JPH08123035A - Photosensitive material - Google Patents

Abstract

PURPOSE: To enhance the bonding strength of a curable layer to a hydrophilic layer and to obtain a photosensitive material less liable to peel by incorporating amino-alcohol into one of the layers. CONSTITUTION: Silver halide, a reducing agent, a polymerizable compd., a precursor of a base, a hydrophobic polymer having acidic groups and a hydrophilic polymer are uniformly contained in two or more layers on a substrate without using microcapsules, the polymerizable compd. and the hydrophobic polymer are contained in the same layer to form a curable layer and a hydrophilic layer contg. the hydrophilic polymer is formed as a layer adjacent to the curable layer. Amino-alcohol is incorporated into the curable layer or the hydrophilic layer to obtain the objective photosensitive material. The amino-alcohol is a compd. represented by the formula (where R<1> is alkylene or a divalent group contg. two or more alkylene groups combined by an ether bond and each of R<2> and R<3> is H or alkyl).

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to a photosensitive material for forming a cured image of a polymerizable compound by utilizing the photosensitivity of silver halide or a photopolymerization initiator.

[0002]

2. Description of the Related Art A method of forming a polymer image by imagewise exposing a light-sensitive material containing a silver halide, a reducing agent and a polymerizable compound to develop the silver halide and thereby polymerizing the polymerizable compound in an image form. However, Japanese Patent Publication Nos. 3-12307 and 3-12308 (U.S. Pat. No. 4,629,67).
No. 6 and European Patent No. 0174634). In this method, the polymerization is initiated by an oxidant radical of a reducing agent that has reduced silver halide (which may be a radical generated by decomposition of an oxidant of the reducing agent; hereinafter, simply referred to as an oxidant radical). . Specifically, the photosensitive material is heated to develop the silver halide,
Thermal development is performed to form a cured image of the polymerizable compound.

The image forming method described above can also be applied to the production of printing plates. A light-sensitive material suitable for producing a printing plate is disclosed in JP-A-5-249667 (US Pat.
22443 and European Patents 0426192) and JP-A-4-191856 (US Pat. No. 5)
No. 290659). In a light-sensitive material used for producing a printing plate, generally two or more layers are provided on a support. Then, the silver halide, the reducing agent, the polymerizable compound, the base precursor, the hydrophobic polymer having an acidic group and the hydrophilic polymer are uniformly contained in any layer without using microcapsules. Further, adjacent to the curable layer containing a polymerizable compound and a hydrophobic polymer,
A hydrophilic layer containing a hydrophilic polymer (for example, a photosensitive layer in which silver halide is dispersed in a hydrophilic polymer) is often provided. In the method for producing a printing plate, after curing the polymerizable compound by heat development, the hydrophilic layer is removed from the curable layer,
The uncured portion of the curable layer is removed using the eluent, and the remaining cured image is used as the image on the printing plate.

On the other hand, a method of exposing a light-sensitive material containing a photopolymerization initiator and a polymerizable compound to an image to polymerize the polymerizable compound in an image-wise manner to form a polymer image is disclosed in West German Patent Publication No. 3807378, Switzerland. National Patent Publication 97
23/781, U.S. Pat. No. 4,147,552 and International Patent Publication No. 86-05777. The image forming method using a photopolymerization initiator can also be applied to the production of printing plates. In the production of a printing plate, two or more layers are provided on a support, and a photopolymerization initiator, a polymerizable compound, a hydrophobic polymer having an acidic group and a hydrophilic polymer are used in any one of the layers. It is uniformly contained without using a capsule, the polymerizable compound and the hydrophobic polymer are contained in the same layer to form a curable layer, and the curable layer is adjacent to the curable layer. A photosensitive material provided with a hydrophilic layer containing a hydrophilic polymer can be used. In the method for producing a printing plate using a photopolymerization initiator, after curing the polymerizable compound by exposure, the hydrophilic layer is removed from the curable layer, the uncured portion of the curable layer is removed using an eluent, The remaining cured image is used as the image on the printing plate.

[0005]

DISCLOSURE OF THE INVENTION The inventor of the present invention relates to a light-sensitive material which can be preferably used for producing a printing plate.
Further research was advanced. In the above light-sensitive material, a curable layer containing a polymerizable compound and a hydrophobic polymer and a hydrophilic layer containing a hydrophilic polymer are provided adjacent to each other. Therefore, the adhesive force between these two layers is generally weak, and there is a problem that the photosensitive material is destroyed by peeling at the interface between the two layers in handling the photosensitive material. For example, when the photosensitive material is cut with a cutter, when the surface of the photosensitive material is strongly rubbed, or when the photosensitive material is taken up in a roll or stacked and then taken out from a roll or a laminate, Is applied to cause peeling between the above two layers.

An object of the present invention is to provide a light-sensitive material in which the adhesive force between a curable layer and a hydrophilic layer is strengthened and peeling hardly occurs.

[0007]

The above objects have been achieved by the following light-sensitive materials (1) and (2). (1) Two or more layers are provided on a support, and a silver halide, a reducing agent, a polymerizable compound, a base precursor, a hydrophobic polymer having an acidic group and a hydrophilic polymer,
It is uniformly contained in any layer without using microcapsules, the polymerizable compound and the hydrophobic polymer are contained in the same layer to form a curable layer, and A photosensitive material, wherein a hydrophilic layer containing the hydrophilic polymer is provided adjacent to the layer, wherein the curable layer or the hydrophilic layer further contains amino alcohol.

(2) Two or more layers are provided on a support, and a photopolymerization initiator, a polymerizable compound, a hydrophobic polymer having an acidic group, and a hydrophilic polymer have microcapsules in either layer. It is contained uniformly without use, the polymerizable compound and the hydrophobic polymer are contained in the same layer to form a curable layer, and the hydrophilic compound is adjacent to the curable layer. A photosensitive material provided with a hydrophilic layer containing a polymer, wherein the curable layer or the hydrophilic layer further contains amino alcohol.

The light-sensitive materials (1) and (2) described above can be implemented in the following modes (3) to (6). (3) The photosensitive material according to (1) or (2), wherein the amino alcohol is a compound represented by the following formula (I).

[0010]

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In the formula, R ¹ is an alkylene group or a divalent group in which two or more alkylene groups are linked by an ether bond; R ² and R ³ are each a hydrogen atom or an alkyl group; The alkylene group and the alkyl group may have a substituent. (4) The amino alcohol is contained in the curable layer, and the amount of amino alcohol in the curable layer is 0.1 to 30% by weight of the amount of the hydrophobic polymer. (1) or (2) Photosensitive material. (5) The amino alcohol is contained in the hydrophilic layer, and the amount of amino alcohol in the hydrophilic layer is 0.1 to 30% by weight of the amount of the hydrophilic polymer. (1) or (2) Photosensitive material. (6) The photosensitive material according to (1), wherein the hydrophilic layer containing the hydrophilic polymer further contains silver halide and functions as a photosensitive layer. (7) The photosensitive material according to (2), wherein the curable layer containing the polymerizable compound and the hydrophobic polymer further contains a photopolymerization initiator and functions as a photosensitive curable layer.

[0012]

When the amino alcohol is added to the curable layer or the hydrophilic layer according to the present invention, the adhesive force between the curable layer and the hydrophilic layer is significantly enhanced. The following two reasons can be inferred for the action of amino alcohol. (A) The hydroxyl group of amino alcohol strongly interacts with the hydrophilic polymer in the hydrophilic layer, and at the same time, the amino group of amino alcohol forms a salt with the acidic group of the hydrophobic polymer in the curable layer, or electrostatically. Interacts with and strengthens the adhesive force. (B) When the amino group of amino alcohol forms a salt with the acidic group of the hydrophobic polymer in the curable layer, the hydrophobic polymer becomes hydrophilic, and this partially diffuses and permeates into the hydrophilic layer. , The two layers of polymer are entangled, resulting in enhanced adhesion between the two layers. Since the adhesive force between the curable layer and the hydrophilic layer is strengthened by the action of the amino alcohol as described above, the photosensitive material of the present invention hardly breaks due to peeling between the two layers.

[0013]

DETAILED DESCRIPTION OF THE INVENTION The light-sensitive material of the present invention is characterized in that amino alcohol is added to a curable layer or a hydrophilic layer. The amino alcohol in the present specification means an organic compound having an amino group and an alcoholic hydroxyl group in the same molecule, as in the general definition in organic chemistry. An alcoholic hydroxyl group is a hydroxyl group that is bonded to an aliphatic hydrocarbon (not aromatic). In the present invention, like the hydroxyl group, the amino group is preferably bound to the aliphatic hydrocarbon. A plurality of amino groups and alcoholic hydroxyl groups may be present in the same molecule.
A preferred amino alcohol is a compound represented by the following formula (I).

