JP4287821B2 - Inkjet recording medium - Google Patents

Description

  The present invention relates to an inkjet recording medium, and more specifically, a liquid ink such as an aqueous ink (using a dye or pigment as a coloring material) and an oil-based ink, or a solid state that is solid at room temperature and melted and liquefied for printing. More particularly, the present invention relates to an ink jet recording medium that is excellent in ink receiving performance, has little aging of an image area, and has excellent water resistance and ozone resistance.

In recent years, with the rapid development of the information technology industry, various information processing systems have been developed, and recording methods and recording apparatuses suitable for the information processing systems have been developed and put into practical use.
Among these recording methods, the inkjet recording method is capable of recording on a variety of recording materials, has advantages such as being relatively inexpensive and compact in hardware (device), and excellent in quietness. It has also been widely used for so-called home use.

In addition, with the recent increase in resolution of inkjet printers, it has become possible to obtain so-called photographic-like high-quality recorded matter. With the progress of such hardware (devices), recording for inkjet recording has become possible. Various seats have been developed.
The characteristics required for this recording sheet for ink jet recording are generally (1) fast drying (high ink absorption speed), and (2) ink dot diameter is appropriate and uniform. (No blurring), (3) good graininess, (4) high dot roundness, (5) high color density, (6) high chroma (dullness) (7) The water resistance, light resistance, and ozone resistance of the print portion are good, (8) the whiteness of the recording sheet is high, and (9) the storage stability of the recording sheet is good ( Does not cause yellowing coloring even after long-term storage, does not blur images after long-term storage (good aging over time), and (10) resists deformation and has good dimensional stability (curl is sufficiently small) (11) Good hard running performance It is.
Furthermore, in the use of photo glossy paper used for the purpose of obtaining so-called photographic-like high-quality recorded matter, in addition to the above properties, gloss, gloss of printed area, surface smoothness, similar to silver salt photography A photographic paper-like texture is also required.

  In recent years, an ink jet recording sheet having a porous structure in an ink receiving layer has been developed and put into practical use for the purpose of improving the various properties described above. Such an ink jet recording medium has a porous structure, so that it has excellent ink receptivity (fast drying property) and high gloss.

For example, a gazette or the like (see Patent Document 1) proposes an ink jet recording sheet that contains fine inorganic pigment particles and a water-soluble resin and has an ink receiving layer having a high porosity on a support. .
These recording sheets, particularly ink jet recording sheets provided with an ink receiving layer having a porous structure using silica as inorganic pigment fine particles, are excellent in ink absorptivity and can form high resolution images. It has high ink receiving performance and can exhibit high gloss.

  However, since these are porous coatings, they have a high oxygen permeability and may promote deterioration of components contained in the ink receiving layer. Furthermore, with the moisture adsorption on the silica surface, image blurring with time (hereinafter referred to as “aging blurring”) may occur.

  On the other hand, an inkjet recording material using a cationic resin has been proposed for the purpose of preventing blurring with time (see Patent Document 2, Patent Document 3, and Patent Document 4). However, these products are not always satisfactory in terms of aging blurring, and have a tendency to deteriorate ozone resistance (particularly cyan).

Japanese Patent Laid-Open No. 10-217601 JP 63-115780 A Japanese Patent Laid-Open No. 11-3210794 JP 2004-167784 A

  An object of the present invention is to solve the above conventional problems and achieve the following objects. That is, the object of the present invention is to form a high-resolution and high-density image, excellent in water resistance, and without causing aging blur even when stored in a high-temperature and high-humidity environment for a long time after printing. An object of the present invention is to provide an ink jet recording medium having a high ozone property and capable of stably holding an image.

In view of such a situation, the present inventors have conducted intensive research and found that an ink jet recording medium containing the following cationic resin in the ink receiving layer on the support solves the above problems. It came to be completed.
That is, the present invention provides the following.

〔Ｒは水素原子またはメチル基、Ｒ₁、Ｒ₂はそれぞれ独立にアルキレン基を表す。Ｒ₃〜Ｒ₅はそれぞれ独立に水素原子、アルキル基、アラルキル基、又はアリール基を表す。Ｑはエチレン性二重結合を有する単量体から与えられる少なくとも１種の単位であり有機概念図の無機性／有機性比（Ｉ／Ｏ値）が０．５未満である。Ｚはアミド結合、ウレタン結合、ウレア結合を表し、Ｘ^-は陰イオンを表す。ｐは２０〜８０モル％、ｑは２０〜８０モル％である。ｒは０または１である〕
＜２＞ 前記式（１）で表されるカチオン性樹脂のＩ／Ｏ値が２．３以下である＜１＞に記載のインクジェット記録媒体。
＜３＞ 前記式（１）であらわされるカチオン性樹脂がさらに分子鎖末端にアルコキシシリル基を有する重合体であることを特徴とする＜１＞または＜２＞に記載のインクジェット記録媒体。
＜４＞ 前記インク受容層が、シリカ微粒子、コロイダルシリカ、アルミナ微粒子、擬ベーマイトの少なくとも１種を含有することを特徴とする＜１＞乃至＜３＞いずれかに記載のインクジェット記録媒体
＜５＞ 前記インク受容層が多価金属塩を含有することを特徴とする＜１＞乃至＜４＞のいずれかに記載のインクジェット記録媒体。
＜６＞ 前記インク受容層が、少なくとも微粒子、水溶性樹脂、および式（１）で表されるカチオン性樹脂を含有する塗布液を塗布した塗布層を架橋硬化させた層であることを特徴とする＜１＞乃至＜５＞のいずれかに記載のインクジェット記録媒体。 <1> An ink jet recording medium having an ink receiving layer on a support, wherein the ink receiving layer contains at least a cationic resin represented by the following general formula (1) .

[R represents a hydrogen atom or a methyl group, and R ₁ and R ₂ each independently represents an alkylene group. R _{3 to} R ₅ each independently represents a hydrogen atom, an alkyl group, an aralkyl group, or an aryl group. Q is at least one unit given from a monomer having an ethylenic double bond, and the inorganic / organic ratio (I / O value) of the organic conceptual diagram is less than 0.5. Z represents an amide bond, a urethane bond, or a urea bond, and X ⁻ represents an anion. p is 20 to 80 mol%, and q is 20 to 80 mol%. r is 0 or 1]
<2> The inkjet recording medium according to <1>, wherein the cationic resin represented by the formula (1) has an I / O value of 2.3 or less.
<3> The inkjet recording medium according to <1> or <2>, wherein the cationic resin represented by the formula (1) is a polymer further having an alkoxysilyl group at a molecular chain terminal.
<4> The ink jet recording medium <5> according to any one of <1> to <3>, wherein the ink receiving layer contains at least one of silica fine particles, colloidal silica, alumina fine particles, and pseudoboehmite. The ink jet recording medium according to any one of <1> to <4>, wherein the ink receiving layer contains a polyvalent metal salt.
<6> The ink receiving layer is a layer obtained by crosslinking and curing a coating layer coated with a coating solution containing at least fine particles, a water-soluble resin, and a cationic resin represented by the formula (1). The inkjet recording medium according to any one of <1> to <5>.

  According to the ink jet recording medium of the present invention, it is possible to form a high-resolution and high-density image, excellent in water resistance, and after printing, even when stored in a high-temperature and high-humidity environment for a long time without causing blurring over time, Moreover, it has high ozone resistance and can hold images stably.

The ink jet recording medium of the present invention is an ink jet recording medium having an ink receiving layer on a support, wherein the ink receiving layer contains at least a cationic resin represented by the general formula (1) .

(Cationic resin)
[Cationic resin having a unit represented by the general formula (1)]
In the present invention, the cationic resin contained in the ink receiving layer has a unit represented by the following general formula (1) .

In general formula (1) , R represents a hydrogen atom or a methyl group, and R ₁ and R ₂ each independently represents an alkylene group. R _{3 to} R ₅ each independently represents a hydrogen atom, an alkyl group, an aralkyl group, or an aryl group. Q is at least one unit given from a monomer having an ethylenic double bond, and the inorganic / organic ratio (I / O value) of the organic conceptual diagram is less than 0.5. Z represents an amide bond, a urethane bond, or a urea bond, and X ⁻ represents an anion. p is 20 to 80 mol%, and q is 20 to 80 mol%. r is 0 or 1;

Hereinafter, this compound will be described in detail.
R ₁ and R ₂ each independently represents an alkylene group. The alkylene group is preferably an alkylene group having 8 or less carbon atoms, more preferably 6 or less carbon atoms, and particularly preferably 4 or less carbon atoms. Further, it may have a substituent (for example, an alkoxy group, an aryloxy group, a halogen atom, a hydroxyl group, a carbamoyl group, an amino group, etc.). Specific examples of the alkylene group include a methylene group, an ethylene group, a propylene group, a trimethylene group, a tetramethylene group, a hexamethylene group, an octamethylene group, a 2-hydroxyethylene group, a 2-hydroxypropylene group, and a 2-methoxypropylene group. Methylene group, ethylene group, propylene group, trimethylene group and 2-hydroxypropylene group are particularly preferable.

R _{3 to} R ₅ each independently represents a hydrogen atom, a good alkyl group, an aralkyl group, or an aryl group. Examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, t-butyl group, n-hexyl group, cyclohexyl group, 2-ethylhexyl group, n-octyl group, Examples include n-nonyl group, n-decyl group, n-dodecyl group, n-octadecyl group, hydroxyethyl group, 1-hydroxypropyl group and the like. Among these, as R _{3 to} R ₅ , a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, and an n-butyl group are particularly preferable, and a hydrogen atom and a methyl group are particularly preferable.

Examples of the aralkyl group optionally having a substituent of R _{3 to} R ₅ include a benzyl group, a phenylethyl group, a vinylbenzyl group, a hydroxyphenylmethyl group, a diphenylmethyl group, a trityl group, and a styryl group. Of these, a benzyl group is preferred.
The aryl group which may have a substituent includes a phenyl group, an alkylphenyl group (for example, a methylphenyl group, an ethylphenyl group, an n-propylphenyl group, an n-butylphenyl group), a cumenyl group, a mesityl group, and a tolyl group. Xylyl group, naphthyl group, chlorophenyl group, dichlorophenyl group, trichlorophenyl group, bromophenyl group, hydroxyphenyl group, methoxyphenyl group, acetoxyphenyl group, cyanophenyl group and the like. Of these, a phenyl group and a naphthyl group are particularly preferable.

Q is at least one unit given from a monomer having an ethylenic double bond, and represents a unit having an inorganic / organic ratio (I / O value) of less than 0.5 in the organic conceptual diagram. Specific examples of the monomer include, for example, styrene, vinyltoluene, t-butyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl (meth) acrylate, and benzyl (meth) acrylate, and styrene. Or vinyl toluene is particularly preferable.
Here, the I / O value is a parameter representing the scale of hydrophilicity / lipophilicity of a compound or a substituent, and there is a detailed explanation in “Organic Conceptual Diagram” (Yoshio Koda, Sankyo Publishing, 1984). I represents inorganic and O represents organic, and the larger the I / O value, the greater the inorganicity (high polarity and high hydrophilicity).

