JP2006056234A - Inkjet recording method/device - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an inkjet recording method which can generate a high definition image showing excellent bronzing resistance, gloss, fretting resistance and color turbidity resistance by printing in an irregularly thinning-out pattern, and an inkjet recording device. <P>SOLUTION: In this inkjet recording method, an irregularly thinning-out image is formed by scanning one recording region of a recording medium with a recording head having 10 to 50 μm nozzle interval. The pigmented ink contains pigment, a high boiling point organic solvent and water and is composed of each color ink i.e. C, M, Y and K and not less than one special color ink. In addition, the diameter of an ink dot discharged from the recording head on the recording medium, is 10 to 50 μm and the recording medium has a void layer which indicates not less than 10 ml/m<SP>2</SP>transition level for 0.04 sec absorption time by the Bristow process and contains an inorganic microparticle with 15 to 100 nm average particle diameter and a hydrophilic binder. Besides, the recording medium has 20 to 45% 20° mirror surface glossiness. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a novel ink jet recording method and ink jet recording apparatus, and more particularly to an ink jet recording method and an ink jet recording apparatus that can improve bronzing resistance, gloss, and scratch resistance, and provide a high-definition image without color turbidity.

  The ink jet recording method is a method in which minute ink droplets are ejected by various operating principles and adhered to a recording medium such as paper to record images / characters. It has advantages such as being easy to make. In the ink jet recording system, various improvements have been made in each field of ink, ink jet recording medium, and ink jet recording apparatus, and now, they are rapidly spreading in various fields such as various printers, facsimiles, computer terminals and the like. In particular, recently, the image quality of printers has been improved and the image quality has been reached.

  As an ink jet recording apparatus used in the ink jet recording system, an ink discharge port (nozzle portion) and an ink liquid path are provided as a recording head (hereinafter also referred to as a multi-head) in which a plurality of recording elements are arranged in an integrated manner in order to improve printing speed. A plurality of integrated ones are used. Furthermore, a printer equipped with a plurality of recording heads having the above-described configuration is often used for color correspondence. In that case, the heads that eject ink of each color are generally arranged in parallel in the main scanning direction.

  As described above, when printing a color image, unlike a monochrome printer that prints only characters, various factors such as color development, gradation, and uniformity are important in obtaining a high-quality image. . In particular, with regard to uniformity, slight nozzle unit variations that occur due to differences in the multihead production process affect the amount of ink discharged from each nozzle and the direction of the discharge direction. As a result, the image quality is deteriorated as uneven density. In addition, fluctuations in speed during main scanning of the carriage on which the head is mounted, fluctuations in the sub-scan paper feed amount of the medium, fluctuations in the distance between the medium surface and the nozzle surface on the medium, and the like also cause image degradation.

To solve the above problem, a recording head having a plurality of nozzle portions is scanned a plurality of times with respect to the same recording area of the ink jet recording medium, and in each scan, an image is formed according to a complementary thinning pattern. A so-called multi-pass recording method has been proposed that reduces image deterioration due to variations and various variations. As a mask used at this time, as described in Japanese Patent Laid-Open No. 60-107975, a method using a complementary pattern having a certain thinning rate according to a certain rule is the most general.
However, as will be described later, in such a regular mask, uneven color, streaky irregularities, white spots, etc. may appear conspicuously, and an irregular mask pattern was used as an improvement measure. A method has been proposed. By forming a thinned image according to this thinning pattern without regularity, density unevenness and color unevenness caused by the synergistic effect of the regularity of the image and the regularity of the mask are prevented, and high-quality printing and high-speed printing are realized to some extent. be able to. (For example, refer patent documents 1-3.).

  However, when using a specific ink and recording medium, particularly when high-quality printing equivalent to that of a silver salt photograph is required, it is possible to obtain sufficient image quality only with these proposed thinning printing methods. Found by a person. This will be described below.

  Inks used in the ink jet recording method are roughly classified into dye inks in which a color material is dissolved in a solvent and dispersed inks in which a color material, mainly a pigment is dispersed in a solvent. The dye is soluble in a solvent, the pigment molecule is colored in a molecular state or a cluster state, its absorption spectrum is sharp, and it exhibits a clear color with high purity. Furthermore, since there is no granular pattern due to the particles, and no scattered light or reflected light is generated, an ink-jet image having a high transparency and a clear hue can be obtained, and since there are no colorant particles, scratch resistance is obtained. It has excellent characteristics. However, on the other hand, when the molecule is destroyed by a photochemical reaction or the like, the decrease in the number of molecules reflects the color density as it is, so that the light resistance and the fading property are poor. Ink-jet recording images using dye ink have high image quality, but the image quality is greatly deteriorated by storage over time, and there is no technology that surpasses silver salt photography yet from the viewpoint of image storage stability.

  As a method for solving this problem, a pigment ink using a pigment having good light resistance as a colorant has been used for an application requiring an image resistant to fading due to light.

  When such a pigment ink is used, when the ink adhesion amount is increased, aggregation of the pigment in the ink occurs, which causes a problem that a high-quality and high-definition color image cannot be obtained. In order to solve such a problem, a method of forming a color image using an ink set in which special colors such as red and violet are added to yellow, magenta, cyan and black inks can be applied (for example, Patent Document 4). reference.).

  However, when ink jet image recording is performed using a pigment ink according to a thinning pattern having no regularity, the ink droplets of cyan, magenta, yellow, black, etc. are not regular because the dot positions formed in each scan have no regularity. However, there are many cases where printing is performed adjacent to the ink jet recording medium by the same scanning. As a result, ink droplets are mixed with each other to cause agglomeration of pigment particles and the like, causing a phenomenon called bronzing, which has hardly occurred in dye ink, and a problem that a color image cannot be accurately reproduced occurs.

  In particular, when an inkjet recording medium having a void layer containing inorganic fine particles having an average particle diameter of 100 nm or less in order to form a high-definition image such as a silver salt photograph, the ink absorption rate is fast, Aggregation of pigment particles existing on the recording medium is more likely to occur. In addition, since a non-regular mask pattern is used, there is a high probability that dots of different colors are printed adjacent to each other, and pigment particles having different color tones are mixed on the recording medium. It has been found that the formation of is difficult.

This is because, when a regular thinning pattern is used, the position of each ink formed on the medium in one scan can be finely controlled, and such mixing of dots can be effectively suppressed. However, this is because such control is difficult to perform in an irregular case. In addition, when the printing rate in one scan by thinning is low, the probability that dots are formed adjacent to each other on the medium is low even when an irregular mask is used, and thus these image quality problems are reduced. Is done.
JP 7-52390 A JP 2002-96461 A JP 2002-144552 A JP 2003-266913 A

  The present invention has been made in view of the above problems, and its object is to achieve a bronzing resistance even when a pigment ink is printed on a recording medium having a relatively high absorption speed to form a color image in accordance with an irregular thinning pattern. The present invention provides an inkjet recording method and an inkjet recording apparatus that can improve gloss and scratch resistance and obtain a high-definition image without color turbidity.

  The above object of the present invention is achieved by the following configurations.

(Claim 1)
A recording head having a plurality of nozzles for discharging colored ink is scanned a plurality of times with respect to the same recording area of the recording medium, and a thinned image according to a thinning pattern having no regularity is formed in each scanning, and the colored ink is applied to the recording medium. An ink jet recording method for forming a color image by printing on
The nozzle pitch of the recording head is 10 to 50 μm,
The colored ink is composed of cyan, magenta, yellow and black color inks and at least one special color ink,
The colored ink contains a pigment, a high boiling point organic solvent, and water, and the dot diameter formed by being ejected from the recording head is 10 to 50 μm on the recording medium,
The recording medium has a void layer containing inorganic fine particles having an average particle size of 15 to 100 nm and a hydrophilic binder having a transition amount of 10 ml / m ² or more at an absorption time of 0.04 seconds according to the Bristow method, And the 20-degree specular glossiness of this recording medium by JIS-Z-8741 is 20 to 45%, The inkjet recording method characterized by the above-mentioned.

(Claim 2)
2. The ink jet recording method according to claim 1, wherein the special color ink is at least one ink selected from a red ink, an orange ink, a blue ink, a violet ink, and a green ink.

(Claim 3)
The ink jet recording method according to claim 1 or 2, wherein a print allowable rate by the thinning pattern is 15 to 35%.

(Claim 4)
The inkjet recording method according to any one of claims 1 to 3, wherein a surface tension of the colored ink is 30 to 50 mN / m.

(Claim 5)
The inkjet recording method according to claim 1, wherein the pigment of the colored ink is dispersed with a polymer dispersant.

(Claim 6)
The inkjet recording method according to claim 1, wherein the recording medium is a medium in which the gap layer is provided on a water-absorbing support.

(Claim 7)
The inkjet recording method according to claim 1, wherein the hydrophilic binder is polyvinyl alcohol or a derivative thereof.

(Claim 8)
The inkjet recording method according to claim 1, wherein the hydrophilic binder is hardened.

(Claim 9)
The ink jet recording method according to claim 1, wherein the void ratio of the void layer is 30 to 70%.

(Claim 10)
The inkjet recording method according to claim 1, wherein the inorganic fine particles are silica or alumina.

(Claim 11)
The inkjet recording method according to claim 1, wherein the inorganic fine particles have an average particle size of 20 to 80 nm.

(Claim 12)
The inkjet recording method according to claim 1, wherein the colored ink contains urea or a urea derivative.

(Claim 13)
An inkjet recording apparatus that forms a color image by discharging colored ink onto a recording medium,
A recording head in which a plurality of nozzle portions for discharging the colored ink are arranged at a pitch of 10 to 50 μm;
Scanning means for scanning the recording head a plurality of times for the same recording area of the recording medium;
The dot diameter formed by the colored ink discharged from the recording head is 10 to 50 μm on the recording medium, and a thinned image according to a thinning pattern having no regularity is formed on the recording medium in each scan. And control means for discharging colored ink from a plurality of nozzle portions,
The colored ink is composed of cyan, magenta, yellow and black color inks and at least one special color ink,
The colored ink contains a pigment, a high boiling point organic solvent, and water,
The recording medium has a void layer containing inorganic fine particles having an average particle size of 15 to 100 nm and a hydrophilic binder having a transition amount of 10 ml / m ² or more at an absorption time of 0.04 seconds according to the Bristow method, and An inkjet recording apparatus, wherein the recording medium has a 20-degree specular glossiness of 20 to 45% according to JIS-Z-8741.

(Claim 14)
14. The inkjet recording apparatus according to claim 13, wherein the special color ink is at least one ink selected from a red ink, an orange ink, a blue ink, a violet ink, and a green ink.

(Claim 15)
The ink jet recording apparatus according to claim 13 or 14, wherein a print allowable rate by the thinning pattern is 15 to 35%.

(Claim 16)
The inkjet recording apparatus according to any one of claims 13 to 15, wherein a surface tension of the colored ink is 30 to 50 mN / m.

(Claim 17)
The inkjet recording apparatus according to claim 13, wherein the pigment of the colored ink is dispersed with a polymer dispersant.

(Claim 18)
The inkjet recording apparatus according to any one of claims 13 to 17, wherein the recording medium is provided with the gap layer on a water-absorbing support.

(Claim 19)
The inkjet recording apparatus according to claim 13, wherein the hydrophilic binder is polyvinyl alcohol or a derivative thereof.

(Claim 20)
The inkjet recording apparatus according to claim 13, wherein the hydrophilic binder is hardened.

(Claim 21)
21. The ink jet recording apparatus according to claim 13, wherein the void ratio of the void layer is 30 to 70%.

(Claim 22)
The inkjet recording apparatus according to any one of claims 13 to 21, wherein the inorganic fine particles are silica or alumina.

(Claim 23)
The inkjet recording apparatus according to any one of claims 13 to 22, wherein an average particle diameter of the inorganic fine particles is 20 to 80 nm.

(Claim 24)
The inkjet recording apparatus according to any one of claims 13 to 23, wherein the colored ink contains urea or a urea derivative.

  According to the present invention, even when a pigment ink is printed on an inkjet recording medium according to an irregular thinning pattern to form a color image, the bronzing resistance, gloss and scratch resistance are improved, and a high-definition image free from color turbidity. An ink jet recording method and an ink jet recording apparatus can be provided.

As a result of intensive studies in view of the above problems, the present inventors have made a recording head having a plurality of nozzles for ejecting ink scan the same recording area of the recording medium a plurality of times, and that each scan has regularity. In a multi-pass ink jet recording method for forming a thinned color image according to a thinning pattern, 1) a recording head having a nozzle pitch of 10 to 50 μm, 2) each color ink of cyan, magenta, yellow and black, and at least one special color ink A colored ink containing at least a pigment, a high-boiling organic solvent, and water, and having a dot diameter of 10 to 50 μm formed on the recording medium (hereinafter, also simply referred to as ink). When, 3) transferred amount at 0.04 sec of absorption time is not more 10 ml / m ² or more, an average particle diameter of 15~100nm inorganic By combining with a recording medium having a void layer containing particles and a hydrophilic binder and having a 20-degree specular gloss of 20 to 40% according to JIS-Z-8741, bronzing resistance, gloss and scratch resistance Has been improved, and it has been found that inkjet recording capable of obtaining a high-definition image free of color turbidity can be realized.

  Hereinafter, the best mode for carrying out the present invention will be described in detail, but the present invention is not limited thereto.

  First, an ink jet printer to which the ink jet recording method of the present invention can be applied will be described with reference to FIG.

  FIG. 1 is a perspective view showing main components of an ink jet printer.

  As shown in the figure, the ink jet printer 1 is provided with an image forming section 2 that ejects ink onto a recording medium to form an image. In the image forming unit 2, a platen 21 that supports the back surface (the surface opposite to the recording surface side) of the recording medium P in a predetermined range on the upper surface is disposed substantially horizontally. In addition, the image forming unit 2 is provided with a guide member 25 that moves along the scanning direction X and moves the carriage 23 that scans in the scanning direction X above the platen 21.

  The carriage 23 reads the optical pattern of the linear scale 26 which extends along the scanning direction X and has an optical pattern with a 300 dpi period in the longitudinal direction. A linear encoder sensor 27 that outputs as a clock signal is mounted. In addition, dpi as used in the field of this invention represents the number of dots per 2.54 cm. The printing operation is performed at a printing density of 1200 dpi, for example, by dividing the encoder signal. The movement direction of the carriage 23 is changed in accordance with the rotation direction of the carriage drive motor 231, whereby the carriage 23 reciprocates in the scanning direction X. Further, during image formation, the carriage 23 moves forward, backward, or reciprocally in the scanning direction X when the recording medium is stopped. The moving speed at this time is, for example, 705 mm / sec at the highest speed.

  Next, the recording head 22 will be described with reference to FIGS. FIG. 2 is an enlarged perspective view of the carriage 23, and FIG. 3 is a bottom view of the recording head 22.

  The recording head 22 may be either a piezo method or a thermal method, but the thermal method is preferable from the viewpoint of arranging the nozzles at a high density, and in this embodiment, a thermal method recording head is used. The recording head 22 is disposed so that the recording surface of the recording medium P conveyed on the platen 21 and the nozzle surface 222 on which the nozzles 221 of the recording head 22 are formed face each other during image recording. .

  As shown in FIG. 2, a total of 256 nozzles 221 are formed on the nozzle surface 222 of the recording head 22 in two rows of 128 at a pitch of 42.3 μm (600 dpi) in the recording medium conveyance direction. The rows are arranged 21.2 μm apart. This corresponds to one pixel at 1200 dpi. The distance between the two rows is about 500 microns. Each nozzle 221 is provided with a thermal ink jet element therein, and ejects ink separately as droplets by the operation of the ejection means.

  Each recording head 22 is supplied with ink from a recording ink cartridge (not shown) through a tube for piping. Eight recording heads 22 are arranged along the scanning direction. For each of the four colors of cyan (C), magenta (M), yellow (Y), and black (K) and three special color inks, respectively. Used for. In this embodiment, four types of inks of C, M, Y, and K and three colors of special color inks are used as recording inks. However, using light colors, eight colors of shades C, M, Y, and K are used. The effect of the present invention is the same in an ink jet printer that records with three special color inks. In FIG. 1, the heads for eight colors are mounted, but in this embodiment, printing is performed using seven of them.

  Next, the control unit of the inkjet printer 1 will be described with reference to FIG. FIG. 4 is a block diagram illustrating a control unit of the inkjet printer 1.