[0014]

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In the formula, R ¹ is an alkylene group or a divalent group in which two or more alkylene groups are linked by an ether bond. R ² and R ³ are each a hydrogen atom or an alkyl group. The alkylene group and the alkyl group may have a substituent. The alkylene group and the alkyl group may be linear, branched, or cyclic. Examples of the substituent of the alkylene group and alkyl group include (alcoholic) hydroxyl group, amino group, substituted amino group, alkoxy group, substituted alkoxy group, aryl group, substituted aryl group, aryloxy group and substituted aryloxy group. included. Two or more compounds represented by formula (I) may be combined to form a polymer. For example, polymers with alcoholic hydroxyl groups (eg polyvinyl alcohol, cellulose)
In addition, a derivative having an amino group introduced as a substituent can also be used as the amino alcohol in the present invention. Specific examples of amino alcohol are shown below.

[0016]

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[0017]

[Chemical 4]

[0018]

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[0019]

[Chemical 6]

[0020]

[Chemical 7]

[0021]

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[0022]

[Chemical 9]

[0023]

[Chemical 10]

As an example in which the amino alcohol forms a polymer, a polymer in which a polymer having an alcoholic hydroxyl group (eg, polyvinyl alcohol, cellulose derivative) is substituted with an amino group can be mentioned. The molecular weight of amino alcohol is preferably in the range of 500,000 to 500,000. Amino alcohol is added to the curable layer or hydrophilic layer. Amino alcohol may be added to both the curable layer and the hydrophilic layer. When the amino alcohol is added to the curable layer, the amount of amino alcohol in the curable layer is 0.1 to 3 times the amount of the hydrophobic polymer.
0% by weight is preferred, 0.5 to 20% by weight
Is more preferable, and 1 to 10% by weight is the most preferable. When amino alcohol is added to the hydrophilic layer, the amount of amino alcohol in the hydrophilic layer is preferably 0.1 to 30% by weight, and preferably 0.5 to 20% by weight, of the amount of hydrophilic polymer. More preferably, it is most preferably 1 to 10% by weight.

[Layer Structure of Photosensitive Material] The layer structure of the photosensitive material is determined according to the application and the type of the optical sensor. When silver halide is used as an optical sensor, it is preferable to add silver halide to a hydrophilic layer containing a hydrophilic polymer so that the hydrophilic layer functions as a photosensitive layer. The photosensitive layer is preferably provided on the curable layer. Further, the photosensitive material may have a constitution of three or more layers including a curable layer, a photosensitive layer and an overcoat layer. The reducing agent and the base precursor can be added to any layer. The amino alcohol and base precursor can be added in different layers. When using a photopolymerization initiator as an optical sensor,
It is preferable to add a photopolymerization initiator to the curable layer so that the curable layer functions as a photosensitive curable layer. The hydrophilic layer containing the hydrophilic polymer is preferably provided on the curable layer as an overcoat layer. Specifically, the hydrophilic layer can function to block oxygen in the air (having a polymerization inhibiting action) and protect the curable layer. The above components are uniformly contained in the layer without using microcapsules. The photosensitive material may be provided with a functional layer other than the above. Other functional layers include an adhesive layer, a release layer and an undercoat layer.

[Support] As the material of the support, paper, synthetic paper, synthetic resin (eg, polyethylene, polypropylene,
Polystyrene laminated paper, plastic film (eg polyethylene terephthalate, polycarbonate, polyimide, nylon, cellulose triacetate), metal plate (eg aluminum, aluminum alloy,
Zinc, iron, copper), paper or plastic film in which these metals are laminated or vapor-deposited can be used. When the light-sensitive material is used for producing a lithographic printing plate, preferable support materials are aluminum plate, polyethylene terephthalate film, polycarbonate film, paper and synthetic paper. A composite sheet in which an aluminum sheet is laminated on a polyethylene terephthalate film is also preferable. Aluminum plates are particularly preferred.

The case where the aluminum plate is used as the support will be further described. The aluminum support is subjected to surface treatment such as surface roughening treatment (graining treatment) or surface hydrophilization treatment, if necessary. The surface roughening treatment is performed by an electrochemical graining method (for example, a method in which a current is applied to an aluminum plate in a hydrochloric acid or nitric acid electrolytic solution to grain the grain) and / or a mechanical graining method. (For example, a wire brush grain method of scratching an aluminum surface with a metal wire, a ball grain method of sanding the aluminum surface with a polishing ball and an abrasive, and a brush grain method of sanding the surface with a nylon brush and an abrasive. Law).

Next, the grained aluminum plate is chemically etched with acid or alkali. An industrially advantageous method is etching using an alkali. Examples of alkaline agents include sodium carbonate, sodium aluminate, sodium metasilicate, sodium phosphate, sodium hydroxide, potassium hydroxide and lithium hydroxide. The concentration of the alkaline solution is preferably in the range of 1 to 50% by weight. The temperature of alkali treatment is preferably in the range of 20 to 100 ° C. Furthermore, it is preferable to adjust the treatment conditions so that the amount of aluminum dissolved is 5 to 20 g / m ² . Usually, after alkaline etching, the aluminum plate is washed with acid to remove stains (smuts) left on the surface.
Preferred acids are nitric acid, sulfuric acid, phosphoric acid, chromic acid, hydrofluoric acid and borofluoric acid. The smut removal treatment after the electrochemical graining treatment can be carried out by a known method such as a method of contacting with sulfuric acid having a concentration of 15 to 65% by weight at 50 to 90 ° C.

The aluminum plate surface-roughened as described above may be subjected to anodizing treatment or chemical conversion treatment, if necessary. The anodizing treatment can be performed by a known method. Specifically, in an acid solution,
A direct current or an alternating current is applied to the aluminum plate to form an anodized film on the aluminum surface. Examples of acids include sulfuric acid, phosphoric acid, chromic acid, oxalic acid, sulfamic acid and benzene sulfonic acid. Anodizing conditions vary depending on the electrolyte solution used. Generally, the concentration of the electrolytic solution is 1 to 80% by weight, the temperature of the electrolytic solution is 5 to 70 ° C., and the current density is 0.5.
It is preferable that the range is from 60 to 60 amps / dm ² , the voltage is from 1 to 100 v, and the electrolysis time is from 10 to 100 seconds. Particularly preferred anodizing methods are a method of anodizing in sulfuric acid at a high current density and a method of anodizing phosphoric acid as an electrolytic bath. After the anodizing treatment, the aluminum plate may be subjected to an alkali metal silicate treatment (for example, a treatment of immersing the aluminum plate in an aqueous sodium silicate solution). An undercoat layer may be provided on the surface of the support in order to improve the adhesion between the aluminum support and the curable layer and the printing characteristics.

[Undercoat layer] As a component constituting the undercoat layer, a polymer (eg, casein, polyvinyl alcohol, ethyl cellulose, phenol resin, styrene-maleic anhydride resin, polyacrylic acid); amine (eg, monoethanolamine, Diethanolamine, triethanolamine, tripropanolamine) and their hydrochlorides; monoaminomonocarboxylic acids (eg oxalates,
Phosphate, aminoacetic acid, alanine); Oxyamino acid (eg, serine, threonine, dihydroxyethylglycine); Sulfur-containing amino acid (eg, cysteine, cystine); Monoaminodicarboxylic acid (eg, aspartic acid, glutamic acid); Diaminomono Carboxylic acid (eg, lysine); Amino acid having aromatic nucleus (eg, p-hydroxyphenylglycine, phenylalanine, anthranil); Aliphatic aminosulfonic acid (eg, sulfamic acid, cyclohexylsulfamic acid); and (poly) aminopolyacetic acid (Eg,
And ethylenediaminetetraacetic acid, nitrilotriacetic acid, iminodiacetic acid, hydroxyethyliminodiacetic acid, hydroxyethylethylenediamineacetic acid, ethylenediaminediacetic acid, cycloethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, glycol etherdiaminetetraacetic acid). It is also possible to use a compound in which some or all of the acid groups of the above compounds are salts (eg, sodium salt, potassium salt, ammonium salt). The above components may be used in combination of two or more.

[Hydrophilic layer and photosensitive layer] The hydrophilic layer is
It is provided adjacent to the curable layer containing a hydrophilic polymer.
When silver halide is used as an optical sensor, it is preferable to add silver halide to a hydrophilic layer containing a hydrophilic polymer so that the hydrophilic layer functions as a photosensitive layer. The photosensitive layer generates radicals by imagewise exposure and thermal development. The generated radicals diffuse and enter the curable layer to cure the curable layer. The thickness of the hydrophilic layer (and the photosensitive layer containing silver halide) is preferably 0.1 to 20 μm, more preferably 0.5 to 10 μm.

[Curable Layer and Photosensitive Curable Layer] The curable layer contains a polymerizable compound and a hydrophobic polymer having an acidic group. To obtain an image with a high degree of curing (strength),
The hydrophobic polymer preferably has crosslinkability.
When the photopolymerization initiator is used as an optical sensor, it is preferable to add the photopolymerization initiator to the curable layer so that the curable layer functions as a photosensitive curable layer. The thickness of the curable layer (and the photosensitive curable layer containing a photopolymerization initiator) is preferably 0.1 to 20 μm, more preferably 0.3 to 7 μm.

