JP5399013B2 - Ink composition for inkjet color filter excellent in inkjet ejection stability, and color filter cured film and color filter obtained using this ink composition - Google Patents

Description

  The present invention relates to a color filter ink composition suitable for producing a color filter by an ink jet method, a color filter cured film obtained using this ink composition, and a color filter.

  Conventional methods for producing color filters used in color liquid crystal display devices include photopolymerization initiators, various additives, and red (R), green (G), and blue (B) colorants for photosensitive resins. In general, a color resist prepared with a solvent is applied, dried, and then a pixel pattern is formed by a photolithographic method through a series of steps. However, with the recent increase in size of mother glass, technical problems have begun to occur in each process such as the coating process in the conventional color filter manufacturing method using the photolithography method.

  For example, coating methods using spin coating have been mainly used so far, but as the mother glass as the base becomes larger, it becomes technically difficult to apply by spin coating, and instead a slit coater is used. The coating method used is employed. However, even with a coating method using a slit coater, it is difficult to form a uniform coating film on the entire surface due to further enlargement of the mother glass. This problem is even more conspicuous particularly in super large mother glasses such as 8G and 10G classes. become. In addition, since the photolithographic method requires coating, drying, exposure, development, and curing processes for every three colors, there is a problem that the number of steps increases and the cost is high. Another pixel forming means is desired.

  Therefore, as a color filter manufacturing method replacing the photolithography method, for example, image formation using an offset printing method as disclosed in Patent Document 1 has been proposed and implemented. However, with respect to the offset printing method, it is difficult to form a stable pixel on a sufficiently large mother glass, and its practical application is delayed. On the other hand, it is a well-known fact that the pixel forming method by the ink jet method has been attracting attention and implemented in recent years and has a certain track record. And several patents are shown about the ink used in the inkjet method (refer patent documents 2-4).

  By the way, in order to realize a good image that can be used for a television application with a liquid crystal display device, a great technical improvement is required for the liquid crystal display device itself and a circuit. Among them, a color filter has a larger NTSC ratio, One of the requirements is to achieve good display specifications such as contrast. For that purpose, it is necessary to contain more pigments in the ink composition for color filters. However, as the pigment content in the ink composition increases, the solid content increases and the drying speed increases. This is a cause of nozzle clogging in an ink jet system that ejects minute droplets.

Here, the ink composition used in the inkjet method generally includes a pigment that acts as a colorant, a polyfunctional monomer for curing, and a binder resin that acts as a binder for the colorant. Each component is dissolved in a solvent. For example, in the invention described in Patent Document 2, diethylene glycol mono-n-butyl ether acetate (boiling point 247 ° C.) is used as a solvent. In the described invention, a solvent having two acetate structures (propylene glycol diacetate (boiling point 190 ° C.), 1,3-butylene glycol diacetate (boiling point 232 ° C.)) is used. As described above, when only a high-boiling solvent is used, the drying speed is delayed, and the probability of blockage and contamination around the nozzle is reduced. As a result, the discharge performance and the like are improved, and problems such as nozzle clogging are solved. However, in the ink composition, in addition to the solvent for dissolving each component such as a pigment, a polyfunctional monomer, and a binder resin, each component that is used for dissolving the dispersant for dispersing the pigment and the resin component There are solvents brought in due to the above, and it is not always possible to use only high-boiling solvents. Further, in the drying process after the ink composition is ejected by the ink jet method, there is a tendency that high-speed drying is desired from the viewpoint of productivity. On the other hand, a patent that guarantees ejection stability by a solvent configuration including an alcohol component as in Patent Document 4 has been proposed, but this is mainly based on a solvent of 200 ° C. or lower, and therefore, at the time of intermittent ejection test. There is a concern of clogging or contamination of a part of the head nozzle.
JP-A-11-58921 Japanese Patent No. 3826561 JP 2006-299090 A JP 2008-50456 A

The present invention is suitable for forming a pixel pattern on a glass substrate whose size is increasing in the manufacture of a color filter, and is suitable for discharging an ink composition used in an inkjet method capable of reducing cost and mass production. The object of the present invention is to provide an ink composition for a color filter which has good properties and is less likely to cause nozzle clogging, and a color filter cured film and a color filter obtained using this ink composition.