  As shown in FIG. 4, the control unit 100 includes a transport motor 101 for transporting a recording medium, a CPU 103, an interface 104, a carriage drive motor 231, a memory write controller 105, an image memory 106, a memory read controller 107, a mask. A processing circuit 108 is configured to be connected via a bus 110. The detailed configuration of the mask processing circuit 108 will be described later. Note that the control unit 100 is connected to the recording head 22 of the ink jet printer 1 and each driving unit.

  The control unit 100 controls the conveyance of the recording medium, the carriage 23 scanning operation, the ink ejection of the recording head 22, and the like. As shown in FIGS. 4 and 5, an image forming apparatus 200 such as a computer is connected to the control unit 100. The image forming apparatus 200 forms a multicolor image based on the input signal. In this example, the application program 201 operating inside the image forming apparatus 200 displays an image on the monitor 300 via the video driver 202 while processing the image. When the application program 201 issues an image formation instruction, the printer driver 203 for the image forming apparatus 200 receives image data for image formation from the application program 201 and converts the image data into a signal that can be formed by the inkjet printer 1. .

  A printer driver 203 includes a rasterizer 204 that converts image data handled by the application program 201 into color information in dot units, and color development of the inkjet printer 1 with respect to image gradation data converted into color information in dot units. Color gradation correction module 205 that performs correction according to characteristics and gradation characteristics, so-called halftone image that expresses density in a certain area based on the presence or absence of recording ink in dot units from image data after color correction A halftone module 206 for generating data is provided. A module 207 that performs thinning mask processing can also be incorporated in this printer driver. In this case, for example, the mask setting corresponding to the type of medium used for printing is changed. Even flexible control is possible. When the mask processing circuit 108 in the printer is used, the processing at 207 is not performed. Conversely, when the mask process is performed at 207, the process at the circuit 108 is not performed. In addition to the print data, a mask pattern can be downloaded from the image processing apparatus 200 for each printing.

  Next, the multipass inkjet recording method will be described. As described above, various elements such as color developability, gradation, and uniformity are required in inkjet image recording, particularly when forming a color image. In particular, with regard to uniformity, that is, the uniformity of the image to be formed, slight variations in nozzle units that occur due to differences in the multihead production process affect the ink discharge amount and direction of each nozzle when printing. Or a band-like unevenness due to the mechanical accuracy of the movement of the recording medium occurs, which ultimately causes the image quality to deteriorate as unevenness in the density of the printed image. Therefore, in this embodiment, in order to solve such a problem, a color image is formed by using a multi-pass inkjet recording method in which the head scans the same recording area of the inkjet recording medium a plurality of times.

  As a multi-pass printing jet recording method, for example, a method as disclosed in JP-A-60-107975 can be used. The method will be described with reference to FIGS.

  According to this method, the multi-head 1101 is scanned three times to complete the print area shown in FIGS. 8 and 9, but the half-pixel unit area is completed in two passes. In this case, the 8 nozzles of the multi-head are divided into groups of 4 upper nozzles and 4 lower nozzles, and the dots printed by one nozzle in one scan are defined image data in accordance with a predetermined image data arrangement. It is thinned out to about half. Then, dots are embedded in the remaining half of the image data at the time of the second scan, and printing of the 4-pixel unit area is completed.

  When such a recording method is used, even if the same one as the multi-head shown in FIG. 9 is used, the influence on the print image unique to each nozzle is halved. As a result, black stripes and white stripes as shown in FIG. Therefore, the density unevenness is considerably reduced as compared with the case of FIG. 9C as shown in FIG.

  When performing such recording, the first scan and the second scan are divided in such a manner that the image data are filled with each other according to a certain arrangement. Usually, this image data arrangement (decimation pattern) is vertically and horizontally as shown in FIG. It is most common to use a pixel that has exactly a houndstooth per pixel.

  Therefore, in the unit print area (here, in units of four pixels), the printing is completed by the first scan for printing the staggered lattice and the second scan for printing the reverse staggered lattice.

  7-a, 7-b, and 7-c in FIG. 7 have 8 nozzles in the same manner as in FIG. 6 to show how recording in a certain area is completed when the staggered pattern and reverse zigzag pattern are used, respectively. This is described using a multi-head. First, in the first scan, staggered patterns (hatched circles) are recorded using the lower four nozzles (7-a). Next, in the second scan, paper feed is performed by 4 pixels (1/2 of the head length), and an inverted zigzag pattern (white circles) is recorded (7-b). Further, in the third scan, the paper is fed again by 4 pixels (1/2 of the head length), and the staggered pattern is recorded again (7-c).

  In this manner, paper feeding in units of four pixels and recording of a staggered pattern and a reverse staggered pattern are alternately performed, thereby completing a recording area in units of four pixels for each scan. As described above, it is possible to obtain a high-quality image without density unevenness by completing printing with two different types of nozzles in the same region.

  However, even when such multi-pass printing is performed, the density unevenness is not eliminated at all depending on the duty, or new density unevenness is confirmed particularly in the halftone. The phenomenon will be described below.

  Usually, image data to be recorded in a certain area received by the printer is already regularly arranged. The recording device stores a certain amount of the data in a buffer, applies a new mask (image arrangement pattern) such as zigzag or reverse zigzag as described above, and prints the pixel for the first time when both are turned on. It is supposed to be done.

  10 to 12 explain this state. In FIG. 10, 1710 is the already arranged data stored in the buffer, 1720 is a staggered pattern mask indicating pixels that are allowed to print in the first pass, and 1730 is an inverted staggered pattern indicating pixels that are allowed to be printed in the second pass. Pattern masks 1740 and 1750 represent pixels printed in the first pass and the second pass, respectively.

  In FIG. 10, already arranged data for printing 25% in a certain area is stocked in the buffer. In general, this data is arranged in a state in which print data varies as much as possible in order to maintain a uniform density in a specified fixed region. The image arrangement of these depends on what area gradation method is used during image processing before being transferred to the printer body. What is shown at 1710 is an example of a certain image arrangement for 25% data, but if such data is printed with the masks 1720 and 1730 respectively, the first pass and the second pass will be As shown by 1740 and 1750, the data is recorded in an equally divided state.

  However, as shown in FIG. 11, when just 50% of data comes, the data 1810 arranged in the most dispersed state and either the staggered pattern mask (1802) or the inverted staggered pattern mask (1830) It can be easily imagined that the arrangement state is exactly the same.

  When this occurs, printing of all image data is completed in the first pass (1840), and no recording is performed in the second pass (1850). That is, all the print data (1810) is printed by the same nozzle. Accordingly, the influence of nozzle variation is directly reflected in density unevenness, and the original purpose of the divided recording method cannot be achieved.

  FIG. 12 shows the printing state when array image data having a higher duty than those in FIGS. 10 and 11 is input. Even in this case, the number of prints is considerably large in the first pass and the second pass. It can be seen that there is a difference. As described above, the density unevenness which has been improved at a high duty of nearly 100% has a disadvantage that it appears again in the data from the low duty to around 50%.

  When thinning printing is performed using a specific mask pattern, the print data and the mask pattern may have the same cycle. The amplitude of the density resulting from the arrangement of the print pixels and the non-print pixels by the mask pattern overlaps with the amplitude of the print data, resulting in resonance. Thus, the dot arrangement of the formed image has a pattern with a specific direction. Usually, this phenomenon is called moire. This is easily noticeable when there are a plurality of lines using the same mask pattern, and is easily recognized by the user. This moire largely depends on the periodicity of the mask pattern.

  In addition to the above problems, the following problems occur when bidirectional printing is performed.

  FIG. 13A shows a state in which the head is ejecting ink drops at a constant speed v onto a smooth paper surface while moving at a constant speed V in the forward or backward direction. If the paper surface is smooth as shown in the figure and the distance d between the paper surface and the head face surface is kept constant at a predetermined value, the discharge timing is uniquely adjusted in the forward path and the return path, so that the paper surface On the top, as shown in the figure below, the dots printed in the forward path and the dots printed in the backward path are landed at the same position. However, if the paper surface itself is lifted from the actual position as shown in FIG. 13B for some reason, the distance between the head face surface and the paper surface is reduced to d ', and the ink drop arrives on the paper surface after the head discharges. Since the time required to do this is shortened for both the forward and backward passes, the printed dots are landed at different positions that are shifted from the target position, as shown in the figure below. Similarly, if the distance d between the paper surface and the head face surface at the time of forward printing for the same image area and the distance d at the time of backward printing are changed due to local paper floating or the like, a larger landing position deviation is caused. May occur.

  When a 100% duty image is printed in both directions using a staggered thinning mask in this state, the dot landing state is as shown in FIG. Here, a state where each dot is shifted by 1/4 pixel from the normal position is shown, and a portion where adjacent dots overlap more than necessary and a portion where a gap is opened between adjacent dots differ depending on the thinning mask. Appears in the arrangement. In FIG. 14, since all dots are printed in the opposite direction to the adjacent dots, a gap of one dot is generated for each dot, and the overall density is low.

  Such landing position misalignment during bi-directional printing is caused not only by the partial ups and downs of the paper surface shown in FIG. 13, but also due to various causes such as uneven discharge speed of the recording head and uneven carriage moving speed. . Since the values of these factors are not always constant with respect to the traveling direction of the carriage, it is difficult to control the ejection timing during bidirectional printing. In addition, since the distance between the head and the paper surface in the recording apparatus may vary greatly from one apparatus to another, there is a limit to the reciprocal landing position control by adjusting the ejection timing.

  Due to the above-described adverse effects, multi-pass printing using a conventional regular thinning pattern that has been performed to correct nozzle variation or the like does not always provide sufficient image quality with respect to density unevenness. . These adverse effects of density unevenness have periodicity that appears alternately in a print area of a certain width, and therefore promote human vision that is recognized as density unevenness.

  The present inventors have found that the above problems occur when a regular mask pattern is used. Therefore, in this embodiment, instead of using a regular mask pattern, the above problem is solved by performing multi-pass printing using a thinning pattern having no regularity. As the thinning pattern without regularity, for example, a random pattern of a predetermined size created using random numbers can be used. Specifically, as described in, for example, Japanese Patent No. 3176182, non-recording A plurality of random mask patterns of a predetermined size in which pixels and recording pixels are randomly arranged are generated, and the generated random mask pattern can be used as a thinning pattern for each recording area as a mask for thinning out recording data.

  By forming an image with print pixels according to such a random mask pattern, the pattern period of the thinning array is eliminated, and the density unevenness caused by the multi-pass printing method using the conventional regular mask Can be overcome by eliminating the periodicity of density unevenness.

  Further, instead of such a random mask using random numbers, a dot arrangement pattern having so-called blue noise characteristics may be used as a thinning pattern without regularity. This pattern was developed for halftone quantization processing. When dither processing is performed using this pattern, the generated dots have few low-frequency components and an image with reduced graininess can be obtained. There are features.

  The image formation according to the thinning pattern without regularity of the present invention is not limited to the method using a random mask using random numbers or a dot arrangement pattern with blue noise characteristics, and thinning out according to a thinning pattern without regularity. Other similar patterns for forming an image can be used.

  Next, regarding the method of performing multi-pass printing using a mask having no regularity as described above, refer to FIGS. 15 and 16 when performing a 4-pass printing using a dot arrangement pattern having a blue noise characteristic as a mask. This will be described below.

  In the actual nozzle form of the head used for recording, as shown in FIG. 3, nozzle rows of 128 nozzles arranged at a pitch of 600 dpi are arranged 500 microns apart in the main scanning direction.

  Hereinafter, in order to simplify the description of multi-pass printing, 16 nozzles per color are divided into four, and the number of nozzles per divided area is 4, and the corresponding mask size is 4 × 16. The corresponding divided areas are shown as 501 to 504 in FIG. Four-pass printing is realized by operating each of the divided areas 501 to 504 separately.

  In each pass, a thinned-out mask pattern with a duty of about 25%, that is, a mask pattern with a print allowance of about 25% is set as print data for each divided region, and a 100% image is created by four scans. A1 to A4, which are examples of 4 × 16 mask patterns used for this, are shown in FIG. Each of the mask patterns A1 to A4 has mask data at positions on the grids indicated by the net pattern in the figure. When the mask patterns A1 to A4 are overlapped, all the 4 × 16 squares are mask data. It is configured to be filled with.

  The mask patterns A1 to A4 are set for the print data 800 shown in FIG. 15 (the hatched portion indicates that there is print data). Here, with respect to the print data 800, 1 is set when there is print data, 0 is set when there is no print data, and with respect to the mask patterns A1 to A4, 1 is set when there is mask data, and 0 is set when there is no print data. The logical sum at the same position of each mask pattern A1 to A4 is taken, and print head ejection data 801 to 804 are generated, respectively. When the four ejection data 801 to 804 are overlaid, the same print image 805 as the original print data 800 is formed.

  FIG. 16 is a diagram for explaining multi-pass printing. Four types of mask data groups, that is, a group of A1 to A4, a group of B1 to B4, a group of C1 to C4, and a group of D1 to D4, are used as one cycle. All the patterns in each group are such that 100% of the image is completed when the four are superimposed. In multi-pass printing, such mask data is set for each of the divided regions 501 to 504 of the print head 500 in each print scan.

  Printing is performed as follows.

  In the first print area on the print image, in the first recording scan, the mask pattern A1 is set in the divided area 504 of the recording head, and recording is performed. Subsequently, in the second recording scan, the mask pattern A2 is used in the divided area 503 of the recording head in the first printing area. In the second printing area, the first printing area is defined in the divided area 504 of the recording head. Printing is performed using a mask pattern B1 of a different group.

  Further, in the third recording scan, the first print area is mask pattern A3 in the print head divided area 502, the second print area is mask pattern B2 in the print head divided area 503, and in the third print area. In the divided area 504 of the recording head, printing is performed using a mask pattern C1 of a group different from these.

  In the fourth print scan, in the first print area, the mask pattern A4 is formed in the divided area 501 of the print head, and in the second print area, the mask pattern B3 is formed in the divided area 502 of the print head. Then, printing is performed using the mask pattern C2 in the divided area 503 of the recording head, and using the mask pattern D1 in a different group in the divided area 504 of the recording head in the fourth printing area. At this time, the first print area is scanned a total of four times using four mask patterns, A1, A2, A3, and A4, and image printing for this area is completed.

  In the same procedure, the second print area uses B1, B2, B3, and B4, the third print area uses C1, C2, C3, and C4, and the fourth print area uses D1, D2, D3, and D4. The image is formed using. After this, the fifth print area is repeated using A1, A2, A3, and A4, and the sixth print area is printed using B1, B2, B3, and B4, and these four groups of patterns are repeated. Operation and printing continue.

  In addition, as shown in FIG. 18, when these patterns are arranged in the order of A4B3C2D1, B4C3D2A1, C4D3A2B1, and D4A3B2C1, and four 16 × 16 masks are configured, each becomes a mask pattern having blue noise characteristics. . These four 16 × 16 masks are arranged so that 0-255 has blue noise characteristics in a 16 × 16 cell, and values of 0-63, 64-127, 128-191, 191-255 of the mask. The portion corresponding to is used as a print permitting pixel. Those obtained by dividing these four masks into four of 4 × 16 correspond to A1 to A4, B1 to B4, C1 to C4, and D1 to D4. For example, Japanese Patent No. 2622429 describes how to create such a pattern.

  As described above, when the dot pattern itself formed in one scan has a blue noise characteristic, there is an effect of reducing the occurrence of repetitive patterns and deterioration of graininess compared to the case of using a pattern generated by random numbers. This is described in, for example, JP-A-2002-96461.

  Further, when changing the allowable printing rate of the mask, it can be easily obtained by changing the value of 0-255 according to the printing rate. For example, when two sets of 40% and 10% masks are to be created, a mask having pixels corresponding to 0-102, 103-127, 128-230, and 231-255 as print allowable pixels may be created. Examples of such a mask are shown in FIGS.

  FIG. 22 is a block diagram showing the configuration of the mask processing circuit used in practicing the present invention, and describes the mask processing circuit 108 of FIG. 4 in detail.

  In FIG. 22, 301 is a data register connected to the memory data bus for reading out print data stored in the image memory 106 in the memory and temporarily storing it, and 302 is the data stored in the data register 301. A parallel-serial converter for converting serial data, 303 is an AND gate for masking the serial data, and 304 is a counter for managing the number of data transfers.

