JP5191255B2 - Method for manufacturing ink jet recording medium - Google Patents

Description

  The present invention relates to a method for manufacturing an ink jet recording medium having an ink receiving layer for receiving ink.

  As an ink jet recording method, an ink jet recording medium in which a recording layer for receiving ink has a porous structure has been proposed and put into practical use for the purpose of improving various characteristics. For example, there is an ink jet recording medium in which a recording layer containing inorganic pigment particles and a water-soluble binder and having a high porosity is provided on a support. Such an ink jet recording medium is widely used as a material that has a porous structure and is excellent in ink acceptability (quick drying), has high gloss, and can record a photographic-like image.

  A recording layer with a high porosity formed using inorganic pigment particles and a water-soluble binder generally has small particles and a large amount of particles, so that the film is cracked in the process of drying the coating film after applying the coating liquid. May occur. This crack is likely to occur especially when drying at a relatively high temperature in order to shorten the drying time, for example, during the drying after coating, specifically at the time of transition from constant rate drying to reduced rate drying. Prone to occur.

  Conventionally known methods for preventing cracking include increasing the viscosity of the binder in the coating solution, but an increase in viscosity is not desirable in terms of coating unevenness. There is also a technique for preventing cracking when drying after coating by using a binder such as acetoacetyl-modified polyvinyl alcohol together with a crosslinking agent.

  On the other hand, from the viewpoint of recording a photographic-like image, it is important that the ink (that is, the image) does not bleed after recording. As a method for preventing ink bleed, the recording layer on which the ink is deposited is cationic. A technique for containing a cationic polymer such as an emulsion or a polyvalent metal compound is known.

In relation to the above-mentioned cracks and ink bleeding, an ink comprising two coating layers by simultaneously applying an ink receiving layer containing a resin binder having a keto group and an ink receiving layer containing a crosslinking agent so as to be adjacent to each other Ink-jet recording material provided with a receiving layer (see, for example, Patent Document 1), an ink receiving material containing a resin binder having a keto group, a cationic emulsion, and a water-soluble zirconium compound, and the resin binder is crosslinked with a crosslinking agent An inkjet recording material having a layer (see, for example, Patent Document 2) is disclosed. The former has no cracks and is excellent in water resistance and the like, and the latter has low bleeding and no surface defects in a high humidity environment, and is excellent in coating properties.
JP 2005-199671 A JP 2006-272797 A

However, using acetoacetyl-modified polyvinyl alcohol and its cross-linking agent and a cationic polymer to alleviate brittleness such as cracks and to suppress ink (image) bleeding due to moisture, an ink receiving layer is actually used. The stability of the coating solution for forming is significantly deteriorated, and in the drying process after coating, coating film failures such as cracks and water resistance are greatly reduced. Improvement effect cannot be obtained.
Also, in the above-mentioned ink jet recording material using a cationic emulsion, although various resin systems such as styrene-acrylic system are mentioned, it is desirable to be composed of a urethane system in terms of preventing bleeding, whereas a urethane resin However, since the stability of the coating liquid is deteriorated due to an increase in the viscosity of the coating liquid, there is a problem that a coating failure tends to occur.

  On the other hand, in the drying process after coating, it is important to increase the film strength of the coating film as soon as possible in the constant rate drying state before the reduced rate drying state starts.

  The present invention has been made in view of the above, and improves the brittleness after coating (particularly during drying) while maintaining the stability of the coating solution, thereby preventing the occurrence of coating film failures such as cracks, and ink after recording. It aims at providing the manufacturing method of the inkjet recording medium which produces the inkjet recording medium which can suppress bleeding, and makes it a subject to achieve this objective.

Specific means for achieving the above object are as follows.
<1> On a support, a first solution containing at least inorganic fine particles and acetoacetyl-modified polyvinyl alcohol, and a second solution containing at least inorganic fine particles and polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol), A coating film forming step of simultaneously coating the first solution so that the second solution is positioned and forming a coating film, and simultaneously with forming the coating film or during dry coating of the coating film A solution applying step of applying a third solution containing a water-soluble polyfunctional compound having two or more amino groups in the molecule on the coating film before the coating film exhibits reduced-rate drying; And at least one of the first solution and the second solution further comprises a cationic polyurethane.

  <2> The third solution further includes inorganic fine particles and polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol), and the first solution, the second solution, and the third solution. A multilayer coating is applied simultaneously on the support so that the first solution, the second solution, and the third solution are in order from the support side, and a coating film is formed on the support. The method for producing an ink jet recording medium according to the item <1>, wherein at least one of the second solution, the second solution, and the third solution further contains a cationic polyurethane.

  <3> The method for producing an ink jet recording medium according to <1> or <2>, wherein the second solution further contains a water-soluble aluminum compound.

  According to the present invention, an ink jet capable of improving the brittleness after coating (particularly during drying) while preventing the occurrence of a coating film failure such as cracking and suppressing ink bleeding after recording while maintaining the coating solution stability. An ink jet recording medium manufacturing method for producing a recording medium can be provided.

Hereinafter, the first aspect of the method for producing an ink jet recording medium of the present invention will be described in detail.
<First aspect>
According to a first aspect of the method for producing an inkjet recording medium of the present invention, a first solution containing at least inorganic fine particles and acetoacetyl-modified polyvinyl alcohol on a support, at least inorganic fine particles and polyvinyl alcohol (acetoacetyl-modified polyvinyl alcohol). A coating film forming step of simultaneously coating a second solution containing (except for alcohol) on the first solution so that the second solution is positioned on the first solution, and forming a coating film; simultaneously forming a film, or the before a during drying middle of a coating film coated film exhibits a decreasing rate of drying, water-soluble polyfunctional compound having two or more amino groups in the molecule (hereinafter, "water-soluble A solution applying step of applying a third solution containing a polyfunctional cross-linking agent ”) on the coating film, and at least a small amount of the first solution and the second solution. To Kutomo one in which further has a configuration moistened with cationic polyurethane.

  In the first aspect of the present invention, when an ink receiving layer is formed by using acetoacetyl-modified polyvinyl alcohol and cationic polyurethane together, acetoacetyl-modified polyvinyl alcohol (and preferably cationic polyurethane) and a crosslinking agent are used. Since the ink receiving layer can be formed so that it does not come into direct contact with the “water-soluble polyfunctional compound having two or more amino groups in the molecule”, acetoacetyl-modified polyvinyl alcohol is used (particularly acetoacetyl). When combined with a modified polyvinyl alcohol and a cationic polyurethane, the thickening that appears greatly and the decrease in coating properties that accompanies this increase are effectively reduced. , The brittleness after application (especially during drying) is improved, and coating failure such as cracks occurs. It can be prevented, occurrence of ink bleeding (image) after recording is suppressed. Furthermore, when a water-soluble aluminum compound is used in combination, it is possible to more effectively prevent a thickening that worsens due to the coexistence with the cationic polyurethane, and a decrease in coating properties that accompanies this.

Hereafter, each process in the 1st aspect of this invention is explained in full detail.
-Coating film formation process-
The coating film forming step includes a first solution containing at least inorganic fine particles and acetoacetyl-modified polyvinyl alcohol (hereinafter also referred to as “first ink-receiving layer coating solution”), at least inorganic fine particles, and a support on the support. A second solution containing polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol) (hereinafter also referred to as “second ink-receiving layer coating solution”) is placed on the first solution. Multi-layer coating is performed simultaneously so that the solution is positioned, and a coating film is formed.
In the coating film forming step, as a coating film, a first coating film (hereinafter sometimes simply referred to as “first coating film”) formed with a first solution in order from the side closer to the support, and a second one. A second coating film formed of a solution (hereinafter, simply referred to as “second coating film”) is formed. Hereinafter, the first and second ink receiving layer coating liquids may be simply referred to as “ink receiving layer coating liquids”.

(First solution)
Components such as inorganic fine particles, acetoacetyl-modified polyvinyl alcohol, and cationic polyurethane constituting the first solution, a preparation method, and the like will be described.

  The first solution is prepared using at least inorganic fine particles and acetoacetyl-modified polyvinyl alcohol, and can be further prepared using cationic polyurethane. The first solution constitutes an ink receiving layer that absorbs and receives ink applied from the outside. Further, the first solution can further contain other components as necessary.

  The first solution (first ink-receiving layer coating solution) is prepared, for example, by adding silica fine particles having an average primary particle size of 10 nm or less to water (example: 10 to 15% by mass), which is wetted at high speed. After being dispersed for 20 minutes (preferably 10 to 30 minutes) in a colloid mill (example: Claremix (M Technique Co., Ltd.)) under high speed rotation conditions of, for example, 10,000 rpm (preferably 5000 to 20000 rpm), aceto It is obtained by adding an aqueous solution containing acetyl-modified PVA and cationic polyurethane, and further carrying out dispersion under the same conditions as described above to obtain an aqueous dispersion. The obtained aqueous dispersion is a uniform sol, and a porous layer having a three-dimensional network structure can be obtained by coating this on a support by the following coating method.

