JP2002196447A - Heat developable photosensitive material - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a heat developable photosensitive material excellent in photographic performance, image stability and block resistance. SOLUTION: The heat developable photosensitive material comprises at least one of each photosensitive layer containing photosensitive silver halide and non-photosensitive protecting layer on the one side of a base. The photosensitive layer contains at least one of each photosensitive silver halide, non- photosensitive organic silver salt, reducing agent for silver ions and binder, The non-photosensitive protecting layer contains plural natural polymers such as polysaccharides and others except for gelatin. It is preferable that the non- photosensitive protecting layer contains organic acid of two or more valences.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a photothermographic material, particularly for medical diagnosis, industrial photography, printing, and COM.
The present invention relates to a photothermographic material suitable for use.

[0002]

2. Description of the Related Art In recent years, in the field of medical diagnostic films and photoengraving films, there has been a strong demand for reduction of processing waste liquid from the viewpoint of environmental protection and space saving. Therefore, heat development is possible as a medical diagnostic film and a photoengraving film that can be efficiently exposed by a laser imagesetter or a laser imager and can form a clear black image having high resolution and sharpness. There is a need for techniques relating to photosensitive materials. According to these photothermographic materials, a photothermographic processing system that does not require solution-based processing chemicals and is simpler and does not damage the environment can be supplied to customers.

There is a similar requirement in the field of general image forming materials. Particularly, medical diagnostic images require high-quality images with excellent sharpness and granularity due to the need for fine description. There is a feature that a cool black image is preferred from the viewpoint of easiness. At present, various hard copy systems using pigments and dyes, such as ink jet printers and electrophotographs, are distributed as general image forming systems, but none of them is satisfactory as a medical image output system.

On the other hand, a thermal image forming system using an organic silver salt is disclosed in, for example, US Pat. Nos. 3,152,904 and 345.
No. 7075 and D.C. Crosta Bohr (Klos
terboer) "Heat Treated Silver System (Therm)
ally Processed Silver Systems) "(Imaging
Processings and Materials (Imaging Proc
esses and Materials) Neblette 8th edition, J.M. Sturge, V.S. Walworth, A.M.
Edited by Shepp, Chapter 9, p. 279, 198
9 years). In particular, photothermographic materials generally include a catalytically active amount of a photocatalyst (eg, silver halide),
It has a photosensitive layer in which a reducing agent, a reducible silver salt (for example, an organic silver salt), and if necessary, a color tone agent for controlling the color tone of silver are dispersed in a binder matrix. After the image exposure, the photothermographic material is heated to a high temperature (for example, 80 ° C. or higher), and a black silver image is formed by a redox reaction between a reducible silver salt (which functions as an oxidizing agent) and a reducing agent. Form. The oxidation-reduction reaction is promoted by the catalytic action of the latent image of silver halide generated by exposure. Therefore, a black silver image is formed in the exposed area. U.S. Patent 2,910,377
And Japanese Patent Publication No. 43-4924.

However, in these photothermographic materials, there is no fixing step after thermal development, so that there is a problem of image deterioration due to an increase in density of an undeveloped portion in image preservability. In addition, since the photothermographic material described above does not require wet processing, a crosslinking agent is often not used, and a problem may occur when special handling is performed in which water or an organic solvent may adhere. there were.

[0006]

SUMMARY OF THE INVENTION An object of the present invention is to solve the above-mentioned conventional problems and achieve the following objects. That is, an object of the present invention is to provide a photothermographic material excellent in photographic performance, image storability and blocking property.

[0007]

Means for solving the above problems are as follows. That is, <1> on one surface of a support, there is provided at least one photosensitive layer containing photosensitive silver halide and a non-photosensitive protective layer, wherein the photosensitive layer comprises at least one kind of photosensitive layer. Photothermographic material containing a photosensitive silver halide, a non-photosensitive organic silver salt, a reducing agent for silver ions and a binder, characterized in that a natural polymer polysaccharide is contained on the side having the photosensitive layer. Is a photothermographic material. <2> The photothermographic material according to <1>, further including a divalent or higher valent organic acid on the side having the photosensitive layer. <3> On one surface of the support, there is provided at least one photosensitive layer containing photosensitive silver halide and a non-photosensitive protective layer, wherein the photosensitive layer is formed of at least one photosensitive halogen. A photothermographic material containing silver chloride, a non-photosensitive organic silver salt, a reducing agent for silver ions and a binder, wherein the non-photosensitive protective layer contains a natural polymer other than gelatin. It is a developed photosensitive material. <4> The photothermographic material according to <3>, wherein the side having the photosensitive layer contains a divalent or higher organic acid. <5> On one surface of a support, there is provided at least one photosensitive layer containing photosensitive silver halide and a non-photosensitive protective layer, wherein the photosensitive layer comprises at least one kind of photosensitive halogen. A photothermographic material containing silver halide, a non-photosensitive organic silver salt, a reducing agent for silver ions and a binder, wherein the non-photosensitive protective layer contains a plurality of natural polymers. It is a photosensitive material. <6> The photothermographic material according to <5>, wherein the side having the photosensitive layer contains a divalent or higher valent organic acid.

[0008]

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. In the photothermographic material of the present invention, it is preferable to use a natural polymer polysaccharide from the viewpoint of image storability and blocking property. It is preferable from the viewpoint of image storability and blocking property. The natural high molecular polysaccharide is not particularly limited, and examples thereof include agar, carrageenan, furcellulan, gum arabic, guar gum, tragacanth gum, karaya gum, pectin, larch gum, locust bean gum, guasseed gum, syllium seed gum, kinsseed gum, tamarind Gum, xanthan gum, gellan gum, tara gum, dextran and the like can be mentioned. Among them, agar, carrageenan, guar gum, locust bean gum, xanthan gum and dextran can be more preferably used. Among them, those having high water solubility are preferred, and those which undergo sol-gel modification by temperature are more preferred. Here, the term "water-soluble" means that 1% by weight or more is dissolved in water at 25 ° C. Also,
The polysaccharide may be a single polysaccharide or a complex polysaccharide. In addition, sol-gel denaturation depending on temperature means that
It means that a sol to a gel and a gel to a sol are denatured within 24 hours at a temperature of 5 ° C. or more and 95 ° C. or less in a weight% aqueous solution. Incidentally, the natural high molecular polysaccharide in the present invention,
It may be used in combination with other water-soluble polymers and polymer latexes as appropriate. Although the natural high molecular polysaccharide in the present invention can be used in a desired amount, 0.001 to 3 g
/ M ² , more preferably 0.01 to 2.2.
g / m ² .

In the photothermographic material of the present invention, the non-photosensitive protective layer preferably contains a natural polymer other than gelatin in view of image storability and blocking property. There is no particular limitation on natural polymers other than gelatin, for example, corn starch, wheat starch, potato starch, potato starch, tapioca starch, rice starch, seaweed,
Agar, sodium alginate, carrageenan, furcellane, gum arabic, guar gum, tragacanth gum,
Karaya Gum, Pectin, Larch Gum, Locust Bean Gum, Gua Seed Gum, Psyllium Seed Gum, Kins Seed Gum, Tamarind Gum, Xanthan Gum, Gellan Gum, Tara Gum, Trolo-Aoi, Konjac, Pullulan, Dextran, glue, casein, collagen,
Chitin, chitosan and the like can be mentioned. Among them, agar, carrageenan, guar gum, locust bean gum, xanthan gum, dextran, collagen, and chitosan can be more preferably used. Among them, those having high water solubility are preferable, and sol-
Those that undergo gel denaturation are more preferred. The natural polymer other than gelatin in the present invention may be used in combination with another water-soluble polymer and polymer latex as appropriate. Natural polymers other than gelatin in the present invention can be used in a desired amount, preferably 0.001~3g / m ^2, more preferably from 0.01~2.2g / m ^2.

In the photothermographic material of the present invention, it is preferred that the non-photosensitive protective layer contains a plurality of natural polymers in view of image storability and blocking property. There is no particular limitation on the natural polymer in the case of containing a plurality of types, for example, corn starch, wheat starch, potato starch, potato starch, tapioca starch, rice starch, seaweed, agar, sodium alginate, carrageenan, furcellane, gum arabic , Guar gum, tragacanth gum, karaya gum, pectin, larch gum, locust bean gum, guay seed gum, syllium seed gum, kins seed gum, tamarind gum, xanthan gum, gellan gum, tara gum, trollo aoi, konjac, pullulan, dextran, glue, gelatin, casein, collagen, Chitin, chitosan and the like can be mentioned. Among them, agar, carrageenan, guar gum, locust bean gum, xanthan gum, dextran, gelatin, collagen, and chitosan can be more preferably used. Among them, those having high water solubility are preferred, and those which undergo sol-gel modification by temperature are more preferred. In the present invention, the natural polymer containing a plurality of types may be used in combination with other water-soluble polymers and polymer latex as appropriate. Natural polymers when containing plural species in the present invention can be used in a desired amount, preferably 0.001~3g / m ^2, more preferably from 0.01~2.2g / m ^2.

In the present invention, it is preferable to use a divalent or higher valent organic acid from the viewpoint of image storability and blocking property. It is preferable in terms of image preservability and blocking property. There is no particular limitation on divalent or higher organic acids,
Examples of divalent or higher organic acids include phthalic acids, oxalic acids,
Examples include succinic acids, maleic acids, fumaric acids, and the like. Among these, phthalic acids (for example, phthalic acid, 4-methylphthalic acid, 4-nitrophthalic acid, diammonium phthalate, sodium phthalate, potassium phthalate and tetrachlorophthalic anhydride) are preferred, and phthalic acid is particularly preferred. The divalent or higher valent organic acid in the present invention can be used in a desired amount, but is preferably 0.01 to 1 g / m ^2.
And more preferably 0.05 to 0.5 g / m.
²

Non-photosensitive organic silver salt usable in the present invention (hereinafter sometimes simply referred to as "organic silver salt")
Is relatively stable to light, but when heated to 80 ° C. or higher in the presence of an exposed photocatalyst (such as a latent image of photosensitive silver halide) and a reducing agent, the silver image It is a silver salt that forms. The organic silver salt can be any organic substance including a source capable of reducing silver ions. Such non-photosensitive organic silver salts are described in JP-A-10-62899, paragraphs 0048 to 0049, European Patent Publication No. 080.
3764A1, page 18, line 24 to page 19, line 37, EP-A-0 962 812 A1, JP-A-11-34991, JP-A-2000-7683,
No. 2000-72711. Silver salts of organic acids, in particular (10 to 30 carbon atoms, preferably 15 to
Silver salts of 28) long chain aliphatic carboxylic acids are preferred. Preferred examples of the organic silver salt include silver behenate, silver arachidate, silver stearate, silver oleate, silver laurate, silver caproate, silver myristate, silver palmitate, and mixtures thereof. In the present invention, among these organic silver salts, it is preferable to use an organic silver salt having a silver behenate content of 75 mol% or more.

The shape of the organic silver salt that can be used in the present invention is not particularly limited, and may be needle-like, rod-like, plate-like, or flake-like. In the present invention, scaly organic silver salts are preferred. In the present specification, the scaly organic silver salt is defined as follows. The organic silver salt was observed with an electron microscope, and the shape of the organic silver salt particles was approximated to a rectangular parallelepiped.
May be the same as ) Then, calculation is performed using the shorter numerical values a and b, and x is obtained as follows. x = b / a

In this way, x is obtained for about 200 particles, and when the average value x (average) is obtained, those satisfying the relationship of x (average) ≧ 1.5 are scaly. Preferably 30 ≧ x (average) ≧ 1.5, more preferably 2
0 ≧ x (average) ≧ 2.0. By the way, needle shape is 1 ≦ x
(Average) <1.5.

In the scaly particle, a can be regarded as the thickness of a tabular particle having a principal plane with b and c as sides. The average of a is preferably 0.01 μm or more and 0.23 μm, more preferably 0.1 μm or more and 0.20 μm or less.
The average of c / b is preferably 1 or more and 6 or less, more preferably 1.05 or more and 4 or less, further preferably 1.1 or more and 3 or less, and particularly preferably 1.1 or more and 2 or less.

The particle size distribution of the organic silver salt is preferably monodispersed. The monodispersion is preferably 100% or less, more preferably 80% or less, and still more preferably 50% of the value obtained by dividing the standard deviation of the length of each of the minor axis and major axis by the minor axis and major axis, respectively. It is as follows. The shape of the organic silver salt can be measured from a transmission electron microscope image of the organic silver salt dispersion. Another method for measuring monodispersity is to determine the standard deviation of the volume-weighted average diameter of the organic silver salt, and the percentage (coefficient of variation) divided by the volume-weighted average diameter is preferably 100% or less. It is preferably at most 80%, more preferably at most 50%. As a measuring method, for example, an organic silver salt dispersed in a liquid is irradiated with laser light, and the particle size (volume weighted average diameter) obtained by obtaining an autocorrelation function with respect to a time change of fluctuation of the scattered light is obtained. be able to.

Known methods and the like can be applied to the production of the organic silver salt used in the present invention and its dispersion method. For example, JP-A-10-62899, European Patent Publication No. 0803763A1, and European Patent Publication No. 0962812A described above.
No. 1, JP-A-11-34991, JP-A-2000-7
No. 683, No. 2000-72711, Japanese Patent Application No. 11-3
No. 48228-30, No. 11-203413, Japanese Patent Application No. 2
000-90093, 2000-195621,
Nos. 2000-191226 and 2000-21381
No. 3, 2000-214155, 2000-19
No. 1226 can be referred to.

In addition, when a photosensitive silver salt is present in the dispersion of the organic silver salt, fog increases and the sensitivity is remarkably lowered. Therefore, it is more preferable that the photosensitive silver salt is not substantially contained at the time of dispersion. In the present invention, the amount of the photosensitive silver salt in the aqueous dispersion to be dispersed is 0.1 to 1 mol of the organic silver salt in the liquid.
The content is 1 mol% or less, and the photosensitive silver salt is not positively added.

In the present invention, it is possible to produce a photosensitive material by mixing an aqueous dispersion of an organic silver salt and an aqueous dispersion of a photosensitive silver salt, but the mixing ratio of the organic silver salt to the photosensitive silver salt may vary depending on the purpose. You can choose, but the ratio of photosensitive silver salt to organic silver salt is 1
~ 30 mol% is preferable, and further 3 ~ 20 mol%,
Particularly, a range of 5 to 15 mol% is preferable. 2 when mixing
Mixing an aqueous dispersion of at least one kind of organic silver salt with an aqueous dispersion of at least two kinds of photosensitive silver salt is a method preferably used for adjusting photographic characteristics.

The organic silver salt in the [0020] present invention can be used in a desired amount, preferably 0.1-5 g / m ² as silver amount, more preferably from 1 to 3 g / m ^2.

The photothermographic material of the present invention preferably contains a reducing agent for an organic silver salt. The reducing agent for the organic silver salt may be any substance (preferably an organic substance) that reduces silver ions to metallic silver. Such a reducing agent is
Paragraph Nos. 0043 to 004 of JP-A-11-65021
5, page 7, line 34 to page 18, line 12 of EP-A-0803764A1.
In the present invention, the reducing agent is preferably a hindered phenols reducing agent or a bisphenols reducing agent, and more preferably a compound represented by the following general formula (I).

[0022]

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In the general formula (I), R ¹¹ and R ^{11 ′}
Each independently represents an alkyl group having 1 to 20 carbon atoms. R
¹² and R ^{12 ′} each independently represent a hydrogen atom or a substituent that can be substituted on a benzene ring. L is a -S- group or-
Represents a CHR ¹³ — group. R ¹³ is a hydrogen atom or carbon atom 1
-20 represents an alkyl group. X ¹ and X ^{1 ′} each independently represent a hydrogen atom or a group that can be substituted on a benzene ring.