  The inventors of the present invention have studied the ink composition for a color filter that contains a pigment at a high concentration to achieve a large NTSC ratio, has good ejection properties, and is less likely to cause nozzle clogging, and the ink composition. In addition to the solvent used to dissolve each component that forms the ink composition, such as pigments, polyfunctional monomers, and binder resins, the presence of a solvent derived from each component contained in each of these components In view of this, the inventors have found that by optimizing the amount and combination of so-called high-boiling solvent and low-boiling solvent, it has stable ejection characteristics and can achieve high-speed drying.

That is, the present invention, in an ink composition used for producing a color filter by an inkjet method, contains 70 to 99% by weight of a solvent having a boiling point in the range of 200 to 300 ° C. in all the solvents, and has a boiling point. 1 to 6 % by weight of a solvent having a temperature of less than 150 ° C.

  The ink composition in the present invention will be described below by being divided into a solid component and a solvent component.

First, as a solid component, an unsaturated compound (A) represented by the following general formula (1), a polyfunctional acrylate compound (B) having four or more functions, and a pigment (D) are essential components in a solvent, The bifunctional or higher polyfunctional epoxy compound (C) is blended in the range of 0 to 20% by weight with respect to the sum of the components (A) + (B) . At this time, the ratio (A) / (B) of the weight of the component (A) and the component (B) is set in the range of 10/90 to 90/10 .
[Wherein, R ₁ , R ₂ , R ₃ and R ₄ independently represent a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a halogen atom or a phenyl group, and R ₅ represents a hydrogen atom or a methyl group. . A is -CO-, -SO _2- , -C (CF ₃ ) _2- , -Si (CH ₃ ) _2- , -CH _2- , -C (CH ₃ ) _2- , -O-, 9 , 9-fluorenyl group or a direct bond, X represents a tetravalent carboxylic acid residue, Y ₁ and Y ₂ independently represent a hydrogen atom or -OC-Z- (COOH) _m (Z is an m-valent It is a carboxylic acid residue, m represents a number of 1 to 3, and n represents a number of 1 to 200. ]

  Here, the component (A) is prepared by reacting (meth) acrylic acid with an epoxy compound having two glycidyl ether groups derived from bisphenols, and adding the resulting hydroxy group to a polybasic acid. One kind each of a certain dicarboxylic acid or an acid anhydride thereof (hereinafter sometimes referred to as “dicarboxylic acids”) and a tetracarboxylic acid or an acid dianhydride thereof (hereinafter sometimes referred to as “tetracarboxylic acids”) It is an epoxy (meth) acrylate acid adduct obtained by reacting with the above. In the present specification, (meth) acrylic acid means acrylic acid, methacrylic acid or both.

The component (A) is preferably derived from an epoxy compound represented by the following general formula (2). This epoxy compound is derived from bisphenols, and when bisphenols are converted to glycidyl ether, oligomer units will be mixed. However, if the average value of l in the general formula (2) is in the range of 0-10. There is no problem in the performance as an ink composition.

In the general formula (2), R ₁ , R ₂ , R ₃ , R ₄ and A represent the same meaning as in the general formula (1), but are preferably R ₁ , R ₂ , R ₃ and R ₄ . Is a hydrogen atom, and A is preferably a 9,9-fluorenyl group. l is an integer of 0 to 10, preferably 0 or an integer of 0 to 2. Here, the 9,9-fluorenyl group refers to a group represented by the following general formula (3).

  In the present invention, the reaction between the epoxy compound and (meth) acrylic acid for obtaining the component (A) is preferably performed using about 2 moles of (meth) acrylic acid per mole of the epoxy compound. . The reaction product obtained by this reaction is an epoxy (meth) acrylate compound represented by the following general formula (5). Then, the hydroxy group in the epoxy (meth) acrylate compound molecule is reacted with a) dicarboxylic acid and b) tetracarboxylic acid to obtain an acid adduct of epoxy (meth) acrylate.

  In addition, in order to react the epoxy (meth) acrylate compound represented by the general formula (5) when obtaining the component (A) with a) dicarboxylic acids and b) tetracarboxylic acids, a known method should be adopted. However, it is preferable to carry out the reaction quantitatively so that the acid component is 3/4 mol per 1 mol of the hydroxy group in the epoxy (meth) acrylate compound molecule. The reaction temperature is 90 to 130 ° C, preferably 95 to 125 ° C.

