleus containing five to six members at least one of which is oxygen, sulfur or nitrogen such as a pyridine nucleus, a quinoline nucleus, etc.;

(c) an aryl radical including a substituted aryl radical, e.g., phenyl, naphthyl, tolyl, hydroxyphenyl, halophenyl such as chlorophenyl, 2,4,6-trichlorophenyl, nitrophenyl, carboxyphenyl, alkoxyphenyl such as methoxyphenyl, ethoxyphenyl, etc.;

(d) a heterocyclic nucleus containing five to six members in the nucleus at least one member being a nitrogen, sulfur, selenium or oxygen atom including a substituted heterocyclic nucleus such as a pyridine nucleus, a quinoline nucleus, a benzothiazole nucleus, etc.;

(e) joined together to complete a five to six membered heterocyclic nucleus including a substituted heterocyclic nucleus such as a 4H-1,2,4-triazolyl, an alkyl substituted 4H-1,2,4-triazolyl, an aryl substituted 4H-1,2,4-triazolyl, a morpholino group, an imidazole group, a piperidino group, a pyrrole group, a pyrrolidino group, etc.;

Q 1 represents the non-metallic atoms necessary to complete a (saturated, unsaturated, or aromatic) heterocyclic nucleus containing five to fifteen atoms in the heterocyclic ring (including fused heterocyclic ring structures), which nucleus can contain at least one additional hetero atom such as oxygen, sulfur, selenium or nitrogen, i.e., a nucleus of the type used in the production of cyanine dyes, and which heterocyclic nucleus can be substituted or unsubstituted by up to 5 independently selected substituents, preferably 0 to 3 substituents, such as the following representative substituted or unsubstituted nuclei: a thiazole nucleus, which may be substituted, e.g., thiazole, 4-methylthiazole, 3-ethylthiazole, 4-phenylthiazole, 5-methylthiazole, 5-phenylthiazole, 4,5-dimethylthiazole, 4,5-diphenylthiazole, 4-(2-thienyl)-thiazole, benzothiazole, 4-chlorobenzothiazole, 5-chlorobenzothiazole, 6-chlorobenzothiazole, 7-chlorobenzothiazole, 4-methylbenzothiazole, 5-methylbenzothiazole, 6-methylbenzothiazole, 6-nitrobenzothiazole, 5-bromobenzothiazole, 6-bromobenzothiazole, 5-chloro-6-nitrobenzothiazole, 4-phenylbenzothiazole, 4-methoxybenzothiazole, 5-methoxybenzothiazole, 6-methoxybenzothiazole, 5-iodobenzothiazole, 6-iodobenzothiazole, 4-ethoxybenzothiazole, 5-ethoxybenzothiazole, a tetrahydrobenzothiazole nucleus, which may be substitued, e.g., 5,6-dimethoxybenzothiazole, 5,6-methylenedioxybenzothiazole, 5-hydroxybenzothiazole, 6-hydroxybenzothiazole; a naphthothiazole nucleus, alpha-naphthothiazole, beta-naphthothiazole, beta, beta-naphthothiazole, which nucleus can be substituted, for example, 5-methoxy-beta, beta-naphthothiazole, 5-ethoxy-beta-naphthothiazole, 8-methoxy-alpha-naphthothiazole, 7-methoxy-alpha-naphthothiazole, 4′-methoxythianaphtheno-7′,6′, 4,5-thiazole, nitro group substituted naphthothiazoles, etc.; an oxazole or benzoxazole or naphthoxazole nucleus, which may be substituted, e.g., 4-methyloxazole, 4-nitro-oxazole, 5-methyloxazole, 4-phenyloxazole, 4,5-diphenyloxazole, 4-ethyloxazole, 4,5-dimethyloxazole, 5-phenyloxazole, benzoxazole, 5-chlorobenzoxazole, 5-methylbenzoxazole, 5-phenylbenzoxazole, 5- or 6-nitrobenzoxazole, 5-chloro-6-nitrobenzoxazole, 6-methylbenzoxazole, 5,6-dimethylbenzoxazole, 4,6-dimethylbenzoxazole, 5-methoxybenzoxazole, 5-ethoxybenzoxazole, 5-chlorobenzoxazole, 6-methoxybenzoxazole, 5-hydroxybenzoxazole, 6-hydroxybenzoxazole, alpha-naphthoxazole, beta-naphthoxazole, nitro group substituted naphthoxazoles, etc.; a selenazole or benzoselenazole or naphthoselenazole nucleus, which may be substituted, e.g., 4-methylselenazole, 4-nitroselenazole, 4-phenylselenazole, benzoselenazole, 5-chlorobenzoselenazole, 5-methoxybenzoselenazole, 5-hydroxybenzoselenazole, 5- or 6-nitrobenzoselenazole, 5-chloro-6-nitrobenzoselenazole, tetrahydrobenzoselenazole, alpha-naphthoselenazole, beta-naphthoselenazole, nitro group substituted naphthoselenazoles, etc.; an oxazoline nucleus, which may be substituted, e.g., 4,4-dimethyloxazoline, etc.; a thiazoline nucleus, which may be subsituted, e.g., 4-methylthiazoline, etc.; a pyridine nucleus, which may be substituted, e.g., 2-pyridine, 5-methyl-2-pyridine, 4-pyridine, 3-methyl-4-pyridine, nitro group substituted pyridines, etc.; a quinoline nucleus, which may be substituted, e.g., 2-quinoline, 3-methyl-2-quinoline, 6-methyl-2-quinoline, 6-chloro-2-quinoline, 6-nitro-2-quinoline, 8-chloro-2-quinoline, 6-methoxy-2-quinoline, 8-ethoxy-2-quinoline, 8-hydroxy-2-quinoline, 4-quinoline, 6-methoxy-4-quinoline, 6-nitro-4-quinoline, 7-methyl-4-quinoline, 8-chloro-4-quinoline, 1-isoquinoline, 6-nitro-1-isoquinoline, 3,4-dihydro-1-isoquinoline, 3-isoquinoline, etc.; a 3,3-dialkylindolenine nucleus, typically having a nitro or cyano substituent, e.g., 3,3-dimethyl-5 or 6-nitroindolenine, 3,3-dimethyl-5 or 6-cyanoindolenine, etc.; and, an imidazole or benzimidazole or naphthimidazole nucleus, which may be substituted, e.g., 1-alkylimidazole, 1-alkyl-4-phenylimidazole, 1-alkyl-4,5-dimethylimidazole, benzimidazole, 1-alkylbenzimidazole, 1-alkyl-5-nitrobenzimidazole, 1-aryl-5,6-dichlorobenzimidazole, 1-alkyl-alpha-naphthimidazole, 1-aryl-beta-naphthimidazole, 1-alkyl-5-methoxy-alpha-naphthimidazole, or, an imidazo[4,5-b]quinoxaline nucleus, which may be substituted, e.g., 1-alkylimidazo[4,5-b]quinoxaline such as 1-ethylimidazo[4,5-b]quinoxaline, 6-chloro-1-ethylimidazo[4,5-b]quinoxaline, etc., 1-alkenylimidazo[4,5-b]quinoxaline such as 1-allylimidazo[4,5-b]quinoxaline, 6-chloro-1-allylimidazo[4,5-b]quinoxaline, etc., 1-arylimidazo[4,5-b]quinoxaline such as 1-phenylimidazo[4,5-b]quinoxaline, 6-chloro-1-phenylimidazo[4,5-b]quinoxaline, etc.; a 3,3-dialkyl-3H-pyrrolo[2,3-b]pyridine, e.g., 3,3-dimethyl-3H-pyrrolo[2,3-b]pyridine, 3,3-diethyl-3H-pyrrolo[2,3-b]pyridine, etc.; a subsituted or unsubstituted thiazolo[4,5-b]quinoline nucleus; an indolyl nucleus including substituted indolyl nuclei such as a 2-phenyl-3-indole, 1-methyl-2-phenyl-3-indole; and the like. Preferred substituents are alkyl, aryl, alkoxy, and heterocyclic, all preferably having 1 to 12 carbon atoms, halogen, hydroxy, and nitro.

Y represents an alkyl group including substituted alkyl (preferably a lower alkyl containing from one to four carbon atoms), e.g., methyl, ethyl, propyl, isopropyl, butyl, hexyl, cyclohexyl, decyl, dodecyl, etc., and substituted alkyl groups (preferably a substituted lower alkyl containing from one to four carbon atoms), such as a hydroxyalkyl group, e.g., beta-hydroxyethyl, omega-hydroxybutyl, etc., an alkoxyalkyl group, e.g., beta-methoxyethyl, omega-butoxybutyl, etc., a carboxyalkyl group, e.g., beta-carboxyethyl, omega-carboxybutyl, etc., an amino or substituted amino group, e.g., dimethylamino, diethylamino, etc., a sulfoalkyl group, e.g. sulfopropyl, beta-sulfoethyl, alpha-sulfobutyl, omega-sulfatobutyl, etc., an acyloxyalkyl group, e.g., beta-acetoxyethyl, gamma-acetoxypropyl, omega-butyryloxybutyl, etc., an alkoxycarbonylalkyl group, e.g., beta-methoxycarbonylethyl, omega-ethoxycarbonylbutyl, etc. or an aralkyl group, e.g., benzyl, phenethyl, etc.; an alkenyl group, e.g., allyl, 1-propenyl, 2-butenyl, etc., or an aryl group, e.g., phenyl, tolyl, naphthyl, methoxyphenyl, chlorophenyl, etc.;

X − can be an acid anion, e.g., chloride, bromide, iodide, perchlorate, sulfate, thiocyanate, p-toluenesulfonate, methyl sulfate, tetrafluoroborate, etc.

In the event, Y contains an anionic group such as a sulfate, phosphate, sulfonate, phosphonate and carboxyl group, then the compound is zwitterionic and an acid anion is unnecessary.

Preferred filter dye compounds are as disclosed in commonly assigned, copending U.S. Ser. No. 09/940,204, hereby incorporated by reference in its entirety. Preferably the Y is an sulfoalkyl group

n is one or two;

p represents the number of double bonds in the heterocylic ring between the N atom and the first methine linkage and is zero or one, preferably 0;

L represents a methine linkage having the formula

wherein T can be hydrogen, halogen, carboxyamides, lower alkyl of one to four carbon atoms or aryl such as phenyl, e.g., —CH, —C(CH 3 ), —C(C 6 H 5 ), etc.;

R 7 and R 8 each can be (1) a hydrogen atom, (2) an alkyl group (preferably a lower alkyl containing from one to four carbon atoms) including a substituted alkyl group such as aralkyl, hydroxyalkyl, e.g., methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, dodecyl, benzyl, hydroxypropyl, hydroxyethyl, etc. or (3) an aryl group including a substituted aryl group such as an alkaryl, haloaryl, alkoxyaryl, aminoaryl, etc. e.g., phenyl, tolyl, naphthyl, methoxyphenyl, chlorophenyl, diethylaminophenyl, etc.;

The preferred light-absorbing photographic layers of this invention contain a 1-aminopyridinium dyes represented by the following structure II:

wherein Q 1 , R 1 , R 2 , R 7 , R 8 and p are as defined and Y is preferably a sulfoalkyl, carboxyalkyl, or phosphoalkyl group, in which Y preferably has 1 to 4 carbon atoms.

More preferably, light-absorbing photothermographic layers of this invention contain 1-aminopyridinium dyes having the following structure III:

wherein R 1 , R 2 , R 7 , R 8 , and Y are as defined above and R 9 is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkoxy, substituted or unsubstituted aryl or alkylaryl, nitro, hydroxy, or halogen, which carbon containing groups preferably have 1 to 8 carbon atoms.

More preferably, the 1-aminopyridinium dye is represented by structure IV:

wherein R 1 , R 2 , R 7 , R 8 , R 9 and Y are as defined above and R 10 and R 11 are independently selected from the R 9 groups mentioned above.

A representative 1-aminopyridiniume compound according to the present invention is as follows:

If desired, a combination of 1-aminopyridinium compounds can be used. Selection of the 1-aminopyridinium dye or combination of such compounds will depend upon such factors as the processing conditions, desired degree of bleaching in the layer containing the dye or dyes, solubility characteristics of the components, spectral absorption characteristics, and the like.

For antihalation layer purposes, it is desirable that the heat bleachable layer have substantially uniform absorption in the spectral region in which the imaging composition is sensitive. The antihalation dye or dye precursor should also be changed to the extent that at least about 40%, and preferably at least 50%, more preferably at least 60%, still more preferably at least 80%, and most preferably at least 90% of the layer absorption is changed from colored to colorless according to a standard test using Status M density. Thus, the antihalation or filter layer, after bleaching, has minimal or substantially no optical density that will adversely affect the Dmin of the product during scanning, or during overall picture production using the photothermographic element.

More than one filter dye can be used in the same AHU or filter layer. Combinations of different filter dyes can be used in the same layer or in different layers, depending on the purpose of the dye. Preferably, the filter dyes useful in an antihalation layer according to the present invention absorbs mainly from about 400 to about 850 nm. Preferably, the dyes absorbing mainly (and relatively uniformly) at from about 500 to about 850 nm are used. In the case of filter layers, a yellow filter dye useful in an yellow filter layer according to the present invention absorbs mainly from about 400 to about 500 nm and will transmit most of the light in the range 500 to 850 nm. Preferably, a yellow filter dye will absorb mainly at from about 420 to about 480 nm and will transmit most of the light in the range 490 to 850 nm. Similarly, a magenta filter dye will absorb light mostly from 500 to 600 nm and preferably from 520 to 580 nm while transmitting most of the light shorter than 500 nm and longer than 600 nm.

The filter dyes within the photothermographic elements of the present invention are irreversibly bleached upon exposure to heat of adequate intensity, including dry processing.

For black & white or monochromatic imaging elements, the phototographic elements are typically based on organic silver salt oxidizing agents and organic reducing agents are described in Owen U.S. Pat. No. 2,910,377, wherein are included silver behenate and silver stearate as well as the silver salts of a number of other organic acids, viz oleic, lauric, hydroxystearic, acetic, phthalic, terephthalic, butyric, m-nitrobenzoic, salicylic, phenylacetic, pyromellitic, p-phenylbenzoic, undecylenic, camphoric, furoic, acetamidobenzoic, and o-aminobenzoic. Other organic silver salts capable of providing similar effects include the silver salts of saccharin, benzotriazole, phthalazinone, 4′-n-octadecyloxydiphenyl-4-carboxylic acid, 10,12,14-octadecatrienoic acid, and benzoic acid. The silver salts of those organic acids which are water-insoluble and normally solid are preferred, since the byproducts do not adversely affect the coating.