  A register 305 is connected to the CPU 103 via the CPU data bus and stores a mask pattern. A selector 306 selects a digit position of the mask pattern. A selector 307 selects a row position of the mask pattern. is there. Reference numeral 311 denotes a counter for managing digit positions.

  The data transfer circuit shown in FIG. 22 serially transfers print data to the print head in response to a print command signal sent from the CPU 103. The print data stored in the image memory 106 in the memory is temporarily stored in the data register 301 and converted into serial data by the parallel-serial converter 302. The converted serial data is masked by the AND gate 303 and then transferred to the print head. A transfer counter 304 counts the number of transfer bits and transfers data for 16 nozzles.

  The mask register 305 includes four mask registers A, B, C, and D, and stores a mask pattern written by the CPU 103. Each register stores a mask pattern of vertical 16 bits × horizontal 16 bits. The selector 306 selects mask pattern data corresponding to the digit position by using the value of the column counter 311 as a selection signal. The selector 307 selects mask pattern data corresponding to the row position by using the value of the transfer counter 304 as a selection signal. The transfer data is masked using the AND gate 303 by the mask pattern data selected by the selectors 306 and 307.

  This data is used for the ejection control of each nozzle, and ejection is performed in synchronization with the timing signal generated from the encoder signal during the main scanning of the carriage. Hereinafter, this operation is performed in accordance with the printing resolution in the width direction of the medium. In this embodiment, since the mask size is 16 in the horizontal direction, the same mask pattern is repeatedly used for every 16 pixels. However, the size in the horizontal direction of the mask can be the same as the width of the medium. . By repeatedly using the same mask pattern as in this embodiment, the capacity of the register for storing the mask can be reduced.

  In the ink jet recording method and the ink jet recording apparatus of the present invention, one of the characteristics is that the nozzle pitch of the recording head is 10 to 50 μm. When the nozzle pitch is 50 μm or less, there is a high probability that the ejected ink droplets are printed side by side, so problems such as bronzing due to adjacent dots are likely to occur, and the effect of applying the present invention is great. Further, by shortening the nozzle pitch to 50 μm or less, the entire head length can be kept short even when a multi-nozzle exceeding 500 nozzles per head is manufactured. As a result, the landing position deviation on the medium due to the change in the flight distance of the ink droplet from the nozzle in the head length direction due to the inclination between the recording medium surface and the recording head surface can be suppressed, and high printing accuracy can be maintained. be able to. In addition, by making the nozzle pitch 10 μm or more, it is possible to suppress obstacles in manufacturing aptitude, and as a result, it is possible to suppress landing position deviation, and it is difficult to cause dot overlap due to shortening of the dot interval in the nozzle length direction. Problems such as bronzing can be suppressed.

  The nozzle pitch here is a distance between nozzles of a nozzle group arranged in a substantially line. As shown in FIG. 3, when two rows of nozzle groups are arranged with a half-pitch shift, a certain time difference occurs when dots adjacent in the sub-scanning direction on the medium are formed in the A row and the B row. When the distance between the A row and the B row is relatively long, since the next dot adheres after the first adhering dot is absorbed by the medium, bronzing due to ink aggregation is unlikely to occur. As described above, when the distance between the A row and the B row is relatively long, the nozzle pitch is set to the pitch of each of the A row and the B row. On the other hand, when the distance is short, the nozzle pitch is the distance between adjacent nozzles in the A and B rows, and is usually half the pitch of each of the A and B rows.

  Therefore, in the present invention, the distance (N1 and Nn) between the nozzle arrays that are the farthest apart from the nozzle groups of a plurality of rows (N rows of N1, N2,. If the distance between the rows and the third row) is 4 mm or less between the rows, it is preferable to consider the influence on aggregation. Therefore, the nozzle pitch is 1 / n of the pitch of each row, When the distance is larger than 4 mm, the nozzle pitch is set to the pitch of each row.

  In the ink jet recording method of the present invention, it is preferable that the print allowance rate by the thinning pattern is 15 to 35%. Here, in the present invention, when the thinning pattern is used, the print allowable rate is a ratio of the number of dots allowed to eject ink in one main scan with respect to the total number of dots in the pattern.

  When printing is performed using a plurality of thinning patterns having different print allowance rates in one image, the image quality after printing is high due to the thinning pattern having the highest print allowance rate. Therefore, in the present invention, when a plurality of thinning patterns having different print allowance rates are used in one image, the thinning pattern allowance rate having the highest allowance among the thinning patterns used in one image is set as the print allowance. Rate.

  By setting the print allowance rate by the thinning pattern to 15% or more, the probability that the ejected ink droplets are printed side by side is increased. Therefore, the effect of applying the ink and medium characteristics and the recording method as in the present invention. By applying the present invention, a high-quality image with little bronzing or the like can be obtained. On the other hand, by setting it to 35% or less, a high-quality image can be obtained in a portion where the amount of liquid to be adhered is large, such as red, blue, and dark gray.

  In the ink jet recording method of the present invention, the dot diameter formed by the colored ink discharged from the recording head is 10 to 50 μm on the medium. By setting the dot diameter formed by the colored ink to 10 μm or more, it is possible to maintain a printing efficiency above a certain level and to accurately control the ink droplet size. Moreover, by setting it as 50 micrometers or less, bronzing by the ink droplets printed adjacently can be suppressed, and a high-definition image can be obtained.

  In the present invention, at least one special color ink is used together with yellow, magenta, cyan, and black color inks. Here, the special color ink is an ink having a hue between one of the basic colors (cyan, magenta and yellow) and the other one of the basic colors, for example, red, green, It means inks such as violet, orange and blue. By using special color inks together with yellow, magenta, cyan and black color inks, the amount of ink discharged can be reduced. As a result, aggregation of pigment particles in the landed ink droplets can be prevented, and glossiness can be reduced. High-definition and high-definition color images can be realized in which deterioration, bronzing or color turbidity is suppressed.

  When such special colors are used, the number of ink types increases as compared with normal CMYK ink printing. Therefore, a method for separating input image data (RGB, CMYK, etc.) into each ink color is established as a general theory. However, know-how according to the ink to be used is required. In this regard, if the technique disclosed in Japanese Patent Application Laid-Open No. 2000-32284 by the present applicant is used, color separation can be performed in accordance with the spot color to be used. According to this method, the expanded color gamut with the special color ink can be used as effectively as possible, and color continuity can be ensured in colorimetry.

  In addition to this, the spot color data can be generated by the method described in Japanese Patent No. 2711081. According to this method, data for blue ink is generated from cyan and magenta data values, and cyan and magenta data are reduced accordingly to reduce the total ink amount. The amount of ink can be easily controlled by reducing the roughness using cyan and magenta.

  Next, the colored ink according to the present invention will be described.

  The colored ink according to the present invention is characterized by containing a pigment, a high-boiling organic solvent and water, and further has a surface tension of 30 to 50 mN / m, and the pigment is dispersed by a polymer dispersant. Preferably it is.

  As the pigment that can be used in the present invention, a known colored organic or colored inorganic pigment can be used. For example, azo pigments such as azo lakes, insoluble azo pigments, condensed azo pigments, chelate azo pigments, phthalocyanine pigments, perylene and perylene pigments, anthraquinone pigments, quinacridone pigments, dioxazine pigments, thioindigo pigments, isoindolinone pigments, quinophthalonine pigments, etc. Examples include polycyclic pigments, dye lakes such as basic dye type lakes and acid dye type lakes, organic pigments such as nitro pigments, nitroso pigments, aniline black, daylight fluorescent pigments, and inorganic pigments such as carbon black. However, the present invention is not limited to these.

  Specific organic pigments are exemplified below.

  Examples of the magenta pigment include C.I. I. Pigment red 2, C.I. I. Pigment red 3, C.I. I. Pigment red 5, C.I. I. Pigment red 6, C.I. I. Pigment red 7, C.I. I. Pigment red 15, C.I. I. Pigment red 16, C.I. I. Pigment red 48: 1, C.I. I. Pigment red 53: 1, C.I. I. Pigment red 57: 1, C.I. I. Pigment red 122, C.I. I. Pigment red 123, C.I. I. Pigment red 139, C.I. I. Pigment red 144, C.I. I. Pigment red 166, C.I. I. Pigment red 202, C.I. I. Pigment red 222, C.I. I. Pigment violet 19 and the like.

  Examples of red pigments include C.I. I. Pigment red 17, C.I. I. Pigment red 49: 2, C.I. I. Pigment red 112, C.I. I. Pigment red 149, C.I. I. Pigment red 177, C.I. I. Pigment red 178, C.I. I. Pigment red 188, C.I. I. Pigment red 255, C.I. I. And CI Pigment Red 264.

  Examples of yellow pigments include C.I. I. Pigment orange 31, C.I. I. Pigment yellow 12, C.I. I. Pigment yellow 13, C.I. I. Pigment yellow 14, C.I. I. Pigment yellow 15, C.I. I. Pigment yellow 17, C.I. I. Pigment yellow 74, C.I. I. Pigment yellow 93, C.I. I. Pigment yellow 94, C.I. I. Pigment yellow 128, C.I. I. And CI Pigment Yellow 138.

  Examples of orange pigments include C.I. I. Pigment orange 36, C.I. I. Pigment orange 43, C.I. I. And CI Pigment Orange 61.

  Examples of cyan pigments include C.I. I. Pigment blue 15, C.I. I. Pigment blue 15: 2, C.I. I. Pigment blue 15: 3, C.I. I. Pigment blue 16 or the like.

  Examples of green pigments include C.I. I. Pigment green 7, C.I. I. And CI Pigment Green 36.

  Examples of blue pigments include C.I. I. Pigment blue 60, C.I. I. And CI Pigment Violet 23.

  Examples of black pigments include C.I. I. Pigment black 1, C.I. I. Pigment black 6, C.I. I. Pigment black 7 and the like.

  As a method for dispersing the pigment, for example, various dispersing machines such as a ball mill, a sand mill, an attritor, a roll mill, an agitator, a Henschel mixer, a colloid mill, an ultrasonic homogenizer, a pearl mill, a wet jet mill, and a paint shaker can be used. It is also preferable to use a centrifugal separator or a filter for the purpose of removing the coarse particles of the pigment dispersion.

  In the ink according to the present invention, it is preferable to use a polymer dispersant for dispersing the pigment. The polymer dispersant according to the present invention is not particularly limited, and a water-soluble resin or a water-insoluble resin is used. Examples of these polymers include styrene, styrene derivatives, vinyl naphthalene derivatives, acrylic acid, acrylic acid derivatives, methacrylic acid, methacrylic acid derivatives, maleic acid, maleic acid derivatives, itaconic acid, itaconic acid derivatives, fumaric acid, fumaric acid. Examples thereof include a polymer composed of a single monomer selected from acid derivatives, a copolymer composed of two or more monomers, and salts thereof. Water-soluble polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, cellulose derivatives, gelatin, and polyethylene glycol can also be used.

  These polymers preferably have both a hydrophilic part and a hydrophobic part. The hydrophilic portion has a function of stabilizing dispersion in water, which is the main component of the ink, and the hydrophobic portion has a function of enhancing adsorption to the pigment surface. Among these, acrylic polymer dispersants are preferably used because of their features such as easy molecular structure design and easy performance as a dispersant. The acrylic polymer dispersant refers to a polymer dispersant containing at least 30 mol% of an acrylic monomer.

  As such an acrylic polymer dispersant, the following polymer composed of a hydrophobic monomer and a hydrophilic monomer, or a copolymer composed of two or more monomers and salts thereof are preferable. . Examples of the hydrophobic monomer include styrene, α-methylstyrene, methyl methacrylate (MMA), ethyl methacrylate (EMA), propyl methacrylate, n-butyl methacrylate (BMA or NBMA), hexyl methacrylate, 2-ethylhexyl methacrylate ( EHMA), octyl methacrylate, lauryl methacrylate (LMA), stearyl methacrylate, phenyl methacrylate, hydroxylethyl methacrylate (HEMA), hydroxypropyl methacrylate, 2-ethoxyethyl methacrylate, methacrylonitrile, 2-trimethylsiloxyethyl methacrylate, glycidyl methacrylate (GMA) ), P-tolyl methacrylate, sorbyl methacrylate, methyl acrylate, ethyl Acrylate, propyl acrylate, butyl acrylate, hexyl acrylate, 2-ethylhexyl acrylate, octyl acrylate, lauryl acrylate, stearyl acrylate, phenyl acrylate, hydroxyethyl acrylate, hydroxypropyl acrylate, acrylonitrile, 2-trimethylsiloxyethyl acrylate, glycidyl acrylate, p- Examples include, but are not limited to, tolyl acrylate, sorbyl acrylate, benzyl acrylate, benzyl methacrylate, and 2-phenylethyl methacrylate.

  As the hydrophobic monomer, styrene, methyl methacrylate, butyl methacrylate, 2-ethylhexyl methacrylate, benzyl methacrylate, 2-phenylethyl methacrylate or benzyl acrylate is particularly preferable.

  Examples of the hydrophilic monomer include methacrylic acid (MAA), acrylic acid, maleic acid, dimethylaminoethyl methacrylate (DMAEMA), diethylaminoethyl methacrylate, 3-butylaminoethyl methacrylate, dimethylaminoethyl acrylate, and diethylamino. Examples include, but are not limited to, ethyl acrylate, dimethylaminopropyl methacrylamide, methacrylamide, acrylamide, dimethylacrylamide and the like.

  The hydrophilic monomer is preferably methacrylic acid, acrylic acid or dimethylaminoethyl methacrylate.

  Polymers containing acids can be produced directly from unsaturated acids or from blocked monomers with blocking groups that can be removed after polymerization. Examples of blocked monomers that yield acrylic acid or methacrylic acid after removal of the blocking group include trimethylsilyl methacrylate (TMS-MAA), trimethylsilyl acrylate, 1-butoxyethyl methacrylate, 1-ethoxyethyl methacrylate, 1-butoxyethyl Examples include acrylate, 1-ethoxyethyl acrylate, 2-tetrahydropyranyl acrylate, and 2-tetrahydropyranyl methacrylate.

  Examples of the structure of these polymers include random polymers, random copolymers, block copolymers, branched polymers or copolymers, graft polymers, and copolymers. Among these, a block copolymer and a branched copolymer are preferable for the purpose of the present invention because the design and control of the hydrophilic portion and the hydrophobic portion are easy.

  Examples of the block polymer include AB, BAB, and ABC type structures (here, A, B, and C schematically indicate polymer blocks having different structures from each other), but there is a block portion. If there is, there is no structural restriction. In particular, a block polymer having a hydrophobic block and a hydrophilic block, and having a balanced block size that contributes to dispersion stability is preferable. Functional groups can be incorporated into the hydrophobic block (block to which the colorant is attached), thereby further enhancing the specific interaction between the dispersant and the colorant to improve dispersion stability.

  These polymers can be synthesized by a conventionally known method, for example, US Pat. Nos. 5,085,698, 5,221,334, 5,272,201, and 5,519,085. No. 6,117,921, JP-A Nos. 10-279873, 11-269418, JP-A Nos. 2001-115065, 2001-13949, Nos. 2001-247796, 2003-260348 Can be synthesized by the methods disclosed in each of the above publications, particularly in the examples.

  Examples of the hydrophobic monomer that can be used in the block copolymer include monomers similar to the hydrophobic monomers that can be used in the acrylic polymer dispersant.

  As the hydrophobic monomer monomer, methyl methacrylate, butyl methacrylate, 2-ethylhexyl methacrylate, benzyl methacrylate, 2-phenylethyl methacrylate or benzyl acrylate is particularly preferable. The hydrophobic polymer block is preferably a polymer composed of the single monomer or a copolymer block composed of two or more monomers.

  Moreover, as a hydrophilic monomer monomer which can be used for a block copolymer, the monomer similar to the hydrophilic monomer which can be used for the said acrylic polymer dispersing agent can be mentioned, for example. .

  The hydrophilic monomer monomer is preferably methacrylic acid, acrylic acid or dimethylaminoethyl methacrylate, and the hydrophilic polymer polymer block is a polymer composed of a single monomer of the above monomers, or Copolymer homopolymers and copolymers composed of two or more monomers are preferred.

