JPH07120011B2 - Dye fixing element - Google Patents

Description

Description: FIELD OF THE INVENTION This invention relates to dye-fixing elements for receiving potential dyes that have been imagewise distributed in a photosensitive element by heat development.

(Prior art and its problems) Regarding the method of obtaining a color image (color image) by heat development,
Many methods have already been proposed.

For the method of forming a color image by combining an oxidant of a developing agent and a coupler, U.S. Pat. No. 3,531,286, U.S. Pat.No. 3,761,270, Belgian Pat.No. 802,519, Research Disclosure, September 1975, pages 31-32 Page, U.S. Pat. No. 4,021,240 and the like.

For the method of forming a positive color image by the light-sensitive silver dye bleaching method, see, for example, Research Disclosure, April 1976, pp. 30-32 (RD-14433), 12: 1976.
Monthly pages 14 to 15 (RD-15227), U.S. Pat. No. 4,235,957 and the like.

However, the above method has a problem that a clear dye image cannot be obtained because the formed dye image and silver image are mixed.

Various methods have been proposed to remedy this drawback.
For example, a method of releasing a mobile dye imagewise by heating, transferring the mobile dye to a dye fixing material having a mordant with a solvent such as water, a method of transferring to the dye fixing material with a high boiling organic solvent, a dye Examples include a method of transferring to a dye fixing material by a hydrophilic thermal solvent incorporated in the fixing material, and a method of transferring to a dye receiving material such as a support where the movable dye is heat diffusible or sublimable (US Patent No. 4,463,079, No. 4,474,867, No. 4,478,927,
No. 4,507,380, No. 4,500,626, No. 4,483,914; JP-A-58-149046, 58-149047, 59-152440,
59-154445, 59-165054, 59-180548, and
59-168439, 59-174832, 59-174833, 59
-174834, 59-174835, 59-218443, Japanese Patent Application 60-79
No. 709).

In the above image forming method, a dye fixing element containing a mordant is used to fix the movable dye.

These mordants are usually used by coating them on a support or another coating film using a hydrophilic colloid such as gelatin as a binder. However, a coating film having this type of polymer mordant and a hydrophilic colloid exhibits significantly different mechanical properties as compared with a coating film formed by a hydrophilic colloid alone. That is, it has been found that a mixed film of a polymer mordant and gelatin, for example, has a significantly reduced tensile strength and breaking elongation as compared with a film of gelatin alone, resulting in a brittle film. The deterioration of the brittleness of the coating film is
This causes cracks due to thermal and mechanical strains that occur in the film coating process and drying process, and significantly restricts manufacturing conditions such as coating and drying.

It has also been found that the mordant layer in the dye-fixing element causes layer breakage (cracking) when thermal and mechanical strain is applied during handling of the dye-fixing element.

When the above-mentioned image forming method is carried out by using such a cracked dye fixing element, unevenness occurs in the development and / or the transfer of the dye, or a cut is formed in the image, resulting in a remarkable image quality. to degrade. In particular, this crack is likely to occur under low humidity conditions. On the other hand, since the heat developing device has a heat developing portion, the inside of the device is likely to have low humidity. Therefore, cracks in the dye fixing element are particularly likely to occur in the thermal developing device, and a solution thereof is desired.

In the above-mentioned image forming method, a base or a base precursor is often used.However, a large amount of such a salt is added to the dye fixing element, or a salt is added to the dye fixing element from the photosensitive element during processing. It has been found that the occurrence of the above-mentioned cracks becomes particularly remarkable when it enters.

OBJECT OF THE INVENTION It is an object of the present invention to provide a dye fixing element for use in dye image formation by thermal development which is less susceptible to cracking and has improved film brittleness.

(Constitution of the Invention) An object of the present invention is a dye-fixing element for receiving a movable dye formed or released in a light-sensitive element by heat development, wherein the dye-fixing element is at least 2 on a support separate from the light-sensitive element. A dye-fixing element having a hydrophilic colloid layer as a layer, and containing a compound having an organic / inorganic value of 3 or more as an oil droplet in a hydrophilic colloid layer other than the uppermost layer. It was

The dye fixing element of the present invention has at least two hydrophilic colloid layers. One of them is a mordant layer containing a mordant. In the present invention, the layer containing the oil droplets is a layer other than the uppermost layer of these hydrophilic colloid layers,
That is, it is a layer below the outermost layer. Here, the uppermost layer refers to the layer in contact with the photosensitive element. Specific examples of the layer suitable for containing oil droplets include a mordant layer which is not the uppermost layer, a layer provided between the uppermost layer and the mordant layer, and a layer provided below the mordant layer. The preferred layer structure of the dye-fixing element of the present invention is: -top layer-mordant layer containing oil droplets-top layer-mordanting layer-layer containing oil droplets-top layer-mordanting layer containing oil droplets- Layers containing oil droplets, and the like. In the above, the uppermost layer is a hydrophilic colloid layer and may have a function as a protective layer.

In the present invention, the oil droplets are oil-based independent systems finely dispersed in a hydrophilic colloid, and are substantially water-insoluble liquid particles. The finer the size of the oil droplets, the better, preferably the average particle size is 3 μm or less, especially 1 μm or less, and further 0.5
μm or less is preferable. The amount of oil droplets added is preferably 5 vol.% To 60 vol.%, Particularly 10 vol.% To 5%, based on the total amount of polymer components (polymer components such as binder and mordant) in the additive layer
It is 0 vol.%, And further 20 vol.% To 40 vol.%. If the amount is too small, the effect of preventing cracking is difficult to be exhibited, and if the amount is too large, problems such as reduction in film strength, film peeling, and bleeding of oil on the surface layer may occur.

Oil droplets in the present invention can be obtained, for example, from US Patent No. 2,322,027.
No. 2,533,514, 2,882,157, Japanese Patent Publication No. 46-23
No. 233, British Patent Nos. 958,441, 1,222,753, JP-A-50-82078, U.S. Patents 2,353,262, 3,676,14.
No. 2, No. 3,600,454, JP-A No. 51-28921, No. 51-1
41623, Japanese Patent Application No. 60-148489 and the like (esters such as phthalates, phosphates and fatty acid esters), amides (such as fatty acid amides and sulfamides), ethers It is preferable to use a high-boiling-point organic solvent that is liquid at room temperature and does not evaporate at the heat treatment temperature, such as compounds, alcohols, and paraffins.

Further, even if it is a solid by itself, it is also included as an oil droplet that is a liquid droplet in the coating film due to the melting point lowering by using two or more kinds in combination.

Also, what is solid at room temperature, but exists as a liquid droplet when included in a hydrophilic binder or when incorporated with various photographic additives is also included as an oil droplet. For example, stilbene used as a whitening agent,
Triazine, oxazole and coumarin compounds,
Examples thereof include benzotriazole, thiazoline, and cinnamic acid ester compounds used as an ultraviolet absorber.

The oil droplets suitable for use in the present invention include saturated or unsaturated hydrocarbons having 10 or more carbon atoms (including those in which a part or all of hydrogen is replaced with a halogen atom), or the following general formula (A ) To (G).

Formula _{^{(E) (R 8 -O 3}} P = 0 General formula (G) R _G —COO—R ¹² {In the above general formula (A), R _A represents a m + n-valent substituted or unsubstituted aliphatic hydrocarbon group, and R ¹ represents a substituted or unsubstituted aliphatic group. It represents a hydrocarbon group, an alicyclic hydrocarbon group or an aromatic hydrocarbon group, and m and n each represent an integer of 1 to 5.

In the above general formula (B), R _B represents a p + q-valent substituted or unsubstituted aliphatic hydrocarbon group or alicyclic hydrocarbon group, and R ² and R ³ may be the same or substituted. Or, it represents an unsubstituted aliphatic hydrocarbon group or an alicyclic hydrocarbon group, p is 0, 1, 2 or 3, and q
Represents 0, 1, 2 or 3, and p + q is 1 or more.

