JP4704496B2 - Photoreactive compound for color-splitting light transmission structure and color-splitting light transmission structure - Google Patents

Description

The present invention relates to a light-reactive compound for a color-splitting light-transmitting structure that has good floatability and that can be effectively used after the film is formed, and a color-splitting light-transmitting structure using this light-reactive compound And a method for manufacturing a color-splitting light transmission structure.

Conventionally, colored layers and transparent layers in color-divided light transmission structures have been manufactured by a projection exposure type pattern transfer method. In this projection exposure type pattern transfer method, a light-reactive compound for a color division light transmission structure is used. A film forming step of forming a film on the core material (hereinafter sometimes simply referred to as a photoreactive compound) may be performed. In general, a liquid dropping film forming method is used in this film forming process. A film forming method by this liquid dropping type film forming method is a method in which an appropriate amount of a photoreactive compound is dropped on a fixed core material, and then the core material is rotated, and a centrifugal force generated by the rotation is used to make the core material. This is a method of spreading the photoreactive compound throughout and curing the photoreactive compound. In such a film formation method by the liquid dropping type film forming method, the amount of the photoreactive compound actually cured on the core material is about several percent of the amount of the photoreactive compound dripped on the core material. It is. That is, the remaining photoreactive compound jumps out of the core material by centrifugal force, and the photoreactive compound that jumps out of the core material is collected as waste liquid and disposed as industrial waste. This is because when the photoreactive compound jumps out of the core material, it is in a fine granular state, so it adsorbs moisture and dust in the atmosphere, and is collected from the influence of moisture and dust. This is because the change in the liquid property of the photoreactive compound after being applied cannot be ignored. In addition, the material suspended by the colored granular material floating method such as the colored layer has a problem such as bonding.

The cause of these bonds and the like includes the presence of alcoholic free radicals in the polymer. As the photoreactive compound, one containing a high molecular polymer, a monomer, an initiator and the like is usually used, and a film is formed by polymerizing these materials by exposure. In this case, a carbon-carbon double bond may be introduced into the side chain of the polymer from the viewpoint of improving the film strength and the like by contributing the polymer to the polymerization. In such a case, a carbon-carbon double bond is usually introduced into the side chain by opening the epoxy group of a compound having an epoxy group. At this time, an alcoholic free radical is simultaneously introduced. . However, the alcoholic free radicals in such a high molecular weight polymer are bonded to the high molecular weight polymer or colored granular material by hydrogen bonding with water molecules when the photoreactive compound absorbs moisture. It is thought to be a cause.

The situation where most of the photoreactive compound is discarded without being effectively used is not preferable from the viewpoints of cost reduction, effective use of resources, material efficiency, environmental pollution due to waste liquid, and the like.

Therefore, as a method for effectively using such a photoreactive compound, for example, Patent Document 1 discloses a viscosity adjusting tank to which a waste liquid of the photoreactive compound is supplied, and a liquid medium for the viscosity adjusting tank. Based on the medium tank to be supplied, the viscometer for measuring the viscosity of the photoreactive compound liquid in the viscosity adjusting tank, the measurement result of the viscometer and the temperature of the photoreactive compound liquid in the viscosity adjusting tank A controller that calculates the resin concentration of the photoreactive compound liquid, determines the amount of the liquid medium to be supplied to the photoreactive compound liquid based on the difference between the calculated resin concentration and a preset resin concentration, and viscosity There is disclosed a photoreactive compound processing apparatus characterized by having a filter for removing foreign substances in the adjusted photoreactive compound.

Further, Patent Document 2 discloses a regeneration container that stores and regenerates the photoreactive compound collected from the photoreactive compound film forming apparatus, and evaporates the liquid component from the photoreactive compound in the regenerator. And a control device for controlling the operation of the fluid removal device, and the control device has a target viscosity that can effectively use the viscosity of the photoreactive compound. Until now, there has been disclosed a photoreactive compound preparation system characterized by operating a liquid removal device so as to remove a liquid component from the photoreactive compound.

Patent Document 3 collects an excessive photoreactive compound solution obtained from the film formation step, and prepares the solid content to be suitable for use as a film formation composition. after,
Particles and contaminants are removed from the solution. Next, a technique that is effectively used for forming a film of the photoreactive compound on a support is disclosed.

However, the method of adjusting the viscosity or the solid content concentration of the photoreactive compound collected in this way often cannot be effectively used.

Japanese Patent Laid-Open No. 2001-1000042 JP-A-11-245226 JP-A-11-133619

From the above, the light-reactive compound for a color-splitting light transmission structure that can be effectively used and has good floatability even when effectively used, and further, the color using the light-reactive compound It is desired to provide a split light transmission structure.

The present invention has been made in view of the above circumstances, and is a photoreactive compound for a color-splitting light transmission structure containing at least a polymer having an alcoholic free radical, a monomer, and an initiator. The alcoholic free radicals contained in the high molecular weight polymer in the solid content of the photoreactive compound for color-splitting light transmission structure are in the range of 0.1 mmol / g to 2.5 mmol / g. There is provided a photoreactive compound for color-splitting light-transmitting structures.

When the alcoholic free radical contained in the polymer is within the above range, the water molecule and polymer contained in the photoreactive compound when the photoreactive compound absorbs moisture. It is possible to prevent the high molecular polymer and the colored particulate matter from being bonded by hydrogen bonding or the like with the alcoholic free radical of the polymer. Thus, for example, the above-mentioned photoreactive compound is formed into a film on the transparent core material by a liquid dropping type stretching device or the like, and then the collected regenerated light reactive compound for color-splitting light transmission structure (hereinafter referred to as regenerated light). In some cases, it may be abbreviated as a reactive compound).

It was Hama present invention, even without low molecular weight polymer contains a monomer and initiator, and when manufacturing a color splitting optical transmission structure, taken after being film formed on at least once the core material A regenerated light reactive compound for color-splitting light transmissive structures, wherein the alcoholic free radicals contained in the polymer are contained in the solid content of the regenerated light reactive compound for color-splitting light transmissive structures. 2.5 mmol / g or less, a regenerated photoreactive compound for color-splitting light transmission structures is provided.