The first solution containing the inorganic fine particles and the acetoacetyl-modified PVA may be prepared by preparing an aqueous dispersion of inorganic fine particles (for example, vapor phase silica) in advance and adding the prepared aqueous dispersion to the PVA-containing aqueous solution. Alternatively, the PVA-containing aqueous solution may be added to the inorganic fine particle aqueous dispersion, or may be mixed at the same time. Further, instead of the aqueous dispersion of inorganic fine particles, powdery inorganic fine particles may be added to the PVA-containing aqueous solution as described above.
After the inorganic fine particles and acetoacetyl-modified PVA are mixed, the mixture is refined using a disperser, whereby an aqueous dispersion having an average particle size of 50 nm or less can be obtained.
For the preparation of the first solution, a solvent can be used in each step, and water, an organic solvent, or a mixed solvent thereof can be used as the solvent. Examples of organic solvents that can be used for coating include alcohols such as methanol, ethanol, n-propanol, i-propanol, and methoxypropanol, ketones such as acetone and methyl ethyl ketone, tetrahydrofuran, acetonitrile, ethyl acetate, and toluene. It is done.
These points are the same when a second solution described later is prepared.

  Application | coating of a 1st solution can be performed using a well-known application | coating method. Examples of known coating methods include methods using an extrusion die coater, an air doctor coater, a bread coater, a rod coater, a knife coater, a squeeze coater, a reverse roll coater, a bar coater, and the like.

  The drying after the application of the ink receiving layer coating liquid is generally performed at 50 to 180 ° C. for 0.5 to 10 minutes (particularly 0.5 to 5 minutes). The drying time naturally varies depending on the coating amount, but the above range is appropriate.

  The thickness of the first coating film is preferably in the range of 10 to 40 μm and more preferably in the range of 20 to 35 μm from the viewpoint of brittleness and improvement of bleeding.

(Inorganic fine particles)
The first solution contains at least one kind of inorganic fine particles. By including inorganic fine particles together with a binder component, a porous ink receiving layer can be formed.

  The inorganic fine particles are preferably selected from those having an average secondary particle diameter of 500 nm or less, such as amorphous synthetic silica, alumina, alumina hydrate, calcium carbonate, magnesium carbonate, titanium dioxide and the like. Various fine particles can be used. In particular, amorphous synthetic silica, alumina, or alumina hydrate is preferable.

Amorphous synthetic silica can be roughly classified into wet method silica, gas phase method silica, and others depending on the production method. Wet method silica is further classified into precipitation method silica, gel method silica, and sol method silica according to the production method.
Precipitated silica is produced by reacting sodium silicate and sulfuric acid under alkaline conditions, and the silica particles that have grown are agglomerated and settled, and are then commercialized through filtration, water washing, drying, pulverization and classification. Precipitated silica is commercially available, for example, as a nip seal from Tosoh Silica Co., Ltd. and from Tokuyama Co., Ltd.
Gel silica is produced by reacting sodium silicate and sulfuric acid under acidic conditions. During the ripening, the fine particles dissolve and reprecipitate so as to bond the other primary particles, so that the clear primary particles disappear and relatively hard aggregated particles having an internal void structure are formed. For example, it is commercially available as nip gel from Tosoh Silica Co., Ltd., and as syloid and silo jet from Grace Japan Co., Ltd. The sol method silica is also called colloidal silica, and is obtained by heating and aging a silica sol obtained through metathesis of sodium silicate acid or through an ion exchange resin layer. For example, it is commercially available as Snowtex from Nissan Chemical Industries, Ltd. Yes.

  Gas phase method silica is also called dry method silica with respect to wet method silica, and is generally produced by flame hydrolysis. Specifically, a method of making silicon tetrachloride by burning with hydrogen and oxygen is generally known. However, silanes such as methyltrichlorosilane and trichlorosilane can be used alone or tetrachlorosilane instead of silicon tetrachloride. It can be used in a mixed state with silicon. Vapor phase method silica is commercially available as Aerosil from Nippon Aerosil Co., Ltd. and QS type from Tokuyama Co., Ltd.

  Vapor phase silica is suitably used by dispersing the average secondary particle size of the vapor phase silica in the presence of a cationic compound to 500 nm or less, preferably 10 to 300 nm, more preferably 20 to 200 nm. . As a dispersion method, pre-mixed gas phase method silica and dispersion medium by ordinary propeller stirring, turbine type stirring, homomixer type stirring, etc., then media mill such as ball mill, bead mill, sand grinder, high pressure homogenizer, ultra high pressure homogenizer It is preferable to perform dispersion using a pressure disperser such as a pressure disperser, an ultrasonic disperser, a thin film swirl disperser, or the like. The average secondary particle diameter is an average value of particle diameters of dispersed aggregated particles observed by observing the obtained ink receiving layer with an electron microscope.

In addition, wet process silica pulverized to an average secondary particle diameter of 500 nm or less can also be preferably used.
As the wet process silica, wet process silica having an average primary particle diameter of 50 nm or less, preferably 3 to 40 nm and an average aggregate particle diameter of 5 to 50 μm is preferable, and this is averaged in the presence of a cationic compound. It is preferable to use wet method silica fine particles finely pulverized to a secondary particle size of 500 nm or less, preferably about 20 to 200 nm.

  Since the wet process silica produced by a normal method has an average aggregated secondary particle diameter of 1 μm or more, it can be used after being finely pulverized. The pulverization method is preferably a wet dispersion method in which silica dispersed in an aqueous medium is mechanically pulverized. At this time, since the increase in the initial viscosity of the dispersion is suppressed, high concentration dispersion is possible, and the pulverization / dispersion efficiency is increased so that it can be further pulverized into fine particles. Precipitated silica having a particle diameter of 5 μm or more is preferred. By using the high concentration dispersion, the productivity of the ink jet recording medium is also improved. The oil absorption is measured based on the description of JIS K-5101.

  As a specific method for obtaining wet-process silica fine particles having an average secondary particle diameter of 500 nm or less, first, wet silica and a cationic compound are mixed in water (whichever is added first or at the same time). Or the respective dispersions or aqueous solutions may be mixed and dispersed using at least one dispersion device such as a sawtooth blade type dispersion device, a propeller blade type dispersion device, or a rotor stator type dispersion device. Thus, a preliminary dispersion is obtained. At this time, if necessary, an appropriate low boiling point solvent or the like may be added. A higher solid content concentration of the preliminary dispersion is preferable, but dispersion becomes impossible when the concentration is too high. Therefore, a preferable range is 15 to 40% by mass, and more preferably 20 to 35% by mass. Next, by applying stronger mechanical energy, a dispersion of wet-process silica fine particles having an average secondary particle diameter of 500 nm or less is obtained. Examples of means for imparting mechanical energy include known media mills such as ball mills, bead mills and sand grinders, pressure dispersers such as high pressure homogenizers and ultrahigh pressure homogenizers, ultrasonic dispersers, and thin film swirl dispersers. Means can be employed.

A cationic compound can be used for the dispersion of the vapor phase method silica and the wet method silica. Examples of the cationic compound include a cationic polymer and a water-soluble metal compound.
As the cationic polymer, polyethyleneimine, polydiallylamine, polyallylamine, alkylamine polymer, JP-A-59-20696, JP-A-59-33176, JP-A-59-33177, JP-A-59-155088, 60-11389, 60-49990, 60-83882, 60-109894, 62-198493, 63-49478, 63-115780, No. 63-280681, No. 1-40371, No. 6-234268, No. 7-125411, No. 10-193976, etc. The polymer which has is preferable. In particular, diallylamine derivatives are preferred as the cationic polymer. In terms of dispersibility and dispersion viscosity, the molecular weight of these cationic polymers is preferably about 2000 to 100,000, and particularly preferably about 2000 to 30,000.

  Examples of the water-soluble metal compound include water-soluble polyvalent metal salts, and among them, a compound of aluminum or a Group 4A metal (for example, zirconium or titanium) in the periodic table is preferable. Particularly preferred is a water-soluble aluminum compound. Examples of the water-soluble aluminum compound include, as inorganic salts, aluminum chloride or a hydrate thereof, aluminum sulfate or a hydrate thereof, ammonium alum and the like. Furthermore, a basic polyaluminum hydroxide compound which is an inorganic aluminum-containing cationic polymer is also preferable. Details of the basic polyaluminum hydroxide compound will be described later.

  As alumina, γ-alumina, which is a γ-type crystal of aluminum oxide, is preferable, and among them, a δ group crystal is preferable. Although γ-alumina can reduce the primary particles to about 10 nm, the secondary particle crystals of several thousands to several tens of thousands of nanometers are usually averaged by ultrasonic waves, a high-pressure homogenizer, a counter collision type jet crusher, or the like. Those obtained by pulverizing the secondary particle diameter to 500 nm or less, preferably about 20 to 300 nm are preferred.

