JPH09230583A - Photosensitive planographic printing master plate and production of planographic printing plate using the same - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a photosensitive planographic printing master plate having high ink repelling property for which pure water can be used as a dampening water by using a hydrophilic polymer essentially comprising silicone. SOLUTION: This master plate has a hydrophilic swellable layer on a substrate, and the hydrophilic swellable layer has a phase separation structure of at least two phases comprising a phase essentially comprising a hydrophilic polymer and a phase essentially comprising a hydrophobic polymer. The hydrophobic polymer essentially consists of silicone. Silicone is preferable because the hydrophilic swellable layer has both of proper swelling property with water and printing durability and silicone has rubber elasticity, ink repelling property and an effect to form a proper phase separation structure of the hydrophilic polymer. Silicone means a well-known org. silicon compd. which has siloxane bonds in a part or whole of the skeleton and org. groups directly bonded to the silicon atoms. Silicone oil, silicone rubber, silicone resin, and silicone powder can be preferably used.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a photosensitive lithographic printing plate precursor, which is particularly easy to develop, has high ink repulsion without desensitizing treatment, and is pure water as fountain solution. The present invention relates to a novel photosensitive lithographic printing plate precursor which can be used.

[0002]

2. Description of the Related Art In planographic printing, the image area and the non-image area are basically on the same plane, and the image area is ink-receptive and the non-image area is ink repellent. After applying ink to only the image area using the difference in adhesion,
It means a method of printing by transferring ink to a printing medium such as paper. A PS plate is usually used for such lithographic printing.

[0003] The PS plate mentioned here means the following.

[0004] That is, Teruhiko Yonezawa, "PS Version Overview"
As described in pp. 18-81 of the Printing Society of Japan (1993), a lipophilic photosensitive resin layer is applied on an aluminum substrate that has been subjected to hydrophilic treatment, and the image portion is formed by photolithography. The photosensitive layer remains, while the non-image area exposes the surface of the aluminum substrate described above, forms a dampening solution layer on the surface, repels ink, and forms a PS plate with water for forming an image and a dampening solution layer. Instead, a waterless PS plate using a silicone rubber layer as an ink repellent layer, a so-called waterless planographic plate.

[0005] The term "waterless lithographic printing plate" used herein means that the non-image area is made of a substance having ink repellency to oil-based ink used in normal lithographic printing, such as silicone rubber or a fluorine-containing compound. This means a printing plate that can be used to form an image between an ink-impartable image portion and print without using the same.

The former PS plate with water is a printing plate which is excellent in practical use, and aluminum is usually used for the support, and the surface of the aluminum has water retentivity and a lipophilic photosensitive resin layer is formed on the surface during printing. It was necessary to have excellent adhesiveness to the photosensitive layer so as not to peel off. Therefore, the aluminum surface is usually grained, and if necessary, a treatment such as anodizing is performed on the grained surface to improve water retention and reinforce adhesion to the photosensitive resin layer. I have been. Further, in order to obtain the storage stability of the photosensitive resin layer, the aluminum surface is generally subjected to a chemical treatment such as zirconium fluoride or sodium silicate.

As described above, the PS plate with water has a complicated manufacturing process and its simplification has been desired. However, the PS plate has been widely used because of its excellent printing characteristics (printing durability, image reproducibility, etc.). I have.

In order to solve the above-mentioned problem, there is a proposal of a new planographic material having printing characteristics equal to or higher than that of an aluminum substrate, and having a low material cost and different from an aluminum substrate by a simple manufacturing process. For example, Japanese Patent Publication No. Sho 56-2938 proposes a method of forming a photosensitive layer on a support using an ink repellent layer made of a hydrophilic polymer material instead of an aluminum substrate. ing. However, in this method, since a urea resin is simply applied as a hydrophilic layer on a water-resistant layer of an aldehyde condensate of polyvinyl chloride, polyurethane, or polyvinyl alcohol, the layer has insufficient ink repellency. In addition, the adhesiveness to the photosensitive resin layer was poor, and the printing durability was insufficient. Also,
JP-A-57-179852 discloses a method in which a hydrophilic radical polymerizable compound is coated on a support, the surface of the support is hydrophilized by irradiation with actinic rays, and a photosensitive resin layer is coated. Proposed. However, the hydrophilic surface layer formed by this method is also rigid, the ink repulsion property is insufficient, and the printing durability is also poor. Further, in the development of these PS plates with water, since the photosensitive layer is dissolved to expose the surface of the aluminum substrate, it is essential that the components of the photosensitive layer be dissolved in the developing solution. Therefore, a large amount of developing waste liquid is generated because the composition is greatly changed and fatigue occurs.

Therefore, the developer has to be frequently maintained and replaced. In addition, a great deal of labor and cost are required for treating the generated developing waste liquid.

Also, as a simple form of the PS plate with water,
An image receiving layer such as toner is formed on a support such as paper
A direct-drawing lithographic printing plate precursor that forms an image using a PC, desensitizes non-image areas with an etchant or the like, and converts the image receiving layer into an ink repellent layer for use is widely used. . Specifically, an image receiving layer comprising a water-soluble binder polymer, an inorganic pigment, a water-proofing agent and the like is generally provided on a water-resistant support, and is disclosed in US Pat. No. 2,532,865, Japanese Patent Publication No. 40-23581, and JP-A-48-9802, JP-A-57-205196, JP-A-60-2
309, JP-A-57-1791, JP-A-5-1791
JP-A-7-15998, JP-A-57-96900, JP-A-57-205196, JP-A-63-1
66590, JP-A-63-166593,
JP-A-63-317388, JP-A-1-1144
No. 88, JP-A-4-366868, and the like. These direct-drawing lithographic printing plate precursors include PVA, starch, hydroxyethylcellulose, casein, gelatin, polyvinylpyrrolidone, vinyl acetate-crotonic acid copolymer, styrene-maleic acid copolymer as an image receiving layer to be converted into an ink repellent layer. Water-dispersible polymers such as water-soluble binder polymers and acrylic resin emulsions that exhibit hydrophilicity before the desensitization treatment such as coalescence, inorganic pigments such as silica and calcium carbonate, and melamine-formaldehyde resin condensates There are proposals made of such a waterproofing agent. Also, JP-A-63-2
Japanese Patent No. 56493 proposes a direct drawing type lithographic printing plate precursor using as a main component a hydrophobic polymer which is hydrolyzed by a desensitizing treatment to generate a hydrophilic group.

In order to convert the image receiving layer into an ink repellent layer, the direct drawing type lithographic printing plate requires a desensitizing treatment, and without such a treatment, shows little ink repellency. It was.

That is, in order to obtain a practical level of ink repellency, it is necessary to desensitize the ink and to use a large amount of a hydrophilic binder polymer. However, the water resistance tends to be poor, and the printing durability deteriorates. . Further, when the hydrophilicity is increased, there is a problem that the adhesiveness to an image such as a toner tends to decrease. On the other hand, if the water resistance is increased by increasing the amount of a water-proofing agent or by adding a hydrophobic polymer in order to improve printing durability, the hydrophilicity is reduced, and the ink repellency is greatly reduced. There was a problem.

A so-called one-step exposure-only technology developed by Union Carbide, which does not require development, lacquer embossing and desensitization treatment utilizing a hydrophilic / hydrophobic conversion reaction, is disclosed in No. 131, Japanese Patent Publication No. Sho 4
No. 2-5365, Japanese Patent Publication No. 42-14328,
JP-B-42-20127, US Pat. No. 3,321,377
JP, USP3231381, USP3231
No. 382, for example. The plate is formed by coating an association of polyethylene oxide and a phenolic resin together with a photosensitizer. However, the non-image portion is rigid and inferior in flexibility, and the ink repellency is insufficient. The difference in ink repulsion / ink deposition between the line and
It was not practical.

Further, the PS plate with water needs to constantly control the amount of dampening solution at the time of printing, and considerable skill and experience have been required to control an appropriate amount of dampening solution. IPA added as an essential component to the fountain solution
In recent years, the use of (isopropanol) has been strictly regulated from the standpoint of the occupational health environment and wastewater treatment, and countermeasures are urgently needed.

On the other hand, in the case of a waterless PS plate in which a silicone rubber layer is used as an ink repellent layer instead of the fountain solution, JP-B-54-26923, JP-B-57-3060, and JP-B-56-12682. No., JP-B-56-23
No. 150, JP-B-56-30856, JP-B-60-60051, JP-B-61-54220, JP-B-61-54222, and JP-B-61-54.
No. 223, Japanese Patent Publication No. 61-616, Japanese Patent Publication No. 63
JP-A-23544, JP-B-2-25498, JP-B3-56622, JP-B4-28098, JP-B5-1934, and JP-A-2-63050.
As described in Japanese Patent Publication No. 2-63051 and Japanese Patent Laid-Open No. 2-63051, it is possible to print without using dampening water, so the former printing with PS plate does not require any dampening water control work. Since the work is extremely simple, it is a plate material with high practicality that is rapidly spreading in recent years, but due to the use of a silicone rubber layer with weak mechanical strength as the ink repellent layer, lack of durability is pointed out. There is a strong demand for ink repellent materials with excellent durability. Further, at the time of development, it is necessary to mechanically peel and remove the silicone rubber layer by brush rubbing, so that a large amount of development waste liquid containing the peeled and removed silicone rubber residue is generated. Therefore, the service life of the brush is short and it is necessary to frequently replace the brush, and maintenance measures such as collecting and discarding the silicone rubber residue have been required.

[0016]

DISCLOSURE OF INVENTION Problems to be Solved by the Invention The inventors of the present invention have expanded the control range of the fountain solution in the conventional lithographic printing of PS plates with water, and made IPA-less from the fountain solution, which has hitherto been impossible. In addition, a waterless planographic printing plate in which a silicone rubber layer is used as an ink repellent layer is provided without a complicated plate making process such as image formation by a PPC method and desensitizing treatment like a direct drawing planographic printing original plate. As a result of diligent studies to develop an ideal lithographic material that can solve the shortcoming of lack of durability, which does not require the development and maintenance that was necessary for conventional PS plates, and has a simple manufacturing process, a specific material It was found that this can be achieved by using a lithographic printing plate in which a hydrophilic swelling layer having a phase-separated structure consisting of groups is used as an ink repellent layer.