[Overcoat Layer] The overcoat layer has a function of protecting the light-sensitive material and preventing the ingress of oxygen in the air to enhance the curing degree of the curable layer. Further, the overcoat layer is a component that accelerates image formation (eg,
A base precursor, a reducing agent, a thermal development accelerator) can be included. The overcoat layer may further contain a matting agent. The matting agent reduces the tackiness of the surface of the photosensitive material and prevents adhesion when the photosensitive materials are stacked. When the photopolymerization initiator is used as an optical sensor, the hydrophilic layer adjacent to the curable layer can function as an overcoat layer. The overcoat layer is generally formed by using a hydrophilic polymer. The thickness of the overcoat layer is 0.3
To 20 μm, preferably 0.5 to 10 μm
m is more preferable, and 0.7 to 5 μm is most preferable.

[Intermediate Layer] An intermediate layer can be provided between the layers. The intermediate layer can also function as an antihalation layer or a barrier layer. The barrier layer has a function of preventing components from moving between layers and diffusing or mixing during storage of the light-sensitive material. The material of the intermediate layer is determined according to the application. You may use the hydrophilic polymer used for a photosensitive layer and an overcoat layer. A hydrophilic layer provided adjacent to the curable layer can also function as an intermediate layer. The thickness of the intermediate layer is preferably 10 μm or less.

[Silver Halide] As the silver halide,
Grains of silver chloride, silver bromide, silver iodide, or silver chlorobromide, silver chloroiodide, silver iodobromide, and silver chloroiodobromide can be used. The shape of the silver halide grains is preferably cubic or tetradecahedral, but not limited to those having a regular crystal form, those having an irregular crystal form, or a composite form thereof. Anomalous crystal forms include potato, spherical, plate and plate crystal forms. In tabular grains, the grain size is generally 5 times or more the grain thickness. There is no particular limitation on the grain size of silver halide. Fine particles of 0.01 μm or less can also be used. On the other hand, large particles of about 10 μm can also be used. Regarding the grain size distribution, monodisperse grains are preferable to polydisperse emulsions. For monodisperse emulsions, see US Pat.
628, 3655394 and British Patent 1413.
No. 748 is described in each specification.

The crystal structure of the silver halide grains may be uniform or may have different halogen compositions inside and outside. It may have a layered structure. Further, silver halides having different compositions may be joined by epitaxial joining. Further, it may be bonded to a compound other than silver halide. Examples of compounds other than silver halide include silver rhodanide and lead oxide. The silver halide grains may contain salts of other elements. Examples of other elements include copper, thallium, lead, bismuth, cadmium, zinc, chalcogen (eg, sulfur, selenium, tellurium), gold and Group VIII noble metals (eg, rhodium, iridium, iron, platinum, palladium). Can be mentioned. Salts of these elements can be added during or after the formation of silver halide grains and included in the grains. Specific methods are described in U.S. Pat. Nos. 1,195,432, 1,195,933, 2,448,060 and 26,281.
No. 67, No. 2950972, No. 3488709, No. 3737313, No. 3772031, No. 42699.
No. 27 and Research Disclosure (RD), Vol. 134, No. 27. 13452 (June 1975).

Iridium ions can be introduced into silver halide grains by adding an aqueous solution of an iridium compound to the emulsion during the preparation of the silver halide emulsion. Examples of water-soluble iridium compounds include hexachloroiridium (III) acid salts and hexachloroiridium (IV) acid salts. Similarly, rhodium ions may be introduced into the silver halide grains by adding an aqueous solution of a rhodium compound to the emulsion. Examples of water-soluble rhodium compounds include rhodium ammonium chloride, rhodium trichloride and rhodium chloride. The iridium compound or rhodium compound may be used by dissolving it in an aqueous solution of a halide for forming silver halide grains. Further, the aqueous solution of the iridium compound or the rhodium compound may be added before the particles are formed or may be added while the particles are formed. Further, it may be added between the grain formation and the chemical sensitization treatment. It is particularly preferred to add it while the particles are being formed. Iridium ion or rhodium ion is preferably used in an amount of 10 ^{−8 to} 10 ⁻³ mol, and more preferably 10 ^{−7 to} 10 ⁻⁵ mol, per mol of silver halide. In addition, when using a rhodium compound and an iridium compound together, it is preferable that the former use is performed before the latter use.

Two or more kinds of silver halide grains having different halogen compositions, crystal habits, and grain sizes can be used in combination. It is preferable to use silver halide as an emulsion. The silver halide emulsion is described in Research Disclosure (RD) No. 17643 (December 1978)
Mon., pp. 22-23, "I. Emulsion prepa
ration and types) ", and No. 18716 (19)
(November 1979), p.648. The silver halide emulsion is usually subjected to chemical sensitization after physical ripening, but chemical sensitization may not be performed. It is preferred to use silver halide grains having a relatively low fog value. Additives used in such processes are described in Research Disclosure, No. 17643 and No. 17643. 18716. No. for chemical sensitizers. 17643 (page 23) and No. 187
16 (page 648, right column). In addition, other known additives other than those mentioned above are
It is described in Disclosure Magazine. For example, regarding the sensitivity enhancer, No. 18716 (page 648, right column)
No. 1 for antifoggants and stabilizers. 176
43 (pages 24 to 25) and No. 18716 (Page 649, right column).

The silver halide emulsion is usually used after spectral sensitization. The sensitizing dye used in the light-sensitive material may be a silver halide sensitizing dye known in the photographic art and the like. Examples of sensitizing dyes include cyanine dyes, merocyanine dyes, complex merocyanine dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes and hemioxonol dyes. Spectral sensitizing dyes are used for various lasers (eg, semiconductor laser,
Helium-neon laser, argon-ion laser, helium-cadmium laser, YAG laser) and light-emitting diodes can be used to adapt the spectral sensitivity of the photosensitive material to different light source wavelengths. For example, plural kinds of spectral sensitizing dyes having different spectral wavelengths are applied to the same light-sensitive layer or silver halide in different light-sensitive layers to enable writing to the same light-sensitive material using light sources having different wavelengths. You can also Along with the sensitizing dye, a dye having no spectral sensitizing effect or a compound that does not substantially absorb visible light and exhibits supersensitization (supersensitizer) may be added to the emulsion. Good.

[Organic metal salt] In addition to the silver halide, an organic metal salt can be added to the light-sensitive material. As such an organic metal salt, it is particularly preferable to use an organic silver salt. The organic compound used to form the organic silver salt, triazoles, tetrazoles, imidazoles, indazoles, thiazoles, thiadiazoles, azaindenes, aliphatic having a mercapto group as a substituent, aromatic or Heterocyclic compounds can be mentioned. Further, a silver salt of carboxylic acid or silver acetylene can be used as the organic silver salt. Two or more kinds of organic silver salts may be used in combination. The organic silver salt is used in an amount of 10 ^{−5 to} 10 mol, preferably 10 ^{−4 to} 1 mol, per mol of silver halide. Further, instead of the organic silver salt, an organic compound constituting the organic silver salt may be added to the photosensitive layer and partially reacted with silver halide in the photosensitive layer to be converted into an organic silver salt.

[Photopolymerization Initiator] The photopolymerization initiator is a compound capable of generating a free radical which can be added to the polymerizable compound upon exposure. When silver halide is not used, a photopolymerization initiator is used as an optical sensor.
For the photopolymerization initiator, see “Chemical Revie” by Oster et al.
w ”p. 125-151, 68, 1968, Kosa
"Light-Sensitive System" by John Wiley & Sons,
Pp. 158-193, 1965), JP-A-61-1753.
42 and Japanese Patent Laid-Open No. 2-207254. Examples of the photopolymerization initiator include carbonyl compounds, halogen-containing compounds, redox couples of photoreducible dyes and reducing agents, organic sulfur compounds, peroxides, optical semiconductors and metal compounds. The photopolymerization initiator is preferably used in the range of 0.001 to 0.5 g, and more preferably 0.01 to 0.2 g, per 1 g of the polymerizable compound.

[Reducing Agent] The reducing agent has a function of reducing silver halide or a function of accelerating (or suppressing) the polymerization of the polymerizable compound. There are various kinds of substances as the reducing agent having the above function. Examples of the reducing agent include hydroquinones, catechols, p-aminophenols,
p-phenylenediamines, 3-pyrazolidones, 3-
Aminopyrazoles, 4-amino-5-pyrazolones,
5-aminouracils, 4,5-dihydroxy-6-aminopyrimidines, reductones, aminoreductones, o- or p-sulfonamidophenols, o-
Or p-sulfonamidonaphthols, 2,4-disulfonamidophenols, 2,4-disulfonamidonaphthols, o- or p-acylaminophenols, 2-sulfonamidoindanones, 4-sulfonamido-5 -Pyrazolones, 3-sulfonamidoindoles, sulfonamide pyrazolobenzimidazoles,
Included are sulfonamide pyrazolotriazoles, α-sulfonamido ketones and hydrazines.

The above reducing agent is disclosed in JP-A-61-18364.
No. 0, No. 61-188535, No. 61-228441
No. 62-70836, 62-86354, 62-86355, 62-206540, 62.
-264041, ibid. 62-109437, ibid. 63-
254442, JP-A-1-267536, 2-1.
No. 41756, No. 2-141757, No. 2-2072.
No. 54, No. 2-262662, and No. 2-269352 (including those described as a developer or a hydrazine derivative). Regarding the reducing agent, see “The Theory of the Photographic Pro” by T. James.
cess ”4th edition, pages 291-334 (1977), Research Disclosure, Vol. 170, 1702.
No. 9, pp. 9-15 (June 1978), and ibid.
Vol. 176, No. 17643, pages 22-31, (197
(December 8th). Also, JP-A-62-210
As in the light-sensitive material described in Japanese Patent No. 446, a reducing agent precursor that releases the reducing agent under heating conditions, contact with a base, or the like may be used instead of the reducing agent.