The general formula (I) will be described in detail. R
¹¹ and R ^{11 ′} are each independently a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, and the substituent of the alkyl group is not particularly limited, but is preferably an aryl group or a hydroxy group. , An alkoxy group, an aryloxy group,
Examples thereof include an alkylthio group, an arylthio group, an acylamino group, a sulfonamide group, a sulfonyl group, a phosphoryl group, an acyl group, a carbamoyl group, an ester group, and a halogen atom.

R ¹² and R ^{12 ′} are each independently a hydrogen atom or a substituent that can be substituted on a benzene ring, and X ¹ and X ^{1 ′} are each independently a hydrogen atom or a substituent that can be substituted on a benzene ring. Represents Preferred examples of the group that can be substituted on a benzene ring include an alkyl group, an aryl group, a halogen atom, an alkoxy group, and an acylamino group.

L represents a —S— group or a —CHR ¹³ — group. R ¹³ represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms, and the alkyl group may have a substituent. R
Specific examples of the unsubstituted alkyl group represented by ¹³ include methyl, ethyl, propyl, butyl, heptyl, undecyl, isopropyl, 1-ethylpentyl, 2,4,4-trimethyl And a pentyl group. Examples of the substituent for the alkyl group can include, similar to substituent of R ^11, halogen atom, alkoxy group, alkylthio group, aryloxy group, arylthio group, an acylamino group, a sulfonamido group, a sulfonyl group, a phosphoryl group, an oxycarbonyl group, Examples include a carbamoyl group and a sulfamoyl group.

R ¹¹ and R ^{11 ′} are preferably a secondary or tertiary alkyl group having 3 to 15 carbon atoms, specifically, isopropyl, isobutyl, t-butyl,
Examples thereof include a t-amyl group, a t-octyl group, a cyclohexyl group, a cyclopentyl group, a 1-methylcyclohexyl group, and a 1-methylcyclopropyl group. R ¹¹ and R
^{11 ′} is more preferably a tertiary alkyl group having 4 to 12 carbon atoms, and among them, t-butyl group, t-amyl group,
A -methylcyclohexyl group is more preferred, and a t-butyl group is most preferred.

R ¹² and R ^{12 ′} are each preferably an alkyl group having 1 to 20 carbon atoms, specifically, a methyl group,
Ethyl group, propyl group, butyl group, isopropyl group, t
-Butyl group, t-amyl group, cyclohexyl group, 1-methylcyclohexyl group, benzyl group, methoxymethyl group, methoxyethyl group and the like. More preferably methyl group, ethyl group, propyl group, isopropyl group,
t-butyl group. X ¹ and X ^{1 ′} are preferably a hydrogen atom, a halogen atom, or an alkyl group, and more preferably a hydrogen atom.

L is preferably a —CHR ¹³ — group.
R ¹³ is preferably a hydrogen atom or an alkyl group having 1 to 15 carbon atoms. As the alkyl group, a methyl group, an ethyl group, a propyl group, an isopropyl group, and a 2,4,4-trimethylpentyl group are preferable. Particularly preferred as R ¹³ are a hydrogen atom, a methyl group, a propyl group and an isopropyl group.

R¹³Is a hydrogen atom, R¹²And R
^{12 '}Is preferably an alkyl group having 2 to 5 carbon atoms,
Ethyl group and propyl group are more preferable, and ethyl group is most preferable.
preferable. R¹³Is a primary or secondary alkyl having 1 to 8 carbon atoms
When it is a kill group¹²And R ^{12 '}Is preferably a methyl group
New R¹³Represented by a primary or secondary carbon number of 1 to 8
Examples of the alkyl group include a methyl group, an ethyl group, and a propyl
Group, isopropyl group is more preferable, methyl group, ethyl group
And propyl groups are more preferred. R¹¹, R^{11 '}, R¹²You
And R^{12 '}Is a methyl group, R¹³Is
It is preferably a secondary alkyl group. In this case, R
¹³As the secondary alkyl group represented by
Group, isobutyl group, 1-ethylpentyl group is preferred,
An isopropyl group is more preferred.

Hereinafter, specific examples of the reducing agent used in the present invention, including the compound represented by the general formula (I), are shown, but the present invention is not limited to these.

[0032]

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[0033]

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[0034]

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[0035]

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In the present invention, the amount of the reducing agent added is 0.01
To 5.0 g / m ² , preferably 0.1 to 3.0 g / m ² .
0 g / m ² , more preferably 5 to 50 mol% with respect to 1 mol of silver on the surface having a photosensitive layer (hereinafter sometimes referred to as “image forming layer”), More preferably, the content is 10 to 40 mol%. The reducing agent is preferably contained in the image forming layer.

The reducing agent may be contained in the coating solution by any method such as a solution form, an emulsified dispersion form and a solid fine particle dispersion form, and may be contained in the light-sensitive material. Well-known emulsification dispersion methods include oils such as dibutyl phthalate, tricresyl phosphate, glyceryl triacetate or diethyl phthalate, and dissolution using an auxiliary solvent such as ethyl acetate or cyclohexanone, and mechanically dispersing the emulsified dispersion. There is a method of manufacturing.

As a method for dispersing solid fine particles, a powder of a reducing agent is dispersed in a suitable solvent such as water by a ball mill, a colloid mill, a vibrating ball mill, a sand mill, a jet mill, a roller mill or ultrasonic waves to obtain a solid dispersion. Is produced. In this case, a protective colloid (for example, polyvinyl alcohol) and a surfactant (for example, an anionic surfactant such as sodium triisopropylnaphthalenesulfonate (a mixture of three isopropyl groups having different substitution positions)) may be used. Good. The aqueous dispersion can contain a preservative (eg, benzoisothiazolinone sodium salt).

In the photothermographic material of the present invention, a phenol derivative represented by the formula (A) described in Japanese Patent Application No. 11-73951 is preferably used as a development accelerator.

When the reducing agent in the present invention has an aromatic hydroxyl group (—OH), especially in the case of the above-mentioned bisphenols, a non-reducing agent having a group capable of forming a hydrogen bond with these groups is used. It is preferable to use a compound having an acidic property. Examples of the group that forms a hydrogen bond with a hydroxyl group or an amino group include a phosphoryl group, a sulfoxide group, a sulfonyl group, a carbonyl group, an amide group, an ester group, a urethane group, a ureido group, a tertiary amino group, and a nitrogen-containing aromatic group. No. Among them, preferred are a phosphoryl group, a sulfoxide group, and an amide group (provided that they have no> NH group,
> N-Ra (Ra is a substituent other than H). ), A urethane group (provided that it does not have a> NH group and is blocked like> N-Ra (Ra is a substituent other than H)), a ureido group (where a> NH group is And is a compound having> N-Ra (Ra is a substituent other than H). In the present invention, a particularly preferred hydrogen bonding compound is represented by the following general formula (I)
It is a compound represented by I).

[0041]

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In the general formula (II), R ^{21 to} R ²³ each independently represent an alkyl group, an aryl group, an alkoxy group, an aryloxy group, an amino group or a heterocyclic group, and these groups are unsubstituted. And may have a substituent.
When R ^{21 to} R ²³ have a substituent, examples of the substituent include a halogen atom, an alkyl group, an aryl group, an alkoxy group,
Amino group, acyl group, acylamino group, alkylthio group, arylthio group, sulfonamide group, acyloxy group, oxycarbonyl group, carbamoyl group, sulfamoyl group, sulfonyl group, phosphoryl group, and the like,
Preferred as the substituent are an alkyl group and an aryl group, for example, a methyl group, an ethyl group, an isopropyl group, a t-
Examples thereof include a butyl group, a t-octyl group, a phenyl group, a 4-alkoxyphenyl group, and a 4-acyloxyphenyl group. The alkyl group represented by R ²¹ to R ^23, for example, methyl, ethyl, butyl, octyl,
Examples include a dodecyl group, an isopropyl group, a t-butyl group, a t-amyl group, a t-octyl group, a cyclohexyl group, a 1-methylcyclohexyl group, a benzyl group, a phenethyl group, and a 2-phenoxypropyl group. Examples of the aryl group include a phenyl group, a cresyl group, a xylyl group, a naphthyl group, a 4-t-butylphenyl group, a 4-t-octylphenyl group, a 4-anisidyl group, and a 3,5-dichlorophenyl group. Examples of the alkoxy group include a methoxy group, an ethoxy group, a butoxy group, an octyloxy group,
Examples include an ethylhexyloxy group, a 3,5,5-trimethylhexyloxy group, a dodecyloxy group, a cyclohexyloxy group, a 4-methylcyclohexyloxy group, and a benzyloxy group. Examples of the aryloxy group include a phenoxy group, a cresyloxy group, an isopropylphenoxy group, a 4-t-butylphenoxy group, a naphthoxy group, a biphenyloxy group, and the like. As the amino group,
Examples include a dimethylamino group, a diethylamino group, a dibutylamino group, a dioctylamino group, an N-methyl-N-hexylamino group, a dicyclohexylamino group, a diphenylamino group, and an N-methyl-N-phenylamino group.

As R ^{21 to} R ²³ , an alkyl group, an aryl group, an alkoxy group and an aryloxy group are preferred. From the viewpoint of the effect of the present invention, at least one of R ^{21 to} R ²³ is preferably an alkyl group or an aryl group, and more preferably two or more are an alkyl group or an aryl group. In addition, it is preferable that R ^{21 to} R ²³ are the same group in that they can be obtained at low cost.

Hereinafter, the general formula (II) used in the present invention will be described.
Specific examples of the hydrogen bonding compound including the compound of the following are shown, but the present invention is not limited thereto.

[0045]

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[0046]

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Specific examples of the hydrogen bonding compound are described in Japanese Patent Application Nos. 2000-192191 and 2000-1948 in addition to those described above.
No. 11 are mentioned. The compound of the general formula (II) used in the present invention can be contained in a coating solution in the form of a solution, an emulsified dispersion, or a solid-dispersed fine particle dispersion as in the case of the reducing agent, and used in a photosensitive material. The compound forms a hydrogen bonding complex with a compound having a phenolic hydroxyl group and an amino group in a solution state, and depending on the combination of the reducing agent and the compound of the general formula (II),
It can be isolated in crystalline form as a complex. It is particularly preferable to use the crystal powder isolated in this way as a solid dispersion fine particle dispersion in order to obtain stable performance.
Further, a method in which the reducing agent and the compound of the formula (II) are mixed in powder form, and a suitable dispersant is used to form a complex at the time of dispersion with a sand grinder mill or the like can also be preferably used. The compound of the above general formula (II) has 1
It is preferably used in the range of ~ 200 mol%, more preferably in the range of 10 ~ 150 mol%, and still more preferably in the range of 30 ~ 100 mol%.

The photosensitive silver halide used in the present invention is not particularly limited as a halogen composition, and silver chloride, silver chlorobromide, silver bromide, silver iodobromide, and silver iodochlorobromide can be used. . Among them, silver bromide and silver iodobromide are preferred. The distribution of the halogen composition in the grains may be uniform, the halogen composition may change stepwise, or may change continuously. Further, silver halide grains having a core / shell structure can be preferably used. The preferred structure is a two- to five-layer structure, and more preferably, a core / shell particle having a two- to four-layer structure is used. Further, a technique for localizing silver bromide on the surface of silver chloride or silver chlorobromide grains can also be preferably used.

Methods for forming photosensitive silver halide are well known in the art and are described, for example, in Research Disclosure No. 17029, June 1978, and US Pat. No. 3,700,458. Specifically, a method of preparing a photosensitive silver halide by adding a silver supply compound and a halogen supply compound to gelatin or another polymer solution, and then mixing the organic silver salt with an organic silver salt. Used. Also, Japanese Patent Application Laid-Open
The methods described in paragraphs 0217 to 0224 of JP-A-119374, the methods described in Japanese Patent Application Nos. 11-98708 and 2000-42336 are also preferable.

The grain size of the photosensitive silver halide is preferably small for the purpose of suppressing the white turbidity after image formation, specifically 0.20 μm or less, more preferably 0.01 μm or more and 0.15 μm or less. And more preferably, 0.02 μm or more and 0.12 μm or less. The grain size as used herein refers to a diameter when converted into a circular image having the same area as the projected area of a silver halide grain (projected area of a main plane in the case of a tabular grain).

The shape of the silver halide grains is cubic,
Octahedral, tabular particles, spherical particles, rod-like particles, potato-like particles and the like can be mentioned. In the present invention, cubic particles are particularly preferable. Grains having rounded corners of silver halide grains can also be preferably used. The surface index (mirror index) of the outer surface of the photosensitive silver halide grains is not particularly limited. However, the spectral sensitization efficiency when the spectral sensitizing dye is adsorbed is high. preferable. The ratio is preferably at least 50%, more preferably at least 65%, even more preferably at least 80%. The ratio of the Miller index {100} plane is determined by T. Tani; J. Imaging Sci., 29, 165 (1985) using the dependence of the adsorption of the sensitizing dye on the {111} plane and the {100} plane. Can be determined by the method described in (1).

In the present invention, silver halide grains having a hexacyano metal complex present on the outermost surface of the grains are preferred. Hexacyano metal complexes include [Fe (CN) ₆ ] ^4- , [Fe (CN) ₆ ] ^3- , [R
u (CN) ₆ ] ^4- , [Os (CN) ₆ ] ^4- , [Co (CN) ₆ ] ^3- , [Rh (CN) ₆ ] ^3- , [Ir
(CN) ₆ ] ^3- , [Cr (CN) ₆ ] ^3- , [Re (CN) ₆ ] ^{3- and the} like.
In the present invention, a hexacyano Fe complex is preferred.

The hexacyano metal complex is present in the form of ions in an aqueous solution, so that the counter cation is not important. However, the hexacyano metal complex is easily miscible with water and is suitable for sodium ion and potassium ions suitable for the precipitation operation of a silver halide emulsion. Use of alkali metal ions such as ions, rubidium ions, cesium ions, and lithium ions, ammonium ions, and alkylammonium ions (for example, tetramethylammonium ion, tetraethylammonium ion, tetrapropylammonium ion, and tetra (n-butyl) ammonium ion) Is preferred.

The hexacyano metal complex is prepared by mixing a water-miscible organic solvent (eg, alcohols, ethers, glycols, ketones, esters, amides, etc.) or gelatin with water. And can be added as a mixture.

The addition amount of the hexacyano metal complex is preferably from 1 × 10 ⁻⁵ mol to 1 × 10 ⁻² mol, more preferably from 1 × 10 ⁻⁴ mol to 1 × 10 ⁻³ mol, per mol of silver. It is.

In order for the hexacyano metal complex to be present on the outermost surface of the silver halide grains, the addition of the hexacyano metal complex to the silver nitrate aqueous solution used for grain formation is completed, and then sulfur sensitization, selenium sensitization, and tellurium sensitization are performed. It is added directly before the completion of the preparation step before the chemical sensitization step for performing noble metal sensitization such as chalcogen sensitization or gold sensitization, during the water washing step, during the dispersion step, or before the chemical sensitization step. In order not to grow the silver halide fine grains, it is preferable to add the hexacyano metal complex immediately after the grain formation, and it is preferable to add the hexacyano metal complex before the completion of the charging step.

Incidentally, the addition of the hexacyano metal complex may be started after 96% by mass of the total amount of silver nitrate added for grain formation is added, or started after 98% by mass is added. More preferably, it is particularly preferable after adding 99% by mass.