In the general formula (C), R _C is a hydrogen atom, or a substituted or unsubstituted aliphatic hydrocarbon group, alicyclic hydrocarbon group,
Aromatic hydrocarbon group, acyl group, amino group, acyloxy group, carbovamoyl group, ureido group, alkoxycarbonyl group, aryloxycarbonyl group or cycloalkyloxycarbonyl group, or halogen atom, hydroxyl group, carboxyl group, nitro group or cyano group Represents a group.

R ⁴ represents a substituted or unsubstituted aliphatic hydrocarbon group, alicyclic hydrocarbon group or aromatic hydrocarbon group.

r represents an integer of 1 to 5, s represents an integer of 1 to 4, and r + s is 6 or less.

When r is 2 or more, R _C may be the same or different.

When s is 2 or more, R ⁴ may be the same or different.

In the general formula (D), R ⁵ and R ⁶ each represent a substituted or unsubstituted alkyl group, a monocyclic or polycyclic alicyclic hydrocarbon group, an aryl group or an aralkyl group.

R ⁷ represents a substituted or unsubstituted alkyl group, aryl group, aralkyl group or amino group, or a halogen atom. Z represents an atomic group for forming a carbon ring condensed with a benzene ring.

l represents 0 or 1. v is an integer of 0 to 2 and w is 0
Each represents an integer of 7 and v + w is 7 or less.

R ⁶ O-and / or R ⁷ - is substituted carbocycles benzene ring and / or condensation in the general formula (D).

In the above general formula (E), R ⁸ represents a substituted or unsubstituted alkyl group, cycloalkyl group, alkenyl group or aryl group.

R ⁸ may be the same or different.

In the general formula (F), R ⁹ represents a hydrogen atom or an n′-valent substituted or unsubstituted aliphatic hydrocarbon group.

R ¹⁰ and R ¹¹ each represent a hydrogen atom or a substituted or unsubstituted aliphatic hydrocarbon group or aromatic hydrocarbon group, and R ¹⁰ and R ¹¹ may be the same or different.

R ⁹ and R ¹⁰ and R ¹⁰ and R ¹¹ may be linked to each other to form a heterocycle.

n'represents 1 or 2.

In the general formula (G), R _G represents a substituted or unsubstituted aliphatic hydrocarbon group, and R ¹² represents a substituted or unsubstituted aliphatic hydrocarbon group, alicyclic hydrocarbon group or aromatic hydrocarbon group. Represents } For a more detailed explanation of the above general formulas (A) to (G), see
59-178455, 59-178454, 59-178452, 59
-178453, 59-178451, 59-178457 and the like.

Specific examples of the compound used to form the oil droplets are given below.

(1) Liquid paraffin (2) Chlorinated paraffin Furthermore, as an example of the compound of the formula (A) of the present invention, 1971 (Maruzen), Oil and Fat Chemistry Handbook (revised second edition), pp. 108-115 (Table 2-31, 2-34, 2-36, 2-39). 2-47).

(13) C ₁₃ H ₂₇ COOC ₁₈ H ₃₇ −iso (32) (C ₄ H ₉ O ₃ P = 0 (34) (C ₈ H ₁₇ O ₃ P = 0 (35) (iso-C ₁₀ H _{21 3} P = 0 (36) (nC ₁₆ H ₃₃ O ₃ P = 0 (37) (nC ₁₈ H ₃₇ O ₃ P = 0 (39) C ₈ H ₁₇ CH ＝ CH (CH ₂ ) ₁₁ CONH ₂ (42) C ₁₁ H ₂₃ CONC ₂ H ₄ OCH ₃ ) ₂ These compounds are known and can be obtained as commercial products, or can be easily synthesized by a known synthesis method.

Among the above compounds, those having a low polarity are particularly effective in improving brittleness because the coating liquid (especially the coating liquid for the mordant layer) is less likely to aggregate. Among them, those having an organic / inorganic value of 6 or more are preferable. preferable. Here, the organic / inorganic value is a concept for predicting the property of a compound, and the details thereof are described in, for example, “Chemical Area”, Vol. 11, page 719 (1957).

Various known methods can be used to form hot water droplets, but as a typical example, the above compound is dissolved in a low boiling point organic solvent such as methyl acetate or ethyl acetate, if necessary, Examples include a method in which an aqueous solution of a hydrophilic colloid such as gelatin is mixed with a surfactant, stirred and emulsified and dispersed, and this dispersion is added to a coating solution for the hydrophilic colloid layer and coating is performed.

In the present invention, the brittleness of the constituent layers of the dye-fixing element (particularly the mordant layer) is improved, and cracks are less likely to occur. In particular, when hot water drops are added to the layers other than the uppermost layer, the surface glossiness of the dye fixing element is not deteriorated. Further, according to the present invention, it is possible to obtain an advantage that the fog density (Dmin) of the transfer dye image is lowered.

There is no particular limitation on the mordant used in the mordant layer of the dye-fixing element of the present invention, and any of the polymer mordants known in the art can be used. Preferably the following general formula (I)
Polymers containing a vinyl monomer unit having a tertiary amino group or a quaternary ammonio group represented by (IV) to (IV) are used.

General formula (I) [In the formula, R ₁ represents a hydrogen atom or a lower alkyl group having 1 to 6 carbon atoms. L represents a divalent linking group having 1 to 20 carbon atoms. E represents a heterocycle containing a nitrogen atom having a double bond with a carbon atom as a constituent. n is 0 or 1. ] General formula (II) [In the formula, R ₁ , L and n represent the same as those in the general formula (II). R ₄ and R ₅ are the same or different and each represent an alkyl group having 1 to 12 carbon atoms or an aralkyl group having 7 to 20 carbon atoms, and R ₄ and R ₅ are connected to each other to form a nitrogen atom. You may form a cyclic structure with an atom. ] In the general formulas (I) to (IV), R ₁ is a hydrogen atom or a carbon number 1
~ 6 lower alkyl groups such as methyl, ethyl,
It represents an n-propyl group, an n-butyl group, an n-amyl group, an n-hexyl group and the like, and a hydrogen atom or a methyl group is particularly preferable.

L is a divalent linking group having 1 to about 20 carbon atoms, such as an alkylene group (eg, methylene group, ethylene group, trimethylene group, hexamethylene group, etc.), phenylene group (eg, o-phenylene group, p-phenylene group). Group, m-phenylene group, etc.), arylene alkylene group (eg, Such.

However, R ₂ represents an alkylene group having 1 to about 12 carbon atoms. ), —CO ₂ —, —CO ₂ —R ₃ — (wherein R ₃ represents an alkylene group, a phenylene group, an arylenealkylene group), —CONH—R ₃ — (wherein R ₃ represents the same as above). .), (However, R ₁ and R ₃ are the same as the above.) _{-CO 2 -, - CONH-, -CO} 2 -CH 2 CH 2 -, - CO 2 -CH 2 CH 2 CH 2 -, -CONHCH 2 -, - CONHCH 2 CH 2 -, -CONHCH 2 CH 2 CH 2 And the like are particularly preferable.

General formula (III)[R in the formula₁, L, and n are the same as those in formula (I).
G Is quaternized and has a double bond with a carbon atom
Represents a heterocycle containing a nitrogen atom as a constituent. X
Represents a monovalent anion. ] General formula (IV)[R in the formula₁, L, and n are the same as those in formula (I).
R_Four, R_FiveRepresents the same as general formula (II). R₆Is R_Four, R_Five
Is chosen from the same ones that represent. X Is the general formula
Represents the same as (III). R_Four, R_Five, R₆Are interconnected
To form a ring structure together with the nitrogen atom. ] In the general formula (I), E is nitrogen having a double bond with a carbon atom.
Heterocycles containing atoms as constituents, eg imidazo
Ring (egSuch. ), A triazole ring (egSuch. ), A pyrazole ring (eg,Such. ), A pyridine ring (eg Such. ), A pyrimidine ring (eg,Such. ) Etc., and the imidazole ring and pyridine ring are
Particularly preferred.