[0017]

That is, the present invention has the following constitution.

(1) A hydrophilic swelling layer having a phase-separated structure composed of at least two phases, a phase containing a hydrophilic polymer as a main component and a phase containing a hydrophobic polymer as a main component, is provided on a substrate. A photosensitive lithographic printing plate precursor, wherein the hydrophobic polymer is mainly composed of silicone.

(2) The photosensitive lithographic printing plate precursor as described in (1) above, wherein the hydrophobic polymer is mainly composed of a silicone emulsion.

(3) The water absorption of the hydrophilic swelling layer is 10 to 1
000%, The photosensitive lithographic printing plate precursor as described in (1) above.

(4) Hydrophobic polymer in hydrophilic swelling layer 6
The photosensitive lithographic printing plate precursor as described in (1) above, which is 0 to 95% by weight.

(5) A method for producing a lithographic printing plate, which comprises irradiating an active ray on the plate surface of the photosensitive lithographic printing plate precursor as described in any of (1) to (4) above.

[0023]

BEST MODE FOR CARRYING OUT THE INVENTION The photosensitive lithographic printing plate precursor according to the invention is characterized by having a hydrophilic swelling layer on a substrate.

The hydrophilic swelling layer is characterized by having a phase-separated structure composed of at least two phases, a phase containing a hydrophilic polymer as a main component and a phase containing a hydrophobic polymer as a main component.

The hydrophilic polymer used in the hydrophilic swelling layer of the present invention will be described.

The hydrophilic polymer is a known water-soluble polymer (meaning one completely soluble in water) or a pseudo-water-soluble polymer (amphiphilic polymer) which is substantially insoluble in water and shows water swelling property. The macro means that it is soluble in water, but the micro means that it contains an insoluble portion, and the water-swellable polymer (means that it swells in water but does not dissolve).
That is, it means a polymer that adsorbs or absorbs water under normal use conditions, and a polymer that dissolves in water or swells in water.

Known hydrophilic polymers can be used in the present invention, and include animal polymers, plant polymers and synthetic polymers. For example, "Function
nal Monomers ”(Y. Nyquist,
Dekker), "Water-soluble polymer" (Nakamura, Kagaku Kogyo Co., Ltd.), "Comprehensive technical data collection of the latest processing and modification technology and application development of water-soluble polymer water-dispersible resin" (Business Development Center Publishing Department), Hydrophilic polymers described in "Applications and markets of new water-soluble polymers" (CMC) and the like can be mentioned.
Specific examples are given below.

(A) Natural polymers Starch-acrylonitrile graft polymer hydrolyzate, starch-acrylic acid graft polymer, starch-styrene sulfonic acid graft polymer, starch-
Vinyl sulfonic acid type graft polymer, starch-acrylamide type graft polymer, carboxylated methyl cellulose, methyl cellulose, hydroxypropyl methyl cellulose, hydroxyethyl cellulose, cellulose xanthate, cellulose-acrylonitrile type graft polymer, cellulose-styrene sulfonic acid type graft polymer , Carboxymethyl cellulose cross-linked product,
Hyaluronic acid, agarose, collagen, milk casein, acid casein, rennet casein, ammonia casein, potash casein, borax casein, glue, gelatin, gluten, soy protein, alginate, ammonium alginate, potassium alginate, sodium alginate arabia gum , Tragacanth gum, karaya gum, guar gum, locust bean gum, Irish moss,
Soy lecithin, pectic acid, starch, carboxylated starch, agar, dextrin, mannan, etc.

(B) Synthetic Polymers Polyvinyl alcohol, polyethylene oxide, poly (ethylene oxide-co-propylene oxide), aqueous urethane resin, water-soluble polyester, ammonium polyacrylate, sodium polyacrylate, ammonium polymethacrylate, Acrylic copolymer, acrylic emulsion copolymer, polyvinyl alcohol cross-linked polymer, sodium polyacrylate cross-linked product, polyacrylonitrylyl saponified polymer, hydroxyethyl (meth) acrylate-based polymer ((meth) □ □
□□ stands for □□□□ or meta □□□□. ), Poly (vinyl methyl ether-co-maleic anhydride), maleic anhydride copolymer, vinylpyrrolidone copolymer, polyethylene glycol di (meth)
Acrylate-based crosslinked polymers, polypropylene glycol di (meth) acrylate-based crosslinked polymers and the like.

The above-mentioned hydrophilic compounds may contain monomers or copolymerization components having different substituents for the purpose of imparting flexibility or controlling the hydrophilicity, as long as the effects of the invention are not changed. is there.

Further, as a hydrophilic polymer which effectively exhibits the effect of the present invention, a carboxylate-based copolymer can be mentioned.

The carboxylate type copolymer preferably used in the present invention is, from the viewpoint of water absorption and durability,
Α, β-unsaturated compounds having one or two carboxyl groups or carboxyl group-derived groups such as carboxyl groups, carboxylate salts, carboxylic acid amides, carboxylic acid imides, carboxylic anhydrides, etc. A saponification reaction product of a carboxylic acid copolymer contained as a component is exemplified.

Specific examples of the α, β-unsaturated compound include:
Acrylic acid, methacrylic acid, acrylamide, methacrylamide, maleic anhydride, maleic acid, maleic amide, maleic imide, itaconic acid, crotonic acid, fumaric acid, mesaconic acid, and the like, which are necessary for the present invention. It is possible to combine with another monomer component copolymerizable within a range showing hydrophilicity.

Examples of other copolymerizable monomer components include ethylene, propylene, isobutylene, 1-butylene, diisobutylene, methyl vinyl ether, styrene, vinyl acetate, acrylic acid ester, methacrylic acid ester and acrylonitrile. Examples thereof include olefins, vinyl compounds and vinylidene compounds.

When combined with other monomers, the α, β-unsaturated compound containing a carboxyl group or a group convertible to this is usually 10 mol% or more in all the monomer components,
More preferably, it is at least 40 mol%.

A polymer containing an α, β-unsaturated compound containing a carboxyl group or a group convertible to the carboxyl group as a monomer is usually prepared by radical polymerization. The degree of polymerization is not particularly limited.

Among the polymers thus prepared, a polymer or copolymer of acrylic acid or methacrylic acid, a copolymer of α-olefin or vinyl compound and maleic anhydride is preferable.

These polymers or copolymers are prepared by using compounds such as hydroxides, oxides or carbonates of alkali metals or alkaline earth metals such as sodium, potassium, magnesium and barium, ammonia, amines and the like. Hydrophilicity is preferably imparted by carrying out a saponification reaction. In these reactions, the polymer or the copolymer is dissolved or dispersed in various organic solvents or water, and the above-mentioned alkali metal compound, alkaline earth metal compound, ammonia, amine, etc. are added thereto with stirring. It is carried out by

Among such carboxylate type copolymers, particularly vinyl ester / (meth) acrylic acid ester copolymers, the hydrophilic swelling layer exhibits appropriate water swelling property, printing durability and ink. It is preferable in that both of the resilience are satisfied.

The vinyl ester / (meth) acrylic acid ester copolymer preferably used in the present invention can be produced by a known method. For example, polymer chemistry, 7
Vol. 142, p. 1950. That is, it is appropriately selected depending on the polymerization method, for example, polymerization initiation of peroxides such as di-t-butyl peroxide and benzoyl peroxide, persulfates such as ammonium persulfate, and azo compounds such as azobisisobutyronitrile. It is synthesized by radical polymerization using an agent. As the polymerization method,
Solution polymerization, emulsion polymerization, suspension polymerization and the like are required. When the amount of the (meth) acrylic acid ester component in the copolymer is small, the water absorption is small. When the amount is too large, the water absorption state is high and the film strength tends to be extremely lowered.

The proportion of the (meth) acrylic acid ester component in the coalescence is generally preferably in the range of 20 to 80 mol%, and in order to achieve both water absorption and mechanical strength when containing water, it is 30 to 70 mol%. It is preferable.

The vinyl ester used in the present invention includes vinyl acetate, vinyl propionate, vinyl stearate and the like. As the (meth) acrylic acid ester, an alkyl ester of (meth) acrylic acid,
Specific examples include methyl ester, ethyl ester, n-propyl ester, isopropyl ester, n-butyl ester and t-butyl ester.

The above-described copolymer preferably undergoes a saponification reaction in the presence of an alkali catalyst. As the solvent used for the saponification reaction, alcohol and an aqueous alcohol solution are preferable. As the catalyst used for the saponification reaction, a known alkali catalyst is used, and an alkali metal hydroxide such as sodium hydroxide or potassium hydroxide is particularly preferable. The saponification reaction is completed at 20 to 80 ° C for 1 to 10 hours. The salt of the saponification reaction product of the present invention can be arbitrarily changed by a known method. Commonly used salt-forming substances include sodium hydroxide, potassium hydroxide, ammonium hydroxide, monomethylamine, dimethylamine, trimethylamine, monoethylamine, diethylamine, triethylamine, monoisopropylamine, diisopropylamine, triisopropylamine, and monoethanolamine. , Diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, triisopropanolamine, N, N-dimethylethanolamine, N, N-
Examples include dimethylisopropanolamine, cyclohexylamine, benzylamine, aniline, pyridine and the like.

It is also possible to add polyvalent metal salts of alkaline earth metal salts such as magnesium and calcium in the form of a mixed salt with the above-mentioned salts.