When these hexacyano metal complexes are added after the addition of an aqueous solution of silver nitrate immediately before the completion of grain formation, they can be adsorbed on the outermost surface of silver halide grains, and most of them are hardly soluble in silver ions on the grain surface. Forms salt. Since the hexacyanoiron (II) silver salt is a salt which is harder to dissolve than AgI, re-dissolution by fine particles can be prevented, and silver halide fine particles having a small particle size can be produced. .

The photosensitive silver halide grains in the present invention can contain a metal or a metal complex of Group 8 to Group 10 of the periodic table (showing Groups 1 to 18).
Rhodium, ruthenium, and iridium are preferably the metals of Groups 8 to 10 of the periodic table or the central metal of the metal complex. One kind of these metal complexes may be used, or two or more kinds of complexes of the same metal and different metals may be used in combination.
The preferred content is from 1 × 10 ^-9 mol to 1 mol per mol of silver.
A range of × 10 ^-3 mol is preferred. These heavy metals and metal complexes and their addition methods are described in JP-A-7-2254.
No. 49, JP-A-11-65021, paragraph No. 0018-
0024, JP-A-11-119374, paragraph number 022
7 to 0240.

Further, metal atoms (for example, [Fe (C)
N) ₆ ] ^4- ), desalting and chemical sensitization of silver halide emulsions are described in JP-A-11-84574, paragraph number 0046.
0050, JP-A-11-65021, paragraph number 002
5-0031, paragraph number 0 of JP-A-11-119374
242 to 0250.

Various gelatins can be used as the gelatin contained in the photosensitive silver halide emulsion used in the present invention. In order to maintain a good dispersion state of the photosensitive silver halide emulsion in the coating solution containing an organic silver salt, it is preferable to use low molecular weight gelatin having a molecular weight of 500 to 60,000. These low molecular weight gelatins may be used at the time of particle formation or at the time of dispersion after desalting, but are preferably used at the time of dispersion after desalting.

The sensitizing dye applicable to the present invention is a sensitizing dye capable of spectrally sensitizing silver halide grains in a desired wavelength region when adsorbed on silver halide grains, and having a spectral sensitivity suitable for the spectral characteristics of an exposure light source. Can be advantageously selected. As for the sensitizing dyes and the method of addition, compounds described in paragraphs 0103 to 0109 of JP-A-11-65021, compounds represented by formula (II) of JP-A-10-186572, and compounds represented by formula (I) of JP-A-11-119374 are described. ) And paragraph No. 0106, US Pat.
Nos. 0,236 and 3,871,887 The dyes described in Example 5, JP-A-2-96131, JP-A-59-48
No. 753, EP 080
No. 3764A1, page 19, line 38 to page 20, line 35, Japanese Patent Application No. 2000-86865, Japanese Patent Application No. 2000
No. 102560, Japanese Patent Application No. 2000-205399, and the like. These sensitizing dyes may be used alone or in combination of two or more. In the present invention, the time when the sensitizing dye is added to the silver halide emulsion is preferably after the desalting step and before coating, and more preferably after desalting and before the start of chemical ripening. The addition amount of the sensitizing dye in the present invention can be a desired amount according to the sensitivity and the performance of fogging, but is preferably 10 ^-6 to 1 mol, more preferably 1 mol per mol of silver halide in the photosensitive layer. Is 10 ^-4 to 10 ^-1 mol.

In the present invention, in order to improve the spectral sensitization efficiency,
Supersensitizers can be used. Examples of the supersensitizer used in the present invention include EP 587,338, U.S. Pat. Nos. 3,877,943 and 4,873,18.
4, JP-A-5-341432, 11-11954
No. 7, No. 10-111543 and the like.

The photosensitive silver halide grains in the present invention are preferably chemically sensitized by a sulfur sensitization method, a selenium sensitization method, or a tellurium sensitization method. As compounds preferably used in the sulfur sensitization method, the selenium sensitization method, and the tellurium sensitization method, known compounds, for example, JP-A-7-1287
Compounds described in No. 68 and the like can be used. Particularly in the present invention, tellurium sensitization is preferable.
Compounds described in the document described in paragraph No. 0030 of JP-A-65021, the compound represented by formula (II) in JP-A-5-313284,
Compounds represented by (III) and (IV) are more preferred.

In the present invention, chemical sensitization can be performed at any time after grain formation and before coating, and after desalting, (1) before spectral sensitization, (2) simultaneously with spectral sensitization, 3)
After spectral sensitization, there may be (4) just before coating. In particular, it is preferably performed after spectral sensitization. The amount of the sulfur, selenium and tellurium sensitizers used in the present invention varies depending on the silver halide grains to be used, the conditions of chemical ripening, etc., but is preferably 10 ^-8 to 10 ^-2 mol, preferably 10 ^-8 mol, per mol of silver halide. About 10 ^-7 to 10 ^-3 mol is used. The conditions for the chemical sensitization in the present invention are not particularly limited, but the pH is 5 to 8, the pAg is 6 to 11, and the temperature is 40 to 40.
It is about 95 ° C. A thiosulfonate compound may be added to the silver halide emulsion used in the present invention by the method described in EP-A-293,917.

The light-sensitive silver halide emulsion in the light-sensitive material used in the present invention may be only one kind or two or more kinds (for example, those having different average grain sizes, different halogen compositions, different crystal habits). And those having different chemical sensitization conditions) may be used in combination. The gradation can be adjusted by using a plurality of photosensitive silver halides having different sensitivities. The technology relating to these is disclosed in Japanese Patent Application Laid-Open No.
No. 41, No. 53-106125, No. 47-3929
Nos. 48-55730, 46-5187, 5
Nos. 0-73627 and 57-150841. The sensitivity difference was 0.2 log for each emulsion.
It is preferable to have a difference of E or more.

The amount of the photosensitive silver halide added is 0.03 to 0.6 g, expressed as the amount of silver applied per m ² of the light-sensitive material.
/ M ² , preferably 0.04 to 0.4 g / m ²
More preferably, 0.05 to 0.3 g / m ²
It is most preferable that the photosensitive silver halide is used in an amount of 0.01 to 0.5 mol, more preferably 0.02 to 0.3 mol, per mol of the organic silver salt.

The mixing method and mixing conditions of the separately prepared photosensitive silver halide and organic silver salt are described below. Mills, a method of mixing with a homogenizer, etc., or a method of preparing an organic silver salt by mixing photosensitive silver halide prepared at any timing during the preparation of the organic silver salt, etc. There is no particular limitation as long as the effect appears sufficiently. In addition, mixing two or more kinds of aqueous dispersions of organic silver salts and two or more kinds of aqueous dispersions of photosensitive silver salts is a preferable method for adjusting photographic characteristics.

The preferred timing of adding the silver halide to the coating solution for the image forming layer in the present invention is from 180 minutes to immediately before coating, preferably from 60 minutes to 10 seconds before coating.
The mixing method and mixing conditions are not particularly limited as long as the effects of the present invention are sufficiently exhibited. As a specific mixing method, a method of mixing in a tank such that the average residence time calculated from the addition flow rate and the amount of liquid sent to the coater is a desired time and N. Harnby, MFEdwards, AWNienow,
"Liquid mixing technology" translated by Koji Takahashi (Nikkan Kogyo Shimbun, 19
(1989), a method using a static mixer or the like described in Chapter 8 or the like.

The binder for the organic silver salt-containing layer in the present invention may be any polymer, and suitable binders are transparent or translucent, generally colorless, and include natural resins and polymers and copolymers, synthetic resins and polymers and Copolymers and other film-forming media such as gelatins, rubbers, poly (vinyl alcohol) s, hydroxyethyl celluloses, cellulose acetates,
Cellulose acetate butyrate, poly (vinylpyrrolidone), casein, starch, poly (acrylic acid)
, Poly (methyl methacrylic acid) s, poly (vinyl chloride) s, poly (methacrylic acid) s, styrene-maleic anhydride copolymers, styrene-acrylonitrile copolymers, styrene-butadiene copolymers, Poly (vinyl acetal) s (eg, poly (vinyl formal) and poly (vinyl butyral)), poly (esters),
Poly (urethane), phenoxy resin, poly (vinylidene chloride), poly (epoxide), poly (carbonate), poly (vinyl acetate), poly (olefin)
, Cellulose esters and poly (amides).
The binder may be coated from water or an organic solvent or an emulsion.

In the present invention, the binder in the layer containing the organic silver salt preferably has a glass transition temperature of from 10 ° C. to 80 ° C. (hereinafter sometimes referred to as a high Tg binder), and from 20 ° C. to 70 ° C. Is more preferable, and it is still more preferable that it is 23 to 65 degreeC.

In this specification, Tg was calculated by the following equation. 1 / Tg = Σ (Xi / Tgi) Here, it is assumed that the polymer has copolymerized n monomer components from i = 1 to n. Xi is the weight fraction of the i-th monomer (ΣXi = 1), and Tgi is the glass transition temperature (absolute temperature) of the homopolymer of the i-th monomer.
Where Σ is the sum of i = 1 to n. The homopolymer glass transition temperature (Tgi) of each monomer is calculated by Polyme.
r Handbook (3rd Edition) (by J. Brandrup, EHImmergut
(Wiley-Interscience, 1989)).

The polymer serving as a binder may be used alone or in combination of two or more as required.
Further, those having a glass transition temperature of 20 ° C. or higher and those having a glass transition temperature of less than 20 ° C. may be used in combination.
When two or more polymers having different Tg are blended and used, the weight average Tg preferably falls within the above range.

In the present invention, when the organic silver salt-containing layer is formed by applying a coating solution containing 30% by mass or more of water with water and drying, the binder of the organic silver salt-containing layer is further added. The performance is improved when it is soluble or dispersible in an aqueous solvent (aqueous solvent), especially when it is composed of a latex of a polymer having an equilibrium water content of 2% by mass or less at 25 ° C. and 60% RH. The most preferred form has an ionic conductivity of 2.5 m
It is prepared so as to be S / cm or less. As such a preparation method, a method of purifying using a separation functional membrane after polymer synthesis can be mentioned.

The aqueous solvent in which the polymer is soluble or dispersible is water or a mixture of water and 70% by mass or less of a water-miscible organic solvent. Examples of the water-miscible organic solvent include, for example, alcohols such as methyl alcohol, ethyl alcohol, and propyl alcohol;
Examples thereof include cellosolves such as methyl cellosolve, ethyl cellosolve, and butyl cellosolve, ethyl acetate, and dimethylformamide.

The term "aqueous solvent" is used herein even in the case where the polymer is not thermodynamically dissolved but exists in a so-called dispersed state.

The “equilibrium water content at 25 ° C. and 60% RH” is defined as the weight W1 of the polymer in the moisture-conditioning equilibrium under the atmosphere of 25 ° C. and 60% RH and the weight W0 of the polymer in the dry state at 25 ° C. It can be expressed as follows. Equilibrium moisture content at 25 ° C. and 60% RH = ｛(W1-W
0) / W0｝ × 100 (% by mass) For the definition and measurement method of the water content, for example, Polymer Engineering Course 14, Polymer Material Testing Method (Polymer Society, Jinjinshokan)
Can be referred to.

In the present invention, the binder polymer 25
The equilibrium water content at 60 ° C. and 60% RH is preferably 2% by mass or less, more preferably 0.01% by mass or more and 1.5% by mass or less, still more preferably 0.02% by mass or more and 1% by mass or less. is there.

In the present invention, a polymer dispersible in an aqueous solvent is particularly preferred. Examples of the dispersion state include a latex in which fine particles of a water-insoluble hydrophobic polymer are dispersed, and a dispersion state in which polymer molecules are dispersed in a molecular state or in the form of micelles. The average particle size of the dispersed particles is 1 to 50000 nm, more preferably 5 to 50000 nm.
The range is about 1000 nm. The particle size distribution of the dispersed particles is not particularly limited, and may have a wide particle size distribution or a monodispersed particle size distribution.

In the present invention, preferred embodiments of the polymer dispersible in an aqueous solvent include acrylic polymers, poly (esters), rubbers (for example, SBR resin), poly (urethane) s, poly (vinyl chloride) s, Hydrophobic polymers such as poly (vinyl acetate) s, poly (vinylidene chloride) s and poly (olefins) can be preferably used. These polymers may be a linear polymer, a branched polymer, a crosslinked polymer, a so-called homopolymer obtained by polymerizing a single monomer, or a copolymer obtained by polymerizing two or more types of monomers. In the case of a copolymer, it may be a random copolymer or a block copolymer. These polymers have a number average molecular weight of 5,000 to 1,000,000, preferably 10,000 to 200,000. If the molecular weight is too small, the mechanical strength of the emulsion layer is insufficient, and if it is too large, the film-forming properties are poor, which is not preferable.

Specific examples of preferable polymer latex include the following. In the following, the raw material monomers are used, and the numerical value in parentheses is% by mass, and the molecular weight is the number average molecular weight. When a polyfunctional monomer is used, the concept of molecular weight cannot be applied because a crosslinked structure is formed. Tg represents a glass transition temperature.

Latex of P-1; -MMA (70) -EA (27) -MAA (3)-(molecular weight 37000) P-2; -MMA (70) -2EHA (20) -St (5) -AA (5)-latex (molecular weight 40
000) P-3; -St (50) -Bu (47) -MAA (3)-latex (crosslinkable) P-4; -St (68) -Bu (29) -AA (3)-latex (Crosslinking) P-5; -St (71) -Bu (26) -AA (3)-latex (Crosslinking, Tg24 ° C) P-6; -St (70) -Bu (27) -IA ( 3) -Latex (crosslinkable) P-7; -St (75) -Bu (24) -AA (1) -Latex (crosslinkable) P-8; -St (60) -Bu (35)- Latex of DVB (3) -MAA (2)-(crosslinkable) P-9; Latex of -St (70) -Bu (25) -DVB (2) -AA (3)-(crosslinkable) P-10 ; -VC (50) -MMA (20) -EA (20) -AN (5) -AA (5)-latex (MW 80000) P-11; -VDC (85) -MMA (5) -EA ( 5) -MAA (5)-latex (molecular weight 67
000) P-12; -Et (90) -MAA (10)-latex (Mw 12000) P-13; -St (70) -2EHA (27) -AA (3) latex (Mw 130000) P- 14; -MMA (63) -EA (35)-AA (2) latex (molecular weight 33000) P-15; -St (70.5) -Bu (26.5) -AA (3)-latex (crosslinkable, Tg23
° C) P-16; -St (69.5) -Bu (27.5) -AA (3)-latex (crosslinkable, Tg20.
(5 ℃)

The abbreviations of the above structures represent the following monomers.
MMA; methyl methacrylate, EA; ethyl acrylate, MAA; methacrylic acid, 2EHA; 2-ethylhexyl acrylate, St; styrene, Bu; butadiene, AA; acrylic acid, DVB;
C; vinyl chloride, AN; acrylonitrile, VDC; vinylidene chloride, Et; ethylene, IA; itaconic acid.

The polymer latex described above is also commercially available, and the following polymers can be used. Examples of acrylic polymers include Sebian A-463.
5, 4718, 4601 (Daicel Chemical Industries, Ltd.)
Nipol Lx811, 814, 821, 82
Examples of poly (esters) such as 0, 857 (all manufactured by Zeon Corporation) are FINETEX ES65.
Examples of poly (urethane) s such as 0, 611, 675, and 850 (all manufactured by Dainippon Ink and Chemicals, Inc.), WD-size, and WMS (all manufactured by Eastman Chemical) include HYDRAN AP10, 20, 30, Examples of rubbers such as 40 (all manufactured by Dainippon Ink and Chemicals, Inc.) include LACSTAR 7310K, 3307B, 470
0H, 7132C (all manufactured by Dainippon Ink and Chemicals, Inc.),
Nipol Lx416, 410, 438C, 2507
(Nippon Zeon Co., Ltd.) and other poly (vinyl chloride)
Examples of poly (olefin) s include G351 and G576 (all manufactured by Zeon Corporation), and examples of poly (vinylidene chloride) s include L502 and L513 (all manufactured by Asahi Chemical Industry Co., Ltd.). For example, Chemipearl S
120, SA100 (all manufactured by Mitsui Petrochemical Co., Ltd.) and the like.