According to the present invention, when the alcoholic free radical contained in the high molecular weight polymer in the reproduction light reaction type compound is within the above range, the reproduction light reaction type compound is converted into a color-splitting light transmission structure. When the color-splitting light transmissive structure constituting layer is made of, there is no bonding of a polymer or the like, and the floatability is good, so the light and darkness is good, and it is uncured when forming a certain pattern This is because it is easy to remove the photoreactive compound, so that a photoreactive compound capable of forming a very clear and constant pattern can be obtained.

The present invention further provides a color splitting optical transmission structures characterized by using the color splitting optical transmission structure for photoreactive formulation or the color splitting optical transmission structure for reproducing photoreactive formulation . According to the present invention, by using the photoreactive compound or the regenerated photoreactive compound, it is possible to effectively utilize an extra photoreactive compound at the time of film formation that has been conventionally discarded, As a result, a low-cost color-divided light transmission structure can be obtained.

The present invention was Saranima, A alcohol soluble free radicals, 0.04mmol / g~1.8mmol / g Color split light transmitting structure and having a color splitting optical transmission structure component layer is in the range of Offer things.

According to the present invention, when the alcoholic free radicals in the color-splitting light transmitting structure constituting layer are within the above range, the high molecular polymer is bound by water molecules resulting from having many alcoholic free radicals. Because it has good floatability, it has good light and darkness, and it is easy to remove the uncured photoreactive compound when forming a certain pattern. A color-split light transmissive structure having a color-split light transmissive structure constituting layer can be obtained.

The present invention, high molecular polymer even without low, the solid content of the monomer and initiator color split light transmitting structure for photoreactive formulation containing, alcoholic free included in the high molecular weight polymer The polymer is selected so that the content of the group is within a predetermined range, and the selected polymer is mixed with the monomer and the initiator to form a color-splitting light transmission structure A color-splitting light-transmitting structure is produced using the light-reactive compound-preparing step for preparing a color-splitting light-transmitting structure and the above-mentioned photo-reactive-type compound for color-splitting light-transmitting structure. There is provided a method for manufacturing a color-splitting light transmissive structure, comprising: a color-splitting light transmissive structure manufacturing step.

A photoreactive compound containing a small amount of alcoholic free radicals contained in a high molecular weight polymer is contained in a photoreactive compound that has absorbed moisture, such as when this photoreactive compound is placed in a hygroscopic environment. It is possible to prevent problems such as bonding of a plurality of high molecular polymers due to hydrogen bonding between water molecules contained and alcoholic free radicals. Therefore, according to the present invention, the photoreactive compound preparation step of selecting the type of the polymer in the photoreactive compound and preparing the photoreactive compound using the selected polymer. In the subsequent color-splitting light transmission structure manufacturing process, the regenerated photoreactive compound collected after the film is once formed on the core material is again used for manufacturing the color-splitting light transmission structure. This is because it is possible to manufacture a color-splitting light transmission structure at a low cost.

In the above invention, the solid content of the upper Symbol color split light transmitting structure for photoreactive formulation, alcoholic radicals contained in the high molecular weight polymer, 0.1. It is preferable to be within the range of mmol / g to 2.5 mmol / g. As a result, regardless of the type of the photoreactive compound, it is possible to use the regenerated photoreactive compound collected after film formation on the core material once again for the production of a color-splitting light transmission structure. This is because the sex becomes higher.

According to the present invention, the alcoholic free radical contained in the high molecular weight polymer is included in the photoreactive compound when the photoreactive compound absorbs moisture or the like due to being in the above range. In addition, it is possible to prevent the high molecular polymer and the colored particulate matter from being bonded by hydrogen bonding between the water molecule and the alcoholic free radical of the high molecular polymer. Thus, for example, the above-mentioned photoreactive compound is formed into a film on the transparent core material by a liquid dropping type stretching device or the like, and then the collected regenerated light reactive compound for color-splitting light transmission structure (hereinafter referred to as regenerated light). It may be abbreviated as a reactive compound).

It is process drawing which shows an example of the manufacturing method of the color division light transmissive structure using the photoreactive type compound of this invention.

The present invention uses a photoreactive compound that can be used effectively in the production of a color-splitting light transmission structure, or a regenerated photoreactive compound, or a photoreactive compound or a regenerated photoreactive compound. The present invention relates to a color division light transmission structure and a method for manufacturing the color division light transmission structure.
Hereinafter, each will be described in detail.

A. First, the photoreactive compound of the present invention will be described. The photoreactive compound according to the present invention is a photoreactive compound for a color-splitting light transmission structure containing at least a polymer having an alcoholic free radical, a monomer, and an initiator, The alcoholic free radicals contained in the high molecular weight polymer in the solid content of the photoreactive compound for light transmissive structures are 0.1 mmol / g to
It is characterized by being in the range of 2.5 mmol / g.

The photoreactive compound of the present invention is used for a color-splitting light transmission structure constituting layer constituting a color-splitting light transmission structure. Here, the color-splitting light-transmitting structure constituting layer constituting the color-splitting light-transmitting structure in the present invention refers to, for example, a colored layer, a polymer plastic light blocking film, a transparent layer, and a spacing-holding projection forming photoreaction. It shall refer to a mold compound or the like.

The color-splitting light-transmitting structure constituting layer constituting such a color-splitting light-transmitting structure is uniformly applied by centrifugal force by rotating the core material after dropping an appropriate amount of the photoreactive compound on the core material. It is formed by a liquid dropping film forming method for forming a transparent film. At this time, the excess photoreactive compound is ejected out of the core material by centrifugal force and collected. When such a photoreactive compound is repelled by centrifugal force, it becomes fine droplets, so it easily absorbs moisture in the air, and there is a problem with the floating property of the collected photoreactive compound. Some have been disposed of as industrial waste. As a result, there are problems such as low material efficiency, increased cost, and environmental pollution due to waste.

The cause of problems in the floating property of the collected photoreactive compound is, for example, that water molecules that have been absorbed bind to alcoholic free radicals of the polymer in the photoreactive compound by hydrogen bonding or the like. In the case of the colored granular material floating method by binding a plurality of high molecular polymers and also by this hydrogen bond, the colored granular material is suspended due to the surrounding high molecular polymer, The distance between the colored particles is reduced by the polymer chains of the surrounding polymer being shrunk within the suspended particles due to the action of the water molecules or by being bonded to each other between adjacent suspended particles. Therefore, it is presumed that the colored granular materials are combined.