The filter dyes of the present invention have good incubation stability, allowing their incorporation into elements requiring prolonged storage. The dyes contained in the novel photothermographic elements of this invention are irreversibly bleached upon exposure. The amount of heat required to cause bleaching of the layers is somewhat dependent upon the particular dye incorporated in the layer; higher temperatures require shorter times to bring about bleaching while lower temperatures require longer times. Generally, temperatures of at least 100° C. for a period of at least 5 seconds are required to bring about any noticeable bleaching. For color photothermography, temperatures of 130° C. and above and times in excess of 10 seconds are generally preferred.

The dyes incorporated in the novel layers of this invention are characterized by their good spectral absorption properties. The maximum absorption of the various individual dyes ranges throughout the visible regions of the spectrum. Also, the dyes are further characterized by the fact that they are readily incorporated in hydrophilic layers used in photographic elements. The dyes are soluble in most of the common organic solvents including halogenated aliphatic hydrocarbons such as chloroform, ketones such as acetone, aliphatic alcohols such as methanol, ethanol, etc., amides such as dimethylformamide, nitrogen-containing heterocyclic solvents such as pyridine, etc. The dyes may also be mordanted with basic mordants, dissolved in a dispersed organic phase, emulsified, or in the form of solid particles.

The dyes described herein are valuable for use in photothermographic light-sensitive material employing one or more sensitive silver halide layers. The dyes can be used to make light-absorbing layers including antihalation as well as filter layers with or without dyes of other classes and can be incorporated readily in colloidal binders used for forming such layers. They are especially useful in gelatin layers lying adjacent to silver halide layers, since they can be mordanted with organic polymeric substances having excellent non-wandering characteristics in gelatin. The dyes can also be readily bleached without removing the layers containing them. Furthermore, they can be mordanted in layers coated in contact with light-sensitive silver halide emulsion layers since the mordanted dyes have very good stability at the pH of the most sensitive silver halide emulsions and have little or no undesirable effect on the silver halide itself As a result, the dyes can be used as light-absorbing dyes in layers coated directly on top of the sensitive silver halide emulsion layers or between two sensitive silver halide emulsion layers or between the support and a sensitive silver halide emulsion layers or between the support and a sensitive silver halide emulsion layer or on the back of a support as an antihalation layer.

As indicated above, the N-aminopyridiniumcarbocyanine dyes are used in association with the melt-formers. In a preferred embodiment, the bleachable AHU Composition containing the above dye is in combination with salicylanilide.

In a preferred embodiment, the melt former is a phenolic compound. Such compounds are advantageous for use with a filter or AHU dye because it provides improved decolorization compared to other melt formers or thermal solvents.

The amount of melt former that should be available to, or within, the light-absorbing layer containing the filter or AHU dye according to the present invention is preferably at least 0.10 g/m 2 . The melt former can be in the same or in a proximate layer, including optionally in an adjacent imaging layer, so long as the melt former can diffuse into the light-absorbing layer during thermal development. In the case where the melt former is not in the light-absorbing layer, the melt former to gel ratio for the combined layers (the dye-containing layer and the melt-former-containing layer) is preferably at least 1%.

Such solvents may also be solids at temperatures above the thermal processing temperature. Preferred examples include compounds which can act as a solvent for the developing agent and compounds having a high dielectric constant which accelerate physical development of silver salts. Thermal solvents include the alkyl and aryl amides disclosed as “heat solvents” by Komamura et al. (U.S. Pat. No. 4,770,981), the variety of benzarnides disclosed as “heat solvents” by Ohbayashi et al. (U.S. Pat. No. 4,983,502). the polyglycols, derivatives of polyethylene oxides, beeswax, monostearin, high dielectric constant compounds having an —SO 2 — or —CO— group such as acetamide, ethylcarbamate, urea, methylsulfonamide, polar substances described in U.S. Pat No. 3,667,959, lactone of 4-hydroxybutanoic acid, methyl anisate, and related compounds are disclosed as thermal solvents in such systems, the methyl anisate and the like disclosed by Masukawa and Koshizuka disclose (in U.S. Pat. No. 4,584,267), the phenolic compounds disclosed in U.S. Pat. No. 5,352,561 to Bailey et al., for example, hydroxybenzene derivatives, the preceeding patents of which are incorporated by reference in their entirety.

Preferably, the thermal solvents have a phenolic-OH group that is believed to function as a hydrogen bond donating functional group as a separate and distinct functional group in the same compound. By “phenolic” is meant that the —OH group is a substituent on an aromatic ring. In one embodiment of the invention, the thermal solvent also contains a hydrogen bond accepting functional group as a separate and distinct functional group in the same compound. In one embodiment, thermal solvents are provided according to structure V:

wherein the substituent B is independently selected from a substituent where an oxygen; carbon, nitrogen, phosphorus, or sulfur atom is linked to the ring as part of a ketone, aldehyde, ester, amido, carbamate, ether, aminosulfonyl, sulfamoyl, sulfonyl, amine (through —NH— or —NR 2 —), phosphine (through —PH— or —PR 2 —), or (preferably through a nitrogen atom) an aromatic heterocyclic group, where R 2 is defined below; m is 0 to 4; and wherein the substituent R is independently selected from a substituted or unsubstituted alkyl, cycloalkyl, aryl, alkylaryl, or forms a ring (for example, a substituted or unsubstituted: aliphatic ring, aryl ring or aromatic heterocyclic ring) with another substituent on the ring; and wherein n is 0 to 4 and m+n is 1 to 5.

Substituents on R or B can include any substituent that does not adversely affect the melt former or thermal solvent, for example, a halogen. The substituents R or B can also comprise another phenolic group.

The phenolic compound should have a melting point of at least 80° C., preferably 80° C. to 300° C., more preferably between 100 and 250° C. Preferably, m+n is 1 or 2. In one embodiment, when m is 0, there is a second phenolic group on an R substituent.

In a preferred class of compounds, in the compound of Structure V, B is selected from the group consisting of —C(═O)NHR 2 , —NHC(═O)R 2 , —NHSO 2 R 2 , —SO 2 NHR 2 , —SO 2 R 2 , and —C(═O)R 2 , —C(═O)OR 2 , and —OR 2 , wherein R 2 is substituted or unsubstituted alkyl, cycloalkyl, aryl, alkylaryl, heterocyclic group and can optionally comprise a phenolic hydroxyl group. More preferably, n is 1 and R 2 is a substituted or unsubstituted phenyl. Preferably, any substituents on the phenyl group have 1 to 10 carbon atoms.

It is noted that in the case of two bulky alkyl (for example, tertiary C 4 ) substituents ortho to the phenolic group, melt-forming activity will be unsatisfactory. Therefore, compounds with two ortho C 4 groups and the like, not being effective melt formers, are excluded.

In general, it is desirable that water solubility of the compound is low enough that the melt former can be dispersed as an aqueous solid particle dispersion without recrystallization leading to ripening and loss of fine particles. Although not necessarily required, tendencies are such that preferably the clogP of the phenolic compounds is above 0.0.

The log of the partition coefficient, logP, characterizes the octanol/water partition equilibrium of the compound in question. Partition coefficients can be experimentally determined. As an estimate, clogP values can be calculated by fragment additivity relationships. These calculations are relatively simple for additional methylene unit in a hydrocarbon chain, but are more difficult in more complex structural variations. The clogP values used herein are estimated using KowWin® software from Syracuse Research Corporation, a not-for-profit organization, headquartered in Syracuse, N.Y. (USA).

In one preferred embodiment of the invention, the color photothermographic element comprises a radiation sensitive silver halide, and a thermal solvent represented by the following structure VI:

wherein B and R is as described above.

In one embodiment, the phenolic thermal solvent (“melt former”) has the following structure VII:

Wherein LINK can be —C(═O)NH—, —NHC(═O)—, —NHSO 2 —, —C(═O)—, —C(═O)O—, —O—, —SO 2 NH—, and —SO 2 —; R and n are as defined above, and p is 0 to 4. Preferably R is independently selected from substituted or unsubstituted alkyl, preferably a C1 to C10 alkyl group. In one embodiment n and p are independently 0 or 1. In another embodiment, n+p=1.

Typically, the thermal solvent is present in an imaging layer of the photothermographic element in the amount of 0.01 times to 0.5 times the amount by weight of coated gelatin per square meter.

The following are some representative examples of melt formers according to the present invention:

TS-1 clogP 3.30 mp ° C. 136-138 87-17-2 ComA
TS-2 clogP 3.84 mp ° C. 193-195 16670-64-7
TS-3 clogP 7.26 mp ° C. 157-9
TS-4 clogP 4.47 mp ° C. 246-251 92-77-3 ComA
TS-5 clogP 5.06 mp ° C. 200-202
TS-6 clogP 3.84 mp ° C. 160 53938-41-3
TS-7 clogP 3.84 mp ° C. 117 16670-62-5
TS-8 ClogP 6.08 mp ° C. 224-226 3236-71-3 ComA
TS-9 clogP 3.64 mp ° C. 158-159 80-05-7 ComA
TS-10 clogP 4.27 mp ° C. 102 2549-50-0
TS-11 clogP 3.33 mp ° C. 193 17177-36-5
TS-12 clogP 2.02 mp ° C. 120-123 96549-95-0 ComA
TS-13 clogP 3.00 mp ° C. 128-133 2440-22-4 ComA
TS-15 clogP 2.67 mp ° C. 132-135 1137-42-4 ComA
TS-16 clogP 3.30 mp ° C. 120-122 103-16-2
TS-17 clogP 2.22 mp ° C. 153 27559-45-1
TS-18 clogP 5.00 mp ° C. 129-132 7260-11-9 ComA
TS-19 clogP 0.18 mp ° C. 152-154 3077-65-4
TS-20 clogP 2.38 mp ° C. 153-161 30988-95-5
TS-21 clogP 1.79 mp ° C. 144-146 51110-60-2
TS-22 clogP 3.87 mp ° C. 168-170

In the above Table, all the values of clogP values were calculated using SRC's LogKow® (KowWin®) software. CAS Registry Numbers are included when available. Also, indication of commercial availability (ComA=commercially available) is provided when known. Sources of commercially available compounds are Aldrich Chemical Company, Inc (Milwaukee, Wis. 53233); Acros Organics, at Janssen Pharmaceuticalaan 3a, B-2440, Geel, Belgium; and Trans World Chemicals Inc., 14674 Southlawn Lane, Rockville, Md. 20850.

As will be appreciated by the skilled artisan, many phenolic compounds according to the present invention may be made by simple reactions between appropriate intermediates, for example, melt former MF-2 can be prepared by treating 4-methyl salicylic acid with aniline. Methods for synthesizing phenolic compounds according to the present invention can be found in a variety of patent or literature references. For example, synthetic methods for making hydroxynaphthoic acid derivatives are disclosed by Ishida, Katsuhiko; Nojima, Masaharu; Yamamoto, Tamotsu; and Okamoto, Tosaku in Japanese Patent JP 61041595 A2 (1986) and JP 04003759 (1992) and Japanese Kokai JP 84-163718 (1984). Synthetic methods for making N-Substituted salicylamides are disclosed by Ciampa, Giuseppe and Grieco, Ciro., Univ. Naples, Rend. Accad. Sci. Fis. Mat. (Soc. Naz. Sci., Lett. Arti Napoli) (1966), 33(Dec.), 396-403.

Methods for the preparation of the anilides of phenolcarboxylic acids are disclosed by Burmistrov, S. I. and Limarenko, L. I., in U.S.S.R. Patent SU 189869 (1966) and Application SU 19660128. For example, anilides were prepared by treating phenolates with phenylurethane in a high-boiling organic solvent, e.g., cumene or the diethylbenzene fraction from the production of PhEt, with heating. Such a method can be used in the synthesis of melt former MF-2 above.

A Friedel-Crafts reaction, involving the synthesis of salicylanilides via ortho-aminocarbonylation of phenols with phenyl isocyanate can be used in the synthesis of melt former MF-6 and MF-7 above. Such a method is reported by Balduzzi, Gianluigi; Bigi, Franca; Casiraghi, Giovanni; Casnati, and Giuseppe; Sartori, Giovanni, Ist. Chim. Org., Univ. Parma, Parma, Italy, in the journal Synthesis (1982), (10), 879-81. For example, the reaction of “a” below with PhNCO in the presence of AlCl 3 in xylene gave “b,” where R, R 1 , R 2 , R 3 =H, H, H, H or Me, H, H, H or H, H, Me, H or H, MeO, H, H or H, H, MeO, H or H, Me, H, Me, or H, OH, H, H or H, H, R 2 R 3 =(CH:CH) 2 .

Iwakura, Ken and Igarashi, Akira, in Japanese Patent JP 62027172 A2 (1987) and Kokai JP 1985-165514 (1985) disclose amethod of making a 1,3-bis(4-hydroxyphenyl)propane, which method can be used, for example, in the preparation of melt-former MF-10 and the like. The preparation of benzimidazoles and analogs is disclosed by Oku, Teruo; Kayakiri, Hiroshi; Satoh, Shigeki; Abe, Yoshito; Sawada, Yuki; Inoue, Takayuki; and Tanaka, Hirokazu, in PCT Int. Appl. WO 9604251 A1 (1996) and WO 95-JP1478 (1995). Such methods can be used in preparing, for example, the melt former MF-21 above.

Methods of preparing bisphenol compounds are disclosed in Japanese Patent JP 56108759 A2 (1981) and Application: JP 80-8234 (1980). For example, bisphenol disulfonamides were prepared from bis(benzotriazolyl sulfonates). Thus, in one case, bis(1-benzotriazolyl)diphenyl ether-4,4′-disulfonate was added to 4-H 2 NC 6 H 4 OH in pyridine with ice cooling and the mixture stirred 24 hours at room temperature to give N′-bis(p-hydroxyphenyl)diphenyl ether-4,4′-disulfonamide. Such methods can be used, for example, to make melt former MF-11 above and the like.