Preferred specific examples of the polymer represented by the general formula (I) and containing a vinyl monomer unit having a tertiary amino group include U.S. Pat. Nos. 4,282,305, 4,115,124 and 3,14.
Including the mordants described in No. 8,061 and the like, the following can be mentioned.

Such. (Number: mol%) In the general formula (II), R ₄ and R ₅ are alkyl groups having 1 to 12 carbon atoms, for example, unsubstituted alkyl groups (methyl group, ethyl group, n-propyl group, n-butyl). Group, n-amyl group, hexyl group, n-nonyl group, n-decyl group, n-dodecyl group, etc.), substituted alkyl group (methoxyethyl group, 3-
Cyanopropyl group, ethoxycarbonylethyl group, acetoxyethyl group, hydroxyethyl group, 2-butenyl group and the like. ) Or an aralkyl group having 7 to 20 carbon atoms, for example, an unsubstituted aralkyl group (benzyl group, phenethyl group, diphenylmethyl group, naphthylmethyl group, etc.), substituted aralkyl group (4-methylbenzyl group, 4
-Isopropylbenzyl group, 4-methoxybenzyl group,
4- (4-methoxyphenyl) benzyl group, 3-chlorobenzyl group and the like. ) Etc.

Further, as an example in which R ₄ and R ₅ are connected to each other to form a cyclic structure with a nitrogen atom, for example, (However, m represents an integer of 4 to 12.), And so on.

Specific preferred examples of the polymer containing a vinyl monomer unit having a tertiary amino group represented by the general formula (II) include the following.

Such.

In the general formula (III), G Is quaternized and with carbon
Heterocycle containing nitrogen atom having heavy bond as constituent
For example, an imidazolium salt ( Such. ), Triazolium salts (egPyridinium salts (eg Such. ), Of which imidazolium salt, pyri
Dinium salts are particularly preferred. Where R_FourIs the general formula (II)
Represents the same thing, and methyl group, ethyl group, benzyl group
Particularly preferred.

X in the general formulas (III) and (IV) Represents an anion, eg
For example, halogen ions (for example, chlorine ion, bromine ion,
Iodine ion), alkyl sulfate ion (eg methyl sulfate)
Acid ion, ethyl sulfate ion), alkyl or ant
Sulfonic acid ion (eg methanesulfonic acid, ethanol
Sulfonic acid, benzene sulfonic acid, p-toluene sulphate
(Fonic acid), acetate ion, sulfate ion, etc.
Especially chlorine ion and p-toluenesulfonate ion
preferable.

Preferred specific examples of the polymer containing a vinyl monomer unit having a quaternary ammonio group represented by the general formula (III) include British Patent Nos. 2,056,101, 2,093,041 and 1,59.
4,961, U.S. Pat.Nos. 4,124,386, 4,115,124,
Including the mordants described in 4,273,853, 4,450,224 and JP-A-48-28225, the following can be mentioned.

Such.

Represents In the general formula (IV), examples of R ₄ and R ₅ interconnected with each other to form a cyclic structure with a nitrogen atom include (However, m represents an integer of 4 to 12.), As an example of forming a cyclic structure by R ₄ , R ₅ and R ₆ , for example, And so on.

It is represented by the general formula (IV). Preferred specific examples of the polymer containing a vinyl monomer unit having a quaternary ammonio group include U.S. Pat.Nos. 3,709,690, 3,898,088 and 3,898,088.
Including the mordants described in 958,995 and the like, the followings can be mentioned.

Such.

Other usable polymer mordants include US Pat.
No. 2,548,564, No. 2,484,430, No. 3,148,061, No.
Vinyl pyridine polymers and vinyl pyridinium cationic polymers disclosed in, for example, 3,756,814;
U.S. Pat.Nos. 3,625,694, 3,859,096, 4,128,538
No. 1, British Patent 1,277,453, and the like, a polymer mordant capable of crosslinking with gelatin and the like; US Pat. No. 3,95
No. 8,995, No. 2,721,852, No. 2,798,063, JP-A-5
Aqueous sol type mordants disclosed in, for example, 4-115228, 54-145529, and 54-126027; U.S. Pat. No. 3,89
A water-insoluble mordant disclosed in U.S. Pat. No. 8,088; a reactive mordant capable of forming a covalent bond with the dye disclosed in U.S. Pat. No. 4,168,976 (JP-A-54-137333) and the like;
Furthermore, U.S. Pat.Nos. 3,709,690, 3,788,855, and 3,64
No. 2,482, No. 3,488,706, No. 3,557,066, No. 3,2
71,147, 3,271,148, JP-A-50-71332, 53-
30328, 52-155528, 53-125, and 53-1024, the mordants disclosed in U.S. Pat.
And the mordants described in JP-A Nos. 2,882,156.

The molecular weight of the polymer mordant used in the present invention is preferably
1,000 to 1,000,000, especially 10,000 to 200,000.

Such a polymer mordant is used in combination with a hydrophilic colloid as a binder in the mordant layer in the dye fixing element. Typical examples of hydrophilic colloids include gelatin, proteins such as gelatin derivatives, cellulose derivatives, starch, natural substances such as polysaccharides such as gum arabic, and synthetic polymers such as polyvinyl alcohol, polyvinylpyrrolidone, and polyacrylamide. Including.

Of these, gelatin and polyvinyl alcohol are particularly preferable.

The mixing ratio of the polymer mordant and the hydrophilic colloid and the coating amount of the polymer mordant are easily determined by those skilled in the art according to the amount of the dye to be mordant, the type and composition of the polymer mordant, and the image forming method to be applied. However, a mordant / hydrophilic colloid ratio of 20/80 to 80/20 (weight ratio) and a mordant coating amount of about 0.2 to about 15 g / m ² are suitable, of which 0.5 to 8 g / m ² It is preferable to use.

Polymer mordants can be used in combination with metal ions in the dye fixing element to increase the transfer density of the dye. This metal ion can be added to a mordant layer containing a mordant or a layer adjacent thereto (either on the side closer to the support carrying the mordant layer or on the side farther from the support). The metal ion used here is preferably colorless and stable to heat and light. That is, Cu ²⁺ , Zn ²⁺ , Ni ²⁺ , Pt
Multivalent ions of a transfer metal such as ²⁺ , Pd ²⁺ and Co ³⁺ ions are preferable, and Zn ²⁺ is particularly preferable. This metal ion is usually in the form of a water-soluble compound, such as ZnSO ₄ , Zn (CH ₃ CO ₂ ) ₂ ,
In is added, the amount added is suitably from about 0.01 to about 5 g / m ^2, preferably from 0.1 to 1.5 g / m ^2.

A hydrophilic polymer can be used as a binder in the layer to which these metal ions are added. As the hydrophilic binder, the hydrophilic colloids specifically listed above for the mordant layer are useful.

The mordant layer containing the polymer mordant may contain various surfactants for the purpose of enhancing coatability.

A gelatin hardener may be used in combination in the mordant layer.