An example of a method for producing the component (A) is as follows when 9,9-bis (4-hydroxyphenyl) fluorene is used as a starting material. First, 9,9-bis (4-hydroxyphenyl) fluorene and epichlorohydrin are reacted to synthesize a bisphenolfluorene type epoxy compound represented by the following general formula (4). A bisphenolfluorene type epoxy acrylate resin represented by the following general formula (5) is synthesized by reacting with (meth) acrylic acid represented by CH ₂ = CR ₅ -COOH, and then bisphenolfluorene in a propylene glycol monomethyl solvent. An alkali-soluble resin represented by the formula (1), which is a component (A), by reacting an epoxy acrylate resin with the acid component [a) dicarboxylic acid and b) tetracarboxylic acid] under heating. it can.

Here, R ₁ , R ₂ , R ₃ , R ₄ , and R ₅ in general formulas (4) and (5) are the same as in general formula (1), and A represents a 9,9-fluorenyl group. .

  In addition, as the polyfunctional acrylate compound of the component (B) in the present invention, for example, ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) Acrylate, tetramethylene glycol di (meth) acrylate, trimethylolpropane tri (meth) acrylate, trimethylolethane tri (meth) acrylate, pentaerythritol di (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) ) Acrylate, dipentaerythritol tetra (meth) acrylate, dipentaerythritol hexa (meth) acrylate, glycerol (meth) acrylate and other (meth) acrylic acid esters. Rukoto can. These may be used alone or in combination of two or more thereof, but it is more preferable to contain a polyfunctional acrylate having 4 or more functional groups.

  In the present invention, the weight ratio (A) / (B) of the component (A) to the component (B) is 10/90 to 90/10, preferably 70/30 to 50/50. Good. When (A) / (B) is out of the range of 10/90 to 90/10, the ink composition is not sufficiently cured, or the light transmittance of the obtained cured film is lowered, and the color filter There is a risk of affecting the color developability and reducing the reliability. Here, the weight average molecular weight (Mw) of the component (A) is preferably in the range of 2000 to 20000.

  Moreover, in this invention, it is a preferable aspect to contain 20 weight% or less of polyfunctional epoxy compounds (C) more than bifunctional with respect to the sum of (A) component and (B) component. Here, the polyfunctional epoxy compound (C) is composed of an epoxy compound having two or more epoxy groups in one molecule. Typical examples include novolak epoxy resins such as phenol novolac type epoxy and cresol novolak type epoxy, bis type epoxy resins such as bisphenol A type epoxy and bisphenol F type epoxy, biphenyl type epoxy resins, and alicyclic epoxy resins. It can be illustrated. In the ink composition of the present invention, the content of the polyfunctional epoxy compound (C) may be 0% by weight.

  In addition, the pigment of component (D) may be an organic pigment or an inorganic pigment. Organic pigments include, for example, azo lakes, insoluble azo (PY-150) s, cyanines including phthalocyanines (PG-7, PG-36 & PB-15.6), quinophthalones (PY138), quinacrines, dioxazines (PV-23) ), Isoindolinone (PY-139), berylone, anthraquinone (PR-177), pyrrolopyrrole (PR-254), perylene, etc., one or more of these Can also be used together. Examples of inorganic pigments include miloli blue, iron oxide, cobalt-based, manganese-based, ultramarine blue, bitumen, cobalt blue, cerulean blue, pyridian, emerald green, cobalt green, and the like. It can also be used together. These pigments are preferably dispersed with an average particle diameter of 0.4 μm or less, which is the lower limit of the wavelength of visible light, in order to color while maintaining the transparency of the coating film. More preferably, the range is 0.01 to 0.25 μm. The component (D) may contain a dispersant necessary for finely dispersing and stabilizing the pigment to form a pigment composition composed of the pigment [component (D)] and the dispersant. Good. Moreover, about the ratio of a pigment (D), it is preferable that it is 0.3 or more by the ratio of the weight of the pigment (D) with respect to the total weight of solid content except the solvent in an ink composition.

  Moreover, you may make it mix | blend a photoinitiator or a thermal-polymerization initiator (F) with the ink composition of this invention. Here, as photo or thermal polymerization initiator (F), acetophenones such as acetophenone and p-tert-butylacetophenone, benzophenones such as benzophenone, 2-chlorobenzophenone, p, p'-bis (dimethylamino) benzophenone Benzoin ethers such as benzoin methyl ether, benzoin isopropyl ether, benzoin butyl ether, 2-methyl-1- [4- (methylthio) phenyl] -2-morpholinopropan-1-one, 2-benzyl-2-dimethylamino Α-aminoalkylphenones such as -1- (4-morpholinophenyl) -butanone-1, bisacylphosphine oxides such as bis (2,4,6-trimethylbenzoyl) -phenyl-phosphine-oxide, Glycines such as N-phenylglycine, 2,4-trichloromethyl- (piperonyl) -6-triazine, 2,4-trichloromethyl- (4'- And triazines such as methoxystyryl) -6-triazine. These may be used alone or in combination of two or more. In addition, this light or thermal polymerization initiator (F) can be used in combination with known photopolymerization accelerators (sensitizers) such as p-dimethylaminobenzoic acid isoamyl ester and p-dimethylaminobenzoic acid ethyl ester. . About the usage-amount of (F) component, it is preferable that it is 0.1-20 weight part with respect to 100 weight part of total amounts of (A) component and (B) component.