Of these reducing agents, those which have a basicity to form a salt with an acid can also be used in the form of a salt with a suitable acid. These reducing agents may be used alone, or as described in each of the above publications, two or more reducing agents may be used in combination. When two or more reducing agents are used in combination, the reducing agents may interact with each other by first promoting the reduction of silver halide (and / or organic silver salt) by so-called superadditivity. Cause the polymerization of the polymerizable compound via an oxidation-reduction reaction with another reducing agent in which the oxidant of the first reducing agent produced by reduction of silver halide (and / or organic silver salt) coexists (Or suppressing polymerization) is considered. However,
In actual use, it is difficult to specify which of the above actions because the above reactions can occur simultaneously. The reducing agent is preferably used in the range of 0.1 to 10 mol, and more preferably in the range of 0.25 to 2.5 mol, per mol of silver halide.

By adjusting the kind and amount of the above reducing agent, the polymerizable compound in the portion where the latent image of silver halide is formed or the portion where the latent image is not formed is selectively polymerized. be able to. The reducing agent develops silver halide and is itself oxidized to an oxidant. When the oxidant of this reducing agent decomposes in the layer to generate radicals,
Polymerization occurs in the area where the latent image of silver halide is formed. Examples of such reducing agents include hydrazines. On the other hand, when the oxidant does not generate (or does not easily generate) radicals and the reducing agent itself or the oxidant has a polymerization suppressing function, it is necessary to include a polymerization initiator (radical generator) with the reducing agent. The part where the latent image of silver halide is not formed (when the oxidation inhibitor has a stronger polymerization inhibiting function than the reducing agent) or the latent image is formed (the reducing agent has a polymerization inhibiting function than the oxidizing agent) When it is strong, polymerization occurs. Examples of the reducing agent having the above functions include 1-phenyl-3-pyrazolidones and hydroquinones. In this case, it is necessary to add a thermal polymerization initiator or a photopolymerization initiator as described below to the photosensitive material.

[Polymerization Initiator] The thermal polymerization initiator is a compound capable of decomposing upon heating to generate free radicals which can be added to the polymerizable compound or the crosslinkable polymer. Regarding the thermal polymerization initiator, "Addition Polymerization / Ring-Opening Polymerization" edited by The Society of Polymer Science and the Society for Polymer Experiments Editorial Committee (1983,
Kyoritsu Shuppan), pages 6-18 and JP-A-61-24344.
It is described in Japanese Patent Publication No. 9. Examples of thermal polymerization initiators include azo compounds (eg, azobis (isobutyronitrile), 1,
1'-azobis (1-cyclohexanecarbonitrile)
And peroxides. The photopolymerization initiator is a compound capable of generating a free radical that can be added to the polymerizable compound upon exposure to light. Regarding the photopolymerization initiator, see Oster et al., "Chemical Review", No. 68.
125-151, Volume (1968), by Kosar, "Ligh
t-Sensitive System "(John Wiley & Sons, 1965
Pp. 158-193, JP-A-61-75342 and JP-A-2-207254.
Examples of the photopolymerization initiator include carbonyl compounds, halogen-containing compounds, redox couples of photoreducible dyes and reducing agents, organic sulfur compounds, peroxides, optical semiconductors and metal compounds. The polymerization initiator is preferably used in the range of 0.001 to 0.5 g, and more preferably 0.01 to 0.2 g, per 1 g of the total amount of the polymerizable compound and the crosslinkable polymer.

[Polymerizable Compound] As the polymerizable compound,
A compound capable of addition polymerization by free radicals, particularly a compound having an ethylenically unsaturated group (monomer or oligomer) is used. The polymerizable compound is described in JP-A-5-249667. Examples of the compound having an ethylenically unsaturated group include acrylic acid and salts thereof, acrylic acid esters, acrylamides, methacrylic acid and salts thereof, methacrylic acid esters, methacrylamides, maleic anhydride, maleic acid esters. , Itaconic acid esters, styrenes, vinyl ethers, vinyl esters, N-vinyl heterocycles, allyl ethers, allyl esters and derivatives thereof. Acrylic acid esters or methacrylic acid esters are preferred. Specific examples of acrylic acid esters include pentaerythritol tetraacrylate, trimethylolpropane triacrylate,
Mention may be made of dipentaerythritol hexaacrylate, polyester acrylates and polyurethane acrylates. The polymerizable compound is contained in the curable layer in an amount of preferably 3 to 90% by weight, more preferably 15 to 60% by weight, based on the total amount of the layer. You may use together 2 or more types of polymerizable compounds.

[Hydrophobic Polymer Having Acidic Group] The curable layer contains a hydrophobic polymer having an acidic group. Hydrophobic means substantially insoluble in water (neutral).
Specifically, the solubility in water at 25 ° C. is 1% or less. The solubility is preferably 0.3% or less,
It is more preferably 0.1% or less. Examples of the acidic group contained in the hydrophobic polymer include a carboxyl group, an acid anhydride group, a phenolic hydroxyl group, a sulfonic acid group, a sulfonamide group and a sulfonimide group. Carboxyl groups are particularly preferred. Specifically, monomers of (meth) acrylic acid, styrene sulfonic acid, or maleic anhydride can be copolymerized at the time of synthesizing the polymer described later, and these acidic groups can be incorporated into the polymer of the curable layer. The molar content of the monomer having an acidic group in the copolymer is preferably 1 to 60%, more preferably 5 to 50%,
Most preferably, it is 10 to 40%. The hydrophobic polymer preferably further has crosslinkability. As the crosslinkable polymer, a polymer having an ethylenically unsaturated group in the main chain or side chain of the molecule is preferably used. The crosslinkable polymer may be a copolymer. Examples of the polymer having an ethylenically unsaturated group in the main chain of the molecule include poly-1,4-butadiene and poly-1,4-
Mention may be made of isoprene, natural and synthetic rubber. Examples of polymers having an ethylenically unsaturated group in the side chain of the molecule include poly-1,2-butadiene and poly-1,2-isoprene.

Further, a polymer of an ester or amide of acrylic acid or methacrylic acid, to which a specific residue (R group of --COOR or --CONHR) is bonded, can be used as the crosslinkable polymer. Examples of the specific residue (R group) include-(CH ₂ ) _n -CR ¹ = CR ² R
³ ,-(CH ₂ O) _n -CH ₂ CR ¹ = CR ² R ³ ,-(CH ₂ CH ₂ O) _n -CH ₂ CR ¹ = CR ²
R ³ ,-(CH ₂ ) _n -NH-CO-O-CH ₂ CR ¹ = CR ² R ³ ,-(CH ₂ ) _n -O-CO-CR ¹
= CR ² R ³ and-(CH ₂ CH ₂ O) ₂ -X (R ^{1 to} R ³ are each a hydrogen atom, a halogen atom, an alkyl group having 1 to 20 carbon atoms, an aryl group, an alkoxy group, or aryl. Is an oxy group, R ¹ and R ² or R ³ may combine with each other to form a ring, n is an integer of 1 to 10, and X is a dicyclopentadienyl residue). Can be mentioned. Specific examples of the ester residue, -CH ₂ CH = CH ₂ (JP 64-17
047 JP allyl (meth) corresponding to the polymer of the _{acrylate), - CH 2 CH 2 O} -CH 2 CH = CH 2, -CH 2 C (CH 3) = CH 2,
-CH ₂ CH = CH-C ₆ H ₅ , -CH ₂ CH ₂ OCOCH = CH-C ₆ H ₅ , -CH ₂ CH ₂ -NHCO
O-CH ₂ CH = CH ₂ and -CH ₂ CH ₂ OX (X is a dicyclopentadienyl residue) are included. Specific examples of amide residues include -C
H ₂ CH = CH ₂ , -CH ₂ CH ₂ -1-Y (Y is a cyclohexene residue) and -CH ₂ CH ₂ -OCO-CH = CH ₂ are included.

In the crosslinkable polymer as described above, free radicals (polymerization initiation radicals or growing radicals during the polymerization process of the polymerizable compound) are added to its unsaturated bond group to directly polymerize or polymerize the polymerizable compound. Addition polymerization is carried out through chains, and crosslinks are formed between polymer molecules to cure. Alternatively, atoms in the polymer (eg, hydrogen atoms on the carbon atom adjacent to the unsaturated bond group) are abstracted by free radicals to form polymer radicals, which bond to each other to form crosslinks between polymer molecules. Is cured. Examples of non-crosslinkable polymers (polymers that are not crosslinkable or weakly crosslinkable) are polyacrylic acid ester, polymethacrylic acid ester, polyvinyl acetate, polyvinyl chloride, polyvinylidene chloride, polyacrylonitrile, polymethacryloyl ester. Nitrile, polyethylene, polyvinyl pyridine, polyvinyl imidazole, polyvinyl butyral, polyvinyl formal, polyvinyl pyrrolidone, chlorinated polyethylene, chlorine polypropylene, polyester, polyamide, polyurethane,
Mention may be made of polycarbonate, ethyl cellulose, triacetyl cellulose, diacetyl cellulose and cellulose acetate butyrate. Among the repeating units of these polymers, copolymerizable units can be arbitrarily combined and used as a copolymer.