According to the present invention, when the alcoholic free radicals contained in the high molecular weight polymer are within a predetermined range, the color-splitting light transmission structure constituting layer is formed by the liquid dropping film forming method or the like. In addition, it is possible to prevent the effect of moisture absorption of the photoreactive compound that has been ejected out of the core material, and the collected photoreactive compound can be used effectively.

In the present invention, the alcoholic free radicals contained in the polymer are in the range of 0.1 mmol / g to 2.5 mmol / g in the solid in the photoreactive compound,
In particular, within the range of 0.1 mmol / g to 0.7 mmol / g, particularly 0.1 mmol / g to 0
. It is preferably within the range of 5 mmol / g. As a result, for example, when the color-splitting light transmitting structure forming layer is formed by the liquid dropping type film forming method, even when the photoreactive compound ejected out of the core material of the color-splitting light transmitting structure is collected, This is because it is possible to prevent the binding of granular materials, high molecular polymers and the like, and it can be used as a regenerative photoreactive compound.

In this case, the amount of alcoholic free radicals contained in the polymer is a value calculated from the composition by a theoretical value.

The photoreactive compound of the present invention contains at least a polymer, a monomer and an initiator,
As long as the amount of alcoholic free radicals in the polymer is not more than the above-mentioned predetermined amount, the composition thereof is not particularly limited, but additionally contains, for example, a liquid medium or colored particulate matter. It may be.

As described above, the polymer used in the photoreactive compound of the present invention is contained in the polymer in the solid content of the photoreactive compound when used as a photoreactive compound. The amount of alcoholic free radicals is within a predetermined range. Since such a high molecular polymer is used as a photoreactive compound, a monomer having an acid such as acrylic acid or methacrylic acid as a main chain is polymerized, and an alcoholic free radical is present. If it has, it will not specifically limit. As what has such an alcoholic free radical, what carried out ring-opening polymerization of epoxy-type acrylates, such as glycidyl methacrylate, etc. in a side chain can be mentioned, for example.

The main chain may be, for example, a polymer of an acid-containing monomer such as methacrylic acid and an ester-based monomer. Examples of these ester-based monomers include ε- Caprolactam-modified tetrahydrofurfuryl acrylate, phenoxyethyl acrylate, phenoxy polyethylene acrylate, ethylene oxide modified nonyl phenol acrylate, alkylphenol polyethylene glycol acrylate, ethylene and propylene oxide modified phenol acrylate, 4-hydroxybutyl acrylate, 2
-Hydroxypropyl acrylate, 2-hydroxy-3-phenoxypropyl acrylate, carboxypolycaprolactone monoacrylate, 2-acryloyloxyethyl hydrogen phthalate, 2-acryloyloxypropyl hydrogen phthalate, 2-
Acryloyloxypropyl hexahydrohydrogen phthalate, β-acryloyloxyethyl hydrogen succinate, 2-acryloyloxyethyl 2-hydroxyethyl hydrogen phthalate, isobutyl acrylate, t-butyl acrylate, lauryl acrylate, alkyl acrylate, cetyl acrylate, stearyl acrylate, Isoamyl acrylate, ethylene oxide modified lauryl acrylate, 2-methoxyethyl acrylate, 3-methoxybutyl acrylate, ethyl carbitol acrylate, 2-ethylhexyl carbitol acrylate, methoxytriethylene glycol acrylate, butoxyethyl acrylate, methoxypolyethylene glycol acrylate, methoxy Dipropi Glycol acrylate, isobornyl acrylate, cyclohexyl acrylate, benzyl acrylate, dicyclopentenyl acrylate,
Examples thereof include ethylene oxide-modified dicyclopentenyl acrylate, tetrahydrofurfuryl acrylate, dimethylaminoethyl acrylate, butylene glycol monovinyl ether, acryloylmorpholine, and methacrylates of the above acrylates.

In addition to the above polymer, the photoreactive compound of the present invention includes polyamide resins, polyurethane resins, epoxy resins, polyamide resins, phenol resins, fluorine resins, cellulose resins, vinyls. System resin etc. may be contained.

Such a polymer is preferably used in the range of 3 to 50% by weight, particularly 10 to 40% by weight in the solid component.

The photoreactive compound of the present invention further contains a monomer and an initiator. Specific examples of such monomers include allyl acrylate, benzyl acrylate, butoxyethyl acrylate, butoxyethylene glycol acrylate, cyclohexyl acrylate, dicyclopentanyl acrylate, 2-ethylhexyl acrylate, glycerol acrylate, glycidyl acrylate, 2 -Hydroxyethyl acrylate, 2-hydroxypropyl acrylate, isobornyl acrylate, isodexyl acrylate,
Isooctyl acrylate, lauryl acrylate, 2-methoxyethyl acrylate,
Methoxyethylene glycol acrylate, phenoxyethyl acrylate, stearyl acrylate, ethylene glycol diacrylate, diethylene glycol diacrylate, 1,4-butanediol diacrylate, 1,5-pentanediol diacrylate, 1,6-hexanediol diacrylate, 1, 3-propanediol acrylate,
1,4-cyclohexanediol diacrylate, 2,2-dimethylolpropane diacrylate, glycerol diacrylate, tripropylene glycol diacrylate, glycerol triacrylate, trimethylolpropane triacrylate, polyoxyethylated trimethylolpropane triacrylate, penta Erythritol triacrylate, pentaerythritol tetraacrylate, triethylene glycol diacrylate, polyoxypropyltrimethylolpropane triacrylate, butylene glycol diacrylate, 1,2,4-butanetriol triacrylate, 2,2,4-trimethyl-1, 3-pentanediol diacrylate, diallyl fumarate, 1,10-decanediol dimethyl acrylate , Dipentaerythritol hexaacrylate, and,
Those obtained by replacing the above acrylate groups with methacrylate groups, γ-methacryloxypropyltrimethoxysilane, 1-vinyl-2-pyrrolidone, 2-hydroxyethylacryloyl phosphate, tetrahydrofurfuryl acrylate, dicyclopentenyl acrylate, dicyclopentenyl Oxyethyl acrylate, 3-butanediol diacrylate, neopentyl glycol diacrylate, polyethylene glycol diacrylate, hydroxypivalate ester neopentyl glycol diacrylate, phenol-ethylene oxide modified acrylate, phenol-propylene oxide modified acrylate, N-vinyl- 2-pyrrolidone, bisphenol A-ethylene oxide modified diacrylate, pentaerythritol Acrylate monostearate, tetraethylene glycol diacrylate, polypropylene glycol diacrylate, trimethylolpropane propylene oxide modified triacrylate, isocyanuric acid ethylene oxide modified triacrylate, trimethylolpropane ethylene oxide modified triacrylate, pentaerythritol pentaacrylate, penta Acrylate monomers such as erythritol hexaacrylate and pentaerythritol tetraacrylate, and those obtained by substituting these acrylate groups with methacrylate groups, urethane acrylate oligomers in which an acrylate group is bonded to an oligomer having a polyurethane structure, and oligomers having a polyester structure Polyester copolymer with acrylate group bonded to Acrylate oligomer, epoxy acrylate oligomer with epoxy group bonded to acrylate group, urethane methacrylate oligomer with methacrylate structure bonded to oligomer with polyurethane structure, polyester methacrylate with methacrylate group bonded to oligomer with polyester structure Oligomers, epoxy methacrylate oligomers in which methacrylate groups are bonded to oligomers having epoxy groups, polyurethane acrylates having acrylate groups, polyester acrylates having acrylate groups, epoxy acrylate resins having acrylate groups, polyurethane methacrylates having methacrylate groups, methacrylate groups Has polyester methacrylate, methacrylate group Epoxy methacrylate resin or the like having the like.