Another hydrophilic polymer that effectively exhibits the effects of the present invention is an N-vinylcarboxylic acid amide copolymer. The N-vinylcarboxylic acid amide-based copolymer is a copolymer having an N-vinylcarboxylic acid amide (hereinafter, abbreviated as NVA) represented by the following general formula (I) as an essential repeating unit (hereinafter, NVA-based copolymer). (Abbreviated as copolymer)
Means

[0046]

Embedded image (Where R1 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, R2 is a hydrogen atom, a methyl group, a phenyl group, R3
Represents a hydrogen atom or a linear or branched alkyl group having 1 to 8 carbon atoms. Examples of NVA include N-vinylacetamide and N-vinylacetamide.
-Vinylformamide, N-vinylpropionamide, N-vinylbenzoamide, N-methyl-N-vinylbenzoamide, N-phenyl-N-vinylacetamide, N-phenyl-N-vinylbenzoamide and the like. However, the present invention is not limited to these examples.

From the viewpoint of water absorption and durability, the NVA copolymer preferably used in the present invention is a carboxyl group such as a carboxyl group, a carboxylic acid salt, a carboxylic acid amide, a carboxylic acid imide, or a carboxylic acid anhydride, or a carboxyl group. It is preferable to contain, as a copolymerized unit, an α, β-unsaturated compound having one or two groups capable of being induced to a group in the molecule.

Specific examples of the α, β-unsaturated compound include:
Acrylic acid, methacrylic acid, acrylamide, methacrylamide, maleic anhydride, maleic acid, maleic amide, maleic imide, itaconic acid, crotonic acid, fumaric acid, mesaconic acid, and the like, which are necessary for the present invention. It is possible to combine with another monomer component copolymerizable within a range showing hydrophilicity.

Examples of other copolymerizable monomer components include ethylene, propylene, isobutylene, 1-butylene, diisobutylene, methyl vinyl ether, styrene, vinyl acetate, acrylic acid ester, methacrylic acid ester, and acrylonitrile. Examples thereof include olefins, vinyl compounds and vinylidene compounds.

When combined with other monomers, the NVA unit is usually not less than 10 mol% and not more than 40 mol% in all the monomer components.
More preferably, it is the above.

Polymers containing NVA are usually prepared by radical polymerization. The degree of polymerization is not particularly limited.

Specific examples of the NVA-based copolymer include the following polymers.

Poly (N-vinylacetamide), N-vinylacetamide / (meth) acrylic acid copolymer ((meth) □□□□ in the following description means □□□□ or meta □□□ Is an abbreviation for □) and its partially or completely neutralized product (“partially or fully neutralized product” means hydrogen in a polymerizable functional group such as carboxylic acid, sulfonic acid, phosphoric acid in the copolymer). Some or all of the ions are sodium,
Alkali metal salts such as potassium, and metal earth chlorides such as calcium and barium are substituted), N
-Vinylacetamide / crotonic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / maleic acid copolymer and its partially or completely neutralized product, N-
Vinyl acetamide / fumaric acid copolymer and partially or completely neutralized product thereof, N-vinyl acetamide / citraconic acid copolymer and partially or completely neutralized product thereof, N-vinyl acetamide / cinnamic acid copolymer and partially thereof Or a completely neutralized product, an N-vinylacetamide / vinyl sulfonic acid copolymer and a partially or completely neutralized product thereof, N
-Vinylacetamide / maleic anhydride copolymer and its partially or completely neutralized product, N-vinylacetamide /
Itaconic acid copolymer and its partially or completely neutralized product,
N-vinylacetamide / aconitic acid copolymer and its partially or completely neutralized product, N-vinylacetamide /
3-butenoic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / 4-pentenoic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / allylsulfonic acid copolymer and its Partially or completely neutralized product, N-vinylacetamide / methallyl sulfonic acid copolymer and partially or completely neutralized product thereof, N
-Vinylacetamide / allylphosphoric acid copolymer and its partially or completely neutralized product, N-vinylacetamide / carboxyethyl acrylate copolymer and its partially or completely neutralized product, N-vinylacetamide / 2-acroylethylphosphoric acid Copolymer and its partially or completely neutralized product, N-vinylacetamide / 3-acroylpropylphosphoric acid copolymer and its partially or completely neutralized product, N
-Vinylacetamide / 8-methacryloyloctylphosphoric acid copolymer and its partially or completely neutralized product, N-vinylacetamide / 2-acrylamido-n-propanesulfonic acid copolymer and its partially or completely neutralized product, N- Vinylacetamide / 2-acrylamide-n
-Octansulphonic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / 2-acrylamido-2-methylpropanesulfonic acid copolymer and its partially or completely neutralized product, N-vinylacetamide /
Acrylic acid / itaconic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / methacrylic acid /
Aconitic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid / 3-butenoic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / methacrylic acid / 4-pentenoic acid Copolymer and partially or completely neutralized product thereof, N-vinylacetamide / vinylsulfonic acid / itaconic acid copolymer and partially or completely neutralized product thereof, N-vinylacetamide / acrylic acid / allylsulfonic acid copolymer and Partially or completely neutralized product, N-vinylacetamide / maleic acid / allylphosphoric acid copolymer and its partially or completely neutralized product, N-vinylacetamide / fumaric acid / carboxyethyl acrylate copolymer and its part or complete medium Japanese products, N-vinylacetamide / methacrylic acid / 2-acryloyl Tyruphosphoric acid copolymer and its partially or completely neutralized product, N-vinylacetamide / methacrylic acid / 3-acryloylpropylphosphoric acid copolymer and its partially or completely neutralized product, N-vinylacetamide / fumaric acid / 2- Acrylamide-n-propanesulfonic acid copolymer and its partially or completely neutralized product, N-
Vinylacetamide / cinnamic acid / 2-acrylamide-
n-octane sulfonic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid /
2-Acrylamido-2-methylpropanesulfonic acid copolymer and its partially or completely neutralized product, N-vinylacetamide / propylene copolymer, N-vinylacetamide / 1-pentene copolymer, N-vinylacetamide / chlorinated Allyl copolymer, N-vinylacetamide / allyl alcohol copolymer, N-vinylacetamide / methallylamine copolymer, N-vinylacetamide / N,
N-diethylallylamine copolymer, N-vinylacetamide / vinyl chloride copolymer, N-vinylacetamide / acrylonitrile copolymer, N-vinylacetamide / allyl acetate copolymer, N-vinylacetamide / methyl vinyl ketone copolymer Combined, N-vinylacetamide /
Methyl (meth) acrylate copolymer, N-vinylacetamide / t-butyl acrylate copolymer, N-vinylacetamide / hydroxyethyl methacrylate copolymer, N-vinylacetamide / ethyl crotonate copolymer, N-vinyl acetamide / dimethylaminoethyl acrylate copolymer, N-vinyl acetamide / diethylene glycol ethoxy acrylate copolymer, N-vinyl acetamide / methoxy polyethylene glycol #
1000 methacrylate copolymer, N-vinylacetamide / acrylamide copolymer, N-vinylacetamide / N-methylacrylamide copolymer, N-vinylacetamide / N-methylolacrylamide copolymer,
N-vinylacetamide / N, N-diethylacrylamide copolymer, N-vinylacetamide / N, N-dimethylaminoethylmethacrylamide copolymer, N-vinylacetamide / N-vinyl-N, N-dimethylamine copolymer Coalesce, N-vinylacetamide / methyl vinyl ether copolymer, N-vinylacetamide / vinyl acetate copolymer, N-vinylacetamide / styrene copolymer,
N-vinylacetamide / p-methylstyrene copolymer, N-vinylacetamide / p-hydroxystyrene copolymer, N-vinylacetamide / p-aminostyrene copolymer, N-vinylacetamide / N-vinylpyrrolidone copolymer Combined, N-vinylacetamide / N-vinylpropionamide copolymer, N-vinylacetamide / N-phenyl-N-vinylacetamide copolymer, N
-Vinylacetamide / acrylic acid / allyl alcohol copolymer and its partially or completely neutralized product, N-vinylacetamide / maleic acid / methallylamine copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid / N, N-dimethylallylamine copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid / acrylonitrile copolymer and its partially or completely neutralized product, N-vinylacetamide /
Methacrylic acid / allyl acetate copolymer and its partially or completely neutralized products, N-vinylacetamide / crotonic acid /
Methyl vinyl ketone copolymer and its partially or completely neutralized product, N-vinyl acetamide / vinyl sulfonic acid / methyl acrylate copolymer and its partially or completely neutralized product, N-vinyl acetamide / maleic acid / methacrylic acid- t-Butyl copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid / hydroxyethyl methacrylate copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid / methacrylic acid hydroxy Propyl copolymer and partially or completely neutralized product thereof, N-vinylacetamide / acrylic acid / diethylaminoethyl methacrylate copolymer and partially or completely neutralized product thereof, N-vinylacetamide / fumaric acid / diethylene glycol ethoxyacrylate copolymer and Partially or completely neutralized product, N-vinylacetamide / acrylic acid / methoxy polyethylene glycol # 1000 methacrylate copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid / acrylamide copolymer and its part or Completely neutralized product, N-vinylacetamide / vinylphosphoric acid /
N-methylacrylamide copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid /
N-methylolacrylamide copolymer and its partially or completely neutralized product, N-vinylacetamide / methacrylic acid / N, N-diethylacrylamide copolymer and its partially or completely neutralized product, N-vinylacetamide /
Maleic acid / N, N-dimethylaminoethyl methacrylamide copolymer and its partially or completely neutralized product, N-
Vinylacetamide / Fumaric acid / N-vinyl-N, N-
Dimethylamine copolymer and partially or completely neutralized product thereof, N-vinylacetamide / methacrylic acid / methylvinylether copolymer and partially or completely neutralized product thereof, N-vinylacetamide / acrylic acid / vinyl acetate copolymer and Partial or complete neutralized product, N-vinylacetamide / methacrylic acid / styrene copolymer and partial or complete neutralized product, N-vinylacetamide /
Vinyl sulfonic acid / p-hydroxystyrene copolymer and its partially or completely neutralized product, N-vinylacetamide / acrylic acid / N-vinylpyrrolidone copolymer and its partially or completely neutralized product, N-vinylacetamide / croton Acid / N-vinylpropionamide copolymer and its partially or completely neutralized product, N-vinylacetamide / itaconic acid / allyl alcohol copolymer and its partially or completely neutralized product, N-vinylacetamide / aconitic acid / N, N-dimethylallylamine copolymer and its partially or completely neutralized product, N-vinylacetamide / 3-butenoic acid / acrylonitrile copolymer and its partially or completely neutralized product, N-vinylacetamide /
Allyl sulfonic acid / allyl acetate copolymer and its partially or completely neutralized product, N-vinyl acetamide / allyl phosphoric acid / methyl vinyl ketone copolymer and its partially or completely neutralized product, N-vinyl acetamide / itaconic acid / acrylic Methyl acid copolymer and its partially or completely neutralized product, N-vinylacetamide / itaconic acid / hydroxyethyl methacrylate copolymer and its partially or completely neutralized product, N-vinylacetamide / 3-butenoic acid / methacrylic acid Hydroxypropyl copolymer and its partially or completely neutralized product, N-vinylacetamide / 4-
Pentenoic acid / diethylaminoethyl methacrylate copolymer and its partially or completely neutralized product, N-vinylacetamide / 2-acryloylethylphosphoric acid / diethylene glycol ethoxyacrylate copolymer and its partially or completely neutralized product, N-vinylacetamide / 2-Acrylamido-2-methylpropane sulfonic acid / methoxy polyethylene glycol # 1000 methacrylate copolymer and its partially or completely neutralized product, N-vinylacetamide / itaconic acid / N-methylol acrylamide copolymer and its partially or completely medium Sulfonate, N-vinylacetamide / 2-acrylamido-2-methylpropanesulfonic acid / N, N-dimethylaminoethylmethacrylamide copolymer and partially or completely neutralized product thereof, N-vinylacetate Toamido / aconitic acid / methyl vinyl ether copolymer and its partially or completely neutralized product, N- vinylacetamide / allyl sulfonic acid / vinyl acetate copolymer and its partially or completely neutralized product, N
-Vinylacetamide / allylphosphoric acid / styrene copolymer and its partially or completely neutralized product, N-vinylacetamide / itaconic acid / N-vinylpyrrolidone copolymer and its partially or completely neutralized product, N-vinylacetamide / 2 -Acrylamido-2-methylpropanesulfonic acid / N-vinylpropionic acid amide copolymer and partially or completely neutralized products thereof.