Examples of gelatin hardeners that can be used in the present invention include:
For example, aldehydes (formaldehyde, glyoxal, glutaraldehyde, etc.), N-methylol compounds (dimethylolurea, methyloldimethylhydantoin, etc.), dioxane derivatives (2,3-dihydroxydioxane, etc.), active vinyl compounds [1,3,5- Triacryloyl-hexahydro-s-triazine, bis ((vinylsulfonyl) methyl ether, N, N'-ethylene-bis (vinylsulfonylacetamide), N, N'-trimethylene-bis (vinylsulfonylacetamide), etc. ], An active halogen compound (2,4-dichloro-6-hydroxy-
s-triazine etc.), mucohalogen acids (mucochromic acid, mucophenoxycyclo acid etc.), epoxy compounds (eg Examples thereof include isoxazoles, dialdehyde starch, 1-chloro-6-hydroxytriazinylated gelatin and the like. A specific example is U.S. Pat. No. 1,870,354.
No., No. 2,080,019, No. 2,726,162, No. 2,870,013,
2,983,611, 2,992,109, 3,047,394, 3,0
57,723, 3,103,437, 3,321,313, 3,325,28
No. 7, No. 3,362,827, No. 3,490,911, No. 3,539,644,
3,543,292, British Patents 676,628, 825,544,
1,270,578, German Patent 872,153, 1,090,427,
No. 2,749,260, Japanese Patent Publication No. 34-7133, No. 46-1872, etc.

These hardeners may be added directly to the mordant layer coating solution, or may be added to another coating solution so as to diffuse into the mordant layer during the process of multilayer coating.

The amount of the gelatin hardener used in the present invention can be arbitrarily selected according to the purpose. Usually, about 0.1 to about 20 wt% of the binder such as gelatin used is suitable, and preferably 1 to 8 wt%.

The dye fixing element of the present invention is in the form of being coated on a support separate from the light-sensitive element. Regarding the relationship between the photosensitive element and the dye fixing element, the relationship with the support, and the relationship with the white reflective layer, Japanese Patent Application No.
The relationships described on pages 58 to 59 of the -268926 specification and column 57 of U.S. Pat. No. 4,500,626 are also applicable to the present application. In the present invention, the dye fixing element is coated on a support separate from the light-sensitive material. If necessary, the dye fixing element can be provided with auxiliary layers such as a protective layer, a peeling layer and an anti-curl layer.
In particular, it is useful to provide a protective layer. One or more of the above layers may include a hydrophilic thermal solvent, a plasticizer, an antifade agent,
A UV absorber, a slipping agent, a matting agent, an antioxidant, a dispersed vinyl compound for increasing dimensional stability, a surfactant, an optical brightening agent and the like may be contained. Specific examples of these additives are described on pages 101 to 120 of Japanese Patent Application No. 59-209563.

The present invention is particularly effective for improving the brittleness of the dye-fixing element when a base and / or a base precursor is added to the dye-fixing element to improve the storage stability of the light-sensitive material. Here, examples of the base and / or the base precursor include the following.

Examples of the base used in the present invention include alkali metal, alkaline earth metal, ammonium, quaternary alkylammonium hydroxide, carbonate, bicarbonate, borate, secondary and tertiary phosphates, and quinoline. Salts, inorganic bases such as metaborates; aliphatic amines (trialkylamines, hydroxylamines, aliphatic polyamines), aromatic amines (N-alkyl substituted aromatic amines, N-hydroxylalkyl substituted) Aromatic amines and bis [p- (dialkylamino) phenyl] methanes), heterocyclic amines, amidines, cyclic amidines, guanidines, cyclic guanidines and other organic bases, and their carbonates and bicarbonates , Borate, secondary and tertiary phosphates, and the like, and betaine tetramethylammonium iodide in US Pat. No. 2,410,644. Diaminobutane dihydrochloride is, U.S. Patent No. 3,506,444 urea is useful is described organic compound containing amino acids such as 6-aminocaproic acid. In the present invention, a pka value of 8 or more is particularly useful.

The base precursor used in the present invention is one that releases or produces a base by thermal decomposition, electrolysis or complex formation reaction.

As a base precursor, a salt of an organic acid and a base that is decarboxylated by heating to decompose, a compound that decomposes to release an amine by Rossen rearrangement, Beckmann rearrangement, etc. that causes some reaction by heating and releases a base. Is mentioned.

Examples of the base used for the salt of an organic acid and a base include the above-mentioned inorganic bases and organic bases. Examples of the organic acid include trichloroacetic acid, trifluoroacetic acid, propiolic acid, cyanoacetic acid, sulfonylacetic acid, acetoacetic acid and the like, and 2-carboxycarboxamide described in US Pat. No. 4,088,496.

In addition to salts of organic acids and bases, for example, hydroxam carbamates described in JP-A-59-168440 utilizing the Rossen rearrangement, aldoxime carbamates described in JP-A-59-157637 that form nitriles, etc. are effective. The amine imides described in Research Disclosure, May 1977, No. 15776, and the aldonamides described in JP-A No. 50-22625 are preferably those which decompose to form a base at high temperature. Used.

The following can be mentioned as base precursors that generate a base by electrolysis.

For example, electrolysis of various fatty acid salts can be mentioned as a representative method using electrolytic oxidation. By this reaction, carbonates of organic bases such as alkali metals, guanidines and amidines can be obtained very efficiently.

As a method using electrolytic reduction, amines are produced by reduction of nitro and nitroso compounds; amines are produced by reduction of nitriles; nitro compounds, azo compounds,
Examples include production of p-aminophenols, p-phenylenediamines, and hydrazines by reduction of azoxy compounds and the like. p-aminophenols, p-
The phenylenediamines and hydrazines can be used not only as bases but also directly as color image forming substances.

Further, it is of course possible to use an alkaline component produced by electrolysis of water in the presence of various inorganic salts.

Next, as a base precursor for producing a base by using a complex formation reaction, for example, a complex formation reaction is performed with a sparingly soluble metal compound described in Japanese Patent Application No. 60-169585 and a metal ion constituting the sparingly soluble metal compound. And a compound capable of forming a complex (referred to as a complex forming compound). For example, the sparingly soluble metal compound includes carbonates, hydroxides and oxides of zinc, aluminum, calcium, barium and the like. Further, regarding the complex-forming compound, for example, AEMartell, R.M.
M. Smith), "Critical Stability Gonstants," Volumes 4-5, Plenum Press. Specifically, aminocarboxylic acids, iminodiacetic acids, pyridylcarboxylic acids, aminophosphoric acids, carboxylic acids (mono, di, tri, tetracarboxylic acids and further phosphono, hydroxy, oxo, ester, amide, alkoxy, mercapto, alkylthio, phosphino Compounds having substituents such as), hydroxamic acids,
Examples thereof include salts with alkali metals such as polyacrylates and polyphosphoric acids, guanidines, amidines and quaternary ammonium salts.

The sparingly soluble metal compound and the complex-forming compound are advantageously added separately to the light-sensitive element and the dye-fixing element.

The base and / or the base precursor may be used alone or in combination of two or more kinds.

The amount of the base and / or base precursor used in the present invention can be used within a wide range. Usually, it is useful that the total coating film of the light-sensitive element and the dye-fixing element is 50% by weight or less in terms of weight, particularly in the range of 1% by weight to 40% by weight.

In the present invention, the light-sensitive element used in combination with the above dye-fixing element has at least a light-sensitive silver halide, a dye-donating substance, a binder and, if necessary, an organic silver salt or a reducing agent on a support. is there.

The silver halide that can be used in the present invention includes silver chloride, silver bromide,
Alternatively, any of silver chlorobromide, silver chloroiodide and silver chloroiodobromide may be used.

Specifically, U.S. Pat. No. 4,500,626, column 50, Research Disclosure, June 1978, pages 9-10 (RD
17029), Japanese Patent Application Nos. 59-228551, 60-225176, and 60
Any of the silver halide emulsions described in -228267 etc. can be used.

The silver halide emulsion used in the present invention may be either a surface latent image type in which a latent image is mainly formed on the grain surface or an internal latent image type in which a latent image is formed inside the grain. It may be a so-called core-shell emulsion in which the inside of the grain and the surface layer of the grain have different phases. Further, in the present invention, a direct reversal emulsion in which an internal latent image type emulsion and a nucleating agent are combined can be used.