Alumina hydrate is represented by Al ₂ O ₃ .nH ₂ O (n = 1 to 3), where n is 1 is a boehmite-structured alumina hydrate, and n is greater than 1 and 3 or less. Is an alumina hydrate having a pseudo boehmite structure. It can be obtained by a known production method such as hydrolysis of an aluminum alkoxide such as aluminum isopropoxide, neutralization of an aluminum salt with an alkali, hydrolysis of an aluminate. The average secondary particle diameter of the alumina hydrate is preferably 500 nm or less, more preferably 20 to 300 nm.

  The above alumina and alumina hydrate can be used in the form of a dispersion dispersed by a known dispersant such as acetic acid, lactic acid, formic acid, nitric acid and the like.

  The content of the inorganic fine particles in the first solution is 5 to 5% of the solid content in the first solution from the viewpoint of forming a porous structure with a high porosity and imparting ink absorbability. A range of 15% by weight is preferred.

(Acetoacetyl-modified polyvinyl alcohol)
The first solution contains at least one kind of acetoacetyl-modified polyvinyl alcohol (hereinafter sometimes abbreviated as “acetoacetyl-modified PVA”). By including acetoacetyl-modified PVA, it is possible to prevent cracking of the ink-receiving layer that is finally formed and deterioration of water resistance.

The acetoacetyl-modified PVA can be produced by a known method such as a reaction between polyvinyl alcohol and diketene. The degree of acetoacetylation is preferably from 0.1 to 20 mol%, more preferably from 1 to 15 mol%, and the degree of saponification is preferably at least 80 mol% in terms of reducing brittleness such as cracks and improving water resistance. Furthermore, 85 mol% or more is preferable.
The average degree of polymerization of acetoacetyl-modified PVA is preferably 500 to 5000, and particularly preferably 1000 to 4500.

  As content in the 1st solution of acetoacetyl modified PVA, the range of 10-30 mass% is preferable with respect to inorganic fine particles, and the range of 15-25 mass% is more preferable. When the content of the acetoacetyl-modified PVA is 10% by mass or more, coating failure such as cracking after coating (particularly during drying) can be prevented, and bleeding (particularly water resistance) after recording can be suppressed. When it is 30% by mass or less, it is advantageous in terms of ink absorbability.

(Cationic polyurethane)
At least one layer of the ink receiving layer constituting the ink jet recording medium in the present invention is constituted by using cationic polyurethane, and the first solution in the first aspect may contain at least one kind of cationic polyurethane. Good. By including the cationic polyurethane, a good coated surface state can be obtained at the time of coating, and bleeding (water resistance) after image recording on the ink receiving layer can be suppressed.

Cationic polyurethane is a polymer compound having a urethane bond and a cationic group in which an isocyanate group and an alcohol group are condensed, such as polymerizing a monomer having a cationic group or introducing a cationic group after the polymerization of the monomer. Obtained by the method. Here, as the cationic group, for example, ammonium salt, amine salt, polyamine salt, pyridinium salt, pyrrole salt, pyrimidine salt and the like are preferable.
As the cationic polyurethane, commercially available products may be used. Examples of commercially available products include Superflex 600 (manufactured by Daiichi Kogyo Seiyaku Co., Ltd.), Pateracol IJ-21 (Dainippon Ink Chemical Co., Ltd.). Manufactured).

  In the first aspect, the cationic polyurethane may be contained in either the first solution or the second solution described later. However, the cationic solution is used in the first solution in terms of preventing image bleeding and keeping the image density high. It is preferably contained.

  As content in the 1st solution of cationic polyurethane, the range of 5-40 mass% is preferable with respect to the total amount of the water-soluble binder of a 1st solution, and the range of 10-35 mass% is more preferable. When the content of the cationic polyurethane is 5% by mass or more, coating failure such as cracks after coating (particularly during drying) can be prevented, and bleeding (particularly water resistance) after recording can be suppressed. It is advantageous in terms of coating solution stability when the content is less than or equal to mass%.

(Ingredients other than the above)
In the first solution, as long as the effects of the present invention are not impaired, a cationic mordant such as a cationic polymer, a cationic system, an anionic system, a nonionic system, an amphoteric system, and a fluorine system are added as necessary. , Other components such as a silicone-based surfactant, a high-boiling organic solvent, and the like can be contained.

(Second solution)
Next, each component such as inorganic fine particles and polyvinyl alcohol constituting the second solution, a preparation method, and the like will be described.

The second solution is prepared using at least inorganic fine particles and polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol), and can be further prepared using a cationic polyurethane and a water-soluble aluminum compound. The second solution constitutes an ink receiving layer that absorbs and receives ink applied from the outside. Further, the second solution can further use other components as necessary.
The second solution (second ink-receiving layer coating solution) can be prepared by the same method as that for preparing the first solution (first ink-receiving layer coating solution).

Application | coating of a 2nd solution can be performed using a well-known application | coating method, and the application | coating method similar to the case in the said 1st solution can be applied. The second solution may be applied simultaneously with the first solution, and in this case, for example, an application method using an extrusion die coater, a curtain flow coater or the like is preferable.
The drying after the application of the second solution can be performed in the same manner as in the first solution.

The thickness of the second coating film is preferably in the range of 1 to 10 μm and more preferably in the range of 2 to 5 μm from the viewpoint of ink absorbability and suppression of coating failure.
Further, the film thickness ratio between the first coating film and the second coating film (second coating film / first coating film) is not particularly limited, but from the viewpoint of coexistence of ink absorbability and brittleness improvement, 1 / 9 to 5/5 is preferable, and 1/9 to 3/7 is more preferable.

(Inorganic fine particles)
The second solution contains at least one kind of inorganic fine particles. Examples of the inorganic fine particles that can be used in the second solution include the same inorganic fine particles that can be used in the preparation of the first solution. Among these, silica particles are preferable, and vapor phase method silica is more preferable.

  The content of the inorganic fine particles in the second solution is 5 to 5% of the solid content in the second solution from the viewpoint of forming a porous structure with a high porosity and imparting ink absorbability. A range of 15% by weight is preferred.

(Polyvinyl alcohol)
The second solution contains at least one polyvinyl alcohol other than acetoacetyl-modified PVA (hereinafter sometimes simply referred to as “PVA”). When the acetoacetyl-modified PVA is included, the “water-soluble polyfunctional compound having two or more amino groups in the molecule” in the third solution is formed when the third solution is applied in the solution application step described later. In this case, the viscosity is increased by direct contact with the acetoacetyl-modified PVA contained in the second solution, and the coating property, that is, the coated surface state after coating is deteriorated.

  Polyvinyl alcohol (PVA) contained in the second solution is a “molecule” described later from the viewpoint of avoiding thickening at the time of application by contact with a third solution described later, and thus deterioration of the coating surface condition and application failure. Any PVA that does not contain an acetoacetyl group that can react with a water-soluble polyfunctional compound having two or more amino groups therein may be used. Examples of such PVA include various modified polyvinyl alcohols other than polyvinyl alcohol and acetoacetyl-modified PVA. Among these, polyvinyl alcohol is preferable, and polyvinyl alcohol having an average degree of polymerization of 1500 or more is particularly preferable. When such PVA is used, the coating strength of the ink receiving layer is improved.

  As content in the 2nd solution of polyvinyl alcohol (except acetoacetyl modified PVA), the range of 15-30 mass% is preferable with respect to an inorganic fine particle from the point of the brittleness in application | coating, and an ink absorptivity, The range of 15-25 mass% is more preferable.

(Cationic polyurethane)
In the method for producing an ink jet recording medium of the present invention, the first solution may or may not contain cationic polyurethane, and the second solution may contain at least one cationic polyurethane. When the second solution or the first and second solutions contain cationic polyurethane, coating failure such as cracking after coating (particularly during drying) is prevented, and bleeding (particularly water resistance) after recording is prevented. It is suppressed.
Examples of the cationic polyurethane that can be used in the second solution include those that can be used in the preparation of the first solution.

(Water-soluble aluminum compound)
The second solution preferably contains a water-soluble aluminum compound. By including the water-soluble aluminum compound, water resistance is improved, and bleeding of ink (image) due to the influence of moisture such as under high humidity is suppressed. Further, when the cationic polyurethane is contained in the first solution, when the acetoacetyl-modified polyvinyl alcohol and the cationic polyurethane are used in combination, a thickening that appears greatly when the water-soluble aluminum compound comes into contact with the first solution is received. A drop in applicability is particularly suppressed. This makes it possible to stabilize the coating liquid when such a composition system is used, and to suppress the deterioration of the coated surface due to coating film failure such as cracks after coating (particularly during drying) and the occurrence of ink (image) bleeding.
“Water-soluble” means that 1% by mass or more dissolves in 20 ° C. water.

  Examples of the water-soluble aluminum compound include inorganic salts such as aluminum chloride or a hydrate thereof, aluminum sulfate or a hydrate thereof, and ammonium alum. Furthermore, the basic polyaluminum hydroxide compound which is an inorganic aluminum-containing cationic polymer is mentioned. From the viewpoint of ozone resistance of the dye, a basic polyaluminum hydroxide compound is particularly preferable.