  Next, the solvent component of the color filter ink composition of the present invention will be described. First, in the present invention, in addition to the components (A), (B) and (D) to be blended as a preferred embodiment, the components (C) and (F) to be added as necessary are dissolved in a solvent to obtain a predetermined form. An ink composition can be obtained. In this case, for example, the pigment of the component (D) is dissolved in a solvent in advance together with a dispersant having a role of dispersing the pigment to obtain a pigment dispersion, and the other (A) , (B) and the like may be dissolved in a solvent to obtain an ink composition.

  In the present invention, 70 to 99% by weight of the solvent having a boiling point in the range of 200 to 300 ° C. is contained in the total solvent in the ink composition. The reason why a relatively high boiling point solvent having a boiling point of 200 to 300 ° C. is contained in the entire solvent in an amount of 70 to 99% by weight is to delay the drying rate and prevent nozzle clogging and contamination. Moreover, the thing whose boiling point is less than 150 degreeC is made to contain 1 to 10weight% in all the solvents. The reason why a relatively low boiling point solvent having a boiling point of less than 150 ° C. is contained in the total amount of 1 to 10% by weight is to stably dissolve the dispersant for dispersing the pigment and the resin component. From the viewpoint of preventing problems such as nozzle clogging, it is desirable that the solvent having a boiling point of less than 150 ° C. is not present as much as possible, but contains 10% by weight as an upper limit in order to stably dissolve resin components and the like. Let

  Among these, the solvent having a boiling point in the range of 200 to 300 ° C. is not particularly limited as long as the boiling point is in the above range, but preferably diethylene glycol monoalkyl ether and its terminal acetates, dipropylene glycol monoalkyl ether And terminal acetates or diethers thereof, diethylene glycol dialkyl ethers, diethylene glycol monoalkyl ethers and terminal acetates thereof, and at least one selected from the group consisting of polyethylene glycol dialkyl ethers.

  As the solvent having a boiling point of less than 150 ° C., the solvents include ketones such as methyl ethyl ketone, cellosolves such as methyl cellosolve and cellosolve acetate, propylene such as propylene glycol monomethyl ether, propylene glycol monoethyl ether and propylene glycol n-propyl ether. Examples include organic solvents such as glycol monoalkyl ethers, propylene glycol monoalkyl ether acetates such as propylene glycol monomethyl ether acetate, lactic acid esters such as methyl lactate and ethyl lactate, and acetates such as n-butyl acetate. it can.

  In the present invention, it is more preferable that the solvent used has a boiling point in the range of 100 to 350 ° C. However, the ratio of the solvent having a boiling point of 200 to 300 ° C. must be in the range of 70 to 99%, and the ratio of the solvent having a boiling point of 150 ° C. or less must be 1 to 10%. If these two conditions are satisfied, the remaining solvent component may be selected from more than 150 ° C. and less than 200 ° C. The preferred range of the solvent component in the color filter ink composition of the present invention is an ink composition in which the solvent is blended in an amount of 5 to 2000 parts by weight, particularly preferably 50 to 1000 parts by weight with respect to 100 parts by weight of the solid content. It is preferable that it is a thing.

  If the ink composition contains 10% or more of a solvent with a boiling point of 150 ° C or lower, the evaporation rate of the solvent becomes too fast, and the surface of the ink waiting in the head is dried, etc. This causes the nozzle to be blocked and ink droplets to fly obliquely. On the other hand, when the solvent composition at 200 ° C. or higher is less than 70%, the same phenomenon as described above occurs.

  On the other hand, to achieve the ink composition only with a solvent having a boiling point of 200 ° C. or higher, when a pigment is dispersed, a highly effective dispersant cannot be used, or an effective amount of binder or cured resin cannot be dissolved. And high-performance hue and contrast cannot be achieved.