These polymer latexes may be used alone or, if necessary, may be blended in two or more kinds.

The polymer latex used in the present invention is particularly preferably a styrene-butadiene copolymer latex. The weight ratio of the styrene monomer unit to the butadiene monomer unit in the styrene-butadiene copolymer is preferably from 40:60 to 95: 5. The proportion of the copolymer of styrene monomer units and butadiene monomer units is 60 to 99% by mass.
It is preferred that The preferred molecular weight range is the same as described above.

Styrene which is preferably used in the present invention
As the latex of butadiene copolymer, the above-mentioned P-
3-P-8, 14, 15; LACSTAR, a commercial product
−3307B, 7132C, Nipol Lx416 and the like.

The organic silver salt-containing layer of the photothermographic material of the present invention may optionally contain a hydrophilic polymer such as gelatin, polyvinyl alcohol, methylcellulose, hydroxypropylcellulose and carboxymethylcellulose. The addition amount of these hydrophilic polymers is 30% by mass or less, more preferably 20% by mass or less of the total binder in the organic silver salt-containing layer.

The organic silver salt-containing layer (that is, image forming layer) in the invention is preferably formed using a polymer latex. The amount of the binder in the organic silver salt-containing layer is
Weight ratio of total binder / organic silver salt is 1/10 to 10 /
1, more preferably in the range of 1/5 to 4/1.

Such an organic silver salt-containing layer is usually a photosensitive layer (emulsion layer) containing a photosensitive silver halide, which is a photosensitive silver salt. / Weight ratio of photosensitive silver halide is 400-5,
More preferably, the range is 200 to 10.

The total amount of the binder in the image forming layer in the present invention is 0.2 to 30 g / m ² , more preferably 1 to 15 g / m ² .
/ M ² is preferred. A crosslinking agent for crosslinking, a surfactant for improving coating properties, and the like may be added to the image forming layer in the invention.

In the present invention, the solvent of the coating solution for the organic silver salt-containing layer of the light-sensitive material (the solvent and the dispersion medium are collectively referred to as a solvent for simplicity) is preferably an aqueous solvent containing 30% by mass or more of water. . As a component other than water, any water-miscible organic solvent such as methyl alcohol, ethyl alcohol, isopropyl alcohol, methyl cellosolve, ethyl cellosolve, dimethylformamide, and ethyl acetate may be used. The water content of the solvent in the coating liquid is preferably 50% by mass or more, more preferably 70% by mass or more. Preferred examples of the solvent composition include water and water / methyl alcohol = 90 in addition to water.
/ 10, water / methyl alcohol = 70/30, water / methyl alcohol / dimethylformamide = 80/15 /
5. Water / methyl alcohol / ethyl cellosolve = 85 /
10/5, water / methyl alcohol / isopropyl alcohol = 85/10/5, etc. (the numerical values are% by mass).

Antifoggants, stabilizers and stabilizer precursors which can be used in the present invention are described in JP-A-10-628.
No. 99, paragraph number 0070, EP-A-08037.
Patent No. 64A1, page 20, line 57 to page 21, line 7, JP-A-9-281637 and JP-A-9-32
No. 9864. The antifoggant preferably used in the present invention is an organic halide, and examples thereof include those disclosed in the patents described in paragraphs 0111 to 0112 of JP-A-11-65021. In particular, an organic halogen compound represented by the formula (P) of Japanese Patent Application No. 11-87297,
Preferred are the organic polyhalogen compounds represented by the general formula (II) of JP-A-339934 and the organic polyhalogen compounds described in Japanese Patent Application No. 11-205330.

Hereinafter, preferred organic polyhalogen compounds in the present invention will be specifically described. The preferred polyhalogen compound in the present invention is a compound represented by the following general formula (III). General formula (III) Q- (Y) _n -C (Z ₁ ) (Z ₂ ) X In the general formula (III), Q represents an alkyl group, an aryl group or a heterocyclic group, and Y is a divalent linking group And n
Represents 0 or 1, Z ₁ and Z ₂ represent a halogen atom, and X represents a hydrogen atom or an electron-withdrawing group. In the general formula (III), Q preferably represents a phenyl group substituted by an electron-withdrawing group having a positive Hammett's substituent constant σp. For Hammett's substituent constant, see Jour
nal of Medicinal Chemistry, 1973, Vol.16, No.11,1207-
1216 etc. can be referred to. Examples of such an electron-withdrawing group include a halogen atom (a fluorine atom (σp
Value: 0.06), chlorine atom (σp value: 0.23), bromine atom (σp value: 0.23), iodine atom (σp value: 0.23).
18)), trihalomethyl group (tribromomethyl (σp
Value: 0.29), trichloromethyl (σp value: 0.3)
3), trifluoromethyl (σp value: 0.54)), cyano group (σp value: 0.66), nitro group (σp value: 0.
78), an aliphatic / aryl or heterocyclic sulfonyl group (for example, methanesulfonyl (σp value: 0.72)),
Aliphatic / aryl or heterocyclic acyl group (for example, acetyl (σp value: 0.50), benzoyl (σp value:
0.43)), an alkynyl group (for example, C≡CH (σp
Value: 0.23)), an aliphatic / aryl or heterocyclic oxycarbonyl group (for example, methoxycarbonyl (σp
Value: 0.45), phenoxycarbonyl (σp value: 0.
44)), a carbamoyl group (σp value: 0.36), a sulfamoyl group (σp value: 0.57), a sulfoxide group,
Examples include a heterocyclic group and a phosphoryl group. The σp value is preferably in the range of 0.2 to 2.0, and more preferably in the range of 0.4 to 1.0. Particularly preferred as the electron-withdrawing group are a carbamoyl group, an alkoxycarbonyl group, an alkylsulfonyl group, and an alkylphosphoryl group, among which a carbamoyl group is most preferred.

X is preferably an electron-withdrawing group, more preferably a halogen atom, an aliphatic / aryl or heterocyclic sulfonyl group, an aliphatic / aryl or heterocyclic acyl group, an aliphatic / aryl or heterocyclic oxycarbonyl. Group, carbamoyl group, sulfamoyl group,
Particularly preferred is a halogen atom. Among the halogen atoms, a chlorine atom, a bromine atom and an iodine atom are preferred, a chlorine atom and a bromine atom are more preferred, and a bromine atom is particularly preferred. Y is preferably -C (= O)
-, - SO- or -SO ₂ -; more preferably, -C (= O) -, - SO 2 - , and particularly preferably -
SO ₂ —. n represents 0 or 1, and is preferably 1.

Hereinafter, the general formula (II) used in the present invention will be described.
Specific examples of the compound (I) are shown below, but the present invention is not limited to these specific examples.

[0097]

Embedded image

[0098]

Embedded image

[0099] In the present invention, the non-photosensitive organic silver salt per mol of the compound represented by formula (III) is the image forming layer, preferably used in an amount of 10 ^-4 to 1 mol, 10 ^- It is more preferably used in the range of ^{3 to} 0.8 mol, particularly preferably in the range of 5 × 10 ^{−3 to} 0.5 mol. In the present invention, as a method for incorporating the antifoggant into the light-sensitive material, the method described in the above-mentioned method for containing the reducing agent can be mentioned, and the organic polyhalogen compound is preferably added in the form of a solid fine particle dispersion.

Other antifoggants include those described in JP-A-1
No. 1-65021, paragraph No. 0113, mercury (II) salt, paragraph No. 0114, benzoic acid, JP-A-2000-20
No. 6642, salicylic acid derivative, JP-A-2000-221
No. 634, the formalin scavenger compound represented by the formula (S), the triazine compound according to claim 9 of JP-A-11-352624, the compound represented by the general formula (III) of JP-A-6-11791, 4- Hydroxy-6-methyl-1,3,3a, 7-tetrazaindene and the like.

The photothermographic material of the present invention may contain an azolium salt for the purpose of preventing fog. Examples of the azolium salt include compounds represented by the general formula (XI) described in JP-A-59-193449, compounds described in JP-B-55-12581, and compounds represented by the general formula (II) described in JP-A-60-153039. And the compounds represented. The azolium salt may be added to any part of the photosensitive material, but it is preferably added to the layer having the photosensitive layer, and more preferably to the organic silver salt-containing layer.
The azolium salt may be added at any step in the preparation of the coating solution, and when it is added to the organic silver salt-containing layer, any step from the preparation of the organic silver salt to the preparation of the coating solution may be used. It is preferable after preparation and immediately before application. The azolium salt may be added by any method such as powder, solution, and fine particle dispersion. Also, sensitizing dyes,
It may be added as a solution mixed with other additives such as a reducing agent and a color tone agent. In the present invention, the azolium salt may be added in any amount.
^It is preferably from ^-6 mol to 2 mol, more preferably from 1 × 10 ^-3 mol to 0.5 mol.

The present invention contains a mercapto compound, a disulfide compound, and a thione compound in order to suppress or accelerate the development to control the development, to improve the spectral sensitization efficiency, and to improve the storage stability before and after the development. Paragraph No. 00 of JP-A-10-62899
67-0069, compounds represented by the general formula (I) of JP-A-10-186572 and specific examples thereof, paragraphs [0033] to [0052], and European Patent Publication No. 0803764A.
No. 1, page 20, lines 36-56, Japanese Patent Application No. 11-27
No. 3670 and the like. Among them, mercapto-substituted heteroaromatic compounds are preferred.

In the photothermographic material of the present invention, a toning agent is preferably added, and as to the toning agent, see JP-A-10-6289.
No. 9, paragraphs 0054 to 0055, European Patent Publication No. 0
No. 803764A1, page 21, lines 23-48, JP-A-2000-356317 and Japanese Patent Application No. 2000-1872.
No. 98, particularly phthalazinones (phthalazinone, phthalazinone derivatives or metal salts; for example, 4- (1-naphthyl) phthalazinone, 6-chlorophthalazinone, 5,7-dimethoxyphthalazinone and 2,3
Phthalazinones and phthalic acids (eg, phthalic acid, 4-methylphthalic acid, 4-nitrophthalic acid, diammonium phthalate,
Combinations with sodium phthalate, potassium phthalate and tetrachlorophthalic anhydride; phthalazines (phthalazine, phthalazine derivatives or metal salts;
(1-naphthyl) phthalazine, 6-isopropylphthalazine, 6-t-butylfuratazine, 6-chlorophthalazine, 5,7-dimethoxyphthalazine and 2,3-dihydrophthalazine); phthalazines and phthalic acids Are particularly preferable, and a combination of phthalazines and phthalic acids is particularly preferable.

The plasticizers and lubricants that can be used in the photosensitive layer in the present invention are described in JP-A-11-65.
Paragraph No. 0117 of paragraph No. 021, paragraph No. 0118 of paragraph No. 0118 of paragraph No. 0118 of paragraph No. 0118 of paragraph No. 0118 of JP-A-11-2223898, and details of a super-high contrast agent for forming a super-high contrast image and the addition method and amount thereof
6 to 0193, Formula (H) of Japanese Patent Application No. 11-87297,
Compounds of formulas (1) to (3), formulas (A) and (B), compounds of general formulas (III) to (V) described in Japanese Patent Application No. 11-91652 (specific compounds: ) And Japanese Patent Application Laid-Open No. 11-65021, paragraph number 010
2, paragraph number 0194-0 of JP-A-11-223898
195.

In order to use formic acid or formate as a strong fogging substance, it is necessary to contain 5 mmol or less, more preferably 1 mmol or less, per mole of silver on the side having the image forming layer containing photosensitive silver halide. preferable.

When a super-high contrast agent is used in the photothermographic material of the present invention, it is preferable to use an acid or a salt thereof formed by hydration of diphosphorus pentoxide in combination. Acids or salts thereof formed by hydration of diphosphorus pentoxide include metaphosphoric acid (salt), pyrophosphoric acid (salt), orthophosphoric acid (salt), triphosphoric acid (salt), tetraphosphoric acid (salt), hexametaline Acids (salts) and the like can be mentioned. Particularly preferred acids and salts thereof formed by hydration of diphosphorus pentoxide include orthophosphoric acid (salt) and hexametaphosphoric acid (salt). Specific salts include sodium orthophosphate, sodium dihydrogen orthophosphate,
Examples include sodium hexametaphosphate and ammonium hexametaphosphate. The amount of the acid or a salt of phosphorus pentoxide obtained by hydration (coating amount per photographic material 1 m ²⁾
May be in a desired amount in accordance with performance such as sensitivity and fog, but is preferably 0.1 to 500 mg / m ² , and 0.5 to 1 mg / m ^2.
00 mg / m ² is more preferred.

The photothermographic material of the present invention can be provided with a non-photosensitive protective layer (also referred to as a surface protective layer) for the purpose of preventing adhesion of the image forming layer. The surface protective layer may be a single layer or a plurality of layers. For the surface protection layer,
JP-A-11-65021, paragraph numbers 0119 to 012
0, Japanese Patent Application No. 2000-171936.
As the binder of the surface protective layer in the present invention, a hydrophilic binder is required, and as the hydrophilic binder, the above-described natural polymer polysaccharides, natural polymers other than gelatin, and a plurality of types of natural polymers are preferable. However, it is also preferable to use gelatin or polyvinyl alcohol (PVA) in combination. As gelatin, inert gelatin (for example, Nitta Gelatin 750), phthalated gelatin (for example, Nitta Gelatin 801) and the like can be used. Examples of the PVA include those described in paragraphs 0009 to 0020 of JP-A-2000-171936, in which PVA-105 as a completely saponified product and P as a partially saponified product are used.
VA-205, PVA-335, MP-203 of modified polyvinyl alcohol (the above are trade names manufactured by Kuraray Co., Ltd.)
And the like. Preferably 0.3 to 4.0 g / m ² as a coating amount of polyvinyl alcohol protective layer (per one layer) (per support 1 m ^2), 0.3 to 2.
0 g / m ² is more preferred.

In particular, when the photothermographic material of the present invention is used for printing applications in which dimensional change is a problem, it is preferable to use a polymer latex for the surface protective layer and the back layer.
For such polymer latex, see "Synthetic Resin Emulsion (edited by Tadashi Okuda and Hiroshi Inagaki, published by Kobunshi Kanko (1978))", "Application of Synthetic Latex (Edited by Takaaki Sugimura, Yasuo Kataoka, Soichi Suzuki, Keiji Kasahara, Published by Kobunshi Kankokai (1993)), "Synthesis of Synthetic Latex (Souichi Muroi, published by Kobunshi Kankokai (1970))", and specifically, methyl methacrylate (33.5% by mass) ) / Ethyl acrylate (50% by weight) / latex of methacrylic acid (16.5% by weight) copolymer, methyl methacrylate (47.5% by weight) / butadiene (4%)
Latex of 7.5% by mass) / itaconic acid (5% by mass) copolymer, latex of ethyl acrylate / methacrylic acid copolymer, methyl methacrylate (58.9%)
Mass%) / 2-ethylhexyl acrylate (25.4
Mass%) / styrene (8.6 mass%) / 2-hydroxyethyl methacrylate (5.1 mass%) / latex of acrylic acid (2.0 mass%) copolymer, methyl methacrylate (64.0 mass%) / styrene Latex of (9.0% by mass) / butyl acrylate (20.0% by mass) / 2-hydroxyethyl methacrylate (5.0% by mass) / acrylic acid (2.0% by mass). Furthermore, as a binder for the surface protective layer,
Combinations of polymer latex described in Japanese Patent Application No. 11-6872, techniques described in paragraphs 0021 to 0025 of Japanese Patent Application No. 11-143058, and Japanese Patent Application No. 11-6.
No. 872, paragraphs 0027 to 0028, and Japanese Patent Application No. 10-199626, paragraph 0
The technology described in O.23 to 0041 may be applied. The ratio of the polymer latex in the surface protective layer was 1 for all binders.
0 mass% or more and 90 mass% or less are preferable, and especially 20 mass% or more and 80 mass% or less are preferable. The amount of the binder (including the water-soluble polymer and the latex polymer) applied to the surface protective layer (per layer) (per 1 m ^{2 of the} support) is preferably 0.3 to 5.0 g / m ² , and 0.3 to ² g / m ^2. .0
g / m ² is more preferred.