Specific examples of non-crosslinkable polymers include:
Addition polymerization type synthetic homopolymers and copolymers (eg,
Mention may be made of homopolymers and copolymers of various vinyl monomers), synthetic homopolymers and copolymers of the polycondensation type (eg polyesters, polyamides, polyurethanes, polyester-polyamides). In the present invention, the crosslinkable or non-crosslinkable polymer as described above,
The acidic group described above is introduced and used. The molecular weight of the hydrophobic polymer is preferably in the range of 1,000 to 500,000. You may use together 2 or more types of polymers. The amount of the hydrophobic polymer is preferably 10 to 90% by weight, more preferably 30 to 80% by weight, based on the entire curable layer.

[Hydrophilic Polymer] The hydrophilic layer (including the photosensitive layer and the overcoat layer) provided adjacent to the curable layer contains a hydrophilic polymer as a binder. The hydrophilic polymer is a polymer compound having a hydrophilic group or a hydrophilic bond in the molecular structure. Examples of hydrophilic groups include carboxyl, alcoholic hydroxyl group, phenolic hydroxyl group, sulfo, sulfonamide group, sulfonimide and amide. Examples of hydrophilic bonds include urethane bonds, ether bonds and amide bonds. It is preferable to use a water-soluble polymer or a water-swellable polymer as the hydrophilic polymer. A water-swellable polymer is one that has an affinity for water but is not completely soluble in water due to the cross-linked structure of the polymer. As the water-soluble or water-swellable polymer, natural, synthetic or semi-synthetic polymer compounds can be used. For hydrophilic polymers, see JP-A-5-24
It is described in Japanese Patent No. 9667. Polyvinyl alcohol is a particularly preferred hydrophilic polymer. Polyvinyl alcohol having various degrees of saponification can be used. However,
In order to reduce the oxygen transmission rate, saponification degree should be 50%.
It is necessary to be at least 80%, preferably at least 80%, more preferably at least 90%, most preferably at least 95%. Copolymer modified polyvinyl alcohol can also be used. Copolymerization modification is a method of synthesizing modified polyvinyl alcohol by saponifying a copolymer of vinyl acetate and another monomer. Examples of copolymerizable monomers include ethylene, higher vinyl carboxylates, higher alkyl vinyl ethers, methyl methacrylate and acrylamide.

Post-modified polyvinyl alcohol can also be used. The post-modification is a method in which a compound having reactivity with a hydroxyl group of polyvinyl alcohol is used and then modified by a polymer reaction after the synthesis of polyvinyl alcohol. Specifically, the hydroxyl group of polyvinyl alcohol is modified by etherification, esterification or acetalization. Furthermore, crosslinked polyvinyl alcohol can also be used. As the crosslinking agent, an aldehyde, a methylol compound, an epoxy compound, a diisocyanate, a divinyl compound, a dicarboxylic acid or an inorganic crosslinking agent (eg boric acid, titanium, copper) can be used. The molecular weight of the hydrophilic polymer is preferably in the range of 3000 to 500,000. The amount of hydrophilic polymer used is 0.05
To 20 g / m ² , preferably 0.1 to 1
More preferably, it is 0 g / m ² . When gelatin is used in combination with another hydrophilic polymer in the layer containing silver halide, the pH of the layer containing silver halide is 1.2 or less or 1.2 or more than the isoelectric point of gelatin. It is preferable to adjust

[Base Precursor] As the base precursor, precursors of inorganic bases and organic bases (decarboxylation type, thermal decomposition type, reaction type, complex salt forming type, etc.)
Can be used. Examples of preferable base precursors include salts of organic acids and bases that are decarboxylated by heating (JP-A-63 / 1988).
-316760, 64-68746, 59-1
80537 and 61-313431) and urea compounds (described in JP-A-63-96159) that release a base upon heating. Further, as a method of releasing a base by utilizing a reaction, a reaction with a transition metal acetylide or a salt containing an anion having an affinity higher than that of the acetylide anion for the transition metal ion (described in JP-A-63-25208) Or a basic metal compound which is poorly soluble in water and a compound capable of undergoing a complex formation reaction with a metal ion constituting the basic metal compound in water as a medium, and between these two compounds in the presence of water. Of releasing a base by the reaction of
-3282 gazette). The base precursor preferably releases the base at 50 to 200 ° C, more preferably 80 to 160 ° C. The base precursor is preferably used in the range of 0.1 to 20 mol per mol of silver halide,
The range is more preferably 0.2 to 10 mol.

[Heat Development Accelerator] The photosensitive material may contain a heat development accelerator in any of the layers in order to accelerate the heat development and perform the heat development processing in a shorter time. The thermal development accelerator may be a compound having a plasticizing action at room temperature or upon heating with respect to the binder used in any layer of the light-sensitive material, or a compound having no plasticizing action but capable of being melted in the layer by heating. Any of these can be used. As the compound having a plasticizing effect on the binder used in any layer of the light-sensitive material at room temperature or at the time of heating, all known compounds known as plasticizers for polymer compounds can be used. As such a plasticizer,
"Plastic compounding agents" Taiseisha, P21-63; "Plastics Additives, 2nd edition"
2nd Edition) Hanser Publishers, Chap.5 P251-296;
"Thermoplastic Additives" (Thermoplas
tics Additives) Marcel Dekker Inc. Chap. 9 P345-37
9; "Plastics Additives An Industri"
al Guide) Noyes Publications, Section-14 P333-485
"The Technology of Solvents and
The Plasticizers "(The Technology of Solvents
and Plasticizers) John Wiley & Sons Inc. Chap.15
P903-1027); "Industrial Plasticizers, Pergamon Press"
); "Plasticizer Technology Volume 1" (P
lasticizer Technology Vol.1, Reinhold Publishing C
orp.); "Plasticization and Plusizer Process" (Plusticization and Plu
The plasticizers described in sticizer Process, American Chemistry) can be used. Preferred thermal development accelerators include glycols (eg, ethylene glycol, polyethylene glycol), polyhydric alcohols (eg, glycerin, butanediol, hexanediol), sugars, formic acid esters,
Examples thereof include ureas (eg, urea, diethylurea, ethyleneurea, propyleneurea), urea resins, phenol resins, amide compounds (eg, acetamide, propionamide), sulfamides and sulfonamides.
Further, two or more of the above thermal development accelerators can be used in combination. It is also possible to add it by dividing it into two or more layers. The addition amount of the thermal development accelerator is preferably 0.05 to 2 g / m ² , and 0.1 to 1 g / m 2.
More preferably, it is ² .

[Colorant] A colorant may be added to the light-sensitive material for the purpose of preventing halation and irradiation or coloring the cured image. As the colorant, known pigments and dyes can be used as long as they do not significantly impede the curing reaction of the curable layer or significantly impair the photosensitivity and developability of silver halide. When using a colorant for the purpose of preventing halation or coloring the image,
It is preferably added to the curable layer. Further, when it is used for the purpose of preventing irradiation, it is preferably added to the photosensitive layer. When a coloring agent is added to prevent halation and irradiation, it is preferable that the coloring agent can absorb light in the photosensitive wavelength region of silver halide. As the colorant, the pigments or dyes described in JP-A-5-249667, "Color Index Handbook", and "Dye Handbook" (edited by the Society of Synthetic Organic Chemistry, 1975) can be used. Dyes for preventing irradiation which have little influence on sensitivity are disclosed in Japanese Examined Patent Publication No. 41-20389 and 4
No. 3-3504, No. 43-13168, and Japanese Patent Laid-Open No. Hei 2
-39042 and U.S. Pat. No. 3697037.
No. 3,423,207, British Patent Nos. 1030392 and 1100546. The content of the colorant is preferably 0.01 to 2 g / m ² , more preferably 0.05 to 1 g / m ² .

[Antifoggant, Development Accelerator, Stabilizer] In order to improve photographic characteristics, an additive such as an antifoggant, a silver development accelerator that promotes silver development, and a stabilizer is contained in any layer. You may let me. Examples of these include azoles and azaindenes (Research Disclosure N.
o. 17643, pages 24 to 25 (1978)), nitrogen-containing carboxylic acids and phosphoric acids (described in JP-A-59-168442), cyclic amides (described in JP-A-61-151841), thioethers (special JP-A-62-151842), polyethylene glycol derivative (JP-A-62-151843), thiol (JP-A-62-151844), acetylene compound (JP-A-62-87957). ) And sulfonamide (JP-A-62-1782).
No. 32 publication). An aromatic ring (carbon ring or heterocycle) mercapto compound is also preferably used as an antifoggant or a development accelerator. Aromatic heterocyclic mercapto compounds, particularly mercaptotriazole derivatives, are preferred. The mercapto compound may be added to the photosensitive material as a mercapto silver compound (silver salt). The amount of these compounds used is in the range of 10 ^{-7 to} 1 mol per mol of silver halide.