In the present invention, trimethylolpropane triacrylate, pentaerythritol tetraacrylate, dipentaerythritol hexaacrylate and the like can be mentioned as preferable examples.

The amount of the monomer component used in the solid component is preferably in the range of 30% to 80% by weight, particularly 30% to 40% by weight.

Specific examples of the initiator that can be used in the photoreactive compound of the present invention include benzophenone, Michler's ketone, N, N′tetramethyl-4,4′-diaminobenzophenone, and 4-methoxy-4. '-Dimethylaminobenzophenone, 4,4'-diethylaminobenzophenone, 2-ethylanthraquinone, aromatic ketones such as phenanthrene, benzoin ethers such as benzoin methyl ether, benzoin ethyl ether, benzoin phenyl ether, methyl benzoin, ethyl benzoin, etc. Benzoin, 2- (o-chlorophenyl) -4,5-phenylimidazole dimer, 2- (o-chlorophenyl)-
4,5-di (m-methoxyphenyl) imidazole dimer, 2- (o-fluorophenyl) -4,5-diphenylimidazole dimer, 2- (o-methoxyphenyl) -4,5-
Diphenylimidazole dimer, 2,4,5-triarylimidazole dimer, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone, 2-trichloromethyl-5-styryl-1 , 3,4-oxadiazole, 2-trichloromethyl-
5- (p-cyanostyryl) -1,3,4-oxadiazole, 2-trichloromethyl-
Halomethylthiazole compounds such as 5- (p-methoxystyryl) -1,3,4-oxadiazole, 2,4-bis (trichloromethyl) -6-p-methoxystyryl-S-triazine, 2,4- Bis (trichloromethyl) -6- (1-p-dimethylaminophenyl-1
, 3-Butadienyl) -S-triazine, 2-trichloromethyl-4-amino-6-p-
Methoxystyryl-S-triazine, 2- (naphth-1-yl) -4,6-bis-trichloromethyl-S-triazine, 2- (4-ethoxy-naphth-1-yl) -4,6-bis- Trichloromethyl-S-triazine, 2- (4-butoxy-naphth-1-yl) -4,
Halomethyl-S-triazine compounds such as 6-bis-trichloromethyl-S-triazine, 2,2-dimethoxy-1,2-diphenylethane-1-one, 2-methyl-1- [4-
(Methylthio) phenyl] -2-morpholinopropanone, 1,2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1,1-hydroxy-cyclohexyl-phenylketone, Irgacure 369 ( Examples include initiators such as Ciba Geigy), Irgacure 651 (Ciba Geigy), Irgacure 907 (Ciba Geigy), Irgacure 184 (Ciba Geigy). In the present invention, these initiators can be used alone or in admixture of two or more.
Among these, Irgacure 184 (manufactured by Ciba Geigy), Irgacure 369 (manufactured by Ciba Geigy), and Irgacure 907 (manufactured by Ciba Geigy) can be cited as preferred examples.

The amount of such initiator used in the solid component is 10% by weight to 30% by weight, particularly 10%.
It is preferable to be within the range of 20% by weight to 20% by weight.

The photoreactive compound of the present invention may further contain other components such as a liquid medium and colored particles added depending on the type of the color-splitting light-transmitting structure constituting layer to be formed.

The liquid medium used in the photoreactive compound of the present invention is not particularly limited as long as it is a liquid medium that can dissolve or float the above-described polymer and can have a predetermined viscosity. Specifically, cyclohexanone, methyl amyl ketone, 3-methoxy-1-butyl acetate, 3-methoxy-3-methyl-1-butyl acetate, ethylene glycol monoethyl ether acetate, ethylene glycol monobutyl ether acetate, propylene glycol monomethyl ether Acetate, propylene glycol monoethyl ether acetate, chloroform, methylene chloride, dichloroethane, tetrahydrofuran,
Examples include toluene, xylene, diethylene glycol dimethyl ether, 3-methoxybutyl acetate, ethyl 3-ethoxypropionate, 4-hydroxy-4-methyl-2-pentane, and the like.

In addition, a surfactant or a polymer additive can be added as an additive. Examples of the surfactant that can be used include polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether, polyoxyethylene octylphenyl ether, polyoxyethylene nonylphenyl ether, polyethylene glycol dilaurate, and polyethylene glycol. Examples include distearate, sorbitan fatty acid esters, fatty acid-modified polyesters, and tertiary amine-modified polyurethanes.

