JP2005225151A - Inkjet recording medium - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an inkjet recording medium which brings about the good quality of inkjet recording and a good feeling of gloss in the use of a rewetting method. <P>SOLUTION: In this inkjet recording medium, at least one ink absorbing layer is provided on a substrate; a gloss developing layer is provided on the surface of the ink absorbing layer; and after that, the gloss is imparted by the rewetting and cast-coating method. The gloss developing layer is mainly composed of a binding agent and flocculated colloidal silica wherein two or three spheroidal primary particles are flocculated. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to an ink jet recording medium used in an ink jet recording method, and more particularly to an ink jet recording medium provided with a surface gloss by a so-called rewet cast coating method.

  2. Description of the Related Art In recent years, as a recording medium used for ink jet recording in which technological progress is remarkable, a plain paper type and a coated paper type have been developed. This coated paper type inkjet recording medium has a type (so-called absorption type) in which the ink is absorbed by the porous pigment in the coating layer and the ink in the coating layer is swelled by the ink solvent to fix the ink. Type (so-called swelling type).

  In particular, when a high-quality image comparable to a silver salt photograph is to be reproduced, the ink discharge amount of the printer increases, so that the above-described absorption recording medium is mainly used. In the case of the absorption type, an ink receiving layer containing a porous pigment such as silica or alumina and a binder is provided on the surface of a support such as paper, and ink droplets are fixed on the ink receiving layer. .

  Further, in order to obtain an image comparable to a silver salt photograph, it is necessary to impart high gloss to the surface of the ink jet recording medium, but a cast coat method using a cast coater is common from the viewpoint of manufacturing cost. In the cast coating method, a coating liquid mainly composed of a pigment and a binder is applied onto a base paper to provide a coating layer that serves as an ink-receiving layer, and the wet coating layer is cast on a cast drum (mirror finish). Is a method of pressing and gloss finishing (see, for example, Patent Documents 1 to 3 and Non-Patent Document 1).

  The cast coating method further includes (1) a wet casting method (direct method) in which a coating layer is pressed onto a mirror-finished heating drum while the coating layer is in a wet state, and then dried (2). (Semi-) Rewetting cast method (rewetting method) in which it is swelled and plasticized with a rewetting liquid after drying, and pressed onto a mirror-finished heated drum (drying method). (3) The wet coating layer is made into a gel state by coagulation treatment. In general, it can be divided into three types: a gelled cast method (coagulation method) in which a heated mirror drum is pressed and dried. Each method is based on the same principle as described above, but is actually treated as a different technique.

  In other words, the direct method and the solidification method press-dry on the mirror drum while the coating layer is in a wet state, which increases the drying load on the mirror drum, but there is a limit to improving the drying capability of the mirror drum. , Forced to operate at low speed. On the other hand, in the rewetting method, the coating layer after drying is rewet with the rewetting liquid and then brought into pressure contact with the mirror drum, so that the drying itself can be performed in the previous step, and the mirror drum has a small drying load. The coating speed is easy to increase compared to the coating method and solidification method.

For this reason, the rewetting method has attracted attention. However, since the rewetting method wets the coated layer once dried again, it is difficult to obtain a high gloss as compared with the direct method or the coagulation method. Therefore, techniques for improving gloss by adding a surfactant to the rewetting liquid, optimizing the wetting time, and the like have been reported (see Patent Documents 4 and 5).
Further, in order to impart high glossiness to the coating layer, it is advantageous that the particle size of the pigment in the coating layer is small, and a technique for containing colloidal silica having a small particle size as the pigment of the gloss developing layer is proposed. Are known.
JP-A-6-305237 JP 9-156210 A Japanese Patent Laid-Open No. 11-48604 JP 2001-191636 A Japanese Patent Laid-Open No. 8-300804 “Paper and Pulp Manufacturing Technology Series (8) Coating”, edited by Paper and Pulp Technology Association, August 17, 1993, Chapter 9 “Cast Coated Paper”

However, in the ink-jet cast coated paper obtained by the rewet method, when colloidal silica having a small particle size is used as the pigment of the glossy layer, there is a problem that the ink absorbability is inferior although high gloss is obtained. Further, when a pigment having a large particle size such as synthetic amorphous silica is used for the purpose of improving ink absorbability, high gloss cannot be obtained. That is, in the case of the techniques of the above-mentioned patent documents and non-patent documents, high gloss is obtained, but the ink absorbency is not satisfied.
Accordingly, an object of the present invention is to provide an ink jet recording medium having good ink jet recording quality and glossiness similar to that of a silver salt photograph when the rewetting method is used.