[Development Stopping Agent] Various development stopping agents can be used for the purpose of always obtaining a constant image with respect to the processing temperature and processing time during heat 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 layer to stop development after proper development, or inhibits development by interacting with silver and a silver salt. It is a compound that causes. Specific examples thereof include an acid precursor that releases an acid when heated, an electrophilic compound that causes a substitution reaction with a coexisting base when heated, or a nitrogen-containing heterocyclic compound, a mercapto compound and a precursor thereof. The heat development stopper is described in JP-A-62-253159, JP-A-2-42447 and JP-A-2-262661.

[Surfactant] A surfactant can be added to any layer. Known surfactants can be used as the surfactant. Examples include nonionic activators, anionic activators, cationic activators, fluorine activators, JP-A-2-19.
The surfactant described in Japanese Patent No. 5356 can be mentioned. In particular, sorbitans, polyoxyethylenes, and nitrogen-containing surfactants are preferable.

[Matting Agent] A matting agent may be added to the back layer or the uppermost layer of the light-sensitive material for the purpose of lowering the tackiness of the front or back surface of the light-sensitive material and preventing adhesion when the light-sensitive materials are stacked. it can. As the matting agent, inorganic or organic solid particles that can be dispersed in a hydrophilic polymer are used. Such grains are well known in the ordinary silver salt photography art. Examples of materials for the matting agent include oxides (eg, silicon dioxide), alkaline earth metal salts, natural polymers (eg, starch, cellulose) and synthetic polymers. The particle size of the matting agent is 1 to 50
The range of μm is preferred. Matting agent is 0.01 to 1 g
It is preferably used in the range of 0.1 / m ² and 0.1 to 0.
It is more preferable to use it in the range of 7 g / m ² .

[Polymerization Inhibitor] A polymerization inhibitor may be added to the curable layer in order to prevent the polymerizable compound from polymerizing during storage of the light-sensitive material. Conventionally known polymerization inhibitors can be used. Examples of the polymerization inhibitor include nitrosamine compounds, urea compounds, thiourea compounds, thioamide compounds, phenol derivatives and amine compounds.

[Exposure Step] Image exposure is carried out by using a light source which emits light having a wavelength corresponding to the spectral sensitivity of a silver halide (sensitizing dye) or a photopolymerization initiator which is a photosensor. When the silver halide is a photosensor, various light sources can be used. Examples of light sources that can be used for silver halide include tungsten lamps, halogen lamps, xenon lamps, xenon flash lamps, mercury lamps, carbon arc lamps and other lamps, various lasers (eg, semiconductor lasers, helium neon lasers,
Examples thereof include an argon ion laser, a helium cadmium laser, a YAG laser), a light emitting diode, and a cathode ray tube. The exposure wavelength is generally visible light, near-ultraviolet light, or near-infrared light, but X-rays or electron beams may be used. When the photopolymerization initiator is an optical sensor,
The same light source as above is used, but in particular ultra high pressure, high pressure,
Medium and low pressure mercury lamps, chemical lamps, carbon arc lamps, xenon lamps, metal halide lamps, and various visible and ultraviolet lasers are preferable. The amount of exposure is determined by the sensitivity of the optical sensor. When the silver halide is an optical sensor, it is generally 0.01 to 10000 ergs / cm.
² , more preferably 0.1 to 1000 erg / cm ²
Range. When the photopolymerization initiator is an optical sensor, it is generally in the range of 10 ² to 10 ⁷ ergs / cm ² , and more preferably 10 ³ to 10 ⁵ erg / cm ² . When the support is transparent, it is also possible to expose through the support from the back side of the support.

In general, the process of exposing silver halide, that is, the process of forming a latent image, is affected by temperature and humidity during exposure,
It is known that the sensitivity of photosensitive materials changes. Therefore, it is desirable that the temperature and humidity of the atmosphere of the light-sensitive material and the light source at the time of exposure are controlled within a constant range as much as possible. Specific adjusting means of the image recording apparatus for achieving the above object is disclosed in JP-A-3-63143 and JP-A-3-63143.
It is described in each publication of No. -63637. In the image formation using silver halide as an optical sensor, 5 to 40 ° C.
It is preferable to set one point in the range (preferably 10 to 35 ° C.) as a set temperature and control the temperature within ± 5 ° C. from the set temperature. It is preferable to similarly control the atmospheric humidity in the apparatus including the photosensitive material and the optical system. The humidity is preferably in the range of 10 to 80% (relative humidity), more preferably in the range of 15 to 75%, and 2
The range of 5 to 70% is the most preferable.

In a light-sensitive material using a photopolymerization initiator as an optical sensor, the above-mentioned image exposure causes the polymerizable compound to polymerize to form a cured image. For a light-sensitive material using silver halide as an optical sensor, the following development processing is performed,
Form a cured image.

[Development Processing] The development of the light-sensitive material is generally carried out by a dry method (heat development) by heating. However, a wet development process using a developing solution may be adopted. The thermal development can be carried out by a method of bringing the light-sensitive material into close contact with a heated object (for example, a metal plate, a block, a roller), a method of immersing it in a heated liquid, a method of irradiating infrared rays, or the like. The heating temperature is 60 to 200 ° C., more preferably 10
It is in the range of 0 to 150 ° C. Heating time is 1 to 180
Seconds, more preferably 5 to 60 seconds. The photosensitive material may be preheated at a temperature higher than the main heating temperature for a short time before the exposure step or after the exposure step, or may be postheated after the main heating. Pre-heating or post-heating can improve the sensitivity and the curing degree of the image. The post-heating may be performed after the post-treatment of image formation, for example, after the elution step. When a cured image is formed by utilizing the polymerization inhibiting action of the reducing agent or its oxidant, it is necessary to uniformly generate radicals from the polymerization initiator. When a thermal polymerization initiator is used, radicals can be generated by heating at the time of thermal development, so heating is required only once. When a photopolymerization initiator is used, it is necessary to expose the entire surface after thermal development in order to generate radicals. The light at this time must have a wavelength that can be absorbed by the photopolymerization initiator. The light source can be appropriately selected from those exemplified as the light source used for the image exposure.
The exposure dose is in the range of 10 ^{3 to} 10 ⁷ ergs / cm ² . A cured image can be formed on the photosensitive material by the above heat development step.

[Removing Step] In the removing step, the uncured portion of the curable layer is removed. The hydrophilic layer is preferably removed before removing the curable layer. Removal of the hydrophilic layer can be easily carried out using water (preferably warm water). The removal process includes a method using an eluate and a method using a removal sheet. First, the method using the eluate will be described. As the eluent (or etching solution) for removing the uncured portion, any solvent can be used as long as it can remove the uncured portion of the curable layer. Preferably an alkaline solvent is used. The alkaline solvent is an aqueous solution containing an alkaline compound, an organic solvent containing an alkaline compound, or a mixture of an aqueous solution containing an alkaline compound and an organic solvent. As the alkaline compound, various organic and inorganic compounds can be used. Examples of alkaline compounds include sodium hydroxide, potassium hydroxide, sodium carbonate, sodium silicate, potassium silicate, sodium metasilicate, potassium metasilicate, sodium phosphate, potassium phosphate, ammonia and amino alcohols (eg, Monoethanolamine, diethanolamine, triethanolamine). As the solvent of the eluate, water or various organic solvents can be used as described above. The solvent of the eluate is preferably mainly composed of water. If necessary, an organic solvent can be added to the eluate mainly containing water. As the organic solvent, alcohols or ethers are preferable. Examples of alcohols include lower alcohols (eg, methanol, ethanol, propanol, butanol), alcohols having an aromatic group (eg, benzyl alcohol, phenethyl alcohol), polyhydric alcohols (eg, ethylene glycol, diethylene glycol, triethylene). Glycol, polyethylene glycol) and amino alcohols (eg, monoethanolamine, diethanolamine, triethanolamine). Examples of ethers include cellosolves. The eluate may contain a surfactant, an antifoaming agent, and other various additives as required.

Next, a method of using the removal sheet will be described. When the removal sheet is brought into close contact with the surface of the curable layer, the adhesive force between the interface between the curable layer and the removal sheet becomes different between the uncured portion and the cured portion. When the curable layer and the removal sheet are peeled off, the adhesive force at the interface between the uncured portion and the adhesive layer is greater than the adhesive force at the removal sheet side, and the adhesive force at the interface between the cured portion and the adhesive layer is at the removal sheet side. When the adhesion is smaller than that, only the cured portion is transferred to the removal sheet. Conversely, when the adhesive force at the interface between the uncured portion and the adhesive layer is smaller than the adhesive force at the removal sheet side, and the adhesive force at the interface between the cured portion and the adhesive layer is greater than the adhesive force at the removal sheet side, Only the uncured portion is transferred to the removal sheet. Whether the cured part is transferred or the uncured part is transferred depends on the property of the polymerizable compound in the curable layer, the amount of the polymerizable compound added, the property of the binder in the curable layer, and the property of the curable layer. The adhesive strength may vary depending on the properties of other components and the addition amount thereof, as well as various conditions of the removing step (heating temperature, time, pressurizing temperature, etc.).
As a result of the above, the cured portion or the uncured portion selectively remains in an image form. When the curable layer contains a coloring material, a color image is formed on the photosensitive material.

