JPS6367176B2 - - Google Patents

Description

[Detailed description of the invention]

The present invention relates to a water-developable polyamide photosensitive resin composition. Conventionally, printing convex plates have been produced by exposing the photosensitive layer of a photosensitive original plate consisting of a layer of a photosensitive resin composition (hereinafter referred to as a photosensitive layer) and a support through a negative film or a positive film having a transparent image area. conduct,
After the photosensitive resin composition in the exposed areas is cured and made insolubilized, the resin composition in the unexposed areas is dissolved and removed using a suitable developer. Such photosensitive resin compositions usually contain a monomer having a photopolymerizable unsaturated bond, a polymer that is soluble in a suitable developer and becomes insolubilized by photopolymerization of the monomer, and a photointensifier. Contains a sensitizer and a thermal polymerization inhibitor. In the unexposed areas, the photosensitive resin composition, particularly the polymer, is soluble in a suitable developer;
The exposed areas become insoluble in the same solvent. Further, the polymer has high mechanical strength after photopolymerization of a monomer having a photopolymerizable unsaturated bond, and is not swollen by organic solvents. As such a polymer, an alcohol-soluble copolymer polyamide has been proposed, for example,
Publication No. 14719, Special Publication No. 15513, Publication No. 15513, Special Publication No. 15513
- Described in Publication No. 7330, etc. However, all of these polyamide-based photosensitive resin compositions are soluble in alcohol but insoluble in water, so the polyamide-based plate material is
An organic solvent such as alcohol must be used as a developer to dissolve and remove all unexposed areas of the resin layer. The use of these organic solvents as developing solutions not only poses problems in terms of handling, storage, waste liquid, and expensive explosion-proof developing equipment, but also
The above-mentioned polyamide has drawbacks such as a slow dissolution rate in organic solvents such as alcohol, and therefore a relatively long time is required for development of a composition prepared from it. Therefore, as a method to solve these problems, a water-developable polyamide-based photosensitive resin composition using a water-soluble polyamide-based polymer was developed by Tokko Sho.
It is described in Publication No. 54-22229. The water-developable polyamide-based photosensitive resin plate produced by this method has good reproducibility with respect to the original image, further improves ink acceptance and transfer properties, and has excellent printing durability during printing. However, since the cured product produced by photocuring the photosensitive resin composition (hereinafter referred to as photocured product) is hard, this type of photosensitive resin is used in flatbed printing machines with slow printing speeds, and Printing is also limited to paper with a relatively flat surface, such as coated paper. However, in recent years, with the aim of saving labor and speeding up printing, the use of high-speed rotary printing presses has progressed, and printing applications have also expanded to include slips and computer forms. It is spreading to papers with rough surfaces such as high-quality paper. For such new applications, if we use a relatively hard material like the conventional photocured material,
Ink is transferred only to the convex portions of the uneven portion of the paper surface, resulting in printed matter (usually referred to as ink smearing) in which no ink is applied to the concave portions. In order to solve this problem, the hardness of the photocured material is relatively soft, and the pressure applied during printing causes the photocured material in the part that is in contact with the paper surface to deform according to the unevenness of the paper, resulting in poor adhesion. We have to make sure that the parts disappear. In order to eliminate the above drawbacks, the present inventors
A water developable product that has a soft hardness of the photocured material and produces good prints without ink fading even when used for high-speed printing or printing on paper with a rough surface, and has excellent mechanical strength and printing durability. As a result of various intensive studies on photosensitive polyamide-based resin compositions, the present invention has been completed. That is, the present invention provides a photosensitive resin composition comprising a polyamide having basic nitrogen, a monomer having a photopolymerizable unsaturated bond, and a photopolymerization initiator. This is a photosensitive resin composition characterized by containing a compound represented by the following general formula (1) as all or a part of the compound. In the formula, X is the number of carbon atoms, a divalent hydrocarbon group of 1 to 24, or -O-, -COO-, - in the molecule
A divalent hydrocarbon group having 1 to 24 carbon atoms having NHCO-, Y is -SO ₃ H,

【formula】

[Formula] is shown, and R represents an alkyl group having 1 to 10 carbon atoms or a phenyl group. In the photosensitive resin composition of the present invention, the main material polyamide is a polyamide having basic nitrogen and the general formula
It is an ammonium salt-type nitrogen atom-containing polymer produced by partially or fully ionic bonding with the photopolymerizable unsaturated bond-containing monomer shown in (1), so it easily dissolves in water. Development with water becomes possible. Furthermore, due to the ionic bonding with the compound represented by general formula (1), the hydrogen bonds in the polyamide, which is the main material, are reduced due to steric hindrance, and the photosensitive resin composition becomes flexible due to the plasticizing effect, and furthermore, the photosensitive resin composition becomes flexible and photosensitive. When cured, the compound represented by formula (1) is polymerized alone or copolymerized with other photopolymerizable monomers having unsaturated bonds, so that the three-dimensional bond network of the photopolymerized product is It becomes coarser and therefore more flexible.