Among the polymers prepared as described above, particularly NVA and carboxylic acid salt-based copolymers such as acrylic acid, methacrylic acid and maleic anhydride, the hydrophilic swelling layer exhibits an appropriate water swelling property. In addition, it is preferable from the viewpoint of satisfying both printing durability and ink repellency. The N-vinylacetamide / (meth) acrylic acid salt type copolymer is more preferable.

The hydrophilic polymers used in the present invention can be used alone or in admixture of two or more.

Next, the hydrophobic polymer used in the hydrophilic swelling layer of the present invention will be described.

The present invention is characterized in that the hydrophobic polymer is mainly composed of silicone. Silicone has rubber elasticity and ink repellency from the viewpoint that the hydrophilic swelling layer has an appropriate water swelling property and simultaneously achieves printing durability, and also has a suitable phase with a hydrophilic polymer. It is preferable from the viewpoint of forming a separated structure.

The silicone referred to in the present invention means a known organosilicon compound having a siloxane bond in a part or all of the skeleton and having an organic group directly bonded to the silicon atom thereof. Examples of the silicone preferably used in the present invention include silicone oil, silicone rubber, silicone resin, and silicone powder from the aspect of form.

Specific examples of the silicone oil include dimethyl silicone oil, phenylmethyl silicone oil, alkyl modified silicone oil, fluorosilicone oil, polyether modified silicone oil, fatty acid ester modified silicone oil, methyl hydrogen silicone oil, silanol group-containing. Silicone oil,
Examples thereof include alkoxy group-containing silicone oil, amino-modified silicone oil, carboxylic acid-modified silicone oil, carbinol-modified silicone oil, epoxy-modified silicone oil and mercapto-modified silicone oil.

Specific examples of the silicone rubber include heat vulcanizing type silicone rubber, fluorosilicone rubber, room temperature curing type silicone rubber and the like.

Specific examples of the silicone resin include straight silicone resin, silanol functional group type silicone resin, methoxy group functional group type silicone resin, silicone modified alkyd resin, silicone modified epoxy resin, silicone modified polyester resin, silicone modified acrylic resin, Examples thereof include silicone-modified phenol resin.

Among these silicones, from the viewpoint of advantageously forming the hydrophilic swelling layer of the present invention, it is preferably used in the form of a silicone emulsion. The emulsion referred to here means a hydrophobic polymer suspension aqueous solution in which fine polymer particles and, if necessary, particles comprising a protective layer surrounding the particles are dispersed in water.

In many cases, the emulsion can be easily dispersed in water, which is a good solvent for the hydrophilic polymer, and a preferable phase separation structure that the hydrophilic swelling layer of the present invention should have is provided. It is advantageous in that it is formed.

That is, it means a self-emulsification or forced emulsification aqueous solution basically composed of emulsion particles composed of polymer particles as a dispersoid and a protective layer formed as necessary, and a dilute aqueous solution as a dispersion medium. That is, as a specific example of the silicone emulsion preferably used in the present invention, the above silicone oil is mixed with water together with an emulsifier, an additive, an organic solvent, a homogenizer,
A product obtained by applying a shearing force using a homomixer, a colloid mill, a sand grinder or the like to emulsify is preferably used. The emulsification method used to obtain the silicone emulsion preferably used in the present invention includes the following (1)
The methods (3) to (3) are mentioned.

(1) Agent-in-water method A method in which an emulsifier and the like are dissolved in advance in an aqueous phase and silicone oil is added to this aqueous phase. (2) agent-in-oi
Method 1 A method in which an emulsifier or the like is dissolved in an oil phase containing silicone oil as a main component and an aqueous phase is added to this oil phase.

(3) Phase inversion method An emulsifier or the like is dissolved in an oil phase, and an aqueous phase is added little by little to the oil phase to prepare a W / O emulsion, and then an aqueous phase is further added to the O / W emulsion. How to invert.

Among the silicone oils which are the raw materials for these silicone emulsions, the silicone oil having a reactive functional group is preferably used from the viewpoint of effectively carrying out a crosslinking reaction with a hydrophilic polymer or another hydrophobic polymer. To be

That is, methyl hydrogen silicone oil, silanol group-containing silicone oil, alkoxy group-containing silicone oil, amino-modified silicone oil, carboxylic acid-modified silicone oil, carbinol-modified silicone oil, epoxy-modified silicone oil, mercapto-modified silicone oil, etc. Is mentioned.

In addition to silicone oil, the above-mentioned known silicone rubber, silicone resin, silicone powder and the like can be optionally mixed in preparing an emulsion.

Specific product groups include SH703 as a dimethylpolysiloxane silicone emulsion.
6, SH8706, SH8710, SM8701, SM
8705, SM8755, BY12-803, SM70
25, BY22-849, BY22-835, BY22
-836 (all manufactured by Toray Dow Corning Silicone Co., Ltd.) and the like. As a methyl hydrogen polysiloxane silicone emulsion, SM
8707, SH8200, SH8241, BY22-8
61 (all Toray Dow Corning Silicone Co., Ltd.)
Manufactured). Amino-modified silicone-based silicone emulsions include SM8702, SM870
9, SM8711, BY22-812, BY22-81
6, BY22-819, BY22-823, BY22-
830, BY22-842, BY22-850, BY2
2-854 (all manufactured by Toray Dow Corning Silicone Co., Ltd.) and the like. As a carboxy-modified silicone-based silicone emulsion, BY22-84
0 (manufactured by Toray Dow Corning Silicone Co., Ltd.) and the like. Other aqueous coating emulsions such as BY22-826, BY22-827, BY2
2-856 (all manufactured by Toray Dow Corning Silicone Co., Ltd.) and the like.

In addition to these silicone emulsions, it is also preferable to add known emulsions, latexes and the like.

Specific examples thereof include vinyl polymer latex, conjugated diene polymer latex and aqueous or water dispersed polyurethane resin.

Examples of the vinyl polymer type latex include acrylic type, vinyl acetate type and vinylidene chloride type. Examples of the conjugated diene polymer-based latex include styrene / butadiene-based (hereinafter abbreviated as SB-based), acrylonitrile / butadiene-based (hereinafter abbreviated as NB-based), methyl methacrylate / butadiene-based (hereinafter abbreviated as MB-based),
Chloroprenes and the like can be mentioned.

Examples of the acrylic latex include copolymers containing acrylic acid ester and methacrylic acid ester as essential components. Specific examples include those obtained by copolymerizing at least one or more of methyl methacrylate, ethyl acrylate, butyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, and styrene.

Examples of the vinyl acetate type latex include vinyl acetate alone or copolymers with acrylic acid ester, higher vinyl acetate, ethylene and the like.

Examples of the vinylidene chloride latex include copolymers of vinylidene chloride and methyl acrylate, octyl acrylate, 2-ethylhexyl acrylate, acrylonitrile, vinyl chloride and the like.

As the SB type latex, styrene and butadiene as essential components, methyl methacrylate,
Examples include higher acrylic acid esters, acrylonitrile, acrylamide, hydroxyethyl acrylate, and copolymers with unsaturated carboxylic acids (such as itaconic acid, maleic acid, acrylic acid, and methacrylic acid).

Other examples include latexes containing conjugated diene compounds such as NB type, MB type and chloroprene type.