The silver halide emulsion may be used as it is without ripening, but it is usually chemically sensitized before use. Well-known sulfur sensitizing methods, reduction sensitizing methods, noble metal sensitizing methods and the like can be used alone or in combination for the emulsions for conventional type light-sensitive materials. These chemical sensitizations can also be carried out in the presence of a nitrogen-containing heterocyclic compound (JP-A-58-126526 and JP-A-58-215644).

The coating amount of the photosensitive silver halide used in the present invention is in the range of 1 mg to 10 g / m ² in terms of silver.

In the present invention, an organic metal salt may be used as an oxidizing agent together with the photosensitive silver halide. in this case,
It is necessary that the photosensitive silver halide and the organic metal salt are in contact with each other or in close proximity.

Among such organic metal salts, organic silver salts are particularly preferably used.

Examples of the organic compound that can be used to form the above organic silver salt oxidizing agent include those described in Japanese Patent Application No. 59-228551, pages 37 to 39, U.S. Pat.No. 4,500,626, columns 52 to 53, etc. There is a compound. Further, silver salts of carboxylic acids having an alkynyl group such as silver phenylpropiolate described in Japanese Patent Application No. 60-113235 and silver acetylene described in Japanese Patent Application No. 60-90089 are also useful. Two or more kinds of organic silver salts may be used in combination.

The above organic silver salts are
0.01 to 10 mol, preferably 0.01 to 1 mol can be used in combination. The total coating amount of the photosensitive silver halide and the organic silver salt is preferably 50 mg to 10 g / m ² in terms of silver.

The silver halide used in the present invention may be spectrally sensitized with methine dyes and the like. The dyes used include cyanine dyes, merocyanine dyes, complex cyanine dyes, complex merocyanine dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes and hemioxonol dyes.

Specifically, the sensitizing dyes described in JP-A-59-180550 and JP-A-60-140335, Research Disclosure June 1978, pages 12 to 13 (RD 17029), and JP-A-60- 111239
And heat-decolorizing sensitizing dyes described in Japanese Patent Application No. 60-172967.

These sensitizing dyes may be used alone or in combination thereof, and the combination of sensitizing dyes is often used especially for the purpose of supersensitization.

A dye that does not itself have a spectral sensitizing effect or a substance that does not substantially absorb visible light together with a sensitizing dye,
A substance exhibiting supersensitization may be contained in the emulsion (for example, US Pat. Nos. 2,933,390, 3,635,721, and 3,743,510).
No. 3,615,613, 3,615,641, 3,617,295,
No. 3,635,721).

These sensitizing dyes may be added to the emulsion at the time of chemical ripening or before or after chemical ripening, and U.S. Pat. No. 4,183,756.
No. 4,225,666, before or after nucleation of silver halide grains.

The addition amount is generally 10 ^-8 to 10 per mol of silver halide.
^-It is about ² mol.

In the present invention, when the silver ion is reduced to silver as an image forming substance under a high temperature condition, a compound that produces or releases a mobile dye in response to this reaction or in the opposite response, that is, a dye Use donating substances.

Examples of dye-donor substances that can be used in the present invention are as follows.
A compound (coupler) that forms a dye by an oxidative coupling reaction can be mentioned. This coupler is 4
It may be an equivalent coupler or a two equivalent coupler. A 2-equivalent coupler having a diffusion resistant group as a leaving group and forming a diffusible dye by an oxidative coupling reaction is also preferable. Specific examples of developing agents and couplers are described in James, "The Theory of the Photographic Process," 4th Edition (TH
James “The Theory of the Photographic Process”) 29
1 to 334 and 354 to 361, JP-A-58-123533,
58-149046, 58-149047, 59-111148, 59
-124399, 59-174835, 59-231539, 59-
231540, 60-2950, 60-2951, 60-14242
No. 60-23474, No. 60-66249 and the like.

As another example of the dye-donating substance, a compound having a function of releasing or diffusing a diffusible dye in an image form can be mentioned. This type of compound can be represented by the following general formula [LI].

(Dye-X) _n -Y [LI] Dye represents a dye group, a temporarily shortened dye group or a dye precursor group, X represents a mere bond or linking group, and Y represents an image latent image. Corresponding to or opposite to the photosensitive silver salt having a difference in the diffusivity of the compound represented by (Dye-X) _n- Y, or releasing Dye and releasing D
ye and (Dye-X) _n -Y represent a group having a property of causing a difference in diffusibility, n represents 1 or 2, and when n is 2, two Dye-X are It may be the same or different.

Specific examples of the dye-donating substance represented by the general formula [LI] include, for example, dye developers in which a hydroquinone-based developer and a dye component are linked to each other are disclosed in U.S. Patent Nos. 3,134,764 and 3,3.
62,819, 3,597,200, 3,544,545, 3,
No. 482,972, etc. In addition, a substance that releases a diffusible dye by an intramolecular nucleophilic substitution reaction is disclosed in US Pat.
No. 3,980,479, a substance that releases a diffusible dye by an intramolecular rewinding reaction of an isoxazolone ring is disclosed in JP-A-49-
No. 111,628, etc.

As another example, a dye-releasing compound is made into an oxidant type having no dye-releasing ability to coexist with a reducing agent or its precursor, and after development, the diffusible dye is reduced by the reducing agent remaining unoxidized. A method of releasing a dye has also been devised, and specific examples of dye-donor substances used therein are disclosed in JP-A-53-
110,827, 54-130,927, 56-164,342, 53
-35,533. Japanese Patent Application No. 60-244873 describes a compound that releases a diffusible dye by cleaving the N—O bond by the remaining reducing agent as a dye-donor substance that releases the diffusible dye by the same mechanism. There is.

Further, as described in JP-A-59-185333, a donor-acceptor reaction occurs in the presence of a base to release a diffusible dye, but when it reacts with an oxidant of a reducing agent, the dye is not substantially released. A non-diffusible compound (LDA compound) can also be used.

In all of these methods, the diffusible dye is released or diffused in a portion where development has not occurred, and the dye is neither released nor diffused where development has occurred.

On the other hand, as a substance that releases the diffusible dye in the developed portion, it is a coupler that has the diffusible dye as a leaving group and that releases the diffusible dye by the reaction with the oxidant of the reducing agent (DDR coupler). However, British Patent No. 1,330,524, Japanese Patent Publication Sho
It is described in 48-39165, U.S. Pat. No. 3,443,940 and the like and is preferably used in the present invention.

Further, in the method using these reducing agents, the image contamination due to the oxidative decomposition product of the reducing agents becomes a serious problem, and for the purpose of improving this problem, a reducing agent is not essential, and a dye having a reducing property itself. Releasing compounds (DRR compounds) have also been devised and are used particularly advantageously in the present invention. Representative examples thereof are U.S. Pat.Nos. 3,928,312, 4,053,312, and 4,
055,428, 4,336,322, JP-A-59-65839, 5
No. 9-69839, No. 53-3819, No. 51-104343, Research Disclosure No. 17465, U.S. Patent No. 3,725,062.
No. 3,728,113, No. 3,443,939, JP-A-58-11
6537, 57-179840, U.S. Pat. No. 4,500,626 and the like. Specific examples of this type of dye-donating substance include the aforementioned U.S. Pat. No. 4,500,626.
The compounds described in Columns 22 to 44 of No. 4 can be mentioned. Among them, the compounds (1) to
(3), (10)-(13), (16)-(19), (28)-
(30), (33) ~ (35), (38) ~ (40), (42) ~
(64) is preferable. Further, the compounds described on pages 80 to 87 of Japanese Patent Application No. 59-246468 are also useful.