In addition, in the photosensitive resin after photocuring, the polyamide and the monomer photopolymer having photopolymerizable unsaturated bonds are ionicly bonded, so it has good moisture resistance, solvent resistance, and mechanical properties. In particular, products with excellent abrasion resistance can be obtained. In the present invention, the compound represented by the general formula (1) used as all or part of the monomer having a photopolymerizable unsaturated bond is, for example, a compound represented by the following formula. and so on. These monomers may be used alone or in combination. These monomers react as quaternizing agents for polyamides containing basic nitrogen. In addition to the compound represented by general formula (1) as a quaternizing agent, inorganic acids such as hydrochloric acid and sulfuric acid, and organic acids such as formic acid, acetic acid, chloroacetic acid, maleic acid, phthalic acid, adipic acid, acrylic acid, and methacrylic acid Also available. Further, the amount of the quaternizing agent containing the compound represented by the general formula (1) can be appropriately selected in consideration of the amount of basic nitrogen present in the polyamide, the solubility in water, and the like. The amount of the compound represented by general formula (1) is 5 mol% or more, especially 50 to 100 mol%, based on the amount of basic nitrogen present in the polyamide.
It is necessary to exist. If the amount of the compound represented by general formula (1) is less than 5 mol %, the photosensitive resin composition after photocrosslinking will lack the necessary flexibility, which is not preferred. In the present invention, monomers having a photopolymerizable unsaturated bond other than the compound represented by the general formula (1) that can be used in combination include, for example, methyl acrylate, methyl methacrylate, benzyl acrylate, tribromphenyl acrylate. , cyclohexyl acrylate, 2-hydroxypropyl acrylate, acrylamide, methacrylamide, N-methylolacrylamide, n-butoxymethylacrylamide, iso-butoxymethylacrylamide, Nt-butylacrylamide, acrylonitrile, styrene, vinylpyridine, etc. Monomers having one heavy bond, or allyl methacrylate, ethylene glycol diacrylate, ethylene glycol dimethacrylate, 1,3-propanediol diacrylate, 1,3-propanediol methacrylate, 1,4-butanediol diacrylate,
1,4-butanediol methacrylate, 1,
6-hexanediol diacrylate, 1,6-
Hexanediol dimethacrylate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, tetramethylolmethane triacrylate, triacryloyloxyethyl phosphate, methylenebisacrylamide, ethylenebisacrylamide, propylenebisacrylamide, butylenebisacrylamide, methylenebis There are monomers having two or more unsaturated double bonds, such as methacrylamide, ethylenebismethacrylamide, and propylenebismethacrylamide. In addition, when the ratio of the sum of the quaternizing agent used in combination with the compound represented by general formula (1) to the amount of basic nitrogen present in the polyamide is 100 mol% or more, the basic nitrogen For convenience, in the present invention, the compound of formula (1) in an amount equal to or more than the equivalent molar amount of the compound of formula (1) after subtracting the molar amount of the quaternizing agent used in combination from the molar amount of nitrogen, It is included in the category of monomers having photopolymerizable unsaturated bonds other than quaternizing agents that can be used in combination. In the present invention, the polyamide having basic nitrogen is obtained, for example, by using monomers represented by the following general formulas () to () as polymerization raw materials. (In the above general formulas () to (), R,