Polymer additives include Polyflow No. 75, No 90, No, 95 (trade name, manufactured by Kyoeisha Yushi Chemical Co., Ltd.), MegaFuck F171, F172, F173 (trade name, manufactured by Dainippon Ink & Chemicals, Inc.) , Florard Fc403, Fc431 (trade name, manufactured by Sumitomo 3M Limited), Sol Sparse 13240, 2
0000, 24000GR, 26000, 28000, 33500 (trade name, manufactured by Avidia), Disperbyk 111, 161,
162, 163, 164, 182, 2000, 2001 (trade name, manufactured by Big Chemie), Addisper PB711, PB4
11, PB111, PB821, PB822 (trade name, manufactured by Ajinomoto Fine Techno Co., Ltd.) and the like.

Further, when forming the colored layer of the color-splitting light transmission structure using the photoreactive compound of the present invention, a colored granular material is further used, and the photoreactive type for the colored layer is used to float it. It can be a blend. The organic colored granular materials that can be used in the present invention are shown in Tables 1 and 2 below.

In addition, as inorganic colored granular materials that can be used, titanium oxide, zinc white, lead sulfate, yellow lead, zinc yellow, bengara, cadmium red, ultramarine blue, bitumen, chromium oxide green, cobalt green, amber, titanium black, synthetic Examples thereof include iron black and carbon black.

On the other hand, when forming the polymer plastic light blocking film of the color-splitting light transmission structure using the photoreactive compound of the present invention, the photoreactive compound of the present invention is added by adding a light-shielding granular material. It is possible to form a black matrix using a material. Specific examples of the light-shielding granular material include carbon fine particles, metal oxides, inorganic colored granular materials, and organic colored granular materials.

B. Next, the reproduction light reaction type compound for color-splitting light transmission structure will be described. The regenerated photoreactive compound of the present invention contains at least a polymer, a monomer, and an initiator, and was formed into a film on the core material at least once when producing a color-splitting light transmission structure. A regenerated photoreactive compound collected later, wherein the alcoholic free radicals contained in the polymer in the solid content of the regenerated photoreactive compound are within a predetermined range. It is what.

According to the present invention, when the alcoholic free radical is within the predetermined range, the regenerated photoreactive compound collected after the film is formed on the core material by, for example, a liquid dropping type stretching device. Even in such cases, the polymer in the regenerated photoreactive compound is less likely to be affected by the water molecules absorbed in the regenerated photoreactive compound, and it must have good floatability when used as a film. From this, it is possible to form a very clear and constant pattern because the light and darkness is good and it is easy to remove the uncured photoreactive compound when forming a certain pattern. .

The alcoholic free radicals contained in the high molecular weight polymer in the solid content in the regenerated photoreactive compound of the present invention are 2.5 mmol / g or less, preferably 0.1 mmol / g to 2.5 mmol /
in the range of g, in particular in the range of 0.1 mmol / g to 0.7 mmol / g, in particular 0.1 mm.
It is preferable to be within the range of ol / g to 0.5 mmol / g. The amount of alcoholic free radicals is a value calculated from the composition by a theoretical value.

In the present invention, the regenerated light-reactive compound may be collected and used in the production process of the color-splitting light transmission structure a plurality of times, and the number of times is not particularly limited.

The composition of the regenerated photoreactive compound of the present invention is not particularly limited as long as it contains at least a polymer, a monomer and an initiator. Since these compositions and the like are the same as those described in the section of “A. Photoreactive compound for color-splitting light transmission structure”, description thereof is omitted here.

C. Next, the color division light transmission structure of the present invention will be described. The color-splitting light transmissive structure of the present invention uses the above-described photoreactive compound or regenerated photoreactive compound (hereinafter referred to as the first embodiment) and the color-splitting light transmissive structure component layer. There are two modes when the amount of the alcoholic free radical is within a predetermined range (hereinafter referred to as the second mode).

In both aspects, since the amount of alcoholic free radicals is within a predetermined range, as described above, the possibility of being affected by water molecules is low, and the color-splitting light transmission has good floating properties and smoothness. A color-splitting light transmission structure having a structure constituting layer can be obtained.

Here, the color-splitting light transmission structure constituting layer refers to a colored layer, a black matrix, a transparent layer, a spacing projection, etc. of the color-splitting light transmission structure as described above. Hereinafter, each aspect will be described separately.

1. First Aspect First, a first aspect in the color-divided light transmission structure of the present invention will be described. The first aspect of the color-splitting light transmitting structure of the present invention is the photoreactive compound described in the above-mentioned section “A. Photoreactive compound for color-splitting light transmitting structure” or “B. This is characterized by using a “regenerative light reaction type compound for split light transmission structures”.

As described above, the color-splitting light transmission structure of this embodiment can be less affected by moisture absorption or the like as described above by using the above-mentioned photoreactive compound or regenerated photoreactive compound. When forming a color-splitting light transmission structure component layer using a drop-type stretching device, etc., it is possible to collect and use the light-reactive compound ejected out of the core of the color-splitting light transmission structure again. Thus, a low-cost color-divided light transmission structure can be obtained.

The color-splitting light transmission structure of this aspect is not particularly limited as long as it has at least a core material and a colored layer formed in a certain pattern on the core material. In addition,
A black matrix, a transparent layer, or the like is laminated.

In this embodiment, the above-described photoreactive compound or regenerated photoreactive compound may be used as a photoreactive compound for a colored layer that forms a colored layer, and light for black matrix that forms a black matrix. It may be used as a reactive compound, used as a photoreactive compound for a transparent layer for forming a transparent layer, a photoreactive compound for a protrusion for spacing and a projection for forming a spacing, etc. Also good. Hereinafter, the core material, the colored layer, the black matrix, and other configurations constituting the color-divided light transmission structure of this aspect will be described.

(1) Core material As the core material used in the color-divided light transmission structure of this aspect, a core material normally used in a color-division light transmission structure can be used. As such a core material, for example, A core material, a glass film, a synthetic resin core material, a synthetic resin film, etc. can be used, and it is preferable that it is excellent in heat resistance, smoothness, and translucency.

(2) Colored layer Normally, the colored layer in the color-divided light transmission structure is formed of a single color or a plurality of colors with various constant patterns, and the same applies to this aspect. .