These monomers may be used alone or as a copolymerizable two or more monomers.
p is 20 to 80 mol%, preferably 25 to 75 mol%, particularly 30 to 70 mol%.
Is preferred. q is 20 to 80 mol%, preferably 25 to 75 mol%, particularly preferably 30 to 70 mol%.

X ⁻ represents an anion. Specific examples thereof include halogen ions (Cl ⁻ , Br ⁻ , I ⁻ ), sulfonate ions, alkyl sulfonate ions, aryl sulfonate ions, alkyl carboxylate ions, and aryl carboxylate ions.

These copolymerizable components may be used alone or in combination of two or more.
The molecular weight of the polymer represented by the above formula (1) is preferably about 1,000 to 500,000, more preferably 2,000 to 100,000, as a weight average molecular weight. If the molecular weight is less than 1000, water resistance may be insufficient, and image blurring over time may not be suppressed. Further, when the molecular weight is 500,000 or more, handling suitability may be poor.

Furthermore, the polymer represented by the general formula (1) is preferably a polymer having an alkoxysilyl group at the molecular chain terminal. Preferred examples of the alkoxysilyl group include a trimethoxysilyl group, a triethoxysilyl group, a tripropoxysilyl group, a methyldimethoxysilyl group, an ethyldimethoxysilyl group, a methyldiethoxysilyl group, and an ethyldiethoxysilyl group. Among these, a trimethoxysilyl group, a triethoxysilyl group, and a methyldimethoxysilyl group are preferable.
The polymer is preferably soluble in an organic solvent that is water-soluble or miscible with water, but can also be used in the form of a water-dispersible latex.

The polymer represented by the general formula (1) preferably has an inorganic / organic ratio (I / O value) of 2.3 or less in the organic conceptual diagram, more preferably 2.0 or less, and further Preferably it is 1.8 or less.
Further, it is preferable to select the content of the structure / copolymerization component so that the cation equivalent is 1.5 to 8 meq / g. When the I / O value is larger than 2.3 or the cation equivalent is larger than 8 meq / g, the water-soluble property of the cationic resin is too high, and the effect of preventing blurring with time may be insufficient. On the other hand, when the cation equivalent is less than 1.5 meq / g, the ratio of the mordanting part is relatively small, and thus the immobilization of the dye may be insufficient.
Here, the cation equivalent is an equivalent (mmol) of a cationic group (total of amino group and ammonium group) contained per 1 g of the polymer, and is a value represented by meq / g.

Preferred specific examples of the cationic resin having a unit represented by the general formula (1) are shown below.

The total content in the inkjet recording medium of a cationic resin having a unit represented by the general formula (1), preferably 0.01-5 g / m ^2, more preferably 0.1 to 3 g / m ^2. If the total content is less than 0.01 g / m ² , the effect of preventing aging blur may be insufficient, and if it exceeds 5 g / m ² , the ink absorbability may be lowered.

(Fine particles)
The ink receiving layer of the ink jet recording medium of the present invention contains fine particles.
The ink receiving layer of the ink jet recording medium has a porous structure by containing fine particles, thereby improving the ink absorption performance. In particular, when the solid content of the fine particles in the ink receiving layer is 50% by mass or more, more preferably more than 60% by mass, it becomes possible to form a more favorable porous structure, and sufficient ink absorptivity. This is preferable because an ink jet recording medium having the above can be obtained. Here, the solid content in the ink receiving layer of fine particles is a content calculated based on components other than water in the composition constituting the ink receiving layer.
The fine particles used in the present invention are preferably inorganic fine particles, but organic fine particles can also be used as long as the effects of the present invention are not impaired.

  Preferred examples of the organic fine particles include polymer fine particles obtained by emulsion polymerization, microemulsion polymerization, soap-free polymerization, seed polymerization, dispersion polymerization, suspension polymerization, and the like. Specifically, polyethylene, polypropylene, Examples include polystyrene, polyacrylate, polyamide, silicon resin, phenol resin, natural polymer powder, latex or emulsion polymer fine particles, and the like.

Examples of the inorganic fine particles include silica fine particles, colloidal silica, titanium dioxide, barium sulfate, calcium silicate, zeolite, kaolinite, halloysite, mica, talc, calcium carbonate, magnesium carbonate, calcium sulfate, pseudoboehmite, zinc oxide, water. Examples thereof include zinc oxide, alumina, aluminum silicate, calcium silicate, magnesium silicate, zirconium oxide, zirconium hydroxide, cerium oxide, lanthanum oxide, and yttrium oxide. Among these, silica fine particles, colloidal silica, alumina fine particles, or pseudoboehmite are preferable from the viewpoint of forming a good porous structure. The fine particles may be used as primary particles or in a state where secondary particles are formed. The average primary particle size of these fine particles is preferably 2 μm or less, and more preferably 200 nm or less.
Further, silica fine particles having an average primary particle size of 20 nm or less, colloidal silica having an average primary particle size of 30 nm or less, alumina fine particles having an average primary particle size of 20 nm or less, or pseudoboehmite having an average pore radius of 2 to 15 nm is more preferable. In particular, silica fine particles, alumina fine particles, and pseudoboehmite are preferable.

  Silica fine particles are generally roughly classified into wet method particles and dry method (gas phase method) particles according to the production method. In the above wet method, a method is mainly used in which activated silica is produced by acid decomposition of a silicate, and this is appropriately polymerized and agglomerated and precipitated to obtain hydrous silica. On the other hand, the gas phase method is a method by high-temperature gas phase hydrolysis of silicon halide (flame hydrolysis method), a method in which silica sand and coke are heated and reduced by an arc in an electric furnace and oxidized with air. The method of obtaining anhydrous silica by the (arc method) is the mainstream, and “gas phase method silica” means anhydrous silica fine particles obtained by the gas phase method. As the silica fine particles used in the present invention, gas phase method silica fine particles are particularly preferable.

The gas phase method silica is different from hydrous silica in terms of the density of silanol groups on the surface, the presence or absence of vacancies, etc., and exhibits different properties, but is suitable for forming a three-dimensional structure with a high porosity. The reason for this is not clear, but in the case of hydrous silica, the density of silanol groups on the fine particle surface is high at 5 to 8 / nm ² , and the silica fine particles tend to aggregate (aggregate) easily. In the case of the method silica, the density of silanol groups on the surface of the fine particles is 2 to 3 / nm ² , so that it is sparse soft agglomeration (flocculate), resulting in a structure with a high porosity. Is done.

  The above-mentioned vapor phase silica has a particularly large specific surface area, so the ink absorption and retention efficiency is high, and the refractive index is low. Therefore, if the dispersion is made to an appropriate particle size, transparency can be imparted to the receiving layer. It is characterized by high color density and good color development. The transparency of the receiving layer is not only for applications that require transparency such as OHP, but also in terms of obtaining high color density and good color development gloss even when applied to recording sheets such as photo glossy paper. is important.

  The average primary particle diameter of the vapor phase silica is preferably 30 nm or less, more preferably 20 nm or less, particularly preferably 10 nm or less, and most preferably 3 to 10 nm. Since the vapor phase silica is easily adhered to each other by hydrogen bonding with a silanol group, a structure having a large porosity can be formed when the average primary particle diameter is 30 nm or less, and ink absorption characteristics are effectively improved. Can be improved.

  Silica fine particles may be used in combination with the other fine particles described above. When the other fine particles and the vapor phase silica are used in combination, the content of the vapor phase silica in all the fine particles is preferably 30% by mass or more, and more preferably 50% by mass or more.

As the inorganic fine particles used in the present invention, alumina fine particles, alumina hydrate, a mixture or a composite thereof are also preferable. Of these, alumina hydrate is preferable because it absorbs and fixes ink well, and pseudoboehmite (Al ₂ O ₃ .nH ₂ O) is particularly preferable. Alumina hydrates can be used in various forms, but it is preferable to use sol boehmite as a raw material because a smooth layer can be easily obtained.

About the pore structure of pseudo boehmite, the average pore radius is preferably 1 to 30 nm, and more preferably 2 to 15 nm. The pore volume is preferably 0.3 to 2.0 cc / g, more preferably 0.5 to 1.5 cc / g. Here, the pore radius and pore volume are measured by a nitrogen adsorption / desorption method, and can be measured by, for example, a gas adsorption / desorption analyzer (for example, trade name “Omni Soap 369” manufactured by Coulter). .
Among alumina fine particles, vapor-phase method alumina fine particles are preferable because of their large specific surface area. The average primary particle size of the vapor phase alumina is preferably 30 nm or less, and more preferably 20 nm or less.

  When the above-mentioned fine particles are used in an inkjet recording medium, for example, JP-A-10-81064, JP-A-10-119423, JP-A-10-157277, JP-A-10-217601, JP-A-11-348409, JP-A-2001-138621. No. 2000-43401, No. 2000-212235, No. 2000-309157, No. 2001-96897, No. 2001-138627, JP-A-11-91242, No. 8-2087, No. 8-2090 8-2091, 8-2093, 8-174992, 11-192777, JP-A-2001-301314, and the like can also be preferably used.

(Water-soluble resin)
In the ink jet recording medium of the present invention, the ink receiving layer further contains a water-soluble resin.
As this water-soluble resin, for example, a polyvinyl alcohol resin which is a resin having a hydroxy group as a hydrophilic structural unit [polyvinyl alcohol (PVA), acetoacetyl-modified polyvinyl alcohol, cation-modified polyvinyl alcohol, anion-modified polyvinyl alcohol, silanol-modified) Polyvinyl alcohol, polyvinyl acetal, etc.], cellulosic resins [methyl cellulose (MC), ethyl cellulose (EC), hydroxyethyl cellulose (HEC), carboxymethyl cellulose (CMC), hydroxypropyl cellulose (HPC), hydroxyethyl methyl cellulose, hydroxypropyl methyl cellulose, etc.] , Chitins, chitosans, starch, resins with ether linkages [polyethylene oxide (PEO), Propylene oxide (PPO), polyethylene glycol (PEG), poly ether (PVE)], and resins having carbamoyl groups [polyacrylamide (PAAM), polyvinyl pyrrolidone (PVP), polyacrylic acid hydrazide, etc.] and the like.
Moreover, the polyacrylic acid salt which has a carboxyl group as a dissociable group, maleic acid resin, alginate, gelatins, etc. can be mentioned.

Among these, polyvinyl alcohol resin is particularly preferable. Examples of the polyvinyl alcohol include Japanese Patent Publication No. 4-52786, Japanese Patent Publication No. 5-67432, Japanese Patent Publication No. 7-29479, Japanese Patent No. 2537827, Japanese Patent Publication No. 7-57553, Japanese Patent No. 2502998, and Japanese Patent No. 3053231. JP-A-63-176173, JP-A-2604367, JP-A-7-276787, JP-A-9-207425, JP-A-11-58941, JP-A-2000-135858, JP-A-2001-205924, JP 2001-287444, JP 62-278080, JP 9-39373, JP 2750433, JP 2000-18801, JP 2001-213045, JP 2001-328345, JP 8 -324105, JP-A-11-348417, etc. It is below.
Examples of water-soluble resins other than polyvinyl alcohol resins include compounds described in “0011” to “0014” of JP-A No. 11-165461.
These water-soluble resins may be used alone or in combination of two or more.