  As will be described later, the ink composition of the present invention is applied to a glass substrate such as mother glass using an inkjet method, and then dried and thermally cured to form a predetermined image to obtain a color filter cured film. However, this does not exclude the image formation of the ink composition of the present invention by photocuring.

  Furthermore, the color filter ink composition of the present invention may contain components other than the solvent as long as the effects of the present invention are not impaired. For example, a surfactant (E) component may be used to improve wettability, and a coupling agent (E) component is preferably used to improve adhesion. In this case, the surfactant is preferably contained in the range of 0.01 to 0.5% by weight with respect to 100 parts by weight of the solid content. The component (E) is not included in the solvent referred to in the present invention.

  About the ink composition in this invention, after apply | coating to the predetermined | prescribed area | regions, such as a glass substrate, by the inkjet method, the drying process is performed for 1 to 60 minutes at room temperature (23 degreeC) -130 degreeC, for example, and then at 200-260 degreeC A predetermined image can be formed by performing thermosetting for 0.5 to 2 hours. In this case, generally used means can be adopted as the ink jet method. For example, a predetermined black matrix is formed in a concave colored pattern shape, and the ink composition is applied to this portion by ink jet, and then dried and cured. There is a way.

  The color filter ink composition of the present invention is suitable for forming a pixel pattern on a glass substrate whose size is increasing, and is an ink composition used for an inkjet method capable of reducing cost and mass production. . The ink composition of the present invention is an ink composition for a color filter that can achieve high productivity because it has excellent viscosity stability and drying properties while maintaining such stable ejection characteristics.

  EXAMPLES Hereinafter, although an Example demonstrates this invention in more detail, this invention is not limited to this. In addition, unless otherwise indicated in an Example, a part represents a weight part and% represents weight%. Moreover, the preparation method of each dispersion liquid containing the pigment of (D) component is described below.

[Red dispersion adjustment]
142g of pigment PR254 and PY150 mixed in 80/20 were collected in a 2L stainless steel container, and 160g of PB823 (dispersant made by Ajinomoto Co., Inc.) and 20g of BC (butyl carbitol) that had been previously made into a 50% butylcarbitol solution. In addition, this is kneaded with a three roll coated with ceramic coating until it becomes fluid. Further, 278 g of BCA (butyl carbitol acetate) is added and mixed, and then the kneaded product is dispersed with a horizontal sand mill until the average particle size of the pigment is 100 nm or less. After the dispersion was completed, it was diluted with 400 g of BCA to obtain a solid content of 22.2%, and a test dispersion was obtained.

[Green dispersion adjustment]
150g of pigment PG36 and PY150 mixed in 60/40 was collected in a 2L stainless steel container, 17.8g of ethyl carbitol acetate, and PB827 (manufactured by Ajinomoto Co., Inc.) made into a 1,3-butylene glycol diacetate 50% solution in advance. Add 150g of (dispersing agent), and knead it with a three roll coated with ceramic coating until it becomes fluid. Further, after adding and mixing 182.2 g of 1,3-butylene glycol diacetate (1,3BGDA), the kneaded product is dispersed with a horizontal sand mill, and dispersed until the average particle size of the pigment is 100 nm or less. After the dispersion was completed, it was diluted with 500 g of 1,3BGDA to give a solid content of 22.5%, and a test dispersion was obtained.

[Blue dispersion adjustment]
Pigment PB; 15.6 (122 g) is collected in a 2 L stainless steel container, and 130.6 g of PB824 (dispersant manufactured by Ajinomoto Co., Inc.) previously prepared as a 50% solution of butyl carbitol is added to 108 g of butyl carbitol. This is kneaded with three rolls coated with ceramic coating until fluidity comes out. 239 g of butyl carbitol acetate is further added to and mixed with this kneaded product, and then dispersed in a horizontal sand mill until the average particle size of the pigment is 100 nm or less. After the dispersion was completed, it was diluted with 400 g of butyl carbitol acetate to obtain a solid dispersion having a solid content of 17.8%.