The photographic elements prepared according to the instant invention can be used in various kinds of photothermographic systems. In addition to being useful in X-ray and other non-optically sensitized systems, they can also be used in orthochromatic, panchromatic and infrared sensitive systems. The sensitizing addenda can be added to photographic systems before or after any sensitizing dyes which are used.

The dyes of this invention can be used in emulsions intended for color photothermography, for example, emulsions containing color-forming couplers or other color-generating materials, emulsions of the mixed-packet type such as described in U.S. Pat. No. 2,698,794 of Godowsky issued Jan. 4, 1955; in silver dye-bleach systems; and emulsions of the mixed-grain type such as described in U.S. Pat. No. 2,592,243 of Carroll and Hanson issued Apr. 8, 1952.

Photographic layers containing the dyes of this invention can be used in diffusion transfer processes which utilize undeveloped silver halide in the non-image areas of the negative to form a positive by dissolving the undeveloped silver halide and precipitating it on a receiving layer in close proximity to the original silver halide emulsion layer. Such processes are described in Rott, U.S. Pat. No. 2,352,014, Land U.S. Pat. No. 2,543,181 and Yackel et al. U.S. Pat. No. 3,020,155. Photographic layers containing the dyes of this invention can also be used in color transfer processes which utilize the diffusion transfer of an imagewise distribution of developer, coupler or dye from a light-sensitive layer to a second layer while the two layers are in close proximity to one another. Color transfer processes of this type are described in Yutzy, U.S. Pat. No. 2,856,142; Land et al. U.S. Pat. No. 2,983,606; Whitmore et al. British Pat. Nos. 904,364 and 840,731; and Whitmore et al. U.S. Pat. No. 3,227,552.

In general, intermediates for, the dyes incorporated in the light-absorbing layers are obtained by reacting an appropriate hydrazine with a pyrylium salt. Representative dyes are illustrated by the following examples which are not intended to limit the invention.

Depending on the choice of the filter dye, it can be in the antihalation or filter layer in the form of solid particles, dissolved in a dispersed organic phase, emulsified, or dissolved in the aqueous matrix of the antihalation or filter layer. Although dissolving a water-soluble dye in the aqueous matrix is easiest, it is not universally preferred since one would generally prefer that the dye remain in the layer in which it was coated.

The coverages and proportions of the components which comprise the described antihalation or filter component of the present invention can vary over wide ranges depending upon such factors as the particular use, location in the element of the antihalation or filter component, the desired degree of absorption, processing temperatures, and the like. For example, in some photothermographic elements the concentration of dye is sufficient to provide a peak optical density of at least about 0.05. For antihalation purposes, it is desirable that the concentration of the dye be sufficient to provide an optical density of at least about 0.2 such as about 0.3 to about 2.0, throughout the visible spectrum. Particles of the 1-aminopyridinium filter dyes can be made by conventional dispersion techniques, such as milling, by preparing the particles by a limited coalescence procedure, or other procedures known in the art. Milling processes that can be used include, for example, processes described in U.K. Patent No. 1,570,632, and U.S. Pat. Nos. 3,676,147, 4,006,025, 4,474,872 and 4,948,718, the entire disclosures of which are incorporate herein by reference. Limited coalescence procedures that can be used include, for example, the procedures described in U.S. Pat. Nos. 4,994,3132, 5,055,371, 2,932,629, 2,394,530, 4,833,060, 4,834,084, 4,965,131 and 5,354,799, the entire disclosures of which are incorporated herein by reference. A suitable average size of the particles are 10 to 5000 nm, preferably 20 to 1000 nm, most preferably 30 to 500 nm.

In a preferred embodiment, the 1-aminopyridinium filter dye is dispersed in the binder in the form of a solid particle dispersion. Such dispersions can be formed by either milling the dye in solid form until the desired particle size range is reached, or by precipitating (from a solvent solution) the dye directly in the form of a solid particle dispersion. In the case of solid particle milling dispersal methods, a coarse aqueous premix, containing the 1-aminopyridinium compound and water, and optionally, any desired combination of water soluble surfactants and polymers, is made, and added to this premix prior to the milling operation. The resulting mixture is then loaded into a mill. The mill can be, for example, a ball mill, media mill, jet mill, attritor mill, vibratory mill, or the like. The mill is charged with the appropriate milling media such as, for example, beads of silica, silicon nitride, sand, zirconium oxide, yttria-stabilized zirconium oxide, alumina, titanium, glass, polystyrene, etc. The bead sizes typically range from 0.25 to 3.0 mm in diameter, but smaller media may be used if desired. The solid 1-aminopyridinium in the slurry are subjected to repeated collisions with the milling media, resulting in crystal fracture and consequent particle size reduction.

The aqueous dispersion can further contain appropriate surfactants and polymers previously disclosed for use in making pH precipitated dispersions. For solvent precipitation, a solution of the dye is made in some water miscible, organic solvent. The solution of the dye is added to an aqueous solution containing appropriate surfactants and polymers to cause precipitation as previously disclosed for use in making solvent precipitated dispersions.

Surfactants and other additional conventional addenda may also be used in the dispersing process described herein in accordance with prior art solid particle dispersing procedures. Such surfactants, polymers and other addenda are disclosed in U.S. Pat. Nos. 5,468,598, 5,300,394, 5,278,037, 4,006,025, 4,924,916, 4,294,917, 4,940,654, 4,950,586, 4,927,744, 5,279,931, 5,158,863, 5,135,844, 5,091,296, 5,089,380, 5,103,640, 4,990,431,4,970,139, 5,256,527, 5,015,564, 5,008,179, 4,957,857, and 2,870,012, British Patent specifications Nos. 1,570,362 and 1,131,179 referenced above, the disclosures of which are hereby incorporated by reference, in the dispersing process of the filter dyes.

Additional surfactants or other water soluble polymers may be added after formation of the 1-aminopyridinium dispersion, before or after subsequent addition of the small particle dispersion to an aqueous coating medium for coating onto a photographic element support. The aqueous medium preferably contains other compounds such as stabilizers and dispersants, for example, additional anionic nonionic, zwitterionic, or cationic surfactants, and water soluble binders such as gelatin as is well known in the photographic element art. The aqueous coating medium may further contain other dispersion or emulsions of compounds useful in photography. Another technique for forming solid 1-aminopyridinium particles involves solvent precipitation. For example, a solution of the 1-aminopyridinium dye can be made in some water miscible, organic solvent, after which the solution of the 1-aminopyridinium dye can be added to an aqueous solution containing appropriate surfactants and polymers to cause precipitation.

Various techniques for forming a liquid dispersion of the 1-aminopyridinium dye, including oil-in-water emulsions, are well known by the skilled artisan. An oil-in-water dispersion of the 1-aminopyridinium dye may be prepared by dissolving the 1-aminopyridinium dye in an organic liquid, forming a premix with an aqueous phase containing dispersing aids such as water-soluble surfactants, polymers and film forming binders such as gelatin, and passing the premix through a mill until the desired particle size is obtained. The mill can be any high energy device such as a colloid mill, high pressure homogenizer, ultrasonic device, or the like. Preparation of conventional oil-in-water dispersions are well known in the art and are described in further detail, for example, in Jelly and Vittum U.S. Pat. No. 2,322,027. Alternatively, the filter dye can be loaded into a latex polymer, either during or after polymerization, and the latex can be dispersed in a binder. Additional disclosure of loaded latexes can be found in Milliken U.S. Pat. No. 3,418,127.

Combinations of bleachable filter or antihalation dyes can be used or one or more bleachable dyes can be used in combination with other non-bleachable dyes in the present invention to obtain a broader spectrum of absorption, if desired. For example, when the filter dye is used to provide antihalation properties or to permit room light loading, the filter dye should be selected to provide an absorption envelope that matches the sensitization envelope of the light sensitive layer(s) of the photographic element. Other filter dyes that can be used include, for example, the filter dyes disclosed in U.S. Pat. Nos. 2,538,008, 2,538,009, and 4,420,555, and UK Patents Nos. 695,873 and 760,739. It is preferred to use the filter dyes as solid particle dispersions as disclosed in U.S. Pat. Nos. 4,950,586, 4,948,718, 4,948,717, 4,940,654, 4,923,788, 4,900,653, 4,861,700, 4,857,446, 4,855,221, 5,213,956 and 5,213,957, and European Patent No. 430,186. The entire disclosures of the above patents are incorporated herein by reference.

For aqueous imaging systems, the binders used in the aqueous dispersion or coating composition should be transparent or translucent and include those materials which do not adversely affect the reaction which changes the dye from colored to colorless and which can withstand the processing temperatures employed. These polymers include, for example, proteins such as gelatin, gelatin derivatives, cellulose derivatives, polysaccharides such as dextran and the like; and synthetic polymeric substances such as water soluble polyvinyl compounds like poly(vinyl alcohol), poly(vinyl pyrrolidone), acrylamide polymers and the like. Other synthetic polymeric compounds which can be useful include dispersed vinyl compounds such as styrene butadiene rubbers in latex form. Effective polymers include high molecular weight materials, polymers and resins which are compatible with the imaging materials of the element. Combinations of the described colloids and polymers can also be useful if desired.

The antihalation layer as described can be useful in a variety of photothermographic elements. Useful photothermographic elements include those which are designed to provide an image from photographic silver halide, such as color images. Photothermographic color elements which are designed for consumer film are especially useful with the antihalation materials according to the invention.

The described combination of the 1-aminopyridinium dye can be in any suitable location in the photothermographic element which provides the desired bleaching of the dye upon heating. When the invention is utilized as an antihalation layer of a photographic material coated on a transparent support (such as photographic film), the inventive layer can be coated on the same side or the opposite of the support as the radiation sensitive layers. When the invention is utilized as an antihalation layer of a photographic material coated on a reflective support (such as photographic paper), then the inventive layer must be coated on the same side of the support as the radiation sensitive layers. When the invention is utilized as a filter layer of a photographic material, the same requirements apply depending upon the type of support used.

In one embodiment of the invention, the dye is in association with a melt former or thermal solvent to promote the desired heat bleaching in the antihalation or filter component. The term “in association” as employed herein is intended to mean that the described materials are in a location with respect to each other which enables the desired processing and heat bleaching and provides a more useful developed image. The term is also employed herein to mean that the filter dye and the melt former are in a location with respect to each other which enables the desired change of the dye from colored to colorless upon heating as described. In general, the two components should be in the same layer, meaning there is no significant barrier or distance between them even if not uniformly dispersed together. Preferably, however, the filter dye and the melt former are uniformly inter-dispersed. Alternatively, however, a sufficient amount of melt former may transfer from an adjacent imaging layer before and during thermal processing.

A preferred embodiment of the invention is a photothermographic element comprising (a) a support having thereon (b) a photothermographic layer, and on the support or in the support (c) at least one antihalation dye compound represented by the formula (I), as described, wherein the dye becomes at least about 50, preferably at least 90% colorless within about 30 seconds upon heating to a temperature of at least about 120° C., as determined by standard testing described herein.

The antihalation or filter layer materials comprising the described dye can be present in a suitable transparent support. However, it is more preferred that an antihalation layer according to the invention should comprise binders which adhere suitably to the support or other layer of the photothermographic element upon which the antihalation or filter layer is coated. Selection of optimum binders for adhesion purposes will depend upon such factors as the particular support, processing conditions, the particular photosensitive layer, and the like.

A visible image can be developed in a photothermographic element according to the invention within a short time after imagewise exposure merely by uniformly heating the photothermographic element to moderately elevated temperatures. For example, the photothermographic element can be heated, after imagewise exposure, to a temperature within the range which provides development of the latent image and also provides the necessary temperature to cause the antihalation or filter layer to change from colored to colorless. Heating is typically carried out until a desired image is developed and until the antihalation or filter layer is bleached to a desired degree. This heating time is typically a time within about 1 second to about 20 minutes, such as about 1 second to about 90 seconds.

A simple exemplary photothermographic element, showing one embodiment comprising filter and AHU layers and their placement in the element, can be represented as follows:

UV Overcoat
Blue Sensitive Layer
Yellow Filter Layer
Green Sensitive Layer
Magenta Filter Layer
Red Sensitive Layer
AHU Layer
Support

As indicated above, the invention is especially useful in a dry photothermographic process (or “dry thermal process”). By a “dry thermal process” is meant herein a process involving, after imagewise exposure of the photographic element, development of the resulting latent image by the use of heat to raise the temperature of the photothermographic element or film to a temperature of at least about 80° C., preferably at least about 100° C., more preferably at about 120° C. to 180° C., in a dry process or an apparently dry process. By a “dry process” is meant without the external application of any aqueous solutions. By an “apparently dry process” is meant a process that, while involving the external application of at least some aqueous solutions, does not involve an amount more than the uniform saturation of the film with aqueous solution.

This dry thermal process typically involves heating the photothermographic element until a developed image is formed, such as within about 0.5 to about 60 seconds. By increasing or decreasing the thermal processing temperature a shorter or longer time of processing is useful. Heating means known in the photothermographic arts are useful for providing the desired processing temperature for the exposed photothermographic element. The heating means can, for example, be a simple hot plate, iron, roller, heated drum, microwave heater, heated air, vapor or the like. Thermal processing is preferably carried out under ambient conditions of pressure and humidity, for simplicity sake, although conditions outside of normal atmospheric pressure and humidity are also useful.

A dry thermal process for the development of a color photothermographic film for general use with respect to consumer cameras provides significant advantages in processing ease and convenience, since they are developed by the application of heat without wet processing solutions. Such film is especially amenable to development at kiosks or at home, with the use of essentially dry equipment. Thus, the dry photothermographic system opens up new opportunities for greater convenience, accessibility, and speed of development (from the point of image capture by the consumer to the point of prints in the consumer's hands), even essentially “immediate” development in the home for a wide cross-section of consumers.

Preferably, during thermal development an internally located blocked developing agent, in reactive association with each of three light-sensitive units, becomes unblocked to form a developing agent, whereby the unblocked developing agent is imagewise oxidized on development. It is necessary that the components of the photographic combination be “in association” with each other in order to produce the desired image. The term “in association” herein means that. in the photothermographic element, the photographic silver halide and the image-forming combination are in a location with respect to each other that enables the desired processing and forms a useful image. This may include the location of components in different layers.