  Polymers containing acids can be produced directly from unsaturated acids or from blocked monomers with blocking groups that can be removed after polymerization. Examples of blocked monomers that yield acrylic acid or methacrylic acid after removal of the blocking group include trimethylsilyl methacrylate (TMS-MAA), trimethylsilyl acrylate, 1-butoxyethyl methacrylate, 1-ethoxyethyl methacrylate, 1-butoxyethyl Examples include acrylate, 1-ethoxyethyl acrylate, 2-tetrahydropyranyl acrylate, and 2-tetrahydropyranyl methacrylate.

  As the monomer that can be used in the branched polymer or copolymer, and the graft polymer or copolymer, those listed as monomers that can be used in the block copolymer may be used. it can. In addition, a macromer having a polymerizable functional group at one end, for example, a silicone macromer, a styrenic macromer, a polyester macromer, a polyurethane macromer, a polymer or copolymer easily branched by using a polyalkyl ether macromer, and a graft A polymer or copolymer can be synthesized. Examples of the macromer include styrene macromers AS-6 and AN-6 manufactured by Toagosei, silicone macromers FM-0711 and FM-0721 manufactured by Chisso, polyethylene glycol acrylate, polyethylene glycol methacrylate, and the like.

  These polymers preferably have a weight average molecular weight in the range of 1,000 to 30,000, more preferably in the range of 1,500 to 15,000. The acid value is preferably in the range of 10 to 500, and more preferably in the range of 50 to 250.

  In the ink according to the present invention, together with the above-described polymer dispersant, known pigment dispersants such as higher fatty acid salts, alkyl sulfates, alkyl ester sulfates, alkyl sulfonates, sulfosuccinates, naphthalene sulfonates, Combined use of activator such as alkyl phosphate, polyoxyalkylene alkyl ether phosphate, polyoxyalkylene alkyl phenyl ether, polyoxyethylene polyoxypropylene glycol, glycerin ester, sorbitan ester, polyoxyethylene fatty acid amide, amine oxide It does not prevent.

  In the water-based ink according to the present invention, the volume average particle size of the pigment dispersion is preferably 20 to 200 nm from the viewpoint of obtaining a preferable color tone, high density or good gloss, and further 40 to 140 nm. In addition, it is preferable from the viewpoint of improving light resistance.

  In the present invention, the volume average particle size of the pigment dispersion can be determined by a commercially available particle size measuring device using a light scattering method, electrophoresis method, laser Doppler method, etc. For example, Malvern Zetasizer 1000HS can be mentioned.

  Specific examples of water-soluble organic solvents that can be used in the present invention include alcohols (for example, methanol, ethanol, propanol, isopropanol, butanol, isobutanol, secondary butanol, tertiary butanol, pentanol, hexanol, and cyclohexanol. , Benzyl alcohol, etc.), polyhydric alcohols (for example, ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycol, butylene glycol, hexanediol, pentanediol, glycerin, hexanetriol, thio Diglycol, etc.), polyhydric alcohol ethers (eg, ethylene glycol monomethyl ether, ethylene glycol) Cole monoethyl ether, ethylene glycol monobutyl ether, ethylene glycol monophenyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, diethylene glycol dimethyl ether, propylene glycol monomethyl ether, propylene glycol monobutyl ether, ethylene glycol monomethyl ether acetate, triethylene Glycol monomethyl ether, triethylene glycol monoethyl ether, triethylene glycol monobutyl ether, triethylene glycol dimethyl ether, dipropylene glycol monopropyl ether, tripropylene glycol dimethyl ether, etc.), amines (for example, Tanolamine, diethanolamine, triethanolamine, N-methyldiethanolamine, N-ethyldiethanolamine, morpholine, N-ethylmorpholine, ethylenediamine, diethylenediamine, triethylenetetramine, tetraethylenepentamine, polyethyleneimine, pentamethyldiethylenetriamine, tetramethylpropylene Diamines, etc.), amides (eg, formamide, N, N-dimethylformamide, N, N-dimethylacetamide, etc.), heterocyclics (eg, 2-pyrrolidone, N-methyl-2-pyrrolidone, N-cyclohexyl-2) -Pyrrolidone, 2-oxazolidone, 1,3-dimethyl-2-imidazolidinone, etc.), sulfoxides (eg, dimethyl sulfoxide, etc.), sulfones (eg, sulfora ), Sulfonates (for example, 1-butanesulfonic acid sodium salt), acetonitrile, acetone and the like.

  The ink according to the present invention preferably contains urea or a urea derivative. By including urea or a urea derivative in the ink according to the present invention, aggregation of pigment particles in ink droplets that have landed on a recording medium can be prevented, and as a result, glossiness and texture can be improved. preferable. Since this urea or urea derivative expresses a desired effect by an interaction such as a hydrogen bond, it is preferable that the interaction has an appropriate strength. As such a compound, urea, thiourea, and urea derivatives substituted with lower alkyl groups (for example, methylurea, dimethylurea, butylurea, ethyleneurea, phenylurea, etc.) are preferable, and urea and ethyleneurea are particularly preferable. .

  In the colored ink according to the present invention, the content of urea is preferably 1 to 20% by mass from the viewpoint of obtaining an image having good emission stability and high gloss at a high density.

  The pH of the ink according to the present invention is preferably 7.0 or more, more preferably 8.05 to 10.0. By setting the above pH, the emission stability is good and the concentration is high. It is preferable from the viewpoint that an image having a preferable gloss can be obtained. Examples of the pH adjuster used in the ink according to the present invention include various organic amines such as monoethanolamine, diethanolamine, and triethanolamine, and alkali metal hydroxides such as sodium hydroxide, lithium hydroxide, and potassium hydroxide. Inorganic alkaline agents such as organic acids and mineral acids.

  The surface tension of the ink according to the present invention is preferably 30 to 50 mN / m. When the surface tension of the ink is less than 30 mN / m, the absorption speed to the recording medium is increased, causing aggregation due to the pigment particles, resulting in the occurrence of bronzing, gloss, and scratch resistance. On the other hand, when the surface tension of the ink exceeds 50 mN / m, the ink droplets that have landed on the recording medium cause color turbidity due to staying for a long time, and a high-definition image cannot be obtained.

  The surface tension defined in the present invention can be adjusted to a desired surface tension by appropriately adjusting the type and amount added, for example, using the various water-soluble organic solvents described above and the various surfactants described below. .

  The method for measuring the surface tension is described in general interface chemistry, colloid chemistry reference books, etc., for example, New Experimental Chemistry Course Vol. 18 (Interface and Colloid), The Chemical Society of Japan, edited by Maruzen. Issued by P .: 68-117 can be referred to, and specifically, it can be determined by using a ring method (Dunoi method) or a vertical plate method (Wilhelmy method).

  Various surfactants can be used as one means for achieving the surface tension. Each surfactant that can be used in the present invention is not particularly limited, and examples thereof include anionic surfactants such as dialkyl sulfosuccinates, alkyl naphthalene sulfonates, fatty acid salts, polyoxyethylene alkyl ethers, polyoxyethylene alkyl ethers, and the like. Nonionic surfactants such as oxyethylene alkyl allyl ethers, acetylene glycols, polyoxyethylene / polyoxypropylene block copolymers, and cationic surfactants such as alkylamine salts and quaternary ammonium salts . In particular, an anionic surfactant and a nonionic surfactant can be preferably used.

  In the present invention, an acetylene-based surfactant is used as the surfactant from the viewpoint of obtaining an image having good emission stability, favorable gloss at a high concentration, and excellent uniformity. preferable.

  The acetylene surfactant is not particularly limited, and examples thereof include acetylene glycols and acetylene alcohols. More preferable are surfactants having an acetylene group and an alkylene oxide chain. Nord 465 (manufactured by Nissin Chemical Industry Co., Ltd.) can be mentioned.

  In addition to the above description, the ink according to the present invention is publicly known depending on the purpose of improving the emission stability, print head and ink cartridge compatibility, storage stability, image storage stability, and other various performances as necessary. Various additives, such as viscosity modifiers, specific resistance regulators, film forming agents, UV absorbers, antioxidants, anti-fading agents, anti-fouling agents, rust inhibitors, etc. can be appropriately selected and used, For example, oil droplet fine particles such as liquid paraffin, dioctyl phthalate, tricresyl phosphate, silicone oil, ultraviolet absorbers described in JP-A-57-74193, JP-A-57-87988, and JP-A-62-261476, 57-74192, 57-87989, 60-72785, 61-146591, JP-A-1-95091 and 3-13376, etc. Anti-fading agents, fluorescent brightening agents described in JP-A-59-42993, JP-A-59-52689, JP-A-62-280069, JP-A-61-228771, JP-A-4-219266, etc. Can be mentioned.

  Next, the recording medium according to the present invention will be described.

  In general, the ink absorbing layer is roughly divided into a swelling type and a void type. As the swelling type, a water-soluble binder such as gelatin, polyvinyl alcohol, polyvinyl pyrrolidone, polyethylene oxide or the like is applied alone or in combination to form an ink absorbing layer. In order to adapt to printing, it is suitable that the ink absorption speed of the recording medium is faster. From this point, it is preferable to use an ink jet recording medium having a void-type ink absorbing layer.

One of the characteristics of the recording medium having a void-type ink absorption layer (also referred to as a void layer) according to the present invention is that the transition amount at an absorption time of 0.04 seconds according to the Bristow method is 10 ml / m ² or more. Yes, preferably 10 ml / m ² or more and 25 ml / m ² or less. When the transfer amount is less than 10 ml / m ² , the ink absorption speed of the recording medium is decreased, causing color turbidity when the ejected ink droplets are printed side by side, and a high-definition image cannot be obtained. .

  In the recording medium according to the present invention, the method for achieving the transition amount specified above is not particularly limited. The film thickness of the void layer, the average particle diameter of the inorganic fine particles (F) constituting the void layer, the hydrophilic binder ( This can be achieved by appropriately adjusting the type of B), the ratio (F / B) of the inorganic fine particles (F) to the hydrophilic binder (B), the type of support used, and the like.

The Bristow method referred to in the present invention is a method for measuring the liquid absorption behavior of paper and paperboard in a short time. TAPPI paper pulp test method no. It is measured according to the liquid absorptivity test method (Bristow method) of 51-87 paper or paperboard, and is represented by a transfer amount (ml / m ² ) at an absorption time of 0.04 seconds. In the above measurement method, pure water (ion-exchanged water) is used for the measurement, but in order to easily determine the measurement area, in the present invention, C.I. I. Measured using 2% water solubility of Acid Red 52.

  An example of a specific measurement method will be described below.

  As a method for measuring the amount of transition, the recording medium is allowed to stand for 12 hours or more in an atmosphere of 25 ° C. and 50% RH, and then, for example, a Bristow tester which is a liquid dynamic absorbency tester manufactured by Kumagai Riki Kogyo Co., Ltd. Measure using type II (pressure type). In the measurement, as described above, C.I. I. By using 2% water-soluble acid red 52 and measuring the area of the dyed portion on the recording medium after a specified contact time, the transfer amount can be determined.

  Further, the recording medium according to the present invention is characterized in that the 20-degree specular gloss according to JIS-Z-8741 is 20 to 45%.

  The 20-degree specular gloss referred to in the present invention is a 20-degree specular gloss value (%) measured according to the method defined in JIS-Z-8741. The specular gloss level correlates with the smoothness of the surface of the recording medium. The smoother the surface, the higher the specular gloss value. For this reason, if the 20 ° specular gloss is less than 20%, the smoothness of the surface of the recording medium is insufficient, and if a pigment image is formed thereon, the gloss of the entire image is lowered. Also, the specular gloss increases as the amount of pigment ink attached increases. At this time, if the specular gloss of the white background portion (the surface of the recording medium) where the pigment ink is not adhered is smaller than 20%, the difference in gloss between the image portion and the non-image portion becomes large, and only the image portion is It will appear floating.

  On the other hand, when trying to manufacture a recording medium having a 20-degree specular gloss exceeding 45%, enormous energy is required to smooth the surface, which is not practical. Further, if the surface is smoothed so that the specular gloss of 20 degrees exceeds 45%, the void layer of the recording medium is crushed, causing a decrease in absorption capacity and absorption speed, resulting in the color during image formation. It becomes cloudy and it becomes impossible to obtain a high-definition image. Therefore, by setting the 20-degree specular gloss between 20% and 45%, it is possible to suppress a phenomenon in which only an image portion peculiar to an image formed with pigment ink appears to be lifted, and to improve the sense of depth of the entire image. it can. In addition, a high-definition image can be formed without causing color turbidity. As a result, an image that approximates a silver salt photograph can be provided.

  The 20-degree specular gloss according to the present invention is, for example, a precision gloss meter GM-26D, True Gross GM-26DPRO, a variable angle gloss meter GM-3D (above, manufactured by Murakami Color Research Laboratory), a variable angle gloss meter VGS. -1000DP, VG-2000 (manufactured by Nippon Denshoku Industries Co., Ltd.), a digital variable gloss meter (manufactured by Suga Test Instruments Co., Ltd.), etc.

  In the recording medium according to the present invention, there is no particular limitation as a means for realizing the 20-degree specular gloss value (%) within the range specified in the present invention. For example, the support surface is smoothed in advance, and ink is formed thereon. A method of forming an absorption layer, a method of providing an ink absorption layer on a smooth support previously impregnated with boric acid, a method of forming a polymer fine particle layer on the surface of the ink absorption layer, and smoothing by heating and pressurizing treatment, ink A desired 20-degree specular gloss value (%) is obtained by a method of providing a gloss layer composed of inorganic fine particles and a binder on the surface of the absorption layer, a method of performing a smoothing process such as a calendar process after coating the ink absorption layer, and the like. Can do. For example, in the case of surface smoothing with a mirror roll, the calendar conditions are usually about 20 to 100 ° C., linear pressure 0.5 to 4 kN / cm, transport speed 10 to 500 m / min, and drying is performed at a temperature of 20 to 100 ° C. It is preferable to carry out in about 0.1 to 10 minutes.

  Hereinafter, details of each component of the ink jet recording medium according to the present invention will be described.

  Conventionally, various methods for forming voids in a film are known. For example, a uniform coating solution containing two or more kinds of polymers is applied on a support, and these polymers are mutually bonded in a drying process. A method of forming voids by phase separation, a coating liquid containing solid fine particles and a hydrophilic or hydrophobic resin is coated on a support, and after drying, the ink jet recording medium is changed to water or a liquid containing an appropriate organic solvent. A method of creating voids by immersing and dissolving solid fine particles, and a method of forming voids in a film by applying a coating solution containing a compound having a property of foaming during film formation and then foaming this compound in the drying process , A method in which a coating liquid containing porous solid fine particles and a hydrophilic binder is coated on a support to form voids in the porous fine particles or between the fine particles; Yes That solid particulates and or a coating solution containing a particulate oil and a hydrophilic binder is coated on a support, and a method of forming an air gap between the solid particles are known.

  The void layer according to the present invention is preferably an ink receiving layer formed mainly from inorganic fine particles and a small amount of a hydrophilic binder and having a porosity of 30 to 70%. If the porosity is 30% or more, a desired ink absorption rate can be achieved without unnecessarily increasing the film thickness, and if it is 70% or less, the ink absorption rate is not excessively high. In addition, failures (cracks) in the coating and drying processes can be prevented, and high-definition images can be obtained stably.

  In the present invention, the void layer is formed by containing inorganic fine particles having an average particle diameter of 15 to 100 nm, preferably the average particle diameter is 20 to 80 nm. When the average particle diameter exceeds 100 nm, the surface gloss of the coating film is deteriorated.

  Examples of the inorganic fine particles used for the above purpose include light calcium carbonate, heavy calcium carbonate, magnesium carbonate, kaolin, clay, talc, calcium sulfate, barium sulfate, titanium dioxide, zinc oxide, zinc hydroxide, zinc sulfide. , Zinc carbonate, hydrotalcite, aluminum silicate, diatomaceous earth, calcium silicate, magnesium silicate, synthetic amorphous silica, colloidal silica, alumina, colloidal alumina, pseudoboehmite, aluminum hydroxide, lithopone, zeolite, magnesium hydroxide, etc. A white inorganic pigment etc. can be mentioned.

  The average particle size of the inorganic fine particles in the present invention is determined by observing the cross section and surface of the void layer of the recording medium with an electron microscope, measuring the particle size of 1,000 arbitrary particles, and calculating the simple average value (number average). As required. Here, the particle diameter of each particle is represented by a diameter assuming a circle equal to the projected area. Silica or alumina is preferably used as the inorganic fine particles.