  As content of the water-soluble resin of this invention, 9-40 mass% is preferable with respect to the total solid content mass of an ink receiving layer, and 12-33 mass% is more preferable.

The water-soluble resin and the fine particles, which mainly constitute the ink receiving layer of the present invention, may each be a single material, or a mixed system of a plurality of materials may be used.
From the viewpoint of maintaining transparency, the type of water-soluble resin to be combined with fine particles, particularly silica fine particles, is important. When the gas phase method silica is used, the water-soluble resin is preferably a polyvinyl alcohol resin, more preferably a polyvinyl alcohol resin having a saponification degree of 70 to 100%, and a saponification degree of 80 to 99.5. % Of polyvinyl alcohol resin is particularly preferable.

The polyvinyl alcohol-based resin has a hydroxyl group in its structural unit, and since this hydroxyl group and the surface silanol group of the silica fine particle form a hydrogen bond, a three-dimensional network having a secondary particle of the silica fine particle as a network chain unit. It becomes easy to form a structure. By forming this three-dimensional network structure, it is considered that a porous ink receiving layer having a high porosity and sufficient strength is formed.
In ink jet recording, the porous ink receiving layer obtained as described above can absorb ink rapidly by a capillary phenomenon, and can form dots with good roundness without ink bleeding.

  In addition, the polyvinyl alcohol resin may be used in combination with the other water-soluble resin. When the other water-soluble resin and the polyvinyl alcohol resin are used in combination, the content of the polyvinyl alcohol resin in the total water-soluble resin is preferably 50% by mass or more, and more preferably 70% by mass or more.

<Content ratio of fine particles to water-soluble resin>
The mass content ratio [PB ratio (x / y)] between the fine particles (x) and the water-soluble resin (y) greatly affects the film structure and film strength of the ink receiving layer. That is, as the mass content ratio [PB ratio] increases, the porosity, pore volume, and surface area (per unit mass) increase, but the density and strength tend to decrease.

  The ink receiving layer of the present invention prevents the decrease in film strength and cracking during drying caused by the PB ratio being too large as the mass content ratio [PB ratio (x / y)], and When the PB ratio is too small, the gap is easily blocked by the resin, and from the viewpoint of preventing the ink absorbency from being lowered due to the decrease in the porosity, 1.5 to 10 is preferable.

  Since stress may be applied to the recording sheet when passing through the conveyance system of the inkjet printer, the ink receiving layer needs to have sufficient film strength. Further, when cutting into a sheet shape, the ink receiving layer needs to have sufficient film strength in order to prevent cracking or peeling of the ink receiving layer. Considering these cases, the mass ratio (x / y) is more preferably 5 or less, while it is more preferably 2 or more from the viewpoint of ensuring high-speed ink absorbency in an inkjet printer.

For example, a coating solution in which gas phase method silica fine particles having an average primary particle size of 20 nm or less and a water-soluble resin are completely dispersed in an aqueous solution at a mass ratio (x / y) of 2 to 5 is applied on a support. When the coating layer is dried, a three-dimensional network structure in which the secondary particles of silica fine particles are network chains is formed, the average pore diameter is 30 nm or less, the porosity is 50 to 80%, and the pore specific volume is 0.00. A translucent porous film having a specific surface area of 5 ml / g or more and a specific surface area of 100 m ² / g or more can be easily formed.

(Crosslinking agent)
The ink receiving layer of the inkjet recording medium of the present invention includes a coating layer containing fine particles and a water-soluble resin, and further contains a crosslinking agent capable of crosslinking the water-soluble resin, and is cured by a crosslinking reaction between the crosslinking agent and the water-soluble resin. The aspect which is the made porous layer is preferable.

Boron compounds are preferred for crosslinking the above water-soluble resins, particularly polyvinyl alcohol resins. Examples of the boron compound include borax, boric acid, borates (for example, orthoborate, InBO ₃ , ScBO ₃ , YBO ₃ , LaBO ₃ , Mg ₃ (BO ₃ ) ₂ , Co ₃ (BO ₃ ) ₂ , two Borate (eg, Mg ₂ B ₂ O ₅ , Co ₂ B ₂ O ₅ ), metaborate (eg, LiBO ₂ , Ca (BO ₂ ) ₂ , NaBO ₂ , KBO ₂ ), tetraborate (eg, Na _{2 B 4 O 7 · 10H 2} O), can be mentioned five borate _{(e.g., KB 5 O 8 · 4H 2} O, Ca 2 B 6 O 11 · 7H 2 O, CsB 5 O 5) or the like. Among them, Of these, borax, boric acid, and borate are preferable, and boric acid is particularly preferable in that a crosslinking reaction can be promptly caused.

The following compounds other than the boron compound can also be used as the crosslinking agent for the water-soluble resin.
For example, aldehyde compounds such as formaldehyde, glyoxal and glutaraldehyde; ketone compounds such as diacetyl and cyclopentanedione; bis (2-chloroethylurea) -2-hydroxy-4,6-dichloro-1,3,5- Active halogen compounds such as triazine and 2,4-dichloro-6-S-triazine sodium salt; divinylsulfonic acid, 1,3-vinylsulfonyl-2-propanol, N, N′-ethylenebis (vinylsulfonylacetamide) ), Active vinyl compounds such as 1,3,5-triacryloyl-hexahydro-S-triazine; N-methylol compounds such as dimethylolurea and methyloldimethylhydantoin; melamine resins (for example, methylolmelamine, alkylated methylolmelamine) ;Epoxy resin;

Isocyanate compounds such as 1,6-hexamethylene diisocyanate; Aziridine compounds described in US Pat. Nos. 3,017,280 and 2,983611; Carboximide compounds described in US Pat. No. 3,100,704; Glycerol triglycidyl Epoxy compounds such as ether; Ethyleneimino compounds such as 1,6-hexamethylene-N, N′-bisethyleneurea; Halogenated carboxaldehyde compounds such as mucochloric acid and mucophenoxycyclolic acid; 2,3-dihydroxy Dioxane-based compounds such as dioxane; titanium-containing aluminum sulfate, chromium alum, potassium alum, metal-containing compounds such as zirconyl acetate, chromium acetate, polyamine compounds such as tetraethylenepentamine, hydrazide compounds such as adipic acid dihydrazide, A low molecule or polymer containing two or more oxazoline groups.
The above crosslinking agents may be used singly or in combination of two or more.

In the crosslinking and curing, a crosslinking agent is added to a coating solution containing fine particles, a water-soluble resin, etc. (hereinafter sometimes referred to as “coating solution A”) and / or the following basic solution, and (1) the coating solution And (2) at any time during the drying of the coating layer formed by coating the coating solution and before the coating layer exhibits reduced-rate drying. The above basic solution (hereinafter sometimes referred to as “coating liquid B”) is preferably applied to the coating layer. The application of the cross-linking agent is preferably performed as described below when a boron compound is taken as an example. That is, when the ink receiving layer is a layer obtained by crosslinking and curing a coating layer coated with a coating solution (coating solution A) containing a water-soluble resin containing fine particles and polyvinyl alcohol, crosslinking curing is performed by (1) the coating described above. (2) When the coating layer formed by coating the coating solution is being dried and before the coating layer exhibits reduced drying, a basic pH of 8 or higher This is performed by applying a solution (coating liquid B) to the coating layer. The boron compound as the cross-linking agent may be contained in either the coating liquid A or the coating liquid B, and may be contained in both the coating liquid A and the coating liquid B.
1-50 mass% is preferable with respect to water-soluble resin, and, as for the usage-amount of a crosslinking agent, 5-40 mass% is more preferable.

(mordant)
In the present invention, it is preferable to add a mordant to the ink receiving layer in order to further improve the water resistance and aging resistance of the formed image.
As such a mordant, a cationic polymer (cationic mordant) or an inorganic mordant is preferable as an organic mordant, and the liquid ink having an anionic dye as a coloring material can be obtained by making the mordant present in the ink receiving layer. It can interact with each other to stabilize the coloring material and improve water resistance and aging resistance. The organic mordant and the inorganic mordant may be used alone or in combination with the organic mordant and the inorganic mordant.

As the cationic mordant, a polymer mordant having a primary to tertiary amino group or a quaternary ammonium base as a cationic group is generally used. On the other hand, in the present invention, a cationic non-polymer mordant can also be used.
Examples of the polymer mordant include a homopolymer of a monomer having a primary to tertiary amino group and a salt thereof, or a quaternary ammonium base (mordant monomer), the mordant monomer and other monomers (hereinafter, What is obtained as a copolymer or condensation polymer with “non-mordant monomer”). Moreover, these polymer mordants can be used in any form of a water-soluble polymer or water-dispersible latex particles.

  Examples of the monomer (mordant monomer) include trimethyl-p-vinylbenzylammonium chloride, trimethyl-m-vinylbenzylammonium chloride, triethyl-p-vinylbenzylammonium chloride, triethyl-m-vinylbenzylammonium chloride, N , N-dimethyl-N-ethyl-Np-vinylbenzylammonium chloride, N, N-diethyl-N-methyl-Np-vinylbenzylammonium chloride, N, N-dimethyl-Nn-propyl-N -P-vinylbenzylammonium chloride, N, N-dimethyl-Nn-octyl-Np-vinylbenzylammonium chloride, N, N-dimethyl-N-benzyl-Np-vinylbenzylammonium chloride, N, N-die Ru-N-benzyl-Np-vinylbenzylammonium chloride, N, N-dimethyl-N- (4-methyl) benzyl-Np-vinylbenzylammonium chloride, N, N-dimethyl-N-phenyl-N -P-vinylbenzylammonium chloride;

  Trimethyl-p-vinylbenzylammonium bromide, trimethyl-m-vinylbenzylammonium bromide, trimethyl-p-vinylbenzylammonium sulfonate, trimethyl-m-vinylbenzylammonium sulfonate, trimethyl-p-vinylbenzylammonium acetate, trimethyl-m-vinyl Benzylammonium acetate, N, N, N-triethyl-N-2- (4-vinylphenyl) ethylammonium chloride, N, N, N-triethyl-N-2- (3-vinylphenyl) ethylammonium chloride, N, N-diethyl-N-methyl-N-2- (4-vinylphenyl) ethylammonium chloride, N, N-diethyl-N-methyl-N-2- (4-vinylphenyl) ethylammonium chloride Tate;

  N, N-dimethylaminoethyl (meth) acrylate, N, N-diethylaminoethyl (meth) acrylate, N, N-dimethylaminopropyl (meth) acrylate, N, N-diethylaminopropyl (meth) acrylate, N, N- Methyl chloride, ethyl chloride, methyl bromide of dimethylaminoethyl (meth) acrylamide, N, N-diethylaminoethyl (meth) acrylamide, N, N-dimethylaminopropyl (meth) acrylamide, N, N-diethylaminopropyl (meth) acrylamide , Quaternized products of ethyl bromide, methyl iodide or ethyl iodide, or sulfonates, alkyl sulfonates, acetates or alkyl carboxylates substituted with their anions.