Such photothermographic elements are used in the field of microfilming, health imaging, graphic arts, consumer products, and the like. It is especially useful where the element is exposed to visible light, directly or indirectly, in the field of health or medical imaging involving phosphorescent light, the originating exposure may be X-ray, for example. A preferred use of the present invention is in consumer color photothermographic film.

A typical photothermographic element will now be described. The support for the photothermographic element can be either reflective or transparent, which is usually preferred. When reflective, the support is white and can take the form of any conventional support currently employed in color print elements. When the support is transparent, it can be colorless or tinted and can take the form of any conventional support currently employed in color negative elements-e.g., a colorless or tinted transparent film support. Details of support construction are well understood in the art. Examples of useful supports are poly(vinylacetal) film, polystyrene film, poly(ethyleneterephthalate) film, poly(ethylene naphthalate) film, polycarbonate film, and related films and resinous materials, as well as paper, cloth, glass, metal, and other supports that withstand the anticipated processing conditions. The element can contain additional layers, such as filter layers, interlayers, overcoat layers, subbing layers, antihalation layers and the like. Transparent and reflective support constructions, including subbing layers to enhance adhesion, are disclosed in Section XV of Research Disclosure I.

Photographic elements may also usefully include a magnetic recording material as described in Research Disclosure , Item 34390, November 1992, or a transparent magnetic recording layer such as a layer containing magnetic particles on the underside of a transparent support as in U.S. Pat. No. 4,279,945, and U.S. Pat. No. 4,302,523.

In an example (one embodiment) of a color negative film construction, each of blue, green and red recording layer units BU, GU and RU are formed of one or more hydrophilic colloid layers and contain at least one radiation-sensitive silver halide emulsion and coupler, including at least one dye image-forming coupler. It is preferred that the green, and red recording units are subdivided into at least two recording layer sub-units to provide increased recording latitude and reduced image granularity. In the simplest contemplated construction each of the layer units or layer sub-units consists of a single hydrophilic colloid layer containing emulsion and coupler. When coupler present in a layer unit or layer sub-unit is coated in a hydrophilic colloid layer other than an emulsion containing layer, the coupler containing hydrophilic colloid layer is positioned to receive oxidized color developing agent from the emulsion during development. Usually the coupler containing layer is the next adjacent hydrophilic colloid layer to the emulsion containing layer.

BU contains at least one yellow dye image-forming coupler, GU contains at least one magenta dye image-forming coupler, and RU contains at least one cyan dye image-forming coupler. Any convenient combination of conventional dye image-forming couplers can be employed. Conventional dye image-forming couplers are illustrated by Research Disclosure I, cited above, X. Dye image formers and modifiers, B. Image-dye-forming couplers. The photographic elements may further contain other image-modifying compounds such as “Development Inhibitor-Releasing” compounds (DIR's). Useful additional DIR's for elements of the present invention, are known in the art and examples are described in U.S. Pat. Nos. 3,137,578; 3,148,022; 3,148,062; 3,227,554; 3,384,657; 3,379,529; 3,615,506; 3,617,291; 3,620,746; 3,701,783; 3,733,201; 4,049,455; 4,095,984; 4,126,459; 4,149,886; 4,150,228; 4,211,562; 4,248,962; 4,259,437; 4,362,878; 4,409,323; 4,477,563; 4,782,012; 4,962,018; 4,500,634; 4,579,816; 4,607,004; 4,618,571; 4,678,739; 4,746,600; 4,746,601; 4,791,049; 4,857,447; 4,865,959; 4,880,342; 4,886,736; 4,937,179; 4,946,767; 4,948,716; 4,952,485; 4,956,269; 4,959,299; 4,966,835; 4,985,336 as well as in patent publications GB 1,560,240; GB 2,007,662; GB 2,032,914; GB 2,099,167; DE 2,842,063, DE 2,937,127; DE 3,636,824; DE 3,644,416 as well as the following European Patent Publications: 272,573; 335,319; 336,411; 346,899; 362,870; 365,252; 365,346; 373,382; 376,212; 377,463; 378,236; 384,670; 396,486; 401,612; 401,613.

DIR compounds are also disclosed in “Developer-Inhibitor-Releasing (DIR) Couplers for Color Photography,” C. R. Barr, J. R. Thirtle and P. W. Vittum in Photographic Science and Engineering , Vol. 13, p. 174 (1969), incorporated herein by reference.

It is common practice to coat one, two or three separate emulsion layers within a single dye image-forming layer unit. When two or more emulsion layers are coated in a single layer unit, they are typically chosen to differ in sensitivity. When a more sensitive emulsion is coated over a less sensitive emulsion, a higher speed is realized than when the two emulsions are blended. When a less sensitive emulsion is coated over a more sensitive emulsion, a higher contrast is realized than when the two emulsions are blended. It is preferred that the most sensitive emulsion be located nearest the source of exposing radiation and the slowest emulsion be located nearest the support.

One or more of the layer units of the photothermographic element is preferably subdivided into at least two, and more preferably three or more sub-unit layers. It is preferred that all light sensitive silver halide emulsions in the color recording unit have spectral sensitivity in the same region of the visible spectrum. In this embodiment, while all silver halide emulsions incorporated in the unit have spectral absorptances according to invention, it is expected that there are minor differences in spectral absorptance properties between them. In still more preferred embodiments, the sensitizations of the slower silver halide emulsions are specifically tailored to account for the light shielding effects of the faster silver halide emulsions of the layer unit that reside above them, in order to provide an imagewise uniform spectral response by the photographic recording material as exposure varies with low to high light levels. Thus higher proportions of peak light absorbing spectral sensitizing dyes may be desirable in the slower emulsions of the subdivided layer unit to account for on-peak shielding and broadening of the underlying layer spectral sensitivity.

The photothermographic element may have interlayers that are hydrophilic colloid layers having as their primary function color contamination reduction-i.e., prevention of oxidized developing agent from migrating to an adjacent recording layer unit before reacting with dye-forming coupler. The interlayers are in part effective simply by increasing the diffusion path length that oxidized developing agent must travel. To increase the effectiveness of the interlayers to intercept oxidized developing agent, it is conventional practice to incorporate a reducing agent capable of reacting with oxidized developing agent. Antistain agents (oxidized developing agent scavengers) can be selected from among those disclosed by Research Disclosure I, X. Dye image formers and modifiers, D. Hue modifiers/stabilization, paragraph (2). When one or more silver halide emulsions in GU and RU are high bromide emulsions and, hence have significant native sensitivity to blue light, it is preferred to incorporate a yellow filter, such as Carey Lea silver or a yellow processing solution decolorizable dye, in IL1. Suitable yellow filter dyes can be selected from among those illustrated by Research Disclosure I, Section VIII. Absorbing and scattering materials, B. Absorbing materials. In elements of the instant invention, magenta colored filter materials are absent from IL2 and RU.

A photothernographic element may comprise a surface overcoat SOC which is a hydrophilic colloid layer that is provided for physical protection of the color negative elements during handling and processing. Each SOC also provides a convenient location for incorporation of addenda that are most effective at or near the surface of the color negative element. In some instances the surface overcoat is divided into a surface layer and an interlayer, the latter functioning as spacer between the addenda in the surface layer and the adjacent recording layer unit. In another common variant form, addenda are distributed between the surface layer and the interlayer, with the latter containing addenda that are compatible with the adjacent recording layer unit. Most typically the SOC contains addenda, such as coating aids, plasticizers and lubricants, antistats and matting agents, such as illustrated by Research Disclosure I, Section IX. Coating physical property modifying addenda. The SOC overlying the emulsion layers additionally preferably contains an ultraviolet absorber, such as illustrated by Research Disclosure I, Section VI. UV dyes/optical brighteners/luminescent dyes, paragraph (1).

Alternative layer units sequences can be employed and are particularly attractive for some emulsion choices. Using high chloride emulsions and/or thin (<0.2 μm mean grain thickness) tabular grain emulsions all possible interchanges of the positions of BU, GU and RU can be undertaken without risk of blue light contamination of the minus blue records, since these emulsions exhibit negligible native sensitivity in the visible spectrum. For the same reason, it is unnecessary to incorporate blue light absorbers in the interlayers.

A number of modifications of color negative elements have been suggested for accommodating scanning, as illustrated by Research Disclosure I, Section XIV. Scan facilitating features. These systems to the extent compatible with the color negative element constructions described above are contemplated for use in the practice of this invention.

It is also contemplated that the imaging element of this invention may be used with non-conventional sensitization schemes. For example, instead of using imaging layers sensitized to the red, green, and blue regions of the spectrum, the light-sensitive material may have one white-sensitive layer to record scene luminance, and two color-sensitive layers to record scene chrominance. Following development, the resulting image can be scanned and digitally reprocessed to reconstruct the full colors of the original scene as described in U.S. Pat No. 5,962,205. The imaging element may also comprise a pan-sensitized emulsion with accompanying color-separation exposure. In this embodiment, the developers of the invention would give rise to a colored or neutral image which, in conjunction with the separation exposure, would enable full recovery of the original scene color values. In such an element, the image may be formed by either developed silver density, a combination of one or more conventional couplers, or “black” couplers such as resorcinol couplers. The separation exposure may be made either sequentially through appropriate filters, or simultaneously through a system of spatially discreet filter elements (commonly called a “color filter array”).

The imaging element of the invention may also be a black and white image-forming material comprised, for example, of a pan-sensitized silver halide emulsion and a developer of the invention. In this embodiment, the image may be formed by developed silver density following processing, or by a coupler that generates a dye which can be used to carry the neutral image tone scale.

The photothermographic elements of the present invention are preferably of type B as disclosed in Research Disclosure I. Type B elements contain in reactive association a photosensitive silver halide, a reducing agent or developer, optionally an activator, a coating vehicle or binder, and a salt or complex of an organic compound with silver ion. In these systems, this organic complex is reduced during development to yield silver metal. The organic silver salt will be referred to as the silver donor. References describing such imaging elements include, for example, U.S. Pat. No. 3,457,075; 4,459,350; 4,264,725 and 4,741,992. In the type B photothermographic material it is believed that the latent image silver from the silver halide acts as a catalyst for the described image-forming combination upon processing. In these systems, a preferred concentration of photographic silver halide is within the range of 0.01 to 100 moles of photographic silver halide per mole of silver donor in the photothermographic material.

The Type B photothermographic element comprises an oxidation-reduction image forming combination that contains an organic silver salt oxidizing agent. The organic silver salt is a silver salt which is comparatively stable to light, but aids in the formation of a silver image when heated to 80° C. or higher in the presence of an exposed photocatalyst (i.e., the photosensitive silver halide) and a reducing agent.

Suitable organic silver salts include silver salts of organic compounds having a carboxyl group. Preferred examples thereof include a silver salt of an aliphatic carboxylic acid and a silver salt of an aromatic carboxylic acid. Preferred examples of the silver salts of aliphatic carboxylic acids include silver behenate, silver stearate, silver oleate, silver laureate, silver caprate, silver myristate, silver palmitate, silver maleate, silver fumarate, silver tartarate, silver furoate, silver linoleate, silver butyrate and silver camphorate, mixtures thereof, etc. Silver salts which are substitutable with a halogen atom or a hydroxyl group can also be effectively used. Preferred examples of the silver salts of aromatic carboxylic acid and other carboxyl group-containing compounds include silver benzoate, a silver-substituted benzoate such as silver 3,5-dihydroxybenzoate, silver o-methylbenzoate, silver m-methylbenzoate, silver p-methylbenzoate, silver 2,4-dichlorobenzoate, silver acetamidobenzoate, silver p-phenylbenzoate, etc., silver gallate, silver tannate, silver phthalate, silver terephthalate, silver salicylate, silver phenylacetate, silver pyromellilate, a silver salt of 3-carboxymethyl-4-methyl-4-thiazoline-2-thione or the like as described in U.S. Pat. No. 3,785,830, and silver salt of an aliphatic carboxylic acid containing a thioether group as described in U.S. Pat. No. 3,330,663. Preferred examples of organic silver donors include a silver salt of benzotriazole and a derivative thereof as described in Japanese patent publications 30270/69 and 18146/70, for example a silver salt of benzotriazole or methylbenzotriazole, etc., a silver salt of a halogen substituted benzotriazole, such as a silver salt of 5-chlorobenzotriazole, etc., a silver salt of 1,2,4-triazole, a silver salt of 3-amino-5-mercaptobenzyl-1,2,4-triazole, of 1H-tetrazole as described in U.S. Pat. No. 4,220,709, a silver salt of imidazole and an imidazole derivative, and the like.

It is also found convenient to use silver half soap, of which an equimolar blend of a silver behenate with behenic acid, prepared by precipitation from aqueous solution of the sodium salt of commercial behenic acid and analyzing about 14.5 percent silver, represents a preferred example. Transparent sheet materials made on transparent film backing require a transparent coating and for this purpose the silver behenate full soap, containing not more than about 4 or percent of free behenic acid and analyzing about 25.2 percent silver may be used. A method for making silver soap dispersions is well known in the art and is disclosed in Research Disclosure October 1983 (23419) and U.S. Pat. No. 3,985,565.

Silver salts complexes may also be prepared by mixture of aqueous solutions of a silver ionic species, such as silver nitrate, and a solution of the organic ligand to be complexed with silver. The mixture process may take any convenient form, including those employed in the process of silver halide precipitation. A stabilizer may be used to avoid flocculation of the silver complex particles. The stabilizer may be any of those materials known to be useful in the photographic art, such as, but not limited to, gelatin, polyvinyl alcohol or polymeric or monomeric surfactants.

The photosensitive silver halide grains and the organic silver salt are coated so that they are in catalytic proximity during development. They can be coated in contiguous layers, but are preferably mixed prior to coating.

Conventional mixing techniques are illustrated by Research Disclosure , Item 17029, cited above, as well as U.S. Pat. No. 3,700,458 and published Japanese patent applications Nos. 32928/75, 13224/74, 17216/75 and 42729/76.