[Example 1]
The rotor was placed in a beaker (1000 ml) and placed on a magnetic stirrer. As solvent, 2.3 g of 1,3-butylene glycol diacetate (1,3BGDA), 206.5 g of diethylene glycol monoethyl ether acetate (also known as ethyl carbitol acetate (ECA)), 1.7 g of propylene glycol monomethyl ether acetate (PEGMEA) While weighing and stirring, 4.0 g of YX4000HK (manufactured by Japan Epoxy Resin Co., Ltd.) was added as component (C). After confirming these dissolutions, a PGMEA (propylene glycol monomethyl ether acetate) solution of the fluorene type epoxy acrylate / acid anhydride polymerization adduct of component (A) (V259ME resin component 56.5%, manufactured by Nippon Steel Chemical Co., Ltd.) 42.5 g of PGMEA) and 16.0 g of component (B) dipentaerythritol hexaacrylate DPHA (manufactured by Nippon Kayaku Co., Ltd.) were added and stirred. Next, 227.0 g of the green dispersion of component (D), which was previously dispersed and adjusted, was added and further stirred. Finally, 2.5 g and 0.3 g of the additive silane coupling agent and surfactant were added, and the mixture was further stirred for 30 minutes to obtain a test ink composition. Table 1 shows the composition of this ink composition and the boiling point of the contained solvent.

  The test ink composition obtained above was evaluated for various performances according to the following methods. The results are shown in Table 1.

[Evaluation method]
<Viscosity stability test>
The prepared ink composition was previously measured for its viscosity at 50 rpm and 23 ° C. using an E-type viscometer. Thereafter, 100 g was transferred to a container that could be sealed, and after accelerated aging at 40 ° C. for one week, the viscosity was measured under the same conditions, and a viscosity increase of 1 mPa · sec or less from the initial viscosity was accepted.

<Discharge test>
Connected to Toshiba Tec head (CA-3), purged and washed, checked ink composition ejection status with strobe camera, no droplets ejected, flight trajectory not clearly vertical, etc. If there was no defect, it was judged as “good”. FIG. 1 shows an example of a stroboscopic photograph when it is determined to be “good”.

<Continuous discharge test>
After continuously discharging for 1 hour in the above discharge test, print solidly on A4 size inkjet paper in the range of 50mm in width and 200mm in length (execute a program that discharges all ink from all nozzles at the highest density). went. This was repeated 10 times, and a case where there was no ejection defect in the printed portion was marked as ◯.

<Intermittent discharge test>
Execute a program to discharge all ink from all nozzles at the highest density, discharge continuously for 1 hour, pause for 10 minutes, discharge after head maintenance by ink purging and cleaning procedures, and print on A4 size inkjet paper A case where printing was performed in a range of 50 mm in width and 200 mm in length and there was no discharge defect in the printed portion was marked as ◯.

[Example 2]
The rotor was placed in a beaker (1000 ml) and placed on a magnetic stirrer. Weigh 131g of diethylene glycol butyl ether acetate (also known as butyl carbitol acetate (BCA)), 4g of diethylene glycol monobutyl ether (also known as butyl carbitol (BC)), and 8g of propylene glycol monomethyl ether acetate (PEGMEA) as a solvent. However, PGMEA solution of component (A) fluorene type epoxy acrylate / acid anhydride polymerization adduct (V259ME resin component 56.5%, PGMEA made by Nippon Steel Chemical Co., Ltd.) 38.5g and component (B) dipenta 9.5 g of erythritol hexaacrylate DPHA (manufactured by Nippon Kayaku Co., Ltd.) was added and stirred. Next, 309 g of the Blue dispersion of component (D), which was previously dispersed and adjusted, was added and further stirred. Finally, 2.5 g and 0.3 g of the additive silane coupling agent and surfactant were added, and the mixture was further stirred for 30 minutes to obtain a test ink composition. Table 1 shows the evaluation results of the ink composition carried out in the same manner as in Example 1, together with the composition of this ink composition and the boiling point of the solvent contained.

[Example 3]
The rotor was placed in a beaker (1000 ml) and placed on a magnetic stirrer. Diethylene glycol butyl ether acetate (also known as butyl carbitol acetate (BCA)) as a solvent 176.9g, diethylene glycol monobutyl ether (also known as butyl carbitol (BC)) 0.2g, propylene glycol monomethyl ether acetate (PEGMEA) 0.9g, weighed Then, 2.5 g of YX4000HK (manufactured by Japan Epoxy Resin Co., Ltd.) was added as component (C) while stirring. After confirming these dissolutions, 26.0 g of PGMEA solution (V259ME resin component 56.5%, PGMEA made by Nippon Steel Chemical Co., Ltd.) of (A) component fluorene type epoxy acrylate / acid anhydride polymerization adduct ( B) Component dipentaerythritol hexaacrylate DPHA (manufactured by Nippon Kayaku Co., Ltd.) 10.0 g was added and stirred. Next, 283.5 g of the Red dispersion of component (D), which was previously dispersed and adjusted, was added and further stirred. Finally, 2.5 g and 0.3 g of the additive silane coupling agent and surfactant were added, and the mixture was further stirred for 30 minutes to obtain a test ink composition. Table 1 shows the evaluation results of the ink composition carried out in the same manner as in Example 1, together with the composition of this ink composition and the boiling point of the solvent contained.