The conjugated diene rubber referred to here is
1,3-butadiene, 2-methyl-1,3-butadiene (isoprene), 2,3-dimethyl-1,3-butadiene, 2-chloro-1,3-butadiene (chloroprene)
Means a compound having an unsubstituted or substituted 1,3-butadiene skeleton having a carbon-carbon double bond at the 1,3-position, such as a homo- or block copolymer rubber (polymer) having these as essential components. .

Block copolymer rubbers include 1,3-dienes such as 1,3-butadiene and 2-methyl-1,3-butadiene (isoprene), and styrene and α-methyl which give glassy polymers at room temperature. Examples thereof include block copolymers with monovinyl-substituted aromatic compounds such as styrene and vinyltoluene.

As such a copolymer rubber, various known types can be exemplified, but an ABA type block copolymer rubber (where A is a monovinyl-substituted aromatic compound, preferably a glass transition) is used. An amorphous polymer segment having a point of 70 ° C. or higher and a degree of polymerization of 10 to 2500, B means 1,3-diene, and preferably a number average molecular weight of 500 to 25,000. (Meaning) and the like. The same applies to the hydrogenated product of the block copolymer rubber.

Specific examples of the homo- and copolymer rubbers used in the present invention include polybutadiene, polyisoprene (including natural rubber), polychloroprene, styrene-butadiene copolymer, carboxy-modified styrene-butadiene copolymer, and acrylic. Acid ester-butadiene copolymer (for example, butadiene-2-ethylhexyl acrylate copolymer, butadiene-n-octadecyl acrylate copolymer), methacrylic acid ester-butadiene copolymer, isobutylene-isoprene copolymer, acrylonitrile-butadiene copolymer Polymer, carboxy-modified acrylonitrile-butadiene copolymer, acrylonitrile-isoprene copolymer, vinylpyridine-butadiene copolymer, vinylpyridine-styrene-butadiene copolymer,
Examples thereof include a styrene-chloroprene copolymer and a styrene-isoprene copolymer.

As the aqueous or water-dispersed polyurethane resin, a hydrophobic polyurethane resin composed of polyester polyol, polyether polyol, poly (ester / ether) polyol and polyisocyanate is compulsorily emulsified by using a surfactant. Emulsion type, a hydrophilic group or a hydrophilic segment is added to the resin itself, and self-emulsifying type obtained by self-dispersing and emulsifying. In both cases, a non-reactive one and a blocking group such as an isocyanate group are reactive groups. The reactive ones that are blocked are mentioned.

These emulsions can be used alone or in admixture of two or more.

The hydrophilic swelling layer of the present invention is formed by laminating on the substrate by mixing the above-mentioned hydrophilic polymer and hydrophobic polymer, cross-linking or pseudo-cross-linking them if necessary, and insolubilizing them in water.

For the cross-linking, it is preferable to carry out the cross-linking reaction by using the reactive functional groups of the hydrophilic polymer and the hydrophobic polymer.

The cross-linking reaction may be covalent cross-linking or ionic bond cross-linking.

Examples of the compound used in the crosslinking reaction include known polyfunctional compounds having a crosslinking property, such as polyepoxy compounds, polyisocyanate compounds, poly (meth) acrylic compounds, polymercapto compounds, polyalkoxysilyl compounds, Polyvalent metal salt compounds, polyamine compounds, aldehyde compounds, polyvinyl compounds, hydrazine and the like can be mentioned. The crosslinking reaction is carried out by adding a known catalyst,
The reaction is promoted.

When preparing a silicone emulsion preferably used as the hydrophobic polymer of the present invention, a reactive functional group such as a carboxyl group, a hydroxyl group, a methylolamide group, an epoxy group, an arbonyl group, an amino group, etc. is present and self-existing. Examples thereof include a method of crosslinking and a method of forming a crosslinked structure by using the above polyfunctional compound as a crosslinking agent.

Specific examples of known polyfunctional compounds having crosslinkability include the following compounds.

(1) Sublimation sulfur, by-product sulfur produced by oxidizing hydrogen sulfide, colloidal sulfur produced by wet-oxidizing hydrogen sulfide, etc. In addition, thiuram compounds such as dithiomorpholine, thioplast tetramethyl thiuram disulfide, tetramethyl thiuram monosulfide, dipentamethylene thiuram tetrasulfide, which decompose to generate sulfur when heated, piperidine pentamethylene thiocarbamate, pipecoline pipecolic Dithiocarbamate compounds such as ludithiocarbamate and sodium dimethyldithiocarbamate, xanthate compounds such as sodium isopropylxanthogenate and zinc butylxanthate, thiourea compounds such as thiourea and thiocarbanilide, zinc salts of thiazole such as diphenylguanidine, and mercaptobenzothiazole Sodium salt, dibenzothiazyl disulfide, cyclohexylamine salt of mercaptobenzothiazole Such as thiazole-based compound.

(2) Butyraldehyde-monobutylamine condensate, butyraldehyde-aniline condensate, heptaaldehyde-aniline reaction product, salt ethyl-formaldehyde-ammonia reaction product, and other aldehyde amine compounds, zinc oxide, tellurium, selenium, Zirconium carbonate ammonia, organic peroxides such as benzoyl peroxide and dicumyl peroxide.

Further, examples of the crosslinking accelerator include zinc carbonate, stearic acid, oleic acid, lauric acid, zinc stearate, dibutylammonium oleate, diethanolamine, triethanolamine and diethylene glycol.

(3) Polyepoxy compound, urea resin, polyamine, melamine resin, benzoguanamine resin, acid anhydride and the like.

Specific examples of the polyepoxy compound include glycerin dipolylysidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, trimethylolpropane polyglycidyl ether, trimethylolpropane polyglycidyl ether, sorbitol polyglycidyl ether and the like. Is mentioned.

Specific examples of the polyamine include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, polyethyleneimine,
And polyamidoamine.

(4) Polyisocyanate compounds and the like.

Examples of polyisocyanate compounds include:
Tolylene diisocyanate, hexamethylene diisocyanate, diphenylmethane isocyanate, liquid diphenylmethane diisocyanate, polymethylene polyphenyl isocyanate, xylylene diisocyanate, cyclohexyl diisocyanate, cyclohexane phenylene diisocyanate, naphthalene-1,5-diisocyanate, isopropylbenzene-2,4-diisocyanate, polypropylene Glycol / tolylene diisocyanate addition reactants.

(5) Silane compounds and the like.

Examples of the silane compound include aminoisopropenoxytrimethoxysilane, epoxypropyltrimethoxysilane, methyltrimethoxysilane and the like.

These cross-linking agents can be used alone or in admixture of two or more. Water is mainly used as the dispersion medium, but a known organic solvent can be added as necessary. As a method of adding the organic solvent, a method of adding as a polymerization solvent and a method of adding as a mixed solvent to an emulsion solution after emulsion polymerization are possible.

As a method for mixing the hydrophilic polymer and the hydrophobic polymer of the hydrophilic swelling layer of the present invention, a kneading method using a mixer such as a roll mixer with three rolls, a kneader, a homogenizer, a ball mill, etc. The mixing is preferably carried out by a known method used for producing a paint or putty, such as a method of wet mixing and dispersing using a disperser.

As a method for forming the hydrophilic swelling layer of the present invention, since an aqueous silicone emulsion is preferably used as the hydrophobic polymer, each component (hydrophilic polymer, hydrophobic polymer, etc.) is mixed in an aqueous solution system. However, a method in which a crosslinking agent is added as necessary is preferable from the viewpoint of realizing a uniform phase-separated structure and improving ink repulsion.

Therefore, it is particularly preferable to use a water-soluble polyfunctional compound as the crosslinking agent. That is, it is preferable to use a water-soluble polyepoxy compound, polyamine compound, melamine compound, or the like.

Next, the phase separation structure of the hydrophilic swelling layer according to the present invention will be described.

The hydrophilic swelling layer used in the present invention has a phase-separated structure composed of at least two phases of the above-mentioned hydrophilic polymer as a main component and hydrophobic polymer as a main component. It has a feature.

By adopting a phase-separated structure composed of a phase containing a hydrophilic polymer as a main component and a phase containing a hydrophobic polymer as a main component, both ink repulsion and printing durability are realized in a wide composition range. It becomes possible.

The composition ratio of the hydrophilic polymer phase and the hydrophobic polymer phase constituting the phase-separated structure is free, and (1) either one is a continuous phase and the other is a dispersed phase, (2) hydrophilic A form in which the hydrophilic and hydrophobic polymer phases have a continuous phase and a dispersed phase, respectively (3) A form in which the hydrophilic and hydrophobic polymer phases are both continuous phases can be freely selected. The above (1)-
FIG. 1 is a schematic diagram showing an example of the phase separation structure of (3).
3 are shown.

That is, when a material in which the hydrophilic polymer exhibits relatively strong hydrophilicity is selected (such as a water-soluble polymer and a pseudo-water-soluble polymer), the ratio of the hydrophilic polymer contained in the hydrophilic swelling layer is determined by the ink repulsion property. In addition, a relatively small amount is sufficient from the viewpoint of printing durability, and the proportion of the hydrophobic polymer is relatively large, so that the form of (1) or (2) above in which the hydrophilic polymer is used as the dispersed phase is obtained. Is preferred. On the other hand, when a material whose hydrophilic polymer shows relatively weak hydrophilicity (such as a water-swellable polymer) is selected, the ratio of the hydrophilic polymer contained in the hydrophilic swelling layer is determined in terms of ink repellency and printing durability. From a relatively large amount, and the proportion of the hydrophobic polymer is relatively small.
It is preferable to take the form of (2) or (3).

That is, the preferred phase-separated structure of the hydrophilic swelling layer used in the present invention varies depending on the rubber elasticity and water swelling property of the layer, but it depends on the degree of hydrophilicity of the hydrophilic polymer.