The basic polyaluminum hydroxide compound has a main component represented by the following formula 1, formula 2, or formula 3, for example, [Al ₆ (OH) ₁₅ ] ³⁺ , [Al ₈ (OH) ₂₀ ] ⁴⁺ , It is a water-soluble polyaluminum hydroxide that stably contains a basic and high-molecular polynuclear condensed ion such as [Al ₁₃ (OH) ₃₄ ] ⁵⁺ and [Al ₂₁ (OH) ₆₀ ] ³⁺ .
[Al ₂ (OH) _n Cl _6-n ] _m Formula 1
[Al (OH) ₃ ] _n AlCl ₃ Formula 2
Al _n (OH) _m Cl _{(3 nm)} [0 <m <3n] Formula 3

  These are named as polyaluminum chloride (PAC) as a water treatment agent from Taki Chemical Co., Ltd., named as polyaluminum hydroxide (Paho) from Asada Chemical Co., Ltd., and Purakem from Riken Green Co., Ltd. It is also marketed under the name of WT and by other manufacturers for the same purpose, and various grades can be used.

  As content in the 2nd solution of a water-soluble aluminum compound, the range of 2-20 mass% is preferable with respect to the inorganic fine particle of a 2nd solution, and the range of 3-15 mass% is more preferable. When the content of the water-soluble aluminum compound is 2% by mass or more, the water resistance is improved, and bleeding caused by the influence of the environment after recording (particularly under high humidity) can be suppressed, and the content is 20% by mass or less. It is advantageous in terms of coating solution stability.

(Ingredients other than the above)
In the second solution, as in the first solution, a cationic mordant such as a cationic polymer, cationic, anionic, nonionic, amphoteric, Other components such as fluorine-based and silicone-based surfactants and high-boiling organic solvents can be contained.

  In the first aspect, from the viewpoint of obtaining high image density, coating solution stability, image bleeding, and coating failure, (1) at least the first solution contains cationic polyurethane, and the second solution Is a form containing a water-soluble aluminum compound, (2) the first solution contains a cationic polyurethane, and the content ratio of the cationic polyurethane (x) and the acetoacetyl-modified PVA (y) in the first solution (X: y) is 1:10 to 4:10, and the second solution contains a water-soluble aluminum compound (preferably in the range of 3 to 15% by mass with respect to the inorganic fine particles), The water-soluble polyfunctional crosslinking agent in the solution of adipic acid dihydrazide (preferably the content of the water-soluble polyfunctional crosslinking agent in the third solution is 1 with respect to the amount of acetoacetyl-modified PVA in the first solution. ~ 3 mass ) In a form particularly preferred.

-Solution application step-
The solution application step is the same as the formation of the coating film (first coating film and second coating film) in the coating film forming step, or during the dry coating of the coating film (first coating film and second coating film). Before the coating film shows reduced-rate drying, a third containing a water-soluble polyfunctional compound having two or more amino groups in the molecule (hereinafter sometimes referred to as “water-soluble polyfunctional crosslinking agent”). A solution is applied on the second coating film.

  By providing this step, the water-soluble polyfunctional crosslinking agent does not come into direct contact with the acetoacetyl-modified PVA, and the constant rate before the reduced drying state of the applied second coating film and the first coating film starts. In the dry state, the film strength of the coating film is increased. In other words, the ink-receiving layer is excellent in ink-resistant (image) bleeding (especially water resistance), maintaining the coating properties that can provide a good coated surface, reducing the brittleness such as cracks after coating (especially during drying). Is obtained.

The third solution is prepared using at least a water-soluble polyfunctional crosslinking agent, and is used as a crosslinking agent solution for crosslinking and curing at least the first coating film. In addition, the 3rd solution may also contain other components, such as a crosslinking agent and surfactant of binder components other than acetoacetyl modified PVA, as needed. The third solution is prepared, for example, by mixing a water-soluble polyfunctional crosslinking agent and a solvent. As the solvent, water, an organic solvent, or a mixed solvent thereof can be used. As examples of the organic solvent, those used for the preparation of the first solution can be used.
The pH of the third solution is preferably a basic solution of 7.1 or more, and the pH of the first solution and the second solution described above is in the range of 3 to 5.5 in terms of promoting crosslinking. preferable.

  In the solution application step according to the present invention, the third solution is during the dry coating of the coating films (first coating film and second coating film), and the coating films (first coating film and second coating film) are reduced. It can be applied before showing rate drying. After application, the ink receiving layer is obtained by drying to give a cross-linked and cured first coating film and second coating film.

  The application of the third solution (crosslinking agent solution) can be performed by a method such as dipping the support after coating in the crosslinking agent solution, application of the crosslinking agent solution, spraying by spraying, or the like.

  “Before showing reduced-rate drying” is usually a few minutes immediately after coating, and during this time, constant-rate drying indicates a phenomenon in which the content of the solvent in the coating film decreases in proportion to time. . About the period which shows such constant rate drying, it is described in the chemical engineering handbook (707-712 pages, Maruzen Co., Ltd. issue, October 25, 1980).

  When the coating film of the ink receiving layer coating liquid is applied in multiple layers, after the application of the first ink receiving layer coating liquid and the second ink receiving layer coating liquid described above, or in the case of sequential application, After application of the second ink-receiving layer coating solution, the coating film (first coating film and second coating film) is immersed in the third solution as described above while the coating film (first coating film and second coating film) shows constant rate drying. The solution of 3 is applied and sprayed.

  When the third solution (crosslinking agent-containing solution) is applied by coating, the coating is applied in addition to the above method, such as curtain flow coater, extrusion die coater, air doctor coater, bread coater, rod coater, knife coater, squeeze coater, A known coating method using a reverse roll coater, a bar coater or the like can be used. Among them, it is preferable to use an extrusion die coater, curtain flow coater, bar coater or the like so that the coater does not directly contact the coating film.

The application amount of the third solution on the coating film is generally in the range of 0.01 to 10 g / m ² in terms of a crosslinking agent (including a water-soluble polyfunctional crosslinking agent and other crosslinking agents such as boric acid). The range of 0.05-5 g / m < ² > is preferable. After the application of the third solution, the coating film is generally heated at 40 to 180 ° C. for 0.5 to 30 minutes, and dried and cured. It is preferable to heat at 40 to 150 ° C. for 1 to 20 minutes.

  Further, in the solution application step in the present invention, the third solution is formed as described above, ie, the formation of the coating film (first coating film and second coating film), that is, the application of the first solution and the second solution. It can be given at the same time. In this case, the first solution, the second solution (ink receiving layer coating solution), and the third solution (crosslinking agent-containing solution) are placed on the support so that the first solution is in contact with the support. Are simultaneously applied to cure the first solution and the second solution. At this time, simultaneous multilayer coating of the ink receiving layer coating liquid and the crosslinking agent-containing solution can be performed by a coating method using, for example, an extrusion die coater or a curtain flow coater. Moreover, drying after simultaneous multilayer coating is generally performed by heating at 40 to 150 ° C. for 0.5 to 10 minutes, and the coating film is cured. Furthermore, it is preferable to heat at 40-100 degreeC for 0.5-5 minutes.

  When simultaneous multilayer coating is performed, for example, with an extrusion die coater, two or three solutions are formed on the extrusion die coater, i.e. before being transferred onto the support. Therefore, in the method for producing an ink jet recording medium of the present invention, a better effect can be obtained by simultaneous multilayer coating.

The ink receiving layer obtained after coating and drying can improve surface smoothness, transparency and coating strength by, for example, using a super calender, gloss calender, etc. and passing between roll nips under heating and pressure. Is possible. However, in order to reduce the void ratio (that is, the ink absorbability is lowered), it is important to perform such treatment under conditions that cause a small decrease in the void ratio.
The thickness of one ink receiving layer formed on the support is preferably in the range of 15 to 40 μm, and the total thickness of the ink receiving layer composed of two or more layers is preferably in the range of 10 to 50 μm.

Here, each component such as a water-soluble polyfunctional crosslinking agent constituting the third solution will be described.
(Water-soluble polyfunctional compound)
The 3rd solution in this invention contains at least 1 sort (s) of the water-soluble polyfunctional compound (water-soluble polyfunctional crosslinking agent) which has a 2 or more amino group in a molecule | numerator. This water-soluble polyfunctional crosslinking agent functions as a crosslinking agent for crosslinking the acetoacetyl-modified PVA described above. In the present invention, this water-soluble polyfunctional cross-linking agent is contained in the third solution so that it does not come into direct contact with the acetoacetyl-modified PVA when forming the ink receiving layer. Film failure is prevented, and bleeding (particularly water resistance) after recording can be suppressed.