R' is a hydrogen atom or a hydrocarbon residue having 1 to 10 carbon atoms, R ₁ , R ₂ , and R ₃ are alkylene groups having 1 to 15 carbon atoms, and R ₄ and R ₅ are 1 to 1 carbon atoms. 10 hydrocarbon residues, A and B are -NH ₂ , -COOH, -
COOR'', and A and B may be the same or different at the same time.R'' represents a hydrocarbon residue having 1 to 10 carbon atoms. ) (In the above general formula (), R ₆ and R ₇ represent hydrocarbon residues having 1 to 10 carbon atoms. R ₆ and R ₇
may join together to form a ring or a heterocyclic ring. Also
R ₈ is a lower alkyl group having 1 to 3 carbon atoms or

[Formula] is shown. Here, R ₆ and R ₇ are the aforementioned groups. Y represents a γ-aminopropyl group. ) Specific monomers represented by the above general formula () include N,N'-bis(aminomethyl)-piperazine, N,N'-bis(β-aminoethyl)-piperazine, N,N'- Bis(β-aminoethyl)
-Methylpiperazine, N-(aminomethyl)-
N′-(β-aminoethyl)-piperazine, N,
Diamines such as N'-bis(γ-aminopropyl)-piperazine, N,N'-bis-(carboxymethyl)-piperazine, N,N'-bis(carboxymethyl)-methylpiperazine, N,N'- Bis(carboxymethyl)-2,6-dimethylpiperazine, N,N'-bis(β-carboxyethyl)
-Dicarboxylic acids such as piperazine, N,N'-bis(γ-carboxypropyl)-piperazine, N-(β-carboxyethyl)-N'-(carboxymethyl)-piperazine, or their lower alkyl esters and acid halides and N-
(aminomethyl)-N'-(carboxymethyl)-
Piperazine, N-(aminomethyl)-N'-(β
-carboxyethyl)-piperazine, N-(β-
aminoethyl)-N′-(β-carboxyethyl)
-Piperazine, N-(aminomethyl)-N'-
(carboxymethyl)-2-methylpiperazine and other ω-amino acids. Specific monomers represented by the above general formula () include N-(β-aminoethyl)piperazine,
N-(γ-aminopropyl)piperazine, N-
(ω-aminohexyl)piperazine, N-(δ-
aminocyclohexyl)piperazine, N-(β-
aminoethyl)-3-methylpiperazine, N-
(β-aminoethyl)-2,5-dimethylpiperazine, N-(β-aminopropyl)-3-methylpiperazine, N-(γ-aminopropyl)-2,
Diamines such as 5-dimethylpiperazine, N-
Carboxymethylpiperazine, N-(β-carboxyethyl)-piperazine, N-(γ-carboxypropyl)piperazine, N-(ω-carboxyhexyl)piperazine, N-(δ-carboxycyclohexyl)piperazine, N-(β- carboxyethyl)-3-methylpiperazine, N-(β-
These include ω-amino acids such as (carboxyethyl)-2,5-dimethylpiperazine, or lower alkyl esters thereof. Specific monomers represented by the general formula () include N,N-di(β-aminoethyl)ethylamine, N,N-di(γ-aminopropyl)methylamine, and N,N-di( β-aminoethyl)-methylamine, N,N'-di(γ-aminopropyl)
-Ethylamine, N,N-di(γ-aminopropyl)isopropylamine, N,N-di(γ-aminopropyl)-cyclohexylamine, N,N-
di(δ-amino-n-butyl)phenylamine,
N-methyl-N-(β-aminoethyl)-1,3
-Diamines such as propanediamine, N,N-
Di(carboxymethyl)-methylamine, N,N
-di(β-carboxyethyl)methylamine,
N,N-di(β-carboxyethyl)-methylamine, N,N-di(β-carboxyethyl)-isopropylamine, N-carboxymethyl-N-
Dicarboxylic acids such as (β-carboxyethyl)-methylamine or their lower alkyl esters, acid halides, and N-(aminomethyl)-N-(carboxymethyl)-methylamine, N-(β-aminoethyl) -N-(β-carboxyethyl)-methylamine, N-(aminomethyl)-N-(β-carboxylethyl)-isopropylamine, N-(γ-aminopropyl)-
N-(γ-carboxypropyl)-isopropylamine, N-(γ-aminopropyl)-N-(β
-Carboxyethyl)-ω of methylamine, etc.-
They are amino acids. A specific monomer represented by the general formula () is N,N'-dimethyl-N,N'-di-(γ
-aminopropyl)-ethylenediamine, N,
N'-dimethyl-N,N'-di-(γ-aminopropyl)-tetramethylenediamine, N,N'-diisobutyl-N,N'-di-(γ-aminopropyl)-hexamethylenediamine, N, N'-dicyclohexyl-N,N'-di-(γ-aminopropyl)-hexamethylenediamine, N,N'-di-(γ-aminopropyl)-2,2,4-trimethyl-hexamethylenediamine, etc. Diamines, N,N'-dimethyl-N,N'-di(carboxymethyl)-ethylenediamine, N,N'-dimethyl-N,N'-di-(β-carboxyethyl)