In the case of the form (1), in order that the hydrophobic polymer phase is mainly a continuous phase, the composition of the hydrophobic polymer is 50% by weight or more, preferably 60 to 95% by weight, It is more preferably 70 to 90% by weight. When the composition ratio of the hydrophobic polymer is 50% by weight or less, the performance of the hydrophilic swelling layer as an ink repellent layer is improved in the initial stage of printing, but the printing durability tends to sharply decrease. On the other hand, when the composition ratio of the hydrophobic polymer exceeds 95% by weight, the hydrophilic polymer in the hydrophilic swelling layer cannot sufficiently absorb water, and the hydrophilicity is insufficient, and the ink repulsion tends to be extremely reduced.

In the cases of the forms (2) and (3), both the hydrophilic polymer and the hydrophobic polymer are 20% by weight or more, preferably 40% by weight or more.

The hydrophilic swelling layer preferably has rubber elasticity.

The rubber elasticity of the hydrophilic swelling layer is characterized by the value of the initial elastic modulus measured by the method described below.

[Method of measuring initial elastic modulus of hydrophilic swelling layer]
A solution having the same composition as the hydrophilic swelling layer of the photosensitive lithographic printing plate precursor to be measured is spread on a Teflon dish and dried and cured at 60 ° C. for 24 hours. The obtained dried and cured film is 40 mm long and 1.95 wide using a razor blade or the like.
mm, and a thickness of about 0.2 mm.

The test piece obtained was measured at 25 ° C. before measurement.
After being left to stand in an environment of 50% RH for 24 hours or more to adjust the humidity, the thickness was measured with a micro gauge, and the initial elastic modulus was measured under the following tensile conditions. Data processing is JIS K6
It was carried out according to 301.

Tensile speed 200 mm / min Distance between chucks 20 mm Number of repetitions 4 times Measuring machine “RTM-100” manufactured by Orientec Co., Ltd. The initial elastic modulus of the hydrophilic swelling layer used in the present invention is 0.
The range of 01 to 10 kgf / mm @ 2 is preferable from the viewpoint of ink repulsion and shape retention. It is preferably in the range of 0.01 to 5 kgf / mm @ 2, and 0.0
The range of 1 to 2 kgf / mm2 is more preferable.

That is, the initial elastic modulus is 0.01 kgf /
If it is less than mm 2, the shape retention of the hydrophilic swelling layer tends to be extremely lowered, and the durability during printing tends to be extremely lowered.

On the other hand, when the initial elastic modulus is more than 10 kgf / mm 2, the rubber elasticity is insufficient and the ink repulsion tends to be extremely lowered.

The hydrophilic swelling layer used in the present invention preferably has a water absorption value measured according to the following definition within a specific range.

[0121]

[Equation 1] However, the water absorption amount means a value measured according to the following definition.

Water absorption (g / m ² ) = W _WET −W _DRY W _DRY : Weight in dry state (g / m 2) W _WET : Weight after immersion in water at 25 ° C. for 10 minutes (g
/ M2) [Measurement method of water absorption amount] The photosensitive lithographic printing plate precursor to be measured is cut into a predetermined area and immersed in purified water at 25 ° C. After soaking for 10 minutes, excess water adhering to the front and back surfaces of the hydrophilic swelling layer of the original plate was quickly wiped off with "Hize Gauze" (cotton cloth: Asahi Chemical Industry Co., Ltd.),
The swelling weight WWET of the original plate is weighed. Then, the original plate is dried in an oven at 60 ° C. for about 30 minutes to obtain a dry weight WDR.
Weigh Y.

The hydrophilic swelling layer used in the present invention may have a water absorption rate of 10 to 1000%, but is preferably 5 from the viewpoint of ink repellency and shape retention.
0 to 500%. When the water absorption rate is less than 10%,
Ink repellency tends to be extremely lowered, and defects such as pinholes are likely to occur during coating. Again 1000
When it is more than%, the shape retention tends to be extremely lowered.

The hydrophilic swelling layer thickness referred to in the present invention means a value measured by a gravimetric method after peeling off the coating layer of the hydrophilic swelling layer of the dried photosensitive lithographic printing plate precursor coated on the substrate. means. The thickness of the hydrophilic swelling layer was measured according to the following equation.

Hydrophilic swelling layer thickness (g / m 2) = (W−W 0) / α W: Dry weight of the photosensitive lithographic printing plate precursor (g) W ₀ : The hydrophilic swelling layer was peeled off from W. Dry weight after (g) α: Measurement area of photosensitive lithographic printing plate precursor (m 2) [Measuring method of hydrophilic swelling layer thickness] After cutting the photosensitive lithographic printing plate precursor to be measured into a predetermined area α Dry in an oven at 60 ° C. for about 30 minutes, and weigh dry weight W. Then, the original plate is immersed in purified water to swell the hydrophilic swelling layer, and the swelling layer is peeled off using a scraper or the like. The original plate from which the hydrophilic swelling layer was peeled off and dropped again 60
Dry in an oven at ℃ for about 30 minutes and weigh dry weight W0.

The thickness of the hydrophilic swelling layer used in the present invention is
It is possible to use 0.1 to 100 g / m2,
From the viewpoint of ink repellency and shape retention, it is preferably 0.3 to 10 g / m @ 2. The thickness is 0.3 g / m2
If it is less than 1, the ink repellency tends to be extremely reduced, and defects such as pinholes are likely to occur during coating. On the other hand, if it is 10 g / m @ 2 or more, the shape-retaining property tends to deteriorate when swollen with water, which is economically disadvantageous.

In the hydrophilic swelling layer used in the present invention, in addition to the above-mentioned hydrophilic polymer, hydrophobic polymer and crosslinking agent optionally added, known anti-aging agents usually added in rubber compositions It is possible to add antioxidants, antiozonants, ultraviolet absorbers, dyes, pigments, plasticizers, etc. within a range that does not impair the effects of the present invention.

For the purpose of improving the adhesiveness with the lower layer,
Known silane coupling agents and isocyanate compounds,
It is also possible to add a catalyst or the like or to provide an intermediate layer between the substrate and the substrate.

Next, an example of a method for producing a lithographic printing plate using the photosensitive lithographic printing plate precursor according to the invention will be described, but the invention is not limited thereto.

The lithographic printing plate can be prepared from the photosensitive lithographic printing plate precursor of the invention by irradiating it with an actinic ray. That is, the difference between the image area and the non-image area is caused by the irradiation of the actinic ray.

Preferably, the photosensitive lithographic printing plate precursor according to the invention is subjected to negative working image formation. That is, the initial elastic modulus of a portion of the hydrophilic swelling layer (hereinafter referred to as an unexposed portion) that is not exposed to the actinic ray (hereinafter referred to as an unexposed portion) is increased. As a result, it becomes an ink-receptive image area, and the unexposed area becomes an ink repellent non-image area.

A known photosensitive compound is used for such image formation.

That is, a known photocrosslinking or photocurable photosensitive compound is contained in the hydrophilic swelling layer of the original plate, and the exposed area is selectively crosslinked and / or cured to increase the initial elastic modulus. Formation is achieved.

Specific examples of the following (1) to (6) can be given as known photocrosslinking or photocurable photosensitive compounds.

(1) Photopolymerizable monomer or oligomer Alcohols (ethanol, propanol, hexanol, octanol, cyclohexanol, glycerin,
(Meth) acrylic acid of trimethylolpropane, pentaerythritol, isoamyl alcohol, lauryl alcohol, stearyl alcohol, butoxyethyl alcohol, ethoxyethylene glycol, methoxyethylene glycol, methoxypropylene glycol, phenoxyethanol, phenoxydiethylene glycol, tetrahydrofurfuryl alcohol, etc. Esters, carboxylic acids (acetic acid, propionic acid, benzoic acid, acrylic acid,
An addition reaction product of methacrylic acid, succinic acid, maleic acid, phthalic acid, tartaric acid, citric acid, etc.) with glycidyl (meth) acrylate or tetraglycidyl-m-xylylenediamine or tetraglycidyl-m-tetrahydroxylylenediamine; Examples include amide derivatives (acrylamide, methacrylamide, n-methylolacrylamide, methylenebisacrylamide, and the like), addition products of an epoxy compound and (meth) acrylic acid, and the like.

More specifically, Japanese Examined Patent Publication No. 48-4170.
No. 8, JP-B-50-6034, JP-A-51-
Urethane acrylates described in JP-A-37193, JP-A-48-64183, JP-B-49-43
No. 191 and JP-B-52-30490, polyfunctional epoxy (meth) acrylate obtained by reacting an epoxy resin with (meth) acrylic acid, and N-methylol described in U.S. Pat. No. 4,540,649. Acrylamide derivatives and the like can be mentioned. Furthermore, Japan Adhesion Association Magazine VOL.20, No.7, p300-308
Photocurable monomers and oligomers described in (1) can be used.

Among them, the photopolymerizable monomer or oligomer preferably used in the present invention is a lipophilic ethylenically unsaturated compound (20) from the viewpoint of ink receptivity of the image area.
It means a photopolymerizable monomer or oligomer having a solubility in water at 8 ° C of 8% by weight or less. Is preferred.

Specific examples of the lipophilic ethylenically unsaturated compound preferably used include compounds represented by the following general formula (II).

CH2 = C (R1) -CO-O- (CH2) n-R2 (II) (wherein R1 represents hydrogen or a methyl group. R2 represents hydrogen, a substituted or unsubstituted group having 1 to 20 carbon atoms). Alkyl group, nitro group, azido group, C2-C20 alkenyl group, C4-C20 substituted or unsubstituted aryl group,
Represents a substituted or unsubstituted aralkyl group, acryloxy group or methacryloyloxy group. n is an integer of 1 to 30. Specific examples include the following compounds.

[0140]

Embedded image n means the average value of the compound represented by the above general formula. That is, the compound represented by the above general formula comprises a mixture having a distribution of n.

From the viewpoint of ink receptivity, these compounds are n
Is preferably an integer of 4 to 30, and more preferably 8 to 13. When n is 3 or less, the lipophilicity tends to be insufficient, and the ink deposition property tends to be insufficient. If n is 31 or more, the equivalent weight of the unsaturated group per weight is insufficient, and the photosensitivity is reduced. For example, n is 4, 5, 6, 7, 8, 9, 10, 1
Compounds such as 3,22 can be used.