Any convenient selection from among conventional radiation-sensitive silver halide emulsions can be incorporated within the layer units and used to provide the spectral absorptances of the invention. Most commonly high bromide emulsions containing a minor amount of iodide are employed. To realize higher rates of processing, high chloride emulsions can be employed. Radiation-sensitive silver chloride, silver bromide, silver iodobromide, silver iodochloride, silver chlorobromide, silver bromochloride, silver iodochlorobromide and silver iodobromochloride grains are all contemplated. The grains can be either regular or irregular (e.g., tabular). Illustrations of conventional radiation-sensitive silver halide emulsions are provided by Research Disclosure I, cited above, I. Emulsion grains and their preparation. Chemical sensitization of the emulsions, which can take any conventional form, is illustrated in section IV. Chemical sensitization. The emulsion layers also typically include one or more antifoggants or stabilizers, which can take any conventional form, as illustrated by section VII. Antifoggants and stabilizers.

The silver halide grains to be used in a photothermographic element may be prepared according to methods known in the art, such as those described in Research Disclosure I, cited above, and James, The Theory of the Photographic Process. These include methods such as ammoniacal emulsion making, neutral or acidic emulsion making, and others known in the art. These methods generally involve mixing a water soluble silver salt with a water soluble halide salt in the presence of a protective colloid, and controlling the temperature, pAg, pH values, etc, at suitable values during formation of the silver halide by precipitation. In the course of grain precipitation one or more dopants (grain occlusions other than silver and halide) can be introduced to modify grain properties.

In a photothermographic element, the silver halide is typically provided in the form of an emulsion, including a vehicle for coating the emulsion as a layer of the element. Useful vehicles include both naturally occurring substances such as proteins, protein derivatives, cellulose derivatives (e.g., cellulose esters, ethers, and both anionically and cationically substituted cellulosics), gelatin (e.g., alkali-treated gelatin such as cattle bone or hide gelatin, or acid treated gelatin such as pigskin gelatin), deionized gelatin, gelatin derivatives (e.g., acetylated gelatin, phthalated gelatin, and the like), and others as described in Research Disclosure , I. Also useful as vehicles or vehicle extenders are hydrophilic water-permeable colloids. These include synthetic polymeric peptizers, carriers, and/or binders such as poly(vinyl alcohol), poly(vinyl lactams), acrylamide polymers, polyvinyl acetals, polymers of alkyl and sulfoalkyl acrylates and methacrylates, hydrolyzed polyvinyl acetates, polyamides, polyvinyl pyridine, methacrylamide copolymers. The vehicle can be present in the emulsion in any amount useful in photographic emulsions. The emulsion can also include any of the addenda known to be useful in photographic emulsions.

While any useful quantity of light sensitive silver, as silver halide, can be employed in the elements useful in this invention, it is preferred that the total quantity be less than 10 g/m 2 of silver. Silver quantities of less than 7 g/m 2 are preferred, and silver quantities of less than 5 g/m 2 are even more preferred. The lower quantities of silver improve the optics of the elements, thus enabling the production of sharper pictures using the elements.

Because in one embodiment of the invention only silver development is required, color developers (p-phenylene diamines or p-aminophenolics) are not obligatory. Other developers that are capable of forming a silver image may also be used, without regard to their ability to form a colored dye. Such developers include, in addition to p-phenylene diamine developers and substituted p-aminophenols (3,5-dichloroaminophenol and 3,5-dibromoaminophenol are particularly preferred choices) but also p-sulfonamidophenols, ascorbic acid, low valent metal compounds, particularly those containing Fe(Il), Cu(I), Co(II), Mn(II), V(II), or Ti(III), hydrazine derivatives, hydroxylamine derivatives, phenidones. For incorporated developers, thermally unblocking blocked developers are preferred.

In some cases, a development activator, also known as an alkali-release agent, base-release agent or an activator precursor can be useful in the described photothermographic element of the invention. A development activator, as described herein, is intended to mean an agent or a compound which aids the developing agent at processing temperatures to develop a latent image in the imaging material. Useful development activators or activator precursors are described, for example, in Belgian Pat. No. 709, 967 published Feb. 29, 1968, and Research Disclosure, Volume 155, Mar. 1977, Item 15567, published by Industrial Opportunities Ltd., Homewell, Havant, Hampshire, PO9 1EF, UK. Examples of useful activator precursors include guanidinium compounds such as guanidinium trichloroacetate, diguanidinium glutarate, succinate, malonate and the like; quaternary ammonium malonates; amino acids, such as 6-aminocaproic acid and glycine; and 2-carboxycarboxamide activator precursors.

Examples of blocked developers that can be used in photographic elements of the present invention include, but are not limited to, the blocked developing agents described in U.S. Pat. No. 3,342,599, to Reeves; Research Disclosure (129 (1975) pp. 27-30) published by Kenneth Mason Publications, Ltd., Dudley Annex, 12a North Street, Emsworth, Hampshire P010 7DQ, ENGLAND; U.S. Pat. No. 4,157,915, to Hamaoka et al.; U.S. Pat. No. 4,060,418, to Waxman and Mourning; and in U.S. Pat. No. 5,019,492. Particularly useful are those blocked developers described in U.S. application Ser. No. 09/476,234, filed Dec. 30, 1999, IMAGING ELEMENT CONTAINING A BLOCKED PHOTOGRAPICALLY USEFUL COMPOUND; U.S. application Ser. No. 09/475,691, filed Dec. 30, 1999, IMAGING ELEMENT CONTAINING A BLOCKED PHOTOGRAPHICALLY USEFUL COMPOUND; U.S. application Ser. No. 09/475,703, filed Dec. 30, 1999, IMAGING ELEMENT CONTAINING A BLOCKED PHOTOGRAPHICALLY USEFUL COMPOUND; U.S. application Ser. No. 09/475,690, filed Dec. 30, 1999, IMAGING ELEMENT CONTAINING A BLOCKED PHOTOGRAPHICALLY USEFUL COMPOUND; and U.S. application Ser. No. 09/476,233, filed Dec. 30, 1999, PHOTOGRAPHIC OR PHOTOTHERMOGRAPHIC ELEMENT CONTAINING A BLOCKED PHOTOGRAPHICALLY USEFUL COMPOUND.

In one embodiment of the invention, the blocked developer is preferably incorporated in one or more of the imaging layers of the imaging element. The amount of blocked developer used is preferably 0.01 to 5 g/m 2 , more preferably 0.1 to 2 g/m 2 and most preferably 0.3 to 2 g/m 2 in each layer to which it is added. These may be color forming or non-color forming layers of the element. The blocked developer can be contained in a separate element that is contacted to the photographic element during processing.

After image-wise exposure of the imaging element, the blocked developer can be activated during processing of the imaging element by the presence of acid or base in the processing solution, by heating the imaging element during processing of the imaging element, and/or by placing the imaging element in contact with a separate element, such as a laminate sheet, during processing. The laminate sheet optionally contains additional processing chemicals such as those disclosed in Sections XIX and XX of Research Disclosure , September 1996, Number 389, Item 38957 (hereafter referred to as (“ Research Disclosure I”). All sections referred to herein are sections of Research Disclosure I, unless otherwise indicated. Such chemicals include, for example, sulfites, hydroxyl amine, hydroxamic acids and the like, antifoggants, such as alkali metal halides, nitrogen containing heterocyclic compounds, and the like, sequestering agents such as an organic acids, and other additives such as buffering agents, sulfonated polystyrene, stain reducing agents, biocides, desilvering agents, stabilizers and the like.

A reducing agent may be included in the photothermographic element. The reducing agent for the organic silver salt may be any material, preferably organic material, that can reduce silver ion to metallic silver. Conventional photographic developers such as 3-pyrazolidinones, hydroquinones, p-aminophenols, p-phenylenediamines and catechol are useful, but hindered phenol reducing agents are preferred. The reducing agent is preferably present in a concentration ranging from 5 to 25 percent of the photothermographic layer.

A wide range of reducing agents has been disclosed in dry silver systems including amidoximes such as phenylamidoxime, 2-thienylamidoxime and p-phenoxy-phenylamidoxime, azines (e.g., 4-hydroxy-3,5-dimethoxybenzaldehydeazine); a combination of aliphatic carboxylic acid aryl hydrazides and ascorbic acid, such as 2,2′-bis(hydroxymethyl)propionylbetaphenyl hydrazide in combination with ascorbic acid; an combination of polyhydroxybenzene and hydroxylamine, a reductone and/or a hydrazine, e.g., a combination of hydroquinone and bis(ethoxyethyl)hydroxylamine, piperidinohexose reductone or formyl-4-methylphenylhydrazine, hydroxamic acids such as phenylhydroxamic acid, p-hydroxyphenyl-hydroxamic acid, and o-alaninehydroxamic acid; a combination of azines and sulfonamidophenols, e.g., phenothiazine and 2,6-dichloro-4-benzenesulfonamidophenol; α-cyano-phenylacetic acid derivatives such as ethyl α-cyano-2-methylphenylacetate, ethyl α-cyano-phenylacetate; bis-β-naphthols as illustrated by 2,2′-dihydroxyl-1-binaphthyl, 6,6′-dibromo-2,2′-dihydroxy-1,1′-binaphthyl, and bis(2-hydroxy-1-naphthyl)methane; a combination of bis-o-naphthol and a 1,3-dihydroxybenzene derivative, (e. g., 2,4-dihydroxybenzophenone or 2,4-dihydroxyacetophenone); 5-pyrazolones such as 3-methyl-1-phenyl-5-pyrazolone; reductones as illustrated by dimethylaminohexose reductone, anhydrodihydroaminohexose reductone, and anhydrodihydro-piperidone-hexose reductone; sulfamidophenol reducing agents such as 2,6-dichloro-4-benzene-sulfon-amido-phenol, and p-benzenesulfonamidophenol; 2-phenylindane-1,3-dione and the like; chromans such as 2,2-dimethyl-7-t-butyl-6-hydroxychroman; 1,4-dihydropyridines such as 2,6-dimethoxy-3,5-dicarbethoxy-1,4-dihydropyridene; bisphenols, e.g., bis(2-hydroxy-3-t-butyl-5-methylphenyl)-methane; 2,2-bis(4-hydroxy-3-methylphenyl)-propane; 4,4-ethylidene-bis(2-t-butyl-6-methylphenol); and 2,2-bis(3,5-dimethyl-4-hydroxyphenyl)propane; ascorbic acid derivatives, e.g., 1-ascorbyl-palmitate, ascorbylstearate and unsaturated aldehydes and ketones, such as benzyl and diacetyl; pyrazolidin-3-ones; and certain indane-1,3-diones.

An optimum concentration of organic reducing agent in the photothermographic element varies depending upon such factors as the particular photothermographic element, desired image, processing conditions, the particular organic silver salt and the particular oxidizing agent.

It is useful to include a melt-forming compound or melt former (also sometimes referred to as a “thermal solvent”) in a photothermographic element, such as in the imaging layers and in the antihalation layer or filter layer, as described. Combinations of melt-forming compounds or melt-formers can also be useful if desired. The term “melt-forming compound” or “melt former” as employed herein is intended to mean a compound which upon heating to the described processing temperature provides an improved reaction medium, typically a molten medium, wherein the described reaction combination can provide a better image. The exact nature of the reaction medium at processing temperatures described is not fully understood; however, it is believed that at reaction temperatures a melt occurs which permits the reaction components to better interact. Useful melt-forming compounds are typically separate components from the reaction combination, although the reaction combination can enter into the melt formation. Typically useful melt-forming compounds are amides, imides, cyclic ureas and triazoles which are compatible with other of the components of the materials of the invention. Useful melt-forming compounds or melt formers are described, for example, in Research Disclosure, Vol. 150, October 1976, Item 15049 of LaRossa and Boettcher, published by Industrial Opportunities Ltd., Homewell, Havant, Hampshire, PO9 1EF, UK. As described, the antihalation or filter layers of the invention can comprise a melt-forming compound if desired. A preferred melt-former is salicylanilide and similar compounds. Examples of thermal solvents, for example, salicylanilide, phthalimide, N-hydroxyphthalimide, N-potassium-phthalimide, succinimide, N-hydroxy-1,8-naphthalimide, phthalazine, 1-(2H)-phthalazinone, 2-acetylphthalazinone, benzanilide, and benzenesulfonamide. Prior-art thermal solvents are disclosed, for example, in U.S. Pat. No. 6,013,420 to Windender.

Examples of toning agents and toning agent combinations are described in, for example, Research Disclosure , June 1978, Item No. 17029 and U.S. Pat. No. 4,123,282.

A range of concentration of melt-forming compound or melt-forming compound combination is useful in the heat developable photographic materials described. The optimum concentration of melt-forming compound will depend upon such factors as the particular imaging material, desired image, processing conditions and the like.

The photothermographic elements according to the invention can contain an image toner or toning agent in order to provide a more neutral or black tone image upon processing. The optimum image toner or toning agent will depend upon such factors as the particular imaging material, the desired image, particular processing conditions and the like. In some cases certain image toning agents or toners provide much better results with certain imaging materials than with others. Combinations of toning agents or toners can be useful if desired. The optimum concentration of toning agent or toning agent combination will depend upon such factors as the particular imaging material, processing conditions, desired image and the like.

Post-processing image stabilizers and latent image keeping stabilizers are useful in the photothermographic element. Any of the stabilizers known in the photothermographic art are useful for the described photothermographic element. Illustrative examples of useful stabilizers include photolytically active stabilizers and stabilizer precursors as described in, for example, U.S. Pat. No. 4,459,350. Other examples of useful stabilizers include azole thioethers and blocked azolinethione stabilizer precursors and carbamoyl stabilizer precursors, such as described in U.S. Pat. No. 3,877,940.

Photothermographic elements as described can contain addenda that are known to aid in formation of a useful image. The photothermographic element can contain development modifiers that function as speed increasing compounds, sensitizing dyes, hardeners, anti-static agents, plasticizers and lubricants, coating aids, brighteners, absorbing and filter dyes, such as described in Research Disclosure , December 1978, Item No. 17643 and Research Disclosure , June 1978, Item No. 17029.

The layers of the photothermographic element are coated on a support by coating procedures known in the photographic art, including dip coating, air knife coating, curtain coating or extrusion coating using hoppers. If desired, two or more layers are coated simultaneously.