  Specifically, for example, monomethyl diallyl ammonium chloride, trimethyl-2- (methacryloyloxy) ethylammonium chloride, triethyl-2- (methacryloyloxy) ethylammonium chloride, trimethyl-2- (acryloyloxy) ethylammonium chloride, triethyl- 2- (acryloyloxy) ethylammonium chloride, trimethyl-3- (methacryloyloxy) propylammonium chloride, triethyl-3- (methacryloyloxy) propylammonium chloride, trimethyl-2- (methacryloylamino) ethylammonium chloride, triethyl-2- (Methacryloylamino) ethylammonium chloride, trimethyl-2- (acryloylamino) ethyl Ammonium chloride, triethyl-2- (acryloylamino) ethylammonium chloride, trimethyl-3- (methacryloylamino) propylammonium chloride, triethyl-3- (methacryloylamino) propylammonium chloride, trimethyl-3- (acryloylamino) propylammonium chloride Triethyl-3- (acryloylamino) propylammonium chloride;

N, N-dimethyl-N-ethyl-2- (methacryloyloxy) ethylammonium chloride, N, N-diethyl-N-methyl-2- (methacryloyloxy) ethylammonium chloride, N, N-dimethyl-N-ethyl- 3- (acryloylamino) propylammonium chloride, trimethyl-2- (methacryloyloxy) ethylammonium bromide, trimethyl-3- (acryloylamino) propylammonium bromide, trimethyl-2- (methacryloyloxy) ethylammonium sulfonate, trimethyl-3- And (acryloylamino) propylammonium acetate.
In addition, examples of copolymerizable monomers include N-vinylimidazole and N-vinyl-2-methylimidazole.

The non-mordant monomer does not contain a basic or cationic moiety such as a primary to tertiary amino group and a salt thereof, or a quaternary ammonium base, and does not show an interaction with a dye in an inkjet ink. Or the monomer which interaction is substantially small is said.
Examples of the non-mordant monomer include (meth) acrylic acid alkyl ester; (meth) acrylic acid cycloalkyl ester such as cyclohexyl (meth) acrylate; (meth) acrylic acid aryl ester such as phenyl (meth) acrylate; Aralkyl esters such as (meth) benzyl acrylate; Aromatic vinyls such as styrene, vinyl toluene and α-methylstyrene; Vinyl esters such as vinyl acetate, vinyl propionate and vinyl versatic acid; Allyl esters such as allyl acetate Halogen-containing monomers such as vinylidene chloride and vinyl chloride; vinyl cyanide such as (meth) acrylonitrile; olefins such as ethylene and propylene; and the like.

The (meth) acrylic acid alkyl ester is preferably a (meth) acrylic acid alkyl ester having 1 to 18 carbon atoms in the alkyl moiety, for example, methyl (meth) acrylate, ethyl (meth) acrylate, (meth) Propyl acrylate, isopropyl (meth) acrylate, n-butyl (meth) acrylate, isobutyl (meth) acrylate, t-butyl (meth) acrylate, hexyl (meth) acrylate, octyl (meth) acrylate, Examples include 2-ethylhexyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, and the like.
Of these, methyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate, and hydroxyethyl methacrylate are preferable.
The non-mordant monomers can also be used singly or in combination of two or more.

Further, as the polymer mordant, polydiallyldimethylammonium chloride, polymethacryloyloxyethyl-β-hydroxyethyldimethylammonium chloride, polyethyleneimine, polyallylamine and derivatives thereof, polyamide-polyamine resin, cationized starch, dicyandiamide formalin condensate, dimethyl Addition of 2-hydroxypropylammonium salt polymer, polyamidine, polyvinylamine, dicyandiamide-formalin polycondensate, dicyanamide-cachinic resin represented by dicyanamide-diethylenetriamine polycondensate, polyamine-type katine resin, epichlorohydrin-dimethylamine addition polymer, dimethyldiallylammonium phosphorus chloride -SO ₂ copolymers, diallylamine salt -SO ₂ copolymer, Quaternary ammonium base-substituted alkyl group having an ester moiety (meth) acrylate-containing polymers, styryl polymers having a quaternary ammonium base-substituted alkyl group can also be mentioned.

  As the organic mordant in the present invention, polyallylamine having a weight average molecular weight of 100,000 or less and derivatives thereof are particularly preferable from the viewpoint of preventing aging stains.

(Water-soluble polyvalent metal salt compound)
The ink receiving layer of the ink jet recording medium of the present invention contains a water-soluble polyvalent metal compound.
By containing the water-soluble polyvalent metal compound in the ink receiving layer, it is possible to improve the water resistance and aging resistance of the formed image, and further improve the gas resistance, light resistance, etc. Become.
Examples of the water-soluble polyvalent metal salt compound used in the present invention include a water-soluble metal selected from calcium, barium, manganese, copper, cobalt, nickel, aluminum, iron, zinc, zirconium, chromium, magnesium, tungsten, and molybdenum. Salt.
Specifically, calcium acetate, calcium chloride, calcium formate, calcium sulfate, barium acetate, barium sulfate, barium phosphate, manganese chloride, manganese acetate, manganese formate dihydrate, manganese ammonium sulfate hexahydrate, second chloride Copper, ammonium chloride (II) chloride dihydrate, copper sulfate, cobalt chloride, cobalt thiocyanate, cobalt sulfate, nickel sulfate hexahydrate, nickel chloride hexahydrate, nickel acetate tetrahydrate, nickel ammonium sulfate Hexahydrate, nickel amidosulfate tetrahydrate, aluminum sulfate, aluminum sulfite, aluminum thiosulfate, polyaluminum chloride, aluminum nitrate nonahydrate, aluminum chloride hexahydrate, ferrous bromide, ferrous chloride Iron, ferric chloride, ferrous sulfate, ferric sulfate, zinc bromide, zinc chloride, zinc nitrate hexahydrate , Zinc sulfate, zirconium acetate, zirconium chloride, zirconium chloride octahydrate, hydroxy zirconium chloride, chromium acetate, chromium sulfate, magnesium sulfate, magnesium chloride hexahydrate, magnesium citrate nonahydrate, sodium phosphotungstate Sodium tungsten citrate, 12 tungstophosphoric acid n hydrate, 12 tungstosilicic acid 26 hydrate, molybdenum chloride, 12 molybdophosphoric acid n hydrate, and the like.

The water-soluble polyvalent metal salt compound is particularly preferably at least one selected from water-soluble aluminum compounds, zirconium compounds and titanium compounds.
As the aluminum compound, for example, aluminum chloride or a hydrate thereof, aluminum sulfate or a hydrate thereof, ammonium alum or the like is known as an inorganic salt. Furthermore, there is a basic polyaluminum hydroxide compound which is an inorganic aluminum-containing cationic polymer. In particular, a basic polyaluminum hydroxide compound is preferable.

  The basic polyaluminum hydroxide compound is represented by the following formula 1, 2 or 3, for example, [Al6 (OH) 15] 3+, [Al8 (OH) 20] 4+, [Al13 ( OH) 34] 5+, [Al21 (OH) 60] 3+, and the like, which are water-soluble polyaluminum hydroxides stably containing basic and high-molecular polynuclear condensed ions.

[Al2 (OH) nCl6-n] m Formula 1
[Al (OH) 3] nAlCl3 Formula 2
Aln (OH) mCl (3n-m) 0 <m <3n Formula 3

  These are water treatment agents from Taki Chemical Co., Ltd. under the name of polyaluminum chloride (PAC), from Asada Chemical Co., Ltd. under the name of polyaluminum hydroxide (Paho), and from Riken Green Co., Ltd. It is marketed under the name of Purachem WT and from other manufacturers for the same purpose, and various grades can be easily obtained. In the present invention, these commercially available products can be used as they are, but there are also products having an inappropriately low pH, and in that case, the pH can be appropriately adjusted and used.

The zirconium compound used in the present invention is not particularly limited and various compounds can be used. For example, zirconium acetate, zirconium chloride, zirconium oxychloride, hydroxy zirconium chloride, zirconium nitrate, basic zirconium carbonate, zirconium hydroxide Zirconium carbonate / ammonium, zirconium carbonate / potassium, zirconium sulfate, zirconium fluoride compound and the like.
The titanium compound is not particularly limited, and various compounds can be used. Examples thereof include titanium chloride and titanium sulfate.
Some of these compounds have an inappropriately low pH. In that case, the pH can be appropriately adjusted and used. In the present invention, the term “water-soluble” means that 1% by mass or more dissolves in water at room temperature and normal pressure.

  In the present invention, the content of the water-soluble polyvalent metal salt compound in the ink receiving layer is preferably 0.1 to 10% by mass, and more preferably 1 to 5% by mass with respect to the fine particles.

Although the water-soluble polyvalent metal salt compound can be used alone, it is preferable to use two or more kinds in combination.
Mordant amount contained in the ink receiving layer in the present invention is preferably from ^{0.01g / m 2 ~5g / m 2} , 0.1g / m 2 ~3g / m 2 is more preferable.

(Other ingredients)
The ink jet recording medium of the present invention may further contain various known additives, such as acids, ultraviolet absorbers, antioxidants, fluorescent whitening agents, monomers, polymerization initiators, polymerization inhibitors, and anti-bleeding agents, as necessary. , Antiseptics, viscosity stabilizers, antifoaming agents, surfactants, antistatic agents, matting agents, anti-curling agents, water-proofing agents, and the like.

  In the present invention, the ink receiving layer may contain an acid. By adding an acid, the surface pH of the ink receiving layer is adjusted to 3 to 8, preferably 5 to 7.5. This is preferable because yellowing resistance of the white background portion is improved. The surface pH is measured by the A method (coating method) of the surface PH measurement defined by the Japan Paper Pulp Technology Association (J.TAPPI). For example, the measurement can be performed by using a paper PH measurement set “Type MPC” manufactured by Kyoritsu Riken Co., Ltd. corresponding to the method A.

Specific examples of acids include formic acid, acetic acid, glycolic acid, oxalic acid, propionic acid, malonic acid, succinic acid, adipic acid, maleic acid, malic acid, tartaric acid, citric acid, benzoic acid, phthalic acid, isophthalic acid , Glutaric acid, gluconic acid, lactic acid, aspartic acid, glutamic acid, salicylic acid, salicylic acid metal salts (salts such as Zn, Al, Ca, Mg), methanesulfonic acid, itaconic acid, benzenesulfonic acid, toluenesulfonic acid, trifluoromethanesulfone Acid, styrenesulfonic acid, trifluoroacetic acid, barbituric acid, acrylic acid, methacrylic acid, cinnamic acid, 4-hydroxybenzoic acid, aminobenzoic acid, naphthalenedisulfonic acid, hydroxybenzenesulfonic acid, toluenesulfinic acid, benzenesulfinic acid, Sulfanilic acid, sulfamic acid, α-le Examples include ricinic acid, β-resorcinic acid, γ-resorcinic acid, gallic acid, phloroglicin, sulfosalicylic acid, ascorbic acid, erythorbic acid, bisphenolic acid, hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, polyphosphoric acid, boric acid, boronic acid, etc. It is done. What is necessary is just to determine the addition amount of these acids so that the surface PH of an ink receiving layer may be set to 3-8.
The above acids can be metal salts (eg sodium, potassium, calcium, cesium, zinc, copper, iron, aluminum, zirconium, lanthanum, yttrium, magnesium, strontium, cerium, etc.) or amine salts (eg ammonia, triethylamine, tri Butylamine, piperazine, 2-methylpiperazine, polyallylamine, etc.).