Specific examples of the lipophilic ethylenically unsaturated compound preferably used in the present invention other than the above general formula (II) include 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, neopentyl glycol diacrylate and neopentyl. Examples thereof include glycol dimethacrylate, isooctyl acrylate, isooctyl methacrylate and the like.

These lipophilic ethylenically unsaturated compounds can be used alone or in admixture of two or more.

These lipophilic ethylenically unsaturated compounds preferably used in the present invention are added to the composition at the time of forming the hydrophilic swelling layer and allowed to exist in the layer, or the hydrophilic swelling layer is added. After formation, the compound is added onto the layer by diluting with a suitable solvent which easily penetrates into the hydrophilic swelling layer, if necessary, and impregnating into the layer.

When a relatively high molecular weight oligomer or the like is used, the former method of simultaneous addition at the time of forming the hydrophilic swelling layer is advantageously performed, and when a relatively low molecular weight monomer or oligomer is used, the latter method is used. The method of impregnation is advantageous.

(2) Photodimerization type photosensitive resin composition A photosensitive layer containing, for example, polyvinyl cinnamate, for example, P
1: 1 polycondensed unsaturated polyester of phenylenediacrylic acid and 1,4-dihydroxyethyloxycyclohexane, photosensitive polyester derived from cinnamylidene malonic acid and difunctional glycols, polyvinyl alcohol , Cinnamic acid esters of hydroxyl group-containing polymers such as Denn Pun, Cellulose, etc.

(3) A composition comprising a combination of a monomer, oligomer or polymer having an epoxy group and a known photo-acid generator. This is because the photo-acid generator produces a Lewis acid or Bronsted acid upon exposure to give an epoxy compound. The groups undergo cationic polymerization to crosslink. As the photoacid generator, allyldiazonium salt compounds, diallyliodonium salt compounds, triallylsulfonium salt compounds, triallylselenonium salt compounds,
Dialkylphenacylsulfonium salt compound, dialkyl-4-phenacylsulfonium salt compound, α-hydroxymethylbenzoin sulfonate, N-
Hydroxyiminosulfonate, α-sulfonyloxy ketone, β-sulfonyloxy ketone, iron-arene complex compound (benzene-cyclopentadienyl-iron (I
I) hexafluorophosphate), o-nitrobenzylsilyl ether compound and the like.

The following are preferably used as the monomer, oligomer or polymer having an epoxy group.

Examples thereof include methyl glycidyl ether, ethyl glycidyl ether, propyl glycidyl ether, n-butyl glycidyl ether, isobutyl glycidyl ether, pentyl glycidyl ether, cyclohexyl glycidyl ether and 2-ethylhexyl glycidyl ether.

(4) Composition of Monomer, Oligomer or Polymer Having Allyl Group and / or Vinyl Group and Monomer, Oligomer or Polymer Having Mercapto Group This is because the mercapto group is added to the allyl group and / or vinyl group when exposed to light. Crosslink.

(5) Composition of Diazonium Salt Compound and Hydroxyl Group-Containing Compound The diazo compound used in the present invention is a water-insoluble organic solvent-soluble diazo resin represented by a condensation product of p-diazodiphenylamine and formaldehyde. And so on.

Specific examples include those described in JP-B-47-1167 and JP-B-57-43890.

Examples of the diazo monomer in the diazo resin preferably used in the present invention include 4-diazo-diphenylamine, 1-diazo-4-N, N-dimethylaminobenzene and 1-diazo-4-N, N-diethylaminobenzene. , 1-diazo-4-N-ethyl-N-hydroxyethylaminobenzene, 1-diazo-4-N-methyl-N-hydroxyethylaminobenzene, 1-diazo-2,5-diethoxy-4-benzoylaminobenzene , 1-diazo-4-N-benzylaminobenzene, 1
-Diazo-4-N, N-dimethylaminobenzene, 1-
Diazo-4-morpholinobenzene, 1-diazo-2,
5-dimethoxy-4-p-tolylmercaptobenzene,
1-diazo-2-ethoxy-4-N, N-dimethylaminobenzene, p-diazo-dimethylaniline, 1-diazo-2,5-dibutoxy-4-morpholinobenzene,
1-diazo-2,5-diethoxy-4-morpholinobenzene, 1-diazo-2,5-dimethoxy-4-morpholinobenzene, 1-diazo-2,5-diethoxy-4
-P-tolylmercaptobenzene, 1-diazo-4-N
-Ethyl-N-hydroxyethylaminobenzene, 1-
Diazo-3-ethoxy-4-N-methyl-N-benzylaminobenzene, 1-diazo-3-chloro-4-diethylaminobenzene, 1-diazo-3-methyl-4-pyrrolidinobenzene, 1-diazo-2 -Chloro-4-N, N
-Dimethylamino-5-methoxybenzene, 1-diazo-3-methoxy-4-pyrrolidinobenzene, 3-methoxy-4-diazodiphenylamine, 3-ethoxy-4-
Diazodiphenylamine, 3- (n-propoxy) -4
-Diazodiphenylamine, 3- (isopropoxy)-
4-diazodiphenylamine and the like.

Examples of the aldehyde used as a condensing agent with these diazo monomers include formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, isobutyraldehyde, benzaldehyde and the like. Furthermore, as anions,
A water-soluble diazo resin can be obtained by using chloride ion, trichlorozinc acid, or the like, and boron tetrafluoride, hexafluorophosphoric acid, triisopropylnaphthalenesulfonic acid, 4,4′-biphenylsulfonic acid, 2, 5
By using -dimethylbenzenesulfonic acid, 2-nitrobenzenesulfonic acid, 2-methoxy-4-hydroxy-5-benzoyl-benzenesulfonic acid, or the like, an organic solvent-soluble diazo resin can be obtained.

In addition, these diazo resins are usually mixed with a polymer compound having a hydroxyl group as described below.

That is, as the polymer compound having a hydroxyl group, a monomer having an alcoholic hydroxyl group, for example, 2-hydroxyethyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 2,3-hydroxypropyl (meth) acrylate is used. , 2-hydroxyethyl (meth) acrylamide, triethylene glycol mono (meth) acrylate, tetraethylene glycol mono (meth) acrylate, 1,3-propanediol mono (meth) acrylate, 1,4-butanediol mono (meth) Acrylate, di (2-hydroxyethyl)
Copolymers of at least one or more monomers selected from maleates and other monomers having no hydroxyl group, and monomers having a phenolic hydroxyl group, for example, N- (4-hydroxyphenyl) (meta ) Acrylamide, N- (4-hydroxyphenyl) maleimide, o-, m-, p-hydroxystyrene, o-, m
-, A copolymer with p-hydroxyphenyl (meth) acrylate, or the like; a ring-opening reaction product of p-hydroxybenzoic acid with glycidyl (meth) acrylate; salicylic acid and 2-hydroxyethyl (meth) acrylate; And a copolymer with a hydroxyl group-containing monomer such as a reaction product of the above. Further, polyvinyl alcohol, cellulose, polyethylene glycol, polypropylene glycol, glycerin, pentaerythritol, and the like, an epoxy addition reaction product thereof, and other hydroxyl-containing natural polymer compounds can also be used.

(6) Polyisoprene rubber or polybutadiene rubber cyclized with a bisazide compound, or a photosensitive composition containing a cresol novolac resin as a main component.

These photosensitive compounds are added to the composition when the hydrophilic swelling layer is formed on the substrate so that they are present in the composition, or after the hydrophilic swelling layer is formed, the photosensitive composition is added to the composition. It is added using a method of coating on the layer and impregnating the layer.

In the case of a photosensitive composition using a polymer or an oligomer having a relatively high molecular weight, the former method of simultaneous addition at the time of forming the hydrophilic swelling layer is advantageously performed, and a monomer or an oligomer having a relatively low molecular weight is used. The latter impregnation method is advantageous in the case of a photosensitive composition using, for example,

Further, a known photosensitizer can be added to the hydrophilic swelling layer of the original plate for the purpose of sensitizing these photosensitive compounds. As the known photosensitizer, a known photosensitizer can be freely selected, and various substituted benzophenone-based compounds, substituted thioxanthone-based compounds, and substituted acridone-based compounds are preferably used. Also, substituted with a vicinal polyketaldonyl compound described in U.S. Pat.No. 236766, an .alpha.-carbonyl compound disclosed in U.S. Pat.No. 2367661, U.S. Pat. Aromatic acyloin compounds, U.S. Pat. No. 3,046,127, polynuclear quinone compounds disclosed in U.S. Pat. Benzothiazole compounds, US Pat. No. 423985
Benzothiazole compound / trihalomethyl-s-triazine compound disclosed in US Pat.
Acridine and phenazine compounds disclosed in US Pat. No. 259, oxadiazole compounds disclosed in US Pat. No. 4212970, trihalomethyl-s-containing chromophore groups disclosed in US Pat. No. 3,954,475, US Pat.
Specific examples include a triazine-based compound and a benzophenone group-containing peroxyester compound disclosed in JP-A-59-197401 and JP-A-60-76503.

The substrate of the lithographic printing plate used in the present invention is not limited at all except that it must be flexible enough to be attached to an ordinary lithographic printing machine and capable of withstanding the load applied during printing.

Typical examples are aluminum, copper, iron,
Examples thereof include a metal plate, a plastic film such as a polyester film and a polypropylene film, coated paper, and a rubber sheet. Further, the substrate may be a composite of the above materials.

Further, the surface of the substrate may be subjected to various surface treatments such as electrochemical treatment, acid-base treatment and corona discharge treatment for the purpose of improving plate inspection property and adhesiveness.

It is also possible to form a primer layer on these substrates by coating or the like for the purpose of improving the adhesiveness and preventing halation, to obtain substrates.