  As the silica that can be used in the present invention, silica synthesized by a usual wet method, colloidal silica, silica synthesized by a gas phase method, or the like is preferably used. In particular, colloidal silica or fine particle silica synthesized by a gas phase method is preferable. Among them, fine particle silica synthesized by a gas phase method forms a so-called soft agglomerated structure by coexisting with a hydrophilic binder and gives a high porosity. Have Furthermore, when added to a cationic polymer used for the purpose of fixing the coloring material, coarse aggregates are hardly formed, which is preferable.

  The alumina or alumina hydrate that can be used in the present invention may be crystalline or amorphous, and those having an arbitrary shape such as amorphous particles, spherical particles, and acicular particles are used. be able to. Among these, alumina hydrate having a plate-like shape with an average aspect ratio of 1 to 4 is particularly preferable. Alumina hydrate has a fibrous shape and a plate-like shape, but when fibrous alumina hydrate is used, it tends to be oriented parallel to the substrate surface during coating. Therefore, the formed pores are small. On the other hand, in the case of plate-like alumina hydrate, the tendency to be oriented in a certain direction by coating is small, and a relatively large porosity can be obtained.

  Examples of the hydrophilic binder that can be used in the void layer according to the present invention include polyvinyl alcohol, gelatin, polyethylene oxide, polyvinyl pyrrolidone, polyacrylic acid, polyacrylamide, polyurethane, dextran, dextrin, color ginnan (κ, ι, λ Etc.), agar, pullulan, water-soluble polyvinyl butyral, hydroxyethyl cellulose, carboxymethyl cellulose and the like. These water-soluble binders can be used in combination of two or more. However, the hygroscopic property of the binder is relatively small, the curling of the recording medium is small, and the binder ability of the inorganic fine particles is high and cracked with a small amount of use. In particular, polyvinyl alcohol or a derivative thereof is particularly preferable from the viewpoint of excellent film adhesion.

  As polyvinyl alcohol preferably used in the present invention, in addition to ordinary polyvinyl alcohol obtained by hydrolyzing polyvinyl acetate, modified polyvinyl alcohol such as polyvinyl alcohol having a cation-modified terminal or anion-modified polyvinyl alcohol having an anionic group. Alcohol is also included.

  The polyvinyl alcohol obtained by hydrolyzing vinyl acetate preferably has an average degree of polymerization of 300 or more, particularly preferably an average degree of polymerization of 1,000 to 5,000, and a saponification degree of 70. -100% is preferable, and 80-99.8% is particularly preferable.

  Examples of the cation-modified polyvinyl alcohol include primary to tertiary amino groups and quaternary amino groups in the main chain or side chain of the polyvinyl alcohol as described in JP-A-61-10383. Polyvinyl alcohol, which is obtained by saponifying a copolymer of an ethylenically unsaturated monomer having a cationic group and vinyl acetate.

  Examples of the ethylenically unsaturated monomer having a cationic group include trimethyl- (2-acrylamido-2,2-dimethylethyl) ammonium chloride and trimethyl- (3-acrylamido-3,3-dimethylpropyl) ammonium chloride. N-vinylimidazole, N-methylvinylimidazole, N- (3-dimethylaminopropyl) methacrylamide, hydroxyethyltrimethylammonium chloride, trimethyl- (3-methacrylamidopropyl) ammonium chloride, and the like.

  The ratio of the cation-modified group-containing monomer of the cation-modified polyvinyl alcohol is 0.1 to 10 mol%, preferably 0.2 to 5 mol%, relative to vinyl acetate.

  Examples of the anion-modified polyvinyl alcohol include polyvinyl alcohol having an anionic group described in JP-A-1-206088, vinyl described in JP-A-61-237681 and JP-A-63-330779. Examples thereof include a copolymer of an alcohol and a vinyl compound having a water-soluble group, and a modified polyvinyl alcohol having a water-soluble group described in JP-A-7-285265.

  Nonionic modified polyvinyl alcohol includes, for example, a polyvinyl alcohol derivative obtained by adding a polyalkylene oxide group described in JP-A-7-9758 to a part of vinyl alcohol, and described in JP-A-8-25795. And a block copolymer of a vinyl compound having a hydrophobic group and vinyl alcohol.

  Polyvinyl alcohol can be used in combination of two or more, such as the degree of polymerization and the type of modification. In particular, when using polyvinyl alcohol having a degree of polymerization of 2,000 or more, the degree of polymerization is from 0.05 to 10% by weight, preferably 0.1 to 5% by weight, based on the inorganic fine particles. Addition of 2,000 or more polyvinyl alcohol is preferred because there is no significant thickening.

  The ratio of the inorganic fine particles to the hydrophilic binder in the void layer is preferably 2 to 20 by mass ratio. If the mass ratio is 2 times or more, a porous film having a sufficient porosity can be obtained, it becomes easy to obtain a sufficient void volume, and does not cause a situation where the voids are blocked by swelling during ink jet recording with a hydrophilic binder that can be maintained. As a result, a high ink absorption speed can be maintained. On the other hand, if this ratio is 20 times or less, cracks are less likely to occur when the gap layer is applied as a thick film. The ratio of the inorganic fine particles to the particularly preferred hydrophilic binder is 2.5 to 12 times, most preferably 3 to 10 times.

In the void layer, the total amount of voids (void volume) is preferably 16 ml or more per 1 m ² of the recording medium. By setting the void volume to 16 ml / m ² or more, the ink absorbability can be improved even when the amount of ink increases, so that the image quality can be improved and the decrease in the drying property can be suppressed.

On the other hand, the upper limit of the void volume is preferably 25 ml / m ² or less. As the number of voids increases, the absorption rate and the absorption capacity increase, but on the other hand, it becomes brittle against external pressure. Therefore, when it is going to enlarge a film thickness, it has the difficulty that it will become easy to produce a crack at the time of manufacture. Although it is possible to increase the absorption rate and the absorption capacity by increasing the porosity even if the film thickness remains as it is, it is also vulnerable to cracking. Various studies have been made to overcome these difficulties, but at present, when the film thickness or porosity is such that the absorption capacity per unit area exceeds 25 ml / m ² , microcracks are generated during manufacturing. As a result, a high-quality image cannot be formed. Therefore, a recording medium having a void layer is preferably designed and manufactured so that the absorption capacity per unit area is such that the film thickness or void ratio exceeds 25 ml / m ² .

  In the present invention, the void volume refers to the saturated water absorption determined by the Bristow method. When the transfer amount obtained by the Bristow method is plotted against the square root of the absorption time, a line having a certain slope is obtained. This indicates a change in the amount of absorption with respect to the absorption time of the recording medium, and when the ink (herein, 2% aqueous solution of CI Acid Red 52) is absorbed to the full void volume, there is no room, so the slope is 0. It becomes. The water absorption at this time is regarded as a value representing the void volume, with the saturated water absorption. In the case of a recording medium having a water-absorbing support preferably used in the present invention, the support may be absorbed in addition to ink absorption by the ink absorbing layer. In the recording medium used in the present invention, the ink absorption speed of the ink absorption layer is overwhelmingly faster than that of the support, so even if the absorption of the support is measured, the curve has a two-step slope. Discrimination is easy.

The porosity in the present invention refers to the ratio of the total volume of voids to the volume of the void layer. As the total volume of the voids, the void volume determined by the Bristow method can be used as it is. The volume of the void layer can be obtained as a volume per 1 m ² of the recording medium by measuring the dry film thickness. The target porosity can be obtained by calculation as a ratio of both volumes. Further, the total volume of the voids can be easily obtained by measuring the saturation transition amount or water absorption amount by Bristow measurement.

  In addition to inorganic fine particles and binders, various additives can be used for the void layer. Among them, cationic polymers, curing agents, urea or derivatives thereof improve bleeding resistance, bronzing resistance, and scratch resistance. Play an important role in terms.

Examples of cationic polymers include polyethyleneimine, polyallylamine, polyvinylamine, dicyandiamide polyalkylene polyamine condensate, polyalkylene polyamine dicyandiamide ammonium salt condensate, dicyandiamide formalin condensate, epichlorohydrin-dialkylamine addition polymer, diallyldimethylammonium Chloride polymer, diallyldimethylammonium chloride / SO ₂ copolymer, polyvinyl imidazole, vinyl pyrrolidone / vinyl imidazole copolymer, polyvinyl pyridine, polyamidine, chitosan, cationized starch, vinyl benzyl trimethyl ammonium chloride polymer, (2-metachlor Yloxyethyl) trimethylammonium chloride polymer, dimethylaminoethyl methacrylate Such as theft polymerization products thereof.

  Examples include the cationic polymers described in Chemical Industry Times, August 15 and 25, 1998, and polymer dye fixing agents described in “Introduction to Polymer Drugs” issued by Sanyo Chemical Industries, Ltd.

  In the recording medium according to the present invention, it is preferable to add a curing agent of a water-soluble binder that forms a void layer.

  The curing agent that can be used for the hardening of the water-soluble binder that forms the void layer in the present invention is not particularly limited as long as it causes a curing reaction with the water-soluble binder. Although other known compounds can be used, they are generally compounds having a group capable of reacting with a water-soluble binder or compounds that promote the reaction between different groups of a water-soluble binder. It is appropriately selected depending on the type of binder. Specific examples of the curing agent include, for example, epoxy curing agents (diglycidyl ethyl ether, ethylene glycol diglycidyl ether, 1,4-butanediol diglycidyl ether, 1,6-diglycidyl cyclohexane, N, N-diglycidyl- 4-glycidyloxyaniline, sorbitol polyglycidyl ether, glycerol polyglycidyl ether, etc.), aldehyde curing agents (formaldehyde, glioxal, etc.), active halogen curing agents (2,4-dichloro-4-hydroxy-1,3,5) -S-triazine, etc.), active vinyl compounds (1,3,5-trisacryloyl-hexahydro-s-triazine, bisvinylsulfonylmethyl ether, etc.), aluminum alum and the like.

  Boric acid or a salt thereof refers to an oxygen acid having a boron atom as a central atom and a salt thereof, specifically, orthoboric acid, diboric acid, metaboric acid, tetraboric acid, pentaboric acid, and octaboron. Examples include acids and their salts.

  Boric acid having a boron atom and a salt thereof as a curing agent may be used as a single aqueous solution or as a mixture of two or more. Particularly preferred is a mixed aqueous solution of boric acid and borax. The aqueous solutions of boric acid and borax can be added only in relatively dilute aqueous solutions, respectively, but by mixing them both can be made into a concentrated aqueous solution and the coating solution can be concentrated. Further, there is an advantage that the pH of the aqueous solution to be added can be controlled relatively freely. The total amount of the curing agent used is preferably 1 to 600 mg per 1 g of the water-soluble binder.

  The recording medium according to the present invention can contain a polyvalent metal ion. The polyvalent metal ion is not particularly limited as long as it is a divalent or higher-valent metal ion, but preferable polyvalent metal ions include aluminum ions, zirconium ions, titanium ions, and the like. These polyvalent metal ions can be contained in the void layer in the form of a water-soluble or water-insoluble salt.

  These polyvalent metal ions may be used alone or in combination of two or more different kinds. The compound containing polyvalent metal ions may be added to the coating solution for forming the void layer, or after the void layer is once coated, in particular after the void layer is once coated and dried, an overcoat method is applied to the void layer. You may supply. When adding a compound containing polyvalent metal ions to the coating solution for forming the ink absorbing layer as in the former, a method of uniformly dissolving in water, an organic solvent or a mixed solvent thereof, or wet grinding such as a sand mill A method of dispersing and adding to fine particles by a method such as a method or emulsification dispersion can be used. When the void layer is composed of a plurality of layers, only one layer may be added, or it may be added to a coating solution of two or more layers or all of the constituent layers. In addition, when a void layer is once formed and then added by an overcoat method as in the latter case, it is preferable that a compound containing a polyvalent metal ion is uniformly dissolved in a solvent and then supplied to the void layer.

These polyvalent metal ions are generally used in an amount of 0.05 to 20 mmol, preferably 0.1 to 10 mmol, per 1 m ² of the recording medium.

  Various additives other than those described above can be added to the void layer according to the present invention. For example, organic latex fine particles such as polystyrene, polyacrylic acid esters, polymethacrylic acid esters, polyacrylamides, polyethylene, polypropylene, polyvinyl chloride, polyvinylidene chloride, or a copolymer thereof, urea resin, or melamine resin , Various cationic or nonionic surfactants, ultraviolet absorbers described in JP-A-57-74193, JP-A-57-87988, and JP-A-62-261476, JP-A-57-74192, JP-A-57-87989, JP-A-60-27285, JP-A-61-146591, JP-A-1-95091 and JP-A-3-13376, etc., and JP-A-59-42993, JP-A-59-52689, JP-A-62. -280069, 61-242871 and JP-A-4-219266. Brighteners, sulfuric acid, phosphoric acid, citric acid, sodium hydroxide, potassium hydroxide, potassium carbonate and other pH adjusters, antifoaming agents, preservatives, thickeners, antistatic agents, mats Various known additives such as an agent can also be contained.

  As the support for the recording medium according to the present invention, either an absorptive support or a non-absorbent support can be used. From the viewpoint of fully achieving the object effects of the present invention, for example, plain paper, baryta It is preferable to use an absorbent support that is a paper support such as paper, art paper, coated paper, and cast coated paper.

  Examples of the water-absorbing support of the present invention include sheets and plates having general paper, synthetic paper, cloth, wood and the like, but especially paper is excellent in water absorption of the substrate itself and is cost-effective. It is most preferable because it is excellent. The paper support will be described below.

The raw material for paper support is mainly made of wood pulp such as chemical pulp such as LBKP and NBKP, mechanical pulp such as GP, CGP, RMP, TMP, CTMP, CMP and PGW, and waste paper pulp such as DIP. Can be used, but it is preferred to use hardwood pulp. As hardwood pulp, kraft pulp, sulfite pulp, chemi-thermomechanical pulp, chemimechanical pulp or the like may be used alone or in combination. Further, if necessary, paper is made using synthetic pulp such as polypropylene or synthetic fiber such as nylon or polyester in addition to wood pulp.

  Moreover, it is preferable that the pulp which is a raw material is bleached with a peroxide etc. from the point of the improvement of whiteness. Bleaching treatment involves cooking pulp, chlorination, alkali treatment or extraction or refining, hypochlorite bleaching, chlorine dioxide bleaching, and combinations thereof, multistage bleaching treatment, and hydrosulfite, borohydride as necessary It is preferably applied after reductive bleaching with sodium or the like. More preferably, the alkaline peroxide bleaching treatment may be performed as a final pulp bleaching treatment after cooking the pulp and after the conventionally known pulp bleaching treatment, but with alkali treatment or extraction or purification. Also good.

  In the paper support, various conventionally known additives such as sizing agents, pigments, paper strength enhancers, fixing agents, fluorescent whitening agents, wet paper strength agents, and cationizing agents may be added as necessary. Can do. As the sizing agent, a sizing agent such as higher fatty acid, alkyl ketene dimer, rosin, paraffin wax, alkenyl succinic acid, petroleum resin emulsion and the like can be added as necessary. Examples of the pigment include calcium carbonate, talc, titanium oxide, and urea resin fine particles, examples of the paper strength enhancer include starch, polyacrylamide, and polyvinyl alcohol, and examples of the fixing agent include a sulfate band and a cationic polymer electrolyte. It is not limited to this.

  The paper support can be produced by mixing various fiber materials such as wood pulp and various additives with various paper machines such as a long net paper machine, a circular net paper machine, and a twin wire paper machine. Further, if necessary, a size press treatment with starch, polyvinyl alcohol or the like, a various coating treatment, or a calendar treatment can be performed at the paper making stage or after paper making.

The paper density is generally 0.7 to 1.2 g / cm ³ (JIS-P-8118). Furthermore, the base paper stiffness is preferably 20 to 200 g under the conditions specified in JIS-P-8143.

  The pH of the paper is preferably 5 to 9 when measured by the hot water extraction method defined in JIS-P-8113.

  In the present invention, for the purpose of increasing the adhesive strength between the support and the ink receiving layer, the support is subjected to corona discharge treatment, subbing treatment, intermediate layer coating, etc. prior to application of the ink receiving layer. be able to.

  Next, the manufacturing method of the inkjet recording medium of this invention is demonstrated.