  As a result of intensive studies on the above problems, the inventors of the present invention laminated an ink receiving layer on a support, and then laminated a gloss developing layer mainly composed of a specific colloidal silica and a binder, and then rewet cast coating. -It has been found that the above-mentioned problems can be solved by applying gloss by the G method. That is, the ink jet recording medium of the present invention is provided with at least one ink receiving layer on a support, and after providing a gloss developing layer on the surface of the ink receiving layer, the gloss is imparted by a rewet cast coating method. In the ink jet recording medium, the glossy layer is characterized in that the main component is an agglomerated colloidal silica in which 2 to 3 primary particles are aggregated and a binder. It is preferable that the binder is an acrylic urethane resin or a urethane resin.

  In addition, the ink jet recording medium of the present invention is provided with at least one ink receiving layer on a support, and after providing a gloss developing layer on the surface of the ink receiving layer, the gloss is imparted by a rewet cast coating method. In the ink jet recording medium, the glossy layer is mainly composed of agglomerated colloidal silica in which a plurality of primary particles are aggregated in a tuft shape and a binder.

  It is preferable that the binder is an acrylic urethane resin or a urethane resin. The primary particles preferably have a particle size of 10 to 100 nm.

  According to the present invention, an excellent image quality can be obtained, and an inkjet recording medium having a glossiness equivalent to that of a silver salt photograph can be obtained. In particular, the color developability of the image and the ink absorbability are increased.

  Hereinafter, embodiments of the present invention will be described. The ink jet recording medium of the present invention is one in which the following ink receiving layer and gloss developing layer are provided on at least one surface of a support, and gloss is given by a rewet method.

(Support)
The support used in the present invention may be any material as long as it has air permeability, but preferably paper (coated paper, uncoated paper, etc.) is used. The raw material pulp of the paper includes chemical pulp (conifer bleached or unbleached kraft pulp, hardwood bleached or unbleached kraft pulp, etc.), mechanical pulp (ground pulp, thermomechanical pulp, chemisermomechanical pulp, etc.), deinking Pulp or the like can be used alone or mixed at an arbitrary ratio. The pH of the paper may be any of acidic, neutral and alkaline. In addition, when a filler is included in the paper, the opacity of the paper tends to be improved. Therefore, it is preferable to include a filler. Examples of the filler include hydrated silicic acid, white carbon, talc, kaolin, clay, calcium carbonate. Well-known fillers such as titanium oxide and synthetic resin fillers can be used.

(Ink receiving layer)
In the present invention, the ink-absorbing property is insufficient only with the glossy layer, and the ink absorption required for the ink jet recording medium cannot be ensured. Therefore, an ink receiving layer having a large absorption capacity is essential. The ink receiving layer is a layer intended to absorb ink or an ink solvent, and is a layer mainly composed of a pigment and a binder. As the pigment of the ink receiving layer, known pigments used in the ink receiving layer such as silica, alumina, calcium carbonate, and fired clay can be used alone or in combination. In addition, as the binder, PVA (polyvinyl alcohol), EVA (ethylene / vinyl acetate copolymer resin), SBR (styrene / butadiene rubber), etc., known binders used in the ink receiving layer are used. be able to. In addition, a known auxiliary agent such as a sizing agent, an ink fixing agent, a surfactant, or a dye may be appropriately added to the ink receiving layer as necessary. In the present invention, it is desirable that the ink receiving layer itself has a certain degree of inkjet suitability (specifically, the ink drying speed is high, the printing density is high, and there is no ink overflow or bleeding).

  From the viewpoint of improving the ink absorption of the ink receiving layer, the average oil absorption amount of the entire pigment in the ink receiving layer is preferably 100 ml / 100 g or more. Moreover, it is preferable that the solid content weight ratio of pigment / binder is 100/3 to 100/50. When the weight ratio of the solid content of the pigment / binder is within this range, the ink receiving layer can satisfy both ink absorbability and coating strength.

The coating amount of the ink receiving layer can be arbitrarily adjusted within the range where the surface of the support is covered and sufficient ink absorptivity is obtained, but from the viewpoint of satisfying both the recording density and the ink absorptivity, It is preferably 5 to 30 g / m ^{2 in} terms of solid content (when the ink receiving layer has a multilayer structure, the total amount of each layer). More preferably, it is 10-25 g / m < ² >. When it exceeds 30 g / m ² , the peelability from the mirror drum decreases, and problems such as adhesion of the coating layer to the mirror drum occur.