In the present invention, it is preferable that a preservability improving agent such as an ultraviolet absorbent, an antioxidant, or a bleeding inhibitor is contained in the ink receiving layer.
These ultraviolet absorbers, antioxidants and anti-bleeding agents include alkylated phenol compounds (including hindered phenol compounds), alkylthiomethylphenol compounds, hydroquinone compounds, alkylated hydroquinone compounds, tocopherol compounds, thiodiphenyl ether compounds, 2 Compounds having the above thioether bonds, bisphenol compounds, O-, N- and S-benzyl compounds, hydroxybenzyl compounds, triazine compounds, phosphonate compounds, acylaminophenol compounds, ester compounds, amide compounds, ascorbic acid, amine antioxidants Agent, 2- (2-hydroxyphenyl) benzotriazole compound, 2-hydroxybenzophenone compound, acrylate, water-soluble or hydrophobic metal salt, organometallic compound, metal complex, Ndardamine compounds (including TEMPO compounds), 2- (2-hydroxyphenyl) 1,3,5, -triazine compounds, metal deactivators, phosphite compounds, phosphonite compounds, hydroxyamine compounds, nitrone compounds, peroxidation Scavenger, polyamide stabilizer, polyether compound, basic auxiliary stabilizer, nucleating agent, benzofuranone compound, indolinone compound, phosphine compound, polyamine compound, thiourea compound, urea compound, hydrazide compound, amidine compound, sugar compound, hydroxybenzoic acid Acid compounds, dihydroxybenzoic acid compounds, trihydroxybenzoic acid compounds and the like can be mentioned.

  Among these, alkylated phenol compounds, compounds having two or more thioether bonds, bisphenol compounds, ascorbic acid, amine-based antioxidants, water-soluble or hydrophobic metal salts, organometallic compounds, metal complexes, hindered amine compounds, Hydroxyamine compounds, polyamine compounds, thiourea compounds, hydrazide compounds, hydroxybenzoic acid compounds, dihydroxybenzoic acid compounds, trihydroxybenzoic acid compounds and the like are preferable.

  Specific examples of the compound include Japanese Patent Application Nos. 2002-13005, 10-182621, 2001-260519, 4-34953, 4-34513, and 11-170686. No. 4-34512, EP 1138509, JP-A-60-67190, JP-A-7-276808, JP-A-2001-94829, JP-A-47-10537, JP-A-58-111942, JP-A-58-212844. 59-19945, 59-46646, 59-109055, 63-53544, JP 36-10466, 42-26187, 48-30492, 48-31255, 48-41572, 48-54965, 50-10726, U.S. Pat.Nos. 2,719,086, 3, 707,375, 3,754,919, 4,220,711,

  Japanese Patent Publication Nos. 45-4699, 54-5324, European Published Patent Nos. 223739, 309401, 309402, 3105301, 310552, 459416, German Published Patent No. 3435443, Kaisho 54-48535, 60-107384, 60-107383, 60-125470, 60-125471, 60-125472, 60-287485, 60-287486, 60-287487, 60-287488, 61-160287, 61-18854, 61-2111079, 62-146678, 62-146680, 62-146679, 62- No. 282885, No. 62-262047, No. 63-051174, Nos. 63-89877, 63-88380 same issue, same 66-88381 JP, same 63-113536 issue,

  63-163351, 63-203372, 63-224989, 63-251282, 63-267594, 63-182484, JP-A-1-239282, JP-A-2-262654, 2-71262, 3-121449, 4-291865, 4-291684, 5-611166, 5-119449, 5-188687, 5-188686, 5 No. 110490, No. 5-110437, No. 5-170361, No. 48-43295, No. 48-33212, US Pat. Nos. 4,814,262, No. 4,980,275, and the like. .

The other components may be used alone or in combination of two or more. These other components may be added after being water-solubilized, dispersed, polymer-dispersed, emulsified or oil-dropped, or may be encapsulated in microcapsules. In the inkjet recording medium of the present invention, the addition amount of the other components is preferably 0.01 to 10 g / m ² .

  Further, the surface of the inorganic fine particles may be treated with a silane coupling agent for the purpose of improving the dispersibility of the inorganic fine particles. Examples of the silane coupling agent include an organic functional group (for example, vinyl group, amino group (primary to tertiary amino group, quaternary ammonium base), epoxy group, mercapto, in addition to the site for coupling treatment. A group having a group, a chloro group, an alkyl group, a phenyl group, an ester group, or the like).

In the present invention, the ink receiving layer coating solution (coating solution A) preferably contains a surfactant. As the surfactant, any of cationic, anionic, nonionic, amphoteric, fluorine and silicon surfactants can be used.
Examples of the nonionic surfactant include polyoxyalkylene alkyl ethers and polyoxyalkylene alkyl phenyl ethers (for example, diethylene glycol monoethyl ether, diethylene glycol diethyl ether, polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene Ethylene nonylphenyl ether), oxyethylene / oxypropylene block copolymer, sorbitan fatty acid esters (for example, sorbitan monolaurate, sorbitan monooleate, sorbitan trioleate, etc.), polyoxyethylene sorbitan fatty acid esters (for example, polyoxyethylene) Sorbitan monolaurate, polyoxyethylene sorbitan monooleate, polyoxyethylene sorbitan Lyolate, etc.), polyoxyethylene sorbitol fatty acid esters (eg, polyoxyethylene sorbitol tetraoleate), glycerin fatty acid esters (eg, glycerol monooleate), polyoxyethylene glycerin fatty acid esters (polyoxymonostearate) Ethylene glycerol, monooleic acid polyoxyethylene glycerin, etc.), polyoxyethylene fatty acid esters (polyethylene glycol monolaurate, polyethylene glycol monooleate, etc.), polyoxyethylene alkylamine, acetylene glycols (eg, 2, 4, 7) , 9-tetramethyl-5-decyne-4,7-diol, and ethylene oxide adducts, propylene oxide adducts, etc. of the diols). Xylene alkylene alkyl ethers are preferable. The nonionic surfactant can be used in the coating liquid A and the coating liquid B. Moreover, the said nonionic surfactant may be used independently and may use 2 or more types together.

  Examples of the amphoteric surfactants include amino acid type, carboxyammonium betaine type, sulfoammonium betaine type, ammonium sulfate betaine type, imidazolium betaine type, etc., for example, U.S. Pat. No. 3,843,368, Those described in JP-A-59-49535, JP-A-63-236546, JP-A-5-303205, JP-A-8-262742, and JP-A-10-282619 can be suitably used. As the amphoteric surfactant, an amino acid type amphoteric surfactant is preferable, and as the amino acid type amphoteric surfactant, as described in JP-A-5-303205, for example, an amino acid (glycine, glutamic acid, Histidine acid etc.), specifically, N-aminoacyl acid and salts thereof into which a long chain acyl group has been introduced. The amphoteric surfactants may be used alone or in combination of two or more.

Examples of the anionic surfactant include fatty acid salts (for example, sodium stearate, potassium oleate), alkyl sulfate esters (for example, sodium lauryl sulfate, triethanolamine lauryl sulfate), and sulfonates (for example, sodium dodecylbenzenesulfonate). Alkyl sulfosuccinate (for example, sodium dioctyl sulfosuccinate), alkyl diphenyl ether disulfonate, alkyl phosphate, and the like.
Examples of the cationic surfactant include alkylamine salts, quaternary ammonium salts, pyridinium salts, imidazolium salts, and the like.

Examples of the fluorosurfactant include compounds derived from an intermediate having a perfluoroalkyl group using a method such as electrolytic fluorination, telomerization, or oligomerization.
Examples thereof include perfluoroalkyl sulfonates, perfluoroalkyl carboxylates, perfluoroalkyl ethylene oxide adducts, perfluoroalkyl trialkyl ammonium salts, perfluoroalkyl group-containing oligomers, and perfluoroalkyl phosphate esters.

  The silicone surfactant is preferably silicone oil modified with an organic group, which has a structure in which the side chain of the siloxane structure is modified with an organic group, a structure in which both ends are modified, and a structure in which one end is modified. obtain. Examples of the organic group modification include amino modification, polyether modification, epoxy modification, carboxyl modification, carbinol modification, alkyl modification, aralkyl modification, phenol modification, and fluorine modification.

  In the present invention, the content of the surfactant is preferably 0.001 to 2.0%, and more preferably 0.01 to 1.0% with respect to the ink receiving layer coating liquid (coating liquid A). Further, when coating is performed using two or more liquids as the ink receiving layer coating liquid, it is preferable to add a surfactant to each coating liquid.

In the present invention, the ink receiving layer preferably contains a high boiling point organic solvent for curling prevention. The high-boiling organic solvent is an organic compound having a boiling point of 150 ° C. or higher at normal pressure, and is a water-soluble or hydrophobic compound. These may be liquid or solid at room temperature, and may be low molecules or polymers.
Specifically, aromatic carboxylic acid esters (for example, dibutyl phthalate, diphenyl phthalate, phenyl benzoate, etc.), aliphatic carboxylic acid esters (for example, dioctyl adipate, dibutyl sebacate, methyl stearate, dibutyl maleate) , Dibutyl fumarate, triethyl acetyl citrate, etc.), phosphate esters (eg, trioctyl phosphate, tricresyl phosphate, etc.), epoxies (eg, epoxidized soybean oil, epoxidized fatty acid methyl, etc.), alcohols (eg, stearyl) Alcohol, ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, glycerol, diethylene glycol monobutyl ether (DEGMBE), triethylene glycol monobutyl ether, glycerol Methyl ether, 1,2,3-butanetriol, 1,2,4-butanetriol, 1,2,4-pentanetriol, 1,2,6-hexanetriol, thiodiglycol, triethanolamine, polyethylene glycol, etc. ), Vegetable oils (eg, soybean oil, sunflower oil, etc.) and higher aliphatic carboxylic acids (eg, linoleic acid, oleic acid, etc.).

(Support)
As the support 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. In order to make use of the transparency of the ink receiving layer, it is preferable to use a transparent support or a highly glossy opaque support.

The material that can be used for the transparent support is preferably a material that is transparent and can withstand radiant heat when used in an OHP or a backlight display. Examples of the material include polyesters such as polyethylene terephthalate (PET); polysulfone, polyphenylene oxide, polyimide, polycarbonate, polyamide and the like. Of these, polyesters are preferable, and polyethylene terephthalate is particularly preferable.
Although there is no restriction | limiting in particular as thickness of the said transparent support body, 50-200 micrometers is preferable at the point which is easy to handle.