  As the method for producing the ink jet recording medium of the present invention, each component layer including the ink absorbing layer is selected from a known coating method, either individually or simultaneously, and coated and dried on a support. Can do. Examples of the coating method include a roll coating method, a rod bar coating method, an air knife coating method, a spray coating method, a curtain coating method, and U.S. Pat. Nos. 2,761,419 and 2,761,791. A slide bead coating method using a hopper, an extrusion coating method or the like is preferably used.

  When the slide bead coating method is used, the viscosity of each coating solution at the time of simultaneous multilayer coating is preferably in the range of 5 to 100 mPa · s, more preferably in the range of 10 to 70 mPa · s. Moreover, when using a curtain application | coating system, the range of 5-1200 mPa * s is preferable, More preferably, it is the range of 25-500 mPa * s.

  Further, the viscosity at 15 ° C. of the coating solution is preferably 100 mPa · s or more, more preferably 100 to 30,000 mPa · s, further preferably 3,000 to 30,000 mPa · s, and most preferably 10 , 30,000 to 30,000 mPa · s.

  As a coating and drying method, the coating liquid is heated to 30 ° C. or higher, and after simultaneous multilayer coating is performed, the temperature of the formed coating film is once cooled to 1 to 15 ° C. and dried at 10 ° C. or higher. Is preferred. More preferably, the drying conditions are a wet bulb temperature of 5 to 50 ° C. and a film surface temperature of 10 to 50 ° C. Moreover, as a cooling method immediately after application | coating, it is preferable to carry out by a horizontal set system from a viewpoint of the formed coating-film uniformity.

  EXAMPLES Hereinafter, the present invention will be specifically described with reference to examples, but the present invention is not limited thereto.

Example 1
<Production of recording medium>
[Preparation of recording medium 1]
(Production of support)
1 part of polyacrylamide, 4 parts of ash (talc), 2 parts of cationized starch, 0.5 part of polyamide epichlorohydrin resin and 100 parts of wood pulp (LBKP / NBSP = 50/50) Slurry liquids containing various addition amounts of alkyl ketene dimer (sizing agent) were prepared, and base paper was made using a long paper machine so that the basis weight was 170 g / m ² . The base paper was supercalendered to produce a support that is a water-absorbing support having a smooth surface. Further, 3% boric acid aqueous solution was applied and dried with a roll coater to prepare a support 1 impregnated with 0.1 g / m ² boric acid.

After corona discharge is applied to the support 1, a gelatin subbing layer containing a hardener is 0.04 g / m ² as a solid content, and on the back side, silica fine particles (matting agent) having an average particle size of about 1 μm and a small amount A styrene / acrylic emulsion containing a cationic polymer (conductive agent) was applied so that the dry film thickness was about 0.5 μm.

[Preparation of coating liquid for ink absorbing layer]
A coating solution for an ink absorbing layer (void layer) was prepared according to the following procedure.

(Preparation of titanium oxide dispersion)
20 kg of titanium oxide having an average particle size of about 0.25 μm (Ishihara Sangyo: W-10), 150 g of sodium tripolyphosphate with pH = 7.5, 500 g of polyvinyl alcohol (Kuraray Co., Ltd .: PVA235), cationic It is added to 90 L of an aqueous solution containing 150 g of polymer (P-1) and 10 g of antifoam SN381 manufactured by Sannobuco, and dispersed with a high-pressure homogenizer (Sanwa Kogyo Co., Ltd.). A uniform titanium oxide dispersion was obtained.

(Preparation of silica dispersion 1)
Water 71L
Boric acid 0.27kg
Borax 0.24kg
Ethanol 2.2L
25% aqueous solution of cationic polymer P-1 17L
Anti-fading agent (AF1 * 1) 10% aqueous solution 8.5L
Optical brightener (* 2) aqueous solution 0.1L
The entire amount was finished to 100 L with pure water.

  As inorganic fine particles, 50 kg of silica fine particles (average primary particle diameter of about 35 nm) are prepared, and after adding the above-mentioned additives, the fine particles are dispersed by the dispersion method described in Example 5 of JP-A-2002-47454. Silica dispersion 1 was obtained.

* 1: anti-fading agent (AF-1) HO-N (C 2 H 4 SO 3 Na) 2
* 2: UVITEX NFW LIQUID manufactured by Ciba Specialty Chemicals
(Preparation of silica dispersion 2)
In the preparation of the silica dispersion 1, the silica dispersion 2 was prepared in the same manner except that the cationic polymer (P-1) was changed to the cationic polymer (P-2).

(Preparation of coating solution)
Each coating solution of the first layer, the second layer, the third layer, and the fourth layer was prepared by the following procedure.

<Coating liquid for first layer>
The following additives were sequentially mixed with 610 ml of silica dispersion 1 while stirring at 40 ° C.

5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA235)
220ml
5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA245)
80ml
Titanium oxide dispersion 30ml
15 ml of polybutadiene dispersion (average particle size: about 0.5 μm, solid content: 40%)
Surfactant (SF1) 5% aqueous solution 1.5ml
The whole amount was finished to 1000 ml with pure water.

<Second layer coating solution>
The following additives were sequentially mixed with 630 ml of silica dispersion 1 while stirring at 40 ° C.

5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA235)
180ml
5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA245)
80ml
15 ml of polybutadiene dispersion (average particle size: about 0.5 μm, solid content: 40%)
The whole amount was finished to 1000 ml with pure water.

<Coating liquid for third layer>
The following additives were sequentially mixed with 650 ml of silica dispersion 2 while stirring at 40 ° C.

5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA235)
180ml
5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA245)
80ml
The whole amount was finished to 1000 ml with pure water.

<Fourth layer coating solution>
The following additives were sequentially mixed with 650 ml of silica dispersion 2 while stirring at 40 ° C.

5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA235)
180ml
5% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA245)
80ml
Saponin 50% aqueous solution 4ml
Surfactant (SF1) 5% aqueous solution 6ml
The whole amount was finished to 1000 ml with pure water.

  Each coating solution prepared as described above was subjected to two-stage filtration with a filter capable of collecting 20 μm.

  Each of the above coating solutions is 30 to 80 mPa · s at 40 ° C. and 30000 to 100,000 mPa.s at 15 ° C. The viscosity characteristic of s was shown.

(Application)
Each coating solution obtained in this way was placed on the front side of the support 1 produced above on the first layer (35 μm), the second layer (45 μm), the third layer (45 μm), and the fourth layer (40 μm). Each layer was simultaneously applied so that In addition, the numerical value in the parenthesis of each layer shows each wet film thickness. For coating, each coating solution was simultaneously coated at a coating width of about 1.5 m and a coating speed of 100 m / min using a four-layer curtain coater at 40 ° C., and then subjected to a calendar process using a mirror roll. .

Immediately after coating, the film is cooled for 20 seconds in a cooling zone maintained at 8 ° C., then 20 to 30 ° C., relative humidity 20% or less for 30 seconds, 60 ° C., relative humidity 20% or less for 120 seconds, 55 ° C., relative humidity 20%. It dried by blowing each drying wind for 60 seconds below. Thereafter, the surface was calendered, further conditioned in a humidity control zone at 23 ° C. and a relative humidity of 40 to 60%, and wound into a roll to obtain a recording medium 1. The obtained recording medium 1 was then heated and stored at 40 ° C. for 5 days in the form of a roll, and then cut into a predetermined size. The porosity of the recording medium 1 was 55% as a result of measurement by the method described later. Further, the amount of transfer at an absorption time of 0.04 seconds according to the Bristow method was determined according to the method described later, and as a result, it was 16 ml / m ² . In addition, according to JIS-Z-8741, the 20-degree specular glossiness on the ink absorption layer coating surface side was measured using a digital variable angle gloss meter (manufactured by Suga Test Instruments Co., Ltd.) and found to be 24%.

[Preparation of recording medium 2]
In the production of the recording medium 1, the support 1 is changed to the following support 2, and the composition ratio (F / B) of the silica fine particles (F) and the polyvinyl alcohol (B) in each ink absorption layer is appropriately changed. Thus, a recording medium 2 having a transfer amount of 8 ml / m ² at an absorption time of 0.04 seconds according to the Bristow method was produced.

(Preparation of support 2)
1 part of polyacrylamide, 4 parts of ash (talc), 2 parts of cationized starch, 0.5 part of polyamide epichlorohydrin resin and 100 parts of wood pulp (LBKP / NBSP = 50/50) Slurry liquids containing various addition amounts of alkyl ketene dimer (sizing agent) were prepared, and base paper was made using a long paper machine so that the basis weight was 170 g / m ² . After calendering the base paper, a low-density polyethylene resin having a density of 0.92 containing 7% anatase-type titanium oxide and a small amount of a color tone adjusting agent is melt-extruded and coated at 320 ° C. to a thickness of 28 μm. And coated one side of the base paper. Immediately after melt extrusion coating, a cooling roll having various regular unevenness heights was pressure-cooled on the surface, and various fine grain surface forming treatments were performed on the polyethylene surface. The difference in the molding was made by adjusting the density and the height of the unevenness.

  Next, the opposite surface is a high density polyethylene with a density of 0.96 / low density polyethylene with a density of 0.92 = 70/30. A support 2 that is a non-water-absorbing support was produced by coating.

After performing corona discharge on the titanium oxide-containing layer surface side of the support 2, a gelatin subbing layer containing a hardener is 0.04 g / m ² as a solid content, and on the back surface is a silica fine particle having an average particle diameter of about 1 μm. A styrene / acrylic emulsion containing (matting agent) and a small amount of a cationic polymer (conductive agent) was applied so that the dry film thickness was about 0.5 μm.

[Preparation of recording medium 3]
In the production of the recording medium 2, the composition ratio (F / B) of silica fine particles and polyvinyl alcohol in each ink absorption layer is appropriately changed so that the transfer amount at an absorption time of 0.04 seconds by the Bristow method is 16 ml / m ² . A recording medium 3 was produced.

[Preparation of recording medium 4]
In the production of the recording medium 1, the composition ratio (F / B) of silica fine particles and polyvinyl alcohol in each ink absorption layer is appropriately changed, and the transfer amount at an absorption time of 0.04 seconds by the Bristow method is 11 ml / m ² . A recording medium 4 was produced. Moreover, when the porosity was measured by the method described later, it was 35%.

[Preparation of recording medium 5]
(Preparation of coating solution)
Alumina hydrate (manufactured by Sasol: Dispersal HP18) 0.50 kg
10L of pure water
1 mol / L hydrochloric acid was added to the dispersion to adjust the pH to 4, and the mixture was stirred at 95 ° C. for 2 hours. Subsequently, 1 mol / L sodium hydroxide aqueous solution was added, pH was adjusted to 10, and also it stirred for 8 hours. After stirring, the mixture was cooled to room temperature, the pH was adjusted to 7-8, desalted, and acetic acid was further added for peptization. After concentrating to a solid content of 17%, a 9% aqueous solution of polyvinyl alcohol (Kuraray Industrial Co., Ltd .: PVA117) was mixed so that the solid content ratio of alumina to polyvinyl alcohol was 10: 1 by mass ratio. The mixture was stirred to obtain a coating solution.

The coating solution prepared as described above was filtered through a 20 μm-capable filter. This coating solution was applied onto a base material (whiteness 89%) of a base material having a variator layer subjected to a supercalender treatment so that the dry film thickness was 30 g / m ² by a die coater. The substrate was previously coated with an aqueous boric acid solution and dried so that the boric acid content was 0.5 g / m ² . The coating speed at this time was 50 m / min, and the recording medium 5 was produced by drying at a temperature of 150 ° C.

The average particle diameter of the alumina particles in this recording medium 5 was 30 nm. Further, the transfer amount at an absorption time of 0.04 seconds by the Bristow method was 22 ml / m ² , and the porosity was 55%.

[Preparation of recording media 6 to 8]
In the production of the recording medium 1, the silica fine particles (average primary particle size of about 35 nm) used for the preparation of each ink absorption layer coating solution were changed to silica fine particles having the average particle size shown in Table 1 in the same manner. Thus, recording media 6 to 8 were produced. Table 1 shows the transfer amount and porosity of each recording medium.

[Preparation of recording medium 9]
A recording medium 9 was produced in the same manner as in the production of the recording medium 1 except that boric acid and borax used for the preparation of each ink absorption layer coating solution were omitted.

[Preparation of recording media 10 and 11]
In the production of the recording medium 1, the same except that the composition ratio (F / B) of silica fine particles and polyvinyl alcohol in each ink absorption layer was appropriately changed so that the porosity of the ink absorption layer was 25% and 75%, respectively. Thus, recording media 10 and 11 were produced. The porosity of each recording medium was as shown in Table 1.

[Preparation of recording media 12 to 15]
In the production of the recording medium 1, except that the treatment temperature and linear pressure of the calendar treatment performed immediately after coating and drying were appropriately changed so that the 20-degree specular gloss was 18%, 22%, 42%, and 47%, respectively. In the same manner, recording media 12 to 15 were produced.

<Preparation of ink>
[Preparation of colored ink set 1]
(Preparation of pigment dispersion)
<Preparation of Yellow Pigment Dispersion 1>
After adding 1.5 g of anthranilic acid to 10 g of 6 mol / L hydrochloric acid solution, the mixture was cooled to 5 ° C., and 1.8 g of sodium nitrite was added and stirred. There, C.I. I. 5 g of Pigment Yellow 74 powder was added, the temperature of the solution was raised to 80 ° C. while stirring, and heating was continued until no nitrogen gas was generated, followed by cooling. Next, acetone is added, and the pigment particles are filtered and washed with ion-exchanged water. Then, ion-exchanged water is added to perform ion exchange, ultrafiltration, and centrifugation, and the pigment content is 20 with ion-exchanged water. A yellow pigment dispersion 1 was obtained by adjusting to a mass%.

<Preparation of magenta pigment dispersion 1>
After adding 1.5 g of anthranilic acid to 10 g of 6 mol / L hydrochloric acid solution, the mixture was cooled to 5 ° C., and 1.8 g of sodium nitrite was added and stirred. There, C.I. I. 5 g of Pigment Red 122 powder was added, the temperature of the solution was raised to 80 ° C. while stirring, and heating was continued until no nitrogen gas was generated, followed by cooling. Next, acetone is added, and the pigment particles are filtered and washed with ion-exchanged water. Then, ion-exchanged water is added to perform ion exchange, ultrafiltration, and centrifugation, and the pigment content is 25 with ion-exchanged water. The magenta pigment dispersion 1 was obtained by adjusting the mass%.

<Preparation of Cyan Pigment Dispersion 1>
After adding 1.5 g of anthranilic acid to 10 g of 6 mol / L hydrochloric acid solution, the mixture was cooled to 5 ° C., and 1.8 g of sodium nitrite was added and stirred. There, C.I. I. 5 g of Pigment Blue 15: 3 powder was added, the temperature of the solution was raised to 80 ° C. while stirring, and heating was continued until generation of nitrogen gas disappeared, followed by cooling. Next, acetone is added, and the pigment particles are filtered and washed with ion-exchanged water. Then, ion-exchanged water is added to perform ion exchange, ultrafiltration, and centrifugation, and the pigment content is 25 with ion-exchanged water. The cyan pigment dispersion 1 was obtained by adjusting the amount to be mass%.

<Preparation of Black Pigment Dispersion 1>
After adding 1.5 g of anthranilic acid to 10 g of 6 mol / L hydrochloric acid solution, the mixture was cooled to 5 ° C., and 1.8 g of sodium nitrite was added and stirred. Thereto, 5 g of carbon black powder was added, the liquid temperature was raised to 80 ° C. while stirring, and heating was continued until no nitrogen gas was generated, followed by cooling. Next, acetone is added, and the pigment particles are filtered and washed with ion-exchanged water. Then, ion-exchanged water is added to perform ion exchange, ultrafiltration, and centrifugation, and the pigment content is 20 with ion-exchanged water. The black pigment dispersion 1 was obtained by adjusting the amount to be mass%.

<Preparation of Blue Pigment Dispersion 1>
After adding 1.5 g of anthranilic acid to 10 g of 6 mol / L hydrochloric acid solution, the mixture was cooled to 5 ° C., and 1.8 g of sodium nitrite was added and stirred. There, C.I. I. 5 g of the powder of Pigment Violet 23 was added, the temperature of the liquid was raised to 80 ° C. while stirring, and heating was continued until no nitrogen gas was generated, followed by cooling. Next, acetone is added, and the pigment particles are filtered and washed with ion-exchanged water. Then, ion-exchanged water is added to perform ion exchange, ultrafiltration, and centrifugation, and the pigment content is 25 with ion-exchanged water. The blue pigment dispersion 1 was obtained by adjusting the amount to be mass%.