In this embodiment, the photoreactive compound for a colored layer forming the colored layer is referred to as “A. Photoreactive compound for color-splitting light transmission structure” or “B. Reproduction light for color-splitting light transmission structure”. Reactive compound "
It is preferable to use a photoreactive compound containing the colored granular material described in the column of this, and even when the photoreactive compound absorbs moisture, the possibility that the floating property of the colored granular material will change is low. For example, when forming a colored layer, the photoreactive compound ejected out of the core material by a liquid dropping type stretching apparatus or the like may be collected and used as a photoreactive compound that forms a colored layer again. It becomes possible. Thereby, a colored layer can be formed advantageously in terms of environment and cost.

(3) Black matrix In this embodiment, a black matrix may be formed. Such a black matrix may be made of a metal thin film such as chromium, or may be made of a resin. In the case of a black matrix made of resin, the photoreactive compound or regenerated photoreactive compound containing the above-mentioned light-shielding granular material should be used as the black matrix photoreactive compound for forming the black matrix. Is possible.

When a black matrix made of a metal thin film such as chromium is formed, a metal thin film such as chromium having a thickness of about 1000 to 2000 mm is formed by, for example, sputtering or vacuum deposition, and the thin film is patterned. can do.

(4) Others In the color-divided light transmission structure in this embodiment, not only the colored layer and the black matrix are laminated, but also a transparent layer, a spacing holding projection, and the like may be provided. Such a transparent layer and spacing holding protrusions can also be formed using the above-described photoreactive compound or regenerated photoreactive compound. As a result, preferable effects such as cost reduction, effective use of resources, material efficiency, and reduction of environmental load due to waste liquid can be further obtained.

2. Second Embodiment Next, a second embodiment of the color division light transmission structure of the present invention will be described. The 2nd aspect in the color division light transmission structure of this invention is a case characterized by having a color division light transmission structure structure layer in which alcoholic free radicals are within a predetermined range.

According to the present invention, the amount of alcoholic free radicals in the color-splitting light transmission structure constituting layer is within a predetermined range, and as described above, due to alcoholic free radicals and hydrogen bonds of water molecules. It has a color-splitting light-transmitting structure constituting layer in which a smooth surface having good floatability is formed without binding of a polymer in the photoreactive compound forming the color-splitting light-transmitting structure constituting layer A color-splitting light transmission structure can be obtained.

The amount of alcoholic free radicals in the color-splitting light transmission structure constituting layer is 0.04 mmol / g.
It is preferable to be within the range of -1.8 mmol / g. The amount of alcoholic free radicals in this case is a value calculated from the composition by a theoretical value.

The color-divided light transmission structure of this embodiment is not particularly limited as long as it has at least a core material and a colored layer formed in a certain pattern on the core material. In addition, a black matrix, a transparent layer, or the like may be laminated, and the material, the formation method, and the like are the same as those in the first aspect described above, and thus the description thereof is omitted here.

D. Next, the manufacturing method of the color division | segmentation light transmission structure of this invention is demonstrated. The method for producing a color-splitting light-transmitting structure of the present invention comprises an alcoholic substance contained in the polymer in the solid content of a photoreactive compound containing at least a polymer, a monomer, and an initiator. A polymer is selected so that the content of free radicals is within a predetermined range, and the selected polymer is mixed with the above monomer and the above initiator to produce a photoreactive compound. A method comprising: a photoreactive compound preparation step for preparing a product; and a color-splitting light transmitting structure manufacturing step for manufacturing a color-splitting light transmitting structure using the photoreactive compound. .

According to the present invention, as described above, by selecting a polymer having a low content of alcoholic free radicals, the binding of the polymer is prevented when the photoreactive compound absorbs moisture. Therefore, it is possible to use the photoreactive compound collected after the film is formed on the core material once again for the production of the color-splitting light transmission structure, and the color-splitting light at a low cost. It is possible to manufacture a transmissive structure. Hereinafter, each process of the present invention will be described.

(1) Photoreactive compound preparation step for color-splitting light transmissive structure First, the photoreactive compound preparation step in the method for producing a color-splitting light transmissive structure of the present invention will be described. The photoreactive compound preparation step in the method for producing a color-splitting light transmissive structure of the present invention includes the above-described high reaction in the solid content of the photoreactive compound containing at least a polymer, a monomer, and an initiator. The polymer is selected such that the content of alcoholic free radicals contained in the molecular polymer is within a predetermined range, the selected polymer, the monomer, and the initiator, Are mixed to prepare a photoreactive compound.

This step has a great feature in that the polymer is selected so that the content of alcoholic free radicals contained in the polymer is within a predetermined range. As a specific selection criterion, when a photoreactive compound is used as a regenerative photoreactive compound,
The content of alcoholic free radicals that does not cause a problem due to contained moisture is set to a predetermined value, and a polymer having a content below this is selected. The relationship between whether the malfunction occurs due to the hydroxyl group content and the contained moisture is determined in advance by conducting an experiment according to the system of the photoreactive compound. In the present invention, the predetermined value is determined according to the value of the experiment conducted in advance as described above, and the polymer to be used is selected from the types of polymer suitable for the system based on this value. It is characterized in that it is selected and used.

In the present invention, the alcoholic free radicals contained in the polymer in the solid content of the photoreactive compound are particularly in the range of 0.1 mmol / g to 2.5 mmol / g, in particular, 0.
Within the range of 1 mmol / g to 0.7 mmol / g, especially 0.1 mmol / g to 0.5 mmo
It is preferred to select a high molecular polymer that is in the range of 1 / g. By selecting a high molecular weight polymer containing a hydroxyl group within this range, various types of photoreactive compounds cause problems due to moisture when used as regenerated photoreactive compounds. This is because the possibility can be extremely reduced.

Calculations for selecting a photoreactive formulation in which the alcoholic free radical is within the above range are performed according to theoretical values from the composition.

In addition, as the photoreactive compound prepared in this step, other compositions may be used as long as they contain the polymer selected by the above-described method and further contain a monomer and an initiator. Is not particularly limited, and is determined according to the type of the color-splitting light transmission structure constituting layer in which the photoreactive compound is used. For example, when the photoreactive compound selected in this step is used for a colored layer, it may contain a monomer, a colored granule, an initiator, etc. in addition to the above-mentioned polymer. it can.

The method for preparing the photoreactive compound in the present invention is prepared by a conventionally used method. Specifically, the above-described polymer, monomer and initiator are used. A method of preparing a photoreactive compound by mixing and dissolving it, and adding a colored granular material or the like to the compound if necessary is used.