Examples of the water-soluble polyfunctional compound having two or more amino groups in the molecule include amine compounds and hydrazine compounds.
Examples of the amine compound include ethylenediamine, propylenediamine, trimethylenediamine, tetramethylenediamine, pentamethylenediamine, hexamethylenediamine, isophoronediamine, dicyclohexylmethane-4,4'-diamine, phenylenediamine, diethylenetriamine, and triethylenetetramine. , Triaminopropane, polymers having an amino group (for example, polyvinylamine, polyethyleneimine, polyallylamine), and the like.

  Examples of the hydrazine compound include carbohydrazide, thiocarbohydrazide, ethylene-1,2-dihydrazine, propylene-1,3-dihydrazine, butylene-1,4-dihydrazine, oxalic acid dihydrazide, propionic acid dihydrazide, Malonic acid dihydrazide, succinic acid dihydrazide, glutaric acid dihydrazide, adipic acid dihydrazide, sebacic acid dihydrazide, maleic acid dihydrazide, fumaric acid dihydrazide, itaconic acid dihydrazide, salicylic acid dihydrazide, isophthalic acid dihydrazide, 4,4'-dihydrazide And vinyl polymers having a group (for example, aminopolyacrylamide).

  The content of the water-soluble polyfunctional crosslinking agent in the third solution varies depending on the film thickness of the first coating film and the second coating film, the amount of acetoacetyl-modified PVA, and the like, but preferably in the first solution It is the range of 0.1-5 mass% with respect to the quantity of acetoacetyl modified PVA, More preferably, it is the range of 1-3 mass%. When the content of the water-soluble polyfunctional crosslinking agent is 0.1% by mass or more, coating failure such as cracking after coating (particularly during drying) is prevented, and bleeding (particularly water resistance) after recording is suppressed. If it is 5% by mass or less, it is advantageous in terms of suppressing coating failure.

  The solution application step in the first aspect includes two or more layers by simultaneously applying the first solution and the second solution in the above-described coating film forming step and simultaneously applying a multilayer coating for applying the third solution. A method of forming an ink receiving layer is more preferable.

  In this case, in the solution application step, when the water-soluble polyfunctional crosslinking agent is applied on the second coating film using the third solution, the second coating film is applied on the second coating film from the viewpoint of ink absorbability. The solution 3 may further contain inorganic fine particles and polyvinyl alcohol (excluding acetoacetyl-modified PVA), and a third coating film may be further formed on the second coating film. In this case, an ink jet recording medium in which an ink receiving layer having a three-layer structure is provided on a support is obtained.

  That is, from the viewpoint of maintaining the bridging and curing reaction of the first coating film and the second coating film and avoiding brittleness such as cracks and ink bleeding (particularly a decrease in water resistance), together with the first solution and the second solution It is preferable that a third solution containing at least a water-soluble polyfunctional crosslinking agent, inorganic fine particles, and polyvinyl alcohol (excluding acetoacetyl-modified PVA) is simultaneously coated on the support. At this time, the cationic polyurethane used in combination with the acetoacetyl-modified polyvinyl alcohol preferably forms a composition in which the water-soluble polyfunctional crosslinking agent does not coexist in the mixed state with the acetoacetyl-modified polyvinyl alcohol. Although it can be contained in one layer or two or more layers selected from three layers of the solution and the second solution and the third solution, it is preferably contained in at least the first solution.

  Specifically, a first solution containing at least inorganic fine particles and acetoacetyl-modified polyvinyl alcohol, a second solution containing at least inorganic fine particles and polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol), and at least in the molecule A third solution containing a water-soluble polyfunctional compound having two or more amino groups, inorganic fine particles, and polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol) is placed on the support in order from the support side. A step of simultaneously applying multiple layers so as to be in a positional relationship between the second solution and the third solution, and forming a first coating film, a second coating film, and a third coating film on the support; It is possible to provide a method in which at least one of the first solution, the second solution, and the third solution further includes a cationic polyurethane. That.

  At this time, the third solution is prepared using at least a water-soluble polyfunctional crosslinking agent, inorganic fine particles, and polyvinyl alcohol (excluding acetoacetyl-modified PVA), and other components can be used as necessary. . The preparation of the third solution (third ink receiving layer coating solution) containing inorganic fine particles and polyvinyl alcohol is the same as the case of preparing the first solution (first ink receiving layer coating solution). It can be done by the method.

The details of the inorganic fine particles constituting the third solution, polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol), and other components are the same as those in the first solution and the second solution described above, The preferred embodiment is also the same.
The content of inorganic fine particles (preferably silica particles (particularly, vapor phase silica)) in the third solution is in the range of 5 to 15% by mass with respect to the third solution from the viewpoint of ink absorbability. Preferably, the range of 6-13 mass% is more preferable.
The content of polyvinyl alcohol (excluding acetoacetyl-modified PVA) in the third solution is preferably in the range of 15 to 30% by mass with respect to the inorganic fine particles from the viewpoint of brittleness and ink absorbability. A range of mass% is more preferred.

  The thicknesses of the first coating film, the second coating film, and the third coating film in the case of multilayer coating are not particularly limited, but the film thickness ratio of the third coating film / second coating film / first coating film is not particularly limited. Is preferably 1/8 to 3/2/5 in terms of brittleness, water resistance and coating failure.

-Support-
In the method for producing an inkjet recording medium of the present invention, any of a transparent support made of a transparent material such as plastic and an opaque support made of an opaque material such as paper can be used as the support. Among these, resin-coated paper in which a resin layer is provided on both sides of a substrate such as paper is preferable.

In the present invention, polyolefin resin-coated paper is preferable as the resin-coated paper.
The base paper constituting the polyolefin resin-coated paper is not particularly limited, and commonly used paper can be used. However, a smooth base paper used for, for example, a photographic support is preferable. As the pulp constituting the base paper, natural pulp, regenerated pulp, synthetic pulp or the like can be used alone or in combination.

  In the base paper, additives such as a sizing agent, a paper strength enhancer, a filler, an antistatic agent, a fluorescent brightening agent, and a dye generally used in papermaking can be blended. Further, a surface sizing agent, surface paper strengthening agent, fluorescent brightening agent, antistatic agent, dye, anchor agent and the like may be applied on the surface.

Although there is no restriction | limiting in particular in the thickness of a base paper, The thing with good surface smoothness which applied the pressure with a calendar | calender etc. during papermaking or after papermaking is preferable. The basis weight is preferably from 30 to 250 g / m ^2, especially 50 to 250 g / m ² is preferred.

  The polyolefin resin of the polyolefin resin-coated paper includes olefin homopolymers such as low density polyethylene, high density polyethylene, polypropylene, polybutene, and polypentene, or a copolymer composed of two or more olefins such as an ethylene-propylene copolymer, and These mixtures are mentioned. As the polyolefin resin, those having various densities and melt viscosity indexes (melt index) can be used alone or in combination of two or more.

  In addition, in polyolefin resin of polyolefin resin-coated paper, white pigments such as titanium oxide, zinc oxide, talc and calcium carbonate, fatty acid amides such as stearic acid amide and arachidic acid amide, zinc stearate, calcium stearate and aluminum stearate , Fatty acid metal salts such as magnesium stearate, antioxidants such as Irganox 1010 and Irganox 1076, blue pigments and dyes such as cobalt blue, ultramarine blue, cecilian blue, phthalocyanine blue, cobalt violet, fast violet, manganese purple, etc. It is preferable to add various additives such as magenta pigments and dyes, fluorescent brighteners and ultraviolet absorbers in appropriate combinations.

  The polyolefin resin-coated paper can be produced by a so-called extrusion coating method in which a heated and melted polyolefin resin is cast on a traveling base paper, and one or both sides thereof are coated with the polyolefin resin. Further, before the base paper is coated with the polyolefin resin, the base paper surface is preferably subjected to an activation treatment such as corona discharge treatment or flame treatment.

The resin-coated paper is preferably configured by coating a polyolefin resin on the surface (front side) on which the ink receiving layer is applied and formed, but the back surface on the opposite side does not necessarily have to be coated with the polyolefin resin. However, from the viewpoint of curling prevention, the back surface is preferably coated with a polyolefin resin. In this case, activation treatment such as corona discharge treatment or flame treatment can be applied to the front side or the front / back side as required.
Moreover, the thickness in the case of coating polyolefin resin has the preferable range of 5-50 micrometers, and the range of 10-45 micrometers is especially preferable.

  Various back coat layers can be coated on the polyolefin resin-coated paper for antistatic properties, transport properties, anticurling properties, and the like. The backcoat layer can contain an appropriate combination of inorganic antistatic agent, organic antistatic agent, hydrophilic binder, latex, curing agent, pigment, surfactant and the like. An ink receiving layer may be provided on both sides of the polyolefin resin-coated paper.

<Second aspect>
Next, a second aspect of the method for manufacturing an ink jet recording medium will be described as a reference aspect .
In the second embodiment, a solution containing at least inorganic fine particles, acetoacetyl-modified polyvinyl alcohol and cationic polyurethane is coated on a support (ink-receiving layer coating solution; hereinafter also referred to as “solution A”). a coating film forming step of forming a coating film, even during dry developing the formed the coating layer before coating film exhibits a decreasing rate of drying, water-soluble having two or more amino groups in the molecule multi A solution application step of applying a solution containing a functional compound (crosslinking agent-containing solution; hereinafter, also referred to as “solution B”) onto the coating film.