  As the highly glossy opaque support, one having a glossiness of 40% or more on the surface on which the ink receiving layer is provided is preferable. The glossiness is a value determined according to the method described in JIS P-8142 (75-degree specular gloss test method for paper and paperboard). Specifically, the following supports are mentioned.

For example, high gloss paper support such as art paper, coated paper, cast coated paper, baryta paper used for silver salt photographic support, etc .; polyesters such as polyethylene terephthalate (PET), nitrocellulose, cellulose acetate , Cellulose esters such as cellulose acetate butyrate, and plastic films such as polysulfone, polyphenylene oxide, polyimide, polycarbonate, and polyamide are made opaque by adding a white pigment or the like (surface calendering may be applied). Glossy film; or a support in which a polyolefin coating layer containing or not containing a white pigment is provided on the surface of a highly glossy film containing the various paper supports, the transparent support or the white pigment. Etc.
A white pigment-containing foamed polyester film (for example, foamed PET containing polyolefin fine particles and forming voids by stretching) can also be suitably exemplified. Furthermore, resin-coated paper used for silver salt photographic printing paper is also suitable.

  Although there is no restriction | limiting in particular also about the thickness of the said opaque support body, 50-300 micrometers is preferable at the point of handleability.

  The surface of the support may be subjected to corona discharge treatment, glow discharge treatment, flame treatment, ultraviolet irradiation treatment or the like in order to improve wettability and adhesion.

Next, the base paper used for the resin-coated paper will be described in detail.
The base paper is made from wood pulp as a main raw material and, if necessary, paper using synthetic pulp such as polypropylene or synthetic fibers such as nylon or polyester in addition to wood pulp. As the above-mentioned wood pulp, any of LBKP, LBSP, NBKP, NBSP, LDP, NDP, LUKP, NUKP can be used, but more LBKP, NBSP, LBSP, NDP, LDP with more short fibers are used. preferable.
However, the ratio of LBSP and / or LDP is preferably 10% by mass or more and 70% by mass or less.

  The pulp is preferably a chemical pulp (sulfate pulp or sulfite pulp) with few impurities, and a pulp having a whiteness improved by bleaching is also useful.

  In the base paper, sizing agents such as higher fatty acids and alkyl ketene dimers, white pigments such as calcium carbonate, talc and titanium oxide, paper strength enhancing agents such as starch, polyacrylamide and polyvinyl alcohol, fluorescent whitening agents, polyethylene glycols A water retaining agent such as a dispersant, a softening agent such as a quaternary ammonium, and the like can be appropriately added.

  The freeness of the pulp used for papermaking is preferably 200 to 500 ml as defined by CSF, and the fiber length after beating is a 24 mesh residual mass% and a 42 mesh residual as defined in JIS P-8207. 30 to 70% of the sum with the mass% of is preferable. In addition, it is preferable that the mass% of 4 mesh remainder is 20 mass% or less.

The basis weight of the base paper is preferably 30 to 250 g, and particularly preferably 50 to 200 g. The thickness of the base paper is preferably 40 to 250 μm. The base paper can be given a high smoothness by calendering at the paper making stage or after paper making. The density of the base paper is generally 0.7 to 1.2 g / m ² (JIS P-8118).
Furthermore, the base paper stiffness is preferably 20 to 200 g under the conditions specified in JIS P-8143.

A surface sizing agent may be applied to the surface of the base paper. As the surface sizing agent, a sizing agent similar to the size that can be added to the base paper can be used.
The pH of the base paper is preferably 5 to 9 when measured by a hot water extraction method defined in JIS P-8113.

  The polyethylene covering the front and back surfaces of the base paper is mainly low-density polyethylene (LDPE) and / or high-density polyethylene (HDPE), but some other LLDPE, polypropylene, etc. can also be used.

  In particular, the polyethylene layer on the side that forms the ink receiving layer is added with rutile or anatase type titanium oxide, fluorescent whitening agent, ultramarine, and polyethylene, as is widely done in photographic paper. Those having improved whiteness and hue are preferred. Here, as a titanium oxide content, about 3-20 mass% is preferable with respect to polyethylene, and 4-13 mass% is more preferable. Although the thickness of a polyethylene layer does not have limitation in particular, 10-50 micrometers is suitable for both front and back layers. Further, an undercoat layer can be provided on the polyethylene layer in order to provide adhesion to the ink receiving layer. As the undercoat layer, aqueous polyester, gelatin and PVA are preferable. Moreover, as thickness of this undercoat layer, 0.01-5 micrometers is preferable.

  Polyethylene-coated paper can be used as glossy paper, or when it is melt-extruded onto the surface of the base paper and coated, the matte surface or silky surface that can be obtained with ordinary photographic printing paper by so-called molding Can also be used.

A back coat layer can be provided on the support, and examples of components that can be added to the back coat layer include a white pigment, an aqueous binder, and other components.
Examples of white pigments contained in the backcoat layer include light calcium carbonate, heavy calcium carbonate, kaolin, talc, calcium sulfate, barium sulfate, titanium dioxide, zinc oxide, zinc sulfide, zinc carbonate, satin white, and aluminum silicate. , Diatomaceous earth, calcium silicate, magnesium silicate, synthetic amorphous silica, colloidal silica, colloidal alumina, pseudoboehmite, aluminum hydroxide, alumina, lithopone, zeolite, hydrous halloysite, magnesium carbonate, magnesium hydroxide, white inorganic pigment, styrene And organic pigments such as polyethylene plastic pigments, acrylic plastic pigments, polyethylene, microcapsules, urea resins, and melamine resins.

Examples of the aqueous binder used in the backcoat layer include styrene / maleate copolymer, styrene / acrylate copolymer, polyvinyl alcohol, silanol-modified polyvinyl alcohol, starch, cationized starch, casein, gelatin, carboxy Examples thereof include water-soluble polymers such as methyl cellulose, hydroxyethyl cellulose, and polyvinyl pyrrolidone, and water-dispersible polymers such as styrene butadiene latex and acrylic emulsion.
Examples of other components contained in the backcoat layer include an antifoaming agent, an antifoaming agent, a dye, a fluorescent brightening agent, a preservative, and a water-proofing agent.

(Preparation of inkjet recording medium)
The ink receiving layer of the ink jet recording medium of the present invention is formed, for example, by applying a coating liquid A containing at least fine particles and a water-soluble resin on the surface of a support, and (1) simultaneously with the coating and (2) the coating. By applying the coating solution B having a pH of 8 or more to the coating layer during drying of the coating layer and before the coating layer exhibits a decreasing drying rate, and then crosslinking and curing the coating layer to which the coating solution B has been applied. Preferably it is formed. Here, the cationic resin having a unit represented by the general formula (1) may be contained in at least one of the coating liquid A or the coating liquid B.
Further, a crosslinking agent capable of crosslinking the water-soluble resin may be contained in at least one of the coating liquid A and the coating liquid B.
Providing an ink receiving layer that has been crosslinked and cured in this manner is preferable from the viewpoints of ink absorptivity and prevention of film cracking.

  In the above manner, since a large amount of mordant is present in a predetermined portion of the ink receiving layer, the ink-jet coloring material is sufficiently mordanted, color density, aging blur, gloss of the printed part, and water resistance of characters and images after printing. This is preferable because ozone resistance is improved. Part of the mordant may be contained in the layer initially provided on the support, and in that case, the mordant to be applied later may be the same or different.

In the present invention, an ink-receiving layer coating solution (coating solution A) containing at least fine particles (for example, vapor-phase process silica) and a water-soluble resin (for example, polyvinyl alcohol) is prepared, for example, as follows. be able to. That is,
Fine particles such as vapor phase silica and a dispersant (a cationic resin having a unit represented by the general formula (1) may be used) are added to water (for example, 10 to 20 mass of silica fine particles in water is used). %) Using a high-speed rotating wet colloid mill (for example, “CLEARMIX” manufactured by M Technique Co., Ltd.), for example, under a high-speed rotation condition of 10,000 rpm (preferably 5000 to 20000 rpm), for example for 20 minutes (preferably 10 After dispersion over ~ 30 minutes, an aqueous polyvinyl alcohol (PVA) solution (for example, PVA having a mass of about 1/3 of the vapor phase silica) is added, and dispersion is performed under the same rotational conditions as above. It can be prepared by performing. In order to impart stability to the coating solution, it is preferable to adjust the pH to about 9.2 with aqueous ammonia or the like, or to use a dispersant. The obtained coating liquid is in a uniform sol state, and a porous ink-receiving layer having a three-dimensional network structure can be formed by coating this on a support by the following coating method and drying it.

In addition, the preparation of the aqueous dispersion composed of the above-mentioned vapor phase method silica and a dispersant may be carried out by preparing a vapor phase method silica aqueous dispersion in advance and adding the aqueous dispersion to the aqueous dispersant solution. The aqueous solution may be added to the vapor phase silica aqueous dispersion, or may be mixed simultaneously. Further, instead of vapor phase silica aqueous dispersion, powder vapor phase silica may be used and added to the aqueous dispersant as described above.
After mixing said vapor phase silica and a dispersing agent, the mixed liquid is refined using a disperser, whereby an aqueous dispersion having an average particle diameter of 50 to 300 nm can be obtained. As a disperser used for obtaining the aqueous dispersion, various types of conventionally known dispersers such as a high-speed rotary disperser, a medium agitating disperser (ball mill, sand mill, etc.), an ultrasonic disperser, a colloid mill disperser, and a high pressure disperser. Although a disperser can be used, a medium agitation disperser, a colloid mill disperser, or a high pressure disperser is preferable from the viewpoint of efficiently dispersing the formed fine particles.

  Moreover, water, an organic solvent, or these mixed solvents can be used as a solvent in each process. Examples of the organic solvent that can be used for this 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.

Further, a dispersant may be added to improve the dispersibility of the coating solution. As the dispersant, the aforementioned chaotic polymer is preferably used.
The amount of the dispersant added to the fine particles is preferably 0.1% to 30%, more preferably 1% to 10%.

  The ink receiving layer coating liquid is applied by a known coating method such as, for example, an extrusion die coater, an air doctor coater, a bread coater, a rod coater, a knife coater, a squeeze coater, a reverse roll coater, or a bar coater. it can.

  The coating liquid B is applied to the coating layer at the same time as or after the coating of the ink receiving layer coating liquid (coating liquid A), and the coating layer after coating has a reduced drying rate. It may be given before it becomes shown. That is, after the application of the ink receiving layer coating liquid (coating liquid A), the coating liquid B is preferably introduced while the coating layer exhibits a constant rate of drying. The coating liquid B may contain a mordant.

  Here, “before the coating layer comes to exhibit a decreasing rate of drying” usually refers to a process of several minutes immediately after the coating of the coating liquid for the ink-receiving layer. This shows the phenomenon of “constant rate drying rate” in which the content of the solvent (dispersion medium) in the medium decreases in proportion to time. About the time which shows this "constant rate drying speed", it describes in chemical engineering handbook (pages 707-712, Maruzen Co., Ltd. issue, October 25, 1980), for example.