(Glossy layer pigment)
The gloss developing layer is formed on the surface of the ink receiving layer, and gloss is imparted by a rewet cast coating method described later. The glossy layer is mainly composed of the following agglomerated colloidal silica and a binder. Here, according to the study by the present inventors, it has been found that the ink coloring property of the recording medium is improved by increasing the transparency of the glossy layer. In other words, if the pigment of the glossy layer contains only relatively large particles (average particle size of about several μm) such as silica, alumina, calcium carbonate, and calcined clay, not only high gloss is not obtained. The transparency of the glossy layer is impaired, and the clarity of the recorded image is impaired. Therefore, in the present invention, aggregated colloidal silica having a relatively small particle size (average particle size (secondary particle size) of about several tens to several hundreds nm) is contained as a pigment of the glossy layer. When aggregated colloidal silica is used, not only the transparency of the gloss developing layer but also the gloss can be improved.
In addition, the glossy layer contains particles having a relatively large particle size (average particle size of about several μm) such as silica, alumina, calcium carbonate, calcined clay, etc. as pigments to such an extent that the gloss is not lowered. Can do. The ratio of the particles in the glossy layer pigment is preferably 30% by mass or less.

  The aggregation state of colloidal silica will be described later.

The agglomerated colloidal silica is an aggregate of a plurality of primary particles, synthesized by sol-gel method using alkoxysilane as a raw material, and depending on the synthesis conditions, the primary particle size (BET method particle size) or secondary particle size (dynamic light scattering method) It is preferable to control the particle diameter. As such colloidal silica, trade name Quatron manufactured by Fuso Chemical Industry Co., Ltd. can be mentioned. The colloidal silica of the present invention is obtained by colloidal particles obtained by subdividing the aggregates of primary particles into secondary particles having an average particle diameter of several tens to several hundreds of nanometers by mechanical means (excluding dry pulverization). Not included.
The primary particles are single particles that are not agglomerated, and when the dispersed particles are observed with a microscope, no joints (or boundary lines due to the joints) with other particles are observed, and the particles are usually spherical. However, non-spherical blocks and rocks are also included.

  The primary particles (spherical colloidal silica) preferably have an average primary particle size of 10 to 100 nm. When the primary particle diameter is less than 10 nm, the transparency of the glossy layer is increased, but the voids between the particles are impaired and the ink absorbability is lowered. When the primary particle diameter exceeds 100 nm, moderate voids are formed between the particles, but the opacity of the glossy layer increases and the color developability of the recorded image decreases.

  Furthermore, as long as the transparency of the glossy layer, the ink coloring property and glossiness of the recorded image are not impaired, the pigments of the glossy layer are different from the above, such as colloidal silica, silica, alumina, calcium carbonate, baked clay, etc. It is also possible to blend particles. In order to secure the transparency of the gloss developing layer, these pigments are preferably 10% by mass or less, more preferably 5% by mass or less in terms of solid content with respect to the entire pigment of the gloss developing layer.

(Binder for glossy layer)
The binder is not particularly limited, but examples of water-based binders include urethane resins derived from urethane resin emulsion, styrene-acrylic resins and derivatives thereof, styrene-butadiene resin latex, acrylic resin emulsion, vinyl acetate resin emulsion, and chloride. Vinyl resin emulsion, urea resin emulsion, alkyd resin emulsion and derivatives thereof, polyvinyl alcohol and modified products thereof, polyvinylpyrrolidone and modified products thereof, starches such as oxidized starch and esterified starch, cellulose such as carboxymethyl cellulose and hydroxyethyl cellulose Derivatives, casein, gelatin, and soy protein. In particular, an acrylic urethane resin and a urethane resin are preferable because the gloss developing layer has high transparency and good storage stability. Here, the acrylic urethane resin is obtained by copolymerizing an acrylic acid monomer, an isocyanate monomer, and a polyol monomer. The urethane resin is obtained by polymerizing an acrylic monomer. When using a urethane resin, a glass transition temperature of 10-70 degreeC is preferable at the point from which high gloss is acquired.