A photothermographic element as described preferably comprises a thermal stabilizer to help stabilize the photothermographic element prior to exposure and processing. Such a thermal stabilizer provides improved stability of the photothermographic element during storage. Preferred thermal stabilizers are 2-bromo-2-arylsulfonylacetamides, such as 2-bromo-2-p-tolysulfonylacetamide; 2-(tribromomethyl sulfonyl)benzothiazole; and 6-substituted-2,4-bis(tribromomethyl)-s-triazines, such as 6-methyl or 6-phenyl-2,4-bis(tribromomethyl)-s-triazine.

Photographic elements of the present invention are preferably imagewise exposed using any of the known techniques, including those described in Research Disclosure I, Section XVI. This typically involves exposure to light in the visible region of the spectrum, and typically such exposure is of a live image through a lens, although exposure can also be exposure to a stored image (such as a computer stored image) by means of light emitting devices (such as light emitting diodes, CRT and the like). The photothermographic elements are also exposed by means of various forms of energy, including ultraviolet and infrared regions of the electromagnetic spectrum as well as electron beam and beta radiation, gamma ray, x-ray, alpha particle, neutron radiation and other forms of corpuscular wave-like radiant energy in either non-coherent (random phase) or coherent (in phase) forms produced by lasers. Exposures are monochromatic, orthochromatic, or panchromatic depending upon the spectral sensitization of the photographic silver halide. Imagewise exposure is preferably for a time and intensity sufficient to produce a developable latent image in the photothermographic element.

Once yellow, magenta, and cyan dye image records have been formed in the processed photographic elements of the invention, conventional techniques can be employed for retrieving the image information for each color record and manipulating the record for subsequent creation of a color balanced viewable image. For example, it is possible to scan the photographic element successively within the blue, green, and red regions of the spectrum or to incorporate blue, green, and red light within a single scanning beam that is divided and passed through blue, green, and red filters to form separate scanning beams for each color record. A simple technique is to scan the photographic element point-by-point along a series of laterally offset parallel scan paths. The intensity of light passing through the element at a scanning point is noted by a sensor which converts radiation received into an electrical signal. Most generally this electronic signal is further manipulated to form a useful electronic record of the image. For example, the electrical signal can be passed through an analog-to-digital converter and sent to a digital computer together with location information required for pixel (point) location within the image. In another embodiment, this electronic signal is encoded with calorimetric or tonal information to form an electronic record that is suitable to allow reconstruction of the image into viewable forms such as computer monitor displayed images, television images, printed images, and so forth.

In one embodiment, a photothermographic elements can be scanned prior to any removal of silver halide from the element. The remaining silver halide yields a turbid coating, and it is found that improved scanned image quality for such a system can be obtained by the use of scanners that employ diffuse illumination optics. Any technique known in the art for producing diffuse illumination can be used. Preferred systems include reflective systems, that employ a diffusing cavity whose interior walls are specifically designed to produce a high degree of diffuse reflection, and transmissive systems, where diffusion of a beam of specular light is accomplished by the use of an optical element placed in the beam that serves to scatter light. Such elements can be either glass or plastic that either incorporate a component that produces the desired scattering, or have been given a surface treatment to promote the desired scattering.

In view of advances in the art of scanning technologies, it has now become natural and practical for photothermographic color films such as disclosed in EP 0762 201 to be scanned, which can be accomplished without the necessity of removing the silver or silver-halide from the negative, although special arrangements for such scanning can be made to improve its quality. See, for example, Simmons U.S. Pat. No. 5,391,443. Method for the scanning of such films are also disclosed in commonly assigned U.S. Ser. No.60/211,364 (docket 81246) and U.S. Ser. No. 60/211,061 (docket 81247), hereby incorporated by reference in their entirety.

For example, it is possible to scan the photographic element successively within the blue, green, and red regions of the spectrum or to incorporate blue, green, and red light within a single scanning beam that is divided and passed through blue, green, and red filters to form separate scanning beams for each color record. If other colors are imagewise present in the element, then appropriately colored light beams are employed. A simple technique is to scan the photographic element point-by-point along a series of laterally offset parallel scan paths. A sensor that converts radiation received into an electrical signal notes the intensity of light passing through the element at a scanning point. Most generally this electronic signal is further manipulated to form a useful electronic record of the image. For example, the electrical signal can be passed through an analog-to-digital converter and sent to a digital computer together with location information required for pixel (point) location within the image. The number of pixels collected in this manner can be varied as dictated by the desired image quality.

The electronic signal can form an electronic record that is suitable to allow reconstruction of the image into viewable forms such as computer monitor displayed images, television images, optically, mechanically or digitally printed images and displays and so forth all as known in the art. The formed image can be stored or transmitted to enable further manipulation or viewing, such as in U.S. Ser. No. 09/592,816 (Docket 81040) titled AN IMAGE PROCESSING AND MANIPULATION SYSTEM to Richard P. Szajewski, Alan Sowinski and John Buhr.

Illustrative systems of scan signal manipulation, including techniques for maximizing the quality of image records, are disclosed by Bayer U.S. Pat. No. 4,553,156; Urabe et al U.S. Pat. No. 4,591,923; Sasaki et al U.S. Pat. No. 4,631,578; Alkofer U.S. Pat. No. 4,654,722; Yamada et al U.S. Pat. No. 4,670,793; Klees U.S. Pat. Nos. 4,694,342 and 4,962,542; Powell U.S. Pat. No. 4,805,031; Mayne et al U.S. Pat. No. 4,829,370; Abdulwahab U.S. Pat. No. 4,839,721; Matsunawa et al U.S. Pat. Nos. 4,841,361 and 4,937,662; Mizukoshi et al U.S. Pat. No. 4,891,713; Petilli U.S. Pat. No. 4,912,569; Sullivan et al U.S. Pat. Nos. 4,920,501 and 5,070,413; Kimoto et al U.S. Pat. No. 4,929,979; Hirosawa et al U.S. Pat. No. 4,972,256; Kaplan U.S. Pat. No. 4,977,521; Sakai U.S. Pat. No. 4,979,027; Ng U.S. Pat. No. 5,003,494; Katayama et al U.S. Pat. No. 5,008,950; Kimura et al U.S. Pat. No. 5,065,255; Osamu et al U.S. Pat. No. 5,051,842; Lee et al U.S. Pat. No. 5,012,333; Bowers et al U.S. Pat. No. 5,107,346; Telle U.S. Pat. No. 5,105,266; MacDonald et al U.S. Pat. 5,105,469; and Kwon et al U.S. Pat. No. 5,081,692. Techniques for color balance adjustments during scanning are disclosed by Moore et al U.S. Pat. No. 5,049,984 and Davis U.S. Pat. No. 5,541,645.

The digital color records once acquired are in most instances adjusted to produce a pleasingly color balanced image for viewing and to preserve the color fidelity of the image bearing signals through various transformations or renderings for outputting, either on a video monitor or when printed as a conventional color print. Preferred techniques for transforming image bearing signals after scanning are disclosed by Giorgianni et al U.S. Pat. No. 5,267,030, the disclosures of which are herein incorporated by reference. Further illustrations of the capability of those skilled in the art to manage color digital image information are provided by Giorgianni and Madden Digital Color Management, Addison-Wesley, 1998.

For illustrative purposes, a non-exhaustive list of photothermographic film processes involving a common dry heat development step are as follows:

1. heat development→scan→stabilize (for example, with a laminate)→scan→obtain returnable archival film.

2. heat development→fix bath→water wash→dry→scan→obtain returnable archival film

3. heat development→scan→blix bath→dry→scan→recycle all or part of the silver in film

4. heat development→bleach laminate→fix laminate→scan→(recycle all or part of the silver in film)

5. heat development→bleach→wash→fix→wash→dry→relatively slow, high quality scan

In a preferred embodiment of a photothermographic film according to the present invention, the processing time to first image (either hard or soft display for customer/consumer viewing), including (i) thermal development of a film, (ii) scanning, and (iii) the formation of the positive image from the developed film, is suitably less than 5 minutes, preferably less than 3.5 minutes, more preferably less than 2 minutes, most preferably less than about 1 minute. In one embodiment, such film might be amenable to development at kiosks, with the use of simple dry or apparently dry equipment. Thus, it is envisioned that a consumer could bring an imagewise exposed photographic film, for development and printing, to a kiosk located at any one of a number of diverse locations, optionally independent from a wet-development lab, where the film could be developed and printed without any manipulation by third-party technicians. A photothermographic color film, in which a silver-halide-containing color photographic element after imagewise exposure can be developed merely by the external application of heat and/or relatively small amounts of alkaline or acidic water, but which same film is also amenable to development in an automated kiosk, preferably not requiring third-party manipulation, would have significant advantages. Assuming the availability and accessibility of such kiosks, such photothermographic films could potentially be developed at any time of day, “on demand,” in a matter minutes, without requiring the participation of third-party processors, multiple-tank equipment and the like. Optional, such photographic processing could potentially be done on an “as needed” basis, even one roll at a time, without necessitating the high-volume processing that would justify, in a commercial setting, equipment capable of high-throughput. Color development and subsequent scanning of such a film could readily occur on an individual consumer basis, with the option of generating a display element corresponding to the developed color image. By kiosk is meant an automated free-standing machine, self-contained and (in exchange for certain payments) capable of developing a roll of imagewise exposed film on a roll-by-roll basis, without the intervention of technicians or other third-party persons such as necessary in wet chemical laboratories. Typically, the customer will initiate and control the carrying out of film processing and optional printing by means of a computer interface. Such kiosks typically will be less than 6 cubic meters in dimension, preferably 3 cubic meters or less in dimension, and hence commercially transportable to diverse locations. Such kiosks may optionally comprise a heater for color development, a scanner for digitally recording the color image, and a device for transferring the color image to a display element.

The following examples are presented to illustrate the practice of this invention, but are not meant to limit it in any way. All percentages are by weight unless otherwise indicated.

COMPARATIVE EXAMPLE 1

This Example is for comparative purposes using bleachable dyes without a melt former. Dyes D-1 to D-7 are described in Table 1-1 below. Most of the dyes are cationic and, therefore, they have negative counter ions associated with them. One example, dye D-7, is zwittterionic in nature, where the negative charge is a part of the dye molecule. In the table below, the arrow designates the coupling position of the fragment to the basic structure.

TABLE 1-1
Dye	Counterion	R 1	R 2
D-1	BF 4 −		—CH 3
D-2	BF 4 −		—CH 3
D-3	BF 4 −		—CH 3
D-4	BF 4 −		—CH 3
D-5	B 4 −		—COCH 3
D-6	ClO 4 −		—COCH 3
D-7	none		—CH 3

All of the dyes in Table 1-1 were evaluated in a single layer coating. The dyes were ball-milled with poly vinyl pyrrolidone surfactant and added to a coating melt preparation to yield the coverages indicated in Table 1-2. The coating melts were coated onto polyethylene terephthalate support.

TABLE 1-2
          Laydown,
Component g/m                                                                        2
dye       0.30
gelatin   4.31

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. The Status M density (see table for filter used) of the coatings was recorded before and after the above tests. The results are listed in Table 1-3.

TABLE 1-3
Coating	Dye	Filter used	Before process	After process
C-1-1	D-1	red	0.69	0.37
C-1-2	D-2	red	0.56	0.26
C-1-3	D-3	red	0.93	0.46
C-1-4	D-4	red	0.74	0.32
C-1-5	D-5	Red	0.71	0.41
C-1-6	D-6	Green	0.80	0.79
C-1-7	D-7	Red	0.69	0.49

In this format, none of the dyes bleached very effectively.

EXAMPLE 2

All of the dyes of the previous example were evaluated in a single layer coating containing a melt former according to the present invention. The dyes were ball-milled and added to a coating melt preparation to yield the coverages indicated in Table 2-1. The melt former MF-1 was a ball-milled dispersion of solid particles. The coating melts were coated onto polyethylene terephthalate support.

.
Compound Structure
MF-1

TABLE 2-1
          Laydown,
Component g/m                                                                        2
dye       0.30
MF-1      1.08
gelatin   4.31

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. The Status M density (see table for filter used) of the coatings was recorded before and after the above tests. The results are listed in Table 2-2.

TABLE 2-2
Coating	Dye	Filter	Before process	After process
1-2-1	D-1	red	0.75	0.07
I-2-2	D-2	red	0.51	0.07
I-2-3	D-3	red	0.87	0.07
I-2-4	D-4	red	0.64	0.09
I-2-5	D-5	red	0.41	0.12
I-2-6	D-6	green	0.56	0.30
I-2-7	D-7	red	0.81	0.10

In this format, all of the dyes bleached much better than in example 1 where no melt former was coated. The comparative data is shown in Table 2-3.

TABLE 2-3
	Coating without	% Bleached	Coating with	% Bleached
Dye	melt former	at 10″/160° C.	melt former	at 10″/160° C.
D-1	C-1-1	46.4	I-2-1	90.7
D-2	C-1-2	53.6	I-2-2	86.3
D-3	C-1-3	50.5	I-2-3	92.0
D-4	C-1-4	56.8	I-2-4	85.9
D-5	C-1-5	42.3	I-2-5	70.7
D-6	C-1-6	1.3	I-2-6	46.4
D-7	C-1-7	29.0	I-2-7	87.7

EXAMPLE 3

Two melt formers were evaluated in this example. One melt former was salicylanilide MF-1, and the other was benzanilide MF-2. The results show the additional, dual purpose of melt formers containing a phenol constituent.

Compound Structure
MF-2

The coatings contained dye D-1 and gelatin at laydowns of 0.30, and 4.31 g/m 2 respectively. Table 3-1 describes the melt former components in the melts. The coating melts were coated onto polyethylene terephthalate support.

TABLE 3-1
		laydown,
coating	melt former	g/m 2
I-3-1	MF-1	1.08
I-3-2	MF-2	1.08

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. The Status M densities of the coatings were recorded before and after thermal processing. The results are listed in Table 3-2.