Next, a plate making method using the photosensitive lithographic printing plate precursor will be described.

The photosensitive lithographic printing plate precursor can be made into a printing plate through a plate making process for negative working.
That is, image exposure is performed through a negative original image film by a normal exposure light source.

As a light source used in this exposure step,
For example, a high-pressure mercury lamp, a carbon arc lamp, a xenon lamp, a metal halide lamp, a fluorescent lamp and the like can be mentioned. After such a normal exposure, rinsing with water or a developing solution dissolves or removes the photosensitive compound present in the hydrophilic swelling layer in the unexposed portion, or renders the photosensitive compound unsuitable for repelling the ink. The non-image area has a separation structure and water swelling, and the exposed area has a higher initial elastic modulus and a lower water swelling property than the unexposed area when the photosensitive compound is photocrosslinked and cured. Becomes

As described above, the photosensitive lithographic printing plate precursor is
The image is formed by changing the rubber elasticity and water swelling property of the phase separation structure of the hydrophilic swelling layer with the help of the photochemical reaction of the photosensitive compound.

Next, a printing method using the lithographic printing plate obtained according to the present invention will be described.

A known lithographic printing machine is used for such lithographic printing. That is, sheet-fed and rotary printing machines of the offset and direct printing type are used.

After image formation of the lithographic printing plate according to the present invention, the lithographic printing plate is mounted on the plate cylinders of these lithographic printing presses, and the plate surface is supplied with ink from an inking roller which comes into contact therewith.

The non-image area having the hydrophilic swelling layer on the plate surface swells with the dampening water supplied from the dampening water supply device to repel the ink. On the other hand, the image area receives the ink and supplies the ink to the surface of the offset blanket cylinder or the surface of the printing medium to form a printed image.

The fountain solution used when printing the lithographic printing plate of the present invention can of course be the etchant used in PS plates with water, but drinking water containing no additives at all. Etc. can be used arbitrarily.

Hereinafter, the present invention will be described in more detail with reference to examples.

[0175]

【Example】

Example 1 [Synthesis example of hydrophilic polymer] n-butyl methacrylate 60
g and 40 g of methyl acrylate and 0.5 g of azobisisobutyronitrile as a polymerization initiator were added to DMF3
Dissolved in 00 ml.

The solution was stirred at 65 ° C. for 8 hours to carry out solution polymerization. The obtained copolymer was precipitated in water. The methyl acrylate component was identified by NMR spectrum to be 40 mol%. The intrinsic viscosity in a benzene solution at 30 ° C. was 1.87.

Next, 8.6 g of the copolymer was added to a saponification reaction solution consisting of 200 g of methanol, 10 g of water and 40 ml of 5N NaOH, and the mixture was stirred and suspended at 25 ° C.
After performing the saponification reaction for 1 hour, the temperature was raised to 65 ° C., and the saponification reaction was further performed for 5 hours.

The saponification reaction product obtained was thoroughly washed with methanol and freeze-dried. The saponification degree was 95.2 mol%, and as a result of measurement of an infrared absorption spectrum, 1570 cm
It was confirmed that -1 had a strong absorption attributed to the -COO- group.

An aluminum plate (made by Sumitomo Light Metal Co., Ltd.) having a thickness of 0.2 mm was coated with the following composition using the hydrophilic polymer shown above, and then heat-treated at 150 ° C. for 60 minutes to 2 g / m 2 Was coated with a hydrophilic swelling layer having a thickness of.

<Hydrophilic swelling layer composition (parts by weight)> (1) Hydrophilic polymer 28 parts by weight (2) Tetraethylene glycol diglycidyl ether 5 parts by weight (3) Silicone emulsion "BY22-840" 65 parts by weight [carboxy Modified silicone emulsion: manufactured by Toray Dow Corning Silicone Co., Ltd.] (4) 2-aminopropyltrimethoxysilane 2 parts by weight (5) Purified water 900 parts by weight On the hydrophilic swelling layer coated as described above Then, a photosensitive composition having the following composition was applied and heat-treated at 100 ° C. for 3 minutes to impregnate the hydrophilic swelling layer with 0.5 g / m 2 of the photosensitive composition.

Thereafter, a 12-micron-thick single-sided matted biaxially oriented polypropylene film was laminated with a calendar roller so that the non-matted surface was in contact with the hydrophilic swelling layer, and a negative type lithographic printing plate precursor was laminated. Got

The lithographic printing plate obtained was a PCW (PLATE CONTOROL WEDGE: manufactured by KALLE) using a high-pressure mercury lamp "Jetlight 3303kW: manufactured by Oak Manufacturing Co., Ltd."
For 90 seconds through a negative film with
6 mW / cm2). Next, rinse the entire plate with tap water,
The unexposed portion of the photosensitive composition was washed and removed to obtain a printing plate.

After swelling the hydrophilic swelling layer corresponding to the ink repellent portions of the printing plates obtained in Examples 1 to 7 with water, Os was added.
It was stained with O4 and observed under a TEM (transmission electron microscope).

As a result of observation, it was confirmed to have a phase-separated structure composed of a phase containing a hydrophilic polymer as a main component and a phase containing a hydrophobic polymer as a main component as shown in FIG.

(1) 1/2/2 mol ratio reaction product of xylylenediamine / glycidyl methacrylate / methylglycidyl ether 5 parts by weight (2) 1,9-nonanediacrylate 10 parts by weight (3) 1,9-no Nandimethacrylate 5 parts by weight (4) Michler's ketone 2 parts by weight (5) 2,4-Diethylthioxanthone 2 parts by weight (6) Ethyl Cellosolve 76 parts by weight The printing plate obtained was a sheet-fed offset printing machine "Sprint 2".
5: Komori Corporation Co., Ltd. "
While supplying commercially available purified water as dampening water, use high quality paper (62.5
kg / chrysanthemum). The non-image area exhibited excellent ink repellency, and the image area to which the above-described photosensitive composition was exposed and fixed exhibited a sufficient ink deposition property to obtain a printed matter having a clear contrast.

After printing about 5,000 sheets, ink stains did not occur on each printing plate, and clear printed matter having sufficient contrast was obtained.

Example 2 A negative type lithographic printing plate precursor was prepared in the same manner as in Example 1 except that the following silicone was used in place of the silicone emulsion, and a printing plate was prepared and printed in the same manner as in Example 1. The same result was obtained.

Silicone of Example 2 Silicone emulsion "BY22-854" amino-modified silicone Example 3 A negative type lithographic printing plate precursor was prepared in the same manner except that the following silicone was used in place of the silicone emulsion of Example 1. Then, a printing plate was prepared and printed in the same manner as in Example 1, and similar results were obtained.

Silicone of Example 2 Carboxy-modified silicone oil "BY16-880" Example 4 A negative type lithographic printing plate precursor was prepared in the same manner except that the following polymer was used in place of the hydrophilic polymer of Example 1. Then
When a printing plate was prepared and printed in the same manner as in Example 1,
Similar results were obtained.

Hydrophilic polymer of Example 2 Melpol F-220: PEG urethane elastomer manufactured by Sanyo Kasei Co., Ltd. Example 5 The planographic printing plate used in Example 1 and a normal PS plate (FPQ;
A plate obtained by exposing and developing Fuji Photo Film Co., Ltd. to a printing plate was mounted on the same plate cylinder, and printing was performed in the same manner as in Example 1 while supplying commercially available purified water as dampening water. went.

When the supply amount of dampening water was increased from the standard condition, the ink density in the image area was extremely reduced in the area where the PS plate was used, and so-called "water loss" caused defective ink inking. did. On the other hand, in the portion where the planographic printing plate used in Example 1 was used, the degree of inking failure was slight.

When the amount of dampening water supplied was reduced from the standard conditions, ink stains were generated on the entire surface of the portion using the PS plate. On the other hand, good printed matter was obtained in the area where the planographic printing plate used in Example 1 was used.

[0193]

[Table 1]

[0194]

The lithographic printing plate of the present invention uses a hydrophilic swelling layer having a phase separation structure as a non-image area.
The ink can be repelled efficiently with a small amount of dampening water supply, and the control range of dampening water is expanded. Further, printing can be performed without using a solvent such as isopropanol which is usually added to the fountain solution.

When an image is formed from the photosensitive lithographic printing plate of the present invention with the aid of a photosensitive compound, a conventional PS
The plate-making process is extremely simple because no physical development is required for the plate. In addition, it is possible to manufacture an inexpensive photosensitive lithographic printing plate because no special surface treatment is required on the substrate for developing ink repellency.

[Brief description of drawings]

FIG. 1 is a schematic view showing an example of a phase separation structure of a hydrophilic swelling layer of a lithographic printing plate according to the invention.

FIG. 2 is a schematic view showing an example of a phase separation structure of a hydrophilic swelling layer of a lithographic printing plate according to the invention.

FIG. 3 is a schematic diagram showing an example of a phase separation structure of a hydrophilic swelling layer of a lithographic printing plate according to the invention.

Claims (5)

[Claims] 1. At least two of a phase mainly composed of a hydrophilic polymer and a phase mainly composed of a hydrophobic polymer on a substrate.
A photosensitive lithographic printing plate precursor comprising a hydrophilic swelling layer having a phase-separated structure composed of phases, wherein the hydrophobic polymer is mainly composed of silicone. 2. The photosensitive lithographic printing plate precursor according to claim 1, wherein the hydrophobic polymer is mainly composed of a silicone emulsion. 3. The water absorption of the hydrophilic swelling layer is 10 to 1000.
%, The photosensitive lithographic printing plate precursor according to claim 1. 4. The hydrophobic polymer comprises 60 to 9 in the hydrophilic swelling layer.
It is 5% by weight, and the photosensitive lithographic printing plate precursor according to claim 1. 5. A method for producing a lithographic printing plate, which comprises irradiating the plate surface of the photosensitive lithographic printing plate precursor according to claim 1 with an actinic ray.