  As described above, after the coating solution A is applied, the coating layer is dried until the coating layer exhibits a reduced rate of drying. This drying is generally performed at 40 to 180 ° C. for 0.5 to 10 minutes (preferably, 0 .5-5 minutes). The drying time naturally varies depending on the coating amount, but the above range is usually appropriate.

  As a method of giving before the said 1st application layer comes to show a decreasing rate drying rate, (1) The method of further apply | coating the coating liquid B on an application layer, (2) Spraying by methods, such as spraying. And (3) a method of immersing the support on which the coating layer is formed in the coating solution B, and the like.

  In the method (1), examples of the coating method for coating the coating liquid B include a curtain flow coater, an extrusion die coater, an air doctor coater, a bread coater, a rod coater, a knife coater, a squeeze coater, a reverse roll coater, and a bar. A known coating method such as a coater can be used. However, it is preferable to use a method in which the coater does not directly contact the already formed first coating layer, such as an extrusion die coater, a curtain flow coater, a bar coater or the like.

  After application of coating liquid B, it is generally heated at 40 to 180 ° C. for 0.5 to 30 minutes, and dried and cured. Especially, it is preferable to heat at 40-150 degreeC for 1 to 20 minutes.

  When the coating liquid B is applied simultaneously with the application of the ink receiving layer coating liquid (coating liquid A), the coating liquid A and the coating liquid B are placed on the support so that the coating liquid A is in contact with the support. The ink receiving layer can be formed by simultaneously coating (multilayer coating) and then drying and curing.

  The simultaneous coating (multilayer coating) can be performed by a coating method using, for example, an extrusion die coater or a curtain flow coater. After the simultaneous coating, the formed coating layer is dried. In this case, the drying is generally performed by heating the coating layer at 40 to 150 ° C. for 0.5 to 10 minutes, preferably 40 to 100. It is carried out by heating at a temperature of 0.5 to 5 minutes.

  When the above simultaneous coating (multilayer coating) is performed by, for example, an extrusion die coater, the two types of coating liquid discharged at the same time are close to the discharge port of the extrusion die coater, that is, before moving onto the support. A multilayer is formed, and in that state, it is coated on the support. Since the two-layer coating liquid that has been layered before coating is likely to cause a crosslinking reaction at the interface between the two liquids when transferred to the support, the two liquids to be discharged are mixed in the vicinity of the discharge port of the extrusion die coater. As a result, thickening is likely to occur, which may hinder the application operation. Therefore, when applying simultaneously as described above, it is preferable to apply the coating solution A and the coating solution B together with the barrier layer solution (intermediate layer solution) interposed between the two solutions.

  The barrier layer solution can be selected without particular limitation. For example, an aqueous solution containing a trace amount of water-soluble resin, water, and the like can be given. The water-soluble resin is used in consideration of applicability for the purpose of a thickener and the like. For example, a cellulose resin (for example, hydroxypropylmethylcellulose, methylcellulose, hydroxyethylmethylcellulose) And polymers such as polyvinylpyrrolidone and gelatin. The barrier layer solution may contain the above mordant.

  After forming the ink receiving layer on the support, surface smoothness, glossiness, transparency and coating strength are obtained by applying a calender treatment through the roll nip under heat and pressure using, for example, super calender, gloss calender, etc. It is possible to improve. However, the calendar process may cause a decrease in the porosity (that is, the ink absorptivity may be decreased), so it is necessary to set conditions under which the decrease in the porosity is small.

As roll temperature in the case of performing a calendar process, 30-150 degreeC is preferable and 40-100 degreeC is more preferable.
Moreover, as a linear pressure between rolls at the time of a calendar process, 50-400 kg / cm is preferable and 100-200 kg / cm is more preferable.

In the case of ink jet recording, the thickness of the ink receiving layer needs to have an absorption capacity sufficient to absorb all of the droplets, and therefore needs to be determined in relation to the porosity in the layer. For example, if the ink amount is 8 nL / mm ² and the porosity is 60%, a film having a layer thickness of about 15 μm or more is required.
Considering this point, in the case of ink jet recording, the layer thickness of the ink receiving layer is preferably 10 to 50 μm.

Further, the pore diameter of the ink receiving layer is preferably 0.005 to 0.030 μm, more preferably 0.01 to 0.025 μm in terms of median diameter.
The porosity and pore median diameter can be measured using a mercury porosimeter (trade name “Bore Sizer 9320-PC2” manufactured by Shimadzu Corporation).

In addition, the ink receiving layer is preferably excellent in transparency, as a guide, the haze value when the ink receiving layer is formed on a transparent film support is preferably 30% or less, More preferably, it is 20% or less.
The haze value can be measured using a haze meter (HGM-2DP: Suga Test Instruments Co., Ltd.).

A polymer fine particle dispersion may be added to a constituent layer (for example, an ink receiving layer or a back layer) of the ink jet recording medium of the present invention. This polymer fine particle dispersion is used for the purpose of improving film properties such as dimensional stabilization, curling prevention, adhesion prevention, and film cracking prevention. The polymer fine particle dispersion is described in JP-A Nos. 62-245258, 62-1316648, and 62-110066. If a polymer fine particle dispersion having a low glass transition temperature (40 ° C. or lower) is added to the layer containing the mordant, cracking and curling of the layer can be prevented. Further, even when a polymer fine particle dispersion having a high glass transition temperature is added to the back layer, curling can be prevented.
The ink jet recording medium of the present invention is disclosed in JP-A-10-81064,
10-119423, 10-157277, 10-217601, 11-348409, JP-A-2001-138621, 2000-43401, 2000-212235, 2000-309157, Also produced by the methods described in JP-A Nos. 2001-96897, 2001-138627, JP-A Nos. 11-91242, 8-2087, 8-2090, 8-2091, and 8-2093. Is possible.

  In the present invention, the support for the ink jet recording medium can be either a transparent support made of a transparent material such as plastic or an opaque support made of an opaque material such as paper. In particular, in order to take advantage of the transparency of the ink receiving layer, it is preferable to use a transparent support or a highly glossy opaque support. Further, a read-only optical disk such as a CD-ROM or DVD-ROM, a write-once optical disk such as a CD-R or DVD-R, or a rewritable optical disk can be used as a support, and an ink receiving layer can be provided on both sides of the label. .

[Synthesis Example 1]
24.8 parts of (3-acrylamidopropyl) trimethylammonium chloride and 12.5 parts of styrene (I / O value = 0.11) are dissolved in 86 parts of ethanol. This was heated to 70 ° C. under a nitrogen stream, 0.133 parts of 2,2′-azobis (2-amidinopropane) dihydrochloride (V-50, manufactured by Wako Pure Chemical Industries, Ltd.) was added, and 70 ° C. And stirred with heating. After 2 hours, 0.133 part of 2,2′-azobis (2-amidinopropane) dihydrochloride [V-50, manufactured by Wako Pure Chemical Industries, Ltd.] was further added, and the mixture was heated and stirred at 70 ° C. for 4 hours.
The reaction solution was poured into 2000 parts of acetone while stirring, and the resulting viscous solid was dried to obtain 32.6 parts of a white solid of the polymer 1 (I / O value = 1.81) according to the present invention.

[Synthesis Example 2]
15.6 parts of N- (3-dimethylaminopropyl) acrylamide is dissolved in 30 parts of ethanol, and 12.8 parts of benzyl chloride are added dropwise while maintaining the temperature at 25 ° C. After stirring at 40 ° C. for 2 hours, 10.4 parts of styrene was added and heated to 70 ° C. under a nitrogen stream, and 2,2′-azobis (2-amidinopropane) dihydrochloride [V-50, Wako Pure Chemical ( Co., Ltd.] was added, and the mixture was heated and stirred at 70 ° C. Two hours later, 0.054 parts of 2,2′-azobis (2-amidinopropane) dihydrochloride [V-50, manufactured by Wako Pure Chemical Industries, Ltd.] was further added, and the mixture was heated and stirred at 70 ° C. for 4 hours.
The reaction solution was poured into 2000 parts of acetone while stirring, and the resulting viscous solid was dried to obtain 32.6 parts of a white solid of the polymer 2 (I / O value = 1.37) according to the present invention.

[Synthesis Example 3]
23.3 parts of 2-methacryloyloxyethyl isocyanate is dissolved in 75 parts of acetonitrile, and 14.1 parts of N, N-dimethylethylenediamine is added dropwise while maintaining the temperature at 5 ° C. After 1 hour, the reaction solution is concentrated with an evaporator and dissolved in 75 parts of ethanol. While maintaining this solution at 25 ° C., 18.9 parts of benzyl chloride was added dropwise, and the mixture was heated and stirred at 60 ° C. for 3 hours to obtain a cationic monomer having a urea bond.
22.2 parts of the obtained cationic monomer and 6.25 parts of styrene were dissolved in 66 parts of ethanol, heated to 70 ° C. under a nitrogen stream, and 2,2′-azobis (2-amidinopropane) dihydrochloride [ 0.067 part of V-50, manufactured by Wako Pure Chemical Industries, Ltd.] was added, and the mixture was heated and stirred at 70 ° C. Two hours later, 0.067 parts of 2,2′-azobis (2-amidinopropane) dihydrochloride [V-50, manufactured by Wako Pure Chemical Industries, Ltd.] was further added, and the mixture was heated and stirred at 70 ° C. for 4 hours.
The reaction solution was poured into 2000 parts of acetone while stirring, and the resulting viscous solid was dried to obtain 21.4 parts of a white solid of the polymer 3 (I / O value = 1.37) according to the present invention.

[Synthesis Example 4]
Polymer 4 according to the present invention (I / O value = 1.37) in the same manner as in Synthesis Example 2 except that 1.96 parts of 3-mercaptopropyltrimethoxysilane was further added to the raw material composition of Synthesis Example 2. An ethanol solution of was obtained.

[Synthesis Example 5]
Polymer 5 (I / O) for Comparative Example was used in the same manner as in Synthesis Example 1 except that 12.5 parts of styrene in Synthesis Example 1 was changed to 12.0 parts of methyl methacrylate (I / O value = 0.62). Value = 2.36).

[Synthesis Example 6]
A polymer 6 for comparative example (I / O value = 3.04) was obtained in the same manner as in Synthesis Example 1 except that 12.5 parts of styrene in Synthesis Example 1 were changed to 1.39 parts.

[Synthesis Example 7]
A polymer for a comparative example in the same manner as in Synthesis Example 1 except that 24.8 parts of (3-acrylamidopropyl) trimethylammonium chloride in Synthesis Example 1 were changed to 24.9 parts of (2-methacryloyloxyethyl) trimethylammonium chloride. 7 (I / O value = 1.40) was obtained.

  EXAMPLES Hereinafter, although an Example demonstrates this invention concretely, this invention is not limited to these Examples. In the examples, “parts” and “%” represent “parts by mass” and “mass%” unless otherwise specified, and “average molecular weight” and “degree of polymerization” are “weight average molecular weight” and “weight”. It represents “average degree of polymerization”.