(2) Color-splitting light transmission structure manufacturing process Next, a color-splitting light transmission structure manufacturing process in the method for manufacturing a color-splitting light transmission structure of the present invention will be described. The color-splitting light transmitting structure manufacturing process in the present invention is a manufacturing process for manufacturing a color-splitting light transmitting structure using the photoreactive compound prepared by the above-described photoreactive compound preparing process.

FIG. 1 is a process diagram showing an example of a method for producing a color-splitting light transmission structure of the present invention. First,
As shown in FIG. 1 (a), the photoreactive compound 2 for black matrix is cured on the core material 1. This black matrix photoreactive compound 2 is a photoreaction in which the alcoholic free radicals in the polymer component contained in the photoreactive compound in the photoreactive compound preparation step are within a predetermined range. This is a photoreactive compound obtained by containing a light-shielding granular material in a mold compound.

The black matrix photoreactive compound 2 is subjected to pattern exposure through a mask 3 formed along a predetermined pattern of the black matrix. The black matrix photoreactive compound 2 subjected to pattern exposure in this way is developed and washed to obtain a black matrix 4 formed in a fixed pattern as shown in FIG.

Next, as shown in FIG.1 (c), the photoreactive type compound 5 for colored layers is film-formed on the core material 1 which has the black matrix 4 formed in the fixed pattern shape. The colored layer photoreactive compound 5 is a photoreactive compound using a polymer having an alcoholic free radical content within a predetermined range selected in the above-described photoreactive compound preparation step. This is a photoreactive compound in which colored particles according to the color of the colored layer to be formed are suspended in the product. This colored layer photoreactive compound 5 is subjected to pattern exposure through a mask 3 ′ formed along a certain pattern of the colored layer.
By developing and washing the photoreactive compound 5 for the colored layer that has been subjected to pattern exposure in this manner, a colored layer 5 ′ formed in a certain pattern is obtained as shown in FIG. 1 (d). .

In the case of a color-divided light transmission structure having a plurality of colors (for example, three colors), the same process is repeated three times, so that a colored layer 5 ′ composed of three colors as shown in FIG. Can be formed.

Next, as shown in FIG. 1 (f), a transparent layer 6 is formed by forming a film of the photoreactive compound for transparent layer on the colored layer 5 ′ formed in a certain pattern. In the present invention, this transparent layer 6 can also be formed using the above-mentioned photoreactive compound.

Furthermore, as shown in FIG. 1 (g), the photoreactive compound 7 for spacing retention protrusions on the transparent layer 6.
A film is formed, and this light-reactive compound 7 for spacing projections is subjected to pattern exposure through a mask 3 '' formed along a certain pattern of spacing projections. By developing and washing the photoreactive compound 7 for spacing holding projections thus pattern-exposed, the photoreactive compound 7 for spacing holding projections is formed into a certain pattern. As shown in FIG. 1 (h), a spacing holding projection 7 ′ can be obtained.

As described above, in the method for producing a color-splitting light transmission structure of the present invention, the above-mentioned photoreactive compound is added to a colored granular material or a light-shielding granular material as necessary for each color-splitting light transmission structure constituting layer. A color-splitting light transmission structure can be manufactured using a photoreactive compound in which an object or the like is floating.
Therefore, when forming these color-splitting light-transmitting structure constituting layers, the photoreactive compound that has been disposed of in the past can be used as a regenerated photoreactive compound, which greatly reduces the waste of materials. Can be reduced. Therefore, it is effective in improving material efficiency, and cost can be reduced. Also, in terms of the environment, since the amount of waste can be reduced, the burden on the environment can be reduced. Furthermore, since the amount of alcoholic free radicals in the photoreactive compound is within a predetermined range as described above, the photoreactive compound can be affected by water molecules even when moisture is absorbed, for example. Because it is low in susceptibility and less buoyant, etc., it has good buoyancy, so it has good light and darkness, and it is easy to remove uncured photoreactive compound when forming a certain pattern Therefore, it is possible to form a constituent layer having a very clear and constant pattern.

About each member in the manufacturing method of such a color division | segmentation light transmissive structure, "C.
Since it is the same as that described in the column of “color-splitting light transmission structure”, description thereof is omitted here.

The present invention is not limited to the above embodiment. The above-described embodiment is an exemplification, and the present invention has any configuration that has substantially the same configuration as the technical idea described in the claims of the present invention and that exhibits the same effects. Are included in the technical scope.

  The following examples further illustrate the invention.

1. Preparation of colored granular suspended liquid According to the composition shown in Table 3, the colored granular substance, the additive, and the medium were weighed and mixed. After mixing, zirconia beads (made by Showa Shell Sekiyu Co., Ltd., trade name: Microhaika Z Z300) are added, and suspended in a paint shaker (Asada Tekko Co., Ltd., trade name: PAINT SHAKER) for 3 hours. , C, D, and E were obtained.

2. Polymer Synthesis [Polymer Polymer Synthesis Example 1]
42.5 parts by weight of benzylmethacrylic acid (BzMA) in the synthesis tank, methacrylic acid (MA)
26 parts by weight, 6 parts by weight of methyl methacrylate (MMA) and 230 parts by weight of diethylene glycol dimethyl ether (DMDG) were added, and the mixture was stirred and dissolved uniformly, and then 2,2-azobis (2-methylbutyronitrile) was added to 4 parts. Part by weight was added and dissolved uniformly. Then, it stirred at 85 degreeC under nitrogen stream for 2 hours, and also was made to react at 100 degreeC for 1 hour. Further, 25.5 parts by weight of glycidyl methacrylate (GMA) and 0.03 of triethylamine were added to the obtained solution.
5 parts by weight and 0.1 part by weight of hydroquinone were added and stirred at 100 ° C. for 5 hours to obtain the desired copolymer resin solution 1 (solid content 40%). The amount of alcoholic free radicals of the obtained resin was 1.8 mmol / g.