Also in the second aspect, as in the first aspect described above, when the ink receiving layer is formed by using acetoacetyl-modified polyvinyl alcohol and cationic polyurethane together, acetoacetyl-modified polyvinyl alcohol (and preferably, The ink-receiving layer can be applied and formed so that the cationic polyurethane) and the “water-soluble polyfunctional compound having two or more amino groups in the molecule” as a crosslinking agent are not in direct contact. Therefore, thickening that appears greatly when acetoacetyl-modified polyvinyl alcohol is used (especially when acetoacetyl-modified polyvinyl alcohol and cationic polyurethane are used in combination), and the decrease in coating properties that accompanies this, is effectively reduced. Therefore, the stability of the coating liquid when such a composition system is maintained, the brittleness after coating (particularly during drying) is improved, and the occurrence of coating failure such as cracks can be prevented, and ink bleeding after recording ( In particular, water resistance) is suppressed.

  In the coating film forming step of the second aspect, a coating film is formed by applying a solution A (ink receiving layer coating solution) containing at least inorganic fine particles, acetoacetyl-modified polyvinyl alcohol and cationic polyurethane on a support. To do. The ink receiving layer coating liquid may further contain other components as required.

Details of the inorganic fine particles, acetoacetyl-modified PVA, cationic polyurethane, and other components contained in the ink-receiving layer coating solution (solution A) are as described above in the first embodiment. The same applies to the preferred embodiment.
The details of the coating method of the ink receiving layer coating liquid are also as described above.

The content of the inorganic fine particles (preferably silica particles (particularly, vapor phase silica)) in the ink receiving layer coating liquid of the second aspect is set to the mass of the ink receiving layer coating liquid from the viewpoint of ink absorptivity. On the other hand, the range of 5-20 mass% is preferable, and the range of 6-15 mass% is more preferable.
The content of the acetoacetyl-modified PVA in the coating liquid for the ink-receiving layer of the second aspect is preferably in the range of 15 to 230% by mass with respect to the inorganic fine particles from the viewpoint of brittleness, water resistance and suppression of coating failure. The range of 15-25 mass% is more preferable.
The content of the cationic polyurethane in the coating liquid for the ink receiving layer of the second aspect is preferably in the range of 5 to 40% by mass with respect to the inorganic fine particles from the viewpoint of improving bleeding (moisture resistance). A range of 35% by mass is more preferred.

  In the solution application step of the second aspect, two or more amino groups are present in the molecule during the dry coating of the coating film formed in the coating film forming step and before the coating film exhibits reduced drying. A solution B (crosslinking agent-containing solution) containing the water-soluble polyfunctional compound (water-soluble polyfunctional crosslinking agent) is applied on the coating film.

  Solution B (crosslinking agent-containing solution) preferably further contains a water-soluble aluminum compound. By including the water-soluble aluminum compound, water resistance is improved, and bleeding of ink (image) due to the influence of moisture such as under high humidity is suppressed. On the other hand, since the water-soluble aluminum compound is contained in the solution B and the ink receiving layer can be formed as a separate liquid so as not to come into direct contact with the cationic polymer in the liquid, the acetoacetyl-modified PAV and the cationic polyurethane are used in combination. In particular, the increase in viscosity and the resulting decrease in coating properties can be suppressed. As a result, the stability of the coating liquid is improved when such a composition system is used, and coating failure such as cracks after application (particularly during drying) and occurrence of ink (image) bleeding are suppressed.

The solution B can be prepared in the same manner as the third solution in the first aspect described above. The details of each component such as the water-soluble polyfunctional crosslinking agent constituting the solution B are as described in the third solution, and the preferred embodiments, contents, and the like are also the same.
In addition, the method to be applied “before the coating film is being dried and before the coating film shows reduced-rate drying” is also as described above for the application of the third solution, and the preferred embodiment is also the same. is there. The crosslinker solution (solution B) in this embodiment may also contain inorganic fine particles and PVA as in the third solution.

  The support used in the second aspect can be the same as the support usable in the first aspect, and is preferably a resin-coated paper in which resin layers are provided on both sides of a substrate such as paper. is there.

  EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to the following examples unless it exceeds the gist thereof. Unless otherwise specified, “part” is based on mass.

( Reference Example 1)
-Production of support-
50 parts of LBKP made of acacia and 50 parts of LBKP made of aspen were each beaten to 300 ml of Canadian freeness by a disc refiner to prepare a pulp slurry. Subsequently, to the obtained pulp slurry, 1.3% by mass of cationic starch (manufactured by Nippon NSC Co., Ltd., CATO 304L), anionic polyacrylamide (manufactured by Seiko Chemical Co., Ltd., polyaclon ST-13) per pulp. 0.15% by mass, alkyl ketene dimer (Arakawa Chemical Co., Ltd., size pine K) 0.29% by mass, epoxidized behenamide 0.29% by mass, polyamide polyamine epichlorohydrin (Arakawa Chemical Co., Ltd., Arakawa Chemical Co., Ltd.) Fix 100) After adding 0.32 mass%, antifoaming agent 0.12 mass% was further added.

This pulp slurry is made with a long paper machine, the web felt surface is pressed against the drum dryer cylinder through the dryer canvas, the dryer canvas is set at a tensile force of 1.6 kg / cm, and dried. Then, 1 g / m ^{2 of} polyvinyl alcohol (manufactured by Kuraray Co., Ltd., KL-118) was applied on both sides of this base paper with a size press and dried, and a calendar process was performed to obtain a base paper. The basis weight of the obtained base paper was 166 g / m ² and the thickness was 160 μm.

After performing corona discharge treatment on the wire surface (back surface) side of the obtained base paper, using a melt extruder, high density polyethylene is coated to a thickness of 25 μm, and a thermoplastic resin layer comprising a mat surface (Hereinafter, this thermoplastic resin layer surface is referred to as a “back surface”). After further corona discharge treatment on the back surface, as an antistatic agent, aluminum oxide (“Alumina sol 100” manufactured by Nissan Chemical Industries, Ltd.) and silicon dioxide (Snowtex O, manufactured by Nissan Chemical Industries, Ltd.) are used. )) Was dispersed in water at a mass ratio of 1: 2 so that the dry mass was 0.2 g / m ² .

  Further, after the corona discharge treatment is performed on the felt surface (surface) side where the thermoplastic resin layer is not provided, 10% by mass of anatase type titanium dioxide and 0.3% of ultramarine made by Tokyo Ink Co., Ltd. MFR (melt flow rate) adjusted to have a content of 0.08% by mass with a whitening agent “Whitefloor PSN conc” manufactured by Nippon Chemical Industry Co., Ltd. 8 low-density polyethylene is extruded to a thickness of 25 μm using a melt extruder to form a high-gloss thermoplastic resin layer (hereinafter, this high-gloss surface is referred to as “front side”), and water resistance. A support was prepared. This water-resistant support was made into a long roll body with a width of 1.5 m and a winding length of 3000 m.

-Preparation of coating liquid A1 for ink receiving layer-
After mixing (1) gas phase method silica fine particles, (2) ion-exchanged water, and (3) Charol DC-902P in the following composition and dispersing them using an ultrasonic disperser (manufactured by SMT Co., Ltd.) The dispersion was heated to 45 ° C. and held for 20 hours. Thereafter, (4) boric acid and (5) 7% by mass aqueous solution of acetoacetyl-modified polyvinyl alcohol, (6) cationic polyurethane resin, and (7) polyaluminum chloride (8) surfactant 10 in the following composition: A mass% aqueous solution was added at 30 ° C. to prepare an ink-receiving layer coating solution A1 (solution A).

<Composition of coating liquid A1 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) ... 0.37 parts (5) 7% by mass aqueous solution of acetoacetyl-modified polyvinyl alcohol (Z210, manufactured by Nippon Synthetic Chemical Co., Ltd.) ... 29 parts (6) Cationic Polyurethane resin (Superflex 600, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) ... 2 parts (7) Polyaluminum chloride ... 1.5 parts (Alphain 83, manufactured by Daimei Chemical Industry Co., Ltd.)
(8) 10% by mass aqueous solution of surfactant (Emulgen 109P, manufactured by Kao Corporation) 0.6 parts

-Preparation of crosslinker solution 1-
Components having the following composition were dissolved and mixed at room temperature to prepare a crosslinker solution 1 (solution B).
<Composition of crosslinking agent solution 1>
(1) Ion-exchanged water: 30 parts (2) Adipic acid dihydrazide (water-soluble polyfunctional crosslinking agent): 1 part (3) 10% by mass of surfactant (Emulgen 109P, manufactured by Kao Corporation) Aqueous solution: 0.5 part

−Preparation of inkjet recording medium−
After the corona discharge treatment was performed on the front surface of the support obtained above, the ink receiving layer coating liquid A1 was applied with a slide bead coater so as to be 200 cc / m ^2, and 80 ° C. (wind speed 3 m) with a hot air dryer. / Sec) for 3 minutes. During this time, the coating film exhibited constant rate drying. Immediately after drying for 3 minutes, this coating film was immersed in the crosslinking agent solution 1 for 1 second and dried at 80 ° C. for 10 minutes. In this way, an ink jet recording medium was produced.