  In the glossy layer, the total of the aggregated colloidal silica and the binder is preferably 80% or more, more preferably 90% or more in terms of the solid content weight ratio. In the glossy layer, 3 to 50 parts by mass of the binder is preferably added to 100 parts by mass of the pigment, and more preferably 5 to 30 parts by mass of the binder. When the blending amount of the binder is less than 3 parts by mass, it is difficult to obtain a glossy feeling, and the strength is lowered to deteriorate the productivity. When the amount of the binder exceeds 50 parts by mass, the gloss increases but the ink absorbability deteriorates.

The coating amount of the glossy layer is preferably ² to 10 g / m ² , more preferably 4 to 8 g / m ² . If the coating amount is less than 2 g / m ² , the white paper glossiness is not improved, and if it is more than 10 g / m ² , the white paper glossiness is improved, but the print density is lowered.

  For the glossy layer, pigment dispersants, water retention agents, thickeners, antifoaming agents, antiseptics, colorants, water resistance agents, wetting agents, fluorescent dyes, UV absorbers, cationic polymer electrolytes, etc., as necessary Can be added as appropriate. However, in order to maintain high transparency, it is desirable that the water-insoluble resin and the water-insoluble component are as few as possible.

(Rewetting liquid)
The rewetting liquid (rewetting liquid) usually comprises an aqueous liquid mainly composed of a fatty acid such as stearic acid or oleic acid or a salt thereof, or a release agent such as polyethylene wax or lecithin. The main effect of the rewetting liquid is to wet plasticize the upper layer of the dry coating layer with the water that accounts for the majority of this liquid. This makes it possible to apply the wet coating layer to the mirror drum by the rewetting cast coating method. The mirror surface is copied with close contact, and the recording medium is given high gloss. In addition to the above releasing agent, a fluorescent dye, a dye, an ink fixing agent, a colloidal pigment, a surfactant, and the like may be added to the rewetting liquid as long as the effects of the present invention are not impaired. In addition, a pigment dispersant, a water retention agent, a thickening agent, an antifoaming agent, a preservative, a coloring agent, a water resistant agent, a wetting agent, an ultraviolet absorber, a cationic polymer electrolyte, and the like may be appropriately added as necessary. it can.

(Coating method)
The ink receiving layer and the gloss developing layer can be provided by applying a predetermined coating liquid with a known coater and then drying it. The coating method can be appropriately selected from methods using known coating machines such as blade coaters, air knife coaters, roll coaters, brush coaters, kiss coaters, squeeze coaters, curtain coaters, die coaters, bar coaters, and gravure coaters. Examples of the method for applying the rewetting liquid or the coagulating liquid include, but are not limited to, a roll, a spray, and a curtain system.

(Form of agglomerated colloidal silica)
Next, various forms of the aggregated colloidal silica used in the present invention will be described.

<First Embodiment Peanut Colloidal Silica>
This agglomerated colloidal silica has a shape in which two to three primary particles are bonded when the dispersion state is observed with a microscope, and this is appropriately referred to as “peanut shape”. In the case of a single spherical colloidal silica that is not aggregated (aggregated), the ink absorptivity is inferior, but the colloidal silica aggregated in a peanut shape can satisfy both glossiness, ink coloring property, and ink absorptivity.

In the peanut-shaped colloidal silica, the ratio of the secondary particle diameter to the primary particle diameter of the colloidal silica ((secondary particle diameter) / (primary particle diameter)) is preferably 1.5 to 2.5. When the ratio is less than 1.5, the glossy layer is improved in transparency, but the ink absorbability is deteriorated because there are few voids. On the other hand, if the ratio exceeds 2.5, voids increase and ink absorbency improves, but opacity increases and ink color developability deteriorates. The primary particle size and secondary particle size of colloidal silica can be measured by the BET method, dynamic light scattering method, or the like. A value obtained by averaging the number of bonded (aggregated) primary particles is a value substantially corresponding to the above ratio.
Moreover, it is preferable that the secondary particle diameter of peanut-like colloidal silica is about 20-1000 nm.

  In this embodiment, when the dispersion state of the colloidal silica is observed with a microscope, it is not necessary that no colloidal silica other than the peanut-like colloidal silica is observed, and the ratio of the secondary particle diameter to the primary particle diameter is measured. If the value (macro physical properties) does not exceed 2.5 (usually 5), other colloidal silica or a single primary particle may be included.