In the present invention, a crosslinking agent can be preferably used. There is no particular limitation on the crosslinking agent,
“THE THEORY OF THE P” by TH James
HOTOGRAPHIC PROCESS FOURTH EDITION ”(Macmillan Pub
lishing Co., Inc., published in 1977), pages 77 to 87, chromium alum, 2,4-dichloro-6
-Hydroxy-s-triazine sodium salt, N, N-
Ethylenebis (vinylsulfoneacetamide), N,
N-propylene bis (vinyl sulfone acetamide)
And polyisocyanates described in U.S. Pat. No. 4,281,060 and JP-A-6-208193, and U.S. Pat.
Epoxy compounds such as No. 2 and JP-A-62-89048
And vinylsulfone-based compounds such as

The crosslinking agent is added as a solution, and this solution is added to the coating solution for the protective layer from 180 minutes to immediately before coating, preferably from 60 minutes to 10 seconds before coating. The conditions are not particularly limited as long as the effects of the present invention are sufficiently exhibited. As a specific mixing method, there is a method of mixing in a tank in which the average residence time calculated from the addition flow rate and the amount of liquid sent to the coater is set to a desired time, Harnby, M .; F. Edward
s, A.S. W. There is a method using a static mixer or the like described in Chapter 8 of Nienow, "Liquid Mixing Technology" translated by Koji Takahashi (Nikkan Kogyo Shimbun, 1989).

The preparation temperature of the coating solution for the image forming layer in the present invention is preferably from 30 ° C. to 65 ° C., more preferably from 35 ° C. to less than 60 ° C., particularly preferably 35 ° C.
Not less than 55 ° C. It is preferable that the temperature of the coating solution for the image forming layer immediately after the addition of the polymer latex is maintained at 30 ° C. or higher and 65 ° C. or lower.

The image forming layer in the present invention comprises one or more layers on a support. When it is composed of one layer, it consists of an organic silver salt, a light-sensitive silver halide, a reducing agent and a binder, and contains, if necessary, additional materials such as a toning agent, a coating auxiliary and other auxiliary agents. When it comprises two or more layers, the first image-forming layer (usually a layer adjacent to the support) contains an organic silver salt and a photosensitive silver halide, and the second image-forming layer or both layers contain some. Other components must be included. The construction of a multicolor photothermographic material may include a combination of these two layers for each color, and all components in a single layer as described in U.S. Pat. No. 4,708,928. May be included. In the case of a multi-dye, multi-color photothermographic material, each emulsion layer generally comprises a functional or non-functional layer between the light-sensitive layers, as described in U.S. Pat. No. 4,460,681. Are kept distinct from each other by using the barrier layer.

The photothermographic material of the present invention preferably has a pH of 7.0 or less, more preferably 6.6 or less, before heat development. The lower limit is not particularly limited, but is about 3. The most preferred pH range is 4-6.
2 range. The adjustment of the film surface pH is preferably performed using an organic acid such as a phthalic acid derivative, a nonvolatile acid such as sulfuric acid, or a volatile base such as ammonia from the viewpoint of reducing the film surface pH. In particular, ammonia is preferable in achieving a low film surface pH since ammonia is easily volatilized and can be removed before the application step and the heat development. It is also preferable to use ammonia in combination with a non-volatile base such as sodium hydroxide, potassium hydroxide, and lithium hydroxide. The method for measuring the film surface pH is described in Japanese Patent Application No. 11-87.
No. 297, paragraph 0123.

In the present invention, the photosensitive layer has a color tone improvement,
Various dyes and pigments (for example, CI Pigment Blue) can be used to prevent interference fringes during laser exposure and irradiation.
60, CI Pigment Blue 64, CI Pigment Blue 15: 6) can be used. About these, WO98 / 363
No. 22, JP-A Nos. 10-268465 and 11-338
No. 098 and the like.

In the photothermographic material of the present invention, an antihalation layer can be provided on the side farther from the light source than the photosensitive layer.

A photothermographic material generally has a non-photosensitive layer in addition to a photosensitive layer. The non-photosensitive layer is composed of (1) a protective layer provided on the photosensitive layer (on the side farther than the support) from the disposition thereof, and (2) a protective layer between a plurality of photosensitive layers or between the photosensitive layer and the protective layer. It can be classified into an intermediate layer provided therebetween, (3) an undercoat layer provided between the photosensitive layer and the support, and (4) a back layer provided on the opposite side of the photosensitive layer. The filter layer is
It is provided on the photosensitive material as the layer (1) or (2).
The antihalation layer is provided on the photosensitive material as the layer (3) or (4).

The antihalation layer is disclosed in
Paragraph Nos. 0123 to 0124 of 1-65021, JP-A Nos. 11-223898, 9-230531, and 10
-36695, 10-104779, 11-2
No. 31457, No. 11-352625, No. 11-35
No. 2626 and the like. The antihalation layer contains an antihalation dye having absorption at the exposure wavelength. When the exposure wavelength is in the infrared region, an infrared absorbing dye may be used, and in that case, a dye having no absorption in the visible region is preferable. When using a dye having absorption in the visible region to prevent halation, it is preferable that substantially no color of the dye remains after image formation, and a means for decoloring by the heat of heat development is used. It is particularly preferable to add a thermal decoloring dye and a base precursor to the non-photosensitive layer to function as an antihalation layer. These techniques are described in Japanese Patent Application Laid-Open No. 11-2
No. 31,457.

The amount of the decolorizable dye is determined depending on the use of the dye. Generally, the optical density (absorbance) measured at the target wavelength is used in an amount exceeding 0.1. The optical density is preferably from 0.2 to 2. The amount of the dye used to obtain such an optical density is generally 0.00
It is about 1 to 1 g / m ² .

When the dye is decolored in this manner, the optical density after thermal development can be reduced to 0.1 or less. Two or more decolorizable dyes may be used in combination in a heat-decolorable recording material or a photothermographic material. Similarly, two or more base precursors may be used in combination. In thermal decoloring using such a decoloring dye and a base precursor,
The use of a substance (for example, diphenylsulfone, 4-chlorophenyl (phenyl) sulfone) which lowers the melting point by 3 ° C. (deg) or more when mixed with a base precursor as described in JP-A-11-352626 can be used in combination with thermal decoloration. It is preferable from the point of view.

In the present invention, a colorant having an absorption maximum at 300 to 450 nm can be added for the purpose of improving the silver tone and the aging of the image. Such coloring agents are described in JP-A-62-210458 and JP-A-63-10404.
No. 6, No. 63-103235, No. 63-208846
Nos. 63-306436 and 63-314535
No. JP-A-01-61745, Japanese Patent Application No. 11-2767.
No. 51, etc. Such a coloring agent is usually added in the range of 0.1 mg / m ^{2 to 1} g / m ² , and the layer to be added is preferably a back layer provided on the side opposite to the photosensitive layer.

The photothermographic material of the present invention is a so-called single-sided photosensitive material having at least one photosensitive layer containing a silver halide emulsion on one side of a support and a back layer on the other side. Preferably, there is.

In the present invention, it is preferable to add a matting agent for improving transportability.
JP-A-11-65021, paragraph numbers 0126 to 0127
It is described in. The matting agent is preferably 1 to 400 mg / m ² when expressed in a coating amount per m ² of the photosensitive material.
m ² , more preferably 5 to 300 mg / m ² . The matting degree of the emulsion surface may be any value as long as stardust failure does not occur, but the Beck smoothness is preferably 30 seconds or more and 2000 seconds or less, and particularly preferably 40 seconds or more and 1500 seconds or less. The Beck smoothness is based on Japanese Industrial Standard (JIS) P811.
9 "Smoothness test method for paper and paperboard using Beck tester" and TAPPI standard method T479.

In the present invention, the matting degree of the back layer is preferably such that the Bekk smoothness is 1200 seconds or less and 10 seconds or more, more preferably 800 seconds or less and 20 seconds or more, and particularly preferably 500 seconds or less and 40 seconds or more.

In the present invention, the matting agent is preferably contained in the outermost surface layer of the light-sensitive material, a layer functioning as the outermost surface layer, or a layer close to the outer surface. Preferably, it is contained.

The back layer applicable to the present invention is described in paragraph No. 0128 of JP-A-11-65021.
To 0130.

The surfactant applicable to the present invention is described in paragraph No. 0132 of JP-A-11-65021, the solvent is the same paragraph No. 0133, the support is the same paragraph No. 0134, and the antistatic or conductive layer is the same. The same paragraph No. 0135, the method for obtaining a color image is the same paragraph No. 0136, and the slipping agent is disclosed in
-84573, paragraph numbers 0061 to 0064 and Japanese Patent Application No.
No. 1-106881, paragraphs 0049 to 0062.

The transparent support was heat-treated at a temperature in the range of 130 to 185 ° C. in order to alleviate the internal strain remaining in the film during biaxial stretching and to eliminate the heat shrinkage distortion generated during the heat development processing. Polyester, especially polyethylene terephthalate, is preferably used. In the case of a photothermographic material for medical use, the transparent support may be colored with a blue dye (for example, Dye-1 described in Examples of JP-A-8-240877) or may be uncolored. As the support, water-soluble polyester disclosed in JP-A-11-84574, 10-1
No. 86565, styrene-butadiene copolymer
It is preferable to apply an undercoating technique such as a vinylidene chloride copolymer described in paragraph Nos. 0063 to 0080 of JP-A-00-39684 and Japanese Patent Application No. 11-106881. Japanese Patent Application Laid-Open No. 56-143430 discloses an antistatic layer or an undercoat.
No., No. 56-143431, No. 58-62646,
Nos. 56-120519, JP-A-11-84573, paragraphs 0040 to 0051, U.S. Pat.
957, JP-A-11-223898, paragraph number 00
The techniques described in 78 to 0084 can be applied.

The photothermographic material is preferably of a monosheet type (a type capable of forming an image on the photothermographic material without using another sheet such as an image receiving material).

The photothermographic material further comprises an antioxidant,
Stabilizers, plasticizers, ultraviolet absorbers or coating aids may be added. Various additives are added to either the photosensitive layer or the non-photosensitive layer. WO98 about them
No./36322, EP803376A1, JP-A-10
Nos. 186567 and 10-18568 can be referred to.

The photothermographic material of the present invention may be applied by any method. Specifically, extrusion coating, slide coating, curtain coating, dip coating, knife coating, flow coating, or US Pat. No. 2,681,294.
A variety of coating operations including extrusion coating using a hopper of the type described in U.S. Pat.
“LIQUID FILM COATIN” by istler and Petert M. Schweizer
G ”(published by CHAPMAN & HALL, 1997), page 399 to 5
Extrusion coating or slide coating described on page 36 is preferably used, and particularly preferably slide coating is used. An example of the shape of a slide coater used for slide coating is shown in FIG. In one. Also,
If desired, the method described in ibid., Pages 399 to 536, U.S. Pat. No. 2,761,791 and British Patent 837,
No. 095, two or more layers can be coated simultaneously.

The coating solution for the organic silver salt-containing layer in the present invention comprises:
Preferably, it is a so-called thixotropic fluid. For this technique, reference can be made to JP-A-11-52509. The organic silver salt-containing layer coating solution of the present invention has a viscosity of 400 mPa · s at a shear rate of 0.1 S ⁻¹ .
s or more and 100,000 mPa · s or less, more preferably 500 mPa · s or more and 20,000 mPa · s or less.
s or less. Further, at a shear rate of 1000 S ^−1, it is preferably from 1 mPa · s to 200 mPa · s, more preferably from 5 mPa · s to 80 mPa · s.

Techniques that can be used for the photothermographic material of the present invention include EP803376A1 and EP88.
No. 3022A1, WO98 / 36322, JP-A-56
-62648, 58-62644, JP-A-9-4
3766, 9-281637, 9-297367
No. 9-304869, No. 9-31405, No. 9-329865, No. 10-10669, No. 10-
No. 62899, No. 10-69023, No. 10-186
No. 568, No. 10-90823, No. 10-17106
No. 3, No. 10-186565, No. 10-186567
Nos. 10-186569 to 10-186572
No. 10-197974, No. 10-197982
No. 10-197983, No. 10-197985 to No. 10-197987, No. 10-207001,
Nos. 10-207004, 10-221807, 10-282601, 10-288823, 1
Nos. 0-288824, 10-307365, and 10
No.-312038, No.10-339934, No.11-
No. 7100, No. 11-15105, No. 11-2420
No. 0, No. 11-24201, No. 11-30832,
11-84574, 11-65021, 11
Nos. 109547, 11-125880, 11-
Nos. 129629 and 11-133536 to 11-1
No. 33538, No. 11-133542, No. 11-13
No. 3543, No. 11-223898, No. 11-352
No. 627, No. 11-305377, No. 11-3053
No. 78, No. 11-305384, No. 11-30538
No. 0, No. 11-316435, No. 11-327076
No. 11-338096 and No. 11-338098
No. 11-338099 and No. 11-343420
No., Japanese Patent Application No. 2000-187298, 2000-10
No. 229, No. 2000-47345, No. 2000-2
No. 06624, No. 2000-98530, No. 2000
-98531, 2000-112059, 20
00-112060, 2000-112104,
Nos. 2000-11204 and 2000-17193
No. 6 is also mentioned.

The photothermographic material of the present invention may be developed by any method, but is usually developed by raising the temperature of the photothermographic material exposed imagewise. The preferred development temperature is 80 to 250 ° C, more preferably 10 to 250 ° C.
0-140 ° C. The development time is preferably 1 to 60 seconds, more preferably 5 to 30 seconds, and particularly preferably 10 to 20 seconds.

As a method of thermal development, a plate heater method is preferable. The heat development method using a plate heater method is preferably a method described in JP-A-11-133572, in which a heat-developable photosensitive material on which a latent image is formed is brought into contact with a heating means in a heat development section to obtain a visible image. A developing device, wherein the heating means comprises a plate heater, and a plurality of pressing rollers are provided to face each other along one surface of the plate heater, and the heating means is provided between the pressing roller and the plate heater. A thermal developing apparatus for performing thermal development by passing a developing photosensitive material. It is preferable to divide the plate heater into two to six stages and lower the temperature at the tip part by about 1 to 10 ° C. Such a method is also described in JP-A-54-30032, in which water and organic solvents contained in the photothermographic material can be excluded from the system. The change in the shape of the support of the photothermographic material due to the heating of the photothermographic material can also be suppressed.

The photothermographic material of the present invention may be exposed by any method, but a laser beam is preferred as an exposure light source. As the laser beam according to the present invention, a gas laser (Ar ⁺ , He—Ne), a YAG laser, a dye laser, a semiconductor laser, or the like is preferable. Further, a semiconductor laser and a second harmonic generation element can be used. Preferably, a gas or semiconductor laser emitting red to infrared light is used.