[Reference Example 1]
The rotor was placed in a beaker (1000 ml) and placed on a magnetic stirrer. Diethylene glycol butyl ether acetate (other name: butyl carbitol acetate (BCA)) 110.5g, diethylene glycol monobutyl ether (other name: butyl carbitol (BC)) 4g, propylene glycol monomethyl ether acetate (PEGMEA) 8g, ethoxypropanol (solvent) Weigh 12.5g of Kanto Chemical Co., Ltd. and 8g of methoxypropanol (Kanto Chemical Co., Ltd.) and stir them while stirring. PGMEA solution of component (A) fluorene type epoxy acrylate / acid anhydride polymerization adduct (Shinichi) 38.5 g of V259ME resin component 56.5%, PGMEA) manufactured by Sakai Chemical Co., Ltd. and 9.5 g of dipentaerythritol hexaacrylate DPHA (manufactured by Nippon Kayaku Co., Ltd.) as component (B) were added and stirred. Next, 309 g of the Blue dispersion of component (D), which was previously dispersed and adjusted, was added and further stirred. Finally, 2.5 g and 0.3 g of the additive silane coupling agent and surfactant were added, and the mixture was further stirred for 30 minutes to obtain a test ink composition. Table 1 shows the evaluation results of the ink composition carried out in the same manner as in Example 1, together with the composition of this ink composition and the boiling point of the solvent contained.

[Comparative Example 1]
The rotor was placed in a beaker (1000 ml) and placed on a magnetic stirrer. Diethylene glycol butyl ether acetate (also known as butyl carbitol acetate (BCA)) 14.3 g, diethylene glycol monobutyl ether (also known as butyl carbitol (BC)) 32.2 g, propylene glycol monomethyl ether acetate (PEGMEA) 49.9 g as solvents 40.8 g of propanol (Kanto Chemical Co., Ltd.) and 40.8 g of methoxypropanol (Kanto Chemical Co., Ltd.) were weighed and 2.5 g of YX4000HK (Japan Epoxy Resin Co., Ltd.) was added as component (C) while stirring. After confirming these dissolutions, 26.0 g of PGMEA solution (V259ME resin component 56.5%, PGMEA made by Nippon Steel Chemical Co., Ltd.) of (A) component fluorene type epoxy acrylate / acid anhydride polymerization adduct ( B) Component dipentaerythritol hexaacrylate DPHA (manufactured by Nippon Kayaku Co., Ltd.) 10.0 g was added and stirred. Next, 283.5 g of the Red dispersion of component (D), which was previously dispersed and adjusted, was added and further stirred. Finally, 2.5 g and 0.3 g of the additive silane coupling agent and surfactant were added, and the mixture was further stirred for 30 minutes to obtain a test ink composition. Table 1 shows the evaluation results of the ink composition carried out in the same manner as in Example 1, together with the composition of this ink composition and the boiling point of the solvent contained.

[Comparative Example 2]
The rotor was placed in a beaker (1000 ml) and placed on a magnetic stirrer. 9.7 g of diethylene glycol butyl ether acetate (also known as butyl carbitol acetate (BCA)), 3.5 g of diethylene glycol monobutyl ether (also known as butyl carbitol (BC)), 52.5 g of butoxypropanol (a reagent manufactured by Kanto Chemical Co., Inc.) Weigh 50.7 g of propylene glycol monomethyl ether acetate (PEGMEA), 20.3 g of ethoxypropanol (Kanto Chemical Co., Ltd.), and 20.3 g of methoxypropanol (Kanto Chemical Co., Ltd.) and stir the fluorene type of component (A). 42.0g of PGMEA solution of epoxy acrylate / acid anhydride polymer adduct (V259ME resin component 56.5%, PGMEA made by Nippon Steel Chemical Co., Ltd.) and (B) component dipentaerythritol hexaacrylate DPHA (Nippon Kayaku Co., Ltd.) 16.0 g) was added and stirred. Next, 285.0 g of the Blue dispersion of component (D), which was previously dispersed and adjusted, was added and further stirred. Finally, 2.5 g and 0.3 g of the additive silane coupling agent and surfactant were added, and the mixture was further stirred for 30 minutes to obtain a test ink composition. Table 1 shows the evaluation results of the ink composition carried out in the same manner as in Example 1, together with the composition of this ink composition and the boiling point of the solvent contained.