  When peanut-like colloidal silica is used for the pigment, it is preferable to use an acrylic urethane resin (with aliphatic isocyanate as a monomer component) and / or a urethane resin having a glass transition temperature of 10 to 70 ° C. as the binder. As the aliphatic isocyanate, for example, 4,4′-dicyclehexylmethane diisocyanate (HMDI) can be used. Moreover, as an acrylic urethane resin having an aliphatic isocyanate as a monomer component, a hybridurur series (model number 560 to 580) manufactured by Air Products can be exemplified.

Second Embodiment Tufted Colloidal Silica
The aggregated colloidal silica has a shape in which four or more primary particles are bonded when the dispersion state is observed with a microscope, and this is appropriately referred to as “tuft shape”. In the case of a single spherical colloidal silica that is not aggregated (aggregated), the ink absorptivity is inferior, but colloidal silica aggregated in a tuft shape can satisfy both glossiness, ink color development, and ink absorptivity.

  Here, “tufted” means that when the dispersion state of the aggregated colloidal silica is observed, when viewed from the short direction of the aggregated colloidal silica (the direction perpendicular to the longest direction of the aggregate), at least two It means that there is a part where spherical colloidal silica is bonded. In addition, there is only one spherical colloidal silica in the short direction, and silica aggregates in a chain form are not included in the “tuft shape”. When this chain colloidal silica is observed with a microscope, usually at least 5 spherical colloidal silicas are bonded in series, usually 10 or more, and the ratio described below is 5 or more.

  In “tufted”, the number of silica bonds in the short direction decreases from the top to the bottom of the agglomerated colloidal silica, resulting in an agglomerated state like a cocoon of bunch, or the short direction and the long side of the agglomerated silica. Also included are those with approximately equal lengths in the direction. In addition, “substantially” means that when the dispersion state of colloidal silica is observed, it indicates that the chain silica is hardly observed, and that a single colloidal silica that does not aggregate may be present. .

  The secondary particle diameter of the tufted colloidal silica is preferably 50 to 800 nm. When the secondary particle diameter is less than 50, the ink absorbability of the ink receiving layer decreases, and when it exceeds 800 nm, the gloss of the ink receiving layer tends to decrease.

  In the tufted colloidal silica, the ratio of the secondary particle diameter to the primary particle diameter of the colloidal silica ((secondary particle diameter) / (primary particle diameter)) is preferably 4 to 10. Here, when the ratio is less than 4, the transparency of the glossy layer increases, but the ink absorbability deteriorates because there are few voids. On the other hand, when the ratio exceeds 10, voids increase and ink absorbency improves, but opacity increases and ink color developability deteriorates. The primary particle diameter of colloidal silica can be measured by a BET method, a dynamic light scattering method, or the like. The secondary particle size can usually be measured by a dynamic light scattering method. It is also possible to measure the length of the agglomerated silica in the short side direction and the long side direction with a micrograph. A value obtained by averaging the number of bonded (aggregated) primary particles is a value substantially corresponding to the above ratio.

  In this embodiment, when the dispersion state of the colloidal silica is observed with a microscope, it is not necessary that no colloidal silica other than the tufted colloidal silica is observed, and the ratio of the secondary particle diameter to the primary particle diameter is measured. As long as the value (macro physical properties) exceeds 4 (usually), other colloidal silica or a single primary particle may be included.

  When tufted colloidal silica is used for the pigment, it is preferable to use a urethane resin having a glass transition temperature of 10 to 70 ° C. as the binder.

  The present invention will be described more specifically with reference to the following examples. However, the present invention is not limited to these examples. “Part” and “%” represent “part by mass” and “% by mass”, respectively, unless otherwise specified.

(Production of support)
100 parts of pulp slurry made of hardwood bleached kraft pulp (L-BKP) with a beating degree of 285 ml, 10 parts of talc, 1.0 part of aluminum sulfate, 0.1 part of synthetic sizing agent, and 0.02 part of yield improver are added. Paper was made with a paper machine. Starch was applied to both sides of this base paper so that the solid content per side was 2.5 g / m ² to obtain a support having a basis weight of 170 g / m ² .
(Coating of ink receiving layer)
On one side of the support, the following coating liquid A was applied with a blade coater so that the coating amount was 12 g / m ² and dried by blowing at 140 ° C. to form an ink receiving layer.
Coating liquid A: 100 parts of synthetic silica (fine seal X-37: trade name manufactured by Tokuyama Co., Ltd.) as a pigment, 5 parts of latex (LX438C: trade name of Sumitomo Chemical Co., Ltd.), polyvinyl as a binder Alcohol (PVA117: trade name of Kuraray Co., Ltd.) 24 parts and sizing agent (Polymaron 360: trade name of Arakawa Chemical Co., Ltd.) 5 parts were blended to prepare an aqueous coating solution having a concentration of 20%. .