As a medical laser imager having an exposure section and a heat development section, Fuji Medical Dry Laser Imager FM-DPL can be mentioned. Regarding FM-DPL, Fuji Medic
al Review No. 8, pages 39 to 55, and it goes without saying that those techniques are applied as a laser imager for the photothermographic material of the present invention. Further, as a network system conforming to the DICOM standard, it can be applied as a photothermographic material for a laser imager in “AD network” proposed by Fuji Medical System.

The photothermographic material of the present invention forms a black-and-white image by a silver image, and is used for medical diagnosis, photothermographic material for industrial photography, photothermographic material for printing, and COM.
Is preferably used as a photothermographic material.

[0138]

EXAMPLES Hereinafter, the present invention will be described specifically with reference to examples, but the present invention is not limited to these examples. (Example 1) [Preparation of PET support] Using terephthalic acid and ethylene glycol, an intrinsic viscosity IV = 0.66 (phenol / tetrachloroethane = 6/4 (weight ratio) 25) according to a conventional method.
(Measured in ° C.). After pelletizing this 1
It was dried at 30 ° C. for 4 hours, melted at 300 ° C., extruded from a T-die, and quenched to prepare an unstretched film having a thickness of 175 μm after heat setting.

This was performed by using rolls having different peripheral speeds in 3.3.
The film was longitudinally stretched by a factor of 2, and then transversely stretched by a factor of 4.5. The temperatures at this time were 110 ° C. and 130 ° C., respectively. After that, it was heat-set at 240 ° C. for 20 seconds, and relaxed 4% in the horizontal direction at the same temperature. Then, after slitting the chuck portion of the tenter, knurling was performed on both ends, and it was wound up at 4 kg / cm ² (4 × 10 ⁴ Pa) to obtain a roll having a thickness of 175 μm.

[Surface Corona Treatment] Using a solid state corona treatment machine 6KVA model manufactured by Pillar Co., both surfaces of the support were treated at room temperature at 20 m / min. From the current and voltage readings at this time, 0.375 kV was applied to the support.
-It turned out that the processing of A * minute / m < ² > was performed.
The processing frequency at this time was 9.6 kHz, and the gap clearance between the electrode and the dielectric roll was 1.6 mm.

[Preparation of Undercoat Support] (1) Preparation of Coating Solution for Undercoat Layer Formulation (for undercoat layer on photosensitive layer side) ・ Pesthresin A-515GB manufactured by Takamatsu Yushi Co., Ltd. (30% by mass solution) 234 g ・ Polyethylene Glycol monononyl phenyl ether (average ethylene oxide number = 8.5) 10% by mass solution 21.5 g ・ Soken Chemical Co., Ltd. MP-1000 (polymer fine particles, average particle diameter 0.4 μm) 0.91 g

Formulation (for back surface first layer) 158 g of styrene-butadiene copolymer latex (solid content 40% by mass, styrene / butadiene weight ratio = 68/32) 2,4-dichloro-6-hydroxy-S -Triazine sodium salt 8% by mass aqueous solution 20g-1% by mass aqueous solution of sodium laurylbenzenesulfonate 10ml-Distilled water 854ml

Formulation (for the back surface side second layer): SnO ₂ / SbO (9/1 mass ratio, average particle size: 0.038 μm, 17 mass% dispersion) 84 g ・ Gelatin (10 mass% aqueous solution) 89.2 g 8.6 g of Metroze TC-5 (2 mass% aqueous solution) manufactured by Shin-Etsu Chemical Co., Ltd.-0.01 g of MP-1000 manufactured by Soken Chemical Co., Ltd.-10 ml of 1 mass% aqueous solution of sodium dodecylbenzenesulfonate-NaOH (1 mass%) %) 6 ml ・ Proxel (manufactured by ICI) 1 ml ・ Distilled water 805 ml

[Preparation of Undercoating Support] The above thickness of 175 μm
m, the corona discharge treatment was applied to both sides of the biaxially stretched polyethylene terephthalate support, and the undercoating solution formulation was wet-coated on one surface (photosensitive layer surface) with a wire bar at a wet application amount of 6.6 ml / m ² ( (Per side) and dried at 180 ° C for 5 minutes. Then, the undercoating liquid formulation was applied to the back surface (back surface) with a wire bar so that the wet application amount was 5.7 ml / m ^2. After drying at 180 ° C. for 5 minutes, the undercoating composition was further applied to the back surface (back surface) with a wire bar so that the wet application amount was 7.7 ml / m ^2.
After drying at 0 ° C. for 6 minutes, an undercoat support was prepared.

[Preparation of back surface coating solution] (Preparation of solid fine particle dispersion (a) of base precursor)
64 g of the base precursor compound 11, 28 g of diphenylsulfone, and 10 g of surfactant Demol N manufactured by Kao Corporation were mixed with 220 ml of distilled water, and the mixture was subjected to a sand mill (1/4 Gallon sand grinder mill,
The beads were dispersed using IMEX Co., Ltd.) to obtain a solid fine particle dispersion (a) of a base precursor compound having an average particle diameter of 0.2 μm.

(Preparation of Dye Solid Fine Particle Dispersion) 9.6 g of cyanine dye compound 13 and 5.8 g of sodium p-dodecylbenzenesulfonate were added to 305 ml of distilled water.
The mixture was mixed using a sand mill (1/4 Gallon Sand Grinder Mill, manufactured by IMEX Co., Ltd.) to obtain a dispersion of fine solid dye particles having an average particle diameter of 0.2 μm.

(Preparation of antihalation layer coating solution) Gelatin (17 g), polyacrylamide (9.6 g), base precursor solid fine particle dispersion (a) 70 g, dye solid fine particle dispersion (56 g), monodispersed polymethyl methacrylate fine particles (average) Particle size 8 μm, particle size standard deviation 0.
4) 1.5 g, benzoisothiazolinone 0.03 g, sodium polyethylene sulfonate 2.2 g, blue dye compound 14 0.2 g, yellow dye compound 15 3.9.
g and water (844 ml) were mixed to prepare an antihalation layer coating solution.

(Preparation of back surface protective layer coating solution)
The mixture was kept at 0 ° C., and gelatin 50 g, polystyrene sodium sulfonate 0.2 g, N, N-ethylenebis (vinylsulfoneacetamide) 2.4 g, sodium t-octylphenoxyethoxyethaneethanesulfonate 1 g,
Benzoisothiazolinone 30 mg, fluorinated surfactant (F-1: N-perfluorooctylsulfonyl-N
37 mg of a fluorinated surfactant (F-2: polyethylene glycol mono (N-
Perfluorooctylsulfonyl-N-propyl-2-
Aminoethyl) ether [average degree of polymerization of ethylene oxide 15]) 0.15 g, fluorinated surfactant (F-3)
64 mg, fluorine-based surfactant (F-4) 32 mg, acrylic acid / ethyl acrylate copolymer (copolymerization weight ratio 5/95) 8.8 g, Aerosol OT (manufactured by American Cyanamid Co.) 0.6 g, The liquid paraffin emulsion was mixed with 1.8 g of liquid paraffin and 950 ml of water to prepare a coating liquid for the back surface protective layer.

<< Preparation of Silver Halide Emulsion 1 >> Distilled Water 14
While adding 3.1 ml of a 1% by mass potassium bromide solution to 21 ml, further adding 3.5 ml of 0.5 mol / L sulfuric acid, and 31.7 g of phthalated gelatin, the mixture was stirred in a stainless steel reaction bottle. The solution temperature was maintained at 30 ° C., and a solution A diluted to 95.4 ml with distilled water added to 22.22 g of silver nitrate, 15.3 g of potassium bromide and 0.1 ml of potassium iodide were added.
Solution B, which was 8 g diluted with distilled water to a volume of 97.4 ml, was added at a constant flow rate over 45 seconds. afterwards,
10 ml of a 3.5% by mass aqueous solution of hydrogen peroxide was added, and a 10% by mass aqueous solution of benzimidazole was added to 10.8 m
1 was added. Further, a solution C diluted to 317.5 ml by adding distilled water to 51.86 g of silver nitrate, and potassium bromide 4
4.2 g of potassium iodide and 2.2 g of potassium iodide in distilled water
Solution D diluted to 00 ml and solution C at a constant flow rate of 2 ml.
The whole amount was added over 0 minutes, and solution D was added by a controlled double jet method while maintaining the pAg at 8.1. The total amount of potassium hexachloride (III) acid salt was added 10 minutes after starting to add the solution C and the solution D so as to be 1 × 10 ⁻⁴ mol per mol of silver. Five seconds after the completion of the addition of the solution C, an aqueous solution of potassium hexairon cyanide (II) was added in a total amount of 3 × 10 ^-4 mol per mol of silver. The pH was adjusted to 3.8 using sulfuric acid at a concentration of 0.5 mol / L.
, The stirring was stopped, and a settling / desalting / water washing step was performed. PH using 1 mol / L sodium hydroxide
The mixture was adjusted to 5.9 to prepare a silver halide dispersion having a pAg of 8.0.

While stirring the above silver halide dispersion, 3
While maintaining the temperature at 8 ° C., 5 ml of a 0.34 mass% 1,2-benzisothiazolin-3-one methanol solution was added,
After 40 minutes, a methanol solution having a molar ratio of spectral sensitizing dye A to spectral sensitizing dye B of 1: 1 was added at 1.2 × 10 ⁻³ mol per mol of silver as a total of spectral sensitizing dyes A and B. After a minute, the temperature was raised to 47 ° C. Twenty minutes after the temperature was raised, 7.6 × 10 ⁻⁵ mol of sodium benzenethiosulfonate was added to 1 mol of silver with a methanol solution, and further 5 minutes later, tellurium sensitizer C was added with 2 mol / mol of silver with a methanol solution. .9 × 10 ^-4
Mol was added and the mixture was aged for 91 minutes. 1.3 ml of a 0.8% by weight methanol solution of N, N′-dihydroxy-N ″ -diethylmelamine was added, and after another 4 minutes, 5-methyl-2-methyl-2-methyl-2-methyl-N-diethylmelamine.
Mercaptobenzimidazole in methanol with silver 1
4.8 × 10 ^-3 mole per mole and 1-phenyl-2-
Heptyl-5-mercapto-1,3,4-triazole was added in a methanol solution at 5.4 × 10 ⁻³ mol per mol of silver to prepare a silver halide emulsion 1.

The grains in the prepared silver halide emulsion were as follows:
The silver iodobromide particles contained 3.5 mol% of iodine having an average equivalent sphere diameter of 0.042 μm and a coefficient of variation of equivalent sphere diameter of 20% uniformly. The particle size and the like were measured using an electron microscope.
It was determined from the average of 0 particles. The {100} plane ratio of the particles was determined to be 80% using the Kubelka-Munk method.

<< Preparation of Silver Halide Emulsion 2 >> In the preparation of silver halide emulsion 1, a liquid temperature of 30 ° C. during grain formation was adjusted to 4 ° C.
The temperature was changed to 7 ° C., the solution B was changed to dilute 15.9 g of potassium bromide to a volume of 97.4 ml with distilled water, and the solution D was prepared by diluting 45.8 g of potassium bromide with a volume of 400 m in distilled water.
The silver halide emulsion 2 was prepared in the same manner except that the dilution was changed to 1 and the addition time of the solution C was changed to 30 minutes to remove potassium hexacyanoferrate (II). Precipitation / desalting / washing / dispersion was carried out in the same manner as in silver halide emulsion 1. Further, the addition amount of a methanol solution having a molar ratio of 1: 1 between the spectral sensitizing dye A and the spectral sensitizing dye B is 7.5 × 10 5 as the total amount of the spectral sensitizing dye A and the spectral sensitizing dye B per mole of silver.
^-4 mol, the tellurium sensitizer C was added in an amount of 1.
Silver halide except that 1 × 10 ^-4 mol, 1-phenyl-2-heptyl-5-mercapto-1,3,4-triazole was changed to 3.3 × 10 ^-3 mol per mol of silver. Emulsion 1, chemical sensitization and 5-methyl-
2-mercaptobenzimidazole, 1-phenyl-2
-Heptyl-5-mercapto-1,3,4-triazole was added to obtain a silver halide emulsion 2. The emulsion grains of the silver halide emulsion 2 had an average sphere equivalent diameter of 0.080 μm.
m, pure silver bromide cubic grains having a sphere equivalent diameter variation coefficient of 20%.

<< Preparation of Silver Halide Emulsion 3 >> In the preparation of silver halide emulsion 1, a liquid temperature of 30 ° C. during grain formation was adjusted to 2 ° C.
Except that the temperature was changed to 7.degree.
Was prepared. Further, precipitation / desalting / washing / dispersion / dispersion was carried out in the same manner as in silver halide emulsion 1. The addition amount of the solid dispersion (aqueous gelatin solution) having a molar ratio of 1: 1 between the spectral sensitizing dye A and the spectral sensitizing dye B is 6 × as the total amount of the spectral sensitizing dye A and the spectral sensitizing dye B per mole of silver. 10 ^-3 moles, except that the amount of tellurium sensitizer C was changed to 5.2 × 10 ^-4 mol per 1 mol of silver, in the same manner as the silver halide emulsion 1, to obtain a silver halide emulsion 3 . The emulsion grains of the silver halide emulsion 3 were:
The silver iodobromide particles contained 3.5 mol% of iodine having an average equivalent sphere diameter of 0.034 μm and a coefficient of variation of equivalent sphere diameter of 20%.

<< Preparation of Silver Halide Mixed Emulsion A for Coating Solution >> Silver halide emulsion 1 was dissolved in 70% by mass, silver halide emulsion 2 in 15% by mass and silver halide emulsion 3 in 15% by mass. Zolium iodide was added as a 1% by mass aqueous solution in an amount of 7 × 10 ⁻³ mol per mol of silver. Further, water was added so that the silver halide content per 1 kg of the silver halide mixed emulsion for the coating solution was 38.2 g as silver.

<< Preparation of Organic Silver Salt Dispersion >> Behenic acid manufactured by Henkel (product name: Edenor C22-85R)
6 Kg, 423 L of distilled water, 5 mol / L concentration of NaOH
49.2 L of an aqueous solution and 120 L of tert-butanol were mixed and reacted by stirring at 75 ° C. for 1 hour to obtain a sodium behenate solution. Separately, 206.2 L (pH 4.0) of an aqueous solution containing 40.4 kg of silver nitrate was prepared and kept at 10 ° C. The reaction vessel containing 635 L of distilled water and 30 L of tert-butanol was kept at 30 ° C., and with sufficient stirring, the total amount of the sodium behenate solution and the total amount of the silver nitrate aqueous solution were respectively 93 minutes and 15 seconds at a constant flow rate. Added over 90 minutes. At this time, only the aqueous silver nitrate solution was added for 11 minutes after the addition of the aqueous silver nitrate solution was started, and then the addition of the sodium behenate solution was started. After the addition of the aqueous silver nitrate solution was completed, only the sodium behenate solution was added for 14 minutes and 15 seconds. I was doing it. At this time, the temperature inside the reaction vessel was set at 30 ° C., and the external temperature was controlled so that the liquid temperature became constant. Further, the piping of the addition system of the sodium behenate solution was kept warm by circulating hot water outside the double tube, and the liquid temperature at the outlet of the addition nozzle tip was adjusted to 75 ° C. Also, the piping for the addition system of the silver nitrate aqueous solution is 2
The temperature was maintained by circulating cold water outside the heavy pipe. The addition position of the sodium behenate solution and the addition position of the aqueous silver nitrate solution were arranged symmetrically with respect to the stirring axis, and were adjusted to a height such that they did not come into contact with the reaction solution.

After the completion of the addition of the sodium behenate solution, the mixture was left to stir at the same temperature for 20 minutes, and then stirred for 35 minutes.
C., and aging was performed for 210 minutes. Immediately after the ripening, the solid content was separated by centrifugal filtration, and the solid content was washed with water until the conductivity of the filtered water became 30 μS / cm. Thus, an organic silver salt was obtained. The obtained solid content was stored as a wet cake without drying.