[Comparative Example 3]
The rotor was placed in a beaker (1000 ml) and placed on a magnetic stirrer. As a solvent, 51 g of 1,3-butylene glycol diacetate (1,3BGDA), 88 g of diethylene glycol monoethyl ether acetate (also known as ethyl carbitol acetate (ECA)), 5.8 g of propylene glycol monomethyl ether acetate (PEGMEA), ethoxypropanol 64.7 g of a reagent (manufactured by Kanto Chemical Co., Inc.) was weighed, and 4.0 g of YX4000HK (manufactured by Japan Epoxy Resin Co., Ltd.) was added as component (C) while stirring. After confirming these dissolutions, 42.5 g of PGMEA solution (V259ME resin component 56.5%, PGMEA made by Nippon Steel Chemical Co., Ltd.) of (A) component fluorene type epoxy acrylate / acid anhydride polymerization adduct ( B) 16.0 g of component dipentaerythritol hexaacrylate DPHA (manufactured by Nippon Kayaku Co., Ltd.) was added and stirred. Next, 228.0 g of the component (D) Green dispersion previously dispersed and adjusted was added and further stirred. Finally, 2.5 g and 0.3 g of the additive silane coupling agent and surfactant were added, and the mixture was further stirred for 30 minutes to obtain a test ink composition. Table 1 shows the evaluation results of the ink composition carried out in the same manner as in Example 1, together with the composition of this ink composition and the boiling point of the solvent contained.

FIG. 1 is an example of a stroboscopic photograph when it is determined that the discharge test is good.

Claims (6)

In the ink composition used to create a color filter by the inkjet method,
As a solid component, it contains an unsaturated compound (A) represented by the following general formula (1), a tetrafunctional or higher polyfunctional acrylate compound (B), and a pigment (D) as essential components, and has a bifunctional or higher functionality. The polyfunctional epoxy compound (C) is blended in the range of 0 to 20% by weight with respect to the sum of the components (A) + (B), and the weight ratio of the components (A) and (B) (A ) / (B) is in the range of 10/90 to 90/10,
Further, as the solvent component in the total solvent, the boiling point contains a solvent in the range of 200 to 300 [° C. 70 to 99 wt%, boiling point and a solvent 1-6% by weight less than 0.99 ° C., the boiling point The solvent having a temperature of 200 to 300 ° C. is diethylene glycol monoalkyl ether and its terminal acetate, dipropylene glycol monoalkyl ether and its terminal acetate or diether, diethylene glycol dialkyl ether, diethylene glycol monoalkyl ether and its terminal acetate And an ink composition for an inkjet color filter, wherein the ink composition is at least one selected from the group consisting of dialkyl ethers of polyethylene glycol .
[Wherein, R ₁ , R ₂ , R ₃ and R ₄ independently represent a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a halogen atom or a phenyl group, and R ₅ represents a hydrogen atom or a methyl group. A is -CO-, -SO _2- , -C (CF ₃ ) _2- , -Si (CH ₃ ) _2- , -CH _2- , -C (CH ₃ ) _2- , -O-, 9 , 9-fluorenyl group or a direct bond, X represents a tetravalent carboxylic acid residue, Y ₁ and Y ₂ independently represent a hydrogen atom or -OC-Z- (COOH) _m It is an acid residue, m represents a number of 1 to 3, and n represents a number of 1 to 200. ] A surfactant and / or coupling agent (E), a light or thermal polymerization initiator (F), and a viscosity modifier (G) are further added to the color filter ink composition according to claim 1 . Ink composition for color filter. The ink composition for an inkjet color filter according to claim 2 , wherein the amount of the solvent used is 50 to 1000 parts by weight based on 100 parts by weight of the total of components (A) to (G). The ink composition for a color filter according to any one of claims 1 to 3 , wherein the ratio of the weight of the pigment (D) to the total weight of the solid content excluding the solvent in the ink composition is 0.3 or more. Using the color filter ink composition according to any one of claims 1-4, color filters cured film, which was obtained by drying and curing the pixels formed by an inkjet method. A color filter comprising the cured color filter film according to claim 5 .