-ethylenediamine, N,N'-dimethyl-N,
Dicarboxylic acids such as N'-di-(γ-carboxypropyl)-hexamethylene diamine or their lower alkyl esters, acid halides, and N,N'-dimethyl-N-(aminomethyl)
-N'-(carboxymethyl)-ethylenediamine, N,N'-dimethyl-N-(βaminoethyl)
-N'-(β-carboxyethyl)-ethylenediamine, N,N'-dimethyl-N-(aminomethyl)-N'-(carboxyethyl)-hexamethylenediamine, and other ω-amino acids. Specific monomers represented by the above general formula () include 6-methyl-6-(N,N'-dimethylaminomethyl)-4,8-dioxa-undecanediamine, 6-methyl-6-( N,N'-diethylaminomethyl)-4,8-dioxa-undecanediamine, 6-ethyl-6-(N,N-dimethylaminomethyl)-4,8-dioxa-undecanediamine, 6,6-bis(N , N-dimethylaminomethyl)-4,8-dioxane undecane diamine. Polyamide is formed by condensation polymerization using one or more of these monomers containing basic nitrogen. That is, monomers that can form polyamide by homopolymerization, such as ω-amino acids or alkyl esters thereof, can be used alone. On the other hand, if the monomer is a dicarboxylic acid, its alkyl esters, acid halides, etc., it can be condensed with a diamine, and if the monomer is a diamine, it can be condensed with a dicarboxylic acid or a derivative thereof to form a polyamide. to form. Furthermore, as polymerization raw materials for polyamide used in the present invention, in addition to the monomers represented by the above general formulas () to (), aliphatic and/or aromatic dicarboxylic acids and diamines used in ordinary polyamide polymerization are used. , ω-amino acids, lactams, etc. may be used in combination. Examples of dicarboxylic acids that can be used in combination include aliphatic and/or aromatic dicarboxylic acids such as succinic acid, adipic acid, glutaric acid, azelaic acid, sebacic acid, decanedicarboxylic acid, terephthalic acid, isophthalic acid, and cyclohexanedicarboxylic acid; Lower alkyl esters, acid halides, etc. of these acids are used.
Examples of diamines include linear saturated aliphatic diamines such as tetramethylene diamine, pentamethylene diamine, hexamethylene diamine, heptamethylene diamine, octamethylene diamine, nonamethylene diamine, and decamethylene diamine, metaxylylene diamine, and paraxylylene diamine. Aromatic diamines such as cyclohexane bismethylamine, aliphatic diamines such as cyclohexane bismethylamine, etc. are used. ω
- As the amino acid, for example, aminocaproic acid, aminoheptanoic acid, aminocaprylic acid, aminocaproic acid, aminolauric acid, etc. are used.
Examples of the lactam used include ε-caprolactam, α-methyl-ε-caprolactam, ε-methyl-ε-caprolactam, cycloheptanone isoxime, and cyclooctanone isoxime. Polyamides having basic nitrogen atoms obtained from the above-mentioned monomers can be polymerized according to conventionally known methods for producing polyamides. The monomer component containing basic nitrogen accounts for 5 to 100 mol% of the total polyamide constituents, especially 20 to 50 mol%.
It is preferable that In addition to the basic nitrogen-containing monomers shown above, general formula ()
Any nitrogen-containing monomer that reacts with the compound represented by to form a quaternary ammonium salt can be used. The above monomers may be used alone or in combination of two or more. In particular, it is desirable to use a single monomer having at least two or more unsaturated double bonds or to use a monomer mixture containing at least one kind. The amount of the monomer used is 5 to 150% by weight, especially 5 to 150% by weight, based on the polyamide in the photosensitive resin composition.