In addition to the above-mentioned dye-donating substances, dye silver compounds in which an organic silver salt and a dye are bound (Research Disclosure, May 1978, p. 54-58, etc.), heat-developable silver dye bleaching method Azo dyes used (U.S. Pat.
957, Research Disclosure, April 1976, pages 30-32, etc.), Leuco dyes (US Pat. No. 3,985,565)
No., No. 4,022,617, etc.) can also be used.

The above dye-providing compounds and hydrophobic additives such as the image-forming accelerators described below can be incorporated into the layers of the light-sensitive element by known methods such as the method described in US Pat. No. 2,322,027. In this case, JP-A-59-83154
59-178451, 59-178452, 59-178453, 59
59-178454, 59-178455, 59-178457, such as a high-boiling organic solvent, as described in the boiling point 50 ℃
It can be used in combination with an organic solvent having a low boiling point of up to 160 ° C.

The amount of the high-boiling organic solvent is 10 g or less, preferably 5 g or less, with respect to 1 g of the dye-donor substance used.

Further, a dispersion method using a polymer described in JP-B-51-39853 and JP-A-51-59943 can also be used.

In the case of a compound which is substantially insoluble in water, fine particles can be dispersed and contained in a binder in addition to the above method.

When dispersing the hydrophobic substance in the hydrophilic colloid, various surfactants can be used. For example, JP-A-59-15
The surfactants listed on pages (37) to (38) of 7636 can be used.

In the present invention, it is desirable that the light-sensitive element contains a reducing substance. Examples of the reducing substance include those generally known as a reducing agent, and the dye-donating substance having the above-described reducing property. Further, a reducing agent precursor which does not have reducing property itself but exhibits reducing property by the action of a nucleophile or heat during the development process is also included.

Examples of the reducing agent used in the present invention include U.S. Pat.
Columns 49-50 of 500,626, Columns 30-31 of 4,483,914,
JP-A-60-140335, pages (17) to (18), JP-A-60-
128438, 60-128436, 60-128439, 60-12
The reducing agents described in 8437 and the like can be used. In addition, JP-A-56
The reducing agent precursors described in, for example, -138736, 57-40245, and U.S. Pat. No. 4,330,617 can also be used.

Combinations of various reducing agents such as those disclosed in US Pat. No. 3,039,869 can also be used.

In the present invention, the amount of reducing agent added is 0.
The amount is 01 to 20 mol, particularly preferably 0.1 to 10 mol.

In the present invention, a compound capable of activating development and stabilizing an image at the same time can be used in the light-sensitive element. For specific compounds that are preferably used, see US Pat.
Various antifoggants or photographic stabilizers can be used in the present invention described in No. 6, columns 51 to 52. For example, research
Disclosure, December 1978, pages 24 to 25, azoles and azaindenes, nitrogen-containing carboxylic acids and phosphoric acids described in JP-A-59-168442, or mercapto described in JP-A-59-111636. Compounds and metal salts thereof, and acetylene compounds described in Japanese Patent Application No. 60-228267 are used.

In the present invention, the light-sensitive element may contain an image toning agent, if necessary. Specific examples of effective toning agents include compounds described in Japanese Patent Application No. 59-268926, pages 92 to 93.

In order to obtain a wide range of colors in the chromaticity diagram by using the three primary colors of yellow, magenta and cyan, it is necessary to use a light-sensitive element having at least three silver halide emulsion layers having light-sensitivity in different spectral regions. Good. For example, the blue layer,
A combination of three layers of green-sensitive layer and red-sensitive layer, green-sensitive layer, red-sensitive layer,
There are combinations of infrared photosensitive layers. Each of these photosensitive layers may be divided into two or more layers if necessary.

The photosensitive element used in the present invention is, if necessary, various additives known for heat-developable photosensitive elements and layers other than the photosensitive layer, such as a protective layer, an intermediate layer, an antistatic layer, an antihalation layer and a dye. It may have a release layer, a matte layer or the like for facilitating release from the fixing element. Examples of various additives include plasticizers, matting agents, sharpness improving dyes and antihalation dyes described in Research Disclosure, June 1978, pages 9 to 15 and Japanese Patent Application No. 59-209563. There are additives such as surfactants, optical brighteners, anti-slip agents, antioxidants and anti-fading agents.

In particular, the protective layer usually contains an organic or inorganic matting agent to prevent adhesion. Further, this protective layer may contain a mordant and an ultraviolet absorber. The protective layer and the intermediate layer may each be composed of two or more layers.

Further, the intermediate layer may contain a reducing agent for preventing discoloration or color mixture, an ultraviolet absorber, or a white pigment such as titanium dioxide. The white pigment may be added to the emulsion layer as well as the intermediate layer for the purpose of improving the sensitivity.

In the present invention, an image formation accelerator can be used in the light-sensitive element and / or the dye fixing element. The image formation accelerator includes a redox reaction between a silver salt oxidizing agent and a reducing agent, a reaction such as generation of a dye from a dye-donor substance, decomposition of the dye or release of a diffusible dye, and a light-sensitive material layer. Has a function of accelerating the transfer of the dye from the dye to the dye fixing layer, and from the physicochemical function, the above-mentioned base or base precursor, nucleophilic compound, high boiling point organic solvent (oil), thermal solvent, surfactant , And compounds that interact with silver or silver ions. However, these substance groups generally have a composite function, and usually have some of the above-mentioned accelerating effects together. For details of these, Japanese Patent Application No. 59
-213978, pages 67-71.

In the light-sensitive element and / or the dye-fixing element of the present invention, various development terminators can be used for the purpose of always obtaining a constant image against variations in processing temperature and processing time during development.

The term "development terminating agent" as used herein refers to a compound that immediately neutralizes or reacts with a base to reduce the concentration of the base in the film to stop the development after proper development, or inhibits development by interacting with silver and a silver salt. Compound. Specific examples thereof include acid precursors that release an acid upon heating, electrophilic compounds that undergo a substitution reaction with a coexisting base upon heating, or nitrogen-containing heterocyclic compounds, mercapto compounds and precursors thereof (for example, Japanese Patent Application No. 58-216928, 59-48305, 59
-85834 or 59-85836, etc.).

Further, a compound which releases a mercapto compound by heating is also useful, for example, Japanese Patent Application Nos. 59-190173 and 59-268926.
No. 59-246468, No. 60-26038, No. 60-22602,
60-26039, 60-24665, 60-29892, 59
-176350, there is a compound described.

A hydrophilic binder may be used as the binder of the photosensitive element and / or the dye fixing element of the present invention. As the hydrophilic binder, a transparent or translucent hydrophilic binder is typical, and for example, gelatin, proteins such as gelatin derivatives, cellulose derivatives, starch, natural substances such as polysaccharides such as arabic gum, and polyvinyl alcohol,
Includes synthetic polymeric materials such as polyvinylpyrrolidone, water soluble polyvinyl compounds such as acrylamide polymers. It is also possible to use a dispersed vinyl compound which is used in the form of a latex and which increases the dimensional stability of the photographic material. These binders can be used alone or in combination.

In the present invention, the binder is applied in an amount of 20 g or less per 1 m ² , preferably 10 g or less, more preferably 7 g or less.

The ratio of the high-boiling organic solvent and the binder dispersed together with the hydrophobic compound such as the dye-providing substance in the binder is 1 cc or less of the solvent per 1 g of the binder, preferably 0.5 cc or less, and more preferably 0.3 cc or less. is there.

The constituent layers (photographic emulsion layer, dye fixing layer, etc.) of the light-sensitive element and / or dye fixing element of the present invention may contain an inorganic or organic hardener.

Specific examples of the hardener include those described in Japanese Patent Application No. 59-268926, pages 94 to 95 and Japanese Patent Application No. 59-157636, page (38), which may be used alone or in combination. Can be used.