The following processing may be optionally performed. [Transfer Processing] In the transfer processing, the cured image is attached to another sheet (image receiving material) and transferred. As a result, the portion transferred to the image receiving material is used as an image. The image receiving material may be laminated with the photosensitive material before image exposure or development. Further, the toner image obtained may be transferred by first performing the following toner development processing.

[Toner Development Processing] A coloring substance (toner) is attached to the cured image to visualize the image. It is also possible to provide an adhesive layer on the photosensitive material, selectively remove the uncured portion, and then attach the toner to the exposed adhesive layer. Further, the toner developing process can be performed on the image receiving material to which the cured portion is selectively transferred.

[Staining process] The cured image is dyed and the image is visualized. You may perform dyeing processing with respect to the image receiving material which transferred the cured image. The image obtained as described above can be used for printing plates, color proofs, hard copies, reliefs and the like.

[0071]

【Example】

[Example 1] Preparation of photosensitive material " Preparation of aluminum support" JI having a thickness of 0.24 mm
The surface of the aluminum plate according to S-A-1050 was grained with a nylon brush and an aqueous suspension of pumicetone (400 mesh), and then thoroughly washed with water. Next, 10%
It was immersed in the aqueous solution of sodium hydroxide for 30 minutes at 70 ° C. for etching, and then washed with running water. It was neutralized and washed with a 20% nitric acid aqueous solution, and then washed with water. The obtained aluminum plate was subjected to a rectangular alternating current (conditions: voltage at anode 12.7 v, ratio of electricity at cathode to electricity at anode was 0.9, electricity at anode was 160 coulomb / dm ² ). Then, electrolytic surface roughening treatment was performed in a 1% nitric acid aqueous solution containing 0.5% aluminum nitrate. The surface roughness of the obtained plate was 0.6 μm (Ra indication). Following this treatment, it was immersed in a 1% aqueous sodium hydroxide solution at 40 ° C. for 30 seconds and then treated in a 30% aqueous sulfuric acid solution at 55 ° C. for 1 minute. Next, so that the thickness becomes 2.5 g / dm ² ,
Current density 2A using direct current in 20% sulfuric acid aqueous solution
Anodizing treatment was performed under the condition of / dm ² . This was immersed in a 2% aqueous sodium silicate solution at 70 ° C. for 1 minute. The obtained aluminum plate was washed with water and dried to prepare a support.

[Formation of Curable Layer] The following coating solution was applied onto a support and dried to form a curable layer having a dry film thickness of about 1.8 μm.

──────────────────────────────────── Curable layer coating liquid ────── ────────────────────────────── Pentaerythritol tetraacrylate 3.0 g Allyl methacrylate / methacrylic acid copolymer (copolymerization molar ratio = 70 / 30) 20 wt% propylene glycol monomethyl ether solution 30.0 g Pigment dispersion liquid 29.0 g Propylene glycol monomethyl ether 122.0 g ───────────────────── ────────────────

──────────────────────────────────── Pigment dispersion ──────── ──────────────────────────── Pigment (Chromophtal red A2B, Ciba Geigy) 10 g Allyl methacrylate / methacrylic acid copolymer (copolymerization mole) Ratio = 80/20) 10 g Methyl ethyl ketone 80 g ─────────────────────────────────────

[Preparation of Silver Halide Emulsion] The following thioether compound was added to a container containing gelatin, potassium bromide, and water and heated at 55 ° C. in an amount of 2.0 × with respect to the amount of silver nitrate added.
It was added in an amount corresponding to 10 ^-3 mol. While maintaining the pAg value of the reaction vessel at 9.2, the molar ratio of rhodium to the total amount of silver nitrate aqueous solution and potassium iodide and silver nitrate was 4 ×.
An aqueous potassium bromide solution containing rhodium ammonium chloride in an amount of 10 ^-8 mol was added by a pAg control double jet method to form silver iodobromide particles. Further subsequently, at the same temperature, pAg = 8.
At 9, the aqueous solution of silver nitrate and hexachloroiridium (I) were added so that the molar ratio of iridium to silver was 10 ^-7 mol.
II) The potassium bromide solution to which the acid salt was added was added in two stages by the double jet method to prepare a core / shell type silver iodobromide emulsion having the following composition.

[0076]

[Chemical 11]

Core: silver iodobromide (silver iodide content: 7.5 mol%) Shell: pure silver bromide Core / shell: 3/7 (silver mol ratio) Average silver iodide content: 2.3 Mol% Average particle size: 0.28 μm

The obtained emulsion grains were monodisperse, and 98% of the total number of grains were present within ± 40% of the average grain size. Then, after desalting the emulsion, spectral sensitizing dyes 1 methanol solution of the following ^(10-2 mol / l) and a spectral sensitizing dye 2 in methanol the following ^(10-2 mol /
A mixture of 100 ml of each liter) was added at 40 ° C. to an emulsion corresponding to 1 mol of silver nitrate to adjust pH to 6.5 and pAg to 8.3 to prepare a silver halide emulsion.

The spectral sensitizing dye 1 has a spectral sensitivity corresponding to an argon ion laser writing light source (488 nm). Further, the spectral sensitizing dye 2 corresponds to an FD-YAG laser writing light source (532 nm). By using the above silver halide emulsion, writing on the same light-sensitive material by light sources of different wavelengths becomes possible.

[0080]

[Chemical 12]

[0081]

[Chemical 13]

[Preparation of Reducing Agent Dispersion] 10 g of a 10% by weight aqueous solution of polynivir alcohol (manufactured by Kuraray Co., Ltd.) was added to 10 g of the following reducing agent powder using a Dynomill disperser.
Dispersed inside. The particle size of the reducing agent was about 0.5 μm or less.

[0083]

Embedded image

[Formation of Photosensitive Layer] The following coating solution was prepared, coated on the curable layer and dried to form a photosensitive layer having a dry film thickness of about 1.2 μm.

──────────────────────────────────── Photosensitive layer coating liquid ────── ────────────────────────────── Polyvinyl alcohol (trade name: PVA-405, manufactured by Kuraray Co., Ltd., saponification degree: 81.5%) 10% by weight aqueous solution 42.0 g The above reducing agent dispersion solution 8.0 g 0.1% by weight methanol solution of the following additives 5.5 g 0.5% by weight aqueous solution of potassium bromide 1.7 g Silver halide emulsion of 2.8 g 5% by weight aqueous solution of the following surfactant 2.7 g Amino alcohol (shown in Table 1 below) (Amount shown in Table 1 below) Water 70.7 g ──────── ─────────────────────────────

[0086]

[Chemical 15]

[0087]

Embedded image

Table 1 ──────────────────────────────────── Sample amino alcohol number Type Quantity ── ────────────────────────────────── 1 None 2 Monoethanolamine 3% 3 Diethanolamine 5% 4 Triethanolamine 7% 5 6-amino-1-hexanol 6% 6 1-amino-2-propanol 4% 7 2-amino-2-hydroxymethyl-1,3-propanediol 6% 8 2- (ethylamino) ethanol 4% 9 2- (2-aminoethoxy) ethanol 5% 10 N-aminoethylethanolamine 5% ─────────────────────────────── ─────── Note: The amount depends on the polyvinyl alcohol in the photosensitive layer. Weight%

[Preparation of Base Precursor Dispersion] 250 g of the powder of the following base precursor was dispersed in 750 g of a 3% by weight aqueous solution of polyvinyl alcohol (manufactured by Kuraray Co., Ltd.) using a Dynomill disperser. The particle size of the base precursor was about 0.5 μm or less.

[0090]

[Chemical 17]

[Formation of Overcoat Layer] The following coating solution was prepared, coated on the photosensitive layer and dried to form an overcoat layer having a dry film thickness of about 3.3 μm.

───────────────────────────────────── Coating solution for the overcoat layer ───── ─────────────────────────────── Acid-modified polyvinyl alcohol (Kuraray Co., Ltd., saponification degree: 98%) 10 wt% aqueous solution 100.0 g The above base precursor dispersion 6.3 g 5 wt% aqueous solution of the above surfactant 2.0 g ────────────────────── ───────────────

(Image formation) A 200 lpi halftone image original and a bandpass filter (transmitting light having a wavelength of about 500 nm) are brought into close contact with the photosensitive material (printing original plate) prepared as described above, and a tungsten lamp is used. Image exposure was performed for 10 seconds with an illumination of 3 lux. Next, the back surface (support side) of the photosensitive material was brought into close contact with a hot plate heated to 150 ° C., and heat development was performed for 30 seconds while the surface of the photosensitive material was opened to the air. After removing the photosensitive layer and the overcoat layer by washing with water, it is immersed in an eluate (Fuji PS Developer DP-4 manufactured by Fuji Photo Film Co., Ltd.) at 30 ° C. for 1 minute to elute the uncured portion, followed by washing with water. As a result, a polymer image in which the exposed portion was colored red was formed. When printing was performed using this as a printing plate, good printed matter was obtained.