<Preparation of Red Pigment Dispersion 1>
After adding 1.5 g of anthranilic acid to 10 g of 6 mol / L hydrochloric acid solution, the mixture was cooled to 5 ° C., and 1.8 g of sodium nitrite was added and stirred. There, C.I. I. 5 g of Pigment Red 177 powder was added, the temperature of the solution was raised to 80 ° C. while stirring, and heating was continued until no nitrogen gas was generated, followed by cooling. Next, acetone is added, and the pigment particles are filtered and washed with ion-exchanged water. Then, ion-exchanged water is added to perform ion exchange, ultrafiltration, and centrifugation, and the pigment content is 20 with ion-exchanged water. The red pigment dispersion 1 was obtained by adjusting the amount to be mass%.

(Preparation of colored ink set)
Using each of the prepared pigment dispersions, a colored ink set 1 composed of yellow ink 1, magenta ink 1, cyan ink 1, black ink 1, blue ink 1 and red ink 1 was prepared according to the following procedure. .

<Preparation of yellow ink 1>
Yellow pigment dispersion 1 15% by mass
Ethylene glycol 4% by mass
Glycerin 3.75% by mass
2-pyrrolidone 5% by mass
Surfactant (Surfinol 465 manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount Ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare yellow ink 1 as a pigment ink. The average particle size of the pigment in the ink was 131 nm.

<Preparation of magenta ink 1>
Magenta pigment dispersion 1 15% by mass
Glycerin 8% by mass
Diethylene glycol 1.75% by mass
2-pyrrolidone 3% by mass
Surfactant (Surfinol 465 manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount Ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare magenta ink 1 as a pigment ink. The average particle size of the pigment in the ink was 129 nm.

<Preparation of cyan ink 1>
Cyan pigment dispersion 1 10% by mass
8% by mass of ethylene glycol
Diethylene glycol 4% by mass
Glycerin 5% by mass
2-pyrrolidone 2% by mass
Surfactant (Surfinol 465 manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount Ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare cyan ink 1 as a pigment ink. The average particle size of the pigment in the ink was 104 nm.

<Preparation of black ink 1>
Black pigment dispersion 1 10% by mass
Glycerin 5% by mass
Diethylene glycol 7% by mass
2-pyrrolidone 2% by mass
Surfactant (Surfinol 465 manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount Ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare black ink 1 as a pigment ink. The average particle size of the pigment in the ink was 98 nm.

<Preparation of Blue Ink 1>
Blue pigment dispersion 1 15% by mass
Glycerin 8% by mass
Diethylene glycol 1.75% by mass
2-pyrrolidone 3% by mass
Surfactant (Surfinol 465 manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount Ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare Blue Ink 1 as a pigment ink. The average particle size of the pigment in the ink was 129 nm.

<Preparation of Red Ink 1>
Red pigment dispersion 1 15% by mass
Glycerin 8% by mass
Diethylene glycol 1.75% by mass
2-pyrrolidone 3% by mass
Surfactant (Surfinol 465 manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount Ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare red ink 1 as a pigment ink. The average particle size of the pigment in the ink was 123 nm.

[Preparation of colored ink set 2]
In the preparation of the colored ink set 1, only the basic inks (yellow ink 1, magenta ink 1, cyan ink 1 and black ink 1) except for the blue ink 1 and red ink 1, which are special color inks, are formed. Colored ink set 2 was obtained.

[Preparation of colored ink set 3]
(Preparation of pigment dispersion)
<Preparation of Green Pigment Dispersion 1>
After adding 1.5 g of anthranilic acid to 10 g of 6 mol / L hydrochloric acid solution, the mixture was cooled to 5 ° C., and 1.8 g of sodium nitrite was added and stirred. There, C.I. I. 5 g of pigment green 7 powder was added, the temperature of the solution was raised to 80 ° C. while stirring, and heating was continued until no nitrogen gas was generated, followed by cooling. Next, acetone is added, and the pigment particles are filtered and washed with ion-exchanged water. Then, ion-exchanged water is added to perform ion exchange, ultrafiltration, and centrifugation, and the pigment content is 25 with ion-exchanged water. The green pigment dispersion 1 was obtained by adjusting the mass%.

<Preparation of green ink 1>
Green pigment dispersion 1 15% by mass
Glycerin 8% by mass
Diethylene glycol 1.75% by mass
2-pyrrolidone 3% by mass
Surfactant (Surfinol 465 manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount Ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare Green Ink 1 as a pigment ink. The average particle size of the pigment in the ink was 104 nm.

(Preparation of colored ink set)
In the preparation of the colored ink set 1, the green ink 1 was used in place of the red ink 1 and the blue ink 1 which are the special color inks, and this was designated as the colored ink set 3.

[Preparation of ink set 4]
(Preparation of pigment dispersion)
<Preparation of Yellow Pigment Dispersion 2>
C. I. Pigment Yellow 74 20% by mass
Polymer dispersant SA-1 10% by mass (as solid content)
Glycerin 15% by mass
Ion-exchanged water 55% by mass
The above additives were mixed and dispersed using a horizontal bead mill (System Zetamini manufactured by Ashizawa Co., Ltd.) filled with 60% by volume of 0.3 mm zirconia beads to obtain Yellow Pigment Dispersion 2. The average particle size of the obtained yellow pigment was 112 nm.

<Preparation of magenta pigment dispersion 2>
C. I. Pigment Red 122 25% by mass
Polymer dispersant SA-2 16% by mass (as solid content)
Glycerin 15% by mass
Ion-exchanged water 44% by mass
The above additives were mixed and dispersed using a horizontal bead mill (System Zeta Mini manufactured by Ashizawa Co., Ltd.) filled with 0.3 mm zirconia beads at a volume ratio of 60% to obtain a magenta pigment dispersion 2. The average particle size of the obtained magenta pigment was 105 nm.

<Preparation of Cyan Pigment Dispersion 2>
C. I. Pigment Blue 15: 3 25% by mass
Polymer dispersing agent SA-1 13% by mass (as solid content)
Diethylene glycol 10% by mass
Ion-exchanged water 52% by mass
The above additives were mixed and dispersed using a horizontal bead mill (System Zetamini manufactured by Ashizawa Co., Ltd.) filled with 60% by volume of 0.3 mm zirconia beads to obtain cyan pigment dispersion 2. The average particle diameter of the obtained cyan pigment was 87 nm.

<Preparation of Black Pigment Dispersion 2>
Carbon black 20% by mass
Polymer dispersant SA-2 9% by mass (as solid content)
Glycerin 10% by mass
Ion-exchanged water 61% by mass
Each of the above additives was mixed and dispersed using a horizontal bead mill (System Zetamini manufactured by Ashizawa Co., Ltd.) filled with 0.3 mm zirconia beads at a volume ratio of 60% to obtain a black pigment dispersion 2. The average particle size of the obtained black pigment was 75 nm.

<Preparation of Blue Pigment Dispersion 2>
C. I. Pigment Violet 23 25% by mass
Polymer dispersing agent SA-1 13% by mass (as solid content)
Ethylene glycol 10% by mass
Ion-exchanged water 52% by mass
The above additives were mixed and dispersed using a horizontal bead mill (System Zeta Mini manufactured by Ashizawa Co., Ltd.) filled with 0.3% zirconia beads at a volume ratio of 60% to obtain Blue Pigment Dispersion 2. The average particle size of the obtained blue pigment was 107 nm.

<Preparation of Red Pigment Dispersion 2>
C. I. Pigment Red 177 20% by mass
Polymer dispersant SA-2 16% by mass (as solid content)
Glycerin 15% by mass
49% by mass of ion-exchanged water
Each of the above additives was mixed and dispersed using a horizontal bead mill (System Zetamini manufactured by Ashizawa Co., Ltd.) filled with 0.3 mm zirconia beads at a volume ratio of 60% to obtain Red Pigment Dispersion 2. The average particle diameter of the obtained red pigment was 98 nm.

  In addition, each polymer dispersing agent used for preparation of each said pigment dispersion was prepared according to the following method.

<Preparation of polymer dispersant SA-1>
A dropping funnel fitted with a three-one motor, a thermometer, a nitrogen inlet tube, and a drying tube was attached to a 3 L four-head flask. Tetrahydrofuran (780.0 g) and p-xylene (3.6 g) were introduced while flowing dry nitrogen gas. While stirring, tetrabutylammonium m-benzoate (1 mol / L solution: 3.2 ml) was added, and 1,1-bis (trimethylsiloxy) -2-methylpropene (144.0 g) was further added.

  Next, tetrabutylammonium m-benzoate (1 mol / L solution: 3.2 ml) was dropped from the dropping funnel with stirring over 130 minutes. After dropping, a mixture of benzyl methacrylate (272.6 g) and trimethylsilyl methacrylate (489.8 g) was added dropwise from a dropping funnel over 40 minutes with stirring. After stirring for 30 minutes, benzyl methacrylate (545.4 g) was added dropwise from the dropping funnel over 30 minutes with stirring.

  After stirring for 240 minutes, anhydrous methanol (216 g) was added and stirred. The dropping funnel was replaced with a Liebig condenser, the entire vessel was heated, and the fraction having a boiling point of 55 ° C. or lower (210 g) was removed. Further upstream, when the boiling point reached 76 ° C., 2-propanol (900 g) was added, and heating and distillation were continued. Heating was continued until 1440 g of the solvent had flowed out in total, to obtain a solution 1 of the target block copolymer (BzMA // BzMA / MAA = 5 // 2.5 / 5). When a part was dried and the molecular weight and acid value were measured, they were 1,500 and 70, respectively.

  The solution 1 was neutralized by adding N, N-dimethylethanolamine to obtain a target polymer dispersant SA-1 solution.

<Preparation of polymer dispersant SA-2>
The polymer dispersant SA-2 was prepared in the same manner as in the preparation of the polymer dispersant SA-2 except that it was neutralized with potassium hydroxide instead of N, N-dimethylethanolamine.

(Preparation of pigment ink set)
In the preparation of the colored ink set 1, instead of the yellow pigment dispersion 1, the magenta pigment dispersion 1, the cyan pigment dispersion 1, the black pigment dispersion 1, the blue pigment dispersion 1, and the red pigment dispersion 1, the above preparation is performed. A colored ink set 4 was prepared in the same manner except that the yellow pigment dispersion 2, the magenta pigment dispersion 2, the cyan pigment dispersion 2, the black pigment dispersion 2, the blue pigment dispersion 2, and the red pigment dispersion 2 were used. Prepared.

[Preparation of ink set 5]
Ink set 5 was prepared in the same manner as in the preparation of ink set 3, except that cyan ink 2 was changed to cyan ink 3 prepared according to the following procedure.

(Preparation of pigment dispersion)
<Preparation of Cyan Pigment Dispersion 3>
C. I. Pigment Blue 15: 3 26g
SA-3 solution 28g
13.6 g of 1 mol / L potassium hydroxide aqueous solution
20g of methyl ethyl ketone
Ion exchange water 30g
The above additives were mixed and kneaded 20 times using a three-roll mill. The obtained paste was added to ion-exchanged water (200 g), and after sufficiently stirring, methyl ethyl ketone and water were distilled off using a rotary evaporator so that the solid content was 20%. Obtained.

  The polymer dispersant SA-3 used for the preparation of the cyan pigment dispersion 3 was prepared according to the following method.

<Preparation of polymer dispersant SA-3>
A 1 L four-head flask was equipped with a three-one motor, a thermometer, a reflux tube with a nitrogen inlet tube, and a dropping funnel. The following monomer mixture 1 was introduced while flowing dry nitrogen gas thereto, and the temperature was raised to 65 ° C.

  Next, the following monomer mixture 2 was added dropwise over 2.5 hours while stirring. Further, a mixed solution of azobisdimethylvaleronitrile (0.8 g) and methyl ethyl ketone (22 ml) was added dropwise over 0.5 hours. Azobisdimethylvaleronitrile (0.8 g) was added, and the mixture was further stirred with heating for 1 hour.

  After completion of the reaction, methyl ethyl ketone (450 ml) was added to obtain a solution of polymer dispersant SA-3 having a solid content of 50%. When a part was dried and the molecular weight and acid value were measured, they were 15,000 and 55, respectively.

(Monomer mixture 1)
Styrene 11.2g
Lauryl methacrylate 12.0g
Polyethylene glycol methacrylate (Kyoeisha Chemical: Light Ester 130MA)
4.0g
Styrene macromer (manufactured by Toagosei Co., Ltd .: Macromonomer AS-6) 4.0 g
Acrylic acid 2.8g
Mercaptoethanol 0.4g
(Monomer mixture 2)
Styrene 100.8g
Lauryl methacrylate 108.0g
Hydroxyethyl methacrylate 60.0g
Polyethylene glycol methacrylate (Kyoeisha Chemical: Light Ester 130MA)
36.0g
Styrene macromer (manufactured by Toagosei: AS-6) 36.0 g
Acrylic acid 25.2g
Mercaptoethanol 3.6g
Azobisdimethylvaleronitrile 2.4g
22 ml of methyl ethyl ketone
<Preparation of cyan ink 3>
Cyan pigment dispersion 3 10% by mass
8% by mass of ethylene glycol
Diethylene glycol 6% by mass
Glycerin 4% by mass
2-pyrrolidone 3% by mass
Urea 3% by mass
Surfactant (Surfinol 465, manufactured by Nissin Chemical Industry Co., Ltd.) The following required amount of ion-exchanged water residue A surfactant is added so that the surface tension is 38 mN / m, and the total amount is 100% by mass with ion-exchanged water. Prepared. The above compositions were mixed, stirred, and filtered through a 1 μm filter to prepare cyan ink 3 as a pigment ink. The average particle size of the pigment in the ink was 98 nm.

[Preparation of ink set 6]
(Preparation of pigment dispersion)
In the preparation of the yellow pigment dispersion 2, the magenta pigment dispersion 2, the cyan pigment dispersion 2, the black pigment dispersion 2, the blue pigment dispersion 2, and the red pigment dispersion 2, the polymer dispersants SA-1 and SA In the same manner except that sodium naphthalene sulfonate was used instead of -2, yellow pigment dispersion 3, magenta pigment dispersion 3, cyan pigment dispersion 4, black pigment dispersion 3, blue pigment dispersion 3, and red Pigment dispersion 3 was prepared.

(Preparation of colored ink set)
In the preparation of the colored ink set 1, instead of the yellow pigment dispersion 1, the magenta pigment dispersion 1, the cyan pigment dispersion 1, the black pigment dispersion 1, the blue pigment dispersion 1, and the red pigment dispersion 1, the above preparation is performed. A colored ink set 6 was prepared in the same manner except that the yellow pigment dispersion 3, the magenta pigment dispersion 3, the cyan pigment dispersion 4, the black pigment dispersion 3, the blue pigment dispersion 3, and the red pigment dispersion 3 were used. Prepared.

[Preparation of ink sets 7-9]
In the preparation of the ink set 1 described above, the amount of the surfactant used for preparing the ink was appropriately adjusted so that the surface tension of each color ink was 28 mN / m, 48 mN / m, and 55 mN / m, respectively. Ink sets 7 to 9 were prepared.

[Preparation of ink set 10]
A colored ink set 10 was prepared in the same manner as in the preparation of the colored ink set 3 except that 5% by mass of ethylene urea was added to each color ink.

<Measurement of each characteristic value of recording medium and ink>
[Recording medium: Measurement of transfer amount]
The amount of transition of each of the produced recording media at an absorption time of 0.04 seconds according to the Bristow method was measured according to the following method.

  The amount of transition was measured by allowing each recording medium to stand for 12 hours or more in an atmosphere of 25 ° C. and 50% RH, and then using a Bristow tester type II which is a liquid dynamic absorbency tester manufactured by Kumagai Riki Kogyo Co., Ltd. (Pressurization type) was used for measurement. For measurement, C.I. I. Using 2% water solubility of Acid Red 52, the amount of transfer was determined by measuring the area of the magenta-stained portion on the recording medium after an absorption time of 0.04 seconds.