(Example 2)
-Preparation of coating liquid A2 for ink receiving layer-
In the preparation of the ink receiving layer coating liquid A1 of Reference Example 1, an ink receiving layer coating liquid A2 was prepared in the same manner as the ink receiving layer coating liquid A1, except that the composition was changed as follows.
<Composition of coating liquid A2 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) ... 0.37 parts (5) 7% by mass aqueous solution of acetoacetyl-modified polyvinyl alcohol (Z210, manufactured by Nippon Synthetic Chemical Co., Ltd.) ... 29 parts (6) Cationic Polyurethane resin (Superflex 600, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) 2 parts (7) 10% by weight aqueous solution of surfactant (Emulgen 109P, Kao Corporation) 0.6 parts

-Preparation of coating liquid B1 for ink receiving layer-
In the preparation of the ink-receiving layer coating liquid A1 of Reference Example 1, the ink-receiving layer coating liquid B1 (the second coating liquid B1) was prepared in the same manner as the ink-receiving layer coating liquid A1 except that the composition was changed as follows. Solution) was prepared.
<Composition of coating liquid B1 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) ... 0.37 parts (5) 7% by mass aqueous solution of polyvinyl alcohol (manufactured by Kuraray Co., Ltd., PVA-235) ... 29 parts (6) Surfactant (Emulgen 109P, 10% by weight aqueous solution of Kao Corp. 0.6 parts

-Preparation of crosslinker solution 1-
In the same manner as in Reference Example 1, a crosslinking agent solution 1 (third solution) was prepared.

−Preparation of inkjet recording medium−
After the corona discharge treatment is performed on the front surface opposite to the back surface of the support obtained above, the ink receiving layer coating solution B1 is formed as an upper layer so that the ink receiving layer coating solution A2 is 160 cc / m ^2. As a result, the first coating film composed of the ink-receiving layer coating liquid A2 and the second coating film composed of the ink-receiving layer coating liquid B1 are sequentially applied from the support side so as to be 40 cc / m ^2. Then, it was dried with a hot air dryer at 80 ° C. (wind speed 3 m / sec) for 3 minutes. During this time, the first coating film and the second coating film exhibited constant rate drying. Immediately after drying for 3 minutes, this coating film was immersed in the crosslinking agent solution 1 for 1 second and dried at 80 ° C. for 10 minutes. Immediately after drying for 3 minutes, this coating layer was immersed in the crosslinking agent solution 1 for 1 second and dried at 80 ° C. for 10 minutes. In this way, an ink jet recording medium was produced.

(Example 3)
In Example 2, except that the ink-receiving layer coating liquid A2 for forming the lower layer was replaced with the ink-jet receiving layer coating liquid A1 (first solution) prepared in Reference Example 1, in the same manner as in Example 2, An ink jet recording medium was produced.

Example 4
In Example 2, the ink-receiving layer coating liquid A2 for forming the lower layer is replaced with the coating liquid A3 for ink-jet receiving layer having the following composition (first solution), and the ink-receiving layer coating liquid B1 for forming the upper layer is ink-jet having the following composition An ink jet recording medium was produced in the same manner as in Example 2 except that the receiving layer coating liquid B2 (second solution) was used.

<Composition of coating liquid A3 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) 0.37 part (5) 7% by mass aqueous solution of acetoacetyl-modified polyvinyl alcohol (Z210, manufactured by Nippon Synthetic Chemical Co., Ltd.) 29 parts (6) Surface activity 10% by weight aqueous solution of an agent (Emulgen 109P, manufactured by Kao Corp.) 0.6 parts

<Composition of coating liquid B2 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) 0.37 part (5) 7% by mass aqueous solution of polyvinyl alcohol (PVA-235, manufactured by Kuraray Co., Ltd.) 29 parts (6) Cationic polyurethane resin ( Superflex 600, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) 2 parts (7) Polyaluminum chloride (Alphain 83, manufactured by Daimei Chemical Co., Ltd.) 1.5 parts (8) Surfactant 10% by weight aqueous solution (Emulgen 109P, manufactured by Kao Corporation) 0.6 parts

(Example 5)
An ink jet recording medium was obtained in the same manner as in Example 2 except that the ink receiving layer coating liquid B1 for forming the upper layer was replaced with the ink receiving layer coating liquid B3 (second solution) having the following composition in Example 2. Was made.

<Composition of coating liquid B3 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (cross-linking agent) 0.37 part (5) 7% by mass aqueous solution of polyvinyl alcohol (PVA-235, manufactured by Kuraray Co., Ltd.) 29 parts (6) Polyaluminum chloride・ 1.5 parts (Alphain 83, manufactured by Daimei Chemical Co., Ltd.)
(7) 10% by mass aqueous solution of surfactant (Emulgen 109P, manufactured by Kao Corporation) 0.6 parts

(Example 6)
-Preparation of coating liquid A2 for ink receiving layer-
In the same manner as in Example 2, an ink receiving layer coating solution A2 (first solution) was prepared.

-Preparation of coating liquid C1 for ink receiving layer-
In the preparation of the ink-receiving layer coating liquid A1 of Reference Example 1, the ink-receiving layer coating liquid C1 (the second receiving liquid C1) was prepared in the same manner as the ink-receiving layer coating liquid A1, except that the composition was changed as follows. Solution) was prepared.
<Composition of coating liquid C1 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) ... 0.37 parts (5) 7% aqueous solution of polyvinyl alcohol (manufactured by Kuraray Co., Ltd., PVA-235) ... 29 parts (6) Surfactant (Emulgen 109P , Made by Kao Corporation) 10% aqueous solution ... 0.6 parts

-Preparation of coating liquid B4 for ink receiving layer-
In the preparation of the ink-receiving layer coating liquid B1 of Example 2, the ink-receiving layer coating liquid B4 (the third liquid coating layer B3) was used in the same manner as the ink-receiving layer coating liquid B1 except that the composition was changed as follows. Solution) was prepared.
<Composition of coating liquid B4 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent): 0.37 parts (5) 7% aqueous solution of polyvinyl alcohol (manufactured by Kuraray Co., Ltd., PVA-235): 29 parts (6) Adipic acid dihydrazide (water-soluble) Multifunctional cross-linking agent) ... 1 part (7) Surfactant (Emulgen 109P, manufactured by Kao Corporation) 10% aqueous solution ... 0.6 part

−Preparation of inkjet recording medium−
Was subjected to corona discharge treatment on the front surface of the support obtained above, 20 cc / m of the ink receiving layer coating solution A2 so as to 140 cc / m ² as a bottom layer, the ink-receiving layer coating liquid C1 as an intermediate layer ^The three liquids are simultaneously applied by a slide bead coater so that the ink receiving layer coating liquid B4 is 40 cc / m ² with the ink receiving layer coating liquid B4 being the uppermost layer, and the ink receiving layer coating liquid A2 is formed from the support side. 1 coating film, a second coating film made of the ink receiving layer coating liquid C1, and a third coating film made of the ink receiving layer coating liquid B4 were formed and dried for 10 minutes at 80 ° C. (wind speed 3 m / sec) with a hot air dryer. . In this way, an ink jet recording medium was produced.

(Example 7)
An ink jet recording medium was produced in the same manner as in Example 6 except that the ink receiving layer coating liquid A2 for forming the lower layer was replaced with the ink receiving layer coating liquid A1 prepared in Reference Example 1 in Example 6. did.

(Example 8)
An ink jet recording medium was obtained in the same manner as in Example 6 except that the ink receiving layer coating liquid B4 for forming the upper layer was replaced with the ink receiving layer coating liquid B5 (second solution) having the following composition in Example 6. Was made.

<Composition of coating liquid B5 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) ... 0.37 parts (5) 7% by mass aqueous solution of polyvinyl alcohol (PVA-235, manufactured by Kuraray Co., Ltd.) ... 29 parts (6) Adipic acid dihydrazide (water-soluble) (1) (7) Cationic polyurethane resin (Superflex 600, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) ... 2 parts (8) Polyaluminum chloride ... 1.5 parts (Alphain 83, manufactured by Daimei Chemical Industry Co., Ltd.)
(9) 10% by mass aqueous solution of surfactant (Emulgen 109P, manufactured by Kao Corporation) 0.6 parts

Example 9
An ink jet recording medium was obtained in the same manner as in Example 6, except that the ink receiving layer coating liquid B4 for forming the upper layer was replaced with the ink receiving layer coating liquid B6 (second solution) having the following composition in Example 6. Was made.