[Polymer Polymer Synthesis Example 2]
In the synthesis tank, 29 parts by weight of benzylmethacrylic acid (BzMA) and 3 methacrylic acid (MA)
After charging 2.2 parts by weight, 2.8 parts by weight of methyl methacrylate (MMA), and 230 parts by weight of diethylene glycol dimethyl ether (DMDG), and stirring and dissolving uniformly, 2,
4 parts by weight of 2-azobis (2-methylbutyronitrile) was added and dissolved uniformly. Then, it stirred at 85 degreeC under nitrogen stream for 2 hours, and also was made to react at 100 degreeC for 1 hour. Furthermore, 36.0 parts by weight of glycidyl methacrylate (GMA), 0.5 part by weight of triethylamine and 0.1 part by weight of hydroquinone were added to the obtained solution, and the mixture was stirred at 100 ° C. for 5 hours.
The objective copolymer resin solution 2 (solid content 40%) was obtained. The amount of alcoholic free radicals of the obtained resin was 2.55 mmol / g.

3. Preparation of photoreactive formulation A photoreactive formulation was prepared according to the formulation shown in Table 4 below. A polymer using the copolymer resin solution 1 as a high molecular weight polymer was designated as a photoreactive compound a, and a polymer using the copolymer resin solution 2 was designated as a photoreactive compound b.

4). Preparation of Photoreactive Formulations for Colored Layers Photoreactive type formulations for colored layers of Examples 1 to 3 and Comparative Examples 1 to 3 were prepared according to the formulation shown in Table 5 below.

Table 6 below summarizes the alcoholic free radical content in the photoreactive formulations of Examples 1 to 3 and Comparative Examples 1 to 3 and the hydroxyl content in the case of a colored layer that is a cured product.

  In addition, the amount of hydroxyl groups is calculated from the composition by a theoretical value.

5. Preparation of Reproduction Photoreactive Formulation for Colored Layer Examples 1 to 3 and Comparative Examples 1 to 3 of the above photoreactive type formulation for the colored layer are each 1.
A predetermined amount was dropped on a 1 mm core material (AL material manufactured by Asahi Glass Co., Ltd.) to form a spin film. The liquid splashed by the spin was collected, the solid content was adjusted, and filtration was performed to obtain a regenerated photoreactive compound for the colored layer. The solid content was obtained by accurately weighing an arbitrary amount of the photoreactive compound and calculating the weight after evaporating the medium at 70 ° C. Filtration is performed by Nippon Millipore AN25 (47m with a pore size of 2.5μm).
m disk type) was set in a pressure filter, and the pressure was 0.10 MPa.

6). Preparation of color-splitting light transmission structure Examples 1 to 3 and Comparative Examples 1 to 3 of the colored layer photoreactive compound on the transparent core material on which a black matrix is formed by sputtering, and a colored layer corresponding to each. A predetermined amount of the regenerated photoreactive compound was dropped, and a film was uniformly formed by spin coating to form a film-forming film. A photomask was placed at a distance of 100 μm from this film forming film, and a region corresponding to the colored layer formation region was irradiated with ultraviolet rays for 10 seconds using a 2.0 kW super high pressure mercury lamp by a proxy milliliner.

Next, it was immersed in a 1 wt% aqueous potassium hydroxide solution (30 ° C.) for 1 minute and alkali-developed to remove uncured portions. Thereafter, the core material was allowed to stand for 30 minutes in an atmosphere at 200 ° C. to form a certain pattern of the colored layer.

7). Evaluation (1) Floatability The average particle diameter of the photoreactive compound for colored layers of Examples 1 to 3 and Comparative Examples 1 to 3 was determined by a dynamic light scattering method (Otsuka Electronics Co., Ltd .: FPAR-1000 (trade name)). It was measured by. Before and after each collection, that is, the change in the average particle diameter between the photoreactive compound for the colored layer and the regenerated photoreactive compound for the colored layer was calculated. The results are summarized in Table 7. In the table, ◯ indicates that the amount of change is less than 100 nm, and x indicates that the amount of change is 100 nm or more.

(2) Residue In the above “6. Preparation of color-splitting light transmission structure”, alkali development was performed without irradiating ultraviolet rays. Thereafter, the residue adhered on the core material was visually confirmed and evaluated before and after collection, that is, by the change between the colored layer photoreactive compound and the colored layer regenerated photoreactive compound. The results are summarized in Table 7. In the table, ◯ indicates that the degree of the residue does not change between the two, and X indicates that the residue is increased in the colored layer regenerating photoreactive compound.

(3) Brightness and darkness A deflecting plate (manufactured by Nitto Denko Corporation, trade name: NPF-G1220DU) is arranged in parallel, and during this time, the color-splitting light transmission structure obtained in the above-mentioned “6. Preparation of color-splitting light transmission structure”. The brightness of transmitted light was measured by applying light from one side of the object. Thereafter, the deflection plate was rotated 90 °, and the brightness of the transmitted light was measured in the same manner. After the measurement, the ratio between the parallel luminance and the vertical luminance was calculated to make it light and dark. Measurement was performed in Example 1.
To 3 and Comparative Examples 1 to 3 and the respective color layer reproducing light reaction-type blends were used. Differences in brightness before and after sampling, that is, the brightness of the color-splitting light transmission structure using the photoreactive compound for the colored layer and the color-splitting light transmitting structure using the regenerated photoreactive compound for the colored layer. The difference was calculated. The results are summarized in Table 7. In the table, ◯ indicates that the difference in brightness is 100 or less, and X indicates that the difference in brightness is 100 or more.

Claims (2)

The polymer contains at least an alcoholic free radical, a colored particulate, a monomer and an initiator, and the alcoholic free radical contained in the polymer in a solid content is 0.1 mmol / g to Preparing a photoreactive formulation for a color-splitting light transmissive structure that is in the range of 2.5 mmol / g;
Using the photoreactive compound for color-splitting light transmissive structure, forming a film on a core material, and then collecting the photoreactive compound for color-splitting light transmissive structure that was not used for the film; A method for producing a regenerative photoreactive compound for color-splitting light transmission structures. The polymer contains at least an alcoholic free radical, a colored particulate, a monomer and an initiator, and the alcoholic free radical contained in the polymer in a solid content is 0.1 mmol / g to Preparing a photoreactive formulation for a color-splitting light transmissive structure that is in the range of 2.5 mmol / g;
Using the photoreactive compound for color-splitting light transmissive structure, forming a film on a core material, and then collecting the photoreactive compound for color-splitting light transmissive structure that was not used for the film; ,
And a step of producing a color-splitting light transmissive structure using the collected light-reactive compound for the color-splitting light transmissive structure.

Images