(Production of support)
Wood pulp composed of 100 parts of LBKP is beaten to 300 ml Canadian freeness with a double disc refiner, 0.5 parts of epoxidized behenamide, 1.0 part of anionic polyacrylamide, 0.1 part of polyamide polyamine epichlorohydrin, 0.5 part of cationic polyacrylamide All the parts were added at an absolutely dry mass ratio to the pulp, and weighed with a long net paper machine to make a base paper of 170 g / m2.

In order to adjust the surface size of the base paper, 0.04% of a fluorescent whitening agent (“Whiteex BB” manufactured by Sumitomo Chemical Co., Ltd.) is added to a 4% aqueous solution of polyvinyl alcohol, and this is 0 in terms of absolute dry mass. The base paper was impregnated so as to have a density of 0.5 g / m ² , dried, and then subjected to a calendering process to obtain a base paper adjusted to a density of 1.05 g / cc.

After the corona discharge treatment was performed on the wire surface (back surface) side of the obtained base paper, high-density polyethylene was coated to a thickness of 19 μm using a melt extruder to form a resin layer composed of a mat surface. (Hereinafter, the resin layer surface is referred to as “back surface”). The resin layer on the back side is further subjected to corona discharge treatment, and thereafter, as an antistatic agent, aluminum oxide (“Alumina sol 100” manufactured by Nissan Chemical Industries, Ltd.) and silicon dioxide (“Nissan Chemical Industry Co., Ltd.” “ Snowtex O ") and a 1: a dispersion dispersed in water at 2 weight ratio, dry mass was coated to a 0.2 g / m ^2.

  Furthermore, after the corona discharge treatment is applied to the felt surface (surface) side where the resin layer is not provided, anatase-type titanium dioxide 10%, a trace amount of ultramarine blue, and a fluorescent whitening agent 0.01% (vs. polyethylene) A low-density polyethylene containing MFR (melt flow rate) 3.8 is extruded using a melt extruder to a thickness of 29 μm, and a high gloss thermoplastic resin layer is formed on the surface side of the base paper. (Hereinafter, this high-gloss surface is referred to as a “front side”), which was used as a support.

[ Reference Example 1]
(Preparation of coating liquid A for ink receiving layer)
(1) Gas phase method silica fine particles, (2) ion-exchanged water, and (3) polymer 1 in the following composition were mixed and dispersed using KD-P (manufactured by Shinmaru Enterprises Co., Ltd.). Thereafter, a solution containing the following (4) zirconyl acetate, (5) boric acid water, (6) polyvinyl alcohol, (7) surfactant, and (8) ion-exchanged water is added to prepare a coating liquid A for ink receiving layer. did.
The mass ratio between the silica fine particles and the water-soluble resin (PB ratio = (1) :( 6)) is 4.5: 1, and the pH of the coating liquid A for the ink receiving layer is 3.8, indicating acidity. It was.

<Composition of ink receiving layer coating liquid A>
(1) Gas phase method silica fine particles (inorganic fine particles) 10.0 parts (“Leosil QS-30” manufactured by Tokuyama Corporation, average primary particle size 7 nm)
(2) Ion-exchanged water 51.6 parts (3) Polymer 1 (25% aqueous solution) 2.0 parts (4) Zirconyl acetate (25% aqueous solution) 0.3 part (5) Borate water (5% aqueous solution, (Crosslinking agent) 8.0 parts (6) polyvinyl alcohol (8% aqueous solution, water-soluble resin) 27.8 parts ("PVA235" manufactured by Kuraray Co., Ltd., saponification degree 88%, polymerization degree 3500)
(7) Surfactant ("Emulgen 109P" (10% aqueous solution) manufactured by Kao Corporation, HLB value 13.6) 0.1 part (8) 24.6 parts ion-exchanged water

(Preparation of inkjet recording medium)
After the corona discharge treatment is applied to the front surface of the support, the coating liquid A for the ink receiving layer obtained above is applied to the front surface of the support at an application amount of 200 ml / m ² using an extrusion die coater. (Applying step), and dried with a hot air dryer at 80 ° C. (wind speed of 3 to 8 m / sec) until the solid content concentration of the coating layer reached 20%. This coating layer exhibited a constant rate of drying during this period. Immediately thereafter, it was immersed in coating solution B having the following composition for 30 seconds to deposit 20 g / m ² on the coating layer, and further dried at 80 ° C. for 10 minutes (drying step). Thus, an inkjet recording medium (1) of the present invention provided with an ink receiving layer having a dry film thickness of 32 μm was produced.

<Composition of coating liquid B>
(1) Boric acid (crosslinking agent) 0.65 parts (2) Ammonium zirconium carbonate 6.5 parts ("Zircozol AC-7" manufactured by Daiichi Rare Element Chemical Co., Ltd., 28% aqueous solution)
(3) Ammonium carbonate 6.0 parts (4) Ion exchange water 83.8 parts (5) Surfactant (Megafac F-1405, manufactured by Dainippon Ink & Chemicals, Inc.) 0.2 part

[Reference Example 2, Example 1, Reference Example 3]
Inkjet recording medium Similarly invention all Reference Example 1 except that the polymer 1 was changed respectively to each polymer 2,3,4 in <Composition of ink receiving layer coating solution A> Reference Example 1 (2 ) To (4) were produced.

[ Reference Example 4, Reference Example 5, Example 2, Reference Example 6 ]
In Reference Example 1, Reference Example 2, Example 1 and Reference Example 3 <Composition of Coating Solution A>, polyaluminum chloride (40% aqueous solution, basic structural formula: Al ₂ (OH) ₅ Cl) 0.6 part The inkjet recording media (5) to (8) of the present invention were obtained in the same manner except that was added.

[Comparative Examples 1-4 ]
Reference All of Reference Example 1 Polymer 1 in <Composition of ink receiving layer coating solution A> was changed to each polymer 5-7, or "SHALLOL DC-902P" (manufactured by Nitto Boseki Co.) Example Comparative inkjet recording media (9) to (12) were prepared in the same manner as in Example 1.

(Evaluation test)
The following evaluation tests were conducted on each of the inkjet recording media (1) to (8) of the present invention obtained above and the comparative inkjet recording media (9) to ( 12 ). The test results are shown in Table 1 below.

<Ink absorbability>
Using an inkjet printer (“PM-970C” manufactured by Seiko Epson Corporation), Y (yellow), M (magenta), C (cyan), K (black), B ( A solid image of blue, G (green), and R (red) is printed, and immediately after that (about 10 seconds later), the paper is pressed against the image to visually transfer the ink onto the paper. Observed and evaluated according to the following criteria: If the transfer of ink onto paper is not observed, the ink absorption rate is good.
A case where no transfer of ink onto the paper was observed was evaluated as A, a case where transfer of the ink was partially recognized was evaluated as B, and a case where transfer of the ink was recognized considerably and there was no practical applicability was evaluated as C.

<Print density>
Using an inkjet printer (“PM-970C” manufactured by Seiko Epson Corporation), a black solid image is printed on each inkjet recording medium, and after left for 3 hours, the reflection density of the printed surface is measured by a reflection density meter. ("Xrite 938" manufactured by Xrite). The case where the reflection density was 2.3 or higher was evaluated as A, the case of 2.0 to 2.3 was evaluated as B, and the case of less than 2.0 was evaluated as C.

<Water resistance>
Using an inkjet printer ("PM-970C" manufactured by Seiko Epson Corporation), Y (yellow), M (magenta), C (cyan), K (black), B (blue) on each inkjet recording medium , G (green), and R (red) solid images were printed, allowed to stand for 3 hours, then immersed in water for 1 hour, and the degree of ink outflow into water was visually evaluated. The case where no dye run-out was observed was evaluated as A, the portion where the dye flowed out was observed and the color density was lowered, B, and the case where the dye flowed almost completely into the water was evaluated as C.

<Burning over time>
Using an inkjet printer (“PM-970C” manufactured by Seiko Epson Corporation), a grid-like linear pattern (line width 0.28 nm) in which magenta ink and black ink are adjacent to each other on each inkjet recording medium. After printing, the visual density (ODfresh) was measured with X-Light 310TR (manufactured by X-Light Co., Ltd.) After the measurement, each printed inkjet recording medium was put in a clear file and placed in a constant temperature and humidity chamber at 35 ° C. and a relative humidity of 80%. After storage for 3 days, the visual density (ODthermo) was measured again and the density change rate ((ODthermo-ODfresh) / ODfresh × 100) was calculated. B, 30-45% was evaluated as C, and 45% or more was evaluated as D. The smaller the density change rate, the less aging blurring (good). It is.

<Ozone resistance>
Using an inkjet printer (“PM-G800” manufactured by Seiko Epson Corporation), a solid cyan image was printed on each inkjet recording sheet, and stored for 40 hours in an environment with an ozone concentration of 10.0 ppm. The magenta and cyan densities before and after storage were measured with a reflection densitometer (“Xrite 938” manufactured by Xrite), and the residual ratio of the cyan density was calculated.
The case where the residual ratio was 80% or more was evaluated as A, the case of 70 to less than 80% as B, the case of 60 to less than 80% as C, and the case of less than 60% as D.
An evaluation result is shown.

  From the results shown in Table 1, the ink jet recording media of the examples of the present invention have performances equivalent to or better than those of the comparative examples with respect to the ink absorbability and the image density, and the water resistance, aging blur, and ozone resistance are comparative examples. Shows that it is better than

Claims (6)

An ink jet recording medium having an ink receiving layer on a support, wherein the ink receiving layer contains at least a cationic resin represented by the following general formula (1).

In the general formula (1), R represents a hydrogen atom or a methyl group, and R ₁ and R ₂ each independently represents an alkylene group. R _{3 to} R ₅ each independently represents a hydrogen atom, an alkyl group, an aralkyl group, or an aryl group. Q is at least one unit given from a monomer having an ethylenic double bond, and the inorganic / organic ratio (I / O value) of the organic conceptual diagram is less than 0.5. Z represents an amide bond, a urethane bond, or a urea bond, and X ⁻ represents an anion. p is 20 to 80 mol%, and q is 20 to 80 mol%. r is 0 or 1;   The inkjet recording medium according to claim 1, wherein the cationic resin represented by the formula (1) has an I / O value of 2.3 or less.   The inkjet recording medium according to claim 1 or 2, wherein the cationic resin represented by the formula (1) is a polymer further having an alkoxysilyl group at a molecular chain terminal. The ink jet recording medium according to any one of claims 1 to 3, wherein the ink receiving layer contains at least one of silica fine particles, colloidal silica, alumina fine particles, and pseudoboehmite.   The ink jet recording medium according to claim 1, wherein the ink receiving layer contains a polyvalent metal salt.   The ink receiving layer is a layer obtained by crosslinking and curing a coating layer coated with a coating solution containing at least fine particles, a water-soluble resin, and a cationic resin represented by the formula (1). The inkjet recording medium according to any one of claims 1 to 5.