In order to pay attention to dye transfer, a hydrophilic thermal solvent that is solid at room temperature and dissolves at high temperature may be incorporated in the photosensitive element or the dye fixing element. The hydrophilic thermal solvent may be incorporated in either the photosensitive element or the dye fixing element, or may be incorporated in both. The layer to be incorporated may be any of an emulsion layer, an intermediate layer, a protective layer and a dye fixing layer, but it is preferably incorporated in the dye fixing layer and / or its adjacent layer. Examples of hydrophilic thermal solvents include ureas, pyridines, amides,
There are sulfonamides, imides, alcohols, oximes and other heterocycles. Further, a high-boiling point organic solvent may be contained in the light-sensitive element and / or the dye-fixing element in order to promote dye transfer.

The support used in the light-sensitive element and / or the dye-fixing element of the present invention can withstand the processing temperature.
As a general support, not only glass, paper, polymer film, metal and its analogues are used,
What is described as a support on pages 95 to 96 of Japanese Patent Application No. 59-268926 can be used.

The light-sensitive element and / or the dye-fixing element may have a form having a conductive heating element layer as a heating means for heat development or diffusion transfer of a dye.

In this case, the transparent or opaque heating element can be manufactured by using a conventionally known technique as a resistance heating element. As the resistance heating element, there are a method of using a thin film of a semiconductive inorganic material and a method of using an organic thin film in which conductive fine particles are dispersed in a binder. Materials usable in these methods include those described in Japanese Patent Application No. 59-151815.

In the present invention, the coating method of the photothermographic layer, protective layer, intermediate layer, undercoat layer, back layer, dye fixing layer and other layers can be applied the method described in US Pat. No. 4,500,626, columns 55 to 56. .

Radiation that also contains visible light can be used as a light source for image exposure for recording an image on the photosensitive element. Generally, light sources used for ordinary color printing, such as halogen lamps such as tungsten lamps, mercury lamps, iodine lamps, xenon lamps, laser light sources, CRT light sources,
A light source such as a light emitting diode (LED) described in Japanese Patent Application No. 59-268926, page 100, or US Pat. No. 4,500,626, column 56 can be used.

In the present invention, the steps of heat development and dye transfer may be independent or simultaneous. Further, it may be continuous in the sense that the scratch transfer is performed for the development in one step.

For example, (1) after imagewise exposing the photosensitive element and heating,
There are a method of stacking dye-fixing elements and heating as required to transfer the movable dye to the dye-fixing element, and a method of (2) image-exposing the photosensitive element and stacking and heating the dye-fixing elements.
The above methods (1) and (2) can be carried out in the substantially absence of water, or can be carried out in the presence of a trace amount of water.

The heating temperature in the heat development step is about 50 ° C. to about 250 ° C., and development is possible, but about 80 ° C. to about 180 ° C. is particularly useful. When heating in the presence of a trace amount of water, the upper limit of the heating temperature is the boiling point or lower. When the transfer step is carried out after the completion of the heat development step, the heating temperature in the transfer step can be transferred in the range from the temperature in the heat development step to room temperature, but especially at 50 ° C or higher, about 10 ° C higher than the temperature in the heat development step. Up to a lower temperature is more preferable.

In the present invention, the preferred image forming method is heating in the presence of a trace amount of water and a base and / or a base precursor after or at the same time as the image exposure, and at the same time as the development, the diffusion generated in the portion corresponding to or inversely corresponding to the silver image. The sex dye is transferred to the dye fixing layer. According to this method
The generation or release reaction of the diffusible dye proceeds extremely quickly,
The migration of the diffusible dye to the dye-fixing layer also progresses rapidly, so that a high-density color image can be obtained in a short time.

The amount of water used in this embodiment is at least 0.1 times the weight of the total coating film of the light-sensitive element and the dye-fixing element, preferably 0.1.
It may be as small as or more than twice the weight of the solvent corresponding to the maximum swelling volume of the entire coated film (particularly less than or equal to the weight of the solvent corresponding to the maximum swelling volume of the entire coated film minus the weight of the entire coated film).

The state of the film at the time of swelling is unstable, and local bleeding may occur depending on the conditions. Or less is preferable. Specifically, the total area of the photosensitive element and the dye fixing element is 1 g to 50 per 1 square meter.
The range of g, especially 2 g to 35 g, and further 3 g to 25 g is preferable.

The base and / or base precursor used in this embodiment can be incorporated in both the light-sensitive element and the dye-fixing element. It can also be dissolved in water and supplied.

In the above aspect, the image-forming reaction system, as a base precursor, a water-insoluble basic metal compound and a metal ion constituting the hardly-soluble metal compound and a compound capable of a complex formation reaction in water as a medium, It is preferred to raise the pH of the system by the reaction of these two compounds on heating.
Here, the image reaction system means a region where an image forming reaction occurs. Specific examples include layers belonging to both the light-sensitive element and the dye-fixing element. When there are two or more layers, any of them may be used.

The sparingly soluble metal compound and the complex-forming compound must be added to at least another layer in order to prevent them from reacting before the development processing. For example, in a so-called monosheet material in which a light-sensitive element and a dye-fixing element are provided on the same support, it is preferable that the additive layers of the both are separate layers and that one or more layers are interposed therebetween. In addition, a more preferable form is
The sparingly soluble metal compound and the complex-forming compound are contained in layers provided on separate supports. For example, it is preferable that the poorly soluble metal compound is contained in the light-sensitive element and the complex-forming compound is contained in the dye-fixing element having a support different from that of the light-sensitive element. The complex-forming compound may be dissolved in water to be coexistent and supplied. The sparingly soluble metal compound is disclosed in JP-A-56-174830.
No. 53-102733, etc., and it is desirable to include it as a fine particle dispersion prepared by the method described in JP-A No. 53-102733. The average particle size thereof is preferably 50 microns or less, particularly preferably 5 microns or less. The sparingly soluble metal compound may be added to any layer of the photosensitive element such as the photosensitive layer, the intermediate layer and the protective layer, or may be added by dividing it into two or more layers.

The amount of the sparingly soluble metal compound or complex-forming compound to be added to the layer on the support depends on the compound species, the particle size of the sparingly soluble metal compound, the complex formation reaction rate, etc. It is suitable to use it in an amount of 50% by weight or less, more preferably 0.01% by weight to 40% by weight. When the complex-forming compound is dissolved in water and supplied, a concentration of 0.005 mol to 5 mol, particularly 0.05 mol to 2 mol per liter is preferable. Further, in the present invention, the content of the complex-forming compound in the reaction system is 1 / molar ratio with respect to the content of the sparingly soluble compound.
100 times to 100 times, particularly preferably 1/10 times to 20 times.

As a method of applying water to the photosensitive layer or the dye fixing layer,
For example, there is a method described in Japanese Patent Application No. 59-268926, page 101, line 9 to page 102, line 4.

As a heating means in the developing and / or transferring process, a heating plate, an iron, a heating roller, or the like is disclosed in Japanese Patent Application No. 59-2689.
There are means described in No. 26, page 102, line 14 to page 103, line 11. Further, a layer of a conductive material such as graphite, carbon black or metal may be superposed on the photosensitive element and / or the dye fixing element, and a current may be passed through the conductive layer to directly heat the conductive layer. .

The pressure condition and the method of applying pressure when the photosensitive element and the dye fixing element are superposed and brought into close contact are described in Japanese Patent Application No. 59-268926.
The method described on pages 103 to 104 can be applied.

Any of a variety of thermal development apparatus can be used in processing the photographic elements of this invention. For example, JP-A-59-75247 and 59-1.
77547, 59-181353, 60-18951, Jpn.
The devices described in 116734 and the like are preferably used.

(Examples) Hereinafter, the present invention will be described in more detail by showing specific examples of the present invention.