The morphology of the obtained silver behenate particles was evaluated by electron microscopic photographing. The average value was a = 0.14 μm.
m, b = 0.4 μm, c = 0.6 μm, average aspect ratio 5.2, average sphere equivalent diameter 0.52 μm, and a flake-like crystal with a sphere equivalent diameter variation coefficient of 15% (a, b) , C are provisions in the text).

A wet cake having a dry solid content of 260 kg was added to polyvinyl alcohol (trade name: PVA-2).
17) 19.3 Kg and water were added, and the total amount was 100
0 kg, and then slurried with a dissolver blade. Further, a pipeline mixer (PM-10 manufactured by Mizuho Industries, Ltd.)
).

Next, the pre-dispersed stock solution was subjected to a pressure of 1 with a dispersing machine (trade name: Microfluidizer M-610, manufactured by Microfluidics International Corporation, using a Z-type interaction chamber).
The pressure was adjusted to 260 kg / cm ² (12.6 MPa), and the mixture was treated three times to obtain a silver behenate dispersion. In the cooling operation, a coiled heat exchanger was mounted before and after the interaction chamber, and the dispersion temperature was set at 18 ° C. by adjusting the temperature of the refrigerant.

<< Preparation of Reducing Agent-1 Dispersion >> Reducing Agent-1
(1,1-bis (2-hydroxy-3,5-dimethylphenyl) -3,5,5-trimethylhexane) 10 kg
And 10 kg of a 20% by mass aqueous solution of denatured polyvinyl alcohol (manufactured by Kuraray Co., Ltd., Poval MP203),
kg, and mixed well to form a slurry. This slurry is fed by a diaphragm pump and has an average diameter of 0.5
mm zirconia beads filled horizontal sand mill (U
VM-2: manufactured by IMEX Co., Ltd.) for 3 hours and 30 minutes, and then dispersed with sodium benzoisothiazolinone sodium salt 0.1.
2 g and water were added to adjust the concentration of the reducing agent to 25% by mass to obtain a reducing agent-1 dispersion. The reducing agent particles contained in the thus obtained reducing agent-1 dispersion have a median diameter of 0.1.
42 μm and the maximum particle size was 2.0 μm or less. The resulting reducing agent-1 dispersion was filtered through a polypropylene filter having a pore size of 10.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Reducing Agent-2 Dispersion >> Reducing Agent-2
10 kg of (2,2'-isobutylidene-bis- (4,6-dimethylphenol)) and 20% by mass of modified polyvinyl alcohol (Poval MP203, manufactured by Kuraray Co., Ltd.)
16 kg of water was added to 10 kg of the aqueous solution and mixed well to form a slurry. This slurry was sent by a diaphragm pump and dispersed in a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm for 3 hours and 30 minutes, and then benzoisothiazolinone sodium salt was added. 0.2 g and water were added to adjust the concentration of the reducing agent to 25% by mass to obtain a reducing agent-2 dispersion. The reducing agent particles contained in the reducing agent-2 dispersion thus obtained had a median diameter of 0.38 μm and a maximum particle diameter of 2.0 μm or less. The obtained reducing agent-2 dispersion was filtered through a polypropylene filter having a pore size of 10.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Dispersion of Reducing Agent Complex-3 >> Reducing Agent Complex-3 (2,2'-methylenebis- (4-ethyl-6-
10 kg of 1: 1 complex of tert-butylphenol) and triphenylphosphine oxide, 0.12 kg of triphenylphosphine oxide and 10 kg of modified polyvinyl alcohol (Poval MP203, manufactured by Kuraray Co., Ltd.)
7.2 kg of water was added to 16 kg of a mass% aqueous solution and mixed well to form a slurry. This slurry was sent by a diaphragm pump and dispersed in a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm for 4 hours and 30 minutes, and then benzoisothiazolinone sodium salt was added. 0.2 g and water were added to adjust the concentration of the reducing agent to 25% by mass to obtain a reducing agent complex-3 dispersion. The reducing agent complex particles contained in the thus obtained dispersion of the reducing agent complex-3 had a median diameter of 0.46 μm.
m, and the maximum particle diameter was 1.6 μm or less. The obtained reducing agent complex-3 dispersion was filtered through a polypropylene filter having a pore size of 3.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Reducing Agent-4 Dispersion >> Reducing Agent-4
(2,2′-methylenebis- (4-ethyl-6-ter
t-butylphenol)) 10 kg and 1 of modified polyvinyl alcohol (Poval MP203, manufactured by Kuraray Co., Ltd.)
6 kg of water was added to 20 kg of a 0 mass% aqueous solution and mixed well to form a slurry. This slurry was sent by a diaphragm pump and dispersed in a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm for 3 hours and 30 minutes, and then benzoisothiazolinone sodium salt was added. 0.2 g and water were added to adjust the concentration of the reducing agent to 25% by mass.
A dispersion was obtained. The reducing agent particles contained in the thus obtained reducing agent-4 dispersion had a median diameter of 0.40 μm and a maximum particle diameter of 1.5 μm or less. The obtained reducing agent-4 dispersion was filtered through a polypropylene filter having a pore size of 3.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Dispersion of Reducing Agent-5 >> Reducing Agent-5
(2,2′-methylenebis- (4-methyl-6-ter
t-butylphenol)) 10 kg and 1 of modified polyvinyl alcohol (Poval MP203, manufactured by Kuraray Co., Ltd.)
6 kg of water was added to 20 kg of a 0 mass% aqueous solution and mixed well to form a slurry. This slurry was sent by a diaphragm pump and dispersed in a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm for 3 hours and 30 minutes, and then benzoisothiazolinone sodium salt was added. 0.2 g and water were added to adjust the concentration of the reducing agent to 25% by mass.
A dispersion was obtained. The reducing agent particles contained in the thus obtained reducing agent-5 dispersion had a median diameter of 0.38 μm and a maximum particle diameter of 1.5 μm or less. The resulting reducing agent-5 dispersion was filtered through a polypropylene filter having a pore size of 3.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Hydrogen Bonding Compound-2 Dispersion >> Hydrogen bonding compound-2 (tri (4-t-butylphenyl))
10 kg of water was added to 10 kg of a 10 mass% aqueous solution of 10 kg of a phosphine oxide) and a 10 mass% aqueous solution of a modified polyvinyl alcohol (manufactured by Kuraray Co., Ltd., Poval MP203), and mixed well to form a slurry. This slurry was sent by a diaphragm pump and dispersed in a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm for 3 hours and 30 minutes, and then benzoisothiazolinone sodium salt was added. 0.2 g and water were added to adjust the concentration of the hydrogen bonding compound to 22% by mass to obtain a hydrogen bonding compound-2 dispersion. The hydrogen bonding compound particles contained in the hydrogen bonding compound-2 dispersion thus obtained had a median diameter of 0.35 μm and a maximum particle diameter of 1.5 μm or less. The obtained hydrogen bonding compound-2 dispersion was filtered through a polypropylene filter having a pore size of 3.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Dispersion of Organic Polyhalogen Compound-1 >> 10 kg of organic polyhalogen compound-1 (2-tribromomethanesulfonylnaphthalene) and modified polyvinyl alcohol (Poval MP203, manufactured by Kuraray Co., Ltd.)
10 kg of 0 mass% aqueous solution and 0.4 kg of 20 mass% aqueous solution of sodium triisopropylnaphthalenesulfonate
And 16 kg of water were added and mixed well to form a slurry. This slurry was sent by a diaphragm pump and dispersed in a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm for 5 hours, and then sodium benzoisothiazolinone sodium salt was added. 2 g and water were added to adjust the concentration of the organic polyhalogen compound to 23.5% by mass to obtain an organic polyhalogen compound-1 dispersion. The organic polyhalogen compound particles contained in the thus obtained organic polyhalogen compound-1 dispersion had a median diameter of 0.36 μm and a maximum particle diameter of 2.0 μm.
m or less. Obtained organic polyhalogen compound-1
The dispersion was filtered with a polypropylene filter having a pore size of 10.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Dispersion of Organic Polyhalogen Compound-2 >> 10 kg of organic polyhalogen compound-2 (tribromomethanesulfonylbenzene) and 10 kg of a 20% by mass aqueous solution of modified polyvinyl alcohol (Poval MP203, manufactured by Kuraray Co., Ltd.) Then, 0.4 kg of a 20% by mass aqueous solution of sodium triisopropylnaphthalenesulfonate and 14 kg of water were added and mixed well to form a slurry. This slurry was sent by a diaphragm pump and dispersed in a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm for 5 hours, and then sodium benzoisothiazolinone sodium salt was added.
2 g and water were added to reduce the concentration of the organic polyhalogen compound to 26.
% By weight of an organic polyhalogen compound
Two dispersions were obtained. Organic polyhalogen compound particles contained in the organic polyhalogen compound-2 dispersion thus obtained are:
The median diameter was 0.41 μm and the maximum particle diameter was 2.0 μm or less. The resulting organic polyhalogen compound-2 dispersion was filtered through a polypropylene filter having a pore size of 10.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Dispersion of Organic Polyhalogen Compound-3 >> 10 kg of a chronological polyhalogen compound-3 (N-butyl-3-tribromomethanesulfonylbenzamide) and modified polyvinyl alcohol (Poval M, manufactured by Kuraray Co., Ltd.)
20 kg of a 10 mass% aqueous solution of P203), 0.4 kg of a 20 mass% aqueous solution of sodium triisopropylnaphthalenesulfonate, and 8 kg of water were added and mixed well to form a slurry. This slurry is fed by a diaphragm pump, and a horizontal sand mill (UVM-2: IMEX Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm.
After dispersing for 5 hours, 0.2 g of benzoisothiazolinone sodium salt and water were added to adjust the concentration of the organic polyhalogen compound to 25% by mass. This dispersion was heated at 40 ° C. for 5 hours to obtain an organic polyhalogen compound-3 dispersion. The organic polyhalogen compound particles contained in the thus obtained organic polyhalogen compound-3 dispersion had a median diameter of 0.36 μm and a maximum particle diameter of 1.5 μm or less. The resulting organic polyhalogen compound-3 dispersion was filtered through a polypropylene filter having a pore size of 3.0 μm to remove foreign substances such as dust, and stored.

<< Preparation of Phthalazine Compound-1 Solution >> 8K
g modified Kuraray Co., Ltd. modified polyvinyl alcohol MP20
Was dissolved in 174.57 kg of water, and 3.15 kg of a 20% by mass aqueous solution of sodium triisopropylnaphthalenesulfonate and 14.28 kg of a 70% by mass aqueous solution of phthalazine compound-1 (6-isopropylphthalazine) were added. A 5% by mass solution of compound-1 was prepared.

<< Preparation of Mercapto Compound-1 Aqueous Solution >> Mercapto compound-1 (1- (3-sulfophenyl) -5
7 g of mercaptotetrazole sodium salt) in water 99
3 g to give a 0.7% by mass aqueous solution.

<< Preparation of Pigment-1 Dispersion >> I. Pig
To 64 g of Ment Blue 60 and 6.4 g of Demol N manufactured by Kao Corporation, 250 g of water was added and mixed well to form a slurry. 800 g of zirconia beads having an average diameter of 0.5 mm is prepared, put into a vessel together with the slurry, and dispersed with a dispersing machine (1 / 4G sand grinder mill: manufactured by IMEX Co., Ltd.) for 25 hours to obtain a pigment-1 dispersion. Obtained. The pigment particles contained in the pigment-1 dispersion thus obtained had an average particle size of 0.21 μm.

<< Preparation of SBR Latex Liquid >> Tg = 23
C. SBR latex was prepared as follows. Using ammonium persulfate as a polymerization initiator and an anionic surfactant as an emulsifier, styrene (70.5 mass), butadiene (26.5 mass) and acrylic acid (3 mass) were emulsion-polymerized and then aged at 80 ° C. for 8 hours. Then 40 ° C
Then, the pH was adjusted to 7.0 with aqueous ammonia, and Sandet BL manufactured by Sanyo Kasei Co., Ltd. was further added to 0.22%. Next, a 5% aqueous solution of sodium hydroxide was added to adjust the pH to 8.3, and further to pH 8.4 with aqueous ammonia.
It was adjusted to become. The molar ratio of Na ⁺ ion to NH ₄ ⁺ ion used at this time was 1: 2.3. Furthermore,
0.15 ml of a 7% aqueous solution of sodium salt of benzoisothiazolinone was added to 1 kg of this solution to prepare an SBR latex solution.

(SBR latex: -St (70.5)
-Bu (26.5) -AA (3)-latex) Tg
23 ° C, average particle size 0.1 µm, concentration 43% by mass, 25 ° C 60% R
Equilibrium water content in H: 0.6% by mass, ionic conductivity: 4.
2 mS / cm (Ion conductivity is measured using a conductivity meter CM-30S manufactured by Toa Denpa Kogyo Co., Ltd., and a latex stock solution (43% by mass) is measured at 25 ° C.), SBR latex having a different pH of 8.4 Tg Was prepared in a similar manner by changing the ratio of styrene and butadiene appropriately.

<< Preparation of Emulsion Layer (Photosensitive Layer) Coating Solution-1 >>
1000 g of the organic silver salt dispersion obtained above, 125 ml of water,
113 g of reducing agent-1 dispersion, 91 g of reducing agent-2 dispersion,
Pigment-1 Dispersion 27g, Organic Polyhalogen Compound-1 Dispersion 82g, Organic Polyhalogen Compound-2 Dispersion 40
g, phthalazine compound-1 solution 173 g, SBR latex (Tg: 20.5 ° C.) solution 1082 g, and mercapto compound-1 aqueous solution 9 g were added sequentially, and immediately before coating, 158 g of a silver halide mixed emulsion A for a coating solution was added. The well-mixed emulsion layer coating solution-1 was directly sent to a coating die and coated.

The viscosity of the above emulsion layer coating solution-1 was measured at 40 ° C. (No. 1 rotor, 6
At 0 rpm) was 85 [mPa · s].

25 ° C. using an RFS fluid spectrometer manufactured by Rheometrics Far East Co., Ltd.
The viscosity of the coating solution at the shear rate is 0.1, 1, 10, 1
For 00 and 1000 [1 / sec], 150
0, 220, 70, 40, and 20 [mPa · s].

<< Preparation of Emulsion Layer (Photosensitive Layer) Coating Solution-2 >>
1000 g of the organic silver salt dispersion obtained above, 104 ml of water,
Pigment-1 dispersion 30 g, organic polyhalogen compound-2 dispersion 21 g, organic polyhalogen compound-3 dispersion 69
g, phthalazine compound-1 solution 173 g, SBR latex (Tg: 23 ° C.) solution 1082 g, reducing agent complex-3 dispersion 258 g, and mercapto compound-1 solution 9 g were sequentially added. Emulsion A11
0 g was added, and the well-mixed emulsion layer coating solution-2 was directly sent to a coating die and coated.

<< Preparation of Emulsion Layer (Photosensitive Layer) Coating Solution-3 >>
1000 g of the organic silver salt dispersion obtained above, 95 ml of water, reducing agent-4 dispersion 73, reducing agent-5 dispersion 68 g, pigment-
30 g of 1 dispersion, organic polyhalogen compound-2 dispersion 2
1 g, organic polyhalogen compound-3 dispersion 69 g, phthalazine compound-1 solution 173 g, SBR core-shell type latex (core Tg: 20 ° C./shell Tg: 30 ° C. = 7)
0/30 weight ratio) 1082 g of liquid, hydrogen bonding compound-2
124 g of the dispersion and 9 g of the mercapto compound-1 solution were sequentially added, and immediately before coating, a silver halide mixed emulsion A1 for a coating solution was added.
10 g was added, and the well-mixed emulsion layer coating solution-3 was directly sent to a coating die and coated.