(Glossy layer coating)
On the surface of the ink receiving layer, 5 g / m ² of the following coating liquid B was applied with a roll coater, and air-dried at 140 ° C. to form a glossy layer.
Coating liquid B: 100 parts of peanut-shaped agglomerated colloidal silica (PL-2: trade name, primary particle diameter 23 nm, secondary particle diameter 51 nm, manufactured by Fuso Chemical Industry Co., Ltd.) as a pigment, acrylic urethane resin (hybrid as a binder) A coating solution having a concentration of 20% was prepared by blending 30 parts (Dure 570: trade name of Air Products).
(Rewet cast coating treatment)
The surface of the gloss developing layer is rewet using the following rewet liquid C, and the gloss developing layer is pressure-bonded to the heated mirror-finished surface via a press roll, and the mirror surface is copied, and the basis weight is 170 g / m ² . A cast coated paper for inkjet recording was obtained.
Rewetting liquid C: 0.2 parts of polyethylene wax (Maycatex HP50: trade name, manufactured by Meisei Chemical Co., Ltd.) as a release agent was blended to prepare a rewetting liquid having a concentration of 0.2%.

  In the coating liquid B of Example 1, a cast coated paper for ink jet recording was obtained in exactly the same manner as in Example 1 except that the blending amount of the acrylic urethane resin as the binder was 20 parts.

  In the coating liquid B of Example 1, except that 30 parts of urethane resin (Superflex 110: trade name, manufactured by Daiichi Kogyo Seiyaku Co., Ltd., Tg = 48 ° C.) was used as a binder instead of acrylic urethane resin. In the same manner as in Example 1, a cast coated paper for ink jet recording was obtained.

  Instead of the colloidal silica used in Example 3, 100 parts of tufted aggregated colloidal silica (HS-M-20: trade name, primary particle diameter 23 nm, secondary particle diameter 240 nm, manufactured by Nissan Chemical Industries, Ltd.) was used. Except for the above, a cast coated paper for inkjet recording was obtained in the same manner as in Example 3.

  Instead of the colloidal silica used in Example 1, 100 parts of tufted aggregated colloidal silica (HS-M-20: trade name, primary particle diameter 23 nm, secondary particle diameter 240 nm, manufactured by Nissan Chemical Industries, Ltd.) was used. Except for the above, a cast coated paper for inkjet recording was obtained in the same manner as in Example 1.

  In the coating liquid B of Example 1, an inkjet was carried out in the same manner as in Example 1 except that 30 parts of SBR resin (0613: trade name of JSR) was used as a binder instead of acrylic urethane resin. A cast coated paper for recording was obtained.

<Comparative Example 1>
In place of the colloidal silica used in Example 1, 100 parts of non-aggregated single spherical colloidal silica (ST-50: trade name of Nissan Chemical Industries, Ltd., primary particle size 23 nm) was used. In the same manner as in No. 1, a cast coated paper for inkjet recording was obtained.
<Comparative example 2>
In place of the colloidal silica used in Example 3, 100 parts of non-aggregated single spherical colloidal silica (ST-50: trade name of Nissan Chemical Industries, Ltd., primary particle diameter: 23 nm) was used. In the same manner as in No. 3, a cast coated paper for ink jet recording was obtained.
<Comparative Example 3>
Instead of the colloidal silica used in Example 1, 100 parts of chain colloidal chain colloidal silica (ST-UP: product name, primary particle diameter 12 nm, secondary particle diameter 50 nm, manufactured by Nissan Chemical Industries, Ltd.) A cast coated paper for ink jet recording was obtained in the same manner as in Example 1 except that.
<Comparative example 4>
Instead of the colloidal silica used in Example 1, synthetic silica (Fine Seal X-37B): trade name manufactured by Tokuyama Corporation, primary particle diameter 10-30 nm, secondary particle diameter 3.7 μm) for 100 parts A cast coated paper for ink jet recording was obtained in the same manner as in Example 1 except that.