Example 1 A method for producing a dispersion (V-1) of oil droplets will be described.

To 100 g of a 10% aqueous gelatin solution, 5 ml of a 5% aqueous solution of sodium dodecylbenzenesulfonate was added, and 20 g of the compound (1) shown in Table 2 was further added. A dispersion (Y-1) was obtained.

Using the oil droplet dispersion (Y-1) thus prepared, a dye fixing material R-1 as shown in Table 1 was prepared.

In the dye fixing material R-1, the addition amount of the oil droplet dispersion (Y-1) (that is, the coating amount of the compound (1)) was changed as shown in Table-2, and the dye fixing materials R-2 to R- were used. 5 was produced.

Further, in the oil drop dispersion (Y-1), the oil drop dispersion (Y-1) was prepared in the same manner as the oil drop dispersion (Y-1) except that the compounds shown in Table 2 were used instead of the compound (1). -2) to (Y-
9) was produced. These oil droplet dispersions (Y-2) to (Y-
Dye fixing materials R-6 to R-13 were produced in the same manner as the dye fixing material R-1 except that 9) was used. The coating amount of each compound is shown in Table 2.

Further, the dye fixing material R-1 is the same as the dye fixing material R-1 except that it does not contain oil droplets.
14 was produced.

By using the obtained dye fixing materials R-1 to R-14, the brittleness of the coating film and the glossiness of the coating film surface were examined. The results are shown in Table-2.

As is clear from Table-2, it can be seen that the dye-fixing material containing oil droplets in the dye-fixing layer is greatly improved in cracking. In addition, the compound (organic /
The larger the (inorganic) value, the better the surface gloss of the dye fixing material. Further, the effect of improving brittleness is large when the content of oil droplets is 5 vol% or more, and is particularly remarkable when it is 10 vol% or more. Again 60vol
% Or less, the glossiness is excellent.

Example 2 Pigment fixing materials R-21, R-22, R having the constitution as shown in Table 3
-23 was made and tested as in Example 1. The results are summarized in Table-3.

It can be seen from Table 3 that brittleness and glossiness are both satisfied by adding oil droplets to the layers other than the uppermost layer.

Example 3 A method for producing a benzotriazole silver emulsion will be described.

28 g of gelatin and 13.2 g of benzotriazole were dissolved in 300 ml of water. This solution was kept at 40 ° C. and stirred. A solution prepared by dissolving 17 g of silver nitrate in 100 ml of water was added to this solution over 2 minutes.

The pH of this benzotriazole silver emulsion was adjusted and allowed to settle to remove excess salt. Then adjust the pH to 6.30,
A yield of 400 g of benzotriazole silver emulsion was obtained.

Next, how to make an acetylene silver emulsion will be described.

28 g of gelatin and 26.7 g of potassium 4-acetylaminophenylpropiolate were dissolved in 500 ml of water. 40 this lysis
The mixture was kept at ℃ and stirred. A solution prepared by dissolving 17 g of silver nitrate in 100 ml of water was added to this solution over 2 minutes, and the mixture was further stirred for 10 minutes.

The pH of this emulsion was adjusted to 6.30 and the yield was 400 g by centrifugation.
To obtain a silver acetylene emulsion.

A method for preparing a silver halide emulsion for the fifth layer and the first layer will be described.

600 ml of an aqueous solution containing sodium chloride and potassium bromide in a well-stirred aqueous gelatin solution (containing 20 g of gelatin and 3 g of sodium chloride in 1,000 ml of water and kept at 75 ° C) and an aqueous solution of silver nitrate (600 ml of water and silver nitrate) 0.59 mol dissolved) was added simultaneously at an equal flow rate over 40 minutes. In this way, a monodisperse cubic silver chlorobromide emulsion (bromine 50 mol%) having an average grain size of 0.40 μm was prepared.

After washing with water and desalting, 5 mg of sodium thiosulfate and 20 mg of 4-hydroxy-6-methyl-1,3,3a, 7-tetrazaindene were added, and chemical sensitization was performed at 60 ° C. Emulsion yield is 600g
Met.

Next, how to prepare a silver halide emulsion for the third layer will be described.

600 ml of an aqueous solution containing sodium chloride and potassium bromide in a well-stirred aqueous gelatin solution (containing 20 g of gelatin and 3 g of sodium chloride in 1,000 ml of water and kept at 75 ° C) and an aqueous solution of silver nitrate (600 ml of water and silver nitrate) 0.59 mol dissolved) was added simultaneously at an equal flow rate over 40 minutes. Thus, a monodisperse cubic silver chlorobromide emulsion (bromine 80 mol%) having an average grain size of 0.35 μm was prepared.

After washing with water and desalting, 5 mg of sodium thiosulfate and 20 mg of 4-hydroxy-6-methyl-1,3,3a, 7-tetrazaindene were added, and chemical sensitization was performed at 60 ° C. Emulsion yield is 600g
Met.

Next, a method for preparing a gelatin dispersion of a dye-donor substance will be described.

5 g of the yellow dye-donor substance (A), 0.5 g of sodium succinate-2-ethyl-hexyl ester sulfonate as a surfactant, and 10 g of triisononyl phosphate were weighed and added with 30 ml of ethyl acetate, Dissolve by heating to 60 ℃,
A homogeneous solution was obtained. 10% of this solution and lime-processed gelatin
After stirring and mixing 30 g of the solution, the mixture was dispersed at 10,000 rpm for 10 minutes with a homogenizer. This dispersion is called a yellow dye-donor substance dispersion.

A dispersion of a magenta dye-donor substance was prepared in the same manner as described above, except that the magenta dye-donor substance (B) was used and 3.75 g of tricresyl phosphate was used as the high boiling point solvent.

A cyan dye dispersion was prepared using the cyan dye-donor (C) in the same manner as the yellow dye dispersion.

From these, a color light-sensitive material having a multilayer structure as shown in the following table was produced.

Dye donating substance Sensitizing dye Reducing agent The multilayer color photosensitive material was exposed for 10 ⁻⁴ seconds using a xenon flash tube. At that time, it was exposed through G, R, and IR3 color separation filters whose densities were continuously changed.

The emulsion surface of the exposed light-sensitive material was coated with 11 ml / m ² of water with a wire bar, and then the dye fixing material R described in Example 1 was used.
-3, R-13, and R-14 were laminated so that the film surface was in contact with each other. Then, using a heat roller whose temperature has been adjusted so that the water-absorbed film has a temperature of 93 ° C., the dye fixing material is heated for 35 seconds and then peeled off from the dye fixing material.
Clear images of yellow, magenta, and cyan were obtained corresponding to the color separation filters.

Table 4 shows the results of measuring the maximum density (D _max ) and the minimum density (D _min ) of each color using a Macbeth reflection densitometer (RD-519).

Further, the degree of cracking of the dye fixing material after the above treatment was examined in the same manner as in Example 1. The results are also shown in Table-4.

From Table 4, it can be seen that the inclusion of oil droplets does not lower D _max , improves cracking, and lowers D _{min, which} is a preferable effect.

 ─────────────────────────────────────────────────── ─── Continuation of front page (56) Reference JP-A-59-224844 (JP, A) JP-A-61-11741 (JP, A) JP-A-54-94319 (JP, A) JP-A-58- 147734 (JP, A) JP 62-215953 (JP, A) JP 62-89037 (JP, A) JP 5-73225 (JP, B2) JP 59-37816 (JP, B2)

Claims (1)

[Claims] 1. A dye-fixing element for receiving a movable dye formed or released in a light-sensitive element by heat development, wherein at least two hydrophilic colloid layers are provided on a support separate from the light-sensitive element. And a hydrophilic colloid layer other than the uppermost layer, containing a compound having an organic / inorganic value of 3 or more as oil droplets, a dye fixing element.