(Test of Strength of Photosensitive Material) The strength of the photosensitive material was tested by the following two methods. (1) Cross-Peeling Test The photosensitive material was cut into 3 cm × 12 cm, and the surface thereof was cut with a cutter knife at intervals of 5 mm to make cuts reaching the support. However, the support is not cut. A commercially available adhesive tape was strongly adhered onto it, and then the tape was peeled off in the 180 ° direction. The grids (squares of 5 mm on each side) of the grid are independently peeled or broken on any of the following surfaces. A: Peeling at the interface between the curable layer and the photosensitive layer (photosensitive material is destroyed) B: Cohesive breakdown inside the curable layer (photosensitive material is destroyed) C: Peeling at the interface between the surface of the photosensitive material and the tape (No breakage of photosensitive material) Peeling at the interface between the photosensitive layer and the overcoat layer,
And no cohesive failure occurred within these layers.
Table 2 shows the numbers of A, B and C per 100 squares.

(2) Measurement of Peeling Force A commercially available adhesive tape was attached to a photosensitive material having a width of 2 cm, and a tensile tester (Tensilon, manufactured by Orientec Co., Ltd.) was used to measure 180 ° direction at a pulling speed of 40 mm / min. After peeling, the tensile force (peeling force) was measured. Table 2 shows the results of the peeled surface (A, B, and C are as defined above) and the peeling force.

Table 2 ──────────────────────────────────── Sample test (1) Test (2 ) Number A B C Peeling surface Peeling force ──────────────────────────────────── 1 100 0 0 A 15 2 0 10 90 C 450 3 0 0 100 C 450 4 0 0 100 C 460 5 0 20 80 C 500 6 0 10 90 C 440 7 0 30 30 70 C 470 8 0 10 10 90 C 460 9 0 40 40 60 B 200 10 0 20 80 C 460 ─────────────────────────────────────

As is clear from the results shown in Table 2, in the light-sensitive materials 2 to 10 using amino alcohol according to the present invention, peeling occurs mainly on the surfaces of the tape and the light-sensitive material, and the light-sensitive material is hardly destroyed. It was From these results, it can be seen that the action of amino alcohol improved the adhesive force between the layers of the light-sensitive material and significantly increased the strength of the light-sensitive material.

Example 2 In the preparation of the light-sensitive material of Sample No. 1 (containing no amino alcohol) of Example 1, alcohols shown in Table 3 below were added to the coating solution for the curable layer.

Table 3 ──────────────────────────────────── Sample amino alcohol number Type Quantity ── ────────────────────────────────── 22 Monoethanolamine 3.5% 23 Diethanolamine 6% 24 Triethanolamine 8.4% ──────────────────────────────────── Note: The amount is in the curable layer. The light-sensitive material having a weight percentage of allyl methacrylate / methacrylic acid copolymer of not less than the same was evaluated in the same manner as in Example 1.
The results are shown in Table 4.

Table 4 ──────────────────────────────────── Sample test (1) Test (2 ) Number A B C Peeling surface Peeling force ──────────────────────────────────── 22 0 22 78 B 350 23 0 25 75 C 460 24 0 20 80 C 450 ─────────────────────────────────────

[Example 3] "Formation of photosensitive curable layer" The following coating solution was applied onto the support used in Example 1 and dried to give a dry film thickness of about 1.4 µm.
m photosensitive curable layer was provided.

──────────────────────────────────── Photosensitive curable layer coating liquid ──── ──────────────────────────────── Trimethylolpropane tri (acryloyloxypropyl) ether 2.0g Allyl methacrylate / methacrylic acid Copolymer (copolymerization ratio = 80/20) 2.0 g Photosensitizer below 0.13 g Initiator below 0.10 g Sensitization aid below 0.40 g Fluorine-based nonionic surfactant 0.03 g Methyl ethyl ketone 20. 0g Propylene glycol monomethyl ether 20.0g ─────────────────────────────────────

[0103]

Embedded image

[0104]

[Chemical 19]

[0105]

Embedded image

[Formation of Overcoat Layer] The following coating solution was prepared, coated on the photosensitive curable layer and dried,
An overcoat layer having a dry film thickness of about 2.0 μm was provided.

──────────────────────────────────── Coating solution for the overcoat layer ───── ─────────────────────────────── Polyvinyl alcohol (Kuraray Co., Ltd., saponification degree: 98%) 125g Amino alcohols listed in Table 5 (amounts listed in Table 5 below) Water 4050 g ────────────────────────────────── ───

Table 5 ──────────────────────────────────── Sample aminoalcohol number Type Quantity ── ────────────────────────────────── 31 None 32 Monoethanolamine 3.5% 33 Diethanolamine 6% 34 Tri Ethanolamine 8.4% ──────────────────────────────────── Note: The amount is the overcoat layer Weight% to polyvinyl alcohol in

(Image formation) A 200 lpi screen image original was brought into close contact with the photosensitive material (printing original plate) prepared as described above,
0.013 mW / cm ² through a filter (BP-49 manufactured by Kenko Optical Co., Ltd.) using a xenon lamp as a light source.
Image exposure for 20 seconds with the illuminance of. Next, when the light-sensitive material was newly coughed in the following developer at 25 ° C. for 1 minute, a polymer image was formed on the exposed area. When printing was performed using this as a printing plate, good printed matter was obtained.

──────────────────────────────────── Developer ────────── ─────────────────────────── sodium 30g potassium hydroxide silicate _{15g C 12 H 25 -C 6 H} 4 -O-C 6 H _4- SO ₃ Na 3 g Water 1000 g ─────────────────────────────────────

(Test of Strength of Photosensitive Material) The strength of the photosensitive material was tested by the following two methods. (1) Cross-Peeling Test The photosensitive material was cut into 3 cm × 12 cm, and the surface thereof was cut with a cutter knife at intervals of 5 mm to make cuts reaching the support. However, the support is not cut. A commercially available adhesive tape was strongly adhered onto it, and then the tape was peeled off in the 180 ° direction. The grids (squares of 5 mm on each side) of the grid are independently peeled or broken on any of the following surfaces. A: Peeling at the interface between the photosensitive curable layer and the overcoat layer (the photosensitive material is destroyed) B: Cohesive destruction inside the photosensitive curable layer (the photosensitive material is destroyed) C: Between the surface of the photosensitive material and the tape Peeling at the interface (no destruction of the photosensitive material) No cohesive failure occurred inside the overcoat layer. The number of A, B and C per 100 squares is 6th
Shown in the table.

(2) Measurement of Peeling Force A commercially available adhesive tape was attached to a photosensitive material having a width of 2 cm, and a tensile tester (Tensilon, manufactured by Orientec Co., Ltd.) was used to measure 180 ° direction at a pulling speed of 40 mm / min. After peeling, the tensile force (peeling force) was measured. Table 6 shows the results of the peeled surface (A, B and C are as defined above) and the peeling force.

Table 6 ──────────────────────────────────── Sample test (1) Test (2 ) No. ABC C Peeling surface Peeling force ──────────────────────────────────── 31 100 0 0 A 15 32 0 5 95 C 450 333 0 70 30 B 230 230 34 0 25 75 C 430 ──────────────────────────────── ─────

[Comparative Example 1] A curable layer and a photosensitive layer (containing 3% of monoethanolamine) were provided on a support in the same manner as in the preparation of Sample No. 2 of Example 1. Next, instead of the overcoat layer of Example 1, the following coating liquid was applied onto the photosensitive layer to form an overcoat layer containing no base precursor and having a dry film thickness of about 3.3 μm. The material (printing original plate) was created.

──────────────────────────────────── Coating solution for the overcoat layer ───── ─────────────────────────────── Acid-modified polyvinyl alcohol (Kuraray Co., Ltd., saponification degree: 98%) 10 wt% aqueous solution 100.0 g 5 wt% aqueous solution of the surfactant used in Example 1 2.0 g ─────────────────────────── ───────────

With respect to the prepared light-sensitive material, the peeling force was measured and the image forming process was carried out in the same manner as in Example 1. As a result, the adhesive force between the curable layer and the photosensitive layer is large (C
It was found that the surface peeled off and the peeling force was 450 g). However,
Little image was formed. This result shows that amino alcohol has a very weak function of promoting image formation.

Claims (2)

[Claims] 1. A support is provided with two or more layers, and a silver halide, a reducing agent, a polymerizable compound, a base precursor, a hydrophobic polymer having an acidic group and a hydrophilic polymer are any layers. In the same layer without the use of microcapsules, the polymerizable compound and the hydrophobic polymer are contained in the same layer to form a curable layer, and adjacent to the curable layer. A photosensitive material provided with a hydrophilic layer containing the hydrophilic polymer, wherein the curable layer or the hydrophilic layer further contains amino alcohol. 2. A support is provided with two or more layers, wherein a photopolymerization initiator, a polymerizable compound, a hydrophobic polymer having an acidic group and a hydrophilic polymer are microcapsules in any layer. Without being uniformly contained, the polymerizable compound and the hydrophobic polymer are contained in the same layer to form a curable layer, and the hydrophilic polymer is adjacent to the curable layer. A photosensitive material provided with a hydrophilic layer containing: wherein the curable layer or the hydrophilic layer further contains amino alcohol.