TABLE 3-2
Coating	Process	Red density	Green density	Blue density
I-3-1	no process	0.60	0.34	0.28
I-3-1	10″/160° C.	0.10	0.16	0.17
I-3-2	no process	0.73	0.39	0.31
I-3-2	10″/160° .C	0.10	0.26	0.32

The above results show that both melt formers resulted in excellent bleaching of the cyan dye color (red channel density). The melt former with the phenol resulted in lower post-process green and blue density. In an additional test, the processed coating I-3-2 was immersed for 10 seconds in a water solution containing phenol. The orange hue of the dye stain was immediately removed. This supports the notion that the phenol portion of the salicylanilide melt former is responsible for removal of the residual green and blue density after the heat process.

EXAMPLE 4

Dye D-1 was coated with varying levels of salicylanilide melt former. The dye was ball-milled and added to a coating melt preparation. The melt former MF-1 was a ball-milled dispersion of solid particles and added to yield the coverages indicated in Table 4-1. The dye and gelatin coverages were held constant at 0.30 and 4.31 g/m 2 respectively. The coating melts were coated onto polyethylene terephthalate support.

TABLE 4-1
		Melt former,
Coating	Dye	g/m 2
C-4-1	D-1	0.00
I-4-1	D-1	0.22
I-4-2	D-1	0.43
I-4-3	D-1	0.65

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. The Status M red density of the coatings was recorded before and after the above tests. The results are listed in Table 4-2.

		Melt former,
	Coating	g/m 2	Before process	After process
	C-4-1	0.00	0.67	0.37
	I-4-1	0.22	0.59	0.06
	I-4-2	0.43	0.56	0.09
	I-4-3	0.65	0.50	0.09

It is clear from the data in the table that the melt former at reasonably low levels greatly improved the bleaching performance of the dye over the case where no melt former was coated.

EXAMPLE 5

Dye D-7 was coated with even lower levels of melt former MF-1 than in the previous example. The dye was ball-milled and added to a coating melt preparation. The melt former was a ball-milled dispersion of solid particles and added to yield the coverages indicated in Table 5-1. The dye and gelatin coverages were held constant at 0.30 and 4.31 g/m 2 respectively. The coating melts were coated onto polyethylene terephthalate support.

TABLE 5-1
		Melt former,
Coating	Dye	g/m 2
C-5-2	D-7	0.000
I-5-5	D-7	0.054
I-5-6	D-7	0.108
I-5-7	D-7	0.161
I-5-8	D-7	1.076

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. In addition, the coatings were evaluated for incubation (raw stock keeping, or RSK) by sealing the coatings into MYLAR polymeric bags and placing them into a heated oven at 50° C. for I week. The Status M red density of the coatings was recorded before and after the above tests. The results are listed in Table 5-2.

TABLE 5-2
	Melt former,
Coating	g/m 2	Before tests	After process	After RSK
C-5-2	0.000	0.80	0.57	0.73
I-5-5	0.054	0.84	0.20	0.66
I-5-6	0.108	0.68	0.13	0.54
I-5-7	0.161	0.81	0.13	0.71
I-5-8	1.076	0.77	0.11	0.51

The data in the above table show that only a small amount of MF-1 is necessary to make such compositions useful.

EXAMPLE 6

Another dye was synthesized for evaluation. The structure for dye D-8 is shown below. The dye was ball-milled and added to a coating melt preparation to yield the coverages indicated in Table 6-1. The coating melt was coated onto polyethylene terephthalate support.

Dye Structure
D-8

Dye Structure
D-8

The coating was evaluated for thermal bleaching by placing the dried coating onto a heated 180° C. platen for 10 seconds. The Status M red density of the coating was recorded before and after the thermal process. The results are listed in Table 6-2.

TABLE 6-2
Coating	Dye	Before process	After process	% Bleaching
I-6-2	D-8	0.36	0.07	80.6

The data in the table show good bleaching for dye D-8.

EXAMPLE 7

In this example, it is shown that the delivery of the melt former to the dye layer can be made by coating the melt former in another layer that may or may not be adjacent to the layer containing the thermally bleachable dye. In this experiment, a total of six coatings were prepared. All of the coatings contained a dye layer and up to two additional layers as shown in the figure below. In all cases, the bottom coated layer was the dye layer.

overcoat
interlayer (optional)
dye layer
support

The melt former was added to the overcoat layer. In some cases, the interlayer was omitted. The dye layer was the same in all coatings and contained 0.30 and 4.31 g/m 2 of dye D-7 and gelatin respectively. The coating melts were coated onto polyethylene terephthalate support.

TABLE 7-1
	Interlayer gel	Overcoat gel	Overcoat melt former
Coating	g/m 2	g/m 2	g/m 2
C-7-1	3.23	4.31	0.00
I-7-1	3.23	4.31	1.08
I-7-2	3.23	4.31	3.23
C-7-2	0.00	4.31	0.00
I-7-3	0.00	4.31	1.08
I-7-4	0.00	4.31	3.23

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. The Status M red density of the coatings was recorded before and after processing. The results are listed in Table 7-2.

TABLE 7-2
	Interlayer	OC melt former
Coating	g/m 2	g/m 2	Before process	After process
C-7-1	3.23	0.00	0.75	0.34
I-7-1	3.23	1.08	0.74	0.07
I-7-2	3.23	3.23	0.77	0.08
C-7-2	0.00	0.00	0.81	0.33
I-7-3	0.00	1.08	0.75	0.08
I-7-4	0.00	3.23	0.71	0.09

It is clear from the data in the table that the melt former delivered from another layer improved the bleaching of the layer containing the dye, even when the two layers were separated by a third layer.

EXAMPLE 8

Several other phenolic melt formers were combined with the heat bleachable dye D-7. This series of melt formers varied in clogP, which characterizes the octanol/water partition equilibrium of the compound in question. Partition coefficients can be experimentally determined. As an estimate, clogP values can be calculated by fragment additivity relationships. These calculations are relatively simple for additional methylene units in a hydrocarbon chain, but are more difficult in more complex structural variations. An expert computer program, MEDCHEM, Pomona Medchem Software, Pomona College, California (ver. 3.54), permits consistent calculation of partition coefficients as the log value, clogP, from molecular structure inputs and is used in the present invention to calculate these values as a first estimate. The melt former compounds are listed below.

Compound Structure
MF-3
MF-4
MF-5
MF-6
MF-7

Dye D-7 was coated with the above melt formers. The dye was ball-milled and added to a coating melt preparation. The melt formers were uniformly ball-milled dispersions of solid particles and added to yield a coverage of 0.65 g/m 2 . The dye and gelatin coverages were held constant at 0.30 and 4.31 g/m 2 respectively. The coating melts were coated onto polyethylene terephthalate support. The coating variations are described in Table 8-1.

TABLE 8-1
Coating	Melt former	clogP
I-8-1	MF-1	2.95
I-8-2	MF-3	3.45
I-8-3	MF-4	3.98
I-8-4	MF-5	5.04
I-8-5	MF-6	4.48
I-8-6	MF-7	5.54

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. The Status M red density of the coatings was recorded before and after processing. The results are listed in Table 8-2.

TABLE 8-2
Coating	Melt former	Before process	After process	% Bleaching
I-8-1	MF-1	0.59	0.17	71.1
I-8-2	MF-3	0.60	0.16	73.3
I-8-3	MF-4	0.57	0.16	71.9
I-8-4	MF-5	0.54	0.31	42.6
I-8-5	MF-6	0.56	0.20	64.3
I-8-6	MF-7	0.57	0.30	47.4

All of the tested melt formers facilitated bleaching of the dye.

EXAMPLE 9

Several other melt formers were combined with the heat bleachable dye D-7. The melt former compounds are listed below.

Compound Structure
MF-8
MF-9
MF-10
MF-l1
MF-12
MF-13

Dye D-7 was coated without melt former and with the above melt formers. The dye was ball-milled and added to a coating melt preparation. The melt formers were uniformly ball-milled dispersions of solid particles and added to yield a coverage of 1.08 g/m 2 . The dye and gelatin coverages were held constant at 0.30 and 4.31 g/m 2 respectively. The coating melts were coated onto polyethylene terephthalate support. The coating variations are described in Table 9-1.

TABLE 9-1
Coating Melt former
C-9-1   none
I-9-1   MF-1
I-9-2   MF-8
I-9-3   MF-9
I-9-4   MF-10
I-9-5   MF-11
I-9-6   MF-12
I-9-7   MF-13

The coatings were evaluated for thermal bleaching by placing the dried coatings onto a heated 160° C. platen for 10 seconds. The Status M red density of the coatings was recorded before and after processing. The results are listed in Table 9-2.

TABLE 9-2
Coating	Melt former	Before process	After process	% Bleaching
C-9-1	none	0.54	0.42	22.2
I-9-1	MF-1	0.73	0.17	76.7
I-9-2	MF-8	0.75	0.11	85.3
I-9-3	MF-9	0.58	0.06	89.7
I-9-4	MF-10	0.55	0.18	67.3
I-9-5	MF-11	0.54	0.35	35.2
I-9-6	MF-12	0.60	0.31	48.3
I-9-7	MF-13	0.55	0.08	85.5

All of the tested melt formers facilitated bleaching of the dye over the coating that did not contain melt former.

EXAMPLE 10

Dye D-7 was evaluated in a multilayer coating. The following components were used in this example.

Silver Salt Dispersion SS-1:

A stirred reaction vessel was charged with 480 g of lime processed gelatin and 5.6 1 of distilled water. A solution containing 0.7 M silver nitrate was prepared (Solution A). A solution containing 0.7 M benzotriazole and 0.7 M NaOH was prepared (Solution B). The mixture in the reaction vessel was adjusted to a pAg of 7.25 and a pH of 8.00 by additions of Solution B, nitric acid, and sodium hydroxide as needed.

Solution A was added with vigorous mixing to the kettle at 38 cc/minute, and the pAg was maintained at 7.25 by a simultaneous addition of solution B. This process was continued until the quantity of silver nitrate added to the vessel was 3.54 M, at which point the flows were stopped and the mixture was concentrated by ultrafiltration. The resulting silver salt dispersion contained fine particles of silver benzotriazole.

Silver Salt Dispersion SS-2:

A stirred reaction vessel was charged with 480 g of lime processed gelatin and 5.6 1 of distilled water. A solution containing 0.7 M silver nitrate was prepared (Solution A). A solution containing 0.7 M 1-phenyl-5-mercaptotetrazole and 0.7 M NaOH was also prepared (Solution B). The mixture in the reaction vessel was adjusted to a pAg of 7.25 and a pH of 8.00 by additions of Solution B, nitric acid, and sodium hydroxide as needed.

Solution A was added to the kettle at 19.6 cc/minute, and the pAg was maintained at 7.25 by a simultaneous addition of solution B. This process was continued until the 3.54 moles of silver nitrate had been added to the vesses, at which point the flows were stopped and mixture was concentrated by ultrafiltration. The resulting silver salt dispersion contained fine particles of the silver salt of 1-phenyl-5-mercaptotetrazole.

Melt Former MF-1 Dispersion:

A dispersion of salicylanilide was prepared by the method of ball milling. To a total 20 g sample was added 3.0 gm salicylanilide solid, 0.20 g polyvinyl pyrrolidone, 0.20 g TRITON X-200 surfactant, 1.0 g gelatin, 15.6 g distilled water, and 20 ml of zirconia beads. The slurry was ball milled for 48 hours. Following milling, the zirconia beads were removed by filtration. The slurry was refrigerated prior to use.

Developer Dev-1 Dispersion:

A slurry was milled in water containing developer Dev-1 and Olin 10 G as a surfactant. The Olin 10 G was added at a level of 10% by weight of the Dev-1. To the resulting slurry was added water and dry gelatin in order to bring the final concentrations to 13% Dev-1 and 4% gelatin. The gelatin was allowed to swell by mixing the components at 15 C for 90 minutes. After this swelling process, the gelatin was dissolved by bringing the mixture to 40C for 10 minutes, followed by cooling to the chill set the dispersion.

Coupler Dispersion MC-1:

A coupler dispersion was prepared by conventional means containing coupler M-1 at 5.5% and gelatin at 8%. The dispersion contained coupler solvents tricresyl phosphate and CS-1 at weight ratios of 0.8 and 0.2 relative to the coupler M-1, respectively.

Coupler Dispersion CC-1:

An oil based coupler dispersion was prepared by conventional means containing coupler C-1 at 6% and gelatin at 6%. Coupler solvent tricresyl phosphate was included at a weight ratio of 1:1 relative to coupler C-1.

Coupler Dispersion YC-1:

An oil based coupler dispersion was prepared by conventional means containing coupler Y-1 at 6% and gelatin at 6%. Coupler solvent CS-2 was included at a weight ratio of 1:1 relative to coupler Y-1.

The multilayer structure as shown in Table 10-1 was coated on a polyethylene terephthalate support. The coating was accomplished using an extrusion hopper that applied each layer in a sequential process.