The glossiness and ink jet recording quality of the cast coated paper for ink jet recording of each Example and Comparative Example were evaluated by the following methods.
(1) Glossiness The 75 degree specular glossiness of the cast coated paper surface was measured according to ISO 8254-1 and evaluated according to the following criteria.
○: Highly transparent gloss (75 degree specular gloss is 75% or more)
Δ: Cloudy gloss (75 degree mirror gloss is less than 75% and 50% or more)
X: Low gloss or uneven coating (75 degree specular gloss less than 50%)

(2) Inkjet recording quality A predetermined pattern was recorded on each recording sheet with an inkjet printer (PM-970C: trade name, manufactured by Epson Corporation) using a dye ink, and evaluated according to the following criteria.
(2-a) Ink absorbability (bleeding)
The blur at the boundary of the solid print portion mixed with red and green was visually evaluated.
○: The color boundary portion is clearly separated Δ: The color boundary portion has a slight blur ×: The color boundary portion has a large blur (2-b) Print density (ink color development)
The vividness of the recorded image area was evaluated by the print density (total print density of cyan, magenta, yellow, and black). If it is more than Δ, normal use is possible.
◎: Total print density is 7.0 or more ○: Total print density is less than 7.0 6.5 or more △: Total print density is less than 6.5 6.0 or more ×: Total print density is less than 6.0

In addition, the primary particle diameter of each colloidal silica obtained | required the specific surface area first by the nitrogen adsorption method, and calculated | required by calculation from the following formula.
Specific surface area = 4πr ² / ((4πr ³ /3)*2.2)
(Here, “2.2” is the true specific gravity of silica, and r is the particle diameter (nm))
The secondary particle size was measured with a Coulter N4 meter (trade name, manufactured by Coulter), and the number average value was adopted.

  The obtained results are shown in Table 1. In addition, during evaluation of 75 degree | times white paper glossiness of a table | surface, a number shows a measured value and a parenthesis shows an evaluation parameter | index ((double-circle) -x).

As is clear from Table 1, the ink jet recording paper of each example was highly evaluated in all of operability, glossiness, and ink jet recording quality (ink absorbability, print density (ink color development)).
When peanut-shaped colloidal silica was used as the pigment of the glossy layer, when the acrylic urethane resin was used as the binder (Examples 1 and 2), both the glossiness of the blank paper and the print density were good values. In general, changing the binder to increase the gloss level tends to decrease the print density, and increasing the print density tends to decrease the gloss level. However, in the above examples, both the gloss level and the print density are improved. . Further, when peanut-like colloidal silica is used as the pigment of the glossy layer and a urethane resin is used as the binder (Example 3), the printing density is greatly improved. Further, when tufted colloidal silica is used as the pigment of the glossy layer, if a urethane resin is used as the binder (Example 4), both glossiness and print density are greatly improved.

  On the other hand, in Comparative Example 1, Comparative Example 2 using spherical colloidal silica that was not associated (aggregated), and Comparative Example 3 using chain colloidal silica aggregated in a chain, the gloss was high. The ink absorbency was very poor. In the case of Comparative Example 4 using synthetic amorphous silica having a very large particle size (secondary particle size), the printing density was improved, but the glossiness of the blank paper was greatly reduced. In general, in the case of colloidal silica having a particle size of about several hundreds of nanometers, it is considered that the glossy expression layer becomes opaque as the particle size increases, resulting in a decrease in print density. On the other hand, when the secondary particle diameter is very large (for example, 3700 nm) as in the case of synthetic amorphous silica, it is considered that the ink is absorbed by the glossy layer and the printing density is improved.

Claims (4)

  An ink jet recording medium provided with at least one ink receiving layer on a support, and after providing a gloss developing layer on the surface of the ink receiving layer, the gloss is imparted by a rewet cast coating method, An ink jet recording medium characterized in that the glossy layer is composed mainly of aggregated colloidal silica in which 2 to 3 primary particles are aggregated and a binder.   An ink jet recording medium provided with at least one ink receiving layer on a support, and after providing a gloss developing layer on the surface of the ink receiving layer, the gloss is imparted by a rewet cast coating method, An ink jet recording medium, wherein the glossy layer is composed mainly of agglomerated colloidal silica in which a plurality of primary particles are aggregated in a tuft shape and a binder.   The ink jet recording medium according to claim 1, wherein the binder is an acrylic urethane resin or a urethane resin.   4. The ink jet recording medium according to claim 1, wherein the primary particles have a particle size of 10 to 100 nm.