<Composition of coating liquid B6 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5 mass% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) ... 0.37 parts (5) 7% by mass aqueous solution of polyvinyl alcohol (PVA-235, manufactured by Kuraray Co., Ltd.) ... 29 parts (6) Adipic acid dihydrazide (water-soluble) (1) (7) Polyaluminum chloride ... 1.5 parts (Alphain 83, manufactured by Daimei Chemical Co., Ltd.)
(8) 10% by mass aqueous solution of surfactant (Emulgen 109P, manufactured by Kao Corporation) 0.6 parts

(Comparative Example 1)
After using the support obtained in Reference Example 1 and subjecting the front side of the support to corona discharge treatment, the ink-receiving layer coating liquid A2 prepared in Example 2 is used as a lower layer so that the amount is 160 cc / m ^2. The two liquids were simultaneously applied by a slide bead coater so that the ink receiving layer coating liquid B6 prepared in Example 9 was 40 cc / m ² as the upper layer, and the coating film formed by coating was applied with a hot air dryer to 80 Drying was performed at a temperature of 3 ° C. (wind speed of 3 m / sec) for 10 minutes. In this way, an ink jet recording medium was produced.

(Comparative Example 2)
An ink jet recording medium was produced in the same manner as in Comparative Example 1 except that the ink receiving layer coating liquid A2 in Comparative Example 1 was replaced with the ink receiving layer coating liquid A1 prepared in Reference Example 1.

(Comparative Example 3)
Using the support obtained in Reference Example 1, the front side of the support was subjected to corona discharge treatment, and then the following ink receiving layer coating solution A4 was applied to 200 cc / m ² and dried with hot air. The film was dried at 80 ° C. (wind speed 3 m / sec) for 10 minutes. In this way, an ink jet recording medium was produced.

-Preparation of coating liquid A4 for ink receiving layer-
In the preparation of the ink receiving layer coating liquid A1 of Reference Example 1, an ink receiving layer coating liquid A4 was prepared in the same manner as the ink receiving layer coating liquid A1 except that the composition was changed as follows.
<Composition of coating liquid A4 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (crosslinking agent) ... 0.37 part (5) 7% aqueous solution of acetoacetyl-modified polyvinyl alcohol (Z210, manufactured by Nippon Synthetic Chemical Co., Ltd.) ... 29 parts (6) Cationic polyurethane Resin (Superflex 600, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) 2 parts (7) Adipic acid dihydrazide (water-soluble polyfunctional crosslinking agent) 0.2 part (8) Surfactant (Emulgen 109P , Made by Kao Corporation) 10% aqueous solution ... 0.6 parts

(Comparative Example 4)
An ink receiving layer coating solution A5 having the following composition was prepared. This coating solution had a high viscosity immediately after preparation and was difficult to handle and could not be applied.
<Composition of coating liquid A5 for ink receiving layer>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (AEROSIL300SV, manufactured by Nippon Aerosil Co., Ltd.)
(2) Ion-exchanged water: 56 parts (3) “Charol DC-902P” (51.5% aqueous solution): 0.87 parts (dispersant, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
(4) Boric acid (cross-linking agent) 0.37 part (5) 7% aqueous solution of acetoacetyl-modified polyvinyl alcohol (Z210, manufactured by Nippon Synthetic Chemical Co., Ltd.) 29 parts (6) Cationic polyurethane Resin (Superflex 600, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.) 2 parts (7) Adipic acid dihydrazide (water-soluble polyfunctional cross-linking agent) 0.2 part (8) Polyaluminum chloride 1.5 parts (Alphain 83, manufactured by Daimei Chemical Industry Co., Ltd.)
(9) 10% aqueous solution of surfactant (Emulgen 109P, manufactured by Kao Corporation) 0.6 parts

(Comparative Example 5)
In Example 4, an ink jet recording medium was prepared in the same manner as in Example 4 except that the ink receiving layer coating liquid B2 for forming the upper layer was replaced with the ink receiving layer coating liquid B3 prepared in Example 5. did.

(Evaluation)
The following evaluations and measurements were performed on the respective ink jet recording media obtained in the above examples and comparative examples. The results of measurement and evaluation are shown in Table 1 below.

-1. Moisture resistance (bleeding)
Using an inkjet printer MP970 (manufactured by Canon Inc.), in a 23 ° C., 50% RH environment, a magenta and black adjacent lattice pattern on each inkjet recording medium (the length of one side of the lattice is 0.28 mm). ) Was printed to form a 3 cm square. Immediately after printing, the inkjet recording medium was moved to an environment of 23 ° C. and 90% RH and left for 7 days. Seven days later, after sufficiently drying in an environment of 23 ° C. and 50% RH, the degree of bleeding was visually evaluated and ranked according to the following evaluation criteria.
<Evaluation criteria>
A: Bleeding could not be recognized.
B: Slightly blurred.
C: Bleeding was large and practically unacceptable.

-2. Water resistance
Using an inkjet printer MP970 (manufactured by Canon Inc.), yellow, magenta, cyan, red, green, blue, and black in a size of 2 cm square on each inkjet recording medium in an environment of 23 ° C. and 50% RH. A solid image was printed. After printing, it was dried at 23 ° C. and 50% RH for 24 hours, and then immersed in ion-exchanged water for 10 minutes. Thereafter, the degree of bleeding of the solid image was visually observed and ranked according to the following evaluation criteria.
<Evaluation criteria>
A: Bleeding could not be recognized.
B: Bleeding was hardly noticeable.
C: Slight bleeding was observed, but this was practically acceptable.
D: Bleeding was large and practically unacceptable.

-3. Concentration-
A black solid image was printed on each inkjet recording medium using an inkjet printer A820 (manufactured by Seiko Epson Corporation) in an environment of 23 ° C. and 50% RH. After printing, the sample was left overnight at 23 ° C. in a 50% environment, and the visual reflection density was measured with a densitometer (X-rite 310TR).

-4. Coating solution stability
The ink image-receiving layer coating liquids A1 to A4 and B1 to B6 were each left in an environment of 30 ° C., and evaluated according to the following evaluation criteria from the time when the viscosity increased with time and reached 300 mPs or more.
<Evaluation criteria>
A: After preparing the coating solution for the ink image-receiving layer, there was no problem in handling even if it was left overnight.
B: There was no problem in handling within 1 hour after the preparation of the ink image-receiving layer coating solution.
C: The handleability was poor except immediately after the preparation of the ink image-receiving layer coating solution.
D: Viscosity was remarkable and handling was impossible.

-5. Coating surface-
About each inkjet recording medium, the film cracking generate | occur | produced on the ink receptive layer surface at the time of application | coating drying, the generation | occurrence | production degree of a blister failure was confirmed visually, and it ranked according to the following references | standards.
<Evaluation criteria>
A: Neither film cracking nor failure occurred.
B: Although film cracking and failure occurred slightly, they were inconspicuous.
C: The occurrence of film cracking and failure could be confirmed, which was in an unacceptable range for practical use.
D: The occurrence of film cracking and failure was remarkable.

As shown in Table 1, in the examples, an ink receiving layer having a good coated surface and reduced brittleness was obtained while maintaining the stability of the coating solution used for coating. Further, it was excellent in moisture resistance and water resistance, and the concentration was high and bleeding after recording could be suppressed.
On the other hand, in the comparative example, when the adipic acid dihydrazide used as the cross-linking agent is in direct contact with the acetoacetyl-modified PVA, the coating surface state is significantly deteriorated in the system in which the cationic polyurethane coexists, and particularly water-soluble. In the system in which the aluminum compound further coexists (Comparative Example 2), the stability of the coating solution was significantly reduced. Further, in Comparative Examples 3 and 4 of one liquid system, the coating liquid stability could not be maintained, and the formed coating surface condition was also deteriorated. When the system did not contain cationic polyurethane (Comparative Example 5), image bleeding was greatly reduced.

Claims (3)

On the support, a first solution containing at least inorganic fine particles and acetoacetyl-modified polyvinyl alcohol, and a second solution containing at least inorganic fine particles and polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol) are used as the first solution. A coating film forming step of simultaneously applying multiple layers so that the second solution is positioned on the solution and forming a coating film;
At the same time to form the coating film, or the before showing a dry even during developing the coating film decreasing rate of drying of the coating film, a third containing a water-soluble polyfunctional compound having two or more amino groups in the molecule A solution application step of applying a solution of
And at least one of the first solution and the second solution further comprises a cationic polyurethane. The third solution further contains inorganic fine particles and polyvinyl alcohol (excluding acetoacetyl-modified polyvinyl alcohol),
The first solution, the second solution, and the third solution are placed on a support in order from the support side so that the first solution, the second solution, and the third solution are in a positional relationship. In addition to the simultaneous multilayer coating, a coating film is formed on the support,
The method for producing an ink jet recording medium according to claim 1, wherein at least one of the first solution, the second solution, and the third solution further contains a cationic polyurethane.   The method for producing an ink jet recording medium according to claim 1, wherein the second solution further contains a water-soluble aluminum compound.