[Calculation of porosity]
The porosity of each of the produced recording media was calculated from the void volume determined by the Bristow method and the total volume of the void layer determined from the dry film thickness.

[Ink set: Measurement of surface tension]
For the surface tension of the ink constituting each ink set, the surface tension value (mN / m) at an ink temperature of 25 ° C. is measured by a platinum plate method using a surface tension meter (manufactured by Kyowa Interface Science: CBVP-Z). did.

[20 degree specular gloss]
According to JIS-Z-8741, the 20-degree specular glossiness on the ink absorbing layer coating surface side of each recording medium was measured with a digital variable gloss meter (manufactured by Suga Test Instruments Co., Ltd.).

<Printing method>
[Printing method 1]
For each ink set prepared above, a nozzle row having a nozzle hole diameter of 15 μm, a driving frequency of 20 kHz, an ink droplet amount of 3 pl, a dot diameter after landing of a recording medium of 35 μm, a number of nozzles in one row of 128, and a nozzle pitch of 42.3 μm. 2 rows spaced 1 mm apart, with a thermal type head capable of effectively forming 256 dots on the medium at a 1200 dpi pitch by shifting the 2 rows by 21.2 μm in the sub-scanning direction, and the maximum recording density main scan It was set in an on-demand type ink jet printer of 1200 × sub-scan 1200 dpi, and one-pass printing was performed without using a thinning pattern. As used herein, dpi represents the number of dots per 2.54 cm. The image data was developed using the method described in paragraphs [0038] to [0059] of JP-A-2000-32284.

  The relationship between the image data and the amount of ink used in this case is shown in FIG. 24 by taking a blue hue as an example.

In FIG. 24, as the gradation level increases, the amount of cyan ink A and magenta ink B increases, but after gradation level 7, blue ink C is used and magenta ink B decreases. . Although the cyan ink A does not decrease, the amount of increase is smaller than when the blue ink C is not used. At the gradation level 16, the blue ink C is solid, and the total ink use amount is 20.5 ml / m ² . Note that even if the blue ink C is solid, the cyan ink A and some magenta ink B are used in order to produce a visually favorable color.

[Printing method 2]
Each of the ink sets prepared above has a nozzle hole diameter of 15 μm, a drive frequency of 20 kHz, an ink droplet amount that causes a dot diameter of 35 μm after landing on the recording medium, an ink droplet amount of 3 pl, a dot diameter after landing of the recording medium of 35 μm, and a row. Two nozzle rows each having 128 nozzles and a nozzle pitch of 42.3 μm are arranged 1 mm apart, and 2 rows are shifted by 21.2 μm in the sub-scanning direction, and 256 dots are effectively formed on the medium at a 1200 dpi pitch. It has a thermal type head that can be formed, and is set in an on-demand type ink jet printer with a maximum recording density of main scanning of 1200 × sub scanning of 1200 dpi, and using a regular thinning pattern, with a print allowance of 25%, A thinned image was formed by 4-pass printing. The mask used is shown in FIG. The image data development method was the same as the printing method 1.

[Printing method 3]
For each ink set prepared above, a nozzle row having a nozzle hole diameter of 15 μm, a driving frequency of 20 kHz, an ink droplet amount of 3 pl, a dot diameter after landing of a recording medium of 35 μm, a number of nozzles in one row of 128, and a nozzle pitch of 42.3 μm. 2 rows spaced 1 mm apart, with a thermal type head capable of effectively forming 256 dots on the medium at a 1200 dpi pitch by shifting the 2 rows by 21.2 μm in the sub-scanning direction, and the maximum recording density main scan A thinned image was formed by four-pass printing with a printing tolerance of 25% using a thinning pattern with no regularity, set in an on-demand type inkjet printer of 1200 × sub-scanning 1200 dpi. The used mask is shown in FIG.

[Printing method 4]
In the above printing method 3, the nozzle hole diameter is appropriately changed so that the dot diameter after landing on the recording medium is 15 μm as the ink droplet volume (about 0.75 pl), and the nozzle pitch of one row is 21 This is the same as the printing method 4 except that a head of 2400 dpi is effectively created by setting the shift amount between 2 μm and 2 rows to 10.6 μm, and the print resolution is the maximum recording density main scanning 2400 × sub scanning 2400 dpi. did. The image data development method was the same as the printing method 1.

[Printing method 5]
In the above printing method 3, printing is performed in the same manner except that the nozzle hole diameter is appropriately changed so that the ink droplet amount is about 40 μm after the landing of the recording medium as the ink droplet amount (about 5 pl). Method 5 was adopted. The image data was adjusted in advance so that the ink adhesion amount on the medium was substantially the same as that of the printing method 3. The image data development method was the same as the printing method 1.

[Printing method 6]
In the above printing method 3, the ink droplet amount is printed in the same manner except that the nozzle hole diameter is appropriately changed so that the ink droplet amount after landing on the recording medium is 60 μm (about 14 pl). Method 6 was adopted. The image data was adjusted in advance so that the ink adhesion amount on the medium was substantially the same as that of the printing method 3. The image data development method was the same as the printing method 1.

[Printing method 7]
In the above printing method 3, this was designated as printing method 7 except that the head was changed to a head having a nozzle pitch of 15 μm and 256 nozzles arranged in a row and the maximum recording density was 850 × sub scanning 1690 dpi. The sub-scanning resolution corresponds to the head nozzle pitch, and the main scanning resolution was changed so that the amount of ink deposited on the other printing methods and the medium was substantially the same as that of the printing method 3 according to this. The image data development method was the same as the printing method 1.

[Printing method 8]
In the printing method 3 described above, a nozzle group having a nozzle pitch of 55 μm and 256 nozzles arranged in a row is separated by 2 cm, arranged in two rows for each color by shifting in the 27.5 μm sub-scanning direction, and 512 nozzles per color. This was designated as printing method 8 in the same manner except that the head was changed to the maximum recording density main scanning 1570 × sub scanning 920 dpi. In this case, the nozzle pitch is 55 μm. Note that the sub-scanning resolution corresponds to the dot pitch on the medium, and the main scanning resolution is changed so that the ink adhesion amount on the medium is substantially the same as that of the printing method 3 according to this. The image data development method was the same as the printing method 1.

[Printing method 9]
In the printing method 3 described above, this is the same as the printing method 9 except that the printing allowance is changed to four types of repetition of 40%, 40%, 10%, and 10% (that is, the printing allowance is 40%). did. The image data development method was the same as the printing method 1.

[Printing method 10]
In the printing method 3 described above, a nozzle group having a nozzle pitch of 42.3 μm and 256 nozzles arranged in a row is spaced 2 cm apart and arranged in two rows of each color by shifting in the 21.2 μm sub-scanning direction, and 512 per color. This was designated as the printing method 10 in the same manner except that the nozzle head was changed to the maximum recording density main scanning 1200 × sub scanning 1200 dpi. The nozzle pitch in this case is 42.3 μm. The image data development method was the same as the printing method 1.

<Formation of inkjet recording image>
Each of the above printing methods and the produced recording medium and ink set are printed in solid colors for each color of yellow, magenta, cyan, green, red, blue, and black in the combinations shown in Table 1, Table 2, and Table 3. Images 1-42 were prepared, and the following evaluations were performed on the obtained images.

<Evaluation of inkjet recording image>
[Evaluation of gloss difference]
Visually observe the image of the high-definition color digital standard image data “N5 Bicycle” (issued in December 1995) issued by the Foundation / Japan Standards Association, obtained by a combination of the above (printing method, recording medium, ink). The image quality was evaluated according to the following criteria.

◎: The difference between the gloss of the watch with high image density and the color chart and the gloss of the surrounding white part is not felt, and the watch / color chart looks uniform without lifting from the surroundings ○: With the watch with high image density Although there is a slight difference between the gloss of the color chart part and the surrounding white background part, the clock / color chart looks uniform without lifting from the surroundings. △: The gloss of the clock and color chart part with high image density There is a difference in glossiness from the surrounding white background, and the clock and color chart appear to slightly lift from the surroundings, but there is no problem in practical use. ×: The gloss of the watch and color chart with high image density and the surrounding white background A large difference in gloss is felt during the period, and the clock and color chart rise from the surroundings. [Evaluation of image quality (high definition)]
High-definition color digital standard image data “N5 Bicycle” (issued in December 1995) issued by the Japan Standards Association, a combination of the above (printing method, recording medium, ink), and the resulting image The image quality was evaluated according to the following criteria.

A: There is no occurrence of color turbidity and the image is extremely high definition. ○: Generation of color turbidity is slightly observed, but the image is high definition. Δ: Slight color turbidity is observed and the sharpness is slightly lacking. No problem for practical use ×: Image with clear color turbidity and lack of clarity [Evaluation of feeling of depth] Foundation obtained by a combination of the above (printing method, recording medium, ink) The image of high-definition color digital standard image data “N2 Cafeteria” (issued in December 1995) published by the Japanese Standards Association was visually observed, and the sense of depth was evaluated according to the following criteria.

◎: A feeling of deep depth is felt and is an image approximated to a silver salt photograph image ○: A feeling of depth is felt and is an image somewhat approximated to a silver salt photograph image △: Although the image is slightly lacking in depth feeling, In practically acceptable range ×: The image clearly has poor depth and cannot be used practically [Evaluation of scratch resistance]
The green and red solid images created above were subjected to 10 reciprocating frictions on the surface with an office eraser (manufactured by MONO Tonbo Pencil Co., Ltd.), and the presence or absence of smudges on the printed portion was visually determined.

◎: No stain on the printed part is observed ○: Some stain on the printed part is observed △: Stain on the printed part is clearly observed, but is within a practically acceptable range ×: The density of the printed part is clearly reduced The results obtained as described above are shown in Table 4.

  As is apparent from the results in Table 4, the ink jet recording method comprising the combination of the recording head, ink and recording medium defined in the present invention can provide good printing efficiency, and the obtained image can be bronzed in comparison with the comparative example. It can be seen that a high-definition image having excellent resistance, gloss, scratch resistance and image uniformity can be obtained.

It is a perspective view showing the main components of an inkjet printer. It is the perspective view which expanded the carriage of the inkjet printer. It is a bottom view of a recording head of an ink jet printer. It is a block diagram showing the control part of an inkjet printer. 1 is a block diagram illustrating a configuration of an image forming apparatus. It is a schematic diagram showing an example of a multipass printing jet recording method. It is a schematic diagram showing another example of the multipass printing jet recording method. It is a schematic diagram showing another example of the multipass printing jet recording method. It is a schematic diagram showing another example of the multipass printing jet recording method. It is a schematic diagram showing an example of the image arrangement pattern regularly arranged. It is a schematic diagram showing another example of the image arrangement pattern regularly arranged. It is a schematic diagram which shows a printing state when arrangement | sequence image data of the state which raised the duty are input. FIG. 6 is a schematic diagram illustrating a state in which an ink drop is ejected at a constant speed v on a smooth paper surface while the head moves at a constant speed V in a forward or backward path direction. It is a schematic diagram showing a dot landing state when a 100% duty image is printed in both directions using a staggered thinning mask. It is a schematic diagram which shows an example of the method of performing multipass printing using a mask without regularity. It is a schematic diagram which shows another example of the method of performing multipass printing using a mask without regularity. It is a schematic diagram which shows an example of the nozzle arrangement | sequence corresponding to a mask pattern. It is a schematic diagram which shows an example of the mask pattern with a blue noise characteristic. It is a schematic diagram which shows an example of a mask pattern. It is a schematic diagram which shows another example of a mask pattern. It is a schematic diagram which shows another example of a mask pattern. It is a block diagram which shows an example of a mask processing circuit. It is a schematic diagram which shows an example of the mask pattern used by the comparative example. It is a graph which shows an example of the relationship between image data and the ink amount to be used.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Inkjet printer 2 Image formation part 22 Recording head 23 Carriage 200 Image formation apparatus 221 Nozzle 222 Nozzle surface 501-504 Division | segmentation area | region

Claims (24)

A recording head having a plurality of nozzles for discharging colored ink is scanned a plurality of times with respect to the same recording area of the recording medium, and a thinned image according to a thinning pattern having no regularity is formed in each scanning, and the colored ink is applied to the recording medium. An ink jet recording method for forming a color image by printing on
The nozzle pitch of the recording head is 10 to 50 μm,
The colored ink is composed of cyan, magenta, yellow and black color inks and at least one special color ink,
The colored ink contains a pigment, a high boiling point organic solvent, and water, and the dot diameter formed by being ejected from the recording head is 10 to 50 μm on the recording medium,
The recording medium has a void layer containing inorganic fine particles having an average particle size of 15 to 100 nm and a hydrophilic binder having a transition amount of 10 ml / m ² or more at an absorption time of 0.04 seconds according to the Bristow method, And the 20-degree specular glossiness of this recording medium by JIS-Z-8741 is 20 to 45%, The inkjet recording method characterized by the above-mentioned. 2. The ink jet recording method according to claim 1, wherein the special color ink is at least one ink selected from a red ink, an orange ink, a blue ink, a violet ink, and a green ink. The ink jet recording method according to claim 1 or 2, wherein a print allowable rate by the thinning pattern is 15 to 35%. The inkjet recording method according to any one of claims 1 to 3, wherein a surface tension of the colored ink is 30 to 50 mN / m. The inkjet recording method according to claim 1, wherein the pigment of the colored ink is dispersed with a polymer dispersant. The inkjet recording method according to claim 1, wherein the recording medium is a medium in which the gap layer is provided on a water-absorbing support. The inkjet recording method according to claim 1, wherein the hydrophilic binder is polyvinyl alcohol or a derivative thereof. The inkjet recording method according to claim 1, wherein the hydrophilic binder is hardened. The ink jet recording method according to claim 1, wherein the void ratio of the void layer is 30 to 70%. The inkjet recording method according to claim 1, wherein the inorganic fine particles are silica or alumina. The inkjet recording method according to claim 1, wherein the inorganic fine particles have an average particle size of 20 to 80 nm. The inkjet recording method according to claim 1, wherein the colored ink contains urea or a urea derivative. An inkjet recording apparatus that forms a color image by discharging colored ink onto a recording medium,
A recording head in which a plurality of nozzle portions for discharging the colored ink are arranged at a pitch of 10 to 50 μm;
Scanning means for scanning the recording head a plurality of times for the same recording area of the recording medium;
The dot diameter formed by the colored ink discharged from the recording head is 10 to 50 μm on the recording medium, and a thinned image according to a thinning pattern having no regularity is formed on the recording medium in each scan. And control means for discharging colored ink from a plurality of nozzle portions,
The colored ink is composed of cyan, magenta, yellow and black color inks and at least one special color ink,
The colored ink contains a pigment, a high boiling point organic solvent, and water,
The recording medium has a void layer containing inorganic fine particles having an average particle size of 15 to 100 nm and a hydrophilic binder having a transition amount of 10 ml / m ² or more at an absorption time of 0.04 seconds according to the Bristow method, and An inkjet recording apparatus, wherein the recording medium has a 20-degree specular glossiness of 20 to 45% according to JIS-Z-8741. 14. The inkjet recording apparatus according to claim 13, wherein the special color ink is at least one ink selected from a red ink, an orange ink, a blue ink, a violet ink, and a green ink. The ink jet recording apparatus according to claim 13 or 14, wherein a print allowable rate by the thinning pattern is 15 to 35%. The inkjet recording apparatus according to any one of claims 13 to 15, wherein a surface tension of the colored ink is 30 to 50 mN / m. The inkjet recording apparatus according to claim 13, wherein the pigment of the colored ink is dispersed with a polymer dispersant. The inkjet recording apparatus according to any one of claims 13 to 17, wherein the recording medium is provided with the gap layer on a water-absorbing support. The inkjet recording apparatus according to claim 13, wherein the hydrophilic binder is polyvinyl alcohol or a derivative thereof. The inkjet recording apparatus according to claim 13, wherein the hydrophilic binder is hardened. 21. The ink jet recording apparatus according to claim 13, wherein the void ratio of the void layer is 30 to 70%. The inkjet recording apparatus according to any one of claims 13 to 21, wherein the inorganic fine particles are silica or alumina. The inkjet recording apparatus according to any one of claims 13 to 22, wherein an average particle diameter of the inorganic fine particles is 20 to 80 nm. The inkjet recording apparatus according to any one of claims 13 to 23, wherein the colored ink contains urea or a urea derivative.

Images