TABLE 10-1
Overcoat
Gelatin	1.2960	g/m 2
Silicone Polymer DC-200 (Dow Corning)	0.0389
Matte Beads	0.1134
Dye-1 (UV)	0.0972
FC-135 Fluorinated Surfactant	0.1058
HAR-1	0.5108
Fast Yellow
Gelatin	1.9980	g/m 2
SS-1	0.1512
SS-2	0.1512
YC-1	0.2160
MF-1	0.5184
Dev-1	0.5184
Yellow Sens. Emulsion: 3.5 × 0.128 micron	0.4860
AF-1	0.0079
Slow Yellow
Gelatin	2.7540	g/m 2
SS-1	0.2376
SS-2	0.2376
YC-1	0.3780
MF-1	0.5832
Dev-1	0.5832
Yellow Sens. Emulsion: 1.5 × 0.129 micron	0.2160
Yellow Sens. Emulsion: 0.6 × 0.139 micron	0.0756
Yellow Sens. Emulsion: 0.5 × 0.13 micron	0.1512
Yellow Sens. Emulsion: 0.55 × 0.08 micron	0.1512
AF-1	0.0096
Interlayer 2
Gelatin	1.0800	g/m 2
CA-1	0.0022
Dye-2	0.0864
Fast Magenta
Gelatin	1.7820	g/m 2
SS-1	0.1512
SS-2	0.1512
MC-1	0.2160
MF-1	0.2160
Dev-1	0.2160
Magenta Sens. Emulsion: 2.1 × 0.131 micron	0.4860
AF-1	0.0079
Mid Magenta
Gelatin	1.1340	g/m 2
SS-1	0.1188
SS-2	0.1188
MC-1	0.1944
MF-1	0.1188
Dev-1	0.1188
Magenta Sens. Emulsion: 1.37 × 0.119 micron	0.0648
Magenta Sens. Emulsion: 0.6 × 0.139 micron	0.1728
AF-1	0.0039
Slow Magenta
Gelatin	1.1340	g/m 2
SS-1	0.1188
SS-2	0.1188
MC-1	0.1944
MF-1	0.1188
Dev-1	0.1188
Magenta Sens. Emulsion: 0.5 × 0.13 micron	0.1080
Magenta Sens. Emulsion: 0.55 × 0.08 micron	0.1404
AF-1	0.0049
Interlayer 1
Gelatin	1.0800	g/m 2
CA-1	0.0022
Fast Cyan
Gelatin	2.2140	g/m 2
SS-1	0.1512
SS-2	0.1512
CC-1	0.2592
MF-1	0.5184
Dev-1	0.5184
Cyan Sens. Emulsion: 2.3 × 0.13 micron	0.4860
AF-1	0.0079
Mid Cyan
Gelatin	1.7280	g/m 2
SS-1	0.1188
SS-2	0.1188
CC-1	0.2322
MF-1	0.2916
Dev-1	0.2916
Cyan Sens. Emulsion: 1.37 × 0.119 micron	0.1512
Cyan Sens. Emulsion: 0.6 × 0.139 micron	0.1512
AF-1	0 0039
Slow Cyan
Gelatin	1.7280	g/m 2
SS-1	0.1188
SS-2	0.1188
CC-1	0.2322
MF-1	0.2916
Dev-1	0.2916
Cyan Sens. Emulsion: 0.55 × 0.08 micron	0.1512
Cyan Sens. Emulsion: 0.5 × 0.13 micron	0.1512
AF-1	0.0049
AHU-01 [01]
Gelatin	1.6200	g/m 2
CA-2	0.0076
CA-3	0.2700
CA-4	0.0005
CA-5	0.0008
AF-1	0.0022

Three variations were made off of the above coating structure. Variations consisted of changing the AHU dye that was present in the AHU layer. For each of these variations, the Status M Red Dmin of the coating was measured for the unprocessed film, as well as a sample of the film processed at 140C for 18 seconds using a heated drum processor. Table 10-2 shows the results of these measurements.

TABLE 10-2
			Processed red
	Additional components	Unprocessed red	Dmin
Coating	to AHU	Dmin	(140° C./18″)
C-10-1	None	0.37	0.19
C-10-2	0.043	g/m 2 Dye-3	0.74	0.66
I-10-1	0.22	g/m 2 D-7	0.70	0.25
	0.11	g/m 2 MF-1

The data in Table 10-2 indicate that while the inventive D-7 and the comparative Dye-3 were coated at levels that formed very similar amounts of density in the unprocessed film, there was significant bleaching of the inventive dye during the process of heating the multilayer coating.

The invention has been described in detail with particular reference to certain preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention.

Claims

1. A photothermographic element comprising a support having thereon at least one aqueous coatable light-sensitive imaging layer and at least one aqueous coatable light-absorbing layer comprising a 1-aminopyridinium dye having a methine linkage terminated by a substituted or unsubstituted heterocyclic nucleus, which dye is in bleaching association with an effective amount of a melt former.

2. The photothermographic element of claim 1 wherein the melt former is a substantially non-hydrolyzable organic material which is a solid at an ambient temperature but substantially mixes with the binder phase and dissolves or melts, or both, with the dye at a temperature suitable for photothermographic development or below but higher than 80° C.

3. The photothermographic element of claim 1 wherein the presence of the melt former increases dye bleaching by at least 10% at a time and temperature corresponding to 50% bleaching, which time is between 5 seconds and 1 minute and which temperature is between 90° C. to 180° C.

4. The photothermographic element of claim 1 wherein the melt former is selected from the group consisting of substituted or unsubstituted aryl amides, benzamides, polyglycols, polyethylene oxides, ureas, sulfonamides, benzophenones, anisates, hydroxy-substituted aryl compound, and derivatives thereof.

5. The photothermographic element of claim 4 wherein the melt former is selected from the group consisting of substituted or unsubstituted benzamides, ureas, sulfonamides, benzophenones, hydroxy-substituted aryl compound, and derivatives thereof.

6. The photothermographic element of claim 5 wherein the melt former is a substituted phenolic compound.

7. The photothermographic element of claim 1 comprising a support having thereon at least one light-sensitive silver halide emulsion layer and at least one light-absorbing layer comprising a dye represented by the following structure: wherein:R1 and R2 can independently be selected from the group consisting of (a) an alkyl group, (b) an acyl group, (c) an aryl group, (d) a heterocyclic nucleus containing five to six members in the nucleus, (e) together form a five to six membered heterocyclic nucleus, Q1 represents the non-metallic atoms necessary to complete a saturated, unsaturated, or aromatic heterocyclic nucleus containing five to fifteen atoms in the heterocyclic ring, which nucleus can contain at least one additional heteroatom, and which heterocyclic nucleus can be substituted or unsubstituted by up to 5 independently selected substituents, W is a linking group selected from substituted or unsubstituted alkylene, alkoxyalkylene, alkoxycarbonylalkylene, aralkylene, alkenylene, allylene, and arylene group, Y represents an alkyl group, alkyl group, carboxyalkyl group, amino group, sulfoalkyl group, acyloxyalkyl group, alkoxycarbonylalkyl group, aralkyl group, alkenyl group, or aryl group, which Y groups may be substituted or unsubstituted, n is one or two; p represents the number of double bonds in the heterocylic ring between the N atom and the first methine linkage is zero or one, L represents a methine linkage having the formula  wherein T can be hydrogen, halogen, carboxyamide, lower alkyl of one to four carbon atoms or aryl, R7 and R8 each can be a hydrogen atom, an alkyl group, or an aryl group, which compound can be zwitterionic or in salt form, X— can be an acid anion or can be absent when Y contains a negatively charged group.

8. The photothermographic element of claim 7 wherein the dye has the following structure: wherein Q1, R1, R2, R7, R8 and p are as defined, and Y is a sulfoalkyl, carboxyalkyl, or phosphoalkyl group, in which Y has 1 to 10 carbon atoms.

9. The photothermographic element of claim 8 wherein Y is a sulfoalkyl group.

10. The photographic element of claim 8 wherein the dye is a 1-aminopyridinium compound having the following structure: wherein R1, R2, R7, R8, X, and Y are as defined above and R9 is hydrogen, subsituted or unsubstituted alkyl, substituted or unsubstituted alkoxy, substituted or unsubstituted aryl or alkylaryl, nitro, hydroxy, or halogen.

11. The photographic element of claim 8 wherein the dye is a 1-aminopyridinium compound having the following structure: wherein R1, R2, R7, R8, R9 X and Y are as defined above and R10 and R11 are independently selected from the R9 groups mentioned above.

12. The photothermographic element of claim 1 wherein the melt former has a melting point of at least 80° C. and is represented by the following structure wherein the substituent B is independently selected from a substituent where an oxygen, carbon, nitrogen, phosphorus or sulfur atom is linked to the ring as part of a ketone, aldehyde, ester, amido, carbamate, ether, aminosulfonyl, sulfamoyl, sulfonyl, amine, phosphine, or aromatic heterocyclic group; m is 0 to 4; andwherein the substituent R is independently selected from a substituted or unsubstituted alkyl, cycloalkyl, aryl, alkylaryl, or forms a ring with another substituent on the ring; n is 0 to 4; and wherein m+n is 1 to 5.

13. The photothermographic element of claim 12 wherein B is selected from the group consisting of —C(═O)NHR2, —NHC(═O)R2, —NHSO2R2, —SO2NHR2, —SO2R2, —C(═O)R2, —C(═O)OR2, and —OR2, wherein R2 is substituted or unsubstituted alkyl, cycloalkyl, aryl, alkylaryl, heterocyclic group and can optionally comprise a phenolic hydroxyl group.

14. The photothermographic element of claim 12 wherein when m is 0, n is at least 1 and there is a second phenolic group on an R substituent.

15. The photothermographic element of claim 12 wherein n is 1 and R2 is a substituted or unsubstituted phenyl substituent.

16. The photothemographic element of claim 12 wherein the melt former has the following structure: wherein LINK is selected from the group consisting of —C(═O)NH—, —NHC(═O)—, —NHSO2—, —C(═O)—, —C(═O)O—, —O(R3)—, —SO2NH—, and —SO2—; where R3 is an alkyl group and R and n is as defined above; and p is 0 to 4.

17. The photothermographic element of claim 16 wherein R is independently selected from substituted or unsubstituted C1 to C10 alkyl group.

18. The photothermographic element of claim 16 wherein n+p is 1 and R is a C1 to C6 alkyl group.

19. The photothermographic element of claim 1 wherein the melt former is 2-hydroxy-N-phenylbenzamide or a derivative thereof.

20. The photothermographic element of claim 1 in which the melt former is present in the of 0.01 times to 0.5 times the amount by weight of coated gelatin per square meter in the light-absorbing layer or in a proximate layer containing melt former in bleaching association with the light-absorbing layer.

21. A photothermographic element according to claim 1 wherein the photothermographic element contains an imaging layer comprising a blocked developer, a light-sensitive silver halide emulsion, and a non-light sensitive silver salt oxidizing agent.

22. A photothermographic element according to claim 1 that is capable of dry development without the application of aqueous solutions.

23. A photothermographic element according to claim 1 comprising a mixture of at least two organic silver salts, at least one of which is a non-light sensitive silver salt oxidizing agent.

24. The photothermographic element of claim 1 wherein said light-sensitive layer and said light-absorbing layer comprise an aqueous composition comprising a hydrophilic binder.

25. The photothermographic element of claim 24 wherein the hydrophilic binder is a polymer is selected from the group consisting of gelatin, poly(vinyl alcohol), poly(vinyl pyrrolidone), poly(amides), and derivatives thereof.

26. The photothermographic element of claim 24 wherein the hydrophilic binder is gelatin.

27. The photothermographic element of claim 24 wherein the light absorbing layer and the imaging layer are both at least 5 percent by weight water.

28. The photothermographic element of claim 1 wherein the dye is in the form of particles having an average diameter of 0.01 to 5 microns.

29. A color photothermographic element comprising (a) a support, having thereon (b) at least three aqueous-coatable light-sensitive imaging layers which have their individual sensitivities in different wavelength regions and (c) an aqueous-coatable antihalation layer, below the imaging layers, comprising (i) at least one 1-aminopyridinium anitihalation dye having a methine linkage terminated by a substituted or unsubstituted heterocyclic nucleus, in the form of a dispersion of solid particles having an average size of 0.01 to 5 microns, in association with an effective amount of a melt former, wherein said antihalation dye becomes at least about 50% colorless within about 5 minutes upon heating to a temperature of at least about 90° C.

30. The color photothermographic element of claim 29, wherein the photothermographic imaging layers further comprise a non-light-sensitive organic, silver salt oxidizing agent, further in combination with an incorporated developing agent or precursor thereof.

31. A color photothermographic element as in claim 29 wherein said antihalation layer is between said support and said imaging layers.

32. A color photothermographic element as in claim 29 wherein said antihalation layer is on the side of said support opposite the side containing said imaging layers.

33. A photothermographic process for preparing visible photographic images comprising the steps of:(a) providing a photothermographic element comprising a support having coated thereon (i) at least one aqueous-coatable layer containing photosensitive silver halide, a water-insoluble organic silver salt as an oxidizing agent, a reducing agent for silver ion, and (ii) a aqueous-coatable light-absorbing layer comprising a 1-aminopyridinium filter dye having a methine linkage terminated by a substituted or unsubstituted heterocyclic nucleus, which dye is in association with an effective amount of a melt former, and (b) thermally developing the film step without any externally applied developing agent, comprising heating said film to an average temperature of at least 90° C. for at least 0.5 seconds, wherein said antihalation dye becomes at least about 50% colorless.

34. The photothermographic method according to claim 33 wherein thermal development is conducted under substantially dry process conditions without the application of aqueous solutions.

35. The photothermographic process of claim 33 wherein said antihalation or filter layer becomes substantially colorless within 2 minutes upon heating to a temperature of at least 90° C.

36. A method according to claim 33, wherein said development step comprises treating said imagewise exposed element at a temperature between about 100° C. and about 180° C. for a time ranging from about 0.5 to about 60 seconds.

37. A method according to claim 33 wherein image formation comprises the step of scanning an imagewise exposed and developed imaging element to form a first electronic image representation of said imagewise exposure.

38. A method according to claim 33 wherein the image formation comprises the step of digitizing the first electronic image representation formed from the imagewise exposed, developed, and scanned imaging element to form the digital image.

39. A method according to claim 38 wherein the image formation comprises the step of modifying a first electronic image representation formed from and imagewise exposed, developed, and scanned imaging element formulated to form a second electronic image representation.

40. A method according to claim 38 comprising storing, transmitting, printing, or displaying and electronic image representation of an image derived from an imagewise exposed, developed, scanned imaging element.

41. A method according to claim 38, wherein printing the image is accomplished with any of the following printing technologies: electrophotography; inkjet; thermal dye sublimation; or CRT or LED printing to sensitized photographic paper.

42. The method of claim 38 wherein the melt former has the following formula: wherein the substituent B is independently selected from a substituent where an oxygen, carbon, nitrogen phosphorus or sulfur atom is linked to the ring as part of of a ketone, aldehyde, ester, amido, carbamate, ether, aminosulfonyl, sulfamoyl, sulfonyl, amine, phosphine, or aromatic heterocylcic group;m is 0 to 4; and wherein the substituent R is independently selected from a substituted or unsubstituted alkyl, cycloalkyl, aryl, alkylaryl, or forms a ring with another substituent on the ring; n is 0 to 4; and wherein m+n is 1 to 5.

43. The method of claim 42 wherein the substituent B is linked to the ring as part of an ester, amido, ether, aminosulfonyl, sulfamoyl, sulfonyl or sulfone group.