<< Preparation of Emulsion Surface Intermediate Layer Coating Solution >> 772 g of a 10% by mass aqueous solution of polyvinyl alcohol PVA-205 (manufactured by Kuraray Co., Ltd.) and a 20% by mass dispersion of a pigment 5.3.
g, methyl methacrylate / styrene / butyl acrylate / hydroxyethyl methacrylate / acrylic acid copolymer (copolymerization weight ratio 64/9/20/5/2) latex 27.5 mass% liquid in 226 g of aerosol OT (American Siana) 5% aqueous solution of
1, 20 mass% aqueous solution of diammonium phthalate
0.5 ml, water was added to make the total amount 880 g, pH
Was adjusted to 7.5 with NaOH to prepare a coating solution for the intermediate layer, and the solution was fed to a coating die at 10 ml / m ² . The viscosity of the coating solution was 40 ° C. using a B-type viscometer (No. 1).
Rotor, 60 rpm) was 21 [mPa · s].

<< Preparation of Coating Solution for First Layer of Emulsion Surface Protective Layer >> Inert gelatin (64 g) was dissolved in water, and methyl methacrylate / styrene / butyl acrylate / hydroxyethyl methacrylate / acrylic acid copolymer (copolymer weight ratio: 6)
4/9/20/5/2) 27.5% by mass latex liquid 8
0 g, 10% methanol solution of phthalic acid in 23m
1, 23 ml of a 10% by mass aqueous solution of 4-methylphthalic acid,
28 ml of 0.5 mol / L sulfuric acid, 5 ml of a 5% by mass aqueous solution of aerosol OT (manufactured by American Cyanamid), 0.5 g of phenoxyethanol and 0.1 g of benzoisothiazolinone are added to make a total amount of 750 g. Was added to water to form a coating solution, and a mixture prepared by mixing 26 ml of 4% by mass chrome alum with a static mixer immediately before coating was sent to a coating die at 18.6 ml / m ² . The viscosity of the coating solution was measured at 40 ° C. using a B-type viscometer (No.
It was 17 [mPa · s] with one rotor at 60 rpm.

<< Preparation of Coating Solution for Second Layer of Emulsion Surface Protecting Layer >> Inert gelatin (80 g) was dissolved in water, and methyl methacrylate / styrene / butyl acrylate / hydroxyethyl methacrylate / acrylic acid copolymer (copolymer weight ratio: 6)
4/9/20/5/2) 27.5% by mass latex liquid 1
3.2 g of a 5% by mass solution of a fluorine-based surfactant (F-1: potassium salt of N-perfluorooctylsulfonyl-N-propylalanine) (F-2: polyethylene glycol mono (F-2)) N-perfluorooctylsulfonyl-N-propyl-2-aminoethyl) ether [average degree of polymerization of ethylene oxide = 1
5]), 32 ml of a 2% by weight aqueous solution of aerosol OT
(American Cyanamid Co.) 5% by mass solution
ml, fine particles of polymethyl methacrylate (average particle size of 0.
7 μm) 4 g, polymethyl methacrylate fine particles (average particle size 4.5 μm) 21 g, 4-methylphthalic acid 1.6
g, phthalic acid 4.8 g, sulfuric acid 4 having a concentration of 0.5 mol / L
4 ml, benzoisothiazolinone 10 mg, total amount 650
g of water and an aqueous solution 445 containing 4% by mass of chromium alum and 0.67% by mass of phthalic acid.
Immediately before coating, a mixture prepared by a static mixer was used as a coating solution for the surface protective layer, and the solution was fed to a coating die at 8.3 ml / m ² . The viscosity of the coating solution was 9 mP with a B-type viscometer at 40 ° C. (No. 1 rotor, 60 rpm).
a · s].

<< Preparation of Photothermographic Material-101 >> On the back surface side of the undercoating support, an antihalation layer coating solution was applied so that the coating amount of the solid fine particle dye was 0.04 g / m ^2. The coating solution for the back surface protective layer was simultaneously coated in a multilayer so that the coating amount of gelatin was 1.7 g / m ^2, and dried to form a back layer.

The emulsion layer (using emulsion layer coating solution-1), the intermediate layer, the first protective layer,
The protective layer was coated in the second layer in the same order by a slide bead coating method to prepare a photothermographic material. At this time, the temperature of the emulsion layer and the intermediate layer was 31 ° C, and the temperature of the first protective layer was 36 ° C.
The temperature of the second protective layer was adjusted to 37 ° C. The coating amount (g / m ² ) of each compound in the emulsion layer is as follows.

• Silver behenate (organic silver salt) 6.19 • Reducing agent-1 0.67 • Reducing agent-2 0.54 • Pigment (CIPigment Blue 60) 0.032 • Organic polyhalogen compound-10 .46-Organic polyhalogen compound-2 0.25-Phthalazine compound-1 0.21-SBR latex 11.1-Mercapto compound-1 0.002-Silver halide (as Ag) 0.145

The coating and drying conditions are as follows. The coating was performed at a speed of 160 m / min, the gap between the tip of the coating die and the support was set to 0.10 to 0.30 mm, and the pressure in the decompression chamber was set 196 to 882 Pa lower than the atmospheric pressure. The support was neutralized with ion wind before coating. In the subsequent chilling zone, the coating liquid is cooled by air having a dry-bulb temperature of 10 to 20 ° C., and is transferred in a non-contact type. It was dried with a dry air having a wet bulb temperature of 15 to 21 ° C. After drying, 25 ° C
After adjusting the humidity at 40-60% RH, the membrane surface is
Heated to 0 ° C. After heating, the film surface was cooled to 25 ° C.

The matte degree of the produced photothermographic material was as follows:
The Beck smoothness was 550 seconds on the photosensitive layer side and 1 on the back side.
30 seconds. Further, the pH of the film surface on the photosensitive layer surface side was measured and found to be 6.0.

<< Preparation of Photothermographic Materials-102 to 119 >> Photothermographic materials 102 to 119 were prepared in the same manner as Sample 101 except that Sample 101 of the photothermographic material was changed as shown in Table 1. Produced.

<Evaluation of Photo Performance> Fuji Medical Dry Laser Imager FM-DP L (Max.
Exposure and thermal development of the photographic material with (IIIB) output 660 nm semiconductor laser) (112 ° C-119 ° C-121)
4 panel heaters set to ℃ -121 ℃ total 24
Sec), and the obtained image was evaluated using a densitometer.

<Evaluation of Image Preservation> Fuji Medical Dry Laser Imager FM-DP L (60 mW max.)
(IIIB) The photographic material is exposed and thermally developed (approximately 120 ° C.) with a 660 nm semiconductor laser having an output, and then 30 ° C.
The image was stored by a densitometer after being stored for 24 hours under an illuminance of 1000 L under a fluorescent lamp in an environment of 70% RH under an illuminance, and the difference from the result obtained by the photographic performance evaluation method was calculated.

<Evaluation of Blocking Property> After the photothermographic material was heat-developed in the same manner as in the evaluation of photographic performance, 25
Humidity control at 75 ° C. for 16 hours, and the photosensitive layer surface and the back layer surface are superimposed on each other to obtain an area of 35 mm × 35 mm.
A load of g was applied, and the peeled area when peeled off at 50 ° C. for 48 hours was evaluated as follows. A: There is no blocking at all. ：: There is a slight trace on the surface but no blocking. Δ: There is a slight blocking trace. ×: Blocking traces exist in nearly half the area. XX: Blocking marks are present in almost all areas.

Table 1 shows the evaluation results.

[0192]

[Table 1]

As shown in Table 1, it can be seen that the photothermographic materials of the present invention (samples 102 to 119) are excellent in photographic performance, image storability and blocking property. It can be seen that more effects can be obtained by using the binder and the divalent or higher organic acid in the present invention together in the protective layer. In a configuration other than the present invention, the fluidity of the binder under high humidity is large, so it is presumed that the blocking property is inferior.

<< Preparation of Photothermographic Materials-201 to 219 >> In the preparation of photothermographic materials-101 to 119,
Photothermographic material-201 was prepared in the same manner as photothermographic materials-101 to 119, except that emulsion layer coating solution-1 was changed to emulsion layer coating solution-2 and yellow dye compound 15 was removed from the antihalation layer. To 219. The coating amount (g / m ² ) of each compound in the emulsion layer at this time is as follows.

-Silver behenate (organic silver salt) 6.19-Pigment (CIPigment Blue 60) 0.036-Organic polyhalogen compound-2 0.13-Organic polyhalogen compound-3 0.41-Phthalazine compound- 1 0.21 ・ SBR latex 11.1 ・ Reducing agent complex-3 1.54 ・ Mercapto compound-1 0.002 ・ Silver halide (as Ag) 0.10

The resulting photothermographic materials 201 to 219
Was evaluated in the same manner as in the photothermographic materials 101 to 119. Table 2 shows the evaluation results.

[0197]

[Table 2]

As shown in Table 2, it can be seen that the photothermographic materials of the present invention (samples 202 to 219) are excellent in photographic performance, image storability and blocking ability.

<< Preparation of Photothermographic Materials-301-319 >> In the preparation of photothermographic materials-101-119,
Emulsion layer coating solution-1 was changed to emulsion layer coating solution-3, and yellow dye compound 15 was removed from the antihalation layer.
Further, the fluorine-based surfactants F-1, F-2, F-3 and F-4 of the protective layer second layer and the back surface protective layer were the same weights of F-5, F-6, F-7 and F-7, respectively. Changed to F-8. Otherwise, the photothermographic materials 301 to 319 were prepared in the same manner as the photothermographic materials 101 to 119. The coating amount (g / m ² ) of each compound in the emulsion layer at this time is as follows.

• Silver behenate (organic silver salt) 5.57 • Pigment (CIPigment Blue 60) 0.032 • Reducing agent-4 0.40 • Reducing agent-5 0.36 • Organic polyhalogen compound-20 .12 ・ organic polyhalogen compound-3 0.37 ・ phthalazine compound-1 0.19 ・ SBR latex 10.0 ・ hydrogen bonding compound-2 0.59 ・ mercapto compound-1 0.002 ・ silver halide (Ag) 0.09)

For the photothermographic materials -301 to 319,
As a result of the evaluation in the same manner as the photothermographic materials 101 to 119, the photothermographic materials of the invention (samples 302 to 319) were obtained.
Showed good results with regard to photographic performance, image storability and blocking ability.

<< Preparation of Photothermographic Materials-401-419 >> In the preparation of photothermographic materials-201-219,
Each of the photothermographic materials was prepared in the same manner as the photothermographic materials 201 to 219, except that 7.8 g of the following development accelerator-1 dispersion was added to the emulsion layer coating solution-2. Materials -401 to 419 were produced.

<< Preparation of Development Accelerator-1 Dispersion >> 1 kg of the development accelerator-1 and a 10% by mass aqueous solution of a modified polyvinyl alcohol (Poval MP203, manufactured by Kuraray Co., Ltd.)
To 5 kg of water, 5 kg of water was added and mixed well to form a slurry. This slurry was sent by a diaphragm pump, and was fed with a horizontal sand mill (UVM-2: manufactured by Imex Co., Ltd.) filled with zirconia beads having an average diameter of 0.5 mm.
After dispersing for a time, 0.02 g of sodium benzoisothiazolinone and water were added to adjust the concentration of the development accelerator to 10% by mass to obtain a development accelerator-1 dispersion.
The development accelerator particles contained in the thus obtained development accelerator-1 dispersion had a median diameter of 0.32 μm and a maximum particle diameter of 1.5 μm.
m or less. The obtained development accelerator-1 dispersion was filtered through a polypropylene filter having a pore size of 3.0 μm to remove foreign substances such as dust, and stored. The coating amount (g / m ² ) of each compound in the emulsion layer at this time is as follows.

-Silver behenate (organic silver salt) 6.19-Pigment (CIPigment Blue 60) 0.036-Organic polyhalogen compound-2 0.13-Organic polyhalogen compound-3 0.41-Phthalazine compound- 1 0.21 ・ SBR latex 11.1 ・ Reducing agent complex-3 1.54 ・ Development accelerator-1 0.028 ・ Mercapto compound-1 0.002 ・ Silver halide (as Ag) 0.10

For the photothermographic materials -401 to 419,
The evaluation was performed in the same manner as the photothermographic materials-201 to 219 except that the heat development time was changed from 24 seconds to 14 seconds. As a result, the photothermographic material of the present invention (samples 402 to 419)
Showed good results with regard to photographic performance, image storability and blocking ability.

<< Preparation of Photothermographic Materials-501-519 >> In the preparation of photothermographic materials-301-319,
7.8 of the above-mentioned development accelerator-1 dispersion was added to the emulsion layer coating solution-3.
The photothermographic materials -501 to 519 were prepared in the same manner as the photothermographic materials -301 to 319, except that the emulsion layer coating solution to which g was added was used. The coating amount (g / m ² ) of each compound in the emulsion layer at this time is as follows.

・ Silver behenate (organic silver salt) 5.57 ・ Pigment (CIPigment Blue 60) 0.032 ・ Reducing agent-4 0.40 ・ Reducing agent-5 0.36 ・ Organic polyhalogen compound-20 .12 ・ organic polyhalogen compound-3 0.37 ・ phthalazine compound-1 0.19 ・ SBR latex 10.0 ・ hydrogen bonding compound-2 0.59 ・ development accelerator-1 0.028 ・ mercapto compound-1 0.002-silver halide (as Ag) 0.09

For the photothermographic materials -501 to 519,
The evaluation was performed in the same manner as in the photothermographic materials-301 to 319, except that the heat development time was changed from 24 seconds to 14 seconds. As a result, the photothermographic material of the present invention (samples 502 to 519)
Showed good results with regard to photographic performance, image storability and blocking ability.

The chemical structures of the compounds used in the examples of the present invention are shown below.

[0210]

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[0211]

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[0212]

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[0213]

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[0214]

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[0215]

According to the present invention, a photothermographic material excellent in photographic performance, image storability and blocking property can be provided.

Claims (6)

[Claims] 1. A support comprising, on one surface of a support, at least one photosensitive layer containing photosensitive silver halide and a non-photosensitive protective layer, wherein the photosensitive layer comprises at least one photosensitive layer. Silver halide, a non-photosensitive organic silver salt, a photothermographic material containing a reducing agent and a binder for silver ions,
A photothermographic material comprising a natural polymer polysaccharide on the side having the photosensitive layer. 2. The photothermographic material according to claim 1, further comprising a divalent or higher organic acid on the side having the photosensitive layer. 3. A support comprising, on one surface of a support, at least one photosensitive layer containing a photosensitive silver halide and a non-photosensitive protective layer, wherein the photosensitive layer comprises at least one photosensitive layer. Silver halide, a non-photosensitive organic silver salt, a photothermographic material containing a reducing agent and a binder for silver ions,
A photothermographic material, wherein the non-photosensitive protective layer contains a natural polymer other than gelatin. 4. The photothermographic material according to claim 3, wherein the side having the photosensitive layer contains a divalent or higher valent organic acid. 5. A support comprising, on one surface of a support, at least one photosensitive layer containing photosensitive silver halide and a non-photosensitive protective layer, wherein the photosensitive layer comprises at least one photosensitive layer. Silver halide, a non-photosensitive organic silver salt, a photothermographic material containing a reducing agent and a binder for silver ions,
A photothermographic material comprising a plurality of natural polymers in the non-photosensitive protective layer. 6. The photothermographic material according to claim 5, wherein the side having the photosensitive layer contains a divalent or higher valent organic acid.