It is preferably 10 to 100% by weight. If the monomer content is less than 5% by weight, the exposed area will not be sufficiently insolubilized in the solvent. Moreover, if it exceeds 150% by weight, the mechanical strength of the photosensitive layer will be impaired after exposure. A photosensitizer is added to accelerate the polymerization reaction of the monomers within the polyamide matrix. As such a photosensitizer, conventionally known ones can be used. For example, 9,10-anthraquinone, 1-chloranthraquinone, 2-
anthraquinones such as chloranthraquinone,
benzophenone, p-aminobenzophenone, p
- Benzophenones such as chlorbenzophenone, benzoins such as benzoin, benzoin methyl ether, benzoin ethyl ether, α-methylbenzoin, and benzyls. The amount of the photosensitizer to be used is 0.01 to 5% relative to the total amount of the polyamide, the compound represented by the general formula (), and the monomer having a photopolymerizable unsaturated bond.
It is preferably 0.1 to 2% by weight, especially 0.1 to 2% by weight. Thermal polymerization inhibitors prevent thermal polymerization of monomers having photopolymerizable unsaturated groups due to heating during preparation, molding, and processing of photosensitive resin compositions, or dark reactions during storage of the photosensitive resin compositions. Add to.
As such a thermal polymerization inhibitor, conventionally known ones can be used. For example, hydroquinones such as hydroquinone, mono-t-butylhydroquinone, benzoquinone, 2,5-di-p-
Examples include benzoquinones such as benzoquinone, catechols such as catechol and pt-butylcatechol, and picric acids. The amount of thermal polymerization inhibitor used is 0.001 to 2% by weight, especially 0.05% by weight, based on the total amount of the polyamide, the compound represented by formula (), and the monomer having a photopolymerizable unsaturated bond.
~0.5% by weight is preferred. As described above, the photosensitive resin composition of the present invention contains a compound represented by the general formula (), a polyamide having basic nitrogen, a monomer having a photopolymerizable unsaturated bond, a photosensitizer, and a thermal polymerization inhibitor. The compound can be easily obtained by dissolving it in a solvent such as water, methanol, ethanol, carbon tetrachloride, toluene, or xylene, evaporating only the solvent from this solution, and mixing uniformly. The photosensitive resin composition of the present invention is usually formed into a sheet-like material and used as a photosensitive resin original plate. That is, a mixture having the above-mentioned composition is formed into a sheet-like product such as a plate, film, or foil having a desired thickness by a method such as hot pressing, casting, or melt extrusion. Further, this sheet-like material is laminated on a support with or without an adhesive. Any material such as steel, aluminum, glass, or plastic film can be used as the support. When the obtained photosensitive resin original plate is closely stacked with a negative film or a positive film having a transparent image area on the photosensitive layer and active light is irradiated from above, only the exposed area becomes insolubilized and hardened. As a light source that emits such actinic rays, various mercury lamps, carbon arc lamps, xenon lamps, ultraviolet rays, fluorescent lamps, etc. can be used. After irradiation with light, the non-exposed areas are dissolved and removed using a suitable solvent to obtain a relief plate with clear image areas. In the present invention, since an ammonium salt-type polyamide having a nitrogen atom, which is produced by the reaction of a compound represented by the general formula () with a polyamide having a basic nitrogen, is used as the base material, it can be easily and quickly treated with just water. It can be developed easily. Of course, development can also be carried out using various acid aqueous solutions, mixtures of water and alcohol, lower aliphatic alcohols, lower paper aliphatic alcohols, and solvents that can solubilize the polyamide binder, such as calcium chloride or zinc chloride. Since the relief plate of the present invention obtained in this way has extremely short exposure and development times, the resulting image has very sharp edges. Moreover, the letterpress is extremely flexible due to the effect of the compound represented by the formula (), and the ink is transferred neatly even to paper with a rough surface such as high-quality paper, and the ink does not smear even when printed at high speed with a rotary printing press. It is very clear. The present invention will be explained in detail below with reference to Examples. In addition, in the examples, all parts simply indicate parts by weight. Reference Example 1 40 parts of N,N-bis(γ-aminopropyl)piperazine adipate and 60 parts of ε-caprolactam were added to a reaction vessel, and after sufficient nitrogen purging, the vessel was sealed and gradually heated. From the time the internal pressure reached 10Kg/ ^m2 , water was distilled out until the pressure could no longer be maintained, and the pressure returned to normal pressure in about 1 hour.
The reaction was carried out at normal pressure for a period of time. The resulting polymer has a specific viscosity of
1.59, is a milky white polyamide with a softening point of 110℃,
It was virtually insoluble in neutral water. Example 1 34 parts of a compound represented by the following formula (), Reference Example 1
100 parts of the polyamide obtained above, 30 parts of a 1:2 condensate of ethylene glycol diglycidyl ether and acrylic acid, 2 parts of benzophenone and 0.2 parts of hydroquinone were added to 300 parts of methanol and dissolved by heating. When this solution is cast onto a glass plate and left under reduced pressure to completely remove methanol, the thickness becomes 0.6 mm.
A transparent film-like photosensitive resin composition with a diameter of 1.0 mm was obtained. This composition was easily dissolved in water at room temperature. The obtained film was adhered onto a 0.25 mm thick polyester film to obtain a photosensitive original plate. A 133-line mesh-resolved photographic image negative film was brought into close contact with the photosensitive layer of this original plate, and exposed for 4 minutes using an exposure machine P-113-D manufactured by Dainippon Screen. After exposure, the film was developed for 2 minutes using Dainippon Screen's Printite Washer BR-A3, dried, and then post-exposed.
The resulting letterpress faithfully reproduced the original image. Next, when this letterpress was attached to a letterpress rotary printing machine BF-201 manufactured by Ukita Kogyo and printed, very good prints were obtained, with no fading in the shadow areas and no thickening in the highlight areas. . Also, 20 of the above letterpress
The hardness at 65% RH was 28° (Shore D) and it was quite flexible. Example 2 63 parts of the compound represented by the following formula (2), 100 parts of the polyamide obtained in Reference Example 1, 1:2 condensate of ethylene glycol diglycidyl ether and acrylic acid
30 parts, 2 parts of benzophenone, 0.2 parts of hydroquinone
1 part was added to 300 parts of methanol and heated to dissolve.
A photosensitive original plate was obtained from this solution in the same manner as in Example 1, and subjected to exposure, development, drying, and post-exposure. The obtained letterpress reproduced the original image, and a good printed matter was obtained. In addition, the hardness was 30° (Shore D). Example 3 29 parts of the compound represented by the following formula (3), 100 parts of the polyamide obtained in Reference Example 1, 30 parts of a 1:2 condensate of ethylene glycol diglycidyl ether and acrylic acid
1 part, 2 parts of benzophenone, and 0.2 parts of hydroquinone were added to 300 parts of methanol and dissolved by heating. A photosensitive original plate was obtained from this solution in the same manner as in Example 1, and subjected to exposure, development, drying, and post-exposure. The resulting letterpress reproduced the original image. When this relief was printed in the same manner as in Example 1, very good printed matter was obtained. The hardness of the letterpress was 33°. Comparative Example 1 10 parts of methacrylic acid, 100 parts of the polyamide obtained in Reference Example 1, 30 parts of a 1:2 condensate of ethylene glycol diglycidyl ether and acrylic acid, 2 parts of benzophenone, and 0.2 parts of hydroquinone were added to 300 parts of methanol and heated. and dissolved. A photosensitive original plate was obtained from this solution in the same manner as in Example 1, exposed to light,
Development, drying, and post-exposure were performed. When printing was performed using the obtained letterpress in the same manner as in Example 1,
Fading occurred in the shadow areas, and the printed matter was not good. Furthermore, the hardness of the letterpress was 50° (Shore D) and lacked flexibility. Example 4 21 parts of the compound represented by the following formula (4), 100 parts of the polyamide obtained in Reference Example 1, 30 parts of a 1:2 condensate of ethylene glycol diglycidyl ether and acrylic acid
1 part, 2 parts of benzophenone, and 0.2 parts of hydroquinone were added to 300 parts of methanol and dissolved by heating. A photosensitive original plate was obtained from this solution in the same manner as in Example 1, and subjected to exposure, development, drying, and post-exposure. The resulting letterpress reproduced the original image. When this relief was printed in the same manner as in Example 1, very good printed matter was obtained. The hardness of the letterpress was 33°.

Claims (1)

[Scope of Claims] 1. In a photosensitive resin composition comprising a polyamide having basic nitrogen, a monomer having a photopolymerizable unsaturated bond, and a photopolymerization initiator, a monomer having a photopolymerizable unsaturated bond 1. A photosensitive resin composition comprising a compound represented by the following general formula (1) as all or part of the polymer. In the formula, X is a divalent hydrocarbon group having 1 to 24 carbon atoms or -O-, -COO-, -
A divalent hydrocarbon group having 1 to 24 carbon atoms and having NHCO-, Y is -SO ₃ H, [Formula] [Formula], and R is an alkyl group or phenyl group having 1 to 10 carbon atoms. .